XDH, xanthine dehydrogenase, 7498

N. diseases: 165; N. variants: 24
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: C4025600
Disease: Reduced xanthine dehydrogenase activity
Reduced xanthine dehydrogenase activity 		phenotype Finding 2 0.100 None 0
CUI: C0220988
Disease: Xanthinuria
Xanthinuria 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 0.140 None 1.000 4 1995 2012
CUI: C0268120
Disease: Adenine phosphoribosyltransferase deficiency
Adenine phosphoribosyltransferase deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 3 11 0.010 None 1.000 1 2018 2018
CUI: C0553718
Disease: Renal artery occlusion
Renal artery occlusion 		disease Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C1863688
Disease: Xanthinuria, Type II
Xanthinuria, Type II 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 8 0.100 None 1.000 1 4 1997 1997
CUI: C3811915
Disease: SUCLA2
SUCLA2 		disease Disease or Syndrome 3 1 0.010 None 1.000 1 1 2016 2016
CUI: C1848431
Disease: Xanthine nephrolithiasis
Xanthine nephrolithiasis 		phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 3 0.100 None 0
CUI: C0007020
Disease: Carbon Monoxide Poisoning
Carbon Monoxide Poisoning 		disease Chemically-Induced Disorders Injury or Poisoning 4 0.200 None 1.000 2 1993 2007
CUI: C0855230
Disease: Food hoarding
Food hoarding 		disease Disease or Syndrome 4 0.010 None 1.000 1 2018 2018
CUI: C0268118
Disease: Xanthinuria, Type I
Xanthinuria, Type I 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 5 4 0.760 strong 1.000 7 4 1997 2013
CUI: C0029823
Disease: Other specified peritonitis
Other specified peritonitis 		disease Digestive System Diseases; Infections Disease or Syndrome 8 0.200 None 1.000 2 1992 1993
CUI: C0268119
Disease: Combined molybdoflavoprotein enzyme deficiency
Combined molybdoflavoprotein enzyme deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 13 0.020 None 1.000 2 2009 2012
CUI: C1412000
Disease: Mesenteric vascular insufficiency
Mesenteric vascular insufficiency 		disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 13 0.010 None 1.000 1 2018 2018
CUI: C0221333
Disease: Hypouricemia
Hypouricemia 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 14 8 0.010 None 1.000 1 2012 2012
CUI: C2697766
Disease: Interleukin 18 Measurement
Interleukin 18 Measurement 		phenotype Laboratory Procedure 16 25 0.100 None 1.000 1 1 2017 2017
CUI: C0020636
Disease: underdevelopment
underdevelopment 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 22 0.010 None 1.000 1 2015 2015
CUI: C0011574
Disease: Involutional Depression
Involutional Depression 		disease Mental Disorders Mental or Behavioral Dysfunction 25 0.300 None 1.000 1 2011 2011
CUI: C0026766
Disease: Multiple Organ Failure
Multiple Organ Failure 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 25 0.300 None 1.000 1 2016 2016
CUI: C0036974
Disease: Shock
Shock 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 25 0.200 None 1.000 1 1991 1991
CUI: C1571983
Disease: Involutional paraphrenia
Involutional paraphrenia 		disease Mental Disorders Mental or Behavioral Dysfunction 25 0.300 None 1.000 1 2011 2011
CUI: C1571984
Disease: Psychosis, Involutional
Psychosis, Involutional 		disease Mental Disorders Mental or Behavioral Dysfunction 25 0.300 None 1.000 1 2011 2011
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 28 32 0.010 None 1.000 1 2019 2019
CUI: C0032320
Disease: Pneumoperitoneum
Pneumoperitoneum 		disease Digestive System Diseases Disease or Syndrome 28 0.200 None 1.000 1 2009 2009
CUI: C0010073
Disease: Coronary Artery Vasospasm
Coronary Artery Vasospasm 		disease Cardiovascular Diseases Disease or Syndrome 30 9 0.010 None 1.000 1 2019 2019
CUI: C0029531
Disease: Other cataract
Other cataract 		disease Eye Diseases Disease or Syndrome 32 0.200 None 1.000 1 2016 2016