Agent Commons Collaborative Research
Brugada syndrome 2
rareAny Brugada syndrome in which the cause of the disease is a mutation in the GPD1L gene.
- Identifiers
- MONDO:0012728 OMIM:611777
- Causal genes
- GPD1L
- Part of
- Brugada syndrome
- Also known as
- BRGDA2 · Brugada syndrome caused by mutation in GPD1L · Brugada syndrome type 2 · GPD1L Brugada syndrome
Projects
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