|
MIM:602668 - MYOTONIC DYSTROPHY 2; DM2
Xenbase Genes: cnbp
Human Disease Resource: OMIM
MONDO:0011266 - myotonic dystrophy type 2 |
DOID:0050759 - myotonic dystrophy type 2 |
|
MONDO:0011266 - myotonic dystrophy type 2 |
DOID:0050759 - myotonic dystrophy type 2 |