Pheochromocytoma/paraganglioma syndrome 4

MONDO:0007273

An autosomal dominant tumor predisposition disorder caused by pathogenic variants in the SDHB 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: SDHB paraganglioma, SDHB-related tumor predisposition, paraganglioma caused by mutation in SDHB, paragangliomas 4, paragangliomas type 4, pheochromocytoma/paraganglioma syndrome 4, PGL4, SDHB-related hereditary paraganglioma-pheochromocytoma syndrome

1350 clinical trials for this condition and its sub-types.

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