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
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Hope for kids with rare bone disorder: new drug shows promise in Long-Term trial
Disease control By invitation onlyThis study is for children with hypochondroplasia, a condition that causes short stature and bone differences. Researchers are testing a drug called infigratinib to see if it is safe and helps improve growth over the long term. Participants must have already completed a previous …
Phase 2 • Sponsor: QED Therapeutics, a BridgeBio company • Aim: Disease control
Last updated Aug 28, 2026 00:00 UTC
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Could a daily pill boost growth in kids with hypochondroplasia?
Disease control By invitation onlyThis study tests an oral drug called infigratinib in children with hypochondroplasia, a condition that causes short stature. The trial has two parts: first, all children receive the drug to see if it safely increases their growth rate; then, some will switch to a placebo to confi…
Phase 2/3 • Sponsor: QED Therapeutics, a BridgeBio company • Aim: Disease control
Last updated Jul 18, 2026 00:00 UTC
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Growth drug shows promise for kids with dwarfism
Disease control OngoingThis study tests a drug called BMN 111 in children with achondroplasia, the most common form of dwarfism. The goal is to see if it safely helps them grow taller over several years. About 119 children who completed an earlier study will take the drug and be monitored for growth, d…
Phase 3 • Sponsor: BioMarin Pharmaceutical • Aim: Disease control
Last updated Jun 27, 2026 11:00 UTC
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New drug aims to help short-statured children grow taller
Disease control OngoingThis study tests a drug called vosoritide to see if it can safely help children with hypochondroplasia grow faster. About 80 children aged 3 to 17 with a confirmed genetic diagnosis and very short stature will receive either the drug or a placebo for one year. The main goal is to…
Phase 3 • Sponsor: BioMarin Pharmaceutical • Aim: Disease control
Last updated Jun 27, 2026 08:13 UTC
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New oral drug shows promise for helping children with dwarfism grow
Disease control By invitation onlyThis study tests a daily oral drug called infigratinib in 300 children with achondroplasia, the most common form of dwarfism. The drug aims to improve bone growth by targeting a specific protein. Researchers will monitor safety and growth over several years, including children wh…
Phase 2 • Sponsor: QED Therapeutics, a BridgeBio company • Aim: Disease control
Last updated Jun 27, 2026 07:56 UTC