Disease #04623

Official abbreviation MRD-36
Name mental retardation, autosomal dominant, type 36 (MRD-36)
OMIM ID 616362
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PPP2R1A
Associated tissues -
Disease features -
Remarks -