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Hereditary inclusion-body myopathy

MONDO:0016112

Also known as: inclusion myopathy, cytoplasmic body myopathy

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

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Sub-types

GNE myopathy (2) Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 (2) Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2 (1) Inclusion body myopathy with Paget disease of bone and frontotemporal dementia (1) Childhood-onset autosomal recessive myopathy with external ophthalmoplegia (0) Desmin-related myopathy with Mallory body-like inclusions (0) Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome (0) Hereditary inclusion body myopathy type 4 (0) Inclusion body myopathy and brain white matter abnormalities (0) Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3 (0) Myopathy, autophagic vacuolar, infantile-onset (0) Myopathy, myofibrillar, 9, with early respiratory failure (0) X-linked myopathy with excessive autophagy (0)

Broader categories

Disease (618) Musculoskeletal system disorder (196) Hereditary disease (172) Muscle tissue disorder (53) Human disease (14) Myopathy (11) Skeletal muscle disorder (8) Disease of genetic or genomic mechanism (2) Hereditary skeletal muscle disorder (1) Disease by body system or component (0)
Trials to join now! 17 Not yet recruiting 7 Not yet finished but already full! 5 Completed 10 Terminated 1
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