Neuroendocrine neoplasm

MONDO:0019496

Endocrine tumors, also referred to as neuroendocrine tumors (NETs), are defined by a common phenotype which is characterized by the expression of general markers (neuron specific enolase, chromogranin, synaptophysin) and hormone secretion products. These tumors may be localized in any part of the body and are generally discovered in non-specific situations, i.e. not immediately suggestive of NETs (tests for inherited predisposition to tumors or for a clinical syndrome caused by abnormal hormone secretion).

Also known as: APUDoma, neuroendocrine neoplasm, neuroendocrine tumor, neuroendocrine tumour

2350 clinical trials for this condition and its sub-types, 181 tagged with Neuroendocrine neoplasm itself.

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Sub-types of Neuroendocrine neoplasm

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