Search results for Menadione

214 hits were found for Menadione

# Family MCID Name MIFTS Score
1
P EXN002 Exanthem 62 0.099
2
P PNC035 Pancreatic Cancer 89 0.090
3
P BRS047 Breast Cancer 100 0.081
4
P LNG032 Lung Cancer 99 0.081
5
P CLR023 Colorectal Cancer 98 0.081
6
END072 Endotheliitis 46 0.081
7
FXF002 Fox-Fordyce Disease 40 0.081
8
P HPT021 Hepatitis 75 0.057
9
MLN008 Melanoma 72 0.057
10
P ADN016 Adenocarcinoma 71 0.057
11
P PNC044 Pancreatitis 64 0.057
12
HYP266 Hypoxia 61 0.057
13
FCH001 Fuchs' Endothelial Dystrophy 48 0.057
14
CRN025 Corneal Dystrophy 42 0.057
15
RDC016 Reducing Body Myopathy, X-Linked 1a, Severe, with Infantile or Early Childhood Onset 20 0.057
16
RDC012 Reducing Body Myopathy, X-Linked 1b, with Late Childhood or Adult Onset 18 0.057
17
P ALZ034 Alzheimer Disease 95 0.040
18
P HPT023 Hepatocellular Carcinoma 94 0.040
19
P RHM011 Rheumatoid Arthritis 91 0.040
20
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.040
21
P PRS040 Prostate Cancer 88 0.040
22
OST012 Osteoarthritis 88 0.040
23
MLR004 Malaria 86 0.040
24
P MLT020 Multiple Sclerosis 85 0.040
25
CYS001 Cystic Fibrosis 85 0.040
26
STR067 Stroke, Ischemic 84 0.040
27
INS024 Insulin-Like Growth Factor I 83 0.040
28
P MYC007 Myocardial Infarction 81 0.040
29
CRH001 Crohn's Disease 80 0.040
30
P HRT032 Heart Disease 80 0.040
31
P PLM037 Pulmonary Hypertension 79 0.040
32
P ART022 Arthritis 77 0.040
33
P LVR013 Liver Disease 76 0.040
34
P NRV007 Nervous System Disease 75 0.040
35
P OST002 Osteoporosis 75 0.040
36
P LKM002 Leukemia 75 0.040
37
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.040
38
GST019 Gastrointestinal Stromal Tumor 74 0.040
39
CNG034 Congestive Heart Failure 74 0.040
40
GLB002 Glioblastoma 74 0.040
41
c HPT073 Hepatitis C Virus 73 0.040
42
SCK003 Sickle Cell Anemia 73 0.040
43
ISC006 Ischemic Heart Disease 73 0.040
44
c HPT001 Hepatitis C 73 0.040
45
P NRB001 Neuroblastoma 73 0.040
46
LVR012 Liver Cirrhosis 73 0.040
47
PSY004 Psychotic Disorder 72 0.040
48
ANX010 Anxiety 72 0.040
49
P DBT009 Diabetes Mellitus 72 0.040
50
c CHR089 Chronic Kidney Failure 72 0.040
51
VSC007 Vascular Disease 71 0.040
52
P PNM007 Pneumonia 70 0.040
53
WRN001 Werner Syndrome 70 0.040
54
P KDN018 Kidney Disease 69 0.040
55
P NRF023 Neurofibromatosis, Type Ii 69 0.040
56
P CRN018 Coronary Artery Anomaly 69 0.040
57
GLB015 Glioblastoma Multiforme 68 0.040
58
c HPT016 Hepatitis B 68 0.040
59
P ORT004 Orthostatic Intolerance 68 0.040
60
P ATR011 Atrial Fibrillation 68 0.040
61
CRB039 Cerebrovascular Disease 68 0.040
62
DMN002 Dementia 68 0.040
63
SKN016 Skin Disease 68 0.040
64
P ART023 Arthropathy 68 0.040
65
c HMP004 Hemophilia B 67 0.040
66
LNG099 Lung Disease 67 0.040
67
P AST007 Astrocytoma 66 0.040
68
ATM095 Autoimmune Disease 66 0.040
69
c MLG068 Malignant Glioma 66 0.040
70
P ENC004 Encephalitis 66 0.040
71
ISC004 Ischemia 66 0.040
72
GST050 Gastrointestinal System Disease 66 0.040
73
ACQ007 Acquired Immunodeficiency Syndrome 65 0.040
74
GST045 Gastroenteritis 65 0.040
75
P TXP001 Toxoplasmosis 65 0.040
76
P INT068 Intestinal Disease 65 0.040
77
P PSR002 Psoriasis 65 0.040
78
c CNT035 Central Nervous System Disease 65 0.040
79
CNN005 Connective Tissue Disease 65 0.040
80
P THR014 Thrombocytopenia 65 0.040
81
AGN016 Aging 65 0.040
82
c ART101 Aortic Valve Disease 2 65 0.040
83
VRL011 Viral Infectious Disease 64 0.040
84
HYP066 Hyperglycemia 64 0.040
85
c ACT075 Acute Myocardial Infarction 64 0.040
86
GST092 Gastroesophageal Reflux 64 0.040
87
WLL001 Williams-Beuren Syndrome 63 0.040
88
RSP006 Respiratory System Disease 63 0.040
89
c HPT003 Hepatitis a 63 0.040
90
SKN019 Skin Melanoma 63 0.040
91
CRD119 Cardiac Arrest 63 0.040
92
P ART021 Arteriosclerosis 62 0.040
93
RHM027 Rheumatic Disease 62 0.040
94
PLM033 Pulmonary Embolism 62 0.040
95
DFC004 Deficiency Anemia 62 0.040
96
THR024 Thrombosis 61 0.040
97
P HMP007 Hemophilia 61 0.040
98
WVR001 Weaver Syndrome 61 0.040
99
P HMR003 Hemorrhagic Disease 61 0.040
100
GLS001 Gliosarcoma 61 0.040
101
c THR092 Thrombophilia Due to Thrombin Defect 61 0.040
102
ANR040 Aneurysm 61 0.040
103
P GLM045 Glioma 61 0.040
104
P CTR002 Cataract 60 0.040
105
MNT002 Mental Depression 60 0.040
106
ORL011 Oral Cancer 60 0.040
107
P DRR001 Diarrhea 60 0.040
108
ALP103 Alpha-1-Antitrypsin Deficiency 60 0.040
109
JNT002 Joint Disorders 60 0.040
110
CCC001 Coccidioidomycosis 60 0.040
111
P INF032 Infertility 59 0.040
112
P ANT006 Antiphospholipid Syndrome 59 0.040
113
RHM001 Rheumatic Fever 59 0.040
114
P PLM034 Pulmonary Emphysema 59 0.040
115
END030 End Stage Renal Failure 59 0.040
116
LPD008 Lipid Metabolism Disorder 59 0.040
117
ALL026 Allergic Hypersensitivity Disease 59 0.040
118
PNC034 Pancreas Disease 59 0.040
119
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.040
120
TRN015 Transient Cerebral Ischemia 58 0.040
121
P HYP069 Hyperparathyroidism 58 0.040
122
P ENC018 Encephalopathy 58 0.040
123
CRT016 Carotid Artery Disease 58 0.040
124
NRN004 Neuroendocrine Tumor 58 0.040
125
DMY004 Demyelinating Disease 58 0.040
126
P THR015 Thrombophilia 58 0.040
127
URN009 Urinary System Disease 58 0.040
128
GLC003 Glucose Intolerance 58 0.040
129
P CRN300 Coronary Heart Disease 1 57 0.040
130
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.040
131
HMR039 Hemorrhage, Intracerebral 57 0.040
132
IMM136 Immune System Disease 57 0.040
133
BRN106 Burns 57 0.040
134
BNF002 Bone Fracture 56 0.040
135
PRS042 Prostate Disease 56 0.040
136
HYP060 Hyperinsulinism 56 0.040
137
GRD007 Grade Iii Astrocytoma 56 0.040
138
FDL002 Food Allergy 55 0.040
139
CLN019 Colonic Disease 55 0.040
140
IRN001 Iron Deficiency Anemia 55 0.040
141
HPT022 Hepatoblastoma 55 0.040
142
PNM001 Pneumocystosis 55 0.040
143
SPS003 Spastic Diplegia 55 0.040
144
SPR004 Supravalvular Aortic Stenosis 54 0.040
145
P TRC086 Trichohepatoenteric Syndrome 1 54 0.040
146
PGM001 Pigmented Villonodular Synovitis 54 0.040
147
RHM028 Rheumatic Heart Disease 54 0.040
148
SCK005 Sickle Cell Disease 54 0.040
149
c INF071 Inflammatory Bowel Disease 1 54 0.040
150
CLC001 Calciphylaxis 53 0.040
151
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.040
152
OVR063 Overnutrition 53 0.040
153
P VNS003 Venous Insufficiency 53 0.040
154
P CLL015 Collagen Disease 53 0.040
155
HYP005 Hypokalemia 53 0.040
156
HMG005 Hemoglobinopathy 53 0.040
157
CLN015 Colon Adenocarcinoma 53 0.040
158
P HRD018 Hair Disease 53 0.040
159
PST095 Post-Thrombotic Syndrome 52 0.040
160
CRD223 Cardiac Arrhythmia 52 0.040
161
ILT001 Ileitis 52 0.040
162
CRT013 Carotid Stenosis 52 0.040
163
P INF037 Inflammatory Bowel Disease 52 0.040
164
PRN014 Paronychia 52 0.040
165
CCC002 Coccidiosis 52 0.040
166
CLC006 Calcinosis 51 0.040
167
ATN002 Autonomic Nervous System Disease 51 0.040
168
ATN005 Autonomic Dysfunction 51 0.040
169
ART140 Arteries, Anomalies of 51 0.040
170
c ART115 Aortic Valve Disease 1 51 0.040
171
FLL008 Folliculitis 50 0.040
172
P GNT008 Giant Cell Tumor 49 0.040
173
MTC069 Mitochondrial Disorders 49 0.040
174
EWN002 Ewing's Family of Tumors 49 0.040
175
HDN002 Head Injury 48 0.040
176
SKN027 Skin Conditions 48 0.040
177
CRB085 Cerebral Hemorrhage 47 0.040
178
P DYS021 Dysautonomia 47 0.040
179
MLK006 Milk Allergy 46 0.040
180
PRD004 Prediabetes Syndrome 46 0.040
181
c MTR002 Mitral Valve Insufficiency 46 0.040
182
HRT012 Heart Valve Disease 45 0.040
183
EXC002 Exocrine Pancreatic Insufficiency 45 0.040
184
IRN002 Iron Metabolism Disease 45 0.040
185
BRN080 Brain Ischemia 45 0.040
186
MRG013 Mirage Syndrome 44 0.040
187
ACT058 Active Peptic Ulcer Disease 43 0.040
188
ACT088 Acute Insulin Response 43 0.040
189
c CHR579 Chiari Malformation Type Ii 42 0.040
190
CWM001 Cow Milk Allergy 42 0.040
191
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.040
192
STT004 Steatorrhea 41 0.040
193
PNG002 Pain Agnosia 41 0.040
194
PST055 Postural Hypotension 40 0.040
195
PHT003 Phototoxic Dermatitis 39 0.040
196
GLC008 Glucose Metabolism Disease 38 0.040
197
TNS001 Tenosynovial Giant Cell Tumor 38 0.040
198
AMN002 Amino Acid Metabolic Disorder 38 0.040
199
ANG016 Angiokeratoma 38 0.040
200
RCT017 Rectal Disease 38 0.040
201
P BLD051 Blood Coagulation Disease 38 0.040
202
ENT004 Enthesopathy 38 0.040
203
CND006 Candida Glabrata 38 0.040
204
VSC008 Vascular Hemostatic Disease 36 0.040
205
P ART106 Arterial Calcification, Generalized, of Infancy, 1 36 0.040
206
VTM001 Vitamin K Deficiency Hemorrhagic Disease 35 0.040
207
RHM035 Rheumatic Fever-Related Antigen 34 0.040
208
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.040
209
NDL002 Nodular Tenosynovitis 29 0.040
210
MNS002 Mini Stroke 23 0.040
211
ACT094 Acute Articular Rheumatism 21 0.040
212
HRP008 Herpes Simiae 16 0.040
213
INB001 Inborn Amino Acid Metabolism Disorder 16 0.040
214
AMN012 Aminoacidopathies 15 0.040
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