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- Bc4c014bd1d6c5f9ae8e5ed74bad6a5fd hasDbXref "Orphanet:213731" @default.
- Bc4c014bd1d6c5f9ae8e5ed74bad6a5fd type Axiom @default.
- Bc4c014bd1d6c5f9ae8e5ed74bad6a5fd annotatedProperty IAO_0000115 @default.
- Bc4c014bd1d6c5f9ae8e5ed74bad6a5fd annotatedSource MONDO_0016269 @default.
- Bc4c014bd1d6c5f9ae8e5ed74bad6a5fd annotatedTarget "High-grade neuroendocrine carcinoma of the corpus uteri is an extremely rare, aggressive, primary uterine neoplasm, originating from neuroendocrine cells scattered within the endometrium, characterized, macroscopically, by a bulky, frequently polypoid, mass with abundant necrosis located in the uterus and, histologically, by rosette-like and cord-like structures consisting of small, rounded cells with oval nuclei and scarce cytoplasm. Patients often present with dysfunctional uterine bleeding, pelvic or abdominal mass and, especially in later stages of the disease, abdominal pain. Symptomatic metastatic spread or symptoms related to a paraneoplastic syndrome, such as retinopathy, or Cushing syndrome due to ectopic ACTH production, may be associated." @default.