Search results for Menadione

396 hits were found for Menadione

# Family MCID Name MIFTS Score
1
P EXN002 Exanthem 57 0.078
2
P PNC035 Pancreatic Cancer 84 0.071
3
P BRS047 Breast Cancer 100 0.064
4
P CLR023 Colorectal Cancer 95 0.064
5
P LNG032 Lung Cancer 94 0.064
6
c CLR085 Colorectal Cancer 1 46 0.064
7
FXF002 Fox-Fordyce Disease 37 0.064
8
c PNC095 Pancreatic Cancer 3 31 0.064
9
c CLR079 Colorectal Cancer 2 30 0.064
10
c PNC111 Pancreatic Cancer 2 29 0.064
11
c CLR075 Colorectal Cancer 3 29 0.064
12
c PNC094 Pancreatic Cancer 1 27 0.064
13
END072 Endotheliitis 41 0.055
14
MLN008 Melanoma 70 0.045
15
P ADN016 Adenocarcinoma 69 0.045
16
P HPT021 Hepatitis 68 0.045
17
P PNC044 Pancreatitis 60 0.045
18
ORL011 Oral Cancer 56 0.045
19
HYP266 Hypoxia 55 0.045
20
RDC011 Reducing Body Myopathy, X-Linked 1a, Severe, Infantile or Early Childhood Onset 22 0.045
21
RDC012 Reducing Body Myopathy, X-Linked 1b, with Late Childhood or Adult Onset 17 0.045
22
P OBS005 Obesity 91 0.032
23
P HPT023 Hepatocellular Carcinoma 89 0.032
24
P PRS040 Prostate Cancer 88 0.032
25
P RHM011 Rheumatoid Arthritis 87 0.032
26
CYS001 Cystic Fibrosis 86 0.032
27
MLR004 Malaria 82 0.032
28
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.032
29
P OST012 Osteoarthritis 79 0.032
30
P MYC007 Myocardial Infarction 77 0.032
31
P PLM037 Pulmonary Hypertension 77 0.032
32
P ALZ034 Alzheimer Disease 76 0.032
33
INS024 Insulin-Like Growth Factor I 75 0.032
34
P HRT032 Heart Disease 75 0.032
35
GST019 Gastrointestinal Stromal Tumor 74 0.032
36
P CRN211 Coronary Artery Disease 73 0.032
37
CRH001 Crohn's Disease 73 0.032
38
P ART022 Arthritis 72 0.032
39
STR067 Stroke, Ischemic 72 0.032
40
P LVR013 Liver Disease 72 0.032
41
P LKM002 Leukemia 72 0.032
42
SCK003 Sickle Cell Anemia 71 0.032
43
P NRB001 Neuroblastoma 71 0.032
44
c HPT073 Hepatitis C Virus 70 0.032
45
CNG034 Congestive Heart Failure 70 0.032
46
P NRV007 Nervous System Disease 70 0.032
47
WRN001 Werner Syndrome 68 0.032
48
PCK002 Pick Disease 68 0.032
49
P CRD011 Cardiomyopathy 67 0.032
50
PSY004 Psychotic Disorder 67 0.032
51
ANX002 Anxiety Disorder 66 0.032
52
LVR012 Liver Cirrhosis 66 0.032
53
P PNM007 Pneumonia 66 0.032
54
P GLB002 Glioblastoma 66 0.032
55
CNT098 Central Core Disease 66 0.032
56
VSC007 Vascular Disease 65 0.032
57
P ATR011 Atrial Fibrillation 65 0.032
58
P KDN018 Kidney Disease 65 0.032
59
ALX003 Alexander Disease 65 0.032
60
ATH003 Atherosclerosis 65 0.032
61
c CHR089 Chronic Kidney Failure 65 0.032
62
SKN016 Skin Disease 64 0.032
63
P PSR002 Psoriasis 64 0.032
64
P ORT004 Orthostatic Intolerance 63 0.032
65
P AST007 Astrocytoma 63 0.032
66
P THR014 Thrombocytopenia 63 0.032
67
P OST002 Osteoporosis 63 0.032
68
CRB039 Cerebrovascular Disease 63 0.032
69
c HPT001 Hepatitis C 62 0.032
70
c HPT016 Hepatitis B 62 0.032
71
MTH009 Mouth Disease 62 0.032
72
P INF037 Inflammatory Bowel Disease 62 0.032
73
HMT002 Hematologic Cancer 62 0.032
74
GST092 Gastroesophageal Reflux 62 0.032
75
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.032
76
c HMP004 Hemophilia B 62 0.032
77
P ART023 Arthropathy 62 0.032
78
WLL001 Williams-Beuren Syndrome 62 0.032
79
GLB015 Glioblastoma Multiforme 61 0.032
80
RBR001 Roberts Syndrome 61 0.032
81
P SHR029 Short Syndrome 61 0.032
82
LNG099 Lung Disease 61 0.032
83
P ENC004 Encephalitis 61 0.032
84
P HML002 Hemolytic Anemia 61 0.032
85
CNN005 Connective Tissue Disease 61 0.032
86
DFC004 Deficiency Anemia 60 0.032
87
RSP006 Respiratory System Disease 60 0.032
88
P TXP001 Toxoplasmosis 60 0.032
89
P WVR001 Weaver Syndrome 60 0.032
90
c CNT035 Central Nervous System Disease 60 0.032
91
ACQ007 Acquired Immunodeficiency Syndrome 60 0.032
92
ISC004 Ischemia 59 0.032
93
HYP066 Hyperglycemia 59 0.032
94
P INT068 Intestinal Disease 59 0.032
95
P NRV006 Nervous System Cancer 59 0.032
96
ACN011 Acne 59 0.032
97
CHL071 Child Syndrome 59 0.032
98
c ACT075 Acute Myocardial Infarction 59 0.032
99
P GLM045 Glioma 59 0.032
100
PLM033 Pulmonary Embolism 59 0.032
101
P GST049 Gastrointestinal System Cancer 59 0.032
102
FCT003 Factor X Deficiency 59 0.032
103
P DRR001 Diarrhea 59 0.032
104
VRL011 Viral Infectious Disease 59 0.032
105
CRD119 Cardiac Arrest 59 0.032
106
WST001 West Syndrome 58 0.032
107
P MTR012 Mitral Valve Disease 58 0.032
108
P THR015 Thrombophilia 58 0.032
109
c VRL010 Viral Hepatitis 58 0.032
110
WLL006 Wells Syndrome 58 0.032
111
GST045 Gastroenteritis 57 0.032
112
P HYP060 Hyperinsulinism 57 0.032
113
P INF032 Infertility 57 0.032
114
ART021 Arteriosclerosis 57 0.032
115
P ORL007 Oral Cavity Cancer 57 0.032
116
ANR040 Aneurysm 57 0.032
117
P CTR002 Cataract 57 0.032
118
KDS001 Kid Syndrome 57 0.032
119
ADL002 Adult Syndrome 57 0.032
120
LPD008 Lipid Metabolism Disorder 57 0.032
121
RHM027 Rheumatic Disease 57 0.032
122
ART017 Aortic Disease 57 0.032
123
P HYP069 Hyperparathyroidism 56 0.032
124
CRT016 Carotid Artery Disease 56 0.032
125
c HPT003 Hepatitis a 56 0.032
126
ETN001 Eating Disorder 56 0.032
127
JNT002 Joint Disorders 55 0.032
128
PNC034 Pancreas Disease 55 0.032
129
GLS001 Gliosarcoma 55 0.032
130
P HMR003 Hemorrhagic Disease 55 0.032
131
ART111 Artery Disease 55 0.032
132
P MTC069 Mitochondrial Disorders 55 0.032
133
c ART115 Aortic Valve Disease 1 55 0.032
134
P HMP007 Hemophilia 55 0.032
135
NRN004 Neuroendocrine Tumor 55 0.032
136
c PND001 Pain Disorder 55 0.032
137
P ANT006 Antiphospholipid Syndrome 54 0.032
138
c ART101 Aortic Valve Disease 2 54 0.032
139
GLC003 Glucose Intolerance 54 0.032
140
PLN006 Poland Syndrome 54 0.032
141
RLP002 Relapsing-Remitting Multiple Sclerosis 54 0.032
142
RHM001 Rheumatic Fever 54 0.032
143
PLS007 Plasmodium Falciparum Malaria 54 0.032
144
HPT022 Hepatoblastoma 54 0.032
145
PLM034 Pulmonary Emphysema 54 0.032
146
MLN007 Male Infertility 54 0.032
147
c FML001 Familial Atrial Fibrillation 54 0.032
148
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.032
149
CND002 Conduct Disorder 53 0.032
150
GST050 Gastrointestinal System Disease 53 0.032
151
PRP019 Peripheral Nervous System Disease 53 0.032
152
DMY004 Demyelinating Disease 53 0.032
153
IMM136 Immune System Disease 53 0.032
154
ISC006 Ischemic Heart Disease 53 0.032
155
CSY001 C Syndrome 53 0.032
156
CCC001 Coccidioidomycosis 53 0.032
157
TRN015 Transient Cerebral Ischemia 53 0.032
158
HMR039 Hemorrhage, Intracerebral 52 0.032
159
CRS005 Crest Syndrome 52 0.032
160
VSC006 Vascular Cancer 52 0.032
161
P SPS003 Spastic Diplegia 52 0.032
162
P VNS003 Venous Insufficiency 52 0.032
163
MNT002 Mental Depression 52 0.032
164
BRN106 Burns 52 0.032
165
DMN002 Dementia 52 0.032
166
P MSC033 Muscle Disorders 52 0.032
167
c VRL007 Viral Encephalitis 51 0.032
168
SCT005 Scott Syndrome 51 0.032
169
c HPT007 Hepatitis E 51 0.032
170
END030 End Stage Renal Failure 51 0.032
171
PRS042 Prostate Disease 51 0.032
172
FDL002 Food Allergy 51 0.032
173
PRT014 Protein S Deficiency 51 0.032
174
HMG005 Hemoglobinopathy 51 0.032
175
BNF002 Bone Fracture 51 0.032
176
P TRC086 Trichohepatoenteric Syndrome 1 51 0.032
177
IRN001 Iron Deficiency Anemia 51 0.032
178
CLN019 Colonic Disease 51 0.032
179
SCK005 Sickle Cell Disease 51 0.032
180
P HRD018 Hair Disease 50 0.032
181
INT007 Intermediate Coronary Syndrome 50 0.032
182
PRS055 Pierson Syndrome 50 0.032
183
HYP005 Hypokalemia 50 0.032
184
DGN001 Degenerative Disc Disease 50 0.032
185
P CLL015 Collagen Disease 50 0.032
186
URN009 Urinary System Disease 49 0.032
187
CLN015 Colon Adenocarcinoma 49 0.032
188
PRT011 Protein C Deficiency 49 0.032
189
PGM001 Pigmented Villonodular Synovitis 49 0.032
190
VND001 Vein Disease 49 0.032
191
HYP037 Hyperhomocysteinemia 49 0.032
192
CRN030 Coronary Stenosis 49 0.032
193
CLC006 Calcinosis 49 0.032
194
CCC002 Coccidiosis 49 0.032
195
c HYP071 Hypersensitivity Reaction Type Ii Disease 48 0.032
196
PST095 Post-Thrombotic Syndrome 48 0.032
197
P GNT008 Giant Cell Tumor 48 0.032
198
DRG003 Drug Dependence 48 0.032
199
ALP007 Alpha 1-Antitrypsin Deficiency 48 0.032
200
c ACT071 Acute Kidney Failure 48 0.032
201
OVR063 Overnutrition 48 0.032
202
ATN002 Autonomic Nervous System Disease 48 0.032
203
RHM028 Rheumatic Heart Disease 48 0.032
204
PRP021 Peripheral Nervous System Neoplasm 48 0.032
205
STM006 Stomach Disease 47 0.032
206
PRT030 Parathyroid Gland Disease 47 0.032
207
CRN017 Coronary Thrombosis 47 0.032
208
PNM001 Pneumocystosis 47 0.032
209
NTR005 Nutritional Deficiency Disease 47 0.032
210
CLC001 Calciphylaxis 47 0.032
211
P RNL015 Renal Hypertension 47 0.032
212
SKN023 Skin Tag 46 0.032
213
HRT007 Heart Cancer 46 0.032
214
PRN014 Paronychia 46 0.032
215
LKC003 Leukocyte Disease 46 0.032
216
BLD053 Blood Platelet Disease 46 0.032
217
UPP004 Upper Respiratory Tract Disease 46 0.032
218
GDS001 Good Syndrome 46 0.032
219
CRB085 Cerebral Hemorrhage 45 0.032
220
P DYS021 Dysautonomia 45 0.032
221
FLL008 Folliculitis 45 0.032
222
ATN005 Autonomic Dysfunction 45 0.032
223
HMN014 Human Immunodeficiency Virus Infectious Disease 45 0.032
224
CRD118 Cardiovascular Cancer 45 0.032
225
BNN003 Bone Inflammation Disease 45 0.032
226
VTM002 Vitamin B12 Deficiency 45 0.032
227
CRT017 Cartilage Disease 45 0.032
228
c MTR002 Mitral Valve Insufficiency 45 0.032
229
P PLM025 Pulmonary Venoocclusive Disease 44 0.032
230
GLC008 Glucose Metabolism Disease 44 0.032
231
c ADL096 Adult Hepatocellular Carcinoma 44 0.032
232
SNS023 Sensory System Cancer 44 0.032
233
HDN002 Head Injury 44 0.032
234
RBF001 Riboflavin Deficiency 44 0.032
235
BRT030 Birth Defects 44 0.032
236
SKN027 Skin Conditions 44 0.032
237
RPR002 Reproductive System Disease 43 0.032
238
INT145 Intracranial Hemorrhage in Brain Cerebrovascular Malformations 43 0.032
239
THR024 Thrombosis 43 0.032
240
P BLD051 Blood Coagulation Disease 43 0.032
241
c LNG031 Lung Benign Neoplasm 43 0.032
242
MLK006 Milk Allergy 43 0.032
243
P HYP729 Hypersensitivity Reaction Disease 43 0.032
244
PRD004 Prediabetes Syndrome 43 0.032
245
PHY002 Physical Disorder 43 0.032
246
ART031 Aortic Coarctation 43 0.032
247
c HMG003 Hemoglobin E Disease 43 0.032
248
CRB008 Cerebral Atherosclerosis 43 0.032
249
PRS036 Parasitic Protozoa Infectious Disease 42 0.032
250
IRN002 Iron Metabolism Disease 42 0.032
251
BNC003 Bone Cancer 42 0.032
252
PRM025 Primary Bacterial Infectious Disease 42 0.032
253
EXC002 Exocrine Pancreatic Insufficiency 42 0.032
254
RNL097 Renal Artery Disease 42 0.032
255
c PRM225 Primary Thrombocytopenia 42 0.032
256
c VRL005 Viral Pneumonia 42 0.032
257
CRN025 Corneal Dystrophy 41 0.032
258
c INF087 Inflammatory Bowel Disease 4 41 0.032
259
DRG001 Drug Psychosis 41 0.032
260
CHR413 Chronic Myocardial Ischemia 41 0.032
261
BRN080 Brain Ischemia 40 0.032
262
c CLL012 Cell Type Benign Neoplasm 40 0.032
263
NSL022 Nasal Cavity Disease 40 0.032
264
MDY003 Mody, Type Ii 40 0.032
265
HRT012 Heart Valve Disease 40 0.032
266
MNR003 Mineral Metabolism Disease 40 0.032
267
STT004 Steatorrhea 40 0.032
268
WTH001 Withdrawal Disorder 40 0.032
269
c PRS116 Prostate Cancer 1 39 0.032
270
CWM001 Cow Milk Allergy 39 0.032
271
BLD054 Blood Protein Disease 39 0.032
272
PNG002 Pain Agnosia 39 0.032
273
BND014 Bone Development Disease 39 0.032
274
FNC002 Functional Diarrhea 39 0.032
275
BNR001 Bone Remodeling Disease 38 0.032
276
ADJ001 Adjustment Disorder 38 0.032
277
ACT088 Acute Insulin Response 38 0.032
278
RCT017 Rectal Disease 38 0.032
279
GRM001 Germ Cell and Embryonal Cancer 38 0.032
280
ANG016 Angiokeratoma 38 0.032
281
ADL053 Adult Astrocytic Tumour 37 0.032
282
c MLG067 Malignant Giant Cell Tumor 37 0.032
283
c THR037 Thrombocytopenia 2 37 0.032
284
CRB070 Cerebral Folate Deficiency 37 0.032
285
PHT003 Phototoxic Dermatitis 37 0.032
286
MSC004 Muscle Tissue Disease 37 0.032
287
SBS006 Sebastian Syndrome 37 0.032
288
c THR111 Thrombocytopenia 3 37 0.032
289
INT078 Intracranial Thrombosis 37 0.032
290
P CRC039 Coarctation of Aorta 36 0.032
291
IMP003 Impaired Renal Function Disease 36 0.032
292
MRG013 Mirage Syndrome 36 0.032
293
PST055 Postural Hypotension 36 0.032
294
IMM078 Immunodeficiency 21 36 0.032
295
c HYP311 Hyperparathyroidism 3 36 0.032
296
BNS002 Bone Structure Disease 36 0.032
297
MLR007 Male Reproductive System Disease 36 0.032
298
INT010 Intracranial Embolism 35 0.032
299
PYR016 Pyridoxine Deficiency 35 0.032
300
INT084 Intrinsic Cardiomyopathy 35 0.032
301
PLS010 Plasma Protein Metabolism Disease 35 0.032
302
CRT013 Carotid Stenosis 35 0.032
303
FLC001 Folic Acid Deficiency Anemia 35 0.032
304
TNS001 Tenosynovial Giant Cell Tumor 34 0.032
305
P HRT017 Heart Tumor 34 0.032
306
c CLR080 Colorectal Cancer 5 34 0.032
307
PNC028 Pancreatic Steatorrhea 34 0.032
308
CND006 Candida Glabrata 34 0.032
309
P GRM010 Germ Cells Tumors 34 0.032
310
c HMG004 Hemoglobin D Disease 33 0.032
311
c CLR077 Colorectal Cancer 10 33 0.032
312
c DRR009 Diarrhea 6 33 0.032
313
c PLM130 Pulmonary Venoocclusive Disease 1 33 0.032
314
WRF003 Warfarin Syndrome 32 0.032
315
VSC008 Vascular Hemostatic Disease 32 0.032
316
c PSR017 Psoriasis 2 32 0.032
317
CRN006 Coronary Aneurysm 32 0.032
318
c ALZ046 Alzheimer's Disease 5 31 0.032
319
P ACT080 Acute Pulmonary Heart Disease 31 0.032
320
VTM001 Vitamin K Deficiency Hemorrhagic Disease 31 0.032
321
VTM003 Vitamin Metabolic Disorder 31 0.032
322
c DRR007 Diarrhea 7 30 0.032
323
c PLM132 Pulmonary Venoocclusive Disease 2 30 0.032
324
c NRV012 Nervous System Benign Neoplasm 30 0.032
325
HNS001 Hansen's Disease 29 0.032
326
c GLB007 Glioblastoma 3 29 0.032
327
c MYC058 Myocardial Infarction 2 28 0.032
328
c ALZ047 Alzheimer's Disease 10 28 0.032
329
c ALZ015 Alzheimer Disease 6 28 0.032
330
ATM052 Autoimmune Disease 1 27 0.032
331
NDL002 Nodular Tenosynovitis 27 0.032
332
RSP004 Respiratory System Benign Neoplasm 27 0.032
333
c ATM007 Autoimmune Disease of Central Nervous System 27 0.032
334
ATM059 Autoimmune Disease 6 27 0.032
335
c CLR083 Colorectal Cancer 8 26 0.032
336
c MLT094 Multiple Sclerosis 3 26 0.032
337
HRT006 Heart Aneurysm 26 0.032
338
c ATR038 Atrial Fibrillation, Familial, 3 26 0.032
339
c ATR075 Atrial Fibrillation 15 26 0.032
340
NLL002 Null Syndrome 26 0.032
341
PLM027 Pulmonary Embolism and Infarction 25 0.032
342
c MLT124 Multiple Sclerosis 5 25 0.032
343
c ATR069 Atrial Fibrillation, Familial, 12 25 0.032
344
c ATR035 Atrial Fibrillation, Familial, 6 24 0.032
345
c ALZ014 Alzheimer Disease 16 23 0.032
346
BNR002 Bone Resorption Disease 23 0.032
347
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 23 0.032
348
c ATR039 Atrial Fibrillation, Familial, 4 23 0.032
349
c RNL016 Renal Infectious Disease 23 0.032
350
c INF073 Inflammatory Bowel Disease 12 23 0.032
351
P CRN178 Coronary Heart Disease 6 22 0.032
352
ATR024 Atrial Fibrillation and Stroke 22 0.032
353
c CRN214 Coronary Heart Disease 5 22 0.032
354
MND006 Mondor Disease 22 0.032
355
c DYS033 Dysautonomia Like Disorder 22 0.032
356
c CRN174 Coronary Heart Disease 2 21 0.032
357
c CRN177 Coronary Heart Disease 7 21 0.032
358
PRM227 Primary Orthostatic Hypotension 20 0.032
359
MNS002 Mini Stroke 20 0.032
360
c CRN172 Coronary Heart Disease 3 20 0.032
361
VSC009 Vascular Skin Disease 20 0.032
362
ACT228 Acute Radiation Syndrome 20 0.032
363
c ALZ043 Alzheimer's Disease 15 20 0.032
364
c CRN175 Coronary Heart Disease 4 20 0.032
365
CYT018 Cytochrome P450 2d6 Variant 20 0.032
366
P HMG016 Hemoglobin Sd 20 0.032
367
c MLT093 Multiple Sclerosis 2 19 0.032
368
c WVR003 Weaver Syndrome 1 19 0.032
369
c MLT095 Multiple Sclerosis 4 18 0.032
370
c CRN176 Coronary Heart Disease 9 18 0.032
371
WSC001 Wisconsin Syndrome 18 0.032
372
ATM053 Autoimmune Disease 2 18 0.032
373
ACT094 Acute Articular Rheumatism 18 0.032
374
ATM054 Autoimmune Disease 3 18 0.032
375
ATM055 Autoimmune Disease 4 18 0.032
376
c ATR027 Atrial Fibrillation, Familial, 5 17 0.032
377
BNM008 Bone Mineral Density, Low 17 0.032
378
PYR009 Pyridoxine Deficiency Anemia 16 0.032
379
AML037 Amelia of Upper Limb 16 0.032
380
c ATR025 Atrial Fibrillation, Familial, 2 16 0.032
381
IMM151 Immunodeficiency 53 16 0.032
382
CGL001 Coagulation Protein Disease 16 0.032
383
NVD002 Nevada Syndrome 16 0.032
384
PRT114 Prothrombin Thrombophilia 16 0.032
385
NVS004 Nova Syndrome 15 0.032
386
c ATR028 Atrial Fibrillation, Familial, 8 15 0.032
387
CMP052 Complication in Hemodialysis 15 0.032
388
HRP008 Herpes Simiae 15 0.032
389
INB001 Inborn Amino Acid Metabolism Disorder 14 0.032
390
c BCT003 Bacterial Exanthem 13 0.032
391
TCK005 Tucker Syndrome 13 0.032
392
HRP012 Herpesvirus Simiae B Virus 13 0.032
393
CLC050 Calciphylaxis Cutis 12 0.032
394
BNJ001 Benjamin Syndrome 11 0.032
395
AML035 Amelia of Upper Limb, Bilateral 11 0.032
396
PRT104 Protein S Acquired Deficiency 9 0.032
Content
Loading form....