Search results for "[genes] IGF2"

99 hits were found for '[genes] IGF2'

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 97 18.827
2
P BRS047 Breast Cancer 100 17.750
3
P BCK002 Beckwith-Wiedemann Syndrome 56 16.604
4
P PRS040 Prostate Cancer 90 15.372
5
RHB003 Rhabdomyosarcoma 57 15.372
6
P SLV001 Silver-Russell Syndrome 54 15.372
7
P HPT023 Hepatocellular Carcinoma 92 14.033
8
ACR007 Acromegaly 66 14.033
9
HYP056 Hypoglycemia 61 14.033
10
EMB004 Embryonal Carcinoma 57 14.033
11
ADR005 Adrenal Carcinoma 57 14.033
12
P HYP050 Hyperinsulinemic Hypoglycemia 56 14.033
13
P LMY004 Leiomyosarcoma 55 14.033
14
HPT022 Hepatoblastoma 55 14.033
15
CHR029 Choroid Plexus Papilloma 55 14.033
16
P EMB005 Embryonal Rhabdomyosarcoma 54 14.033
17
LMY002 Leiomyoma 54 14.033
18
c CLR017 Clear Cell Sarcoma 46 14.033
19
SMN007 Seminoma 45 14.033
20
c CNG029 Congenital Mesoblastic Nephroma 37 14.033
21
GRW027 Growth Restriction, Severe, with Distinctive Facies 11 14.033
22
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 12.551
23
P MDL005 Medulloblastoma 77 12.551
24
INS024 Insulin-Like Growth Factor I 75 12.551
25
EWN003 Ewing Sarcoma 66 12.551
26
P ANR002 Aniridia 64 12.551
27
WLM007 Wilms Tumor Susceptibility-5 63 12.551
28
ADR016 Adrenal Cortical Carcinoma 61 12.551
29
LRN004 Laron Dwarfism 58 12.551
30
UTR039 Uterine Fibroid 57 12.551
31
PPL022 Papilloma 55 12.551
32
ATY005 Atypical Teratoid Rhabdoid Tumor 52 12.551
33
ISL001 Islet Cell Tumor 50 12.551
34
RHB001 Rhabdoid Cancer 50 12.551
35
OST016 Osteochondrosis 50 12.551
36
UMB002 Umbilical Hernia 44 12.551
37
HYP299 Hyperostosis, Endosteal 43 12.551
38
P HMN036 Hemangiopericytoma, Malignant 42 12.551
39
FTL021 Fetal Macrosomia 41 12.551
40
SKL003 Skeletal Muscle Cancer 39 12.551
41
HYP026 Hypoglycemic Coma 39 12.551
42
P OBS005 Obesity 92 10.870
43
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 10.870
44
P NRB001 Neuroblastoma 70 10.870
45
OST085 Osteosarcoma, Somatic 63 10.870
46
c MNN043 Meningioma, Familial 59 10.870
47
PNC034 Pancreas Disease 58 10.870
48
PRT093 Proteus Syndrome, Somatic 56 10.870
49
P HLL001 Hallermann-Streiff Syndrome 53 10.870
50
ADL002 Adult Syndrome 52 10.870
51
P SMP003 Simpson-Golabi-Behmel Syndrome 51 10.870
52
MSC072 Muscle Cancer 49 10.870
53
FRZ001 Frozen Shoulder 45 10.870
54
SPN021 Spinal Meningioma 44 10.870
55
CMP034 Complete Androgen Insensitivity Syndrome 43 10.870
56
c FTL006 Fetal Alcohol Spectrum Disorder 43 10.870
57
MNN006 Meninges Hemangiopericytoma 42 10.870
58
HYP691 Hypomelanosis of Ito 42 10.870
59
HMH002 Hemihypertrophy 41 10.870
60
END038 Endocrine Pancreas Disease 41 10.870
61
c MCP026 Mucopolysaccharidosis Type Iiib 40 10.870
62
FST010 Fasting Hypoglycemia 39 10.870
63
PHY007 Phyllode Tumor 37 10.870
64
c HRD009 Hereditary Wilms' Tumor 36 10.870
65
CRB024 Cerebral Neuroblastoma 35 10.870
66
SML014 Small Intestine Leiomyosarcoma 34 10.870
67
RBS002 Rubeosis Iridis 34 10.870
68
PSD008 Pseudopapilledema 34 10.870
69
GST036 Gastric Leiomyosarcoma 34 10.870
70
PRS029 Periosteal Osteogenic Sarcoma 33 10.870
71
JXT003 Juxtacortical Osteosarcoma 32 10.870
72
SML015 Small Intestinal Sarcoma 32 10.870
73
ORB007 Orbital Cyst 32 10.870
74
OCL004 Ocular Hyperemia 32 10.870
75
IRS003 Iris Disease 31 10.870
76
P PTT002 Potter's Syndrome 30 10.870
77
c BNG012 Benign Mesenchymoma 28 10.870
78
MNN011 Meninges Sarcoma 25 10.870
79
P BLD040 Bladder Benign Neoplasm 23 10.870
80
HMH004 Hemihyperplasia, Isolated 23 10.870
81
P SPN039 Spinal Canal and Spinal Cord Meningioma 20 10.870
82
BLD023 Bladder Leiomyoma 18 10.870
83
BRS067 Breast Cancer, Childhood 12 10.870
84
c BCK012 Beckwith-Wiedemann Syndrome Due to Imprinting Defect of 11p15 12 10.870
85
c SLV022 Silver-Russell Syndrome Due to an Imprinting Defect of 11p15 11 10.870
86
SLV018 Silver-Russell Syndrome Due to 11p15 Microduplication 9 10.870
87
CHR333 Chromosome 11p15.5-Related Russell-Silver Syndrome 2 10.870
88
P GST049 Gastrointestinal System Cancer 60 8.875
89
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 55 8.875
90
ACN001 Acinar Cell Carcinoma 48 8.875
91
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 43 8.875
92
c CNG420 Congenital Muscular Dystrophy Due to Lmna Mutation 41 8.875
93
ALB001 Albright's Hereditary Osteodystrophy 41 8.875
94
c SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 40 8.875
95
WLS004 Wilson-Turner Syndrome 38 8.875
96
LMY013 Leiomyoma, Uterine, Somatic 34 8.875
97
SLV005 Silver Spastic Paraplegia Syndrome 32 8.875
98
c DBT055 Diabetes Mellitus, Insulin-Dependent, 3 26 8.875
99
c SLV020 Silver-Russell Syndrome Due to a Point Mutation 13 6.276