Chondrodysplasia   205465004

SNOMED CT code


SNOMED code205465004
nameChondrodysplasia
statusactive
date introduced2002-01-31
fully specified name(s)Chondrodysplasia (disorder)
synonymsChondrodysplasia
attributes - group1
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Associated morphologyDysplasia   25723000
Finding siteBone structure   272673000
parents
children
  • Achondroplasia   86268005
  • Bone dysplasia lethal Holmgren type   732249002
  • Brachydactylous dwarfism Mseleni type   715470008
  • Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome   720600004
  • Chondrodysplasia with disorder of sex development syndrome   720851007
  • Chondrodysplasia with joint dislocations gPAPP type   782882009
  • Chondrodysplasia, unspecified   205466003  removed: 2010-01-31
  • Dyschondroplasia NOS   205471005  removed: 2010-01-31
  • Fibrochondrogenesis   17144009
  • Lethal chondrodysplasia with fragmented bone   389260001
  • Lethal recessive chondrodysplasia   719404009
  • Lethal retarded ossification syndromes   205482002
  • Multiple exostosis syndromes   240186007  removed: 2004-07-31
  • QRICH1-related intellectual disability, chondrodysplasia syndrome   1220568003
  • X-linked dominant chondrodysplasia Chassaing Lacombe type   719837003
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
            Chondrodysplasia   205465004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Disorder of bone development   371521007
          Congenital anomaly of skeletal bone   8447006
            Chondrodysplasia   205465004

ancestors
sorted most to least specific
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