Disease #05836 (MRD51 (mental retardation, autosomal dominant, type 51 (MRD51)), OMIM:617788)

Official abbreviation MRD51
Name mental retardation, autosomal dominant, type 51 (MRD51)
OMIM ID 617788
Human Phenotype Ontology Project (HPO) HPO
Inheritance AD
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SUV420H1
Associated tissues -
Disease features -
Remarks -