OMOP Concept 4121285
Phagocytic cell defect
StandardConditionSNOMED234573000Disorder
Maps from
1
Descendants
122
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Phagocytic cell defect via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 234573000 | Phagocytic cell defect | Non-standard |
Synonyms
Alternative names recorded for Phagocytic cell defect across source vocabularies.
- defecto de célula fagocítica
- defecto de célula fagocítica (trastorno)
- Phagocytic cell defect (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(5)Roll up to these when you need a wider cohort.
Narrower concepts
(122)Included automatically when you query with descendants.
- 1Disorder of phagocytic cell number
- 1Functional disorder of polymorphonuclear neutrophil
- 1Phagocytic cell dysfunction
- 2Combined phagocytic defect
- 2Defective phagocytic cell adhesion
- 2Defective phagocytic cell chemotaxis
- 2Defective phagocytic cell killing
- 2Defective phagocytic cell opsonization
- 2Lichtenstein syndrome
- 2Lipochrome histiocytosis - familial
- 2Quantitative abnormality of granulocytes
- 2Susceptibility to localized juvenile periodontitis
- 3Agranulocytosis
- 3Chédiak-Higashi syndrome
- 3Chronic granulomatous disease
- 3Glutathione synthetase deficiency
- 3Gluthathione peroxidase deficiency
- 3Hemolytic erythrophagocytic syndrome
- 3Leukocyte adhesion deficiency
- 3Leukocyte glucose-6-phosphate dehydrogenase deficiency
- 3Mannan-binding protein deficiency
- 3Monocytopenia with susceptibility to infections
- 3Myeloperoxidase deficiency
- 3Neutrophil lactoferrin deficiency
- 3Neutrophil secondary granule deficiency
- 3Periodic fever, immunodeficiency, thrombocytopenia syndrome
- 3Quantitative disorder of neutrophils
- 4Agranulocytosis caused by antithyroid agent
- 4Agranulocytosis co-occurrent with human immunodeficiency virus infection
- 4Agranulocytosis due to and following administration of antineoplastic agent
- 4Attenuated Chédiak-Higashi syndrome
- 4Chronic granulomatous disease, type I
- 4Chronic granulomatous disease, type IA
- 4Chronic granulomatous disease, type II
- 4Chronic granulomatous disease, type IIA
- 4Chronic granulomatous disease, type III
- 4Chronic granulomatous disease, type IV
- 4Chronic granulomatous disease, type IVA
- 4Glutathione synthase deficiency with 5-oxoprolinuria
- 4Glutathione synthase deficiency without 5-oxoprolinuria
- 4Hemophagocytic lymphohistiocytosis
- 4Leukocyte adhesion deficiency - type 1
- 4Leukocyte adhesion deficiency - type 2
- 4Leukocyte adhesion deficiency type III
- 4Neutropenic disorder
- 4Neutrophilia disorder
- 4Pseudoneutrophilia
- 4Secondary agranulocytosis
- 5Acquired neutropenia
- 5Acquired neutrophilia
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