Sinus bradycardia

Symptom Information:

Symptom ID: HPO:0001688
Synonyms:
Sinus bradycardia [OMIM:Sinus bradycardia]
Sinus bradycardia [MedDRA:10040741]
Quality:
Cross references:
OMIM: "Sinus bradycardia" [OMIM:Sinus bradycardia]
Is a (Direct Parents):
HPO         Abnormal electrophysiology of sinoatrial node origin
MedDRA Supraventricular arrhythmia
HPO         Bradycardia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of cardiovascular system physiology(HPO:0011025)
             Arrhythmia(HPO:0011675)
                Bradycardia(HPO:0001662)
                   Sinus bradycardia(HPO:0001688)
                Abnormal electrophysiology of sinoatrial node origin(HPO:0011702)
                   Sinus bradycardia(HPO:0001688)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Arrhythmia(HPO:0011675)
       Supraventricular arrhythmia(HPO:0005115)
          Sinus bradycardia(HPO:0001688)
Investigations(MedDRA:10022891)
    Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512)
       ECG investigations(MedDRA:10053104)
          Arrhythmia(HPO:0011675)
             Supraventricular arrhythmia(HPO:0005115)
                Sinus bradycardia(HPO:0001688)
       Heart rate and pulse investigations(MedDRA:10053103)
          Arrhythmia(HPO:0011675)
             Supraventricular arrhythmia(HPO:0005115)
                Sinus bradycardia(HPO:0001688)
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Atrial fibrillation, familial, 7 (OMIM:612240)
Cardiac arrhythmia, ankyrin-B-related (OMIM:600919)
Cardiomyopathy, dilated, 1DD (OMIM:613172)
Cardiomyopathy, familial hypertrophic, 6 (OMIM:600858)
Cardiomyopathy, familial restrictive, 3 (OMIM:612422)
Catecholaminergic polymorphic ventricular tachycardia (Orphanet:3286)
Chronic atrial and intestinal dysrhythmia syndrome (Orphanet:435988)
DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERALVASCULATURE (OMIM:126320)
Fabry disease (Orphanet:324)
Familial long QT syndrome (Orphanet:768)
Familial progressive cardiac conduction defect (Orphanet:871)
Familial sick sinus syndrome (Orphanet:166282)
Holt-Oram syndrome (Orphanet:392)
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency (Orphanet:314637)
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II (OMIM:140400)
Sick sinus syndrome 1, autosomal recessive (OMIM:608567)
Sick sinus syndrome 2, autosomal dominant (OMIM:163800)
X-linked Emery-Dreifuss muscular dystrophy (Orphanet:98863)