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inclusion body myopathy with Paget disease of bone and frontotemporal dementia
MONDO:0000507
X-linked myopathy with excessive autophagy
MONDO:0010684
myopathy, myofibrillar, 9, with early respiratory failure
MONDO:0011362
GNE myopathy
MONDO:0011603
hereditary inclusion body myopathy type 4
MONDO:0017931
childhood-onset autosomal recessive myopathy with external ophthalmoplegia
MONDO:0018206