| # | Disease Name | Mondo ID | Direct Associated Targets | |
|---|---|---|---|---|
| 1. | epilepsy, familial temporal lobe, 1 | MONDO:0700090 | 3 | |
| 2. | paroxysmal nonkinesigenic dyskinesia 1 | MONDO:0700089 | 2 | |
| 3. | paroxysmal nonkinesigenic dyskinesia | MONDO:0700088 | 2 | |
| 4. | Usher syndrome type 1B | MONDO:0700087 | 7 | |
| 5. | trisomy | MONDO:0700065 | 2 | |
| 6. | aneuploidy | MONDO:0700064 | 5 | |
| 7. | megacystis-microcolon-intestinal hypoperistalsis syndrome 1 | MONDO:0100354 | 4 | |
| 8. | episodic kinesigenic dyskinesia 1 | MONDO:0100352 | 1 | |
| 9. | COACH syndrome | MONDO:0100349 | 3 | |
| 10. | Bartter disease type 1 | MONDO:0100344 | 3 | |
| 11. | malignant glioma | MONDO:0100342 | 4998 | |
| 12. | Friedreich ataxia 1 | MONDO:0100340 | 1 | |
| 13. | Friedreich ataxia | MONDO:0100339 | 1 | |
| 14. | urinary tract infection | MONDO:0100338 | 2 | |
| 15. | microcephaly, epilepsy, and diabetes syndrome | MONDO:0100328 | 1 | |
| 16. | Glanzmann thrombasthenia | MONDO:0100326 | 2 | |
| 17. | long QT syndrome 1 | MONDO:0100316 | 12 | |
| 18. | hereditary ataxia | MONDO:0100309 | 36 | |
| 19. | Olmsted syndrome 1 | MONDO:0100296 | 2 | |
| 20. | mitochondrial complex II deficiency, nuclear type 1 | MONDO:0100294 | 4 |
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