| Disease | cystadenoma |
| Phenotype | C0019562|von hippel-lindau syndrome |
| Sentences | 1 |
| PubMedID- 24901398 | Covered briefly are familial conditions such as the peutz-jeghers syndrome and its association with tubal mucinous metaplasia, clear cell papillary cystadenoma associated with von hippel-lindau syndrome, and the li fraumeni syndrome's germline p53 mutation and its association with distal tubal p53 signatures. |
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