TMEM127-related tumor predisposition

MONDO:0700345

An autosomal dominant tumor predisposition disorder caused by pathogenic variants in the TMEM127 gene, characterized by an increased risk of paraganglioma and pheochromocytoma, as well as an increased risk of renal cell carcinoma.

Also known as: TMEM127-related tumor predisposition

1487 clinical trials for this condition and its sub-types, 0 tagged with TMEM127-related tumor predisposition itself.

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↑ Autosomal dominant disease (699) ↑ Benign endocrine neoplasm (60) ↑ Pheochromocytoma (59) ↑ Hereditary pheochromocytoma-paraganglioma (6)

Including sub-types (1487) Tagged with TMEM127-related tumor predisposition (0)

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