VEGFA, vascular endothelial growth factor A, 7422

N. diseases: 1899; N. variants: 59
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: C0043407
Disease: Yersinia infections
Yersinia infections
group Infections Disease or Syndrome 17 0.010 None 1.000 1 2003 2003
CUI: C0750466
Disease: Yeast infection
Yeast infection
disease Infections Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C1337035
Disease: Xanthogranulomatous cholecystitis
Xanthogranulomatous cholecystitis
disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 6 0.010 None 1.000 1 2013 2013
CUI: C0043144
Disease: Wheezing
Wheezing
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 132 54 0.030 None 1.000 3 2014 2019
Wet age-related macular degeneration
disease Disease or Syndrome 20 2 0.100 None 1.000 23 2008 2019
Well Differentiated Pancreatic Endocrine Tumor
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 117 3 0.020 None 1.000 2 2013 2017
Well Differentiated Oligodendroglioma
disease Neoplasms Neoplastic Process 270 22 0.020 None 1.000 2 1998 2017
CUI: C0024419
Disease: Waldenstrom Macroglobulinemia
Waldenstrom Macroglobulinemia
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 162 15 0.010 None 1.000 1 2019 2019
CUI: C1264041
Disease: von Willebrand Disease, Type 3
von Willebrand Disease, Type 3
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 11 17 0.010 None 1.000 1 2018 2018
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 174 187 0.100 None 0.955 22 1 1995 2018
CUI: C1858805
Disease: Vohwinkel Syndrome, Variant Form
Vohwinkel Syndrome, Variant Form
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 4 0.010 None 1.000 1 2010 2010
CUI: C3161192
Disease: Vitreomacular traction
Vitreomacular traction
disease Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C2748203
Disease: Vitreomacular adhesion
Vitreomacular adhesion
phenotype Anatomical Abnormality 6 0.010 None 1.000 1 2017 2017
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
disease Skin and Connective Tissue Diseases Disease or Syndrome 302 92 0.010 None 1.000 1 1 2019 2019
CUI: C0042900
Disease: Vitiligo
Vitiligo
disease Skin and Connective Tissue Diseases Disease or Syndrome 395 249 0.010 None 1.000 1 1 2019 2019
CUI: C0042870
Disease: Vitamin D Deficiency
Vitamin D Deficiency
disease Nutritional and Metabolic Diseases Disease or Syndrome 153 37 0.020 None 1.000 2 2018 2018
Visually threatening diabetic retinopathy
disease Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 8 4 0.010 None < 0.001 1 2015 2015
CUI: C0422943
Disease: Visual symptoms
Visual symptoms
phenotype Sign or Symptom 17 5 0.010 None 1.000 1 2018 2018
Visual impairment and blindness (excl colour blindness)
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C0042769
Disease: Virus Diseases
Virus Diseases
group Infections Disease or Syndrome 1471 42 0.090 None 0.889 9 1999 2019
CUI: C0042749
Disease: Viremia
Viremia
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 56 3 0.010 None 1.000 1 2008 2008
CUI: C0243010
Disease: Viral Encephalitis
Viral Encephalitis
group Infections; Nervous System Diseases Disease or Syndrome 35 0.010 None 1.000 1 2008 2008
CUI: C4551858
Disease: Vesicoureteral Reflux 1
Vesicoureteral Reflux 1
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 47 10 0.030 None 1.000 3 2007 2019
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 187 23 0.020 None 1.000 2 2007 2019
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 426 87 0.010 None 1.000 1 2007 2007