Search results for Menadione

473 hits were found for Menadione

# Family MCID Name MIFTS Score
1
P EXN002 Exanthem 58 2.677
2
P NRB001 Neuroblastoma 66 2.117
3
c FNC043 Fanconi Anemia, Complementation Group E 62 2.113
4
GLM045 Glioma 62 1.934
5
GLL048 Glial Tumor 51 1.934
6
OST159 Osteogenic Sarcoma 66 1.917
7
c ACT027 Acute Pancreatitis 60 1.892
8
MND023 Mend Syndrome 49 1.871
9
P HML002 Hemolytic Anemia 62 1.689
10
GLB002 Glioblastoma 67 1.675
11
48X005 48,xyyy 39 1.593
12
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.472
13
P CLR023 Colorectal Cancer 100 1.451
14
P PNC044 Pancreatitis 61 1.451
15
VTM033 Vitamin K Deficiency Bleeding 49 1.439
16
RDC016 Reducing Body Myopathy, X-Linked 1a, Severe, with Infantile or Early Childhood Onset 22 1.437
17
IRN002 Iron Metabolism Disease 56 1.429
18
P RDC012 Reducing Body Myopathy, X-Linked 1b, with Late Childhood or Adult Onset 22 1.385
19
HPT022 Hepatoblastoma 54 1.382
20
HYP266 Hypoxia 56 1.297
21
P MYP004 Myopathy 67 1.268
22
ANX004 Anoxia 40 1.214
23
FCH001 Fuchs' Endothelial Dystrophy 48 1.201
24
CLN015 Colon Adenocarcinoma 64 1.201
25
P CRN025 Corneal Dystrophy 49 1.201
26
P KLZ004 Kala-Azar 1 41 1.200
27
LSH001 Leishmaniasis 63 1.200
28
P CTR002 Cataract 59 1.087
29
P GST053 Gastric Cancer 82 1.049
30
GST040 Gastric Adenocarcinoma 66 1.049
31
P MNC007 Monocytic Leukemia 48 1.049
32
CND006 Candida Glabrata 29 1.049
33
INS001 Insulinoma 59 1.028
34
OVR059 Ovary Adenocarcinoma 49 1.028
35
OVR094 Ovarian Epithelial Cancer 39 1.028
36
ALL003 Allergic Rhinitis 66 1.007
37
PLL012 Pollen Allergy 44 1.007
38
GST023 Gastric Ulcer 52 1.007
39
P MTC133 Mitochondrial Myopathy 51 0.983
40
P MSC005 Muscular Dystrophy 66 0.983
41
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.959
42
P PRK057 Parkinson Disease, Late-Onset 79 0.959
43
ORL011 Oral Cancer 60 0.959
44
c THY107 Thymoma, Familial 42 0.932
45
P THY023 Thymoma 64 0.932
46
P CND004 Candidiasis 57 0.932
47
P HML001 Hemolytic-Uremic Syndrome 52 0.932
48
P MTC069 Mitochondrial Disorders 57 0.932
49
P TRM003 Tremor 50 0.932
50
P HYP265 Hypotonia 42 0.932
51
c HYP836 Hypercholesterolemia, Familial, 1 73 0.902
52
c RDC017 Reducing Body Myopathy 1a 4 0.890
53
c RDC018 Reducing Body Myopathy 1b 4 0.890
54
P PNC035 Pancreatic Cancer 87 0.868
55
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 54 0.868
56
P MYC084 Mycobacterium Tuberculosis 1 68 0.868
57
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.868
58
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.868
59
PRP016 Paraplegia 52 0.868
60
P LKD001 Leukodystrophy 58 0.868
61
ORN004 Ornithinemia 13 0.868
62
MSC157 Muscular Dystrophy, Duchenne Type 78 0.828
63
c LKM063 Leukemia, Chronic Myeloid 70 0.828
64
P ADN016 Adenocarcinoma 63 0.828
65
P BRS044 Breast Adenocarcinoma 58 0.828
66
PLS007 Plasmodium Falciparum Malaria 52 0.828
67
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.775
68
SBC019 Subcutaneous Mycosis 34 0.775
69
P SPP010 Suppressor of Tumorigenicity 3 50 0.775
70
P LMY004 Leiomyosarcoma 62 0.775
71
P ECL001 Eclampsia 52 0.775
72
P CRN026 Corneal Edema 42 0.775
73
c PRC016 Pre-Eclampsia 64 0.775
74
SCH014 Schistosomiasis 56 0.775
75
SPR010 Sporotrichosis 45 0.775
76
P AMY004 Amyloidosis 69 0.775
77
MLR004 Malaria 77 0.732
78
CYS001 Cystic Fibrosis 77 0.732
79
AGN016 Aging 53 0.732
80
ISC004 Ischemia 61 0.705
81
ACQ007 Acquired Immunodeficiency Syndrome 58 0.705
82
HYP001 Hypochromic Microcytic Anemia 36 0.649
83
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 0.649
84
c GRV008 Graves Disease 1 54 0.649
85
ANG016 Angiokeratoma 37 0.649
86
P HYP098 Hypereosinophilic Syndrome 66 0.649
87
P HMR003 Hemorrhagic Disease 59 0.642
88
BCT022 Bacterial Infectious Disease 55 0.642
89
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.602
90
P ALZ034 Alzheimer Disease 87 0.602
91
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.602
92
HMN044 Human Immunodeficiency Virus Type 1 76 0.602
93
P HPT021 Hepatitis 68 0.602
94
DFC004 Deficiency Anemia 74 0.549
95
c PSR023 Psoriasis 1 52 0.549
96
P PRS040 Prostate Cancer 95 0.549
97
HMC014 Homocysteinemia 52 0.549
98
P MYC007 Myocardial Infarction 69 0.549
99
P GLM040 Glioma Susceptibility 1 70 0.549
100
MLG169 Malignant Astrocytoma 57 0.549
101
P VSC007 Vascular Disease 62 0.549
102
PST011 Pustulosis of Palm and Sole 52 0.549
103
HYP066 Hyperglycemia 60 0.549
104
ALL029 Allergic Disease 61 0.549
105
P MLN008 Melanoma 75 0.549
106
P PSR002 Psoriasis 63 0.549
107
SKN019 Skin Melanoma 70 0.549
108
c ACT075 Acute Myocardial Infarction 55 0.549
109
P TXP001 Toxoplasmosis 59 0.549
110
CLT003 Colitis 63 0.423
111
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.423
112
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.423
113
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.423
114
CRH005 Crohn's Colitis 53 0.423
115
c PSR028 Psoriasis 7 42 0.423
116
PNG002 Pain Agnosia 51 0.423
117
P RHM011 Rheumatoid Arthritis 81 0.423
118
ATH013 Atherosclerosis Susceptibility 63 0.423
119
c ART115 Aortic Valve Disease 1 72 0.423
120
BHR001 Behr Syndrome 51 0.423
121
DWN001 Down Syndrome 70 0.423
122
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.423
123
P OST002 Osteoporosis 76 0.423
124
P OVR042 Ovarian Cancer 88 0.423
125
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.423
126
c TYP009 Type 2 Diabetes Mellitus 91 0.423
127
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.423
128
EPT021 Epithelial Recurrent Erosion Dystrophy 45 0.423
129
P HMN038 Human Coronavirus Sensitivity 30 0.423
130
P NJM001 Nijmegen Breakage Syndrome 75 0.423
131
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.423
132
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 0.423
133
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.423
134
c PNS012 Paine Syndrome 60 0.423
135
P ANR048 Aniridia 1 66 0.423
136
P PSD087 Pseudoxanthoma Elasticum 66 0.423
137
c INF071 Inflammatory Bowel Disease 1 65 0.423
138
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.423
139
P MLT020 Multiple Sclerosis 79 0.423
140
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.423
141
SCK003 Sickle Cell Anemia 74 0.423
142
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.423
143
c PSR017 Psoriasis 2 53 0.423
144
c PRS130 Prostate Cancer, Hereditary, 8 32 0.423
145
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.423
146
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.423
147
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.423
148
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.423
149
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.423
150
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.423
151
P PLM037 Pulmonary Hypertension 69 0.423
152
BLC012 Bile Acid Malabsorption, Primary 45 0.423
153
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.423
154
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.423
155
AMD002 Amed Syndrome, Digenic 36 0.423
156
ANG049 Angioedema Induced by Ace Inhibitors 38 0.423
157
c ORT011 Orthostatic Hypotension 1 43 0.423
158
PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.423
159
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 35 0.423
160
IMM167 Immune Deficiency Disease 76 0.423
161
HYP781 Hypoascorbemia 52 0.423
162
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.423
163
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.423
164
c THR092 Thrombophilia Due to Thrombin Defect 74 0.423
165
ALP103 Alpha-1-Antitrypsin Deficiency 67 0.423
166
c PSR018 Psoriasis 13 40 0.423
167
c OVR114 Ovarian Cancer 1 60 0.423
168
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.423
169
c ART101 Aortic Valve Disease 2 65 0.423
170
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.423
171
HMR039 Hemorrhage, Intracerebral 57 0.423
172
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.423
173
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.423
174
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.423
175
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.423
176
c ATR087 Atrial Standstill 1 74 0.423
177
ADL002 Adult Syndrome 69 0.423
178
c BLD140 Blood Group, I System 47 0.423
179
c HYP595 Hypertension, Essential 84 0.423
180
P CNR004 Cone-Rod Dystrophy 2 74 0.423
181
c PNC108 Pancreatitis, Hereditary 68 0.423
182
P HPT023 Hepatocellular Carcinoma 95 0.423
183
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.423
184
c PSR032 Psoriasis 11 47 0.423
185
KRT013 Keratolytic Winter Erythema 45 0.423
186
c PRS136 Prostate Cancer, Hereditary, 6 33 0.423
187
CRN241 Corneal Dystrophy, Congenital Stromal 49 0.423
188
P BND020 Bone Disease 60 0.423
189
SPR126 Superior Semicircular Canal Dehiscence 41 0.423
190
THR024 Thrombosis 56 0.423
191
DSS009 Disseminated Intravascular Coagulation 56 0.423
192
ANT039 Antisynthetase Syndrome 55 0.423
193
FML035 Familial Hyperlipidemia 54 0.423
194
HYP458 Hyper Ige Syndrome 60 0.423
195
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.423
196
P ART021 Arteriosclerosis 53 0.423
197
CRT016 Carotid Artery Disease 52 0.423
198
PNM001 Pneumocystosis 60 0.423
199
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.423
200
BLD051 Blood Coagulation Disease 52 0.423
201
CLC006 Calcinosis 47 0.423
202
EXC002 Exocrine Pancreatic Insufficiency 42 0.423
203
NRN004 Neuroendocrine Tumor 55 0.423
204
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 0.423
205
RHM028 Rheumatic Heart Disease 55 0.423
206
LVR012 Liver Cirrhosis 62 0.423
207
P TRN020 Turner Syndrome 67 0.423
208
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.423
209
FLL008 Folliculitis 45 0.423
210
NTR005 Nutritional Deficiency Disease 60 0.423
211
MXD026 Mixed Glioma 45 0.423
212
LPD008 Lipid Metabolism Disorder 61 0.423
213
c CNT035 Central Nervous System Disease 53 0.423
214
CNG034 Congestive Heart Failure 69 0.423
215
P PNM007 Pneumonia 64 0.423
216
TRN015 Transient Cerebral Ischemia 62 0.423
217
P PST095 Post-Thrombotic Syndrome 51 0.423
218
P HRT032 Heart Disease 84 0.423
219
SVR001 Severe Acute Respiratory Syndrome 68 0.423
220
P ANT006 Antiphospholipid Syndrome 55 0.423
221
P CRV039 Cervicitis 52 0.423
222
ENT004 Enthesopathy 51 0.423
223
HYP005 Hypokalemia 55 0.423
224
CLC001 Calciphylaxis 50 0.423
225
HRT012 Heart Valve Disease 53 0.423
226
HGH043 High Grade Glioma 46 0.423
227
GLS001 Gliosarcoma 63 0.423
228
CRB009 Cerebritis 43 0.423
229
CRN030 Coronary Stenosis 50 0.423
230
PRD004 Prediabetes Syndrome 52 0.423
231
VSL002 Visual Epilepsy 39 0.423
232
GLC003 Glucose Intolerance 53 0.423
233
c HPT003 Hepatitis a 63 0.423
234
RCK004 Rickets 64 0.423
235
CRT013 Carotid Stenosis 51 0.423
236
CVD001 Covid-19 59 0.423
237
PRS047 Prostatitis 57 0.423
238
P PRS038 Personality Disorder 65 0.423
239
P CRD246 Cardiovascular System Disease 55 0.423
240
P ART022 Arthritis 70 0.423
241
P DBT009 Diabetes Mellitus 67 0.423
242
P ENC004 Encephalitis 61 0.423
243
PLM033 Pulmonary Embolism 58 0.423
244
ULC004 Ulcerative Colitis 74 0.423
245
ACT058 Active Peptic Ulcer Disease 55 0.423
246
END086 End Stage Renal Disease 54 0.423
247
CYT018 Cytochrome P450 2d6 Variant 26 0.423
248
P NRV007 Nervous System Disease 65 0.423
249
CRH001 Crohn's Disease 80 0.423
250
ATX019 Ataxia with Vitamin E Deficiency 44 0.423
251
P SCK005 Sickle Cell Disease 56 0.423
252
49X006 49, Xxxxy Syndrome 40 0.423
253
HMN016 Hemangioendothelioma 35 0.423
254
PRT058 Pure Autonomic Failure 58 0.423
255
P SZR006 Seizure Disorder 69 0.423
256
ANR040 Aneurysm 60 0.423
257
CHL079 Children's Interstitial Lung Disease 25 0.423
258
c HMG029 Hemoglobin Se Disease 41 0.423
259
AND005 Androgen Insensitivity Syndrome, Mild 21 0.423
261
CHR682 Chronic Bilirubin Encephalopathy 37 0.423
262
P ENC018 Encephalopathy 62 0.423
263
P HDC001 Headache 56 0.423
264
P RDC010 Reducing Body Myopathy 33 0.419
265
P ASP006 Aspergillosis 71 0.400
266
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.379
267
P CCK001 Cockayne Syndrome 67 0.379
268
CHR074 Choriocarcinoma 46 0.357
269
P BNG032 Benign Mesothelioma 53 0.334
270
P NRP001 Neuropathy 59 0.334
271
HML018 Homologous Wasting Disease 21 0.334
272
STN013 Stenotrophomonas Maltophilia Infection 26 0.334
274
OST017 Osteomyelitis 63 0.309
275
P PRK039 Parkinsonism 55 0.309
276
BRN004 Brain Edema 54 0.309
277
MTC005 Mitochondrial Metabolism Disease 44 0.309
278
P PRD008 Periodontitis 63 0.309
279
DBT010 Diabetic Neuropathy 54 0.309
280
c PCH010 Pachyonychia Congenita 3 43 0.283
281
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.283
282
CHL068 Cholestasis 61 0.283
283
HMS001 Hemosiderosis 48 0.283
284
P LTR001 Lateral Sclerosis 57 0.283
285
P LVR013 Liver Disease 68 0.283
286
GRD001 Giardiasis 46 0.283
287
CHG001 Chagas Disease 65 0.283
288
P RRH023 Rare Hereditary Hemochromatosis 52 0.283
289
PRM329 Premature Aging 36 0.283
290
P SCL018 Scoliosis 57 0.253
291
c MST023 Mesothelioma, Malignant 56 0.253
292
END057 Endometrial Cancer 76 0.253
293
INV001 Invasive Aspergillosis 48 0.253
294
ATN004 Autonomic Neuropathy 42 0.253
295
PLR022 Pleural Disease 45 0.253
296
CRB004 Cerebral Artery Occlusion 45 0.253
297
PLC008 Placenta Disease 48 0.253
298
FTT001 Fatty Liver Disease 61 0.253
299
MLG079 Malignant Pleural Mesothelioma 42 0.253
300
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.253
301
c ACT134 Acute Liver Failure 57 0.253
302
P SCP010 Scapuloperoneal Myopathy 32 0.219
303
SNG007 Sengers Syndrome 45 0.219
304
PPL052 Papillomatosis, Confluent and Reticulated 34 0.219
305
LGH007 Leigh Syndrome 70 0.219
306
PLY150 Polykaryocytosis Inducer 29 0.219
307
P GLC113 Galactosemia I 65 0.219
308
P BLD134 Bladder Cancer 79 0.219
309
INS024 Insulin-Like Growth Factor I 77 0.219
310
MYP056 Myopathy, X-Linked, with Postural Muscle Atrophy 45 0.219
311
ESP021 Esophageal Cancer 84 0.219
312
P INT068 Intestinal Disease 53 0.219
313
ACT098 Acute Erythroid Leukemia 55 0.219
314
NRM005 Neuromuscular Disease 62 0.219
315
P LCT001 Lactic Acidosis 50 0.219
316
LNG031 Lung Benign Neoplasm 51 0.219
317
CHL061 Childhood Leukemia 47 0.219
318
VSC003 Visceral Leishmaniasis 54 0.219
319
LNG099 Lung Disease 62 0.219
320
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 0.219
321
PRS115 Prosthetic Joint Infection 42 0.219
322
ACY005 Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of 54 0.179
323
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 62 0.179
324
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 59 0.179
325
FCT001 Factor Viii Deficiency 61 0.179
326
c PRD040 Periodontitis, Chronic 52 0.179
327
DSS032 Disease by Infectious Agent 55 0.179
328
c HPT073 Hepatitis C Virus 70 0.179
329
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.179
330
c HMP029 Hemophilia a 69 0.179
331
P ATX030 Ataxia-Telangiectasia 80 0.179
332
KRT019 Keratitis, Hereditary 66 0.179
333
MTH071 Methane Production 24 0.179
334
SCP009 Scapuloperoneal Myopathy, X-Linked Dominant 38 0.179
335
c HMP004 Hemophilia B 68 0.179
336
MLD001 Melioidosis 67 0.179
337
c BTT014 Beta-Thalassemia 72 0.179
338
P HNT016 Huntington Disease 73 0.179
339
HRW001 Hair Whorl 35 0.179
340
P PHC003 Pheochromocytoma 70 0.179
341
HLC007 Helicobacter Pylori Infection 67 0.179
342
P LNG064 Lung Cancer Susceptibility 3 69 0.179
343
ADR040 Adrenal Gland Pheochromocytoma 45 0.179
344
P MMP001 Mumps 56 0.179
345
P RSP003 Respiratory Failure 73 0.179
346
P FBR017 Fibrosarcoma 55 0.179
347
P EYD002 Eye Disease 57 0.179
348
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.179
349
c HPT001 Hepatitis C 61 0.179
350
P SKN015 Skin Carcinoma 71 0.179
351
P HYP061 Hypertrophic Cardiomyopathy 68 0.179
352
GTR002 Goiter 52 0.179
353
P ADL010 Adult Respiratory Distress Syndrome 70 0.179
354
MNN009 Meningoencephalitis 47 0.179
355
P VNW001 Von Willebrand's Disease 64 0.179
356
MST005 Mastitis 52 0.179
357
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.179
358
TLN003 Telangiectasis 51 0.179
359
SPT004 Septic Arthritis 58 0.179
360
VRL011 Viral Infectious Disease 60 0.179
361
STM007 Stomatitis 52 0.179
362
P HMP007 Hemophilia 52 0.179
363
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 19 0.179
364
P THL005 Thalassemia 56 0.179
365
CTN007 Cutaneous Leishmaniasis 61 0.179
366
HYP056 Hypoglycemia 65 0.179
367
ACY011 Acyl-Coa Dehydrogenase Deficiency 31 0.179
368
DYS073 Dysphagia 53 0.179
369
BRS102 Breast Abscess 25 0.126
370
c AMY088 Amyotrophic Lateral Sclerosis 3 33 0.126
371
c FNC029 Fanconi Anemia, Complementation Group I 55 0.126
372
P APL001 Aplastic Anemia 72 0.126
373
P PRG013 Paraganglioma 57 0.126
374
ANG061 Angular Cheilitis 27 0.126
375
ORL015 Oral Squamous Cell Carcinoma 43 0.126
376
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.126
377
P RTN024 Retinoblastoma 72 0.126
378
OCL069 Ocular Motor Apraxia 57 0.126
379
P BRS047 Breast Cancer 97 0.126
380
PRS131 Prostate Cancer/brain Cancer Susceptibility 23 0.126
381
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.126
382
c LKM061 Leukemia, Acute Myeloid 83 0.126
383
MTG002 Mutagen Sensitivity 34 0.126
384
HLX001 Helix Syndrome 47 0.126
385
PNC005 Penicilliosis 30 0.126
386
BRT005 Barth Syndrome 55 0.126
387
ENT011 Enterocolitis 55 0.126
388
c TBR025 Tuberous Sclerosis 1 84 0.126
389
c HMC039 Hemochromatosis, Type 1 73 0.126
390
MYL069 Myeloma, Multiple 76 0.126
391
c THY056 Thyroid Dyshormonogenesis 3 32 0.126
392
c MCR115 Microvascular Complications of Diabetes 5 65 0.126
393
c FML347 Familial Adenomatous Polyposis 2 56 0.126
395
P FRD001 Friedreich Ataxia 62 0.126
396
P ORT004 Orthostatic Intolerance 61 0.126
397
CVT001 Cavitary Optic Disc Anomalies 38 0.126
398
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.126
399
P ADL017 Adult T-Cell Leukemia 53 0.126
400
P ANP001 Anaplastic Large Cell Lymphoma 59 0.126
401
MCS002 Mucositis 55 0.126
402
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.126
403
P MYF003 Myofibrillar Myopathy 50 0.126
404
P HYP111 Hyperprolinemia 44 0.126
405
NNL006 Non-Alcoholic Steatohepatitis 54 0.126
406
LMB062 Limb Ischemia 55 0.126
407
ASB001 Asbestosis 47 0.126
408
P CYS018 Cystitis 58 0.126
409
EXT006 Extrahepatic Cholestasis 41 0.126
410
NRL005 Neurilemmoma 60 0.126
411
VCC001 Vaccinia 49 0.126
412
TRN018 Transitional Cell Carcinoma 56 0.126
413
c BSL007 Basal Cell Carcinoma 67 0.126
414
P PRM002 Primary Hyperoxaluria 65 0.126
415
c ACT071 Acute Kidney Failure 60 0.126
416
P GLY013 Glycogen Storage Disease 59 0.126
417
RTN020 Retinal Vascular Disease 45 0.126
418
GLM008 Glomus Tumor 48 0.126
419
SQM006 Squamous Cell Carcinoma 59 0.126
420
P TBR001 Tuberous Sclerosis 69 0.126
421
P MLN007 Male Infertility 56 0.126
422
P SPN046 Spinal Muscular Atrophy 62 0.126
423
DNT008 Denture Stomatitis 35 0.126
424
URT010 Ureteral Obstruction 44 0.126
425
P PRP019 Peripheral Nervous System Disease 57 0.126
426
GST045 Gastroenteritis 58 0.126
427
P INT143 Interstitial Cystitis 59 0.126
428
P HYP086 Hypothyroidism 68 0.126
429
P OPT006 Optic Nerve Disease 57 0.126
430
c VRL010 Viral Hepatitis 52 0.126
431
P END033 Endocarditis 58 0.126
432
CRC021 Carcinosarcoma 62 0.126
433
BLD131 Bladder Urothelial Carcinoma 59 0.126
434
INT066 Interstitial Lung Disease 60 0.126
435
GNG013 Gingivitis 59 0.126
436
P RHB003 Rhabdomyosarcoma 66 0.126
437
P CHR012 Chronic Granulomatous Disease 69 0.126
438
P EMR001 Emery-Dreifuss Muscular Dystrophy 62 0.126
439
AMN003 Amnestic Disorder 53 0.126
440
P RNL015 Renal Hypertension 45 0.126
441
FLR002 Filariasis 55 0.126
442
KRT002 Keratomalacia 54 0.126
443
TXC005 Toxic Shock Syndrome 61 0.126
444
PRT037 Pertussis 49 0.126
445
CRN027 Corneal Neovascularization 47 0.126
446
ATR009 Atrophy of Testis 22 0.126
447
CRY005 Cryptococcosis 61 0.126
448
CHL056 Cheilitis 46 0.126
449
P INF032 Infertility 60 0.126
450
MDS022 Mediastinitis 47 0.126
451
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.126
452
P ATT003 Attenuated Familial Adenomatous Polyposis 57 0.126
453
BRN056 Bronchopulmonary Dysplasia 57 0.126
454
MTC004 Mitochondrial Encephalomyopathy 42 0.126
455
BBS001 Babesiosis 48 0.126
456
P MSC003 Muscular Atrophy 52 0.126
457
OST012 Osteoarthritis 77 0.126
458
PRN019 Perinatal Necrotizing Enterocolitis 60 0.126
459
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.126
460
c CHR684 Chronic Kidney Disease 73 0.126
461
HMP009 Haemophilus Influenzae 41 0.126
462
c LKM005 Leukemia, T-Cell, Chronic 33 0.126
463
NNT024 Neonatal Stroke 31 0.126
464
P HRP006 Herpes Simplex 65 0.126
465
PLS002 Peliosis Hepatis 32 0.126
466
ASB003 Asbestos Intoxication 32 0.126
467
MYH016 Myh-Associated Polyposis 39 0.126
468
MTY003 Mutyh Polyposis 39 0.126
469
P PHC019 Pheochromocytoma-Paraganglioma 35 0.126
470
ISL116 Isolated Complex Iii Deficiency 23 0.126
471
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 18 0.126
472
FTD001 Foot Drop 36 0.126
473
PLS037 Plasma Cell Tumor 20 0.126
Content
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