Hereditary pheochromocytoma-paraganglioma

MONDO:0017366

Neoplasm predisposition characterized by an increased risk of paragangliomas (tumors that arise from neuroendocrine tissues distributed along the paravertebral axis from the base of the skull to the pelvis) and pheochromocytomas (paragangliomas that are confined to the adrenal medulla).

Also known as: familial pheochromocytoma-paraganglioma, hereditary paraganglioma-pheochromocytoma syndrome, hereditary pheochromocytoma-paraganglioma, SDHx-related paraganglioma-pheochromocytoma, hereditary paraganglioma-pheochromocytoma

1454 clinical trials for this condition and its sub-types.

Follow this condition to get notified about new trials

Sub-types

Broader categories

Sort by

Showing the 400 most recently updated of 698 trials in this tab.