Disorder of sulfur-bearing amino acid metabolism   28882002

SNOMED CT code


SNOMED code28882002
nameDisorder of sulfur-bearing amino acid metabolism
statusactive
date introduced2002-01-31
fully specified name(s)Disorder of sulfur-bearing amino acid metabolism (disorder)
synonyms
  • Disorder of sulphur-bearing amino acid metabolism
  • Disorder of transsulfuration
  • Sulfuraminoacidemia
  • Disorder of sulfur-bearing amino acid metabolism
  • Disorder of transsulphuration
  • Sulphuraminoacidaemia
  • Disorder of sulphur-bearing amino acid including those due to folate and B12 disturbance
  • Disorder of sulfur-bearing amino acid including those due to folate and B12 disturbance
parentsDisorder of amino acid and organic acid metabolism   237911005
children
  • 4-Hydroxyphenylpyruvate dioxygenase deficiency   403001  removed: 2005-01-31
  • 5,10-Methylenetetrahydrofolate reductase deficiency   41797007
  • Autosomal recessive extra-oral halitosis   1269235004
  • Beta-mercaptolactate cysteine disulfiduria   784373007
  • Congenital defect of folate absorption   62578003
  • Cystathione gamma-lyase deficiency   367036006  removed: 2020-01-31
  • Cystathionine beta-synthase deficiency   24308003
  • Cystathioninemia   190706001  removed: 2002-07-31
  • Cystathioninemia   6669004
  • Cystathioninuria   13003007
  • Deficiency of dihydrofolate reductase   124178006
  • Disturbance of sulfur-bearing amino acid metabolism NOS   267421004  removed: 2010-01-31
  • Familial methionine malabsorption   45812003
  • Functional defects of methionine synthase   360376008
  • Glutamate formiminotransferase deficiency   59761008
  • Hawkinsinuria   414380008
  • Homocystinemia   52311001
  • Homocystinuria   11282001
  • Hyperhomocysteinemia   419503008
  • Hypermethioninemia   43123004
  • Methionine malabsorption syndrome   237932002  removed: 2009-07-31
  • Other specified disturbance of sulfur-bearing amino acid metabolism   190711004  removed: 2010-01-31
  • Selective malabsorption of cyanocobalamin   234363001
  • Sulfite oxidase deficiency   367368009
  • Sulfite oxidase deficiency syndrome   40873003
  • Tetrahydrofolate methyltransferase deficiency   89579000
  • Transcobalamin I deficiency   237933007
  • Transcobalamin II deficiency   237934001
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of organic acid metabolism   116021002
          Disorder of amino acid metabolism   44779003
            Disorder of amino acid and organic acid metabolism   237911005
              Disorder of sulfur-bearing amino acid metabolism   28882002

ancestors
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