Search results for "[genes] RUNX2"

40 hits were found for '[genes] RUNX2'

# Family MCID Name MIFTS Score
1
P CLD001 Cleidocranial Dysplasia 62 24.828
2
P LKM002 Leukemia 71 18.963
3
P OST002 Osteoporosis 64 17.556
4
MTP023 Metaphyseal Dysplasia with Maxillary Hypoplasia with or Without Brachydactyly 16 17.556
5
P MYL006 Myeloid Leukemia 66 16.026
6
P BRC006 Brachydactyly 54 16.026
7
HYP025 Hyperphosphatemia 47 16.026
8
P PFF001 Pfeiffer Syndrome 73 14.334
9
OST085 Osteosarcoma, Somatic 63 14.334
10
P STH001 Saethre-Chotzen Syndrome 60 14.334
11
ANK001 Ankylosis 51 14.334
12
P SCL048 Sclerosteosis 45 14.334
13
OST003 Osteonecrosis 45 14.334
14
DYS018 Dysostosis 44 14.334
15
GLC086 Glucocorticoid-Induced Osteoporosis 38 14.334
16
HJD001 Hajdu-Cheney Syndrome 59 12.414
17
BNC003 Bone Cancer 58 12.414
18
OSS012 Osseous Heteroplasia, Progressive 54 12.414
19
IMP002 Imperforate Anus 52 12.414
20
c ART115 Aortic Valve Disease 1 50 12.414
21
c TRC092 Trichorhinophalangeal Syndrome, Type I 46 12.414
22
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 44 12.414
23
SYN031 Synovial Chondromatosis 42 12.414
24
CRB138 Core Binding Factor Acute Myeloid Leukemia 42 12.414
25
RTR008 Root Resorption 42 12.414
26
BND014 Bone Development Disease 40 12.414
27
CLR005 Clear Cell Chondrosarcoma 38 12.414
28
BNR001 Bone Remodeling Disease 37 12.414
29
ISC005 Ischemic Bone Disease 36 12.414
30
LCL004 Localized Osteosarcoma 35 12.414
31
ALV001 Alveolar Periostitis 34 12.414
32
SWY001 Swayback 28 12.414
33
PRT043 Parietal Foramina with Cleidocranial Dysplasia 25 12.414
34
BNR002 Bone Resorption Disease 21 12.414
35
c LKM061 Leukemia, Acute Myeloid 73 10.136
36
SDC002 Sed Congenita 53 10.136
37
c WLF009 Wolfram Syndrome 2 45 10.136
38
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 41 10.136
39
MRC001 Marchiafava Bignami Disease 39 10.136
40
c HLP012 Holoprosencephaly-3 39 10.136