FGG, fibrinogen gamma chain, 2266

N. diseases: 70; N. variants: 18
Disease: Hypodysfibrinogenemia ×
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: C0472803
Disease: Hypodysfibrinogenemia
Hypodysfibrinogenemia 		disease Disease or Syndrome 8 1 0.440 strong 1.000 4 1 2015 2019