Disease #05638 (BCDS1 (blepharocheilodontic syndrome, type 1 (BCDS-1)), OMIM:119580)
| Official abbreviation |
BCDS1 |
| Name |
blepharocheilodontic syndrome, type 1 (BCDS-1) |
| OMIM ID |
119580 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CDH1 |
| Associated tissues |
- |
| Disease features |
lower eyelid ectropion, upper eyelid distichiasis, euryblepharon, bilateral cleft lip and palate, conical teeth and (rare) imperforate anus |
| Remarks |
autosomal dominant |
| Date created |
2019-07-29 19:25:26 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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