non-syndromic X-linked intellectual disability

Summary

DOID:0050776 - non-syndromic X-linked intellectual disability

Disease Ontology Definition:A non-syndromic intellectual disability characterized by a X-linked inheritance pattern.

Synonyms: non-specific X-linked mental retardation,

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, il1rapl1, arx, slc9a7, cnksr2, rab39b, mecp2, dmd.2, agtr2, tspan7, syp, zdhhc15, arhgef6, clcn4, znf711, [+]

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0019181 - non-syndromic X-linked intellectual disability

MONDO:0019181 - non-syndromic X-linked intellectual disability

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

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

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