Search results for kcna2

96 hits were found for kcna2

# Family MCID Name MIFTS Score
1
c DVL058 Developmental and Epileptic Encephalopathy 32 25 68.044
2
UND011 Undetermined Early-Onset Epileptic Encephalopathy 44 63.462
3
P SZR006 Seizure Disorder 70 17.795
4
DSS008 Disease of Mental Health 74 17.689
5
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 13.975
6
P EPS003 Episodic Ataxia 59 13.322
7
P DBT009 Diabetes Mellitus 67 12.391
8
c HRD010 Hereditary Spastic Paraplegia 66 12.317
9
c EPS042 Episodic Ataxia, Type 1 58 12.158
10
WST001 West Syndrome 59 11.692
11
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 58 10.117
12
c DVL033 Developmental and Epileptic Encephalopathy 1 56 9.380
13
ERL001 Early Myoclonic Encephalopathy 62 8.814
14
P BNG026 Benign Neonatal Seizures 49 8.075
15
DRV001 Dravet Syndrome 69 7.805
16
P ENC018 Encephalopathy 62 7.594
17
P EPL140 Epilepsy, Idiopathic Generalized 62 7.154
18
CHR222 Chromosome 1p36 Deletion Syndrome 45 7.154
19
PRX015 Paroxysmal Extreme Pain Disorder 56 7.154
20
CHR101 Char Syndrome 53 7.154
21
P ERL057 Early Infantile Epileptic Encephalopathy 60 7.154
22
NNT041 Neonatal Period Electroclinical Syndrome 24 7.154
23
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 7.154
24
c FML001 Familial Atrial Fibrillation 65 7.154
25
c DVL052 Developmental and Epileptic Encephalopathy 26 36 7.154
26
c TBR026 Tuberous Sclerosis 2 71 7.154
27
c LNG044 Long Qt Syndrome 1 66 7.154
28
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 7.154
29
BNG006 Benign Familial Neonatal Epilepsy 55 7.154
30
c ALZ031 Alzheimer Disease 17 28 7.154
31
P LNG028 Long Qt Syndrome 64 7.154
32
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 5.462
33
P EPL164 Epilepsy 68 4.964
34
P DVL113 Developmental and Epileptic Encephalopathy 43 3.733
35
STT001 Status Epilepticus 59 3.205
36
P MCR010 Microcephaly 60 2.887
37
CHC001 Chickenpox 57 2.799
38
HRP004 Herpes Zoster 61 2.799
39
PST053 Postherpetic Neuralgia 40 2.799
40
OST012 Osteoarthritis 77 2.693
41
P ZNC008 Zinc Finger Protein 1 23 2.462
42
P TRM003 Tremor 48 2.334
43
PRP016 Paraplegia 52 2.200
44
HLX001 Helix Syndrome 48 2.060
45
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 2.041
46
P SHR121 Short Sleep, Familial Natural, 1 18 2.041
47
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.041
48
c SZR022 Seizures, Benign Familial Neonatal, 1 43 1.867
49
IQS001 Iqsec2 18 1.660
50
P RTT002 Rett Syndrome 79 1.390
51
c PLM164 Pulmonary Hypertension, Primary, 1 76 1.128
52
P CHR345 Chronic Pain 50 1.128
53
c ATS007 Autism Spectrum Disorder 72 0.921
54
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.921
55
P BRS047 Breast Cancer 98 0.811
56
c PRG011 Progressive Myoclonus Epilepsy 41 0.738
57
P MYC033 Myoclonus 47 0.738
58
P MYC026 Myoclonus Epilepsy 35 0.738
59
SPN186 Spinal Cord Injury 61 0.651
60
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.651
61
CLT003 Colitis 63 0.651
62
APH002 Aphasia 56 0.651
63
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.651
64
c DPH024 Diaphragmatic Hernia, Congenital 64 0.651
65
P SPN301 Spinocerebellar Ataxia 2 59 0.651
66
c CRB191 Cerebral Cavernous Malformations 2 45 0.651
67
c PGM022 Pigmented Nodular Adrenocortical Disease, Primary, 4 24 0.651
68
FRY002 Fryns Syndrome 39 0.651
69
c HYD064 Hydrocephalus, Congenital, 1 51 0.651
70
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.651
71
DNT005 Dentatorubral-Pallidoluysian Atrophy 60 0.651
72
MYC071 Myoclonic-Atonic Epilepsy 31 0.651
73
P PTN014 Patent Ductus Arteriosus 1 59 0.651
74
P LKD001 Leukodystrophy 59 0.651
75
P HRP006 Herpes Simplex 65 0.651
76
ULC004 Ulcerative Colitis 74 0.651
77
c DLT002 Dilated Cardiomyopathy 78 0.651
78
P LTR001 Lateral Sclerosis 58 0.651
79
SNS003 Sensory Peripheral Neuropathy 52 0.651
80
FCL014 Focal Epilepsy 53 0.651
81
P HRT032 Heart Disease 81 0.651
82
CNG034 Congestive Heart Failure 69 0.651
83
c INH020 Inherited Metabolic Disorder 48 0.651
84
P TMP001 Temporal Lobe Epilepsy 49 0.651
85
QDR001 Quadriplegia 50 0.651
86
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.651
87
P BNC003 Bone Cancer 58 0.651
88
STX004 Stxbp1 Encephalopathy with Epilepsy 15 0.651
90
ATS301 Autosomal Dominant Epilepsy with Auditory Features 36 0.651
92
EPL170 Epilepsy-Aphasia Spectrum 21 0.651
93
EPL230 Epilepsy with Myoclonic-Atonic Seizures 23 0.651
94
MLG120 Malignant Migrating Partial Seizures of Infancy 43 0.651
95
P OVR042 Ovarian Cancer 88 0.573
96
P PNC035 Pancreatic Cancer 86 0.573
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