EGF, epidermal growth factor, 1950

N. diseases: 774; N. variants: 33
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: C0086543
Disease: Cataract
Cataract
disease Eye Diseases Acquired Abnormality 878 124 0.010 None 1.000 1 1999 1999
CUI: C0153594
Disease: Malignant neoplasm of testis
Malignant neoplasm of testis
disease Neoplasms; Male Urogenital Diseases; Endocrine System Diseases Neoplastic Process 253 31 0.010 None 1.000 1 2019 2019
CUI: C0153601
Disease: Malignant neoplasm of penis
Malignant neoplasm of penis
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 39 3 0.010 None 1.000 1 2013 2013
Secondary malignant neoplasm of lung
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 1370 20 0.010 None 1.000 1 2005 2005
Secondary malignant neoplasm of bone
disease Pathological Conditions, Signs and Symptoms; Neoplasms; Musculoskeletal Diseases Neoplastic Process 647 18 0.010 None 1.000 1 2014 2014
CUI: C0162830
Disease: Dermatitis, Phototoxic
Dermatitis, Phototoxic
disease Skin and Connective Tissue Diseases Disease or Syndrome 89 0.010 None 1.000 1 2018 2018
CUI: C0175693
Disease: Russell-Silver syndrome
Russell-Silver syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 104 12 0.010 None 1.000 1 2012 2012
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 0.010 None 1.000 1 2010 2010
CUI: C0175754
Disease: Agenesis of corpus callosum
Agenesis of corpus callosum
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 615 45 0.010 None 1.000 1 2016 2016
CUI: C1510420
Disease: Cavitation
Cavitation
disease Anatomical Abnormality 47 0.010 None 1.000 1 2018 2018
CUI: C1444680
Disease: Posterior capsule opacification
Posterior capsule opacification
disease Eye Diseases Disease or Syndrome 20 0.010 None 1.000 1 2018 2018
CUI: C1411966
Disease: Clostridium; difficile (disorder)
Clostridium; difficile (disorder)
disease Disease or Syndrome 106 0.010 None 1.000 1 2011 2011
CUI: C1402291
Disease: Pigmented lesions
Pigmented lesions
disease Disease or Syndrome 18 3 0.010 None 1.000 1 1994 1994
CUI: C0153452
Disease: Malignant neoplasm of gallbladder
Malignant neoplasm of gallbladder
disease Digestive System Diseases; Neoplasms Neoplastic Process 425 81 0.010 None 1.000 1 1 2008 2008
CUI: C1519666
Disease: Tumor-Associated Vasculature
Tumor-Associated Vasculature
disease Acquired Abnormality 84 0.010 None 1.000 1 2017 2017
CUI: C1697878
Disease: BK virus nephropathy
BK virus nephropathy
disease Infections Disease or Syndrome 12 0.010 None 1.000 1 2018 2018
CUI: C1656427
Disease: Early onset schizophrenia
Early onset schizophrenia
disease Mental or Behavioral Dysfunction 15 3 0.010 None 1.000 1 2005 2005
CUI: C0149939
Disease: Obstructive nephropathy
Obstructive nephropathy
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 95 0.010 None 1.000 1 2000 2000
CUI: C0151450
Disease: Secondary Sjögren's syndrome
Secondary Sjögren's syndrome
disease Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases Disease or Syndrome 20 0.010 None 1.000 1 2018 2018
CUI: C0151650
Disease: Renal fibrosis
Renal fibrosis
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 570 1 0.010 None 1.000 1 2019 2019
CUI: C0151718
Disease: Hypocholesterolemia
Hypocholesterolemia
disease Nutritional and Metabolic Diseases Disease or Syndrome 113 22 0.010 None 1.000 1 2010 2010
CUI: C1567741
Disease: Alport Syndrome
Alport Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases Disease or Syndrome 51 314 0.010 None 1.000 1 2018 2018
CUI: C0151971
Disease: Primary ulcer of intestine
Primary ulcer of intestine
disease Digestive System Diseases Disease or Syndrome 13 0.010 None 1.000 1 2019 2019
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 615 42 0.010 None 1.000 1 2018 2018
CUI: C1527349
Disease: Ductal Breast Carcinoma
Ductal Breast Carcinoma
disease Neoplasms Neoplastic Process 196 10 0.010 None 1.000 1 1997 1997