Achromatopsia 2
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
2
|
43
|
0.940 |
None |
1.000 |
26 |
43
|
1998 |
2019 |
Oligocone trichromacy
|
disease |
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |
Color Blindness, Acquired
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
5
|
|
0.300 |
None |
1.000 |
1 |
|
2018 |
2018 |
Color Blindness, Green
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
5
|
|
0.300 |
None |
1.000 |
1 |
|
2018 |
2018 |
Color Blindness, Inherited
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
5
|
|
0.300 |
None |
1.000 |
1 |
|
2018 |
2018 |
Monochromatopsia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
5
|
|
0.300 |
None |
1.000 |
1 |
|
2018 |
2018 |
Abnormal color vision
|
phenotype |
|
Finding
|
5
|
5
|
0.100 |
None |
|
0 |
1
|
|
|
Achromatopsia 3
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
6
|
106
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Progressive Cone Dystrophy
|
disease |
Eye Diseases
|
Disease or Syndrome
|
7
|
2
|
0.050 |
None |
1.000 |
5 |
|
2001 |
2010 |
Granular macular appearance
|
phenotype |
|
Finding
|
8
|
|
0.100 |
None |
|
0 |
|
|
|
Color Blindness, Red
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
9
|
1
|
0.300 |
None |
1.000 |
1 |
|
2018 |
2018 |
Hemeralopia
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
12
|
|
0.100 |
None |
|
0 |
|
|
|
Enhanced S-Cone Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
14
|
21
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Cone monochromatism
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
16
|
9
|
0.120 |
None |
1.000 |
2 |
|
2002 |
2014 |
Dyschromatopsia
|
disease |
|
Disease or Syndrome
|
19
|
1
|
0.100 |
None |
|
0 |
|
|
|
Achromatopsia 1
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
20
|
14
|
0.100 |
None |
0.978 |
46 |
9
|
1998 |
2019 |
Color Blindness, Red-Green
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
24
|
|
0.300 |
None |
1.000 |
1 |
|
2018 |
2018 |
Color Blindness, Blue
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
25
|
12
|
0.300 |
None |
1.000 |
1 |
|
2018 |
2018 |
Cone dysfunction syndrome
|
disease |
|
Disease or Syndrome
|
25
|
2
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Pendular Nystagmus
|
disease |
Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
25
|
2
|
0.100 |
None |
|
0 |
|
|
|
Retinal pigment epithelial atrophy
|
phenotype |
|
Finding
|
25
|
4
|
0.100 |
None |
|
0 |
|
|
|
Foveal hypoplasia (finding)
|
phenotype |
|
Finding
|
25
|
4
|
0.100 |
None |
|
0 |
|
|
|
Achromatopsia
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
26
|
63
|
0.800 |
strong |
0.982 |
56 |
23
|
2000 |
2019 |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
26
|
9
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
obsolete Rod-cone dystrophy
|
disease |
|
Disease or Syndrome
|
29
|
41
|
0.100 |
None |
|
0 |
1
|
|
|