MeSH Browser

MeSH Supplementary: Sick Sinus Syndrome 2, Autosomal Dominant
Unique ID: C563513
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563513
Entry Term(s): Atrial Fibrillation with Bradyarrhythmia; Sinus Bradycardia Syndrome, Familial, Autosomal Dominant; Sinus Node Disease, Familial, Autosomal Dominant
Registry Number: 0
Heading Mapped to: *Sick Sinus Syndrome
Frequency: 4
Date of Entry: 2012/11/05

Sick Sinus Syndrome 2, Autosomal Dominant MeSH Supplementary Concept Data 2024