|
centronuclear myopathy, autosomal dominant
|
8048 |
|
|
heparin-induced thrombocytopenia (disease)
|
18048 |
|
|
myopathy, centronuclear, 1; CNM1
|
http://purl.obolibrary.org/obo/MONDO_0008048 |
|
|
myopathy, centronuclear, autosomal dominant
|
8048 |
|
|
myotubular myopathy, autosomal dominant
|
8048 |
|
|
autosomal dominant centronuclear myopathy
|
8048 |
|
|
DNM2-related centronuclear myopathy
|
8048 |
|
|
sudden unexpected death in epilepsy
|
D000080485 |
|
|
trisomy 17p chromosome 17
|
C538048 |
|
|
myopathy, centronuclear, type 1
|
8048 |
|
|
chromosome 17, trisomy 17p
|
C538048 |
|
|
heparin-induced thrombocytopenia type 2
|
18048 |
|
