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