Disease #05293 (EIEE-37 (encephalopathy, epileptic, early infantile, type 37 (EIEE-37)), OMIM:616981)

Official abbreviation EIEE-37
Name encephalopathy, epileptic, early infantile, type 37 (EIEE-37)
OMIM ID 616981
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FRRS1L
Associated tissues -
Disease features -
Remarks -