| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | LINC01798 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | RBFOX1 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | LINC00364 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | TRIM44 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | ADAMTS13 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | FHIT | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | HULC | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | KIAA1755 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | ZFHX3 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | PKN2-AS1 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | ENOX1 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | AKAP6 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | NXPH4 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | EMX2OS | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | LINC00971 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | SRRM4 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | AUTS2 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | DPH6-DT | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | CAMTA1 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | KLF12 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | PRR5L | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | LINC00461 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | NRG3 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | ESRRG | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | PKNOX2 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | BRWD3 | disease | C1863416 | GeneticVariation | 0.1 | disgenet |
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