Search results for MECP2

83 hits were found for MECP2

# Family MCID Name MIFTS Score
1
MNT208 Mental Retardation, X-Linked Syndromic, Lubs Type 42 17.817
2
P ENC021 Encephalopathy, Neonatal Severe 29 14.105
3
c MCP022 Mecp2-Related Severe Neonatal Encephalopathy 11 11.177
4
P RTT002 Rett Syndrome 77 10.076
5
P MNT135 Mental Retardation, X-Linked, Syndromic 13 35 5.994
6
P ANG001 Angelman Syndrome 61 4.834
7
c ATS044 Autism Susceptibility, X-Linked 3 19 4.310
8
P ENC018 Encephalopathy 59 3.886
9
ATT013 Attention Deficit-Hyperactivity Disorder 69 3.786
10
ATS001 Autistic Disorder 63 3.762
11
PRV006 Pervasive Developmental Disorder 53 3.737
12
P FRG001 Fragile X Syndrome 69 3.709
13
KLN001 Klinefelter's Syndrome 50 3.709
14
SPC010 Speech and Communication Disorders 41 3.709
15
P ATS007 Autism Spectrum Disorder 65 3.425
16
LRN003 Learning Disability 49 3.376
17
MCP017 Mecp2-Related Disorders 6 3.376
18
PRG009 Progressive Multifocal Leukoencephalopathy 52 3.348
19
WST001 West Syndrome 57 3.317
20
BRX001 Bruxism 49 3.317
21
CLS012 Classic Rett Syndrome 23 3.133
22
P HYP265 Hypotonia 38 2.938
23
NNS032 Non-Syndromic X-Linked Intellectual Disability 28 2.908
24
c MCP021 Mecp2-Related Angelman-Like Syndrome 7 2.908
25
P RBN001 Rubinstein-Taybi Syndrome 64 2.873
26
P GLL020 Gallbladder Disease 59 2.873
27
WGR001 Wagr Syndrome 53 2.873
28
DSS008 Disease of Mental Health 52 2.873
29
KBG001 Kbg Syndrome 48 2.873
30
RNP001 Renpenning Syndrome 47 2.873
31
MNN009 Meningoencephalitis 47 2.873
32
PRT003 Partington Syndrome 43 2.873
33
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 2.873
34
SPC003 Specific Developmental Disorder 38 2.873
35
STR015 Stereotypic Movement Disorder 36 2.873
36
GTP001 Gait Apraxia 35 2.873
37
INT304 Interstitial Pneumonitis, Desquamative, Familial 31 2.873
38
P SYN064 Syndromic X-Linked Intellectual Disability 28 2.873
39
c INF065 Infantile Hypotonia 17 2.873
40
P INT063 Intellectual Disability 49 2.611
41
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 38 2.529
42
c EPL029 Epileptic Encephalopathy, Early Infantile, 9 39 2.346
43
PLR009 Pol Iii-Related Leukodystrophies 38 2.346
44
MNT046 Mental Retardation and Microcephaly with Pontine and Cerebellar Hypoplasia 38 2.346
45
BNS002 Bone Structure Disease 37 2.346
46
LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 34 2.346
47
IMM013 Immunodeficiency, Centromere Instability and Facial Anomalies Syndrome 22 2.346
48
NRN002 Neuronitis 41 0.388
49
c SYS001 Systemic Lupus Erythematosus 86 0.159
50
P LPS004 Lupus Erythematosus 64 0.159
51
SPS057 Spasticity 42 0.145
52
P PRS040 Prostate Cancer 90 0.112
53
GST053 Gastric Cancer 78 0.112
54
P MCR010 Microcephaly 58 0.112
55
PRS047 Prostatitis 56 0.112
56
P HPT023 Hepatocellular Carcinoma 92 0.092
57
P SCH015 Schizophrenia 77 0.092
58
P EPL164 Epilepsy 66 0.092
59
P DYS154 Dystonia 65 0.092
60
P ATX004 Ataxia 53 0.092
61
P BRS047 Breast Cancer 100 0.065
62
P CLR023 Colorectal Cancer 97 0.065
63
P LNG032 Lung Cancer 95 0.065
64
END057 Endometrial Cancer 75 0.065
65
P RTN024 Retinoblastoma 74 0.065
66
P PLM036 Pulmonary Fibrosis 71 0.065
67
P RSP003 Respiratory Failure 71 0.065
68
P NRB001 Neuroblastoma 70 0.065
69
P SPN046 Spinal Muscular Atrophy 65 0.065
70
GLL008 Gilles De La Tourette Syndrome 62 0.065
71
P GLM045 Glioma 60 0.065
72
CNT097 Central Hypoventilation Syndrome, Congenital 59 0.065
73
HYP266 Hypoxia 56 0.065
74
DRG011 Drug Addiction 51 0.065
75
P PRC019 Precocious Puberty 51 0.065
76
P MSC003 Muscular Atrophy 50 0.065
77
P SJG001 Sjogren's Syndrome 50 0.065
78
ATN005 Autonomic Dysfunction 49 0.065
79
MYC033 Myoclonus 42 0.065
80
SPS019 Spastic Paraparesis 41 0.065
81
CRB009 Cerebritis 39 0.065
82
c EPL037 Epileptic Encephalopathy, Early Infantile, 1 38 0.065
83
c RTT008 Rett Syndrome, Congenital Variant 24 0.065
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