×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
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
Paragangliomas with Sensorineural Hearing Loss
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
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients.
26269449 2015
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
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
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
Challenges in the diagnosis of pheochromocytoma and paraganglioma syndrome.
25275255 2014
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
Identification of somatic VHL gene mutations in sporadic head and neck paragangliomas in association with activation of the HIF-1α/miR-210 signaling pathway.
23902947 2013
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
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
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations.
23433498 2013
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
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
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
Genetic testing in head and neck paraganglioma: who, what, and why?
24436918 2013
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas.
21945342 2012
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
The endemic paraganglioma syndrome type 1: origin, spread, and clinical expression.
22456618 2012
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas.
22517554 2012
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients.
22241717 2012
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands.
21348866 2012
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
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
Paragangliomas with Sensorineural Hearing Loss
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
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
Molecular analysis of pheochromocytoma after maternal transmission of SDHD mutation elucidates mechanism of parent-of-origin effect.
21937622 2011
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
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
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
Paraganglioma syndrome type 1 in a patient with Carney-Stratakis syndrome.
20098451 2010
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD.
19802898 2010
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational family.
19584903 2010
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
0.100
GeneticVariation
CLINVAR
Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD.
19802898 2010
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients.
19825962 2009
×
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
Paragangliomas with Sensorineural Hearing Loss
0.100
CausalMutation
CLINVAR
Diagnosis and management of hereditary paraganglioma syndrome due to the F933>X67 SDHD mutation.
19072999 2009