Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Hemoglobinopathies
Preferred term
Anemia, Sickle Cell
Type
-
mesh:Descriptor
Definition
- A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S.
Broader concept
Narrower concepts
Entry terms
- HbS Disease
- Hemoglobin S Disease
- Sickle Cell Anemia
- Sickle Cell Disease
- Sickle Cell Disorders
- Sickling Disorder Due to Hemoglobin S
Allowable Qualifier(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
In other languages
-
French
-
Anémie à cellules falciformes
-
Anémie à drépanocytes
-
Anémie à hématies falciformes
-
Anémie drépanocytaire
-
Anémie falciforme
-
Anémie SS
-
Drépanocytose homozygote
-
Hémoglobinopathie à hématies falciformes
-
Hémoglobinose S
-
Hémoglobinose SS
-
Sicklanémie
-
Sicklémie
URI
http://data.loterre.fr/ark:/67375/JVR-HPS8Q007-W
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