SNOMED CT Concept  138875005

Clinical finding  404684003

Integumentary system finding  106077005

Disorder of integument  128598002

Hereditary disorder of the integument  363185004

Hereditary hypermelanosis   403804008

SNOMED CT code


SNOMED code403804008
nameHereditary hypermelanosis
statusactive
date introduced2003-07-31
fully specified name(s)Hereditary hypermelanosis (disorder)
synonymsHereditary hypermelanosis
attributes - group1
Associated morphologyMelanosis   48010006
Finding siteSkin structure   39937001
parents
children
  • Acromelanosis   239089006
  • Arterial dissection and lentiginosis syndrome   720512007
  • Centrofacial lentiginosis syndrome   18822004
  • Familial generalized lentiginosis   765195000
  • Familial progressive hyperpigmentation   715630006
  • Genetic syndrome with hypermelanosis   402780003
  • Hereditary benign acanthosis nigricans   205583005
  • Hereditary benign acanthosis nigricans with insulin resistance   237606005
  • Hereditary diffuse melanosis   402778009
  • Hereditary lentiginosis   402777004  removed: 2018-07-31
  • Hereditary reticulate melanosis   402779001
  • Hypermelanotic pigmentary mosaicism   1254911003
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

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Melanosis   414662006
          Hereditary hypermelanosis   403804008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of pigmentation   414032001
        Disorder of skin pigmentation   46690002
          Hyperpigmentation of skin   49765009
            Hereditary hypermelanosis   403804008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Genetic disorder of skin pigmentation   724839001
          Hereditary hypermelanosis   403804008

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.