autosomal dominant non-syndromic intellectual disability 10

Summary

DOID:0070040 - autosomal dominant non-syndromic intellectual disability 10

Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of CACNG2 on chromosome 22q12.3.

Synonyms: MRD10, autosomal dominant mental retardation 10,

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

: cacng2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013657 - intellectual disability, autosomal dominant 10

MONDO:0013657 - intellectual disability, autosomal dominant 10

OMIM:

OMIM:614256 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 10; MRD10

OMIM:614256 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 10; MRD10

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)