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Results 1 - 10 of 11 for molybdopterin
  1. Molybdenum cofactor deficiency 
    Molybdenum cofactor deficiency is a rare condition characterized by brain dysfunction (encephalopathy) that worsens over time. Babies with this condition appear ...
    https://medlineplus.gov/.../condition/molybdenum-cofactor-deficiency - Genetics
  2. MOCS2 gene 
    ... MOCS2B, which combine to form an enzyme called molybdopterin synthase. Molybdopterin synthase performs the second of a series of ...
    https://medlineplus.gov/genetics/gene/mocs2 - Genetics
  3. MOCS1 gene 
    ... in the formation (biosynthesis) of a molecule called molybdenum cofactor. Specifically, MOCS1A and MOCS1B perform the first of ... of MOCS1B in this process is not understood. Molybdenum cofactor, which contains the element molybdenum, is essential to ...
    https://medlineplus.gov/genetics/gene/mocs1 - Genetics
  4. MOCOS gene 
    ... gene provides instructions for making an enzyme called molybdenum cofactor sulfurase. This enzyme is necessary for the function ... in the breakdown (metabolism) of many different compounds.Molybdenum cofactor sulfurase carries out a chemical reaction that adds ...
    https://medlineplus.gov/genetics/gene/mocos - Genetics
  5. GPHN gene 
    ... in the formation (biosynthesis) of a molecule called molybdenum cofactor, and it also plays a role in communication ... neurons).Gephyrin performs the final two steps in molybdenum cofactor biosynthesis. Molybdenum cofactor, which contains the element molybdenum, ...
    https://medlineplus.gov/genetics/gene/gphn - Genetics
  6. Hereditary xanthinuria 
    ... gene provides instructions for making an enzyme called molybdenum cofactor sulfurase. This enzyme is necessary for the normal ... R, Hosoya T, Nishino T. Mutation of human molybdenum cofactor sulfurase gene is responsible for classical xanthinuria type ...
    https://medlineplus.gov/genetics/condition/hereditary-xanthinuria - Genetics
  7. Genetic Brain Disorders (National Library of Medicine)  
    A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
    https://medlineplus.gov/geneticbraindisorders.html - Health Topics
  8. 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 ...
    https://medlineplus.gov/metabolicdisorders.html - Health Topics
  9. Seizures (National Library of Medicine)  
    Seizures are symptoms of a brain problem. They happen because of sudden, abnormal electrical activity in the brain. When people think of seizures, they often ...
    https://medlineplus.gov/seizures.html - Health Topics
  10. Isolated sulfite oxidase deficiency 
    ... M, Sadek AA, Gleeson JG, Abdel Hamid MS. Molybdenum cofactor and isolated sulphite oxidase deficiencies: Clinical and molecular ...
    https://medlineplus.gov/.../isolated-sulfite-oxidase-deficiency - Genetics
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