×
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
×
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
SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a Multinational Study of the European Network for the Study of Adrenal Tumors (ENS@T).
25720320 2015
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
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
CausalMutation
CLINVAR
Succinate dehydrogenase-deficient gastrointestinal stromal tumors.
25741136 2015
×
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
CausalMutation
CLINVAR
Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort.
25494863 2015
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice.
25695889 2015
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
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
Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.
25300370 2014
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas.
24102379 2014
×
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
CausalMutation
CLINVAR
Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.
25300370 2014
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Pitfalls in genetic analysis of pheochromocytomas/paragangliomas-case report.
24758185 2014
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Krebs cycle metabolite profiling for identification and stratification of pheochromocytomas/paragangliomas due to succinate dehydrogenase deficiency.
25014000 2014
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Challenges in the diagnosis of pheochromocytoma and paraganglioma syndrome.
25275255 2014
×
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
Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations.
23433498 2013
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome.
23175444 2013
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma.
23666964 2013
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing.
23512077 2013
×
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
CausalMutation
CLINVAR
Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients.
22241717 2012