FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term intellectual developmental disorder with dysmorphic facies and behavioral abnormalities ID (Ontology) DOID:0061129 (Human Disease)
Definition An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in FBXO11 gene on chromosome 2p16.
Also Known As "FBXO11-related NDD" ; "FBXO11-related neurodevelopmental disorder" ; "IDDFBA"
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 Genes
 intellectual developmental disorder with dysmorphic facies and behavioral abnormalities       1
 for disease ribbon | intellectual developmental disorder with dysmorphic facies and behavioral abnormalities       1
 model of | intellectual developmental disorder with dysmorphic facies and behavioral abnormalities       1
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autosomal dominant disease
 |__autosomal dominant intellectual developmental disorder__
intellectual disability                                     |
 |__autosomal dominant intellectual developmental disorder__|
disease                                                     |
 |__syndrome________________________________________________|
                                                            intellectual developmental disorder with dysmorphic facies and behavioral abnormalities  1 rec.
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Is a autosomal dominant intellectual developmental disorder
syndrome
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Synonyms
  • "FBXO11-related NDD" EXACT
    "FBXO11-related neurodevelopmental disorder" EXACT
    "IDDFBA" EXACT OMO:0003012
Secondary IDs
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MIM:618089