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Disease Ontology Browser
Gamstorp-Wohlfart syndrome (DOID:0050526)
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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last database update
09/12/2017
MGI 6.10
The Jackson Laboratory