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Summary Literature (0)
DOID:0070072 - autosomal dominant non-syndromic intellectual disability 42


Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of GNB1 on chromosome 1p36.33.

Synonyms: MRD42, autosomal dominant mental retardation 42

Xenbase Genes : gnb1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014855 - intellectual disability, autosomal dominant 42


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)