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 None 0.978 185 4 2000 2020
CUI: C2973725
Disease: Pulmonary arterial hypertension
Pulmonary arterial hypertension
disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 413 70 0.500 None 0.927 55 49 2002 2020
Familial primary pulmonary hypertension
disease Respiratory Tract Diseases Disease or Syndrome 30 2 0.700 None 1.000 48 2 1997 2019
CUI: C0152171
Disease: Idiopathic pulmonary hypertension
Idiopathic pulmonary hypertension
disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 161 5 0.600 None 1.000 43 2000 2019
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
group Cardiovascular Diseases Disease or Syndrome 2322 1085 0.200 None 1.000 40 1 2002 2020
Familial pulmonary arterial hypertension
disease Disease or Syndrome 12 1 0.400 None 1.000 21 1 2005 2018
CUI: C0020542
Disease: Pulmonary Hypertension
Pulmonary Hypertension
phenotype Respiratory Tract Diseases Pathologic Function 156 0.370 None 1.000 16 2001 2013
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.100 None 1.000 16 2002 2014
Hereditary hemorrhagic telangiectasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 42 81 0.080 None 1.000 8 2004 2018
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 267 80 0.060 None 1.000 6 2003 2016
CUI: C0027651
Disease: Neoplasms
Neoplasms
group Neoplasms Neoplastic Process 10161 1644 0.060 None 1.000 6 2004 2017
Pulmonary Veno-Occlusive Disease (disorder)
disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 11 1 0.720 None 1.000 5 1 2003 2016
Sporadic primary pulmonary hypertension
disease Respiratory Tract Diseases Disease or Syndrome 4 0.040 None 1.000 4 2000 2004
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 6941 3417 0.330 None 1.000 4 2007 2015
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 6776 2793 0.330 None 1.000 4 2007 2015
PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT
disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 8 3 0.430 None 1.000 3 2 2003 2016
Associated Pulmonary Arterial Hypertension
disease Respiratory Tract Diseases Disease or Syndrome 22 4 0.030 None 1.000 3 2008 2012
Chronic thromboembolic pulmonary hypertension
disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 76 4 0.030 None 1.000 3 2010 2019
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 5473 1962 0.030 None 1.000 3 2008 2015
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone
disease Neoplasms Neoplastic Process 2247 151 0.020 None 1.000 2 2002 2017
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 6385 327 0.020 None 0.500 2 2015 2017
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
group Neoplasms Neoplastic Process 8221 1374 0.020 None 1.000 2 2 2010 2017
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma
disease Neoplasms Neoplastic Process 2208 151 0.020 None 1.000 2 2002 2017
CUI: C0235833
Disease: Congenital diaphragmatic hernia
Congenital diaphragmatic hernia
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 239 31 0.020 None 0.500 2 2013 2017
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
phenotype Disease or Syndrome 716 25 0.020 None 1.000 2 2015 2019