Search results for MECP2

78 hits were found for MECP2

# Family MCID Name MIFTS Score
1
MNT208 Mental Retardation, X-Linked Syndromic, Lubs Type 41 17.933
2
P ENC021 Encephalopathy, Neonatal Severe 32 12.922
3
c MCP022 Mecp2-Related Severe Neonatal Encephalopathy 11 10.334
4
P RTT002 Rett Syndrome 82 10.284
5
P MNT135 Mental Retardation, X-Linked, Syndromic 13 37 6.113
6
P ANG001 Angelman Syndrome 62 4.923
7
P ENC018 Encephalopathy 52 3.976
8
PRV006 Pervasive Developmental Disorder 50 3.806
9
c ATS044 Autism Susceptibility, X-Linked 3 22 3.659
10
ATT013 Attention Deficit-Hyperactivity Disorder 66 3.464
11
ATS001 Autistic Disorder 63 3.438
12
P FRG001 Fragile X Syndrome 67 3.379
13
SPC010 Speech and Communication Disorders 42 3.379
14
SPS057 Spasticity 42 3.071
15
P ATS007 Autism Spectrum Disorder 65 3.047
16
P MCR010 Microcephaly 58 3.021
17
LRN003 Learning Disability 46 2.993
18
P HYP265 Hypotonia 39 2.993
19
PRG009 Progressive Multifocal Leukoencephalopathy 50 2.962
20
WST001 West Syndrome 58 2.926
21
BRX001 Bruxism 48 2.926
22
IMM011 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 41 2.926
23
P INT063 Intellectual Disability 58 2.678
24
CLS012 Classic Rett Syndrome 23 2.678
25
P SCL018 Scoliosis 56 2.389
26
P SZR006 Seizure Disorder 54 2.389
27
WGR001 Wagr Syndrome 53 2.389
28
DSS008 Disease of Mental Health 53 2.389
29
RNP001 Renpenning Syndrome 52 2.389
30
KBG001 Kbg Syndrome 49 2.389
31
MNN009 Meningoencephalitis 45 2.389
32
MNT046 Mental Retardation and Microcephaly with Pontine and Cerebellar Hypoplasia 44 2.389
33
PRT003 Partington Syndrome 44 2.389
34
c EPL029 Epileptic Encephalopathy, Early Infantile, 9 41 2.389
35
SPC003 Specific Developmental Disorder 38 2.389
36
STR015 Stereotypic Movement Disorder 36 2.389
37
GTP001 Gait Apraxia 36 2.389
38
P SYN064 Syndromic X-Linked Intellectual Disability 26 2.389
39
c INF065 Infantile Hypotonia 17 2.389
40
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 41 1.931
41
MCP017 Mecp2-Related Disorders 6 1.786
42
XLN224 X-Linked Non-Specific Intellectual Disability 19 1.744
43
c MCP021 Mecp2-Related Angelman-Like Syndrome 6 1.744
44
BNS002 Bone Structure Disease 36 1.689
45
NRN002 Neuronitis 39 0.396
46
c SYS001 Systemic Lupus Erythematosus 86 0.162
47
P LPS004 Lupus Erythematosus 63 0.162
48
P PRS040 Prostate Cancer 88 0.114
49
P SCH015 Schizophrenia 71 0.114
50
PRS047 Prostatitis 55 0.114
51
P HPT023 Hepatocellular Carcinoma 89 0.093
52
P EPL164 Epilepsy 65 0.093
53
P DYS154 Dystonia 61 0.093
54
P ATX004 Ataxia 52 0.093
55
P BRS047 Breast Cancer 100 0.066
56
P CLR023 Colorectal Cancer 95 0.066
57
P LNG032 Lung Cancer 94 0.066
58
P RTN024 Retinoblastoma 75 0.066
59
END057 Endometrial Cancer 74 0.066
60
P NRB001 Neuroblastoma 71 0.066
61
P PLM036 Pulmonary Fibrosis 68 0.066
62
P RSP003 Respiratory Failure 68 0.066
63
P SPN046 Spinal Muscular Atrophy 63 0.066
64
GLL008 Gilles De La Tourette Syndrome 63 0.066
65
P GLM045 Glioma 59 0.066
66
CNT097 Central Hypoventilation Syndrome, Congenital 57 0.066
67
HYP266 Hypoxia 55 0.066
68
DRG011 Drug Addiction 51 0.066
69
P PRC019 Precocious Puberty 50 0.066
70
P MSC003 Muscular Atrophy 49 0.066
71
P SJG001 Sjogren's Syndrome 49 0.066
72
ASP001 Asperger Syndrome 49 0.066
73
c ERL020 Early-Onset Schizophrenia 46 0.066
74
ATN005 Autonomic Dysfunction 45 0.066
75
MYC033 Myoclonus 41 0.066
76
CRB009 Cerebritis 39 0.066
77
SPS019 Spastic Paraparesis 34 0.066
78
c RTT008 Rett Syndrome, Congenital Variant 28 0.066
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