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: C0152097
Disease: Disease of diaphragm
Disease of diaphragm 		group Respiratory Tract Diseases Disease or Syndrome 1 0.010 None 1.000 1 2014 2014
CUI: C1096494
Disease: Gastroduodenal haemorrhage
Gastroduodenal haemorrhage 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2007 2007
CUI: C0266807
Disease: Acute gastrointestinal hemorrhage
Acute gastrointestinal hemorrhage 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 2 4 0.020 None 1.000 2 2 2008 2009
CUI: C0030922
Disease: Peptic Ulcer Hemorrhage
Peptic Ulcer Hemorrhage 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Pathologic Function 2 0.300 None 1.000 1 2007 2007
CUI: C2675747
Disease: Coumarin Sensitivity
Coumarin Sensitivity 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 2 0.010 None 1.000 1 2007 2007
CUI: C3888513
Disease: CYP2C9 polymorphism
CYP2C9 polymorphism 		disease Disease or Syndrome 3 0.030 None 1.000 3 2001 2014
CUI: C0750384
Disease: Coumarin Resistance
Coumarin Resistance 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 6 10 0.410 None 1.000 1 1 2016 2016
CUI: C0857493
Disease: Upper gastrointestinal symptoms
Upper gastrointestinal symptoms 		disease Disease or Syndrome 6 0.010 None 1.000 1 2005 2005
CUI: C0017567
Disease: Gingival Hypertrophy
Gingival Hypertrophy 		disease Stomatognathic Diseases Disease or Syndrome 7 0.010 None 1.000 1 2018 2018
CUI: C1844680
Disease: DEAFNESS-HYPOGONADISM SYNDROME
DEAFNESS-HYPOGONADISM SYNDROME 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Endocrine System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 7 0.010 None 1.000 1 2017 2017
CUI: C1709735
Disease: Prosthetic Valve Thrombosis
Prosthetic Valve Thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 8 0.010 None < 0.001 1 2019 2019
CUI: C2921125
Disease: Post traumatic seizures
Post traumatic seizures 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 8 7 0.010 None 1.000 1 2017 2017
CUI: C2608079
Disease: WARFARIN SENSITIVITY (disorder)
WARFARIN SENSITIVITY (disorder) 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 10 8 0.400 None 0.882 17 4 2005 2019
CUI: C0042880
Disease: Vitamin K Deficiency
Vitamin K Deficiency 		disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 19 2 0.010 None 1.000 1 2018 2018
CUI: C0272051
Disease: Xerocytosis
Xerocytosis 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 20 3 0.010 None 1.000 1 2017 2017
CUI: C4476767
Disease: Diffuse alveolar hemorrhage
Diffuse alveolar hemorrhage 		disease Disease or Syndrome 21 0.010 None 1.000 1 2010 2010
CUI: C0019154
Disease: Hepatic Vein Thrombosis
Hepatic Vein Thrombosis 		disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 23 4 0.010 None 1.000 1 2019 2019
CUI: C0850715
Disease: Abnormality of blood and blood-forming tissues
Abnormality of blood and blood-forming tissues 		disease Finding 23 1 0.100 None 0
CUI: C0856761
Disease: Budd-Chiari Syndrome
Budd-Chiari Syndrome 		disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 24 4 0.010 None 1.000 1 2019 2019
CUI: C1319853
Disease: Asthma, Aspirin-Induced
Asthma, Aspirin-Induced 		disease Respiratory Tract Diseases; Immune System Diseases; Chemically-Induced Disorders Disease or Syndrome 25 6 0.010 None 1.000 1 2003 2003
CUI: C3495549
Disease: Patent ductus arteriosus - persisting type
Patent ductus arteriosus - persisting type 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Cardiovascular Diseases Congenital Abnormality 30 10 0.020 None 1.000 2 2017 2019
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 35 11 0.010 None 1.000 1 2014 2014
CUI: C4728082
Disease: Severe hypoglycaemia
Severe hypoglycaemia 		disease Disease or Syndrome 36 2 0.020 None 1.000 2 2005 2011
CUI: C0013182
Disease: Drug Allergy
Drug Allergy 		group Immune System Diseases; Chemically-Induced Disorders Pathologic Function 37 0.300 None 1.000 1 2010 2010
CUI: C0040156
Disease: Thyrotoxicosis
Thyrotoxicosis 		disease Endocrine System Diseases Disease or Syndrome 37 7 0.010 None 1.000 1 2014 2014