Search results for MECP2

100 hits were found for MECP2

# Family MCID Name MIFTS Score
1
LBS001 Lubs X-Linked Mental Retardation Syndrome 41 18.397
2
ENC054 Encephalopathy, Neonatal Severe, Due to Mecp2 Mutations 21 15.384
3
P RTT002 Rett Syndrome 82 10.269
4
P MNT135 Mental Retardation, X-Linked, Syndromic 13 36 6.109
5
MCP022 Mecp2-Related Severe Neonatal Encephalopathy 9 5.087
6
P ANG001 Angelman Syndrome 61 4.909
7
c ATS367 Autism X-Linked 3 20 4.797
8
P ATS364 Autism 70 4.218
9
P ENC018 Encephalopathy 58 4.011
10
PRV006 Pervasive Developmental Disorder 56 3.838
11
P ATT013 Attention Deficit-Hyperactivity Disorder 67 3.488
12
P FRG001 Fragile X Syndrome 69 3.409
13
SPC010 Speech and Communication Disorders 40 3.409
14
c ATS007 Autism Spectrum Disorder 68 3.064
15
P MCR010 Microcephaly 57 3.064
16
P HYP265 Hypotonia 40 3.040
17
LRN003 Learning Disability 49 3.014
18
PRG009 Progressive Multifocal Leukoencephalopathy 55 2.985
19
WST001 West Syndrome 57 2.953
20
BRX001 Bruxism 51 2.953
21
KBG001 Kbg Syndrome 51 2.953
22
IMM011 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 48 2.953
23
HYP748 Hypertelorism 46 2.953
24
P ASP001 Asperger Syndrome 51 2.450
25
P PRD006 Prader-Willi Syndrome 66 2.411
26
P GLL020 Gallbladder Disease 64 2.411
27
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 60 2.411
28
P SCL018 Scoliosis 56 2.411
29
P SZR006 Seizure Disorder 55 2.411
30
RNP003 Renpenning Syndrome 1 53 2.411
31
DSS008 Disease of Mental Health 51 2.411
32
MNN009 Meningoencephalitis 49 2.411
33
PRT052 Partington X-Linked Mental Retardation Syndrome 42 2.411
34
c EPL029 Epileptic Encephalopathy, Early Infantile, 9 41 2.411
35
STR015 Stereotypic Movement Disorder 40 2.411
36
GTP001 Gait Apraxia 38 2.411
37
SPC003 Specific Developmental Disorder 29 2.411
38
P SYN064 Syndromic X-Linked Intellectual Disability 25 2.411
39
c INF065 Infantile Hypotonia 20 2.411
40
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 2.005
41
XLN224 X-Linked Non-Specific Intellectual Disability 21 1.755
42
BNS002 Bone Structure Disease 26 1.705
43
NRN002 Neuronitis 43 0.370
44
c SYS001 Systemic Lupus Erythematosus 86 0.149
45
GST053 Gastric Cancer 84 0.149
46
P LPS004 Lupus Erythematosus 69 0.149
47
SPS057 Spasticity 41 0.149
48
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.122
49
P PRS040 Prostate Cancer 88 0.105
50
P SCH015 Schizophrenia 71 0.105
51
PRS047 Prostatitis 59 0.105
52
P BRS047 Breast Cancer 100 0.086
53
P HPT023 Hepatocellular Carcinoma 94 0.086
54
P EPL164 Epilepsy 70 0.086
55
AGN016 Aging 65 0.086
56
CNT097 Central Hypoventilation Syndrome, Congenital 65 0.086
57
P DYS154 Dystonia 61 0.086
58
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.086
59
P LNG032 Lung Cancer 99 0.061
60
P CLR023 Colorectal Cancer 98 0.061
61
P PNC035 Pancreatic Cancer 89 0.061
62
P RTN024 Retinoblastoma 76 0.061
63
END057 Endometrial Cancer 76 0.061
64
P NRB001 Neuroblastoma 73 0.061
65
ANX010 Anxiety 72 0.061
66
P RSP003 Respiratory Failure 71 0.061
67
P PLM036 Pulmonary Fibrosis 68 0.061
68
GLL008 Gilles De La Tourette Syndrome 64 0.061
69
GST092 Gastroesophageal Reflux 64 0.061
70
P PNC044 Pancreatitis 64 0.061
71
P SPN046 Spinal Muscular Atrophy 63 0.061
72
HYP266 Hypoxia 61 0.061
73
P GLM045 Glioma 61 0.061
74
P SJG008 Sjogren Syndrome 58 0.061
75
P MSC003 Muscular Atrophy 55 0.061
76
CRD223 Cardiac Arrhythmia 52 0.061
77
P PRC019 Precocious Puberty 52 0.061
78
ATN005 Autonomic Dysfunction 51 0.061
79
c ERL020 Early-Onset Schizophrenia 51 0.061
80
THR013 Thoracic Outlet Syndrome 50 0.061
81
CRB009 Cerebritis 41 0.061
82
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.061
83
MYC033 Myoclonus 40 0.061
84
c PCH010 Pachyonychia Congenita 3 38 0.061
85
c BLD140 Blood Group, I System 37 0.061
86
HYP745 Hyperreflexia 36 0.061
87
P ATS366 Autism X-Linked 2 34 0.061
88
SPS019 Spastic Paraparesis 33 0.061
89
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.061
90
c ATR062 Atrial Septal Defect 1 32 0.061
91
APC009 Apocrine Gland Secretion, Variation in 29 0.061
92
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 24 0.061
93
c RTT008 Rett Syndrome, Congenital Variant 24 0.061
94
XP2002 Xp22.13p22.2 Duplication Syndrome 23 0.061
95
RDN004 Radin Blood Group Antigen 23 0.061
96
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.061
97
XQ1001 Xq12-Q13.3 Duplication Syndrome 20 0.061
98
BLD138 Blood Group--Diego System 18 0.061
99
CHR274 Chromosome Xq Duplication 12 0.061
100
MCP017 Mecp2-Related Disorders 4 0.061
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