Disease Term Disease ID Gene Symbol Classification References Source
Hereditary Factor V Deficiency C0015499 F5 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 7910348, 7911872, 8164741, 9694743, 10942390, 11418372, 12393490, 12816860, 16476093, 19486170, 20735394, 22044617, 31064749 -