×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
GeneticVariation
disease
BEFREE
Germline mutations in SDH genes ( SDHA, SDHB, SDHC, or SDHD ) suggest Carney-Stratakis syndrome , a paraganglioma syndrome with predisposition for GIST.
30301441
2019
×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
GeneticVariation
disease
BEFREE
SDH deficiency may result from germline SDHA, SDHB, SDHC, or SDHD mutations and is found in autosomal-dominant familial paraganglioma/pheochromocytoma and Carney-Stratakis syndrome, describing the combination of paraganglioma and gastrointestinal stromal tumor (GIST).
29339836
2018
×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
CausalMutation
disease
CLINVAR
Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients.
27279923
2016
×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
CausalMutation
disease
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
0.760
CausalMutation
disease
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
0.760
CausalMutation
disease
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
0.760
CausalMutation
disease
CLINVAR
Challenges in the diagnosis of pheochromocytoma and paraganglioma syndrome.
25275255
2014
×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
CausalMutation
disease
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
0.760
CausalMutation
disease
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
0.760
CausalMutation
disease
CLINVAR
Genetic testing in head and neck paraganglioma: who, what, and why?
24436918
2013
×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
GeneticVariation
disease
BEFREE
They may be syndromal with some being associated with the Carney Triad or germline SDHA, SDHB, SDHC, or SDHD mutations (Carney-Stratakis syndrome ).
23060355
2013
×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
Biomarker
disease
BEFREE
Some of these patients have germline mutations of SDH subunit genes SDHB, SDHC, or SDHD , known as Carney-Stratakis syndrome when combined with paraganglioma.
23282968
2013
×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
CausalMutation
disease
CLINVAR
Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations.
23433498
2013
×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
CausalMutation
disease
CLINVAR
Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing.
23512077
2013
×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
CausalMutation
disease
CLINVAR
Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas.
22517554
2012
×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
CausalMutation
disease
CLINVAR
High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands.
21348866
2012
×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
CausalMutation
disease
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
0.760
CausalMutation
disease
CLINVAR
The endemic paraganglioma syndrome type 1: origin, spread, and clinical expression.
22456618
2012
×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
GeneticVariation
disease
CLINVAR
Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients.
22241717
2012
×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
CausalMutation
disease
CLINVAR
Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients.
22241717
2012
×
Entrez Id:
6392
Gene Symbol:
SDHD
SDHD
0.760
CausalMutation
disease
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
0.760
GeneticVariation
disease
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
0.760
CausalMutation
disease
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
0.760
CausalMutation
disease
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
0.760
CausalMutation
disease
CLINVAR
Paraganglioma syndrome type 1 in a patient with Carney-Stratakis syndrome.
20098451
2010