ILDS

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

 


ICD sorted by Disorder:
Hyperthyroidism, NOS - Immunoblastic lymphoma

ICD Code Disorder
E05.900:
Hyperthyroidism, NOS
L68.900:
Hypertrichosis
L68.830:
Hypertrichosis due to drug
L68.100:
Hypertrichosis lanuginosa, acquired
Q84.220:
Hypertrichosis lanuginosa, congenital
Q84.210:
Hypertrichosis lanuginosa, congenital
L68.200:
Hypertrichosis localised, NOS
L68.860:
Hypertrichosis, idiopathic
L68.800:
Hypertrichosis, specified, NEC
E67.000:
Hypervitaminosis A, skin disease due to
E29.920:
Hypogonadism
L74.420:
Hypohidrosis
L81.540:
Hypomelanosis, idiopathic guttate
E03.900:
Hypothyroidism, skin signs of
L85.020:
Ichthyosiform reaction to drug
L85.000:
Ichthyosis, acquired
Q80.020:
Ichthyosis, follicular
Q80.200:
Ichthyosis, lamellar
Q80.100:
Ichthyosis, X-linked recessive
L30.240:
Id eruption due to eczema
L30.205:
Ide eruption
D47.300:
Idiopathic hemorrhagic thrombocythemia
D69.300:
Idiopathic thrombocytopenic purpura
I82.830:
Iliac vein thrombosis
C83.410:
Immunoblastic lymphoma
 

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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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