|
DOID:0111384 - inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2
Disease Ontology Definition:An inclusion body myopathy with Paget disease of bone and frontotemporal dementia that has_material_basis_in heterozygous mutation in HNRPA2B1 on 7p15.2.
Synonyms: IBMPFD2, MSP2, multisystem proteinopathy 2,
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)