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DOID:0080235 - autosomal dominant intellectual developmental disorder 48
Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the RAC1 gene on chromosome 7p22.
Synonyms: autosomal dominant mental retardation 48,
Xenbase Genes : rac1
MONDO:0030913 - intellectual disability, autosomal dominant 48 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee