FGF19, fibroblast growth factor 19, 9965

N. diseases: 123; N. variants: 0
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: C0267919
Disease: Primary cholangitis
Primary cholangitis 		disease Digestive System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C4274352
Disease: Chronic intestinal failure
Chronic intestinal failure 		disease Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C4524087
Disease: Bile acid diarrhea
Bile acid diarrhea 		disease Disease or Syndrome 4 0.070 None 1.000 7 2016 2019
CUI: C0156173
Disease: Functional diarrhea
Functional diarrhea 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C0742395
Disease: Cholestasis, chronic
Cholestasis, chronic 		disease Disease or Syndrome 5 0.010 None 1.000 1 2019 2019
CUI: C0863194
Disease: Hepatoma resectable
Hepatoma resectable 		disease Digestive System Diseases; Neoplasms Neoplastic Process 6 0.010 None 1.000 1 2019 2019
CUI: C2747802
Disease: Bile acid malabsorption
Bile acid malabsorption 		disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
CUI: C0432252
Disease: Osteoporosis with pseudoglioma
Osteoporosis with pseudoglioma 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 12 37 0.010 None 1.000 1 1999 1999
CUI: C1306571
Disease: Hepatic Insufficiency
Hepatic Insufficiency 		phenotype Digestive System Diseases Pathologic Function 13 0.200 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: C0001193
Disease: Apert syndrome
Apert syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 20 24 0.010 None 1.000 1 2016 2016
CUI: C0271710
Disease: Reactive hypoglycemia
Reactive hypoglycemia 		disease Nutritional and Metabolic Diseases Disease or Syndrome 23 0.010 None 1.000 1 2019 2019
CUI: C1608426
Disease: Compensated cirrhosis
Compensated cirrhosis 		disease Disease or Syndrome 23 2 0.010 None 1.000 1 2017 2017
CUI: C4522181
Disease: Brachial Amyotrophic Diplegia
Brachial Amyotrophic Diplegia 		disease Nervous System Diseases Disease or Syndrome 28 0.020 None 1.000 2 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 0.010 None 1.000 1 2018 2018
CUI: C0001306
Disease: Acute alcoholic liver disease
Acute alcoholic liver disease 		disease Digestive System Diseases; Chemically-Induced Disorders; Mental Disorders Disease or Syndrome 35 0.200 None 1.000 1 2017 2017
CUI: C4551898
Disease: Cholestasis, progressive familial intrahepatic 1
Cholestasis, progressive familial intrahepatic 1 		disease Digestive System Diseases Disease or Syndrome 38 19 0.010 None 1.000 1 2018 2018
CUI: C0008372
Disease: Intrahepatic Cholestasis
Intrahepatic Cholestasis 		disease Digestive System Diseases Disease or Syndrome 54 3 0.010 None < 0.001 1 2017 2017
CUI: C1262211
Disease: Diarrhoea predominant irritable bowel syndrome
Diarrhoea predominant irritable bowel syndrome 		disease Disease or Syndrome 57 8 0.020 None 1.000 2 2011 2020
CUI: C0860204
Disease: Cholestatic liver disease
Cholestatic liver disease 		disease Digestive System Diseases Disease or Syndrome 58 0.010 None 1.000 1 2020 2020
CUI: C0027540
Disease: Necrosis
Necrosis 		phenotype Pathological Conditions, Signs and Symptoms Organ or Tissue Function 60 0.200 None 1.000 1 2014 2014
CUI: C0920563
Disease: Insulin Sensitivity
Insulin Sensitivity 		phenotype Nutritional and Metabolic Diseases Pathologic Function 62 0.200 None 1.000 1 2017 2017
CUI: C0858617
Disease: Posterior subcapsular cataract
Posterior subcapsular cataract 		disease Eye Diseases Disease or Syndrome 67 9 0.010 None 1.000 1 2016 2016
CUI: C0156147
Disease: Crohn's disease of large bowel
Crohn's disease of large bowel 		disease Digestive System Diseases Disease or Syndrome 96 1 0.010 None 1.000 1 2012 2012
CUI: C0268318
Disease: Cholestasis of pregnancy
Cholestasis of pregnancy 		disease Digestive System Diseases; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 100 24 0.020 None 1.000 2 2014 2019