ORPHA:209978
Alternating hemiplegia
- 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 | Alternating hemiplegia | |
| fr | Hémiplégie alternante | |
| de | Hemiplegie, alternierende | |
| es | Hemiplejia alternante | |
| it | Emiplegia alternante | |
| nl | Alternerende hemiplegie | |
| pt | Hemiplegia alternante | |
| pl | Naprzemienne porażenie połowicze | |
| cs | Alternující hemiplegie | |
| uk | Альтернуюча геміплегія | |
| zh | 交叉性肢体瘫痪 | |
| tr | Alternatif hemipleji |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | MB53.0 | E | specific | validated |
| MONDO | 0016210 | E | validated | |
| MONDO | 16210 | E | validated | |
| UMLS | C0278110 | 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 (3):
- ORPHA:166472Monogenic disease with epilepsy
rare genetic diseases; rare neurological diseases - ORPHA:71859Rare genetic neurological disorder
rare genetic diseases - ORPHA:98006Rare neurologic 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/209978
- This record as JSON: /data/d/209978.json