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myotonic dystrophy

Disease Summary
Associated Targets (6)
Tbio

4

Tclin

1

Tchem

1


GARD Rare
Mondo Description An inherited progressive disorder affecting the muscles. It is characterized by muscle wasting and hypotonia, cataracts, heart conduction defects and endocrinopathies.
Disease Ontology Description A muscular dystrophy that is characterized by progressive muscle wasting and weakness.
Mondo Term and Equivalent IDs
MONDO:0016107:  myotonic dystrophy
DC:0000127: 
GARD:0010419: 
MESH:D009223: 
NCIT:C84914: 
OMIMPS:160900: 
Orphanet:206647: 
SCTID:240104008: 
UMLS:C0027126: