| class of disease | Q112193867 |
| rare disease | Q929833 |
| eye disease | Q3041498 |
| P2888 | exact match | http://www.orpha.net/ORDO/Orphanet_97966 |
| P5270 | Mondo ID | MONDO_0020004 |
| P1550 | Orphanet ID | 97966 |
| P2892 | UMLS CUI | C5681556 |
| Q1106923 | Cogan syndrome |
| Q55786056 | IRVAN syndrome |
| Q55788665 | enthesitis-related juvenile idiopathic arthritis |
| Q18558093 | myopathy of extraocular muscle |
| Q55785265 | rare acquired eye disease |
| Q55785254 | rare genetic eye disease |
| Q7316771 | retinal vasculitis |
| Q55788660 | rheumatoid factor-negative juvenile idiopathic arthritis |
| Q64050244 | Vision for improvement: Expressive writing as an intervention for people with Stargardt's disease, a rare eye disease | main subject | P921 |
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