autosomal dominant non-syndromic intellectual disability 13

Summary

DOID:0070043 - autosomal dominant non-syndromic intellectual disability 13

Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of DYNC1H1 on chromosome 14q32.31.

Synonyms: MRD13, autosomal dominant mental retardation 13, mental retardation, autosomal dominant 13, with neuronal migration defects,

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

: dync1h1

OMIM:

MIM:614563 - mental retardation, autosomal dominant 13; mrd13

MIM:614563 - mental retardation, autosomal dominant 13; mrd13

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)