mental retardation, x-linked 95 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A non-syndromic intellectual disability characterized by a X-linked inheritance pattern. (Human Disease Ontology, DOID_0050776)
External Link
Similar Terms
Downloads & Tools


1 genes associated with the mental retardation, x-linked 95 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
MRX95 Mental retardation, X-linked 95