Search results for "[genes] IGF2"

83 hits were found for '[genes] IGF2'

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 97 18.307
2
P BRS047 Breast Cancer 100 17.125
3
P BCK002 Beckwith-Wiedemann Syndrome 54 15.855
4
P SLV001 Silver-Russell Syndrome 50 15.855
5
P PRS040 Prostate Cancer 90 14.473
6
HYP056 Hypoglycemia 60 14.473
7
RHB003 Rhabdomyosarcoma 58 14.473
8
P OBS005 Obesity 91 12.945
9
HPT023 Hepatocellular Carcinoma 90 12.945
10
ADR005 Adrenal Carcinoma 59 12.945
11
UTR039 Uterine Fibroid 58 12.945
12
LMY002 Leiomyoma 56 12.945
13
P EMB005 Embryonal Rhabdomyosarcoma 55 12.945
14
HPT022 Hepatoblastoma 55 12.945
15
P HMN013 Hemangiopericytoma 55 12.945
16
P HYP050 Hyperinsulinemic Hypoglycemia 53 12.945
17
c CLR017 Clear Cell Sarcoma 51 12.945
18
c CNG029 Congenital Mesoblastic Nephroma 42 12.945
19
GRW027 Growth Restriction, Severe, with Distinctive Facies 12 12.945
20
P OST002 Osteoporosis 80 11.211
21
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 11.211
22
P LFR001 Li-Fraumeni Syndrome 79 11.211
23
INS024 Insulin-Like Growth Factor I 76 11.211
24
P MDL005 Medulloblastoma 74 11.211
25
EWN003 Ewing Sarcoma 66 11.211
26
WLM007 Wilms Tumor Susceptibility-5 63 11.211
27
ANR002 Aniridia 60 11.211
28
LRN004 Laron Dwarfism 59 11.211
29
ADR016 Adrenal Cortical Carcinoma 59 11.211
30
CHR029 Choroid Plexus Papilloma 52 11.211
31
RHB001 Rhabdoid Cancer 52 11.211
32
OST016 Osteochondrosis 52 11.211
33
ISL001 Islet Cell Tumor 52 11.211
34
HYP299 Hyperostosis, Endosteal 49 11.211
35
FBR054 Fibroma 48 11.211
36
HYP026 Hypoglycemic Coma 46 11.211
37
UMB002 Umbilical Hernia 44 11.211
38
SKL003 Skeletal Muscle Cancer 44 11.211
39
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 9.154
40
GST019 Gastrointestinal Stromal Tumor 74 9.154
41
EYD002 Eye Disease 65 9.154
42
OST085 Osteosarcoma, Somatic 61 9.154
43
P PLR004 Pleuropulmonary Blastoma 61 9.154
44
c MNN043 Meningioma, Familial 58 9.154
45
PRL032 Perlman Syndrome 58 9.154
46
PRT093 Proteus Syndrome, Somatic 55 9.154
47
P HLL001 Hallermann-Streiff Syndrome 55 9.154
48
SLT008 Solitary Fibrous Tumor 53 9.154
49
MLK003 Melkersson-Rosenthal Syndrome 53 9.154
50
ADL002 Adult Syndrome 50 9.154
51
P SMP003 Simpson-Golabi-Behmel Syndrome 48 9.154
52
ACN001 Acinar Cell Carcinoma 48 9.154
53
FRZ001 Frozen Shoulder 47 9.154
54
INC001 Incontinentia Pigmenti Achromians 47 9.154
55
MNN006 Meninges Hemangiopericytoma 45 9.154
56
END038 Endocrine Pancreas Disease 44 9.154
57
c HRD009 Hereditary Wilms' Tumor 44 9.154
58
P PTT002 Potter's Syndrome 44 9.154
59
RTR010 Retroperitoneal Sarcoma 43 9.154
60
FST010 Fasting Hypoglycemia 42 9.154
61
c MCP026 Mucopolysaccharidosis Type Iiib 42 9.154
62
OCL004 Ocular Hyperemia 42 9.154
63
FTL021 Fetal Macrosomia 41 9.154
64
BLS003 Blastoma 41 9.154
65
PSD008 Pseudopapilledema 39 9.154
66
PRS029 Periosteal Osteogenic Sarcoma 37 9.154
67
CRB024 Cerebral Neuroblastoma 37 9.154
68
SML014 Small Intestine Leiomyosarcoma 37 9.154
69
JXT003 Juxtacortical Osteosarcoma 37 9.154
70
SML015 Small Intestinal Sarcoma 35 9.154
71
IRS003 Iris Disease 33 9.154
72
RBS002 Rubeosis Iridis 32 9.154
73
ORB007 Orbital Cyst 31 9.154
74
c BNG012 Benign Mesenchymoma 29 9.154
75
BLD023 Bladder Leiomyoma 22 9.154
76
P BLD040 Bladder Benign Neoplasm 21 9.154
77
PNC034 Pancreas Disease 54 6.473
78
MSC072 Muscle Cancer 50 6.473
79
ISL101 Isolated Hemihyperplasia 27 6.473
80
c BCK012 Beckwith-Wiedemann Syndrome Due to Imprinting Defect of 11p15 12 6.473
81
c SLV022 Silver-Russell Syndrome Due to an Imprinting Defect of 11p15 12 6.473
82
SLV018 Silver-Russell Syndrome Due to 11p15 Microduplication 10 6.473
83
CHR333 Chromosome 11p15.5-Related Russell-Silver Syndrome 4 6.473