{"orpha":183469,"name":"Genetic hypopigmentation 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-183469/","orphanet_url":"https://www.orpha.net/en/disease/detail/183469","names":{"fr":{"name":"Hypopigmentation cutanée génétique"},"de":{"name":"Hypopigmentierung der Haut, genetisch bedingte"},"es":{"name":"Hipopigmentación genética de la piel"},"it":{"name":"Ipopigmentazione della cute di origine genetica"},"nl":{"name":"Genetische hypopigmentatie van huid"},"pt":{"name":"Hipopigmentação da pele, genética"},"pl":{"name":"Hipopigmentacja skóry uwarunkowana genetycznie"},"cs":{"name":"Geneticky podmíněné hypopigmentace kůže"},"uk":{"name":"Генетично обумовлена гіпопігментація шкіри"},"zh":{"name":"遗传性皮肤色素沉着过多"},"tr":{"name":"Derinin genetik hipopigmentasyonu"}},"xrefs":[{"source":"UMLS","code":"C5680576","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":183463,"name":"Genetic pigmentation anomaly of the skin","classifications":[156]}],"children":[{"orpha":998,"name":"Albinism-deafness syndrome","type":"Malformation syndrome"},{"orpha":726452,"name":"Combined immunodeficiency with early gray hairing","type":"Disease"},{"orpha":3214,"name":"Deaf blind hypopigmentation syndrome, Yemenite type","type":"Malformation syndrome"},{"orpha":717846,"name":"Developmental delay-facial dysmorphism-Blaschko lines hypopigmentation-obesity-intellectual disability syndrome","type":"Malformation syndrome"},{"orpha":55,"name":"Oculocutaneous albinism","type":"Clinical group"},{"orpha":163746,"name":"Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease","type":"Disease"},{"orpha":2885,"name":"Piebald trait-neurologic defects syndrome","type":"Malformation syndrome"},{"orpha":2884,"name":"Piebaldism","type":"Disease"},{"orpha":284811,"name":"Syndromic oculocutaneous albinism","type":"Category"},{"orpha":42665,"name":"Tietz syndrome","type":"Malformation syndrome"},{"orpha":1493,"name":"Vici syndrome","type":"Malformation syndrome"},{"orpha":3440,"name":"Waardenburg syndrome","type":"Disease"},{"orpha":897,"name":"Waardenburg-Shah syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}