Ectopia lentis, chorioretinal dystrophy, myopia syndrome   722437006

SNOMED CT code


SNOMED code722437006
nameEctopia lentis, chorioretinal dystrophy, myopia syndrome
statusactive
date introduced2017-01-31
fully specified name(s)Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder)
synonymsEctopia lentis, chorioretinal dystrophy, myopia syndrome
attributes - group2
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Associated morphologyCongenital ectopia   416286003
Finding siteLens clear   78076003
attributes - group1
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Associated morphologyDystrophy   4720007
Finding siteRetinal structure   5665001
attributes - group3
Associated morphologyDystrophy   4720007
Finding siteChoroidal structure   68703001
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
parents
  • Congenital chorioretinal degeneration   24210004
  • Retinal dystrophy   314407005
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of the visual system   363343008
  • Congenital ectopic lens   74969002
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Globe finding   246915008
        Choroid finding   247195001
          Disorder of choroid of eye   128468007
            Congenital anomaly of choroid   95490000
              Congenital chorioretinal degeneration   24210004
                Ectopia lentis, chorioretinal dystrophy, myopia syndrome   722437006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Degenerative disorder of eye   62585004
          Degeneration of retina   95695004
            Retinal dystrophy   314407005
              Ectopia lentis, chorioretinal dystrophy, myopia syndrome   722437006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Ectopia lentis, chorioretinal dystrophy, myopia syndrome   722437006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Hereditary disorder of the visual system   363343008
          Ectopia lentis, chorioretinal dystrophy, myopia syndrome   722437006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of sensory organ   1279550006
        Disorder of eye   371405004
          Anomaly of eye   11131000119108
            Lesion of eye   301905003
              Congenital ectopic lens   74969002
                Ectopia lentis, chorioretinal dystrophy, myopia syndrome   722437006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Ectopia lentis, chorioretinal dystrophy, myopia syndrome   722437006

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.