Congenital anomaly of face bones   32003007

SNOMED CT code


SNOMED code32003007
nameCongenital anomaly of face bones
statusactive
date introduced2002-01-31
fully specified name(s)Congenital anomaly of face bones (disorder)
synonyms
  • Face congenital deformities
  • Congenital anomaly of face bones
attributes - group1
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteBone structure of face   91397008
parents
children
  • Acrofacial dysostosis Catania type   720419000
  • Acrofacial dysostosis Kennedy Teebi type   720427009
  • Acrofacial dysostosis Palagonia type   720429007
  • Acrofacial dysostosis Rodriguez type   720430002
  • Anterior perimaxillary faciosynostosis   109402007
  • Antley-Bixler syndrome   62964007
  • Bilateral craniofacial microsomia   254027003
  • Cleft of alveolar ridge   445306000
  • Complete perimaxillary faciosynostosis   109403002
  • Congenital anomaly of lacrimal bone   93009002
  • Congenital anomaly of mandible   128224008
  • Congenital anomaly of maxilla   128223002
  • Congenital anomaly of nasal bone   93011006
  • Congenital anomaly of palatine bone   93014003
  • Congenital anomaly of zygomatic bone   93029001
  • Congenital asymmetry of jaw   90693008
  • Congenital malformation syndromes affecting facial appearance   205797000  removed: 2021-09-30
  • Congenital prognathism   72855002
  • Congenital retrognathism   109515000
  • Craniofacial conodysplasia syndrome   720754008
  • Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome   1217229007
  • Craniofacial dyssynostosis syndrome   720755009
  • Dobrow syndrome   782940006
  • Familial osteodysplasia Anderson type   773278003
  • Freeman-Sheldon syndrome   52616002
  • Hemifacial microsomia   254025006
  • Hirschsprung disease with nail hypoplasia and dysmorphism   721223002
  • Holzgreve syndrome   783159001
  • Mandibulofacial dysostosis with alopecia   1216943004
  • Mandibulofacial dysostosis, macroblepharon, macrostomia syndrome   773557002
  • Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome   723442008
  • Oculodento-osseous dysplasia   254137006
  • Papillon-Lefèvre syndrome   40158001
  • Patterson Stevenson Fontaine syndrome   724069009
  • Posterior perimaxillary faciosynostosis   109404008
  • Teebi Shaltout syndrome   771265006
  • Temtamy syndrome   719947004
  • Whistling face syndrome   205799002  removed: 2003-01-31
  • X-linked mandibulofacial dysostosis   719813003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Bone finding   118953000
        Facial bone finding   248398006
          Disorder of facial bone   128225009
            Congenital anomaly of face bones   32003007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of head   118934005
        Congenital anomaly of head   87290003
          Congenital abnormality of skull and face bones   268239009
            Congenital anomaly of face bones   32003007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of head   118934005
        Disorder of face   118930001
          Congenital anomaly of face   398302004
            Congenital anomaly of face bones   32003007

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

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.