Medium chain acyl CoA dehydrogenase deficiency

An inherited deficiency of medium-chain acyl-CoA dehydrogenase that is characterized by intolerance to prolonged fasting, recurrent episodes of hypoglycemic COMA; medium-chain dicarboxylic aciduria, impaired ketogenesis, and low plasma and tissue CARNITINE levels. The disorder may be severe, and even fatal, in young patients. Germline mutations have been identified in the ACADM gene. OMIM: 201450

Also Known As:

ACADM Deficiency; Acyl-CoA dehydrogenase, medium chain, deficiency of; Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of; Carnitine Deficiency Secondary To Medium-Chain Acyl-Coa Dehydrogenase Deficiency; MCAD Deficiency; MCADH Deficiency; Medium Chain Acyl-Coa Dehydrogenase Deficiency; Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency; Medium-chain Acyl-CoA dehydrogenase deficiency

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Lipid Metabolism
      - Medium chain acyl CoA dehydrogenase deficiency: 410
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Lipid Metabolism
      - Medium chain acyl CoA dehydrogenase deficiency: 410
  - Lipid Metabolism Disorders: 898
    - Inborn Errors Lipid Metabolism
      - Medium chain acyl CoA dehydrogenase deficiency: 410
Enzymes and Coenzymes: 1
- Enzymes: 152586
  - Oxidoreductases: 13671
    - Oxidoreductases Acting on CH-CH Group Donors
      - Acyl-CoA Dehydrogenases: 26
        Acyl-CoA Dehydrogenase: 385
        Medium chain acyl CoA dehydrogenase deficiency: 410
Amino Acids, Peptides, and Proteins: 1
- Proteins: 484843
  - Flavoproteins: 234
    - Acyl-CoA Dehydrogenase: 385
      - Medium chain acyl CoA dehydrogenase deficiency: 410

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