FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term immunodeficiency 80 ID (Ontology) DOID:0061051 (Human Disease)
Definition A primary immunodeficiency disease that is characterized by variable manifestations and that has_material_basis_in compound heterozygous mutation in the MCM10 gene on chromosome 10p13.
Also Known As "immunodeficiency 80 with or without cautosomal recessive inheritancediomyopathy"
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 Genes
 immunodeficiency 80       1
 for disease ribbon | immunodeficiency 80       1
 model of | immunodeficiency 80       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease_______
immune system disease                 |
 |__primary immunodeficiency disease__|
                                      immunodeficiency 80  1 rec.
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Is a autosomal recessive disease
primary immunodeficiency disease
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Synonyms
  • "immunodeficiency 80 with or without cautosomal recessive inheritancediomyopathy" EXACT
Secondary IDs
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MIM:619313