Disease #00077 (BCDS1 (BLEPHAROCHEILODONTIC SYNDROME 1), OMIM:119580)

Official abbreviation BCDS1
Name BLEPHAROCHEILODONTIC SYNDROME 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 -
Remarks -
Date created 2023-06-16 08:53:57 +00:00 (UTC)
Date last edited N/A

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