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Query OMIM entry list
143890
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HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Parkinsonian Disorders
Parkinson Disease
Movement Disorders
Parkinsonian Disorders
Parkinson Disease
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Neuropathy, Ischemic
Neurodegenerative Diseases
Parkinson Disease
Eye Diseases
Optic Nerve Diseases
Optic Neuropathy, Ischemic
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Cardiovascular Diseases
Heart Diseases
Heart Valve Diseases
Myocardial Ischemia
Coronary Disease
Vascular Diseases
Aortic Diseases
Arterial Occlusive Diseases
Arteriosclerosis
Myocardial Ischemia
Coronary Disease
Optic Neuropathy, Ischemic
Hemic and Lymphatic Diseases
Lymphatic Diseases
Histiocytosis
Histiocytosis, Non-Langerhans-Cell
Xanthogranuloma, Juvenile
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fetal Diseases
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hyperlipidemia, Familial Combined
Hyperlipoproteinemia Type II
Hyperlipoproteinemia Type III
Lysosomal Storage Diseases
Skin and Connective Tissue Diseases
Skin Diseases
Xanthogranuloma, Juvenile
Nutritional and Metabolic Diseases
Metabolic Diseases
Lipid Metabolism Disorders
Dyslipidemias
Hyperlipidemias
Hypercholesterolemia
Hyperlipidemia, Familial Combined
Hyperlipoproteinemias
Hyperlipoproteinemia Type II
Hyperlipoproteinemia Type III
Hypertriglyceridemia
Lipid Metabolism, Inborn Errors
Xanthomatosis
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hyperlipidemia, Familial Combined
Hyperlipoproteinemia Type II
Hyperlipoproteinemia Type III
Lysosomal Storage Diseases
Animal Diseases
Disease Models, Animal
Primate Diseases
Monkey Diseases
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
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