eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | osteogenesis imperfecta |
| Comorbidity | C0029456|osteoporosis |
| Sentences | 4 |
| PubMedID- 22487062 | Idiopathic juvenile osteoporosis (ijo) without features of osteogenesis imperfecta (oi) is a rare bone condition that affects children and adolescents. |
| PubMedID- 22589248 | Brittle bones, fractures and osteoporosis are symptoms of osteogenesis imperfecta (oi), a group of inherited connective tissue disorders. |
| PubMedID- 26308295 | The most common indications were osteoporosis (33% of cohort) and osteogenesis imperfecta (27.2%). |
| PubMedID- 23389618 | Low bone mass and strength lead to fragility fractures, for example, in elderly individuals affected by osteoporosis or children with osteogenesis imperfecta. |
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