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: C1862463
Disease: Aryl Hydrocarbon Hydroxylase Inducibility
Aryl Hydrocarbon Hydroxylase Inducibility 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 1 0.030 None 0.667 3 1979 1998
CUI: C0403809
Disease: Primary spermatogenic failure
Primary spermatogenic failure 		disease Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C0003860
Disease: Arteritis
Arteritis 		phenotype Cardiovascular Diseases Pathologic Function 5 0.300 None 1.000 1 2009 2009
CUI: C1304119
Disease: Chronic stable plaque psoriasis
Chronic stable plaque psoriasis 		disease Disease or Syndrome 5 4 0.010 None 1.000 1 2 2016 2016
CUI: C3203671
Disease: CYP2D6 polymorphism
CYP2D6 polymorphism 		disease Disease or Syndrome 7 5 0.020 None 1.000 2 2004 2009
CUI: C0403766
Disease: Acquired phimosis
Acquired phimosis 		disease Skin and Connective Tissue Diseases; Male Urogenital Diseases Acquired Abnormality 7 0.010 None 1.000 1 2018 2018
CUI: C0345326
Disease: Congenital phimosis
Congenital phimosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Male Urogenital Diseases Congenital Abnormality 8 1 0.010 None 1.000 1 2018 2018
CUI: C0858864
Disease: Spot pigmented
Spot pigmented 		disease Disease or Syndrome 8 0.010 None 1.000 1 2019 2019
CUI: C0031347
Disease: Pharyngeal Neoplasms
Pharyngeal Neoplasms 		group Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases Neoplastic Process 9 5 0.010 None 1.000 1 2008 2008
CUI: C0850741
Disease: Smoker's lung
Smoker's lung 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 10 0.030 None 1.000 3 1994 2002
CUI: C0149875
Disease: Primary dysmenorrhea
Primary dysmenorrhea 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 13 3 0.010 None 1.000 1 2007 2007
CUI: C0334233
Disease: Pleomorphic carcinoma
Pleomorphic carcinoma 		disease Neoplasms Neoplastic Process 16 0.010 None 1.000 1 2001 2001
CUI: C0004659
Disease: Bacteriuria
Bacteriuria 		phenotype Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 18 0.010 None 1.000 1 2017 2017
CUI: C3826044
Disease: Lymphoblastic leukemia in children
Lymphoblastic leukemia in children 		disease Neoplastic Process 19 2 0.010 None 1.000 1 2011 2011
CUI: C0013502
Disease: Echinococcosis
Echinococcosis 		disease Infections Disease or Syndrome 21 1 0.010 None 1.000 1 2008 2008
CUI: C0017411
Disease: Female Genital Diseases
Female Genital Diseases 		group Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 21 3 0.010 None 1.000 1 2006 2006
CUI: C1443237
Disease: Healthcare associated pneumonia
Healthcare associated pneumonia 		phenotype Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases Disease or Syndrome 22 2 0.020 None 1.000 2 1 2013 2014
CUI: C0028797
Disease: Occupational Diseases
Occupational Diseases 		group Occupational Diseases Disease or Syndrome 22 1 0.300 None 1.000 1 2006 2006
CUI: C0020540
Disease: Malignant Hypertension
Malignant Hypertension 		disease Cardiovascular Diseases Disease or Syndrome 23 2 0.020 None 1.000 2 2010 2018
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma 		disease Neoplastic Process 24 13 0.020 None 1.000 2 1 2004 2019
CUI: C0019112
Disease: Hemorrhoids
Hemorrhoids 		disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 24 0.010 None 1.000 1 2009 2009
CUI: C0406537
Disease: Morbilliform Drug Reaction
Morbilliform Drug Reaction 		disease Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders Disease or Syndrome 24 0.300 None 1.000 1 2009 2009
CUI: C0949083
Disease: Hospital acquired pneumonia
Hospital acquired pneumonia 		disease Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases Disease or Syndrome 25 2 0.020 None 1.000 2 1 2013 2014
CUI: C1449861
Disease: Micronuclei, Chromosome-Defective
Micronuclei, Chromosome-Defective 		phenotype Pathological Conditions, Signs and Symptoms Cell Component 26 0.300 None 1.000 1 2013 2013
CUI: C1449862
Disease: Micronuclei, Genotoxicant-Induced
Micronuclei, Genotoxicant-Induced 		phenotype Pathological Conditions, Signs and Symptoms Cell Component 26 0.300 None 1.000 1 2013 2013