Disease #00164 (CFC1 (CARDIOFACIOCUTANEOUS SYNDROME 1), OMIM:115150)

Official abbreviation CFC1
Name CARDIOFACIOCUTANEOUS SYNDROME 1
OMIM ID 115150
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene BRAF
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-27 12:56:28 +00:00 (UTC)
Date last edited N/A

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