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: C3536715
Disease: AA amyloidosis
AA amyloidosis
disease Nutritional and Metabolic Diseases Disease or Syndrome 38 10 0.010 None 1.000 1 2006 2006
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 302 18 0.100 None 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
phenotype Finding 75 10 0.100 None 0
CUI: C0159060
Disease: Abnormal bowel sounds
Abnormal bowel sounds
phenotype Finding 5 0.100 None 0
Abnormal cardiac ventricular function
phenotype Finding 6 0.100 None 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 59 4 0.100 None 0
Abnormal liver parenchyma morphology
phenotype Anatomical Abnormality 4 0.100 None 0
CUI: C0392188
Disease: Abnormal rapid eye movement sleep
Abnormal rapid eye movement sleep
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Finding 11 1 0.100 None 0
Abnormal reproductive system morphology
phenotype Anatomical Abnormality 2 0.100 None 0
CUI: C0149772
Disease: Abnormal salivary gland morphology
Abnormal salivary gland morphology
phenotype Stomatognathic Diseases Anatomical Abnormality 5 0.100 None 0
CUI: C4023166
Disease: Abnormality of T cell physiology
Abnormality of T cell physiology
phenotype Pathologic Function 6 3 0.100 None 0
CUI: C4021794
Disease: Abnormality of the adrenal glands
Abnormality of the adrenal glands
disease Anatomical Abnormality 10 0.100 None 0
Abnormality of the gastrointestinal tract
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Anatomical Abnormality 14 1 0.100 None 0
CUI: C4025854
Disease: Abnormality of the nasal mucosa
Abnormality of the nasal mucosa
phenotype Anatomical Abnormality 2 0.100 None 0
CUI: C4025698
Disease: Abnormality of the peritoneum
Abnormality of the peritoneum
disease Anatomical Abnormality 9 0.100 None 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision
disease Finding 127 8 0.100 None 0
CUI: C1321756
Disease: Achalasia
Achalasia
disease Disease or Syndrome 40 5 0.020 None 1.000 2 2000 2018
CUI: C0271907
Disease: Acquired aplastic anemia
Acquired aplastic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 64 12 0.010 None 1.000 1 2012 2012
CUI: C1096116
Disease: Acquired haemophilia
Acquired haemophilia
disease Disease or Syndrome 7 2 0.010 None 1.000 1 2010 2010
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome
group Infections; Immune System Diseases Disease or Syndrome 243 42 0.010 None 1.000 1 2004 2004
CUI: C0406217
Disease: Actinic prurigo
Actinic prurigo
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 4 0.040 None 1.000 4 1997 2016
CUI: C0151332
Disease: Active tuberculosis
Active tuberculosis
disease Infections Disease or Syndrome 116 25 0.010 None 1.000 1 2016 2016
CUI: C0701807
Disease: Acute anterior uveitis
Acute anterior uveitis
disease Eye Diseases Disease or Syndrome 90 30 0.030 None 1.000 3 1997 2011
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 405 135 0.030 None 1.000 3 2007 2017
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
disease Cardiovascular Diseases Disease or Syndrome 440 139 0.030 None 1.000 3 2007 2017