Inclusion body myopathy with paget disease and frontotemporal dementia

Disease Term Disease ID Gene Symbol Classification References Source
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA C1833662 VCP Causal Pathogenic evidence from ClinVar 15034582 ClinVar
HNRNPA1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 23455423 -
HNRNPA2B1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 23455423 -
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia 52430 VCP Causal Pathogenic evidence from ClinVar - ClinVar
HNRNPA1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
HNRNPA2B1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -