Search results for cntnap2

208 hits were found for cntnap2

# Family MCID Name MIFTS Score
1
c PTT029 Pitt-Hopkins-Like Syndrome 1 50 72.446
2
c PTT042 Pitt-Hopkins-Like Syndrome 38 68.497
3
c ATS376 Autism 15 23 35.170
4
P ATS364 Autism 72 23.197
5
c ATS007 Autism Spectrum Disorder 72 22.765
6
BNG009 Benign Epilepsy with Centrotemporal Spikes 60 18.515
7
P EPL164 Epilepsy 70 15.697
8
GLL008 Gilles De La Tourette Syndrome 64 15.322
9
P SCH015 Schizophrenia 74 14.463
10
P PTT014 Pitt-Hopkins Syndrome 63 14.460
11
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 14.019
12
DSS008 Disease of Mental Health 74 12.452
13
P SPC019 Specific Language Impairment 31 11.911
14
FCL014 Focal Epilepsy 53 11.539
15
P ATT013 Attention Deficit-Hyperactivity Disorder 66 11.286
16
SPC010 Speech and Communication Disorders 48 11.266
17
STT041 Stuttering 52 11.222
18
OBS002 Obsessive-Compulsive Disorder 68 10.522
19
EXF001 Exfoliation Syndrome 56 10.391
20
P BPL003 Bipolar Disorder 56 10.373
21
MTS001 Mutism 44 10.116
22
APR001 Apraxia 51 9.798
23
P ENC004 Encephalitis 61 9.069
24
P ALZ034 Alzheimer Disease 87 8.985
25
P PRV006 Pervasive Developmental Disorder 52 8.926
26
P DYS005 Dyslexia 40 8.460
27
SPC005 Speech Disorder 46 8.191
28
CHL109 Childhood Apraxia of Speech 44 7.668
29
P TCD001 Tic Disorder 50 7.513
30
ATS301 Autosomal Dominant Epilepsy with Auditory Features 40 7.192
31
c ATM075 Autoimmune Encephalitis 39 6.616
32
P ERL057 Early Infantile Epileptic Encephalopathy 61 6.561
33
LMB024 Limbic Encephalitis 43 6.497
34
WST001 West Syndrome 64 6.413
35
PHL006 Phelan-Mcdermid Syndrome 62 6.413
36
c DVL029 Developmental and Epileptic Encephalopathy 2 46 6.413
37
LRN003 Learning Disability 49 6.413
38
VLC001 Velocardiofacial Syndrome 57 6.353
39
P FRG001 Fragile X Syndrome 70 6.353
40
P MVM001 Movement Disease 61 6.353
41
ART014 Articulation Disorder 34 6.353
42
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 37 6.210
43
CLR009 Color Agnosia 26 6.210
44
ATM105 Autoimmune Disease of Peripheral Nervous System 25 6.210
45
SPC003 Specific Developmental Disorder 31 6.210
46
c ATM089 Autoimmune Neuropathy 28 6.210
47
LCR004 La Crosse Encephalitis 36 6.210
48
P HYP097 Hyperekplexia 62 6.210
49
c EPL086 Epilepsy, Idiopathic Generalized 9 28 6.210
50
c MRG009 Meier-Gorlin Syndrome 2 33 6.210
51
STF001 Stiff-Person Syndrome 57 6.210
52
P CHL002 Childhood Absence Epilepsy 63 6.210
53
MLL002 Miller Fisher Syndrome 40 6.210
54
CRB023 Cerebellopontine Angle Meningioma 21 6.210
55
VNC001 Von Economo's Disease 41 6.210
56
ACT049 Acute Disseminated Encephalomyelitis 53 6.210
57
ANT019 Anterograde Amnesia 38 6.210
58
AMN003 Amnestic Disorder 54 6.210
59
PST109 Postinfectious Encephalitis 25 6.210
60
DSS002 Dissociative Amnesia 28 6.210
61
LND001 Landau-Kleffner Syndrome 50 6.210
62
CHR073 Choreatic Disease 53 6.210
63
CHR051 Chorea Gravidarum 19 6.210
64
RDN001 Reading Disorder 40 6.210
65
CHL012 Childhood Disintegrative Disease 44 6.210
66
THY025 Thymus Cancer 56 6.210
67
SPN041 Spinal Cord Disease 54 6.210
68
CRB029 Cerebellopontine Angle Tumor 27 6.210
69
c EPL114 Epilepsy, Familial Temporal Lobe, 1 50 6.210
70
DRV001 Dravet Syndrome 70 6.210
71
LNG015 Lingual-Facial-Buccal Dyskinesia 47 6.210
72
ECH002 Echolalia 33 6.210
73
P EPS003 Episodic Ataxia 59 6.210
74
THY026 Thymus Gland Disease 27 6.210
75
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 4.677
76
DYS182 Dysphasia, Familial Developmental 34 3.129
77
P SZR006 Seizure Disorder 69 2.545
78
c MJR024 Major Affective Disorder 9 40 1.591
79
c MJR022 Major Affective Disorder 8 37 1.591
80
c PTT030 Pitt-Hopkins-Like Syndrome 2 41 1.500
81
ALL029 Allergic Disease 61 1.500
82
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 1.498
83
ESP021 Esophageal Cancer 84 1.469
84
ELC001 Elective Mutism 22 1.334
85
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.296
86
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.213
87
c SPC015 Specific Language Impairment 4 12 1.160
88
GST040 Gastric Adenocarcinoma 66 1.134
89
P SCL057 Scoliosis, Isolated 1 40 1.125
90
P SCL018 Scoliosis 57 1.125
91
IDP070 Idiopathic Scoliosis 41 1.125
92
CMP097 Complex Chromosomal Rearrangement 23 1.101
93
P AGN002 Agnosia 53 1.074
96
HND015 Hand Skill, Relative 29 0.982
97
CND002 Conduct Disorder 50 0.982
98
ATS010 Autosomal Recessive Disease 42 0.943
99
P CHR071 Charcot-Marie-Tooth Disease 64 0.935
100
AGN016 Aging 54 0.898
101
c PRC016 Pre-Eclampsia 64 0.898
102
P ECL001 Eclampsia 52 0.898
103
ALC007 Alcohol Dependence 65 0.838
104
P BRS047 Breast Cancer 97 0.767
105
P LKM062 Leukemia, Acute Lymphoblastic 69 0.767
106
VTR016 Vater/vacterl Association 50 0.732
107
VCT001 Vacterl Association 46 0.732
108
P GST053 Gastric Cancer 82 0.693
109
GST103 Gastric Cancer, Hereditary Diffuse 68 0.693
110
SML009 Small Intestine Adenocarcinoma 57 0.693
111
P PNC035 Pancreatic Cancer 86 0.644
112
SPL004 Splenic Marginal Zone Lymphoma 50 0.441
113
P OVR042 Ovarian Cancer 88 0.441
114
P MLN008 Melanoma 75 0.441
115
GLM045 Glioma 62 0.441
116
c NRB010 Neuroblastoma 1 60 0.380
117
c WLM018 Wilms Tumor 5 54 0.380
118
P AGM001 Agammaglobulinemia 67 0.380
119
P INF038 Influenza 68 0.380
120
FRN006 Frontotemporal Dementia 68 0.380
121
P DMN002 Dementia 65 0.380
122
HLX001 Helix Syndrome 47 0.351
123
APH002 Aphasia 55 0.321
124
SQM006 Squamous Cell Carcinoma 59 0.321
125
SCT005 Scott Syndrome 51 0.287
126
P DVL113 Developmental and Epileptic Encephalopathy 45 0.287
127
P EPL196 Epilepsy, Familial Focal, with Variable Foci 1 44 0.287
128
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.287
129
AMN001 Amenorrhea 53 0.287
130
RHB001 Rhabdoid Cancer 68 0.287
131
OHT001 Ohtahara Syndrome 39 0.287
132
CHR178 Chromosomal Triplication 34 0.287
133
47X002 47,xyy 48 0.287
136
P TBR001 Tuberous Sclerosis 69 0.248
137
LVR012 Liver Cirrhosis 62 0.248
138
P MCR010 Microcephaly 59 0.248
139
c HPT016 Hepatitis B 62 0.248
140
P ENC018 Encephalopathy 62 0.248
141
P NRB001 Neuroblastoma 66 0.248
142
c PNS012 Paine Syndrome 60 0.203
143
EPL199 Epilepsy, Progressive Myoclonic, 4, with or Without Renal Failure 36 0.203
144
CRB004 Cerebral Artery Occlusion 46 0.203
145
PRM013 Premature Menopause 57 0.203
146
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.203
147
c EPL103 Epilepsy, Familial Adult Myoclonic, 5 34 0.203
148
WLL001 Williams-Beuren Syndrome 60 0.203
149
c FML363 Familial Adult Myoclonic Epilepsy 45 0.203
150
PRV004 Periventricular Leukomalacia 52 0.203
151
P PRP019 Peripheral Nervous System Disease 57 0.203
152
TTH006 Tooth Disease 51 0.203
153
GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 30 0.203
154
P HRZ002 Horizontal Gaze Palsy with Progressive Scoliosis 37 0.203
155
P TRM003 Tremor 50 0.203
156
P NRP001 Neuropathy 59 0.203
157
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.203
158
SPC030 Specific Language Disorder 25 0.203
159
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.143
160
BRN134 Brain Malformations with or Without Urinary Tract Defects 38 0.143
161
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.143
162
P RST001 Restless Legs Syndrome 52 0.143
163
P ASP001 Asperger Syndrome 48 0.143
164
P PRK039 Parkinsonism 55 0.143
165
c MCR247 Microcephaly 1, Primary, Autosomal Recessive 42 0.143
166
MWT001 Mowat-Wilson Syndrome 57 0.143
167
ORL015 Oral Squamous Cell Carcinoma 43 0.143
168
CHR662 Chromosome 15q13.3 Deletion Syndrome 37 0.143
169
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.143
170
P MJR001 Major Depressive Disorder 68 0.143
171
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.143
172
HYP748 Hypertelorism 46 0.143
173
c HYP836 Hypercholesterolemia, Familial, 1 73 0.143
174
c ATS173 Autism 18 27 0.143
175
c MNT319 Mental Retardation, Autosomal Dominant 20 42 0.143
176
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.143
177
TBC004 Tobacco Addiction 63 0.143
178
c TBR025 Tuberous Sclerosis 1 84 0.143
179
STT001 Status Epilepticus 58 0.143
180
P MYP006 Myopia 55 0.143
181
P ADN016 Adenocarcinoma 63 0.143
182
ADN018 Adenoma 58 0.143
183
MNT002 Mental Depression 56 0.143
184
GST033 Gestational Diabetes 61 0.143
185
PNC129 Pancreatic Adenocarcinoma 65 0.143
186
ERL001 Early Myoclonic Encephalopathy 63 0.143
187
P PTT006 Pituitary Adenoma 55 0.143
188
HMT002 Hematologic Cancer 61 0.143
189
CNS004 Constipation 56 0.143
190
P TMP001 Temporal Lobe Epilepsy 49 0.143
191
MSC157 Muscular Dystrophy, Duchenne Type 79 0.143
192
P TMT001 Timothy Syndrome 55 0.143
193
c LKM061 Leukemia, Acute Myeloid 83 0.143
194
c DFN170 Deafness, Autosomal Recessive 31 39 0.143
195
DPR016 Depression 65 0.143
196
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.143
197
P MYL006 Myeloid Leukemia 60 0.143
198
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 30 0.143
199
SYN116 Syndromic Obesity 27 0.143
200
PTT037 Pituitary Tumors 44 0.143
201
P HYP265 Hypotonia 42 0.143
202
PLY024 Polymicrogyria 46 0.143
203
OST012 Osteoarthritis 77 0.143
204
c SPR009 Sporadic Breast Cancer 42 0.143
205
P MSC005 Muscular Dystrophy 66 0.143
206
P DBT009 Diabetes Mellitus 67 0.143
207
ORL011 Oral Cancer 60 0.143
208
STX004 Stxbp1 Encephalopathy with Epilepsy 14 0.143
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