eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | keratitis |
| Comorbidity | C0010036|corneal dystrophy |
| Sentences | 2 |
| PubMedID- 21217896 | [40] this gene, situated at 11p13, has been implicated in a heterogeneous group of anterior segment anomalies, including peter’s anomaly, autosomal dominant keratitis, congenital cataract with late onset corneal dystrophy, isolated foveal hypoplasia and aniridia. |
| PubMedID- 25821589 | Similar to a previous report [49], in hsv keratitis with underlying granular corneal dystrophy, as-oct allowed the precise localization of microcystic edema and keratic precipitate in the subject patient (figure 9). |
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