SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Developmental disorder  5294002

Congenital malformation  276654001

Congenital malformation syndrome  400038003

Indomethacin embryofetopathy   715430001

SNOMED CT code


SNOMED code715430001
nameIndomethacin embryofetopathy
statusactive
date introduced2016-07-31
fully specified name(s)Embryofetopathy caused by indomethacin (disorder)
synonyms
  • Fetal indomethacin syndrome
  • Foetal indomethacin syndrome
  • Embryofetopathy caused by indomethacin
  • Indomethacin embryofetopathy
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
Causative agentIndomethacin   373513008
OccurrenceCongenital   255399007
Finding siteFetal structure   55460000
parentsCongenital malformation syndrome   400038003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Indomethacin embryofetopathy   715430001

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.