Disease #01123 (MRX88 (mental retardation, X-linked, type 88 (MRX88)), OMIM:300852)

Official abbreviation MRX88
Name mental retardation, X-linked, type 88 (MRX88)
OMIM ID 300852
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene AGTR2
Associated tissues -
Disease features -
Remarks -