SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Autosomal dominant epidermolysis bullosa simplex   60518002

SNOMED CT code


SNOMED code60518002
nameAutosomal dominant epidermolysis bullosa simplex
statusremoved
date introduced2002-01-31
date removed2003-07-31
fully specified name(s)Autosomal dominant epidermolysis bullosa simplex (disorder)
synonyms
  • Autosomal dominant epidermolysis bullosa simplex
  • EBS 1
  • Epidermolysis bullosa simplex, Ogna type
  • Epidermolysis bullosa simplex of Ogna
parentsAutosomal dominant hereditary disorder   11164009
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
              Autosomal dominant epidermolysis bullosa simplex   60518002  removed: 2003-07-31

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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