Disease #05531

Official abbreviation MRD-49
Name mental retardation, autosomal dominant, type 49 (MRD-49)
OMIM ID 617752
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene TRIP12
Associated tissues -
Disease features autosomal dominant
Remarks -