Osteogenesis imperfecta
MONDO:0019019Osteogenesis 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 trialsWhere it sits in the disease tree
Browse by category →Part of
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
-
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
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)