Disease #01217 (PFHB1A (heart block, progressive, familial, type 1A (PFHB1A, heart block, nonprogressive)), OMIM:113900)

Official abbreviation PFHB1A
Name heart block, progressive, familial, type 1A (PFHB1A, heart block, nonprogressive)
OMIM ID 113900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 4
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 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00101843 12574143-? PubMed: Bezzina 2003 data copied from the Inherited arrhythmogenic diseases and cardiac ion channels database; - - Netherlands - - - - - PFHB1A Cardiac conduction defect SCN5A SCN5A 1 1 Johan den Dunnen
00101845 12569159-? PubMed: Viswanathan 2003 data copied from the Inherited arrhythmogenic diseases and cardiac ion channels database; - - - - - - - - PFHB1A Cardiac conduction defect SCN5A SCN5A 1 1 Johan den Dunnen
00101846 11234013-? PubMed: Tan 2001 data copied from the Inherited arrhythmogenic diseases and cardiac ion channels database; - - - - - - - - PFHB1A Cardiac conduction defect SCN5A SCN5A 1 1 Johan den Dunnen
00101847 16379539-? PubMed: Shim 2005 data copied from the Inherited arrhythmogenic diseases and cardiac ion channels database; - - - - - - - - PFHB1A Cardiac conduction defect SCN5A SCN5A 1 1 Johan den Dunnen
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