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DOID:0112019 - non-syndromic X-linked intellectual disability 19
Disease Ontology Definition:A non-syndromic X-linked intellectual disability characterized by mild to moderate intellectual disability that has_material_basis_in hemizygous or heterozygous mutation in the RPS6KA3 gene on chromosome Xp22.12.
Synonyms: MRX19, X-linked mental retardation 19,
Xenbase Genes : rps6ka3
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee