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DOID:0070036 - autosomal dominant intellectual developmental disorder 6
Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the GRIN2B gene on chromosome 12p13.1.
Synonyms: MRD6, autosomal dominant mental retardation 6, autosomal dominant non-syndromic intellectual disability 6,
Xenbase Genes : grin2b
MONDO:0013509 - intellectual disability, autosomal dominant 6 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee