SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Familial disease  111941005

Familial lecithin cholesterol acyltransferase deficiency   1264565005

SNOMED CT code


SNOMED code1264565005
nameFamilial lecithin cholesterol acyltransferase deficiency
statusactive
date introduced2023-02-28
fully specified name(s)Familial lecithin cholesterol acyltransferase deficiency (disorder)
synonyms
  • Familial lecithin cholesterol acyltransferase deficiency
  • Complete LCAT deficiency
  • Norum disease
  • Complete LCAT (lecithin-cholesterol acyltransferase) deficiency
attributes - group2
InterpretsHigh density lipoprotein cholesterol measurement   28036006
Has interpretationBelow reference range   281300000
attributes - group1
Finding siteCorneal structure   28726007
Associated morphologyOpacity   128305008
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Familial disease   111941005
        Familial lecithin cholesterol acyltransferase deficiency   1264565005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Lecithin cholesterol acyltransferase deficiency   238091006
          Familial lecithin cholesterol acyltransferase deficiency   1264565005

ancestors
sorted most to least specific
cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:
  • CPT® to SNOMED Crosswalks

demo
request yours today
 subscribe
start today
 newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.