SOD2, superoxide dismutase 2, 6648

N. diseases: 668; N. variants: 32
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.
Heart failure with reduced ejection fraction [HFrEF]
disease Disease or Syndrome 9 0.010 None 1.000 1 2020 2020
Posterior Circulation Transient Ischemic Attack
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2001 2001
Carotid Circulation Transient Ischemic Attack
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2001 2001
Transient Ischemic Attack, Vertebrobasilar Circulation
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2001 2001
Crescendo Transient Ischemic Attacks
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2001 2001
CUI: C0751022
Disease: Brain Stem Ischemia, Transient
Brain Stem Ischemia, Transient
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2001 2001
Electron Transport Chain Deficiencies, Mitochondrial
disease Nutritional and Metabolic Diseases Disease or Syndrome 10 0.300 None 1.000 1 1999 1999
Transient Ischemic Attack, Anterior Circulation
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2001 2001
CUI: C3714618
Disease: Primary Hyperthyroidism
Primary Hyperthyroidism
disease Endocrine System Diseases Disease or Syndrome 10 0.300 None 1.000 1 2010 2010
CUI: C4721845
Disease: Marfan Syndrome, Type I
Marfan Syndrome, Type I
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 1.000 1 2014 2014
CUI: C0206307
Disease: Canavan Disease
Canavan Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 12 65 0.200 None 1.000 2 1998 2001
CUI: C0014122
Disease: Subacute Bacterial Endocarditis
Subacute Bacterial Endocarditis
disease Infections; Cardiovascular Diseases Disease or Syndrome 12 1 0.010 None 1.000 1 2019 2019
CUI: C0018776
Disease: Hearing Loss, Central
Hearing Loss, Central
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 12 0.200 None 1.000 1 2004 2004
CUI: C0034535
Disease: Radiation Syndrome
Radiation Syndrome
disease Wounds and Injuries Disease or Syndrome 14 0.300 None 1.000 2 2006 2011
Persistent Fetal Circulation Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Disease or Syndrome 14 7 0.010 None 1.000 1 2019 2019
CUI: C1853230
Disease: Aphakia, congenital primary
Aphakia, congenital primary
disease Eye Diseases Congenital Abnormality 14 7 0.010 None 1.000 1 2012 2012
CUI: C4049636
Disease: ROSE Cluster 1
ROSE Cluster 1
disease Neoplastic Process 14 0.010 None 1.000 1 2018 2018
CUI: C4281802
Disease: Spongiform encephalopathy
Spongiform encephalopathy
disease Infections; Nervous System Diseases Disease or Syndrome 14 2 0.010 None 1.000 1 2015 2015
CUI: C0236053
Disease: Mucosal ulcer
Mucosal ulcer
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 15 0.010 None 1.000 1 2005 2005
CUI: C0021367
Disease: Mammary Ductal Carcinoma
Mammary Ductal Carcinoma
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 16 0.300 None 1.000 1 2014 2014
CUI: C0205874
Disease: Papilloma, Squamous Cell
Papilloma, Squamous Cell
disease Neoplasms Neoplastic Process 16 0.300 None 1.000 1 2001 2001
CUI: C2713442
Disease: Polyposis, Adenomatous Intestinal
Polyposis, Adenomatous Intestinal
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms Disease or Syndrome 16 332 0.300 None 1.000 1 2003 2003
CUI: C2713443
Disease: Familial Intestinal Polyposis
Familial Intestinal Polyposis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms Disease or Syndrome 16 0.300 None 1.000 1 2003 2003
CUI: C0014733
Disease: Erysipelas
Erysipelas
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 17 2 0.010 None 1.000 1 2017 2017
CUI: C0014866
Disease: Esophageal Stenosis
Esophageal Stenosis
disease Digestive System Diseases Disease or Syndrome 17 2 0.300 None 1.000 1 2001 2001