SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Disorder of pigmentation  414032001

Disorder of skin pigmentation  46690002

Congenital pigmentary skin anomalies  205564003

Inherited cutaneous hyperpigmentation   239079007

SNOMED CT code


SNOMED code239079007
nameInherited cutaneous hyperpigmentation
statusactive
date introduced2002-01-31
fully specified name(s)Inherited cutaneous hyperpigmentation (disorder)
synonymsInherited cutaneous hyperpigmentation
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyHyperpigmentation   4830009
Finding siteSkin structure   39937001
OccurrenceCongenital   255399007
parents
children
  • Acromelanosis   239089006
  • Dermatopathia pigmentosa reticularis   239088003
  • Dyschromatosis universalis   239082002
  • Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome   771179007
  • Hereditary benign acanthosis nigricans   205583005
  • Hereditary benign acanthosis nigricans with insulin resistance   237606005
  • Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome   1177178005
  • Naegeli-Franceschetti-Jadassohn syndrome   239084001
  • Osteopathia striata, pigmentary dermopathy, white forelock syndrome   787408008
  • Symmetrical dyschromatosis of extremities   239085000
  • Terminal osseous dysplasia and pigmentary defect syndrome   723578001
  • Thumb deformity, alopecia, pigmentation anomaly syndrome   771182002
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of pigmentation   414032001
        Disorder of skin pigmentation   46690002
          Congenital pigmentary skin anomalies   205564003
            Inherited cutaneous hyperpigmentation   239079007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Congenital anomaly of integument   38164009
          Congenital anomaly of skin   199879009
            Genodermatosis   239001006
              Inherited cutaneous hyperpigmentation   239079007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Inherited cutaneous hyperpigmentation   239079007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Hereditary disorder of the integument   363185004
          Inherited cutaneous hyperpigmentation   239079007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of pigmentation   414032001
        Disorder of skin pigmentation   46690002
          Hyperpigmentation of skin   49765009
            Inherited cutaneous hyperpigmentation   239079007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Genetic disorder of skin pigmentation   724839001
          Inherited cutaneous hyperpigmentation   239079007

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:
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