Search Ontology:
Human Disease
familial temporal lobe epilepsy 5
- Term ID
- DOID:0060752
- Synonyms
-
- ETL5
- Definition
- A temporal lobe epilepsy that has_material_basis_in heterozygous mutation in the CPA6 gene on chromosome 8q13. https://www.ncbi.nlm.nih.gov/pubmed/21922598
- References
-
- MIM:614417
- ORDO:163717
- Ontology
- Human Disease ( DOID:0060752 )
- is a type of
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Genes Involved
| Human Gene | Zebrafish Ortholog | OMIM Term | Disease | OMIM Phenotype ID |
|---|---|---|---|---|
| CPA6 | Epilepsy, familial temporal lobe, 5 | familial temporal lobe epilepsy 5 | 614417 |
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Zebrafish Models
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