eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | 22q11.2 deletion syndrome |
| Comorbidity | C0020302|congenital glaucoma |
| Sentences | 1 |
| PubMedID- 24024747 | A case of 22q11.2 deletion syndrome with peters anomaly, congenital glaucoma, and heterozygous mutation in cyp1b1. |
Page: 1