Search results for ATXN3

62 hits were found for ATXN3

# Family MCID Name MIFTS Score
1
P MCH002 Machado-Joseph Disease 63 5.225
2
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 3.103
3
P HNT016 Huntington Disease 71 2.779
4
c SPN301 Spinocerebellar Ataxia 2 59 2.747
5
P DMN002 Dementia 67 2.710
6
P NRC002 Narcolepsy 51 2.710
7
c HRD026 Hereditary Ataxia 48 2.710
8
P PRK057 Parkinson Disease, Late-Onset 76 2.326
9
DNT005 Dentatorubral-Pallidoluysian Atrophy 57 2.256
10
ACR006 Aceruloplasminemia 73 2.213
11
c HRD010 Hereditary Spastic Paraplegia 66 2.213
12
P DYS154 Dystonia 65 2.213
13
c DYS056 Dystonia 12 64 2.213
14
P FRD001 Friedreich Ataxia 63 2.213
15
KRN002 Kearns-Sayre Syndrome 63 2.213
16
P RST001 Restless Legs Syndrome 54 2.213
17
c SPN294 Spinocerebellar Ataxia 1 52 2.213
18
c SPN296 Spinocerebellar Ataxia 17 50 2.213
19
c SPN293 Spinocerebellar Ataxia 12 45 2.213
20
c PRM015 Primary Cerebellar Degeneration 36 2.213
21
MLT157 Multiple System Atrophy 1 70 1.622
22
c MCH013 Machado-Joseph Disease Type 3 17 1.622
23
c MCH012 Machado-Joseph Disease Type 1 17 1.622
24
c MCH014 Machado-Joseph Disease Type 2 17 1.622
25
c AMY091 Amyotrophic Lateral Sclerosis 1 89 1.565
26
c MYT021 Myotonic Dystrophy 1 66 1.565
27
c EPS035 Episodic Ataxia, Type 2 63 1.565
28
P MVM001 Movement Disease 61 1.565
29
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 61 1.565
30
P EPS003 Episodic Ataxia 60 1.565
31
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 1.565
32
P SLP005 Sleep Disorder 59 1.565
33
P SPN309 Spinocerebellar Ataxia 6 59 1.565
34
P PRP019 Peripheral Nervous System Disease 57 1.565
35
c SPN291 Spinocerebellar Ataxia 7 53 1.565
36
CHR073 Choreatic Disease 52 1.565
37
c HNT004 Huntington Disease-Like 2 49 1.565
38
c SPN101 Spinocerebellar Ataxia 29 48 1.565
39
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 46 1.565
40
NRN008 Neuronal Intranuclear Inclusion Disease 45 1.565
41
CRB027 Cerebellar Disease 45 1.565
42
MNT229 Mental Retardation, X-Linked, with Cerebellar Hypoplasia and Distinctive Facial Appearance 43 1.565
43
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 42 1.565
44
c SPN314 Spinocerebellar Ataxia 10 42 1.565
45
OCL011 Ocular Motility Disease 41 1.565
46
c ATS307 Autosomal Recessive Cerebellar Ataxia 41 1.565
47
c SPN284 Spinocerebellar Ataxia 38 41 1.565
48
c SPN304 Spinocerebellar Ataxia 8 41 1.565
49
c SPN103 Spinocerebellar Ataxia 31 38 1.565
50
MYT003 Myotonic Disease 37 1.565
51
c ATS009 Autosomal Genetic Disease 27 1.565
52
XLN228 X-Linked Recessive Disease 26 1.565
53
c XLN230 X-Linked Monogenic Disease 20 1.565
54
XLN191 X-Linked Hereditary Ataxia 19 1.565
55
c ATS461 Autosomal Dominant Cerebellar Ataxia Type I 18 1.565
56
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.293
57
P ATX030 Ataxia-Telangiectasia 83 0.098
58
TLN003 Telangiectasis 51 0.098
59
P BRS047 Breast Cancer 96 0.069
60
P NRB001 Neuroblastoma 71 0.069
61
P MSC003 Muscular Atrophy 52 0.069
62
SPN187 Spinocerebellar Atrophy 26 0.069
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