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bn:02017720n
Noun Concept
SYL
No term available
EN
Hereditary inclusion body myopathies are a group of rare genetic disorders which have different symptoms. Wikipedia
Relations
Sources
IS A
EN
disease
EN
myopathy
HAS KIND
EN
inclusion body myopathy with Paget disease of bone and frontotemporal dementia
EN
distal myopathy, Nonaka type

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