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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


OMIM:
OMIM:300419 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 29; XLID29

Other Model Organisms: AGR, 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)