Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

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

1495 clinical trials for this condition and its sub-types, 0 tagged with Pheochromocytoma/paraganglioma syndrome 4 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by

Showing the 400 most recently updated of 720 trials in this tab.