Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0112021 - non-syndromic X-linked intellectual disability ARX-related


Disease Ontology Definition:A non-syndromic X-linked intellectual disability characterized by moderate to profound intellectual disability with variable additional features that has_material_basis_in hemizygous mutation in ARX on chromosome Xp21.3.

Synonyms: ARX-related intellectual disability, MRXARX, X-linked mental retardation 29, X-linked mental retardation 29 and others, X-linked mental retardation 32, X-linked mental retardation 33, X-linked mental retardation 38, X-linked mental retardation 43, X-linked mental retardation 52, X-linked mental retardation 54, X-linked mental retardation 76, X-linked mental retardation 87, X-linked mental retardation with or without seizures ARX-related

Xenbase Genes : arx



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)