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hereditary continuous muscle fiber activity

Disease Summary
Associated Targets (1)
Tclin

1


GARD Rare
Mondo Description Hereditary continuous muscle fiber activity is a rare, non-dystrophic myopathy characterized by generalized myokymia and increased muscle tone associated with delayed motor milestones, leg stiffness, spastic gait, hyperreflexia and Babinski sign. Symptoms may be worsened by febrile illness or anesthesia.
Mondo Term and Equivalent IDs
MONDO:0019943:  hereditary continuous muscle fiber activity
GARD:0001512: 
Orphanet:972: 
UMLS:C1834559: