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DOID:0070051 - autosomal dominant non-syndromic intellectual disability 21
Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of CTCF on chromosome 16q22.1.
Synonyms: MRD21, autosomal dominant mental retardation 21,
Echinobase Genes : ctcf
MIM:615502 - mental retardation, autosomal dominant 21; mrd21 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee