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207750
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APOLIPOPROTEIN C-II DEFICIENCY
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Digestive System Diseases
Pancreatic Diseases
Pancreatitis
Hemic and Lymphatic Diseases
Lymphatic Diseases
Histiocytosis
Histiocytosis, Non-Langerhans-Cell
Xanthogranuloma, Juvenile
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hyperlipoproteinemia Type I
Skin and Connective Tissue Diseases
Skin Diseases
Xanthogranuloma, Juvenile
Nutritional and Metabolic Diseases
Metabolic Diseases
Lipid Metabolism Disorders
Dyslipidemias
Hyperlipidemias
Hyperlipoproteinemias
Hyperlipoproteinemia Type I
Hypertriglyceridemia
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hyperlipoproteinemia Type I
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
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