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Syndromic disease
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Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Inclusion body myopathy and brain white matter abnormalities
rare
Identifiers
MONDO:0850514
OMIM:619733
Causal genes
ANXA11
Part of
Autosomal dominant disease
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
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