FGG, fibrinogen gamma chain, 2266

N. diseases: 70; N. variants: 18
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: C2584774
Disease: Congenital hypofibrinogenemia
Congenital hypofibrinogenemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 6 10 0.740 strong 1.000 9 3 2000 2018
CUI: C4316812
Disease: Fibrinogen Deficiency
Fibrinogen Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 56 4 0.700 strong 1.000 10 1 2005 2018
CUI: C0272350
Disease: Dysfibrinogenemia, Congenital
Dysfibrinogenemia, Congenital
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 6 8 0.610 strong 1.000 7 5 1986 2018
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 9 0.530 None 1.000 5 2000 2004
CUI: C0472803
Disease: Hypodysfibrinogenemia
Hypodysfibrinogenemia
disease Disease or Syndrome 8 1 0.440 strong 1.000 4 1 2015 2019
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
disease Digestive System Diseases; Neoplasms Neoplastic Process 3806 615 0.310 None 1.000 2 2009 2018
CUI: C0022548
Disease: Keloid
Keloid
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Acquired Abnormality 165 15 0.300 None 1.000 1 2010 2010
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms
group Digestive System Diseases; Neoplasms Neoplastic Process 820 55 0.300 None 1.000 1 2009 2009
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
Hereditary Diffuse Gastric Cancer
disease Digestive System Diseases; Neoplasms Neoplastic Process 312 119 0.300 None 1.000 1 2009 2009
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
disease Digestive System Diseases Disease or Syndrome 502 80 0.200 None 1.000 1 2010 2010
CUI: C0028754
Disease: Obesity
Obesity
disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 2821 1111 0.200 None 1.000 1 2012 2012
CUI: C0023893
Disease: Liver Cirrhosis, Experimental
Liver Cirrhosis, Experimental
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Experimental Model of Disease 870 0.200 None 1.000 1 2006 2006
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism
disease Respiratory Tract Diseases; Cardiovascular Diseases Pathologic Function 93 16 0.200 None 1.000 1 2012 2012
CUI: C0021368
Disease: Inflammation
Inflammation
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 467 0.200 None 1.000 1 2001 2001
CUI: C0160390
Disease: Injury of liver
Injury of liver
disease Digestive System Diseases; Wounds and Injuries Injury or Poisoning 36 0.200 None 1.000 1 2015 2015
CUI: C0553681
Disease: Hypofibrinogenemia
Hypofibrinogenemia
disease Disease or Syndrome 60 14 0.190 None 1.000 10 4 2005 2019
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
phenotype Cardiovascular Diseases Disease or Syndrome 378 408 0.160 None 1.000 8 3 2011 2019
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis
phenotype Cardiovascular Diseases Pathologic Function 117 218 0.110 None 1.000 2 4 2007 2012
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
phenotype Laboratory Procedure 55 143 0.100 None 1.000 2 2 2011 2016
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
phenotype Molecular Function 26 63 0.100 None 1.000 1 1 2011 2011
CUI: C0523677
Disease: Glycine measurement
Glycine measurement
phenotype Laboratory Procedure 32 68 0.100 None 1.000 1 1 2019 2019
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
phenotype Finding 26 63 0.100 None 1.000 1 1 2011 2011
CUI: C1458140
Disease: Bleeding tendency
Bleeding tendency
phenotype Hemic and Lymphatic Diseases Pathologic Function 71 14 0.100 None 1.000 1 1 2019 2019
CUI: C0232943
Disease: Intermenstrual heavy bleeding
Intermenstrual heavy bleeding
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Sign or Symptom 10 1 0.100 None 0
CUI: C0152031
Disease: Joint swelling
Joint swelling
phenotype Pathological Conditions, Signs and Symptoms Finding 33 0.100 None 0