Search results for msx2

120 hits were found for msx2

# Family MCID Name MIFTS Score
1
c PRT059 Parietal Foramina 1 34 5.673
2
c CRN277 Craniosynostosis 2 36 5.596
3
P PRT042 Parietal Foramina 46 4.955
4
P CRN037 Craniosynostosis 68 4.670
5
PRT043 Parietal Foramina with Cleidocranial Dysplasia 27 4.409
6
P CLD001 Cleidocranial Dysplasia 65 3.669
7
NRL016 Neural Tube Defects 82 2.863
8
INV006 Inverted Papilloma 52 2.407
9
SYN005 Synostosis 45 2.407
10
EXN003 Exencephaly 31 2.383
11
P AML002 Amelogenesis Imperfecta 55 2.357
12
CLF027 Cleft Palate, Isolated 64 2.327
13
P HDC001 Headache 57 2.327
14
P OMP004 Omphalocele 50 2.327
15
c ART115 Aortic Valve Disease 1 75 2.292
16
CRZ001 Crouzon Syndrome 68 2.292
17
STH001 Saethre-Chotzen Syndrome 67 2.292
18
FBR011 Fibrodysplasia Ossificans Progressiva 67 2.292
19
ACH004 Achondroplasia 66 2.292
20
P BRC006 Brachydactyly 53 2.292
21
P DNT009 Dentin Dysplasia 40 2.292
22
SYN106 Syndromic Craniosynostosis 33 1.702
23
PFF001 Pfeiffer Syndrome 79 1.667
24
TTH002 Tooth Agenesis 60 1.667
25
DYS018 Dysostosis 44 1.667
26
APR006 Apert Syndrome 70 1.620
27
ODN023 Odontochondrodysplasia 68 1.620
28
HYL004 Hyaline Fibromatosis Syndrome 67 1.620
29
CHR619 Chromosome 2q35 Duplication Syndrome 62 1.620
30
MNK003 Muenke Syndrome 59 1.620
31
P VND007 Van Der Woude Syndrome 1 58 1.620
32
HMF006 Hemifacial Microsomia 55 1.620
33
JCK001 Jackson-Weiss Syndrome 51 1.620
34
c BRC079 Brachydactyly, Type A2 51 1.620
35
HYP059 Hypertelorism, Microtia, Facial Clefting Syndrome 45 1.620
36
P ORF002 Orofacial Cleft 44 1.620
37
P SYN075 Syngnathia 43 1.620
38
TRC118 Trichodentoosseous Syndrome 43 1.620
39
PHY002 Physical Disorder 42 1.620
40
CRP003 Corpus Callosum Lipoma 34 1.620
41
P BND014 Bone Development Disease 33 1.620
42
CRB034 Cerebral Hemisphere Lipoma 26 1.620
43
BST002 Baastrup's Syndrome 21 1.620
44
P PNC035 Pancreatic Cancer 84 0.158
45
BNR002 Bone Resorption Disease 48 0.125
46
WRM002 Warman Mulliken Hayward Syndrome 8 0.125
47
P ADN016 Adenocarcinoma 64 0.111
48
PPL022 Papilloma 54 0.111
49
SQM002 Squamous Cell Papilloma 46 0.111
50
P OST001 Osteopetrosis 70 0.096
51
MCR013 Microphthalmia 57 0.096
52
P BRS047 Breast Cancer 97 0.079
53
OST159 Osteogenic Sarcoma 66 0.079
54
OST003 Osteonecrosis 61 0.079
55
P MCR010 Microcephaly 59 0.079
56
P PLY006 Polydactyly 59 0.079
57
P ANT088 Anterior Segment Dysgenesis 52 0.079
58
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.079
59
HRW001 Hair Whorl 36 0.079
60
CHR178 Chromosomal Triplication 35 0.079
61
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 21 0.079
62
P CLR023 Colorectal Cancer 99 0.056
63
P OVR042 Ovarian Cancer 88 0.056
64
c SPN225 Spondyloarthropathy 1 73 0.056
65
P MLN008 Melanoma 69 0.056
66
CHL065 Cholangiocarcinoma 68 0.056
67
P HYD006 Hydrocephalus 66 0.056
68
P NRV007 Nervous System Disease 66 0.056
69
CLR108 Colorectal Adenoma 64 0.056
70
P PRD008 Periodontitis 64 0.056
71
c PRC016 Pre-Eclampsia 63 0.056
72
PTR032 Peters-Plus Syndrome 63 0.056
73
BRS099 Breast Ductal Carcinoma 62 0.056
74
HYP066 Hyperglycemia 61 0.056
75
P PNC044 Pancreatitis 61 0.056
76
ING001 Inguinal Hernia 60 0.056
77
SPP011 Suppression of Tumorigenicity 12 59 0.056
78
P BND020 Bone Disease 59 0.056
79
P BCL017 B-Cell Lymphoma 58 0.056
80
P FTL001 Fetal Alcohol Syndrome 57 0.056
81
P MYS005 Myositis 56 0.056
82
DBL002 Double Outlet Right Ventricle 56 0.056
83
ANN002 Anencephaly 56 0.056
84
EMB004 Embryonal Carcinoma 56 0.056
85
P SCL048 Sclerosteosis 55 0.056
86
P ALP008 Alopecia 54 0.056
87
P ART021 Arteriosclerosis 54 0.056
88
CLF001 Cleft Lip 53 0.056
89
c CNT035 Central Nervous System Disease 52 0.056
90
P DNT011 Dentinogenesis Imperfecta 52 0.056
91
SPN051 Spondylitis 51 0.056
92
INT079 Intrahepatic Cholangiocarcinoma 51 0.056
93
P ECL001 Eclampsia 50 0.056
94
CHR635 Chromosome 5q Deletion Syndrome 50 0.056
95
DNT045 Dental Anomalies and Short Stature 49 0.056
96
FBR009 Fibrous Dysplasia 48 0.056
97
P ENC008 Encephalocele 47 0.056
98
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.056
99
c CNG216 Congenital Hydrocephalus 47 0.056
100
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.056
101
c SPL067 Split-Hand/foot Malformation 1 46 0.056
102
ISL121 Isolated Split Hand-Split Foot Malformation 45 0.056
103
PTC001 Potocki-Shaffer Syndrome 42 0.056
104
P SYN012 Synpolydactyly 42 0.056
105
MYS001 Myositis Ossificans 41 0.056
106
OST115 Osteonecrosis of the Jaw 40 0.056
107
TTH008 Tooth Resorption 37 0.056
109
c LKM005 Leukemia, T-Cell, Chronic 34 0.056
110
FCL090 Facial Cleft 34 0.056
111
INF009 Inflammatory Spondylopathy 31 0.056
112
c PRT060 Parietal Foramina 2 31 0.056
113
TRD003 Taurodontism 30 0.056
114
P TTH013 Tooth Agenesis, Selective, 4 26 0.056
115
c TTH012 Tooth Agenesis, Selective, 3 26 0.056
116
CRN266 Craniofacial Dyssynostosis with Short Stature 26 0.056
117
MNN022 Meningoencephalocele 21 0.056
118
P SPN237 Spina Bifida Aperta 20 0.056
119
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 17 0.056
120
CRN301 Craniosynostosis with Ocular Abnormalities and Hallucal Defects 9 0.056
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