Search results for cnga3

Showing 25 of 151 hits for cnga3
# Family MCID Name MIFTS Score
1
c ACH020 Achromatopsia 2 52 65.025
2
P ACH003 Achromatopsia 61 47.377
3
FND002 Fundus Dystrophy 55 28.259
4
P CNR004 Cone-Rod Dystrophy 2 78 27.095
5
P CND005 Cone Dystrophy 47 24.660
6
P EYD002 Eye Disease 59 21.987
7
P CLR019 Color Blindness 51 20.888
9
c PRG059 Progressive Cone Dystrophy 51 12.798
10
PTH003 Pathologic Nystagmus 47 10.810
11
P RTN008 Retinitis Pigmentosa 80 9.939
12
ENH001 Enhanced S-Cone Syndrome 59 9.644
13
P RTN209 Retinoschisis 1, X-Linked, Juvenile 60 9.605
14
P AML002 Amelogenesis Imperfecta 55 9.497
15
c ACH021 Achromatopsia 3 47 9.093
16
TRT020 Tritanopia 49 8.641
17
LBR036 Leber Plus Disease 70 8.615
18
PRP026 Peripheral Retinal Degeneration 45 7.985
19
P CNG024 Congenital Nystagmus 40 7.743
20
c RTN055 Retinitis Pigmentosa 26 45 7.620
21
P STR022 Stargardt Disease 62 7.028
22
BLC001 Blue Cone Monochromacy 48 6.941
23
c ACH023 Achromatopsia 4 37 6.941
24
RDG001 Red-Green Color Blindness 33 6.866
25
P CNG010 Congenital Stationary Night Blindness 54 6.866
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