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)