Brugada syndrome 3 Disease Ontology Browser

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Disease Ontology Browser

Brugada syndrome 3 (DOID:0110220)
Alliance: disease page
Synonyms: BRGDA3
Alt IDs: OMIM:611875, ICD10CM:I49.8, MESH:C567509
Definition: A Brugada syndrome that has_material_basis_in heterozygous mutation in the gene encoding the alpha-1C subunit of the L-type voltage-dependent calcium channel (CACNA1C) on chromosome 12p13.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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