Hereditary xanthinuria   54627004

SNOMED CT code


SNOMED code54627004
nameHereditary xanthinuria
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary xanthinuria (disorder)
synonyms
  • Classical xanthinuria
  • Hereditary xanthinuria
attributes - group1
Finding siteKidney structure   64033007
parents
children
  • Combined molybdoflavoprotein enzyme deficiency   29692004
  • Hereditary xanthinuria type 1   836343001
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Metabolic renal disease   106000008
          Deficiency of xanthine oxidase   124147007
            Hereditary xanthinuria   54627004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Hereditary metabolic disease   1821000146108
          Hereditary xanthinuria   54627004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of purine and pyrimidine metabolism   238006008
          Disorder of purine metabolism   32612005
            Hereditary xanthinuria   54627004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Viscus structure finding   406123005
      Abdominal organ finding   249561001
        Kidney finding   249578005
          Kidney disease   90708001
            Hereditary nephropathy   367591000119105
              Hereditary xanthinuria   54627004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Hereditary xanthinuria   54627004

ancestors
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