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: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 1800 680 0.010 None 1.000 1 2019 2019
CUI: C0030283
Disease: Pancreatic Cyst
Pancreatic Cyst 		disease Digestive System Diseases; Neoplasms Disease or Syndrome 60 4 0.010 None 1.000 1 2017 2017
CUI: C0030286
Disease: Pancreatic Diseases
Pancreatic Diseases 		group Digestive System Diseases Disease or Syndrome 100 11 0.010 None 1.000 1 2019 2019
CUI: C0034067
Disease: Pulmonary Emphysema
Pulmonary Emphysema 		disease Respiratory Tract Diseases Disease or Syndrome 352 64 0.010 None 1.000 1 1995 1995
CUI: C0035854
Disease: Rosacea
Rosacea 		disease Skin and Connective Tissue Diseases Disease or Syndrome 41 2 0.010 None 1.000 1 2018 2018
CUI: C0038354
Disease: Stomach Diseases
Stomach Diseases 		group Digestive System Diseases Disease or Syndrome 70 3 0.010 None 1.000 1 2017 2017
CUI: C0041325
Disease: Peritonitis, Tuberculous
Peritonitis, Tuberculous 		disease Digestive System Diseases; Infections Disease or Syndrome 14 2 0.010 None 1.000 1 2017 2017
CUI: C0042870
Disease: Vitamin D Deficiency
Vitamin D Deficiency 		disease Nutritional and Metabolic Diseases Disease or Syndrome 153 37 0.010 None 1.000 1 2018 2018
CUI: C0080032
Disease: Pleural Effusion, Malignant
Pleural Effusion, Malignant 		disease Neoplasms; Respiratory Tract Diseases Disease or Syndrome 119 6 0.010 None 1.000 1 2019 2019
CUI: C0085110
Disease: Severe Combined Immunodeficiency
Severe Combined Immunodeficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases Disease or Syndrome 284 46 0.010 None 1.000 1 2009 2009
CUI: C0221505
Disease: Lesion of brain
Lesion of brain 		group Disease or Syndrome 188 9 0.010 None 1.000 1 2019 2019
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		group Nervous System Diseases Disease or Syndrome 373 95 0.010 None 1.000 1 1999 1999
CUI: C0262660
Disease: VASCULAR EMBOLISM
VASCULAR EMBOLISM 		disease Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 2013 2013
CUI: C0268074
Disease: Indian childhood cirrhosis
Indian childhood cirrhosis 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 67 6 0.010 None 1.000 1 2018 2018
CUI: C0275524
Disease: Coinfection
Coinfection 		phenotype Infections Disease or Syndrome 252 11 0.010 None 1.000 1 1995 1995
CUI: C0276199
Disease: Canarypox (disorder)
Canarypox (disorder) 		disease Disease or Syndrome 32 0.010 None 1.000 1 1997 1997
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia 		disease Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 320 215 0.010 None 1.000 1 1999 1999
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 161 43 0.010 None 1.000 1 2017 2017
CUI: C0566602
Disease: Primary sclerosing cholangitis
Primary sclerosing cholangitis 		disease Digestive System Diseases Disease or Syndrome 264 58 0.010 None 1.000 1 2017 2017
CUI: C0746102
Disease: Chronic lung disease
Chronic lung disease 		disease Respiratory Tract Diseases Disease or Syndrome 133 12 0.010 None 1.000 1 2019 2019
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases 		group Nutritional and Metabolic Diseases Disease or Syndrome 284 84 0.010 None 1.000 1 2018 2018
CUI: C0751956
Disease: Acute Cerebrovascular Accidents
Acute Cerebrovascular Accidents 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 155 2 0.010 None 1.000 1 2020 2020
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction 		phenotype Disease or Syndrome 716 25 0.010 None 1.000 1 2017 2017
CUI: C1301752
Disease: Respiratory morbidity
Respiratory morbidity 		disease Disease or Syndrome 18 0.010 None 1.000 1 2017 2017
CUI: C1536222
Disease: Non STEMI
Non STEMI 		disease Disease or Syndrome 13 0.010 None 1.000 1 2019 2019