Search results for nrxn1

85 hits were found for nrxn1

# Family MCID Name MIFTS Score
1
c PTT030 Pitt-Hopkins-Like Syndrome 2 40 7.963
2
P SCH015 Schizophrenia 74 4.407
3
c PTT042 Pitt-Hopkins-Like Syndrome 35 4.379
4
CHR669 Chromosome 2p16.3 Deletion Syndrome 26 4.239
5
P PTT014 Pitt-Hopkins Syndrome 63 2.874
6
P BPL003 Bipolar Disorder 56 2.874
7
c ATS007 Autism Spectrum Disorder 67 2.744
8
P ATS364 Autism 70 2.529
9
P MCR010 Microcephaly 59 2.427
10
PSY004 Psychotic Disorder 67 2.376
11
CNS004 Constipation 58 2.313
12
HND004 Hand-Foot-Genital Syndrome 48 2.313
13
SCH012 Schizoaffective Disorder 50 2.274
14
PRN009 Paranoid Schizophrenia 50 2.274
15
AST006 Astigmatism 47 2.274
16
RFR003 Refractive Error 43 2.274
17
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 2.092
18
TBC004 Tobacco Addiction 64 1.762
19
GLL008 Gilles De La Tourette Syndrome 66 1.699
20
WLL001 Williams-Beuren Syndrome 60 1.699
21
c OVR102 Ovarian Dysgenesis 3 22 1.699
22
P ERL057 Early Infantile Epileptic Encephalopathy 63 1.659
23
P EPL140 Epilepsy, Idiopathic Generalized 62 1.659
24
PHL006 Phelan-Mcdermid Syndrome 62 1.659
25
P STR020 Strabismus 55 1.659
26
c PTT029 Pitt-Hopkins-Like Syndrome 1 49 1.659
27
P ASP001 Asperger Syndrome 48 1.659
28
P FRG001 Fragile X Syndrome 70 1.608
29
P ANG001 Angelman Syndrome 69 1.608
30
DGR001 Digeorge Syndrome 64 1.608
31
WST001 West Syndrome 61 1.608
32
DSS008 Disease of Mental Health 58 1.608
33
P PRV006 Pervasive Developmental Disorder 57 1.608
34
KFM001 Kaufman Oculocerebrofacial Syndrome 56 1.608
35
VLC001 Velocardiofacial Syndrome 54 1.608
36
P TCD001 Tic Disorder 53 1.608
37
KGM001 Kagami-Ogata Syndrome 51 1.608
38
PTC002 Potocki-Lupski Syndrome 48 1.608
39
CHL012 Childhood Disintegrative Disease 44 1.608
40
ECH002 Echolalia 34 1.608
41
P SPC019 Specific Language Impairment 33 1.608
42
c SCH087 Schizophrenia 18 31 1.608
43
SPC003 Specific Developmental Disorder 31 1.608
44
P CHR084 Chromosomal Disease 30 1.608
45
c CHR565 Chromosomal Deletion Syndrome 25 1.608
46
CHR569 Chromosomal Duplication Syndrome 18 1.608
47
P HYP265 Hypotonia 43 0.139
48
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.124
49
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.108
50
c MJR024 Major Affective Disorder 9 41 0.108
51
c MJR022 Major Affective Disorder 8 38 0.108
52
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.088
53
P BRC006 Brachydactyly 53 0.088
54
P RSP003 Respiratory Failure 74 0.062
55
P NRB001 Neuroblastoma 72 0.062
56
P EPL164 Epilepsy 71 0.062
57
P LKM062 Leukemia, Acute Lymphoblastic 69 0.062
58
P LKM002 Leukemia 68 0.062
59
GST092 Gastroesophageal Reflux 67 0.062
60
CLR108 Colorectal Adenoma 64 0.062
61
MDD011 Mood Disorder 62 0.062
62
P ENC018 Encephalopathy 61 0.062
63
SDD001 Sudden Infant Death Syndrome 61 0.062
64
P SCL018 Scoliosis 60 0.062
65
P PLY006 Polydactyly 59 0.062
66
c ACT073 Acute Leukemia 58 0.062
67
P SZR006 Seizure Disorder 56 0.062
68
SCH003 Schizophreniform Disorder 56 0.062
69
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.062
70
P SCK004 Seckel Syndrome 56 0.062
71
AGN016 Aging 56 0.062
72
HYP706 Hypermobile Ehlers-Danlos Syndrome 53 0.062
73
P FBR031 Febrile Seizures 53 0.062
74
HYP748 Hypertelorism 50 0.062
75
BKR002 Baker-Gordon Syndrome 49 0.062
76
P GND004 Gonadal Dysgenesis 48 0.062
77
SPC010 Speech and Communication Disorders 47 0.062
78
c ERL020 Early-Onset Schizophrenia 44 0.062
79
MCH006 Mechanical Strabismus 42 0.062
80
c SCK015 Seckel Syndrome 2 41 0.062
81
c 46X002 46 Xx Gonadal Dysgenesis 41 0.062
82
JWD001 Jawad Syndrome 40 0.062
83
BNN005 Bunion 33 0.062
84
IMM162 Immunoglobulin E Concentration, Serum 28 0.062
85
c INF065 Infantile Hypotonia 24 0.062
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