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黑色素代谢紊乱

Disorder of melanin metabolism

ORPHA:352728疾病组

相关基因 19来自下位疾病

Orphanet 未在本条目上直接标注致病基因。下表由本组所属的下位疾病汇总而来,「来源条目」列给出基因实际标注在哪一个 ORPHA 条目上。

基因名称来源条目
AP3B1adaptor related protein complex 3 subunit beta 1ORPHA:664500
AP3D1adaptor related protein complex 3 subunit delta 1ORPHA:664511
DCTdopachrome tautomeraseORPHA:597733
GPR143G protein-coupled receptor 143ORPHA:54
HPS1HPS1 biogenesis of lysosomal organelles complex 3 subunit 1ORPHA:231500
HPS3HPS3 biogenesis of lysosomal organelles complex 2 subunit 1ORPHA:231512
HPS4HPS4 biogenesis of lysosomal organelles complex 3 subunit 2ORPHA:231500
HPS5HPS5 biogenesis of lysosomal organelles complex 2 subunit 2ORPHA:231512
HPS6HPS6 biogenesis of lysosomal organelles complex 2 subunit 3ORPHA:231512
LRMDAleucine rich melanocyte differentiation associatedORPHA:352745
LYSTlysosomal trafficking regulatorORPHA:167
MLPHmelanophilinORPHA:79478
MYO5Amyosin VAORPHA:79476
OCA2OCA2 melanosomal transmembrane proteinORPHA:79432
RAB27ARAB27A, member RAS oncogene familyORPHA:79477
SLC24A5solute carrier family 24 member 5ORPHA:370097
SLC45A2solute carrier family 45 member 2ORPHA:79435
TYRtyrosinaseORPHA:79431
TYRP1tyrosinase related protein 1ORPHA:79433

外部标识与链接

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本页数据来源

  • 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
  • 中文病名:Orphanet 中文包,冻结于 2020-06-01
  • 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)