Disease #00285 (epilepsy (epilepsy, focal, dysarthria, intellectual disability, cortical thickening, cerebellar atrophy))

Official abbreviation epilepsy
Name epilepsy, focal, dysarthria, intellectual disability, cortical thickening, cerebellar atrophy
OMIM ID -
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TBC1D24
Associated tissues -
Disease features -
Remarks -
Date created 2013-11-28 15:59:54 +01:00 (CET)
Date last edited N/A