SUDDEN CARDIAC FAILURE, ALCOHOL-INDUCED
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2.
|
27523597 |
2016 |
SUDDEN CARDIAC FAILURE, INFANTILE
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Infancy.
|
27523598 |
2016 |
SUDDEN CARDIAC FAILURE, INFANTILE
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2.
|
27523597 |
2016 |
SUDDEN CARDIAC FAILURE, INFANTILE
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
Body Height
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
Intelligence
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence.
|
29942086 |
2018 |
Intelligence
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence.
|
29326435 |
2019 |
Intelligence
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
|
29844566 |
2018 |
Breast Carcinoma
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Association analysis identifies 65 new breast cancer risk loci.
|
29059683 |
2017 |
Finding of Mean Corpuscular Hemoglobin
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
Mitochondrial Diseases
|
0.020 |
GeneticVariation
|
group |
BEFREE |
Altogether these data demonstrate that PPA2 is an essential gene in yeast and that biallelic mutations in PPA2 cause a mitochondrial disease leading to sudden cardiac arrest in infants.
|
27523598 |
2016 |
Mitochondrial Diseases
|
0.020 |
GeneticVariation
|
group |
BEFREE |
These individuals show a range of severity, indicating that PPA2 mutations may cause a spectrum of mitochondrial disease phenotypes.
|
27523597 |
2016 |
Cardiac Arrest
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Infancy.
|
27523598 |
2016 |
Depletion of mitochondrial DNA
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
We sequenced the PPA2 gene in 13 patients with mitochondrial DNA depletion syndromes (MDS) of unknown cause to determine if mutations in the PPA2 gene of these patients were associated with this disease.
|
16300924 |
2006 |
SUDDEN CARDIAC FAILURE, ALCOHOL-INDUCED
|
0.700 |
Biomarker
|
disease |
CTD_human |
|
|
|
SUDDEN CARDIAC FAILURE, ALCOHOL-INDUCED
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Infancy.
|
27523598 |
2016 |
SUDDEN CARDIAC FAILURE, ALCOHOL-INDUCED
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2.
|
27523597 |
2016 |
SUDDEN CARDIAC FAILURE, INFANTILE
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Infancy.
|
27523598 |
2016 |
SUDDEN CARDIAC FAILURE, INFANTILE
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
SUDDEN CARDIAC FAILURE, INFANTILE
|
0.700 |
Biomarker
|
disease |
CTD_human |
|
|
|
SUDDEN CARDIAC FAILURE, INFANTILE
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2.
|
27523597 |
2016 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Myocarditis
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Myocardial fibrosis
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Bradycardia
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|