Disease #01130 (MRX3 (mental retardation, X-linked, type 3 (MRX3)), OMIM:309541)

Official abbreviation MRX3
Name mental retardation, X-linked, type 3 (MRX3)
OMIM ID 309541
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene HCFC1
Associated tissues -
Disease features -
Remarks -