MeSH Treeview
Query OMIM entry list
608836
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CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Digestive System Diseases
Liver Diseases
Fatty Liver
Nervous System Diseases
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Death
Cardiovascular Diseases
Heart Diseases
Arrhythmias, Cardiac
Cardiomyopathies
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Nutritional and Metabolic Diseases
Metabolic Diseases
Calcium Metabolism Disorders
Calcinosis
Glucose Metabolism Disorders
Hypoglycemia
Metabolism, Inborn Errors
Mitochondrial Diseases
Mitochondrial Myopathies
Water-Electrolyte Imbalance
Hyperkalemia
Nutrition Disorders
Malnutrition
Deficiency Diseases
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Arrhythmias, Cardiac
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Death
Fetal Death
Disease
Syndrome
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