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Up to: Autosomal dominant disease · Paraganglioma · Hereditary pheochromocytoma-paraganglioma
Pheochromocytoma/paraganglioma syndrome 4
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).
This condition has no sub-types.