Search results for pold1

203 hits were found for pold1

# Family MCID Name MIFTS Score
1
c CLR077 Colorectal Cancer 10 32 103.007
2
P ATT003 Attenuated Familial Adenomatous Polyposis 57 90.013
3
P TMR010 Tumor Predisposition Syndrome 69 52.942
4
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 51.243
5
INH023 Inherited Cancer-Predisposing Syndrome 53 51.243
6
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 42.115
7
P CLR023 Colorectal Cancer 100 39.085
8
c FML053 Familial Colorectal Cancer 47 19.914
9
P LYN001 Lynch Syndrome 76 13.543
10
CLT003 Colitis 63 13.327
11
XRD010 Xeroderma Pigmentosum, Variant Type 72 10.881
12
RCT009 Rectosigmoid Cancer 37 10.881
13
P CCK001 Cockayne Syndrome 68 10.881
14
P CWD010 Cowden Syndrome 71 8.842
16
P HRD144 Hereditary Mixed Polyposis Syndrome 54 7.694
17
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 7.694
18
P MLN066 Melanoma, Cutaneous Malignant 1 66 7.694
19
P JVN014 Juvenile Polyposis Syndrome 65 7.694
20
INT253 Intestinal Benign Neoplasm 46 7.694
21
c CLR087 Colorectal Cancer 12 34 4.605
22
END057 Endometrial Cancer 71 4.542
23
P BRS047 Breast Cancer 97 4.281
24
c BRN108 Branchiootic Syndrome 1 63 3.592
25
BLD173 Bladder Small Cell Carcinoma 44 2.826
26
GST103 Gastric Cancer, Hereditary Diffuse 68 2.826
27
SML009 Small Intestine Adenocarcinoma 57 2.622
28
LNG039 Lung Squamous Cell Carcinoma 57 2.484
29
P OLG002 Oligodendroglioma 66 2.427
30
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 2.402
31
ADN018 Adenoma 58 2.367
32
WRN001 Werner Syndrome 69 2.341
33
CLR108 Colorectal Adenoma 63 2.308
34
P BLD134 Bladder Cancer 79 2.202
35
P PRS040 Prostate Cancer 95 2.053
36
CLN015 Colon Adenocarcinoma 64 2.033
37
GST040 Gastric Adenocarcinoma 66 2.033
38
P GST053 Gastric Cancer 82 1.998
39
P LNG032 Lung Cancer 98 1.956
40
P PRG139 Progeroid Syndrome 29 1.944
41
P LNG064 Lung Cancer Susceptibility 3 70 1.909
42
PRM329 Premature Aging 36 1.897
43
ADN011 Adenoid Cystic Carcinoma 68 1.847
44
ADN089 Adenosquamous Lung Carcinoma 49 1.698
45
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 1.698
46
SKN022 Skin Squamous Cell Carcinoma 54 1.697
47
END041 Endometrial Adenocarcinoma 63 1.638
48
P GLM040 Glioma Susceptibility 1 70 1.543
49
ATY016 Atypical Werner Syndrome 29 1.507
50
PPL004 Papillary Squamous Carcinoma 39 1.489
51
c MSM022 Mismatch Repair Cancer Syndrome 1 69 1.481
52
GLM045 Glioma 62 1.481
53
P HYP750 Hypertriglyceridemia, Familial 62 1.413
54
HYP080 Hypogonadism 49 1.385
55
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 1.332
56
c GLM043 Glioma Susceptibility 9 30 1.332
57
c GLM047 Glioma Susceptibility 3 32 1.332
58
c GLM025 Glioma Susceptibility 2 29 1.332
59
MNN043 Meningioma, Familial 79 1.332
60
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 1.332
61
LYN004 Lynch Syndrome I 60 1.315
62
ESP021 Esophageal Cancer 84 1.302
63
c FNC027 Fanconi Anemia, Complementation Group a 81 1.238
64
MTY003 Mutyh Polyposis 38 1.238
65
P FML011 Familial Adenomatous Polyposis 71 1.217
66
c 46X071 46,xy Disorder of Sexual Development Due to Dihydrotestosterone Backdoor Pathway Biosynthesis Defect 42 1.217
67
c FML347 Familial Adenomatous Polyposis 2 56 1.172
68
MYH016 Myh-Associated Polyposis 38 1.172
69
c FML346 Familial Adenomatous Polyposis 1 65 1.148
70
47X002 47,xyy 48 1.148
71
APC006 Apc-Associated Polyposis Conditions 22 1.148
72
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.122
73
SKN005 Skin Atrophy 41 1.122
74
THY029 Thyroid Carcinoma 54 1.095
75
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.066
76
P SNS001 Sensorineural Hearing Loss 59 1.034
77
AGN016 Aging 54 0.999
78
P LKM062 Leukemia, Acute Lymphoblastic 69 0.999
79
P RCT021 Rectum Cancer 54 0.999
80
P LKM002 Leukemia 66 0.999
81
c PRS070 Prostate Cancer, Hereditary, 12 22 0.942
82
c PRS071 Prostate Cancer, Hereditary, 13 25 0.942
83
c PRS117 Prostate Cancer, Hereditary, 11 24 0.942
84
c PRS114 Prostate Cancer, Hereditary, 2 33 0.942
85
c PRS097 Prostate Cancer, Hereditary, 1 38 0.942
86
PRS015 Prostate Signet Ring Cell Adenocarcinoma 25 0.942
87
SQM006 Squamous Cell Carcinoma 59 0.924
88
P CTR002 Cataract 59 0.912
89
GNT142 Genetic Progeroid Syndrome 5 0.912
90
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 64 0.898
91
VNH007 Von Hippel-Lindau Syndrome 73 0.816
92
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.816
93
P BLD062 Bile Duct Cancer 68 0.816
94
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 32 0.816
95
CLR030 Clear Cell Renal Cell Carcinoma 54 0.816
96
MLT165 Multilocular Cystic Renal Neoplasm of Low Malignant Potential 28 0.816
97
P OVR042 Ovarian Cancer 88 0.681
98
P MLN008 Melanoma 75 0.681
99
c BSL024 Basal Cell Carcinoma 1 54 0.666
100
c BSL034 Basal Cell Carcinoma 7 25 0.666
101
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.666
102
RMB001 Rombo Syndrome 29 0.666
103
BSL044 Basal Cell Carcinoma, Infundibulocystic 35 0.666
104
P TRC095 Trichoepithelioma, Multiple Familial, 1 32 0.666
105
P RTH006 Rothmund-Thomson Syndrome, Type 2 67 0.666
106
BRS099 Breast Ductal Carcinoma 61 0.666
107
c BSL007 Basal Cell Carcinoma 68 0.666
108
NDL009 Nodular Basal Cell Carcinoma 40 0.666
109
MTT001 Metatypical Basal Cell Carcinoma 31 0.666
110
PGM002 Pigmented Basal Cell Carcinoma 31 0.666
111
ANL013 Anal Margin Basal Cell Carcinoma 18 0.666
112
SBC013 Sebaceous Basal Cell Carcinoma 13 0.666
113
MCR016 Micronodular Basal Cell Carcinoma 34 0.666
114
ADM002 Adamantinoid Basal Cell Epithelioma 20 0.666
115
CLR015 Clear Cell Basal Cell Carcinoma 39 0.666
116
ADN015 Adenoid Basal Cell Carcinoma 31 0.666
117
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.666
118
INF027 Infiltrative Basal Cell Carcinoma 32 0.666
119
CYS004 Cystic Basal Cell Carcinoma 36 0.666
120
SRC003 Sarcomatoid Basal Cell Carcinoma 28 0.666
121
SGN001 Signet Ring Basal Cell Carcinoma 32 0.666
122
INF057 Inflammatory Linear Verrucous Epidermal Nevus 33 0.666
123
9Q2001 9q22.3 Microdeletion 24 0.666
124
LNR004 Linear Porokeratosis 33 0.666
125
PLM026 Pilomatrixoma 57 0.620
126
P PNC035 Pancreatic Cancer 86 0.573
127
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.557
128
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.471
129
DST001 Distal Biliary Tract Carcinoma 24 0.471
130
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.471
131
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.471
132
THY124 Thyroid Gland Papillary Carcinoma 38 0.471
133
LBL001 Lobular Neoplasia 55 0.471
134
MRK001 Merkel Cell Carcinoma 65 0.471
135
c ALB010 Albinism, Oculocutaneous, Type Ib 52 0.471
136
P LNG021 Lung Occult Small Cell Carcinoma 20 0.471
137
OVR062 Ovary Serous Adenocarcinoma 25 0.471
138
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 20 0.471
139
RCS008 Recessive Dystrophic Epidermolysis Bullosa-Generalized Other 27 0.471
140
PRM126 Primary Peritoneal Carcinoma 61 0.471
141
IMM167 Immune Deficiency Disease 77 0.421
142
ALL029 Allergic Disease 61 0.421
143
CMB007 Combined Immunodeficiency 56 0.364
144
LYM027 Lymphopenia 56 0.364
145
P TRT010 Teratoma 50 0.364
146
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.298
147
P CLR037 Colorectal Cancer, Hereditary Nonpolyposis, Type 5 48 0.298
148
GLB002 Glioblastoma 67 0.298
149
c CLR039 Colorectal Cancer, Hereditary Nonpolyposis, Type 4 40 0.298
150
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.258
151
c SML038 Small Cell Cancer of the Lung 69 0.258
152
c PRG020 Paragangliomas 3 39 0.258
153
HYP457 Hypertrophic Scars 42 0.210
154
MLG169 Malignant Astrocytoma 57 0.210
155
P THR014 Thrombocytopenia 66 0.210
156
P NTR004 Neutropenia 62 0.210
157
MDD011 Mood Disorder 62 0.210
158
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.210
159
P CHR345 Chronic Pain 50 0.210
160
P HRP006 Herpes Simplex 65 0.210
161
FTT001 Fatty Liver Disease 61 0.210
162
THY128 Thyroid Tumor 33 0.210
163
SRR001 Serrated Polyposis Syndrome 42 0.210
164
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.149
165
c SPR119 Spermatogenic Failure, X-Linked, 1 36 0.149
166
HLC007 Helicobacter Pylori Infection 67 0.149
167
P SPP010 Suppressor of Tumorigenicity 3 51 0.149
168
ADR023 Adrenomyodystrophy 32 0.149
169
CRV035 Cervical Cancer 72 0.149
170
c BRS111 Breast-Ovarian Cancer, Familial 2 54 0.149
171
P MLN069 Melanoma, Uveal 59 0.149
172
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.149
173
P MND003 Mandibuloacral Dysplasia with Type a Lipodystrophy 48 0.149
174
P CTN015 Cutaneous T Cell Lymphoma 48 0.149
175
c FML339 Familial Adenomatous Polyposis 4 30 0.149
176
c SPR162 Spermatogenic Failure 50 42 0.149
177
GST086 Gastric Adenocarcinoma and Proximal Polyposis of the Stomach 30 0.149
178
c OVR114 Ovarian Cancer 1 60 0.149
179
c BRS110 Breast-Ovarian Cancer, Familial 1 58 0.149
180
c MST023 Mesothelioma, Malignant 56 0.149
181
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.149
182
c FNC028 Fanconi Anemia, Complementation Group L 46 0.149
183
PTN004 Patent Ductus Venosus 31 0.149
184
LPD008 Lipid Metabolism Disorder 61 0.149
185
ISC004 Ischemia 61 0.149
186
P ADN016 Adenocarcinoma 63 0.149
187
PLM020 Pleomorphic Xanthoastrocytoma 40 0.149
188
TLN003 Telangiectasis 51 0.149
189
AZS001 Azoospermia 45 0.149
190
HMS001 Hemosiderosis 48 0.149
191
HGH043 High Grade Glioma 46 0.149
192
P BNG032 Benign Mesothelioma 53 0.149
193
P GLL018 Gallbladder Cancer 53 0.149
194
SPN035 Spindle Cell Sarcoma 51 0.149
195
GLL048 Glial Tumor 52 0.149
196
c FML311 Familial Colorectal Cancer Type X 37 0.149
197
BSL006 Basaloid Squamous Cell Carcinoma 43 0.149
198
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 68 0.149
199
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.149
200
c SPR009 Sporadic Breast Cancer 42 0.149
201
NTH004 Nthl1 Tumor Syndrome 9 0.149
202
P RRH023 Rare Hereditary Hemochromatosis 53 0.149
203
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.149
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