| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Klippel Feil syndrome dominant type | GDF6 | disease | C1861689 | CausalMutation | 0.73 | disgenet |
| Klippel Feil syndrome dominant type | GDF6 | disease | C1861689 | GeneticVariation | 0.73 | disgenet |
| Klippel Feil syndrome dominant type | GDF6 | disease | C1861689 | Biomarker | 0.73 | disgenet |
| Klippel Feil syndrome dominant type | MEOX1 | disease | C1861689 | GeneticVariation | 0.32 | disgenet |
| Klippel Feil syndrome dominant type | MEOX1 | disease | C1861689 | Biomarker | 0.32 | disgenet |
| Klippel Feil syndrome dominant type | MYO18B | disease | C1861689 | Biomarker | 0.01 | disgenet |
| Klippel Feil syndrome dominant type | GDF3 | disease | C1861689 | Biomarker | 0.01 | disgenet |
| Klippel Feil syndrome dominant type | BRD2 | disease | C1861689 | AlteredExpression | 0.01 | disgenet |
| Klippel Feil syndrome dominant type | PAX1 | disease | C1861689 | Biomarker | 0.01 | disgenet |
| click here to return to the previous page | ||||||