Familial chylomicronemia syndrome   1197489003

SNOMED CT code


SNOMED code1197489003
nameFamilial chylomicronemia syndrome
statusactive
date introduced2022-02-28
fully specified name(s)Familial chylomicronemia syndrome (disorder)
synonymsFamilial chylomicronemia syndrome
attributes - group1
InterpretsLipids measurement   104780002
Has interpretationAbove reference range   281302008
parents
children
  • Familial apolipoprotein C-II deficiency   33513003
  • Hyperlipoproteinemia, type I   275598004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Familial disease   111941005
        Familial chylomicronemia syndrome   1197489003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of lipoprotein AND/OR lipid metabolism   48286001
          Disorder of lipoprotein storage and metabolism   238037008
            Hyperlipidemia   55822004
              Hyperlipidemia with lipid deposition in skin   402725005
                Primary chylomicronemia   402726006
                  Chylomicronemia syndrome   402786009
                    Familial chylomicronemia syndrome   1197489003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Familial chylomicronemia syndrome   1197489003

ancestors
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