Search results for MSX2

46 hits were found for MSX2

# Family MCID Name MIFTS Score
1
c PRT059 Parietal Foramina 1 27 6.075
2
c CRN277 Craniosynostosis 2 35 5.938
3
P PRT042 Parietal Foramina 37 5.847
4
P CRN037 Craniosynostosis 68 5.666
5
PRT043 Parietal Foramina with Cleidocranial Dysplasia 26 5.237
6
P CLD001 Cleidocranial Dysplasia 63 4.352
7
INV006 Inverted Papilloma 36 3.398
8
HDC001 Headache 55 3.364
9
EXN003 Exencephaly 34 3.364
10
CRZ001 Crouzon Syndrome 71 3.326
11
STH001 Saethre-Chotzen Syndrome 64 3.326
12
FBR011 Fibrodysplasia Ossificans Progressiva 64 3.326
13
SYN005 Synostosis 50 3.326
14
P DNT009 Dentin Dysplasia 39 3.326
15
P BRC015 Bruck Syndrome 44 2.716
16
ATS008 Autosomal Dominant Disease 39 2.716
17
OVR051 Ovarian Endodermal Sinus Tumor 38 2.716
18
BND014 Bone Development Disease 31 2.716
19
OVR056 Ovarian Primitive Germ Cell Tumor 23 2.716
20
P ORF002 Orofacial Cleft 41 1.920
21
P PNC044 Pancreatitis 64 0.160
22
P PNC035 Pancreatic Cancer 89 0.143
23
P BRS047 Breast Cancer 100 0.124
24
P ADN016 Adenocarcinoma 71 0.124
25
c PRT060 Parietal Foramina 2 24 0.124
26
NRL016 Neural Tube Defects 79 0.101
27
P OST001 Osteopetrosis 70 0.101
28
PPL022 Papilloma 58 0.101
29
NRL018 Neural Tube Defects, Folate-Sensitive 44 0.101
30
P CLR023 Colorectal Cancer 98 0.072
31
MLN008 Melanoma 72 0.072
32
c SPN225 Spondyloarthropathy 1 71 0.072
33
PNC041 Pancreatic Ductal Adenocarcinoma 67 0.072
34
CLR108 Colorectal Adenoma 60 0.072
35
PRS047 Prostatitis 59 0.072
36
SPN051 Spondylitis 55 0.072
37
RTN023 Retinitis 52 0.072
38
P OMP004 Omphalocele 51 0.072
39
P DNT011 Dentinogenesis Imperfecta 47 0.072
40
P AML002 Amelogenesis Imperfecta 46 0.072
41
SPP011 Suppression of Tumorigenicity 12 41 0.072
42
TTH008 Tooth Resorption 38 0.072
43
c BLD140 Blood Group, I System 37 0.072
44
PPL059 Popliteal Pterygium Syndrome, Lethal Type 37 0.072
45
INF009 Inflammatory Spondylopathy 32 0.072
46
BLD142 Blood Group--Kidd System 18 0.072
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