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DOID:0070050 - mental retardation, autosomal dominant 20
Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of MEF2C on chromosome 5q14.3.
Synonyms: MRD20, autosomal dominant mental retardation 20,
Echinobase Genes :
MIM:613443 - mental retardation, autosomal dominant 20; mrd20 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee