Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation BEFREE This case also provides the first clinical evidence that the p.G360R mutation is pathogenic and responsible for a classic phenotype of Fabry disease. 31634893 2020
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. 27854360 2017
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Alpha-Galactosidase A p.A143T, a non-Fabry disease-causing variant. 27142856 2016
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Functional and Clinical Consequences of Novel α-Galactosidase A Mutations in Fabry Disease. 26415523 2016
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. 25356965 2015
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Guidelines for the primary prevention of stroke: a statement for healthcare professionals from the American Heart Association/American Stroke Association. 25355838 2014
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC). 25173338 2014
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Fabry disease practice guidelines: recommendations of the National Society of Genetic Counselors. 23860966 2013
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. 23788249 2013
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Clinical utility gene card for: Fabry disease. 21934708 2012
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT HFSA 2010 Comprehensive Heart Failure Practice Guideline. 20610207 2010
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Fabry disease: guidelines for the evaluation and management of multi-organ system involvement. 16980809 2006
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Analysis of splice-site mutations of the alpha-galactosidase A gene in Fabry disease. 12786754 2003
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Fabry disease in genetic counseling practice: recommendations of the National Society of Genetic Counselors. 12735292 2002
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Identification of a novel de novo mutation (G373D) in the alpha-galactosidase A gene (GLA) in a patient affected with Fabry disease. 11295840 2001
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Identification of four novel mutations in five unrelated Korean families with Fabry disease. 11076046 2000
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Characterization of two alpha-galactosidase mutants (Q279E and R301Q) found in an atypical variant of Fabry disease. 10838196 2000
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Fabry disease: identification of novel alpha-galactosidase A mutations and molecular carrier detection by use of fluorescent chemical cleavage of mismatches. 10208848 1999
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Twenty novel mutations in the alpha-galactosidase A gene causing Fabry disease. 10666480 1999
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Novel missense mutation (M72V) of alpha-galactosidase gene and its expression product in an atypical Fabry hemizygote. 9452090 1998
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Mutation analysis in 11 French patients with Fabry disease. 9452111 1998
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Screening and detection of gene mutations in Japanese patients with Fabry disease by non-radioactive single-stranded conformation polymorphism analysis. 9105656 1997
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT An atypical variant of Fabry's disease in men with left ventricular hypertrophy. 7596372 1995
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Alpha-galactosidase gene mutations in Fabry disease: heterogeneous expressions of mutant enzyme proteins. 7759078 1995
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
0.810 GeneticVariation UNIPROT Detection of 8 new mutations in the alpha-galactosidase A gene in Fabry disease. 8069316 1994