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Complementation Group C Molybdenum Cofactor Deficiency

Also Known As:

Molybdenum Cofactor Deficiency, Complementation Group C; Molybdenum Cofactor Deficiency Type C

Networked: 0 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Metal Metabolism
      - Complementation Group C Molybdenum Cofactor Deficiency
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Metal Metabolism
      - Complementation Group C Molybdenum Cofactor Deficiency
Enzymes and Coenzymes: 1
- Enzymes: 152586
  - Oxidoreductases: 13671
    - Nitrogenase: 83
      - Molybdoferredoxin: 1
        Complementation Group C Molybdenum Cofactor Deficiency
- Coenzymes: 558
  - Molybdenum Cofactors
    - Molybdoferredoxin: 1
      - Complementation Group C Molybdenum Cofactor Deficiency
Amino Acids, Peptides, and Proteins: 1
- Proteins: 484843