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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,
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)