CPT Changes
Current book and archives back to 2000 Easy-to-read online book format Linked to and from code details
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Robin sequence 4602007 SNOMED CT code SNOMED code 4602007 name Robin sequence status active date introduced 2002-01-31 fully specified name(s) Robin sequence (disorder) synonyms Pierre Robin association Robin sequence Micrognathia-glossoptosis syndrome Pierre Robin syndrome attributes - group1 Associated morphology Morphologically abnormal structure 49755003 Pathological process Pathological developmental process 308490002 Occurrence Congenital 255399007 Finding site Face structure 89545001 parents Multiple 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.
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