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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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory