Disease | n syndrome |
Phenotype | C0020302|congenital glaucoma |
Sentences | 2 |
PubMedID- 21243979 | Infantile primary congenital glaucoma with trisomy 21 (down syndrome) associated with brushfield spots. |
PubMedID- 24024747 | A case of 22q11.2 deletion syndrome with peters anomaly, congenital glaucoma, and heterozygous mutation in cyp1b1. |
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