Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0070059 - autosomal dominant non-syndromic intellectual disability 29


Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of SETBP1 on chromosome 18q12.3.

Synonyms: MRD29, autosomal dominant mental retardation 29

Xenbase Genes : zmynd11, setbp1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014482 - intellectual disability, autosomal dominant 29


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant non-syndromic intellectual disability (is_a)