OMOP Concept 4242755
A-gamma beta+ HPFH AND beta0 thalassemia in cis
StandardConditionSNOMED5967006Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to A-gamma beta+ HPFH AND beta0 thalassemia in cis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 150928 | A gamma beta+ HPFH and beta 0 thalassemia in CIS | Non-standard |
| Nebraska Lexicon | 5967006 | A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Non-standard |
Synonyms
Alternative names recorded for A-gamma beta+ HPFH AND beta0 thalassemia in cis across source vocabularies.
- A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis
- A gamma beta+ hereditary persistence of fetal hemoglobin AND beta0 thalassemia in cis
- A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis (disorder)
- A>gamma< beta^+^ HPFH AND beta^0^ thalassaemia in cis
- A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis
- A gamma beta+ HPFH AND beta0 thalassemia in cis
- A gamma beta<sup>+</sup> hereditary persistence of fetal hemoglobin AND beta<sup>0</sup> thalassemia in cis
- A<sub>gamma</sub> beta<sup>+</sup> HPFH AND beta<sup>0</sup> thalassemia in cis
- persistencia hereditaria de hemoglobina fetal A>gamma< beta^+^ Y talasemia beta^0^ en cis
- persistencia hereditaria de hemoglobina fetal A gamma beta+ Y talasemia beta0 en cis
- persistencia hereditaria de hemoglobina fetal A>gamma< beta^+^ Y talasemia beta^0^ en cis (trastorno)
- persistencia hereditaria de hemoglobina fetal A<sub>gamma</sub> beta<sup>+</sup> Y talasemia beta<sup>0</sup> en cis
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.
- 1HPFH A gamma beta+ thalassemia
- 2Beta plus thalassemia
- 2Hereditary persistence of fetal hemoglobin thalassemia
- 3Beta thalassemia
- 3Thalassemia
- 4Anemia due to disturbance of hemoglobin synthesis
- 4Hereditary hemoglobinopathy
- 5Anemia
- 5Congenital disease
- 5Hemoglobin below reference range
- 5Hemoglobinopathy
- 5Hereditary red blood cell disorder
- 6Disorder of cellular component of blood
- 6Disorder of fetus and/or newborn
- 6Hemoglobin level outside reference range
- 6Hereditary disorder of cellular element of blood
- 6Measurement finding below reference range
- 6Red blood cell disorder
- 7Disease
- 7Disorder of body system
- 7Finding of blood, lymphatics and immune system
- 7Hematology test outside reference range
- 7Hemoglobin finding
- 7Hereditary disorder by system
- 7Measurement finding outside reference range
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