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Summary Literature (0)
MIM:615422 - INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2; IBMPFD2

Xenbase Genes: hnrnpa2b1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000507 - inclusion body myopathy with Paget disease of bone and frontotemporal dementia
MONDO:0014178 - inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2

Disease Ontology (DO):
DOID:0050881 - inclusion body myopathy with Paget disease of bone and frontotemporal dementia