Disease #05605 (EIEE-62 (encephalopathy, epileptic, early infantile, type 62 (EIEE-62)), OMIM:617938)

Official abbreviation EIEE-62
Name encephalopathy, epileptic, early infantile, type 62 (EIEE-62)
OMIM ID 617938
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SCN3A
Associated tissues -
Disease features autosomal dominant
Remarks -