|
DOID:0111385 - inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1
Disease Ontology 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.
Synonyms: IBMPFD1, MSP1, multisystem proteinopathy 1,
Xenbase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
inclusion body myopathy with Paget disease of bone and frontotemporal dementia (is_a)