non-syndromic X-linked intellectual disability 19

Summary

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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: rps6ka3

MIM:

MIM:300844 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 19; XLID19

MIM:300844 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 19; XLID19

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): non-syndromic X-linked intellectual disability (is_a), X-linked dominant disease (is_a)