rs80338844, SDHD

N. diseases: 10
Disease: Pheochromocytoma ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.800 CausalMutation CLINVAR Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort. 25494863 2015
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.800 GeneticVariation UNIPROT Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. 24893135 2014
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.800 GeneticVariation UNIPROT American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers. 24493721 2014
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.800 GeneticVariation UNIPROT Canadian guideline on genetic screening for hereditary renal cell cancers. 24319509 2013
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.800 CausalMutation CLINVAR Genetic testing in head and neck paraganglioma: who, what, and why? 24436918 2013
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.800 CausalMutation CLINVAR Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations. 23433498 2013
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.800 CausalMutation CLINVAR High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands. 21348866 2012
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.800 CausalMutation CLINVAR Molecular analysis of pheochromocytoma after maternal transmission of SDHD mutation elucidates mechanism of parent-of-origin effect. 21937622 2011
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.800 CausalMutation CLINVAR The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. 19454582 2009
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.800 CausalMutation CLINVAR SDHB, SDHC, and SDHD mutation screen in sporadic and familial head and neck paragangliomas. 15479192 2004
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.800 CausalMutation CLINVAR Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas. 11897817 2002
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.800 CausalMutation CLINVAR Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss. 11391796 2001
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.800 CausalMutation CLINVAR Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. 10657297 2000