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Search results for MK-801

370 hits were found for MK-801

# Family MCID Name MIFTS Score
1
P SCH015 Schizophrenia 74 23.315
2
CRB004 Cerebral Artery Occlusion 45 18.772
3
P SZR006 Seizure Disorder 70 18.531
4
AMN003 Amnestic Disorder 54 15.850
5
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 15.131
6
PNG002 Pain Agnosia 51 12.438
7
STT001 Status Epilepticus 59 11.064
8
P PRK039 Parkinsonism 55 9.131
9
CRT015 Carotid Artery Occlusion 45 9.108
10
BRN004 Brain Edema 54 8.977
11
ANX004 Anoxia 40 8.926
12
TRM010 Traumatic Brain Injury 51 8.688
13
SPN186 Spinal Cord Injury 61 8.617
14
BRN071 Brain Injury 50 8.237
15
HYP266 Hypoxia 57 8.046
16
ANX010 Anxiety 70 7.931
17
MRP001 Morphine Dependence 42 7.841
18
P HNT016 Huntington Disease 73 7.790
19
P NRB001 Neuroblastoma 66 7.790
20
ALL029 Allergic Disease 59 7.696
21
48X005 48,xyyy 39 7.696
22
P TRM003 Tremor 48 7.502
23
c DNT047 Dentinogenesis Imperfecta Type 2 35 7.328
24
PRP016 Paraplegia 52 7.268
25
ISC004 Ischemia 61 7.253
26
ADG002 Audiogenic Seizures 25 6.984
27
P CRD119 Cardiac Arrest 67 6.876
28
HDN002 Head Injury 44 6.825
29
HYP056 Hypoglycemia 65 6.766
30
TRN015 Transient Cerebral Ischemia 63 6.392
31
P CHR345 Chronic Pain 50 6.382
32
ALC007 Alcohol Dependence 66 6.264
33
PSY004 Psychotic Disorder 66 6.264
34
ANT019 Anterograde Amnesia 38 6.192
35
c AMY091 Amyotrophic Lateral Sclerosis 1 88 5.765
36
P LTR001 Lateral Sclerosis 58 5.765
37
HPT004 Hepatic Coma 43 5.690
38
HPT019 Hepatic Encephalopathy 59 5.690
39
MNN017 Mononeuropathy 41 5.690
40
c MJR022 Major Affective Disorder 8 38 5.374
41
c MJR024 Major Affective Disorder 9 41 5.374
42
P BPL003 Bipolar Disorder 56 5.374
43
GLL048 Glial Tumor 52 5.305
44
GLM045 Glioma 63 5.305
45
WTH001 Withdrawal Disorder 48 5.226
46
PRT037 Pertussis 65 5.226
47
P ATT013 Attention Deficit-Hyperactivity Disorder 64 5.103
48
CRB090 Cerebral Hypoxia 42 5.090
49
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 5.018
50
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 4.940
51
P DYS154 Dystonia 64 4.934
52
P PRP019 Peripheral Nervous System Disease 58 4.862
53
P BRB001 Beriberi 44 4.843
54
DPR016 Depression 65 4.783
55
P SBS003 Substance Abuse 54 4.751
56
RTN003 Retinal Ischemia 49 4.701
57
PTH003 Pathologic Nystagmus 52 4.701
58
P TMP001 Temporal Lobe Epilepsy 49 4.678
59
P MJR001 Major Depressive Disorder 68 4.618
60
MNT002 Mental Depression 57 4.618
61
P ENC018 Encephalopathy 62 4.577
62
RCK004 Rickets 68 4.444
63
RTR001 Retrograde Amnesia 41 4.380
64
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 4.354
65
HRN029 Hearing Loss, Noise-Induced 37 4.289
66
TTN003 Tetanus 65 4.231
67
PST028 Post-Traumatic Stress Disorder 59 4.206
68
P LVR013 Liver Disease 69 4.063
69
P DMN002 Dementia 66 4.032
70
OPT003 Opiate Dependence 49 4.032
71
OBS002 Obsessive-Compulsive Disorder 68 3.941
72
c ACT134 Acute Liver Failure 59 3.850
73
c ATS007 Autism Spectrum Disorder 72 3.848
74
OCL069 Ocular Motor Apraxia 57 3.848
75
P EPL164 Epilepsy 68 3.848
76
P NRP001 Neuropathy 60 3.751
77
HYP066 Hyperglycemia 61 3.751
78
FCL014 Focal Epilepsy 53 3.751
79
ARG004 Argyria 26 3.737
80
CRB039 Cerebrovascular Disease 66 3.737
81
P MTR014 Motor Neuron Disease 65 3.617
82
SBC016 Subacute Delirium 43 3.617
83
P ALZ034 Alzheimer Disease 87 3.547
84
P PRK057 Parkinson Disease, Late-Onset 80 3.547
85
DWN001 Down Syndrome 70 3.491
86
ACT084 Acute Stress Disorder 54 3.438
87
CHL014 Cholera 62 3.438
88
P MYC033 Myoclonus 47 3.438
89
CHR178 Chromosomal Triplication 34 3.356
90
P LNG032 Lung Cancer 98 3.324
91
P FTL001 Fetal Alcohol Syndrome 55 3.324
92
c SCH082 Schizophrenia 5 23 3.324
93
P HPT023 Hepatocellular Carcinoma 96 3.324
94
P MLG056 Malignant Hyperthermia 66 3.324
95
MDD011 Mood Disorder 62 3.210
96
P PHC003 Pheochromocytoma 69 3.205
97
c SCH079 Schizophrenia 1 44 3.205
98
ADR040 Adrenal Gland Pheochromocytoma 46 3.205
99
P RRH023 Rare Hereditary Hemochromatosis 54 3.205
100
HMS001 Hemosiderosis 48 3.205
101
NRT001 Neurotic Disorder 56 3.205
102
DMY004 Demyelinating Disease 50 3.205
103
ALL014 Allergic Encephalomyelitis 34 3.205
104
INS024 Insulin-Like Growth Factor I 78 3.125
105
c BCT007 Bacterial Meningitis 55 3.079
106
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 3.079
108
MLD018 Mild Cognitive Impairment 48 3.079
109
P ART022 Arthritis 71 3.079
110
P HYP086 Hypothyroidism 69 3.079
111
CHL068 Cholestasis 61 3.079
112
CYT002 Cytokine Deficiency 43 3.079
113
PLY150 Polykaryocytosis Inducer 29 2.946
114
c MGR028 Migraine with or Without Aura 1 64 2.946
115
TRD006 Tardive Dyskinesia 53 2.944
116
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.944
117
P BCL017 B-Cell Lymphoma 59 2.944
118
BLR008 Bilirubin Metabolic Disorder 57 2.944
119
P MNN013 Meningitis 65 2.944
120
HVY002 Heavy Metal Poisoning 22 2.944
121
HMC014 Homocysteinemia 52 2.852
122
IMM167 Immune Deficiency Disease 78 2.852
123
RST023 Resting Heart Rate, Variation in 40 2.799
124
PHN001 Phencyclidine Abuse 22 2.799
125
P PRN023 Prion Disease 60 2.799
126
P ADL010 Adult Respiratory Distress Syndrome 71 2.799
127
LNG015 Lingual-Facial-Buccal Dyskinesia 47 2.799
128
WLL004 Wallerian Degeneration 38 2.799
129
HLX001 Helix Syndrome 48 2.756
130
HMN044 Human Immunodeficiency Virus Type 1 78 2.655
131
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 18 2.655
132
DBT010 Diabetic Neuropathy 54 2.642
133
P ALC033 Alcohol Use Disorder 61 2.642
134
P RTN016 Retinal Degeneration 52 2.642
135
P KRN004 Kernicterus 46 2.642
136
P DYS005 Dyslexia 41 2.642
137
P SLP005 Sleep Disorder 61 2.642
138
DRG003 Drug Dependence 46 2.642
139
WRN002 Wernicke-Korsakoff Syndrome 50 2.468
140
P PNC035 Pancreatic Cancer 86 2.468
141
OCL052 Ocular Dominance 40 2.468
142
RBS001 Rabies 58 2.468
143
SPN033 Spontaneous Ocular Nystagmus 25 2.468
144
DMN012 Dementia - Subcortical 18 2.468
145
NNT024 Neonatal Stroke 33 2.468
146
P FML011 Familial Adenomatous Polyposis 71 2.271
147
c MCR130 Microvascular Complications of Diabetes 6 41 2.271
148
CLT003 Colitis 63 2.271
149
c MCR120 Microvascular Complications of Diabetes 7 47 2.271
150
PRX097 Paroxysmal Dystonia 32 2.271
151
END040 Endogenous Depression 55 2.271
152
c MCR113 Microvascular Complications of Diabetes 3 52 2.271
153
c MCR133 Microvascular Complications of Diabetes 4 41 2.271
154
ATY001 Atypical Depressive Disorder 45 2.271
155
P CRB088 Cerebral Atrophy 33 2.271
156
c ART112 Arthrogryposis, Distal, Type 10 34 2.209
157
P MVM001 Movement Disease 61 2.209
158
CCN009 Cocaine Intoxication 30 2.083
159
TRT001 Teratocarcinoma 42 2.083
160
P PRC019 Precocious Puberty 47 2.083
161
AGN016 Aging 54 2.037
162
P SPR120 Supranuclear Palsy, Progressive, 1 69 2.037
163
ADT003 Auditory System Disease 49 2.037
164
CCN002 Cocaine Abuse 49 2.037
165
IRN002 Iron Metabolism Disease 57 2.037
166
HYP144 Hyperacusis 23 2.037
167
PST047 Post-Traumatic Epilepsy 20 2.037
168
BNR002 Bone Resorption Disease 47 1.949
169
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 1.949
170
CHL045 Choline Deficiency Disease 39 1.949
171
DTR001 Detrusor Sphincter Dyssynergia 37 1.949
172
P RSP003 Respiratory Failure 74 1.949
173
P FBR031 Febrile Seizures 52 1.949
174
SPS057 Spasticity 42 1.804
175
LMB062 Limb Ischemia 55 1.804
176
c CNG006 Congenital Hypothyroidism 63 1.804
177
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 1.804
178
P MTH008 Methylmalonic Acidemia 52 1.804
179
ACQ007 Acquired Immunodeficiency Syndrome 59 1.804
180
P SNS001 Sensorineural Hearing Loss 59 1.804
181
CMP006 Complex Partial Epilepsy 36 1.804
182
CHR073 Choreatic Disease 54 1.804
183
P ENC004 Encephalitis 61 1.804
184
MTH086 Methotrexate Toxicity 32 1.732
185
c HYP836 Hypercholesterolemia, Familial, 1 73 1.732
186
ULC004 Ulcerative Colitis 74 1.732
187
PNM001 Pneumocystosis 61 1.732
188
SRT004 Serotonin Syndrome 54 1.647
189
OTT002 Otitis Media 71 1.647
190
GLT035 Glutaric Acidemia I 57 1.647
191
P NRC002 Narcolepsy 56 1.647
192
P PNC025 Panic Disorder 52 1.647
193
c VRL007 Viral Encephalitis 50 1.647
194
P MGR003 Migraine with Aura 52 1.647
195
NRG002 Neurogenic Bladder 55 1.647
196
ISL099 Isolated Methylmalonic Acidemia 36 1.647
197
STR067 Stroke, Ischemic 80 1.473
198
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.473
199
47X002 47,xyy 48 1.473
200
P CYS018 Cystitis 59 1.473
201
PLR008 Pleurisy 50 1.473
202
PTH002 Pathological Gambling 48 1.473
203
LWC001 Low Compliance Bladder 45 1.473
204
P MCR010 Microcephaly 60 1.473
205
P RTN018 Retinal Disease 53 1.473
206
P TRT010 Teratoma 51 1.473
207
P PTS002 Ptosis 52 1.473
208
GNR004 Generalized Anxiety Disorder 55 1.473
209
P CRB059 Cerebellar Degeneration 36 1.473
210
MSL001 Measles 61 1.473
211
P ATS364 Autism 69 1.276
212
P OVR082 Overgrowth Syndrome 49 1.276
213
CRD223 Cardiac Arrhythmia 63 1.276
214
CRD132 Cardiac Conduction Defect 60 1.276
215
c 2HY001 2-Hydroxyglutaric Aciduria 38 1.276
216
c RTN041 Retinitis Pigmentosa 11 42 1.276
217
PRP001 Propionic Acidemia 65 1.276
218
P STR092 Striatal Degeneration, Autosomal Dominant 2 47 1.276
219
P MPL001 Maple Syrup Urine Disease 70 1.276
220
c TYP009 Type 2 Diabetes Mellitus 92 1.276
221
GLB002 Glioblastoma 67 1.276
222
P SKN015 Skin Carcinoma 71 1.276
223
P PLM036 Pulmonary Fibrosis 66 1.276
224
LNG099 Lung Disease 62 1.276
225
PRV004 Periventricular Leukomalacia 52 1.276
226
P HRT032 Heart Disease 81 1.276
227
c ESS001 Essential Tremor 57 1.276
228
P TCD001 Tic Disorder 49 1.276
229
HYP026 Hypoglycemic Coma 37 1.276
230
P BNC003 Bone Cancer 58 1.276
231
CRB037 Cerebral Palsy 67 1.276
232
VSC002 Vascular Dementia 60 1.276
233
DST006 Diastolic Heart Failure 45 1.276
234
NRN016 Neuronal Migration Disorders 40 1.276
235
PRX035 Paroxysmal Dyskinesia 30 1.042
236
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 1.042
237
NRM022 Neurometabolic Disease 24 1.042
238
SPS019 Spastic Paraparesis 38 1.042
239
LSC001 Lesch-Nyhan Syndrome 62 1.042
240
P FRG001 Fragile X Syndrome 70 1.042
241
P MYS005 Myositis 56 1.042
242
TRT017 Teratoma, Ovarian 28 1.042
243
GLL008 Gilles De La Tourette Syndrome 65 1.042
244
c L2H001 L-2-Hydroxyglutaric Aciduria 49 1.042
245
TND004 Tendinopathy 45 1.042
246
ANG054 Angina Pectoris 66 1.042
247
FTL006 Fetal Alcohol Spectrum Disorder 43 1.042
248
P INF037 Inflammatory Bowel Disease 53 1.042
249
TND005 Tendinitis 54 1.042
250
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.042
251
P ATR011 Atrial Fibrillation 66 1.042
252
c BRN108 Branchiootic Syndrome 1 62 1.042
253
PHN003 Phenylketonuria 76 1.042
254
c TRM024 Tremor, Hereditary Essential, 1 34 1.042
255
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 1.042
256
c SML038 Small Cell Cancer of the Lung 69 1.042
257
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 1.042
258
DSS032 Disease by Infectious Agent 55 1.042
259
P SCL018 Scoliosis 57 1.042
260
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 1.042
261
RPD005 Rapidly Involuting Congenital Hemangioma 46 1.042
262
SCR011 Scrapie 39 1.042
263
INT075 Intracranial Hypertension 53 1.042
264
P PSR002 Psoriasis 63 1.042
265
MNG007 Manganese Poisoning 28 1.042
266
SKN016 Skin Disease 63 1.042
267
ANV001 Anovulation 47 1.042
268
PST011 Pustulosis of Palm and Sole 52 1.042
269
HGH001 High Pressure Neurological Syndrome 27 1.042
270
SPP007 Suppression Amblyopia 38 1.042
271
AMB002 Amblyopia 50 1.042
272
PCD001 Pica Disease 38 1.042
273
RFL002 Reflex Epilepsy 41 1.042
274
P VSC007 Vascular Disease 63 1.042
275
NRT004 Neuritis 53 1.042
276
HGH043 High Grade Glioma 45 1.042
277
ING001 Inguinal Hernia 59 1.042
278
ASP004 Asphyxia Neonatorum 50 1.042
279
OVR109 Ovarian Germ Cell Teratoma 32 1.042
280
LPD008 Lipid Metabolism Disorder 62 1.042
281
PLM010 Pulmonary Edema 55 1.042
282
VRT001 Vertebral Artery Occlusion 29 1.042
283
CRB033 Cerebral Degeneration 39 1.042
284
PLY024 Polymicrogyria 47 1.042
285
ADS004 Aids Dementia Complex 40 1.042
286
HRN003 Heroin Dependence 44 1.042
287
OPD006 Opioid Addiction 48 1.042
288
CHL078 Childhood-Onset Schizophrenia 29 1.042
289
BRN056 Bronchopulmonary Dysplasia 56 1.042
291
P VTR007 Vitreoretinopathy 46 0.736
292
SHK001 Shaken Baby Syndrome 21 0.736
293
NRM021 Neurometabolic Disorder Due to Serine Deficiency 15 0.736
294
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 62 0.736
295
3HY007 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 51 0.736
296
P MYS003 Myasthenia Gravis 68 0.736
297
ANR007 Anorexia Nervosa 60 0.736
298
c LSS005 Lissencephaly 1 57 0.736
299
P D2H002 D-2-Hydroxyglutaric Aciduria 1 52 0.736
300
RTN017 Retinal Detachment 60 0.736
301
P OVR042 Ovarian Cancer 88 0.736
302
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.736
303
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.736
304
P PLM037 Pulmonary Hypertension 72 0.736
305
SRN001 Serine Deficiency 24 0.736
306
MTB004 Metabolic Acidosis 48 0.736
307
P SLP006 Sleep Apnea 69 0.736
308
c MCR115 Microvascular Complications of Diabetes 5 65 0.736
309
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 0.736
310
c NTR051 Neutropenia, Severe Congenital, 2, Autosomal Dominant 27 0.736
311
ATM100 Autoimmune Optic Neuritis 28 0.736
312
ACT098 Acute Erythroid Leukemia 55 0.736
313
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.736
314
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 0.736
315
GLY010 Glycine Encephalopathy 57 0.736
316
c SCH085 Schizophrenia 2 27 0.736
317
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.736
318
GLY094 Glycine Encephalopathy with Normal Serum Glycine 24 0.736
319
c SPN097 Spinocerebellar Ataxia 23 40 0.736
320
WST005 West Nile Virus 57 0.736
321
PLY068 Polysubstance Abuse 41 0.736
322
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.736
323
P MJR007 Major Affective Disorder 1 42 0.736
324
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 47 0.736
325
P GLM040 Glioma Susceptibility 1 71 0.736
326
c DYS151 Dystonia 25 40 0.736
327
ORG002 Organic Acidemia 44 0.736
328
RNL077 Renal Fibrosis 46 0.736
329
c SCH081 Schizophrenia 6 27 0.736
330
ACS001 Acoustic Neuroma 56 0.736
331
ZKF001 Zika Fever 52 0.736
332
P MYP006 Myopia 56 0.736
333
URT010 Ureteral Obstruction 45 0.736
334
PST092 Posttransplant Acute Limbic Encephalitis 28 0.736
335
P BRS044 Breast Adenocarcinoma 58 0.736
336
INS001 Insulinoma 59 0.736
337
OVR059 Ovary Adenocarcinoma 49 0.736
338
NRM005 Neuromuscular Disease 63 0.736
339
c VRL012 Viral Meningitis 46 0.736
340
c PRC016 Pre-Eclampsia 65 0.736
341
P OPT009 Optic Neuritis 57 0.736
342
SHG001 Shigellosis 63 0.736
343
P GLL022 Guillain-Barre Syndrome 60 0.736
344
IMP005 Impotence 52 0.736
345
P CHL002 Childhood Absence Epilepsy 63 0.736
346
NNT012 Neonatal Jaundice 53 0.736
347
MLG169 Malignant Astrocytoma 57 0.736
348
CYS014 Cystadenocarcinoma 51 0.736
349
P ECL001 Eclampsia 52 0.736
350
JPN002 Japanese Encephalitis 61 0.736
351
TCL003 T Cell Deficiency 44 0.736
352
c SVR105 Severe Congenital Neutropenia 2 11 0.736
353
BRN024 Bronchitis 67 0.736
354
c INH020 Inherited Metabolic Disorder 48 0.736
355
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.736
356
EMB004 Embryonal Carcinoma 56 0.736
357
PPL003 Papillary Cystadenocarcinoma 29 0.736
358
c CNT035 Central Nervous System Disease 54 0.736
359
WRN003 Wernicke Encephalopathy 46 0.736
360
CRT004 Carotid Artery Thrombosis 39 0.736
361
DPR002 Depersonalization Disorder 41 0.736
362
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.736
363
NRM004 Neuroma 49 0.736
364
P RTN022 Retinal Vein Occlusion 54 0.736
365
DYT003 Dyt-Gnal 16 0.736
366
IRR002 Irritable Bowel Syndrome 65 0.736
367
P SCK005 Sickle Cell Disease 56 0.736
368
PRS063 Paresthesia 39 0.736
369
P NRV007 Nervous System Disease 67 0.736
370
ETN001 Eating Disorder 59 0.736
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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