Search results for "colorectal cancer, hereditary nonpolyposis, type 3"

The MalaCard for "colorectal cancer, hereditary nonpolyposis, type 3" has been retired.
Searching MalaCards for entries containing "colorectal cancer, hereditary nonpolyposis, type 3"

104 hits were found for 'colorectal cancer, hereditary nonpolyposis, type 3'

# Family MCID Name MIFTS Score
1
P CLR070 Colorectal Cancer, Hereditary Nonpolyposis, Type 1 55 6.437
2
P CLR023 Colorectal Cancer 97 1.667
3
P BRS047 Breast Cancer 100 0.981
4
P GST049 Gastrointestinal System Cancer 60 0.597
5
INT253 Intestinal Benign Neoplasm 50 0.557
6
CLN019 Colonic Disease 50 0.543
7
RCT018 Rectal Neoplasm 55 0.529
8
RCT017 Rectal Disease 39 0.528
9
P OVR042 Ovarian Cancer 75 0.520
10
P PNC035 Pancreatic Cancer 85 0.507
11
P ADN016 Adenocarcinoma 69 0.503
12
c CLR079 Colorectal Cancer 2 31 0.456
13
c CLR085 Colorectal Cancer 1 42 0.422
14
ADN018 Adenoma 59 0.397
15
P PNC044 Pancreatitis 60 0.393
16
P LYN001 Lynch Syndrome 69 0.383
17
c CLR075 Colorectal Cancer 3 30 0.372
18
P INT068 Intestinal Disease 61 0.365
19
c CLR080 Colorectal Cancer 5 35 0.326
20
CLR109 Colorectal Adenocarcinoma 50 0.313
21
P CLR108 Colorectal Adenoma 60 0.306
22
c FML053 Familial Colorectal Cancer 50 0.271
23
c CLR081 Colorectal Cancer 6 24 0.270
24
GST071 Gastrointestinal Carcinoma 41 0.257
25
END057 Endometrial Cancer 75 0.256
26
P SML016 Small Intestine Cancer 54 0.256
27
OCL009 Ocular Cancer 62 0.255
28
P SKN013 Skin Benign Neoplasm 46 0.253
29
P LYM118 Lymphoma 70 0.247
30
SML033 Small Cell Cancer of the Lung, Somatic 53 0.241
31
P SML001 Small Cell Carcinoma 57 0.232
32
P KDN017 Kidney Cancer 67 0.227
33
c HRD169 Hereditary Colorectal Cancer 43 0.226
34
FML039 Female Reproductive System Disease 48 0.225
35
P RNL014 Renal Cell Carcinoma 81 0.224
36
SKN016 Skin Disease 68 0.224
37
c CLR083 Colorectal Cancer 8 27 0.220
38
FML038 Female Reproductive Organ Cancer 51 0.219
39
c CLR077 Colorectal Cancer 10 31 0.216
40
CLN015 Colon Adenocarcinoma 49 0.213
41
PCK002 Pick Disease 67 0.202
42
MLR007 Male Reproductive System Disease 37 0.200
43
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 31 0.194
44
MLR006 Male Reproductive Organ Cancer 47 0.194
45
P OVR049 Ovarian Disease 55 0.193
46
c INH020 Inherited Metabolic Disorder 49 0.180
47
P SPS003 Spastic Diplegia 53 0.177
48
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 0.175
49
c CLR082 Colorectal Cancer 7 23 0.172
50
P UTR038 Uterine Disease 40 0.162
51
SPC010 Speech and Communication Disorders 46 0.160
52
ADJ001 Adjustment Disorder 38 0.157
53
FNC005 Functional Colonic Disease 30 0.151
54
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 30 0.143
55
AND005 Androgen Insensitivity Syndrome, Mild 16 0.140
56
RNL101 Renal Cell Carcinoma, Papillary 67 0.138
57
P NRB001 Neuroblastoma 69 0.134
58
P RTN024 Retinoblastoma 75 0.134
59
CHL071 Child Syndrome 58 0.132
60
BLD087 Bladder Cancer, Somatic 67 0.132
61
KDS001 Kid Syndrome 53 0.131
62
BLD044 Bladder Disease 51 0.131
63
WLL006 Wells Syndrome 56 0.131
64
P RCK004 Rickets 59 0.130
65
UTR033 Uterine Corpus Cancer 50 0.130
66
END080 Endometrial Disease 42 0.129
67
GDS001 Good Syndrome 45 0.128
68
SML036 Small Intestinal Adenocarcinoma 45 0.127
69
c CLR089 Colorectal Cancer, Hereditary Nonpolyposis, Type 8 19 0.126
70
c CLR055 Colorectal Cancer, Hereditary Nonpolyposis, Type 6 25 0.126
71
c CLR039 Colorectal Cancer, Hereditary Nonpolyposis, Type 4 26 0.125
72
c CLR037 Colorectal Cancer, Hereditary Nonpolyposis, Type 5 27 0.123
73
ATS008 Autosomal Dominant Disease 42 0.123
74
CLN008 Colon Small Cell Carcinoma 21 0.122
75
ADL002 Adult Syndrome 53 0.119
76
HDG012 Hodgkin Lymphoma 73 0.118
77
c CLR100 Colorectal Cancer, Hereditary Nonpolyposis, Type 7 19 0.115
78
c CLR041 Colorectal Cancer, Hereditary Nonpolyposis, Type 2 24 0.115
79
P FLL037 Follicular Lymphoma 66 0.110
80
NSY001 N Syndrome 39 0.108
81
c FML303 Familial/multiple Cancer 16 0.106
82
DDN006 Duodenitis 44 0.104
83
MDD011 Mood Disorder 61 0.101
84
c FML311 Familial Colorectal Cancer Type X 36 0.096
85
END041 Endometrial Adenocarcinoma 56 0.092
86
P NMN002 Niemann-Pick Disease 63 0.088
87
VTM003 Vitamin Metabolic Disorder 33 0.088
88
RHB003 Rhabdomyosarcoma 58 0.084
89
LYM006 Lymphoepithelioma-Like Carcinoma 42 0.075
90
P LPS002 Liposarcoma 50 0.074
91
c JVN024 Juvenile Hereditary Hemochromatosis 28 0.073
92
UND005 Undifferentiated Pleomorphic Sarcoma 43 0.072
93
KRT002 Keratomalacia 54 0.072
94
UTR024 Uterine Carcinosarcoma 52 0.070
95
BLD039 Bladder Adenocarcinoma 34 0.066
96
P ATT003 Attenuated Familial Adenomatous Polyposis 45 0.065
97
DSM004 Desmoid Tumor 51 0.065
98
HYP017 Hypophosphatemia 42 0.060
99
PHS001 Phosphorus Metabolism Disease 42 0.059
100
OST011 Osteomalacia 48 0.059
101
LCH009 Lichen Sclerosus 42 0.058
102
P FNG005 Feingold Syndrome 43 0.057
103
ESP020 Esophageal Atresia 49 0.053
104
ONC003 Oncogenic Osteomalacia 40 0.049