OMOP Concept 4121107
Congenital transferrin deficiency
StandardConditionSNOMED234353009Disorder
Maps from
0
Descendants
1
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Synonyms
Alternative names recorded for Congenital transferrin deficiency across source vocabularies.
- Congenital transferrin deficiency (disorder)
- deficiencia congénita de transferrina
- deficiencia congénita de transferrina (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(33)Roll up to these when you need a wider cohort.
- 1Anemia due to disturbance of hemoglobin synthesis
- 1Autosomal recessive hereditary disorder
- 1Congenital anemia
- 1Microcytic anemia
- 2Anemia
- 2Autosomal hereditary disorder
- 2Congenital disease
- 2Hemoglobin below reference range
- 2Microcytosis
- 2Red blood cell count below reference range
- 3Cytopenia
- 3Disorder of cellular component of blood
- 3Fetal and/or neonatal disorder
- 3Hematopoietic system finding
- 3Hemoglobin level outside reference range
- 3Hereditary disease
- 3Measurement finding below reference range
- 3Microscopic specimen observation
- 3Red blood cell count outside reference range
- 4Blood cell count outside reference range
- 4Disease
- 4Evaluation finding
- 4Finding of blood, lymphatics and immune system
- 4Genetic disease
- 4Hematology test outside reference range
Showing 25 of 33. Retrieve the full set via the API.
Narrower concepts
(1)Included automatically when you query with descendants.
Get this concept via the API
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