SLC22A4, solute carrier family 22 member 4, 6583

N. diseases: 90; N. variants: 21
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: C1266159
Disease: Trophoblastic tumor, epithelioid
Trophoblastic tumor, epithelioid 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 4 0.010 None 1.000 1 2019 2019
CUI: C1853438
Disease: INFLAMMATORY BOWEL DISEASE 5
INFLAMMATORY BOWEL DISEASE 5 		disease Digestive System Diseases Disease or Syndrome 5 2 0.020 None 1.000 2 2008 2012
CUI: C0523446
Disease: Acylcarnitines measurement
Acylcarnitines measurement 		phenotype Laboratory Procedure 6 12 0.100 None 1.000 1 2 2015 2015
CUI: C0341332
Disease: Indeterminate colitis
Indeterminate colitis 		disease Digestive System Diseases Disease or Syndrome 13 1 0.010 None 1.000 1 2006 2006
CUI: C0869523
Disease: Carditis
Carditis 		disease Cardiovascular Diseases Disease or Syndrome 13 1 0.300 None 1.000 1 2011 2011
CUI: C4018871
Disease: Abnormality of the respiratory system
Abnormality of the respiratory system 		disease Anatomical Abnormality 16 0.100 None 0
CUI: C0206666
Disease: Trophoblastic Tumor, Placental Site
Trophoblastic Tumor, Placental Site 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 18 0.010 None 1.000 1 2019 2019
CUI: C0850715
Disease: Abnormality of blood and blood-forming tissues
Abnormality of blood and blood-forming tissues 		disease Finding 23 1 0.100 None 0
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity 		phenotype Molecular Function 26 63 0.100 None 1.000 2 2 2009 2011
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		phenotype Finding 26 63 0.100 None 1.000 2 2 2009 2011
CUI: C2931133
Disease: Pediatric Crohn's disease
Pediatric Crohn's disease 		disease Digestive System Diseases Disease or Syndrome 32 6 0.010 None 1.000 1 1 2007 2007
CUI: C4021753
Disease: Abnormality of the immune system
Abnormality of the immune system 		disease Pathologic Function 34 3 0.100 None 0
CUI: C1846647
Disease: DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE (disorder) 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 38 4 0.010 None 1.000 1 2013 2013
CUI: C0014356
Disease: Enterocolitis
Enterocolitis 		disease Digestive System Diseases Disease or Syndrome 40 2 0.010 None 1.000 1 2005 2005
CUI: C0010246
Disease: Coxsackievirus Infections
Coxsackievirus Infections 		group Infections Disease or Syndrome 48 1 0.300 None 1.000 1 2011 2011
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		phenotype Laboratory Procedure 55 143 0.100 None 1.000 3 3 2009 2016
CUI: C0852283
Disease: Respiratory Distress Syndrome
Respiratory Distress Syndrome 		disease Disease or Syndrome 58 9 0.010 None 1.000 1 2017 2017
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 59 123 0.010 None 1.000 1 2012 2012
CUI: C0030524
Disease: Paratuberculosis
Paratuberculosis 		disease Infections; Animal Diseases Disease or Syndrome 61 6 0.010 None 1.000 1 1 2005 2005
CUI: C1859308
Disease: PREMATURE CENTROMERE DIVISION
PREMATURE CENTROMERE DIVISION 		disease Disease or Syndrome 66 2 0.010 None 1.000 1 2012 2012
CUI: C0016169
Disease: pathologic fistula
pathologic fistula 		phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 71 8 0.010 None 1.000 1 1 2011 2011
CUI: C0497552
Disease: Congenital neurologic anomalies
Congenital neurologic anomalies 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 84 4 0.100 None 0
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: C0857490
Disease: Granulocyte count
Granulocyte count 		phenotype Laboratory Procedure 100 150 0.100 None 1.000 1 1 2016 2016