Osteochondrodysplasia

Part of

Sub-types of Osteochondrodysplasia

• Osteogenesis imperfecta 35 trials · 329 incl. sub-types
  10 sub-types

  • Osteogenesis imperfecta and a reduction of bone mineral density. 0 trials · 307 incl. sub-types Sub-types →
  • Brittle bone disorder 4 trials Sub-types →
  • COL1A2-related osteogenesis imperfecta 0 trials
  • High bone mass osteogenesis imperfecta 0 trials
  • Osteogenesis imperfecta type 13 0 trials
  • Osteogenesis imperfecta, IIA 22 0 trials
  • Osteogenesis imperfecta, type 20 0 trials
  • Osteogenesis imperfecta, type 21 0 trials
  • Osteogenesis imperfecta, type 23 0 trials
  • Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome 0 trials
• Achondroplasia 26 trials
• Hypochondroplasia 9 trials
• Spondyloepiphyseal dysplasia 0 trials · 8 incl. sub-types
  44 sub-types

  • Stickler syndrome 2 trials · 4 incl. sub-types Sub-types →
  • COL2A1-related spondyloepiphyseal dysplasia 0 trials · 3 incl. sub-types Sub-types →
  • Roifman syndrome 1 trial
  • Progressive pseudorheumatoid arthropathy of childhood 1 trial
  • Spondyloepiphyseal dysplasia tarda 0 trials · 1 incl. sub-types Sub-types →
  • Spondyloepiphyseal dysplasia, Cantu type 1 trial
  • CODAS syndrome 0 trials
  • Dyggve-Melchior-Clausen disease 0 trials Sub-types →
  • Ehlers-Danlos syndrome, spondylocheirodysplastic type 0 trials
  • MGP-related spondyloepiphyseal dysplasia 0 trials
  • MIR140-related spondyloepiphyseal dysplasia 0 trials
  • Marshall syndrome 0 trials
  • Richieri Costa-da Silva syndrome 0 trials
  • Schimke immuno-osseous dysplasia 0 trials
  • Schwartz-Jampel syndrome 0 trials Sub-types →
  • Silverman-Handmaker type dyssegmental dysplasia 0 trials
  • Smith-McCort dysplasia 0 trials Sub-types →
  • Steel syndrome 0 trials
  • TMEM165-congenital disorder of glycosylation 0 trials
  • Wolcott-Rallison syndrome 0 trials
  • X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome 0 trials
  • X-linked spondyloepimetaphyseal dysplasia 0 trials
  • Anauxetic dysplasia 0 trials Sub-types →
  • Brachydactylous dwarfism, Mseleni type 0 trials
  • Brachyolmia-amelogenesis imperfecta syndrome 0 trials
  • Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome 0 trials
  • Cono-spondylar dysplasia 0 trials
  • Dyssegmental dysplasia, Rolland-Desbuquois type 0 trials
  • Even-plus syndrome 0 trials
  • Hip dysplasia, Beukes type 0 trials
  • Immunoskeletal dysplasia with neurodevelopmental abnormalities 0 trials
  • Metatropic dysplasia 0 trials
  • Otospondylomegaepiphyseal dysplasia 0 trials Sub-types →
  • Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome 0 trials
  • Spondylo-megaepiphyseal-metaphyseal dysplasia 0 trials
  • Spondyloepiphyseal dysplasia with congenital joint dislocations 0 trials
  • Spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability 0 trials
  • Spondyloepiphyseal dysplasia with punctate corneal dystrophy 0 trials
  • Spondyloepiphyseal dysplasia, Holling type 0 trials
  • Spondyloepiphyseal dysplasia, Kimberley type 0 trials
  • Spondyloepiphyseal dysplasia, MacDermot type 0 trials
  • Spondyloepiphyseal dysplasia, Reardon type 0 trials
  • Spondyloepiphyseal dysplasia, kondo-fu type 0 trials
  • Spondyloepiphyseal dysplasia, nishimura type 0 trials
• Spondyloepimetaphyseal dysplasia 0 trials · 4 incl. sub-types
  23 sub-types

  • COL2A1-related spondyloepiphyseal dysplasia 0 trials · 3 incl. sub-types Sub-types →
  • Spondyloepimetaphyseal dysplasia, aggrecan type 1 trial
  • Spondyloepimetaphyseal dysplasia with joint laxity 0 trials Sub-types →
  • Spondyloepimetaphyseal dysplasia, Bieganski type 0 trials
  • Spondyloepimetaphyseal dysplasia, Genevieve type 0 trials
  • Spondyloepimetaphyseal dysplasia, Guo-Campeau type 0 trials
  • Spondyloepimetaphyseal dysplasia, Handigodu type 0 trials
  • Spondyloepimetaphyseal dysplasia, Irapa type 0 trials
  • Spondyloepimetaphyseal dysplasia, Isidor type 0 trials
  • Spondyloepimetaphyseal dysplasia, Isidor-Toutain type 0 trials
  • Spondyloepimetaphyseal dysplasia, Krakow type 0 trials
  • Spondyloepimetaphyseal dysplasia, Li-Shao-Li type 0 trials
  • Spondyloepimetaphyseal dysplasia, Maroteaux type 0 trials
  • Spondyloepimetaphyseal dysplasia, Missouri type 0 trials
  • Spondyloepimetaphyseal dysplasia, PAPSS2 type 0 trials
  • Spondyloepimetaphyseal dysplasia, Shohat type 0 trials
  • Spondyloepimetaphyseal dysplasia, Strudwick type 0 trials
  • Spondyloepimetaphyseal dysplasia, di rocco type 0 trials
  • Spondyloepimetaphyseal dysplasia, matrilin-3 type 0 trials
  • Spondyloepimetaphyseal dysplasia, sponastrime type 0 trials
  • Spondyloepimetaphyseal dysplasia-abnormal dentition syndrome 0 trials
  • Spondyloepimetaphyseal dysplasia-hypotrichosis syndrome 0 trials
  • Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome 0 trials
• Blount disease 2 trials
  2 sub-types

  • Blount disease, infantile 1 trial
  • Blount disease, adolescent 0 trials
• Diastrophic dysplasia 2 trials
• Mesomelic dysplasia 0 trials · 2 incl. sub-types
  6 sub-types

  • Langer mesomelic dysplasia 2 trials
  • Mesomelic dwarfism, Nievergelt type 0 trials
  • Mesomelic dwarfism, Reinhardt-Pfeiffer type 0 trials
  • Mesomelic dysplasia, Kantaputra type 0 trials Sub-types →
  • Mesomelic dysplasia, Savarirayan type 0 trials
  • Upper limb mesomelic dysplasia 0 trials
• Neonatal osteosclerotic dysplasia 0 trials · 2 incl. sub-types
  5 sub-types

  • Desmosterolosis 2 trials
  • Caffey disease 0 trials
  • Chondrodysplasia Blomstrand type 0 trials
  • Dysplastic cortical hyperostosis 0 trials Sub-types →
  • Lethal osteosclerotic bone dysplasia 0 trials
• Cleidocranial dysplasia 1 1 trial
• Metaphyseal chondrodysplasia, Jansen type 1 trial
• Microcephalic osteodysplastic primordial dwarfism type I 1 trial
• Microcephalic osteodysplastic primordial dwarfism type II 1 trial
• Midface dysplasia 1 trial
• Pseudoachondroplasia 1 trial
• Akaba Hayasaka syndrome 0 trials
• Boomerang dysplasia 0 trials
• Desbuquois dysplasia 0 trials
  2 sub-types

  • Desbuquois dysplasia 1 0 trials
  • Desbuquois dysplasia 2 0 trials
• Fairbank disease 0 trials
• Kashin-Beck disease 0 trials
• Kniest dysplasia 0 trials
• Leri-Weill dyschondrosteosis 0 trials
  1 sub-type

  • Madelung deformity 0 trials Sub-types →
• Pyle disease 0 trials
  2 sub-types

  • Chondrodysplasia calcificans Metaphysealis 0 trials
  • Metaphyseal chondrodysplasia 0 trials
• Schmid metaphyseal chondrodysplasia 0 trials
• Acheiropody 0 trials
• Achondrogenesis 0 trials
  5 sub-types

  • Achondrogenesis type IA 0 trials
  • Achondrogenesis type IB 0 trials
  • Achondrogenesis type II 0 trials
  • Acromesomelic dysplasia 2A 0 trials
  • Hypochondrogenesis 0 trials
• Acrocapitofemoral dysplasia 0 trials
• Acromesomelic dysplasia 0 trials
  8 sub-types

  • Osebold-Remondini syndrome 0 trials
  • Acromesomelic dysplasia 1, Maroteaux type 0 trials
  • Acromesomelic dysplasia 2A 0 trials
  • Acromesomelic dysplasia 2B 0 trials
  • Acromesomelic dysplasia 2C, Hunter-Thompson type 0 trials
  • Acromesomelic dysplasia 3 0 trials
  • Acromesomelic dysplasia 4 0 trials
  • Acromesomelic dysplasia, Campailla Martinelli type 0 trials
• Arterial tortuosity-bone fragility syndrome 0 trials
• Atelosteogenesis 0 trials
  3 sub-types

  • Atelosteogenesis type I 0 trials
  • Atelosteogenesis type II 0 trials
  • Atelosteogenesis type III 0 trials
• Bone dysplasia, lethal Holmgren type 0 trials
• Brachyolmia 0 trials
  3 sub-types

  • Autosomal dominant brachyolmia 0 trials
  • Autosomal recessive brachyolmia 0 trials Sub-types →
  • Brachyolmia, Maroteaux type 0 trials
• Campomelic dysplasia 0 trials
• Cleidocranial dysplasia 2 0 trials
• Cleidocranial dysplasia, recessive form 0 trials
• Fibrochondrogenesis 0 trials
  2 sub-types

  • Fibrochondrogenesis 1 0 trials
  • Fibrochondrogenesis 2 0 trials
• Hypertrichotic osteochondrodysplasia Cantu type 0 trials
• Lethal Kniest-like dysplasia 0 trials
• Lethal chondrodysplasia, Seller type 0 trials
• Linkeropathy 0 trials
  3 sub-types

  • Desbuquois dysplasia 2 0 trials
  • Spondylo-ocular syndrome 0 trials
  • Spondylodysplastic Ehlers-Danlos syndrome 0 trials
• Mesomelia-synostoses syndrome 0 trials
• Metaphyseal chondrodysplasia, Kaitila type 0 trials
• Metaphyseal chondrodysplasia, Spahr type 0 trials
• Metaphyseal chondrodysplasia-retinitis pigmentosa syndrome 0 trials
• Multiple epiphyseal dysplasia 0 trials
  10 sub-types

  • Epiphyseal dysplasia, multiple, 7 0 trials
  • Multiple epiphyseal dysplasia due to collagen 9 anomaly 0 trials Sub-types →
  • Multiple epiphyseal dysplasia type 1 0 trials
  • Multiple epiphyseal dysplasia type 4 0 trials
  • Multiple epiphyseal dysplasia type 5 0 trials
  • Multiple epiphyseal dysplasia, Al-Gazali type 0 trials
  • Multiple epiphyseal dysplasia, Beighton type 0 trials
  • Multiple epiphyseal dysplasia, Lowry type 0 trials
  • Multiple epiphyseal dysplasia, with miniepiphyses 0 trials
  • Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia 0 trials
• Pycnodysostosis 0 trials
• Pyknoachondrogenesis 0 trials
• Schneckenbecken dysplasia 0 trials
• Thanatophoric dysplasia 0 trials
  4 sub-types

  • Kozlowski Warren Fisher syndrome 0 trials
  • Thanatophoric dysplasia type 1 0 trials
  • Thanatophoric dysplasia type 2 0 trials Sub-types →
  • Thanatophoric dysplasia, Glasgow variant 0 trials
• Ulna metaphyseal dysplasia syndrome 0 trials