Search Ontology:
Human Disease

familial atrial fibrillation 13

Term ID
DOID:0061381
Synonyms
  • ATFB13
Definition
A familial atrial fibrillation that has_material_basis_in heterozygous mutation in the SCN1B gene on chromosome 19q13.11. https://pubmed.ncbi.nlm.nih.gov/19808477/
References
Ontology
Human Disease   ( DOID:0061381 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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