F5, coagulation factor V, 2153

N. diseases: 369; N. variants: 52
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: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		disease Disease or Syndrome 1075 276 0.050 None 1.000 5 1 1995 2013
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		phenotype Laboratory Procedure 17 44 0.100 None 1.000 2 2 2012 2018
CUI: C1963943
Disease: Atherothrombosis
Atherothrombosis 		disease Acquired Abnormality 115 15 0.020 None 1.000 2 2004 2009
CUI: C4049291
Disease: Postpartum thrombosis
Postpartum thrombosis 		disease Disease or Syndrome 1 0.020 None 1.000 2 1997 2017
CUI: C0220810
Disease: Congenital defects
Congenital defects 		group Congenital Abnormality 126 6 0.010 None 1.000 1 2004 2004
CUI: C0278488
Disease: Carcinoma breast stage IV
Carcinoma breast stage IV 		disease Neoplastic Process 573 14 0.010 None 1.000 1 2004 2004
CUI: C0282666
Disease: Very Low Birth Weight
Very Low Birth Weight 		phenotype Sign or Symptom 42 2 0.010 None 1.000 1 2005 2005
CUI: C0339499
Disease: Central retinal vein occlusion - juvenile
Central retinal vein occlusion - juvenile 		disease Acquired Abnormality 2 0.010 None 1.000 1 1998 1998
CUI: C0340517
Disease: Atrial thrombosis
Atrial thrombosis 		disease Disease or Syndrome 6 0.010 None 1.000 1 2007 2007
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		phenotype Laboratory Procedure 545 1440 0.100 None 1.000 1 2 2012 2012
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		phenotype Laboratory Procedure 283 679 0.100 None 1.000 1 2 2012 2012
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		disease Mental or Behavioral Dysfunction 1825 553 0.010 None 1.000 1 2001 2001
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		disease Disease or Syndrome 6 0.010 None 1.000 1 1999 1999
CUI: C0747845
Disease: early pregnancy
early pregnancy 		phenotype Disease or Syndrome 273 8 0.010 None 1.000 1 2002 2002
CUI: C0867390
Disease: postoperative stroke
postoperative stroke 		disease Disease or Syndrome 2 0.010 None 1.000 1 2000 2000
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		phenotype Laboratory Procedure 62 522 0.100 None 1.000 1 1 2012 2012
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		phenotype Laboratory Procedure 62 522 0.100 None 1.000 1 1 2012 2012
CUI: C1397674
Disease: Persistent foramen ovale
Persistent foramen ovale 		disease Congenital Abnormality 1 0.010 None 1.000 1 2003 2003
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		phenotype Laboratory Procedure 486 1243 0.100 None 1.000 1 2 2012 2012
CUI: C1852242
Disease: Nonarteritic anterior ischemic optic neuropathy (NAION)
Nonarteritic anterior ischemic optic neuropathy (NAION) 		disease Disease or Syndrome 22 6 0.010 None 1.000 1 1 2009 2009
CUI: C2585684
Disease: Heterozygous prothrombin G20210A mutation
Heterozygous prothrombin G20210A mutation 		disease Disease or Syndrome 2 0.010 None 1.000 1 2008 2008
CUI: C2825910
Disease: Stem Cell Factor Measurement
Stem Cell Factor Measurement 		phenotype Laboratory Procedure 4 8 0.100 None 1.000 1 1 2017 2017
CUI: C2873788
Disease: Deficiency of factor XII [Hageman]
Deficiency of factor XII [Hageman] 		disease Disease or Syndrome 2 0.010 None 1.000 1 2000 2000
CUI: C2945695
Disease: Limb ischemia
Limb ischemia 		disease Disease or Syndrome 171 3 0.010 None < 0.001 1 2013 2013
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 1 9 2018 2018