ORPHA:371433
Genetic periodic paralysis
- 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 | Genetic periodic paralysis | |
| fr | Paralysie périodique génétique | |
| de | Periodische Paralyse, genetisch bedingte | |
| es | Parálisis periódica genética | |
| it | Paralisi periodica genetica | |
| nl | Genetische periodieke paralyse | Genetische periodieke verlamming |
| pt | Paralisia periódica genética | |
| pl | Paraliż okresowy uwarunkowany genetycznie | |
| cs | Geneticky podmíněné periodické paralýzy | |
| uk | Генетично обумовлений періодичний параліч | |
| zh | 遗传性周期性麻痹 | |
| tr | Genetik periyodik paraliz |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 8C74.1 | NTBT | specific | validated |
| MONDO | 995 | E | validated | |
| UMLS | C5681151 | 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:206634Genetic skeletal muscle disease
rare genetic 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/371433
- This record as JSON: /data/d/371433.json