MeSH Treeview
Query OMIM entry list
231690
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GLUTARYL-CoA OXIDASE DEFICIENCY
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Signs and Symptoms
Signs and Symptoms, Digestive
Diarrhea
Database Center for Life Science
