Search results for wnt8b

74 hits were found for wnt8b

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 100 20.873
2
P HPT023 Hepatocellular Carcinoma 95 18.646
3
P GST053 Gastric Cancer 82 16.901
4
P ALZ034 Alzheimer Disease 87 14.637
5
c EXD008 Exudative Vitreoretinopathy 1 71 11.951
6
NRR002 Norrie Disease 59 8.451
7
P EXD001 Exudative Vitreoretinopathy 56 8.451
8
P PNC035 Pancreatic Cancer 87 2.705
9
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.720
10
SGN002 Signet Ring Cell Adenocarcinoma 46 1.409
11
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.357
12
P LNG032 Lung Cancer 98 1.344
13
CLB010 Coloboma of Macula 53 1.268
14
P HRS035 Hirschsprung Disease 1 66 1.268
15
FCL014 Focal Epilepsy 53 1.197
16
P RTN016 Retinal Degeneration 52 1.157
17
P PLY011 Polycystic Ovary Syndrome 57 1.110
18
ANV001 Anovulation 46 1.110
19
HYP043 Hyperandrogenism 47 1.110
20
c SML038 Small Cell Cancer of the Lung 68 0.811
21
P OVR042 Ovarian Cancer 88 0.753
22
P BRS047 Breast Cancer 97 0.753
23
c HPT073 Hepatitis C Virus 70 0.560
24
P PRS040 Prostate Cancer 95 0.533
25
IRN008 Iron Overload in Africa 50 0.388
26
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 59 0.388
27
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.388
28
RJS001 Ruijs-Aalfs Syndrome 47 0.388
29
c CLR087 Colorectal Cancer 12 34 0.388
30
GST103 Gastric Cancer, Hereditary Diffuse 68 0.388
31
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.388
32
ADL096 Adult Hepatocellular Carcinoma 60 0.388
33
HPT079 Hepatoid Adenocarcinoma 39 0.388
34
PDT042 Pediatric Hepatocellular Carcinoma 51 0.388
35
CLN015 Colon Adenocarcinoma 64 0.388
36
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.388
37
SML009 Small Intestine Adenocarcinoma 57 0.388
38
FBR086 Fibrolamellar Carcinoma 59 0.388
39
HPT011 Hepatocellular Clear Cell Carcinoma 46 0.388
40
PTY007 Pityriasis Rotunda 27 0.388
41
c HLP023 Holoprosencephaly 1 56 0.299
42
P PLY006 Polydactyly 58 0.299
43
P FML011 Familial Adenomatous Polyposis 70 0.299
44
TRT001 Teratocarcinoma 41 0.299
45
c SPL034 Split-Hand/foot Malformation 4 38 0.244
46
P ECT100 Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/palate Syndrome 1 51 0.244
47
ANK017 Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate 46 0.244
48
SPP011 Suppression of Tumorigenicity 12 61 0.244
49
LMB008 Limb-Mammary Syndrome 34 0.244
50
P ORF002 Orofacial Cleft 43 0.244
51
P LSS002 Lissencephaly 52 0.244
52
ADL002 Adult Syndrome 69 0.244
53
RPP001 Rapp-Hodgkin Syndrome 44 0.244
54
c SPL067 Split-Hand/foot Malformation 1 46 0.244
55
FRY006 Fryns Microphthalmia Syndrome 52 0.244
56
P SPL061 Split Hand-Foot Malformation 43 0.244
57
P ECT006 Ectodermal Dysplasia 62 0.244
58
P ADN016 Adenocarcinoma 63 0.244
59
CLF001 Cleft Lip 54 0.244
61
ISL121 Isolated Split Hand-Split Foot Malformation 42 0.244
62
CLF004 Cleft Lip/palate 56 0.244
63
RNL077 Renal Fibrosis 46 0.173
64
NRL016 Neural Tube Defects 80 0.173
65
P CHN012 Chondrosarcoma 56 0.173
66
ESP021 Esophageal Cancer 84 0.173
67
BLD170 Bladder Exstrophy and Epispadias Complex 43 0.173
68
OBS082 Obstructive Nephropathy 41 0.173
69
P MLN007 Male Infertility 56 0.173
70
BLD129 Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex 41 0.173
71
BLD130 Bladder Exstrophy 44 0.173
72
URT010 Ureteral Obstruction 44 0.173
73
c HPT001 Hepatitis C 61 0.173
74
P HLP001 Holoprosencephaly 68 0.173
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