Hypnic headache
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult, Childhood, Elderly
- Status
- active
A rare headache characterized by recurrent brief, intense headache attacks occurring exclusively during sleep, typically at the same time of the night, causing the patient to wake up. The pain usually lasts more than 15 minutes after waking. It is mostly bilateral and may be associated with nausea, photophobia, or phonophobia, while characteristically no autonomic symptoms are present.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hypnic headache | |
| fr | Céphalée hypnique | |
| de | Kopfschmerz, schlafgebundener | |
| es | Cefalea hípnica | |
| it | Cefalea ipnica | |
| nl | Hypnische hoofdpijn | |
| pt | Cefaleia hipnica | |
| pl | Śródsenny ból głowy | |
| cs | Hypnická bolest hlavy | |
| uk | Гіпнічний головний біль | |
| zh | 睡眠性头痛 | |
| tr | Hipnik baş ağrısı |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G44.8 | NTBT | attributed | validated |
| ICD-11 | 8A83 | NTBT | index | validated |
| MONDO | 0017181 | E | validated | |
| UMLS | C0752150 | E | validated | |
| GARD | 10796 | E | validated | |
| MedDRA | 10088606 | 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:98022Rare headache
rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/276429
- This record as JSON: /data/d/276429.json