Gene: SDHD ×
Source: ALL
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 group 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 group CLINVAR Mediastinal paragangliomas related to SDHx gene mutations. 27785149 2016
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation group CLINVAR Usefulness of Somatostatin Receptor Scintigraphy (Tc-[HYNIC, Tyr3]-Octreotide) and 123I-Metaiodobenzylguanidine Scintigraphy in Patients with SDHx Gene-Related Pheochromocytomas and Paragangliomas Detected by Computed Tomography. 25791839 2015
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation group CLINVAR SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a Multinational Study of the European Network for the Study of Adrenal Tumors (ENS@T). 25720320 2015
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation group 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 group CLINVAR Succinate dehydrogenase-deficient gastrointestinal stromal tumors. 25741136 2015
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 GeneticVariation group 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 GeneticVariation group CLINVAR 15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5. 26273102 2015
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation group 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 group CLINVAR Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice. 25695889 2015
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation group CLINVAR 15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5. 26273102 2015
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 GeneticVariation group CLINVAR Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations. 25300370 2014
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation group CLINVAR Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas. 24102379 2014
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 GeneticVariation group CLINVAR Aberrant DNA hypermethylation of SDHC: a novel mechanism of tumor development in Carney triad. 24859990 2014
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation group CLINVAR Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations. 25300370 2014
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation group CLINVAR Pitfalls in genetic analysis of pheochromocytomas/paragangliomas-case report. 24758185 2014
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation group CLINVAR Krebs cycle metabolite profiling for identification and stratification of pheochromocytomas/paragangliomas due to succinate dehydrogenase deficiency. 25014000 2014
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation group CLINVAR Challenges in the diagnosis of pheochromocytoma and paraganglioma syndrome. 25275255 2014
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation group CLINVAR Sporadic or familial head neck paragangliomas enrolled in a single center: clinical presentation and genotype/phenotype correlations. 22290790 2013
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation group CLINVAR Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations. 23433498 2013
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation group 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 group CLINVAR A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma. 23666964 2013
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.100 CausalMutation group 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 GeneticVariation group 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 group CLINVAR Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients. 22241717 2012