Search results for prph2

67 hits were found for prph2

# Family MCID Name MIFTS Score
1
c MCL059 Macular Dystrophy, Patterned, 1 40 5.339
2
P RTN008 Retinitis Pigmentosa 78 5.232
3
FND001 Fundus Albipunctatus 61 4.942
4
c RTN069 Retinitis Pigmentosa 7 43 4.861
5
c MCL060 Macular Dystrophy, Vitelliform, 3 38 4.529
6
P VTL001 Vitelliform Macular Dystrophy 45 4.266
7
c CHR449 Choroidal Dystrophy, Central Areolar 2 23 4.082
8
RTN023 Retinitis 47 3.760
9
P CHR637 Choroidal Dystrophy, Central Areolar, 1 51 3.420
10
P CNR004 Cone-Rod Dystrophy 2 72 3.270
11
P RTN016 Retinal Degeneration 54 3.247
12
P LBR001 Leber Congenital Amaurosis 68 3.196
13
P STR022 Stargardt Disease 59 2.812
14
P RTN018 Retinal Disease 53 2.751
15
P CND005 Cone Dystrophy 42 2.751
16
BTT011 Butterfly-Shaped Pigment Dystrophy 24 2.751
17
FND002 Fundus Dystrophy 52 2.473
19
c CNR007 Cone-Rod Dystrophy 6 51 2.328
20
P USH001 Usher Syndrome 60 2.260
21
c AMY091 Amyotrophic Lateral Sclerosis 1 90 2.217
22
P NGH001 Night Blindness 48 2.217
23
c RTN172 Retinitis Pigmentosa 1 43 2.217
24
PRP026 Peripheral Retinal Degeneration 29 2.217
25
c INH030 Inherited Retinal Disorder 47 1.859
26
PTT063 Pattern Dystrophy 29 1.763
27
STR046 Stargardt Macular Degeneration 31 1.666
28
MLT117 Multifocal Pattern Dystrophy Simulating Fundus Flavimaculatus 9 1.623
29
P BRD002 Bardet-Biedl Syndrome 66 1.568
30
P ACH003 Achromatopsia 61 1.568
31
EYD002 Eye Disease 59 1.568
32
GYR004 Gyrate Atrophy of Choroid and Retina 57 1.568
33
P CNG010 Congenital Stationary Night Blindness 54 1.568
34
c LBR014 Leber Congenital Amaurosis 4 54 1.568
35
DYN002 Doyne Honeycomb Retinal Dystrophy 48 1.568
36
BST008 Bestrophinopathy, Autosomal Recessive 46 1.568
37
c NNN011 Noonan Syndrome 4 44 1.568
38
SCT002 Scotoma 43 1.568
39
GND002 Gender Identity Disorder 41 1.568
40
c RTN054 Retinitis Pigmentosa 25 40 1.568
41
BSL037 Basal Laminar Drusen 38 1.568
42
CHR079 Choroid Disease 36 1.568
43
c JBR030 Joubert Syndrome 22 36 1.568
44
NWF001 Newfoundland Rod-Cone Dystrophy 35 1.568
45
BTH002 Bothnia Retinal Dystrophy 35 1.568
46
c RTN210 Retinitis Pigmentosa 50 34 1.568
47
c MCL071 Macular Dystrophy, Patterned, 2 33 1.568
48
DGN003 Degeneration of Macula and Posterior Pole 29 1.568
49
HRD019 Hereditary Choroidal Atrophy 24 1.568
50
DGN006 Digenic Disease 21 1.568
51
PRT032 Partial Central Choroid Dystrophy 21 1.568
52
EYD001 Eye Degenerative Disease 19 1.568
53
P PTT054 Patterned Macular Dystrophy 15 1.568
54
EGD001 Ego-Dystonic Sexual Orientation 7 1.568
55
NRR001 Neuroretinitis 43 0.233
56
P PRS040 Prostate Cancer 98 0.095
57
c MCL066 Macular Dystrophy, Vitelliform, 2 42 0.095
58
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.067
59
P SNS001 Sensorineural Hearing Loss 61 0.067
60
c USH036 Usher Syndrome, Type I 60 0.067
61
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.067
62
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 0.067
63
c USH035 Usher Syndrome Type 2 46 0.067
64
HRD016 Hereditary Retinal Dystrophy 37 0.067
65
c RTN064 Retinitis Pigmentosa 35 35 0.067
66
BST007 Best Vitelliform Macular Dystrophy 33 0.067
67
c CHR665 Choroidal Dystrophy, Central Areolar, 3 16 0.067
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