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: C0334337
Disease: Endometrioid adenoma
Endometrioid adenoma 		disease Neoplasms Neoplastic Process 1 0.010 None 1.000 1 1993 1993
CUI: C1096572
Disease: Staphylococcus epidermidis infection
Staphylococcus epidermidis infection 		disease Infections Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C3839044
Disease: Compensated liver disease
Compensated liver disease 		disease Digestive System Diseases Disease or Syndrome 4 0.020 None 0.500 2 2007 2007
CUI: C1861385
Disease: SYMPHALANGISM, PROXIMAL
SYMPHALANGISM, PROXIMAL 		disease Musculoskeletal Diseases Disease or Syndrome 4 1 0.010 None 1.000 1 2006 2006
CUI: C0017145
Disease: Gastric Varix
Gastric Varix 		disease Digestive System Diseases Disease or Syndrome 5 0.010 None 1.000 1 2018 2018
CUI: C0341486
Disease: Cystadenoma of pancreas
Cystadenoma of pancreas 		disease Neoplasms Neoplastic Process 5 0.010 None 1.000 1 1997 1997
CUI: C1566302
Disease: Preterm Premature Rupture of Fetal Membranes
Preterm Premature Rupture of Fetal Membranes 		disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 5 0.010 None 1.000 1 2018 2018
CUI: C4049394
Disease: Chronic hepatitis C genotype 1b
Chronic hepatitis C genotype 1b 		disease Disease or Syndrome 5 0.010 None 1.000 1 2016 2016
CUI: C0013949
Disease: Embryopathies
Embryopathies 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 6 0.010 None 1.000 1 2015 2015
CUI: C0025167
Disease: Megakaryocytic hyperplasia
Megakaryocytic hyperplasia 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 8 1 0.010 None 1.000 1 1996 1996
CUI: C0588006
Disease: Mild depression
Mild depression 		disease Mental Disorders Mental or Behavioral Dysfunction 8 0.010 None 1.000 1 2018 2018
CUI: C0038166
Disease: Staphylococcal Skin Infections
Staphylococcal Skin Infections 		group Infections; Skin and Connective Tissue Diseases Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
CUI: C4049431
Disease: Chronic hepatitis C genotype 4
Chronic hepatitis C genotype 4 		disease Disease or Syndrome 10 3 0.010 None 1.000 1 2011 2011
CUI: C0948775
Disease: High weight
High weight 		phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Sign or Symptom 12 0.010 None 1.000 1 2012 2012
CUI: C0334507
Disease: Synovial sarcoma, biphasic
Synovial sarcoma, biphasic 		disease Neoplasms Neoplastic Process 13 0.010 None 1.000 1 1998 1998
CUI: C0032827
Disease: Potassium Deficiency
Potassium Deficiency 		disease Nutritional and Metabolic Diseases Disease or Syndrome 14 0.010 None 1.000 1 2018 2018
CUI: C0221773
Disease: Hyperamylasemia
Hyperamylasemia 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 14 0.010 None 1.000 1 2017 2017
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 14 9 0.010 None 1.000 1 2017 2017
CUI: C4049392
Disease: Chronic hepatitis C genotype 1
Chronic hepatitis C genotype 1 		disease Disease or Syndrome 14 1 0.010 None 1.000 1 2009 2009
CUI: C0079102
Disease: Cerebral Thrombosis
Cerebral Thrombosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 15 7 0.010 None 1.000 1 2017 2017
CUI: C0401146
Disease: Constipation - functional
Constipation - functional 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 15 0.010 None 1.000 1 2019 2019
CUI: C1136135
Disease: Water Stress
Water Stress 		disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 17 0.030 None 1.000 3 2017 2017
CUI: C0238062
Disease: Chronic intestinal pseudo-obstruction
Chronic intestinal pseudo-obstruction 		disease Digestive System Diseases Disease or Syndrome 17 10 0.020 None 1.000 2 2017 2017
CUI: C0268124
Disease: Adenosine deaminase deficiency
Adenosine deaminase deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases Disease or Syndrome 17 2 0.010 None 1.000 1 1995 1995
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom 		phenotype Sign or Symptom 17 3 0.010 None 1.000 1 2017 2017