Search results for ATXN8OS

38 hits were found for ATXN8OS

# Family MCID Name MIFTS Score
1
c SPN304 Spinocerebellar Ataxia 8 41 4.792
2
P PRK057 Parkinson Disease, Late-Onset 78 3.655
3
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 2.585
4
P MCH002 Machado-Joseph Disease 62 2.543
5
P FRD001 Friedreich Ataxia 64 2.494
6
c SPN301 Spinocerebellar Ataxia 2 58 2.494
7
c SPN294 Spinocerebellar Ataxia 1 53 2.494
8
c HRD026 Hereditary Ataxia 48 2.494
9
c SPN293 Spinocerebellar Ataxia 12 45 2.494
10
c MYT021 Myotonic Dystrophy 1 69 1.763
11
P SPN309 Spinocerebellar Ataxia 6 59 1.763
12
c MYT020 Myotonic Dystrophy 2 57 1.763
13
c SPN291 Spinocerebellar Ataxia 7 52 1.763
14
c HNT004 Huntington Disease-Like 2 50 1.763
15
c HLP028 Holoprosencephaly 5 45 1.763
16
c SPN314 Spinocerebellar Ataxia 10 45 1.763
17
FCH001 Fuchs' Endothelial Dystrophy 44 1.763
18
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 43 1.763
19
c SPN265 Spinocerebellar Ataxia 36 42 1.763
20
c FML363 Familial Adult Myoclonic Epilepsy 41 1.763
21
c SPN266 Spinocerebellar Ataxia 35 39 1.763
22
c SPN283 Spinocerebellar Ataxia 37 36 1.763
23
MYT003 Myotonic Disease 35 1.763
24
c SPS105 Spastic Paraplegia 37, Autosomal Dominant 31 1.763
25
c SPS198 Spastic Paraplegia 16, X-Linked 30 1.763
26
c SPS102 Spastic Paraplegia 25, Autosomal Recessive 30 1.763
27
c SPS110 Spastic Paraplegia 19, Autosomal Dominant 29 1.763
28
c SPS068 Spastic Paraplegia 14, Autosomal Recessive 29 1.763
29
c SPS094 Spastic Paraplegia 29, Autosomal Dominant 28 1.763
30
c SPS111 Spastic Paraplegia 27, Autosomal Recessive 28 1.763
31
c SPS062 Spastic Paraplegia 34, X-Linked 28 1.763
32
XLN191 X-Linked Hereditary Ataxia 18 1.763
33
c 46X050 46,xx Sex Reversal 3 17 1.763
34
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.110
35
P BRS047 Breast Cancer 97 0.077
36
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.077
37
P LTR001 Lateral Sclerosis 54 0.077
38
DNT005 Dentatorubral-Pallidoluysian Atrophy 54 0.077
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