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DOID:0070041 - autosomal dominant intellectual developmental disorder 11
Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the EPB41L1 gene on chromosome 20q11.23.
Synonyms: MRD11, autosomal dominant mental retardation 11, autosomal dominant non-syndromic intellectual disability 11,
Xenbase Genes : epb41l1
MONDO:0013658 - intellectual disability, autosomal dominant 11 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee