|
primary biliary cirrhosis and systemic scleroderma
|
13276 |
|
|
nonarteriosclerotic, idiopathic, childhood-onset cerebral calcification
|
C536276 |
|
|
obsolete arteriosclerotic cardiovascular disease
|
2276.0 |
|
|
ventricular tachycardia, catecholaminergic polymorphic, 2
|
12762 |
|
|
ventricular tachycardia, catecholaminergic polymorphic, 2; CPVT2
|
http://purl.obolibrary.org/obo/MONDO_0012762 |
|
|
ventricular tachycardia, catecholaminergic polymorphic, type 2
|
12762 |
|
|
primary biliary cirrhosis, Scleroderma, Raynaud disease, and telangiectasia
|
13276 |
|
|
capillary malformations, congenital, 1
|
C562760 |
|
|
disorder of defective peroxisomal and mitochondrial fission
|
100276 |
|
|
frontotemporal lobar degeneration
|
17276 |
|
|
age-related macular degeneration caused by mutation in CST3
|
12767 |
|
