Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2751089
Disease: Brugada Syndrome 6
Brugada Syndrome 6 		0.600 CausalMutation disease CLINVAR
CUI: C2751089
Disease: Brugada Syndrome 6
Brugada Syndrome 6 		0.600 Biomarker disease CTD_human
CUI: C0039070
Disease: Syncope
Syncope 		0.110 Biomarker phenotype HPO
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: C0035232
Disease: Respiratory Paralysis
Respiratory Paralysis 		0.100 Biomarker phenotype HPO
CUI: C0037052
Disease: Sick Sinus Syndrome
Sick Sinus Syndrome 		0.100 Biomarker disease 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: C0206667
Disease: Adrenal Cortical Adenoma
Adrenal Cortical Adenoma 		0.100 Biomarker disease HPO
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal 		0.100 Biomarker phenotype HPO
CUI: C0520886
Disease: ST segment elevation (finding)
ST segment elevation (finding) 		0.100 Biomarker phenotype HPO
CUI: C1855520
Disease: Hyperglycemia, Postprandial
Hyperglycemia, Postprandial 		0.100 Biomarker phenotype HPO
CUI: C1855580
Disease: Exercise-induced muscle fatigue
Exercise-induced muscle fatigue 		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: C4020730
Disease: Increased intramyocellular lipid droplets
Increased intramyocellular lipid droplets 		0.100 Biomarker phenotype HPO
CUI: C4021553
Disease: Periodic hypokalemic paresis
Periodic hypokalemic paresis 		0.100 Biomarker disease HPO
CUI: C4022587
Disease: Fatigable weakness of respiratory muscles
Fatigable weakness of respiratory muscles 		0.100 Biomarker phenotype HPO
CUI: C4022754
Disease: Episodic hypokalemia
Episodic hypokalemia 		0.100 Biomarker phenotype HPO
CUI: C4025572
Disease: Episodic flaccid weakness
Episodic flaccid weakness 		0.100 Biomarker phenotype HPO
CUI: C4025578
Disease: Late-onset proximal muscle weakness
Late-onset proximal muscle weakness 		0.100 Biomarker phenotype HPO
CUI: C0030443
Disease: Familial Periodic Paralysis
Familial Periodic Paralysis 		0.040 GeneticVariation disease BEFREE Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation. 15037716 2004