Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Hemoglobinopathies
Terme préférentiel
Anemia, Sickle Cell
Type
-
mesh:Descriptor
Définition
- 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.
Concept générique
Concepts spécifiques
Synonyme(s)
- HbS Disease
- Hemoglobin S Disease
- Sickle Cell Anemia
- Sickle Cell Disease
- Sickle Cell Disorders
- Sickling Disorder Due to Hemoglobin S
Qualificatif(s) autorisé(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)
Traductions
-
français
-
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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