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: C0265029
Disease: Portal vein obstruction
Portal vein obstruction 		disease Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C0266242
Disease: Congenital hypoplasia of bile duct
Congenital hypoplasia of bile duct 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 3 0.010 None 1.000 1 2004 2004
CUI: C0013882
Disease: Elephantiasis
Elephantiasis 		disease Hemic and Lymphatic Diseases Disease or Syndrome 6 6 0.010 None 1.000 1 2003 2003
CUI: C0392663
Disease: Infection by Wuchereria bancrofti
Infection by Wuchereria bancrofti 		disease Infections; Hemic and Lymphatic Diseases Disease or Syndrome 9 2 0.010 None 1.000 1 2003 2003
CUI: C0149841
Disease: Benign recurrent intrahepatic cholestasis
Benign recurrent intrahepatic cholestasis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 10 1 0.020 None 1.000 2 2005 2016
CUI: C0814152
Disease: Viral hepatitis, type G
Viral hepatitis, type G 		disease Infections Disease or Syndrome 11 0.020 None 1.000 2 1996 1999
CUI: C4551984
Disease: Arthrogryposis with renal dysfunction and cholestasis syndrome
Arthrogryposis with renal dysfunction and cholestasis syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 12 0.020 None 1.000 2 2004 2014
CUI: C0861876
Disease: Recurrent Hepatocellular Carcinoma
Recurrent Hepatocellular Carcinoma 		disease Digestive System Diseases; Neoplasms Neoplastic Process 12 0.010 None 1.000 1 2003 2003
CUI: C3839589
Disease: Secondary osteoporosis
Secondary osteoporosis 		disease Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 15 0.010 None 1.000 1 2015 2015
CUI: C1859722
Disease: Arthrogryposis, renal dysfunction, and cholestasis 1
Arthrogryposis, renal dysfunction, and cholestasis 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases Disease or Syndrome 16 13 0.020 None 1.000 2 2004 2014
CUI: C0741281
Disease: atrial fibrillation new onset
atrial fibrillation new onset 		disease Disease or Syndrome 18 0.010 None 1.000 1 2017 2017
CUI: C1112213
Disease: Cholestasis in newborn
Cholestasis in newborn 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Disease or Syndrome 19 0.020 None 1.000 2 2004 2019
CUI: C0221155
Disease: Systolic hypertension
Systolic hypertension 		disease Cardiovascular Diseases Disease or Syndrome 19 1 0.010 None 1.000 1 2006 2006
CUI: C0740340
Disease: Amyloidosis, Familial
Amyloidosis, Familial 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 19 12 0.010 None 1.000 1 2001 2001
CUI: C0014458
Disease: Eosinophilia, Tropical
Eosinophilia, Tropical 		disease Hemic and Lymphatic Diseases Disease or Syndrome 24 0.010 None 1.000 1 2003 2003
CUI: C0748168
Disease: Pulmonary Pathology
Pulmonary Pathology 		disease Disease or Syndrome 29 0.010 None 1.000 1 2003 2003
CUI: C0023886
Disease: Liver Abscess, Amebic
Liver Abscess, Amebic 		disease Digestive System Diseases; Infections Disease or Syndrome 30 1 0.010 None 1.000 1 2017 2017
CUI: C0268312
Disease: Progressive intrahepatic cholestasis (disorder)
Progressive intrahepatic cholestasis (disorder) 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 31 10 0.070 None 1.000 7 1994 2019
CUI: C0268307
Disease: Conjugated hyperbilirubinemia
Conjugated hyperbilirubinemia 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 32 1 0.010 None 1.000 1 2019 2019
CUI: C0022353
Disease: Neonatal Jaundice
Neonatal Jaundice 		phenotype Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 33 2 0.010 None 1.000 1 2010 2010
CUI: C4551898
Disease: Cholestasis, progressive familial intrahepatic 1
Cholestasis, progressive familial intrahepatic 1 		disease Digestive System Diseases Disease or Syndrome 38 19 0.080 None 1.000 8 1994 2019
CUI: C0013884
Disease: Filarial Elephantiases
Filarial Elephantiases 		disease Infections; Hemic and Lymphatic Diseases Disease or Syndrome 38 10 0.010 None 1.000 1 2003 2003
CUI: C0085280
Disease: Alagille Syndrome
Alagille Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases Congenital Abnormality 38 18 0.010 None 1.000 1 2010 2010
CUI: C0008372
Disease: Intrahepatic Cholestasis
Intrahepatic Cholestasis 		disease Digestive System Diseases Disease or Syndrome 54 3 0.040 None 1.000 4 2011 2016
CUI: C0042749
Disease: Viremia
Viremia 		disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 56 3 0.010 None 1.000 1 2002 2002