Disease Term Disease ID Gene Symbol Classification References Source
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3 C3809469 HNRNPA1 Causal Pathogenic evidence from ClinVar 23455423 ClinVar
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2 C3809468 HNRNPA2B1 Causal Pathogenic evidence from ClinVar 23455423 ClinVar
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 C4551951 VCP Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 15034582, 15732117, 16247064, 16321991, 16790606, 16984901, 17889967, 17935506, 19225410, 19237541, 19704082, 20104022, 20335036, 20512113, 21145000, 21249466, 21684747, 21816654, 21822278, 21984748, 22078486, 22270372, 22900631, 22909335, 23029473, 23056506, 23152587, 23333620, 23349634, 23498975, 24196964, 24829604, 25125609, 25388089, 25492614, 25617006, 25878907, 26105173, 26555887, 26627873, 27209344, 27226613, 27753622, 27768726, 28360103, 28692196, 29804830 -