Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 CausalMutation CLINVAR

Entrez Id: 5894
Gene Symbol: RAF1
RAF1
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.410 CausalMutation CLINVAR

Entrez Id: 8048
Gene Symbol: CSRP3
CSRP3
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.370 CausalMutation CLINVAR

Entrez Id: 8048
Gene Symbol: CSRP3
CSRP3
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.370 GeneticVariation CLINVAR

Entrez Id: 84665
Gene Symbol: MYPN
MYPN
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.130 GeneticVariation CLINVAR

Entrez Id: 10529
Gene Symbol: NEBL
NEBL
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.110 GeneticVariation CLINVAR

Entrez Id: 3920
Gene Symbol: LAMP2
LAMP2
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.110 GeneticVariation CLINVAR

Entrez Id: 3920
Gene Symbol: LAMP2
LAMP2
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.110 CausalMutation CLINVAR

Entrez Id: 9464
Gene Symbol: HAND2
HAND2
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.100 CausalMutation CLINVAR

Entrez Id: 3753
Gene Symbol: KCNE1
KCNE1
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.100 GeneticVariation CLINVAR

Entrez Id: 10848
Gene Symbol: PPP1R13L
PPP1R13L
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.100 CausalMutation CLINVAR

Entrez Id: 10102
Gene Symbol: TSFM
TSFM
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.100 CausalMutation CLINVAR

Entrez Id: 145781
Gene Symbol: GCOM1
GCOM1
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.100 GeneticVariation CLINVAR

Entrez Id: 4633
Gene Symbol: MYL2
MYL2
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.100 GeneticVariation CLINVAR

Entrez Id: 122622
Gene Symbol: ADSS1
ADSS1
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.100 CausalMutation CLINVAR

Entrez Id: 79804
Gene Symbol: HAND2-AS1
HAND2-AS1
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.100 CausalMutation CLINVAR

Entrez Id: 100820829
Gene Symbol: MYZAP
MYZAP
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.100 GeneticVariation CLINVAR

Entrez Id: 6558
Gene Symbol: SLC12A2
SLC12A2
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.100 GeneticVariation CLINVAR

Entrez Id: 6901
Gene Symbol: TAZ
TAZ
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.190 CausalMutation CLINVAR Two cases of endocardial fibroelastosis--possible x-linked determination. 4685904

1973

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.490 CausalMutation CLINVAR Human growth hormone stimulates somatomedin C/insulin-like growth factor I production by the human lymphoid cell line, IM-9. 2753225

1989

Entrez Id: 4000
Gene Symbol: LMNA
LMNA
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.500 GeneticVariation CLINVAR An alternative splicing product of the lamin A/C gene lacks exon 10. 8621584

1996

Entrez Id: 6901
Gene Symbol: TAZ
TAZ
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.190 CausalMutation CLINVAR The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies. 9382096

1997

Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.700 CausalMutation CLINVAR Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. 9521325

1998

Entrez Id: 4607
Gene Symbol: MYBPC3
MYBPC3
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.150 CausalMutation CLINVAR Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy. 9562578

1998

Entrez Id: 7273
Gene Symbol: TTN
TTN
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.900 GeneticVariation CLINVAR Familial dilated cardiomyopathy locus maps to chromosome 2q31. 10051295

1999