Search Ontology:
Human Disease

myotonia congenita

Term ID
DOID:2106
Synonyms
  • Congenital myotonia, autosomal dominant form
  • Thomsen and Becker disease
  • Thomsen's disease
Definition
A muscle tissue disease that is characterized by slow muscle relaxation associated with hyperexcitation of the muscle fibres. (3)
References
  • GARD:12301
  • ICD9CM:359.22
  • MESH:D009224
  • NCI:C84912
  • ORDO:614
  • UMLS_CUI:C0027127
Ontology
Human Disease   ( DOID:2106 )
Relationships
is a type of
has subtype
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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