Pheochromocytoma/paraganglioma syndrome 1

MONDO:0008192

An autosomal dominant tumor predisposition disorder caused by pathogenic variants in the SDHD gene, characterized by an increased risk of paraganglioma and pheochromocytoma, as well as an increased risk of renal cell carcinoma and gastrointestinal stromal tumors (GIST).

Also known as: SDHD paraganglioma, SDHD-related tumor predisposition, paraganglioma caused by mutation in SDHD, paragangliomas 1, paragangliomas 1, with or without deafness, paragangliomas type 1, pheochromocytoma/paraganglioma syndrome 1, PGL1

1495 clinical trials for this condition and its sub-types, 0 tagged with Pheochromocytoma/paraganglioma syndrome 1 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal dominant disease (699) ↑ Paraganglioma (57) ↑ Hereditary pheochromocytoma-paraganglioma (6)

Including sub-types (1495) Tagged with Pheochromocytoma/paraganglioma syndrome 1 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.