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.
Anemia, Hypochromic Microcytic, With Iron Overload
disease Hemic and Lymphatic Diseases Disease or Syndrome 4 2 0.630 None 1.000 4 2 2006 2011
ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1
disease Disease or Syndrome 1 3 0.500 strong 1.000 3 3 2005 2006
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
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: 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
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 5473 1962 0.310 None 1.000 1 1 2016 2016
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver
disease Digestive System Diseases; Neoplasms Neoplastic Process 1649 88 0.300 None 1.000 1 2009 2009
CUI: C0023903
Disease: Liver neoplasms
Liver neoplasms
group Digestive System Diseases; Neoplasms Neoplastic Process 1424 7 0.300 None 1.000 1 2009 2009
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders
group Nervous System Diseases Disease or Syndrome 373 95 0.210 None 1.000 3 2008 2010
CUI: C0007786
Disease: Brain Ischemia
Brain Ischemia
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 358 5 0.210 None 1.000 2 2011 2012
Other specified iron deficiency anemias
disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 13 0.200 None 1.000 1 2007 2007
CUI: C0032285
Disease: Pneumonia
Pneumonia
disease Infections; Respiratory Tract Diseases Disease or Syndrome 1032 33 0.200 None 1.000 1 2011 2011
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: C0010474
Disease: Curling Ulcer
Curling Ulcer
disease Digestive System Diseases Disease or Syndrome 12 0.200 None 1.000 1 2009 2009
CUI: C0013295
Disease: Duodenal Ulcer
Duodenal Ulcer
disease Digestive System Diseases Disease or Syndrome 102 33 0.200 None 1.000 1 2009 2009
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: 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: C0855790
Disease: Decreased mean corpuscular volume
Decreased mean corpuscular volume
phenotype Finding 6 0.100 None 0
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: C0030567
Disease: Parkinson Disease
Parkinson Disease
disease Nervous System Diseases Disease or Syndrome 2078 990 0.090 None 1.000 9 1 2009 2018
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