远端关节挛缩
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 |
|---|---|---|
| CHST14 | carbohydrate sulfotransferase 14 | ORPHA:2953 |
| DSE | dermatan sulfate epimerase | ORPHA:2953 |
| ECEL1 | endothelin converting enzyme like 1 | ORPHA:329457 |
| FBN2 | fibrillin 2 | ORPHA:115 |
| MYBPC1 | myosin binding protein C1 | ORPHA:1146 |
| MYH3 | myosin heavy chain 3 | ORPHA:65743 |
| MYH8 | myosin heavy chain 8 | ORPHA:3377 |
| NALCN | sodium leak channel, non-selective | ORPHA:2053 |
| PIEZO2 | piezo type mechanosensitive ion channel component 2 | ORPHA:1154 |
| SLC35A3 | solute carrier family 35 member A3 | ORPHA:370943 |
| TNNI2 | troponin I2, fast skeletal type | ORPHA:1147 |
| TNNT3 | troponin T3, fast skeletal type | ORPHA:1147 |
| TPM2 | tropomyosin 2 | ORPHA: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)