Disease #01158 (MRX32 (mental retardation, X-linked, syndromic, type 32 (MRX32)), OMIM:300886)

Official abbreviation MRX32
Name mental retardation, X-linked, syndromic, type 32 (MRX32)
OMIM ID 300886
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CLIC2
Associated tissues -
Disease features -
Remarks -