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: C0086492
Disease: J-Pouch
J-Pouch
disease Acquired Abnormality 1 0.010 None 1.000 1 2018 2018
CUI: C0270075
Disease: Perinatal disorder
Perinatal disorder
group Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 1 0.010 None 1.000 1 2015 2015
CUI: C2673648
Disease: Hypomagnesemia 4, Renal
Hypomagnesemia 4, Renal
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 1 1 0.600 None 1.000 1 1 2007 2007
CUI: C3828832
Disease: Neural Glioblastoma
Neural Glioblastoma
disease Neoplastic Process 1 0.010 None 1.000 1 2013 2013
CUI: C4324732
Disease: Bladder wall thickening
Bladder wall thickening
disease Disease or Syndrome 1 0.010 None 1.000 1 1999 1999
CUI: C2609319
Disease: Papulopustular Rash
Papulopustular Rash
phenotype Skin and Connective Tissue Diseases Sign or Symptom 2 0.010 None 1.000 1 2020 2020
Familial primary hypomagnesemia with normocalciuria and normocalcemia
disease Disease or Syndrome 2 0.300 None 1.000 1 2007 2007
CUI: C0521483
Disease: Mucous membrane hyperplasia
Mucous membrane hyperplasia
phenotype Sign or Symptom 3 0.010 None 1.000 1 2017 2017
Adult Central Nervous System Neoplasm
group Neoplasms; Nervous System Diseases Neoplastic Process 3 0.010 None 1.000 1 2001 2001
CUI: C1299888
Disease: laminitis
laminitis
disease Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C0553647
Disease: calcifying aponeurotic fibroma
calcifying aponeurotic fibroma
disease Neoplasms Neoplastic Process 5 0.020 None 0.500 2 2016 2019
Papillary and follicular adenocarcinoma
disease Neoplasms Neoplastic Process 5 2 0.010 None 1.000 1 2006 2006
CUI: C0341335
Disease: Cytomegaloviral colitis
Cytomegaloviral colitis
disease Infections Disease or Syndrome 5 0.010 None 1.000 1 2019 2019
CUI: C0862802
Disease: Recurrent lung cancer
Recurrent lung cancer
disease Neoplastic Process 5 0.010 None 1.000 1 2017 2017
Recurrent Lung Carcinoma Cell Type Unspecified
disease Neoplastic Process 6 0.010 None 1.000 1 2017 2017
Spinal muscular atrophy with lower extremity predominance
disease Nervous System Diseases Disease or Syndrome 6 0.010 None 1.000 1 2014 2014
CUI: C2673443
Disease: Hypermagnesiuria
Hypermagnesiuria
phenotype Finding 6 1 0.100 None 0
CUI: C3844293
Disease: Oval fat body
Oval fat body
phenotype Anatomical Abnormality 7 0.040 None 1.000 4 2011 2013
CUI: C0813148
Disease: Metastatic Endometrial Carcinoma
Metastatic Endometrial Carcinoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 7 0.010 None 1.000 1 2015 2015
CUI: C3714873
Disease: Axenfeld-Rieger Syndrome, Type 1
Axenfeld-Rieger Syndrome, Type 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 7 15 0.010 None 1.000 1 1996 1996
CUI: C0237938
Disease: Gastrointestinal ulcer
Gastrointestinal ulcer
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 9 0.020 None 1.000 2 2018 2019
CUI: C0265268
Disease: Adams Oliver syndrome
Adams Oliver syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 9 12 0.010 None 1.000 1 2015 2015
CUI: C0268225
Disease: Aspartylglucosaminuria
Aspartylglucosaminuria
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 9 53 0.010 None 1.000 1 1990 1990
CUI: C0334357
Disease: Papillary cystic tumor
Papillary cystic tumor
disease Neoplasms Neoplastic Process 9 0.010 None 1.000 1 2017 2017
CUI: C0393559
Disease: Troyer syndrome
Troyer syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 9 4 0.010 None 1.000 1 2007 2007