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Distal arthrogryposis

ORPHA:97120疾病组

定义 英文原文(暂无中文)

A group of rare arthrogryposis syndromes characterized by congenital contractures of two or more areas of the body, primarily involving the hands and feet, while the proximal joints are largely spared, in the absence of primary neurologic and/or muscle disease affecting limb function. Diagnostic features include camptodactyly or pseudocamptodactyly, hypoplastic or absent flexion creases, overriding fingers, ulnar deviation at the wrist, talipes equinovarus, calcaneovalgus deformities, vertical talus, and/or metatarsus varus.

相关基因 13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
CHST14carbohydrate sulfotransferase 14ORPHA:2953
DSEdermatan sulfate epimeraseORPHA:2953
ECEL1endothelin converting enzyme like 1ORPHA:329457
FBN2fibrillin 2ORPHA:115
MYBPC1myosin binding protein C1ORPHA:1146
MYH3myosin heavy chain 3ORPHA:65743
MYH8myosin heavy chain 8ORPHA:3377
NALCNsodium leak channel, non-selectiveORPHA:2053
PIEZO2piezo type mechanosensitive ion channel component 2ORPHA:1154
SLC35A3solute carrier family 35 member A3ORPHA:370943
TNNI2troponin I2, fast skeletal typeORPHA:1147
TNNT3troponin T3, fast skeletal typeORPHA:1147
TPM2tropomyosin 2ORPHA:1147

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)