Congenital deficiency of pigment of skin   1953005

SNOMED CT code


SNOMED code1953005
nameCongenital deficiency of pigment of skin
statusactive
date introduced2002-01-31
fully specified name(s)Congenital deficiency of pigment of skin (disorder)
synonymsCongenital deficiency of pigment of skin
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyHypopigmentation   89031001
OccurrenceCongenital   255399007
Finding siteSkin structure   39937001
parents
children
  • Congenital oculocutaneous hypopigmentation   61649007
  • Deaf blind hypopigmentation syndrome Yemenite type   721084001
  • Deafness, vitiligo, achalasia syndrome   733069009
  • Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies   1208985003
  • Oculocerebral hypopigmentation syndrome of Preus type   716174001
  • Phylloid hypomelanosis   403807001
  • Piebald trait with neurologic defects syndrome   773984007
  • Piebaldism   718122005
  • Waardenburg's syndrome   47434006
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
            Congenital deficiency of pigment of skin   1953005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of pigmentation   414032001
        Disorder of skin pigmentation   46690002
          Skin hypopigmented   23006000
            Congenital deficiency of pigment of skin   1953005

ancestors
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