Congenital melanosis   86042009

SNOMED CT code


SNOMED code86042009
nameCongenital melanosis
statusactive
date introduced2002-01-31
fully specified name(s)Congenital melanosis (disorder)
synonymsCongenital melanosis
attributes - group1
OccurrenceCongenital   255399007
Associated morphologyMelanosis   48010006
parents
children
  • Acromelanosis   239089006
  • Arterial dissection and lentiginosis syndrome   720512007
  • Centrofacial lentiginosis syndrome   18822004
  • Congenital melanosis of sclera   51174006
  • Dermal melanocytic hamartoma   897554004
  • Familial generalized lentiginosis   765195000
  • Hereditary benign acanthosis nigricans   205583005
  • Hereditary benign acanthosis nigricans with insulin resistance   237606005
  • Melanosis oculi   45795007
  • Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome   764995008
  • Peutz-Jeghers syndrome   54411001
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Melanosis   414662006
          Congenital melanosis   86042009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital melanosis   86042009

ancestors
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