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Disease Ontology Browser
myotonia congenita (DOID:2106)
Synonyms: Congenital myotonia, autosomal dominant form (disorder); Thomsen disease; Thomsen's disease
Alt IDs: OMIM:160800, OMIM:255700, ICD9CM:359.22, MESH:D009224, NCI:C84912, ORDO:614, UMLS_CUI:C0027127
Definition: A muscle tissue disease that is characterised by slow muscle relaxation associated with hyperexcitation of the muscle fibres.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/08/2017
MGI 6.10
The Jackson Laboratory