Search results for rom1

42 hits were found for rom1

# Family MCID Name MIFTS Score
1
P RTN008 Retinitis Pigmentosa 79 6.122
2
c RTN069 Retinitis Pigmentosa 7 44 4.516
3
RTN023 Retinitis 46 4.194
4
P RTN016 Retinal Degeneration 53 3.289
5
P VTL001 Vitelliform Macular Dystrophy 42 3.136
6
P RTN018 Retinal Disease 53 2.596
7
P CNR004 Cone-Rod Dystrophy 2 73 2.520
8
P JBR020 Joubert Syndrome 1 72 2.472
9
c USH036 Usher Syndrome, Type I 60 2.472
10
EYD002 Eye Disease 58 2.472
11
FND002 Fundus Dystrophy 55 2.050
12
PTT063 Pattern Dystrophy 29 1.899
13
BST007 Best Vitelliform Macular Dystrophy 34 1.811
14
BTT011 Butterfly-Shaped Pigment Dystrophy 24 1.811
15
LBR036 Leber Plus Disease 66 1.748
16
P BRD002 Bardet-Biedl Syndrome 66 1.748
17
c BRD010 Bardet-Biedl Syndrome 1 62 1.748
18
FND001 Fundus Albipunctatus 60 1.748
19
P USH001 Usher Syndrome 60 1.748
20
P STR022 Stargardt Disease 58 1.748
21
ENH001 Enhanced S-Cone Syndrome 57 1.748
22
P CNG010 Congenital Stationary Night Blindness 54 1.748
23
P CHR637 Choroidal Dystrophy, Central Areolar, 1 50 1.748
24
c STR084 Stargardt Disease 1 47 1.748
25
NSS002 Neisseria Meningitidis Infection 47 1.748
26
MNN020 Meningococcal Infection 46 1.748
27
c RTN172 Retinitis Pigmentosa 1 44 1.748
28
P NNP021 Nanophthalmos 36 1.748
29
c EXD006 Exudative Vitreoretinopathy 5 30 1.748
30
PRP026 Peripheral Retinal Degeneration 28 1.748
31
HRD019 Hereditary Choroidal Atrophy 24 1.748
32
EYD001 Eye Degenerative Disease 24 1.748
33
P PTT054 Patterned Macular Dystrophy 22 1.748
34
PRT032 Partial Central Choroid Dystrophy 20 1.748
35
NRR001 Neuroretinitis 42 0.261
36
c INH030 Inherited Retinal Disorder 51 0.214
38
c NNS043 Nonsyndromic Retinitis Pigmentosa 27 0.107
39
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.075
40
P CND005 Cone Dystrophy 43 0.075
41
c MCL066 Macular Dystrophy, Vitelliform, 2 42 0.075
42
c MCL059 Macular Dystrophy, Patterned, 1 32 0.075
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