|
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
MIM:613192 - mental retardation, autosomal recessive 13; mrt13 |
MIM:614202 - mental retardation, autosomal recessive 15; mrt15 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
intellectual disability (is_a)