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DOID:0061129 - intellectual developmental disorder with dysmorphic facies and behavioral abnormalities
Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in FBXO11 gene on chromosome 2p16.
Synonyms: FBXO11-related NDD, FBXO11-related neurodevelopmental disorder, IDDFBA
Xenbase Genes

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee