Disease #01472 (SSS2 (sinus, sick, syndrome, type 2, autosomal dominant), OMIM:163800)

Official abbreviation SSS2
Name sinus, sick, syndrome, type 2, autosomal dominant
OMIM ID 163800
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 HCN4
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-04-07 13:27:55 +02:00 (CEST)


Individuals

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00407390 patient - - M no (Italy) Sicily - - - - SSS2 Sinus bradycardia at 8 years old Paradox Q-T trait prolongation at 13 years old HCN4 HCN4 1 54 Emanuele Micaglio
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