ORPHA:306773
Hyperekplexia
- 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 | Hyperekplexia | |
| fr | Hyperexplexie | |
| de | Hyperekplexie | |
| es | Hiperekplexia | Hiperecplexia · Hiperplexia |
| it | Iperekplexia | |
| nl | Hyperekplexie | |
| pt | Hiperecplexia | |
| pl | Hiperekpleksja | |
| cs | Hyperekplexie | Choroby s úlekovými reakcemi |
| uk | Гіперекплексія | |
| zh | 过度惊吓反应症 | |
| tr | Hiperekpleksi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0017658 | E | validated | |
| MONDO | 17658 | E | validated | |
| MeSH | D000071017 | E | validated | |
| MedDRA | 10058271 | 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:102003Rare movement disorder
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/306773
- This record as JSON: /data/d/306773.json