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Query OMIM entry list
250620
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BETA-HYDROXYISOBUTYRYL CoA DEACYLASE, DEFICIENCY OF
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
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
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Nerve Degeneration
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