intellectual developmental disorder with dysmorphic facies and behavioral abnormalities

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Summary

Literature (0)

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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant intellectual developmental disorder (is_a), syndrome (is_a)