Search results for prph2

33 hits were found for prph2

# Family MCID Name MIFTS Score
1
c MCL059 Macular Dystrophy, Patterned, 1 26 6.768
2
FND001 Fundus Albipunctatus 53 6.609
3
P RTN008 Retinitis Pigmentosa 81 6.229
4
c RTN069 Retinitis Pigmentosa 7 37 5.906
5
P VTL001 Vitelliform Macular Dystrophy 42 5.894
6
c MCL060 Macular Dystrophy, Vitelliform, 3 38 5.709
7
c CHR449 Choroidal Dystrophy, Central Areolar 2 17 5.250
8
P CHR637 Choroidal Dystrophy, Central Areolar, 1 40 5.038
9
RTN023 Retinitis 50 4.671
10
P RTN016 Retinal Degeneration 54 4.520
11
P LBR001 Leber Congenital Amaurosis 64 4.098
12
P STR022 Stargardt Disease 59 3.736
13
CNR004 Cone-Rod Dystrophy 2 67 3.702
14
BTT011 Butterfly-Shaped Pigment Dystrophy 25 3.702
15
RTN018 Retinal Disease 56 3.665
16
c RTN172 Retinitis Pigmentosa 1 39 3.174
17
FND002 Fundus Dystrophy 49 2.937
18
c MCL042 Macular Degeneration, Age-Related, 1 84 2.786
19
STR046 Stargardt Macular Degeneration 30 2.642
20
PRL047 Prolonged Electroretinal Response Suppression 34 2.592
21
P BST001 Bestrophinopathy 33 2.592
22
PRP026 Peripheral Retinal Degeneration 29 2.592
23
HRD019 Hereditary Choroidal Atrophy 25 2.592
24
PRT032 Partial Central Choroid Dystrophy 23 2.592
25
EYD001 Eye Degenerative Disease 20 2.592
26
MLT117 Multifocal Pattern Dystrophy Simulating Fundus Flavimaculatus 6 1.898
27
P PRS040 Prostate Cancer 90 0.157
28
c LTN004 Late-Onset Retinal Degeneration 40 0.157
29
c LBR014 Leber Congenital Amaurosis 4 49 0.136
30
CHR008 Choroiditis 46 0.111
31
P USH001 Usher Syndrome 58 0.079
32
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 45 0.079
33
RTN187 Retinitis Pigmentosa-Deafness Syndrome 43 0.079
Content
Loading form....