autosomal dominant non-syndromic intellectual disability 4

Summary

DOID:0070034 - autosomal dominant non-syndromic intellectual disability 4

Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of KIRREL3 on chromosome 11q24.2.

Synonyms: MRD4, autosomal dominant mental retardation 4

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

: kirrel3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012947 - intellectual disability, autosomal dominant 4

MONDO:0012947 - intellectual disability, autosomal dominant 4

OMIM:

OMIM:612581 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 4; MRD4

OMIM:612581 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 4; MRD4

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

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

Parent(s): autosomal dominant non-syndromic intellectual disability (is_a)