Search results for Nimodipine

259 hits were found for Nimodipine

# Family MCID Name MIFTS Score
1
CRB039 Cerebrovascular Disease 67 0.218
2
ANR040 Aneurysm 59 0.214
3
c MGR028 Migraine with or Without Aura 1 67 0.204
4
CRB004 Cerebral Artery Occlusion 45 0.192
5
VSL002 Visual Epilepsy 59 0.189
6
P SZR006 Seizure Disorder 56 0.189
7
CRB086 Cerebral Aneurysms 40 0.189
8
HDN002 Head Injury 46 0.185
9
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.180
10
P HDC001 Headache 57 0.180
11
STR067 Stroke, Ischemic 81 0.172
12
ISC004 Ischemia 58 0.168
13
P DMN002 Dementia 66 0.163
14
VSC002 Vascular Dementia 57 0.163
15
INT030 Intracranial Aneurysm 56 0.163
16
SPN186 Spinal Cord Injury 60 0.159
17
BRN004 Brain Edema 56 0.154
18
P VSC007 Vascular Disease 63 0.139
19
P INT260 Intracranial Berry Aneurysm 39 0.139
20
P CRD119 Cardiac Arrest 67 0.133
21
OCL069 Ocular Motor Apraxia 51 0.133
22
PNG002 Pain Agnosia 51 0.128
23
P ECL001 Eclampsia 50 0.122
24
DWN001 Down Syndrome 70 0.115
25
NRL005 Neurilemmoma 60 0.115
26
ACS001 Acoustic Neuroma 56 0.115
27
P EPL164 Epilepsy 71 0.109
28
P TRN020 Turner Syndrome 67 0.109
29
P HYD006 Hydrocephalus 66 0.109
30
P NRP001 Neuropathy 56 0.109
31
BRN071 Brain Injury 49 0.109
32
ANX004 Anoxia 40 0.109
33
KHL003 Kohlschutter-Tonz Syndrome 65 0.102
34
TRM010 Traumatic Brain Injury 51 0.102
35
P ALZ034 Alzheimer Disease 88 0.094
36
c HYP595 Hypertension, Essential 84 0.094
37
c PRC016 Pre-Eclampsia 63 0.094
38
MDD011 Mood Disorder 62 0.094
39
P ENC018 Encephalopathy 61 0.094
40
HYP266 Hypoxia 57 0.094
41
AMN003 Amnestic Disorder 54 0.094
42
DBT010 Diabetic Neuropathy 54 0.094
43
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.086
44
ANG054 Angina Pectoris 66 0.086
45
P PRP019 Peripheral Nervous System Disease 58 0.086
46
P INF032 Infertility 57 0.086
47
P EXN002 Exanthem 57 0.086
48
AGN016 Aging 56 0.086
49
c SVR005 Severe Pre-Eclampsia 50 0.086
50
P MGR001 Migraine Without Aura 49 0.086
51
WTH001 Withdrawal Disorder 48 0.086
52
CRT015 Carotid Artery Occlusion 45 0.086
53
RVR002 Reversible Cerebral Vasoconstriction Syndrome 28 0.086
54
P SCH015 Schizophrenia 74 0.077
55
P KDN018 Kidney Disease 72 0.077
56
P NRB001 Neuroblastoma 72 0.077
57
DPR016 Depression 63 0.077
58
ACQ007 Acquired Immunodeficiency Syndrome 60 0.077
59
STT001 Status Epilepticus 60 0.077
60
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.077
61
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.077
62
HMR039 Hemorrhage, Intracerebral 57 0.077
63
P BPL003 Bipolar Disorder 56 0.077
64
ATR057 Atrioventricular Block 55 0.077
65
CCN002 Cocaine Abuse 49 0.077
66
CYT002 Cytokine Deficiency 42 0.077
67
c MJR024 Major Affective Disorder 9 41 0.077
68
ADS004 Aids Dementia Complex 40 0.077
69
c MJR022 Major Affective Disorder 8 38 0.077
70
THN005 Thunderclap Headache 19 0.077
71
c NRF023 Neurofibromatosis, Type Ii 80 0.067
72
IMM167 Immune Deficiency Disease 78 0.067
73
P CNR004 Cone-Rod Dystrophy 2 73 0.067
74
HMN044 Human Immunodeficiency Virus Type 1 71 0.067
75
P FRN006 Frontotemporal Dementia 68 0.067
76
PSY004 Psychotic Disorder 67 0.067
77
c RHB024 Rhabdomyosarcoma 2 67 0.067
78
ALC007 Alcohol Dependence 66 0.067
79
P NRV007 Nervous System Disease 66 0.067
80
PRT037 Pertussis 65 0.067
81
TRN015 Transient Cerebral Ischemia 63 0.067
82
ALL026 Allergic Hypersensitivity Disease 62 0.067
83
MNT002 Mental Depression 58 0.067
84
P PLY011 Polycystic Ovary Syndrome 56 0.067
85
SCH003 Schizophreniform Disorder 56 0.067
86
P MLN007 Male Infertility 55 0.067
88
P RTN016 Retinal Degeneration 53 0.067
89
INT075 Intracranial Hypertension 53 0.067
90
c CNT035 Central Nervous System Disease 52 0.067
91
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.067
92
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.067
93
SBC016 Subacute Delirium 44 0.067
94
BNS003 Binswanger's Disease 42 0.067
95
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.067
96
48X005 48,xyyy 39 0.067
97
ALL014 Allergic Encephalomyelitis 38 0.067
98
P PRC031 Preeclampsia/eclampsia 1 38 0.067
99
c PLY105 Polycystic Ovary Syndrome 1 38 0.067
100
PRP028 Peripheral Vertigo 37 0.067
101
CYT018 Cytochrome P450 2d6 Variant 27 0.067
102
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.067
103
P HRT032 Heart Disease 75 0.054
104
P MLT020 Multiple Sclerosis 72 0.054
105
P HYP086 Hypothyroidism 69 0.054
106
P MJR001 Major Depressive Disorder 68 0.054
107
P MNN013 Meningitis 66 0.054
108
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.054
109
P ADL010 Adult Respiratory Distress Syndrome 65 0.054
110
P NTR004 Neutropenia 63 0.054
111
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.054
112
c BRN108 Branchiootic Syndrome 1 62 0.054
113
HYP066 Hyperglycemia 61 0.054
114
P SNS001 Sensorineural Hearing Loss 60 0.054
115
THY029 Thyroid Carcinoma 59 0.054
116
CMP010 Complex Regional Pain Syndrome 58 0.054
117
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.054
118
P DRR001 Diarrhea 55 0.054
119
P SBS003 Substance Abuse 55 0.054
120
END040 Endogenous Depression 55 0.054
121
HMP005 Hemiplegia 55 0.054
122
RFL001 Reflex Sympathetic Dystrophy 54 0.054
123
P TRM003 Tremor 54 0.054
124
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.054
125
NRT001 Neurotic Disorder 53 0.054
126
PRP016 Paraplegia 52 0.054
127
P MGR003 Migraine with Aura 52 0.054
128
BHR001 Behr Syndrome 51 0.054
129
CCN001 Cocaine Dependence 48 0.054
130
SPS057 Spasticity 45 0.054
131
RTR001 Retrograde Amnesia 44 0.054
132
CRB090 Cerebral Hypoxia 44 0.054
133
PNM013 Pneumococcal Meningitis 42 0.054
134
P CLS010 Cluster Headache 42 0.054
135
ALG001 Algoneurodystrophy 39 0.054
136
HRN029 Hearing Loss, Noise-Induced 37 0.054
137
MST020 Mast Cell Activation Syndrome 26 0.054
138
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.038
139
P OVR042 Ovarian Cancer 88 0.038
140
P PRK057 Parkinson Disease, Late-Onset 78 0.038
141
GLB015 Glioblastoma Multiforme 75 0.038
142
P RSP003 Respiratory Failure 74 0.038
143
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.038
144
ANX010 Anxiety 73 0.038
145
P PHC003 Pheochromocytoma 71 0.038
146
c EXD008 Exudative Vitreoretinopathy 1 71 0.038
147
P MYC007 Myocardial Infarction 70 0.038
148
ADL002 Adult Syndrome 70 0.038
149
CNG034 Congestive Heart Failure 69 0.038
150
ACR008 Acrocallosal Syndrome 69 0.038
151
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.038
152
CRP001 Carpal Tunnel Syndrome 67 0.038
153
P PLM037 Pulmonary Hypertension 67 0.038
154
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.038
155
P ATR011 Atrial Fibrillation 66 0.038
156
CRN036 Craniopharyngioma 65 0.038
157
c FML001 Familial Atrial Fibrillation 65 0.038
158
P ART005 Arteriovenous Malformation 65 0.038
159
P MTR014 Motor Neuron Disease 65 0.038
160
CLN015 Colon Adenocarcinoma 65 0.038
161
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.038
162
P ADN016 Adenocarcinoma 64 0.038
163
LSH001 Leishmaniasis 63 0.038
164
P GLM045 Glioma 63 0.038
165
P END044 Endometriosis 63 0.038
166
c SVR001 Severe Acute Respiratory Syndrome 62 0.038
167
P VSC011 Vasculitis 62 0.038
168
ATM095 Autoimmune Disease 62 0.038
169
CRC021 Carcinosarcoma 62 0.038
170
LVR012 Liver Cirrhosis 62 0.038
171
ALC006 Alcoholic Hepatitis 61 0.038
172
INT066 Interstitial Lung Disease 60 0.038
173
LNG099 Lung Disease 60 0.038
174
c ACT071 Acute Kidney Failure 60 0.038
175
P OPT006 Optic Nerve Disease 60 0.038
176
SPN027 Spinal Stenosis 59 0.038
177
PLM033 Pulmonary Embolism 59 0.038
178
PPT005 Peptic Ulcer Disease 59 0.038
179
P BCL017 B-Cell Lymphoma 58 0.038
180
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.038
181
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.038
182
P URT039 Urticaria 58 0.038
183
NWB001 Newborn Respiratory Distress Syndrome 58 0.038
184
BRN056 Bronchopulmonary Dysplasia 57 0.038
185
MNR012 Meniere Disease 57 0.038
186
THR024 Thrombosis 57 0.038
187
APH002 Aphasia 57 0.038
188
P CRD246 Cardiovascular System Disease 57 0.038
189
P URF003 Urofacial Syndrome 1 57 0.038
190
PNM008 Pneumothorax 56 0.038
191
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.038
192
c ESS001 Essential Tremor 56 0.038
193
P PLY019 Polyneuropathy 56 0.038
194
P SCK002 Sick Sinus Syndrome 55 0.038
195
c PRG126 Progressive Familial Heart Block 55 0.038
196
P DBT005 Diabetes Insipidus 55 0.038
197
URN010 Urinary Tract Obstruction 55 0.038
198
P NRM002 Normal Pressure Hydrocephalus 54 0.038
199
TRD006 Tardive Dyskinesia 54 0.038
200
GLS001 Gliosarcoma 54 0.038
201
P ALP008 Alopecia 54 0.038
202
THR013 Thoracic Outlet Syndrome 54 0.038
203
P ART021 Arteriosclerosis 54 0.038
204
P LTR001 Lateral Sclerosis 54 0.038
205
HMS001 Hemosiderosis 54 0.038
206
P FML023 Familial Hemiplegic Migraine 53 0.038
207
GSG001 Gas Gangrene 53 0.038
208
P PNC025 Panic Disorder 53 0.038
209
APR001 Apraxia 52 0.038
210
ILS001 Ileus 51 0.038
211
SCH012 Schizoaffective Disorder 50 0.038
212
RDC002 Radiculopathy 50 0.038
213
RTN003 Retinal Ischemia 50 0.038
214
DYS073 Dysphagia 50 0.038
215
OPT003 Opiate Dependence 50 0.038
216
47X002 47,xyy 49 0.038
217
INT078 Intracranial Thrombosis 49 0.038
218
c BPL002 Bipolar I Disorder 49 0.038
219
LRN003 Learning Disability 49 0.038
220
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.038
221
URN009 Urinary System Disease 48 0.038
222
c HYD064 Hydrocephalus, Congenital, 1 48 0.038
223
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.038
224
FCL012 Facial Paralysis 46 0.038
225
P BRB001 Beriberi 46 0.038
226
ADR040 Adrenal Gland Pheochromocytoma 46 0.038
227
GLL048 Glial Tumor 45 0.038
228
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.038
229
ATN004 Autonomic Neuropathy 45 0.038
230
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.038
231
TNS014 Tenosynovitis 44 0.038
232
CVD001 Covid-19 44 0.038
233
SDD008 Sudden Sensorineural Hearing Loss 43 0.038
234
P MJR007 Major Affective Disorder 1 43 0.038
235
BCK006 Back Pain 42 0.038
236
ATX019 Ataxia with Vitamin E Deficiency 42 0.038
237
P KLZ004 Kala-Azar 1 41 0.038
238
DBT002 Diabetic Autonomic Neuropathy 41 0.038
239
P RRH023 Rare Hereditary Hemochromatosis 41 0.038
240
LWR018 Lower Urinary Tract Obstruction, Congenital 40 0.038
241
BRC011 Brachial Plexus Neuropathy 39 0.038
242
AML001 Amelanotic Melanoma 39 0.038
243
CDQ001 Cauda Equina Syndrome 38 0.038
244
CRT012 Cortical Blindness 37 0.038
245
SYS071 Systemic Autoimmune Disease 37 0.038
246
MDD003 Middle Cerebral Artery Infarction 36 0.038
247
AMR003 Amaurosis Fugax 34 0.038
248
RTN004 Retinal Microaneurysm 33 0.038
249
VRT003 Vertebrobasilar Insufficiency 30 0.038
250
PLX004 Plexopathy 30 0.038
251
RSP007 Respiratory Distress Syndrome, Infant 30 0.038
252
MNG007 Manganese Poisoning 29 0.038
253
VSD001 Vas Deferens, Congenital Bilateral Aplasia of, X-Linked 28 0.038
254
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.038
255
CCN009 Cocaine Intoxication 27 0.038
256
OGL001 Ogilvie Syndrome 24 0.038
257
NWD001 New Daily-Persistent Headache 21 0.038
258
HDC005 Headache Associated with Sexual Activity 17 0.038
259
c SCN082 Secondary Vasculitis 15 0.038
Content
Loading form....