autosomal dominant intellectual developmental disorder 41

Summary

DOID:0070071 - autosomal dominant intellectual developmental disorder 41

Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the TBL1XR1 gene on chromosome 3q26.32.

Synonyms: MRD41, autosomal dominant mental retardation 41, autosomal dominant non-syndromic intellectual disability 41,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: tbl1xr1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014842 - intellectual disability, autosomal dominant 41

MONDO:0014842 - intellectual disability, autosomal dominant 41

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant intellectual developmental disorder (is_a)