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Items: 8

1.

Arrhythmogenic right ventricular cardiomyopathy

Arrhythmogenic right ventricular cardiomyopathy (ARVC) – previously referred to as arrhythmogenic right ventricular dysplasia (ARVD) – is characterized by progressive fibrofatty replacement of the myocardium that predisposes to ventricular tachycardia and sudden death in young individuals and athletes. It primarily affects the right ventricle, and it may also involve the left ventricle. The presentation of disease is highly variable even within families, and some affected individuals may not meet established clinical criteria. The mean age at diagnosis is 31 years (±13; range: 4-64 years). [from GeneReviews]

MedGen UID:
87618
Concept ID:
C0349788
Congenital Abnormality; Disease or Syndrome
2.

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; Pathologic Function
3.

Arrhythmogenic right ventricular dysplasia

MedGen UID:
894001
Concept ID:
CN239850
Disease or Syndrome
4.

Hypoplastic right heart; intrauterine growth retardation

MedGen UID:
850712
Concept ID:
CN231400
Finding
5.

Hypoplastic right heart; tricuspid atresia; muscular ventricular septal defect; single umbilical artery

MedGen UID:
850701
Concept ID:
CN231394
Finding
6.

Right ventricular outflow

MedGen UID:
628768
Concept ID:
C0455844
Finding
7.

Right

Being located on the right side of the body. [from HPO]

MedGen UID:
619189
Concept ID:
C0444532
Spatial Concept
8.

Dysplasia

Cells that look abnormal under a microscope but are not cancer. [from NCI]

MedGen UID:
87191
Concept ID:
C0334044
Neoplastic Process; Pathologic Function
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