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Disease association ontology term - MONDO:0016107 - myotonic dystrophy

Term summary

ID
MONDO:0016107
Name
myotonic dystrophy
Ontology or CV name
Disease association
Definition
An inherited progressive disorder affecting the muscles. It is characterized by muscle wasting and hypotonia, cataracts, heart conduction defects and endocrinopathies.

Parents

Annotation

Disease association

MONDO:0011266 - myotonic dystrophy type 2

References:

Genes: