This website is for informational and educational purposes only. Please do not self-medicate; contact a medical professional for advice before administration. This website is for informational and educational purposes only. Please do not self-medicate; contact a medical professional for advice before administration.

Gamstorp-Wohlfart Syndrome

Disease ID: disease_node_20383

Connections displayed (default: 10).
Loading graph...

DbxrefGARD:12353, MIM:137200
SubclassofDOID_225
Data SourceDOID
Synonymsautosomal recessive neuromyotonia and axonal neuropathy, myokymia, myotonia and muscle wasting
Doid LabelGamstorp-Wohlfart syndrome
Doid DescriptionA 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. OMIM mapping confirmed by DO. [SN].
Has SymptomSYMP_0000363
Disease Node Iddisease_node_20383
Doid IdDOID_0050526
LabelGamstorp-Wohlfart Syndrome