ORPHA:98819
Familial temporal lobe epilepsy
- Type
- Disease
- Group
- Disorder
- Status
- active
A rare, genetic epilepsy characterized by mostly benign simple or complex partial seizures with autonomic or psychic auras. Seizures occur infrequently, are of short duration and are usually well controlled with medication. Development and cognition are normal.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Familial temporal lobe epilepsy | |
| fr | Epilepsie temporale familiale | |
| de | Temporallappenepilepsie, familiäre | |
| es | Epilepsia familiar del lóbulo temporal | |
| it | Epilessia del lobo temporale familiare | |
| nl | Familiale temporaalkwabepilepsie | Familiale TLE · Familiale epilepsie van de temporale kwab |
| pt | Epilepsia temporal, familiar | |
| pl | Rodzinna padaczka skroniowa | |
| cs | Familiární temporální epilepsie | |
| uk | Сімейна скронева епілепсія | |
| zh | 家族性颞叶癫痫 | |
| tr | Ailesel temporal lob epilepsisi |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 608096 | E | validated | |
| OMIM | 611631 | BTNT | not yet validated | |
| ICD-10 | G40.2 | NTBT | attributed | validated |
| ICD-11 | 8A61.4Y | NTBT | index | validated |
| MONDO | 0005115 | E | validated | |
| MONDO | 5115 | E | validated | |
| MeSH | C536956 | E | validated | |
| UMLS | C1842564 | E | validated | |
| GARD | 5135 | 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:98259Childhood-onset epilepsy syndrome
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98819
- This record as JSON: /data/d/98819.json