Search results for kcnc1

63 hits were found for kcnc1

# Family MCID Name MIFTS Score
1
c EPL134 Epilepsy, Progressive Myoclonic 7 29 55.313
2
P EPL164 Epilepsy 68 19.756
3
P MYC033 Myoclonus 47 17.046
4
c PRG011 Progressive Myoclonus Epilepsy 41 15.306
5
c PRG143 Progressive Myoclonus Epilepsy 7 17 12.412
6
c SPN311 Spinocerebellar Ataxia 13 48 10.958
7
UNV001 Unverricht-Lundborg Syndrome 53 9.693
8
P SZR006 Seizure Disorder 70 8.820
9
c EPS042 Episodic Ataxia, Type 1 58 7.749
10
P BRG001 Brugada Syndrome 69 7.749
11
P ERL057 Early Infantile Epileptic Encephalopathy 60 7.749
12
c FML001 Familial Atrial Fibrillation 65 7.749
13
c SPN247 Spinocerebellar Ataxia Type 19/22 37 7.749
14
DSS008 Disease of Mental Health 74 7.749
15
HRT008 Heart Conduction Disease 44 7.749
16
P EPS003 Episodic Ataxia 59 7.749
17
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 5.767
18
P MYC026 Myoclonus Epilepsy 35 5.145
19
ERL001 Early Myoclonic Encephalopathy 62 3.585
20
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 53 3.368
21
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 3.009
22
P ENC018 Encephalopathy 62 2.695
23
MLD018 Mild Cognitive Impairment 48 2.604
24
P DVL113 Developmental and Epileptic Encephalopathy 43 2.435
25
c RRP028 Rare Epilepsy 17 1.945
26
EPL095 Epilepsy with Myoclonic Absences 13 1.727
27
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 57 1.727
28
c SPN308 Spinocerebellar Ataxia 28 48 1.727
29
EPL199 Epilepsy, Progressive Myoclonic, 4, with or Without Renal Failure 36 1.727
30
c SPS212 Spastic Ataxia 5, Autosomal Recessive 31 1.727
32
P EPL140 Epilepsy, Idiopathic Generalized 62 1.444
33
P TRM003 Tremor 48 1.444
34
c ATS007 Autism Spectrum Disorder 72 1.185
35
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.967
36
P USH001 Usher Syndrome 64 0.967
37
P NRN021 Neuronal Ceroid Lipofuscinosis 65 0.967
38
OPD006 Opioid Addiction 48 0.967
39
P BRS047 Breast Cancer 98 0.811
40
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 0.684
41
c MJR022 Major Affective Disorder 8 38 0.684
42
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.684
43
c MJR024 Major Affective Disorder 9 41 0.684
44
DWN001 Down Syndrome 70 0.684
45
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.684
46
DNT005 Dentatorubral-Pallidoluysian Atrophy 60 0.684
47
P MSC003 Muscular Atrophy 52 0.684
48
P BPL003 Bipolar Disorder 56 0.684
49
P RTN016 Retinal Degeneration 52 0.684
50
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.684
51
P SNS001 Sensorineural Hearing Loss 59 0.684
52
P SPN046 Spinal Muscular Atrophy 63 0.684
53
P GCH001 Gaucher's Disease 70 0.684
54
OPT003 Opiate Dependence 49 0.684
55
TRN018 Transitional Cell Carcinoma 56 0.684
56
GLY031 Glycoproteinosis 49 0.684
57
STT001 Status Epilepticus 59 0.684
58
SBS004 Substance Dependence 47 0.684
60
MD2001 Med23 20 0.684
61
CHR178 Chromosomal Triplication 34 0.684
62
P PNC035 Pancreatic Cancer 86 0.573
63
MYL005 Myelofibrosis 71 0.573
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