autosomal dominant intellectual developmental disorder 13

Summary

DOID:0070043 - autosomal dominant intellectual developmental disorder 13

Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the DYNC1H1 gene on chromosome 14q32.31.

Synonyms: MRD13, autosomal dominant mental retardation 13, autosomal dominant non-syndromic intellectual disability 13, mental retardation, autosomal dominant 13, with neuronal migration defects,

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

: dync1h1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013805 - intellectual disability, autosomal dominant 13

MONDO:0013805 - intellectual disability, autosomal dominant 13

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)