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.
Idiopathic pulmonary arterial hypertension
disease Respiratory Tract Diseases Disease or Syndrome 776 24 0.700 strong 0.952 21 2012 2020
Familial primary pulmonary hypertension
disease Respiratory Tract Diseases Disease or Syndrome 30 2 0.640 strong 1.000 7 2013 2019
CUI: C3809198
Disease: PULMONARY HYPERTENSION, PRIMARY, 4
PULMONARY HYPERTENSION, PRIMARY, 4
disease Disease or Syndrome 1 7 0.600 None 1.000 2 7 2013 2017
CUI: C2973725
Disease: Pulmonary arterial hypertension
Pulmonary arterial hypertension
disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 413 70 0.460 strong 0.857 7 2016 2019
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1658 591 0.400 None 1.000 1 1 2018 2018
CUI: C4552070
Disease: Pulmonary Hypertension, Primary, 1
Pulmonary Hypertension, Primary, 1
disease Respiratory Tract Diseases Disease or Syndrome 9 323 0.400 None 0 1
Familial pulmonary arterial hypertension
disease Disease or Syndrome 12 1 0.320 None 1.000 3 2013 2017
CUI: C0152171
Disease: Idiopathic pulmonary hypertension
Idiopathic pulmonary hypertension
disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 161 5 0.320 strong 1.000 3 2013 2017
CUI: C0751956
Disease: Acute Cerebrovascular Accidents
Acute Cerebrovascular Accidents
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 155 2 0.300 None 1.000 1 2018 2018
CUI: C3887640
Disease: Astrocytosis
Astrocytosis
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 37 0.300 None 1.000 1 2008 2008
2-oxo-hept-3-ene-1,7-dioate hydratase activity
phenotype Molecular Function 14 0.300 strong 1.000 1 2017 2017
CUI: C0017639
Disease: Gliosis
Gliosis
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 102 3 0.300 None 1.000 1 2008 2008
CUI: C0020542
Disease: Pulmonary Hypertension
Pulmonary Hypertension
phenotype Respiratory Tract Diseases Pathologic Function 156 0.300 None 1.000 1 2019 2019
Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia
disease Respiratory Tract Diseases Disease or Syndrome 7 1 0.300 None 0
PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED
disease Respiratory Tract Diseases Disease or Syndrome 7 3 0.300 None 0
Pulmonary Hypertension, Primary, Fenfluramine-Associated
disease Respiratory Tract Diseases Disease or Syndrome 7 0.300 None 0
CUI: C0038220
Disease: Status Epilepticus
Status Epilepticus
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 533 12 0.200 None 1.000 1 2008 2008
CUI: C0011053
Disease: Deafness
Deafness
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Finding 62 37 0.200 None 1.000 1 2007 2007
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
group Cardiovascular Diseases Disease or Syndrome 2322 1085 0.190 None 0.900 10 4 2011 2019
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
phenotype Clinical Attribute 507 1037 0.100 None 1.000 6 6 2016 2019
CUI: C1305855
Disease: Body mass index
Body mass index
phenotype Clinical Attribute 1014 2689 0.100 None 1.000 5 3 2015 2019
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
phenotype Clinical Attribute 843 1931 0.100 None 1.000 5 7 2016 2019
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
phenotype Finding 146 344 0.100 None 1.000 3 6 2018 2018
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1159 704 0.100 None 1.000 1 1 2018 2018
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement
phenotype Diagnostic Procedure 54 95 0.100 None 1.000 1 1 2018 2018