Hereditary inclusion-body myopathy
MONDO:0016112Also known as: inclusion myopathy, cytoplasmic body myopathy
40 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-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)