VCAN, versican, 1462

N. diseases: 205; N. variants: 16
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.
Peripheral tractional retinal detachment
phenotype Finding 1 0.100 None 0
CUI: C4073118
Disease: Optically empty vitreous
Optically empty vitreous
disease Anatomical Abnormality 2 0.100 None 0
CUI: C2242658
Disease: Aortic dissection rupture
Aortic dissection rupture
disease Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C0220996
Disease: Infantile scurvy
Infantile scurvy
disease Nutritional and Metabolic Diseases Disease or Syndrome 4 0.010 None 1.000 1 2018 2018
Hyaloideoretinal degeneration of Wagner
disease Eye Diseases Disease or Syndrome 7 6 0.700 None 0.938 16 6 1999 2018
EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 9 7 0.010 None 1.000 1 2020 2020
CUI: C0221290
Disease: Chondromyxoid fibroma
Chondromyxoid fibroma
disease Neoplasms Neoplastic Process 12 0.010 None 1.000 1 2007 2007
CUI: C3888044
Disease: Nephrogenic Systemic Fibrosis
Nephrogenic Systemic Fibrosis
disease Skin and Connective Tissue Diseases Disease or Syndrome 12 3 0.010 None 1.000 1 2009 2009
Non-Hereditary Clear Cell Renal Cell Carcinoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 15 0.010 None 1.000 1 2012 2012
Snowflake vitreoretinal degeneration
disease Eye Diseases Disease or Syndrome 15 1 0.010 None 1.000 1 2008 2008
CUI: C0344290
Disease: Vitreoretinal degeneration
Vitreoretinal degeneration
disease Disease or Syndrome 20 6 0.120 None 1.000 2 2009 2019
CUI: C0038012
Disease: Spondylitis
Spondylitis
disease Infections; Musculoskeletal Diseases Disease or Syndrome 20 0.010 None 1.000 1 2003 2003
CUI: C4048273
Disease: Chorioretinal atrophy
Chorioretinal atrophy
disease Eye Diseases Disease or Syndrome 24 4 0.100 None 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy
phenotype Finding 25 4 0.100 None 0
CUI: C1568363
Disease: Tendinosis
Tendinosis
disease Musculoskeletal Diseases; Wounds and Injuries Disease or Syndrome 28 0.010 None 1.000 1 2014 2014
CUI: C0862312
Disease: Epithelioid mesothelioma, malignant
Epithelioid mesothelioma, malignant
disease Neoplasms Neoplastic Process 32 0.010 None 1.000 1 2003 2003
CUI: C0206647
Disease: Dermatofibrosarcoma
Dermatofibrosarcoma
disease Neoplasms Neoplastic Process 33 0.010 None 1.000 1 2008 2008
CUI: C0574960
Disease: Sacroiliitis
Sacroiliitis
disease Musculoskeletal Diseases Disease or Syndrome 33 2 0.010 None 1.000 1 2003 2003
CUI: C1314694
Disease: Astrocytoma, low grade
Astrocytoma, low grade
disease Neoplasms Neoplastic Process 34 2 0.010 None 1.000 1 2012 2012
CUI: C0010072
Disease: Coronary Thrombosis
Coronary Thrombosis
disease Cardiovascular Diseases Disease or Syndrome 35 2 0.010 None 1.000 1 2002 2002
CUI: C0265004
Disease: Dilatation of aorta
Dilatation of aorta
phenotype Cardiovascular Diseases Disease or Syndrome 39 2 0.020 None 1.000 2 2001 2018
CUI: C4721413
Disease: Juvenile angiofibroma
Juvenile angiofibroma
disease Neoplasms; Cardiovascular Diseases Neoplastic Process 44 0.010 None 1.000 1 2003 2003
CUI: C0206731
Disease: Angiofibroma
Angiofibroma
disease Neoplasms Neoplastic Process 45 1 0.010 None 1.000 1 2003 2003
CUI: C1519678
Disease: Tumor Expansion
Tumor Expansion
phenotype Neoplastic Process 46 0.010 None 1.000 1 2015 2015
CUI: C3887875
Disease: Visual field defects
Visual field defects
group Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Finding 47 1 0.100 None 0