myeloperoxidase (MPO) deficiency

myeloperoxidase (MPO) deficiency: my·elo·per·ox·i·dase (MPO) de·fi·cien·cy (mi″ə-lo-pər-okґsĭ-dās) an autosomal recessive disorder caused by mutation in the myeloperoxidase gene (MPO, locus:17q23.1), characterized by the complete absence of MPO in azurophil granules of neutrophils and monocytes; the deficiency is usually clinically insignificant although candidiasis may occur, especially in persons with diabetes mellitus.

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Myeloperoxidase — drawn from PDB 1D7W … Wikipedia
Myeloperoxidase deficiency — Classification and external resources Hypochlorous acid is normally produced by myeloperoxidase OMIM … Wikipedia
Myeloperoxidase — Vorhandene Strukturdaten: s. UniProt Masse/Länge … Deutsch Wikipedia
myeloperoxidase — A peroxidase occurring in phagocytic cells that can oxidize halogen ions ( e.g., I−) to the free halogen; an autosomal recessive deficiency of m. leads to impaired bacterial killing. * * * my·e·lo·per·ox·i·dase .mī ə lō pə räk sə .dās, .dāz … Medical dictionary
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