Search results for msx2

275 hits were found for msx2

# Family MCID Name MIFTS Score
1
P PRT042 Parietal Foramina 51 50.619
2
c PRT059 Parietal Foramina 1 32 49.700
3
c CRN277 Craniosynostosis 2 37 47.162
4
PRT043 Parietal Foramina with Cleidocranial Dysplasia 25 31.038
5
P CRN037 Craniosynostosis 67 25.045
6
P CLD001 Cleidocranial Dysplasia 64 16.312
7
NRL016 Neural Tube Defects 81 13.006
8
P AML002 Amelogenesis Imperfecta 56 11.429
9
INV006 Inverted Papilloma 49 11.358
10
SYN005 Synostosis 43 11.331
11
EXN003 Exencephaly 30 11.165
12
CLF027 Cleft Palate, Isolated 64 10.666
13
P OMP004 Omphalocele 47 10.466
14
P HDC001 Headache 56 10.095
15
P BRC006 Brachydactyly 52 9.867
16
STH001 Saethre-Chotzen Syndrome 66 9.844
17
c ART115 Aortic Valve Disease 1 72 9.794
18
FBR011 Fibrodysplasia Ossificans Progressiva 67 9.766
19
P DNT009 Dentin Dysplasia 40 9.700
20
CRZ001 Crouzon Syndrome 64 9.659
21
ACH004 Achondroplasia 66 9.659
22
SYN106 Syndromic Craniosynostosis 32 8.102
23
TTH002 Tooth Agenesis 61 7.667
24
DBL002 Double Outlet Right Ventricle 57 7.641
25
PFF001 Pfeiffer Syndrome 77 7.506
26
DYS018 Dysostosis 43 7.451
27
CHR619 Chromosome 2q35 Duplication Syndrome 64 7.239
28
APR006 Apert Syndrome 69 7.020
29
MNK003 Muenke Syndrome 56 6.992
30
BRT054 Brittle Bone Disorder 74 6.926
31
JCK001 Jackson-Weiss Syndrome 48 6.926
32
P HLP001 Holoprosencephaly 69 6.926
33
HMF006 Hemifacial Microsomia 55 6.884
34
ODN023 Odontochondrodysplasia 70 6.830
35
SPN060 Spondylocarpotarsal Synostosis Syndrome 48 6.699
36
ART035 Arterial Calcification of Infancy 58 6.699
37
c BRC079 Brachydactyly, Type A2 50 6.699
38
HYP059 Hypertelorism, Microtia, Facial Clefting Syndrome 44 6.699
39
TRC118 Trichodentoosseous Syndrome 42 6.699
40
P BND014 Bone Development Disease 33 6.699
41
PHY002 Physical Disorder 41 6.699
42
P ORF002 Orofacial Cleft 42 6.699
43
CRB034 Cerebral Hemisphere Lipoma 25 6.699
44
CRP003 Corpus Callosum Lipoma 33 6.699
45
BST002 Baastrup's Syndrome 20 6.699
46
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 3.765
47
P PNC035 Pancreatic Cancer 86 3.094
48
c CRN278 Craniosynostosis 1 55 2.398
49
WRM002 Warman Mulliken Hayward Syndrome 8 2.351
50
BNR002 Bone Resorption Disease 47 2.259
51
MCR013 Microphthalmia 60 1.924
52
PPL022 Papilloma 53 1.911
53
SQM002 Squamous Cell Papilloma 45 1.911
54
P OST001 Osteopetrosis 70 1.884
55
HRW001 Hair Whorl 35 1.507
56
OST159 Osteogenic Sarcoma 66 1.507
57
P ADN016 Adenocarcinoma 63 1.494
58
HYP066 Hyperglycemia 60 1.450
59
P ART021 Arteriosclerosis 53 1.435
60
P ANT088 Anterior Segment Dysgenesis 53 1.369
61
P PLY006 Polydactyly 58 1.351
62
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 20 1.351
63
OST003 Osteonecrosis 61 1.314
64
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.314
65
P MCR010 Microcephaly 59 1.272
66
P DNT011 Dentinogenesis Imperfecta 52 1.178
67
P VSC007 Vascular Disease 62 1.162
68
CHR178 Chromosomal Triplication 34 1.141
69
TRD003 Taurodontism 30 1.112
70
c PRT060 Parietal Foramina 2 30 1.112
71
CLF001 Cleft Lip 54 1.112
72
c PRC016 Pre-Eclampsia 64 1.094
73
P ECL001 Eclampsia 52 1.094
74
P SCL048 Sclerosteosis 58 1.075
75
P BCL017 B-Cell Lymphoma 57 1.075
76
P FTL001 Fetal Alcohol Syndrome 55 1.056
78
PTC001 Potocki-Shaffer Syndrome 41 1.036
79
P CLR023 Colorectal Cancer 100 1.036
80
SPP011 Suppression of Tumorigenicity 12 61 1.036
81
PTR032 Peters-Plus Syndrome 63 1.015
82
P PRD008 Periodontitis 64 1.015
83
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.005
84
TTH008 Tooth Resorption 37 0.992
85
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.992
86
c LKM005 Leukemia, T-Cell, Chronic 33 0.992
87
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.992
88
P PNC044 Pancreatitis 61 0.968
89
P ALP008 Alopecia 53 0.968
90
c SPL067 Split-Hand/foot Malformation 1 46 0.943
91
c HYP836 Hypercholesterolemia, Familial, 1 73 0.943
92
ANN002 Anencephaly 57 0.943
93
CHL065 Cholangiocarcinoma 58 0.943
94
INT079 Intrahepatic Cholangiocarcinoma 51 0.943
95
P ENC008 Encephalocele 46 0.943
96
FCL090 Facial Cleft 30 0.943
97
P SPN237 Spina Bifida Aperta 19 0.943
98
ISL121 Isolated Split Hand-Split Foot Malformation 42 0.943
99
P BRS047 Breast Cancer 97 0.939
100
P SYN012 Synpolydactyly 38 0.915
101
P HYD006 Hydrocephalus 63 0.915
102
c CNT035 Central Nervous System Disease 53 0.915
103
P NRV007 Nervous System Disease 66 0.915
104
c MCR133 Microvascular Complications of Diabetes 4 41 0.884
105
DNT045 Dental Anomalies and Short Stature 48 0.884
106
FBR009 Fibrous Dysplasia 48 0.884
107
ING001 Inguinal Hernia 59 0.884
108
c MCR113 Microvascular Complications of Diabetes 3 52 0.884
109
c MCR130 Microvascular Complications of Diabetes 6 41 0.884
110
c MCR120 Microvascular Complications of Diabetes 7 47 0.884
111
EMB004 Embryonal Carcinoma 55 0.884
112
OST115 Osteonecrosis of the Jaw 40 0.884
113
P MYS005 Myositis 56 0.848
114
c TTH012 Tooth Agenesis, Selective, 3 25 0.848
115
c TTH013 Tooth Agenesis, Selective, 4 27 0.848
116
MYS001 Myositis Ossificans 44 0.848
117
c CNG216 Congenital Hydrocephalus 50 0.848
118
MNN022 Meningoencephalocele 21 0.848
119
P MLN008 Melanoma 75 0.826
120
CHR635 Chromosome 5q Deletion Syndrome 50 0.807
121
P BND020 Bone Disease 60 0.807
122
c SPN225 Spondyloarthropathy 1 70 0.753
123
CRN301 Craniosynostosis with Ocular Abnormalities and Hallucal Defects 9 0.753
124
SPN051 Spondylitis 51 0.753
125
INF009 Inflammatory Spondylopathy 30 0.753
126
DST103 Distal Muscular Dystrophy with Anterior Tibial Onset 29 0.622
127
CRN266 Craniofacial Dyssynostosis with Short Stature 25 0.622
128
MYP035 Myopathy, Distal, with Anterior Tibial Onset 33 0.622
129
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 19 0.622
130
LPD008 Lipid Metabolism Disorder 61 0.540
131
BRR002 Barrett's Adenocarcinoma 36 0.533
132
P LKM062 Leukemia, Acute Lymphoblastic 69 0.490
133
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.473
134
CLR108 Colorectal Adenoma 63 0.471
135
HYP025 Hyperphosphatemia 47 0.435
136
RCK004 Rickets 65 0.371
137
P KDN018 Kidney Disease 72 0.347
138
INS024 Insulin-Like Growth Factor I 77 0.321
139
c CHR684 Chronic Kidney Disease 74 0.321
140
CLF004 Cleft Lip/palate 57 0.321
141
HLX001 Helix Syndrome 47 0.293
142
c ATS007 Autism Spectrum Disorder 72 0.293
143
AML029 Ameloblastoma 46 0.293
144
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.293
145
RTN020 Retinal Vascular Disease 45 0.293
146
P MNN007 Meningocele 39 0.293
147
FCL014 Focal Epilepsy 53 0.293
148
47X002 47,xyy 48 0.293
149
CRN194 Cranial Meningocele 11 0.293
150
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.262
151
P LFT003 Left Ventricular Noncompaction 57 0.262
152
HYP748 Hypertelorism 46 0.262
153
TNG004 Tongue Disease 43 0.262
154
P INF032 Infertility 60 0.262
155
P ECT006 Ectodermal Dysplasia 62 0.262
156
SPN186 Spinal Cord Injury 61 0.262
157
ORF053 Orofacial Clefting Syndrome 31 0.262
158
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.227
159
c HYP820 Hypogonadotropic Hypogonadism 22 with or Without Anosmia 24 0.227
160
ANK001 Ankylosis 51 0.227
161
HYP014 Hyperuricemia 51 0.227
162
CHR254 Chromosome 5q Duplication 13 0.227
163
P DBT009 Diabetes Mellitus 67 0.227
164
CLF056 Cleft Lip with or Without Cleft Palate 43 0.227
165
ISL089 Isolated Scaphocephaly 26 0.227
166
c FRS014 Fraser Syndrome 1 56 0.185
167
CTS011 Cutis Marmorata Telangiectatica Congenita 34 0.185
168
OLV002 Oliver Syndrome 41 0.185
169
P PSD087 Pseudoxanthoma Elasticum 66 0.185
170
c ORF014 Orofacial Cleft 5 21 0.185
171
P PRX021 Proximal Symphalangism 50 0.185
172
P PLY014 Polycystic Kidney Disease 71 0.185
173
P TRC072 Treacher Collins Syndrome 1 62 0.185
174
MRF001 Marfan Syndrome 76 0.185
175
c BRC078 Brachydactyly, Type A1 53 0.185
176
CLB010 Coloboma of Macula 53 0.185
177
P CNR004 Cone-Rod Dystrophy 2 75 0.185
178
CST001 Costello Syndrome 68 0.185
179
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.185
180
P ADM011 Adams-Oliver Syndrome 59 0.185
181
PRP080 Peripheral Artery Disease 54 0.185
182
c BRC052 Brachydactyly, Type B2 40 0.185
183
c ORF048 Orofacial Cleft 1 30 0.185
184
STP011 Stapes Ankylosis with Broad Thumbs and Toes 28 0.185
185
c SYM022 Symphalangism, Proximal, 1a 28 0.185
186
TTH030 Teeth, Supernumerary 32 0.185
187
ULN023 Ulnar Hypoplasia 25 0.185
188
NPH003 Nephrocalcinosis 49 0.185
189
P HYP040 Hypospadias 51 0.185
190
HRT011 Heart Septal Defect 49 0.185
191
P HYP086 Hypothyroidism 69 0.185
192
P TRT010 Teratoma 50 0.185
193
ODN006 Odontoma 29 0.185
194
DXT001 Dextrocardia 55 0.185
195
RTN123 Retinochoroidal Coloboma 18 0.185
196
ISL109 Isolated Cleft Lip 33 0.185
197
MNT058 Mental Retardation, X-Linked, Syndromic, Turner Type 40 0.131
198
AGN016 Aging 54 0.131
199
CDG001 Cdags Syndrome 26 0.131
200
HMC014 Homocysteinemia 52 0.131
201
P GST053 Gastric Cancer 82 0.131
202
c CRN299 Craniosynostosis Syndrome, Autosomal Recessive 7 0.131
203
c PRT113 Parietal Foramina 3 16 0.131
204
SWN003 Sweeney-Cox Syndrome 39 0.131
205
NVS015 Nevus Comedonicus 38 0.131
206
STR112 Structural Brain Anomalies with Impaired Intellectual Development and Craniosynostosis 23 0.131
207
MTL007 Mutilating Palmoplantar Keratoderma with Periorificial Keratotic Plaques 49 0.131
208
P SPL061 Split Hand-Foot Malformation 42 0.131
209
ATR093 Atrial Heart Septal Defect 7 22 0.131
210
MRF007 Marfanoid Hypermobility Syndrome 50 0.131
211
PLY150 Polykaryocytosis Inducer 29 0.131
212
P FNG006 Feingold Syndrome 1 61 0.131
213
P OST002 Osteoporosis 77 0.131
214
ATR088 Atrial Septal Defect 7 with or Without Atrioventricular Conduction Defects 30 0.131
215
ACN002 Acanthosis Nigricans 56 0.131
216
ATH013 Atherosclerosis Susceptibility 63 0.131
217
P STS008 Sotos Syndrome 1 62 0.131
218
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 60 0.131
219
BLL001 Baller-Gerold Syndrome 58 0.131
220
P BRN042 Branchiootic Syndrome 34 0.131
221
SYN090 Syndromic X-Linked Intellectual Disability Turner Type 30 0.131
222
P BRC015 Bruck Syndrome 48 0.131
223
c BRN128 Branchiootic Syndrome 3 28 0.131
224
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.131
225
JCB001 Jacobsen Syndrome 50 0.131
226
P SYN075 Syngnathia 42 0.131
227
CLF028 Cleft Soft Palate 38 0.131
228
P CMR001 Camurati-Engelmann Disease 59 0.131
229
P ART028 Aortic Aneurysm, Familial Thoracic 4 61 0.131
230
c EXS020 Exostoses, Multiple, Type Ii 38 0.131
231
P FRN036 Frontonasal Dysplasia 1 43 0.131
232
c NRF024 Neurofibromatosis, Type I 76 0.131
233
MCC012 Mccune-Albright Syndrome 69 0.131
234
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.131
235
P LNG064 Lung Cancer Susceptibility 3 70 0.131
236
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.131
237
ANS023 Anus, Imperforate 56 0.131
238
P OLM003 Olmsted Syndrome 1 36 0.131
239
c BSL032 Basal Ganglia Calcification, Idiopathic, 4 25 0.131
240
PLP001 Pulpitis 48 0.131
241
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 50 0.131
242
PRT037 Pertussis 49 0.131
243
P ATR010 Atrial Heart Septal Defect 58 0.131
244
HYP068 Hyperostosis 47 0.131
245
KRT009 Keratosis 52 0.131
246
c BSL007 Basal Cell Carcinoma 68 0.131
247
OBS004 Obstructive Hydrocephalus 45 0.131
248
P VNT002 Ventricular Septal Defect 58 0.131
249
P CHN059 Chondrocalcinosis 51 0.131
250
P LKM002 Leukemia 66 0.131
251
SKN016 Skin Disease 62 0.131
252
TST014 Testicular Cancer 51 0.131
253
c LKM061 Leukemia, Acute Myeloid 83 0.131
254
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 47 0.131
255
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.131
256
P PTN014 Patent Ductus Arteriosus 1 59 0.131
257
SKL017 Skeletal Dysplasias 41 0.131
258
HRT012 Heart Valve Disease 53 0.131
259
CHL149 Childhood Acute Myeloid Leukemia 42 0.131
260
P MYL006 Myeloid Leukemia 60 0.131
261
TRC037 Tracheobronchomalacia 23 0.131
262
TRC052 Trichofolliculoma 17 0.131
263
XLN179 X-Linked Intellectual Disability, Turner Type 19 0.131
264
HYP266 Hypoxia 56 0.131
265
OST012 Osteoarthritis 77 0.131
266
END086 End Stage Renal Disease 54 0.131
267
P NRF002 Neurofibromatosis 60 0.131
268
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 71 0.131
269
PLG004 Plagiocephaly 40 0.131
270
LRN003 Learning Disability 49 0.131
271
CNG284 Congenital Pseudoarthrosis of the Tibia 17 0.131
272
KRT063 Keratocystic Odontogenic Tumor 39 0.131
273
ISL087 Isolated Oxycephaly 35 0.131
274
P OVR082 Overgrowth Syndrome 42 0.131
275
PRP101 Peripheral Pulmonary Stenosis 23 0.131
Content
Loading form....