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: C0729771
Disease: Infective pharyngitis
Infective pharyngitis
group Infections; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 1 0.020 None 1.000 2 2019 2019
CUI: C0265903
Disease: Single coronary artery
Single coronary artery
disease Disease or Syndrome; Congenital Abnormality 1 0.010 None 1.000 1 2018 2018
CUI: C0271930
Disease: Anemia of pregnancy
Anemia of pregnancy
disease Hemic and Lymphatic Diseases Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C0948873
Disease: Flu symptoms
Flu symptoms
disease Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C4531217
Disease: Peripheral arterial calcification
Peripheral arterial calcification
disease Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0271468
Disease: Eustachian tube disorder
Eustachian tube disorder
group Stomatognathic Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C1619733
Disease: Gout flare
Gout flare
disease Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C2939149
Disease: Amyloid of cornea
Amyloid of cornea
disease Disease or Syndrome 4 5 0.010 None 1.000 1 2018 2018
CUI: C0021342
Disease: Infectious enteritis
Infectious enteritis
disease Digestive System Diseases Disease or Syndrome 5 0.010 None 1.000 1 2018 2018
CUI: C0030757
Disease: Pediculus capitis infestation
Pediculus capitis infestation
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 6 0.010 None < 0.001 1 2012 2012
CUI: C0010266
Disease: Cranial nerve diseases
Cranial nerve diseases
group Nervous System Diseases Disease or Syndrome 7 0.010 None 1.000 1 2019 2019
CUI: C0233622
Disease: Ritual compulsion
Ritual compulsion
phenotype Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 8 1 0.010 None 1.000 1 2017 2017
CUI: C0745153
Disease: Hypoglycaemic episode
Hypoglycaemic episode
disease Disease or Syndrome 8 2 0.010 None 1.000 1 2019 2019
CUI: C0729665
Disease: Arteriovenous graft
Arteriovenous graft
disease Acquired Abnormality 10 2 0.010 None 1.000 1 2019 2019
CUI: C0339273
Disease: Corneal dystrophy, Lattice type 3
Corneal dystrophy, Lattice type 3
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases Disease or Syndrome 12 14 0.010 None 1.000 1 2018 2018
CUI: C0679395
Disease: vascular ischemia
vascular ischemia
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 12 0.010 None 1.000 1 2018 2018
CUI: C0242429
Disease: Sore Throat
Sore Throat
phenotype Infections; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Sign or Symptom 18 2 0.020 None 1.000 2 2019 2019
CUI: C0264936
Disease: Secondary pulmonary hypertension
Secondary pulmonary hypertension
disease Respiratory Tract Diseases Disease or Syndrome 19 0.010 None 1.000 1 2018 2018
CUI: C0342335
Disease: insulin resistance in diabetes
insulin resistance in diabetes
disease Nutritional and Metabolic Diseases Disease or Syndrome 21 1 0.010 None 1.000 1 2017 2017
CUI: C0270726
Disease: Alexander Disease
Alexander Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 27 99 0.010 None 1.000 1 2010 2010
CUI: C0312414
Disease: Menstrual spotting
Menstrual spotting
phenotype Sign or Symptom 27 2 0.010 None 1.000 1 2018 2018
CUI: C0031350
Disease: Pharyngitis
Pharyngitis
disease Infections; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 30 0.020 None 1.000 2 2019 2019
CUI: C0271683
Disease: Polyneuropathy, Motor
Polyneuropathy, Motor
disease Nervous System Diseases Disease or Syndrome 32 3 0.010 None 1.000 1 2018 2018
CUI: C0432475
Disease: XX males
XX males
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 32 0.010 None 1.000 1 2011 2011
CUI: C0574960
Disease: Sacroiliitis
Sacroiliitis
disease Musculoskeletal Diseases Disease or Syndrome 33 2 0.010 None 1.000 1 2019 2019