Search results for "[genes] PDGFRB"

44 hits were found for '[genes] PDGFRB'

# Family MCID Name MIFTS Score
1
c MYF007 Myofibromatosis, Infantile, 1 32 19.970
2
P LNG032 Lung Cancer 92 17.295
3
MYL015 Myeloproliferative Disorder with Eosinophilia 34 17.295
4
c BSL032 Basal Ganglia Calcification, Idiopathic, 4 18 17.295
5
PRM206 Premature Aging Syndrome, Penttinen Type 21 17.295
6
KSK002 Kosaki Overgrowth Syndrome 17 17.295
7
MYL009 Myelodysplastic Syndrome 73 15.788
8
P ESN007 Eosinophilia 61 15.788
9
BSL009 Basal Ganglia Calcification 41 15.788
10
P BRS047 Breast Cancer 100 14.121
11
P PRS040 Prostate Cancer 89 14.121
12
GST019 Gastrointestinal Stromal Tumor 73 14.121
13
DRM014 Dermatofibrosarcoma Protuberans 61 14.121
14
GLB015 Glioblastoma Multiforme 63 14.121
15
P ADN016 Adenocarcinoma 69 14.121
16
c CHR285 Chronic Myelomonocytic Leukemia 54 14.121
17
P INF049 Infantile Myofibromatosis 44 14.121
18
P RNL014 Renal Cell Carcinoma 80 12.229
19
P LKM068 Leukemia, Chronic Myeloid, Somatic 65 12.229
20
PLY125 Polycythemia Vera, Somatic 63 12.229
21
EWN003 Ewing Sarcoma 63 12.229
22
P PRM175 Primary Familial Brain Calcification 43 12.229
23
BNC003 Bone Cancer 44 12.229
24
c SYS004 Systemic Mastocytosis 60 12.229
25
c MNN043 Meningioma, Familial 61 9.985
26
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 39 9.985
27
P HYP098 Hypereosinophilic Syndrome 48 9.985
28
DSM004 Desmoid Tumor 55 9.985
29
c CHR092 Chronic Myeloproliferative Disease 50 9.985
30
CRN273 Corneal Dystrophy, Subepithelial Mucinous 29 9.985
31
c CNN010 Connective Tissue Benign Neoplasm 31 9.985
32
DBT008 Diabetic Angiopathy 30 9.985
33
CHR563 Chronic Eosinophilic Leukemia 46 9.985
34
SPN036 Spinal Chordoma 37 9.985
35
P 8P1002 8p11 Myeloproliferative Syndrome 37 9.985
36
HYP048 Hypotropia 30 9.985
37
CLR005 Clear Cell Chondrosarcoma 38 9.985
38
CLL006 Cellular Neurofibroma 32 9.985
39
FBR002 Fibrosarcoma of Bone 41 9.985
40
TND006 Tendinosis 37 9.985
41
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 62 7.061
42
c PRM149 Primary Hypereosinophilic Syndrome 39 7.061
43
MYL042 Myeloid Neoplasm Associated with Pdgfrb Rearrangement 5 7.061
44
c PRM180 Primary Familial Brain Calcification 4 6 7.061