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

Congenital pigmentary skin anomalies   205564003

SNOMED CT code


SNOMED code205564003
nameCongenital pigmentary skin anomalies
statusactive
date introduced2002-01-31
fully specified name(s)Congenital pigmentary skin anomalies (disorder)
synonyms
  • Congenital pigmentary anomaly of skin
  • Congenital pigmentary skin anomalies
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Associated morphologyPigment alteration   79644001
Finding siteSkin structure   39937001
parents
children
  • Birthmark   51089004
  • Carney complex   733491005
  • Carney complex, trismus, pseudocamptodactyly syndrome   766881008
  • Congenital deficiency of pigment of skin   1953005
  • Congenital pigmentary skin anomaly NOS   205568000  removed: 2010-01-31
  • Dermal melanocytic hamartoma   897554004
  • Familial generalized lentiginosis   765195000
  • Familial progressive hyper and hypopigmentation   763368004
  • Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome   733469003
  • Inherited cutaneous hyperpigmentation   239079007
  • McCune Albright syndrome   726029005
  • Neuroectodermal melanolysosomal disease   724091002
  • Pseudoleprechaunism syndrome Patterson type   771262009
hierarchies
a selection of possible paths
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
            Congenital pigmentary skin anomalies   205564003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of pigmentation   414032001
        Disorder of skin pigmentation   46690002
          Congenital pigmentary skin anomalies   205564003

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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