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

Congenital ichthyosis of skin   13059002

SNOMED CT code


SNOMED code13059002
nameCongenital ichthyosis of skin
statusactive
date introduced2002-01-31
fully specified name(s)Congenital ichthyosis of skin (disorder)
synonyms
  • Congenital ichthyosis of skin
  • Ichthyosis congenita
  • Congenital ichthyosis
  • Fish scale disease
  • Fish skin
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyHyperkeratosis   26996000
Finding siteEntire skin   181469002
OccurrenceCongenital   255399007
attributes - group2
InterpretsKeratinization   44138005
Has interpretationAbnormal   263654008
parents
children
  • [X]Other congenital ichthyosis   205974009  removed: 2009-01-31
  • Autosomal dominant ichthyosis   402770002
  • Autosomal recessive ichthyosis   402772005
  • Bullous ichthyosis   254166009  removed: 2019-07-31
  • Congenital ichthyosis, microcephalus, tetraplegia syndrome   1197059004
  • Congenital ichthyosis, unspecified   205547001  removed: 2010-01-31
  • Congenital non bullous ichthyosiform erythroderma   267372009
  • Cutaneous syndrome with ichthyosis   239057002
  • Dominant congenital ichthyosiform erythroderma   20512000  removed: 2015-01-31
  • Erythrokeratodermia variabilis   70041004
  • Follicular ichthyosis   238627002
  • Ichthyosis congenita with biliary atresia   235916001
  • Ichthyosis vulgaris   254157005
  • Keratinopathic ichthyosis   724837004
  • Lamellar ichthyosis   205550003
  • Lamellar ichthyosis AND trichorrhexis invaginata syndrome   34638006
  • Limb reduction-ichthyosis syndrome   68551007
  • Non-bullous ichthyosiform erythroderma   254165008  removed: 2020-01-31
  • Rud's syndrome   2355008
  • Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome   722114007
  • Severe ichthyoses   254159008
  • X-linked ichthyosis with steryl-sulfatase deficiency   72523005
  • X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome   765471005
  • X-linked recessive ichthyosis   402771003  removed: 2016-07-31
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
            Genodermatosis   239001006
              Congenital ichthyosis of skin   13059002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Disorder of keratinization   277905003
          Inherited disorder of keratinization   254214009
            Congenital ichthyosis of skin   13059002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Congenital ichthyosis of skin   13059002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Keratosis   254666005
        Keratoderma   707209001
          Ichthyosis   782957005
            Congenital ichthyosis of skin   13059002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Skin finding   106076001
        Rough skin   816995008
          Congenital ichthyosis of skin   13059002

ancestors
sorted most to least specific
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