Search results for "[genes] IGF2"

85 hits were found for '[genes] IGF2'

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 95 18.229
2
P BRS047 Breast Cancer 100 17.052
3
P SLV001 Silver-Russell Syndrome 58 17.052
4
P BCK002 Beckwith-Wiedemann Syndrome 58 17.052
5
P PRS040 Prostate Cancer 90 15.787
6
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 14.411
7
RHB003 Rhabdomyosarcoma 51 14.411
8
HYP056 Hypoglycemia 49 14.411
9
HPT023 Hepatocellular Carcinoma 90 12.890
10
ACR007 Acromegaly 61 12.890
11
CHR029 Choroid Plexus Papilloma 52 12.890
12
PPL022 Papilloma 49 12.890
13
HPT022 Hepatoblastoma 49 12.890
14
ADR015 Adrenocortical Carcinoma 48 12.890
15
P LMY004 Leiomyosarcoma 47 12.890
16
P EMB005 Embryonal Rhabdomyosarcoma 46 12.890
17
ADR005 Adrenal Carcinoma 46 12.890
18
P HMN013 Hemangiopericytoma 46 12.890
19
UTR039 Uterine Fibroid 45 12.890
20
c CLR017 Clear Cell Sarcoma 43 12.890
21
SMN007 Seminoma 40 12.890
22
P OBS005 Obesity 89 11.163
23
P LFR001 Li-Fraumeni Syndrome 79 11.163
24
ANR002 Aniridia 72 11.163
25
P MDL005 Medulloblastoma 69 11.163
26
INS024 Insulin-Like Growth Factor I 64 11.163
27
WLM007 Wilms Tumor Susceptibility-5 61 11.163
28
LRN004 Laron Dwarfism 59 11.163
29
P RHB017 Rhabdoid Tumor 54 11.163
30
ISL001 Islet Cell Tumor 51 11.163
31
LMY002 Leiomyoma 49 11.163
32
OST016 Osteochondrosis 47 11.163
33
GST010 Gestational Trophoblastic Neoplasm 46 11.163
34
ATY005 Atypical Teratoid Rhabdoid Tumor 45 11.163
35
HMH002 Hemihypertrophy 45 11.163
36
GRM005 Germ Cell Cancer 43 11.163
37
HYP026 Hypoglycemic Coma 37 11.163
38
UMB002 Umbilical Hernia 35 11.163
39
c CNG029 Congenital Mesoblastic Nephroma 35 11.163
40
MLR006 Male Reproductive Organ Cancer 33 11.163
41
SKL002 Skeletal Muscle Neoplasm 32 11.163
42
FTL021 Fetal Macrosomia 31 11.163
43
CHR084 Chromosomal Disease 30 11.163
44
GRW027 Growth Restriction, Severe, with Distinctive Facies 12 11.163
45
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 9.114
46
OST085 Osteosarcoma, Somatic 56 9.114
47
c MNN043 Meningioma, Familial 55 9.114
48
P HLL001 Hallermann-Streiff Syndrome 53 9.114
49
MLK003 Melkersson-Rosenthal Syndrome 53 9.114
50
ALB001 Albright's Hereditary Osteodystrophy 53 9.114
51
PRT093 Proteus Syndrome, Somatic 52 9.114
52
P SMP003 Simpson-Golabi-Behmel Syndrome 51 9.114
53
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 47 9.114
54
CMP034 Complete Androgen Insensitivity Syndrome 45 9.114
55
c MCP026 Mucopolysaccharidosis Type Iiib 43 9.114
56
INC001 Incontinentia Pigmenti Achromians 43 9.114
57
ADL002 Adult Syndrome 43 9.114
58
ACN001 Acinar Cell Carcinoma 41 9.114
59
FRZ001 Frozen Shoulder 38 9.114
60
EMB003 Embryonal Cancer 38 9.114
61
P PTT002 Potter's Syndrome 37 9.114
62
MNN006 Meninges Hemangiopericytoma 35 9.114
63
JXT003 Juxtacortical Osteosarcoma 32 9.114
64
RBS002 Rubeosis Iridis 31 9.114
65
PSD008 Pseudopapilledema 31 9.114
66
PRS029 Periosteal Osteogenic Sarcoma 31 9.114
67
SKL007 Skeletal Muscle Regeneration 31 9.114
68
FST010 Fasting Hypoglycemia 29 9.114
69
c HRD009 Hereditary Wilms' Tumor 29 9.114
70
CHL060 Childhood Kidney Neoplasm 28 9.114
71
CRB024 Cerebral Neuroblastoma 28 9.114
72
END038 Endocrine Pancreas Disease 28 9.114
73
SML014 Small Intestine Leiomyosarcoma 28 9.114
74
ORB007 Orbital Cyst 27 9.114
75
OCL004 Ocular Hyperemia 27 9.114
76
PRP024 Peripheral Osteosarcoma 26 9.114
77
IRS003 Iris Disease 25 9.114
78
SML015 Small Intestinal Sarcoma 25 9.114
79
c BNG012 Benign Mesenchymoma 25 9.114
80
BLD023 Bladder Leiomyoma 16 9.114
81
P BLD040 Bladder Benign Neoplasm 13 9.114
82
c BCK012 Beckwith-Wiedemann Syndrome Due to Imprinting Defect of 11p15 13 6.445
83
c SLV022 Silver-Russell Syndrome Due to an Imprinting Defect of 11p15 11 6.445
84
SLV018 Silver-Russell Syndrome Due to 11p15 Microduplication 10 6.445
85
CHR333 Chromosome 11p15.5-Related Russell-Silver Syndrome 4 6.445