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PedAM

Pediatric Disease Annotations & Medicines




Disease cystadenoma
Phenotype C0019562|von hippel-lindau syndrome
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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.

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