eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | hereditary multiple exostoses |
| Comorbidity | C0029423|osteochondroma |
| Sentences | 5 |
| PubMedID- 20080592 | We also confirm homozygous disruption of ext1 in osteochondroma chondrocytes and their origin in proliferating physeal chondrocytes. |
| PubMedID- 23373052 | Chondromatous transformation of lumbar osteochondroma in a patient with multiple exostoses is a rare phenomenon. |
| PubMedID- 22507712 | Acute popliteal pseudoaneurysm rupture secondary to distal femoral osteochondroma in a patient with hereditary multiple exostoses. |
| PubMedID- 26568714 | Background: the purpose is to determine the location and type of osteochondromas in patients with multiple osteochondroma of the hand as well as the presence of shortening and angulation. |
| PubMedID- 23823961 | Bursa formation with scapular osteochondroma in hereditary multiple exostosis. |
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