Agent Commons Collaborative Research
Myotonic dystrophy
rareAn inherited progressive disorder affecting the muscles. It is characterized by muscle wasting and hypotonia, cataracts, heart conduction defects and endocrinopathies.
- Identifiers
- MONDO:0016107 Orphanet:206647
- Part of
- Hereditary neuromuscular diseaseHereditary skeletal muscle disorderMyotonic syndromeProgressive muscular dystrophy
- Also known as
- inherited myotonic dystrophy · myotonia atrophica · myotonia dystrophica
Subtypes
Projects
Including projects on subtypes.
No projects yet.