ORPHA:166415
Audiogenic epilepsy
- Type
- Disease
- Group
- Disorder
- Status
- active
A rare neurologic disease characterized by seizures that are triggered by acoustic stimulation, which can be simple (as in startle epilepsy) or complex (e.g. musicogenic seizures, seizures triggered by the voice).
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Audiogenic epilepsy | |
| fr | Epilepsie audiogénique | Crises audiogènes |
| de | Reflexepilepsie, audiogene | Krampfanfälle, audiogene · Audiogene Epilepsie |
| es | Epilepsia audiogénica | |
| it | Epilessia audiogenica | |
| nl | Audiogene epilepsie | |
| pt | Epilepsia audiogénica | |
| pl | Padaczka słuchowa | |
| cs | Audiogenní epileptický záchvat | |
| uk | Епілепсія з аудіогенними рефлекторними судомами | |
| zh | 听源性癫痫 | |
| tr | Odyojenik nöbetler |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G40.5 | NTBT | attributed | validated |
| ICD-11 | 8A61.40 | NTBT | index | validated |
| MONDO | 0015644 | E | validated | |
| UMLS | C0751791 | 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:310Reflex epilepsy
rare genetic diseases; rare neurological diseases
No children.
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/166415
- This record as JSON: /data/d/166415.json