OMOP Concept 4009785
Anemia due to membrane defect
StandardConditionSNOMED111575000Disorder
Maps from
2
Descendants
10
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Anemia due to membrane defect via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 148860 | Anaemia due to membrane defect | Non-standard |
| Nebraska Lexicon | 111575000 | Anaemia due to membrane defect | Non-standard |
Synonyms
Alternative names recorded for Anemia due to membrane defect across source vocabularies.
- Anaemia due to membrane defect
- anemia causada por defecto de membrana
- Anemia due to membrane defect (disorder)
- anemia por defecto de la membrana celular eritrocitaria
- anemia por defecto de la membrana celular eritrocitaria (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Anemia due to intrinsic red cell abnormality
- 1Hemolytic anemia
- 2Anemia
- 2Hemolytic disorder
- 2Red blood cell count below reference range
- 3Cytopenia
- 3Disorder of cellular component of blood
- 3Hemolysis
- 3Red blood cell count outside reference range
- 4Blood cell count outside reference range
- 4Disease
- 4Finding of blood, lymphatics and immune system
- 4Measurement finding below reference range
- 4Red blood cell count - finding
- 4Red blood cell destruction finding
- 5Clinical finding
- 5Functional finding
- 5Measurement finding
- 5Measurement finding outside reference range
- 6Evaluation finding
- 7Procedure related finding
Narrower concepts
(10)Included automatically when you query with descendants.
- 1Hereditary spherocytosis
- 1Infantile pyknocytosis
- 2Hereditary spherocytosis due to beta spectrin defect
- 2Hereditary spherocytosis due to deficiency of protein 4.2
- 2Hereditary spherocytosis due to spectrin deficiency
- 3Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
- 3Mild hereditary spherocytosis due to spectrin deficiency
- 3Severe hereditary spherocytosis due to spectrin deficiency
- 4Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
- 4Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
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