myotonia congenita Disease Ontology Browser

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Disease Ontology Browser

myotonia congenita (DOID:2106)
Alliance: disease page
Synonyms: Batten Turner congenital myopathy; Thomsen and Becker disease
Alt IDs: ICD9CM:359.22, MESH:D009224, NCI:C84912, ORDO:614, UMLS_CUI:C0027127
Definition: A muscle tissue disease that is characterized by slow muscle relaxation associated with hyperexcitation of the muscle fibres.

Disease References using Mouse Models (3)

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/30/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Clcn1adr-mto/Clcn1adr-mto	SWR/J-Clcn1^adr-mto/J	J:16954	View
Clcn1adr/Clcn1adr	A2G-Clcn1^adr	J:18371	View
Clcn1m1Btlr/Clcn1m1Btlr	C57BL/6J-Clcn1^m1Btlr	J:307652	View
Clcn1em1Btlr/Clcn1em1Btlr	C57BL/6J-Clcn1^em1Btlr	J:307652	View