Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
0.180 GeneticVariation disease BEFREE In family 1, 12 instances of SDHD gene mutation were detected, eight of which manifested as bilateral carotid body tumor (CBT) with one bilateral malignant CBT. 30484866 2019
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
0.180 AlteredExpression disease BEFREE SDHD protein expression was reduced in SDHD-related carotid body tumor tissues. 25328978 2015
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
0.180 GeneticVariation disease BEFREE Novel germline SDHD mutation in a patient with recurrent familial carotid body tumor and concomitant pheochromocytoma. 24599702 2014
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
0.180 GeneticVariation disease BEFREE Familial carotid body tumors in patients with SDHD mutations: a case series. 22441002 2013
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
0.180 GeneticVariation disease BEFREE A patient with a history of carotid body paragangliomas and an aggressive form of kidney cancer was evaluated from a family with a germline SDHD mutation. 23083876 2012
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
0.180 GeneticVariation disease BEFREE Carotid body paraganglioma and SDHD mutation in a Greek family. 16080474 2005
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
0.180 GeneticVariation disease BEFREE Tumorigenesis of NF1-associated pheochromocytomas remains unknown, as does tumor formation (i.e., carotid body tumor) in patients with germline mutations in SDHB, SDHC, and SDHD, genes that encode subunits of the mitochondrial complex II, the smallest complex in the respiratory chain. 12381538 2002
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
0.180 GeneticVariation disease BEFREE Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss. 11391796 2001
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
0.180 CausalMutation disease CLINVAR
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
0.080 Biomarker disease BEFREE Negative SDHB immunostaining of the carotid body tumour confirmed that it was caused by the SDHB variant. 29292578 2018
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
0.080 GeneticVariation disease BEFREE Mutations in the SDHB gene are associated with worse disease-free survival after resection in patients with carotid body paragangliomas despite earlier intervention. 24169168 2014
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
0.080 GeneticVariation disease BEFREE SDHB gene mutation in a carotid body paraganglioma: case report and review of the paraganglioma syndromes. 24509376 2014
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
0.080 GeneticVariation disease BEFREE Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations. 23433498 2013
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
0.080 Biomarker disease BEFREE Immunohistochemistry with SDHB antibody was performed for a carotid body tumor. 21945342 2012
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
0.080 GeneticVariation disease BEFREE The novel SDHB p.R242C mutation was identified in a sporadic monolateral carotid body tumor. 17102086 2006
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
0.080 GeneticVariation disease BEFREE Location, number of tumors, malignancy, and age were different: more carotid body tumors were found in SDHC (13/22 [59%]) than in sporadic HNPs (29/90 [32%], P = .03), as well as fewer instances of multiple tumors in SDHC (2/22) than in SDHD (24/42; P<.001), 0 malignant tumors in SDHC vs 6/15 in SDHB (P = .002), and younger age at diagnosis in SDHC than in sporadic HNPs (45 vs 52 years; P = .03). 16249420 2005
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
0.080 GeneticVariation disease BEFREE Tumorigenesis of NF1-associated pheochromocytomas remains unknown, as does tumor formation (i.e., carotid body tumor) in patients with germline mutations in SDHB, SDHC, and SDHD, genes that encode subunits of the mitochondrial complex II, the smallest complex in the respiratory chain. 12381538 2002
Entrez Id: 6652
Gene Symbol: SORD
SORD
0.010 GeneticVariation disease BEFREE Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations. 23433498 2013
Entrez Id: 10993
Gene Symbol: SDS
SDS
0.010 GeneticVariation disease BEFREE Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations. 23433498 2013
Entrez Id: 1757
Gene Symbol: SARDH
SARDH
0.010 GeneticVariation disease BEFREE Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations. 23433498 2013
Entrez Id: 7428
Gene Symbol: VHL
VHL
0.010 GeneticVariation disease BEFREE The current case of carotid body paraganglioma in patient with the 393C>A (N131K) missense mutation in the VHL gene, supports association of this specific mutation and VHL disease type 2, and suggests its correlation with susceptibility to paragangliomas. 21384277 2011
Entrez Id: 6391
Gene Symbol: SDHC
SDHC
0.010 Biomarker disease BEFREE Location, number of tumors, malignancy, and age were different: more carotid body tumors were found in SDHC (13/22 [59%]) than in sporadic HNPs (29/90 [32%], P = .03), as well as fewer instances of multiple tumors in SDHC (2/22) than in SDHD (24/42; P<.001), 0 malignant tumors in SDHC vs 6/15 in SDHB (P = .002), and younger age at diagnosis in SDHC than in sporadic HNPs (45 vs 52 years; P = .03). 16249420 2005