Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0040479
Disease: Torsades de Pointes
Torsades de Pointes 		0.180 Biomarker disease HPO
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		0.160 GeneticVariation disease CLINVAR
CUI: C0004245
Disease: Atrioventricular Block
Atrioventricular Block 		0.130 Biomarker disease HPO
CUI: C0036572
Disease: Seizures
Seizures 		0.130 Biomarker phenotype HPO
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		0.120 Biomarker disease HPO
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.120 Biomarker group HPO
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		0.120 Biomarker group HPO
CUI: C0042510
Disease: Ventricular Fibrillation
Ventricular Fibrillation 		0.110 Biomarker disease HPO
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death 		0.110 Biomarker phenotype HPO
CUI: C0266589
Disease: Congenital ear anomaly NOS (disorder)
Congenital ear anomaly NOS (disorder) 		0.110 Biomarker group HPO
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.110 CausalMutation disease CLINVAR
CUI: C1865866
Disease: Congenital sensorineural hearing loss
Congenital sensorineural hearing loss 		0.110 Biomarker disease HPO
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		0.100 Biomarker disease HPO
CUI: C0013363
Disease: Dysautonomia
Dysautonomia 		0.100 Biomarker disease HPO
CUI: C0015300
Disease: Exophthalmos
Exophthalmos 		0.100 Biomarker disease HPO
CUI: C0018800
Disease: Cardiomegaly
Cardiomegaly 		0.100 Biomarker phenotype HPO
CUI: C0018808
Disease: Heart murmur
Heart murmur 		0.100 CausalMutation phenotype CLINVAR
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		0.100 Biomarker phenotype HPO
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0020621
Disease: Hypokalemia
Hypokalemia 		0.100 Biomarker phenotype HPO
CUI: C0024421
Disease: Macroglossia
Macroglossia 		0.100 Biomarker disease HPO
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome 		0.100 GeneticVariation disease CLINVAR
CUI: C0027709
Disease: Nephrocalcinosis
Nephrocalcinosis 		0.100 Biomarker disease HPO
CUI: C0030252
Disease: Palpitations
Palpitations 		0.100 Biomarker phenotype HPO
CUI: C0039231
Disease: Tachycardia
Tachycardia 		0.100 Biomarker phenotype HPO