autosomal dominant intellectual developmental disorder 10

Summary

DOID:0070040 - autosomal dominant intellectual developmental disorder 10

Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the CACNG2 gene on chromosome 22q12.3.

Synonyms: MRD10, autosomal dominant mental retardation 10, autosomal dominant non-syndromic intellectual disability 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

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

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

Parent(s): autosomal dominant intellectual developmental disorder (is_a)