Disease #02517 (PFHB1B (heart block, familial, progressive, type 1B), OMIM:604559)

Official abbreviation PFHB1B
Name heart block, familial, progressive, type 1B
OMIM ID 604559
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene TRPM4
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

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00204304 - PubMed: Brink et al 1977 extensive family, 23 affeteds/35 unaffecteds analysed - - South Africa Afrikaner - - - - PFHB1B - TRPM4 TRPM4 1 23 LOVD
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