Disease #03516 (ATFB10 (fibrillation, atrial, familial, type 10), OMIM:614022)

Official abbreviation ATFB10
Name fibrillation, atrial, familial, type 10
OMIM ID 614022
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene SCN5A
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 22:43:13 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00163024 III.15 Holl et al, submitted 4-generation family, 6 affected (1M, 5F) F no Netherlands - - - yes - ATFB10, VF1 Non-sustained ventricular tachycardia, Paroxysmal atrial tachycardia (HP:0006671) KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, RYR2, SCN5A SCN5A 1 6 Judith Verhagen
00299450 - - - - no (China) Chinese - - - Catheter ablation ATFB10 familial atrial fibrillation and sinus bradycardia ISL1 ISL1 1 6 Yi-Qing Yang
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