NFE2L2, nuclear factor, erythroid 2 like 2, 4780

N. diseases: 823; N. variants: 34
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: C2732697
Disease: Autoimmune inflammation of skeletal muscle
Autoimmune inflammation of skeletal muscle 		disease Musculoskeletal Diseases; Immune System Diseases; Nervous System Diseases Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
CUI: C0152014
Disease: Atrophy of pancreas
Atrophy of pancreas 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 10 0.010 None 1.000 1 2018 2018
CUI: C0472390
Disease: High altitude cerebral edema
High altitude cerebral edema 		disease Nervous System Diseases Disease or Syndrome 10 0.010 None 1.000 1 2018 2018
CUI: C0596452
Disease: disabling disease
disabling disease 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 10 1 0.010 None 1.000 1 2019 2019
CUI: C3888461
Disease: Dry age-related macular degeneration
Dry age-related macular degeneration 		phenotype Anatomical Abnormality 11 1 0.020 None 1.000 2 2019 2019
CUI: C0001420
Disease: Papillary adenocarcinoma
Papillary adenocarcinoma 		disease Neoplasms Neoplastic Process 11 3 0.010 None 1.000 1 2011 2011
CUI: C0281773
Disease: Acute glaucoma
Acute glaucoma 		disease Disease or Syndrome 11 0.010 None 1.000 1 2017 2017
CUI: C0729552
Disease: Genital infection
Genital infection 		group Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 11 0.010 None 1.000 1 2019 2019
CUI: C4534309
Disease: Acute lung injury/Acute respiratory distress syndrome (ARDS)
Acute lung injury/Acute respiratory distress syndrome (ARDS) 		disease Disease or Syndrome 12 0.020 None 1.000 2 2010 2017
CUI: C0155870
Disease: Pneumonia and influenza
Pneumonia and influenza 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 12 2 0.010 None 1.000 1 2018 2018
CUI: C1565321
Disease: Cholera Infantum
Cholera Infantum 		disease Digestive System Diseases Disease or Syndrome 12 0.300 None 1.000 1 2010 2010
CUI: C0520571
Disease: Fibrosis of bile duct
Fibrosis of bile duct 		disease Digestive System Diseases Disease or Syndrome 13 0.020 None 1.000 2 2019 2019
CUI: C0858681
Disease: Vitiligo vulgaris
Vitiligo vulgaris 		disease Skin and Connective Tissue Diseases Disease or Syndrome 13 5 0.010 None 1.000 1 2010 2010
CUI: C1306571
Disease: Hepatic Insufficiency
Hepatic Insufficiency 		phenotype Digestive System Diseases Pathologic Function 13 0.300 None 1.000 1 2018 2018
CUI: C3469605
Disease: PSEUDOHYPOALDOSTERONISM, TYPE IID
PSEUDOHYPOALDOSTERONISM, TYPE IID 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 13 29 0.010 None 1.000 1 2019 2019
CUI: C0333440
Disease: Hyaline body
Hyaline body 		disease Anatomical Abnormality 14 0.010 None 1.000 1 2016 2016
CUI: C0333704
Disease: Chromosome Breaks
Chromosome Breaks 		phenotype Pathological Conditions, Signs and Symptoms Cell or Molecular Dysfunction 14 0.300 None 1.000 1 2017 2017
CUI: C0730321
Disease: Punctate inner choroidopathy
Punctate inner choroidopathy 		disease Eye Diseases Disease or Syndrome 14 0.010 None 1.000 1 2019 2019
CUI: C1321422
Disease: Monoblastic leukemia
Monoblastic leukemia 		disease Neoplastic Process 14 0.010 None 1.000 1 2011 2011
CUI: C0521858
Disease: Decreased drug resistance
Decreased drug resistance 		phenotype Disease or Syndrome 15 0.010 None 1.000 1 2010 2010
CUI: C0008412
Disease: Choline Deficiency
Choline Deficiency 		disease Nutritional and Metabolic Diseases Disease or Syndrome 16 4 0.010 None 1.000 1 2017 2017
CUI: C0679407
Disease: Gastrointestinal dysfunction
Gastrointestinal dysfunction 		phenotype Digestive System Diseases Disease or Syndrome 16 6 0.010 None 1.000 1 2018 2018
CUI: C2936781
Disease: Generalized Myotonia of Thomsen
Generalized Myotonia of Thomsen 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 16 61 0.010 None 1.000 1 2018 2018
CUI: C0018500
Disease: Hair Diseases
Hair Diseases 		group Skin and Connective Tissue Diseases Disease or Syndrome 17 2 0.010 None 1.000 1 2017 2017
CUI: C0019342
Disease: Genital Herpes
Genital Herpes 		disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 17 0.010 None 1.000 1 2019 2019