Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome   722108000

SNOMED CT code


SNOMED code722108000
nameOsteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome
statusactive
date introduced2017-01-31
fully specified name(s)Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome (disorder)
synonymsOsteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome
attributes - group2
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteRetinal structure   5665001
Associated morphologyDystrophy   4720007
attributes - group1
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Finding siteBone structure   272673000
Associated morphologyDysplasia   25723000
attributes - group5
InterpretsHeight / growth measure   271603002
attributes - group3
Finding siteAuditory structure   91159003
attributes - group4
InterpretsHearing   47078008
parents
  • Skeletal dysplasia   105986008
  • Autosomal dominant retinitis pigmentosa   232052009
  • Short stature disorder   237836003
  • Auditory system hereditary disorder   362991006
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of musculoskeletal system   363212003
  • Congenital anomaly of retina   49381001
  • Sensorineural hearing loss   60700002
  • Congenital anomaly of skeletal bone   8447006
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
            Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome   722108000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Autosomal dominant retinitis pigmentosa   232052009
                Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome   722108000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of general physiological development   271616002
      Disorder of stature   237834000
        Short stature disorder   237836003
          Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome   722108000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Ear and auditory finding   118236001
      Disorder of auditory system   362966006
        Auditory system hereditary disorder   362991006
          Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome   722108000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome   722108000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome   722108000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Globe finding   246915008
        Retina finding   399858007
          Retinal disorder   29555009
            Congenital anomaly of retina   49381001
              Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome   722108000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Hearing finding   118230007
        Hearing disorder   128540005
          Hearing loss   15188001
            Sensorineural hearing loss   60700002
              Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome   722108000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Disorder of bone development   371521007
          Congenital anomaly of skeletal bone   8447006
            Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome   722108000

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.