ORPHA:71864
Muscular channelopathy
- Type
- Category
- 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 | Muscular channelopathy | |
| fr | Canalopathie musculaire | |
| de | Ionenkanalkrankheit, muskuläre | |
| es | Canalopatía muscular | |
| it | Canalopatia muscolare | |
| nl | Musculaire kanalopathie | |
| pt | Canalopatia muscular | |
| pl | Kanałopatia plamki | |
| cs | Svalové kanálopatie | |
| uk | Мязова каналопатія | |
| zh | 肌肉离子通道病 | |
| tr | Kas kanalopatisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019119 | E | validated | |
| MONDO | 19119 | E | validated | |
| UMLS | C5681306 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:68381Neuromuscular disease
rare neurological diseases
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/71864
- This record as JSON: /data/d/71864.json