SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Genetic defect of hair shaft  402774006

Congenital wooly hair   254231002

SNOMED CT code


SNOMED code254231002
nameCongenital wooly hair
statusactive
date introduced2002-01-31
fully specified name(s)Congenital wooly hair (disorder)
synonyms
  • Congenital wooly hair
  • Congenital woolly hair
attributes - group1
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
Finding siteHair shaft structure   37111008
OccurrenceCongenital   255399007
parents
children
  • Autosomal dominant familial wooly hair   403794008
  • Autosomal recessive familial wooly hair   403795009
  • Skin fragility, wooly hair, palmoplantar keratoderma syndrome   778010006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Genetic defect of hair shaft   402774006
          Congenital wooly hair   254231002

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 anomaly of hair   65033000
              Congenital wooly hair   254231002

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:
  • CPT® to SNOMED Crosswalks

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