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"

150 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 6.383
2
P CLR023 Colorectal Cancer 97 1.572
3
P BRS047 Breast Cancer 100 0.946
4
P GST049 Gastrointestinal System Cancer 60 0.567
5
INT253 Intestinal Benign Neoplasm 47 0.533
6
CLN019 Colonic Disease 51 0.518
7
RCT018 Rectal Neoplasm 54 0.507
8
RCT017 Rectal Disease 40 0.507
9
P OVR042 Ovarian Cancer 76 0.499
10
P PNC035 Pancreatic Cancer 87 0.494
11
P ADN016 Adenocarcinoma 69 0.478
12
c CLR079 Colorectal Cancer 2 29 0.438
13
c CLR085 Colorectal Cancer 1 45 0.407
14
P PNC044 Pancreatitis 61 0.377
15
ADN018 Adenoma 58 0.373
16
c CLR075 Colorectal Cancer 3 28 0.358
17
P LYN001 Lynch Syndrome 69 0.355
18
P INT068 Intestinal Disease 60 0.337
19
c CLR080 Colorectal Cancer 5 32 0.314
20
CLR109 Colorectal Adenocarcinoma 51 0.294
21
P CLR108 Colorectal Adenoma 60 0.287
22
c CLR081 Colorectal Cancer 6 22 0.262
23
c FML053 Familial Colorectal Cancer 51 0.254
24
GST071 Gastrointestinal Carcinoma 42 0.249
25
OCL009 Ocular Cancer 59 0.245
26
P SML016 Small Intestine Cancer 52 0.243
27
END057 Endometrial Cancer 75 0.241
28
P SKN013 Skin Benign Neoplasm 43 0.240
29
P LYM118 Lymphoma 69 0.236
30
SML033 Small Cell Cancer of the Lung, Somatic 54 0.233
31
MLN008 Melanoma 62 0.224
32
P SML001 Small Cell Carcinoma 56 0.223
33
P KDN017 Kidney Cancer 65 0.218
34
P RNL014 Renal Cell Carcinoma 82 0.212
35
FML038 Female Reproductive Organ Cancer 50 0.212
36
c CLR083 Colorectal Cancer 8 24 0.211
37
c CLR077 Colorectal Cancer 10 29 0.210
38
c HRD169 Hereditary Colorectal Cancer 42 0.210
39
SKN016 Skin Disease 66 0.209
40
CLN015 Colon Adenocarcinoma 50 0.203
41
FML039 Female Reproductive System Disease 48 0.201
42
MLR007 Male Reproductive System Disease 34 0.190
43
P OVR049 Ovarian Disease 56 0.186
44
MLR006 Male Reproductive Organ Cancer 43 0.186
45
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.183
46
c INH020 Inherited Metabolic Disorder 49 0.169
47
P SPS003 Spastic Diplegia 52 0.167
48
c CLR082 Colorectal Cancer 7 20 0.166
49
P FML011 Familial Adenomatous Polyposis 68 0.163
50
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.161
51
SPC010 Speech and Communication Disorders 41 0.156
52
P UTR038 Uterine Disease 37 0.154
53
ADJ001 Adjustment Disorder 38 0.152
54
FNC005 Functional Colonic Disease 27 0.145
55
AND005 Androgen Insensitivity Syndrome, Mild 16 0.139
56
P DRR001 Diarrhea 60 0.136
57
URN008 Urinary Bladder Cancer 66 0.131
58
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 33 0.130
59
RNL101 Renal Cell Carcinoma, Papillary 63 0.129
60
P RTN024 Retinoblastoma 74 0.127
61
P NRB001 Neuroblastoma 70 0.126
62
KDS001 Kid Syndrome 53 0.126
63
BLD044 Bladder Disease 51 0.125
64
CHL071 Child Syndrome 58 0.124
65
WLL006 Wells Syndrome 59 0.124
66
SML036 Small Intestinal Adenocarcinoma 46 0.123
67
UTR033 Uterine Corpus Cancer 49 0.122
68
GDS001 Good Syndrome 44 0.122
69
END080 Endometrial Disease 27 0.118
70
CLN008 Colon Small Cell Carcinoma 19 0.115
71
c CLR089 Colorectal Cancer, Hereditary Nonpolyposis, Type 8 19 0.114
72
c CLR055 Colorectal Cancer, Hereditary Nonpolyposis, Type 6 25 0.114
73
ADL002 Adult Syndrome 52 0.114
74
c CLR039 Colorectal Cancer, Hereditary Nonpolyposis, Type 4 27 0.113
75
CLN045 Colonic Benign Neoplasm 33 0.113
76
c CLR037 Colorectal Cancer, Hereditary Nonpolyposis, Type 5 27 0.112
77
HDG012 Hodgkin Lymphoma 77 0.112
78
P RCK004 Rickets 61 0.111
79
ATS008 Autosomal Dominant Disease 39 0.110
80
c BSL007 Basal Cell Carcinoma 65 0.106
81
c CLR041 Colorectal Cancer, Hereditary Nonpolyposis, Type 2 23 0.105
82
c CLR100 Colorectal Cancer, Hereditary Nonpolyposis, Type 7 18 0.105
83
P FLL037 Follicular Lymphoma 70 0.102
84
c FML303 Familial/multiple Cancer 14 0.101
85
NSY001 N Syndrome 36 0.101
86
DDN006 Duodenitis 42 0.097
87
MDD011 Mood Disorder 61 0.094
88
c FML311 Familial Colorectal Cancer Type X 36 0.089
89
END041 Endometrial Adenocarcinoma 56 0.086
90
VTM003 Vitamin Metabolic Disorder 30 0.082
91
CHR008 Choroiditis 44 0.082
92
RHB003 Rhabdomyosarcoma 57 0.078
93
P PLY014 Polycystic Kidney Disease 53 0.077
94
CMP010 Complex Regional Pain Syndrome 54 0.073
95
APH001 Aphthous Stomatitis 62 0.072
96
P LPS002 Liposarcoma 55 0.071
97
LYM006 Lymphoepithelioma-Like Carcinoma 43 0.070
98
P PLY006 Polydactyly 56 0.070
99
c JVN024 Juvenile Hereditary Hemochromatosis 29 0.069
100
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.068
101
KRT002 Keratomalacia 52 0.067
102
UTR024 Uterine Carcinosarcoma 52 0.063
103
DYS018 Dysostosis 44 0.062
104
SML031 Small Cell Carcinoma of the Bladder 37 0.061
105
P ATT003 Attenuated Familial Adenomatous Polyposis 47 0.060
106
EXT010 Extramedullary Plasmacytoma 49 0.059
107
DSM004 Desmoid Tumor 56 0.058
108
P SPN052 Spondyloarthropathy 60 0.057
109
ATS009 Autosomal Genetic Disease 35 0.055
110
LCH009 Lichen Sclerosus 41 0.054
111
P FNG005 Feingold Syndrome 42 0.052
112
ESP020 Esophageal Atresia 50 0.052
113
PRN049 Paraneoplastic Pemphigus 40 0.052
114
c ANT034 Anterior Uveitis 48 0.050
115
TKY002 Takayasu Arteritis 61 0.050
116
P BRD002 Bardet-Biedl Syndrome 63 0.049
117
P ALG002 Alagille Syndrome 72 0.049
118
HJD001 Hajdu-Cheney Syndrome 59 0.049
119
BSL036 Basal Cell Nevus Syndrome 65 0.048
120
c PLY139 Polycystic Kidney Disease 3 37 0.048
121
c SPN297 Spondylocostal Dysostosis 3, Autosomal Recessive 37 0.048
122
P INT283 Integumentary System Cancer 33 0.047
123
c BRD015 Bardet-Biedl Syndrome 3 42 0.047
124
P HLP001 Holoprosencephaly 63 0.047
125
PST053 Postherpetic Neuralgia 40 0.047
126
HST011 Histoplasmosis 52 0.046
127
GGR001 Geographic Tongue 46 0.046
128
MCK005 Mckusick-Kaufman Syndrome 52 0.046
129
HYP542 Hypersensitivity Syndrome, Carbamazepine-Induced 52 0.045
130
NDL005 Nodular Medulloblastoma 36 0.044
131
SCR003 Secretory Diarrhea 36 0.044
132
CNG048 Congenital Hepatic Fibrosis 44 0.044
133
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 45 0.043
134
VGT001 Vogt-Koyanagi-Harada Disease 55 0.043
135
PLL001 Pallister-Hall Syndrome 55 0.042
136
IDP074 Idiopathic Bronchiectasis 36 0.042
137
c CHR098 Chronic Pyelonephritis 36 0.041
138
LBR025 Lobar Holoprosencephaly 34 0.041
139
VNZ002 Venezuelan Equine Encephalitis 45 0.041
140
c BRD010 Bardet-Biedl Syndrome 1 54 0.040
141
c BRD013 Bardet-Biedl Syndrome 12 45 0.040
142
c BRD011 Bardet-Biedl Syndrome 10 45 0.040
143
c BRD033 Bardet-Biedl Syndrome 13 41 0.040
144
c BRD020 Bardet-Biedl Syndrome 8 40 0.040
145
PTY001 Pityriasis Rosea 42 0.040
146
c BRD012 Bardet-Biedl Syndrome 11 43 0.039
147
P SPN081 Spondylocostal Dysostosis, Autosomal Recessive 35 0.039
148
PHN012 Phenytoin or Carbamazepine Toxicity 23 0.039
149
c SPN310 Spondylocostal Dysostosis 1, Autosomal Recessive 41 0.039
150
c SPN330 Spondylocostal Dysostosis 5 38 0.039