MeSH Treeview
Query OMIM entry list
605019
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HYPOBETALIPOPROTEINEMIA, FAMILIAL, 2
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Smith-Lemli-Opitz Syndrome
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hypolipoproteinemias
Hypobetalipoproteinemias
Smith-Lemli-Opitz Syndrome
Steroid Metabolism, Inborn Errors
Smith-Lemli-Opitz Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Lipid Metabolism Disorders
Dyslipidemias
Hypolipoproteinemias
Hypobetalipoproteinemias
Smith-Lemli-Opitz Syndrome
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hypolipoproteinemias
Hypobetalipoproteinemias
Smith-Lemli-Opitz Syndrome
Steroid Metabolism, Inborn Errors
Smith-Lemli-Opitz Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
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