Disease #05799 (EIEE63 (encephalopathy, epileptic, early infantile, type 63 (EIEE63)), OMIM:617976)

Official abbreviation EIEE63
Name encephalopathy, epileptic, early infantile, type 63 (EIEE63)
OMIM ID 617976
Human Phenotype Ontology Project (HPO) HPO
Inheritance AR
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CPLX1
Associated tissues -
Disease features -
Remarks -