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Summary Literature (0)
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 : 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

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)