Search results for "[genes] IGF2"

84 hits were found for '[genes] IGF2'

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 96 18.172
2
P BRS047 Breast Cancer 100 16.998
3
P BCK002 Beckwith-Wiedemann Syndrome 56 15.737
4
P SLV001 Silver-Russell Syndrome 54 15.737
5
P PRS040 Prostate Cancer 89 14.366
6
HPT023 Hepatocellular Carcinoma 90 12.849
7
CHR029 Choroid Plexus Papilloma 55 12.849
8
HYP056 Hypoglycemia 60 12.849
9
RHB003 Rhabdomyosarcoma 55 12.849
10
GRW027 Growth Restriction, Severe, with Distinctive Facies 11 12.849
11
P OBS005 Obesity 91 11.128
12
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 11.128
13
P MDL005 Medulloblastoma 76 11.128
14
WLM007 Wilms Tumor Susceptibility-5 64 11.128
15
EWN003 Ewing Sarcoma 63 11.128
16
ANR002 Aniridia 62 11.128
17
LRN004 Laron Dwarfism 58 11.128
18
ACR007 Acromegaly 66 11.128
19
HYP299 Hyperostosis, Endosteal 45 11.128
20
ADR005 Adrenal Carcinoma 57 11.128
21
P HMN010 Hemangioma 62 11.128
22
UTR039 Uterine Fibroid 55 11.128
23
P EMB005 Embryonal Rhabdomyosarcoma 56 11.128
24
HPT022 Hepatoblastoma 57 11.128
25
ISL001 Islet Cell Tumor 51 11.128
26
OST016 Osteochondrosis 48 11.128
27
PPL022 Papilloma 54 11.128
28
c CLR017 Clear Cell Sarcoma 48 11.128
29
P HMN013 Hemangiopericytoma 52 11.128
30
ATY005 Atypical Teratoid Rhabdoid Tumor 47 11.128
31
SKL003 Skeletal Muscle Cancer 41 11.128
32
c CNG029 Congenital Mesoblastic Nephroma 37 11.128
33
HYP026 Hypoglycemic Coma 42 11.128
34
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 9.086
35
c MNN043 Meningioma, Familial 61 9.086
36
OST085 Osteosarcoma, Somatic 63 9.086
37
GST019 Gastrointestinal Stromal Tumor 73 9.086
38
ADR016 Adrenal Cortical Carcinoma 60 9.086
39
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 53 9.086
40
PRT093 Proteus Syndrome, Somatic 54 9.086
41
INS024 Insulin-Like Growth Factor I 75 9.086
42
PRL032 Perlman Syndrome 55 9.086
43
MLK003 Melkersson-Rosenthal Syndrome 52 9.086
44
ADL002 Adult Syndrome 53 9.086
45
ALB001 Albright's Hereditary Osteodystrophy 49 9.086
46
P HLL001 Hallermann-Streiff Syndrome 53 9.086
47
c MCP026 Mucopolysaccharidosis Type Iiib 37 9.086
48
HYP691 Hypomelanosis of Ito 44 9.086
49
PNC034 Pancreas Disease 56 9.086
50
PSD008 Pseudopapilledema 39 9.086
51
LMY002 Leiomyoma 56 9.086
52
P PTT002 Potter's Syndrome 42 9.086
53
MSC072 Muscle Cancer 47 9.086
54
CMP034 Complete Androgen Insensitivity Syndrome 42 9.086
55
ACN001 Acinar Cell Carcinoma 48 9.086
56
PHC013 Phaeochromocytoma 47 9.086
57
ORB007 Orbital Cyst 30 9.086
58
SPN021 Spinal Meningioma 39 9.086
59
c HRD009 Hereditary Wilms' Tumor 40 9.086
60
SML014 Small Intestine Leiomyosarcoma 36 9.086
61
FRZ001 Frozen Shoulder 40 9.086
62
OCL004 Ocular Hyperemia 33 9.086
63
JXT003 Juxtacortical Osteosarcoma 34 9.086
64
MNN011 Meninges Sarcoma 25 9.086
65
SML015 Small Intestinal Sarcoma 34 9.086
66
CRB024 Cerebral Neuroblastoma 37 9.086
67
PRS029 Periosteal Osteogenic Sarcoma 33 9.086
68
MNN006 Meninges Hemangiopericytoma 43 9.086
69
END038 Endocrine Pancreas Disease 42 9.086
70
IRS003 Iris Disease 32 9.086
71
RBS002 Rubeosis Iridis 33 9.086
72
BLD023 Bladder Leiomyoma 17 9.086
73
GST036 Gastric Leiomyosarcoma 36 9.086
74
c BNG012 Benign Mesenchymoma 25 9.086
75
P BLD040 Bladder Benign Neoplasm 22 9.086
76
P SPN039 Spinal Canal and Spinal Cord Meningioma 21 9.086
77
FTL021 Fetal Macrosomia 38 9.086
78
FST010 Fasting Hypoglycemia 37 9.086
79
P GST049 Gastrointestinal System Cancer 59 6.425
80
HMH004 Hemihyperplasia, Isolated 23 6.425
81
c BCK012 Beckwith-Wiedemann Syndrome Due to Imprinting Defect of 11p15 10 6.425
82
SLV018 Silver-Russell Syndrome Due to 11p15 Microduplication 8 6.425
83
c SLV022 Silver-Russell Syndrome Due to an Imprinting Defect of 11p15 10 6.425
84
CHR333 Chromosome 11p15.5-Related Russell-Silver Syndrome 3 6.425