SNOMED CT Concept  138875005

Clinical finding  404684003

Integumentary system finding  106077005

Disorder of integument  128598002

Hereditary disorder of the integument  363185004

Hereditary hypermelanosis  403804008

Genetic syndrome with hypermelanosis   402780003

SNOMED CT code


SNOMED code402780003
nameGenetic syndrome with hypermelanosis
statusactive
date introduced2003-07-31
fully specified name(s)Genetic syndrome with hypermelanosis (disorder)
synonymsGenetic syndrome with hypermelanosis
attributes - group2
Associated morphologyMelanosis   48010006
Finding siteSkin structure   39937001
parentsHereditary hypermelanosis   403804008
children
  • Leukonychia totalis, acanthosis-nigricans-like lesions, abnormal hair syndrome   773700005
  • Linear and whorled nevoid hypermelanosis   403803002
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
          Hereditary hypermelanosis   403804008
            Genetic syndrome with hypermelanosis   402780003

ancestors
sorted most to least specific
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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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