osteogenesis imperfecta and a reduction of bone mineral density.
MONDO:0800064Mondo
Findings
No curated finding names osteogenesis imperfecta and a reduction of bone mineral density. yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A skeletal dysplasia characterized by osteogenesis imperfecta and decreased bone density.
Definition from the Mondo Disease Ontology (MONDO:0800064), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
- Narrower terms (33)
- autosomal recessive cutis laxa type 2A
- autosomal recessive cutis laxa type 2B
- Bruck syndrome 2
- calvarial doughnut lesions-bone fragility syndrome
- Cole-Carpenter syndrome 1
- Cole-Carpenter syndrome 2
- Ehlers-Danlos syndrome, spondylodysplastic type, 1
- geroderma osteodysplastica
- gnathodiaphyseal dysplasia
- osteogenesis imperfecta type 1
- osteogenesis imperfecta type 10
- osteogenesis imperfecta type 11
- osteogenesis imperfecta type 12
- osteogenesis imperfecta type 14
- osteogenesis imperfecta type 15
- osteogenesis imperfecta type 16
- osteogenesis imperfecta type 17
- osteogenesis imperfecta type 2
- osteogenesis imperfecta type 3
- osteogenesis imperfecta type 4
- osteogenesis imperfecta type 5
- osteogenesis imperfecta type 6
- osteogenesis imperfecta type 7
- osteogenesis imperfecta type 8
- osteogenesis imperfecta type 9
- osteogenesis imperfecta, type 18
- osteogenesis imperfecta, type 19
- osteoporosis-pseudoglioma syndrome
- short stature-optic atrophy-Pelger-Huët anomaly syndrome
- Singleton-Merten syndrome 1
- Singleton-Merten syndrome 2
- spondylo-ocular syndrome
- Wiedemann-Rautenstrauch syndrome