×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5.
26273102 2015
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5.
26273102 2015
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
A case of familial paraganglioma syndrome type 4 caused by a mutation in the SDHB gene.
17143317 2006
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma.
23666964 2013
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
A Duodenal SDH-Deficient Gastrointestinal Stromal Tumor in a Patient With a Germline SDHB Mutation.
28324028 2017
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas.
16103922 2005
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
A recurrent stop-codon mutation in succinate dehydrogenase subunit B gene in normal peripheral blood and childhood T-cell acute leukemia.
17487275 2007
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
A SDHC Founder Mutation Causes Paragangliomas (PGLs) in the French Canadians: New Insights on the SDHC-Related PGL.
27700540 2016
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Accumulation of Krebs cycle intermediates and over-expression of HIF1alpha in tumours which result from germline FH and SDH mutations.
15987702 2005
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathy.
25736212 2015
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis.
19576851 2009
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Are these compound heterozygous mutations of SDHB really mutations?
20213850 2010
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Association of urinary bladder paragangliomas with germline mutations in the SDHB and VHL genes.
25683602 2015
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Attention Deficit Hyperactivity Disorder in Pediatric Patients with Pheochromocytoma and Paraganglioma.
27171833 2016
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Bilateral adrenal medullary hyperplasia associated with an SDHB mutation.
21172883 2011
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Biochemically silent abdominal paragangliomas in patients with mutations in the succinate dehydrogenase subunit B gene.
18840642 2008
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Biochemically silent abdominal paragangliomas in patients with mutations in the succinate dehydrogenase subunit B gene.
18840642 2008
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Calculating the optimal surveillance for head and neck paraganglioma in SDHB-mutation carriers.
27573198 2017
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Carney triad can be (rarely) associated with germline succinate dehydrogenase defects.
26173966 2016
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Carney triad versus Carney Stratakis syndrome: two cases which illustrate the difficulty in distinguishing between these conditions in individual patients.
20119652 2010
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Cervical paragangliomas: is SDH genetic analysis systematically required?
17987308 2008
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Chromosomal changes in sporadic and familial head and neck paragangliomas.
19393419 2009
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Clinical manifestations of familial paraganglioma and phaeochromocytomas in succinate dehydrogenase B (SDH-B) gene mutation carriers.
18419787 2008
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients.
19825962 2009
×
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out.
19351833 2009