Search results for Menadione

331 hits were found for Menadione

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 99 0.086
2
P EXN002 Exanthem 57 0.086
3
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.086
4
P BRS047 Breast Cancer 97 0.078
5
P PNC035 Pancreatic Cancer 84 0.078
6
MND023 Mend Syndrome 43 0.078
7
P LNG032 Lung Cancer 98 0.070
8
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.070
9
OST159 Osteogenic Sarcoma 66 0.070
10
c SML038 Small Cell Cancer of the Lung 65 0.070
11
P PRS040 Prostate Cancer 97 0.061
12
P OVR042 Ovarian Cancer 88 0.061
13
P BLD134 Bladder Cancer 79 0.061
14
P NRB001 Neuroblastoma 72 0.061
15
c RHB024 Rhabdomyosarcoma 2 67 0.061
16
P GLM045 Glioma 63 0.061
17
P HML002 Hemolytic Anemia 63 0.061
18
c FNC043 Fanconi Anemia, Complementation Group E 62 0.061
19
c ACT027 Acute Pancreatitis 60 0.061
20
HPT022 Hepatoblastoma 56 0.061
21
GLL048 Glial Tumor 45 0.061
22
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.061
23
P HPT023 Hepatocellular Carcinoma 100 0.050
24
P RHM011 Rheumatoid Arthritis 80 0.050
25
GLB015 Glioblastoma Multiforme 75 0.050
26
P MLT020 Multiple Sclerosis 72 0.050
27
P ART022 Arthritis 69 0.050
28
CLN015 Colon Adenocarcinoma 65 0.050
29
P VSC007 Vascular Disease 63 0.050
30
IRN002 Iron Metabolism Disease 57 0.050
31
P END033 Endocarditis 57 0.050
32
P CRN025 Corneal Dystrophy 49 0.050
33
VTM033 Vitamin K Deficiency Bleeding 48 0.050
34
FCH001 Fuchs' Endothelial Dystrophy 44 0.050
35
c RDC016 Reducing Body Myopathy, X-Linked 1a, Severe, with Infantile or Early Childhood Onset 22 0.050
36
P RDC012 Reducing Body Myopathy, X-Linked 1b, with Late Childhood or Adult Onset 22 0.050
37
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.035
38
P ALZ034 Alzheimer Disease 88 0.035
40
c HYP595 Hypertension, Essential 84 0.035
41
P GST053 Gastric Cancer 83 0.035
42
MLR004 Malaria 81 0.035
43
CYS001 Cystic Fibrosis 81 0.035
44
P GLM040 Glioma Susceptibility 1 81 0.035
45
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.035
46
c NRF023 Neurofibromatosis, Type Ii 80 0.035
47
IMM167 Immune Deficiency Disease 78 0.035
48
OST012 Osteoarthritis 78 0.035
49
P PRK057 Parkinson Disease, Late-Onset 78 0.035
50
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.035
51
P HRT032 Heart Disease 75 0.035
52
c ATR087 Atrial Standstill 1 75 0.035
53
c ART115 Aortic Valve Disease 1 75 0.035
54
SCK003 Sickle Cell Anemia 74 0.035
55
P SCH015 Schizophrenia 74 0.035
56
P OST002 Osteoporosis 74 0.035
57
CRH001 Crohn's Disease 74 0.035
58
c HYP836 Hypercholesterolemia, Familial, 1 73 0.035
59
ULC004 Ulcerative Colitis 73 0.035
60
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.035
61
P CNR004 Cone-Rod Dystrophy 2 73 0.035
62
ANX010 Anxiety 73 0.035
63
MSC157 Muscular Dystrophy, Duchenne Type 72 0.035
64
c HPT073 Hepatitis C Virus 72 0.035
65
c LKM063 Leukemia, Chronic Myeloid 72 0.035
66
HMN044 Human Immunodeficiency Virus Type 1 71 0.035
67
P MYC007 Myocardial Infarction 70 0.035
68
DFC004 Deficiency Anemia 70 0.035
69
P AMY004 Amyloidosis 70 0.035
70
GST040 Gastric Adenocarcinoma 70 0.035
71
DWN001 Down Syndrome 70 0.035
72
ADL002 Adult Syndrome 70 0.035
73
c PNC108 Pancreatitis, Hereditary 70 0.035
74
P MYP004 Myopathy 70 0.035
75
CNG034 Congestive Heart Failure 69 0.035
76
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.035
77
P MLN008 Melanoma 69 0.035
78
P OCL013 Oculodentodigital Dysplasia 69 0.035
79
P LVR013 Liver Disease 68 0.035
80
P PNM007 Pneumonia 68 0.035
81
P LKM002 Leukemia 68 0.035
82
SKN019 Skin Melanoma 68 0.035
83
RCK004 Rickets 68 0.035
84
P THR014 Thrombocytopenia 67 0.035
85
GST092 Gastroesophageal Reflux 67 0.035
86
P HPT021 Hepatitis 67 0.035
87
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.035
88
c INF071 Inflammatory Bowel Disease 1 67 0.035
89
ALL003 Allergic Rhinitis 67 0.035
90
P HYP098 Hypereosinophilic Syndrome 67 0.035
91
P PLM037 Pulmonary Hypertension 67 0.035
92
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.035
93
P DMN002 Dementia 66 0.035
94
P MSC005 Muscular Dystrophy 66 0.035
95
P SKN015 Skin Carcinoma 66 0.035
96
P NRV007 Nervous System Disease 66 0.035
97
KHL003 Kohlschutter-Tonz Syndrome 65 0.035
98
P PSD087 Pseudoxanthoma Elasticum 65 0.035
99
PND002 Pendred Syndrome 65 0.035
100
c ART101 Aortic Valve Disease 2 65 0.035
101
ATH013 Atherosclerosis Susceptibility 65 0.035
102
P CTS001 Cutis Laxa 65 0.035
103
P THY023 Thymoma 65 0.035
104
P DBT009 Diabetes Mellitus 64 0.035
105
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.035
106
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.035
107
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.035
108
MSC007 Muscle Hypertrophy 64 0.035
109
P ADN016 Adenocarcinoma 64 0.035
110
LSH001 Leishmaniasis 63 0.035
111
c PRC016 Pre-Eclampsia 63 0.035
112
P HYP069 Hyperparathyroidism 63 0.035
113
P LMY004 Leiomyosarcoma 63 0.035
114
TRN015 Transient Cerebral Ischemia 63 0.035
115
c ALP101 Alpha-Thalassemia 62 0.035
116
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.035
117
LPD008 Lipid Metabolism Disorder 62 0.035
118
CLT003 Colitis 62 0.035
119
c HPT001 Hepatitis C 62 0.035
120
P PSR002 Psoriasis 62 0.035
121
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.035
122
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.035
123
ALL026 Allergic Hypersensitivity Disease 62 0.035
124
LVR012 Liver Cirrhosis 62 0.035
125
NTR005 Nutritional Deficiency Disease 62 0.035
126
HYP066 Hyperglycemia 61 0.035
127
P ENC018 Encephalopathy 61 0.035
128
P ENC004 Encephalitis 61 0.035
129
P PNC044 Pancreatitis 61 0.035
130
APP008 Appendicitis 61 0.035
131
P MYL006 Myeloid Leukemia 60 0.035
132
P TXP001 Toxoplasmosis 60 0.035
133
HPT019 Hepatic Encephalopathy 60 0.035
134
CRD223 Cardiac Arrhythmia 60 0.035
135
ACQ007 Acquired Immunodeficiency Syndrome 60 0.035
136
P ALP009 Alopecia Areata 60 0.035
137
VRC005 Varicose Veins 60 0.035
138
P CTR002 Cataract 60 0.035
139
ORL011 Oral Cancer 60 0.035
140
INS001 Insulinoma 60 0.035
141
P THL005 Thalassemia 60 0.035
142
PRT013 Portal Hypertension 59 0.035
143
P BND020 Bone Disease 59 0.035
144
PNM001 Pneumocystosis 59 0.035
145
c HPT016 Hepatitis B 59 0.035
146
P LKD001 Leukodystrophy 59 0.035
147
PLM033 Pulmonary Embolism 59 0.035
148
PRT058 Pure Autonomic Failure 59 0.035
149
P BRS044 Breast Adenocarcinoma 59 0.035
150
GRD007 Grade Iii Astrocytoma 59 0.035
151
IRN001 Iron Deficiency Anemia 59 0.035
152
ANR040 Aneurysm 59 0.035
153
PPT005 Peptic Ulcer Disease 59 0.035
154
ISC004 Ischemia 58 0.035
155
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.035
156
DSS008 Disease of Mental Health 58 0.035
157
P CND004 Candidiasis 58 0.035
158
DSS009 Disseminated Intravascular Coagulation 57 0.035
159
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.035
160
c ACT075 Acute Myocardial Infarction 57 0.035
161
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.035
162
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.035
163
P CRD246 Cardiovascular System Disease 57 0.035
164
HMR039 Hemorrhage, Intracerebral 57 0.035
165
SCH014 Schistosomiasis 57 0.035
166
P BPL003 Bipolar Disorder 56 0.035
167
CMR002 Coumarin Resistance 56 0.035
168
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.035
169
P MTC069 Mitochondrial Disorders 56 0.035
170
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.035
171
BCT022 Bacterial Infectious Disease 56 0.035
172
P SZR006 Seizure Disorder 56 0.035
173
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.035
174
c GRV008 Graves Disease 1 56 0.035
175
AGN016 Aging 56 0.035
176
c FML035 Familial Hyperlipidemia 55 0.035
177
HYP005 Hypokalemia 55 0.035
178
NRN004 Neuroendocrine Tumor 55 0.035
179
P DRR001 Diarrhea 55 0.035
180
P ANT006 Antiphospholipid Syndrome 55 0.035
181
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.035
182
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 55 0.035
183
ACT058 Active Peptic Ulcer Disease 55 0.035
184
GLS001 Gliosarcoma 54 0.035
185
CRT017 Cartilage Disease 54 0.035
186
GLC003 Glucose Intolerance 54 0.035
187
P ALP008 Alopecia 54 0.035
188
P INF037 Inflammatory Bowel Disease 54 0.035
189
P ART021 Arteriosclerosis 54 0.035
190
P TRM003 Tremor 54 0.035
191
P TCD001 Tic Disorder 53 0.035
192
RHM028 Rheumatic Heart Disease 53 0.035
193
HRT012 Heart Valve Disease 53 0.035
194
P MNC007 Monocytic Leukemia 53 0.035
195
CRH005 Crohn's Colitis 53 0.035
196
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.035
197
P HML001 Hemolytic-Uremic Syndrome 53 0.035
198
INF034 Infective Endocarditis 53 0.035
199
P HMR003 Hemorrhagic Disease 53 0.035
200
GTR002 Goiter 53 0.035
201
HMC014 Homocysteinemia 53 0.035
202
GST023 Gastric Ulcer 53 0.035
203
c PSR017 Psoriasis 2 53 0.035
204
OVR059 Ovary Adenocarcinoma 53 0.035
205
c CNT035 Central Nervous System Disease 52 0.035
206
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.035
207
PRP016 Paraplegia 52 0.035
208
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.035
209
PST011 Pustulosis of Palm and Sole 52 0.035
210
PLS007 Plasmodium Falciparum Malaria 52 0.035
211
CRT016 Carotid Artery Disease 52 0.035
212
c THY107 Thymoma, Familial 52 0.035
213
c PSR023 Psoriasis 1 52 0.035
214
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.035
215
PNG002 Pain Agnosia 51 0.035
216
P HMP007 Hemophilia 51 0.035
217
P SPP010 Suppressor of Tumorigenicity 3 51 0.035
218
OCL069 Ocular Motor Apraxia 51 0.035
219
FCT001 Factor Viii Deficiency 51 0.035
220
FDL002 Food Allergy 51 0.035
221
CLC001 Calciphylaxis 51 0.035
222
ESP002 Esophageal Varix 51 0.035
223
P THR015 Thrombophilia 51 0.035
224
P PST095 Post-Thrombotic Syndrome 51 0.035
225
P AST007 Astrocytoma 51 0.035
226
END086 End Stage Renal Disease 51 0.035
227
HYP781 Hypoascorbemia 51 0.035
228
HYP081 Hypolipoproteinemia 51 0.035
229
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.035
230
P ECL001 Eclampsia 50 0.035
231
CRN030 Coronary Stenosis 50 0.035
232
CRT013 Carotid Stenosis 50 0.035
233
P SCK005 Sickle Cell Disease 50 0.035
234
c INF145 Infantile Liver Failure Syndrome 1 50 0.035
235
RNL011 Renal Osteodystrophy 50 0.035
236
P MTC133 Mitochondrial Myopathy 49 0.035
237
PRN014 Paronychia 49 0.035
238
BNR002 Bone Resorption Disease 48 0.035
239
ATS010 Autosomal Recessive Disease 48 0.035
240
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 48 0.035
241
CLC006 Calcinosis 48 0.035
242
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.035
243
SPL018 Splenomegaly 48 0.035
244
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.035
245
HYP025 Hyperphosphatemia 48 0.035
246
MLK006 Milk Allergy 48 0.035
247
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.035
248
HPR003 Heparin-Induced Thrombocytopenia 48 0.035
249
PRD004 Prediabetes Syndrome 47 0.035
250
c PSR032 Psoriasis 11 47 0.035
251
KRT002 Keratomalacia 47 0.035
252
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.035
253
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.035
254
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.035
255
P BLD051 Blood Coagulation Disease 46 0.035
256
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.035
257
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.035
258
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.035
259
PLL012 Pollen Allergy 46 0.035
260
KRT013 Keratolytic Winter Erythema 46 0.035
261
FLL008 Folliculitis 46 0.035
262
SPR010 Sporotrichosis 46 0.035
263
c DRR009 Diarrhea 6 46 0.035
264
c MLG068 Malignant Glioma 46 0.035
265
VSD002 Vas Deferens, Congenital Bilateral Aplasia of 45 0.035
266
MXD026 Mixed Glioma 45 0.035
267
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.035
268
KTL001 Keutel Syndrome 45 0.035
269
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.035
270
HPT004 Hepatic Coma 45 0.035
271
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.035
272
BLC012 Bile Acid Malabsorption, Primary 45 0.035
273
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.035
274
c ORT011 Orthostatic Hypotension 1 44 0.035
275
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.035
276
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.035
277
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.035
278
ANG011 Angiodysplasia 43 0.035
279
P CRN026 Corneal Edema 43 0.035
280
P HYP265 Hypotonia 43 0.035
281
P MJR007 Major Affective Disorder 1 43 0.035
282
c PSR028 Psoriasis 7 42 0.035
283
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.035
284
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.035
285
EXC002 Exocrine Pancreatic Insufficiency 42 0.035
286
GST020 Gastric Antral Vascular Ectasia 41 0.035
287
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.035
288
P KLZ004 Kala-Azar 1 41 0.035
289
49X006 49, Xxxxy Syndrome 41 0.035
290
c PSR018 Psoriasis 13 41 0.035
291
c MJR024 Major Affective Disorder 9 41 0.035
292
RDN001 Reading Disorder 40 0.035
293
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.035
294
ANX004 Anoxia 40 0.035
295
HPR006 Heparin Cofactor Ii Deficiency 40 0.035
296
SPR126 Superior Semicircular Canal Dehiscence 40 0.035
297
ANG049 Angioedema Induced by Ace Inhibitors 40 0.035
298
48X005 48,xyyy 39 0.035
299
c HMG029 Hemoglobin Se Disease 39 0.035
300
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.035
301
c CHR682 Chronic Bilirubin Encephalopathy 39 0.035
302
ANG016 Angiokeratoma 38 0.035
303
HYP001 Hypochromic Microcytic Anemia 38 0.035
304
OVR094 Ovarian Epithelial Cancer 38 0.035
305
c MJR022 Major Affective Disorder 8 38 0.035
306
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 38 0.035
307
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.035
308
c MJR008 Major Affective Disorder 2 35 0.035
309
HMN016 Hemangioendothelioma 34 0.035
310
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.035
311
SBC019 Subcutaneous Mycosis 34 0.035
312
c MJR023 Major Affective Disorder 7 33 0.035
313
c MJR003 Major Affective Disorder 6 33 0.035
314
c MJR006 Major Affective Disorder 5 33 0.035
315
c PRS136 Prostate Cancer, Hereditary, 6 33 0.035
316
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.035
317
c PRS130 Prostate Cancer, Hereditary, 8 32 0.035
318
CND006 Candida Glabrata 32 0.035
319
DLF001 Dieulafoy Lesion 32 0.035
320
CRD220 Cardiac Valvular Defect, Developmental 29 0.035
321
c MJR004 Major Affective Disorder 4 28 0.035
322
c ATR092 Atrial Fibrillation, Familial, 15 28 0.035
323
MLL004 Mallory-Weiss Syndrome 27 0.035
324
CYT018 Cytochrome P450 2d6 Variant 27 0.035
325
CHL079 Children's Interstitial Lung Disease 26 0.035
326
c RDC017 Reducing Body Myopathy 1a 26 0.035
327
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.035
328
HRP008 Herpes Simiae 25 0.035
329
CRR012 Cirrhotic Cardiomyopathy 24 0.035
330
ORN004 Ornithinemia 17 0.035
331
c RDC018 Reducing Body Myopathy 1b 4 0.035
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