OMOP Concept 4311397
Alpha plus thalassemia deletion type
StandardConditionSNOMED86242003Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Alpha plus thalassemia deletion type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 149050 | Alpha+ thalassaemia, deletion type | Non-standard |
| Nebraska Lexicon | 86242003 | alpha^+^ Thalassaemia, deletion type | Non-standard |
Synonyms
Alternative names recorded for Alpha plus thalassemia deletion type across source vocabularies.
- Alpha plus thalassaemia deletion type
- Alpha plus thalassemia deletion type (disorder)
- deleción tipo talasemia alfa más
- deleción tipo talasemia alfa más (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(38)Roll up to these when you need a wider cohort.
- 1Alpha plus thalassemia
- 1Congenital anemia
- 2Alpha thalassemia
- 2Anemia
- 2Congenital disease
- 2Hemoglobin below reference range
- 2Red blood cell count below reference range
- 3Cytopenia
- 3Disorder of cellular component of blood
- 3Disorder of fetus and/or newborn
- 3Hemoglobin level outside reference range
- 3Measurement finding below reference range
- 3Red blood cell count outside reference range
- 3Thalassemia
- 4Anemia due to disturbance of hemoglobin synthesis
- 4Blood cell count outside reference range
- 4Disease
- 4Finding of blood, lymphatics and immune system
- 4Hematology test outside reference range
- 4Hemoglobin finding
- 4Hereditary hemoglobinopathy
- 4Measurement finding outside reference range
- 4Red blood cell count - finding
- 5Clinical finding
- 5Hematopoietic system finding
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