Search results for "MECP2"

79 hits were found for 'MECP2'

# Family MCID Name MIFTS Score
1
MNT208 Mental Retardation, X-Linked Syndromic, Lubs Type 29 17.353
2
P ENC021 Encephalopathy, Neonatal Severe 30 14.202
3
c MCP022 Mecp2-Related Severe Neonatal Encephalopathy 11 10.241
4
P RTT002 Rett Syndrome 78 9.983
5
P MNT135 Mental Retardation, X-Linked, Syndromic 13 31 5.777
6
P ANG001 Angelman Syndrome 61 4.769
7
PRV006 Pervasive Developmental Disorder 50 3.787
8
c ATS044 Autism Susceptibility, X-Linked 3 19 3.700
9
ATT013 Attention Deficit-Hyperactivity Disorder 68 3.447
10
ATS001 Autistic Disorder 59 3.421
11
P FRG001 Fragile X Syndrome 68 3.362
12
KLN001 Klinefelter's Syndrome 55 3.362
13
SPC010 Speech and Communication Disorders 46 3.362
14
P ATS007 Autism Spectrum Disorder 64 3.032
15
SPS057 Spasticity 42 3.032
16
LRN003 Learning Disability 51 2.978
17
P HYP265 Hypotonia 39 2.978
18
MCP017 Mecp2-Related Disorders 6 2.978
19
WST001 West Syndrome 61 2.912
20
WGR001 Wagr Syndrome 52 2.912
21
BRX001 Bruxism 51 2.912
22
CLS012 Classic Rett Syndrome 22 2.664
23
P INT063 Intellectual Disability 53 2.563
24
PRG009 Progressive Multifocal Leukoencephalopathy 50 2.419
25
NNS032 Non-Syndromic X-Linked Intellectual Disability 29 2.419
26
P RBN001 Rubinstein-Taybi Syndrome 65 2.378
27
P GLL020 Gallbladder Disease 59 2.378
28
DSS008 Disease of Mental Health 55 2.378
29
KBG001 Kbg Syndrome 49 2.378
30
RNP001 Renpenning Syndrome 48 2.378
31
OBS015 Obesity, Hyperphagia, and Developmental Delay 46 2.378
32
MNN009 Meningoencephalitis 45 2.378
33
PRT003 Partington Syndrome 42 2.378
34
SPC003 Specific Developmental Disorder 40 2.378
35
STR015 Stereotypic Movement Disorder 38 2.378
36
GTP001 Gait Apraxia 37 2.378
37
IMM013 Immunodeficiency, Centromere Instability and Facial Anomalies Syndrome 36 2.378
38
INT304 Interstitial Pneumonitis, Desquamative, Familial 32 2.378
39
c INF065 Infantile Hypotonia 15 2.378
40
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 37 1.871
41
PLR009 Pol Iii-Related Leukodystrophies 37 1.812
42
LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 33 1.812
43
c MCP021 Mecp2-Related Angelman-Like Syndrome 7 1.735
44
BNS002 Bone Structure Disease 36 1.681
45
NRN002 Neuronitis 42 0.387
46
P ENC018 Encephalopathy 59 0.185
47
c SYS001 Systemic Lupus Erythematosus 87 0.160
48
P LPS004 Lupus Erythematosus 63 0.160
49
P PRS040 Prostate Cancer 89 0.113
50
PRS047 Prostatitis 56 0.113
51
HPT023 Hepatocellular Carcinoma 91 0.092
52
GST053 Gastric Cancer 77 0.092
53
P SCH015 Schizophrenia 76 0.092
54
P EPL164 Epilepsy 66 0.092
55
P DYS154 Dystonia 64 0.092
56
P ATX004 Ataxia 53 0.092
57
P BRS047 Breast Cancer 100 0.065
58
P CLR023 Colorectal Cancer 97 0.065
59
END057 Endometrial Cancer 75 0.065
60
P RTN024 Retinoblastoma 75 0.065
61
P RSP003 Respiratory Failure 70 0.065
62
P NRB001 Neuroblastoma 69 0.065
63
P PLM036 Pulmonary Fibrosis 68 0.065
64
P SPN046 Spinal Muscular Atrophy 63 0.065
65
GLL008 Gilles De La Tourette Syndrome 62 0.065
66
CNT097 Central Hypoventilation Syndrome, Congenital 60 0.065
67
P MCR010 Microcephaly 58 0.065
68
P GLM045 Glioma 58 0.065
69
HYP266 Hypoxia 55 0.065
70
P SJG001 Sjogren's Syndrome 53 0.065
71
P MSC003 Muscular Atrophy 51 0.065
72
P PRC019 Precocious Puberty 51 0.065
73
DRG011 Drug Addiction 51 0.065
74
ATN005 Autonomic Dysfunction 45 0.065
75
MYC033 Myoclonus 41 0.065
76
CRB009 Cerebritis 38 0.065
77
SPS019 Spastic Paraparesis 34 0.065
78
c EPL037 Epileptic Encephalopathy, Early Infantile, 1 33 0.065
79
c RTT008 Rett Syndrome, Congenital Variant 24 0.065