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Search results for ctnnb1

163 hits were found for ctnnb1

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 98 5.323
2
P HPT023 Hepatocellular Carcinoma 94 4.537
3
P MDL005 Medulloblastoma 76 4.248
4
P OVR042 Ovarian Cancer 82 4.107
5
PLM026 Pilomatrixoma 53 4.083
6
c MNT159 Mental Retardation, Autosomal Dominant 19 20 3.715
7
P BRS047 Breast Cancer 100 3.437
8
P PRS040 Prostate Cancer 88 3.403
9
GST053 Gastric Cancer 84 3.294
10
END057 Endometrial Cancer 76 3.236
11
P LNG032 Lung Cancer 99 2.990
12
CRN036 Craniopharyngioma 63 2.843
13
ADN018 Adenoma 63 2.815
14
HPT022 Hepatoblastoma 55 2.784
15
P ADN016 Adenocarcinoma 71 2.750
16
P EXD001 Exudative Vitreoretinopathy 51 2.732
17
P FML011 Familial Adenomatous Polyposis 71 2.712
18
P PNC035 Pancreatic Cancer 89 2.690
19
c BSL007 Basal Cell Carcinoma 66 2.690
20
GST040 Gastric Adenocarcinoma 60 2.656
21
MLN008 Melanoma 72 2.633
22
FBR019 Fibromatosis 47 2.540
23
DSM004 Desmoid Tumor 63 2.524
24
c WLM013 Wilms Tumor 1 69 2.490
25
ULC004 Ulcerative Colitis 80 2.406
26
THY028 Thyroid Cancer 72 2.406
27
PTZ001 Peutz-Jeghers Syndrome 70 2.406
28
CLT003 Colitis 63 2.406
29
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 57 2.406
30
BRS099 Breast Ductal Carcinoma 55 2.406
31
CLN015 Colon Adenocarcinoma 53 2.406
32
PPL009 Papillary Craniopharyngioma 28 2.406
33
ESP021 Esophageal Cancer 79 2.313
34
CLN045 Colonic Benign Neoplasm 44 2.176
35
PRT029 Parathyroid Adenoma 50 2.157
36
P MCR010 Microcephaly 57 2.135
37
RTN017 Retinal Detachment 59 2.111
38
P SMP003 Simpson-Golabi-Behmel Syndrome 54 2.111
39
CLR109 Colorectal Adenocarcinoma 54 2.111
40
P NRB001 Neuroblastoma 73 2.084
41
PNC041 Pancreatic Ductal Adenocarcinoma 67 2.084
42
TNG003 Tongue Cancer 63 2.084
43
CRV038 Cervical Squamous Cell Carcinoma 61 2.084
44
c MST023 Mesothelioma, Malignant 61 2.084
45
CLR108 Colorectal Adenoma 60 2.084
46
INT079 Intrahepatic Cholangiocarcinoma 60 2.084
47
ORL015 Oral Squamous Cell Carcinoma 59 2.084
48
END041 Endometrial Adenocarcinoma 59 2.084
49
SRC027 Sarcoma, Synovial 58 2.084
50
UTR024 Uterine Carcinosarcoma 57 2.084
51
ATY005 Atypical Teratoid Rhabdoid Tumor 57 2.084
52
TNG009 Tongue Squamous Cell Carcinoma 57 2.084
53
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 56 2.084
54
OST024 Osteoporosis-Pseudoglioma Syndrome 55 2.084
55
STR020 Strabismus 55 2.084
56
ACN001 Acinar Cell Carcinoma 52 2.084
57
URT010 Ureteral Obstruction 49 2.084
58
HPT067 Hepatocellular Adenoma 43 2.084
59
LBL001 Lobular Neoplasia 42 2.084
60
SCL017 Sclerosing Hemangioma 41 2.084
61
PLM018 Pulmonary Sclerosing Hemangioma 37 2.084
62
ADN075 Adenomyoma 36 2.084
63
PSD016 Pseudosarcomatous Fibromatosis 32 2.084
64
OST006 Osteoblastoma 32 2.084
65
ATY009 Atypical Polypoid Adenomyoma 31 2.084
66
GLL029 Gallbladder Adenoma 27 2.084
67
P LNG064 Lung Cancer Susceptibility 3 64 2.033
68
c WLM018 Wilms Tumor 5 49 1.878
69
c EXD012 Exudative Vitreoretinopathy 7 16 1.845
70
P NSP012 Nasopharyngeal Carcinoma 71 1.734
71
P THY109 Thyroid Cancer, Nonmedullary, 1 64 1.734
72
BRT002 Birt-Hogg-Dube Syndrome 54 1.734
73
P OST002 Osteoporosis 75 1.702
74
BRN028 Brain Cancer 72 1.702
75
P LYN001 Lynch Syndrome 71 1.702
76
c FML346 Familial Adenomatous Polyposis 1 63 1.702
77
MSM014 Mismatch Repair Cancer Syndrome 63 1.702
78
P GST049 Gastrointestinal System Cancer 60 1.702
79
P TWN003 Townes-Brocks Syndrome 57 1.702
80
c CRD099 Cardiomyopathy, Dilated, 1e 53 1.702
81
HPT082 Hepatic Adenomas, Familial 52 1.702
82
SML036 Small Intestinal Adenocarcinoma 51 1.702
83
ECT042 Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/palate Syndrome 3 51 1.702
84
P PRS049 Persistent Mullerian Duct Syndrome 50 1.702
85
FRZ001 Frozen Shoulder 48 1.702
86
P CRN013 Craniodiaphyseal Dysplasia 48 1.702
87
SGN002 Signet Ring Cell Adenocarcinoma 47 1.702
88
HMM003 Hemimegalencephaly 47 1.702
89
EMB007 Embryonal Sarcoma 47 1.702
90
CHN010 Chondroma 44 1.702
91
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 42 1.702
92
ARR018 Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 42 1.702
93
PLY040 Polymorphous Low-Grade Adenocarcinoma 42 1.702
94
INT253 Intestinal Benign Neoplasm 42 1.702
95
CLR014 Clear Cell Adenoma 39 1.702
96
INF039 Infratentorial Cancer 38 1.702
97
GBL002 Goblet Cell Carcinoid 37 1.702
98
LRG016 Large Intestine Adenocarcinoma 37 1.702
99
ESP010 Esophageal Basaloid Squamous Cell Carcinoma 36 1.702
100
c SCL042 Sclerosteosis 2 35 1.702
101
FML005 Female Reproductive Endometrioid Cancer 34 1.702
102
PRS016 Periosteal Chondrosarcoma 34 1.702
103
NDL005 Nodular Medulloblastoma 33 1.702
104
c CLL012 Cell Type Benign Neoplasm 32 1.702
105
CYS003 Cystitis Cystica 32 1.702
106
c GST048 Gastrointestinal System Benign Neoplasm 31 1.702
107
PSM001 Psammomatous Meningioma 30 1.702
108
JXT001 Juxtacortical Chondroma 30 1.702
109
ORG010 Organ System Benign Neoplasm 28 1.702
110
CNV003 Conventional Fibrosarcoma 26 1.702
111
ADM001 Adamantinous Craniopharyngioma 26 1.702
112
CNT043 Central Nervous System Organ Benign Neoplasm 23 1.702
113
SKN011 Skin Pilomatrix Carcinoma 22 1.702
114
HRF001 Hair Follicle Neoplasm 22 1.702
115
LNG022 Lung Acinar Adenocarcinoma 19 1.702
116
CLS002 Classic Pulmonary Blastoma 12 1.702
117
c WLM011 Wilms Tumor 6 44 1.405
118
c EXD008 Exudative Vitreoretinopathy 1 65 1.388
119
PNC033 Pancreas Adenocarcinoma 63 1.370
120
c OVR114 Ovarian Cancer 1 54 1.245
121
CHL128 Childhood Hepatocellular Carcinoma 47 1.245
122
c ADL096 Adult Hepatocellular Carcinoma 47 1.245
123
DSM003 Desmoid Disease, Hereditary 40 1.245
124
FML038 Female Reproductive Organ Cancer 42 1.203
125
P RPR003 Reproductive Organ Cancer 38 1.203
126
c CLL013 Cell Type Cancer 37 1.203
127
SPP011 Suppression of Tumorigenicity 12 41 0.237
128
ADR054 Adrenocortical Carcinoma, Hereditary 63 0.226
129
BLD131 Bladder Urothelial Carcinoma 55 0.226
130
P MLN066 Melanoma, Cutaneous Malignant 1 60 0.175
131
P CRV035 Cervical Cancer 72 0.160
132
SQM013 Squamous Cell Carcinoma, Head and Neck 79 0.124
133
P HRD009 Hereditary Wilms' Tumor 46 0.113
134
P HPT021 Hepatitis 75 0.101
135
c HPT016 Hepatitis B 68 0.088
136
P THY032 Thyroiditis 56 0.088
137
c HPT073 Hepatitis C Virus 73 0.071
138
c HPT001 Hepatitis C 73 0.071
139
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.071
140
P CRV039 Cervicitis 49 0.071
141
ALD013 Aldosterone-Producing Adenoma 39 0.071
142
P BLD134 Bladder Cancer 78 0.051
143
P LVR013 Liver Disease 76 0.051
144
SQM006 Squamous Cell Carcinoma 74 0.051
145
c SML038 Small Cell Cancer of the Lung 67 0.051
146
P ESP024 Esophagitis 64 0.051
147
THY111 Thyroid Carcinoma, Familial Medullary 63 0.051
148
CHL068 Cholestasis 60 0.051
149
ORL011 Oral Cancer 60 0.051
150
c PRM005 Primary Hyperparathyroidism 59 0.051
151
P HYP069 Hyperparathyroidism 58 0.051
152
P HYP097 Hyperekplexia 57 0.051
153
P PTT006 Pituitary Adenoma 57 0.051
154
SPP010 Suppressor of Tumorigenicity 3 55 0.051
155
P EPN002 Ependymoma 53 0.051
156
RTN023 Retinitis 52 0.051
157
CHL018 Childhood Medulloblastoma 51 0.051
158
NSP002 Nasopharyngitis 46 0.051
159
PNC019 Pancreatoblastoma 33 0.051
160
BNS004 Bone Squamous Cell Carcinoma 31 0.051
161
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.051
162
PLM177 Pilomatrix Carcinoma 22 0.051
163
SVR061 Severe Intellectual Disability-Progressive Spastic Diplegia Syndrome 6 0.051
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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