Osteochondrodysplasia syndrome   105985007

SNOMED CT code


SNOMED code105985007
nameOsteochondrodysplasia syndrome
statusactive
date introduced2002-01-31
fully specified name(s)Osteochondrodysplasia syndrome (disorder)
synonymsOsteochondrodysplasia syndrome
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
parentsMultiple system malformation syndrome   82354003
children
  • Atelosteogenesis   43814000
  • Chondroectodermal dysplasia   62501005
  • Complex lethal osteochondrodysplasia   1228858000
  • Craniometaphyseal dysplasia   36601008
  • Dysplasias with significant membranous bone involvement   254094003
  • Frontometaphyseal dysplasia   62803002
  • Hajdu-Cheney syndrome   63122002
  • Kenny syndrome   82837002
  • Kniest dysplasia   53974002
  • Kniest-Stickler dysplasia   254059005
  • Lethal Kniest-like syndrome   93132001
  • Metaphyseal chondrodysplasia, Jansen type   24629003
  • Metatropic dysplasia   22764001
  • Osteodysplastic primordial dwarfism   254101001
  • Otospondylomegaepiphyseal dysplasia   254060000
  • Spondylocarpotarsal synostosis syndrome   702351004
  • Spondyloepimetaphyseal dysplasia with joint laxity   254100000  removed: 2023-07-31
  • Spondyloepimetaphyseal dysplasia, Strudwick type   702350003
  • Spondyloepiphyseal dysplasia tarda   51952004
  • Spondyloperipheral dysplasia   702339001
  • Thanatophoric dysplasia   29352008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Multiple system malformation syndrome   82354003
              Osteochondrodysplasia syndrome   105985007

ancestors
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