eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | axenfeld-rieger syndrome |
| Comorbidity | C0019322|umbilical hernia |
| Sentences | 1 |
| PubMedID- 25893250 | Interestingly, all the mutation carriers had also oligodontia, maxillary hypoplasia and iris hypoplasia, and the proband (iii-3) and her father (ii-5) had also congenital umbilical hernia, a phenotype of axenfeld-rieger syndrome (ars). |
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