SNOMED CT Concept  138875005

Clinical finding  404684003

Integumentary system finding  106077005

Disorder of integument  128598002

Hereditary disorder of the integument  363185004

Epidermolysis bullosa  61003004

Epidermolysis bullosa simplex  67144006

Basal epidermolysis bullosa simplex   723163000

SNOMED CT code


SNOMED code723163000
nameBasal epidermolysis bullosa simplex
statusactive
date introduced2017-01-31
fully specified name(s)Basal epidermolysis bullosa simplex (disorder)
synonymsBasal epidermolysis bullosa simplex
attributes - group1
Pathological processPathological developmental process   308490002
Finding siteStratum germinativum   62650009
OccurrenceCongenital   255399007
Associated morphologyEpidermolysis   85269007
parentsEpidermolysis bullosa simplex   67144006
children
  • Epidermolysis bullosa simplex with muscular dystrophy   723308003
  • KRT14 related epidermolysis bullosa simplex   724206005
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Hereditary disorder of the integument   363185004
          Epidermolysis bullosa   61003004
            Epidermolysis bullosa simplex   67144006
              Basal epidermolysis bullosa simplex   723163000

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.

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