autosomal dominant non-syndromic intellectual disability 23

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Summary

Literature (0)

DOID:0070053 - autosomal dominant non-syndromic intellectual disability 23

Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of SETD5 on chromosome 3p25.3.

Synonyms: MRD23, autosomal dominant mental retardation 23,

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

OMIM:

MIM:615761 - mental retardation, autosomal dominant 23; mrd23

MIM:615761 - mental retardation, autosomal dominant 23; mrd23

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)