OMOP Concept 4144746
Hereditary hemoglobinopathy
StandardConditionSNOMED427306008Disorder
Maps from
1
Descendants
131
Valid from
31 Jul 2007
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Hereditary hemoglobinopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| HemOnc | 46106 | Inherited hemoglobinopathy | Non-standard |
Synonyms
Alternative names recorded for Hereditary hemoglobinopathy across source vocabularies.
- hemoglobinopatía hereditaria
- hemoglobinopatía hereditaria (trastorno)
- Hereditary haemoglobinopathy
- Hereditary hemoglobinopathy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Congenital disease
- 1Hemoglobinopathy
- 1Hereditary red blood cell disorder
- 2Fetal and/or neonatal disorder
- 2Hereditary disorder of cellular element of blood
- 2Red blood cell disorder
- 3Disease
- 3Disorder of body system
- 3Disorder of cellular component of blood
- 3Hereditary disorder by system
- 4Clinical finding
- 4Finding of blood, lymphatics and immune system
- 4Hereditary disease
- 5Genetic disease
Narrower concepts
(131)Included automatically when you query with descendants.
- 1Hemoglobinopathy Toms River
- 1Hereditary hemoglobinopathy due to globin chain mutation
- 1Hereditary persistence of fetal hemoglobin
- 1Heterozygous hemoglobinopathy
- 1Homozygous hemoglobinopathy
- 1Thalassemia
- 2Acquired hemoglobin H disease
- 2Alpha-beta thalassemia
- 2Alpha thalassemia
- 2Beta thalassemia
- 2Delta thalassemia
- 2Gamma thalassemia
- 2Hb Lepore thalassemia
- 2Hemoglobin C disease
- 2Hemoglobin C trait
- 2Hemoglobin D disease
- 2Hemoglobin D trait
- 2Hemoglobin E disease
- 2Hemoglobin E trait
- 2Hemoglobin Iraq-Halabja trait
- 2Hemoglobin M disease
- 2Hemoglobin O-Arab trait
- 2Hereditary hemoglobin S
- 2Hereditary persistence of fetal hemoglobin, intellectual disability syndrome
- 2Hereditary persistence of fetal hemoglobin thalassemia
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