eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | dentinogenesis imperfecta |
| Comorbidity | C0029434|osteogenesis imperfecta |
| Sentences | 6 |
| PubMedID- 24371383 | dentinogenesis imperfecta (di) associated with osteogenesis imperfecta (oi) is a genetic disorder that affects the connective tissues and results in dentine dysplasia. |
| PubMedID- 26578979 | dentinogenesis imperfecta type i associated with osteogenesis imperfecta (omim#166200) is caused by genetic defects of col1a1 and col1a2, i.e., the two genes encoding the α1 and α2 chains of type i collagen. |
| PubMedID- 21291557 | Dgi type i is osteogenesis imperfecta with dentinogenesis imperfecta and is caused by mutations in col1a1 and col1a2 [7]. |
| PubMedID- 23162594 | dentinogenesis imperfecta associated with osteogenesis imperfecta. |
| PubMedID- 20384825 | dentinogenesis imperfecta in children with osteogenesis imperfecta: a clinical and ultrastructural study. |
| PubMedID- 23579912 | osteogenesis imperfecta/lobstein syndrome associated with dentinogenesis imperfecta. |
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