Disease #03672 (PMRED (psychomotor retardation, epilepsy, and craniofacial dysmorphism (PMRED)), OMIM:614501)

Official abbreviation PMRED
Name psychomotor retardation, epilepsy, and craniofacial dysmorphism (PMRED)
OMIM ID 614501
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 2
Associated with 1 gene SNIP1
Associated tissues -
Disease features -
Remarks -