| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Cardiomyopathies, Restrictive | TNNI3 | disease | C0007196 | CausalMutation | 0.7 | orphanet , disgenet |
| Cardiomyopathies, Restrictive | TNNI3 | disease | C0007196 | GeneticVariation | 0.7 | orphanet , disgenet |
| Cardiomyopathies, Restrictive | TNNI3 | disease | C0007196 | Biomarker | 0.7 | orphanet , disgenet |
| Cardiomyopathies, Restrictive | TNNI3 | disease | C0007196 | AlteredExpression | 0.7 | orphanet , disgenet |
| Cardiomyopathies, Restrictive | MYPN | disease | C0007196 | GeneticVariation | 0.22 | orphanet , disgenet |
| Cardiomyopathies, Restrictive | MYPN | disease | C0007196 | Biomarker | 0.22 | orphanet , disgenet |
| Cardiomyopathies, Restrictive | CCN2 | disease | C0007196 | Biomarker | 0.2 | disgenet |
| Cardiomyopathies, Restrictive | PRKCD | disease | C0007196 | Biomarker | 0.2 | disgenet |
| Cardiomyopathies, Restrictive | FLNC | disease | C0007196 | GeneticVariation | 0.13 | orphanet , disgenet |
| Cardiomyopathies, Restrictive | FLNC | disease | C0007196 | CausalMutation | 0.13 | orphanet , disgenet |
| Cardiomyopathies, Restrictive | TNNT2 | disease | C0007196 | GeneticVariation | 0.11 | orphanet , disgenet |
| Cardiomyopathies, Restrictive | MYH7 | disease | C0007196 | GeneticVariation | 0.11 | disgenet |
| Cardiomyopathies, Restrictive | MYH7 | disease | C0007196 | CausalMutation | 0.11 | disgenet |
| Cardiomyopathies, Restrictive | TMEM87B | disease | C0007196 | GeneticVariation | 0.1 | disgenet |
| Cardiomyopathies, Restrictive | SLC4A1 | disease | C0007196 | Biomarker | 0.1 | disgenet |
| Cardiomyopathies, Restrictive | SPTB | disease | C0007196 | Biomarker | 0.1 | disgenet |
| Cardiomyopathies, Restrictive | JAG1 | disease | C0007196 | CausalMutation | 0.1 | disgenet |
| Cardiomyopathies, Restrictive | XYLT2 | disease | C0007196 | Biomarker | 0.1 | disgenet |
| Cardiomyopathies, Restrictive | PDGFRA | disease | C0007196 | Biomarker | 0.1 | disgenet |
| Cardiomyopathies, Restrictive | ANK1 | disease | C0007196 | Biomarker | 0.1 | disgenet |
| Cardiomyopathies, Restrictive | ABCC6 | disease | C0007196 | Biomarker | 0.1 | disgenet |
| Cardiomyopathies, Restrictive | SPTA1 | disease | C0007196 | Biomarker | 0.1 | disgenet |
| Cardiomyopathies, Restrictive | XYLT1 | disease | C0007196 | Biomarker | 0.1 | disgenet |
| Cardiomyopathies, Restrictive | MYL3 | disease | C0007196 | Biomarker | 0.1 | disgenet |
| Cardiomyopathies, Restrictive | EPB42 | disease | C0007196 | Biomarker | 0.1 | disgenet |
| Cardiomyopathies, Restrictive | ENPP1 | disease | C0007196 | Biomarker | 0.1 | disgenet |
| Cardiomyopathies, Restrictive | PIGT | disease | C0007196 | Biomarker | 0.1 | disgenet |
| Cardiomyopathies, Restrictive | DES | disease | C0007196 | GeneticVariation | 0.07 | disgenet |
| Cardiomyopathies, Restrictive | DES | disease | C0007196 | Biomarker | 0.07 | disgenet |
| Cardiomyopathies, Restrictive | TTR | disease | C0007196 | GeneticVariation | 0.03 | disgenet |
| Cardiomyopathies, Restrictive | TTR | disease | C0007196 | Biomarker | 0.03 | disgenet |
| Cardiomyopathies, Restrictive | TNNC1 | disease | C0007196 | GeneticVariation | 0.02 | disgenet |
| Cardiomyopathies, Restrictive | TNNC1 | disease | C0007196 | Biomarker | 0.02 | disgenet |
| Cardiomyopathies, Restrictive | BAG3 | disease | C0007196 | GeneticVariation | 0.02 | disgenet |
| Cardiomyopathies, Restrictive | MYBPC3 | disease | C0007196 | GeneticVariation | 0.02 | disgenet |
| Cardiomyopathies, Restrictive | ACE | disease | C0007196 | GeneticVariation | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | RNF19A | disease | C0007196 | Biomarker | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | TTN | disease | C0007196 | GeneticVariation | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | PDE4D | disease | C0007196 | PosttranslationalModification | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | MAPK14 | disease | C0007196 | Biomarker | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | MYL2 | disease | C0007196 | GeneticVariation | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | CRK | disease | C0007196 | Biomarker | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | AIMP2 | disease | C0007196 | Biomarker | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | MAPK8 | disease | C0007196 | AlteredExpression | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | LMNA | disease | C0007196 | GeneticVariation | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | MAPK1 | disease | C0007196 | Biomarker | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | GRAP2 | disease | C0007196 | Biomarker | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | CRYAB | disease | C0007196 | GeneticVariation | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | POLDIP2 | disease | C0007196 | Biomarker | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | AHSA1 | disease | C0007196 | Biomarker | 0.01 | disgenet |
| Cardiomyopathies, Restrictive | KIF20A | NA | C0007196 | NA | NA | orphanet |
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