Hallux varus, preaxial polysyndactyly syndrome   771180005

SNOMED CT code


SNOMED code771180005
nameHallux varus, preaxial polysyndactyly syndrome
statusactive
date introduced2019-01-31
fully specified name(s)Hallux varus, preaxial polysyndactyly syndrome (disorder)
synonyms
  • Kleiner Holmes syndrome
  • Hallux varus, preaxial polysyndactyly syndrome
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyVarus deformity   127562007
OccurrenceCongenital   255399007
Finding siteJoint of hallux   280456006
attributes - group2
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteDigit structure   82680008
Associated morphologySupernumerary structure   91431006
attributes - group3
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteDigit structure   82680008
Associated morphologyCongenital abnormal fusion   37764001
attributes - group4
Pathological processPathological developmental process   308490002
Associated morphologyDysplasia   25723000
OccurrenceCongenital   255399007
Finding siteBone structure of extremity   48566001
parents
  • Dysostosis   109420003
  • Congenital anomaly of bone and joint   237513002
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of musculoskeletal system   363212003
  • Multiple malformation syndrome with limb defect as major feature   41443008
  • Congenital hallux varus   79969004
  • Polysyndactyly   84598000
  • Autosomal recessive hereditary disorder   85995004
  • Congenital dysplasia of limb   88631000119105
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Disorder of bone development   371521007
          Congenital anomaly of skeletal bone   8447006
            Dysostosis   109420003
              Hallux varus, preaxial polysyndactyly syndrome   771180005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Disorder of bone development   371521007
          Congenital anomaly of skeletal bone   8447006
            Congenital anomaly of bone and joint   237513002
              Hallux varus, preaxial polysyndactyly syndrome   771180005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Hallux varus, preaxial polysyndactyly syndrome   771180005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Hallux varus, preaxial polysyndactyly syndrome   771180005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Multiple system malformation syndrome   82354003
              Multiple malformation syndrome with limb defect as major feature   41443008
                Hallux varus, preaxial polysyndactyly syndrome   771180005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Deformity   417893002
      Joint deformity   250087009
        Toe joint deformity   299581004
          Congenital hallux varus   79969004
            Hallux varus, preaxial polysyndactyly syndrome   771180005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Disorder of limb   128605003
        Disorder of digit   128597007
          Congenital anomaly of digit   403855001
            Polydactyly   367506006
              Polysyndactyly   84598000
                Hallux varus, preaxial polysyndactyly syndrome   771180005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Hallux varus, preaxial polysyndactyly syndrome   771180005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Disorder of limb   128605003
        Congenital anomaly of limb   60475009
          Congenital dysplasia of limb   88631000119105
            Hallux varus, preaxial polysyndactyly syndrome   771180005

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.