ORPHA:166430
Micturition-induced epilepsy
- Type
- Disease
- Group
- Disorder
- Status
- active
A rare reflex epilepsy characterized by tonic posturing or clonic movements triggered by micturition, with bilateral or unilateral involvement of the extremities and with or without loss of consciousness. Developmental delay is reported in some cases.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Micturition-induced epilepsy | |
| fr | Epilepsie induite par la miction | |
| de | Krampfanfälle, miktionsinduzierte | |
| es | Crisis epilépticas inducidas por la micción | |
| it | Epilessia indotta dalla minzione | |
| nl | Epilepsie door mictie | Epilepsie door urinelozing |
| pt | Convulsões induzidas pela micção | |
| pl | Padaczka wywołana mikcją | |
| cs | Záchvaty vyvolané močením | |
| uk | Епілепсія з рефлекторними судомами, що викликаються сечовипусканням | |
| zh | 排尿诱发性癫痫 | |
| tr | Miktürasyon kaynaklı 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 | 0015649 | E | validated | |
| UMLS | C4706587 | E | 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:310Reflex epilepsy
rare genetic diseases; rare neurological diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/166430
- This record as JSON: /data/d/166430.json