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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=LP30929-1

Language Variants Get Info

TagLanguageTranslation
zh-CNChinese (China)血红蛋白 G
Synonyms: Hgb G
fr-CAFrench (Canada)Hémoglobine G
et-EEEstonian (Estonia)Hemoglobiin G
es-ESSpanish (Spain)Hemoglobina G
it-ITItalian (Italy)Emoglobina G
tr-TRTurkish (Turkey)Hemoglobin G
ru-RURussian (Russian Federation)Гемоглобин G
nl-NLDutch (Netherlands)hemoglobine G
fr-BEFrench (Belgium)Hémoglobine G
Synonyms: HbG
fr-FRFrench (France)Hémoglobine G
pl-PLPolish (Poland)Hemoglobina G
el-GRGreek (Greece)Αιμοσφαιρίνη G
Synonyms: Αιμοσφαιρίνη G