Combined molybdoflavoprotein enzyme deficiency   29692004

SNOMED CT code


SNOMED code29692004
nameCombined molybdoflavoprotein enzyme deficiency
statusactive
date introduced2002-01-31
fully specified name(s)Combined molybdoflavoprotein enzyme deficiency (disorder)
synonyms
  • Hereditary xanthinuria type 2
  • Molybdenum cofactor deficiency
  • Combined xanthine oxidase and aldehyde oxidase deficiency
  • Xanthine oxidase-sulphite oxidase deficiency
  • Combined xanthine oxidase and sulfite oxidase and aldehyde oxidase deficiency
  • Combined xanthine oxidase and sulphite oxidase and aldehyde oxidase deficiency
  • Combined molybdoflavoprotein enzyme deficiency
  • Hereditary xanthinuria, type 2
  • Deficiency of molybdenum cofactor
  • Xanthine oxidase-sulfite oxidase deficiency
attributes - group1
Finding siteKidney structure   64033007
parentsHereditary xanthinuria   54627004
children
  • Molybdenum cofactor deficiency complementation group A   1003367004
  • Molybdenum cofactor deficiency complementation group B   1003368009
  • Molybdenum cofactor deficiency complementation group C   1003387003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Hereditary metabolic disease   1821000146108
          Hereditary xanthinuria   54627004
            Combined molybdoflavoprotein enzyme deficiency   29692004

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