Genetic metabolic diseases

• mtDNA depletion
  25 June 2011
• congenital defect in bile acid synthesis type 2
  17 May 2011
• unclassified amylopectinosis
  6 April 2011
• cobalamin deficiency type C
  14 March 2011
• mucopolysaccharidosis type 6
  14 March 2011
• neonatal hyperammonemia
  9 February 2011
• glycogen storage disease type 1a
  25 November 2010
• glycogen storage disease type 9a
  7 May 2010
• hereditary fructose intolerance
  7 May 2010
• glycogen storage disease type 0
  29 April 2010

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