Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Hemoglobinopathies
Término preferido
Hemoglobin C Disease
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Tipo
-
mesh:Descriptor
Definición
- A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice.
Concepto genérico
Etiquetas alternativas
- Hemoglobin-C Disease
En otras lenguas
-
francés
-
Hémoglobinopathie C
URI
http://data.loterre.fr/ark:/67375/JVR-NW4B670C-J
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