Search results for pold1

41 hits were found for pold1

# Family MCID Name MIFTS Score
1
c CLR077 Colorectal Cancer 10 32 13.426
2
INH023 Inherited Cancer-Predisposing Syndrome 46 7.789
3
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 6.346
4
P CLR023 Colorectal Cancer 99 6.150
5
CLT003 Colitis 62 3.528
6
P LYN001 Lynch Syndrome 77 3.035
7
XRD010 Xeroderma Pigmentosum, Variant Type 73 2.881
8
RCT009 Rectosigmoid Cancer 37 2.881
9
P CWD010 Cowden Syndrome 67 2.099
11
P MLN066 Melanoma, Cutaneous Malignant 1 70 2.037
12
P JVN014 Juvenile Polyposis Syndrome 68 2.037
13
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 2.037
14
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 2.037
15
P HRD144 Hereditary Mixed Polyposis Syndrome 51 2.037
16
INT253 Intestinal Benign Neoplasm 45 2.037
17
c BRN108 Branchiootic Syndrome 1 62 0.236
18
WRN001 Werner Syndrome 69 0.167
19
ADN018 Adenoma 59 0.167
20
END057 Endometrial Cancer 74 0.149
21
CLR108 Colorectal Adenoma 64 0.149
22
c CLR087 Colorectal Cancer 12 36 0.129
23
PRM329 Premature Aging 35 0.129
24
c FML053 Familial Colorectal Cancer 35 0.129
25
P PRG139 Progeroid Syndrome 28 0.129
26
P HYP750 Hypertriglyceridemia, Familial 62 0.105
27
HYP080 Hypogonadism 50 0.105
28
P ATT003 Attenuated Familial Adenomatous Polyposis 48 0.105
29
ATY016 Atypical Werner Syndrome 31 0.105
30
P BRS047 Breast Cancer 97 0.075
31
c FNC027 Fanconi Anemia, Complementation Group a 81 0.075
32
P FML011 Familial Adenomatous Polyposis 72 0.075
33
P LKM062 Leukemia, Acute Lymphoblastic 69 0.075
34
P OLG002 Oligodendroglioma 67 0.075
35
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.075
36
P SNS001 Sensorineural Hearing Loss 60 0.075
37
P CTR002 Cataract 60 0.075
38
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.075
39
P RCT021 Rectum Cancer 52 0.075
40
SKN005 Skin Atrophy 43 0.075
41
GNT142 Genetic Progeroid Syndrome 5 0.075
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