|
pulmonary arterial hypertension associated with congenital heart disease
|
17152 |
|
|
isolated renal magnesium loss
|
C537152 |
|
|
PAH associated with congenital heart disease
|
17152 |
|
|
TGFB3 arrhythmogenic right ventricular cardiomyopathy
|
7152 |
|
|
familial arrhythmogenic right ventricular dysplasia 1
|
7152 |
|
|
arrhythmogenic right ventricular cardiomyopathy 1
|
7152 |
|
|
arrhythmogenic right ventricular cardiomyopathy caused by mutation in TGFB3
|
7152 |
|
|
cardiomyopathy, right ventricular dilated
|
7152 |
|
|
arrhythmogenic right ventricular dysplasia 1
|
7152 |
|
|
arrhythmogenic right ventricular dysplasia type 1
|
7152 |
|
|
arrhythmogenic right ventricular dysplasia, familial, 1
|
7152 |
|
|
arrhythmogenic right ventricular dysplasia, familial, 1; ARVD1
|
http://purl.obolibrary.org/obo/MONDO_0007152 |
|
