PON1, paraoxonase 1, 5444

N. diseases: 496; N. variants: 29
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: C0001828
Disease: Agricultural Workers' Diseases
Agricultural Workers' Diseases 		group Occupational Diseases Disease or Syndrome 1 0.300 None 1.000 2 2005 2008
CUI: C2257843
Disease: paraoxonase activity
paraoxonase activity 		phenotype Molecular Function 1 3 0.100 None 1.000 2 3 2012 2013
CUI: C0581375
Disease: Double coronary vessel disease
Double coronary vessel disease 		disease Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2003 2003
CUI: C0857256
Disease: Unwell
Unwell 		phenotype Sign or Symptom 1 0.010 None 1.000 1 2011 2011
CUI: C1392046
Disease: Cardiovascular insufficiency
Cardiovascular insufficiency 		disease Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C1827841
Disease: Enzyme activity finding
Enzyme activity finding 		phenotype Pathological Conditions, Signs and Symptoms Finding 1 2 0.100 None 0 2
CUI: C2674665
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding) 		disease Finding 1 1 0.400 None 0 1
CUI: C3149706
Disease: CORONARY ARTERY SPASM 2, SUSCEPTIBILITY TO
CORONARY ARTERY SPASM 2, SUSCEPTIBILITY TO 		phenotype Finding 1 1 0.100 None 0 1
CUI: C0034219
Disease: Alveolar pyorrhea
Alveolar pyorrhea 		disease Stomatognathic Diseases Disease or Syndrome 2 0.300 None 1.000 1 2008 2008
CUI: C0393947
Disease: Cholinergic crisis
Cholinergic crisis 		disease Nervous System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C1840169
Disease: CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO
CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO 		disease Finding 2 3 0.100 None 0 2
CUI: C0003177
Disease: Cutaneous anthrax
Cutaneous anthrax 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C1257753
Disease: Child Malnutrition
Child Malnutrition 		disease Nutritional and Metabolic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C0353676
Disease: Organophosphorus Poisoning
Organophosphorus Poisoning 		disease Chemically-Induced Disorders Injury or Poisoning 4 0.300 None 1.000 7 2000 2017
CUI: C3494247
Disease: Organothiophosphonate Poisoning
Organothiophosphonate Poisoning 		disease Chemically-Induced Disorders Injury or Poisoning 4 0.300 None 1.000 7 2000 2017
CUI: C3494248
Disease: Organothiophosphate Poisoning
Organothiophosphate Poisoning 		disease Chemically-Induced Disorders Injury or Poisoning 4 0.300 None 1.000 7 2000 2017
CUI: C0700359
Disease: Organophosphate poisoning
Organophosphate poisoning 		disease Chemically-Induced Disorders Injury or Poisoning 5 0.300 None 1.000 7 2000 2017
CUI: C0282550
Disease: Persian Gulf Syndrome
Persian Gulf Syndrome 		disease Occupational Diseases Disease or Syndrome 5 0.330 None 1.000 4 1997 2006
CUI: C0003860
Disease: Arteritis
Arteritis 		phenotype Cardiovascular Diseases Pathologic Function 5 0.300 None 1.000 1 2009 2009
CUI: C0877854
Disease: Cerebral Arteriosclerosis
Cerebral Arteriosclerosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 5 0.010 None 1.000 1 2013 2013
CUI: C1257861
Disease: Colonic Inertia
Colonic Inertia 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 6 0.300 None 1.000 1 2009 2009
CUI: C1720821
Disease: Membranoproliferative Glomerulonephritis, Type III
Membranoproliferative Glomerulonephritis, Type III 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 6 0.300 None 1.000 1 2007 2007
CUI: C3665858
Disease: Parenteral nutrition associated liver disease
Parenteral nutrition associated liver disease 		disease Disease or Syndrome 6 0.010 None 1.000 1 2017 2017
CUI: C0237326
Disease: Dyschezia
Dyschezia 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 7 0.300 None 1.000 1 2009 2009
CUI: C0268742
Disease: Membranoproliferative Glomerulonephritis, Type I
Membranoproliferative Glomerulonephritis, Type I 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 7 0.300 None 1.000 1 2007 2007