Hemicrania continua
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
A rare trigeminal autonomic cephalalgia characterized by indomethacin-sensitive, persistent, strictly unilateral headache lasting for more than three months, associated with ipsilateral conjunctival injection, lacrimation, nasal congestion, rhinorrhea, forehead and facial sweating, miosis, ptosis, eyelid edema, and/or restlessness or agitation, and not better accounted for by another type of headache. Migrainous symptoms such as photophobia are often observed. The headache may be continuous (unremitting subtype) or interrupted by remission periods of more than 24 hours (remitting subtype).
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hemicrania continua | |
| fr | Hémicrânie continue | |
| de | Hemicrania continua | |
| es | Hemicránea continua | |
| it | Emicrania continua | |
| nl | Hemicrania continua | |
| pt | Hemicrania continua | |
| pl | Hemikrania ciągła | |
| cs | Hemicrania continua | |
| uk | Постійна геморагія | |
| zh | 连续性半侧颅痛 | |
| tr | Hemikrani kontinua |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G44.0 | NTBT | attributed | validated |
| ICD-11 | 8A82 | NTBT | index | validated |
| MONDO | 0018615 | E | validated | |
| UMLS | C2349425 | E | validated | |
| GARD | 10795 | E | validated | |
| MedDRA | 10090227 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:157843Trigeminal autonomic cephalalgia
rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/443070
- This record as JSON: /data/d/443070.json