HRG, histidine rich glycoprotein, 3273

N. diseases: 72; N. variants: 21
Disease: Prothrombin G20210A mutation ×
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		disease Hemic and Lymphatic Diseases Disease or Syndrome 20 9 0.010 None 1.000 1 1999 1999