Term Name: inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1
Synonyms: IBMPFD1, MSP1, multisystem proteinopathy 1
Definition: An inclusion body myopathy with Paget disease of bone and frontotemporal dementia that has_material_basis_in heterozygous mutation in VCP on chromosome 9p13.3.
Ontology: Human Disease [DOID:0111385]   ( DOID:0111385 )

Relationships
is a type of: autosomal dominant disease inclusion body myopathy with Paget disease of bone and frontotemporal dementia