Search results for "[genes] RUNX2"

33 hits were found for '[genes] RUNX2'

# Family MCID Name MIFTS Score
1
P CLD001 Cleidocranial Dysplasia 65 25.555
2
P OST002 Osteoporosis 76 18.070
3
P BRC006 Brachydactyly 49 16.496
4
P MYL006 Myeloid Leukemia 61 14.754
5
MTP001 Metaphyseal Dysplasia 45 14.754
6
HYP025 Hyperphosphatemia 38 14.754
7
MTP023 Metaphyseal Dysplasia with Maxillary Hypoplasia with or Without Brachydactyly 15 14.754
8
P PFF001 Pfeiffer Syndrome 69 12.777
9
P STH001 Saethre-Chotzen Syndrome 62 12.777
10
OST085 Osteosarcoma, Somatic 61 12.777
11
P SCL048 Sclerosteosis 49 12.777
12
P GNT008 Giant Cell Tumor 44 12.777
13
RTR008 Root Resorption 39 12.777
14
GLC086 Glucocorticoid-Induced Osteoporosis 36 12.777
15
HJD001 Hajdu-Cheney Syndrome 58 10.433
16
SDC002 Sed Congenita 53 10.433
17
BNC003 Bone Cancer 47 10.433
18
c ART115 Aortic Valve Disease 1 47 10.433
19
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 46 10.433
20
CRB138 Core Binding Factor Acute Myeloid Leukemia 39 10.433
21
CLR005 Clear Cell Chondrosarcoma 35 10.433
22
OSS012 Osseous Heteroplasia, Progressive 35 10.433
23
PPL009 Papillary Craniopharyngioma 34 10.433
24
SWY001 Swayback 33 10.433
25
BND014 Bone Development Disease 33 10.433
26
BNR001 Bone Remodeling Disease 33 10.433
27
LCL004 Localized Osteosarcoma 33 10.433
28
BNR002 Bone Resorption Disease 32 10.433
29
ISC005 Ischemic Bone Disease 31 10.433
30
ALV001 Alveolar Periostitis 29 10.433
31
MRC001 Marchiafava Bignami Disease 26 10.433
32
c LKM061 Leukemia, Acute Myeloid 66 7.377
33
MTP030 Metaphyseal Dysplasia-Maxillary Hypoplasia-Brachydacty Syndrome 10 7.377