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Up to: Autosomal dominant disease · Benign endocrine neoplasm · Pheochromocytoma · Hereditary pheochromocytoma-paraganglioma
TMEM127-related tumor predisposition
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.
This condition has no sub-types.