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.
CUI: C1510432
Disease: Radiation Sickness
Radiation Sickness 		disease Wounds and Injuries Injury or Poisoning 1 0.300 None 1.000 2 2006 2011
CUI: C0152497
Disease: Food poisoning caused by Vibrio parahaemolyticus
Food poisoning caused by Vibrio parahaemolyticus 		disease Infections; Chemically-Induced Disorders Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C2675128
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 (finding) 		disease Finding 1 0.300 None 0
CUI: C0340305
Disease: Inferior Wall Myocardial Infarction
Inferior Wall Myocardial Infarction 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2013 2013
CUI: C0018200
Disease: Granuloma, Respiratory Tract
Granuloma, Respiratory Tract 		phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Pathologic Function 4 0.300 None 1.000 1 2000 2000
CUI: C0278837
Disease: Stage IV Prostate Carcinoma
Stage IV Prostate Carcinoma 		disease Neoplasms; Male Urogenital Diseases Neoplastic Process 4 6 0.010 None 1.000 1 1 2015 2015
CUI: C0520574
Disease: Cerebrovascular amyloidosis
Cerebrovascular amyloidosis 		disease Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 2006 2006
CUI: C0751316
Disease: Acquired Meningomyelocele
Acquired Meningomyelocele 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Acquired Abnormality 4 0.300 None 1.000 1 2012 2012
CUI: C0855247
Disease: Sleep attack
Sleep attack 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Mental or Behavioral Dysfunction 4 3 0.010 None 1.000 1 1 2019 2019
CUI: C3146264
Disease: Stage IV Prostate Cancer AJCC v7
Stage IV Prostate Cancer AJCC v7 		disease Neoplastic Process 4 6 0.010 None 1.000 1 1 2015 2015
CUI: C3502298
Disease: Lactic Acidosis, Fatal Infantile
Lactic Acidosis, Fatal Infantile 		disease Nutritional and Metabolic Diseases Disease or Syndrome 4 0.010 None 1.000 1 1996 1996
CUI: C4553752
Disease: Stage IV Prostate Cancer AJCC v8
Stage IV Prostate Cancer AJCC v8 		disease Neoplastic Process 4 6 0.010 None 1.000 1 1 2015 2015
CUI: C0086664
Disease: Myelocele
Myelocele 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 5 1 0.300 None 1.000 1 2012 2012
CUI: C0153658
Disease: Malignant neoplasm of endocrine gland
Malignant neoplasm of endocrine gland 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 5 0.010 None 1.000 1 2018 2018
CUI: C0242992
Disease: Multiple Chemical Sensitivity
Multiple Chemical Sensitivity 		phenotype Immune System Diseases; Disorders of Environmental Origin Disease or Syndrome 5 0.300 None 1.000 1 2013 2013
CUI: C1527168
Disease: Bonnevie-Ullrich Syndrome
Bonnevie-Ullrich Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 5 0.300 None 1.000 1 2014 2014
CUI: C0033074
Disease: Presbycusis
Presbycusis 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Pathologic Function 6 0.200 None 1.000 1 2014 2014
CUI: C0036980
Disease: Shock, Cardiogenic
Shock, Cardiogenic 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 6 0.300 None 1.000 1 2011 2011
CUI: C0268255
Disease: Farber Lipogranulomatosis
Farber Lipogranulomatosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 7 10 0.310 None 1.000 1 1999 1999
CUI: C0395887
Disease: Tympanosclerosis
Tympanosclerosis 		disease Otorhinolaryngologic Diseases Disease or Syndrome 7 1 0.010 None 1.000 1 2016 2016
CUI: C0475802
Disease: Perinatal anoxic-ischemic brain injury
Perinatal anoxic-ischemic brain injury 		disease Nervous System Diseases Disease or Syndrome 7 0.010 None 1.000 1 2016 2016
CUI: C1859317
Disease: Cataract and cardiomyopathy
Cataract and cardiomyopathy 		disease Eye Diseases; Cardiovascular Diseases Disease or Syndrome 7 15 0.300 None 1.000 1 2013 2013
CUI: C2316401
Disease: Chronic kidney disease stage 1
Chronic kidney disease stage 1 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 7 0.010 None 1.000 1 2016 2016
CUI: C0543891
Disease: Neuroleptic-Induced Tardive Dyskinesia
Neuroleptic-Induced Tardive Dyskinesia 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Chemically-Induced Disorders Disease or Syndrome 8 2 0.010 None < 0.001 1 1 2008 2008
CUI: C3830518
Disease: Diabetic embryopathy
Diabetic embryopathy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 9 0.010 None 1.000 1 2018 2018