Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/615424
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Genes

1 genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
HNRNPA1 heterogeneous nuclear ribonucleoprotein A1