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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,
Echinobase Genes :
MIM:614256 - mental retardation, autosomal dominant 10; mrd10 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee