Search results for PTPN13

96 hits were found for PTPN13

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 100 23.743
2
P OVR042 Ovarian Cancer 88 16.246
3
TNG007 Tongue Carcinoma 52 14.070
4
c CLR055 Colorectal Cancer, Hereditary Nonpolyposis, Type 6 39 8.123
5
c CLR039 Colorectal Cancer, Hereditary Nonpolyposis, Type 4 38 8.123
6
LYN004 Lynch Syndrome I 58 8.123
8
SBC003 Subacute Bacterial Endocarditis 33 8.123
9
STR002 Streptococcal Meningitis 24 8.123
10
RCT023 Rectum Squamous Cell Carcinoma 24 8.123
11
RNL114 Renal Cell Carcinoma, Nonpapillary 80 4.215
12
P HPT023 Hepatocellular Carcinoma 96 4.199
13
CLR030 Clear Cell Renal Cell Carcinoma 54 4.130
14
P HPT021 Hepatitis 69 3.423
15
c HPT016 Hepatitis B 62 3.423
16
LNG039 Lung Squamous Cell Carcinoma 57 3.383
17
SQM006 Squamous Cell Carcinoma 60 3.285
18
c SML038 Small Cell Cancer of the Lung 69 3.183
19
SQM013 Squamous Cell Carcinoma, Head and Neck 73 2.961
20
GST103 Gastric Cancer, Hereditary Diffuse 68 2.853
21
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 2.625
22
c CLR087 Colorectal Cancer 12 34 2.625
23
SML009 Small Intestine Adenocarcinoma 57 2.625
24
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 2.575
25
PLM134 Pulmonary Fibrosis, Idiopathic 76 2.488
26
P PLM036 Pulmonary Fibrosis 66 2.488
27
c LKM063 Leukemia, Chronic Myeloid 71 2.392
28
P PLY014 Polycystic Kidney Disease 69 2.392
29
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 2.392
30
HLX001 Helix Syndrome 48 2.392
31
P ADN016 Adenocarcinoma 63 2.392
32
LNG099 Lung Disease 62 2.303
33
INT066 Interstitial Lung Disease 60 2.303
34
ESP021 Esophageal Cancer 83 2.251
35
TRM010 Traumatic Brain Injury 51 2.251
36
P LNG064 Lung Cancer Susceptibility 3 70 2.251
37
P PRS040 Prostate Cancer 95 2.059
38
ALL029 Allergic Disease 59 1.915
39
MYL031 Myeloproliferative Neoplasm 66 1.915
40
GLM045 Glioma 63 1.784
41
INS024 Insulin-Like Growth Factor I 78 1.704
42
P RTN024 Retinoblastoma 73 1.704
43
P LNG032 Lung Cancer 98 1.487
44
CRV035 Cervical Cancer 73 1.429
45
SML031 Small Cell Carcinoma of the Bladder 46 1.119
46
c GLM047 Glioma Susceptibility 3 33 1.119
47
c PRS097 Prostate Cancer, Hereditary, 1 39 1.119
48
c GLM025 Glioma Susceptibility 2 30 1.119
49
c GLM043 Glioma Susceptibility 9 30 1.119
50
c PRS070 Prostate Cancer, Hereditary, 12 22 1.119
51
c PRS071 Prostate Cancer, Hereditary, 13 25 1.119
52
c PRS117 Prostate Cancer, Hereditary, 11 24 1.119
53
P GLM040 Glioma Susceptibility 1 71 1.119
54
c PRS114 Prostate Cancer, Hereditary, 2 33 1.119
55
MNN043 Meningioma, Familial 79 1.119
56
PRS015 Prostate Signet Ring Cell Adenocarcinoma 25 1.119
57
P KDN018 Kidney Disease 72 0.940
58
P CYS039 Cystic Kidney Disease 53 0.940
59
TCL008 T-Cell Lymphoma 1a 17 0.940
60
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.867
61
P BRS047 Breast Cancer 98 0.811
62
VNH007 Von Hippel-Lindau Syndrome 73 0.791
63
PPL049 Papillon-Lefevre Syndrome 66 0.791
64
c MSM022 Mismatch Repair Cancer Syndrome 1 70 0.791
65
MLT165 Multilocular Cystic Renal Neoplasm of Low Malignant Potential 28 0.791
66
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 32 0.791
67
CRN005 Craniofrontonasal Syndrome 57 0.665
68
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.665
69
CYS001 Cystic Fibrosis 78 0.665
70
ATS010 Autosomal Recessive Disease 42 0.665
71
DFF005 Diffuse Large B-Cell Lymphoma 54 0.665
72
BRN032 Brain Glioma 45 0.665
73
IMM167 Immune Deficiency Disease 78 0.665
74
P CRB048 Cerebral Cavernous Malformations 63 0.665
75
c CRB191 Cerebral Cavernous Malformations 2 45 0.665
76
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.665
77
c CRB094 Cerebral Cavernous Malformations 3 41 0.665
78
P GST053 Gastric Cancer 83 0.665
79
P HRS035 Hirschsprung Disease 1 66 0.665
80
IMM011 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 52 0.665
81
MCR004 Macroglobulinemia 49 0.665
82
P BCL017 B-Cell Lymphoma 59 0.665
83
ULC004 Ulcerative Colitis 74 0.665
84
P MYL006 Myeloid Leukemia 61 0.665
85
GLL048 Glial Tumor 52 0.665
86
P LVR013 Liver Disease 69 0.665
87
P SKN015 Skin Carcinoma 71 0.665
88
LMY003 Leiomyomatosis 44 0.665
89
INT020 Intravenous Leiomyomatosis 36 0.665
90
P TRT010 Teratoma 51 0.665
91
c CRB051 Cerebral Cavernous Malformation, Familial 40 0.665
92
CVR010 Cavernous Malformation 30 0.665
93
HYP266 Hypoxia 57 0.665
94
CHR176 Chromophil Renal Cell Carcinoma 23 0.665
95
P PNC035 Pancreatic Cancer 86 0.573
96
MYL005 Myelofibrosis 71 0.573
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