Lecithin cholesterol acyltransferase deficiency   238091006

SNOMED CT code


SNOMED code238091006
nameLecithin cholesterol acyltransferase deficiency
statusactive
date introduced2002-01-31
fully specified name(s)Lecithin cholesterol acyltransferase deficiency (disorder)
synonyms
  • Lecithin cholesterol acyltransferase deficiency
  • LCAT (lecithin-cholesterol acyltransferase) deficiency
  • LCAT deficiency
attributes - group1
Finding siteCorneal structure   28726007
Associated morphologyOpacity   128305008
attributes - group2
InterpretsHigh density lipoprotein cholesterol measurement   28036006
Has interpretationBelow reference range   281300000
parents
children
  • Familial lecithin cholesterol acyltransferase deficiency   1264565005
  • Fish-eye disease   238092004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Procedure related finding   127325009
      Evaluation finding   441742003
        Measurement finding   118245000
          Finding of substance level   785671009
            Protein level - finding   365799007
              Lipoprotein below reference range   124041005
                High density lipoprotein below reference range   1172654005
                  Lecithin cholesterol acyltransferase deficiency   238091006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of lipoprotein AND/OR lipid metabolism   48286001
          Lipoprotein deficiency disorder   267436001
            Hypoalphalipoproteinemia   190785000
              Lecithin cholesterol acyltransferase deficiency   238091006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Procedure related finding   127325009
      Evaluation finding   441742003
        Measurement finding   118245000
          Finding of substance level   785671009
            Lipid level - finding   365791005
              Cholesterol level - finding   365793008
                Lecithin cholesterol acyltransferase deficiency   238091006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Degenerative disorder of eye   62585004
          Corneal degeneration   111521006
            Corneal opacity   64634000
              Lecithin cholesterol acyltransferase deficiency   238091006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Lecithin cholesterol acyltransferase deficiency   238091006

ancestors
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