Search results for smad2

151 hits were found for smad2

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 99 5.504
2
P BRS047 Breast Cancer 97 4.297
3
P GST053 Gastric Cancer 83 4.018
4
P PNC035 Pancreatic Cancer 84 3.986
5
P HPT023 Hepatocellular Carcinoma 100 3.698
6
P OVR042 Ovarian Cancer 88 3.608
7
END057 Endometrial Cancer 74 3.608
8
P PRS040 Prostate Cancer 97 3.274
9
CRV035 Cervical Cancer 76 2.891
10
P INF037 Inflammatory Bowel Disease 54 2.806
11
P OST002 Osteoporosis 74 2.778
12
PNC129 Pancreatic Adenocarcinoma 68 2.778
13
P PLM037 Pulmonary Hypertension 67 2.778
14
CHG001 Chagas Disease 66 2.778
15
P GLM007 Glomerulonephritis 57 2.778
16
CLR003 Clear Cell Adenocarcinoma 50 2.778
17
RNL077 Renal Fibrosis 47 2.414
18
P LYS001 Loeys-Dietz Syndrome 65 2.353
19
SQM013 Squamous Cell Carcinoma, Head and Neck 80 2.301
20
HMT002 Hematologic Cancer 62 2.301
21
BSC001 Buschke-Ollendorff Syndrome 56 2.301
22
MLR003 Melorheostosis 45 2.301
23
OST014 Osteopoikilosis 41 2.301
24
c ART115 Aortic Valve Disease 1 75 2.268
25
HYP457 Hypertrophic Scars 42 2.268
26
OBS082 Obstructive Nephropathy 42 2.268
27
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 1.647
28
URN010 Urinary Tract Obstruction 55 1.647
29
PLM134 Pulmonary Fibrosis, Idiopathic 77 1.604
30
c HRD010 Hereditary Spastic Paraplegia 66 1.604
31
c SPS215 Spastic Paraplegia 3, Autosomal Dominant 61 1.604
32
c LYS021 Loeys-Dietz Syndrome 3 58 1.604
33
c LYS019 Loeys-Dietz Syndrome 1 57 1.604
34
c SPN395 Spinal Muscular Atrophy, Type Ii 55 1.604
35
c LYS017 Loeys-Dietz Syndrome 4 51 1.604
36
c LYS020 Loeys-Dietz Syndrome 5 50 1.604
37
NPH018 Nephrogenic Systemic Fibrosis 50 1.604
38
c ALB025 Albinism, Ocular, with Late-Onset Sensorineural Deafness 49 1.604
39
DYS160 Dyssegmental Dysplasia, Silverman-Handmaker Type 49 1.604
40
P ORF002 Orofacial Cleft 44 1.604
41
URT031 Ureteral Disease 41 1.604
42
VTR005 Vitreous Disease 39 1.604
43
PCM002 Pauci-Immune Glomerulonephritis 30 1.604
44
c ATS417 Autosomal Dominant Non-Syndromic Intellectual Disability 19 28 1.604
45
P ADN016 Adenocarcinoma 64 0.155
46
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.155
47
P LNG032 Lung Cancer 98 0.137
48
SQM006 Squamous Cell Carcinoma 60 0.137
49
c MCR113 Microvascular Complications of Diabetes 3 52 0.116
50
c MCR120 Microvascular Complications of Diabetes 7 47 0.116
51
c MCR130 Microvascular Complications of Diabetes 6 41 0.116
52
c MCR133 Microvascular Complications of Diabetes 4 41 0.116
53
P LNG064 Lung Cancer Susceptibility 3 78 0.103
54
GLB015 Glioblastoma Multiforme 75 0.103
55
P PRD008 Periodontitis 64 0.103
56
ANR040 Aneurysm 59 0.103
57
P PLM036 Pulmonary Fibrosis 65 0.090
58
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.090
59
P OVR082 Overgrowth Syndrome 50 0.090
60
KLD004 Keloid Disorder 40 0.090
61
SVR004 Severe Combined Immunodeficiency 73 0.073
62
P KDN018 Kidney Disease 72 0.073
63
ART016 Aortic Aneurysm 69 0.073
64
P LVR013 Liver Disease 68 0.073
65
OST159 Osteogenic Sarcoma 66 0.073
66
P SKN015 Skin Carcinoma 66 0.073
67
c SML038 Small Cell Cancer of the Lung 65 0.073
68
CLF027 Cleft Palate, Isolated 64 0.073
69
P GLM045 Glioma 63 0.073
70
P BRS044 Breast Adenocarcinoma 59 0.073
71
GLL048 Glial Tumor 45 0.073
72
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.073
73
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.073
74
ESP021 Esophageal Cancer 90 0.052
75
MYL069 Myeloma, Multiple 85 0.052
76
P ATX030 Ataxia-Telangiectasia 82 0.052
77
c DLT002 Dilated Cardiomyopathy 79 0.052
78
INS024 Insulin-Like Growth Factor I 79 0.052
79
OST012 Osteoarthritis 78 0.052
80
MRF001 Marfan Syndrome 77 0.052
81
P RTN024 Retinoblastoma 73 0.052
82
P FML011 Familial Adenomatous Polyposis 72 0.052
83
GST040 Gastric Adenocarcinoma 70 0.052
84
P TTR001 Tetralogy of Fallot 70 0.052
85
P LYM118 Lymphoma 68 0.052
86
P SYS005 Systemic Scleroderma 68 0.052
87
c BSL007 Basal Cell Carcinoma 68 0.052
88
P LKM002 Leukemia 68 0.052
89
P JVN014 Juvenile Polyposis Syndrome 68 0.052
90
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.052
91
P NSP012 Nasopharyngeal Carcinoma 66 0.052
92
ART001 Arterial Tortuosity Syndrome 66 0.052
93
P DRM053 Dermatitis, Atopic 66 0.052
94
CLR108 Colorectal Adenoma 64 0.052
95
MSC007 Muscle Hypertrophy 64 0.052
96
c PRC016 Pre-Eclampsia 63 0.052
97
P VSC007 Vascular Disease 63 0.052
98
SKN016 Skin Disease 63 0.052
99
c HPT001 Hepatitis C 62 0.052
100
CHL068 Cholestasis 61 0.052
101
HYP066 Hyperglycemia 61 0.052
102
DRM006 Dermatitis 61 0.052
103
c SCL052 Scleroderma, Familial Progressive 61 0.052
104
GST033 Gestational Diabetes 61 0.052
105
P MYL006 Myeloid Leukemia 60 0.052
106
P VNT002 Ventricular Septal Defect 60 0.052
107
ADN018 Adenoma 59 0.052
108
P INT070 Intestinal Obstruction 58 0.052
109
P BCL017 B-Cell Lymphoma 58 0.052
110
P INF032 Infertility 57 0.052
111
TTL012 Total Anomalous Pulmonary Venous Return 1 57 0.052
112
BRN056 Bronchopulmonary Dysplasia 57 0.052
113
HYP266 Hypoxia 57 0.052
114
P PLY011 Polycystic Ovary Syndrome 56 0.052
115
BCT022 Bacterial Infectious Disease 56 0.052
116
AGN016 Aging 56 0.052
117
c PRD040 Periodontitis, Chronic 53 0.052
118
P ACT008 Actinic Keratosis 53 0.052
119
c FML008 Familial Retinoblastoma 53 0.052
120
c FBR084 Fibromatosis, Gingival, 1 52 0.052
121
P MSC003 Muscular Atrophy 52 0.052
122
ART074 Aortic Dissection 52 0.052
123
TLN003 Telangiectasis 52 0.052
124
P SPP010 Suppressor of Tumorigenicity 3 51 0.052
125
KRT009 Keratosis 51 0.052
126
CLR109 Colorectal Adenocarcinoma 51 0.052
127
LNG031 Lung Benign Neoplasm 51 0.052
128
GNG012 Gingival Overgrowth 51 0.052
129
P ECL001 Eclampsia 50 0.052
130
P GNG025 Gingival Fibromatosis 50 0.052
131
HYP748 Hypertelorism 50 0.052
132
ART017 Aortic Disease 49 0.052
133
BNR002 Bone Resorption Disease 48 0.052
134
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.052
135
END062 Endometrial Hyperplasia 48 0.052
136
HLX001 Helix Syndrome 47 0.052
137
SYN036 Syncope 45 0.052
138
URT010 Ureteral Obstruction 45 0.052
139
ORL015 Oral Squamous Cell Carcinoma 43 0.052
140
FBR019 Fibromatosis 41 0.052
141
P DYS005 Dyslexia 40 0.052
142
SKL017 Skeletal Dysplasias 40 0.052
143
HTR003 Heterotaxy 39 0.052
144
ALL014 Allergic Encephalomyelitis 38 0.052
145
OVR094 Ovarian Epithelial Cancer 38 0.052
146
DBT081 Diabetic Encephalopathy 37 0.052
147
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 37 0.052
148
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.052
149
CRN270 Coronary Artery Dissection, Spontaneous 32 0.052
150
MLR023 Melorheostosis, Isolated 32 0.052
151
PRM334 Primary Bone Dysplasia with Increased Bone Density 20 0.052
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