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

Echinobase Genes:

Human Disease Resource: OMIM


Disease Ontology (DO):
DOID:0050881 - inclusion body myopathy with Paget disease of bone and frontotemporal dementia
DOID:0111385 - inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1