SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Developmental disorder  5294002

Primary lymphedema  1217009002

Hereditary lymphedema  254199006

German syndrome   733037000

SNOMED CT code


SNOMED code733037000
nameGerman syndrome
statusactive
date introduced2017-07-31
fully specified name(s)German syndrome (disorder)
synonymsGerman syndrome
attributes - group3
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Finding siteFace structure   89545001
attributes - group2
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Associated morphologyContracture   57048009
Finding siteStructure of joint region   785818007
attributes - group1
Has interpretationDecreased   1250004
InterpretsRange of joint movement   364564000
attributes - group4
Finding siteLimb structure   66019005
Pathological processPathological developmental process   308490002
Associated morphologyLymphatic edema   30213001
parents
  • Hereditary lymphedema   254199006
  • Inherited arthrogryposis   28204005
  • Multiple malformation syndrome with facial defects as major feature   65094009
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Primary lymphedema   1217009002
          Hereditary lymphedema   254199006
            German syndrome   733037000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Inherited arthrogryposis   28204005
            German syndrome   733037000

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
              German syndrome   733037000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              German syndrome   733037000

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

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