Disease #03531 (ATFB12 (fibrillation, atrial, familial, type 12), OMIM:614050)

Official abbreviation ATFB12
Name fibrillation, atrial, familial, type 12
OMIM ID 614050
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ABCC9
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-01-03 13:24:24 +01:00 (CET)

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