Phosphoserine aminotransferase deficiency   718603002

SNOMED CT code


SNOMED code718603002
namePhosphoserine aminotransferase deficiency
statusactive
date introduced2017-01-31
fully specified name(s)Deficiency of phosphoserine aminotransferase (disorder)
synonyms
  • Phosphoserine aminotransferase deficiency
  • Deficiency of phosphoserine aminotransferase
parents
  • Autosomal dominant hereditary disorder   11164009
  • Deficiency of aminotransferase   124394008
  • Disorder of serine metabolism   303097007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Phosphoserine aminotransferase deficiency   718603002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Enzymopathy   78548001
          Specific enzyme deficiency   129456006
            Deficiency of aminotransferase   124394008
              Phosphoserine aminotransferase deficiency   718603002

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 serine metabolism   303097007
                Phosphoserine aminotransferase deficiency   718603002

ancestors
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