ORPHA:183509
Rare genetic headache
- 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 | Rare genetic headache | |
| fr | Céphalée rare de cause génétique | |
| de | Kopfschmerzen, genetisch bedingte, seltene | |
| es | Cefalea genética rara | |
| it | Cefalea rara genetica | |
| nl | Zeldzame genetische hoofdpijn | |
| pt | Enxaqueca genética rara | |
| pl | Rzadki ból głowy uwarunkowany genetycznie | |
| cs | Vzácné geneticky podmíněné bolesti hlavy | |
| uk | Рідкісний генетично обумовлений головний біль | |
| zh | 罕见遗传性头痛 | |
| tr | Nadir genetik baş ağrısı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15954 | E | validated | |
| UMLS | C5680565 | 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:71859Rare genetic neurological disorder
rare genetic diseases
Children (1):
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/183509
- This record as JSON: /data/d/183509.json