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DOID:0070056 - autosomal dominant intellectual developmental disorder 26
Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the AUTS2 gene on chromosome 7q11.22.
Synonyms: MRD26, autosomal dominant mental retardation 26, autosomal dominant non-syndromic intellectual disability 26,
Echinobase Genes :
MIM:615834 - mental retardation, autosomal dominant 26; mrd26 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee