Description

An abnormal hemoglobin composed of four beta chains. It is caused by the reduced synthesis of the alpha chain. This abnormality results in ALPHA-THALASSEMIA. Source: National Library of Medicine, MeSH 2006

Basic Part Properties

Part Name
Hemoglobin H
Part Display Name
Hemoglobin H
Part Type
Component (Describes the core component or analyte measured)
Created On
2000-05-04
Construct for LOINC Short Name
Hgb H

LOINC Terminology Service (API) using HL7® FHIR® Get Info

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=LP16434-0

Language Variants Get Info

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