| Disease ID | Source | Name | Description |
| 617681 | OMIM | Blepharocheilodontic syndrome 2 (BCDS2) | A form of blepharocheilodontic syndrome, a rare autosomal dominant disorder. It is characterized by lower eyelid ectropion, upper eyelid distichiasis, euryblepharon, bilateral cleft lip and palate, and features of ectodermal dysplasia, including hair anomalies, conical teeth and tooth agenesis. An additional rare manifestation is imperforate anus. There is considerable phenotypic variability among affected individuals. The disease is caused by variants affecting the gene represented in this entry. |