Gene: SDHB ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease CLINVAR Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling. 27604842 2017
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma. 28738844 2017
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR The phenotype of SDHB germline mutation carriers: a nationwide study. 28490599 2017
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Cardiac Paraganglioma Arising From the Right Atrioventricular Groove in a Paraganglioma-Pheochromocytoma Family Syndrome With Evidence of SDHB Gene Mutation: An Unusual Presentation. 27549546 2016
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 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 		0.710 Biomarker disease GENOMICS_ENGLAND Genetic predisposition to kidney cancer. 27899189 2016
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease CLINVAR Magnetic resonance imaging spectrum of succinate dehydrogenase-related infantile leukoencephalopathy. 26642834 2016
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease CLINVAR SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster Delivery. 26719882 2016
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma. 27539324 2016
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster Delivery. 26719882 2016
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Genetics of Apparently Sporadic Pheochromocytoma and Paraganglioma in a Chinese Population. 26267327 2015
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Superiority of [68Ga]-DOTATATE PET/CT to Other Functional Imaging Modalities in the Localization of SDHB-Associated Metastatic Pheochromocytoma and Paraganglioma. 25873086 2015
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR SDHD immunohistochemistry: a new tool to validate SDHx mutations in pheochromocytoma/paraganglioma. 25405498 2015
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR [Intrapericardical paraganglioma associated with mutation in succinate dehydrogenase enzyme gene]. 24939699 2015
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathy. 25736212 2015
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Association of urinary bladder paragangliomas with germline mutations in the SDHB and VHL genes. 25683602 2015
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Succinate Dehydrogenase (SDH)-Deficient Pancreatic Neuroendocrine Tumor Expands the SDH-Related Tumor Spectrum. 26259135 2015
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Paraganglioma Presenting as Postpartum Fever of Unknown Origin. 26236513 2015
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245 2015
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245 2015
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease CLINVAR Mitochondrial leukoencephalopathy and complex II deficiency associated with a recessive SDHB mutation with reduced penetrance. 26925370 2015
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice. 25695889 2015
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease CLINVAR 15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5. 26273102 2015
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma. 24694336 2014
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Pheochromocytoma and paraganglioma syndromes: genetics and management update. 24523625 2014