SNOMED CT Concept  138875005

Clinical finding  404684003

Digestive system finding  386617003

Finding of mouth region  423066003

Oral cavity finding  116337000

Congenital abnormality of oral cavity  282041002

Congenital anomaly of tooth  422977003

Ectodermal dysplasia with hair-tooth defects   239027006

SNOMED CT code


SNOMED code239027006
nameEctodermal dysplasia with hair-tooth defects
statusactive
date introduced2002-01-31
fully specified name(s)Ectodermal dysplasia with hair-tooth defects (disorder)
synonymsEctodermal dysplasia with hair-tooth defects
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteEctoderm structure   63206006
Associated morphologyDysplasia   25723000
attributes - group2
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
Finding siteTooth structure   38199008
OccurrenceCongenital   255399007
attributes - group3
Pathological processPathological developmental process   308490002
Finding siteHair structure   386045008
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
parents
children
  • Berlin syndrome   239032007
  • Conductive deafness, ptosis, skeletal anomalies syndrome   763213001
  • Contracture with ectodermal dysplasia and orofacial cleft syndrome   720746006
  • Cranioectodermal dysplasia   254093009
  • Ectodermal dysplasia syndactyly syndrome   771335004
  • Ectodermal dysplasia with blindness syndrome   721208007
  • Ectodermal dysplasia with hair-tooth-nail defects   239015008
  • Ectodermal syndrome with hair-tooth-sweating defects   402767001
  • Flynn-Aird syndrome   239056006
  • GAPO syndrome   721843003
  • Hallermann-Streiff syndrome   7903009
  • Johanson-Blizzard syndrome   75979009
  • Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies   1208985003
  • Oculodentodigital syndrome   38215007
  • Oculoosteocutaneous syndrome   722061006
  • Pilodental dysplasia, refractive errors syndrome   771240009
  • Taurodontia with absent teeth and sparse hair syndrome   719945007
  • Teebi Shaltout syndrome   771265006
  • Trichodental syndrome   277810000
  • Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome   719910004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Finding of mouth region   423066003
        Oral cavity finding   116337000
          Congenital abnormality of oral cavity   282041002
            Congenital anomaly of tooth   422977003
              Ectodermal dysplasia with hair-tooth defects   239027006

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
              Ectodermal dysplasia with hair-tooth defects   239027006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of embryonic structure   609521009
        Congenital ectodermal defect   254154003
          Ectodermal dysplasia   8654005
            Ectodermal dysplasia with hair-tooth defects   239027006

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:
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