Brugada syndrome 5 Disease Ontology Browser

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Disease Ontology Browser

Brugada syndrome 5 (DOID:0110222)
Alliance: disease page
Synonyms: BRGDA5
Alt IDs: OMIM:612838, ICD10CM:I49.8, MESH:C567556
Definition: A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN1B gene on chromosome 19q13.

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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