Disease #04645 (ETL-7 (epilepsy, temporal lobe, familial, type 7 (ETL-7)), OMIM:616436)

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Official abbreviation	ETL-7
Name	epilepsy, temporal lobe, familial, type 7 (ETL-7)
OMIM ID	616436
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RELN
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:23 +02:00 (CEST)
Date last edited	N/A