?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/615422
Similar Terms
Downloads & Tools

Genes

1 genes associated with the ?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
HNRNPA2B1 heterogeneous nuclear ribonucleoprotein A2/B1