muscular disease
disease in which the muscle fibers do not function, resulting in muscular weakness
congenital myopathy
human disease
spasticity
muscle paralysis, increased tendon reflex activity, hypertonia
Acquired non-inflammatory myopathy
medical condition
strain
injury to a muscle in which the muscle fibers tear as a result of overstretching
gas gangrene
human disease
muscular atrophy
human disease
muscular dystrophy
diseases that weaken the body's muscles
myoglobinuria
myopathy that is characterized by an increased urinary excretion of myoglobin
spheroid body myopathy
Human disease
metabolic myopathy
group of rare inherited disorders characterized by a deficiency of enzymes that are involved in metabolic pathways that affect muscles. The disorders are characterized by muscle dysfunction
periodic paralysis
human disease
muscle imbalance
medical condition
Statin-associated autoimmune myopathy
medical condition
epidemic pleurodynia
human disease
muscle rigidity
symptom
Hereditary inclusion body myopathy
inherited genetic condition resulting in muscle weakness