OMOP Concept 4207240
Anemia due to intrinsic red cell abnormality
StandardConditionSNOMED323666000Disorder
Maps from
1
Descendants
44
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 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 |
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
(44)Included automatically when you query with descendants.
- 1Anemia due to membrane defect
- 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 cryohydrocytosis with normal stomatin
- 2Hereditary cryohydrocytosis with reduced stomatin
- 2Hereditary elliptocytosis
- 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
- 3Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome
- 3Hemoglobin SS disease with vasoocclusive crisis
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