Disease #01217

Official abbreviation PFHB-1A
Name heart block, progressive, familial, type 1A (PFHB1A, heart block, nonprogressive)
OMIM ID 113900
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene SCN5A
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Disease features -
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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 - - 0 - - PFHB-1A 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; - - - - - 0 - - PFHB-1A 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; - - - - - 0 - - PFHB-1A 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; - - - - - 0 - - PFHB-1A Cardiac conduction defect SCN5A SCN5A 1 1 Johan den Dunnen
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