Search results for neil3

72 hits were found for neil3

# Family MCID Name MIFTS Score
1
c FNC027 Fanconi Anemia, Complementation Group a 81 11.617
2
ATH013 Atherosclerosis Susceptibility 63 1.823
3
c FNC042 Fanconi Anemia, Complementation Group D2 54 1.741
4
GLB002 Glioblastoma 67 1.741
5
P GLM040 Glioma Susceptibility 1 70 1.618
6
DFC004 Deficiency Anemia 74 1.377
7
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.328
8
P ATX030 Ataxia-Telangiectasia 80 1.328
9
P LNG064 Lung Cancer Susceptibility 3 70 1.328
10
TLN003 Telangiectasis 51 1.328
11
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.302
12
BRN032 Brain Glioma 45 1.275
13
P PRN023 Prion Disease 60 1.275
14
PNC129 Pancreatic Adenocarcinoma 65 1.275
15
P AGM001 Agammaglobulinemia 67 1.246
16
MLG169 Malignant Astrocytoma 57 1.182
17
CRD016 Cardiac Rupture 34 1.182
18
P MYC007 Myocardial Infarction 69 1.146
19
HYP266 Hypoxia 56 1.106
20
c FNC029 Fanconi Anemia, Complementation Group I 55 1.007
21
P PRS040 Prostate Cancer 95 0.992
22
P BRS047 Breast Cancer 97 0.992
23
P SBS003 Substance Abuse 54 0.937
24
BRN028 Brain Cancer 73 0.807
25
CNT033 Central Nervous System Cancer 47 0.807
26
P NRV006 Nervous System Cancer 47 0.807
27
BRN049 Brain Tumor, Childhood 28 0.807
28
P HPT023 Hepatocellular Carcinoma 95 0.768
29
P PNC035 Pancreatic Cancer 86 0.753
30
P OVR042 Ovarian Cancer 88 0.701
31
P LNG032 Lung Cancer 98 0.701
32
c MSM022 Mismatch Repair Cancer Syndrome 1 69 0.436
33
c GLM043 Glioma Susceptibility 9 30 0.436
34
c GLM047 Glioma Susceptibility 3 32 0.436
35
c GLM025 Glioma Susceptibility 2 29 0.436
36
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.436
37
P OLG002 Oligodendroglioma 66 0.436
38
LNG039 Lung Squamous Cell Carcinoma 57 0.436
39
MNN043 Meningioma, Familial 79 0.436
40
GLM045 Glioma 62 0.436
41
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 20 0.436
42
CLR108 Colorectal Adenoma 63 0.377
43
ADN018 Adenoma 58 0.377
44
P TMR010 Tumor Predisposition Syndrome 69 0.338
45
HLX001 Helix Syndrome 47 0.338
46
c FML347 Familial Adenomatous Polyposis 2 56 0.338
47
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.338
48
P ATT003 Attenuated Familial Adenomatous Polyposis 57 0.338
49
MTY003 Mutyh Polyposis 38 0.338
50
MYH016 Myh-Associated Polyposis 38 0.338
51
INH023 Inherited Cancer-Predisposing Syndrome 53 0.338
52
ISC004 Ischemia 61 0.292
53
CRB004 Cerebral Artery Occlusion 46 0.239
54
P CLR023 Colorectal Cancer 100 0.239
55
P ADN016 Adenocarcinoma 63 0.239
56
c HPT016 Hepatitis B 62 0.239
57
P HPT021 Hepatitis 68 0.239
58
c BSL007 Basal Cell Carcinoma 68 0.239
59
P BNG032 Benign Mesothelioma 53 0.239
60
STR067 Stroke, Ischemic 79 0.239
61
MLG079 Malignant Pleural Mesothelioma 42 0.239
62
DFF036 Differentiated Thyroid Carcinoma 51 0.239
63
THY029 Thyroid Carcinoma 54 0.239
64
LYN004 Lynch Syndrome I 60 0.169
65
P HNT016 Huntington Disease 73 0.169
66
CHL065 Cholangiocarcinoma 58 0.169
67
P CCK001 Cockayne Syndrome 68 0.169
68
INT079 Intrahepatic Cholangiocarcinoma 51 0.169
69
P LYN001 Lynch Syndrome 76 0.169
70
c FNC032 Fanconi Anemia, Complementation Group B 49 0.169
71
48X005 48,xyyy 39 0.169
72
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.169
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