LP30929-1
Hemoglobin G
Active
Description
Hemoglobin G (Hgb G) is a rare hemoglobin variant that results from particular mutations in either the alpha and beta globin chains. The most common Hgb G variant is Philadelphia, an alpha chain mutation occurring most frequently in individuals of African descent. Hgb G is usually clinically benign but may be associated with mild anemia. Hemoglobins exhibit different migration patterns in alkaline versus acidic electrophoresis conditions. So a combination of 2 procedures can be used in tandem to identify the hemoglobin variants. Source: Regenstrief LOINC
Basic Part Properties
- Part Name
- Hemoglobin G
- Part Display Name
- Hemoglobin G
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2003-02-03
- Construct for LOINC Short Name
- Hgb G
LOINC Terminology Service (API) using HL7® FHIR® Get Info
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- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=LP30929-1
Language Variants Get Info
Tag | Language | Translation |
---|---|---|
zh-CN | Chinese (China) | 血红蛋白 G Synonyms: Hgb G |
es-ES | Spanish (Spain) | Hemoglobina G |
it-IT | Italian (Italy) | Emoglobina G |
et-EE | Estonian (Estonia) | Hemoglobiin G |
tr-TR | Turkish (Turkey) | Hemoglobin G |
ru-RU | Russian (Russian Federation) | Гемоглобин G |
fr-BE | French (Belgium) | Hémoglobine G Synonyms: HbG |
fr-CA | French (Canada) | Hémoglobine G |
nl-NL | Dutch (Netherlands) | hemoglobine G |
pl-PL | Polish (Poland) | Hemoglobina G |
el-GR | Greek (Greece) | Αιμοσφαιρίνη G Synonyms: Αιμοσφαιρίνη G |
LOINC Copyright
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