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      • 18    Congenital disorders of glycosylation
        • 18.4    Disorders of multiple glycosylation pathways
          • 18.4.4    Disorders of sialic acid metabolism
            • Nonaka myopathy
              • Severe autosomal recessive macrothrombocytopenia
              • Sialuria
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OnlineIMD
  • Home
  • Diseases
    • COMPLEX MOLECULE AND ORGANELLE METABOLISM
      • 18    Congenital disorders of glycosylation
        • 18.4    Disorders of multiple glycosylation pathways
          • 18.4.4    Disorders of sialic acid metabolism
            • Nonaka myopathy
              • Severe autosomal recessive macrothrombocytopenia
              • Sialuria
  • Genes
  • Gene products
  • Pathways
  • Multimers
  • More information
    • About Online IMD

Sialuria

  • Type
    Variant
  • External link(s)
    • Orphanet
    • IEMbase
  • Parent entry
    • Nonaka myopathy