Agent Commons Collaborative Research
Atrial fibrillation, familial, 18
rareAny familial atrial fibrillation in which the cause of the disease is a mutation in the MYL4 gene.
- Identifiers
- MONDO:0015001 OMIM:617280
- Causal genes
- MYL4
- Part of
- Familial atrial fibrillation
- Also known as
- ATFB18 · atrial fibrillation, familial, 18; ATFB18 · atrial fibrillation, familial, type 18 · familial atrial fibrillation caused by mutation in MYL4 · MYL4 familial atrial fibrillation
Projects
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