OMOP Concept 4207240
Anemia due to intrinsic red cell abnormality
StandardConditionSNOMED323666000Disorder
Maps from
2
Descendants
42
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 intrinsic red cell abnormality via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 148863 | Anaemia due to intrinsic red cell abnormality | Non-standard |
| Nebraska Lexicon | 323666000 | Anaemia due to intrinsic red cell abnormality | Non-standard |
Synonyms
Alternative names recorded for Anemia due to intrinsic red cell abnormality across source vocabularies.
- Anaemia due to intrinsic red cell abnormality
- anemia debida a alteración intrínseca del eritrocito
- anemia debida a alteración intrínseca del eritrocito (trastorno)
- anemia debida a alteración intrínseca del glóbulo rojo
- Anemia due to intrinsic red cell abnormality (disorder)
- anemia por anomalía intrínseca del eritrocito
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
(42)Included automatically when you query with descendants.
- 1Anemia due to membrane defect
- 1Hereditary elliptocytosis due to abnormal protein 4.1
- 1Hereditary elliptocytosis due to alpha spectrin defect
- 1Hereditary elliptocytosis due to beta spectrin-ankyrin interaction
- 1Hereditary elliptocytosis due to beta spectrin defect in self-association
- 1Hereditary elliptocytosis due to deficiency of protein 4.1
- 1Hereditary elliptocytosis due to glycophorin C deficiency
- 1Hereditary pyropoikilocytosis
- 1Paroxysmal nocturnal hemoglobinuria
- 1Rh deficiency syndrome
- 1Sickle cell-hemoglobin SS disease
- 1Stomatocytosis
- 1Xerocytosis
- 2Acquired stomatocytosis
- 2Dehydrated hereditary stomatocytosis
- 2Familial pseudohyperkalemia
- 2Hemoglobin SS disease with crisis
- 2Hemoglobin SS disease without crisis
- 2Hereditary spherocytosis
- 2Hereditary stomatocytosis
- 2Infantile pyknocytosis
- 2Overhydrated hereditary stomatocytosis
- 2Sickle cell anemia in mother complicating childbirth
- 2Sickle cell anemia with coexistent alpha-thalassemia
- 2Sickle cell anemia with high hemoglobin F
- 2Southeast Asian ovalocytosis
- 3Acute sickle cell splenic sequestration crisis
- 3Hemoglobin SS disease with vasoocclusive crisis
- 3Hereditary cryohydrocytosis with normal stomatin
- 3Hereditary cryohydrocytosis with reduced stomatin
- 3Hereditary spherocytosis due to beta spectrin defect
- 3Hereditary spherocytosis due to deficiency of protein 4.2
- 3Hereditary spherocytosis due to spectrin deficiency
- 3Sickle cell crisis with extensive hemolysis
- 3Vasoocclusive sickle cell crisis
- 4Acute splenic sequestration due to sickle cell hemoglobin C disease with crisis
- 4Acute splenic sequestration of spleen due to sickle cell thalassemia with crisis
- 4Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
- 4Mild hereditary spherocytosis due to spectrin deficiency
- 4Severe hereditary spherocytosis due to spectrin deficiency
- 5Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
- 5Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
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