Osteogenesis imperfecta

MONDO:0019019

Osteogenesis imperfecta (OI) comprises a heterogeneous group of genetic disorders characterized by increased bone fragility, low bone mass, and susceptibility to bone fractures with variable severity.

Also known as: Lobstein disease, OI, Osteopsathyrosis, Porak and Durante disease, brittle bone disease, glass bone disease, Vrolik disease

329 clinical trials for this condition and its sub-types, 35 tagged with Osteogenesis imperfecta itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Osteochondrodysplasia (380)

Sub-types of Osteogenesis imperfecta

Osteogenesis imperfecta and a reduction of bone mineral density. 0 trials · 307 incl. sub-types
34 sub-types
- Osteoporosis 277 trials · 295 incl. sub-types Sub-types →
- Osteogenesis imperfecta type 3 9 trials
- Osteogenesis imperfecta type 1 8 trials Sub-types →
- Osteogenesis imperfecta type 4 7 trials
- Osteogenesis imperfecta type 5 1 trial
- Bruck syndrome 2 0 trials
- Cole-Carpenter syndrome 1 0 trials
- Cole-Carpenter syndrome 2 0 trials
- Ehlers-Danlos syndrome, spondylodysplastic type, 1 0 trials
- Singleton-Merten syndrome 1 0 trials
- Singleton-Merten syndrome 2 0 trials
- Wiedemann-Rautenstrauch syndrome 0 trials
- Autosomal recessive cutis laxa type 2A 0 trials Sub-types →
- Autosomal recessive cutis laxa type 2B 0 trials
- Calvarial doughnut lesions-bone fragility syndrome 0 trials
- Geroderma osteodysplastica 0 trials
- Gnathodiaphyseal dysplasia 0 trials
- Osteogenesis imperfecta type 10 0 trials
- Osteogenesis imperfecta type 11 0 trials
- Osteogenesis imperfecta type 12 0 trials
- Osteogenesis imperfecta type 14 0 trials
- Osteogenesis imperfecta type 15 0 trials
- Osteogenesis imperfecta type 16 0 trials
- Osteogenesis imperfecta type 17 0 trials
- Osteogenesis imperfecta type 2 0 trials
- Osteogenesis imperfecta type 6 0 trials
- Osteogenesis imperfecta type 7 0 trials
- Osteogenesis imperfecta type 8 0 trials
- Osteogenesis imperfecta type 9 0 trials
- Osteogenesis imperfecta, type 18 0 trials
- Osteogenesis imperfecta, type 19 0 trials
- Osteoporosis-pseudoglioma syndrome 0 trials
- Short stature-optic atrophy-Pelger-Huët anomaly syndrome 0 trials
- Spondylo-ocular syndrome 0 trials
Brittle bone disorder 4 trials
1 sub-type
- Brittle bone syndrome lethal type 0 trials
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

Most studied deeper sub-types

Postmenopausal osteoporosis (53) Glucocorticoid-induced osteoporosis (6) Corticosteroid-induced osteoporosis (1) Pregnancy associated osteoporosis (1) Premenopausal osteoporosis (1) Drug-induced osteoporosis (0) Hypophosphatemic nephrolithiasis/osteoporosis 1 (0) Hypophosphatemic nephrolithiasis/osteoporosis 2 (0) Idiopathic juvenile osteoporosis (0) Idiopathic pregnancy-associated osteoporosis (0) Nephrolithiasis/osteoporosis, hypophosphatemic (0) Osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures (0) Wrinkly skin syndrome (0) X-linked osteoporosis with fractures (0)

Including sub-types (329) Tagged with Osteogenesis imperfecta (35)

Trials to join now! 12 Not yet recruiting 4 Not yet finished but already full! 9 Completed 9 Terminated 1

Osteogenesis imperfecta

Where it sits in the disease tree

Most studied deeper sub-types

New Bone-Strengthening device for osteoporosis under review

Could donor stem cells help kids with brittle bones grow taller and stronger?

Dental scans and AI could spot rare bone diseases faster

New study aims to unmask hidden causes of childhood joint stiffness