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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: autosomal dominant mental retardation 10, autosomal dominant non-syndromic intellectual disability 10, MRD10
Xenbase Genes : cacng2
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