Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.760 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.760 Biomarker disease CTD_human
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.760 CausalMutation disease CLINVAR
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.760 Biomarker disease CTD_human
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.760 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.620 Biomarker disease CTD_human
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.620 CausalMutation disease CLINVAR
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.300 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 7428
Gene Symbol: VHL
VHL 		0.300 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 55654
Gene Symbol: TMEM127
TMEM127 		0.300 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.760 CausalMutation disease CLINVAR A Chinese family with familial paraganglioma syndrome due to succinate dehydrogenase deficiency. 17406045 2007
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.760 CausalMutation disease CLINVAR A novel mutation in the SDHD gene in a family with inherited paragangliomas--implications of genetic diagnosis for follow up and treatment. 12509798 2003
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.760 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 		0.760 CausalMutation disease CLINVAR A role for mitochondrial enzymes in inherited neoplasia and beyond. 12612654 2003
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.760 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.760 Biomarker disease BEFREE All GISTs from patients with Carney-Stratakis syndrome and Carney triad were negative for SDHB immunohistochemically. 20890271 2011
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.760 GeneticVariation disease CLINVAR Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect. 12811540 2003
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.760 CausalMutation disease CLINVAR Carotid body paraganglioma and SDHD mutation in a Greek family. 16080474 2005
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.760 CausalMutation disease CLINVAR Challenges in the diagnosis of pheochromocytoma and paraganglioma syndrome. 25275255 2014
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.760 CausalMutation disease CLINVAR Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases. 15066320 2004
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.760 GeneticVariation disease BEFREE Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD. 17667967 2008
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.760 CausalMutation disease CLINVAR Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients. 19825962 2009
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.760 CausalMutation disease CLINVAR Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out. 19351833 2009
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.760 GeneticVariation disease CLINVAR Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. 16317055 2006
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.760 CausalMutation disease CLINVAR Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. 16317055 2006