Epiretinal Membrane
|
disease |
Eye Diseases
|
Acquired Abnormality
|
102
|
|
0.030 |
None |
1.000 |
3 |
|
2015 |
2019 |
Retinal pigment epithelium atrophy
|
disease |
|
Acquired Abnormality
|
7
|
2
|
0.030 |
None |
1.000 |
3 |
|
2002 |
2019 |
Cavitation
|
disease |
|
Anatomical Abnormality
|
47
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Dry age-related macular degeneration
|
phenotype |
|
Anatomical Abnormality
|
11
|
1
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Hereditary macular dystrophy
|
disease |
|
Congenital Abnormality
|
39
|
10
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Autosomal recessive retinitis pigmentosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
82
|
31
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Congenital hypertrophy of retinal pigment epithelium
|
disease |
|
Congenital Abnormality
|
5
|
3
|
0.010 |
None |
1.000 |
1 |
|
1994 |
1994 |
Age related macular degeneration
|
disease |
Eye Diseases
|
Disease or Syndrome
|
685
|
663
|
0.100 |
None |
0.970 |
33 |
2
|
2003 |
2019 |
Drusen
|
disease |
|
Disease or Syndrome
|
57
|
18
|
0.090 |
None |
1.000 |
9 |
|
2005 |
2019 |
Geographic Atrophy
|
disease |
Eye Diseases
|
Disease or Syndrome
|
85
|
81
|
0.070 |
None |
1.000 |
7 |
|
2013 |
2019 |
Choroideremia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
41
|
15
|
0.060 |
None |
1.000 |
6 |
|
1999 |
2019 |
Retinal Diseases
|
group |
Eye Diseases
|
Disease or Syndrome
|
714
|
56
|
0.050 |
None |
1.000 |
5 |
|
2015 |
2019 |
Glycogen storage disease type II
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
194
|
269
|
0.040 |
None |
1.000 |
4 |
2
|
2009 |
2018 |
Diabetic Retinopathy
|
disease |
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
645
|
213
|
0.030 |
None |
1.000 |
3 |
|
2017 |
2019 |
Retinitis Pigmentosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
546
|
541
|
0.030 |
None |
1.000 |
3 |
1
|
2001 |
2016 |
Proliferative vitreoretinopathy
|
disease |
Eye Diseases
|
Disease or Syndrome
|
142
|
14
|
0.030 |
None |
1.000 |
3 |
|
2006 |
2017 |
Atrophic retina
|
disease |
Eye Diseases
|
Disease or Syndrome
|
24
|
2
|
0.030 |
None |
1.000 |
3 |
|
2010 |
2018 |
Cytomegalovirus Infections
|
group |
Infections
|
Disease or Syndrome
|
462
|
26
|
0.020 |
None |
1.000 |
2 |
|
2011 |
2015 |
Retinoschisis
|
disease |
Eye Diseases
|
Disease or Syndrome
|
13
|
6
|
0.020 |
None |
1.000 |
2 |
|
2018 |
2019 |
Hypopigmentation disorder
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
126
|
15
|
0.020 |
None |
1.000 |
2 |
|
2007 |
2008 |
Severe myopia
|
disease |
Eye Diseases
|
Disease or Syndrome
|
184
|
116
|
0.020 |
None |
1.000 |
2 |
|
2019 |
2019 |
Blindness
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
393
|
34
|
0.020 |
None |
1.000 |
2 |
|
2018 |
2019 |
Diabetic macular edema
|
disease |
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
92
|
6
|
0.020 |
None |
1.000 |
2 |
|
2018 |
2019 |
Atrophoderma maculatum
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
39
|
2
|
0.020 |
None |
1.000 |
2 |
|
2007 |
2007 |
FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, OF SORSBY
|
disease |
Eye Diseases
|
Disease or Syndrome
|
16
|
6
|
0.020 |
None |
1.000 |
2 |
|
2000 |
2017 |