OMOP Concept 28396
Hereditary hemolytic anemia
StandardConditionSNOMED38911009Disorder
Maps from
35
Descendants
44
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
35 source codes normalize to Hereditary hemolytic anemia via the OMOP "Maps to" relationship.
Showing 25 of 35 source codes. Retrieve the full set via the API.
Synonyms
Alternative names recorded for Hereditary hemolytic anemia across source vocabularies.
- anemia hemolítica hereditaria
- anemia hemolítica hereditaria (trastorno)
- Hereditary haemolytic anaemia
- Hereditary hemolytic anemia (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.
- 1Hemoglobin below reference range
- 1Hemolytic anemia
- 1Hereditary red blood cell disorder
- 2Anemia
- 2Hemoglobin level outside reference range
- 2Hemolytic disorder
- 2Hereditary disorder of cellular element of blood
- 2Measurement finding below reference range
- 2Red blood cell count below reference range
- 2Red blood cell disorder
- 3Cytopenia
- 3Disorder of body system
- 3Disorder of cellular component of blood
- 3Hematology test outside reference range
- 3Hemoglobin finding
- 3Hemolysis
- 3Hereditary disorder by system
- 3Measurement finding outside reference range
- 3Red blood cell count outside reference range
- 4Blood cell count outside reference range
- 4Disease
- 4Finding of blood, lymphatics and immune system
- 4Hematopoietic system finding
- 4Hereditary disease
- 4Measurement finding
Showing 25 of 34. Retrieve the full set via the API.
Narrower concepts
(44)Included automatically when you query with descendants.
- 1Glutathione synthetase deficiency
- 1Hemolytic anemia due to glutathione metabolism disorder
- 1Hemolytic anemia due to triose phosphate isomerase deficiency
- 1Hereditary elliptocytosis
- 1Hereditary nonspherocytic hemolytic anemia
- 1Hereditary spherocytosis
- 2Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome
- 2Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism
- 2Glutathione synthase deficiency with 5-oxoprolinuria
- 2Glutathione synthase deficiency without 5-oxoprolinuria
- 2Hemolytic anemia due to adenylate kinase deficiency
- 2Hemolytic anemia due to erythrocyte adenosine deaminase overproduction
- 2Hereditary elliptocytosis due to abnormal protein 4.1
- 2Hereditary elliptocytosis due to alpha spectrin defect
- 2Hereditary elliptocytosis due to beta spectrin-ankyrin interaction
- 2Hereditary elliptocytosis due to beta spectrin defect in self-association
- 2Hereditary elliptocytosis due to deficiency of protein 4.1
- 2Hereditary elliptocytosis due to glycophorin C deficiency
- 2Hereditary elliptocytosis with transient poikilocytosis
- 2Hereditary pyropoikilocytosis
- 2Hereditary spherocytosis due to beta spectrin defect
- 2Hereditary spherocytosis due to deficiency of protein 4.2
- 2Hereditary spherocytosis due to spectrin deficiency
- 2HNSHA due to decreased adenosine deaminase activity
- 2HNSHA due to diphosphoglycerate mutase deficiency
Showing 25 of 44. Retrieve the full set via the API.
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