Search results for vangl2

54 hits were found for vangl2

# Family MCID Name MIFTS Score
1
NRL016 Neural Tube Defects 82 6.049
2
P STR020 Strabismus 55 4.104
3
P TTR001 Tetralogy of Fallot 70 2.625
4
ANN002 Anencephaly 56 2.588
5
P MCK013 Meckel Syndrome, Type 1 65 2.543
6
MYL020 Myelomeningocele 51 2.543
7
CRN088 Craniorachischisis 37 2.102
8
c BRC051 Brachydactyly, Type B1 51 1.856
9
CRV062 Cervical Spina Bifida Cystica 19 1.856
10
CRV063 Cervical Spina Bifida Aperta 18 1.856
11
LMB056 Lumbosacral Spina Bifida Cystica 18 1.856
12
LMB057 Lumbosacral Spina Bifida Aperta 18 1.856
13
CRV061 Cervicothoracic Spina Bifida Cystica 17 1.856
14
CRV064 Cervicothoracic Spina Bifida Aperta 17 1.856
15
c TTL008 Total Spina Bifida Cystica 17 1.856
16
c TTL009 Total Spina Bifida Aperta 17 1.856
17
THR084 Thoracolumbosacral Spina Bifida Cystica 17 1.856
18
THR085 Thoracolumbosacral Spina Bifida Aperta 17 1.856
19
UPP007 Upper Thoracic Spina Bifida Cystica 17 1.856
20
UPP008 Upper Thoracic Spina Bifida Aperta 17 1.856
21
ISL155 Isolated Anencephaly 11 1.856
22
ISL154 Isolated Exencephaly 10 1.856
23
P BRD002 Bardet-Biedl Syndrome 66 1.798
24
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 64 1.798
25
P VSC013 Visceral Heterotaxy 52 1.798
26
PHY002 Physical Disorder 42 1.798
27
OCL011 Ocular Motility Disease 42 1.798
28
SPN221 Spina Bifida Occulta 39 1.798
29
c DFN179 Deafness, Autosomal Recessive 62 30 1.798
30
MCH006 Mechanical Strabismus 42 0.122
31
P RBN002 Robinow Syndrome 49 0.099
32
CLP005 Ciliopathy 43 0.099
33
EXN003 Exencephaly 31 0.099
34
P JBR020 Joubert Syndrome 1 72 0.070
35
P NRB001 Neuroblastoma 72 0.070
36
c ATS007 Autism Spectrum Disorder 67 0.070
37
P PLM037 Pulmonary Hypertension 67 0.070
38
P MSC005 Muscular Dystrophy 66 0.070
39
P HYD006 Hydrocephalus 66 0.070
40
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.070
41
P PLY014 Polycystic Kidney Disease 62 0.070
42
c BRN108 Branchiootic Syndrome 1 62 0.070
43
LNG099 Lung Disease 60 0.070
44
P FCL005 Focal Segmental Glomerulosclerosis 57 0.070
45
DBL002 Double Outlet Right Ventricle 56 0.070
46
P BRC006 Brachydactyly 53 0.070
47
P RTN016 Retinal Degeneration 53 0.070
48
P OVR082 Overgrowth Syndrome 50 0.070
49
c BRD020 Bardet-Biedl Syndrome 8 50 0.070
50
STS002 Situs Inversus 45 0.070
51
c ATS082 Autosomal Dominant Robinow Syndrome 41 0.070
52
GLM044 Glomerular Disease 37 0.070
53
ECT089 Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia 27 0.070
54
NRL025 Neural Tube Closure Defect 12 0.070
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