SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Metabolic disease  75934005

Metabolic renal disease  106000008

Primary hyperoxaluria  17901006

Primary hyperoxaluria, type I   65520001

SNOMED CT code


SNOMED code65520001
namePrimary hyperoxaluria, type I
statusactive
date introduced2002-01-31
fully specified name(s)Primary hyperoxaluria, type I (disorder)
synonyms
  • Primary hyperoxaluria, type I
  • Glycolic aciduria
  • Alanine-glyoxylate aminotransferase deficiency
  • 2-Oxoglutarate glyoxylate carboligase deficiency
  • Oxalosis type I
  • Primary hyperoxaluria type I
  • Alanine-glycoxylate aminotransferase deficiency
attributes - group1
OccurrenceCongenital   255399007
attributes - group2
Finding siteKidney structure   64033007
parents
childrenOxaluria NEC   190767007  removed: 2010-01-31
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Metabolic renal disease   106000008
          Primary hyperoxaluria   17901006
            Primary hyperoxaluria, type I   65520001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          Disorder of peroxisomal function   238059005
            Loss of single peroxisomal function   238066006
              Primary hyperoxaluria, type I   65520001

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