PLN, phospholamban, 5350

N. diseases: 90; N. variants: 6
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 Biomarker group HPO
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 GeneticVariation group CLINVAR
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.700 Biomarker group GENOMICS_ENGLAND
CUI: C1835928
Disease: CARDIOMYOPATHY, DILATED, 1P
CARDIOMYOPATHY, DILATED, 1P
0.700 Biomarker disease CTD_human
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18
0.600 CausalMutation disease CLINVAR
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18
0.600 Biomarker disease CTD_human
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.450 Biomarker disease HPO
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
0.400 Biomarker disease HPO
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.200 Biomarker group HPO
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia
0.160 Biomarker disease HPO
Cardiomyopathy, Hypertrophic, Familial
0.110 GeneticVariation disease CLINVAR
CUI: C0008031
Disease: Chest Pain
Chest Pain
0.100 Biomarker phenotype HPO
Sensorineural Hearing Loss (disorder)
0.100 Biomarker disease HPO
CUI: C0018790
Disease: Cardiac Arrest
Cardiac Arrest
0.100 GeneticVariation disease CLINVAR
CUI: C0023787
Disease: Lipodystrophy
Lipodystrophy
0.100 Biomarker disease HPO
CUI: C0026848
Disease: Myopathy
Myopathy
0.100 Biomarker group HPO
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death
0.100 GeneticVariation phenotype CLINVAR
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
0.100 Biomarker disease HPO
Creatine phosphokinase serum increased
0.100 Biomarker phenotype HPO
Ventricular Arrhythmia by ECG Finding
0.100 Biomarker phenotype HPO
CUI: C0427515
Disease: Neutrophil abnormality
Neutrophil abnormality
0.100 Biomarker phenotype HPO
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal
0.100 Biomarker phenotype HPO
CUI: C1280433
Disease: Lipoatrophy
Lipoatrophy
0.100 Biomarker disease HPO
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
0.100 CausalMutation disease CLINVAR
CUI: C1883529
Disease: Ventricular Arrhythmia, CTCAE 3.0
Ventricular Arrhythmia, CTCAE 3.0
0.100 Biomarker phenotype HPO