ILDS

Application to Dermatology of International Classification of Disease (ICD-10)

 


ICD sorted by Disorder:
Kaposi's sarcoma, NOS - Kinky hair disease

ICD Code Disorder
C46.900:
Kaposi's sarcoma, NOS
C46.020:
Kaposi's sarcoma, sporadic
D69.507:
Kasabach-Merritt syndrome
D69.507:
Kasabach-Merritt syndrome
B65.210:
Katayama disease
M30.300:
Kawasaki disease
M30.300:
Kawasaki disease
L91.000:
Keloid
D23.L71:
Keratoacanthoma
M35.010:
Keratoconjunctivitis sicca
L85.110:
Keratoderma climactericum
L85.140:
Keratoderma, acquired
Q82.832:
Keratoderma, progressive palmoplantar (Greither)
Q82.832:
Keratoderma, progressive palmoplantar (Greither)
L08.850:
Keratolysis, pitted
L08.850:
Keratoma plantare sulcatum
B36.100:
Keratomycosis nigricans palmaris
E50.810:
Keratosis follicular due to vitamin A deficiency
B35.020:
Kerion
B35.020:
Kerion (due to tinea elsewhere classified)
C84.040:
Ketron-Goodman disease (pagetoid reticulosis)
C84.420:
Ki-1 positive T cell lymphoma
C84.430:
Ki-1 positive T cell lymphoma
L98.820:
Kimura´s disease
E83.010:
Kinky hair disease
 

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Disorder
Code & Disorder

Abnormal hair shaft, NOSAcne, infantileAcute generalised pustular psoriasisAllergic contact dermatitis - cosmetic or toiletryAlopecia due to pressureAnal fissure, NOSAngiolupoidApocrine adenocarcinomaAtopic dermatitis, prurigoBalanitisBasal cell carcinoma, recurrentBlepharitisBurkitt's lymphoma in HIV diseaseCandida balanitisCapillaritis, NOSChediak Higashi syndromeChronic hyperplastic candidiasisConfluent and reticulate papillomatosis of Gougerot & CarteaudCryptococcosis of skinCysticercosis of skinDermatitis, NECDiabetic microangiopathy, dermatoses due toDrug-induced lupus syndromeEctodermosis erosiva pluriorificialisEndometriosis, cutaneousEpithelioma calcificans MalherbeErythema multiforme, bullousErythropoietic porphyria, congenitalFibrofolliculomas, multipleFistula, pilonidal with abscessFragile hairGeographical tongueGonococcal infection, otherGranuloma of skin or subcutaneous tissue, NOSHaemangiopericytomaHead liceHerpes simplex, primary ocularHistiocytosis, familial sea-blueHurler syndrome (MPS I)Hyperthyroidism, NOSImmunobullous disorder, unclassifiableIododermaKaposi's sarcoma, NOSKlinefelter syndromeLeg ulcer, NOSLeprosy, borderline lepromatousLeukoplakia of lipLichen scrofulosorumLipomatosis (NEC/NOS)Lupus erythematosus(LE)-like syndrome due to drugLymphangioma circumscriptumMadelung's diseaseMalignant melanoma, mucosalMetageriaMorphoeaMucormycosis, rhinocerebralMyiasisNaevus, woolly hairNecrobiotic xanthogranulomaNevus, acantholyticOculocutaneous albinism - tyrosinase-negative (type 1)Oral hairy leucoplakiaPachyonychia congenita type I (Jadasssohn-Lewandowsky)Papulosquamous disorders in diseases classified elsewherePemphigoid, bullousPerlèchePiedra albaPityriasis rubra HebraPoliosisPost-mastectomy lymphedemaPrurigo, subacutePsoriasis, arthropathicPustular bacterid AndrewsReactive perforating collagenosisRingworm of groinSarcoidosis, nodularSclerosing periphlebitis of chest wallSheehan's syndromeSore, tropicalStomatitis aphthosa minor MikuliczSurgical wound, dehiscenceSyphilitic chancre, genitalTattoo, iron saltTinea barbaeToxic shock syndromeTrichonodosisTuberculosis, wartyUlerythema reticulataVagabond's diseaseVerrucous dermatitisWarts, handXanthoma, tendinous
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