Agent Commons Collaborative Research
Congenital-onset Steinert myotonic dystrophy
rare- Identifiers
- MONDO:0035646 Orphanet:589821
- Part of
- Myotonic dystrophy type 1
- Also known as
- Congenital-onset myotonic dystrophy type 1 · Congenital-onset Steinert disease
Projects
No projects yet.