SLC2A9, solute carrier family 2 member 9, 56606

N. diseases: 74; N. variants: 389
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.
URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 2
phenotype Finding 1 3 0.100 None 0 3
CUI: C2677549
Disease: Hypouricemia, Renal, 2
Hypouricemia, Renal, 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 2 8 0.720 None 1.000 5 7 2008 2019
CUI: C0744466
Disease: gout tophaceous
gout tophaceous
disease Disease or Syndrome 2 3 0.020 None 1.000 2 1 2010 2011
CUI: C0268113
Disease: Familial juvenile gout
Familial juvenile gout
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 2 0.010 None 1.000 1 2003 2003
CUI: C0473219
Disease: Renal hypouricemia
Renal hypouricemia
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 4 18 0.600 None 1.000 19 3 2008 2019
CUI: C0155778
Disease: Varicose veins of lower extremity
Varicose veins of lower extremity
disease Cardiovascular Diseases Disease or Syndrome 4 1 0.010 None 1.000 1 2016 2016
CUI: C1861735
Disease: Dementia, familial Danish
Dementia, familial Danish
disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases Disease or Syndrome 10 1 0.010 None 1.000 1 2019 2019
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 0.180 None 1.000 8 3 2011 2020
CUI: C0221248
Disease: Tophus
Tophus
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Acquired Abnormality 14 3 0.020 None 0.500 2 1 2010 2017
CUI: C2751306
Disease: Polycystic kidney disease, type 2
Polycystic kidney disease, type 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 15 41 0.010 None 1.000 1 2012 2012
Posterior reversible encephalopathy syndrome
disease Nervous System Diseases Disease or Syndrome 16 1 0.030 None 1.000 3 2011 2015
CUI: C0019112
Disease: Hemorrhoids
Hemorrhoids
disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 24 0.010 None 1.000 1 2016 2016
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 1 2018 2018
CUI: C0031572
Disease: Phobia, Social
Phobia, Social
disease Mental Disorders Mental or Behavioral Dysfunction 33 8 0.010 None 1.000 1 1 2013 2013
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
phenotype Laboratory Procedure 39 568 0.100 None 1.000 1 8 2011 2011
CUI: C0149896
Disease: Primary gout
Primary gout
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 40 5 0.010 None 1.000 1 2014 2014
CUI: C0032969
Disease: Pregnancy in Diabetics
Pregnancy in Diabetics
phenotype Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 53 1 0.020 None 1.000 2 2011 2017
CUI: C3854173
Disease: Pre-renal acute kidney injury
Pre-renal acute kidney injury
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 67 4 0.050 None 1.000 5 2005 2015
CUI: C0033575
Disease: Prostatic Diseases
Prostatic Diseases
group Male Urogenital Diseases Disease or Syndrome 72 4 0.010 None 1.000 1 2016 2016
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
phenotype Laboratory Procedure 89 111 0.100 None 1.000 1 1 2011 2011
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
phenotype Finding 89 111 0.100 None 1.000 1 1 2011 2011
CUI: C0852949
Disease: Arteriopathic disease
Arteriopathic disease
group Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 101 14 0.010 None 1.000 1 2011 2011
Creatinine measurement, serum (procedure)
phenotype Laboratory Procedure 124 243 0.100 None 1.000 1 1 2018 2018
CUI: C0022650
Disease: Kidney Calculi
Kidney Calculi
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 190 71 0.040 None 1.000 4 4 2010 2018
CUI: C2981150
Disease: Uranostaphyloschisis
Uranostaphyloschisis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Congenital Abnormality 190 75 0.010 None 1.000 1 2014 2014