Disease #01116

Official abbreviation MRX89
Name mental retardation, X-linked, type 89 (MRX89)
OMIM ID 300848
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ZNF41
Associated tissues -
Disease features -
Remarks -