Search results for grk1

60 hits were found for grk1

# Family MCID Name MIFTS Score
1
P OGC005 Oguchi Disease 45 44.954
2
c OGC002 Oguchi Disease 2 35 44.337
3
P CNG010 Congenital Stationary Night Blindness 56 33.254
4
P NGH001 Night Blindness 52 23.855
5
P RTN008 Retinitis Pigmentosa 80 19.222
6
P RTN016 Retinal Degeneration 52 17.366
7
c OGC001 Oguchi Disease 1 39 16.400
8
ENH001 Enhanced S-Cone Syndrome 58 13.240
9
P CNR004 Cone-Rod Dystrophy 2 74 12.078
11
P JBR020 Joubert Syndrome 1 74 11.108
12
P CND005 Cone Dystrophy 47 10.905
13
FND001 Fundus Albipunctatus 55 10.818
14
P RTN209 Retinoschisis 1, X-Linked, Juvenile 60 10.117
15
LBR036 Leber Plus Disease 66 9.370
16
c LBR004 Leber Congenital Amaurosis 1 52 8.721
17
P ACH003 Achromatopsia 62 8.368
18
PRL047 Prolonged Electroretinal Response Suppression 43 7.855
19
c NGH025 Night Blindness, Congenital Stationary, Type 2a 44 7.154
20
c RTN048 Retinitis Pigmentosa 19 39 7.154
21
P STR022 Stargardt Disease 61 7.154
22
P USH001 Usher Syndrome 64 7.154
23
PRT114 Prothrombin Thrombophilia 25 7.154
24
c MYS048 Myasthenic Syndrome, Congenital, 3a, Slow-Channel 34 7.154
25
c USH035 Usher Syndrome Type 2 52 7.154
26
FND002 Fundus Dystrophy 55 7.154
27
ABN003 Abnormal Threshold of Rods 22 7.154
28
EYD001 Eye Degenerative Disease 25 7.154
29
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 6.760
30
NRR001 Neuroretinitis 42 6.393
31
RTN023 Retinitis 46 6.393
32
PPL052 Papillomatosis, Confluent and Reticulated 34 3.512
33
P RTN018 Retinal Disease 53 2.901
34
c RTN162 Retinitis Pigmentosa 2 45 2.365
35
HLX001 Helix Syndrome 48 2.365
36
RTN017 Retinal Detachment 60 1.982
37
GNY003 Guanylate Cyclase 2e, Pseudogene 12 1.401
38
ATS010 Autosomal Recessive Disease 42 1.214
39
CLP005 Ciliopathy 41 0.991
40
HMC014 Homocysteinemia 52 0.991
41
P RTN024 Retinoblastoma 73 0.991
42
P CHR345 Chronic Pain 50 0.991
43
P BRS047 Breast Cancer 98 0.811
44
LTN004 Late-Onset Retinal Degeneration 60 0.747
45
P LBR014 Leber Congenital Amaurosis 4 56 0.747
46
P TRN020 Turner Syndrome 67 0.747
47
SYN149 Syndromic Rod-Cone Dystrophy 21 0.701
48
P MCK013 Meckel Syndrome, Type 1 64 0.701
49
c NGH010 Night Blindness, Congenital Stationary, Autosomal Dominant 2 46 0.701
50
P PLY006 Polydactyly 59 0.701
51
c NPH031 Nephronophthisis 3 46 0.701
52
MVL001 Mevalonic Aciduria 66 0.701
53
P SCL018 Scoliosis 57 0.701
54
P BRD002 Bardet-Biedl Syndrome 66 0.701
55
P NPH005 Nephronophthisis 56 0.701
56
P HRT032 Heart Disease 81 0.701
57
KRT002 Keratomalacia 55 0.701
58
CNG034 Congestive Heart Failure 69 0.701
59
P CLR023 Colorectal Cancer 100 0.573
60
P PNC035 Pancreatic Cancer 86 0.573
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