MeSH Treeview
Query OMIM entry list
600649
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CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE
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Digestive System Diseases
Liver Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Nutritional and Metabolic Diseases
Metabolic Diseases
Glucose Metabolism Disorders
Hypoglycemia
Lipid Metabolism Disorders
Lipid Metabolism, Inborn Errors
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Death
Death, Sudden
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