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134820
FGA
FIBRINOGEN, A ALPHA POLYPEPTIDE
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Neoplasms
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Nephritis
Glomerulonephritis
Glomerulonephritis, IGA
Urination Disorders
Hematuria
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Nephritis
Glomerulonephritis
Glomerulonephritis, IGA
Urination Disorders
Hematuria
Pregnancy Complications
Pregnancy Complications, Hematologic
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Tetralogy of Fallot
Heart Diseases
Cardiomyopathies
Cardiomyopathy, Hypertrophic
Heart Defects, Congenital
Tetralogy of Fallot
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Subvalvular
Cardiomyopathy, Hypertrophic
Vascular Diseases
Arterial Occlusive Diseases
Arteriosclerosis
Embolism and Thrombosis
Thromboembolism
Thrombosis
Thromboembolism
Venous Thrombosis
Thrombophlebitis
Peripheral Vascular Diseases
Phlebitis
Thrombophlebitis
Vasculitis
Phlebitis
Thrombophlebitis
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Afibrinogenemia
Factor V Deficiency
Factor XIII Deficiency
Hemophilia A
Hemophilia B
Coagulation Protein Disorders
Afibrinogenemia
Factor V Deficiency
Factor XIII Deficiency
Hemophilia A
Hemophilia B
Disseminated Intravascular Coagulation
Blood Protein Disorders
Paraproteinemias
Hemorrhagic Disorders
Afibrinogenemia
Disseminated Intravascular Coagulation
Factor V Deficiency
Factor XIII Deficiency
Hemophilia A
Hemophilia B
Pregnancy Complications, Hematologic
Thrombophilia
Disseminated Intravascular Coagulation
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Cardiovascular Abnormalities
Heart Defects, Congenital
Tetralogy of Fallot
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Afibrinogenemia
Factor V Deficiency
Factor XIII Deficiency
Hemophilia A
Hemophilia B
Genetic Diseases, X-Linked
Hemophilia B
Metabolism, Inborn Errors
Amyloidosis, Familial
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amyloidosis, Familial
Proteostasis Deficiencies
Amyloidosis
Amyloidosis, Familial
Immune System Diseases
Autoimmune Diseases
Glomerulonephritis, IGA
Immunoproliferative Disorders
Paraproteinemias
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Translocation, Genetic
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Hemorrhage
Hematuria
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