EPHA2, EPH receptor A2, 1969

N. diseases: 187; N. variants: 10
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: C1861825
Disease: CATARACT, POSTERIOR POLAR, 1
CATARACT, POSTERIOR POLAR, 1 		disease Eye Diseases Disease or Syndrome 1 4 0.900 strong 1.000 6 4 2006 2013
CUI: C0854775
Disease: stage IV pancreatic cancer
stage IV pancreatic cancer 		disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 3 0.010 None 1.000 1 2006 2006
CUI: C4551484
Disease: Leopard Syndrome 1
Leopard Syndrome 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 6 26 0.300 None 1.000 1 2012 2012
CUI: C1955634
Disease: Kaposi's sarcoma-associated herpesvirus infection
Kaposi's sarcoma-associated herpesvirus infection 		disease Disease or Syndrome 8 0.030 None 1.000 3 2017 2018
CUI: C1850191
Disease: Posterior polar cataract
Posterior polar cataract 		phenotype Finding 8 0.100 None 0
CUI: C2880562
Disease: Age-related cortical cataract
Age-related cortical cataract 		disease Acquired Abnormality 9 2 0.320 strong 1.000 2 2009 2011
CUI: C0342500
Disease: Adrenal mass
Adrenal mass 		disease Endocrine System Diseases Disease or Syndrome 9 0.010 None 1.000 1 2017 2017
CUI: C0041409
Disease: Turner Syndrome, Male
Turner Syndrome, Male 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 1.000 1 2012 2012
CUI: C1527404
Disease: Female Pseudo-Turner Syndrome
Female Pseudo-Turner Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Congenital Abnormality 11 0.300 None 1.000 1 2012 2012
CUI: C0035320
Disease: Retinal Neovascularization
Retinal Neovascularization 		phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases Pathologic Function 12 0.200 None 1.000 1 2006 2006
CUI: C1708502
Disease: Induced cataract
Induced cataract 		disease Disease or Syndrome 13 0.010 None 1.000 1 2019 2019
CUI: C0034089
Disease: Pulmonary Valve Stenosis
Pulmonary Valve Stenosis 		disease Cardiovascular Diseases Disease or Syndrome; Anatomical Abnormality 16 2 0.010 None 1.000 1 2013 2013
CUI: C0266539
Disease: Congenital total cataract
Congenital total cataract 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality 16 0.300 None 1.000 1 2009 2009
CUI: C0302254
Disease: Juvenile cataract
Juvenile cataract 		disease Eye Diseases Anatomical Abnormality 16 3 0.010 None 1.000 1 2014 2014
CUI: C1377919
Disease: Stage IV Nasopharyngeal Carcinoma
Stage IV Nasopharyngeal Carcinoma 		disease Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases Neoplastic Process 16 1 0.010 None 1.000 1 2019 2019
CUI: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 23 83 0.300 None 1.000 1 2012 2012
CUI: C1112211
Disease: Hepatic Infection
Hepatic Infection 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Infections Disease or Syndrome 24 0.020 None 1.000 2 2015 2018
CUI: C0919659
Disease: Oropharyngeal candidiasis
Oropharyngeal candidiasis 		disease Infections Disease or Syndrome 27 3 0.020 None 1.000 2 2018 2019
CUI: C0038160
Disease: Staphylococcal Infections
Staphylococcal Infections 		group Infections Disease or Syndrome 37 5 0.010 None 1.000 1 2019 2019
CUI: C0392557
Disease: Nuclear cataract
Nuclear cataract 		disease Eye Diseases Disease or Syndrome 39 11 0.310 None 1.000 2 2013 2018
CUI: C0008525
Disease: Choroideremia
Choroideremia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 41 15 0.100 None 0
CUI: C2882221
Disease: Acute pulmonary embolism
Acute pulmonary embolism 		disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 42 0.010 None 1.000 1 2018 2018
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 47 27 0.310 None 1.000 2 2012 2013
CUI: C0279751
Disease: Adenoid cystic carcinoma of salivary gland
Adenoid cystic carcinoma of salivary gland 		disease Neoplasms; Stomatognathic Diseases Neoplastic Process 47 0.010 None 1.000 1 2013 2013
CUI: C0153567
Disease: Uterine Cancer
Uterine Cancer 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 54 4 0.010 None 1.000 1 2010 2010