Search results for flavone

195 hits were found for flavone

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 99 0.181
2
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.148
3
ISC004 Ischemia 58 0.135
4
P BRS047 Breast Cancer 97 0.113
5
P BRS044 Breast Adenocarcinoma 59 0.113
6
HYP066 Hyperglycemia 61 0.104
7
P KDN017 Kidney Cancer 60 0.104
8
P NRB001 Neuroblastoma 72 0.095
9
P LKM002 Leukemia 68 0.095
10
OST159 Osteogenic Sarcoma 66 0.095
11
CLN015 Colon Adenocarcinoma 65 0.095
12
NWC001 Newcastle Disease 45 0.095
13
c HYP836 Hypercholesterolemia, Familial, 1 73 0.085
14
ORL011 Oral Cancer 60 0.085
15
BCT022 Bacterial Infectious Disease 56 0.085
16
P INF037 Inflammatory Bowel Disease 54 0.085
17
ORL015 Oral Squamous Cell Carcinoma 43 0.085
18
CYT002 Cytokine Deficiency 42 0.085
19
P HPT023 Hepatocellular Carcinoma 100 0.074
20
P PRS040 Prostate Cancer 97 0.074
21
P PNC035 Pancreatic Cancer 84 0.074
22
P LNG064 Lung Cancer Susceptibility 3 78 0.074
23
P OST002 Osteoporosis 74 0.074
24
P RTN024 Retinoblastoma 73 0.074
25
GST040 Gastric Adenocarcinoma 70 0.074
26
P ADN016 Adenocarcinoma 64 0.074
27
P CRN300 Coronary Heart Disease 1 63 0.074
28
LPD008 Lipid Metabolism Disorder 62 0.074
29
HYP266 Hypoxia 57 0.074
30
NNL006 Non-Alcoholic Steatohepatitis 54 0.074
31
c FML008 Familial Retinoblastoma 53 0.074
32
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.074
33
CRB004 Cerebral Artery Occlusion 45 0.074
34
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.074
35
ANX004 Anoxia 40 0.074
36
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.074
37
P OVR042 Ovarian Cancer 88 0.060
38
c LKM061 Leukemia, Acute Myeloid 84 0.060
39
GLB015 Glioblastoma Multiforme 75 0.060
40
CRH001 Crohn's Disease 74 0.060
41
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.060
42
HMN044 Human Immunodeficiency Virus Type 1 71 0.060
43
PNC129 Pancreatic Adenocarcinoma 68 0.060
44
P NSP012 Nasopharyngeal Carcinoma 66 0.060
45
SRC014 Sarcoma 65 0.060
46
P HRP006 Herpes Simplex 65 0.060
47
GT001 Gout 64 0.060
48
P RHB003 Rhabdomyosarcoma 63 0.060
49
SKN016 Skin Disease 63 0.060
50
c HPT003 Hepatitis a 62 0.060
51
P HYP750 Hypertriglyceridemia, Familial 62 0.060
52
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.060
53
FTT001 Fatty Liver Disease 61 0.060
54
P MYL006 Myeloid Leukemia 60 0.060
55
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.060
56
ADN018 Adenoma 59 0.060
57
P BCL017 B-Cell Lymphoma 58 0.060
58
c DWL002 Dowling-Degos Disease 1 58 0.060
59
MCR013 Microphthalmia 57 0.060
60
P FBR017 Fibrosarcoma 56 0.060
61
P NRP001 Neuropathy 56 0.060
62
P DRR001 Diarrhea 55 0.060
63
SPN035 Spindle Cell Sarcoma 53 0.060
64
GST023 Gastric Ulcer 53 0.060
65
DNT012 Dental Caries 53 0.060
66
c MCR113 Microvascular Complications of Diabetes 3 52 0.060
67
HLX001 Helix Syndrome 47 0.060
68
c MCR120 Microvascular Complications of Diabetes 7 47 0.060
69
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.060
70
c PCH010 Pachyonychia Congenita 3 44 0.060
71
c MCR130 Microvascular Complications of Diabetes 6 41 0.060
72
c MCR133 Microvascular Complications of Diabetes 4 41 0.060
73
48X005 48,xyyy 39 0.060
74
HRW001 Hair Whorl 36 0.060
75
c LKM005 Leukemia, T-Cell, Chronic 34 0.060
76
P LNG032 Lung Cancer 98 0.043
77
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.043
78
P ALZ034 Alzheimer Disease 88 0.043
79
MYL069 Myeloma, Multiple 85 0.043
81
CYS001 Cystic Fibrosis 81 0.043
82
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.043
83
P BLD134 Bladder Cancer 79 0.043
84
P LKM071 Leukemia, Chronic Lymphocytic 79 0.043
85
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.043
86
CRV035 Cervical Cancer 76 0.043
87
P HRT032 Heart Disease 75 0.043
88
END057 Endometrial Cancer 74 0.043
89
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.043
90
P MLT020 Multiple Sclerosis 72 0.043
91
P HNT016 Huntington Disease 72 0.043
92
P FML011 Familial Adenomatous Polyposis 72 0.043
93
PLM001 Pulmonary Tuberculosis 69 0.043
94
P LPR021 Leprosy 3 69 0.043
95
P LKM062 Leukemia, Acute Lymphoblastic 69 0.043
96
P INF038 Influenza 68 0.043
97
BRN024 Bronchitis 68 0.043
98
P THR014 Thrombocytopenia 67 0.043
99
CRB039 Cerebrovascular Disease 67 0.043
100
P PLM037 Pulmonary Hypertension 67 0.043
101
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.043
102
ANG054 Angina Pectoris 66 0.043
103
P DMN002 Dementia 66 0.043
104
c SML038 Small Cell Cancer of the Lung 65 0.043
105
IRR002 Irritable Bowel Syndrome 65 0.043
106
ATH013 Atherosclerosis Susceptibility 65 0.043
107
P MST009 Mastocytosis 64 0.043
108
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.043
109
P GLM045 Glioma 63 0.043
110
P NTR004 Neutropenia 63 0.043
111
P VSC007 Vascular Disease 63 0.043
112
c SYS004 Systemic Mastocytosis 63 0.043
113
TRN015 Transient Cerebral Ischemia 63 0.043
114
CLT003 Colitis 62 0.043
115
c SVR001 Severe Acute Respiratory Syndrome 62 0.043
116
ATM095 Autoimmune Disease 62 0.043
117
ALL026 Allergic Hypersensitivity Disease 62 0.043
118
INT002 Intermittent Claudication 61 0.043
119
SQM006 Squamous Cell Carcinoma 60 0.043
120
CHC001 Chickenpox 60 0.043
121
P CTR002 Cataract 60 0.043
122
CHL014 Cholera 59 0.043
123
c HPT016 Hepatitis B 59 0.043
124
VSL002 Visual Epilepsy 59 0.043
125
AVN001 Avian Influenza 59 0.043
126
P DNG005 Dengue Virus 59 0.043
127
P ANP001 Anaplastic Large Cell Lymphoma 58 0.043
128
P PRP019 Peripheral Nervous System Disease 58 0.043
129
P GLM007 Glomerulonephritis 57 0.043
130
c ACT075 Acute Myocardial Infarction 57 0.043
131
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.043
132
APH002 Aphasia 57 0.043
133
VSC002 Vascular Dementia 57 0.043
134
P ADL017 Adult T-Cell Leukemia 56 0.043
135
P PLY011 Polycystic Ovary Syndrome 56 0.043
136
ERY051 Erythroleukemia, Familial 56 0.043
137
P SZR006 Seizure Disorder 56 0.043
138
c GRV008 Graves Disease 1 56 0.043
139
BRN004 Brain Edema 56 0.043
140
AGN016 Aging 56 0.043
141
LMB062 Limb Ischemia 55 0.043
142
P MYP006 Myopia 55 0.043
143
P VNS003 Venous Insufficiency 55 0.043
144
HYP060 Hyperinsulinism 54 0.043
145
PRP030 Purpura 54 0.043
146
GLC003 Glucose Intolerance 54 0.043
147
P ALP008 Alopecia 54 0.043
148
PLM010 Pulmonary Edema 54 0.043
149
P ART021 Arteriosclerosis 54 0.043
150
P LNG035 Lung Large Cell Carcinoma 54 0.043
151
P MNC007 Monocytic Leukemia 53 0.043
152
P RTN016 Retinal Degeneration 53 0.043
153
MST005 Mastitis 53 0.043
154
OVR059 Ovary Adenocarcinoma 53 0.043
155
c VRL010 Viral Hepatitis 52 0.043
156
P RCT021 Rectum Cancer 52 0.043
157
HYP014 Hyperuricemia 52 0.043
158
P BRN035 Brain Stem Glioma 52 0.043
159
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.043
160
P SPP010 Suppressor of Tumorigenicity 3 51 0.043
161
CLR109 Colorectal Adenocarcinoma 51 0.043
162
TNG007 Tongue Carcinoma 51 0.043
163
P AST007 Astrocytoma 51 0.043
164
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.043
165
CHR005 Chorioamnionitis 51 0.043
166
STM007 Stomatitis 50 0.043
167
NTR046 Neutrophil Migration 50 0.043
168
ENT004 Enthesopathy 49 0.043
169
c CHR431 Chronic Venous Insufficiency 49 0.043
170
47X002 47,xyy 49 0.043
171
BRN071 Brain Injury 49 0.043
172
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.043
173
TTR011 Tetraploidy 47 0.043
174
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.043
175
STM006 Stomach Disease 47 0.043
176
MYC005 Myocardial Stunning 46 0.043
177
GLL048 Glial Tumor 45 0.043
178
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.043
179
ATN004 Autonomic Neuropathy 45 0.043
180
GLL017 Gallbladder Adenocarcinoma 43 0.043
181
RTC009 Reticulum Cell Sarcoma 43 0.043
182
MST004 Mast Cell Neoplasm 42 0.043
183
c RTN047 Retinitis Pigmentosa 18 42 0.043
184
KLB003 Klebsiella Pneumonia 41 0.043
185
PLY100 Polyploidy 40 0.043
186
AML001 Amelanotic Melanoma 39 0.043
187
EXT007 Extracutaneous Mastocytoma 38 0.043
188
ALL014 Allergic Encephalomyelitis 38 0.043
189
HNS001 Hansen's Disease 34 0.043
190
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.043
192
c CLR079 Colorectal Cancer 2 32 0.043
193
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.043
194
c RNG015 Ring Chromosome 2 26 0.043
195
c RNG019 Ring Chromosome 3 22 0.043
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