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Primary hyperoxaluria type 1

ORPHA:93598

Classification level: Subtype of disorder
  • Synonym(s):
    • Glycolic aciduria
    • Peroxisomal alanine-glyoxylate aminotransferase deficiency
  • Prevalence: -
  • Inheritance: Autosomal recessive 
  • Age of onset: All ages
  • ICD-10: E74.8
  • ICD-11: 5C51.20
  • OMIM: 259900
  • UMLS: C0268164
  • MeSH: C536414
  • GARD: 2835
  • MedDRA: -

Summary

This disease is described under Primary hyperoxaluria

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