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Items: 6

1.

Tachycardia

A rapid heartrate that exceeds the range of the normal resting heartrate for age. [from HPO]

MedGen UID:
21453
Concept ID:
C0039231
Finding; Finding
2.

Catecholaminergic polymorphic ventricular tachycardia

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is characterized by episodic syncope occurring during exercise or acute emotion. The underlying cause of these episodes is the onset of fast ventricular tachycardia (bidirectional or polymorphic). Spontaneous recovery may occur when these arrhythmias self-terminate. In other instances, ventricular tachycardia may degenerate into ventricular fibrillation and cause sudden death if cardiopulmonary resuscitation is not readily available. The mean onset of symptoms (usually a syncopal episode) is between age seven and 12 years; onset as late as the fourth decade of life has been reported. If untreated, CPVT is highly lethal, as approximately 30% of affected individuals experience at least one cardiac arrest and up to 80% have one or more syncopal spells. Sudden death may be the first manifestation of the disease. [from GeneReviews]

MedGen UID:
1803763
Concept ID:
C5574922
Disease or Syndrome
3.

Effort-induced polymorphic ventricular tachycardia

Polymorphic ventricular arrhythmias of varying morphologythat do not exist under resting conditions but appear only upon physical exercise or catecholamine administration. [from HPO]

MedGen UID:
870838
Concept ID:
C4025298
Finding
4.

Polymorphic ventricular tachycardia

A type of ventricular tachycardia that is characterized by variable QRS complexes within each lead (i.e., QRS complexes may be different from beat to beat). [from HPO]

MedGen UID:
138002
Concept ID:
C0344432
Disease or Syndrome
5.

Ventricular tachycardia

A tachycardia originating in the ventricles characterized by rapid heart rate (over 100 beats per minute) and broad QRS complexes (over 120 ms). [from HPO]

MedGen UID:
12068
Concept ID:
C0042514
Disease or Syndrome; Finding
6.

Conduction disorder of the heart

Any abnormal alteration of atrioventricular conduction. [from SNOMEDCT_US]

MedGen UID:
78114
Concept ID:
C0264886
Disease or Syndrome
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