Search results for CNTNAP2

40 hits were found for CNTNAP2

# Family MCID Name MIFTS Score
1
c ATS376 Autism 15 13 5.554
2
c PTT029 Pitt-Hopkins-Like Syndrome 1 25 5.547
3
P ATS364 Autism 70 4.962
4
GLL008 Gilles De La Tourette Syndrome 64 4.286
5
c ATS007 Autism Spectrum Disorder 68 3.875
6
P PTT014 Pitt-Hopkins Syndrome 52 3.814
7
FCL014 Focal Epilepsy 56 3.778
8
P SCH015 Schizophrenia 71 3.408
9
EXF001 Exfoliation Syndrome 55 3.312
10
STT041 Stuttering 52 3.312
11
MTS001 Mutism 42 3.312
12
P SPC019 Specific Language Impairment 30 3.312
13
c PTT042 Pitt-Hopkins-Like Syndrome 14 3.312
14
PRV006 Pervasive Developmental Disorder 56 3.272
15
THY025 Thymus Cancer 52 3.272
16
SPC010 Speech and Communication Disorders 40 3.272
17
CHL109 Childhood Apraxia of Speech 31 2.719
18
P ATT013 Attention Deficit-Hyperactivity Disorder 67 2.672
19
SPC005 Speech Disorder 44 2.672
20
c ATM075 Autoimmune Encephalitis 40 2.672
21
RDN001 Reading Disorder 36 2.672
22
ART014 Articulation Disorder 31 2.672
23
P EPL164 Epilepsy 70 0.129
24
PSY004 Psychotic Disorder 72 0.105
25
P ALZ034 Alzheimer Disease 95 0.075
26
P INF038 Influenza 77 0.075
27
P NRB001 Neuroblastoma 73 0.075
28
ANX010 Anxiety 72 0.075
29
P AGM001 Agammaglobulinemia 70 0.075
30
OBS002 Obsessive-Compulsive Disorder 68 0.075
31
AGN016 Aging 65 0.075
32
P SCL018 Scoliosis 56 0.075
33
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.075
34
APR001 Apraxia 52 0.075
35
IDP070 Idiopathic Scoliosis 42 0.075
36
P DYS005 Dyslexia 39 0.075
37
DYS182 Dysphasia, Familial Developmental 29 0.075
38
P SCL057 Scoliosis, Isolated 1 28 0.075
39
ATS301 Autosomal Dominant Epilepsy with Auditory Features 16 0.075
40
c SPC015 Specific Language Impairment 4 9 0.075
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