Myeloperoxidase deficiency (Q64636): Difference between revisions
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Este é um transtorno genético comum que apresenta deficiência, em quantidade ou função, de mieloperoxidase, que é uma enzima encontrada em algumas células imunes fagocitárias, especialmente leucócitos polimorfonucleares. | |||
| description / en | description / en | ||
This is a common genetic disorder featuring deficiency, either in quantity or function, of myeloperoxidase, an enzyme found in certain phagocytic immune cells, especially polymorphonuclear leukocytes. | |||
Revision as of 12:20, 14 August 2026
This is a common genetic disorder featuring deficiency, either in quantity or function, of myeloperoxidase, an enzyme found in certain phagocytic immune cells, especially polymorphonuclear leukocytes.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1933575033 |
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| English | Myeloperoxidase deficiency |
This is a common genetic disorder featuring deficiency, either in quantity or function, of myeloperoxidase, an enzyme found in certain phagocytic immune cells, especially polymorphonuclear leukocytes. |
