SLC9A3, solute carrier family 9 member A3, 6550

N. diseases: 58; N. variants: 4
Source: BEFREE ×
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: C0268916
Disease: Atrophy of vas deferens
Atrophy of vas deferens 		phenotype Pathological Conditions, Signs and Symptoms Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C0400875
Disease: Hollow visceral neuropathy
Hollow visceral neuropathy 		disease Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2015 2015
CUI: C0037859
Disease: Spermatocele
Spermatocele 		disease Pathological Conditions, Signs and Symptoms; Male Urogenital Diseases Disease or Syndrome 2 0.010 None 1.000 1 2006 2006
CUI: C4305530
Disease: Dent disease type 1
Dent disease type 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C0268435
Disease: Renal Tubular Acidosis, Type II
Renal Tubular Acidosis, Type II 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 5 3 0.010 None 1.000 1 2002 2002
CUI: C3671887
Disease: Hypernatriuria
Hypernatriuria 		disease Disease or Syndrome 5 0.010 None < 0.001 1 2018 2018
CUI: C1868889
Disease: Irritable bowel syndrome characterized by constipation
Irritable bowel syndrome characterized by constipation 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 8 0.020 None 1.000 2 2017 2019
CUI: C0033817
Disease: Pseudomonas Infections
Pseudomonas Infections 		group Infections Disease or Syndrome 14 1 0.010 None 1.000 1 1 2011 2011
CUI: C0267663
Disease: Congenital secretory diarrhea, sodium type (disorder)
Congenital secretory diarrhea, sodium type (disorder) 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Congenital Abnormality 17 3 0.720 strong 1.000 2 2015 2019
CUI: C0341306
Disease: Microvillus inclusion disease
Microvillus inclusion disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 18 2 0.010 None 1.000 1 2016 2016
CUI: C2939175
Disease: Meconium ileus
Meconium ileus 		disease Digestive System Diseases Disease or Syndrome 20 11 0.010 None 1.000 1 1 2014 2014
CUI: C0277528
Disease: Traveler's diarrhea
Traveler's diarrhea 		disease Digestive System Diseases; Infections Disease or Syndrome 21 2 0.010 None 1.000 1 2019 2019
CUI: C0848676
Disease: Subfertility, Male
Subfertility, Male 		phenotype Male Urogenital Diseases Sign or Symptom 26 2 0.010 None 1.000 1 2006 2006
CUI: C0403814
Disease: Congenital bilateral aplasia of vas deferens
Congenital bilateral aplasia of vas deferens 		disease Male Urogenital Diseases Congenital Abnormality 27 28 0.030 None 1.000 3 2017 2019
CUI: C1290807
Disease: Diarrheal disorder
Diarrheal disorder 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 32 0.010 None 1.000 1 2017 2017
CUI: C0022672
Disease: Acute Kidney Tubular Necrosis
Acute Kidney Tubular Necrosis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 44 0.010 None 1.000 1 2013 2013
CUI: C1443924
Disease: Severe diarrhea
Severe diarrhea 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 47 6 0.010 None 1.000 1 2018 2018
CUI: C0854135
Disease: Pseudomonas aeruginosa infection
Pseudomonas aeruginosa infection 		disease Infections Disease or Syndrome 49 1 0.010 None 1.000 1 2011 2011
CUI: C0085681
Disease: Hyperphosphatemia (disorder)
Hyperphosphatemia (disorder) 		disease Nutritional and Metabolic Diseases Disease or Syndrome 50 1 0.020 None 1.000 2 2017 2019
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases Disease or Syndrome 52 10 0.010 None 1.000 1 2018 2018
CUI: C0343386
Disease: Clostridium difficile infection
Clostridium difficile infection 		disease Infections Disease or Syndrome 53 1 0.010 None 1.000 1 2015 2015
CUI: C0020488
Disease: Hypernatremia
Hypernatremia 		phenotype Nutritional and Metabolic Diseases Disease or Syndrome 55 2 0.010 None 1.000 1 2019 2019
CUI: C4023106
Disease: Obstructive azoospermia
Obstructive azoospermia 		disease Male Urogenital Diseases Disease or Syndrome 59 5 0.030 None 1.000 3 2017 2019
CUI: C0687720
Disease: Central Diabetes Insipidus
Central Diabetes Insipidus 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 100 3 0.020 None 1.000 2 2015 2018
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 131 57 0.030 None 1.000 3 2 2008 2014