Search results for atxn2

71 hits were found for atxn2

# Family MCID Name MIFTS Score
1
c SPN301 Spinocerebellar Ataxia 2 58 6.282
2
P PRK057 Parkinson Disease, Late-Onset 78 4.445
3
P LTR001 Lateral Sclerosis 54 3.758
4
c AMY091 Amyotrophic Lateral Sclerosis 1 89 3.342
5
P DMN002 Dementia 66 2.934
6
P MCH002 Machado-Joseph Disease 62 2.906
7
DNT005 Dentatorubral-Pallidoluysian Atrophy 54 2.875
8
P FRD001 Friedreich Ataxia 64 2.840
9
c HRD026 Hereditary Ataxia 48 2.840
10
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 2.814
11
P FRN006 Frontotemporal Dementia 68 2.480
12
c HRD010 Hereditary Spastic Paraplegia 66 2.361
13
P RTN008 Retinitis Pigmentosa 79 2.319
14
c HMC039 Hemochromatosis, Type 1 74 2.319
15
P RST001 Restless Legs Syndrome 54 2.319
16
P TRM003 Tremor 54 2.319
17
c SPN291 Spinocerebellar Ataxia 7 52 2.319
18
P OLV001 Olivopontocerebellar Atrophy 51 2.319
19
c SPN296 Spinocerebellar Ataxia 17 51 2.319
20
c SPN105 Spinocerebellar Ataxia 4 47 2.319
21
c SPN293 Spinocerebellar Ataxia 12 45 2.319
22
P SPR120 Supranuclear Palsy, Progressive, 1 68 1.771
23
SLT014 Salt and Pepper Developmental Regression Syndrome 43 1.736
24
c PRG001 Progressive Muscular Atrophy 42 1.694
25
c PRM015 Primary Cerebellar Degeneration 36 1.694
26
P CHR071 Charcot-Marie-Tooth Disease 65 1.640
27
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 62 1.640
28
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 61 1.640
29
P EPS003 Episodic Ataxia 59 1.640
30
P SPN309 Spinocerebellar Ataxia 6 59 1.640
31
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 1.640
32
c SPN294 Spinocerebellar Ataxia 1 53 1.640
33
c AMY045 Amyotrophic Lateral Sclerosis 4, Juvenile 48 1.640
34
c SPN314 Spinocerebellar Ataxia 10 45 1.640
35
MNT229 Mental Retardation, X-Linked, with Cerebellar Hypoplasia and Distinctive Facial Appearance 45 1.640
36
CRB027 Cerebellar Disease 44 1.640
37
c SPN265 Spinocerebellar Ataxia 36 42 1.640
38
c SPN304 Spinocerebellar Ataxia 8 41 1.640
39
c AMY069 Amyotrophic Lateral Sclerosis 21 40 1.640
40
DRM021 Dermatopathia Pigmentosa Reticularis 39 1.640
41
MLT177 Multisystem Proteinopathy 30 1.640
42
c SPS118 Spastic Paraplegia 36, Autosomal Dominant 27 1.640
43
XLN191 X-Linked Hereditary Ataxia 18 1.640
44
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.321
45
P MTR014 Motor Neuron Disease 65 0.113
46
P ALZ034 Alzheimer Disease 88 0.093
47
P MSC003 Muscular Atrophy 52 0.093
48
P RHM011 Rheumatoid Arthritis 80 0.065
49
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.065
50
P SCH015 Schizophrenia 74 0.065
51
P HNT016 Huntington Disease 72 0.065
52
c LKM063 Leukemia, Chronic Myeloid 72 0.065
53
MLT157 Multiple System Atrophy 1 70 0.065
54
P HYP086 Hypothyroidism 69 0.065
55
P LKM062 Leukemia, Acute Lymphoblastic 69 0.065
56
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.065
57
c JVN010 Juvenile Rheumatoid Arthritis 64 0.065
58
c GLC092 Glaucoma, Primary Open Angle 62 0.065
59
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.065
60
LPD008 Lipid Metabolism Disorder 62 0.065
61
c JVN061 Juvenile Arthritis 60 0.065
62
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.065
63
APH002 Aphasia 57 0.065
64
P PLY019 Polyneuropathy 56 0.065
65
P ANT006 Antiphospholipid Syndrome 55 0.065
66
PRP016 Paraplegia 52 0.065
67
47X002 47,xyy 49 0.065
68
P OPN001 Open-Angle Glaucoma 49 0.065
69
SPS057 Spasticity 45 0.065
70
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.065
71
SPN050 Spinocerebellar Degeneration 42 0.065
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