Search results for NMNAT1

29 hits were found for NMNAT1

# Family MCID Name MIFTS Score
1
c LBR019 Leber Congenital Amaurosis 9 43 6.684
2
P LBR001 Leber Congenital Amaurosis 67 6.198
3
WLL004 Wallerian Degeneration 39 3.140
4
P RTN016 Retinal Degeneration 53 3.022
5
P CNR004 Cone-Rod Dystrophy 2 71 2.987
6
P KRT007 Keratoconus 49 2.852
7
P PLL002 Pellagra 45 2.852
8
FND002 Fundus Dystrophy 51 2.287
9
P RTN008 Retinitis Pigmentosa 77 2.085
10
P ACH003 Achromatopsia 60 2.016
11
CLB010 Coloboma of Macula 53 2.016
12
c LBR004 Leber Congenital Amaurosis 1 52 2.016
13
PTH003 Pathologic Nystagmus 51 2.016
14
BTT001 Bietti Crystalline Corneoretinal Dystrophy 47 2.016
15
c LBR007 Leber Congenital Amaurosis 12 40 2.016
16
c LBR009 Leber Congenital Amaurosis 14 40 2.016
17
c LBR010 Leber Congenital Amaurosis 15 39 2.016
18
c RTN106 Retinitis Pigmentosa 51 36 2.016
19
c INH030 Inherited Retinal Disorder 47 0.202
20
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.143
21
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.117
22
P RTN018 Retinal Disease 52 0.117
23
c CNR007 Cone-Rod Dystrophy 6 51 0.117
24
P NRV007 Nervous System Disease 66 0.082
25
P NRP001 Neuropathy 56 0.082
26
RTN003 Retinal Ischemia 50 0.082
27
RTN023 Retinitis 46 0.082
28
NRR001 Neuroretinitis 43 0.082
29
IMM165 Immunoglobulin Switch Sequences 15 0.082
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