HFE, homeostatic iron regulator, 3077

N. diseases: 415; N. variants: 59
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: C0524988
Disease: Schnitzler Syndrome
Schnitzler Syndrome
disease Immune System Diseases Disease or Syndrome 14 2 0.010 None 1.000 1 1 2009 2009
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 518 138 0.010 None 1.000 1 2 2007 2007
Conventional (Clear Cell) Renal Cell Carcinoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 2346 222 0.010 None 1.000 1 1 2011 2011
Secondary acquired sideroblastic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 6 2 0.010 None < 0.001 1 2 1999 1999
CUI: C0271979
Disease: Thalassemia Intermedia
Thalassemia Intermedia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 53 8 0.010 None 1.000 1 2004 2004
CUI: C0267809
Disease: Cirrhosis, Cryptogenic
Cirrhosis, Cryptogenic
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 15 5 0.010 None 1.000 1 2 2000 2000
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis
disease Digestive System Diseases Disease or Syndrome 1 1 0.010 None 1.000 1 1 2015 2015
CUI: C0265219
Disease: Miller Dieker syndrome
Miller Dieker syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 182 9 0.010 None 1.000 1 2016 2016
CUI: C0242787
Disease: Malignant neoplasm of male breast
Malignant neoplasm of male breast
disease Neoplasms; Skin and Connective Tissue Diseases; Endocrine System Diseases Neoplastic Process 75 43 0.010 None 1.000 1 2 2006 2006
CUI: C0238158
Disease: Secondary hemochromatosis
Secondary hemochromatosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 6 1 0.010 None 1.000 1 1 2000 2000
CUI: C0238033
Disease: Carcinoma of Male Breast
Carcinoma of Male Breast
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 87 38 0.010 None 1.000 1 2 2006 2006
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 454 44 0.010 None 1.000 1 2016 2016
CUI: C0235653
Disease: Malignant neoplasm of female breast
Malignant neoplasm of female breast
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 71 15 0.010 None 1.000 1 2006 2006
CUI: C0302332
Disease: Poisoning syndrome
Poisoning syndrome
disease Disease or Syndrome 14 0.010 None 1.000 1 2006 2006
CUI: C0302486
Disease: Erythrophagocytosis
Erythrophagocytosis
disease Disease or Syndrome 40 0.010 None 1.000 1 1998 1998
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 1597 326 0.010 None 1.000 1 3 2015 2015
CUI: C0442874
Disease: Neuropathy
Neuropathy
group Nervous System Diseases Disease or Syndrome 484 110 0.010 None 1.000 1 2008 2008
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee
disease Musculoskeletal Diseases Disease or Syndrome 368 150 0.010 None 1.000 1 1 2012 2012
CUI: C0403447
Disease: Chronic Kidney Insufficiency
Chronic Kidney Insufficiency
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 52 12 0.010 None < 0.001 1 2 2005 2005
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 4502 1082 0.010 None 1.000 1 2 2006 2006
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
disease Disease or Syndrome 593 24 0.010 None < 0.001 1 2003 2003
CUI: C0342886
Disease: Primary hypertriglyceridemia
Primary hypertriglyceridemia
disease Nutritional and Metabolic Diseases Congenital Abnormality 2 0.010 None 1.000 1 2009 2009
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 5 4 0.010 None 1.000 1 1 2007 2007
CUI: C0342257
Disease: Complications of Diabetes Mellitus
Complications of Diabetes Mellitus
group Endocrine System Diseases Disease or Syndrome 240 35 0.010 None 1.000 1 2 2002 2002
CUI: C0341299
Disease: Collagenous Sprue
Collagenous Sprue
disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 6 0.010 None 1.000 1 2011 2011