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MIM:167320 - INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1; IBMPFD1
Xenbase Genes: vcp
Human Disease Resource: MIM
MONDO:0008178 - inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 |
DOID:0050881 - inclusion body myopathy with Paget disease of bone and frontotemporal dementia |