non-syndromic X-linked intellectual disability 88

Summary

DOID:0112053 - non-syndromic X-linked intellectual disability 88

Disease Ontology Definition:A non-syndromic X-linked intellectual disability characterized by moderate to severe intellectual disability that has_material_basis_in mutation in a region on chromosome Xq24.

Synonyms: MRX88, X-linked mental retardation 88

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

: agtr2

MIM:

MIM:300852 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 88; XLID88

MIM:300852 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 88; XLID88

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)