Frontonasal dysplasia sequence   86610004

SNOMED CT code


SNOMED code86610004
nameFrontonasal dysplasia sequence
statusactive
date introduced2002-01-31
fully specified name(s)Frontonasal dysplasia sequence (disorder)
synonyms
  • Frontonasal dysplasia sequence
  • Median cleft face syndrome
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteBone structure of cranium   89546000
Associated morphologyDysplasia   25723000
attributes - group2
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
Finding siteFace structure   89545001
parents
  • Dysostosis of bone of skull   128219005
  • Multiple malformation syndrome with facial defects as major feature   65094009
children
  • Craniofrontonasal dysplasia with Poland anomaly syndrome   720757001
  • Craniorhiny   784350004
  • Frontonasal dysplasia with alopecia and genital anomaly syndrome   725029001
  • Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome   1177166006
  • Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome   773628009
  • Frontorhiny   1230021007
  • Hypertelorism Teebi type   724284005
  • Oculoauriculofrontonasal syndrome   782783009
  • Pai syndrome   722201004
  • SIX2-related frontonasal dysplasia   1172632008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of head   118934005
        Disorder of skull   118945008
          Congenital anomaly of skull   51655004
            Dysostosis of bone of skull   128219005
              Frontonasal dysplasia sequence   86610004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of head   118934005
        Disorder of face   118930001
          Congenital anomaly of face   398302004
            Multiple malformation syndrome with facial defects as major feature   65094009
              Frontonasal dysplasia sequence   86610004

ancestors
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