Congenital anomaly of hair   65033000

SNOMED CT code


SNOMED code65033000
nameCongenital anomaly of hair
statusactive
date introduced2002-01-31
fully specified name(s)Congenital anomaly of hair (disorder)
synonyms
  • Congenital anomaly of hair
  • Congenital malformation of hair and hair growth
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
Finding siteHair structure   386045008
OccurrenceCongenital   255399007
parents
children
  • [X]Other congenital malformations of hair   205978007  removed: 2009-01-31
  • Bamforth Lazarus syndrome   722375007
  • Bayonet hair   65950001
  • Beaded hair   69488000
  • Congenital alopecia   2965006
  • Congenital hypertrichosis   56797000
  • Congenital hypotrichia   56558005
  • Congenital ringed hair   254233004
  • Congenital wooly hair   254231002
  • Ectodermal dysplasia with hair-nail defect   239035009
  • Ectodermal dysplasia with hair-tooth defects   239027006
  • Ectodermal syndrome with hair-sweating defects   402768006
  • Ectopic cilia of eyelid   95504004
  • Familial isolated trichomegaly   764523004
  • Hair defect with photosensitivity and intellectual disability syndrome   721007005
  • Intellectual disability, polydactyly, uncombable hair syndrome   763742008
  • Noonan syndrome-like disorder with loose anagen hair   723444009
  • Oculocerebral hypopigmentation syndrome of Preus type   716174001
  • Oliver McFarlane syndrome   719944006
  • Osteopathia striata, pigmentary dermopathy, white forelock syndrome   787408008
  • Osteopenia, intellectual disability, sparse hair syndrome   732954002
  • Persistent lanugo   90575004
  • Pili annulati   21926007
  • Pili torti   17170005
  • Specified hair anomalies NOS   205598007  removed: 2010-01-31
  • Taenzer's hair   205597002
  • Trichodysplasia xeroderma syndrome   766812005
  • Trichothiodystrophy   723551003
  • Uncombable hair syndrome   254230001
  • Waardenburg syndrome type 1   1010606009
  • Waardenburg syndrome type 2   1010636000
  • White forelock with malformations syndrome   763619009
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 anomaly of hair   65033000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Skin finding   106076001
        Hair finding   247522004
          Disorder of hair   279425004
            Congenital anomaly of hair   65033000

ancestors
sorted most to least specific
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