Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome   721229003

SNOMED CT code


SNOMED code721229003
nameHydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome
statusactive
date introduced2017-01-31
fully specified name(s)Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome (disorder)
synonyms
  • Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome
  • Ferlini Ragno Calzolari syndrome
  • Waaler Aarskog syndrome
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Associated morphologySuperior displacement   62470007
Finding siteBone structure of scapula   79601000
attributes - group2
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteBrain cerebrospinal fluid pathway   280371009
Associated morphologyDilatation   25322007
parents
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of musculoskeletal system   363212003
  • Hereditary disorder of nervous system   363235000
  • Congenital hydrocephalus   47032000
  • Congenital elevation of scapula   79120002
  • Multiple system malformation syndrome   82354003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome   721229003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome   721229003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of nervous system   118940003
          Hereditary disorder of nervous system   363235000
            Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome   721229003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Finding of brain   299718000
        Disorder of brain   81308009
          Hydrocephalus   230745008
            Congenital hydrocephalus   47032000
              Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome   721229003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Bone finding   118953000
        Disorder of bone   76069003
          Displacement of bone   1296833008
            Congenital elevation of scapula   79120002
              Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome   721229003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Multiple system malformation syndrome   82354003
              Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome   721229003

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.