{"orpha":79374,"name":"Pigmentation anomaly of the skin","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-79374/","orphanet_url":"https://www.orpha.net/en/disease/detail/79374","names":{"fr":{"name":"Anomalie de la pigmentation cutanée"},"de":{"name":"Pigmentierungsanomalien"},"es":{"name":"Anomalía de la pigmentación"},"it":{"name":"Anomalie della pigmentazione"},"nl":{"name":"Pigmentatie-anomalie van huid"},"pt":{"name":"Anomalia da pigmentação cutânea"},"pl":{"name":"Zaburzenie pigmentacji skóry"},"cs":{"name":"Anomálie kožní pigmentace"},"uk":{"name":"Аномалія пігментації шкіри"},"zh":{"name":"皮肤色素沉着异常"},"tr":{"name":"Derinin pigmentasyon anomalisi"}},"xrefs":[{"source":"MONDO","code":"0019288","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"19288","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681482","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":98700,"name":"OBSOLETE: Pigmentation disorder with eye involvement","status":"inactive"},{"type":"Referred to","orpha":98708,"name":"OBSOLETE: Pigmentation disorder with eye involvement, excluding albinism","status":"inactive"}],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":89826,"name":"Rare skin disease","classifications":[187]}],"children":[{"orpha":280628,"name":"Familial progressive hyper- and hypopigmentation","type":"Disease"},{"orpha":79375,"name":"Hyperpigmentation of the skin","type":"Category"},{"orpha":2435,"name":"Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome","type":"Disease"},{"orpha":79376,"name":"Hypopigmentation of the skin","type":"Category"},{"orpha":447961,"name":"Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}