has characteristic has characteristic has material basis in germline mutation in SDHC Autosomal dominant inheritance autosomal dominant disease paraganglioma pheochromocytoma/paraganglioma syndrome 3 https://github.com/monarch-initiative/mondo/issues/9178 https://rarediseases.info.nih.gov/diseases/10545/paragangliomas-3 https://www.malacards.org/card/pheochromocytoma_paraganglioma_syndrome_3 SDHC-related hereditary paraganglioma-pheochromocytoma syndrome (paragangliomas 3) DOID:0061218 GARD:0010545 MEDGEN:340200 An autosomal dominant tumor predisposition disorder caused by pathogenic variants in the SDHC 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). paragangliomas type 3 OMIM:605373 PGL3 paraganglioma caused by mutation in SDHC pheochromocytoma/paraganglioma syndrome 3 MONDO:0011544 SDHC paraganglioma paragangliomas 3 MESH:C565335 UMLS:C1854336 SDHC-related tumor predisposition hereditary neoplastic syndrome hereditary pheochromocytoma-paraganglioma