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Summary Literature (0)
DOID:0070056 - autosomal dominant non-syndromic intellectual disability 26


Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of AUTS2 on chromosome 7q11.22.

Synonyms: MRD26, autosomal dominant mental retardation 26

Xenbase Genes : auts2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014361 - autism spectrum disorder due to AUTS2 deficiency

OMIM:
OMIM:615834 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 26; MRD26

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)