SLC11A2, solute carrier family 11 member 2, 4891

N. diseases: 99; N. variants: 13
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: C4021780
Disease: Abnormality of the liver
Abnormality of the liver
phenotype Finding 75 8 0.100 None 0
Abnormality of metabolism/homeostasis
phenotype Finding 171 5 0.100 None 0
CUI: C0333912
Disease: Hypochromatism
Hypochromatism
phenotype Finding 5 0.100 None 0
CUI: C0855790
Disease: Decreased mean corpuscular volume
Decreased mean corpuscular volume
phenotype Finding 6 0.100 None 0
Microcytic hypochromic anemia (disorder)
disease Hemic and Lymphatic Diseases Disease or Syndrome 25 3 0.080 None 1.000 8 1998 2014
Iron-Refractory Iron Deficiency Anemia
disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 51 36 0.070 None 0.857 7 3 1998 2012
CUI: C0018995
Disease: Hemochromatosis
Hemochromatosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 93 45 0.350 None 0.833 6 1998 2006
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
HEMOCHROMATOSIS, TYPE 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 83 62 0.050 None 0.800 5 1 1998 2014
CUI: C0002884
Disease: Hypochromic anemia
Hypochromic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 16 0.200 None 1.000 1 1998 1998
CUI: C0282193
Disease: Iron Overload
Iron Overload
disease Nutritional and Metabolic Diseases Disease or Syndrome 241 53 0.100 None 0.920 25 3 1999 2019
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 254 56 0.400 None 0.917 12 1 1999 2019
FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED
disease Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 6 6 0.050 None 1.000 5 1 1999 2018
CUI: C0240066
Disease: Iron deficiency
Iron deficiency
disease Nutritional and Metabolic Diseases Disease or Syndrome 179 13 0.100 None 0.929 14 2000 2020
CUI: C0002871
Disease: Anemia
Anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 847 94 0.100 None 1.000 10 1 2000 2017
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
group Digestive System Diseases Disease or Syndrome 1577 605 0.020 None 1.000 2 2000 2015
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia
disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 83 21 0.350 None 1.000 6 2002 2019
HFE-Associated Hereditary Hemochromatosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 10 3 0.010 None 1.000 1 2003 2003
CUI: C0302486
Disease: Erythrophagocytosis
Erythrophagocytosis
disease Disease or Syndrome 40 0.010 None 1.000 1 2003 2003
CUI: C1623038
Disease: Cirrhosis
Cirrhosis
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 919 110 0.020 None 0.500 2 2004 2008
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 1182 189 0.020 None 0.500 2 2004 2008
CUI: C0023895
Disease: Liver diseases
Liver diseases
group Digestive System Diseases Disease or Syndrome 1019 100 0.010 None < 0.001 1 2004 2004
CUI: C0948120
Disease: Hepatic siderosis
Hepatic siderosis
disease Nutritional and Metabolic Diseases Disease or Syndrome 8 1 0.010 None < 0.001 1 2004 2004
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
disease Infections Disease or Syndrome 1256 328 0.010 None 1.000 1 2004 2004
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
disease Nervous System Diseases; Mental Disorders Disease or Syndrome 3397 1843 0.060 None 0.833 6 1 2005 2018
ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1
disease Disease or Syndrome 1 3 0.500 strong 1.000 3 3 2005 2006