ILDS

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

 


ICD sorted by Disorder:
Apocrine adenocarcinoma - Atopic dermatitis, inverse pattern

ICD Code Disorder
C44.L62:
Apocrine adenocarcinoma
D23.L37:
Apocrine adenoma, tubular
D23.L36:
Apocrine tumour, benign (NEC/NOS)
L29.830:
Aquagenic pruritus
Q87.410:
Arachnodactyly
L81.854:
Argyria
E53.000:
Ariboflavinosis
L98.580:
Arndt Gottron syndrome
L98.120:
Artefact, cutaneous
M31.610:
Arteritis, giant cell
M31.600:
Arteritis, giant cell
M31.610:
Arteritis, temporal
M31.610:
Arteritis, temporal
L98.884:
Ascher´s syndrome
G11.310:
Ataxia telangiectasia
I70.200:
Atherosclerosis of arteries of extremit
I70.240:
Atherosclerotic gangrene
I70.231:
Atherosclerotic ulcer
L20.900:
Atopic dermatitis
L20.802:
Atopic dermatitis, discoid pattern
L20.810:
Atopic dermatitis, flexural
L20.806:
Atopic dermatitis, follicular
L20.840:
Atopic dermatitis, impetiginised
L20.816:
Atopic dermatitis, infantile
L20.804:
Atopic dermatitis, inverse pattern
 

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Code
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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