×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.
15328326 2004
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Novel SDHD gene mutation (H102R) in a patient with metastatic cervical paraganglioma effectively treated by peptide receptor radionuclide therapy.
22025150 2011
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
High prevalence of SDHB mutations in head and neck paraganglioma in Belgium.
18551016 2008
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients.
22241717 2012
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.
25300370 2014
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
19454582 2009
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
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: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Crystal structure of mitochondrial respiratory membrane protein complex II.
15989954 2005
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Aberrant DNA hypermethylation of SDHC: a novel mechanism of tumor development in Carney triad.
24859990 2014
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.
10657297 2000
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
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
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
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
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5.
26273102 2015
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.
16317055 2006
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Mutations associated with succinate dehydrogenase D-related malignant paragangliomas.
17973943 2008
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands.
21348866 2012
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
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
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Is the c.3G>C mutation in the succinate dehydrogenase subunit D (SDHD) gene due to a founder effect in Chinese head and neck paraganglioma patients?
21792967 2011
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Active succinate dehydrogenase (SDH) and lack of SDHD mutations in sporadic paragangliomas.
16080530 2005
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.
10657297 2000
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
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
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas.
11897817 2002
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
A Chinese family with familial paraganglioma syndrome due to succinate dehydrogenase deficiency.
17406045 2007
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients.
27279923 2016
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Mediastinal paragangliomas related to SDHx gene mutations.
27785149 2016