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PedAM

Pediatric Disease Annotations & Medicines




Disease von hippel-lindau syndrome
Phenotype C0010633|cystadenoma
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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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