Robin sequence   4602007

SNOMED CT code


SNOMED code4602007
nameRobin sequence
statusactive
date introduced2002-01-31
fully specified name(s)Robin sequence (disorder)
synonyms
  • Pierre Robin association
  • Robin sequence
  • Micrognathia-glossoptosis syndrome
  • Pierre Robin syndrome
attributes - group1
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteFace structure   89545001
parentsMultiple malformation syndrome with facial defects as major feature   65094009
children
  • Intellectual disability, brachydactyly, Pierre Robin syndrome   763744009
  • Joint contractures, developmental delay, Pierre Robin syndrome   1216940001
  • Pierre Robin sequence faciodigital anomaly syndrome   723461007
  • Robin sequence and oligodactyly syndrome   770681000
  • Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome   723998001
  • Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome   719823007
hierarchies
a selection of possible paths
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
              Robin sequence   4602007

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.