Disease #05638

Official abbreviation BCDS-1
Name syndrome, blepharocheilodontic, type 1 (BCDS-1)
OMIM ID 119580
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
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