Craniofacial microsomia   254026007

SNOMED CT code


SNOMED code254026007
nameCraniofacial microsomia
statusactive
date introduced2002-01-31
fully specified name(s)Craniofacial microsomia (disorder)
synonymsCraniofacial microsomia
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyHypoplasia   55199003
Finding siteBone structure of head   272679001
OccurrenceCongenital   255399007
parentsCongenital abnormality of skull and face bones   268239009
children
  • Acrorenal mandibular syndrome   720414005
  • Antley-Bixler syndrome   62964007
  • Bilateral craniofacial microsomia   254027003
  • Congenital alveolar hypoplasia of mandible   109526006
  • Congenital hypoplasia of alisphenoid bone   93236008
  • Congenital hypoplasia of basioccipital bone   93243002
  • Congenital hypoplasia of exoccipital bone   93253001
  • Congenital hypoplasia of frontal bone   93258005
  • Congenital hypoplasia of interparietal bone   93267005
  • Congenital hypoplasia of lacrimal bone   93270009
  • Congenital hypoplasia of nasal bone   93274000
  • Congenital hypoplasia of palatine bone   93281007
  • Congenital hypoplasia of parietal bone   93282000
  • Congenital hypoplasia of squamosal bone   93293003
  • Congenital hypoplasia of zygomatic bone   93303009
  • Congenital maxillary hypoplasia   27299009
  • Congenital micrognathism   32958008
  • Goldenhar syndrome   205418005
  • Hemifacial microsomia   254025006
  • Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome   723442008
hierarchies
a selection of possible paths
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
            Craniofacial microsomia   254026007

ancestors
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