GPX1, glutathione peroxidase 1, 2876

N. diseases: 290; N. variants: 12
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: C4025283
Disease: Compensated hemolytic anemia
Compensated hemolytic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 3 0.100 None 0
CUI: C0553699
Disease: Heinz body observation
Heinz body observation
phenotype Laboratory or Test Result 6 0.100 None 0
CUI: C2697573
Disease: Heinz-Ehrlich Body Measurement
Heinz-Ehrlich Body Measurement
phenotype Laboratory Procedure 6 0.100 None 0
Glutathione Peroxidase Deficiency, Hemolytic Anemia possibly due to
disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.300 None 0
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 33 15 0.100 None 0
CUI: C0398747
Disease: Gluthathione peroxidase deficiency
Gluthathione peroxidase deficiency
disease Disease or Syndrome 1 0.300 limited 1.000 1 1975 1975
CUI: C0086942
Disease: Rous Sarcoma
Rous Sarcoma
disease Neoplasms; Infections; Animal Diseases Neoplastic Process; Experimental Model of Disease 60 0.010 None 1.000 1 1990 1990
Other specified iron deficiency anemias
disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 13 0.200 None 1.000 1 1995 1995
CUI: C0023903
Disease: Liver neoplasms
Liver neoplasms
group Digestive System Diseases; Neoplasms Neoplastic Process 1424 7 0.010 None 1.000 1 1998 1998
CUI: C1519346
Disease: Skin Carcinogenesis
Skin Carcinogenesis
disease Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 194 7 0.010 None 1.000 1 1999 1999
CUI: C0024530
Disease: Malaria
Malaria
disease Infections Disease or Syndrome 685 148 0.010 None 1.000 1 1999 1999
CUI: C0024535
Disease: Malaria, Falciparum
Malaria, Falciparum
disease Infections Disease or Syndrome 158 19 0.010 None 1.000 1 1999 1999
CUI: C0015695
Disease: Fatty Liver
Fatty Liver
disease Digestive System Diseases Disease or Syndrome 875 35 0.300 None 1.000 1 2000 2000
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis
disease Digestive System Diseases Disease or Syndrome 1143 75 0.300 None 1.000 1 2000 2000
CUI: C0027059
Disease: Myocarditis
Myocarditis
disease Cardiovascular Diseases Disease or Syndrome 285 2 0.010 None 1.000 1 2001 2001
CUI: C0027765
Disease: nervous system disorder
nervous system disorder
group Nervous System Diseases Disease or Syndrome 977 39 0.010 None 1.000 1 2001 2001
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
group Nutritional and Metabolic Diseases Disease or Syndrome 284 84 0.010 None 1.000 1 2001 2001
CUI: C0007786
Disease: Brain Ischemia
Brain Ischemia
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 358 5 0.300 None 1.000 1 2002 2002
CUI: C0917798
Disease: Cerebral Ischemia
Cerebral Ischemia
disease Nervous System Diseases; Cardiovascular Diseases Pathologic Function 120 2 0.300 None 1.000 1 2002 2002
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
group Neoplasms Neoplastic Process 2235 168 0.010 None 1.000 1 2002 2002
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma
disease Neoplasms; Nervous System Diseases Neoplastic Process 2419 231 0.010 None 1.000 1 2003 2003
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma
disease Neoplasms Neoplastic Process 2509 386 0.010 None 1.000 1 2003 2003
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
Complete Trisomy 21 Syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 669 77 0.010 None 1.000 1 2003 2003
CUI: C4704874
Disease: Mammary Carcinoma, Human
Mammary Carcinoma, Human
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 545 0.300 None 1.000 1 2003 2003
CUI: C0013080
Disease: Down Syndrome
Down Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 766 80 0.010 None 1.000 1 2003 2003