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Disease Ontology Browser
Brugada syndrome 3 (DOID:0110220)
Alliance: disease page
Synonyms: BRGDA3
Alt IDs: OMIM:611875, ICD10CM:I49.8
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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory