non-syndromic intellectual disability

Summary

DOID:0050889 - non-syndromic intellectual disability

Disease Ontology Definition:An intellectual disability that is characterized by the absence of associated medical and behavioral signs and symptoms.

Synonyms:

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

: tnik, sox4, rps6ka3, tbl1xr1, smarce1, il1rapl1, sox11, arx, smarca4, ezr, hivep2, mef2c, ctnnb1, syngap1, slc9a7, [+]

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0000509 - non-syndromic intellectual disability

MONDO:0000509 - non-syndromic intellectual disability

MIM:

MIM:613192 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 13; MRT13
MIM:614202 - RAFIQ SYNDROME; RAFQS

MIM:613192 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 13; MRT13

MIM:614202 - RAFIQ SYNDROME; RAFQS

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

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

Parent(s): intellectual disability (is_a)