Disease #00097 (FIME (epilepsy, myoclonic, infantile, familial (FIME)), OMIM:605021)

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Official abbreviation	FIME
Name	epilepsy, myoclonic, infantile, familial (FIME)
OMIM ID	605021
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TBC1D24
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-12-14 10:00:34 +01:00 (CET)
Date last edited	N/A