ORPHA:698005
Epilepsy with generalized tonic-clonic seizures alone
Synonyms: EGTCS · Epilepsy with grand mal seizures on awakening · GTCA
- Type
- Disease
- Group
- Disorder
- Inheritance
- Multigenic/multifactorial
- Age of onset
- Adolescent, Adult, Childhood
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Epilepsy with generalized tonic-clonic seizures alone | EGTCS · Epilepsy with grand mal seizures on awakening · GTCA |
| fr | Epilepsie avec crises tonico-cloniques généralisées seules | |
| de | Epilepsie mit ausschließlich generalisierten tonisch-klonischen Anfällen | Epilepsie mit Grand-Mal-Anfällen beim Aufwachen · GTCA · GTCSA |
| es | Epilepsia con sólo crisis tónico-clónicas generalizadas | EGTCS · Epilepsia con crisis de gran mal al despertar · GTCA |
| it | Epilessia con sole crisi epilettiche tonico-cloniche generalizzate | EGTCS · Epilessia con convulsioni tipo grande male al risveglio · GTCA |
| nl | Epilepsie met enkel gegeneraliseerde tonisch-clonische insulten | EGTCS · Epilepsie met 'grand mal'-insulten bij ontwaken · GTCA |
| pt | Epilepsy with generalized tonic-clonic seizures alone | |
| pl | Epilepsy with generalized tonic-clonic seizures alone | = en |
| cs | Epilepsy with generalized tonic-clonic seizures alone | = en |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G40.3 | NTBT | attributed | not yet validated |
| ICD-11 | 8A61.4Y | NTBT | index | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:699645Variable age-onset epilepsy syndrome
rare genetic diseases; rare neurological diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | 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.
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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/698005
- This record as JSON: /data/d/698005.json