ORPHA:206976
Periodic paralysis
- 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 | Periodic paralysis | |
| fr | Paralysie périodique | |
| de | Periodische Paralyse | |
| es | Parálisis periódica | |
| it | Paralisi periodica | |
| nl | Periodieke paralyse | Periodieke verlamming |
| pt | Paralisia periódica | |
| pl | Paraliż okresowy | |
| cs | Periodická paralýza | |
| uk | Періодичні паралічі | |
| zh | 周期性麻痹 | |
| tr | Periyodik paraliz |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G72.3 | E | specific | validated |
| ICD-11 | 8C74.1 | E | specific | validated |
| MONDO | 0016122 | E | validated | |
| MONDO | 16122 | E | validated | |
| MeSH | D010245 | 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 neurological diseases
Children (6):
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/206976
- This record as JSON: /data/d/206976.json