Search results for CNTN4

29 hits were found for CNTN4

# Family MCID Name MIFTS Score
1
P ATS364 Autism 70 3.923
2
c ATS007 Autism Spectrum Disorder 67 3.341
3
P SCH015 Schizophrenia 74 3.058
4
CHR667 Chromosome 3pter-P25 Deletion Syndrome 41 2.324
5
P PRV006 Pervasive Developmental Disorder 57 2.162
6
c SPN096 Spinocerebellar Ataxia 21 40 2.162
7
c SPN290 Spinocerebellar Ataxia 15 40 2.162
8
CHR390 Chromosome 14q11-Q22 Deletion Syndrome 38 2.162
9
c CFF011 Coffin-Siris Syndrome 6 35 2.162
10
CHR523 Chromosome 15q11.2 Deletion Syndrome 33 2.162
11
c SPN098 Spinocerebellar Ataxia 25 29 2.162
12
c CHR565 Chromosomal Deletion Syndrome 25 2.162
13
LPN002 Lip and Oral Cavity Cancer 19 0.115
14
P NRB001 Neuroblastoma 72 0.081
15
c PRM196 Premature Ovarian Failure 1 67 0.081
16
GT001 Gout 64 0.081
17
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.081
18
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.081
19
ORL011 Oral Cancer 60 0.081
20
VSL002 Visual Epilepsy 59 0.081
21
THR024 Thrombosis 57 0.081
22
P CRD246 Cardiovascular System Disease 57 0.081
23
NPH009 Nephrolithiasis 55 0.081
24
APR001 Apraxia 52 0.081
25
BKR002 Baker-Gordon Syndrome 49 0.081
26
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.081
27
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.081
28
CHR178 Chromosomal Triplication 35 0.081
29
CHR244 Chromosome 3p Duplication 14 0.081
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