CATARACT, COPPOCK-LIKE
|
disease |
Eye Diseases
|
Disease or Syndrome
|
20
|
1
|
0.820 |
None |
1.000 |
7 |
1
|
1999 |
2017 |
CATARACT 2, MULTIPLE TYPES
|
disease |
|
Disease or Syndrome
|
3
|
6
|
0.800 |
None |
1.000 |
9 |
6
|
1999 |
2014 |
Cataract
|
disease |
Eye Diseases
|
Acquired Abnormality
|
878
|
124
|
0.460 |
None |
1.000 |
8 |
6
|
1999 |
2012 |
Nuclear non-senile cataract
|
disease |
Eye Diseases
|
Disease or Syndrome
|
69
|
11
|
0.400 |
None |
1.000 |
2 |
|
2008 |
2014 |
Nuclear cataract
|
disease |
Eye Diseases
|
Disease or Syndrome
|
39
|
11
|
0.400 |
None |
1.000 |
2 |
|
2008 |
2014 |
Congenital cataract
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Nervous System Diseases
|
Congenital Abnormality
|
105
|
104
|
0.360 |
None |
1.000 |
8 |
7
|
2002 |
2017 |
CATARACT, AUTOSOMAL DOMINANT
|
disease |
Eye Diseases
|
Disease or Syndrome
|
14
|
10
|
0.310 |
strong |
1.000 |
2 |
|
2000 |
2013 |
Cataract, Pulverulent
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
12
|
4
|
0.310 |
None |
1.000 |
2 |
|
2000 |
2013 |
Pseudoaphakia
|
disease |
Eye Diseases
|
Disease or Syndrome
|
28
|
|
0.300 |
None |
1.000 |
2 |
|
2000 |
2002 |
Lens Opacities
|
phenotype |
Eye Diseases
|
Finding
|
24
|
|
0.300 |
None |
1.000 |
2 |
|
2000 |
2002 |
Cataract microcornea syndrome
|
disease |
Eye Diseases
|
Disease or Syndrome
|
10
|
5
|
0.300 |
None |
1.000 |
2 |
|
2009 |
2012 |
Retinal Degeneration
|
phenotype |
Eye Diseases
|
Pathologic Function
|
125
|
2
|
0.200 |
None |
1.000 |
1 |
|
2007 |
2007 |
Embryonal nuclear cataract (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
16
|
1
|
0.130 |
None |
1.000 |
3 |
1
|
2008 |
2015 |
Microcornea
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
129
|
10
|
0.110 |
None |
1.000 |
1 |
1
|
2009 |
2009 |
Nystagmus, CTCAE 3.0
|
phenotype |
|
Finding
|
779
|
|
0.100 |
None |
|
0 |
|
|
|
Nystagmus, CTCAE 5.0
|
phenotype |
|
Finding
|
779
|
|
0.100 |
None |
|
0 |
|
|
|
Coloboma of iris
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Anatomical Abnormality
|
153
|
12
|
0.100 |
None |
|
0 |
|
|
|
CATARACT 2, COPPOCK-LIKE
|
disease |
|
Finding
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Nystagmus
|
disease |
Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
833
|
95
|
0.100 |
None |
|
0 |
|
|
|
Congenital coloboma of iris
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
148
|
1
|
0.100 |
None |
|
0 |
|
|
|
Myopia
|
disease |
Eye Diseases
|
Disease or Syndrome
|
490
|
167
|
0.100 |
None |
|
0 |
|
|
|
Corneal Opacity
|
phenotype |
Eye Diseases
|
Finding
|
113
|
5
|
0.100 |
None |
|
0 |
|
|
|
Microphthalmos
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
337
|
40
|
0.100 |
None |
|
0 |
1
|
|
|
Corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
113
|
25
|
0.100 |
None |
|
0 |
|
|
|
Amblyopia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
85
|
29
|
0.100 |
None |
|
0 |
|
|
|