ORPHA:53739
Distal hereditary motor neuropathy
Synonyms: Distal spinal muscular atrophy · dHMN · dSMA
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Distal hereditary motor neuropathy | Distal spinal muscular atrophy · dHMN · dSMA |
| fr | Neuropathie motrice distale héréditaire | dSMA · Amyotrophie spinale distale · dHMN |
| de | Neuropathie, distale hereditäre motorische | Muskelatrophie, distale spinale · dHMN · dSMA |
| es | Neuropatía motora distal hereditaria | Atrofia muscular espinal distal · dHMN · dSMA |
| it | Neuropatia motoria ereditaria distale | Atrofia muscolare spinale distale · dHMN · dSMA |
| nl | Distale erfelijke motorische neuropathie | Distale spinale musculaire atrofie · Distale spinale spieratrofie · dHMN · dSMA |
| pt | Neuropatia motora distal hereditária | |
| pl | Dystalna dziedziczna neuropatia ruchowa | dHMN · dSMA · Dystalny rdzeniowy zanik mięśni |
| cs | Distální dědičná motorická neuropatie | Distální spinální svalová atrofie · dHMN · dSMA |
| uk | Дистальна спадкова моторна нейропатія | dHMN · Дистальна спінальна мязова атрофія · dSMA |
| zh | 远端遗传性运动神经病 | 远端脊髓肌萎缩 |
| tr | Distal kalıtsal motor nöropati | dHMN · dSMA · Distal spinal kas atrofisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0018894 | E | validated | |
| MONDO | 18894 | E | validated | |
| UMLS | C0393541 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:98505Genetic motor neuron disease
rare genetic diseases; rare neurological diseases - ORPHA:98497Genetic peripheral neuropathy
rare genetic diseases; rare neurological diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:206713OBSOLETE: Distal spinal muscular atrophy referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/53739
- This record as JSON: /data/d/53739.json