罕见病知识库 RareSeen

常染色体隐性遗传肢体带状肌营养不良

Autosomal recessive limb-girdle muscular dystrophy

ORPHA:102015疾病组

基本事实

遗传方式
常染色体隐性

相关基因 26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
ANO5anoctamin 5ORPHA:206549
CAPN3calpain 3ORPHA:267
CRPPACDP-L-ribitol pyrophosphorylase AORPHA:352479
DAG1dystroglycan 1ORPHA:280333
DYSFdysferlinORPHA:268
FKRPfukutin related proteinORPHA:34515
FKTNfukutinORPHA:206554
GMPPBGDP-mannose pyrophosphorylase BORPHA:363623
HMGCR3-hydroxy-3-methylglutaryl-CoA reductaseORPHA:653725
LAMA2laminin subunit alpha 2ORPHA:565837
PLECplectinORPHA:257
POGLUT1protein O-glucosyltransferase 1ORPHA:480682
POMGNT1protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)ORPHA:206564
POMKprotein O-mannose kinaseORPHA:445110
POMT1protein O-mannosyltransferase 1ORPHA:86812
POMT2protein O-mannosyltransferase 2ORPHA:206559
POPDC1popeye domain cAMP effector 1ORPHA:476084
SGCAsarcoglycan alphaORPHA:62
SGCBsarcoglycan betaORPHA:119
SGCDsarcoglycan deltaORPHA:219
SGCGsarcoglycan gammaORPHA:353
TCAPtitin-capORPHA:34514
TOR1AIP1torsin 1A interacting protein 1ORPHA:424261
TRAPPC11trafficking protein particle complex subunit 11ORPHA:369840
TRIM32tripartite motif containing 32ORPHA:1878
TTNtitinORPHA:140922

外部标识与链接

发现这一页有错误?告诉我 · 邮件主题会自动带上本页的 ORPHA 编号

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)