Weill-Marchesani syndrome   2884008

SNOMED CT code


SNOMED code2884008
nameWeill-Marchesani syndrome
statusactive
date introduced2002-01-31
fully specified name(s)Weill-Marchesani syndrome (disorder)
synonyms
  • Spherophakia-brachymorphia syndrome
  • Weill-Marchesani syndrome
  • Brachydactyly-spherophakia syndrome
  • Marchesani's syndrome
  • Brachymorphy with spherophakia syndrome
attributes - group3
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteLens clear   78076003
Associated morphologyCongenital abnormal roundness   38022006
attributes - group2
Finding siteBone structure   272673000
Pathological processPathological developmental process   308490002
Associated morphologyDysplasia   25723000
OccurrenceCongenital   255399007
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyAbnormally short growth   11182007
OccurrenceCongenital   255399007
Finding siteEntire digit   361367007
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Disorder of skeletal system   88230002
          Skeletal dysplasia   105986008
            Weill-Marchesani syndrome   2884008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Deformity of limb   445144002
        Longitudinal deficiency of part of limb   716638009
          Brachydactyly   43476002
            Weill-Marchesani syndrome   2884008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of sensory organ   1279550006
        Disorder of eye   371405004
          Disorder of anterior segment of eye   128535002
            Disorder of lens   10810001
              Congenital anomaly of lens   128353007
                Congenital anomaly of lens shape   33521009
                  Lentiglobus   419281007
                    Spherophakia   4465002
                      Weill-Marchesani syndrome   2884008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Disorder of bone development   371521007
          Congenital anomaly of skeletal bone   8447006
            Weill-Marchesani syndrome   2884008

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.