Search results for prph2

37 hits were found for prph2

# Family MCID Name MIFTS Score
1
P RTN008 Retinitis Pigmentosa 80 5.714
2
c MCL059 Macular Dystrophy, Patterned, 1 25 4.975
3
c MCL060 Macular Dystrophy, Vitelliform, 3 38 4.912
4
P RTN016 Retinal Degeneration 54 4.626
5
CHR406 Choriodal Dystrophy, Central Areolar 2 18 4.533
6
RTN023 Retinitis 50 4.413
7
RTN175 Retinitis Pigmentosa 7 and Digenic 38 4.398
8
P FND001 Fundus Albipunctatus 55 3.977
9
P STR022 Stargardt Disease 56 3.949
10
CNR002 Cone-Rod Dystrophy 64 3.886
11
P VTL001 Vitelliform Macular Dystrophy 38 3.512
12
PRT032 Partial Central Choroid Dystrophy 26 3.512
13
BTT011 Butterfly-Shaped Pigment Dystrophy 24 3.512
14
P LBR001 Leber Congenital Amaurosis 61 3.476
15
RTN018 Retinal Disease 53 3.476
16
c RTN172 Retinitis Pigmentosa 1 43 3.476
17
STR046 Stargardt Macular Degeneration 29 3.051
18
c PRP047 Prph2-Related Retinitis Pigmentosa 10 3.051
19
c PRP044 Prph2-Related Adult-Onset Vitelliform Macular Dystrophy 6 3.051
20
MLT117 Multifocal Pattern Dystrophy Simulating Fundus Flavimaculatus 6 3.051
21
c PRP046 Prph2-Related Fundus Albipunctatus 5 3.051
22
CNR035 Cone-Rod Dystrophy, Prph2-Related 3 3.051
23
c MCL042 Macular Degeneration, Age-Related, 1 73 3.010
24
BRD009 Bradyopsia 37 3.010
25
PRP026 Peripheral Retinal Degeneration 34 3.010
26
EYD001 Eye Degenerative Disease 30 3.010
27
CHR080 Choroidal Sclerosis 26 3.010
28
P BST001 Bestrophinopathy 26 3.010
29
HRD019 Hereditary Choroidal Atrophy 25 3.010
30
c RTN087 Retinal Degeneration, Late-Onset, Autosomal Dominant 43 2.458
31
c MCL066 Macular Dystrophy, Vitelliform, 2 43 2.458
32
CNR016 Cone-Rod Dystrophy 7 29 2.458
33
P PTT054 Patterned Macular Dystrophy 22 2.199
34
RHY001 Rhyns Syndrome 32 0.188
35
P USH001 Usher Syndrome 53 0.077
36
c LBR004 Leber Congenital Amaurosis 1 44 0.077
37
CHR008 Choroiditis 44 0.077
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