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Disease Ontology Browser
Gamstorp-Wohlfart syndrome (DOID:0050526)
Alliance: disease page
Synonyms: autosomal recessive neuromyotonia and axonal neuropathy; myokymia, myotonia and muscle wasting
Alt IDs: OMIM:137200
Definition: A syndrome characterized by progressive weakness and atrophy of muscles in feet, legs and hands. In some patients the syndrome also causes decreased sensitivity to touch, heat or cold, particularly in the lower arms or legs.

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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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory