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Anemia, Sickle Cell
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.
推出的年份:
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
diagnosis
diagnostic imaging
diet therapy
drug therapy
economics
embryology
enzymology
epidemiology
ethnology
etiology
genetics
history
immunology
metabolism
microbiology
mortality
nursing
parasitology
pathology
physiopathology
prevention and control
psychology
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veterinary
virology
树号:
C15.378.071.141.150.150, C15.378.420.155, C16.320.070.150, C16.320.365.155
MeSH 单一 ID:
D000755
进入的组:
Anemias, Sickle Cell
Sickle Cell Anemias
Hemoglobin S Disease
Disease, Hemoglobin S
Hemoglobin S Diseases
Sickle Cell Anemia
Sickle Cell Disorders
Cell Disorder, Sickle
Cell Disorders, Sickle
Sickle Cell Disorder
Sickling Disorder Due to Hemoglobin S
HbS Disease
Sickle Cell Disease
Cell Disease, Sickle
Cell Diseases, Sickle
Sickle Cell Diseases
All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Anemia [C15.378.071]
Anemia, Hemolytic [C15.378.071.141]
Anemia, Hemolytic, Congenital [C15.378.071.141.150]
Anemia, Dyserythropoietic, Congenital [C15.378.071.141.150.095]
Anemia, Hemolytic, Congenital Nonspherocytic [C15.378.071.141.150.100]
Anemia, Sickle Cell [C15.378.071.141.150.150]
Acute Chest Syndrome [C15.378.071.141.150.150.219]
Hemoglobin SC Disease [C15.378.071.141.150.150.440]
Sickle Cell Trait [C15.378.071.141.150.150.670]
Elliptocytosis, Hereditary [C15.378.071.141.150.365]
Glucosephosphate Dehydrogenase Deficiency [C15.378.071.141.150.480]
add_circle
Hemoglobin C Disease [C15.378.071.141.150.490]
Spherocytosis, Hereditary [C15.378.071.141.150.785]
Thalassemia [C15.378.071.141.150.875]
add_circle
All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Hemoglobinopathies [C15.378.420]
Anemia, Sickle Cell [C15.378.420.155]
Acute Chest Syndrome [C15.378.420.155.219]
Hemoglobin SC Disease [C15.378.420.155.440]
Sickle Cell Trait [C15.378.420.155.668]
Hemoglobin C Disease [C15.378.420.463]
Thalassemia [C15.378.420.826]
add_circle
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Anemia, Hemolytic, Congenital [C16.320.070]
Anemia, Dyserythropoietic, Congenital [C16.320.070.095]
Anemia, Hemolytic, Congenital Nonspherocytic [C16.320.070.100]
Anemia, Sickle Cell [C16.320.070.150]
Acute Chest Syndrome [C16.320.070.150.219]
Hemoglobin SC Disease [C16.320.070.150.440]
Sickle Cell Trait [C16.320.070.150.670]
Elliptocytosis, Hereditary [C16.320.070.365]
Glucosephosphate Dehydrogenase Deficiency [C16.320.070.480]
add_circle
Hemoglobin C Disease [C16.320.070.490]
Spherocytosis, Hereditary [C16.320.070.785]
Thalassemia [C16.320.070.875]
add_circle
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Hemoglobinopathies [C16.320.365]
Anemia, Sickle Cell [C16.320.365.155]
Acute Chest Syndrome [C16.320.365.155.219]
Hemoglobin SC Disease [C16.320.365.155.440]
Sickle Cell Trait [C16.320.365.155.668]
Hemoglobin C Disease [C16.320.365.463]
Thalassemia [C16.320.365.826]
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