Search results for "[genes] RUNX2"

33 hits were found for '[genes] RUNX2'

# Family MCID Name MIFTS Score
1
P CLD001 Cleidocranial Dysplasia 62 25.555
2
P OST002 Osteoporosis 80 18.070
3
P BRC006 Brachydactyly 51 16.496
4
P MYL006 Myeloid Leukemia 68 14.754
5
MTP001 Metaphyseal Dysplasia 48 14.754
6
HYP025 Hyperphosphatemia 46 14.754
7
MTP023 Metaphyseal Dysplasia with Maxillary Hypoplasia with or Without Brachydactyly 17 14.754
8
P PFF001 Pfeiffer Syndrome 72 12.777
9
OST085 Osteosarcoma, Somatic 61 12.777
10
P STH001 Saethre-Chotzen Syndrome 60 12.777
11
P GNT008 Giant Cell Tumor 54 12.777
12
P SCL048 Sclerosteosis 48 12.777
13
RTR008 Root Resorption 45 12.777
14
GLC086 Glucocorticoid-Induced Osteoporosis 42 12.777
15
BNC003 Bone Cancer 62 10.433
16
HJD001 Hajdu-Cheney Syndrome 57 10.433
17
OSS012 Osseous Heteroplasia, Progressive 54 10.433
18
MRC001 Marchiafava Bignami Disease 54 10.433
19
c ART115 Aortic Valve Disease 1 54 10.433
20
SDC002 Sed Congenita 53 10.433
21
CRB138 Core Binding Factor Acute Myeloid Leukemia 47 10.433
22
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 46 10.433
23
BND014 Bone Development Disease 44 10.433
24
CLR005 Clear Cell Chondrosarcoma 43 10.433
25
BNR001 Bone Remodeling Disease 43 10.433
26
PPL009 Papillary Craniopharyngioma 42 10.433
27
BNR002 Bone Resorption Disease 42 10.433
28
LCL004 Localized Osteosarcoma 41 10.433
29
SWY001 Swayback 40 10.433
30
ISC005 Ischemic Bone Disease 40 10.433
31
ALV001 Alveolar Periostitis 38 10.433
32
c LKM061 Leukemia, Acute Myeloid 71 7.377
33
MTP030 Metaphyseal Dysplasia-Maxillary Hypoplasia-Brachydacty Syndrome 10 7.377