Version 2.78

Description

Sickle-cell anemia is an autosomal recessive genetic blood disorder characterized by the presence of rigid and sickle-shaped red blood cells. The sickling occurs because of a mutation in the hemoglubin gene. In the US, the prevalence of the disease is about 1 in 5000, mostly affecting Americans of Sub-Sahara African descent. One third of all inhabitants of Sub-Sahara Africa carry the gene because in areas where malaria is common there is a survival advantage in carrying only one single sickle-cell gene (sickle-cell trait). Source: Regenstrief Help

Reference Information

Type Source Reference
Webcontent Lab Tests Online®Copyright Copyright © 2021 Lab Tests Online. All rights reserved. Sickle Cell

Basic Part Properties

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

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=LP17228-5

Language Variants Get Info

Tag Language Translation
zh-CN Chinese (China) 镰刀形红细胞
Synonyms: 镰形细胞;镰状红细胞;镰状细胞
fr-CA French (Canada) Drépanocytes
et-EE Estonian (Estonia) Sirprakud
es-ES Spanish (Spain) Drepanocitos
it-IT Italian (Italy) Cellule falciformi
tr-TR Turkish (Turkey) Orak hücreleri
ru-RU Russian (Russian Federation) Серповидные клетки
nl-NL Dutch (Netherlands) sikkelcellen
fr-BE French (Belgium) Drépanocytes
Synonyms: Cellules en faucille, Cellules en forme de faux.