FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Gamstorp-Wohlfart syndrome ID (Ontology) DOID:0050526 (Human Disease)
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.
Also Known As "autosomal recessive neuromyotonia and axonal neuropathy" ; "myokymia, myotonia and muscle wasting"
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 Genes
 Gamstorp-Wohlfart syndrome       1
 for disease ribbon | Gamstorp-Wohlfart syndrome       1
 model of | Gamstorp-Wohlfart syndrome       1
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       |__Gamstorp-Wohlfart syndrome  1 rec.
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Synonyms
  • "autosomal recessive neuromyotonia and axonal neuropathy" EXACT
    "myokymia, myotonia and muscle wasting" EXACT
Secondary IDs
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GARD:12353
MIM:137200