Search results for runx2

235 hits were found for runx2

# Family MCID Name MIFTS Score
1
P CLD001 Cleidocranial Dysplasia 65 6.104
2
P LKM002 Leukemia 68 3.447
3
P OST002 Osteoporosis 74 3.421
4
MTP023 Metaphyseal Dysplasia with Maxillary Hypoplasia with or Without Brachydactyly 26 3.341
5
P BRC006 Brachydactyly 53 3.199
6
P BND020 Bone Disease 59 3.136
7
P PRS040 Prostate Cancer 97 2.918
8
P RTN024 Retinoblastoma 73 2.874
9
P MYL006 Myeloid Leukemia 60 2.858
10
P MTP001 Metaphyseal Dysplasia 36 2.858
11
OST012 Osteoarthritis 78 2.593
12
P CHN012 Chondrosarcoma 56 2.580
13
P SCL018 Scoliosis 60 2.507
14
OST159 Osteogenic Sarcoma 66 2.481
15
c CHR684 Chronic Kidney Disease 70 2.470
16
HYP025 Hyperphosphatemia 48 2.425
17
DYS018 Dysostosis 44 2.425
18
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 21 2.289
19
P CRN037 Craniosynostosis 68 2.212
20
OST003 Osteonecrosis 61 2.122
21
CLF027 Cleft Palate, Isolated 64 2.090
22
P PRD008 Periodontitis 64 2.090
23
P SCL048 Sclerosteosis 55 2.053
24
RTR008 Root Resorption 45 2.053
25
P HYP035 Hypophosphatasia 61 2.032
26
FBR009 Fibrous Dysplasia 48 2.032
27
GLC086 Glucocorticoid-Induced Osteoporosis 43 2.032
28
ODN023 Odontochondrodysplasia 68 2.008
29
STH001 Saethre-Chotzen Syndrome 67 2.008
30
OSS012 Osseous Heteroplasia, Progressive 61 2.008
31
PFF001 Pfeiffer Syndrome 79 1.980
32
c ART115 Aortic Valve Disease 1 75 1.980
33
P OST001 Osteopetrosis 70 1.980
34
WLL001 Williams-Beuren Syndrome 60 1.980
35
P ART021 Arteriosclerosis 54 1.980
36
ANK001 Ankylosis 51 1.980
37
P PRT042 Parietal Foramina 46 1.980
38
BNR002 Bone Resorption Disease 48 1.750
39
TTH030 Teeth, Supernumerary 33 1.750
40
c LKM061 Leukemia, Acute Myeloid 84 1.548
41
MYL069 Myeloma, Multiple 85 1.511
42
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 49 1.490
43
TTH002 Tooth Agenesis 60 1.466
44
CRT017 Cartilage Disease 54 1.466
45
SYN005 Synostosis 45 1.466
46
SYN106 Syndromic Craniosynostosis 33 1.466
47
APR006 Apert Syndrome 70 1.437
48
c ART101 Aortic Valve Disease 2 65 1.437
49
P VNB005 Van Buchem Disease 56 1.437
50
BRT054 Brittle Bone Disorder 72 1.400
51
CRZ001 Crouzon Syndrome 68 1.400
52
CNN005 Connective Tissue Disease 68 1.400
53
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 61 1.400
54
P CMR001 Camurati-Engelmann Disease 59 1.400
55
ENC044 Enchondromatosis, Multiple, Ollier Type 57 1.400
56
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 1.400
57
c OST164 Osteoporosis, Juvenile 53 1.400
58
BNS007 Bone Sarcoma 45 1.400
59
P ORF002 Orofacial Cleft 44 1.400
60
HPT082 Hepatic Adenomas, Familial 44 1.400
61
CRB138 Core Binding Factor Acute Myeloid Leukemia 43 1.400
62
DNT014 Dental Pulp Disease 42 1.400
63
SYN031 Synovial Chondromatosis 42 1.400
64
PHS001 Phosphorus Metabolism Disease 40 1.400
65
MNR003 Mineral Metabolism Disease 39 1.400
66
TTH008 Tooth Resorption 37 1.400
67
CLR005 Clear Cell Chondrosarcoma 34 1.400
68
BNS001 Bone Osteosarcoma 33 1.400
69
P BND014 Bone Development Disease 33 1.400
70
BNR001 Bone Remodeling Disease 28 1.400
71
ISC005 Ischemic Bone Disease 27 1.400
72
PRT043 Parietal Foramina with Cleidocranial Dysplasia 27 1.400
73
BNS002 Bone Structure Disease 24 1.400
74
c ATS476 Autosomal Dominant Non-Syndromic Intellectual Disability 32 21 1.400
75
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.196
76
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.196
77
P BRS047 Breast Cancer 97 0.155
78
THY029 Thyroid Carcinoma 59 0.149
79
P PNC035 Pancreatic Cancer 84 0.119
80
P LNG032 Lung Cancer 98 0.110
81
MSC007 Muscle Hypertrophy 64 0.110
82
P MLN008 Melanoma 69 0.100
83
P GLM045 Glioma 63 0.100
84
HYP266 Hypoxia 57 0.100
85
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.100
86
GLL048 Glial Tumor 45 0.100
87
DWR001 Dwarfism 44 0.100
88
P CLR023 Colorectal Cancer 99 0.090
89
INS024 Insulin-Like Growth Factor I 79 0.090
90
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 65 0.090
91
c FML008 Familial Retinoblastoma 53 0.090
92
P HPT023 Hepatocellular Carcinoma 100 0.078
93
P BLD134 Bladder Cancer 79 0.078
94
P LNG064 Lung Cancer Susceptibility 3 78 0.078
95
SVR004 Severe Combined Immunodeficiency 73 0.078
96
P LKM062 Leukemia, Acute Lymphoblastic 69 0.078
97
P LYM118 Lymphoma 68 0.078
98
HYP066 Hyperglycemia 61 0.078
99
CLF001 Cleft Lip 53 0.078
100
c TRC092 Trichorhinophalangeal Syndrome, Type I 52 0.078
101
BNG036 Bone Giant Cell Tumor 49 0.078
102
HLX001 Helix Syndrome 47 0.078
103
IDP070 Idiopathic Scoliosis 42 0.078
104
P SCL057 Scoliosis, Isolated 1 41 0.078
105
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.078
106
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.078
107
P OVR042 Ovarian Cancer 88 0.063
108
GLB015 Glioblastoma Multiforme 75 0.063
109
MYL009 Myelodysplastic Syndrome 70 0.063
110
P MYP004 Myopathy 70 0.063
111
P SKN015 Skin Carcinoma 66 0.063
112
P ADN016 Adenocarcinoma 64 0.063
113
ALL026 Allergic Hypersensitivity Disease 62 0.063
114
c ACT073 Acute Leukemia 58 0.063
115
P BNC003 Bone Cancer 58 0.063
116
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.063
117
P PLY011 Polycystic Ovary Syndrome 56 0.063
118
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.063
119
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.063
120
HYP748 Hypertelorism 50 0.063
121
DGN001 Degenerative Disc Disease 48 0.063
122
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.063
123
CLF056 Cleft Lip with or Without Cleft Palate 47 0.063
124
THY128 Thyroid Tumor 47 0.063
125
c PCH010 Pachyonychia Congenita 3 44 0.063
126
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.063
127
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.063
128
DND018 Dendritic Cell Tumor 40 0.063
129
BLS007 Blastic Plasmacytoid Dendritic Cell 38 0.063
130
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.063
131
ESP021 Esophageal Cancer 90 0.045
132
P GST053 Gastric Cancer 83 0.045
133
P ATX030 Ataxia-Telangiectasia 82 0.045
134
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.045
135
CRV035 Cervical Cancer 76 0.045
136
CRH001 Crohn's Disease 74 0.045
137
c SPN225 Spondyloarthropathy 1 73 0.045
138
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.045
139
P ART022 Arthritis 69 0.045
140
P OCL013 Oculodentodigital Dysplasia 69 0.045
141
P HYP086 Hypothyroidism 69 0.045
142
ART016 Aortic Aneurysm 69 0.045
143
MNT001 Mantle Cell Lymphoma 69 0.045
144
CHL065 Cholangiocarcinoma 68 0.045
145
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.045
146
P TRN020 Turner Syndrome 67 0.045
147
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.045
148
P MCR115 Microvascular Complications of Diabetes 5 66 0.045
149
MYL031 Myeloproliferative Neoplasm 66 0.045
150
c SML038 Small Cell Cancer of the Lung 65 0.045
151
SRC014 Sarcoma 65 0.045
152
c WLM013 Wilms Tumor 1 65 0.045
153
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.045
154
P DBT009 Diabetes Mellitus 64 0.045
155
P CMP005 Campomelic Dysplasia 64 0.045
156
HYP020 Hyperprolactinemia 64 0.045
157
OST017 Osteomyelitis 64 0.045
158
BRS099 Breast Ductal Carcinoma 62 0.045
159
LVR012 Liver Cirrhosis 62 0.045
160
BLD131 Bladder Urothelial Carcinoma 62 0.045
161
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.045
162
PSR001 Psoriatic Arthritis 61 0.045
163
FTT001 Fatty Liver Disease 61 0.045
164
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.045
165
WLF002 Wolf-Hirschhorn Syndrome 59 0.045
166
DCT002 Ductal Carcinoma in Situ 59 0.045
167
P BRS044 Breast Adenocarcinoma 59 0.045
168
ADN018 Adenoma 59 0.045
169
ANT024 Anthrax Disease 58 0.045
170
P BCL017 B-Cell Lymphoma 58 0.045
171
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.045
172
CHR003 Cherubism 57 0.045
173
P MLT074 Multiple Endocrine Neoplasia 56 0.045
174
PRS047 Prostatitis 56 0.045
175
P CRB154 Cerebrocostomandibular Syndrome 55 0.045
176
CLF004 Cleft Lip/palate 54 0.045
177
GLC003 Glucose Intolerance 54 0.045
178
P ALP008 Alopecia 54 0.045
179
P INF037 Inflammatory Bowel Disease 54 0.045
180
NNL006 Non-Alcoholic Steatohepatitis 54 0.045
181
c EXS019 Exostoses, Multiple, Type I 53 0.045
182
P INS002 in Situ Carcinoma 53 0.045
183
P MNC007 Monocytic Leukemia 53 0.045
184
GTR002 Goiter 53 0.045
185
HMC014 Homocysteinemia 53 0.045
186
SPN035 Spindle Cell Sarcoma 53 0.045
187
OST011 Osteomalacia 52 0.045
188
P RCT021 Rectum Cancer 52 0.045
189
P DNT011 Dentinogenesis Imperfecta 52 0.045
190
TLN003 Telangiectasis 52 0.045
191
SPN051 Spondylitis 51 0.045
192
CLR109 Colorectal Adenocarcinoma 51 0.045
193
INT079 Intrahepatic Cholangiocarcinoma 51 0.045
194
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.045
195
BLD053 Blood Platelet Disease 49 0.045
196
ENT004 Enthesopathy 49 0.045
197
DNT045 Dental Anomalies and Short Stature 49 0.045
198
P CTN015 Cutaneous T Cell Lymphoma 49 0.045
199
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.045
200
BNN003 Bone Inflammation Disease 48 0.045
201
P GND004 Gonadal Dysgenesis 48 0.045
202
LYM009 Lymphocytic Choriomeningitis 47 0.045
203
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.045
204
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.045
205
EXS001 Exostosis 46 0.045
206
URT010 Ureteral Obstruction 45 0.045
207
P CHR345 Chronic Pain 44 0.045
208
PTT037 Pituitary Tumors 44 0.045
209
P BNG095 Benign Giant Cell Tumor 44 0.045
210
AND001 Anodontia 43 0.045
211
LRW001 Leri-Weill Dyschondrosteosis 43 0.045
212
DNT001 Dental Fluorosis 43 0.045
213
OST115 Osteonecrosis of the Jaw 40 0.045
214
ANX004 Anoxia 40 0.045
215
SKL017 Skeletal Dysplasias 40 0.045
216
KLD004 Keloid Disorder 40 0.045
217
c PRG020 Paragangliomas 3 39 0.045
218
OVR094 Ovarian Epithelial Cancer 38 0.045
219
ISL109 Isolated Cleft Lip 38 0.045
220
PLM156 Palmoplantar Carcinoma, Multiple Self-Healing 37 0.045
221
c CRN277 Craniosynostosis 2 36 0.045
222
GPS001 Gapo Syndrome 36 0.045
223
LNG040 Langer Mesomelic Dysplasia 36 0.045
224
HRW001 Hair Whorl 36 0.045
225
MYP035 Myopathy, Distal, with Anterior Tibial Onset 32 0.045
226
INF009 Inflammatory Spondylopathy 31 0.045
227
CRT069 Cortical Malformations, Occipital 30 0.045
228
TRD003 Taurodontism 30 0.045
229
CLF049 Cleft Lip and Alveolus 30 0.045
230
DST103 Distal Muscular Dystrophy with Anterior Tibial Onset 30 0.045
231
CNG092 Congenital Extrahepatic Portosystemic Shunt 23 0.045
232
c JVN025 Juvenile Primary Osteoporosis 22 0.045
233
MD2001 Med23 22 0.045
234
CHR247 Chromosome 4p Deletion 22 0.045
235
BNC005 Bone Chondrosarcoma 19 0.045
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