SNOMED CT Concept  138875005

Context-dependent categories  243796009

Finding with explicit context  413350009

Family history of clinical finding  416471007

Family history of gene mutation  138701000119105

Family history of genetic mutation for Lynch syndrome   1099601000119106

SNOMED CT code


SNOMED code1099601000119106
nameFamily history of genetic mutation for Lynch syndrome
statusactive
date introduced2017-07-31
fully specified name(s)Family history of genetic mutation for hereditary nonpolyposis colon cancer (situation)
synonyms
  • Family history of genetic mutation for Lynch syndrome
  • Family history of genetic mutation for hereditary non-polyposis colon cancer
  • Family history of genetic mutation for hereditary nonpolyposis colon cancer
  • Family history of genetic mutation for HNPCC (hereditary nonpolyposis colon cancer)
attributes - group1
Subject relationship contextPerson in the family   303071001
Associated findingGenetic mutation   55446002
Finding contextKnown present   410515003
Temporal contextCurrent or past   410511007
parentsFamily history of gene mutation   138701000119105
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Context-dependent categories   243796009
    Finding with explicit context   413350009
      Family history of clinical finding   416471007
        Family history of gene mutation   138701000119105
          Family history of genetic mutation for Lynch syndrome   1099601000119106

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

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