Summary Literature (0)

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:

Echinobase Genes : LOC577399, taf2, med23, pgap1, mettl23, smarcb1, dync1h1, kptn, tti2, kansl1, trappc9, ctcf, nsun2


OMIM:

MIM:613192 - mental retardation, autosomal recessive 13; mrt13

MIM:614202 - mental retardation, autosomal recessive 15; mrt15

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

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