FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term immunodeficiency 13 ID (Ontology) DOID:0111987 (Human Disease)
Definition A T cell deficiency characterized by decreased CD4 T-lymphocyte counts that has_material_basis_in heterozygous mutation in the UNC119 gene on chromosome 17q11.2.
Also Known As "ICL" ; "idiopathic CD4 lymphopenia" ; "IMD13"
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DO.org
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 Genes
 immunodeficiency 13       1
 for disease ribbon | immunodeficiency 13       1
 model of | immunodeficiency 13       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease____
primary immunodeficiency disease  |
 |__T cell deficiency_____________|
                                  immunodeficiency 13  1 rec.
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Is a autosomal dominant disease
T cell deficiency
Part of
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Synonyms
  • "ICL" EXACT OMO:0003012
    "idiopathic CD4 lymphopenia" EXACT
    "IMD13" EXACT OMO:0003012
Secondary IDs
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GARD:12375
MIM:615518
ORDO:228000
UMLS_CUI:C3809768