ZFIN Human Disease: familial temporal lobe epilepsy 5

OBO ID: DOID:0060752

Term Name:	familial temporal lobe epilepsy 5		Search Ontology:
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:	OMIM:614417 ORDO:163717
Ontology:	Human Disease ( DOID:0060752 )

Relationships

is a type of:	autosomal dominant disease autosomal recessive disease temporal lobe epilepsy autosomal dominant disease autosomal recessive disease temporal lobe epilepsy Show first 5 Terms

OTHER familial temporal lobe epilepsy 5 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CPA6	cpa6	Epilepsy, familial temporal lobe, 5	614417

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None