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Inclusion body myositis

MONDO:0007827

A slowly progressive degenerative inflammatory disorder of skeletal muscles characterized by late onset weakness of specific muscles and distinctive histopathological features.

Also known as: IBM, Sporadic Inclusion Body Myositis, inclusion body myositis, sIBM, sporadic inclusion body myositis, Ibm, inflammatory myopathy

79 clinical trials for this condition and its sub-types.

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Sub-types

GNE myopathy (2) Childhood-onset autosomal recessive myopathy with external ophthalmoplegia (0) Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome (0) Myopathy, proximal, and ophthalmoplegia (0)

Broader categories

Disease (618) Inflammatory disease (310) Musculoskeletal system disorder (196) Myositis disease (94) Muscle tissue disorder (53) Human disease (14) Myopathy (11) Skeletal muscle disorder (8) Disease by body system or component (0) Disease by developmental or physiological process (0)
Trials to join now! 35 Not yet recruiting 13 Not yet finished but already full! 12 Completed 18 Terminated 1
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