Disease | von hippel-lindau syndrome |
Phenotype | C0010633|cystadenoma |
Sentences | 2 |
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. |
PubMedID- 22296276 | Aims: clear cell papillary cystadenoma (ccpc) is associated with von hippel-lindau disease (vhld), but rarely involves mesosalpinx and broad ligament (m/bl). |
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