Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3809312
Disease: ATRIAL FIBRILLATION, FAMILIAL, 14
ATRIAL FIBRILLATION, FAMILIAL, 14 		0.600 Biomarker disease CTD_human
CUI: C3809312
Disease: ATRIAL FIBRILLATION, FAMILIAL, 14
ATRIAL FIBRILLATION, FAMILIAL, 14 		0.600 CausalMutation disease CLINVAR
CUI: C0018790
Disease: Cardiac Arrest
Cardiac Arrest 		0.100 Biomarker disease HPO
CUI: C0030591
Disease: Paroxysmal ventricular tachycardia
Paroxysmal ventricular tachycardia 		0.100 Biomarker disease HPO
CUI: C0037052
Disease: Sick Sinus Syndrome
Sick Sinus Syndrome 		0.100 Biomarker disease HPO
CUI: C0039070
Disease: Syncope
Syncope 		0.100 Biomarker phenotype HPO
CUI: C0039240
Disease: Supraventricular tachycardia
Supraventricular tachycardia 		0.100 Biomarker disease HPO
CUI: C0042510
Disease: Ventricular Fibrillation
Ventricular Fibrillation 		0.100 Biomarker disease HPO
CUI: C0085614
Disease: First degree atrioventricular block
First degree atrioventricular block 		0.100 Biomarker disease HPO
CUI: C0085615
Disease: Right bundle branch block
Right bundle branch block 		0.100 Biomarker disease HPO
CUI: C0155707
Disease: Trifascicular block
Trifascicular block 		0.100 Biomarker disease HPO
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
Paroxysmal atrial fibrillation 		0.100 Biomarker disease HPO
CUI: C0520886
Disease: ST segment elevation (finding)
ST segment elevation (finding) 		0.100 Biomarker phenotype HPO
CUI: C0600125
Disease: Prolonged PR interval
Prolonged PR interval 		0.100 Biomarker phenotype HPO
CUI: C3715208
Disease: AV Block First Degree by ECG Finding
AV Block First Degree by ECG Finding 		0.100 Biomarker phenotype HPO
CUI: C0270824
Disease: Visual seizure
Visual seizure 		0.200 Biomarker disease RGD mRNA coding for voltage-gated sodium channel beta2 subunit in rat central nervous system: cellular distribution and changes following kainate-induced seizures. 9672387 1998
CUI: C1832399
Disease: Charcot-Marie-Tooth disease, Type 4B1
Charcot-Marie-Tooth disease, Type 4B1 		0.010 GeneticVariation disease BEFREE In addition, a search for mutations in patients affected with CMT4B as well as a refined physical localisation excludes SCN2B as the CMT4B gene. 9887383 1999
CUI: C0029882
Disease: Otitis Media
Otitis Media 		0.200 Biomarker disease RGD Suppression of epithelial ion transport transcripts during pneumococcal acute otitis media in the rat. 12206256 2002
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.100 GeneticVariation phenotype GWASDB A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. 19074352 2008
CUI: C3809312
Disease: ATRIAL FIBRILLATION, FAMILIAL, 14
ATRIAL FIBRILLATION, FAMILIAL, 14 		0.600 GeneticVariation disease UNIPROT Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation. 19808477 2009
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.510 Biomarker disease CLINGEN Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation. 19808477 2009
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder 		0.300 Biomarker phenotype CLINGEN Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation. 19808477 2009
CUI: C0348626
Disease: Other specified cardiac arrhythmias
Other specified cardiac arrhythmias 		0.300 Biomarker phenotype CLINGEN Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation. 19808477 2009
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder) 		0.300 Biomarker disease CLINGEN Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation. 19808477 2009
CUI: C1399226
Disease: Ectopic rhythm
Ectopic rhythm 		0.300 Biomarker phenotype CLINGEN Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation. 19808477 2009