Gene: SDHD ×
Source: CLINVAR ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients. 27279923 2016
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort. 25494863 2015
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients. 26269449 2015
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency. 26008905 2015
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Challenges in the diagnosis of pheochromocytoma and paraganglioma syndrome. 25275255 2014
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Identification of somatic VHL gene mutations in sporadic head and neck paragangliomas in association with activation of the HIF-1α/miR-210 signaling pathway. 23902947 2013
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing. 23512077 2013
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations. 23433498 2013
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. 23175444 2013
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Genetic testing in head and neck paraganglioma: who, what, and why? 24436918 2013
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas. 21945342 2012
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR The endemic paraganglioma syndrome type 1: origin, spread, and clinical expression. 22456618 2012
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas. 22517554 2012
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients. 22241717 2012
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands. 21348866 2012
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 GeneticVariation disease CLINVAR Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients. 22241717 2012
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Is the c.3G>C mutation in the succinate dehydrogenase subunit D (SDHD) gene due to a founder effect in Chinese head and neck paraganglioma patients? 21792967 2011
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Molecular analysis of pheochromocytoma after maternal transmission of SDHD mutation elucidates mechanism of parent-of-origin effect. 21937622 2011
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 GeneticVariation disease CLINVAR Novel SDHD gene mutation (H102R) in a patient with metastatic cervical paraganglioma effectively treated by peptide receptor radionuclide therapy. 22025150 2011
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Paraganglioma syndrome type 1 in a patient with Carney-Stratakis syndrome. 20098451 2010
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD. 19802898 2010
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational family. 19584903 2010
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 GeneticVariation disease CLINVAR Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD. 19802898 2010
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients. 19825962 2009
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation disease CLINVAR Diagnosis and management of hereditary paraganglioma syndrome due to the F933>X67 SDHD mutation. 19072999 2009