FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term myotonia congenita ID (Ontology) DOID:2106 (Human Disease)
Definition A muscle tissue disease that is characterized by slow muscle relaxation associated with hyperexcitation of the muscle fibres.
Also Known As "Batten Turner congenital myopathy" ; "Thomsen and Becker disease"
Comment
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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      10
Human Disease Models (FBhh)  DOID       1
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 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes Human Disease Models
 myotonia congenita      10      4      1
 ameliorates | myotonia congenita       3       --       --
 model of | myotonia congenita       7       --       --
Spanning Tree (Parents/Children)
Only view relationship: 
muscular disease
 |__muscle tissue disease__
disease                    |
 |__physical disorder______|
                           myotonia congenita  16 rec.
                            |__Becker disease 1 rec.
                            |__Thomsen disease 1 rec.
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Is a physical disorder
muscle tissue disease
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Synonyms
  • "Batten Turner congenital myopathy" EXACT
    "Thomsen and Becker disease" EXACT
Secondary IDs
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GARD:12301
ICD9CM:359.22
MESH:D009224
NCI:C84912
ORDO:614
UMLS_CUI:C0027127