Epoophoron   263993001

SNOMED CT code


SNOMED code263993001
nameEpoophoron
statusactive
date introduced2002-01-31
fully specified name(s)Epoophoron (disorder)
synonymsEpoophoron
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Associated morphologyPersistent embryonic structure   31807009
Finding siteEpoophoron   699003003
parents
children
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Embryological remnant   276752006
            Epoophoron   263993001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of trunk structure   302292003
      Disorder of trunk   128121009
        Congenital anomaly of trunk   78626001
          Congenital anomaly of lower trunk   363030001
            Congenital anomaly of the pelvis   47583008
              Epoophoron   263993001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of embryonic structure   609521009
        Epoophoron   263993001

ancestors
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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.

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