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GTR Home > Conditions/Phenotypes > Myeloperoxidase deficiency

Myeloperoxidase deficiency

Synonyms
MPO deficiency; Myeloperoxidase deficiency syndrome

Summary

A rare primary immunodeficiency due to a defect in innate immunity characterized by a marked decrease or absence of myeloperoxidase activity in neutrophils and monocytes. Clinically, most patients are asymptomatic. Occasionally, severe infectious complications may occur, particularly recurrent candida infections, being especially severe in the setting of comorbid diabetes mellitus. [from ORDO]

Available tests

8 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (8 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: , MPO
    Summary: myeloperoxidase

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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