| P2888 | exact match | http://www.orpha.net/ORDO/Orphanet_91483 |
| P4229 | ICD-10-CM | Q13.8 |
| P5270 | Mondo ID | MONDO_0019628 |
| P1550 | Orphanet ID | 91483 |
| P2293 | genetic association | FOXC1 | Q5469819 |
| PITX2 | Q18030562 |
| Q70436172 | Autosomal dominant partial lipodystrophy associated with Rieger anomaly, short stature, and insulinopenic diabetes |
| Q97545443 | Axenfeld Rieger Anomaly Presenting as Spontaneous Hyphema |
| Q68805738 | Familial Wolf-Hirschhorn syndrome associated with Rieger anomaly of the eye |
| Q71493749 | Rieger anomaly and congenital glaucoma in the SHORT syndrome |
| Q68805743 | Rieger anomaly and uveal coloboma with associated anomalies. Third observation of a rare oculo-palato-osseous syndrome--the Abruzzo-Erikson syndrome |
| Q42165385 | Rieger anomaly with bilateral choroidal osteoma: coincidence or association? |
| Q69398183 | The Rieger anomaly concomitant with multiple dental, craniofacial, and somatic midline anomalies and short stature |
| Q82619641 | What's your diagnosis? Axenfeld Rieger anomaly with secondary glaucoma |
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