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ICD 10 || Tabular list of inclusions and four-character subcategories || CHAPTER XII Diseases of the skin and subcutaneous tissue (L00–L99) - CHAPTER XIV Diseases of the genitourinary system (N00–N99)


CHAPTER XII
Diseases of the skin and subcutaneous tissue
(L00–L99)

Excl.: certain conditions originating in the perinatal period (P00–P96) certain infectious and parasitic diseases (A00–B99)
complications of pregnancy, childbirth and the puerperium (O00–O99) congenital malformations, deformations and chromosomal abnormalities (Q00–Q99)
endocrine, nutritional and metabolic diseases (E00–E90)
injury, poisoning and certain other consequences of external causes (S00–T98)
lipomelanotic reticulosis (I89.8) neoplasms (C00–D48)
symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00–R99)
systemic connective tissue disorders (M30–M36)

This chapter contains the following blocks:
L00–L08 Infections of the skin and subcutaneous tissue L10–L14 Bullous disorders
L20–L30 Dermatitis and eczema L40–L45 Papulosquamous disorders L50–L54 Urticaria and erythema
L55–L59 Radiation-related disorders of the skin and subcutaneous tissue L60–L75 Disorders of skin appendages
L80–L99 Other disorders of the skin and subcutaneous tissue

Asterisk categories for this chapter are provided as follows:
L14* Bullous disorders in diseases classified elsewhere
L45* Papulosquamous disorders in diseases classified elsewhere L54* Erythema in diseases classified elsewhere
L62* Nail disorders in diseases classified elsewhere L86* Keratoderma in diseases classified elsewhere
L99* Other disorders of skin and subcutaneous tissue in diseases classified elsewhere
 
Infections of the skin and subcutaneous tissue (L00–L08)
Use additional code (B95–B98), if desired, to identify infectious agent.
Excl.: hordeolum (H00.0)
infective dermatitis (L30.3)
local infections of skin classified in Chapter I, such as:
erysipelas (A46)
erysipeloid (A26.-)
herpesviral [herpes simplex] infection (B00.-)
herpesviral [herpes simplex] infection:
anogenital (A60.-)
molluscum contagiosum (B08.1)
mycoses (B35–B49)
pediculosis, acariasis and other infestations (B85–B89)
viral warts (B07) panniculitis (of):
NOS (M79.3)
lupus (L93.2)
neck and back (M54.0)
relapsing [Weber–Christian] (M35.6) perlèche (due to):
NOS (K13.0)
candidiasis (B37.-)
riboflavin deficiency (E53.0) pyogenic granuloma (L98.0) zoster (B02.-)

  L00 Staphylococcal scalded skin syndrome
Incl.: pemphigus neonatorum Ritter disease
Excl.: toxic epidermal necrolysis [Lyell] (L51.2)

  L01 Impetigo
Excl.: impetigo herpetiformis (L40.1) pemphigus neonatorum (L00)
L01.0 Impetigo [any organism][any site]
Bockhart impetigo
L01.1 Impetiginization of other dermatoses
 

  L02 Cutaneous abscess, furuncle and carbuncle
Incl.: boil
furunculosis
Excl.: anal and rectal regions (K61.-) genital organs (external):
female (N76.4)
male (N48.2, N49.-)
L02.0 Cutaneous abscess, furuncle and carbuncle of face
Excl.: ear, external (H60.0) eyelid (H00.0)
head [any part, except face] (L02.8) lacrimal:
gland (H04.0)
passages (H04.3) mouth (K12.2) nose (J34.0)
orbit (H05.0) submandibular (K12.2)
L02.1 Cutaneous abscess, furuncle and carbuncle of neck L02.2 Cutaneous abscess, furuncle and carbuncle of trunk
Abdominal wall
Back [any part, except buttock] Chest wall
Groin Perineum Umbilicus
Excl.: breast (N61)
hip (L02.4)
omphalitis of newborn (P38)
L02.3 Cutaneous abscess, furuncle and carbuncle of buttock
Gluteal region
Excl.: pilonidal cyst with abscess (L05.0)
L02.4 Cutaneous abscess, furuncle and carbuncle of limb
Axilla Hip Shoulder
L02.8 Cutaneous abscess, furuncle and carbuncle of other sites
Head [any part, except face] Scalp
L02.9 Cutaneous abscess, furuncle and carbuncle, unspecified
Furunculosis NOS
 
  L03 Cellulitis
Incl.: acute lymphangitis
Excl.: cellulitis of:
anal and rectal regions (K61.-)
external auditory canal (H60.1)
external genital organs:
– female (N76.4)
– male (N48.2, N49.-)
eyelid (H00.0)
lacrimal apparatus (H04.3)
mouth (K12.2)
nose (J34.0)
eosinophilic cellulitis [Wells] (L98.3)
febrile neutrophilic dermatosis [Sweet] (L98.2) lymphangitis (chronic)(subacute) (I89.1)
L03.0 Cellulitis of finger and toe
Infection of nail Onychia Paronychia Perionychia
L03.1 Cellulitis of other parts of limb
Axilla Hip Shoulder
L03.2 Cellulitis of face L03.3 Cellulitis of trunk
Abdominal wall
Back [any part] Chest wall Groin Perineum Umbilicus
Excl.: omphalitis of newborn (P38)
L03.8 Cellulitis of other sites
Head [any part, except face] Scalp
L03.9 Cellulitis, unspecified
 

  L04 Acute lymphadenitis
Incl.: abscess (acute)
lymphadenitis, acute any lymph node, except mesenteric
Excl.: enlarged lymph nodes (R59.-)
human immunodeficiency virus [HIV] disease resulting in generalized lymphadenopathy (B23.1)
lymphadenitis:
NOS (I88.9)
chronic or subacute, except mesenteric (I88.1)
mesenteric, nonspecific (I88.0)
L04.0 Acute lymphadenitis of face, head and neck L04.1 Acute lymphadenitis of trunk
L04.2 Acute lymphadenitis of upper limb
Axilla Shoulder
L04.3 Acute lymphadenitis of lower limb
Hip
L04.8 Acute lymphadenitis of other sites L04.9 Acute lymphadenitis, unspecified
  L05 Pilonidal cyst
Incl.: fistula
sinus coccygeal or pilonidal
L05.0 Pilonidal cyst with abscess L05.9 Pilonidal cyst without abscess
Pilonidal cyst NOS

  L08 Other local infections of skin and subcutaneous tissue
L08.0 Pyoderma
Dermatitis:
gangrenosa
purulent
septic
suppurative
Excl.: pyoderma gangrenosum (L88)
L08.1 Erythrasma
L08.8 Other specified local infections of skin and subcutaneous tissue L08.9 Local infection of skin and subcutaneous tissue, unspecified
 
Bullous disorders (L10–L14)
Excl.: benign familial pemphigus [Hailey–Hailey] (Q82.8) staphylococcal scalded skin syndrome (L00)
toxic epidermal necrolysis [Lyell] (L51.2)

  L10 Pemphigus
Excl.: pemphigus neonatorum (L00)
L10.0 Pemphigus vulgaris L10.1 Pemphigus vegetans L10.2 Pemphigus foliaceus
L10.3 Brazilian pemphigus [fogo selvagem]
L10.4 Pemphigus erythematosus
Senear–Usher syndrome
L10.5 Drug-induced pemphigus
Use additional external cause code (Chapter XX), if desired, to identify drug.
L10.8 Other pemphigus
L10.9 Pemphigus, unspecified

  L11 Other acantholytic disorders
L11.0 Acquired keratosis follicularis
Excl.: keratosis follicularis (congenital) [Darier–White] (Q82.8)
L11.1 Transient acantholytic dermatosis [Grover] L11.8 Other specified acantholytic disorders L11.9 Acantholytic disorder, unspecified
  L12 Pemphigoid
Excl.: herpes gestationis (O26.4) impetigo herpetiformis (L40.1)
L12.0 Bullous pemphigoid L12.1 Cicatricial pemphigoid
Benign mucous membrane pemphigoid
L12.2 Chronic bullous disease of childhood
Juvenile dermatitis herpetiformis
L12.3 Acquired epidermolysis bullosa
Excl.: epidermolysis bullosa (congenital) (Q81.-)
L12.8 Other pemphigoid
L12.9 Pemphigoid, unspecified
 

  L13 Other bullous disorders
L13.0 Dermatitis herpetiformis
Duhring’s disease
L13.1 Subcorneal pustular dermatitis
Sneddon–Wilkinson disease
L13.8 Other specified bullous disorders L13.9 Bullous disorder, unspecified
  L14* Bullous disorders in diseases classified elsewhere

Dermatitis and eczema (L20–L30)
Note: In this block, the terms dermatitis and eczema are used synonymously and interchangeably.
Excl.: chronic (childhood) granulomatous disease (D71) dermatitis:
dry skin (L85.3)
factitial (L98.1)
gangrenosa (L08.0)
herpetiformis (L13.0)
perioral (L71.0)
stasis (I83.1–I83.2)
radiation-related disorders of the skin and subcutaneous tissue (L55–L59)

  L20 Atopic dermatitis
Excl.: circumscribed neurodermatitis (L28.0)
L20.0 Besnier prurigo
L20.8 Other atopic dermatitis
Eczema:
flexural NEC
infantile (acute)(chronic)
intrinsic (allergic) Neurodermatitis:
atopic
diffuse
L20.9 Atopic dermatitis, unspecified

  L21 Seborrhoeic dermatitis
Excl.: infective dermatitis (L30.3)
L21.0 Seborrhoea capitis
Cradle cap
 
L21.1 Seborrhoeic infantile dermatitis L21.8 Other seborrhoeic dermatitis
L21.9 Seborrhoeic dermatitis, unspecified

  L22 Diaper [napkin] dermatitis
Incl.: diaper or napkin:
erythema
rash
psoriasiform napkin rash

  L23 Allergic contact dermatitis
Incl.: allergic contact eczema
Excl.: allergy NOS (T78.4) dermatitis (of):
NOS (L30.9)
contact NOS (L25.9)
diaper [napkin] (L22)
due to substances taken internally (L27.-)
eyelid (H01.1)
irritant contact (L24.-)
perioral (L71.0)
eczema of external ear (H60.5)
radiation-related disorders of the skin and subcutaneous tissue (L55–L59)
L23.0 Allergic contact dermatitis due to metals
Chromium Nickel
L23.1 Allergic contact dermatitis due to adhesives L23.2 Allergic contact dermatitis due to cosmetics
L23.3 Allergic contact dermatitis due to drugs in contact with skin
Use additional external cause code (Chapter XX), if desired, to identify drug.
Excl.: allergic reaction NOS due to drugs (T88.7)
dermatitis due to ingested drugs and medicaments (L27.0–L27.1)
L23.4 Allergic contact dermatitis due to dyes
L23.5 Allergic contact dermatitis due to other chemical products
Cement Insecticide Plastic Rubber
L23.6 Allergic contact dermatitis due to food in contact with skin
Excl.: dermatitis due to ingested food (L27.2)
 

L23.7 Allergic contact dermatitis due to plants, except food L23.8 Allergic contact dermatitis due to other agents
L23.9 Allergic contact dermatitis, unspecified cause
Allergic contact eczema NOS

  L24 Irritant contact dermatitis
Incl.: irritant contact eczema
Excl.: allergy NOS (T78.4) dermatitis (of):
NOS (L30.9)
allergic contact (L23.-)
contact NOS (L25.9)
diaper [napkin] (L22)
due to substances taken internally (L27.-)
eyelid (H01.1)
perioral (L71.0)
eczema of external ear (H60.5)
radiation-related disorders of the skin and subcutaneous tissue (L55–L59)
L24.0 Irritant contact dermatitis due to detergents L24.1 Irritant contact dermatitis due to oils and greases L24.2 Irritant contact dermatitis due to solvents
Solvents:
chlorocompound
cyclohexane
ester
glycol
hydrocarbon
ketone
L24.3 Irritant contact dermatitis due to cosmetics
L24.4 Irritant contact dermatitis due to drugs in contact with skin
Use additional external cause code (Chapter XX), if desired, to identify drug.
Excl.: allergic reaction NOS due to drugs (T88.7)
dermatitis due to ingested drugs and medicaments (L27.0–L27.1)
L24.5 Irritant contact dermatitis due to other chemical products
Cement Insecticide
L24.6 Irritant contact dermatitis due to food in contact with skin
Excl.: dermatitis due to ingested food (L27.2)
L24.7 Irritant contact dermatitis due to plants, except food
 
L24.8 Irritant contact dermatitis due to other agents
Dyes
L24.9 Irritant contact dermatitis, unspecified cause
Irritant contact eczema NOS

  L25 Unspecified contact dermatitis
Incl.: unspecified contact eczema
Excl.: allergy NOS (T78.4) dermatitis (of):
NOS (L30.9)
allergic contact (L23.-)
due to substances taken internally (L27.-)
eyelid (H01.1)
irritant contact (L24.-)
perioral (L71.0)
eczema of external ear (H60.5)
radiation-related disorders of the skin and subcutaneous tissue (L55–L59)
L25.0 Unspecified contact dermatitis due to cosmetics
L25.1 Unspecified contact dermatitis due to drugs in contact with skin
Use additional external cause code (Chapter XX), if desired, to identify drug.
Excl.: allergic reaction NOS due to drugs (T88.7)
dermatitis due to ingested drugs and medicaments (L27.0–L27.1)
L25.2 Unspecified contact dermatitis due to dyes
L25.3 Unspecified contact dermatitis due to other chemical products
Cement Insecticide
L25.4 Unspecified contact dermatitis due to food in contact with skin
Excl.: dermatitis due to ingested food (L27.2)
L25.5 Unspecified contact dermatitis due to plants, except food L25.8 Unspecified contact dermatitis due to other agents
L25.9 Unspecified contact dermatitis, unspecified cause
Contact:
dermatitis (occupational) NOS
eczema (occupational) NOS

  L26 Exfoliative dermatitis
Incl.: Hebra pityriasis
Excl.: Ritter disease (L00)
 

  L27 Dermatitis due to substances taken internally
Excl.: adverse:
effect NOS of drugs (T88.7)
food reaction, except dermatitis (T78.0–T78.1) allergy NOS (T78.4)
contact dermatitis (L23–L25) drug:
photoallergic response (L56.1)
phototoxic response (L56.0) urticaria (L50.-)
L27.0 Generalized skin eruption due to drugs and medicaments
Use additional external cause code (Chapter XX), if desired, to identify drug.
L27.1 Localized skin eruption due to drugs and medicaments
Use additional external cause code (Chapter XX), if desired, to identify drug.
L27.2 Dermatitis due to ingested food
Excl.: dermatitis due to food in contact with skin (L23.6, L24.6, L25.4)
L27.8 Dermatitis due to other substances taken internally L27.9 Dermatitis due to unspecified substance taken internally
  L28 Lichen simplex chronicus and prurigo
L28.0 Lichen simplex chronicus Circumscribed neurodermatitis Lichen NOS
L28.1 Prurigo nodularis L28.2 Other prurigo
Prurigo:
NOS
Hebra
mitis
Urticaria papulosa

  L29 Pruritus
Excl.: neurotic excoriation (L98.1) psychogenic pruritus (F45.8)
L29.0 Pruritus ani
L29.1 Pruritus scroti
L29.2 Pruritus vulvae
L29.3 Anogenital pruritus, unspecified L29.8 Other pruritus
L29.9 Pruritus, unspecified
Itch NOS
 
  L30 Other dermatitis
Excl.: dermatitis:
contact (L23–L25)
dry skin (L85.3)
small plaque parapsoriasis (L41.3) stasis dermatitis (I83.1–I83.2)
L30.0 Nummular dermatitis L30.1 Dyshidrosis [pompholyx]
L30.2 Cutaneous autosensitization Candidid [levurid] Dermatophytid
Eczematid
L30.3 Infective dermatitis
Infectious eczematoid dermatitis
L30.4 Erythema intertrigo L30.5 Pityriasis alba
L30.8 Other specified dermatitis
L30.9 Dermatitis, unspecified
Eczema NOS

Papulosquamous disorders (L40–L45)

  L40 Psoriasis
L40.0 Psoriasis vulgaris
Nummular psoriasis Plaque psoriasis
L40.1 Generalized pustular psoriasis
Impetigo herpetiformis Von Zumbusch’s disease
L40.2 Acrodermatitis continua
L40.3 Pustulosis palmaris et plantaris L40.4 Guttate psoriasis
L40.5† Arthropathic psoriasis (M07.0–M07.3*, M09.0*)
L40.8 Other psoriasis
Flexural psoriasis
L40.9 Psoriasis, unspecified
 

  L41 Parapsoriasis
Excl.:  poikiloderma vasculare atrophicans (L94.5)
L41.0 Pityriasis lichenoides et varioliformis acuta
Mucha–Habermann disease
L41.1 Pityriasis lichenoides chronica L41.3 Small plaque parapsoriasis L41.4 Large plaque parapsoriasis L41.5 Retiform parapsoriasis
L41.8 Other parapsoriasis
L41.9 Parapsoriasis, unspecified

  L42 Pityriasis rosea
  L43 Lichen planus
Excl.: lichen planopilaris (L66.1) L43.0 Hypertrophic lichen planus L43.1 Bullous lichen planus
L43.2 Lichenoid drug reaction
Use additional external cause code (Chapter XX), if desired, to identify drug.
L43.3 Subacute (active) lichen planus
Lichen planus tropicus
L43.8 Other lichen planus
L43.9 Lichen planus, unspecified

  L44 Other papulosquamous disorders
L44.0 Pityriasis rubra pilaris L44.1 Lichen nitidus
L44.2 Lichen striatus
L44.3 Lichen ruber moniliformis
L44.4 Infantile papular acrodermatitis [Giannotti–Crosti] L44.8 Other specified papulosquamous disorders
L44.9 Papulosquamous disorder, unspecified

  L45* Papulosquamous disorders in diseases classified elsewhere
 
Urticaria and erythema (L50–L54)
Excl.: Lyme disease (A69.2)
rosacea (L71.-)

  L50 Urticaria
Excl.: allergic contact dermatitis (L23.-) angioneurotic oedema (T78.3) hereditary angio-oedema (D84.1) Quincke oedema (T78.3) urticaria:
giant (T78.3)
neonatorum (P83.8)
papulosa (L28.2)
pigmentosa (Q82.2)
serum (T80.6)
solar (L56.3) L50.0 Allergic urticaria L50.1 Idiopathic urticaria
L50.2 Urticaria due to cold and heat L50.3 Dermatographic urticaria L50.4 Vibratory urticaria
L50.5 Cholinergic urticaria
L50.6 Contact urticaria L50.8 Other urticaria
Urticaria:
chronic
recurrent periodic
L50.9 Urticaria, unspecified

  L51 Erythema multiforme
L51.0 Nonbullous erythema multiforme L51.1 Bullous erythema multiforme
Stevens–Johnson syndrome
L51.2 Toxic epidermal necrolysis [Lyell] L51.8 Other erythema multiforme
L51.9 Erythema multiforme, unspecified

  L52 Erythema nodosum
 

  L53 Other erythematous conditions
Excl.: erythema:
ab igne (L59.0)
due to external agents in contact with skin (L23–L25)
intertrigo (L30.4)
L53.0 Toxic erythema
Use additional external cause code (Chapter XX), if desired, to identify external agent.
Excl.: neonatal erythema toxicum (P83.1) L53.1 Erythema annulare centrifugum L53.2 Erythema marginatum
L53.3 Other chronic figurate erythema
L53.8 Other specified erythematous conditions L53.9 Erythematous condition, unspecified
Erythema NOS Erythroderma NOS

  L54* Erythema in diseases classified elsewhere L54.0* Erythema marginatum in acute rheumatic fever (I00†) L54.8* Erythema in other diseases classified elsewhere

Radiation-related disorders of the skin and subcutaneous tissue
(L55–L59)

  L55 Sunburn
L55.0 Sunburn of first degree L55.1 Sunburn of second degree L55.2 Sunburn of third degree L55.8 Other sunburn
L55.9 Sunburn, unspecified

  L56 Other acute skin changes due to ultraviolet radiation
L56.0 Drug phototoxic response
Use additional external cause code (Chapter XX), if desired, to identify drug.
L56.1 Drug photoallergic response
Use additional external cause code (Chapter XX), if desired, to identify drug.
 
L56.2 Photocontact dermatitis [berloque dermatitis] L56.3 Solar urticaria
L56.4 Polymorphous light eruption
L56.8 Other specified acute skin changes due to ultraviolet radiation L56.9 Acute skin change due to ultraviolet radiation, unspecified
  L57 Skin changes due to chronic exposure to nonionizing radiation
L57.0 Actinic keratosis
Keratosis:
NOS
senile
solar
L57.1 Actinic reticuloid
L57.2 Cutis rhomboidalis nuchae L57.3 Poikiloderma of Civatte L57.4 Cutis laxa senilis
Elastosis senilis
L57.5 Actinic granuloma
L57.8 Other skin changes due to chronic exposure to nonionizing radiation
Farmer’s skin Sailor’s skin Solar dermatitis
L57.9 Skin changes due to chronic exposure to nonionizing radiation, unspecified

  L58 Radiodermatitis
L58.0 Acute radiodermatitis L58.1 Chronic radiodermatitis
L58.9 Radiodermatitis, unspecified

  L59 Other disorders of skin and subcutaneous tissue related to radiation
L59.0 Erythema ab igne [dermatitis ab igne]
L59.8 Other specified disorders of skin and subcutaneous tissue related to radiation
L59.9 Disorder of skin and subcutaneous tissue related to radiation, unspecified
 

Disorders of skin appendages (L60–L75)
Excl.: congenital malformations of integument (Q84.-)

  L60 Nail disorders
Excl.: clubbing of nails (R68.3) onychia and paronychia (L03.0)
L60.0 Ingrowing nail
L60.1 Onycholysis L60.2 Onychogryphosis L60.3 Nail dystrophy
L60.4 Beau’s lines
L60.5 Yellow nail syndrome L60.8 Other nail disorders L60.9 Nail disorder, unspecified
  L62* Nail disorders in diseases classified elsewhere L62.0* Clubbed nail pachydermoperiostosis  (M89.4†) L62.8* Nail disorders in other diseases classified elsewhere
  L63 Alopecia areata
L63.0 Alopecia (capitis) totalis L63.1 Alopecia universalis L63.2 Ophiasis
L63.8 Other alopecia areata
L63.9 Alopecia areata, unspecified

  L64 Androgenic alopecia
Incl.: male-pattern baldness
L64.0 Drug-induced androgenic alopecia
Use additional external cause code (Chapter XX), if desired, to identify drug.
L64.8 Other androgenic alopecia
L64.9 Androgenic alopecia, unspecified
 
  L65 Other nonscarring hair loss
Use additional external cause code (Chapter XX), if desired, to identify drug, if drug-induced.
Excl.: trichotillomania (F63.3)
L65.0 Telogen effluvium L65.1 Anagen effluvium L65.2 Alopecia mucinosa
L65.8 Other specified nonscarring hair loss
L65.9 Nonscarring hair loss, unspecified
Alopecia NOS

  L66 Cicatricial alopecia [scarring hair loss]
L66.0 Pseudopelade L66.1 Lichen planopilaris
Follicular lichen planus
L66.2 Folliculitis decalvans
L66.3 Perifolliculitis capitis abscedens L66.4 Folliculitis ulerythematosa reticulata L66.8 Other cicatricial alopecia
L66.9 Cicatricial alopecia, unspecified

  L67 Hair colour and hair shaft abnormalities
Excl.: monilethrix (Q84.1) pili annulati (Q84.1)
telogen effluvium (L65.0)
L67.0 Trichorrhexis nodosa L67.1 Variations in hair colour
Canities
Greyness, hair (premature) Heterochromia of hair Poliosis:
NOS
circumscripta, acquired
L67.8 Other hair colour and hair shaft abnormalities
Fragilitas crinium
L67.9 Hair colour and hair shaft abnormality, unspecified
 

  L68 Hypertrichosis
Incl.: excess hair
Excl.: congenital hypertrichosis (Q84.2) persistent lanugo (Q84.2)
L68.0 Hirsutism
Use additional external cause code (Chapter XX), if desired, to identify drug, if drug-induced.
L68.1 Acquired hypertrichosis lanuginosa
Use additional external cause code (Chapter XX), if desired, to identify drug, if drug-induced.
L68.2 Localized hypertrichosis L68.3 Polytrichia
L68.8 Other hypertrichosis
L68.9 Hypertrichosis, unspecified

  L70 Acne
Excl.: acne keloid (L73.0)
L70.0 Acne vulgaris L70.1 Acne conglobata L70.2 Acne varioliformis
Acne necrotica miliaris
L70.3 Acne tropica
L70.4 Infantile acne
L70.5 Acné excoriée
Acné excoriée des jeunes filles
L70.8 Other acne
L70.9 Acne, unspecified

  L71 Rosacea
L71.0 Perioral dermatitis
Use additional external cause code (Chapter XX), if desired, to identify drug, if drug-induced.
L71.1 Rhinophyma
L71.8 Other rosacea
L71.9 Rosacea, unspecified
 
  L72 Follicular cysts of skin and subcutaneous tissue
L72.0 Epidermal cyst L72.1 Trichilemmal cyst
Pilar cyst Sebaceous cyst
L72.2 Steatocystoma multiplex
L72.8 Other follicular cysts of skin and subcutaneous tissue
L72.9 Follicular cyst of skin and subcutaneous tissue, unspecified

  L73 Other follicular disorders
L73.0 Acne keloid
L73.1 Pseudofolliculitis barbae L73.2 Hidradenitis suppurativa
L73.8 Other specified follicular disorders
Sycosis barbae
L73.9 Follicular disorder, unspecified

  L74 Eccrine sweat disorders
Excl.: hyperhidrosis (R61.-)
L74.0 Miliaria rubra L74.1 Miliaria crystallina L74.2 Miliaria profunda
Miliaria tropicalis
L74.3 Miliaria, unspecified L74.4 Anhidrosis
Hypohidrosis
L74.8 Other eccrine sweat disorders L74.9 Eccrine sweat disorder, unspecified
Sweat gland disorder NOS

  L75 Apocrine sweat disorders
Excl.: dyshidrosis [pompholyx] (L30.1) hidradenitis suppurativa (L73.2)
L75.0 Bromhidrosis
L75.1 Chromhidrosis L75.2 Apocrine miliaria
Fox–Fordyce disease
L75.8 Other apocrine sweat disorders L75.9 Apocrine sweat disorder, unspecified
 

Other disorders of the skin and subcutaneous tissue (L80–L99)

  L80 Vitiligo
  L81 Other disorders of pigmentation
Excl.: birthmark NOS (Q82.5)
naevus – see Alphabetical index Peutz–Jeghers syndrome (Q85.8)
L81.0 Postinflammatory hyperpigmentation L81.1 Chloasma
L81.2 Freckles
L81.3 Café-au-lait spots
L81.4 Other melanin hyperpigmentation
Lentigo
L81.5 Leukoderma, not elsewhere classified
L81.6 Other disorders of diminished melanin formation L81.7 Pigmented purpuric dermatosis
Angioma serpiginosum
L81.8 Other specified disorders of pigmentation
Iron pigmentation Tattoo pigmentation
L81.9 Disorder of pigmentation, unspecified

  L82 Seborrhoeic keratosis
Incl.: basal cell papilloma
dermatosis papulosa nigra Leser–Trélat disease

  L83 Acanthosis nigricans
Incl.: confluent and reticulated papillomatosis

  L84 Corns and callosities
Incl.: callus
clavus

  L85 Other epidermal thickening
Excl.: hypertrophic disorders of skin (L91.-)
L85.0 Acquired ichthyosis
Excl.: congenital ichthyosis (Q80.-)
 
L85.1 Acquired keratosis [keratoderma] palmaris et plantaris
Excl.: inherited keratosis palmaris et plantaris (Q82.8)
L85.2 Keratosis punctata (palmaris et plantaris) L85.3 Xerosis cutis
Dry skin dermatitis
L85.8 Other specified epidermal thickening
Cutaneous horn
L85.9 Epidermal thickening, unspecified

  L86* Keratoderma in diseases classified elsewhere
Incl.: follicular keratosis xeroderma due to a vitamin A deficiency (E50.8†)
  L87 Transepidermal elimination disorders
Excl.:  granuloma annulare (perforating) (L92.0)
L87.0 Keratosis follicularis et parafollicularis in cutem penetrans [Kyrle]
Hyperkeratosis follicularis penetrans L87.1 Reactive perforating collagenosis L87.2 Elastosis perforans serpiginosa
L87.8 Other transepidermal elimination disorders L87.9 Transepidermal elimination disorder, unspecified
  L88 Pyoderma gangrenosum
Incl.: Phagedenic pyoderma
Excl.: dermatitis gangrenosa (L08.0)

  L89 Decubitus ulcer and pressure area
Note: For multiple sites of differing stages, assign only one code indicating the highest stage.
Incl.: bedsore
plaster ulcer
Excl.: decubitus (trophic) ulcer of cervix (uteri) (N86)
L89.0 Stage I decubitus ulcer and pressure area
The ulcer appears as a defined area of persistent redness (erythema) in lightly pigmented skin, whereas in darker skin tones, the ulcer may appear with persistent red, blue or purple hues, without skin loss.
Decubitus [pressure] ulcer limited to erythema only
 

L89.1 Stage II decubitus ulcer
Decubitus [pressure] ulcer with:
abrasion
blister
partial thickness skin loss involving epidermis and/or dermis
skin loss NOS
L89.2 Stage III decubitus ulcer
Decubitus [pressure] ulcer with full thickness skin loss involving damage or necrosis of subcutaneous tissue extending to underlying fascia
L89.3 Stage IV decubitus ulcer
Decubitus [pressure] ulcer with necrosis of muscle, bone or supporting structures (ie tendon or joint capsule)
L89.9 Decubitus ulcer and pressure area, unspecified
Decubitus [pressure] ulcer without mention of stage

  L90 Atrophic disorders of skin
L90.0 Lichen sclerosus et atrophicus
Excl.:  lichen sclerosus of external genital organs:
female (N90.4)
male (N48.0)
L90.1 Anetoderma of Schweninger–Buzzi L90.2 Anetoderma of Jadassohn–Pellizzari L90.3 Atrophoderma of Pasini and Pierini L90.4 Acrodermatitis chronica atrophicans L90.5 Scar conditions and fibrosis of skin
Adherent scar (skin)
Cicatrix
Disfigurement due to scar Scar NOS
Excl.: hypertrophic scar (L91.0) keloid scar (L91.0)
L90.6 Striae atrophicae
L90.8 Other atrophic disorders of skin L90.9 Atrophic disorder of skin, unspecified
 
  L91 Hypertrophic disorders of skin
L91.0 Hypertrophic scar
Keloid scar Keloid
Excl.: acne keloid (L73.0) scar NOS (L90.5)
L91.8 Other hypertrophic disorders of skin L91.9 Hypertrophic disorder of skin, unspecified
  L92 Granulomatous disorders of skin and subcutaneous tissue
Excl.: actinic granuloma (L57.5)
L92.0 Granuloma annulare
Perforating granuloma annulare
L92.1 Necrobiosis lipoidica, not elsewhere classified
Excl.: associated with diabetes mellitus (E10–E14)
L92.2 Granuloma faciale [eosinophilic granuloma of skin]
L92.3 Foreign body granuloma of skin and subcutaneous tissue L92.8 Other granulomatous disorders of skin and subcutaneous tissue L92.9 Granulomatous disorder of skin and subcutaneous tissue,
unspecified

  L93 Lupus erythematosus
Use additional external cause code (Chapter XX), if desired, to identify drug, if drug-induced.
Excl.: lupus:
exedens (A18.4)
vulgaris (A18.4) scleroderma (M34.-)
systemic lupus erythematosus (M32.-)
L93.0 Discoid lupus erythematosus
Lupus erythematosus NOS
L93.1 Subacute cutaneous lupus erythematosus L93.2 Other local lupus erythematosus
Lupus:
erythematosus profundus
panniculitis
 

  L94 Other localized connective tissue disorders
Excl.:  systemic connective tissue disorders (M30–M36)
L94.0 Localized scleroderma [morphea]
Circumscribed scleroderma
L94.1 Linear scleroderma
En coup de sabre lesion L94.2 Calcinosis cutis L94.3 Sclerodactyly
L94.4 Gottron papules
L94.5 Poikiloderma vasculare atrophicans L94.6 Ainhum
L94.8 Other specified localized connective tissue disorders L94.9 Localized connective tissue disorder, unspecified
  L95 Vasculitis limited to skin, not elsewhere classified
Excl.: angioma serpiginosum (L81.7) Henoch(–Schönlein) purpura (D69.0) hypersensitivity angiitis (M31.0) panniculitis (of):
NOS (M79.3)
lupus (L93.2)
neck and back (M54.0)
relapsing [Weber–Christian] (M35.6) polyarteritis nodosa (M30.0) rheumatoid vasculitis (M05.2)
serum sickness (T80.6) urticaria (L50.-)
Wegener granulomatosis (M31.3)
L95.0 Livedoid vasculitis
Atrophie blanche (en plaque)
L95.1 Erythema elevatum diutinum L95.8 Other vasculitis limited to skin
L95.9 Vasculitis limited to skin, unspecified

  L97 Ulcer of lower limb, not elsewhere classified
Excl.: decubitus [pressure] ulcer and pressure area (L89.-) gangrene (R02)
skin infections (L00–L08)
specific infections classified to A00–B99 varicose ulcer (I83.0, I83.2)
 
  L98 Other disorders of skin and subcutaneous tissue, not elsewhere classified
L98.0 Pyogenic granuloma L98.1 Factitial dermatitis
Neurotic excoriation
L98.2 Febrile neutrophilic dermatosis [Sweet] L98.3 Eosinophilic cellulitis [Wells]
L98.4 Chronic ulcer of skin, not elsewhere classified
Chronic ulcer of skin NOS Tropical ulcer NOS
Ulcer of skin NOS
Excl.: decubitus [pressure] ulcer and pressure area (L89.-) gangrene (R02)
skin infections (L00–L08)
specific infections classified to A00–B99 ulcer of lower limb NEC (L97)
varicose ulcer (I83.0, I83.2)
L98.5 Mucinosis of skin
Focal mucinosis
Lichen myxoedematosus Reticular erythematous mucinosis
Excl.: focal oral mucinosis (K13.7) myxoedema (E03.9)
L98.6 Other infiltrative disorders of skin and subcutaneous tissue
Excl.: hyalinosis cutis et mucosae (E78.8)
L98.7 Excessive and redundant skin and subcutaneous tissue
Loose or sagging skin:
NOS
following weight loss (bariatric surgery)(dietary)
Excl.: excess or redundant skin of eyelid:
acquired (H02.3)
congenital (Q10.3)
skin changes due to chronic exposure to nonionizing radiation (L57.-)
L98.8 Other specified disorders of skin and subcutaneous tissue L98.9 Disorder of skin and subcutaneous tissue, unspecified
 

  L99* Other disorders of skin and subcutaneous tissue in diseases classified elsewhere
L99.0* Amyloidosis of skin (E85.-†)
Lichen amyloidosis Macular amyloid
L99.8* Other specified disorders of skin and subcutaneous tissue in diseases classified elsewhere
Syphilitic:
alopecia (A51.3†)
leukoderma (A51.3†, A52.7†)

Text Box: CHAPTER XIIICHAPTER XIII                                              

Diseases of the musculoskeletal system and connective tissue

(M00–M99)

 

Excl.:           certain conditions originating in the perinatal period (P00–P96) certain disorders of the temporomandibular joint (K07.6) certain infectious and parasitic diseases (A00–B99) compartment syndrome (T79.6)

complications of pregnancy, childbirth and the puerperium (O00–O99) congenital malformations, deformations and chromosomal abnormalities (Q00–Q99)

endocrine, nutritional and metabolic diseases (E00–E90)

injury, poisoning and certain other consequences of external causes (S00–T98)

neoplasms (C00–D48)

symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00–R99)

 

This chapter contains the following blocks:

M00–M25 Arthropathies

M00–M03 Infectious arthropathies M05–M14 Inflammatory polyarthropathies M15–M19 Arthrosis

M20–M25 Other joint disorders M30–M36 Systemic connective tissue disorders M40–M54 Dorsopathies

M40–M43 Deforming dorsopathies M45–M49 Spondylopathies M50–M54 Other dorsopathies

M60–M79 Soft tissue disorders

M60–M63 Disorders of muscles

M65–M68 Disorders of synovium and tendon M70–M79 Other soft tissue disorders

M80–M94 Osteopathies and chondropathies

M80–M85 Disorders of bone density and structure M86–M90 Other osteopathies

M91–M94 Chondropathies

M95–M99 Other disorders of the musculoskeletal system and connective tissue

 

Asterisk categories for this chapter are provided as follows:

M01*          Direct infections of joint in infectious and parasitic diseases classified elsewhere

M03*          Postinfective and reactive arthropathies in diseases classified elsewhere


M07*          Psoriatic and enteropathic arthropathies

M09*          Juvenile arthritis in diseases classified elsewhere M14*              Arthropathies in other diseases classified elsewhere

M36*          Systemic disorders of connective tissue in diseases classified elsewhere M49*      Spondylopathies in diseases classified elsewhere

M63*          Disorders of muscle in diseases classified elsewhere

M68*          Disorders of synovium and tendon in diseases classified elsewhere M73*               Soft tissue disorders in diseases classified elsewhere

M82*          Osteoporosis in diseases classified elsewhere M90*     Osteopathies in diseases classified elsewhere

Site of musculoskeletal involvement

The following  subclassification  to  indicate  the  site  of  involvement  is  provided  for optional use with appropriate categories in Chapter XIII. As local extensions or specialty adaptations may vary in the number of characters used, it is suggested that the supplementary site subclassification be placed in an identifiably separate position (e.g. in an additional box). Different subclassifications for use with derangement of knee, dorsopathies, and biomechanical lesions not elsewhere classified are given at M23, before M40 and at M99 respectively.

0         Multiple sites

1         Shoulder region

acromioclavicular glenohumeral sternoclavicular

 

joints

 

 

clavicle scapula

 

 

 

2         Upper arm humerus elbow joint

3         Forearm radius ulna

wrist joint

4         Hand carpus fingers metacarpus

joints between these bones

5         Pelvic region and thigh

buttock femur pelvis

hip (joint) sacroiliac joint


6         Lower leg fibula knee joint tibia

7         Ankle and foot metatarsus tarsus

toes

ankle joint

other joints in foot

8         Other head neck ribs skull trunk

vertebral column

9         Site unspecified


Arthropathies (M00–M25)

Incl.:            disorders affecting predominantly peripheral (limb) joints

 

Infectious arthropathies (M00–M03)

 

Note:            This block comprises arthropathies due to microbiological agents.

Distinction is made between the following types of etiological relationship:

a)     direct infection of joint, where organisms invade synovial tissue and microbial antigen is present in the joint;

b)    indirect infection, which may be of two types: a reactive arthropathy, where microbial infection of the body is established but neither organisms nor antigens can be identified in the joint, and a postinfective arthropathy, where microbial antigen is present but recovery of an organism is inconstant and evidence of local multiplication is lacking.

 

  M00        Pyogenic arthritis

[See site code at the beginning of this chapter]

Excl.: infection and inflammatory reaction due to internal joint prosthesis (T84.5)

 

M00.0        Staphylococcal arthritis and polyarthritis M00.1         Pneumococcal arthritis and polyarthritis M00.2    Other streptococcal arthritis and polyarthritis

M00.8        Arthritis and polyarthritis due to other specified bacterial agents

Use additional code (B95–B96), if desired, to identify bacterial agent.

M00.9        Pyogenic arthritis, unspecified

Infective arthritis NOS

 

  M01*      Direct infections of joint in infectious and parasitic diseases classified elsewhere

[See site code at the beginning of this chapter]

Excl.: arthropathy in sarcoidosis (M14.8*) postinfective and reactive arthropathy (M03.-*)

M01.0*       Meningococcal arthritis (A39.8†)

Excl.: postmeningococcal arthritis (M03.0*)


M01.1*       Tuberculous arthritis (A18.0†)

Excl.: of spine (M49.0*)

M01.2*       Arthritis in Lyme disease (A69.2†)

M01.3*       Arthritis in other bacterial diseases classified elsewhere

Arthritis in:

  leprosy [Hansen disease] (A30.-†)

  localized Salmonella infection (A02.2†)

  typhoid or paratyphoid fever (A01.-†)

  gonococcal arthritis (A54.4†)

M01.4*       Rubella arthritis (B06.8†)

M01.5*       Arthritis in other viral diseases classified elsewhere

Arthritis in:

  mumps (B26.8†)

  O’nyong-nyong fever (A92.1†)

M01.6*       Arthritis in mycoses (B35–B49†)

M01.8*       Arthritis in other infectious and parasitic diseases classified elsewhere

 

  M02        Reactive arthropathies

[See site code at the beginning of this chapter]

Excl.: Behçet disease (M35.2) rheumatic fever (I00)

M02.0        Arthropathy following intestinal bypass M02.1 Postdysenteric arthropathy

M02.2        Postimmunization arthropathy M02.3    Reiter disease

M02.8        Other reactive arthropathies M02.9       Reactive arthropathy, unspecified

  M03*      Postinfective and reactive arthropathies in diseases classified elsewhere

[See site code at the beginning of this chapter]

Excl.: direct infections of joint in infectious and parasitic diseases classified elsewhere (M01.-*)

M03.0*       Postmeningococcal arthritis (A39.8†)

Excl.: meningococcal arthritis (M01.0*)


M03.1*       Postinfective arthropathy in syphilis

Clutton joints (A50.5†)

Excl.: Charcot or tabetic arthropathy (M14.6*)

M03.2*       Other postinfectious arthropathies in diseases classified elsewhere

Postinfectious arthropathy in:

   enteritis due to Yersinia enterocolitica (A04.6†)

   viral hepatitis (B15–B19†)

Excl.: viral arthropathies (M01.4–M01.5*)

M03.6*       Reactive arthropathy in other diseases classified elsewhere

Arthropathy in infective endocarditis (I33.0†)

 

Inflammatory polyarthropathies (M05–M14)

 

  M05        Seropositive rheumatoid arthritis

[See site code at the beginning of this chapter]

Excl.: rheumatic fever (I00) rheumatoid arthritis (of):

  juvenile (M08.-)

  spine (M45)

M05.0        Felty syndrome

Rheumatoid arthritis with splenoadenomegaly and leukopenia

M05.1†      Rheumatoid lung disease (J99.0*) M05.2         Rheumatoid vasculitis

M05.3†      Rheumatoid arthritis with involvement of other organs and systems

Rheumatoid:

   carditis (I52.8*)

   endocarditis (I39.-*)

   myocarditis (I41.8*)

   myopathy (G73.7*)

   pericarditis (I32.8*)

   polyneuropathy (G63.6*)

M05.8        Other seropositive rheumatoid arthritis

M05.9        Seropositive rheumatoid arthritis, unspecified

 

  M06        Other rheumatoid arthritis

[See site code at the beginning of this chapter]


M06.0        Seronegative rheumatoid arthritis M06.1           Adult-onset Still disease

Excl.: Still disease NOS (M08.2)

M06.2        Rheumatoid bursitis M06.3        Rheumatoid nodule

M06.4        Inflammatory polyarthropathy

Excl.: polyarthritis NOS (M13.0)

M06.8        Other specified rheumatoid arthritis M06.9       Rheumatoid arthritis, unspecified

  M07*      Psoriatic and enteropathic arthropathies

[See site code at the beginning of this chapter]

Excl.: juvenile psoriatic and enteropathic arthropathies (M09.-*) M07.0* Distal interphalangeal psoriatic arthropathy (L40.5†) M07.1*       Arthritis mutilans (L40.5†)

M07.2*       Psoriatic spondylitis (L40.5†)

M07.3*       Other psoriatic arthropathies (L40.5†)

M07.4*       Arthropathy in Crohn disease [regional enteritis] (K50.-†) M07.5*         Arthropathy in ulcerative colitis (K51.-†)

M07.6*       Other enteropathic arthropathies

 

  M08        Juvenile arthritis

[See site code at the beginning of this chapter]

Incl.: arthritis in children, with onset before 16th birthday and lasting longer than 3 months

Excl.: Felty syndrome (M05.0)

juvenile dermatomyositis (M33.0)

M08.0        Juvenile rheumatoid arthritis

Juvenile rheumatoid arthritis with or without rheumatoid factor

M08.1        Juvenile ankylosing spondylitis

Excl.: ankylosing spondylitis in adults (M45)

M08.2        Juvenile arthritis with systemic onset

Still disease NOS

Excl.: adult-onset Still disease (M06.1)

M08.3        Juvenile polyarthritis (seronegative)

Chronic juvenile polyarthritis

M08.4        Pauciarticular juvenile arthritis


M08.8        Other juvenile arthritis

M08.9        Juvenile arthritis, unspecified

 

  M09*      Juvenile arthritis in diseases classified elsewhere

[See site code at the beginning of this chapter]

Excl.: arthropathy in Whipple disease (M14.8*)

M09.0*       Juvenile arthritis in psoriasis (L40.5†)

M09.1*       Juvenile arthritis in Crohn disease [regional enteritis] (K50.-†) M09.2*  Juvenile arthritis in ulcerative colitis (K51.-†)

M09.8*       Juvenile arthritis in other diseases classified elsewhere

 

  M10        Gout

[See site code at the beginning of this chapter]

M10.0        Idiopathic gout

Gouty bursitis Primary gout

Urate tophus of heart† (I43.8*)

M10.1        Lead-induced gout M10.2         Drug-induced gout

Use additional external cause code (Chapter XX), if desired, to identify drug.

M10.3        Gout due to impairment of renal function

Use additional code, if desired, to identify impairment of kidney disease (N17–N19)

M10.4        Other secondary gout M10.9    Gout, unspecified

  M11        Other crystal arthropathies

[See site code at the beginning of this chapter] M11.0 Hydroxyapatite deposition disease M11.1 Familial chondrocalcinosis

M11.2        Other chondrocalcinosis

Chondrocalcinosis NOS

M11.8        Other specified crystal arthropathies M11.9    Crystal arthropathy, unspecified

  M12        Other specific arthropathies

[See site code at the beginning of this chapter]

Excl.: arthropathy NOS (M13.9) arthrosis (M15–M19) cricoarytenoid arthropathy (J38.7)


M12.0        Chronic postrheumatic arthropathy [Jaccoud] M12.1   Kaschin-Beck disease

M12.2        Villonodular synovitis (pigmented) M12.3         Palindromic rheumatism

M12.4        Intermittent hydrarthrosis

M12.5        Traumatic arthropathy

Excl.: post-traumatic arthrosis (of):

   NOS (M19.1)

   first carpometacarpal joint (M18.2–M18.3)

   hip (M16.4–M16.5)

   knee (M17.2–M17.3)

   other single joints (M19.1)

M12.8        Other specific arthropathies, not elsewhere classified

Transient arthropathy

 

  M13        Other arthritis

[See site code at the beginning of this chapter]

Excl.: arthrosis (M15-M19)

M13.0        Polyarthritis, unspecified

M13.1        Monoarthritis, not elsewhere classified M13.8  Other specified arthritis

Allergic arthritis

M13.9        Arthritis, unspecified

Arthropathy NOS

 

  M14*      Arthropathies in other diseases classified elsewhere

Excl.: arthropathy in:

   haematological disorders (M36.2–M36.3*)

   hypersensitivity reactions (M36.4*)

   neoplastic disease (M36.1*) neuropathic spondylopathy (M49.4*)

psoriatic and enteropathic arthropathies (M07.-*) psoriatic and enteropathic arthropathies:

   juvenile (M09.-*)

M14.0*       Gouty arthropathy due to enzyme defects and other inherited disorders

Gouty arthropathy in:

  Lesch–Nyhan syndrome (E79.1†)

  sickle-cell disorders (D57.-†)


M14.1*       Crystal arthropathy in other metabolic disorders

Crystal arthropathy in hyperparathyroidism (E21.-†)

M14.2*       Diabetic arthropathy (E10–E14 with common fourth character .6†)

Excl.: diabetic neuropathic arthropathy (M14.6*)

M14.3*       Lipoid dermatoarthritis (E78.8†) M14.4*           Arthropathy in amyloidosis (E85.-†)

M14.5*       Arthropathies in other endocrine, nutritional and metabolic disorders

Arthropathy in:

   acromegaly and pituitary gigantism (E22.0†)

   haemochromatosis (E83.1†)

   hypothyroidism (E00–E03†)

   thyrotoxicosis [hyperthyroidism] (E05.-†)

M14.6*       Neuropathic arthropathy

Charcot or tabetic arthropathy (A52.1†)

Diabetic neuropathic arthropathy (E10–E14 with common fourth character .6†)

M14.8*       Arthropathies in other specified diseases classified elsewhere

Arthropathy in:

   erythema:

   multiforme (L51.-†)

   nodosum (L52†)

   sarcoidosis (D86.8†)

   Whipple disease (K90.8†)

 

Arthrosis (M15–M19)

 

Note: In this block, the term osteoarthritis is used as a synonym for arthrosis or osteoarthrosis. The term primary has been used with its customary clinical meaning of no underlying or determining condition identified.

Excl.: osteoarthritis of spine (M47.-)

 

  M15        Polyarthrosis

Incl.: arthrosis with mention of more than one site

Excl.: bilateral involvement of single joint (M16–M19)

M15.0        Primary generalized (osteo)arthrosis M15.1    Heberden nodes (with arthropathy) M15.2   Bouchard nodes (with arthropathy) M15.3                 Secondary multiple arthrosis

Post-traumatic polyarthrosis

M15.4        Erosive (osteo)arthrosis


M15.8        Other polyarthrosis

M15.9        Polyarthrosis, unspecified

Generalized osteoarthritis NOS

  M16        Coxarthrosis [arthrosis of hip] M16.0           Primary coxarthrosis, bilateral M16.1          Other primary coxarthrosis

Primary coxarthrosis:

  NOS

  unilateral

M16.2        Coxarthrosis resulting from dysplasia, bilateral M16.3 Other dysplastic coxarthrosis

Dysplastic coxarthrosis:

  NOS

  unilateral

M16.4        Post-traumatic coxarthrosis, bilateral M16.5     Other post-traumatic coxarthrosis

Post-traumatic coxarthrosis:

  NOS

  unilateral

M16.6        Other secondary coxarthrosis, bilateral M16.7  Other secondary coxarthrosis

Secondary coxarthrosis:

  NOS

  unilateral

M16.9        Coxarthrosis, unspecified

  M17        Gonarthrosis [arthrosis of knee] M17.0        Primary gonarthrosis, bilateral M17.1          Other primary gonarthrosis

Primary gonarthrosis:

  NOS

  unilateral

M17.2        Post-traumatic gonarthrosis, bilateral M17.3     Other post-traumatic gonarthrosis

Post-traumatic gonarthrosis:

  NOS

  unilateral

M17.4        Other secondary gonarthrosis, bilateral


M17.5        Other secondary gonarthrosis

Secondary gonarthrosis:

   NOS

   unilateral

M17.9        Gonarthrosis, unspecified

 

  M18        Arthrosis of first carpometacarpal joint

M18.0        Primary arthrosis of first carpometacarpal joints, bilateral M18.1       Other primary arthrosis of first carpometacarpal joint

Primary arthrosis of first carpometacarpal joint:

   NOS

   unilateral

M18.2        Post-traumatic arthrosis of first carpometacarpal joints, bilateral

M18.3        Other post-traumatic arthrosis of first carpometacarpal joint

Post-traumatic arthrosis of first carpometacarpal joint:

   NOS

   unilateral

M18.4        Other secondary arthrosis of first carpometacarpal joints, bilateral

M18.5        Other secondary arthrosis of first carpometacarpal joint

Secondary arthrosis of first carpometacarpal joint:

   NOS

   unilateral

M18.9        Arthrosis of first carpometacarpal joint, unspecified

 

  M19        Other arthrosis

[See site code at the beginning of this chapter]

Excl.: arthrosis of spine (M47.-) hallux rigidus (M20.2) polyarthrosis (M15.-)

M19.0        Primary arthrosis of other joints

Primary arthrosis NOS

M19.1        Post-traumatic arthrosis of other joints

Post-traumatic arthrosis NOS

M19.2        Other secondary arthrosis

Secondary arthrosis NOS


M19.8        Other specified arthrosis M19.9 Arthrosis, unspecified

Other joint disorders (M20–M25)

 

Excl.:           joints of the spine (M40–M54)

 

  M20        Acquired deformities of fingers and toes

Excl.: acquired absence of fingers and toes (Z89.-) congenital:

   absence of fingers and toes (Q71.3, Q72.3)

   deformities and malformations of fingers and toes (Q66.-, Q68–Q70, Q74.-)

M20.0        Deformity of finger(s)

Boutonnière and swan-neck deformities

Excl.: clubbing of fingers (R68.3)

palmar fascial fibromatosis [Dupuytren] (M72.0) trigger finger (M65.3)

M20.1        Hallux valgus (acquired)

Bunion

M20.2        Hallux rigidus

M20.3        Other deformity of hallux (acquired)

Hallux varus

M20.4        Other hammer toe(s) (acquired) M20.5  Other deformities of toe(s) (acquired)

M20.6        Acquired deformity of toe(s), unspecified

 

  M21        Other acquired deformities of limbs

[See site code at the beginning of this chapter]

Excl.: acquired absence of limb (Z89.-)

acquired deformities of fingers or toes (M20.-) congenital:

   absence of limbs (Q71–Q73)

   deformities and malformations of limbs (Q65–Q66, Q68–Q74) coxa plana (M91.2)

M21.0        Valgus deformity, not elsewhere classified

Excl.: metatarsus valgus (Q66.6) talipes calcaneovalgus (Q66.4)


M21.1        Varus deformity, not elsewhere classified

Excl.: metatarsus varus (Q66.2) tibia vara (M92.5)

M21.2        Flexion deformity

M21.3        Wrist or foot drop (acquired) M21.4     Flat foot [pes planus] (acquired)

Excl.:  congenital pes planus (Q66.5)

M21.5        Acquired clawhand, clubhand, clawfoot and clubfoot

Excl.: clubfoot, not specified as acquired (Q66.8)

M21.6        Other acquired deformities of ankle and foot

Excl.:  deformities of toe (acquired) (M20.1–M20.6)

M21.7        Unequal limb length (acquired)

M21.8        Other specified acquired deformities of limbs M21.9  Acquired deformity of limb, unspecified

  M22        Disorders of patella

Excl.: dislocation of patella (S83.0) M22.0  Recurrent dislocation of patella M22.1          Recurrent subluxation of patella M22.2        Patellofemoral disorders

M22.3        Other derangements of patella M22.4  Chondromalacia patellae M22.8       Other disorders of patella

M22.9        Disorder of patella, unspecified

 

  M23        Internal derangement of knee

Excl.: ankylosis (M24.6)

current injury – see injury to the knee and lower leg (S80–S89) deformity of knee (M21.-)

disorders of patella (M22.-) osteochondritis dissecans (M93.2)

recurrent dislocation or subluxation (M24.4) recurrent dislocation or subluxation

  patella (M22.0–M22.1)

The following supplementary subclassification to indicate the site of involvement is provided for optional use with appropriate subcategories in M23.-; see also note at the beginning of this chapter.


0       multiple sites

1       Anterior cruciate ligament or anterior horn of medial meniscus

2       Posterior cruciate ligament or posterior horn of medial meniscus

3       Medial collateral ligament or other and unspecified medial meniscus

4       Lateral collateral ligament or anterior horn of lateral meniscus

5       Posterior horn of lateral meniscus

6       Other and unspecified lateral meniscus

7       Capsular ligament

9     Unspecified ligament or unspecified meniscus

M23.0        Cystic meniscus

M23.1        Discoid meniscus (congenital)

M23.2        Derangement of meniscus due to old tear or injury

Old bucket-handle tear

M23.3        Other meniscus derangements

Degenerate Detached Retained

 

meniscus

M23.4        Loose body in knee

M23.5        Chronic instability of knee

M23.6        Other spontaneous disruption of ligament(s) of knee M23.8     Other internal derangements of knee

Laxity of ligament of knee Snapping knee

M23.9        Internal derangement of knee, unspecified

 

  M24        Other specific joint derangements

[See site code at the beginning of this chapter]

Excl.: current injury – see injury of joint by body region ganglion (M67.4)

snapping knee (M23.8) temporomandibular joint disorders (K07.6)

M24.0        Loose body in joint

Excl.: loose body in knee (M23.4)

M24.1        Other articular cartilage disorders

Excl.: chondrocalcinosis (M11.1–M11.2) internal derangement of knee (M23.-) metastatic calcification (E83.5) ochronosis (E70.2)


M24.2        Disorder of ligament

Instability secondary to old ligament injury Ligamentous laxity NOS

Excl.: familial ligamentous laxity (M35.7) knee (M23.5–M23.8)

M24.3        Pathological dislocation and subluxation of joint, not elsewhere classified

Excl.: dislocation or displacement of joint:

  congenital – see congenital malformations and deformations of the musculoskeletal system (Q65–Q79)

  current injury – see injury of joints and ligaments by body region

  recurrent (M24.4)

M24.4        Recurrent dislocation and subluxation of joint

Excl.: patella (M22.0–M22.1)

vertebral subluxation (M43.3–M43.5)

M24.5        Contracture of joint

Excl.: acquired deformities of limbs (M20–M21)

contracture of tendon (sheath) without contracture of joint (M67.1) Dupuytren’s contracture (M72.0)

M24.6        Ankylosis of joint

Excl.: spine (M43.2)

stiffness of joint without ankylosis (M25.6)

M24.7        Protrusio acetabuli

M24.8        Other specific joint derangements, not elsewhere classified

Excl.: involving iliotibial band syndrome (M76.3)

M24.9        Joint derangement, unspecified

 

  M25        Other joint disorders, not elsewhere classified

[See site code at the beginning of this chapter]

Excl.: abnormality of gait and mobility (R26.-) calcification of:

  bursa (M71.4)

  shoulder (joint) (M75.3)

  tendon (M65.2)

deformities classified to M20–M21 difficulty in walking (R26.2)

M25.0        Haemarthrosis

Excl.: current injury – see injury of joint by body region

M25.1        Fistula of joint M25.2    Flail joint


M25.3        Other instability of joint

Excl.: instability of joint secondary to:

   old ligament injury (M24.2)

   removal of joint prosthesis (M96.8)

M25.4        Effusion of joint

Excl.: hydrarthrosis of yaws (A66.6)

M25.5        Pain in joint

M25.6        Stiffness of joint, not elsewhere classified M25.7          Osteophyte

M25.8        Other specified joint disorders M25.9    Joint disorder, unspecified

 

Systemic connective tissue disorders (M30–M36)

Incl.: autoimmune disease:

   NOS

   systemic

collagen (vascular) disease:

   NOS

   systemic

Excl.:  antiphospholipid syndrome (D68.6)

autoimmune disease, single organ or single cell-type (code to relevant condition category)

 

  M30        Polyarteritis nodosa and related conditions

M30.0        Polyarteritis nodosa

M30.1        Polyarteritis with lung involvement [Churg–Strauss]

Allergic granulomatous angiitis

M30.2        Juvenile polyarteritis

M30.3        Mucocutaneous lymph node syndrome [Kawasaki] M30.8        Other conditions related to polyarteritis nodosa

Polyangiitis overlap syndrome

 

  M31        Other necrotizing vasculopathies

M31.0        Hypersensitivity angiitis

Goodpasture syndrome

M31.1        Thrombotic microangiopathy

Thrombotic thrombocytopenic purpura

M31.2        Lethal midline granuloma


M31.3        Wegener granulomatosis

Necrotizing respiratory granulomatosis

M31.4        Aortic arch syndrome [Takayasu]

M31.5        Giant cell arteritis with polymyalgia rheumatica M31.6           Other giant cell arteritis

M31.7        Microscopic polyangiitis

Microscopic polyarteritis

Excl.: polyarteritis nodosa (M30.0)

M31.8        Other specified necrotizing vasculopathies

Hypocomplementaemic vasculitis

M31.9        Necrotizing vasculopathy, unspecified

 

  M32        Systemic lupus erythematosus

Excl.: lupus erythematosus (discoid)(NOS) (L93.0)

M32.0        Drug-induced systemic lupus erythematosus

Use additional external cause code (Chapter XX), if desired, to identify drug.

M32.1†      Systemic lupus erythematosus with organ or system involvement

Libman–Sacks disease (I39.-*) Lupus pericarditis (I32.8*) Systemic lupus erythematosus with:

   kidney involvement (N08.5*, N16.4*)

   lung involvement (J99.1*)

M32.8        Other forms of systemic lupus erythematosus M32.9 Systemic lupus erythematosus, unspecified

  M33        Dermatopolymyositis M33.0 Juvenile dermatomyositis M33.1     Other dermatomyositis M33.2                 Polymyositis

M33.9        Dermatopolymyositis, unspecified

 

  M34        Systemic sclerosis

Incl.: scleroderma

Excl.: scleroderma:

  circumscribed (L94.0)

  neonatal (P83.8)


M34.0        Progressive systemic sclerosis M34.1  CR(E)ST syndrome

Combination of calcinosis, Raynaud phenomenon, (o)esophageal dysfunction, sclerodactyly, telangiectasia.

M34.2        Systemic sclerosis induced by drugs and chemicals

Use additional external cause code (Chapter XX), if desired, to identify cause.

M34.8        Other forms of systemic sclerosis

Systemic sclerosis with:

  lung involvement† (J99.1*)

  myopathy† (G73.7*)

M34.9        Systemic sclerosis, unspecified

 

  M35        Other systemic involvement of connective tissue

Excl.: reactive perforating collagenosis (L87.1)

M35.0        Sicca syndrome [Sjögren]

Sjögren syndrome with:

  keratoconjunctivitis† (H19.3*)

  lung involvement† (J99.1*)

  myopathy† (G73.7*)

  renal tubulo-interstitial disorders† (N16.4*)

M35.1        Other overlap syndromes

Mixed connective tissue disease

Excl.: polyangiitis overlap syndrome (M30.8)

M35.2        Behçet disease

M35.3        Polymyalgia rheumatica

Excl.: polymyalgia rheumatica with giant cell arteritis (M31.5)

M35.4        Diffuse (eosinophilic) fasciitis M35.5     Multifocal fibrosclerosis

M35.6        Relapsing panniculitis [Weber–Christian]

Excl.: panniculitis:

   NOS (M79.3)

   lupus (L93.2)

M35.7        Hypermobility syndrome

Familial ligamentous laxity

Excl.: Ehlers–Danlos syndrome (Q79.6) ligamentous laxity NOS (M24.2)

M35.8        Other specified systemic involvement of connective tissue


M35.9        Systemic involvement of connective tissue, unspecified

Autoimmune disease (systemic) NOS Collagen (vascular) disease NOS

 

  M36*      Systemic disorders of connective tissue in diseases classified elsewhere

Excl.: arthropathies in diseases classified elsewhere (M14.-*)

M36.0*       Dermato(poly)myositis in neoplastic disease (C00–D48†) M36.1*       Arthropathy in neoplastic disease (C00–D48†)

Arthropathy in:

   leukaemia (C91–C95†)

   malignant histiocytosis (C96.8†)

   multiple myeloma (C90.0†)

M36.2*       Haemophilic arthropathy (D66–D68†)

M36.3*       Arthropathy in other blood disorders (D50–D76†)

Excl.: arthropathy in Henoch(–Schönlein) purpura (M36.4*)

M36.4*       Arthropathy in hypersensitivity reactions classified elsewhere

Arthropathy in Henoch(–Schönlein) purpura (D69.0†)

M36.8*       Systemic disorders of connective tissue in other diseases classified elsewhere

Systemic disorders of connective tissue in:

   hypogammaglobulinaemia (D80.-†)

   ochronosis (E70.2†)

 

Dorsopathies (M40–M54)

The following supplementary subclassification to indicate the site of involvement is provided for optional use with appropriate categories in the block on dorsopathies, except categories M50 and M51; see also note at the beginning of this chapter.

0       Multiple sites in spine

1       Occipito-atlanto-axial region

2       Cervical region

3       Cervicothoracic region

4       Thoracic region

5       Thoracolumbar region

6       Lumbar region


7       Lumbosacral region

8       Sacral and sacrococcygeal region

9       Site unspecified

 

Deforming dorsopathies (M40–M43)

 

  M40        Kyphosis and lordosis

[See site code before M40]

Excl.: kyphoscoliosis (M41.-) kyphosis and lordosis:

   congenital (Q76.4)

   postprocedural (M96.-)

M40.0        Postural kyphosis

Excl.: osteochondrosis of spine (M42.-)

M40.1        Other secondary kyphosis M40.2          Other and unspecified kyphosis M40.3           Flatback syndrome

M40.4        Other lordosis

Lordosis:

  acquired

  postural

M40.5        Lordosis, unspecified

 

  M41        Scoliosis

[See site code before M40]

Incl.: kyphoscoliosis

Excl.: congenital scoliosis:

   NOS (Q67.5)

   due to bony malformation (Q76.3)

   postural (Q67.5)

kyphoscoliotic heart disease (I27.1) postprocedural (M96.-)

M41.0        Infantile idiopathic scoliosis M41.1       Juvenile idiopathic scoliosis

Adolescent scoliosis

M41.2        Other idiopathic scoliosis M41.3           Thoracogenic scoliosis


M41.4        Neuromuscular scoliosis

Scoliosis secondary to cerebral palsy, Friedreich ataxia, poliomyelitis, and other neuromuscular disorders

M41.5        Other secondary scoliosis M41.8         Other forms of scoliosis M41.9     Scoliosis, unspecified

  M42        Spinal osteochondrosis

[See site code before M40]

Excl.: postural kyphosis (M40.0)

M42.0        Juvenile osteochondrosis of spine

   Calvé disease

   Scheuermann disease

Excl.: postural kyphosis (M40.0)

M42.1        Adult osteochondrosis of spine M42.9            Spinal osteochondrosis, unspecified

  M43        Other deforming dorsopathies

[See site code before M40]

Excl.: congenital spondylolysis and spondylolisthesis (Q76.2) hemivertebra (Q76.3–Q76.4)

Klippel–Feil syndrome (Q76.1) lumbarization and sacralization (Q76.4) platyspondylisis (Q76.4)

spina bifida occulta (Q76.0) spinal curvature in:

  osteoporosis (M80–M81)

  Paget disease of bone [osteitis deformans] (M88.-)

M43.0        Spondylolysis M43.1    Spondylolisthesis

M43.2        Other fusion of spine

Ankylosis of spinal joint

Excl.: ankylosing spondylitis (M45) arthrodesis status (Z98.1)

pseudoarthrosis after fusion or arthrodesis (M96.0) M43.3        Recurrent atlantoaxial subluxation with myelopathy M43.4   Other recurrent atlantoaxial subluxation

M43.5        Other recurrent vertebral subluxation

Excl.: biomechanical lesions NEC (M99.-)


M43.6        Torticollis

Excl.: torticollis:

   congenital (sternomastoid) (Q68.0)

   current injury – see injury of spine by body region

   due to birth injury (P15.2)

   psychogenic (F45.8)

   spasmodic (G24.3)

M43.8        Other specified deforming dorsopathies

Excl.: kyphosis and lordosis (M40.-) scoliosis (M41.-)

M43.9        Deforming dorsopathy, unspecified

Curvature of spine NOS

 

Spondylopathies (M45–M49)

 

  M45        Ankylosing spondylitis

[See site code before M40]

Incl.: rheumatoid arthritis of spine

Excl.: arthropathy in Reiter disease (M02.3) Behçet disease (M35.2)

juvenile (ankylosing) spondylitis (M08.1)

 

  M46        Other inflammatory spondylopathies

[See site code before M40]

M46.0        Spinal enthesopathy

Disorder of ligamentous or muscular attachments of spine

M46.1        Sacroiliitis, not elsewhere classified M46.2       Osteomyelitis of vertebra

M46.3        Infection of intervertebral disc (pyogenic)

Use additional code (B95–B98), if desired, to identify infectious agent.

M46.4        Discitis, unspecified

M46.5        Other infective spondylopathies

M46.8        Other specified inflammatory spondylopathies M46.9  Inflammatory spondylopathy, unspecified

  M47        Spondylosis

[See site code before M40]

Incl.: arthrosis or osteoarthritis of spine degeneration of facet joints


M47.0†      Anterior spinal and vertebral artery compression syndromes (G99.2*)

M47.1        Other spondylosis with myelopathy

Spondylogenic compression of spinal cord† (G99.2*)

Cervical spondylosis Lumbosacral spondylosis Thoracic spondylosis

 

without myelopathy or radiculopathy

 

 

Excl.: vertebral subluxation (M43.3–M43.5) M47.2 Other spondylosis with radiculopathy M47.8 Other spondylosis

 

 

 

M47.9        Spondylosis, unspecified

 

  M48        Other spondylopathies

[See site code before M40]

M48.0        Spinal stenosis

Caudal stenosis

M48.1        Ankylosing hyperostosis [Forestier]

Diffuse idiopathic skeletal hyperostosis [DISH]

M48.2        Kissing spine

M48.3        Traumatic spondylopathy M48.4          Fatigue fracture of vertebra

Stress fracture of vertebra

M48.5        Collapsed vertebra, not elsewhere classified

Collapsed vertebra NOS Wedging of vertebra NOS

Excl.: collapsed vertebra in osteoporosis (M80.-)

current injury – see injury of spine by body region

M48.8        Other specified spondylopathies

Ossification of posterior longitudinal ligament

M48.9        Spondylopathy, unspecified

 

  M49*      Spondylopathies in diseases classified elsewhere

[See site code before M40]

Excl.: psoriatic and enteropathic arthropathies (M07.-*, M09.-*)

M49.0*       Tuberculosis of spine (A18.0†)

Pott’s curvature


M49.1*       Brucella spondylitis (A23.-†)

M49.2*       Enterobacterial spondylitis (A01–A04†)

M49.3*       Spondylopathy in other infectious and parasitic diseases classified elsewhere

Excl.: neuropathic spondylopathy in tabes dorsalis (M49.4*)

M49.4*       Neuropathic spondylopathy

Neuropathic spondylopathy in:

  syringomyelia and syringobulbia (G95.0†)

  tabes dorsalis (A52.1†)

M49.5*       Collapsed vertebra in diseases classified elsewhere

Metastatic fracture of vertebra (C79.5†)

M49.8*       Spondylopathy in other diseases classified elsewhere

 

Other dorsopathies (M50–M54)

 

Excl.:           current injury – see injury of spine by body region discitis NOS (M46.4)

 

  M50        Cervical disc disorders

Incl.: cervical disc disorders with cervicalgia cervicothoracic disc disorders

M50.0†      Cervical disc disorder with myelopathy (G99.2*) M50.1 Cervical disc disorder with radiculopathy

Excl.: brachial radiculitis NOS (M54.1) M50.2           Other cervical disc displacement M50.3    Other cervical disc degeneration M50.8                 Other cervical disc disorders M50.9      Cervical disc disorder, unspecified

  M51        Other intervertebral disc disorders

Incl.: thoracic, thoracolumbar and lumbosacral disc disorders

M51.0†      Lumbar and other intervertebral disc disorders with myelopathy (G99.2*)

M51.1†      Lumbar and other intervertebral disc disorders with radiculopathy (G55.1*)

Sciatica due to intervertebral disc disorder

Excl.: lumbar radiculitis NOS (M54.1)


M51.2        Other specified intervertebral disc displacement

Lumbago due to displacement of intervertebral disc M51.3     Other specified intervertebral disc degeneration M51.4    Schmorl nodes

M51.8        Other specified intervertebral disc disorders M51.9    Intervertebral disc disorder, unspecified

  M53        Other dorsopathies, not elsewhere classified

[See site code before M40]

M53.0        Cervicocranial syndrome

Posterior cervical sympathetic syndrome

M53.1        Cervicobrachial syndrome

Excl.: cervical disc disorder (M50.-) thoracic outlet syndrome (G54.0)

M53.2        Spinal instabilities

M53.3        Sacrococcygeal disorders, not elsewhere classified

Coccygodynia

M53.8        Other specified dorsopathies M53.9    Dorsopathy, unspecified

  M54        Dorsalgia

[See site code before M40]

Excl.: psychogenic dorsalgia (F45.4)

M54.0        Panniculitis affecting regions of neck and back

Excl.: panniculitis:

  NOS (M79.3)

  lupus (L93.2)

  relapsing [Weber-Christian] (M35.6)

M54.1        Radiculopathy

Neuritis or radiculitis:

   brachial NOS

   lumbar NOS

   lumbosacral NOS

   thoracic NOS Radiculitis NOS

Excl.: neuralgia and neuritis NOS (M79.2) radiculopathy with:

  cervical disc disorder (M50.1)

  lumbar and other intervertebral disc disorder (M51.1)

  spondylosis (M47.2)


M54.2        Cervicalgia

Excl.: cervicalgia due to intervertebral cervical disc disorder (M50.-)

M54.3        Sciatica

Excl.: lesion of sciatic nerve (G57.0) sciatica:

   due to intervertebral disc disorder (M51.1)

   with lumbago (M54.4)

M54.4        Lumbago with sciatica

Excl.: due to intervertebral disc disorder (M51.1)

M54.5        Low back pain

Loin pain

Low back strain Lumbago NOS

Excl.: lumbago:

   due to intervertebral disc displacement (M51.2)

   with sciatica (M54.4)

M54.6        Pain in thoracic spine

Excl.: pain due to intervertebral disc disorder (M51.-)

M54.8        Other dorsalgia

M54.9        Dorsalgia, unspecified

Backache NOS

 

Soft tissue disorders (M60–M79)

 

Disorders of muscles (M60–M63)

 

Excl.:           dermatopolymyositis (M33.-)

muscular dystrophies and myopathies (G71–G72) myopathy in:

   amyloidosis (E85.-)

   polyarteritis nodosa (M30.0)

   rheumatoid arthritis (M05.3)

   scleroderma (M34.-)

   Sjögren syndrome (M35.0)

   systemic lupus erythematosus (M32.-)


  M60        Myositis

[See site code at the beginning of this chapter]

M60.0        Infective myositis

Tropical pyomyositis

Use additional code (B95–B98), if desired, to identify infectious agent.

M60.1        Interstitial myositis

M60.2        Foreign body granuloma of soft tissue, not elsewhere classified

Excl.: foreign body granuloma of skin and subcutaneous tissue (L92.3)

M60.8        Other myositis

M60.9        Myositis, unspecified

 

  M61        Calcification and ossification of muscle

[See site code at the beginning of this chapter]

M61.0        Myositis ossificans traumatica M61.1  Myositis ossificans progressiva

Fibrodysplasia ossificans progressiva

M61.2        Paralytic calcification and ossification of muscle

Myositis ossificans associated with quadriplegia or paraplegia

M61.3        Calcification and ossification of muscles associated with burns

Myositis ossificans associated with burns

M61.4        Other calcification of muscle

Excl.: calcific tendinitis (M65.2) calcific tendinitis:

  of shoulder (M75.3)

M61.5        Other ossification of muscle

M61.9        Calcification and ossification of muscle, unspecified

 

  M62        Other disorders of muscle

[See site code at the beginning of this chapter]

Excl.: cramp and spasm (R25.2) myalgia (M79.1) myopathy:

  alcoholic (G72.1)

  drug-induced (G72.0) stiff-man syndrome (G25.8)

M62.0        Diastasis of muscle


 

M62.1        Other rupture of muscle (nontraumatic)

Excl.: rupture of tendon (M66.-)

traumatic rupture of muscle – see injury of muscle by body region

M62.2        Ischaemic infarction of muscle

Compartment syndrome, non-traumatic

Excl.: compartment syndrome, traumatic (T79.6) traumatic ischaemia of muscle (T79.6) Volkmann ischaemic contracture (T79.6)

M62.3        Immobility syndrome (paraplegic) M62.4           Contracture of muscle

Excl.: contracture of joint (M24.5)

M62.5        Muscle wasting and atrophy, not elsewhere classified

Disuse atrophy NEC

M62.6        Muscle strain

Excl.: current injury – see injury of muscle by body region

M62.8        Other specified disorders of muscle

Muscle (sheath) hernia

M62.9        Disorder of muscle, unspecified

 

  M63*      Disorders of muscle in diseases classified elsewhere

Excl.: myopathy in:

   endocrine diseases (G73.5*)

   metabolic diseases (G73.6*)

M63.0*       Myositis in bacterial diseases classified elsewhere

Myositis in:

  leprosy [Hansen disease] (A30.-†)

  syphilis (A51.4†, A52.7†)

M63.1*       Myositis in protozoal and parasitic infections classified elsewhere

Myositis in:

  cysticercosis (B69.8†)

  schistosomiasis [bilharziasis] (B65.-†)

  toxoplasmosis (B58.8†)

  trichinellosis (B75†)

M63.2*       Myositis in other infectious diseases classified elsewhere

Myositis in mycosis (B35–B49†)

M63.3*       Myositis in sarcoidosis (D86.8†)

M63.8*       Other disorders of muscle in diseases classified elsewhere


Disorders of synovium and tendon (M65–M68)

 

  M65        Synovitis and tenosynovitis

[See site code at the beginning of this chapter]

Excl.: chronic crepitant synovitis of hand and wrist (M70.0)

current injury – see injury of ligament or tendon by body region soft tissue disorders related to use, overuse and pressure (M70.-)

M65.0        Abscess of tendon sheath

Use additional code (B95–B96), if desired, to identify bacterial agent.

M65.1        Other infective (teno)synovitis M65.2   Calcific tendinitis

Excl.: of shoulder (M75.3)

specified tendinitis (M75–M77)

M65.3        Trigger finger

Nodular tendinous disease

M65.4        Radial styloid tenosynovitis [de Quervain] M65.8        Other synovitis and tenosynovitis

Irritable hip

M65.9        Synovitis and tenosynovitis, unspecified

 

  M66        Spontaneous rupture of synovium and tendon

[See site code at the beginning of this chapter]

Incl.: rupture that occurs when a normal force is applied to tissues that are inferred to have less than normal strength

Excl.: rotator cuff syndrome (M75.1)

rupture where an abnormal force is applied to normal tissue – see injury of tendon by body region

M66.0        Rupture of popliteal cyst M66.1           Rupture of synovium

Rupture of synovial cyst

Excl.: rupture of popliteal cyst (M66.0)

M66.2        Spontaneous rupture of extensor tendons M66.3        Spontaneous rupture of flexor tendons M66.4    Spontaneous rupture of other tendons M66.5                 Spontaneous rupture of unspecified tendon

Rupture at musculotendinous junction, nontraumatic


  M67        Other disorders of synovium and tendon

Excl.: palmar fascial fibromatosis [Dupuytren] (M72.0) tendinitis NOS (M77.9)

xanthomatosis localized to tendons (E78.2)

M67.0        Short Achilles tendon (acquired) M67.1 Other contracture of tendon (sheath)

Excl.: with contracture of joint (M24.5)

M67.2        Synovial hypertrophy, not elsewhere classified

Excl.: villonodular synovitis (pigmented) (M12.2)

M67.3        Transient synovitis

Toxic synovitis

Excl.: palindromic rheumatism (M12.3)

M67.4        Ganglion

Ganglion of joint or tendon (sheath)

Excl.: cyst of:

   bursa (M71.2–M71.3)

   synovium (M71.2–M71.3) ganglion in yaws (A66.6)

M67.8        Other specified disorders of synovium and tendon M67.9        Disorder of synovium and tendon, unspecified

  M68*      Disorders of synovium and tendon in diseases classified elsewhere

M68.0*       Synovitis and tenosynovitis in bacterial diseases classified elsewhere

Synovitis or tenosynovitis in:

  gonorrhoea (A54.4†)

  syphilis (A52.7†)

  tuberculosis (A18.0†)

M68.8*       Other disorders of synovium and tendon in diseases classified elsewhere


Other soft tissue disorders (M70–M79)

 

  M70        Soft tissue disorders related to use, overuse and pressure

[See site code at the beginning of this chapter]

Incl.: soft tissue disorders of occupational origin

Excl.: bursitis (of):

  NOS (M71.9)

  shoulder (M75.5)

decubitus ulcer and pressure area (L89.-) enthesopathies (M76–M77)

M70.0        Chronic crepitant synovitis of hand and wrist M70.1   Bursitis of hand

M70.2        Olecranon bursitis M70.3         Other bursitis of elbow M70.4          Prepatellar bursitis M70.5        Other bursitis of knee

M70.6        Trochanteric bursitis

Trochanteric tendinitis

M70.7        Other bursitis of hip

Ischial bursitis

M70.8        Other soft tissue disorders related to use, overuse and pressure

M70.9        Unspecified soft tissue disorder related to use, overuse and pressure

 

  M71        Other bursopathies

[See site code at the beginning of this chapter]

Excl.: bunion (M20.1)

bursitis related to use, overuse and pressure (M70.-) enthesopathies (M76–M77)

M71.0        Abscess of bursa M71.1          Other infective bursitis

M71.2        Synovial cyst of popliteal space [Baker]

Excl.: with rupture (M66.0)

M71.3        Other bursal cyst

Synovial cyst NOS

Excl.: synovial cyst with rupture (M66.1)


M71.4        Calcium deposit in bursa

Excl.: of shoulder (M75.3)

M71.5        Other bursitis, not elsewhere classified

Excl.: bursitis (of):

   NOS (M71.9)

   shoulder (M75.5)

   tibial collateral [Pellegrini-Stieda] (M76.4)

M71.8        Other specified bursopathies M71.9      Bursopathy, unspecified

Bursitis NOS

 

  M72        Fibroblastic disorders

[See site code at the beginning of this chapter]

Excl.: retroperitoneal fibromatosis (D48.3) M72.0       Palmar fascial fibromatosis [Dupuytren] M72.1     Knuckle pads

M72.2        Plantar fascial fibromatosis

Plantar fasciitis

M72.4        Pseudosarcomatous fibromatosis

Nodular fasciitis

M72.6        Necrotizing fasciitis

Use additional code, if desired, to identify infectious agent

M72.8        Other fibroblastic disorders

Abscess of fascia

Excl.: fasciitis:

   diffuse (eosinophilic) (M35.4)

   necrotizing (M72.6)

   nodular (M72.4)

   perirenal:

– NOS (N13.5)

– with infection (N13.6)

   plantar (M72.2)

M72.9        Fibroblastic disorder, unspecified

Fasciitis NOS Fibromatosis NOS

 

  M73*      Soft tissue disorders in diseases classified elsewhere

[See site code at the beginning of this chapter]

M73.0*       Gonococcal bursitis (A54.4†) M73.1*     Syphilitic bursitis (A52.7†)


M73.8*       Other soft tissue disorders in diseases classified elsewhere

 

  M75        Shoulder lesions

Excl.: shoulder-hand syndrome (M89.0)

M75.0        Adhesive capsulitis of shoulder

Frozen shoulder Periarthritis of shoulder

M75.1        Rotator cuff syndrome

Rotator cuff or supraspinatus tear or rupture (complete)(incomplete), not specified as traumatic

Supraspinatus syndrome

M75.2        Bicipital tendinitis

M75.3        Calcific tendinitis of shoulder

Calcified bursa of shoulder

M75.4        Impingement syndrome of shoulder M75.5      Bursitis of shoulder

M75.8        Other shoulder lesions M75.9  Shoulder lesion, unspecified

  M76        Enthesopathies of lower limb, excluding foot

[See site code at the beginning of this chapter]

Note: The superficially specific terms bursitis, capsulitis and tendinitis tend to be used indiscriminately for various disorders of peripheral ligamentous or muscular attachments; most of these conditions have been brought together as enthesopathies, which is the generic term for lesions at these sites.

Excl.: bursitis due to use, overuse and pressure (M70.-)

M76.0        Gluteal tendinitis M76.1           Psoas tendinitis M76.2    Iliac crest spur

M76.3        Iliotibial band syndrome

M76.4        Tibial collateral bursitis [Pellegrini–Stieda] M76.5       Patellar tendinitis

M76.6        Achilles tendinitis

Achilles bursitis

M76.7        Peroneal tendinitis

M76.8        Other enthesopathies of lower limb, excluding foot

Anterior tibial syndrome Posterior tibial tendinitis

M76.9        Enthesopathy of lower limb, unspecified


  M77        Other enthesopathies

[See site code at the beginning of this chapter]

Excl.: bursitis:

   NOS (M71.9)

   due to use, overuse and pressure (M70.-) osteophyte (M25.7)

spinal enthesopathy (M46.0)

M77.0        Medial epicondylitis M77.1        Lateral epicondylitis

Tennis elbow

M77.2        Periarthritis of wrist M77.3         Calcaneal spur M77.4        Metatarsalgia

Excl.: Morton metatarsalgia (G57.6)

M77.5        Other enthesopathy of foot

M77.8        Other enthesopathies, not elsewhere classified M77.9  Enthesopathy, unspecified

Bone spur NOS Capsulitis NOS Periarthritis NOS Tendinitis NOS

 

  M79        Other soft tissue disorders, not elsewhere classified

[See site code at the beginning of this chapter]

Excl.: soft tissue pain, psychogenic (F45.4)

M79.0        Rheumatism, unspecified

Excl.: fibromyalgia (M79.7) palindromic rheumatism (M12.3)

M79.1        Myalgia

Excl.: myositis (M60.-)

M79.2        Neuralgia and neuritis, unspecified

Excl.: mononeuropathies (G56–G58) radiculitis:

   NOS (M54.1)

   brachial NOS (M54.1)

   lumbosacral NOS (M54.1) sciatica (M54.3–M54.4)

M79.3        Panniculitis, unspecified

Excl.: panniculitis:

   lupus (L93.2)

   neck and back (M54.0)

   relapsing [Weber–Christian] (M35.6)


M79.4        Hypertrophy of (infrapatellar) fat pad M79.5    Residual foreign body in soft tissue

Excl.: foreign body granuloma of:

  skin and subcutaneous tissue (L92.3)

  soft tissue (M60.2)

M79.6        Pain in limb

M79.7        Fibromyalgia Fibromyositis Fibrositis Myofibrositis

M79.8        Other specified soft tissue disorders M79.9    Soft tissue disorder, unspecified

 

Osteopathies and chondropathies (M80–M94)

 

Disorders of bone density and structure (M80–M85)

 

  M80        Osteoporosis with pathological fracture

[See site code at the beginning of this chapter]

Incl.: osteoporotic vertebral collapse and wedging

Excl.: collapsed vertebra NOS (M48.5) pathological fracture NOS (M84.4) wedging of vertebra NOS (M48.5)

M80.0        Postmenopausal osteoporosis with pathological fracture M80.1                 Postoophorectomy osteoporosis with pathological fracture M80.2    Osteoporosis of disuse with pathological fracture

M80.3        Postsurgical malabsorption osteoporosis with pathological fracture

M80.4        Drug-induced osteoporosis with pathological fracture

Use additional external cause code (Chapter XX), if desired, to identify drug.

M80.5        Idiopathic osteoporosis with pathological fracture M80.8       Other osteoporosis with pathological fracture M80.9     Unspecified osteoporosis with pathological fracture


  M81        Osteoporosis without pathological fracture

[See site code at the beginning of this chapter]

Excl.: osteoporosis with pathological fracture (M80.-)

M81.0        Postmenopausal osteoporosis M81.1   Postoophorectomy osteoporosis M81.2 Osteoporosis of disuse

Excl.:    Sudeck atrophy (M89.0)

M81.3        Postsurgical malabsorption osteoporosis M81.4          Drug-induced osteoporosis

Use additional external cause code (Chapter XX), if desired, to identify drug.

M81.5        Idiopathic osteoporosis

M81.6        Localized osteoporosis [Lequesne]

Excl.: Sudeck atrophy (M89.0)

M81.8        Other osteoporosis

Senile osteoporosis

M81.9        Osteoporosis, unspecified

 

  M82*      Osteoporosis in diseases classified elsewhere

[See site code at the beginning of this chapter]

M82.0*       Osteoporosis in multiple myelomatosis (C90.0†) M82.1*           Osteoporosis in endocrine disorders (E00–E34†) M82.8*     Osteoporosis in other diseases classified elsewhere

  M83        Adult osteomalacia

[See site code at the beginning of this chapter]

Excl.: osteomalacia:

  infantile and juvenile (E55.0)

  vitamin-D-resistant (E83.3) renal osteodystrophy (N25.0) rickets (active) (E55.0) rickets (active):

  sequelae (E64.3)

  vitamin-D-resistant (E83.3)

M83.0        Puerperal osteomalacia M83.1   Senile osteomalacia

M83.2        Adult osteomalacia due to malabsorption

Postsurgical malabsorption osteomalacia in adults M83.3         Adult osteomalacia due to malnutrition M83.4     Aluminium bone disease


M83.5        Other drug-induced osteomalacia in adults

Use additional external cause code (Chapter XX), if desired, to identify drug.

M83.8        Other adult osteomalacia

M83.9        Adult osteomalacia, unspecified

 

  M84        Disorders of continuity of bone

[See site code at the beginning of this chapter]

M84.0        Malunion of fracture

M84.1        Nonunion of fracture [pseudarthrosis]

Excl.: pseudarthrosis after fusion or arthrodesis (M96.0)

M84.2        Delayed union of fracture

M84.3        Stress fracture, not elsewhere classified

Stress fracture NOS

Excl.: stress fracture of vertebra (M48.4)

M84.4        Pathological fracture, not elsewhere classified

Pathological fracture NOS

Excl.: collapsed vertebra NEC (M48.5) pathological fracture in osteoporosis (M80.-)

M84.8        Other disorders of continuity of bone M84.9   Disorder of continuity of bone, unspecified

  M85        Other disorders of bone density and structure

[See site code at the beginning of this chapter]

Excl.: osteogenesis imperfecta (Q78.0) osteopetrosis (Q78.2) osteopoikilosis (Q78.8)

polyostotic fibrous dysplasia (Q78.1)

M85.0        Fibrous dysplasia (monostotic)

Excl.: fibrous dysplasia of jaw (K10.8)

M85.1        Skeletal fluorosis M85.2           Hyperostosis of skull M85.3            Osteitis condensans M85.4      Solitary bone cyst

Excl.: solitary cyst of jaw (K09.1–K09.2)

M85.5        Aneurysmal bone cyst

Excl.: aneurysmal cyst of jaw (K09.2)

M85.6        Other cyst of bone

Excl.: cyst of jaw NEC (K09.1–K09.2)

osteitis fibrosa cystica generalisata [von Recklinghausen disease of bone] (E21.0)


M85.8        Other specified disorders of bone density and structure

Hyperostosis of bones, except skull Osteosclerosis, acquired

Excl.: diffuse idiopathic skeletal hyperostosis [DISH] (M48.1) osteosclerosis:

   congenita (Q77.4)

   myelofibrosis (D75.8)

M85.9        Disorder of bone density and structure, unspecified

 

Other osteopathies (M86–M90)

 

Excl.:           postprocedural osteopathies (M96.-)

 

  M86        Osteomyelitis

[See site code at the beginning of this chapter]

Use additional code (B95–B98), if desired, to identify infectious agent.

Excl.: osteomyelitis (of):

   due to Salmonella (A01–A02)

   jaw (K10.2)

   vertebra (M46.2)

M86.0        Acute haematogenous osteomyelitis M86.1      Other acute osteomyelitis

M86.2        Subacute osteomyelitis

M86.3        Chronic multifocal osteomyelitis

M86.4        Chronic osteomyelitis with draining sinus M86.5          Other chronic haematogenous osteomyelitis M86.6         Other chronic osteomyelitis

M86.8        Other osteomyelitis

Brodie’s abscess

M86.9        Osteomyelitis, unspecified

Infection of bone NOS

Periostitis without mention of osteomyelitis

 

  M87        Osteonecrosis

[See site code at the beginning of this chapter]

Incl.: avascular necrosis of bone

Excl.: osteochondropathies (M91–M93)

osteonecrosis of jaw (drug-induced) (radiation induced) (K10.2)


M87.0        Idiopathic aseptic necrosis of bone M87.1      Osteonecrosis due to drugs

Use additional external cause code (Chapter XX), if desired, to identify drug.

M87.2        Osteonecrosis due to previous trauma M87.3  Other secondary osteonecrosis

M87.8        Other osteonecrosis

M87.9        Osteonecrosis, unspecified

 

  M88        Paget disease of bone [osteitis deformans]

[See site code at the beginning of this chapter]

M88.0        Paget disease of skull

M88.8        Paget disease of other bones M88.9    Paget disease of bone, unspecified

  M89        Other disorders of bone

[See site code at the beginning of this chapter]

M89.0        Algoneurodystrophy

Shoulder-hand syndrome Sudeck atrophy

Sympathetic reflex dystrophy

M89.1        Epiphyseal arrest

M89.2        Other disorders of bone development and growth M89.3        Hypertrophy of bone

M89.4        Other hypertrophic osteoarthropathy Marie–Bamberger disease Pachydermoperiostosis

M89.5        Osteolysis

M89.6        Osteopathy after poliomyelitis

Use additional code (B91) , if desired, to identify previous poliomyelitis.

Excl.: postpolio syndrome (G14)

M89.8        Other specified disorders of bone

Infantile cortical hyperostoses

Post-traumatic subperiosteal ossification

M89.9        Disorder of bone, unspecified


  M90*      Osteopathies in diseases classified elsewhere

[See site code at the beginning of this chapter]

M90.0*       Tuberculosis of bone (A18.0†)

Excl.: tuberculosis of spine (M49.0*)

M90.1*       Periostitis in other infectious diseases classified elsewhere

Secondary syphilitic periostitis (A51.4†)

M90.2*       Osteopathy in other infectious diseases classified elsewhere

Osteomyelitis:

  echinococcal (B67.2†)

  gonococcal (A54.4†)

  salmonella (A02.2†)

Syphilitic osteopathy or osteochondropathy (A50.5†, A52.7†)

M90.3*       Osteonecrosis in Caisson disease (T70.3†)

M90.4*       Osteonecrosis due to haemoglobinopathy (D50–D64†) M90.5* Osteonecrosis in other diseases classified elsewhere M90.6*           Osteitis deformans in neoplastic disease (C00–D48†)

Osteitis deformans in malignant neoplasm of bone (C40–C41†)

M90.7*       Fracture of bone in neoplastic disease (C00–D48†)

Excl.: collapse of vertebra in neoplastic disease (M49.5*)

M90.8*       Osteopathy in other diseases classified elsewhere

Osteopathy in renal osteodystrophy (N25.0†)

 

Chondropathies (M91–M94)

 

Excl.:           postprocedural chondropathies (M96.-)

 

  M91        Juvenile osteochondrosis of hip and pelvis

[See site code at the beginning of this chapter]

Excl.: slipped upper femoral epiphysis (nontraumatic) (M93.0)

M91.0        Juvenile osteochondrosis of pelvis

Osteochondrosis (juvenile) of:

  acetabulum

  iliac crest [Buchanan]

  ischiopubic synchondrosis [van Neck]

  symphisis pubis [Pierson]

M91.1        Juvenile osteochondrosis of head of femur [Legg–Calvé– Perthes]

M91.2        Coxa plana

Hip deformity due to previous juvenile osteochondrosis


M91.3        Pseudocoxalgia

M91.8        Other juvenile osteochondrosis of hip and pelvis

Juvenile osteochondrosis after reduction of congenital dislocation of hip

M91.9        Juvenile osteochondrosis of hip and pelvis, unspecified

 

  M92        Other juvenile osteochondrosis

M92.0        Juvenile osteochondrosis of humerus

Osteochondrosis (juvenile) of:

   capitulum of humerus [Panner]

   head of humerus [Haas]

M92.1        Juvenile osteochondrosis of radius and ulna

Osteochondrosis (juvenile) of:

   lower ulna [Burns]

   radial head [Brailsford]

M92.2        Juvenile osteochondrosis of hand

Osteochondrosis (juvenile) of:

   carpal lunate [Kienböck]

   metacarpal heads [Mauclaire]

M92.3        Other juvenile osteochondrosis of upper limb M92.4  Juvenile osteochondrosis of patella

Osteochondrosis (juvenile) of:

   primary patellar centre [Köhler]

   secondary patellar centre [Sinding–Larsen]

M92.5        Juvenile osteochondrosis of tibia and fibula

Osteochondrosis (juvenile) of:

   proximal tibia [Blount]

   tibial tubercle [Osgood–Schlatter] Tibia vara

M92.6        Juvenile osteochondrosis of tarsus

Osteochondrosis (juvenile) of:

   calcaneum [Sever]

   os tibiale externum [Haglund]

   talus [Diaz]

   tarsal navicular [Köhler]

M92.7        Juvenile osteochondrosis of metatarsus

Osteochondrosis (juvenile) of:

   fifth metatarsus [Iselin]

   second metatarsus [Freiberg]


M92.8        Other specified juvenile osteochondrosis

Calcaneal apophysitis

M92.9        Juvenile osteochondrosis, unspecified

Apophysitis Epiphysitis Osteochondritis Osteochondrosis

 

specified as juvenile, of unspecified site

  M93        Other osteochondropathies

Excl.: osteochondrosis of spine (M42.-)

M93.0        Slipped upper femoral epiphysis (nontraumatic) M93.1            Kienböck’s disease of adults

Adult osteochondrosis of carpal lunate

M93.2        Osteochondritis dissecans

Apophysitis Epiphysitis Osteochondritis Osteochondrosis

 

not specified as adult or juvenile, of unspecified site

 

 

M93.8        Other specified osteochondropathies M93.9                 Osteochondropathy, unspecified

 

 

 

 

  M94        Other disorders of cartilage

[See site code at the beginning of this chapter]

M94.0        Chondrocostal junction syndrome [Tietze]

Costochondritis

M94.1        Relapsing polychondritis M94.2                 Chondromalacia

Excl.: chondromalacia patellae (M22.4)

M94.3        Chondrolysis

M94.8        Other specified disorders of cartilage M94.9     Disorder of cartilage, unspecified


Other disorders of the musculoskeletal system and connective tissue

(M95–M99)

 

  M95        Other acquired deformities of musculoskeletal system and connective tissue

Excl.: acquired:

  absence of limbs and organs (Z89–Z90)

  deformities of limbs (M20–M21)

congenital malformations and deformations of the musculoskeletal system (Q65–Q79)

deforming dorsopathies (M40–M43)

dentofacial anomalies [including malocclusion] (K07.-) postprocedural musculoskeletal disorders (M96.-)

M95.0        Acquired deformity of nose

Excl.: deviated nasal septum (J34.2)

M95.1        Cauliflower ear

Excl.: other acquired deformities of ear (H61.1)

M95.2        Other acquired deformity of head M95.3          Acquired deformity of neck

M95.4        Acquired deformity of chest and rib

M95.5        Acquired deformity of pelvis

Excl.: maternal care for known or suspected disproportion (O33.-) M95.8          Other specified acquired deformities of musculoskeletal system M95.9      Acquired deformity of musculoskeletal system, unspecified

  M96        Postprocedural musculoskeletal disorders, not elsewhere classified

Excl.: arthropathy following intestinal bypass (M02.0) disorders associated with osteoporosis (M80–M81)

presence of functional implants and other devices (Z95–Z97)

M96.0        Pseudarthrosis after fusion or arthrodesis

M96.1        Postlaminectomy syndrome, not elsewhere classified M96.2  Postradiation kyphosis

M96.3        Postlaminectomy kyphosis M96.4       Postsurgical lordosis M96.5      Postradiation scoliosis


M96.6        Fracture of bone following insertion of orthopaedic implant, joint prosthesis, or bone plate

Excl.: complication of internal orthopaedic devices, implants or grafts (T84.-)

M96.8        Other postprocedural musculoskeletal disorders

Instability of joint secondary to removal of joint prosthesis

M96.9        Postprocedural musculoskeletal disorder, unspecified

  M99        Biomechanical lesions, not elsewhere classified

Note: This category should not be used if the condition can be classified elsewhere.

The following supplementary subclassification to indicate the site of lesions is provided for optional use with appropriate subcategories in M99.-; see also note at the beginning of this chapter:

0        Head region

occipitocervical

1        Cervical region

cervicothoracic

2        Thoracic region

thoracolumbar

3        Lumbar region

lumbosacral

4        Sacral region sacrococcygeal sacroiliac

5        Pelvic region

hip pubic

6        Lower extremity

7        Upper extremity acromioclavicular sternoclavicular

8        Rib cage costochondral costovertebral sternochondral

9        Abdomen and othe


CHAPTER XIV

Diseases of the genitourinary system (N00–N99)


Excl.: certain conditions originating in the perinatal period (P00–P96) certain infectious and parasitic diseases (A00–B99)

complications of pregnancy, childbirth and the puerperium (O00–O99) congenital malformations, deformations and chromosomal abnormalities (Q00–Q99)

endocrine, nutritional and metabolic diseases (E00–E90)

injury, poisoning and certain other consequences of external causes (S00–T98)

neoplasms (C00–D48)

symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00–R99)


This chapter contains the following blocks:

N00–N08 Glomerular diseases

N10–N16 Renal tubulo-interstitial diseases N17–N19 Renal failure

N20–N23 Urolithiasis

N25–N29 Other disorders of kidney and ureter N30–N39 Other diseases of urinary system N40–N51 Diseases of male genital organs N60–N64 Disorders of breast

N70–N77 Inflammatory diseases of female pelvic organs N80–N98 Noninflammatory disorders of female genital tract N99 Other disorders of the genitourinary system


Asterisk categories for this chapter are provided as follows:

N08* Glomerular disorders in diseases classified elsewhere

N16* Renal tubulo-interstitial disorders in diseases classified elsewhere N22* Calculus of urinary tract in diseases classified elsewhere

N29* Other disorders of kidney and ureter in diseases classified elsewhere N33* Bladder disorders in diseases classified elsewhere

N37* Urethral disorders in diseases classified elsewhere

N51* Disorders of male genital organs in diseases classified elsewhere N74* Female pelvic inflammatory disorders in diseases classified elsewhere

N77* Vulvovaginal ulceration and inflammation in diseases classified elsewhere

 

Glomerular diseases (N00–N08)

Use additional code, if desired, to identify associated chronic kidney disease (N18.-) .

Use additional code, if desired, to identify external cause (Chapter XX) or presence of renal failure, acute (N17.-) or unspecified, (N19).

Excl.: hypertensive renal disease (I12.-)

The following fourth-character subdivisions classify morphological changes and are for use with categories N00–N07. Subdivisions .0–.8 should not normally be used unless these have been specifically identified (e.g. by renal biopsy or autopsy). The three- character categories relate to clinical syndromes.

.0 Minor glomerular abnormality

Minimal change lesion

.1 Focal and segmental glomerular lesions

Focal and segmental:

hyalinosis

sclerosis

Focal glomerulonephritis

.2 Diffuse membranous glomerulonephritis

.3 Diffuse mesangial proliferative glomerulonephritis

.4 Diffuse endocapillary proliferative glomerulonephritis

.5 Diffuse mesangiocapillary glomerulonephritis

Membranoproliferative glomerulonephritis, types 1 and 3, or NOS

.6 Dense deposit disease

Membranoproliferative glomerulonephritis, type 2

.7 Diffuse crescentic glomerulonephritis

Extracapillary glomerulonephritis

.8 Other

Proliferative glomerulonephritis NOS

.9 Unspecified

 

  N00 Acute nephritic syndrome

[See before N00 for subdivisions]

Incl.: acute:

glomerular disease

glomerulonephritis

nephritis

renal disease NOS

Excl.: acute infectious tubulo-interstitial nephritis (N10) nephritic syndrome NOS (N05.-)


  N01 Rapidly progressive nephritic syndrome

[See before N00 for subdivisions]

Incl.: rapidly progressive:

glomerular disease

glomerulonephritis

nephritis

Excl.: nephritic syndrome NOS (N05.-)


  N02 Recurrent and persistent haematuria

[See before N00 for subdivisions]

Incl.: haematuria:

benign (familial)(of childhood)

with morphological lesion specified in .0-.8 before N00.-

Excl.: haematuria NOS (R31)


  N03 Chronic nephritic syndrome

[See before N00 for subdivisions]

Incl.: chronic:

glomerular disease

glomerulonephritis

nephritis

Excl.: chronic tubulo-interstitial nephritis (N11.-) diffuse sclerosing glomerulonephritis (N18.-) nephritic syndrome NOS (N05.-)


  N04 Nephrotic syndrome

[See before N00 for subdivisions]

Incl.: congenital nephrotic syndrome lipoid nephrosis

 

  N05 Unspecified nephritic syndrome

[See before N00 for subdivisions]

Incl.: glomerular disease glomerulonephritis nephritis

NOS

nephropathy NOS and renal disease NOS with morphological lesion specified in .0–.8 before N00.-

Excl.: nephropathy NOS with no stated morphological lesion (N28.9) renal disease NOS with no stated morphological lesion (N28.9) tubulo-interstitial nephritis NOS (N12)


  N06 Isolated proteinuria with specified morphological lesion

[See before N00 for subdivisions]

Incl.: proteinuria (isolated)(orthostatic)(persistent) with morphological lesion specified in .0–.8 before N00.-

Excl.: proteinuria:

NOS (R80)

Bence–Jones (R80)

gestational (O12.1)

isolated NOS (R80)

orthostatic NOS (N39.2)

persistent NOS (N39.1)


  N07 Hereditary nephropathy, not elsewhere classified

[See before N00 for subdivisions]

Excl.: Alport syndrome (Q87.8)

hereditary amyloid nephropathy (E85.0) nail patella syndrome (Q87.2)

non-neuropathic heredofamilial amyloidosis (E85.0)


  N08* Glomerular disorders in diseases classified elsewhere

Incl.: nephropathy in diseases classified elsewhere

Excl.: renal tubulo-interstitial disorders in diseases classified elsewhere (N16.-*)

N08.0* Glomerular disorders in infectious and parasitic diseases classified elsewhere

Glomerular disorders in:

Plasmodium malariae malaria (B52.0†)

mumps (B26.8†)

schistosomiasis [bilharziasis] (B65.-†)

sepsis (A40–A41†)

strongyloidiasis (B78.-†)

syphilis (A52.7†)

 

N08.1* Glomerular disorders in neoplastic diseases

Glomerular disorders in:

multiple myeloma (C90.0†)

Waldenström macroglobulinaemia (C88.0†)

N08.2* Glomerular disorders in blood diseases and disorders involving the immune mechanism

Glomerular disorders in:

cryoglobulinaemia (D89.1†)

disseminated intravascular coagulation [defibrination syndrome] (D65†)

haemolytic-uraemic syndrome (D59.3†)

Henoch(–Schönlein) purpura (D69.0†)

sickle-cell disorders (D57.-†)

N08.3* Glomerular disorders in diabetes mellitus (E10–E14 with common fourth character .2†)

N08.4* Glomerular disorders in other endocrine, nutritional and metabolic diseases

Glomerular disorders in:

amyloidosis (E85.-†)

Fabry(–Anderson) disease (E75.2†)

lecithin cholesterol acyltransferase deficiency (E78.6†)

N08.5* Glomerular disorders in systemic connective tissue disorders

Glomerular disorders in:

Goodpasture syndrome (M31.0†)

microscopic polyangiitis (M31.7†)

systemic lupus erythematosus (M32.1†)

thrombotic thrombocytopenic purpura (M31.1†)

Wegener granulomatosis (M31.3†)

N08.8* Glomerular disorders in other diseases classified elsewhere

Glomerular disorders in subacute bacterial endocarditis (I33.0†)


Renal tubulo-interstitial diseases (N10–N16)

Incl.: pyelonephritis

Use additional code, if desired, to identify associated chronic kidney disease (N18.-) .

Excl.: pyeloureteritis cystica (N28.8)


  N10 Acute tubulo-interstitial nephritis

Incl.: acute:

infectious interstitial nephritis

pyelitis

pyelonephritis

Use additional code (B95–B98), if desired, to identify infectious agent.

 

  N11 Chronic tubulo-interstitial nephritis

Incl.: chronic:

infectious interstitial nephritis

pyelitis

pyelonephritis

Use additional code (B95–B98), if desired, to identify infectious agent.

N11.0 Nonobstructive reflux-associated chronic pyelonephritis

Pyelonephritis (chronic) associated with (vesicoureteral) reflux

Excl.:  vesicoureteral reflux NOS (N13.7)

N11.1 Chronic obstructive pyelonephritis

Pyelonephritis (chronic) associated with:

anomaly

kinking

obstruction

stricture


of

pelviureteric junction pyeloureteric junction ureter

Excl.: calculous pyelonephritis (N20.9) obstructive uropathy (N13.-)

N11.8 Other chronic tubulo-interstitial nephritis

Nonobstructive chronic pyelonephritis NOS

N11.9 Chronic tubulo-interstitial nephritis, unspecified

Chronic:

interstitial nephritis NOS

pyelitis NOS

pyelonephritis NOS


  N12 Tubulo-interstitial nephritis, not specified as acute or chronic

Incl.: interstitial nephritis NOS pyelitis NOS pyelonephritis NOS

Excl.: calculous pyelonephritis (N20.9)


  N13 Obstructive and reflux uropathy

Excl.: calculus of kidney and ureter without hydronephrosis (N20.-) congenital obstructive defects of renal pelvis and ureter (Q62.0–Q62.3)

obstructive pyelonephritis (N11.1)

N13.0 Hydronephrosis with ureteropelvic junction obstruction

Excl.: with infection (N13.6)

 

N13.1 Hydronephrosis with ureteral stricture, not elsewhere classified

Excl.: with infection (N13.6)

N13.2 Hydronephrosis with renal and ureteral calculous obstruction

Excl.: with infection (N13.6)

N13.3 Other and unspecified hydronephrosis

Excl.: with infection (N13.6)

N13.4 Hydroureter

Excl.: with infection (N13.6)

N13.5 Kinking and stricture of ureter without hydronephrosis

Excl.: with infection (N13.6)

N13.6 Pyonephrosis

Conditions in N13.0–N13.5 with infection Obstructive uropathy with infection

Use additional code (B95–B98), if desired, to identify infectious agent.

N13.7 Vesicoureteral-reflux-associated uropathy

Vesicoureteral reflux:

NOS

with scarring

Excl.: reflux-associated pyelonephritis (N11.0)

N13.8 Other obstructive and reflux uropathy

N13.9 Obstructive and reflux uropathy, unspecified

Urinary tract obstruction NOS


  N14 Drug- and heavy-metal-induced tubulo-interstitial and tubular conditions

Use additional external cause code (Chapter XX), if desired, to identify toxic agent.

N14.0 Analgesic nephropathy

N14.1 Nephropathy induced by other drugs, medicaments and biological substances

N14.2 Nephropathy induced by unspecified drug, medicament or biological substance

N14.3 Nephropathy induced by heavy metals N14.4 Toxic nephropathy, not elsewhere classified

  N15 Other renal tubulo-interstitial diseases

N15.0 Balkan nephropathy

Balkan endemic nephropathy

N15.1 Renal and perinephric abscess

 

N15.8 Other specified renal tubulo-interstitial diseases N15.9 Renal tubulo-interstitial disease, unspecified

Infection of kidney NOS

Excl.: urinary tract infection NOS (N39.0)


  N16* Renal tubulo-interstitial disorders in diseases classified elsewhere

N16.0* Renal tubulo-interstitial disorders in infectious and parasitic diseases classified elsewhere

Renal tubulo-interstitial disorders (due to)(in):

brucellosis (A23.-†)

diphtheria (A36.8†)

salmonella infection (A02.2†)

sepsis (A40–A41†)

toxoplasmosis (B58.8†)

N16.1* Renal tubulo-interstitial disorders in neoplastic diseases

Renal tubulo-interstitial disorders in:

leukaemia (C91–C95†)

lymphoma (C81–C85†, C96.-†)

multiple myeloma (C90.0†)

N16.2* Renal tubulo-interstitial disorders in blood diseases and disorders involving the immune mechanism

Renal tubulo-interstitial disorders in:

mixed cryoglobulinaemia (D89.1†)

sarcoidosis (D86.-†)

N16.3* Renal tubulo-interstitial disorders in metabolic diseases

Renal tubulo-interstitial disorders in:

cystinosis (E72.0†)

glycogen storage disease (E74.0†)

Wilson disease (E83.0†)

N16.4* Renal tubulo-interstitial disorders in systemic connective tissue disorders

Renal tubulo-interstitial disorders in:

sicca syndrome [Sjögren] (M35.0†)

systemic lupus erythematosus (M32.1†)

N16.5* Renal tubulo-interstitial disorders in transplant rejection (T86.-†)

N16.8* Renal tubulo-interstitial disorders in other diseases classified elsewhere

 

Renal failure (N17–N19)

Use additional external cause code (Chapter XX), if desired, to identify external agent.

Excl.: congenital renal failure (P96.0)

drug- and heavy-metal-induced tubulo-interstitial and tubular conditions (N14.-)

extrarenal uraemia (R39.2)

haemolytic-uraemic syndrome (D59.3) hepatorenal syndrome (K76.7) hepatorenal syndrome:

postpartum (O90.4) prerenal uraemia (R39.2) renal failure:

complicating abortion or ectopic or molar pregnancy (O00–O07, O08.4)

following labour and delivery (O90.4)

postprocedural (N99.0)


  N17 Acute renal failure

Incl.: acute renal impairment

N17.0 Acute renal failure with tubular necrosis

Tubular necrosis:

NOS

acute

renal

N17.1 Acute renal failure with acute cortical necrosis

Cortical necrosis:

NOS

acute

renal

N17.2 Acute renal failure with medullary necrosis

Medullary [papillary] necrosis:

NOS

acute

renal

N17.8 Other acute renal failure

N17.9 Acute renal failure, unspecified

 

  N18 Chronic kidney disease

Incl.: chronic renal failure

Use additional code, if desired, to identify underlying disease.

Use additional code, if desired, to identify presence of hypertension.

Excl.: chronic renal failure with hypertension (I12.0)

N18.1 Chronic kidney disease, stage 1

Kidney damage with normal or increased GFR (≥ 90 mL/min)

N18.2 Chronic kidney disease, stage 2

Kidney damage with mild decreased GFR (60–89 mL/min)

N18.3 Chronic kidney disease, stage 3

Kidney damage with moderately decreased GFR (30–59 mL/min)

N18.4 Chronic kidney disease, stage 4

Kidney damage with severely decreased GFR (15–29 mL/min)

N18.5 Chronic kidney disease, stage 5

End-stage kidney disease:

in allograft failure

NOS

on dialysis

without dialysis or transplant Renal retinitis (H32.8*) Uraemic:

apoplexia† (I68.8*)

dementia† (F02.8*)

neuropathy† (G63.8*)

paralysis† (G99.8*)

pericarditis† (I32.8*)

N18.9 Chronic kidney disease, unspecified

Chronic uraemia NOS Chronic renal impairment

Diffuse sclerosing glomerulonephritis NOS



  N19 Unspecified kidney failure

Incl.: renal insufficiency NOS Uraemia NOS

Excl.: kidney failure due to hypertension (I12.0) uraemia of newborn (P96.0)

 

Urolithiasis (N20–N23)


  N20 Calculus of kidney and ureter

Incl.: calculous pyelonephritis

Excl.: with hydronephrosis (N13.2)

N20.0 Calculus of kidney

Nephrolithiasis NOS Renal calculus or stone Staghorn calculus Stone in kidney

N20.1 Calculus of ureter

Ureteric stone

N20.2 Calculus of kidney with calculus of ureter N20.9 Urinary calculus, unspecified

  N21 Calculus of lower urinary tract

Incl.: with cystitis and urethritis

N21.0 Calculus in bladder

Calculus in diverticulum of bladder Urinary bladder stone

Excl.: staghorn calculus (N20.0)

N21.1 Calculus in urethra

N21.8 Other lower urinary tract calculus

N21.9 Calculus of lower urinary tract, unspecified


  N22* Calculus of urinary tract in diseases classified elsewhere

N22.0* Urinary calculus in schistosomiasis [bilharziasis] (B65.-†)

N22.8* Calculus of urinary tract in other diseases classified elsewhere


  N23 Unspecified renal colic

 

Other disorders of kidney and ureter (N25–N29)

Excl.: with urolithiasis (N20–N23)


  N25 Disorders resulting from impaired renal tubular function

Excl.: metabolic disorders classifiable to E70–E90

N25.0 Renal osteodystrophy

Azotaemic osteodystrophy Phosphate-losing tubular disorders Renal:

rickets

short stature

N25.1 Nephrogenic diabetes insipidus

N25.8 Other disorders resulting from impaired renal tubular function

Lightwood–Albright syndrome Renal tubular acidosis NOS

Secondary hyperparathyroidism of renal origin

N25.9 Disorder resulting from impaired renal tubular function, unspecified


  N26 Unspecified contracted kidney

Incl.: atrophy of kidney (terminal) renal sclerosis NOS

Excl.: contracted kidney due to hypertension (I12.-) diffuse sclerosing glomerulonephritis (N18.-)

hypertensive nephrosclerosis (arteriolar)(arteriosclerotic) (I12.-) small kidney of unknown cause (N27.-)


  N27 Small kidney of unknown cause

N27.0 Small kidney, unilateral N27.1 Small kidney, bilateral N27.9 Small kidney, unspecified

  N28 Other disorders of kidney and ureter, not elsewhere classified

Excl.: hydroureter (N13.4) renal disease:

acute NOS (N00.9)

chronic NOS (N03.9) ureteric kinking and stricture:

with hydronephrosis (N13.1)

without hydronephrosis (N13.5)

 

N28.0 Ischaemia and infarction of kidney

Renal artery:

embolism

obstruction

occlusion

thrombosis Renal infarct

Excl.: Goldblatt kidney (I70.1) renal artery (extrarenal part):

atherosclerosis (I70.1)

congenital stenosis (Q27.1)

N28.1 Cyst of kidney

Cyst (acquired) (multiple)(solitary) of kidney

Excl.: cystic kidney disease (congenital) (Q61.-)

N28.8 Other specified disorders of kidney and ureter

Hypertrophy of kidney Megaloureter Nephroptosis

Pyelitis

Pyeloureteritis Ureteritis

cystica

Ureterocele

N28.9 Disorder of kidney and ureter, unspecified

Nephropathy NOS Renal disease NOS

Excl.: nephropathy NOS and renal disease NOS with morphological lesion specified in .0–.8 before N00.- (N05.-)


  N29* Other disorders of kidney and ureter in diseases classified elsewhere

N29.0* Late syphilis of kidney (A52.7†)

N29.1* Other disorders of kidney and ureter in infectious and parasitic diseases classified elsewhere

Disorders of kidney and ureter in:

schistosomiasis [bilharziasis] (B65.-†)

tuberculosis (A18.1†)

N29.8* Other disorders of kidney and ureter in other diseases classified elsewhere

Cystine storage disease (E72.0†)

 

Other diseases of urinary system (N30–N39)

Excl.: urinary infection (complicating):

abortion or ectopic or molar pregnancy (O00–O07, O08.8)

pregnancy, childbirth and the puerperium (O23.-, O75.3, O86.2)

with urolithiasis (N20–N23)


  N30 Cystitis

Use additional code, if desired, to identify infectious agent (B95–B98) or responsible external agent (Chapter XX).

Excl.: prostatocystitis (N41.3)

N30.0 Acute cystitis

Excl.: irradiation cystitis (N30.4) trigonitis (N30.3)

N30.1 Interstitial cystitis (chronic) N30.2 Other chronic cystitis N30.3 Trigonitis

Urethrotrigonitis

N30.4 Irradiation cystitis N30.8 Other cystitis

Abscess of bladder

N30.9 Cystitis, unspecified


  N31 Neuromuscular dysfunction of bladder, not elsewhere classified

Excl.: cord bladder NOS (G95.8)

due to spinal cord lesion (G95.8)

neurogenic bladder due to cauda equina syndrome (G83.4) urinary incontinence:

NOS (R32)

specified (N39.3–N39.4)

N31.0 Uninhibited neuropathic bladder, not elsewhere classified N31.1 Reflex neuropathic bladder, not elsewhere classified N31.2 Flaccid neuropathic bladder, not elsewhere classified

Neuropathic bladder:

• atonic (motor)(sensory)

• autonomous

• nonreflex

N31.8 Other neuromuscular dysfunction of bladder

 

N31.9 Neuromuscular dysfunction of bladder, unspecified

Neurogenic bladder dysfunction NOS


  N32 Other disorders of bladder

Excl.: calculus in bladder (N21.0) cystocele (N81.1)

hernia or prolapse of bladder, female (N81.1)

N32.0 Bladder-neck obstruction

Bladder-neck stenosis (acquired)

N32.1 Vesicointestinal fistula

Vesicorectal fistula

N32.2 Vesical fistula, not elsewhere classified

Excl.: fistula between bladder and female genital tract (N82.0–N82.1)

N32.3 Diverticulum of bladder

Diverticulitis of bladder

Excl.: calculus in diverticulum of bladder (N21.0)

N32.4 Rupture of bladder, nontraumatic N32.8 Other specified disorders of bladder

Bladder:

calcified

contracted

overactive

N32.9 Bladder disorder, unspecified


  N33* Bladder disorders in diseases classified elsewhere

N33.0* Tuberculous cystitis (A18.1†)

N33.8* Bladder disorders in other diseases classified elsewhere

Bladder disorder in schistosomiasis [bilharziasis] (B65.-†)


  N34 Urethritis and urethral syndrome

Use additional code (B95–B98), if desired, to identify infectious agent.

Excl.: Reiter disease (M02.3)

urethritis in diseases with a predominantly sexual mode of transmission (A50–A64)

urethrotrigonitis (N30.3)

N34.0 Urethral abscess

Abscess (of):

Cowper gland

Littré gland

periurethral

urethral (gland)

Excl.: urethral caruncle (N36.2)

 

N34.1 Nonspecific urethritis

Urethritis:

nongonococcal

nonvenereal

N34.2 Other urethritis

Meatitis, urethral

Ulcer of urethra (meatus) Urethritis:

NOS

postmenopausal

N34.3 Urethral syndrome, unspecified


  N35 Urethral stricture

Excl.: postprocedural urethral stricture (N99.1)

N35.0 Post-traumatic urethral stricture

Stricture of urethra as a sequela of:

childbirth

injury

N35.1 Postinfective urethral stricture, not elsewhere classified N35.8 Other urethral stricture

N35.9 Urethral stricture, unspecified

Pinhole meatus NOS


  N36 Other disorders of urethra

N36.0 Urethral fistula False urethral passage Fistula:

urethroperineal

urethrorectal

urinary NOS

Excl.: fistula:

urethroscrotal (N50.8)

urethrovaginal (N82.1) N36.1 Urethral diverticulum N36.2 Urethral caruncle

N36.3 Prolapsed urethral mucosa

Prolapse of urethra Urethrocele, male

Excl.: urethrocele:

congenital (Q64.7)

female (N81.0)

 

N36.8 Other specified disorders of urethra N36.9 Urethral disorder, unspecified

  N37* Urethral disorders in diseases classified elsewhere

N37.0* Urethritis in diseases classified elsewhere

Candidal urethritis (B37.4†)

N37.8* Other urethral disorders in diseases classified elsewhere


  N39 Other disorders of urinary system

Excl.: haematuria:

NOS (R31)

recurrent and persistent (N02.-)

with specified morphological lesion (N02.-) proteinuria NOS (R80)

N39.0 Urinary tract infection, site not specified

Use additional code (B95–B98), if desired, to identify infectious agent.

N39.1 Persistent proteinuria, unspecified

Excl.: complicating pregnancy, childbirth and the puerperium (O11–O15) with specified morphological lesion (N06.-)

N39.2 Orthostatic proteinuria, unspecified

Excl.: with specified morphological lesion (N06.-)

N39.3 Stress incontinence

Use additional code (N32.8), if desired, to identify overactive bladder or detrusor muscle hyperactivity.

N39.4 Other specified urinary incontinence

Overflow Reflex

Urge

incontinence

Use additional code (N32.8), if desired, to identify overactive bladder or detrusor muscle hyperactivity.

Excl.: enuresis NOS (R32) urinary incontinence (of):

NOS (R32)

nonorganic origin (F98.0)

N39.8 Other specified disorders of urinary system N39.9 Disorder of urinary system, unspecified

 

Diseases of male genital organs (N40–N51)


  N40 Hyperplasia of prostate

Incl.: adenofibromatous hypertrophy enlargement (benign) hypertrophy (benign)

of prostate

median bar (prostate) prostatic obstruction NOS

Excl.: benign neoplasms, of prostate (D29.1)


  N41 Inflammatory diseases of prostate

Use additional code (B95–B98), if desired, to identify infectious agent.

N41.0 Acute prostatitis N41.1 Chronic prostatitis N41.2 Abscess of prostate N41.3 Prostatocystitis

N41.8 Other inflammatory diseases of prostate

N41.9 Inflammatory disease of prostate, unspecified

Prostatitis NOS


  N42 Other disorders of prostate

N42.0 Calculus of prostate

Prostatic stone

N42.1 Congestion and haemorrhage of prostate N42.2 Atrophy of prostate

N42.3 Dysplasia of prostate

Low-grade dysplasia

Excl.: high-grade dysplasia of prostate (D07.5) N42.8 Other specified disorders of prostate N42.9 Disorder of prostate, unspecified

  N43 Hydrocele and spermatocele

Incl.: hydrocele of spermatic cord, testis or tunica vaginalis

Excl.: congenital hydrocele (P83.5)

N43.0 Encysted hydrocele N43.1 Infected hydrocele

 

Use additional code (B95–B98), if desired, to identify infectious agent.

N43.2 Other hydrocele

N43.3 Hydrocele, unspecified N43.4 Spermatocele

  N44 Torsion of testis

Incl.: torsion of:

epididymis

spermatic cord

testicle


  N45 Orchitis and epididymitis

Use additional code (B95–B98), if desired, to identify infectious agent.

N45.0 Orchitis, epididymitis and epididymo-orchitis with abscess

Abscess of epididymis or testis

N45.9 Orchitis, epididymitis and epididymo-orchitis without abscess

Epididymitis NOS Orchitis NOS


  N46 Male infertility

Incl.: azoospermia NOS oligospermia NOS


  N47 Redundant prepuce, phimosis and paraphimosis

Incl.: adherent prepuce

tight foreskin


  N48 Other disorders of penis

N48.0 Leukoplakia of penis

Balanitis xerotica obliterans Kraurosis of penis

Excl.: carcinoma in situ of penis (D07.4)

N48.1 Balanoposthitis

Balanitis

Use additional code (B95–B98), if desired, to identify infectious agent.

N48.2 Other inflammatory disorders of penis

Abscess Boil Carbuncle Cellulitis

of corpus cavernosum and penis

Cavernitis (penis)

Use additional code (B95–B98), if desired, to identify infectious agent.

 

N48.3 Priapism

Painful erection

N48.4 Impotence of organic origin

Use additional code, if desired, to identify cause.

Excl.: psychogenic impotence (F52.2)

N48.5 Ulcer of penis

N48.6 Induratio penis plastica

Peyronie disease

Plastic induration of penis

N48.8 Other specified disorders of penis

Atrophy Hypertrophy Thrombosis

of corpus cavernosum and penis

N48.9 Disorder of penis, unspecified


  N49 Inflammatory disorders of male genital organs, not elsewhere classified

Use additional code (B95–B98), if desired, to identify infectious agent.

Excl.: inflammation of penis (N48.1–N48.2) orchitis and epididymitis (N45.-)

N49.0 Inflammatory disorders of seminal vesicle

Vesiculitis NOS

N49.1 Inflammatory disorders of spermatic cord, tunica vaginalis and vas deferens

Vasitis

N49.2 Inflammatory disorders of scrotum

N49.8 Inflammatory disorders of other specified male genital organs

Inflammation of multiple sites in male genital organs

N49.9 Inflammatory disorder of unspecified male genital organ

Abscess Boil Carbuncle Cellulitis

of unspecified male genital organ

  N50 Other disorders of male genital organs

Excl.: torsion of testis (N44)

N50.0 Atrophy of testis

N50.1 Vascular disorders of male genital organs

Haematocele NOS Haemorrhage Thrombosis

of male genital organs

 

N50.8 Other specified disorders of male genital organs

Atrophy Hypertrophy Oedema Ulcer

of scrotum, seminal vesicle, spermatic cord, testis [except atrophy], tunica vaginalis and vas deferens

Chylocele, tunica vaginalis (nonfilarial) NOS Fistula, urethroscrotal

Stricture of:

spermatic cord

tunica vaginalis

vas deferens

N50.9 Disorder of male genital organs, unspecified


  N51* Disorders of male genital organs in diseases classified elsewhere

N51.0* Disorders of prostate in diseases classified elsewhere

Prostatitis:

gonococcal (A54.2†)

trichomonal (A59.0†)

tuberculous (A18.1†)

N51.1* Disorders of testis and epididymis in diseases classified elsewhere

Chlamydial:

epididymitis (A56.1†)

orchitis (A56.1†) Gonococcal:

epididymitis (A54.2†)

orchitis (A54.2†) Mumps orchitis (B26.0†) Tuberculosis of:

epididymis (A18.1†)

testis (A18.1†)

N51.2* Balanitis in diseases classified elsewhere

Balanitis:

amoebic (A06.8†)

candidal (B37.4†)

N51.8* Other disorders of male genital organs in diseases classified elsewhere

Filarial chylocele, tunica vaginalis (B74.-†)

Herpesviral [herpes simplex] infection of male genital tract (A60.0†) Tuberculosis of seminal vesicle (A18.1†)

 

Disorders of breast (N60–N64)

Excl.: disorders of breast associated with childbirth (O91–O92)


  N60 Benign mammary dysplasia

Incl.: fibrocystic mastopathy

N60.0 Solitary cyst of breast

Cyst of breast

N60.1 Diffuse cystic mastopathy

Cystic breast

Excl.: with epithelial proliferation (N60.3)

N60.2 Fibroadenosis of breast

Excl.: fibroadenoma of breast (D24)

N60.3 Fibrosclerosis of breast

Cystic mastopathy with epithelial proliferation

N60.4 Mammary duct ectasia

N60.8 Other benign mammary dysplasias N60.9 Benign mammary dysplasia, unspecified

  N61 Inflammatory disorders of breast

Incl.: abscess (acute)(chronic)(nonpuerperal) of:

areola

breast

carbuncle of breast

mastitis (acute)(subacute)(nonpuerperal):

NOS

infective

Excl.: neonatal infective mastitis (P39.0)


  N62 Hypertrophy of breast

Incl.: gynaecomastia

hypertrophy of breast:

NOS

massive pubertal


  N63 Unspecified lump in breast

Incl.: nodule(s) NOS in breast


  N64 Other disorders of breast

N64.0 Fissure and fistula of nipple

 

N64.1 Fat necrosis of breast

Fat necrosis (segmental) of breast

N64.2 Atrophy of breast

N64.3 Galactorrhoea not associated with childbirth N64.4 Mastodynia

N64.5 Other signs and symptoms in breast

Induration of breast Nipple discharge Retraction of nipple

N64.8 Other specified disorders of breast

Galactocele

Subinvolution of breast (postlactational)

N64.9 Disorder of breast, unspecified


Inflammatory diseases of female pelvic organs (N70–N77)

Excl.: those complicating:

abortion or ectopic or molar pregnancy (O00–O07, O08.0)

pregnancy, childbirth and the puerperium (O23.-, O75.3, O85, O86.-)


  N70 Salpingitis and oophoritis

Incl.: abscess (of):

fallopian tube

ovary

tubo-ovarian pyosalpinx salpingo-oophoritis

tubo-ovarian inflammatory disease

Use additional code (B95–B98), if desired, to identify infectious agent.

N70.0 Acute salpingitis and oophoritis N70.1 Chronic salpingitis and oophoritis

Hydrosalpinx

N70.9 Salpingitis and oophoritis, unspecified


  N71 Inflammatory disease of uterus, except cervix

Incl.: endo(myo)metritis

metritis

myometritis

pyometra

uterine abscess

Use additional code (B95–B98), if desired, to identify infectious agent.

 

N71.0 Acute inflammatory disease of uterus N71.1 Chronic inflammatory disease of uterus

N71.9 Inflammatory disease of uterus, unspecified


  N72 Inflammatory disease of cervix uteri

Incl.: cervicitis

endocervicitis exocervicitis

with or without erosion or ectropion

Use additional code (B95–B98), if desired, to identify infectious agent.

Excl.: erosion and ectropion of cervix without cervicitis (N86)


  N73 Other female pelvic inflammatory diseases

Use additional code (B95–B98), if desired, to identify infectious agent.

N73.0 Acute parametritis and pelvic cellulitis

Abscess of:

broad ligament

parametrium

Pelvic cellulitis, female

specified as acute

N73.1 Chronic parametritis and pelvic cellulitis

Any condition in N73.0 specified as chronic

N73.2 Unspecified parametritis and pelvic cellulitis

Any condition in N73.0 unspecified whether acute or chronic

N73.3 Female acute pelvic peritonitis N73.4 Female chronic pelvic peritonitis

N73.5 Female pelvic peritonitis, unspecified

N73.6 Female pelvic peritoneal adhesions

Excl.:  postprocedural pelvic peritoneal adhesions (N99.4)

N73.8 Other specified female pelvic inflammatory diseases N73.9 Female pelvic inflammatory disease, unspecified

Female pelvic infection or inflammation NOS


  N74* Female pelvic inflammatory disorders in diseases classified elsewhere

N74.0* Tuberculous infection of cervix uteri (A18.1†)

N74.1* Female tuberculous pelvic inflammatory disease (A18.1†)

Tuberculous endometritis

N74.2* Female syphilitic pelvic inflammatory disease (A51.4†, A52.7†) N74.3* Female gonococcal pelvic inflammatory disease (A54.2†)

 

N74.4* Female chlamydial pelvic inflammatory disease (A56.1†)

N74.8* Female pelvic inflammatory disorders in other diseases classified elsewhere


  N75 Diseases of Bartholin gland

N75.0 Cyst of Bartholin gland N75.1 Abscess of Bartholin gland

N75.8 Other diseases of Bartholin gland

Bartholinitis

N75.9 Disease of Bartholin gland, unspecified


  N76 Other inflammation of vagina and vulva

Use additional code (B95–B98), if desired, to identify infectious agent.

Excl.: senile (atrophic) vaginitis (N95.2)

N76.0 Acute vaginitis

Vaginitis NOS Vulvovaginitis:

NOS

acute

N76.1 Subacute and chronic vaginitis

Vulvovaginitis:

chronic

subacute

N76.2 Acute vulvitis

Vulvitis NOS

N76.3 Subacute and chronic vulvitis N76.4 Abscess of vulva

Furuncle of vulva

N76.5 Ulceration of vagina N76.6 Ulceration of vulva

N76.8 Other specified inflammation of vagina and vulva


  N77* Vulvovaginal ulceration and inflammation in diseases classified elsewhere

N77.0* Ulceration of vulva in infectious and parasitic diseases classified elsewhere

Ulceration of vulva in:

herpesviral [herpes simplex] infection (A60.0†)

tuberculosis (A18.1†)

 

N77.1* Vaginitis, vulvitis and vulvovaginitis in infectious and parasitic diseases classified elsewhere

Vaginitis, vulvitis and vulvovaginitis in:

candidiasis (B37.3†)

herpesviral [herpes simplex] infection (A60.0†)

pinworm infection (B80†)

N77.8* Vulvovaginal ulceration and inflammation in other diseases classified elsewhere

Ulceration of vulva in Behçet disease (M35.2†)


Noninflammatory disorders of female genital tract (N80–N98)


  N80 Endometriosis

N80.0 Endometriosis of uterus

Adenomyosis

N80.1 Endometriosis of ovary

N80.2 Endometriosis of fallopian tube N80.3 Endometriosis of pelvic peritoneum

N80.4 Endometriosis of rectovaginal septum and vagina N80.5 Endometriosis of intestine

N80.6 Endometriosis in cutaneous scar

N80.8 Other endometriosis

Endometriosis of thorax

N80.9 Endometriosis, unspecified



  N81 Female genital prolapse

Excl.: genital prolapse complicating pregnancy, labour or delivery (O34.5)

prolapse and hernia of ovary and fallopian tube (N83.4) prolapse of vaginal vault after hysterectomy (N99.3)

N81.0 Female urethrocele

Excl.: congenital (Q64.7) urethrocele with:

cystocele (N81.1)

prolapse of uterus (N81.2–N81.4)

N81.1 Cystocele

Cystocele with urethrocele

 

Prolapse of (anterior) vaginal (wall) NOS

Excl.: cystocele with prolapse of uterus (N81.2–N81.4)

N81.2 Incomplete uterovaginal prolapse

Prolapse of cervix NOS Uterine prolapse:

first–degree

second–degree

N81.3 Complete uterovaginal prolapse

Procidentia (uteri) NOS Third–degree uterine prolapse

N81.4 Uterovaginal prolapse, unspecified

Prolapse of uterus NOS

N81.5 Vaginal enterocele

Excl.: enterocele with prolapse of uterus (N81.2–N81.4)

N81.6 Rectocele

Prolapse of posterior vaginal wall

Excl.: rectal prolapse (K62.3)

rectocele with prolapse of uterus (N81.2–N81.4)

N81.8 Other female genital prolapse

Deficient perineum

Old laceration of muscles of pelvic floor

N81.9 Female genital prolapse, unspecified


  N82 Fistulae involving female genital tract

Excl.: vesicointestinal fistulae (N32.1)

N82.0 Vesicovaginal fistula

N82.1 Other female urinary-genital tract fistulae

Fistula:

cervicovesical

ureterovaginal

urethrovaginal

uteroureteric

uterovesical

N82.2 Fistula of vagina to small intestine N82.3 Fistula of vagina to large intestine

Rectovaginal fistula

N82.4 Other female intestinal-genital tract fistulae

Intestinouterine fistula

N82.5 Female genital tract-skin fistulae

Fistula:

uterus to abdominal wall

vaginoperineal

 

N82.8 Other female genital tract fistulae N82.9 Female genital tract fistula, unspecified

  N83 Noninflammatory disorders of ovary, fallopian tube and broad ligament

Excl.: hydrosalpinx (N70.1)

N83.0 Follicular cyst of ovary

Cyst of graafian follicle

Haemorrhagic follicular cyst (of ovary)

N83.1 Corpus luteum cyst

Haemorrhagic corpus luteum cyst

N83.2 Other and unspecified ovarian cysts

Retention cyst Simple cyst of ovary

Excl.: ovarian cyst:

developmental (Q50.1)

neoplastic (D27)

polycystic ovarian syndrome (E28.2)

N83.3 Acquired atrophy of ovary and fallopian tube N83.4 Prolapse and hernia of ovary and fallopian tube

N83.5 Torsion of ovary, ovarian pedicle and fallopian tube

Torsion:

accessory tube

hydatid of Morgagni

N83.6 Haematosalpinx

Excl.: haematosalpinx with:

haematocolpos (N89.7)

haematometra (N85.7)

N83.7 Haematoma of broad ligament

N83.8 Other noninflammatory disorders of ovary, fallopian tube and broad ligament

Broad ligament laceration syndrome [Allen–Masters]

N83.9 Noninflammatory disorder of ovary, fallopian tube and broad ligament, unspecified


  N84 Polyp of female genital tract

Excl.: adenomatous polyp (D28.-) placental polyp (O90.8)

 


N84.0 Polyp of corpus uteri

Polyp of:

endometrium

uterus NOS

Excl.: polypoid endometrial hyperplasia (N85.0)

N84.1 Polyp of cervix uteri

Mucous polyp of cervix

N84.2 Polyp of vagina N84.3 Polyp of vulva

Polyp of labia

N84.8 Polyp of other parts of female genital tract N84.9 Polyp of female genital tract, unspecified

  N85 Other noninflammatory disorders of uterus, except cervix

Excl.: endometriosis (N80.-)

inflammatory diseases of uterus (N71.-) noninflammatory disorders of cervix except malposition (N86–N88)

polyp of corpus uteri (N84.0) uterine prolapse (N81.-)

N85.0 Endometrial glandular hyperplasia

Hyperplasia of endometrium:

NOS

cystic

glandular-cystic

polypoid

N85.1 Endometrial adenomatous hyperplasia

Hyperplasia of endometrium, atypical (adenomatous)

N85.2 Hypertrophy of uterus

Bulky or enlarged uterus

Excl.: puerperal hypertrophy of uterus (O90.8)

N85.3 Subinvolution of uterus

Excl.: puerperal subinvolution of uterus (O90.8)

N85.4 Malposition of uterus

Anteversion Retroflexion Retroversion

of uterus

Excl.: that complicating pregnancy, labour or delivery (O34.5, O65.5)

 

N85.5 Inversion of uterus

Excl.: current obstetric trauma (O71.2) postpartum inversion of uterus (O71.2)

N85.6 Intrauterine synechiae N85.7 Haematometra

Haematosalpinx with haematometra

Excl.: haematometra with haematocolpos (N89.7)

N85.8 Other specified noninflammatory disorders of uterus

Atrophy of uterus, acquired Fibrosis of uterus NOS

N85.9 Noninflammatory disorder of uterus, unspecified

Disorder of uterus NOS


  N86 Erosion and ectropion of cervix uteri

Incl.: decubitus (trophic) ulcer eversion of cervix

Excl.: with cervicitis (N72)


  N87 Dysplasia of cervix uteri

Excl.: carcinoma in situ of cervix (D06.-)

N87.0 Mild cervical dysplasia

Cervical intraepithelial neoplasia [CIN], grade I Low-grade squamous intraepithelial lesion (LSIL)

N87.1 Moderate cervical dysplasia

Cervical intraepithelial neoplasia [CIN], grade II

N87.2 Severe cervical dysplasia, not elsewhere classified

Severe cervical dysplasia NOS

Excl.: cervical intraepithelial neoplasia [CIN], grade III, with or without mention of severe dysplasia (D06.-)

N87.9 Dysplasia of cervix uteri, unspecified


  N88 Other noninflammatory disorders of cervix uteri

Excl.: inflammatory disease of cervix (N72) polyp of cervix (N84.1)

N88.0 Leukoplakia of cervix uteri N88.1 Old laceration of cervix uteri

Adhesions of cervix

Excl.: current obstetric trauma (O71.3)

 

N88.2 Stricture and stenosis of cervix uteri

Excl.: complicating labour (O65.5)

N88.3 Incompetence of cervix uteri

Investigation and management of (suspected) cervical incompetence in a nonpregnant woman

Excl.: affecting fetus or newborn (P01.0) complicating pregnancy (O34.3)

N88.4 Hypertrophic elongation of cervix uteri

N88.8 Other specified noninflammatory disorders of cervix uteri

Excl.: current obstetric trauma (O71.3)

N88.9 Noninflammatory disorder of cervix uteri, unspecified


  N89 Other noninflammatory disorders of vagina

Excl.: carcinoma in situ of vagina (D07.2) inflammation of vagina (N76.-) senile (atrophic) vaginitis (N95.2) trichomonal leukorrhoea (A59.0)

N89.0 Mild vaginal dysplasia

Vaginal intraepithelial neoplasia [VAIN], grade I

N89.1 Moderate vaginal dysplasia

Vaginal intraepithelial neoplasia [VAIN], grade II

N89.2 Severe vaginal dysplasia, not elsewhere classified

Severe vaginal dysplasia NOS

Excl.: vaginal intraepithelial neoplasia [VAIN], grade III, with or without mention of severe dysplasia (D07.2)

N89.3 Dysplasia of vagina, unspecified N89.4 Leukoplakia of vagina

N89.5 Stricture and atresia of vagina

Vaginal:

adhesions

stenosis

Excl.: postoperative adhesions of vagina (N99.2)

N89.6 Tight hymenal ring

Rigid hymen Tight introitus

Excl.: imperforate hymen (Q52.3)

N89.7 Haematocolpos

Haematocolpos with haematometra or haematosalpinx

 

N89.8 Other specified noninflammatory disorders of vagina

Leukorrhoea NOS Old vaginal laceration

Pessary ulcer of vagina

Excl.: current obstetric trauma (O70.-, O71.4, O71.7–O71.8) old laceration involving muscles of pelvic floor (N81.8)

N89.9 Noninflammatory disorder of vagina, unspecified


  N90 Other noninflammatory disorders of vulva and perineum

Excl.: carcinoma in situ of vulva (D07.1)

current obstetric trauma (O70.-, O71.7–O71.8) inflammation of vulva (N76.-)

N90.0 Mild vulvar dysplasia

Vulvar intraepithelial neoplasia [VIN], grade I

N90.1 Moderate vulvar dysplasia

Vulvar intraepithelial neoplasia [VIN], grade II

N90.2 Severe vulvar dysplasia, not elsewhere classified

Severe vulvar dysplasia NOS

Excl.: vulvar intraepithelial neoplasia grade III, [VIN] with or without mention of severe dysplasia (D07.1)

N90.3 Dysplasia of vulva, unspecified N90.4 Leukoplakia of vulva



N90.5 Atrophy of vulva

Stenosis of vulva

N90.6 Hypertrophy of vulva

Hypertrophy of labia

N90.7 Vulvar cyst

N90.8 Other specified noninflammatory disorders of vulva and perineum

Adhesions of vulva Hypertrophy of clitoris

N90.9 Noninflammatory disorder of vulva and perineum, unspecified


  N91 Absent, scanty and rare menstruation

Excl.: ovarian dysfunction (E28.-)

N91.0 Primary amenorrhoea

Failure to start menstruation at puberty.

 

N91.1 Secondary amenorrhoea

Absence of menstruation in a woman who had previously menstruated.

N91.2 Amenorrhoea, unspecified

Absence of menstruation NOS

N91.3 Primary oligomenorrhoea

Menstruation which is scanty or rare from the start.

N91.4 Secondary oligomenorrhoea

Scanty and rare menstruation in a woman with previously normal periods.

N91.5 Oligomenorrhoea, unspecified

Hypomenorrhoea NOS


  N92 Excessive, frequent and irregular menstruation

Excl.: postmenopausal bleeding (N95.0)

N92.0 Excessive and frequent menstruation with regular cycle

Heavy periods NOS Menorrhagia NOS Polymenorrhoea

N92.1 Excessive and frequent menstruation with irregular cycle

Irregular intermenstrual bleeding

Irregular, shortened intervals between menstrual bleeding Menometrorrhagia

Metrorrhagia

N92.2 Excessive menstruation at puberty

Excessive bleeding associated with onset of menstrual periods Pubertal menorrhagia

Puberty bleeding

N92.3 Ovulation bleeding

Regular intermenstrual bleeding

N92.4 Excessive bleeding in the premenopausal period

Menorrhagia or metrorrhagia:

climacteric

menopausal

preclimacteric

premenopausal

N92.5 Other specified irregular menstruation N92.6 Irregular menstruation, unspecified

Irregular:

bleeding NOS

periods NOS

Excl.: irregular menstruation with:

lengthened intervals or scanty bleeding (N91.3–N91.5)

shortened intervals or excessive bleeding (N92.1)

 

  N93 Other abnormal uterine and vaginal bleeding

Excl.: neonatal vaginal haemorrhage (P54.6) pseudomenses (P54.6)

N93.0 Postcoital and contact bleeding

N93.8 Other specified abnormal uterine and vaginal bleeding

Dysfunctional or functional uterine or vaginal bleeding NOS

N93.9 Abnormal uterine and vaginal bleeding, unspecified


  N94 Pain and other conditions associated with female genital organs and menstrual cycle

N94.0 Mittelschmerz

N94.1 Dyspareunia

Excl.: psychogenic dyspareunia (F52.6)

N94.2 Vaginismus

Excl.: psychogenic vaginismus (F52.5) N94.3 Premenstrual tension syndrome N94.4 Primary dysmenorrhoea

N94.5 Secondary dysmenorrhoea N94.6 Dysmenorrhoea, unspecified

N94.8 Other specified conditions associated with female genital organs and menstrual cycle

N94.9 Unspecified condition associated with female genital organs and menstrual cycle


  N95 Menopausal and other perimenopausal disorders

Excl.: excessive bleeding in the premenopausal period (N92.4) postmenopausal:

osteoporosis (M81.0)

osteoporosis

– with pathological fracture (M80.0)

urethritis (N34.2)

premature menopause NOS (E28.3)

N95.0 Postmenopausal bleeding

Excl.: that associated with artificial menopause (N95.3)

N95.1 Menopausal and female climacteric states Symptoms such as flushing, sleeplessness, headache, lack of concentration, associated with menopause

Excl.: those associated with artificial menopause (N95.3)

 

N95.2 Postmenopausal atrophic vaginitis

Senile (atrophic) vaginitis

Excl.: that associated with artificial menopause (N95.3)

N95.3 States associated with artificial menopause

Post-artificial-menopause syndrome

N95.8 Other specified menopausal and perimenopausal disorders N95.9 Menopausal and perimenopausal disorder, unspecified

  N96 Habitual aborter

Incl.: investigation or care in a nonpregnant woman relative infertility

Excl.: currently pregnant (O26.2)

with current abortion (O03–O06)


  N97 Female infertility

Incl.: inability to achieve a pregnancy sterility, female NOS

Excl.: relative infertility (N96)

N97.0 Female infertility associated with anovulation N97.1 Female infertility of tubal origin

Associated with congenital anomaly of tube

Tubal:

block

occlusion

stenosis

N97.2 Female infertility of uterine origin Associated with congenital anomaly of uterus Nonimplantation of ovum

N97.3 Female infertility of cervical origin

N97.4 Female infertility associated with male factors N97.8 Female infertility of other origin

N97.9 Female infertility, unspecified


  N98 Complications associated with artificial fertilization

N98.0 Infection associated with artificial insemination N98.1 Hyperstimulation of ovaries

Hyperstimulation of ovaries:

NOS

associated with induced ovulation

 

N98.2 Complications of attempted introduction of fertilized ovum following in vitro fertilization

N98.3 Complications of attempted introduction of embryo in embryo transfer

N98.8 Other complications associated with artificial fertilization

Complications of artificial insemination by:

donor

husband

N98.9 Complication associated with artificial fertilization, unspecified


Other disorders of the genitourinary system (N99)


  N99 Postprocedural disorders of genitourinary system, not elsewhere classified

Excl.: irradiation cystitis (N30.4)

post-oophorectomy osteoporosis (M81.1) post-oophorectomy osteoporosis:

with pathological fracture (M80.1)

states associated with artificial menopause (N95.3)

N99.0 Postprocedural renal failure N99.1 Postprocedural urethral stricture

Postcatheterization urethral stricture

N99.2 Postoperative adhesions of vagina

N99.3 Prolapse of vaginal vault after hysterectomy N99.4 Postprocedural pelvic peritoneal adhesions N99.5 Malfunction of external stoma of urinary tract

N99.8 Other postprocedural disorders of genitourinary system

Residual ovary syndrome

N99.9 Postprocedural disorder of genitourinary system, unspecified






 




Hajriah Fajar Hajriah Fajar (lahir pada bulan Desember 1987) adalah seorang seniman, penulis, dan kreator konten asal Indonesia. Ia lahir dan dibesarkan di sebuah kampung di Kabupaten Bogor. Sebelum terjun ke dunia seni dan tulis-menulis, Fajar pernah bekerja sebagai tukang parkir profesional di beberapa tempat, antara lain Gedung Hijau Arkadia, Plaza Senayan, dan Kafe Lacodefin Kemang. Setelah lulus dari Sekolah Menengah Atas, Fajar melanjutkan pendidikannya di Universitas Nusamandiri, di mana ia memperoleh gelar S1 Komputer Program Dual Degree pada tahun 2019. Setelah lulus, ia bekerja di berbagai perusahaan teknologi dan IT, dan saat ini bekerja di salah satu rumah sakit swasta di Jakarta sebagai IT. Selain bekerja di dunia IT, Fajar juga aktif di media sosial seperti Instagram, Twitter, dan Facebook, di mana ia sering membagikan pemikiran, karya seni, serta konten-konten menarik lainnya. Ia juga menulis di blog pribadinya di hajriahfajar.com dan membuat konten video di kanal YouTube bernama Hajriah Fajar.Fajar diakui sebagai salah satu sosok yang inspiratif dan memotivasi banyak orang untuk berkreasi dan berinovasi dalam bidang seni dan teknologi.

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