FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term myotonic disease ID (Ontology) DOID:450 (Human Disease)
Definition A muscular dystrophy that is characterized by progressive muscle wasting and weakness.
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       2
Human Disease Models (FBhh)  DOID       1
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes Human Disease Models
 myotonic disease       2      2      1
 ameliorates | myotonic disease       1       --       --
 model of | myotonic disease       1       --       --
Spanning Tree (Parents/Children)
Only view relationship: 
  myopathy
   |__muscular dystrophy
       |__myotonic disease  66 rec.
           |__myotonic dystrophy type 1 42 rec.
           |__myotonic dystrophy type 2 25 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a muscular dystrophy
Part of
hide Synonyms & Secondary IDs
Synonyms
Secondary IDs
hide External Crossreferences & Linkouts
ICD10CM:G71.1
ICD9CM:359.2
MESH:D020967
NCI:C84913
SNOMEDCT_US_2023_03_01:155096007
UMLS_CUI:C0553604