Search results for "[genes] RUNX2"

34 hits were found for '[genes] RUNX2'

# Family MCID Name MIFTS Score
1
P CLD001 Cleidocranial Dysplasia 62 25.322
2
MTP023 Metaphyseal Dysplasia with Maxillary Hypoplasia with or Without Brachydactyly 17 17.905
3
P OST002 Osteoporosis 64 16.345
4
P BRC006 Brachydactyly 52 16.345
5
P MYL006 Myeloid Leukemia 67 14.619
6
HYP025 Hyperphosphatemia 46 14.619
7
P PFF001 Pfeiffer Syndrome 73 12.661
8
OST085 Osteosarcoma, Somatic 63 12.661
9
P STH001 Saethre-Chotzen Syndrome 59 12.661
10
ANK001 Ankylosis 52 12.661
11
OST003 Osteonecrosis 45 12.661
12
P SCL048 Sclerosteosis 45 12.661
13
DYS018 Dysostosis 44 12.661
14
GLC086 Glucocorticoid-Induced Osteoporosis 37 12.661
15
HJD001 Hajdu-Cheney Syndrome 58 10.337
16
OSS012 Osseous Heteroplasia, Progressive 53 10.337
17
c ART115 Aortic Valve Disease 1 53 10.337
18
IMP002 Imperforate Anus 52 10.337
19
MRC001 Marchiafava Bignami Disease 50 10.337
20
BNC003 Bone Cancer 45 10.337
21
c TRC092 Trichorhinophalangeal Syndrome, Type I 45 10.337
22
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 44 10.337
23
BND014 Bone Development Disease 42 10.337
24
CRB138 Core Binding Factor Acute Myeloid Leukemia 41 10.337
25
SYN031 Synovial Chondromatosis 41 10.337
26
BNR001 Bone Remodeling Disease 40 10.337
27
LCL004 Localized Osteosarcoma 38 10.337
28
CLR005 Clear Cell Chondrosarcoma 38 10.337
29
ISC005 Ischemic Bone Disease 38 10.337
30
ALV001 Alveolar Periostitis 35 10.337
31
SWY001 Swayback 29 10.337
32
PRT043 Parietal Foramina with Cleidocranial Dysplasia 25 10.337
33
BNR002 Bone Resorption Disease 22 10.337
34
c LKM061 Leukemia, Acute Myeloid 71 7.310