Visualize Submit Comment

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	MIM: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