IRF1, interferon regulatory factor 1, 3659

N. diseases: 257; N. variants: 7
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: C0339434
Disease: Choroidal effusion
Choroidal effusion 		disease Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C0751079
Disease: Diplopia, Vertical
Diplopia, Vertical 		disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C1853438
Disease: INFLAMMATORY BOWEL DISEASE 5
INFLAMMATORY BOWEL DISEASE 5 		disease Digestive System Diseases Disease or Syndrome 5 2 0.010 None 1.000 1 2012 2012
CUI: C0279763
Disease: endometrial adenoacanthoma
endometrial adenoacanthoma 		disease Neoplastic Process 7 12 0.200 None 1.000 1 2009 2009
CUI: C0005683
Disease: Urinary Bladder Calculi (disorder)
Urinary Bladder Calculi (disorder) 		disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 10 0.010 None 1.000 1 2020 2020
CUI: C1264610
Disease: Infectious peritonitis
Infectious peritonitis 		disease Digestive System Diseases; Infections Disease or Syndrome 11 0.010 None 1.000 1 2018 2018
CUI: C4534309
Disease: Acute lung injury/Acute respiratory distress syndrome (ARDS)
Acute lung injury/Acute respiratory distress syndrome (ARDS) 		disease Disease or Syndrome 12 0.010 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: C4703633
Disease: Increased level of L-fucose in urine
Increased level of L-fucose in urine 		phenotype Finding 14 0.100 None 0
CUI: C0153943
Disease: Benign neoplasm of stomach
Benign neoplasm of stomach 		disease Digestive System Diseases; Neoplasms Neoplastic Process 17 0.300 None 0
CUI: C0496905
Disease: Neoplasm of uncertain or unknown behavior of stomach
Neoplasm of uncertain or unknown behavior of stomach 		disease Digestive System Diseases; Neoplasms Neoplastic Process 17 0.300 None 0
CUI: C0574002
Disease: Edema of foot (finding)
Edema of foot (finding) 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 19 0.010 None 1.000 1 2017 2017
CUI: C0154060
Disease: Carcinoma in situ of stomach
Carcinoma in situ of stomach 		disease Digestive System Diseases; Neoplasms Neoplastic Process 19 0.300 None 0
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity 		phenotype Molecular Function 26 63 0.100 None 1.000 1 1 2011 2011
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		phenotype Finding 26 63 0.100 None 1.000 1 1 2011 2011
CUI: C2931826
Disease: Potassium aggravated myotonia
Potassium aggravated myotonia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 27 18 0.010 None 1.000 1 2020 2020
CUI: C0729531
Disease: Viral respiratory infection
Viral respiratory infection 		group Infections; Respiratory Tract Diseases Disease or Syndrome 33 0.010 None 1.000 1 2017 2017
CUI: C0009766
Disease: Allergic Conjunctivitis
Allergic Conjunctivitis 		disease Eye Diseases; Immune System Diseases Disease or Syndrome 38 2 0.200 None 1.000 1 2003 2003
CUI: C1142553
Disease: Primary HIV infection
Primary HIV infection 		disease Infections; Immune System Diseases Disease or Syndrome 38 1 0.010 None 1.000 1 2011 2011
CUI: C0392557
Disease: Nuclear cataract
Nuclear cataract 		disease Eye Diseases Disease or Syndrome 39 11 0.010 None 1.000 1 2018 2018
CUI: C1535950
Disease: Gastrointestinal inflammation
Gastrointestinal inflammation 		disease Disease or Syndrome 39 0.010 None 1.000 1 2009 2009
CUI: C0302180
Disease: Condyloma
Condyloma 		disease Disease or Syndrome 40 0.010 None 1.000 1 2001 2001
CUI: C1292779
Disease: Myelodysplastic Syndrome with Isolated del(5q)
Myelodysplastic Syndrome with Isolated del(5q) 		disease Hemic and Lymphatic Diseases Neoplastic Process 41 1 0.010 None 1.000 1 1993 1993
CUI: C1802398
Disease: Chromosome 5, trisomy 5q
Chromosome 5, trisomy 5q 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 42 1 0.010 None 1.000 1 1993 1993
CUI: C3805043
Disease: Vascular cognitive impairment
Vascular cognitive impairment 		disease Disease or Syndrome 42 1 0.010 None 1.000 1 2018 2018