Search results for nrl

55 hits were found for nrl

# Family MCID Name MIFTS Score
1
P RTN008 Retinitis Pigmentosa 79 6.070
2
c RTN131 Retinitis Pigmentosa 27 33 5.190
3
RTN023 Retinitis 46 4.391
4
ENH001 Enhanced S-Cone Syndrome 57 4.237
5
P RTN016 Retinal Degeneration 53 4.182
6
P RTN018 Retinal Disease 53 2.696
7
LBR036 Leber Plus Disease 66 2.639
8
P NGH001 Night Blindness 48 2.639
9
OCL008 Oculopharyngeal Muscular Dystrophy 53 2.606
11
P CNR004 Cone-Rod Dystrophy 2 73 2.524
12
DGN006 Digenic Disease 25 2.524
13
FND002 Fundus Dystrophy 55 2.238
14
P ACH003 Achromatopsia 61 1.887
15
P STR022 Stargardt Disease 58 1.785
16
EYD002 Eye Disease 58 1.785
17
OPT070 Optic Nerve Hypoplasia, Bilateral 56 1.785
18
P CNG010 Congenital Stationary Night Blindness 54 1.785
19
c NPH031 Nephronophthisis 3 45 1.785
20
c RTN172 Retinitis Pigmentosa 1 44 1.785
21
LTX001 Latex Allergy 41 1.785
23
P NNP021 Nanophthalmos 36 1.785
24
c RTN070 Retinitis Pigmentosa 9 34 1.785
25
DGN003 Degeneration of Macula and Posterior Pole 29 1.785
26
PHS028 Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial 24 1.785
27
HMP030 Haemophilus Meningitis 24 1.785
28
EYD001 Eye Degenerative Disease 24 1.785
29
c DFN177 Deafness, Autosomal Recessive 5 22 1.785
30
VGT003 Vegetable Allergy 14 1.785
31
NRR001 Neuroretinitis 42 0.320
32
c INH030 Inherited Retinal Disorder 51 0.288
33
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.171
34
P RTN024 Retinoblastoma 73 0.121
35
c FML008 Familial Retinoblastoma 53 0.121
36
P CND005 Cone Dystrophy 43 0.121
37
P MSC005 Muscular Dystrophy 66 0.099
38
RTN017 Retinal Detachment 61 0.099
39
ALB002 Albinism 46 0.099
40
P CLR023 Colorectal Cancer 99 0.070
41
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.070
42
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.070
43
P MDL005 Medulloblastoma 77 0.070
44
P ATS364 Autism 70 0.070
45
P TRN020 Turner Syndrome 67 0.070
46
P LTR001 Lateral Sclerosis 54 0.070
47
c LBR004 Leber Congenital Amaurosis 1 52 0.070
48
PTH003 Pathologic Nystagmus 52 0.070
49
c ACH020 Achromatopsia 2 50 0.070
50
ATS010 Autosomal Recessive Disease 48 0.070
51
AST006 Astigmatism 47 0.070
52
CLN045 Colonic Benign Neoplasm 46 0.070
53
RFR003 Refractive Error 43 0.070
54
c RTN035 Retinal Cone Dystrophy 3b 32 0.070
55
GNY003 Guanylate Cyclase 2e, Pseudogene 14 0.070
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