Search results for "[genes] RPGR"

37 hits were found for '[genes] RPGR'

# Family MCID Name MIFTS Score
1
P RTN008 Retinitis Pigmentosa 80 26.116
2
c RTN058 Retinitis Pigmentosa 3 44 22.905
3
RTN023 Retinitis 50 21.729
4
RTN104 Retinitis Pigmentosa, X-Linked, and Sinorespiratory Infections, with or Without Deafness 20 19.164
5
CNR002 Cone-Rod Dystrophy 64 16.196
6
P LBR001 Leber Congenital Amaurosis 61 16.196
7
P RTN016 Retinal Degeneration 54 16.196
8
CND005 Cone Dystrophy 39 16.196
9
ORN006 Ornithine Transcarbamylase Deficiency 61 14.486
10
P PRM011 Primary Ciliary Dyskinesia 57 14.486
11
P STR022 Stargardt Disease 56 14.486
12
RTN018 Retinal Disease 53 14.486
13
c RTN162 Retinitis Pigmentosa 2 48 14.486
14
CNR031 Cone-Rod Dystrophy, X-Linked, 1 26 14.486
15
MCL029 Macular Degeneration, X-Linked Atrophic 16 14.486
16
ALS001 Alstrom Syndrome 53 12.545
17
P SNR012 Senior-Loken Syndrome-1 49 12.545
18
FND002 Fundus Dystrophy 46 12.545
19
c ORF037 Orofaciodigital Syndrome I 46 12.545
20
CNR007 Cone-Rod Dystrophy 6 46 12.545
21
LRN001 Laurence-Moon Syndrome 38 12.545
22
PRP026 Peripheral Retinal Degeneration 34 12.545
23
SPP007 Suppression Amblyopia 26 12.545
24
CNR003 Cone-Rod Dystrophy 1 25 12.545
25
c RPG004 Rpgr-Related Retinitis Pigmentosa 9 12.545
26
c JBR020 Joubert Syndrome 1 60 10.243
27
P ACH003 Achromatopsia 55 10.243
28
P CNG010 Congenital Stationary Night Blindness 53 10.243
29
c RTN087 Retinal Degeneration, Late-Onset, Autosomal Dominant 43 10.243
30
c RTN055 Retinitis Pigmentosa 26 41 10.243
31
c RTN043 Retinitis Pigmentosa 13 40 10.243
32
c USH034 Usher Syndrome, Type 2d 39 10.243
33
c RTN136 Retinitis Pigmentosa 44 37 10.243
34
c RTN088 Retinitis Pigmentosa-50 33 10.243
35
c RTN178 Retinitis Pigmentosa 72 22 10.243
36
c RTN161 Retinitis Pigmentosa, X-Linked Recessive, 6 21 10.243
37
CLR096 Ciliary Dyskinesia, Primary, 1, with or Without Situs Inversus 40 7.243