Search results for NRXN2

84 hits were found for NRXN2

# Family MCID Name MIFTS Score
1
P ATS364 Autism 72 15.328
2
c ATS007 Autism Spectrum Disorder 72 13.456
3
DSS008 Disease of Mental Health 74 11.904
4
P FRG001 Fragile X Syndrome 70 8.340
5
KGM001 Kagami-Ogata Syndrome 54 8.042
6
c PTT029 Pitt-Hopkins-Like Syndrome 1 50 8.042
7
KFM001 Kaufman Oculocerebrofacial Syndrome 55 8.042
8
P PRV006 Pervasive Developmental Disorder 52 8.042
9
PHL006 Phelan-Mcdermid Syndrome 62 8.042
10
CHL012 Childhood Disintegrative Disease 44 8.042
11
P TCD001 Tic Disorder 50 8.042
12
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 5.571
13
P SZR006 Seizure Disorder 69 1.749
14
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.593
15
c DVL033 Developmental and Epileptic Encephalopathy 1 49 1.577
16
WST001 West Syndrome 64 1.577
17
P EPL164 Epilepsy 70 1.577
18
P SCH015 Schizophrenia 74 1.291
19
P SPN046 Spinal Muscular Atrophy 62 1.190
20
CHR669 Chromosome 2p16.3 Deletion Syndrome 22 1.190
21
P MSC003 Muscular Atrophy 52 1.190
22
P ERL057 Early Infantile Epileptic Encephalopathy 61 1.149
23
P RSP003 Respiratory Failure 74 1.149
24
SDD001 Sudden Infant Death Syndrome 60 1.149
25
DPR016 Depression 65 1.149
26
P ENC018 Encephalopathy 62 1.149
27
P FBR031 Febrile Seizures 52 1.149
28
P NRB001 Neuroblastoma 66 0.977
29
IRN008 Iron Overload in Africa 51 0.839
30
RJS001 Ruijs-Aalfs Syndrome 47 0.839
31
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.839
32
HPT079 Hepatoid Adenocarcinoma 39 0.839
33
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.839
34
c HPT073 Hepatitis C Virus 71 0.839
35
P HPT023 Hepatocellular Carcinoma 95 0.839
36
ADL096 Adult Hepatocellular Carcinoma 60 0.839
37
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.839
38
PDT042 Pediatric Hepatocellular Carcinoma 50 0.839
39
PTY007 Pityriasis Rotunda 26 0.839
40
FBR086 Fibrolamellar Carcinoma 59 0.839
41
HPT011 Hepatocellular Clear Cell Carcinoma 45 0.839
42
P BRS047 Breast Cancer 97 0.779
43
c MSM022 Mismatch Repair Cancer Syndrome 1 69 0.751
44
c GLM043 Glioma Susceptibility 9 30 0.751
45
c GLM047 Glioma Susceptibility 3 32 0.751
46
c GLM025 Glioma Susceptibility 2 29 0.751
47
P GLM040 Glioma Susceptibility 1 70 0.751
48
P OLG002 Oligodendroglioma 66 0.751
49
MNN043 Meningioma, Familial 79 0.751
50
GLM045 Glioma 62 0.751
51
P MLN008 Melanoma 75 0.551
52
P PNC035 Pancreatic Cancer 86 0.551
53
LKC005 Leukocyte Adhesion Deficiency, Type Iii 51 0.243
54
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.243
55
LKC009 Leukocyte Adhesion Deficiency, Type I 70 0.243
56
GT001 Gout 63 0.243
57
HYP014 Hyperuricemia 51 0.243
58
P ALZ034 Alzheimer Disease 87 0.172
59
GST092 Gastroesophageal Reflux 60 0.172
60
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.172
61
SLF014 Sulfite Oxidase Deficiency, Isolated 53 0.172
62
ANX010 Anxiety 70 0.172
63
ZLL002 Zollinger-Ellison Syndrome 55 0.172
64
MLY001 Molybdenum Cofactor Deficiency 40 0.172
65
P MDL005 Medulloblastoma 75 0.172
66
P PTT014 Pitt-Hopkins Syndrome 63 0.172
67
P ANG001 Angelman Syndrome 65 0.172
68
c CRN139 Cornelia De Lange Syndrome 1 61 0.172
69
CRT072 Creutzfeldt-Jakob Disease 67 0.172
70
c MJR024 Major Affective Disorder 9 40 0.172
71
MLY010 Molybdenum Cofactor Deficiency, Complementation Group C 41 0.172
72
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.172
73
c MJR022 Major Affective Disorder 8 37 0.172
74
TBC004 Tobacco Addiction 63 0.172
75
P PRN023 Prion Disease 60 0.172
76
PNC027 Pancreatic Gastrinoma 30 0.172
77
P MCR010 Microcephaly 59 0.172
78
P CRN015 Cornelia De Lange Syndrome 67 0.172
79
P MLT074 Multiple Endocrine Neoplasia 58 0.172
80
P BPL003 Bipolar Disorder 56 0.172
81
P TMP001 Temporal Lobe Epilepsy 49 0.172
82
DYS073 Dysphagia 53 0.172
83
GST030 Gastrinoma 45 0.172
84
P OVR082 Overgrowth Syndrome 42 0.172
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