Search results for CNTN2

28 hits were found for CNTN2

# Family MCID Name MIFTS Score
1
c EPL103 Epilepsy, Familial Adult Myoclonic, 5 24 6.717
2
P EPL164 Epilepsy 72 4.378
3
c ADL017 Adult T-Cell Leukemia 57 3.391
4
TRP002 Tropical Spastic Paraparesis 50 3.391
5
P TCL004 T-Cell Leukemia 47 3.391
6
P TRM003 Tremor 54 2.822
7
P PLY019 Polyneuropathy 56 2.769
8
P DMY001 Demyelinating Polyneuropathy 41 2.769
9
c BNG079 Benign Adult Familial Myoclonic Epilepsy 36 2.125
10
P GLM040 Glioma Susceptibility 1 81 1.958
11
SPN041 Spinal Cord Disease 57 1.958
12
c PTT029 Pitt-Hopkins-Like Syndrome 1 48 1.958
13
c HMN021 Human T-Cell Leukemia Virus Type 1 48 1.958
14
MLT075 Multifocal Motor Neuropathy 47 1.958
15
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 44 1.958
16
LMB024 Limbic Encephalitis 41 1.958
17
MYL057 Myelopathy, Htlv-1-Associated 39 1.958
18
c HMN022 Human T-Cell Leukemia Virus Type 2 37 1.958
19
URN011 Urinary Tract Papillary Transitional Cell Benign Neoplasm 27 1.958
20
NNN005 Non-Invasive Bladder Papillary Urothelial Neoplasm 25 1.958
21
BLD046 Bladder Papillary Transitional Cell Neoplasm 20 1.958
22
DFC004 Deficiency Anemia 75 0.083
23
c ATS007 Autism Spectrum Disorder 68 0.083
24
P ATS364 Autism 65 0.083
25
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.083
26
IRN001 Iron Deficiency Anemia 59 0.083
27
IRN002 Iron Metabolism Disease 58 0.083
28
EPL199 Epilepsy, Progressive Myoclonic, 4, with or Without Renal Failure 36 0.083
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