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A reference for what the literature reports. Not medical advice.

Disease

myotonic dystrophy

MONDO:0016107Mondo

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Findings

No curated finding names myotonic dystrophy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

An inherited progressive disorder affecting the muscles. It is characterized by muscle wasting and hypotonia, cataracts, heart conduction defects and endocrinopathies.

Definition from the Mondo Disease Ontology (MONDO:0016107), read 2026-09-29. CC BY 4.0.

Where it sits

A kind of: hereditary neuromuscular disease
hereditary skeletal muscle disorder
myotonic syndrome
progressive muscular dystrophy
Narrower terms (8): adult-onset Steinert myotonic dystrophy
childhood-onset Steinert myotonic dystrophy
congenital myotonic dystrophy
juvenile-onset Steinert myotonic dystrophy
late-onset Steinert myotonic dystrophy
myotonic cataract
myotonic dystrophy type 1
myotonic dystrophy type 2

Other names

1 name

Resolves to: myotonic dystrophy

Also called: inherited myotonic dystrophy