intellectual developmental disorder with dysmorphic facies and behavioral abnormalities Disease Ontology Browser

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Disease Ontology Browser

intellectual developmental disorder with dysmorphic facies and behavioral abnormalities (DOID:0061129)
Alliance: disease page
Synonyms: FBXO11-related NDD; FBXO11-related neurodevelopmental disorder; IDDFBA
Alt IDs: OMIM:618089
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in FBXO11 gene on chromosome 2p16.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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