has characteristic has characteristic has material basis in germline mutation in TMEM127 Autosomal dominant inheritance autosomal dominant disease benign endocrine neoplasm pheochromocytoma hereditary neoplastic syndrome hereditary pheochromocytoma-paraganglioma TMEM127-related tumor predisposition https://github.com/monarch-initiative/mondo/issues/9178 MONDO:0700345 GARD:0028019 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. TMEM127-related tumor predisposition