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Summary Literature (0)
DOID:0070071 - autosomal dominant non-syndromic intellectual disability 41


Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of TBL1XR1 on chromosome 3q26.32.

Synonyms: MRD41, autosomal dominant mental retardation 41


In Mondo Disease Ontology:
MONDO:0014842 - intellectual disability, autosomal dominant 41

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : tbl1xr1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant non-syndromic intellectual disability (is_a)