Search Ontology:
Human Disease

intellectual developmental disorder with dysmorphic facies and behavioral abnormalities

Term ID
DOID:0061129
Synonyms
  • FBXO11-related NDD
  • FBXO11-related neurodevelopmental disorder
  • IDDFBA
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in FBXO11 gene on chromosome 2p16. https://pubmed.ncbi.nlm.nih.gov/30057029/
References
Ontology
Human Disease   ( DOID:0061129 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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