eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | congenital glaucoma |
| Comorbidity | C0012236|22q11.2 deletion syndrome |
| Sentences | 1 |
| PubMedID- 24024747 | A case of 22q11.2 deletion syndrome with peters anomaly, congenital glaucoma, and heterozygous mutation in cyp1b1. |
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