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Summary Literature (0)
OMIM:167320 - INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1; IBMPFD1


Xenbase Genes: vcp

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008178 - inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1

Disease Ontology (DO):
DOID:0050881 - inclusion body myopathy with Paget disease of bone and frontotemporal dementia