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DOID:0070033 - autosomal dominant non-syndromic intellectual disability 3
Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of CDH15 on chromosome 16q24.3.
Synonyms: MRD3, autosomal dominant mental retardation 3,
Echinobase Genes :
MIM:612580 - mental retardation, autosomal dominant 3; mrd3 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee