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.
Abnormality of the respiratory system
disease Anatomical Abnormality 16 0.100 None 0
CUI: C0042384
Disease: Vasculitis
Vasculitis
disease Cardiovascular Diseases Disease or Syndrome 294 24 0.100 None 0
Abnormality of blood and blood-forming tissues
disease Finding 23 1 0.100 None 0
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: C4021753
Disease: Abnormality of the immune system
Abnormality of the immune system
disease Pathologic Function 34 3 0.100 None 0
CUI: C0003864
Disease: Arthritis
Arthritis
disease Musculoskeletal Diseases Disease or Syndrome 1072 69 0.010 None 1.000 1 2003 2003
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
disease Neoplasms Neoplastic Process 1740 140 0.010 None 1.000 1 2004 2004
CUI: C0023418
Disease: leukemia
leukemia
disease Neoplasms Neoplastic Process 2111 144 0.010 None 1.000 1 2004 2004
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 527 263 0.010 None 1.000 1 2004 2004
CUI: C0030524
Disease: Paratuberculosis
Paratuberculosis
disease Infections; Animal Diseases Disease or Syndrome 61 6 0.010 None 1.000 1 1 2005 2005
CUI: C0014356
Disease: Enterocolitis
Enterocolitis
disease Digestive System Diseases Disease or Syndrome 40 2 0.010 None 1.000 1 2005 2005
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 1883 1172 0.030 None 0.667 3 2004 2006
Diabetes Mellitus, Insulin-Dependent
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 1675 954 0.020 None 1.000 2 3 2005 2006
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: 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: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.010 None 1.000 1 2 2010 2010
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
disease Infections Disease or Syndrome 1256 328 0.010 None 1.000 1 2010 2010
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: C0027059
Disease: Myocarditis
Myocarditis
disease Cardiovascular Diseases Disease or Syndrome 285 2 0.300 None 1.000 1 2011 2011
CUI: C0869523
Disease: Carditis
Carditis
disease Cardiovascular Diseases Disease or Syndrome 13 1 0.300 None 1.000 1 2011 2011
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: C0032584
Disease: polyps
polyps
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 390 18 0.010 None 1.000 1 2011 2011
CUI: C0010246
Disease: Coxsackievirus Infections
Coxsackievirus Infections
group Infections Disease or Syndrome 48 1 0.300 None 1.000 1 2011 2011