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Metadata
ID DOID:0060752
Name familial temporal lobe epilepsy 5
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
Xrefs

OMIM:614417

ORDO:163717

Subsets

DO_rare_slim

Synonyms

ETL5 [EXACT]

Parent Relationships

is_a temporal lobe epilepsy

is_a autosomal recessive disease

is_a autosomal dominant disease

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