Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:615424 - INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3; IBMPFD3

Xenbase Genes: hnrnpa1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000507 - inclusion body myopathy with Paget disease of bone and frontotemporal dementia
MONDO:0014179 - inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3

Disease Ontology (DO):
DOID:0050881 - inclusion body myopathy with Paget disease of bone and frontotemporal dementia
DOID:0111386 - inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3