About: Poikiloderma

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Human skin condition.

Attributes	Values
rdf:type	Item
owl:sameAs	Poikiloderma
description	Krankheit (de) malattia (it) хвороба (uk) مرض جلدي (ar) enfermedad de la piel (es) Condição da pele humana. (pt) Condição da pele humana. (pt-br) Human skin condition. (en) syndrome dermatologique (fr)
rdfs:label	Poikiloderma (en) Poichilodermia (it) Poikilodermie (de) Poikilodermie (nl) Poiquilodermia (pt) Poiquilodermia (pt-br) poïkilodermie (fr) تبكل الجلد (ar)
skos:prefLabel	Poikiloderma (en) Poichilodermia (it) Poikilodermie (de) Poikilodermie (nl) Poiquilodermia (pt) Poiquilodermia (pt-br) poïkilodermie (fr) تبكل الجلد (ar)
name	Poikiloderma (en) Poichilodermia (it) Poikilodermie (de) Poikilodermie (nl) Poiquilodermia (pt) Poiquilodermia (pt-br) poïkilodermie (fr) تبكل الجلد (ar)
instance of	wds:Q1307866-16089878-4641-b943-7351-9afdc84c7d66
instance of	disease
subclass of	wds:Q1307866-00787e3e-4b6f-a438-69e2-462da0d2690f
subclass of	skin disease
skos:altLabel	Poikiloderma (nl)
OpenAlex ID	wds:Q1307866-DC34D1F7-9CE1-42D5-8ED9-69080C5CA5CB
NCI Thesaurus ID	wds:Q1307866-405f9101-4608-f380-dc78-ef1aca6dda66
Microsoft Academic ID	wds:Q1307866-6BAF4F4B-D019-4F81-A9C3-839F2C1ADB40
ICD-11 (foundation)	wds:Q1307866-4641CBB6-A581-4208-A415-108E27E99A27
Microsoft Academic ID	https://makg.org/entity/2778163040
OpenAlex ID	C2778163040
NCI Thesaurus ID	C53975
Microsoft Academic ID	2778163040
ICD-11 (foundation)	657613175
is owl:sameAs of	Poikiloderma
is about of	Poikiloderma https://www.wikidata.org/wiki/Special:EntityData/Q1307866 Poikiloderma https://de.wikipedia.org/wiki/Poikilodermie https://fr.wikipedia.org/wiki/Po%C3%AFkilodermie https://it.wikipedia.org/wiki/Poichilodermia https://ar.wikipedia.org/wiki/%D8%AA%D8%A8%D9%83%D9%84_%D8%A7%D9%84%D8%AC%D9%84%D8%AF https://nl.wikipedia.org/wiki/Poikilodermie
is cites work of	Focal dermal hypoplasia. Ocular and general manifestations with a survey of the literature
is cites work of	wds:Q93808985-5451AAD9-F689-423F-A222-861120E9CC66
is subclass of of	Poikiloderma of Civatte Poikiloderma vasculare atrophicans Hereditary sclerosing poikiloderma poikiloderma with neutropenia
is subclass of of	wds:Q7207847-04c19496-4a8f-e46c-3a3f-9ac14650f433 wds:Q16937928-ed6ab47f-4fc7-b043-05f4-344aa487a6c6 wds:Q7207846-d504bc99-456e-6931-5194-7d643b22568f wds:Q26492775-1c75a049-4920-4c2a-1a2d-a84dbfc81dd2
is main subject of	Treatment of poikiloderma of Civatte with an intense pulsed light source Treatment of poikiloderma of Civatte on the neck with an intense pulsed light source Congenital poikiloderma with traumatic bulla formation and progressive cutaneous atrophy Poikiloderma vasculare atrophicans; report of a case due to exposure to cold Poikiloderma vasculare atrophicans; report of a case with observations at autopsy Hereditary acrokeratotic poikiloderma Poikiloderma vasculare atrophicans Poikiloderma with epitheliomata Generalized cutaneous calcinosis and poikiloderma Thomson's syndrome (poikiloderma congenita) The natural history of parapsoriasis en plaques (chronic superficial dermatitis) and prereticulotic poikiloderma Poikiloderma congenitale-an early case of rothmund-thomson's syndrome Congenital poikiloderma with traumatic bulla formation, anhidrosisi, and keratoderma Poikiloderma congenitale (Thomson's disease) Poikiloderma Vasculare of Jacobi Poikiloderma Atrophicans Vasculare Jacobi [Thomson-type congenital poikiloderma with major bone dysplasias] Poikiloderma congenitale; Rothmund-Thomson syndrome Poikiloderma ? Premycosis Mutations in FAM111B cause hereditary fibrosing poikiloderma with tendon contracture, myopathy, and pulmonary fibrosis [An unusual poikiloderma form: lupus erythematosus-like skin changes in dwarfism] Granulomatous slack skin presenting as diffuse poikiloderma and necrotic ulcers, with features of granulomatous vasculitis and response to oral prednisone, acitretin, and oral psoralen plus ultraviolet light therapy-A case report Granulomatous mycosis fungoides presenting as poikiloderma Hypogonadism and parathyroid adenoma in congenital poikiloderma (Rothmund-Thomson syndrome) Rothmund's syndrome; Thomson's syndrome; congenital poikiloderma with or without juvenile cataracts POIKILODERMA CONGENITALE. REPORT OF TWO CASES Mitochondrial complex I and III mutations and neutral-lipid storage in activated mononuclear macrophages and neutrophils: a case presenting with necrotizing myopathy, poikiloderma atrophicans vasculare, and xanthogranulomatous bursitis Poikiloderma congenitale accompanied by megalocornea in one eye. A case report Is poikiloderma a graft-versus-host-like reaction? [Pulmonary fibrosis associated with hereditary fibrosing poikiloderma caused by FAM111B mutation: A case report] Calcinosis cutis, osteoma cutis, poikiloderma and skeletal abnormalities (COPS syndrome)--a new entity? [Forms of congenital poikiloderma]

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