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.
erythrocyte sedimentation rate result
phenotype Laboratory or Test Result 5 5 0.100 None 1.000 1 1 2011 2011
CUI: C0005833
Disease: Blood Sedimentation
Blood Sedimentation
phenotype Laboratory Procedure 7 8 0.100 None 1.000 2 2 2011 2012
CUI: C0036830
Disease: Serum Sickness
Serum Sickness
disease Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders Disease or Syndrome 9 0.010 None 1.000 1 2010 2010
Ovalocytosis, Malaysian-Melanesian-Filipino Type
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 9 5 0.010 None 1.000 1 2010 2010
CUI: C0340968
Disease: Deficiency of pyruvate kinase
Deficiency of pyruvate kinase
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 10 63 0.010 None 1.000 1 2010 2010
CUI: C0003907
Disease: Arthus Reaction
Arthus Reaction
disease Immune System Diseases Disease or Syndrome 12 0.010 None 1.000 1 1991 1991
CUI: C1412000
Disease: Mesenteric vascular insufficiency
Mesenteric vascular insufficiency
disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 13 0.010 None 1.000 1 2004 2004
CUI: C0403367
Disease: proliferative nephritis unspecified
proliferative nephritis unspecified
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 14 0.010 None 1.000 1 1986 1986
CUI: C0235618
Disease: Proliferative glomerulonephritis
Proliferative glomerulonephritis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 15 0.010 None 1.000 1 2010 2010
CUI: C4087273
Disease: C3 glomerulopathy
C3 glomerulopathy
disease Disease or Syndrome 16 1 0.010 None < 0.001 1 2017 2017
CUI: C0221480
Disease: Recurrent depression
Recurrent depression
disease Mental Disorders Mental or Behavioral Dysfunction 19 12 0.010 None 1.000 1 2 2012 2012
Congenital glucose-galactose malabsorption
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome; Congenital Abnormality 19 12 0.010 None 1.000 1 2018 2018
CUI: C0013902
Disease: Elliptocytosis, Hereditary
Elliptocytosis, Hereditary
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 23 1 0.020 None 1.000 2 2008 2010
CUI: C0263314
Disease: Pemphigus and fogo selvagem
Pemphigus and fogo selvagem
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 26 3 0.010 None 1.000 1 2019 2019
CUI: C4543807
Disease: Clinical malaria
Clinical malaria
disease Infections Disease or Syndrome 37 3 0.010 None 1.000 1 2015 2015
CUI: C0020877
Disease: Ileitis
Ileitis
disease Digestive System Diseases Disease or Syndrome 44 0.010 None 1.000 1 2017 2017
CUI: C0263313
Disease: Pemphigus Foliaceus
Pemphigus Foliaceus
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 51 16 0.010 None 1.000 1 2019 2019
CUI: C0343804
Disease: Chronic Chagas' disease
Chronic Chagas' disease
disease Infections Disease or Syndrome 52 4 0.010 None 1.000 1 2018 2018
CUI: C2931788
Disease: Atypical Hemolytic Uremic Syndrome
Atypical Hemolytic Uremic Syndrome
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 56 42 0.010 None 1.000 1 2015 2015
CUI: C0267026
Disease: Actinic cheilitis
Actinic cheilitis
disease Stomatognathic Diseases Disease or Syndrome 64 8 0.010 None 1.000 1 1984 1984
CUI: C0004626
Disease: Pneumonia, Bacterial
Pneumonia, Bacterial
group Infections; Respiratory Tract Diseases Disease or Syndrome 66 2 0.010 None 1.000 1 2006 2006
CUI: C0221026
Disease: X-linked agammaglobulinemia
X-linked agammaglobulinemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 68 69 0.010 None 1.000 1 2007 2007
Deficiency of glucose-6-phosphate dehydrogenase
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 75 20 0.010 None 1.000 1 2010 2010
CUI: C0002880
Disease: Autoimmune hemolytic anemia
Autoimmune hemolytic anemia
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 81 0.010 None 1.000 1 2009 2009
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 86 37 0.010 None 1.000 1 2004 2004