Myeloperoxidase deficiency

Preferred Label : Myeloperoxidase deficiency;

ICD-11 definition : 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.;

Details

Origin ID

1933575033;

UMLS CUI

C0398595;

Currated CISMeF NLP mapping
- Myeloperoxidase deficiency [OMIM Phenotype]
- Myeloperoxidase deficiency [ORDO Disease]
- Myeloperoxidase deficiency [MedDRA Preferred Term]
- Myeloperoxidase deficiency (disorder) [SNOMED CT concept]
- myeloperoxidase deficiency [MeSH Supplementary Concept]
- myeloperoxidase deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Myeloperoxidase deficiency [MedDRA Preferred Term]
- Myeloperoxidase deficiency [OMIM Phenotype]
- Myeloperoxidase deficiency [ORDO Disease]
- Myeloperoxidase deficiency (disorder) [SNOMED CT concept]
- Myeloperoxidase deficiency syndrome (disorder) [SNOMED CT concept]
- myeloperoxidase deficiency [MeSH concept]
- myeloperoxidase deficiency [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients