Disease #02468 (VF-1 (fibrillation, ventricular, paroxysmal, familial, type 1 (VF-1)), OMIM:603829)

Official abbreviation VF-1
Name fibrillation, ventricular, paroxysmal, familial, type 1 (VF-1)
OMIM ID 603829
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene SCN5A
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Disease features -
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Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00101706 9521325-FamK2823 PubMed: Chen 1998 - - - - - - 0 - - VF-1 idiopathic ventricular fibrillation (IVF) SCN5A SCN5A 1 1 Johan den Dunnen
00148148 16922724-? PubMed: Millat 2006 data from Inherited Arrhythmias web site - - - - - 0 - - VF-1 Idiopathic Ventricular Fibrillation SCN5A SCN5A 1 1 Johan den Dunnen
00163024 III.15 Holl et al, submitted 4-generation family, 6 affected (1M, 5F) F no Netherlands - - 0 yes - ATFB-10, VF-1 Non-sustained ventricular tachycardia, Paroxysmal atrial tachycardia (HP:0006671) KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, RYR2, SCN5A SCN5A 1 6 Judith Verhagen
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