Results 1 - 5 of 5 for Deficiency of "isobutyryl-CoA" dehydrogenase
  1. ... PubMed Recent literature OMIM Genetic disorder catalog Conditions > Isobutyryl-CoA dehydrogenase deficiency On this page: Description Genetic changes Inheritance Diagnosis ...
  2. Rare Diseases and Related Terms From the National Institutes of Health (Office of Rare Diseases)  
    ... dehydrogenase deficiency * Acyl-CoaA dehydrogenase family, member 8, deficiency of - See Isobutyryl-CoA dehydrogenase deficiency * AD dRTA - See Renal tubular acidosis, distal, ...
  3. Metabolic Disorders (National Library of Medicine)  
    Metabolism is the process your body uses to get or make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive ...
  4. Newborn Screening (National Library of Medicine)  
    ... treatment should start right away. NIH: National Institute of Child Health and Human Development
  5. Genetics Home Reference: Cardiomyopathy From the National Institutes of Health (National Library of Medicine)  
    ... familial restrictive cardiomyopathy glycogen storage disease type III isobutyryl-CoA dehydrogenase deficiency Kearns-Sayre syndrome neutral lipid storage disease with ...
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