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:0070041 - autosomal dominant non-syndromic intellectual disability 11


Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of EPB41L1 on chromosome 20q11.23.

Synonyms: MRD11, autosomal dominant mental retardation 11

Xenbase Genes : epb41l1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013658 - intellectual disability, autosomal dominant 11

OMIM:
OMIM:614257 - CHROMOSOME 20q11-q12 DELETION SYNDROME

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)