SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Subepithelial mucinous corneal dystrophy   723582004

SNOMED CT code


SNOMED code723582004
nameSubepithelial mucinous corneal dystrophy
statusactive
date introduced2017-07-31
fully specified name(s)Subepithelial mucinous corneal dystrophy (disorder)
synonymsSubepithelial mucinous corneal dystrophy
attributes - group1
Associated morphologyDystrophy   4720007
Finding siteCorneal structure   28726007
parents
  • Autosomal dominant hereditary disorder   11164009
  • Hereditary corneal dystrophy   77797009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Subepithelial mucinous corneal dystrophy   723582004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Hereditary disorder of the visual system   363343008
          Hereditary corneal dystrophy   77797009
            Subepithelial mucinous corneal dystrophy   723582004

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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