OMOP Concept 4312021
Hereditary pyropoikilocytosis
StandardConditionSNOMED9434008Disorder
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 Hereditary pyropoikilocytosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138742 | Hereditary pyropoikilocytosis | Non-standard |
| HPO | HP_0004839 | Pyropoikilocytosis | Non-standard |
| MeSH | C563004 | Pyropoikilocytosis, Hereditary | Non-standard |
Synonyms
Alternative names recorded for Hereditary pyropoikilocytosis across source vocabularies.
- Hereditary pyropoikilocytosis (disorder)
- HPP - hereditary pyropoikilocytosis
- piropoiquilocitosis hereditaria
- piropoiquilocitosis hereditaria (trastorno)
- PPH - piropoiquilocitosis hereditaria
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(48)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Hereditary elliptocytosis
- 2Anemia due to membrane defect
- 2Autosomal hereditary disorder
- 2Congenital hemolytic anemia
- 2Congenital malformation
- 2Developmental hereditary disorder
- 2Erythrocyte membrane abnormality
- 2Hereditary hemolytic anemia
- 3Anemia due to intrinsic red cell abnormality
- 3Congenital anemia
- 3Congenital disease
- 3Developmental disorder
- 3Hemoglobin below reference range
- 3Hemolytic anemia
- 3Hereditary disease
- 3Hereditary red blood cell disorder
- 3Red blood cell disorder
- 4Anemia
- 4Disease
- 4Disorder of body system
- 4Disorder of cellular component of blood
- 4Fetal and/or neonatal disorder
- 4Genetic disease
- 4Hemoglobin level outside reference range
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