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Search results for cox1

382 hits were found for cox1

# Family MCID Name MIFTS Score
1
c BLD154 Bleeding Disorder, Platelet-Type, 12 28 14.921
2
PRS059 Prostaglandin-Endoperoxide Synthase Deficiency 8 9.886
3
ECH003 Echinococcosis 53 9.130
4
CYS008 Cystic Echinococcosis 57 7.768
5
RCH002 Richards-Rundle Syndrome 31 5.188
6
CYS005 Cysticercosis 60 4.178
7
LGH007 Leigh Syndrome 70 3.739
8
SPR006 Sparganosis 35 3.549
9
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 3.470
10
SCH014 Schistosomiasis 56 3.470
11
TNS007 Taeniasis 46 3.284
12
FSC002 Fascioliasis 44 3.245
13
PPL052 Papillomatosis, Confluent and Reticulated 34 3.232
14
ASP030 Aspirin Resistance 40 3.226
15
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 3.149
16
MLR004 Malaria 80 2.897
17
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.705
18
MYS004 Myiasis 39 2.678
19
ALV002 Alveolar Echinococcosis 57 2.571
20
STR008 Strongyloidiasis 52 2.525
21
CLB021 Coloboma, Ocular, with or Without Hearing Impairment, Cleft Lip/palate, and/or Mental Retardation 38 2.426
22
HLX001 Helix Syndrome 48 2.357
23
ASC010 Ascaris Lumbricoides Infection 49 2.286
24
ASC001 Ascaridiasis 36 2.286
25
SRC011 Sarcocystosis 31 2.286
26
CHL065 Cholangiocarcinoma 58 2.143
27
INT079 Intrahepatic Cholangiocarcinoma 51 2.143
28
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.132
29
THL003 Thelaziasis 28 2.132
30
MTC005 Mitochondrial Metabolism Disease 45 2.048
31
HRW001 Hair Whorl 35 2.048
32
CNG034 Congestive Heart Failure 69 2.048
33
CRC001 Cercarial Dermatitis 27 2.048
34
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.960
35
ADN018 Adenoma 59 1.960
36
CLT003 Colitis 63 1.864
37
CRY005 Cryptococcosis 60 1.864
38
P INF032 Infertility 57 1.864
39
SCB001 Scabies 50 1.818
40
c MGR028 Migraine with or Without Aura 1 64 1.761
41
c PHT011 Photoparoxysmal Response 3 12 1.761
42
ULC004 Ulcerative Colitis 74 1.761
43
TRN015 Transient Cerebral Ischemia 63 1.761
44
P ADN016 Adenocarcinoma 63 1.761
45
BRN024 Bronchitis 67 1.761
46
CLN003 Clonorchiasis 43 1.761
47
BBS001 Babesiosis 49 1.752
48
DPH003 Diphyllobothriasis 33 1.683
49
CCC002 Coccidiosis 50 1.683
50
P OVR042 Ovarian Cancer 88 1.646
51
CYS001 Cystic Fibrosis 78 1.646
52
P FML011 Familial Adenomatous Polyposis 71 1.646
53
CNR001 Coenurosis 26 1.612
54
HYP266 Hypoxia 57 1.612
55
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 1.537
56
FBR012 Fabry Disease 70 1.516
57
BRR014 Barrett Esophagus 66 1.516
58
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.516
59
PLS006 Plasmodium Vivax Malaria 51 1.516
60
INT017 Intestinal Schistosomiasis 51 1.458
61
P HYP098 Hypereosinophilic Syndrome 66 1.458
62
OPS001 Opisthorchiasis 41 1.458
63
BRN071 Brain Injury 50 1.458
64
ESN006 Eosinophilic Meningitis 36 1.374
65
TRM010 Traumatic Brain Injury 51 1.374
66
PRS034 Parasitic Helminthiasis Infectious Disease 51 1.374
67
PST092 Posttransplant Acute Limbic Encephalitis 28 1.374
68
c PRC016 Pre-Eclampsia 65 1.374
69
DRF001 Dirofilariasis 32 1.374
70
MTN002 Mite Infestation 35 1.374
71
P SZR006 Seizure Disorder 70 1.361
72
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 1.361
73
GST092 Gastroesophageal Reflux 61 1.361
74
APH002 Aphasia 56 1.361
75
P BLD062 Bile Duct Cancer 67 1.361
76
MTC004 Mitochondrial Encephalomyopathy 42 1.361
77
P LCT001 Lactic Acidosis 51 1.361
78
PPT005 Peptic Ulcer Disease 58 1.361
79
P BRS047 Breast Cancer 98 1.286
80
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.286
81
LCN001 Lice Infestation 41 1.286
82
MTG001 Metagonimiasis 24 1.286
83
ONC002 Onchocerciasis 51 1.286
84
PRG008 Paragonimiasis 37 1.286
85
ISC004 Ischemia 61 1.286
86
CND006 Candida Glabrata 30 1.286
87
P KLZ004 Kala-Azar 1 41 1.190
88
P SPP010 Suppressor of Tumorigenicity 3 51 1.190
89
P MYC007 Myocardial Infarction 70 1.190
90
DSS032 Disease by Infectious Agent 55 1.190
91
LSH001 Leishmaniasis 64 1.190
92
BYL001 Baylisascariasis 30 1.190
93
FLR002 Filariasis 55 1.190
94
LYM017 Lyme Disease 62 1.190
95
MNN009 Meningoencephalitis 48 1.190
96
P CNJ013 Conjunctivitis 66 1.190
97
P TXP001 Toxoplasmosis 60 1.190
98
P ATR011 Atrial Fibrillation 66 1.160
99
ACT058 Active Peptic Ulcer Disease 56 1.160
100
P DBT005 Diabetes Insipidus 54 1.087
101
ART140 Arteries, Anomalies of 53 1.087
102
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.087
103
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.087
104
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.087
105
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 1.087
106
P PLM037 Pulmonary Hypertension 72 1.087
107
LPP008 Lipoprotein Quantitative Trait Locus 65 1.087
108
P PLY014 Polycystic Kidney Disease 69 1.087
109
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.087
110
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 1.087
111
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.087
112
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 1.087
113
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.087
114
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 1.087
115
YLL002 Yellow Fever 61 1.087
116
ART016 Aortic Aneurysm 68 1.087
117
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.087
118
ANC001 Ancylostomiasis 39 1.087
119
P DRR001 Diarrhea 55 1.087
120
P MTC069 Mitochondrial Disorders 57 1.087
121
ANR040 Aneurysm 61 1.087
122
DST016 Distomatosis 22 1.087
123
ANX004 Anoxia 40 0.972
124
AGN016 Aging 54 0.972
125
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.972
126
c OPT053 Optic Atrophy 1 62 0.972
127
c ATR087 Atrial Standstill 1 74 0.972
128
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.972
129
VLV047 Volvulus of Midgut 52 0.972
130
P CLC063 Celiac Disease 1 66 0.972
131
MTC205 Mitochondrial Complex Iv Deficiency, Nuclear Type 1 57 0.972
132
CHK001 Chikungunya 60 0.972
133
END062 Endometrial Hyperplasia 48 0.972
134
CLR108 Colorectal Adenoma 64 0.972
135
KRT019 Keratitis, Hereditary 66 0.972
136
c ART101 Aortic Valve Disease 2 66 0.972
137
PRT037 Pertussis 65 0.972
138
CTN007 Cutaneous Leishmaniasis 62 0.972
139
ENT003 Enterobiasis 38 0.972
140
P KDN018 Kidney Disease 72 0.972
141
P NRP001 Neuropathy 60 0.972
142
ACQ007 Acquired Immunodeficiency Syndrome 59 0.972
143
ACN005 Acanthocephaliasis 17 0.972
144
MTC221 Mitochondrial Complex Iv Deficiency, Nuclear Type 14 14 0.972
145
END080 Endometrial Disease 45 0.972
146
HYM001 Hymenolepiasis 29 0.972
147
DRM006 Dermatitis 62 0.972
148
URN003 Urinary Schistosomiasis 46 0.972
149
P ENC004 Encephalitis 61 0.972
150
CLP006 Clopidogrel Resistance 44 0.972
151
P CRN300 Coronary Heart Disease 1 73 0.842
152
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.842
153
P MLT020 Multiple Sclerosis 79 0.842
154
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.842
155
HYP457 Hypertrophic Scars 42 0.842
156
FTL068 Fatal Infantile Cardioencephalomyopathy Due to Cytochrome C Oxidase Deficiency 35 0.842
157
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.842
158
c CNG413 Congenital Short Bowel Syndrome 42 0.842
159
WLF002 Wolf-Hirschhorn Syndrome 57 0.842
160
P PTN014 Patent Ductus Arteriosus 1 59 0.842
161
ARG004 Argyria 26 0.842
162
PRM329 Premature Aging 36 0.842
163
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.842
164
P LYM024 Lymphatic System Disease 47 0.842
165
47X002 47,xyy 48 0.842
166
P THR014 Thrombocytopenia 66 0.842
167
P LVR013 Liver Disease 69 0.842
168
INS001 Insulinoma 59 0.842
169
P GST044 Gastritis 55 0.842
170
OST012 Osteoarthritis 77 0.842
171
P LNG064 Lung Cancer Susceptibility 3 70 0.842
172
DNG003 Dengue Disease 65 0.842
173
FLR001 Filarial Elephantiasis 59 0.842
174
P LTR001 Lateral Sclerosis 58 0.842
175
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.842
176
LVR012 Liver Cirrhosis 63 0.842
177
P INT068 Intestinal Disease 53 0.842
178
P EYD002 Eye Disease 57 0.842
179
GNT004 Gnathomiasis 29 0.842
180
P ENC018 Encephalopathy 62 0.842
181
TRP014 Triploidy 38 0.842
182
CYT002 Cytokine Deficiency 43 0.842
183
GNT023 Gnathostoma Infection 19 0.842
184
SPN186 Spinal Cord Injury 61 0.687
185
BNG077 Benign Idiopathic Neonatal Seizures 23 0.687
186
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 0.687
187
INS024 Insulin-Like Growth Factor I 78 0.687
188
P DRM053 Dermatitis, Atopic 65 0.687
189
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.687
190
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.687
191
NNL006 Non-Alcoholic Steatohepatitis 54 0.687
192
c LKM061 Leukemia, Acute Myeloid 83 0.687
193
P CHN012 Chondrosarcoma 57 0.687
194
MTC211 Mitochondrial Complex Iv Deficiency, Nuclear Type 13 21 0.687
195
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.687
196
c THR048 Thrombocytopenia 4 28 0.687
197
c SPN308 Spinocerebellar Ataxia 28 48 0.687
198
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.687
199
c HYP836 Hypercholesterolemia, Familial, 1 73 0.687
200
BCT022 Bacterial Infectious Disease 56 0.687
201
HPT004 Hepatic Coma 43 0.687
202
CHL149 Childhood Acute Myeloid Leukemia 43 0.687
203
P BCL017 B-Cell Lymphoma 59 0.687
204
P MSC003 Muscular Atrophy 52 0.687
205
CRV002 Cervix Uteri Carcinoma in Situ 47 0.687
206
P MYL006 Myeloid Leukemia 61 0.687
207
FTT001 Fatty Liver Disease 62 0.687
208
GLL048 Glial Tumor 52 0.687
209
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.687
210
HYP066 Hyperglycemia 61 0.687
211
P BRS044 Breast Adenocarcinoma 58 0.687
212
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 0.687
213
TRY001 Trypanosomiasis 50 0.687
214
CRB004 Cerebral Artery Occlusion 45 0.687
215
PLY003 Polycystic Echinococcosis 24 0.687
216
P UVT001 Uveitis 57 0.687
217
GT001 Gout 64 0.687
218
CHG001 Chagas Disease 66 0.687
219
P HYP061 Hypertrophic Cardiomyopathy 69 0.687
220
TRC012 Trichuriasis 43 0.687
221
HPT019 Hepatic Encephalopathy 59 0.687
222
c BSL007 Basal Cell Carcinoma 68 0.687
223
NRW001 Norwegian Scabies 36 0.687
224
CLN015 Colon Adenocarcinoma 65 0.687
225
PRT013 Portal Hypertension 59 0.687
226
JPN002 Japanese Encephalitis 61 0.687
227
SPT005 Spotted Fever 49 0.687
228
CDQ001 Cauda Equina Syndrome 37 0.687
229
P PRN023 Prion Disease 60 0.687
230
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.687
231
PNN001 Panniculitis 52 0.687
232
LCH001 Leech Infestation 38 0.687
233
STT001 Status Epilepticus 59 0.687
234
SQM006 Squamous Cell Carcinoma 60 0.687
235
RLP003 Relapsing Fever 49 0.687
236
ANS003 Anisakiasis 38 0.687
237
TXC011 Toxocariasis 46 0.687
238
BCK006 Back Pain 47 0.687
239
BNS003 Binswanger's Disease 41 0.687
240
CRV045 Cervical Intraepithelial Neoplasia 39 0.687
241
GLM045 Glioma 63 0.687
242
c SPN225 Spondyloarthropathy 1 70 0.674
243
P CHL066 Cholangitis 52 0.674
244
SPN051 Spondylitis 51 0.674
245
INF009 Inflammatory Spondylopathy 30 0.674
246
P ATS364 Autism 69 0.486
247
P LNG032 Lung Cancer 98 0.486
248
LYM133 Lymphoma, Hodgkin, Classic 74 0.486
249
WND005 Wound Myiasis 16 0.486
250
PLY100 Polyploidy 36 0.486
251
SCR039 Scorpion Envenomation 41 0.486
252
P BLD134 Bladder Cancer 79 0.486
253
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.486
254
P NSP012 Nasopharyngeal Carcinoma 61 0.486
255
P XNC004 X Inactivation, Familial Skewed, 1 17 0.486
256
HMC014 Homocysteinemia 52 0.486
257
ANX010 Anxiety 70 0.486
258
P SCH015 Schizophrenia 74 0.486
259
MRF001 Marfan Syndrome 76 0.486
260
P LKM071 Leukemia, Chronic Lymphocytic 75 0.486
261
ATM095 Autoimmune Disease 61 0.486
262
BSL036 Basal Cell Nevus Syndrome 73 0.486
263
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.486
264
P APL001 Aplastic Anemia 73 0.486
265
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.486
266
HMR023 Hemorrhagic Cystitis 43 0.486
267
c MCR130 Microvascular Complications of Diabetes 6 41 0.486
268
MYL009 Myelodysplastic Syndrome 67 0.486
269
P INF037 Inflammatory Bowel Disease 53 0.486
270
DFC004 Deficiency Anemia 74 0.486
271
PRT251 Proteinuria, Chronic Benign 57 0.486
272
c ATM099 Autoimmune Uveitis 45 0.486
273
P URN019 Urinary Tract Infection 49 0.486
274
c ATS007 Autism Spectrum Disorder 72 0.486
275
BNR002 Bone Resorption Disease 47 0.486
276
THR024 Thrombosis 56 0.486
277
P LYM118 Lymphoma 67 0.486
278
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.486
279
CYS044 Cystic Disease of Lung 20 0.486
280
c BRN108 Branchiootic Syndrome 1 62 0.486
282
CMB048 Combined Oxidative Phosphorylation Deficiency 15 25 0.486
283
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.486
284
c PCH010 Pachyonychia Congenita 3 43 0.486
285
MTC210 Mitochondrial Complex Iv Deficiency, Nuclear Type 9 17 0.486
286
c MCR120 Microvascular Complications of Diabetes 7 47 0.486
287
WST005 West Nile Virus 57 0.486
288
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.486
289
BRL010 Buruli Ulcer 45 0.486
290
DWN001 Down Syndrome 70 0.486
291
OCL069 Ocular Motor Apraxia 57 0.486
292
c SML038 Small Cell Cancer of the Lung 69 0.486
293
P HYP733 Hypercalciuria, Absorptive, 2 45 0.486
294
MMM006 Mammographic Density 39 0.486
295
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.486
296
P SCL018 Scoliosis 57 0.486
297
ORL015 Oral Squamous Cell Carcinoma 43 0.486
298
GLC003 Glucose Intolerance 54 0.486
300
P HML001 Hemolytic-Uremic Syndrome 52 0.486
301
P AMY004 Amyloidosis 70 0.486
302
MNZ001 Monieziasis 14 0.486
303
P NRB001 Neuroblastoma 66 0.486
304
P MYP004 Myopathy 67 0.486
305
SCR011 Scrapie 39 0.486
306
VSC003 Visceral Leishmaniasis 55 0.486
307
P HMC002 Homocystinuria 53 0.486
308
IRD001 Iridocyclitis 53 0.486
309
P RBL001 Rubella 58 0.486
310
P DBT009 Diabetes Mellitus 67 0.486
311
P CYS018 Cystitis 59 0.486
312
SKN016 Skin Disease 63 0.486
313
P EPL164 Epilepsy 68 0.486
314
CHL067 Cholecystitis 60 0.486
315
P CND004 Candidiasis 58 0.486
316
P PLM036 Pulmonary Fibrosis 66 0.486
317
P LYN001 Lynch Syndrome 76 0.486
318
THL004 Theileriasis 31 0.486
319
TCK004 Tick Infestation 30 0.486
320
c VRL007 Viral Encephalitis 50 0.486
321
PRT036 Peritonitis 65 0.486
322
P CRN028 Corneal Ulcer 47 0.486
323
P ART022 Arthritis 71 0.486
325
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.486
326
MTC173 Mitochondrial Complex I Deficiency, Nuclear Type 27 19 0.486
327
P KRT007 Keratoconus 50 0.486
328
P GRF003 Graft-Versus-Host Disease 71 0.486
329
c MCR113 Microvascular Complications of Diabetes 3 52 0.486
330
c MCR133 Microvascular Complications of Diabetes 4 41 0.486
331
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.486
332
PHL002 Philophthalmiasis 5 0.486
333
MTC219 Mitochondrial Complex Iv Deficiency, Nuclear Type 11 16 0.486
334
MTC227 Mitochondrial Complex Iv Deficiency, Nuclear Type 20 16 0.486
335
MND031 Mandibuloacral Dysplasia Progeroid Syndrome 33 0.486
336
P DNG005 Dengue Virus 56 0.486
337
c DLT002 Dilated Cardiomyopathy 78 0.486
338
ECH001 Echinostomiasis 21 0.486
339
PLC002 Plica Syndrome 35 0.486
340
ALL029 Allergic Disease 59 0.486
341
P MLN007 Male Infertility 56 0.486
342
VGN020 Vaginal Disease 48 0.486
343
BRN014 Bronchopneumonia 53 0.486
344
P SPN046 Spinal Muscular Atrophy 63 0.486
345
CNS004 Constipation 56 0.486
346
TXC005 Toxic Shock Syndrome 62 0.486
347
P VSC007 Vascular Disease 63 0.486
348
CHL014 Cholera 62 0.486
349
GST033 Gestational Diabetes 61 0.486
350
MST005 Mastitis 53 0.486
351
RBS001 Rabies 58 0.486
352
STR012 Setariasis 11 0.486
353
STL001 St. Louis Encephalitis 38 0.486
354
P END047 Endophthalmitis 53 0.486
355
P BLP003 Blepharospasm 46 0.486
356
END085 Endometrial Serous Adenocarcinoma 43 0.486
357
P RTN018 Retinal Disease 53 0.486
358
PLC008 Placenta Disease 49 0.486
359
P CYS039 Cystic Kidney Disease 53 0.486
360
SYN007 Synovitis 55 0.486
361
MDD011 Mood Disorder 62 0.486
362
VLV010 Vulvovaginitis 42 0.486
363
P MTR014 Motor Neuron Disease 65 0.486
364
DMY004 Demyelinating Disease 50 0.486
365
PHL003 Phlebotomus Fever 33 0.486
366
KLB003 Klebsiella Pneumonia 50 0.486
367
GST023 Gastric Ulcer 52 0.486
368
P CRD246 Cardiovascular System Disease 56 0.486
369
HYP014 Hyperuricemia 51 0.486
370
c SVR005 Severe Pre-Eclampsia 50 0.486
371
APH001 Aphthous Stomatitis 58 0.486
372
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 17 0.486
373
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 0.486
374
STM007 Stomatitis 54 0.486
375
P SCK005 Sickle Cell Disease 56 0.486
376
48X005 48,xyyy 39 0.486
377
P CHR345 Chronic Pain 50 0.486
378
P HYP265 Hypotonia 42 0.486
379
STT009 Sutton Disease 2 29 0.486
381
CHR178 Chromosomal Triplication 34 0.486
382
OVR094 Ovarian Epithelial Cancer 39 0.486
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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