Search results for cacna1a

77 hits were found for cacna1a

# Family MCID Name MIFTS Score
1
c EPS035 Episodic Ataxia, Type 2 54 8.026
2
c EPL172 Epileptic Encephalopathy, Early Infantile, 42 21 7.045
3
c SPN309 Spinocerebellar Ataxia 6 49 5.909
4
c MGR032 Migraine, Familial Hemiplegic, 1 37 4.810
5
P EPS003 Episodic Ataxia 56 4.270
6
c FML023 Familial Hemiplegic Migraine 51 4.070
7
P HMP006 Hemiplegic Migraine 48 3.963
8
P ATS308 Autosomal Dominant Cerebellar Ataxia 54 3.606
9
ACR006 Aceruloplasminemia 73 3.393
10
P MGR003 Migraine with Aura 53 3.122
11
P ALT001 Alternating Hemiplegia of Childhood 48 3.122
12
P MCH002 Machado-Joseph Disease 62 3.040
13
DNT005 Dentatorubral-Pallidoluysian Atrophy 50 3.040
14
c SPR083 Sporadic Hemiplegic Migraine 36 2.869
15
HDC001 Headache 59 2.748
16
HMP005 Hemiplegia 55 2.748
17
BNG078 Benign Paroxysmal Torticollis of Infancy 16 2.748
18
P CLS010 Cluster Headache 46 2.723
19
EXF001 Exfoliation Syndrome 55 2.696
20
MGR028 Migraine with or Without Aura 1 49 2.667
21
P FRD012 Friedreich Ataxia 1 64 2.633
22
c SPN294 Spinocerebellar Ataxia 1 58 2.633
23
LMB002 Lambert-Eaton Myasthenic Syndrome 57 2.633
24
c EPS042 Episodic Ataxia, Type 1 57 2.633
25
P CHL002 Childhood Absence Epilepsy 56 2.633
26
CRB027 Cerebellar Disease 49 2.633
27
c SPN293 Spinocerebellar Ataxia 12 48 2.633
28
HRD026 Hereditary Ataxia 47 2.633
29
MGR001 Migraine Without Aura 46 2.633
30
c SPN296 Spinocerebellar Ataxia 17 46 2.633
31
P CRB059 Cerebellar Degeneration 39 2.633
32
P TRT019 Torticollis 46 2.280
33
P SPN301 Spinocerebellar Ataxia 2 56 2.224
34
P EPL140 Epilepsy, Idiopathic Generalized 57 2.190
35
P DRR001 Diarrhea 56 2.190
36
RST001 Restless Legs Syndrome 52 2.150
37
c SPN100 Spinocerebellar Ataxia 27 45 2.150
38
MRS004 Marshall-Smith Syndrome 41 2.150
39
c SPN103 Spinocerebellar Ataxia 31 40 2.150
40
P EPL116 Epileptic Encephalopathy, Childhood-Onset 39 2.150
41
c EPS017 Episodic Ataxia, Type 6 37 2.150
42
c SPN094 Spinocerebellar Ataxia 18 36 2.150
43
VST001 Vestibular Neuronitis 34 2.150
44
BNG018 Benign Paroxysmal Positional Nystagmus 34 2.150
45
PRN032 Paraneoplastic Cerebellar Degeneration 33 2.150
46
c SPN099 Spinocerebellar Ataxia 26 31 2.150
47
c EPS015 Episodic Ataxia, Type 7 30 2.150
48
VST006 Vestibulocochlear Nerve Disease 28 2.150
49
c SPN247 Spinocerebellar Ataxia Type 19/22 27 2.150
50
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 1.676
51
c FML306 Familial or Sporadic Hemiplegic Migraine 27 1.572
52
UND011 Undetermined Early-Onset Epileptic Encephalopathy 20 1.572
53
P NRV007 Nervous System Disease 73 1.520
54
c CNT035 Central Nervous System Disease 63 1.520
55
P CNG001 Congenital Myasthenic Syndrome 55 1.520
56
P EPL164 Epilepsy 69 0.200
57
P ATX024 Ataxia-Oculomotor Apraxia 3 40 0.167
58
NRN002 Neuronitis 41 0.141
59
CRB009 Cerebritis 41 0.141
60
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.126
61
P ENC018 Encephalopathy 62 0.126
62
STR020 Strabismus 56 0.126
63
CHR073 Choreatic Disease 37 0.126
64
SPS019 Spastic Paraparesis 35 0.126
65
P ATS364 Autism 70 0.089
66
AGN016 Aging 64 0.089
67
P TRM003 Tremor 54 0.089
68
MGR035 Migraine with Brainstem Aura 19 0.089
69
P RTT002 Rett Syndrome 82 0.063
70
DPR016 Depression 72 0.063
71
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 67 0.063
72
P DYS154 Dystonia 64 0.063
73
MVM001 Movement Disease 60 0.063
74
STT001 Status Epilepticus 60 0.063
75
P INF016 Infantile Epileptic Encephalopathy 54 0.063
76
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 39 0.063
77
IDP067 Idiopathic Hemiconvulsion-Hemiplegia Syndrome 19 0.063
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