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Disease Ontology Browser
myotonia congenita (DOID:2106)
Alliance: disease page
Synonyms: Congenital myotonia, autosomal dominant form; 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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
04/13/2021
MGI 6.16
The Jackson Laboratory