Details of Disease | DrugMAP

General Information of Disease (ID: DISDFYQA)

Disease Name	Atrial fibrillation, familial, 12
Synonyms	ATFB12; ABCC9 familial atrial fibrillation; familial atrial fibrillation caused by mutation in ABCC9; atrial fibrillation, familial, 12; atrial fibrillation, familial, type 12
Definition	Any familial atrial fibrillation in which the cause of the disease is a mutation in the ABCC9 gene.
Disease Hierarchy	DISL4AGF: Familial atrial fibrillation DISDFYQA: Atrial fibrillation, familial, 12
Disease Identifiers	MONDO ID MONDO_0013545 UMLS CUI C3279695 OMIM ID 614050 MedGen ID 481325

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
ABCC9	TTEF5MJ	Limited	Biomarker	[1]
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This Disease Is Related to 1 DTP Molecule(s)

Gene Name	DTP ID	Evidence Level	Mode of Inheritance	REF
ABCC9	DT3JCE6	Limited	Unknown	[2]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
ABCC9	OTGAXLQN	Limited	Unknown	[2]
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References

1	Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.Genet Med. 2017 Feb;19(2):192-203. doi: 10.1038/gim.2016.90. Epub 2016 Aug 17.
2	KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillation. Nat Clin Pract Cardiovasc Med. 2007 Feb;4(2):110-6. doi: 10.1038/ncpcardio0792.