CONE DYSTROPHY 3 (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
3
|
6
|
0.720 |
None |
1.000 |
9 |
6
|
1998 |
2011 |
Cone-Rod Dystrophy 2
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
254
|
51
|
0.370 |
None |
1.000 |
8 |
2
|
2001 |
2019 |
Progressive cone dystrophy (without rod involvement)
|
disease |
Eye Diseases
|
Disease or Syndrome
|
9
|
6
|
0.300 |
None |
1.000 |
2 |
|
1998 |
2005 |
Central areolar choroidal sclerosis
|
disease |
Eye Diseases
|
Disease or Syndrome
|
10
|
5
|
0.300 |
None |
1.000 |
1 |
|
2017 |
2017 |
Disorder of eye
|
group |
Eye Diseases
|
Disease or Syndrome
|
400
|
14
|
0.300 |
None |
|
0 |
|
|
|
Cone-Rod Dystrophies
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
86
|
53
|
0.200 |
None |
1.000 |
10 |
2
|
1999 |
2019 |
Retinitis Pigmentosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
546
|
541
|
0.140 |
None |
1.000 |
5 |
2
|
1998 |
2013 |
Retinal Dystrophies
|
group |
Eye Diseases
|
Disease or Syndrome
|
219
|
227
|
0.120 |
None |
1.000 |
2 |
2
|
2005 |
2019 |
Photophobia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Sign or Symptom
|
227
|
7
|
0.120 |
None |
1.000 |
2 |
|
2002 |
2018 |
Macular dystrophy
|
disease |
Eye Diseases
|
Disease or Syndrome
|
52
|
59
|
0.110 |
None |
1.000 |
3 |
2
|
1998 |
2019 |
Cone Dystrophy
|
disease |
Eye Diseases
|
Disease or Syndrome
|
48
|
31
|
0.100 |
None |
0.900 |
10 |
|
1999 |
2019 |
Usher Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
68
|
74
|
0.100 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Abnormality of retinal pigmentation
|
phenotype |
|
Finding
|
215
|
5
|
0.100 |
None |
|
0 |
|
|
|
Electroretinogram abnormal
|
phenotype |
|
Finding
|
158
|
10
|
0.100 |
None |
|
0 |
|
|
|
Reduced visual acuity
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Finding
|
147
|
10
|
0.100 |
None |
|
0 |
|
|
|
Retinal pigment epithelial mottling
|
phenotype |
|
Finding
|
16
|
2
|
0.100 |
None |
|
0 |
|
|
|
Slow decrease in visual acuity
|
phenotype |
|
Finding
|
27
|
3
|
0.100 |
None |
|
0 |
|
|
|
Dyschromatopsia
|
disease |
|
Disease or Syndrome
|
19
|
1
|
0.100 |
None |
|
0 |
|
|
|
Drusen
|
disease |
|
Disease or Syndrome
|
57
|
18
|
0.100 |
None |
|
0 |
|
|
|
Atrophoderma maculatum
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
39
|
2
|
0.100 |
None |
|
0 |
|
|
|
Progressive visual loss
|
phenotype |
|
Finding
|
77
|
11
|
0.100 |
None |
|
0 |
|
|
|
Atrophic macular change
|
phenotype |
|
Finding
|
24
|
1
|
0.100 |
None |
|
0 |
|
|
|
Color vision defect
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
94
|
4
|
0.100 |
None |
|
0 |
|
|
|
Hyperautofluorescent macular lesion
|
phenotype |
|
Finding
|
4
|
|
0.100 |
None |
|
0 |
|
|
|
Nyctalopia
|
disease |
Eye Diseases
|
Disease or Syndrome
|
168
|
18
|
0.100 |
None |
|
0 |
|
|
|