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Metadata
ID DOID:0110220
Name Brugada syndrome 3
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.
https://www.ncbi.nlm.nih.gov/pubmed/17224476
Xrefs

GARD:10361

ICD10CM:I49.8

OMIM:611875

Synonyms

BRGDA3 [EXACT]

Parent Relationships

is_a Brugada syndrome

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