Osteochondrodysplasia
MONDO:0005516A term referring to disorders characterized by abnormalities in the development of bones and cartilage.
Also known as: skeletal dysplasia, congenital skeletal dysplasia, osteochondrodysplasia, cartilage development disorder, congenital anomaly of cartilage
381 clinical trials for this condition and its sub-types, 12 tagged with Osteochondrodysplasia itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Osteochondrodysplasia
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Osteogenesis imperfecta 35 trials · 330 incl. sub-types
10 sub-types
- Osteogenesis imperfecta and a reduction of bone mineral density. 0 trials · 308 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
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Achondroplasia 26 trials
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Hypochondroplasia 9 trials
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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
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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
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Blount disease 2 trials
2 sub-types
- Blount disease, infantile 1 trial
- Blount disease, adolescent 0 trials
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Diastrophic dysplasia 2 trials
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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
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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
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Cleidocranial dysplasia 1 1 trial
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Midface dysplasia 1 trial
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Pseudoachondroplasia 1 trial
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Akaba Hayasaka syndrome 0 trials
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Boomerang dysplasia 0 trials
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Desbuquois dysplasia 0 trials
2 sub-types
- Desbuquois dysplasia 1 0 trials
- Desbuquois dysplasia 2 0 trials
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Fairbank disease 0 trials
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Kashin-Beck disease 0 trials
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Kniest dysplasia 0 trials
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Leri-Weill dyschondrosteosis 0 trials
1 sub-type
- Madelung deformity 0 trials Sub-types →
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Pyle disease 0 trials
2 sub-types
- Chondrodysplasia calcificans Metaphysealis 0 trials
- Metaphyseal chondrodysplasia 0 trials
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Schmid metaphyseal chondrodysplasia 0 trials
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Acheiropody 0 trials
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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
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Acrocapitofemoral dysplasia 0 trials
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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
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Atelosteogenesis 0 trials
3 sub-types
- Atelosteogenesis type I 0 trials
- Atelosteogenesis type II 0 trials
- Atelosteogenesis type III 0 trials
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Bone dysplasia, lethal Holmgren type 0 trials
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Brachyolmia 0 trials
3 sub-types
- Autosomal dominant brachyolmia 0 trials
- Autosomal recessive brachyolmia 0 trials Sub-types →
- Brachyolmia, Maroteaux type 0 trials
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Campomelic dysplasia 0 trials
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Cleidocranial dysplasia 2 0 trials
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Fibrochondrogenesis 0 trials
2 sub-types
- Fibrochondrogenesis 1 0 trials
- Fibrochondrogenesis 2 0 trials
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Lethal Kniest-like dysplasia 0 trials
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Lethal chondrodysplasia, Seller type 0 trials
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Linkeropathy 0 trials
3 sub-types
- Desbuquois dysplasia 2 0 trials
- Spondylo-ocular syndrome 0 trials
- Spondylodysplastic Ehlers-Danlos syndrome 0 trials
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Mesomelia-synostoses syndrome 0 trials
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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
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Pycnodysostosis 0 trials
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Pyknoachondrogenesis 0 trials
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Schneckenbecken dysplasia 0 trials
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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
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Ulna metaphyseal dysplasia syndrome 0 trials
Most studied deeper sub-types
Osteoporosis
(278)
Postmenopausal osteoporosis
(53)
Osteogenesis imperfecta type 3
(9)
Osteogenesis imperfecta type 1
(8)
Osteogenesis imperfecta type 4
(7)
Glucocorticoid-induced osteoporosis
(6)
Stickler syndrome type 1
(3)
Stickler syndrome type 2
(2)
Corticosteroid-induced osteoporosis
(1)
Osteogenesis imperfecta type 5
(1)
Pregnancy associated osteoporosis
(1)
Premenopausal osteoporosis
(1)
Spondyloepiphyseal dysplasia tarda, X-linked
(1)
Anauxetic dysplasia 1
(0)
Anauxetic dysplasia 2
(0)
Anauxetic dysplasia 3
(0)
Autosomal recessive cutis laxa type 2A
(0)
Autosomal recessive cutis laxa type 2B
(0)
Brachyolmia type 1, Hobaek type
(0)
Brachyolmia type 1, toledo type
(0)