Search results for "[genes] RUNX2"

36 hits were found for '[genes] RUNX2'

# Family MCID Name MIFTS Score
1
P CLD001 Cleidocranial Dysplasia 66 26.278
2
P OST002 Osteoporosis 75 16.297
3
P BRC006 Brachydactyly 48 16.297
4
P MYL006 Myeloid Leukemia 59 14.577
5
MTP001 Metaphyseal Dysplasia 46 14.577
6
HYP025 Hyperphosphatemia 36 14.577
7
MTP023 Metaphyseal Dysplasia with Maxillary Hypoplasia with or Without Brachydactyly 17 14.577
8
P PFF001 Pfeiffer Syndrome 71 12.624
9
P STH001 Saethre-Chotzen Syndrome 65 12.624
10
P HYP035 Hypophosphatasia 58 12.624
11
OST085 Osteosarcoma, Somatic 56 12.624
12
OST003 Osteonecrosis 50 12.624
13
OST015 Osteochondrodysplasia 46 12.624
14
P SCL048 Sclerosteosis 43 12.624
15
ANK001 Ankylosis 43 12.624
16
RTR008 Root Resorption 35 12.624
17
GLC086 Glucocorticoid-Induced Osteoporosis 33 12.624
18
BND014 Bone Development Disease 28 12.624
19
OSS012 Osseous Heteroplasia, Progressive 52 10.307
20
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 47 10.307
21
IMP002 Imperforate Anus 45 10.307
22
c ART115 Aortic Valve Disease 1 43 10.307
23
DYS018 Dysostosis 43 10.307
24
MRC001 Marchiafava Bignami Disease 42 10.307
25
SYN031 Synovial Chondromatosis 38 10.307
26
CRB138 Core Binding Factor Acute Myeloid Leukemia 34 10.307
27
PPL009 Papillary Craniopharyngioma 31 10.307
28
SWY001 Swayback 30 10.307
29
LCL004 Localized Osteosarcoma 30 10.307
30
ISC005 Ischemic Bone Disease 28 10.307
31
BNR002 Bone Resorption Disease 28 10.307
32
CHN003 Chondroblastic Osteosarcoma 27 10.307
33
ALV001 Alveolar Periostitis 25 10.307
34
PRT043 Parietal Foramina with Cleidocranial Dysplasia 25 10.307
35
c LKM061 Leukemia, Acute Myeloid 74 7.288
36
MTP020 Metaphyseal Dysplasia - Maxillary Hypoplasia - Brachydacty 11 7.288