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 Name
Sickle cells
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.