ORPHA:98022
Rare 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 headache | |
| fr | Céphalée rare | |
| de | Kopfschmerz, seltene Form | |
| es | Cefalea rara | |
| it | Cefalea rara | |
| nl | Zeldzame hoofdpijn | |
| pt | Cefaleia rara | |
| pl | Rzadki ból głowy | |
| cs | Vzácné příčiny bolesti hlavy | |
| uk | Рідкісний головний біль | |
| zh | 罕见头痛 | |
| tr | Nadir baş ağrısı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0020011 | E | validated | |
| UMLS | C5681547 | 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:98006Rare neurologic disease
rare neurological diseases
Children (7):
- ORPHA:353253Burning mouth syndrome
- ORPHA:692271Cerebral proliferative angiopathy
- ORPHA:569Familial or sporadic hemiplegic migraine
- ORPHA:276429Hypnic headache
- ORPHA:284388Reversible cerebral vasoconstriction syndrome
- ORPHA:443180Spontaneous intracranial hypotension
- ORPHA:157843Trigeminal autonomic cephalalgia
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/98022
- This record as JSON: /data/d/98022.json