Search results for "[genes] RPGR"

30 hits were found for '[genes] RPGR'

# Family MCID Name MIFTS Score
1
P RTN008 Retinitis Pigmentosa 81 26.931
2
RTN023 Retinitis 51 22.408
3
c RTN058 Retinitis Pigmentosa 3 41 22.408
4
CNR002 Cone-Rod Dystrophy 63 18.296
5
P LBR001 Leber Congenital Amaurosis 61 14.939
6
P MYP006 Myopia 57 14.939
7
P RTN016 Retinal Degeneration 51 14.939
8
CND005 Cone Dystrophy 41 14.939
9
CNR031 Cone-Rod Dystrophy, X-Linked, 1 20 14.939
10
RTN104 Retinitis Pigmentosa, X-Linked, and Sinorespiratory Infections, with or Without Deafness 16 14.939
11
MCL029 Macular Degeneration, X-Linked Atrophic 11 14.939
12
RTN018 Retinal Disease 58 12.937
13
P PRM011 Primary Ciliary Dyskinesia 58 12.937
14
P STR022 Stargardt Disease 52 12.937
15
ALS001 Alstrom Syndrome 50 10.563
16
P SNR012 Senior-Loken Syndrome-1 49 10.563
17
c RTN162 Retinitis Pigmentosa 2 48 10.563
18
CNR007 Cone-Rod Dystrophy 6 47 10.563
19
c ORF037 Orofaciodigital Syndrome I 47 10.563
20
LRN001 Laurence-Moon Syndrome 37 10.563
21
PRP026 Peripheral Retinal Degeneration 36 10.563
22
SPP007 Suppression Amblyopia 25 10.563
23
c JBR020 Joubert Syndrome 1 57 7.469
24
P ACH003 Achromatopsia 51 7.469
25
P CNG010 Congenital Stationary Night Blindness 51 7.469
26
c LBR017 Leber Congenital Amaurosis 7 27 7.469
27
CNR003 Cone-Rod Dystrophy 1 22 7.469
28
c CNG201 Congenital Disorder of Glycosylation, Type Iij 22 7.469
29
c RPG004 Rpgr-Related Retinitis Pigmentosa 12 7.469
30
PRM230 Primary Ciliary Dyskinesia-Retinitis Pigmentosa Syndrome 5 7.469