Antley-Bixler syndrome   62964007

SNOMED CT code


SNOMED code62964007
nameAntley-Bixler syndrome
statusactive
date introduced2002-01-31
fully specified name(s)Antley-Bixler syndrome (disorder)
synonyms
  • Antley-Bixler syndrome
  • Multisynostotic osteodysgenesis
  • Trapezoidcephaly-multiple synostosis
attributes - group4
Pathological processPathological developmental process   308490002
Finding siteBone structure of femur   71341001
Associated morphologyBowing deformity   34058006
OccurrenceCongenital   255399007
attributes - group2
Pathological processPathological developmental process   308490002
Associated morphologyHypoplasia   55199003
OccurrenceCongenital   255399007
Finding siteBone structure of face   91397008
attributes - group5
Associated morphologyCongenital abnormal fusion   37764001
Pathological processPathological developmental process   308490002
Finding siteBone structure of humerus   85050009
OccurrenceCongenital   255399007
attributes - group6
Pathological processPathological developmental process   308490002
Associated morphologyCongenital abnormal fusion   37764001
Finding siteBone structure of radius   62413002
OccurrenceCongenital   255399007
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyCongenital premature fusion   67798003
Finding siteStructure of lambdoid suture of skull   32170006
OccurrenceCongenital   255399007
attributes - group3
Pathological processPathological developmental process   308490002
Associated morphologyCongenital premature fusion   67798003
Finding siteStructure of coronal suture of skull   29012004
OccurrenceCongenital   255399007
parents
  • Humeroradial synostosis   205329008
  • Congenital anomaly of bone and joint   237513002
  • Craniofacial microsomia   254026007
  • Deformity of femur   271092002
  • Congenital anomaly of face bones   32003007
  • Congenital bowing of femur   33534005
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of musculoskeletal system   363212003
  • Craniosynostosis syndrome   57219006
  • 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
    Finding of limb structure   302293008
      Finding of upper limb   116307009
        Finding of bone of upper limb   298756009
          Congenital anomaly of humerus   123558002
            Congenital abnormal fusion of humerus   92859003
              Humeroradial synostosis   205329008
                Antley-Bixler syndrome   62964007

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
              Antley-Bixler syndrome   62964007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of head   118934005
        Congenital anomaly of head   87290003
          Congenital abnormality of skull and face bones   268239009
            Craniofacial microsomia   254026007
              Antley-Bixler syndrome   62964007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Deformity   417893002
      Deformation of bone   298356007
        Deformity of femur   271092002
          Antley-Bixler syndrome   62964007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Bone finding   118953000
        Facial bone finding   248398006
          Disorder of facial bone   128225009
            Congenital anomaly of face bones   32003007
              Antley-Bixler syndrome   62964007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Deformity   417893002
      Congenital deformity   276655000
        Congenital bowing of long bone   716098006
          Congenital bowing of femur   33534005
            Antley-Bixler syndrome   62964007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Antley-Bixler syndrome   62964007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Antley-Bixler syndrome   62964007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Joint finding   118952005
        Cranial suture finding   248387005
          Imperfect fusion of skull   23939000
            Craniosynostosis syndrome   57219006
              Antley-Bixler syndrome   62964007

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
              Antley-Bixler syndrome   62964007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Antley-Bixler syndrome   62964007

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.