MeSH Treeview
Query OMIM entry list
604377
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CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Mitochondrial Encephalomyopathies
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Abortion, Spontaneous
Cardiovascular Diseases
Heart Diseases
Cardiomyopathies
Cardiomyopathy, Hypertrophic
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Subvalvular
Cardiomyopathy, Hypertrophic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Cytochrome-c Oxidase Deficiency
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Mitochondrial Encephalomyopathies
Mitochondrial Diseases
Cytochrome-c Oxidase Deficiency
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
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