OMOP Concept 4009784
Congenital atransferrinemia
StandardConditionSNOMED111571009Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Congenital atransferrinemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 144148 | Congenital atransferrinaemia | Non-standard |
| MeSH | C538259 | Congenital atransferrinemia | Non-standard |
| Nebraska Lexicon | 111571009 | Congenital atransferrinaemia | Non-standard |
Synonyms
Alternative names recorded for Congenital atransferrinemia across source vocabularies.
- atransferrinemia congénita
- atransferrinemia congénita (trastorno)
- Congenital atransferrinaemia
- Congenital atransferrinemia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(34)Roll up to these when you need a wider cohort.
- 1Congenital transferrin deficiency
- 2Anemia due to disturbance of hemoglobin synthesis
- 2Autosomal recessive hereditary disorder
- 2Congenital anemia
- 2Microcytic anemia
- 3Anemia
- 3Autosomal hereditary disorder
- 3Congenital disease
- 3Hemoglobin below reference range
- 3Microcytosis
- 3Red blood cell count below reference range
- 4Cytopenia
- 4Disorder of cellular component of blood
- 4Disorder of fetus and/or newborn
- 4Hematopoietic system finding
- 4Hemoglobin level outside reference range
- 4Hereditary disease
- 4Measurement finding below reference range
- 4Microscopic specimen observation
- 4Red blood cell count outside reference range
- 5Blood cell count outside reference range
- 5Disease
- 5Evaluation finding
- 5Finding of blood, lymphatics and immune system
- 5Genetic disease
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