eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | crest syndrome |
| Comorbidity | C0206754|neuroendocrine tumor |
| Sentences | 7 |
| PubMedID- 25759690 | Neuroblastoma is a neuroendocrine tumor, arising from neural crest element of the sympathetic nervous system and represents the most common extracranial solid cancer in childhood. |
| PubMedID- 24591776 | [1] neuroendocrine tumors (nets) arising from the neural crest, such as neuroblastomas, form a large proportion of childhood malignancies, accounting for 7% to 10% of all pediatric neoplasms. |
| PubMedID- 23754889 | Mtc is a neuroendocrine tumor arising from neural-crest-derived, calcitonin-secreting parafollicular c cells within the thyroid. |
| PubMedID- 24204677 | Neuroblastoma (nb) is a neuroendocrine tumor arising from neural crest element of the sympathetic nervous system. |
| PubMedID- 22250122 | Paragangliomas are rare neuroendocrine tumors arising from the neural crest cells in the extra-adrenal location. |
| PubMedID- 25965060 | Background: sympathetic urinary bladder paragangliomas are rare catecholamine-secreting neuroendocrine tumors arising from neural crest cells. |
| PubMedID- 24991121 | [3] it is a neuroendocrine tumor, arising from any neural crest element of the sympathetic nervous system. |
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