familial atrial fibrillation
An autosomal dominant heart condition that causes disruptions in the heart's normal rhythm. This condition is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular. [ http://en.wikipedia.org/wiki/Familial_atrial_fibrillation ]
Term info
- Orphanet:334 (MONDO:equivalentTo)
- OMIMPS:608583 (MONDO:equivalentTo)
- SCTID:715395008 (MONDO:equivalentTo)
- DOID:0050650 (MONDO:equivalentTo)
- GARD:0009740 (MONDO:equivalentTo)
- UMLS:CN204347 (MONDO:equivalentTo)
ordo_disease
Editor note: DO def states this as being in ATFB but this is not correct
An autosomal dominant heart condition that causes disruptions in the heart's normal rhythm. This condition is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular.
http://purl.obolibrary.org/obo/Orphanet_334, http://purl.obolibrary.org/obo/DOID_0050650, http://linkedlifedata.com/resource/umls/id/CN204347, http://identifiers.org/snomedct/715395008, https://omim.org/phenotypicSeries/PS608583
ATFB, hereditary atrial fibrillation (disease)
atrial fibrillation autosomal dominant, autosomal dominant atrial fibrillation, atrial fibrillation, familial
MONDO:0018054