All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01457 - myotonia congenita, autosomal dominant (Thomsen disease) 160800 - 37 35 CLCN1 - -
01961 - myotonia congenita, autosomal recessive (Becker disease) 255700 - 95 94 CLCN1 - -
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