Search results for cacna1a

76 hits were found for cacna1a

# Family MCID Name MIFTS Score
1
c SPN309 Spinocerebellar Ataxia 6 48 5.591
2
c EPS035 Episodic Ataxia, Type 2 54 5.519
3
c MGR032 Migraine, Familial Hemiplegic, 1 32 4.501
4
c EPL172 Epileptic Encephalopathy, Early Infantile, 42 21 4.418
5
P EPS003 Episodic Ataxia 57 4.257
6
c FML023 Familial Hemiplegic Migraine 51 3.765
7
P HMP006 Hemiplegic Migraine 49 3.620
8
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 3.609
9
MGR028 Migraine with or Without Aura 1 55 3.381
10
P ALT001 Alternating Hemiplegia of Childhood 48 3.169
11
P MGR003 Migraine with Aura 56 3.124
12
P MCH002 Machado-Joseph Disease 63 3.042
13
DNT005 Dentatorubral-Pallidoluysian Atrophy 50 3.042
14
ACR006 Aceruloplasminemia 65 2.854
15
c SPR083 Sporadic Hemiplegic Migraine 33 2.836
16
HDC001 Headache 55 2.751
17
HMP005 Hemiplegia 54 2.751
18
BNG078 Benign Paroxysmal Torticollis of Infancy 9 2.751
19
P CLS010 Cluster Headache 47 2.726
20
EXF001 Exfoliation Syndrome 55 2.699
21
c SPN294 Spinocerebellar Ataxia 1 58 2.635
22
LMB002 Lambert-Eaton Myasthenic Syndrome 58 2.635
23
P FRD012 Friedreich Ataxia 1 58 2.635
24
c EPS042 Episodic Ataxia, Type 1 57 2.635
25
P CHL002 Childhood Absence Epilepsy 56 2.635
26
CRB027 Cerebellar Disease 48 2.635
27
c SPN293 Spinocerebellar Ataxia 12 47 2.635
28
MGR001 Migraine Without Aura 47 2.635
29
c SPN296 Spinocerebellar Ataxia 17 46 2.635
30
P CRB059 Cerebellar Degeneration 40 2.635
31
P TRT019 Torticollis 45 2.283
32
P SPN301 Spinocerebellar Ataxia 2 56 2.226
33
P DRR001 Diarrhea 60 2.192
34
P EPL140 Epilepsy, Idiopathic Generalized 58 2.192
35
RST001 Restless Legs Syndrome 54 2.151
36
c SPN100 Spinocerebellar Ataxia 27 44 2.151
37
HRD026 Hereditary Ataxia 43 2.151
38
MRS004 Marshall-Smith Syndrome 43 2.151
39
P EPL116 Epileptic Encephalopathy, Childhood-Onset 41 2.151
40
c SPN103 Spinocerebellar Ataxia 31 40 2.151
41
MNN006 Meninges Hemangiopericytoma 39 2.151
42
c EPS017 Episodic Ataxia, Type 6 36 2.151
43
c SPN094 Spinocerebellar Ataxia 18 36 2.151
44
PRN032 Paraneoplastic Cerebellar Degeneration 33 2.151
45
BNG018 Benign Paroxysmal Positional Nystagmus 32 2.151
46
VST001 Vestibular Neuronitis 32 2.151
47
c SPN099 Spinocerebellar Ataxia 26 30 2.151
48
c EPS015 Episodic Ataxia, Type 7 27 2.151
49
VST006 Vestibulocochlear Nerve Disease 27 2.151
50
c SPN247 Spinocerebellar Ataxia Type 19/22 26 2.151
51
c FML306 Familial or Sporadic Hemiplegic Migraine 27 1.574
52
UND011 Undetermined Early-Onset Epileptic Encephalopathy 21 1.574
53
P NRV007 Nervous System Disease 75 1.521
54
c CNT035 Central Nervous System Disease 65 1.521
55
P CNG001 Congenital Myasthenic Syndrome 55 1.521
56
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.511
57
P EPL164 Epilepsy 70 0.190
58
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.190
59
CRB009 Cerebritis 41 0.142
60
P ENC018 Encephalopathy 58 0.127
61
NRN002 Neuronitis 43 0.127
62
P ATS364 Autism 70 0.090
63
AGN016 Aging 65 0.090
64
P TRM003 Tremor 54 0.090
65
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.090
66
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.090
67
c BLD140 Blood Group, I System 37 0.090
68
CNT017 Central Nervous System Origin Vertigo 30 0.090
69
P RTT002 Rett Syndrome 82 0.063
70
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 67 0.063
71
P DYS154 Dystonia 61 0.063
72
STT001 Status Epilepticus 60 0.063
73
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.063
74
IDP067 Idiopathic Hemiconvulsion-Hemiplegia Syndrome 19 0.063
75
MGR035 Migraine with Brainstem Aura 17 0.063
76
HMP020 Hemiplegia Alterans 1 0.063
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