DISEASES

Disease-gene associations mined from literature

Human genes for Dravet syndrome

Dravet syndrome [DOID:0080422]

An early infantile epileptic encephalopathy that has_material_basis_in heterozygous mutation in the SCN1A gene on chromosome 2q24.

Synonyms:  Dravet syndrome,  DOID:0080422,  Dravet disease,  Dravet disorder,  Dravet syndromes ...