Search results for "[genes] RPGR"

36 hits were found for '[genes] RPGR'

# Family MCID Name MIFTS Score
1
P RTN008 Retinitis Pigmentosa 79 26.155
2
c RTN058 Retinitis Pigmentosa 3 45 22.940
3
RTN023 Retinitis 49 21.762
4
CNR002 Cone-Rod Dystrophy 68 17.769
5
RTN104 Retinitis Pigmentosa, X-Linked, and Sinorespiratory Infections, with or Without Deafness 20 16.221
6
P MYP006 Myopia 59 14.508
7
P RTN016 Retinal Degeneration 54 14.508
8
CND005 Cone Dystrophy 38 14.508
9
CNR031 Cone-Rod Dystrophy, X-Linked, 1 24 14.508
10
MCL029 Macular Degeneration, X-Linked Atrophic 16 14.508
11
ORN006 Ornithine Transcarbamylase Deficiency 61 12.565
12
P LBR001 Leber Congenital Amaurosis 60 12.565
13
P PRM011 Primary Ciliary Dyskinesia 58 12.565
14
RTN018 Retinal Disease 56 12.565
15
P STR022 Stargardt Disease 54 12.565
16
ALS001 Alstrom Syndrome 52 10.259
17
c RTN162 Retinitis Pigmentosa 2 51 10.259
18
P SNR012 Senior-Loken Syndrome-1 49 10.259
19
FND002 Fundus Dystrophy 46 10.259
20
c ORF037 Orofaciodigital Syndrome I 46 10.259
21
CNR007 Cone-Rod Dystrophy 6 45 10.259
22
c USH003 Usher Syndrome Type Ii 42 10.259
23
LRN001 Laurence-Moon Syndrome 38 10.259
24
PRP026 Peripheral Retinal Degeneration 34 10.259
25
SPP007 Suppression Amblyopia 27 10.259
26
P RFS001 Refsum Disease 62 7.254
27
c JBR020 Joubert Syndrome 1 59 7.254
28
CHY002 Chylomicron Retention Disease 59 7.254
29
P ACH003 Achromatopsia 53 7.254
30
P CNG010 Congenital Stationary Night Blindness 50 7.254
31
c LBR014 Leber Congenital Amaurosis 4 47 7.254
32
c RTN087 Retinal Degeneration, Late-Onset, Autosomal Dominant 43 7.254
33
RHY001 Rhyns Syndrome 33 7.254
34
CRT065 Cortisone Reductase Deficiency 1 32 7.254
35
CNR003 Cone-Rod Dystrophy 1 24 7.254
36
c RPG004 Rpgr-Related Retinitis Pigmentosa 9 7.254