FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term immunodeficiency 118 ID (Ontology) DOID:0061084 (Human Disease)
Definition A primary immunodeficiency disease that is characterized by increased susceptibility to the development of disseminated mycobacterial infections in infancy, notably after BCG vaccination and that has_material_basis_in hemizygous mutation in the MCTS1 gene on chromosome Xq24.
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 Genes
 immunodeficiency 118       1
 for disease ribbon | immunodeficiency 118       1
 model of | immunodeficiency 118       1
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__X-linked recessive disease________
immune system disease                 |
 |__primary immunodeficiency disease__|
                                      immunodeficiency 118  1 rec.
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Is a X-linked recessive disease
primary immunodeficiency disease
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MIM:301115