Source: BEFREE ×
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: C0033847
Disease: Pseudoxanthoma Elasticum
Pseudoxanthoma Elasticum
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 55 15 1.000 None 0.982 150 9 1978 2020
CUI: C1859727
Disease: Arterial calcification of infancy
Arterial calcification of infancy
disease Nutritional and Metabolic Diseases Disease or Syndrome 3 1 0.580 None 1.000 8 2011 2020
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
group Cardiovascular Diseases Disease or Syndrome 1973 871 0.130 None 1.000 3 1 2005 2019
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1515 412 0.130 None 1.000 3 1 2010 2018
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 4264 861 0.110 None 1.000 1 2000 2000
CUI: C0002982
Disease: Angioid Streaks
Angioid Streaks
disease Eye Diseases Disease or Syndrome 6 2 0.110 None 1.000 1 1 2009 2009
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 391 32 0.110 None 1.000 1 2016 2016
CUI: C0473583
Disease: Nevus elasticus
Nevus elasticus
disease Neoplasms Neoplastic Process 37 5 0.100 None 1.000 72 4 2000 2019
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
disease Cardiovascular Diseases Disease or Syndrome 1262 440 0.070 None 1.000 7 2 2002 2018
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
disease Cardiovascular Diseases Disease or Syndrome 1504 1022 0.060 None 1.000 6 2 2002 2013
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
disease Cardiovascular Diseases Disease or Syndrome 1432 769 0.060 None 1.000 6 2 2002 2013
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
disease Neoplasms Neoplastic Process 2428 247 0.050 None 0.800 5 2000 2020
CUI: C0025517
Disease: Metabolic Diseases
Metabolic Diseases
group Nutritional and Metabolic Diseases Disease or Syndrome 937 50 0.050 None 0.800 5 2001 2017
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
group Cardiovascular Diseases Disease or Syndrome 1551 382 0.040 None 1.000 4 1 2002 2018
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 2395 676 0.030 None 1.000 3 1988 2017
CUI: C0023418
Disease: leukemia
leukemia
disease Neoplasms Neoplastic Process 1984 138 0.020 None 1.000 2 1996 2020
Premature coronary artery atherosclerosis
phenotype Cardiovascular Diseases Disease or Syndrome 80 42 0.020 None 0.500 2 1 2002 2005
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
disease Cardiovascular Diseases Disease or Syndrome 585 103 0.020 None 0.500 2 1 2011 2018
CUI: C0333307
Disease: Superficial ulcer
Superficial ulcer
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 242 10 0.010 None 1.000 1 1986 1986
CUI: C0342649
Disease: Vascular calcification
Vascular calcification
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 255 3 0.010 None 1.000 1 2017 2017
Polycystic Kidney, Autosomal Dominant
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 269 20 0.010 None 1.000 1 2008 2008
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal
disease Cardiovascular Diseases Disease or Syndrome 566 78 0.010 None < 0.001 1 2005 2005
Coagulation factor deficiency syndrome
group Hemic and Lymphatic Diseases Disease or Syndrome 12 1 0.010 None 1.000 1 1 2009 2009
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 555 80 0.010 None 1.000 1 2018 2018
CUI: C0268307
Disease: Conjugated hyperbilirubinemia
Conjugated hyperbilirubinemia
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 16 1 0.010 None 1.000 1 2011 2011