http://caligraph.org/ontology/Skin_condition_resulting_from_errors_in_metabolism

Property	Value
rdf:type	owl:Class
rdfs:label	Skin condition resulting from errors in metabolism
rdfs:subClassOf	Cutaneous condition
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Skin_conditions_resulting_from_errors_in_metabolism
is rdf:type of	Amyloid purpura Necrobiosis lipoidica Prolidase deficiency Waxy skin Fabry disease Aminolevulinic acid dehydratase deficiency porphyria Carotenosis Lesch–Nyhan syndrome Hartnup disease Myxedema Calcinosis cutis Diabetic dermopathy Hepatoerythropoietic porphyria Hives Lipoprotein lipase deficiency Diabetic dermadrome Dystrophic calcinosis cutis Xanthoma Apolipoprotein B deficiency Tangier disease Cerebrotendineous xanthomatosis Iatrogenic calcinosis cutis Hyaluronidase deficiency Familial dysbetalipoproteinemia Familial hypertriglyceridemia Combined hyperlipidemia Sialidosis Alkaptonuria Gaucher's disease Gout Fucosidosis Porphyria Xanthoma diabeticorum Ochronosis Secondary systemic amyloidosis Erythropoietic protoporphyria Haemodialysis-associated amyloidosis Transient erythroporphyria of infancy Verruciform xanthoma CADASIL Variegate porphyria Diabetic cheiroarthropathy Subepidermal calcified nodule Secondary cutaneous amyloidosis Citrullinemia Milia-like calcinosis Farber disease Idiopathic scrotal calcinosis Pseudoporphyria Phenylketonuria Metastatic calcinosis cutis Primary cutaneous amyloidosis Traumatic calcinosis cutis Urbach–Wiethe disease Diabetic bulla Sly syndrome Mucopolysaccharidosis type I Heredofamilial amyloidosis Xanthoma striatum palmare Adrenoleukodystrophy Lafora disease Porphyria cutanea tarda Normolipoproteinemic xanthomatosis Xanthomatous biliary cirrhosis Familial amyloid polyneuropathy Gunther disease Niemann–Pick disease Erythropoietic porphyria Familial Amyloidosis, Finnish Type Sitosterolemia Xanthelasma Amyloidosis Hereditary coproporphyria Medication-induced hyperlipoproteinemia Osteoma cutis

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