Disease #00232 (BRGDA3 (BRUGADA SYNDROME 3), OMIM:611875)

Official abbreviation BRGDA3
Name BRUGADA SYNDROME 3
OMIM ID 611875
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2025-10-09 12:38:47 +00:00 (UTC)
Date last edited N/A

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