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Summary Literature (0)
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 : cacng2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013657 - intellectual disability, autosomal dominant 10

OMIM:
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)