SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Developmental disorder  5294002

Congenital malformation  276654001

Congenital malformation syndrome  400038003

Multiple system malformation syndrome  82354003

Shprintzen syndrome   83092002

SNOMED CT code


SNOMED code83092002
nameShprintzen syndrome
statusremoved
date introduced2002-01-31
date removed2018-07-31
fully specified name(s)Shprintzen syndrome (disorder)
synonyms
  • Velocardiofacial syndrome
  • Shprintzen syndrome
  • Velo-cardio-facial syndrome
  • VCF-Velocardiofacial syndrome
  • 22q11 microdeletion with velocardiofacial syndrome phenotype
parentsMultiple system malformation syndrome   82354003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Multiple system malformation syndrome   82354003
              Shprintzen syndrome   83092002  removed: 2018-07-31

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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