{"orpha":183463,"name":"Genetic 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-183463/","orphanet_url":"https://www.orpha.net/en/disease/detail/183463","names":{"fr":{"name":"Anomalie génétique de la pigmentation cutanée"},"de":{"name":"Pigmentanomalien der Haut, genetisch bedingte"},"es":{"name":"Anomalía genética en la pigmentación de la piel"},"it":{"name":"Anomalia della pigmentazione della cute di origine genetica"},"nl":{"name":"Genetische pigmentatie-anomalie van huid"},"pt":{"name":"Anomalia genética da pigmentação da pele"},"pl":{"name":"Zaburzenie pigmentacji skóry uwarunkowane genetycznie"},"cs":{"name":"Geneticky podmíněné anomálie pigmentace kůže"},"uk":{"name":"Генетично обумовлена аномалія пігментації шкіри"},"zh":{"name":"遗传性皮肤色素沉着异常"},"tr":{"name":"Derinin genetik pigmentasyon anomalisi"}},"xrefs":[{"source":"UMLS","code":"C5680578","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":68346,"name":"Rare genetic skin disease","classifications":[156]}],"children":[{"orpha":280628,"name":"Familial progressive hyper- and hypopigmentation","type":"Disease"},{"orpha":183466,"name":"Genetic hyperpigmentation of the skin","type":"Category"},{"orpha":183469,"name":"Genetic hypopigmentation of the skin","type":"Category"},{"orpha":2435,"name":"Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome","type":"Disease"},{"orpha":447961,"name":"Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}