Search results for "[genes] RPGR"

34 hits were found for '[genes] RPGR'

# Family MCID Name MIFTS Score
1
P RTN008 Retinitis Pigmentosa 78 25.329
2
c RTN058 Retinitis Pigmentosa 3 44 23.122
3
RTN023 Retinitis 49 21.936
4
CNR002 Cone-Rod Dystrophy 65 19.346
5
RTN104 Retinitis Pigmentosa, X-Linked, and Sinorespiratory Infections, with or Without Deafness 21 16.350
6
CNR031 Cone-Rod Dystrophy, X-Linked, 1 21 14.624
7
MCL029 Macular Degeneration, X-Linked Atrophic 15 14.624
8
CND005 Cone Dystrophy 37 14.624
9
ORN006 Ornithine Transcarbamylase Deficiency 60 12.665
10
P PRM011 Primary Ciliary Dyskinesia 56 12.665
11
RTN018 Retinal Disease 55 12.665
12
P STR022 Stargardt Disease 48 12.665
13
c RTN164 Retinitis Pigmentosa Autosomal Recessive 46 12.665
14
P SNR012 Senior-Loken Syndrome-1 49 10.341
15
ALS001 Alstrom Syndrome 52 10.341
16
P LBR001 Leber Congenital Amaurosis 61 10.341
17
c ORF037 Orofaciodigital Syndrome I 43 10.341
18
c RTN162 Retinitis Pigmentosa 2 50 10.341
19
LRN001 Laurence-Moon Syndrome 36 10.341
20
P RTN016 Retinal Degeneration 50 10.341
21
c USH003 Usher Syndrome Type Ii 40 10.341
22
PRP026 Peripheral Retinal Degeneration 33 10.341
23
SPP007 Suppression Amblyopia 22 10.341
24
c JBR020 Joubert Syndrome 1 57 7.312
25
P RFS001 Refsum Disease 60 7.312
26
CHY002 Chylomicron Retention Disease 54 7.312
27
c RTN087 Retinal Degeneration, Late-Onset, Autosomal Dominant 40 7.312
28
c LBR014 Leber Congenital Amaurosis 4 41 7.312
29
c CNG201 Congenital Disorder of Glycosylation, Type Iij 26 7.312
30
P ACH003 Achromatopsia 48 7.312
31
c LBR017 Leber Congenital Amaurosis 7 32 7.312
32
RHY001 Rhyns Syndrome 35 7.312
33
CNR003 Cone-Rod Dystrophy 1 23 7.312
34
c RPG004 Rpgr-Related Retinitis Pigmentosa 9 7.312