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.
CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3
disease Disease or Syndrome 2 16 0.600 strong 1.000 4 13 2000 2016
Alanine aminotransferase measurement
phenotype Laboratory Procedure 41 77 0.100 None 1.000 1 1 2018 2018
Low density lipoprotein cholesterol measurement
phenotype Laboratory Procedure 483 1142 0.100 None 1.000 1 1 2018 2018
CUI: C0332853
Disease: Anastomosis
Anastomosis
disease Acquired Abnormality 155 2 0.010 None 1.000 1 2020 2020
CUI: C0742395
Disease: Cholestasis, chronic
Cholestasis, chronic
disease Disease or Syndrome 5 0.010 None 1.000 1 2001 2001
CUI: C0920027
Disease: Cholestatic hepatic disorder
Cholestatic hepatic disorder
disease Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
phenotype Laboratory Procedure 486 1243 0.100 None 1.000 1 1 2018 2018
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.010 None 1.000 1 2012 2012
CUI: C1868683
Disease: B-CELL MALIGNANCY, LOW-GRADE
B-CELL MALIGNANCY, LOW-GRADE
disease Neoplastic Process 350 19 0.010 None 1.000 1 1993 1993
Serum Alanine Aminotransferase Measurement
phenotype Laboratory Procedure 41 77 0.100 None 1.000 1 1 2018 2018
CUI: C2004489
Disease: Regurgitation
Regurgitation
phenotype Sign or Symptom 66 0.010 None 1.000 1 2019 2019
CUI: C3544266
Disease: Hepatobiliary cancer
Hepatobiliary cancer
disease Neoplastic Process 11 1 0.010 None 1.000 1 1 2015 2015
Parenteral nutrition associated liver disease
disease Disease or Syndrome 6 0.010 None 1.000 1 2020 2020
CUI: C3666017
Disease: Cholangiopathy
Cholangiopathy
disease Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.010 None 1.000 1 2018 2018
CUI: C1314665
Disease: Serum alkaline phosphatase raised
Serum alkaline phosphatase raised
phenotype Finding 67 6 0.100 None 0
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase
phenotype Finding 212 9 0.100 None 0
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype Finding 175 0.100 None 0
Increased serum bile acid concentration during pregnancy
phenotype Finding 2 0.100 None 0
Abnormal liver function tests during pregnancy
disease Finding 3 1 0.100 None 0
CUI: C0013146
Disease: Drug abuse
Drug abuse
group Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 405 39 0.010 None 1.000 1 2019 2019
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 757 47 0.010 None 1.000 1 2006 2006
Congenital atresia of extrahepatic bile duct
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 172 19 0.010 None 1.000 1 2017 2017
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 0.010 None 1.000 1 2010 2010
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 586 125 0.020 None 1.000 2 2017 2017