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DOID:0050526 - Gamstorp-Wohlfart syndrome
Disease Ontology 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.
Synonyms: autosomal recessive neuromyotonia and axonal neuropathy, myokymia, myotonia and muscle wasting,
Xenbase Genes : hint1
MONDO:0007646 - Gamstorp-Wohlfart syndrome |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
syndrome (is_a)