Search results for tubb2b
46 hits were found for tubb2b
# |
|
Family |
MCID |
Name |
MIFTS |
Score |
1 |
|
c
|
CRT081 |
Cortical Dysplasia, Complex, with Other Brain Malformations 7 |
31 |
15.373 |
|
2 |
|
|
PLY024 |
Polymicrogyria |
49 |
3.970 |
|
3 |
|
P
|
ALZ034 |
Alzheimer Disease |
88 |
3.229 |
|
4 |
|
|
TKL001 |
Tukel Syndrome |
50 |
2.792 |
|
5 |
|
|
TBL029 |
Tubulin, Beta |
28 |
2.760 |
|
6 |
|
|
TBL023 |
Tubulinopathies |
31 |
2.189 |
|
7 |
|
c
|
CRT070 |
Cortical Dysplasia, Complex, with Other Brain Malformations 1 |
41 |
1.974 |
|
8 |
|
P
|
CRB185 |
Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1 |
55 |
1.927 |
|
9 |
|
|
MCR099 |
Microlissencephaly |
32 |
1.927 |
|
10 |
|
|
TBL027 |
Tubulinopathy-Associated Dysgyria |
17 |
1.927 |
|
11 |
|
|
WLK001 |
Walker-Warburg Syndrome |
63 |
1.864 |
|
12 |
|
|
STR039 |
Sturge-Weber Syndrome |
60 |
1.864 |
|
13 |
|
P
|
STR020 |
Strabismus |
55 |
1.864 |
|
14 |
|
P
|
BND018 |
Band Heterotopia |
53 |
1.864 |
|
15 |
|
c
|
LSS006 |
Lissencephaly 2 |
52 |
1.864 |
|
16 |
|
P
|
PRV002 |
Periventricular Nodular Heterotopia |
52 |
1.864 |
|
17 |
|
|
MLL018 |
Miller-Dieker Lissencephaly Syndrome |
51 |
1.864 |
|
18 |
|
c
|
PRM031 |
Primary Autosomal Recessive Microcephaly |
47 |
1.864 |
|
19 |
|
|
GLD006 |
Goldberg-Shprintzen Syndrome |
47 |
1.864 |
|
20 |
|
P
|
DNR001 |
Duane Retraction Syndrome |
47 |
1.864 |
|
21 |
|
|
ACR012 |
Aicardi Syndrome |
45 |
1.864 |
|
22 |
|
|
HYD001 |
Hydranencephaly |
44 |
1.864 |
|
23 |
|
|
OCL011 |
Ocular Motility Disease |
42 |
1.864 |
|
24 |
|
c
|
MCR122 |
Microphthalmia, Isolated 5 |
39 |
1.864 |
|
25 |
|
|
PRT015 |
Partial Third-Nerve Palsy |
30 |
1.864 |
|
26 |
|
|
PRL014 |
Paralytic Squint |
29 |
1.864 |
|
27 |
|
c
|
SCH052 |
Schizophrenia 14 |
28 |
1.864 |
|
28 |
|
c
|
CNG031 |
Congenital Nervous System Abnormality |
24 |
1.864 |
|
29 |
|
|
PLY183 |
Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome |
41 |
0.225 |
|
30 |
|
|
PCH002 |
Pachygyria |
31 |
0.168 |
|
31 |
|
P
|
MCR010 |
Microcephaly |
59 |
0.130 |
|
32 |
|
P
|
LSS002 |
Lissencephaly |
51 |
0.130 |
|
33 |
|
P
|
NRB001 |
Neuroblastoma |
72 |
0.106 |
|
34 |
|
|
ALC028 |
Alacrima, Achalasia, and Mental Retardation Syndrome |
64 |
0.106 |
|
35 |
|
P
|
CRB045 |
Cerebellar Hypoplasia |
41 |
0.106 |
|
36 |
|
|
NRN016 |
Neuronal Migration Disorders |
40 |
0.106 |
|
37 |
|
P
|
BRS047 |
Breast Cancer |
97 |
0.075 |
|
38 |
|
P
|
DYS154 |
Dystonia |
65 |
0.075 |
|
39 |
|
P
|
FTL069 |
Fetal Akinesia Deformation Sequence 1 |
64 |
0.075 |
|
40 |
|
|
SCH018 |
Schizencephaly |
52 |
0.075 |
|
41 |
|
|
CRP032 |
Corpus Callosum, Agenesis of |
49 |
0.075 |
|
42 |
|
P
|
MYC033 |
Myoclonus |
46 |
0.075 |
|
43 |
|
c
|
CRT089 |
Cortical Dysplasia, Complex, with Other Brain Malformations 10 |
36 |
0.075 |
|
44 |
|
P
|
CMP082 |
Complex Cortical Dysplasia with Other Brain Malformations |
21 |
0.075 |
|
45 |
|
|
SGC002 |
Sgce Myoclonus-Dystonia |
17 |
0.075 |
|
46 |
|
|
PFH001 |
Pafah1b1-Associated Lissencephaly/subcortical Band Heterotopia |
12 |
0.075 |
|