Disease association ontology term - MONDO:0016120 - myotonic syndrome
Term summary
ID
MONDO:0016120
Name
myotonic syndrome
Ontology or CV name
Disease association
Parents
is_a
syndromic disease
is_a
skeletal muscle disorder
Annotation
Disease association
MONDO:0011266
-
myotonic dystrophy type 2
References:
PB_REF:0000006
Genes:
byr3 (SPAC13D6.02c)