FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term immunodeficiency 132A ID (Ontology) DOID:0061101 (Human Disease)
Definition A primary immunodeficiency disease that is characterized by increased susceptibility to infection with certain pathogens and that has_material_basis_in heterozygous dominant-negative mutation in the TRAF3 gene on chromosome 14q32.
Also Known As "IMD132A"
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DO.org
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 Genes
 immunodeficiency 132A       1
 for disease ribbon | immunodeficiency 132A       1
 model of | immunodeficiency 132A       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease________
immune system disease                 |
 |__primary immunodeficiency disease__|
                                      immunodeficiency 132A  1 rec.
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Is a autosomal dominant disease
primary immunodeficiency disease
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Synonyms
  • "IMD132A" EXACT OMO:0003012
Secondary IDs
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MIM:614849