Search results for Dantrolene

167 hits were found for Dantrolene

# Family MCID Name MIFTS Score
1
P MLG056 Malignant Hyperthermia 67 0.639
2
SPS057 Spasticity 45 0.354
3
NRL004 Neuroleptic Malignant Syndrome 56 0.284
4
TTN003 Tetanus 65 0.216
5
STR067 Stroke, Ischemic 81 0.185
6
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.180
7
SPN186 Spinal Cord Injury 60 0.156
8
CRB037 Cerebral Palsy 69 0.135
9
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.135
10
CRB039 Cerebrovascular Disease 67 0.135
11
P MLT020 Multiple Sclerosis 72 0.127
12
P HYP098 Hypereosinophilic Syndrome 67 0.127
13
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.127
14
BRN071 Brain Injury 49 0.127
15
P MYP004 Myopathy 70 0.119
16
P VSC007 Vascular Disease 63 0.119
17
P SZR006 Seizure Disorder 56 0.119
18
P MSC005 Muscular Dystrophy 66 0.110
19
ANR040 Aneurysm 59 0.110
20
MLG086 Malignant Hyperthermia Susceptibility 39 0.110
21
MYT011 Myotonia 34 0.110
22
INT053 Intracranial Vasospasm 24 0.110
23
P ALZ034 Alzheimer Disease 88 0.100
24
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 0.100
25
STT001 Status Epilepticus 60 0.100
26
PNG002 Pain Agnosia 51 0.100
27
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.100
28
P MYG005 Myoglobinuria 44 0.100
29
P HRT032 Heart Disease 75 0.090
30
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.090
31
P HPT021 Hepatitis 67 0.090
32
P TRN020 Turner Syndrome 67 0.090
33
P DYS154 Dystonia 65 0.090
34
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.090
35
TXC005 Toxic Shock Syndrome 62 0.090
36
VSL002 Visual Epilepsy 59 0.090
37
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.090
38
HDN002 Head Injury 46 0.090
39
HYP264 Hypertonia 38 0.090
40
MSC157 Muscular Dystrophy, Duchenne Type 72 0.078
41
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.078
42
P CRD119 Cardiac Arrest 67 0.078
43
P ATR011 Atrial Fibrillation 66 0.078
44
c DBT099 Diabetes Mellitus, Type I 65 0.078
45
P DBT009 Diabetes Mellitus 64 0.078
46
c WLF013 Wolfram Syndrome 1 60 0.078
47
P WLF004 Wolfram Syndrome 60 0.078
48
P OPT006 Optic Nerve Disease 60 0.078
49
BRD001 Brody Myopathy 57 0.078
50
HMR039 Hemorrhage, Intracerebral 57 0.078
51
P DBT005 Diabetes Insipidus 55 0.078
52
PRC013 Pericarditis 54 0.078
53
P TRM003 Tremor 54 0.078
54
PRP016 Paraplegia 52 0.078
55
PLR008 Pleurisy 50 0.078
56
MTB004 Metabolic Acidosis 50 0.078
57
P MYT002 Myotonic Dystrophy 49 0.078
58
c MLG147 Malignant Hyperthermia 1 43 0.078
59
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.078
60
EXR008 Exercise-Induced Malignant Hyperthermia 20 0.078
61
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.064
62
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.064
63
P RSP003 Respiratory Failure 74 0.064
64
P MYS003 Myasthenia Gravis 68 0.064
65
c RHB024 Rhabdomyosarcoma 2 67 0.064
66
P LNG028 Long Qt Syndrome 66 0.064
67
ISC004 Ischemia 58 0.064
68
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.064
69
P CRD246 Cardiovascular System Disease 57 0.064
70
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.064
71
P DRR001 Diarrhea 55 0.064
72
HMP005 Hemiplegia 55 0.064
73
P LTR001 Lateral Sclerosis 54 0.064
74
SPS003 Spastic Diplegia 51 0.064
75
QDR001 Quadriplegia 48 0.064
76
P MYC033 Myoclonus 46 0.064
77
P HYP265 Hypotonia 43 0.064
78
ANG049 Angioedema Induced by Ace Inhibitors 40 0.064
79
SCN049 Second-Degree Atrioventricular Block 35 0.064
80
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.064
81
MLR004 Malaria 81 0.045
82
c NRF023 Neurofibromatosis, Type Ii 80 0.045
83
c DLT002 Dilated Cardiomyopathy 79 0.045
84
c ATR087 Atrial Standstill 1 75 0.045
85
ADR007 Adrenoleukodystrophy 75 0.045
86
P HNT016 Huntington Disease 72 0.045
87
P NRB001 Neuroblastoma 72 0.045
88
OTT002 Otitis Media 72 0.045
89
P PHC003 Pheochromocytoma 71 0.045
90
c GCH015 Gaucher Disease, Type I 70 0.045
91
CNG034 Congestive Heart Failure 69 0.045
92
P LYM118 Lymphoma 68 0.045
93
P SYS005 Systemic Scleroderma 68 0.045
95
HYP056 Hypoglycemia 66 0.045
96
CHG001 Chagas Disease 66 0.045
97
P MTR014 Motor Neuron Disease 65 0.045
98
P HRP006 Herpes Simplex 65 0.045
99
PRT036 Peritonitis 64 0.045
100
NRM005 Neuromuscular Disease 64 0.045
101
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.045
102
P GCH001 Gaucher's Disease 63 0.045
103
c ACT068 Acute Cystitis 63 0.045
104
TRN015 Transient Cerebral Ischemia 63 0.045
105
c LCL006 Localized Scleroderma 62 0.045
106
P MCH002 Machado-Joseph Disease 62 0.045
107
P ENC018 Encephalopathy 61 0.045
108
P ENC004 Encephalitis 61 0.045
109
P PNC044 Pancreatitis 61 0.045
110
CNT105 Central Core Disease of Muscle 60 0.045
111
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.045
112
c ACT027 Acute Pancreatitis 60 0.045
113
CRD223 Cardiac Arrhythmia 60 0.045
114
P SNS001 Sensorineural Hearing Loss 60 0.045
115
STF001 Stiff-Person Syndrome 60 0.045
116
c ACT071 Acute Kidney Failure 60 0.045
117
P MYC008 Myocarditis 59 0.045
118
P CYS018 Cystitis 59 0.045
119
c SPN301 Spinocerebellar Ataxia 2 58 0.045
120
CRD132 Cardiac Conduction Defect 58 0.045
121
CNS004 Constipation 58 0.045
122
c ACT075 Acute Myocardial Infarction 57 0.045
123
BLR008 Bilirubin Metabolic Disorder 57 0.045
124
SPN041 Spinal Cord Disease 56 0.045
125
c MYS033 Miyoshi Muscular Dystrophy 1 56 0.045
126
P MYT023 Myotonia Congenita 56 0.045
127
NRG002 Neurogenic Bladder 55 0.045
128
P HYP076 Hyperthyroidism 55 0.045
129
P TCD001 Tic Disorder 53 0.045
130
INT075 Intracranial Hypertension 53 0.045
131
CHR073 Choreatic Disease 52 0.045
132
IMP005 Impotence 52 0.045
133
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 52 0.045
134
OCL069 Ocular Motor Apraxia 51 0.045
135
P LCT001 Lactic Acidosis 51 0.045
136
TRM010 Traumatic Brain Injury 51 0.045
137
SPN019 Spondylolisthesis 51 0.045
138
c VRL007 Viral Encephalitis 51 0.045
139
P CHL066 Cholangitis 51 0.045
140
DYS073 Dysphagia 50 0.045
141
P SPS133 Spastic Paraplegia 2, X-Linked 49 0.045
142
CCN002 Cocaine Abuse 49 0.045
143
c BPL002 Bipolar I Disorder 49 0.045
144
P CMP008 Compartment Syndrome 49 0.045
145
c MLG069 Malignant Hypertension 47 0.045
146
c INH020 Inherited Metabolic Disorder 47 0.045
147
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.045
148
ATN005 Autonomic Dysfunction 46 0.045
149
ADR040 Adrenal Gland Pheochromocytoma 46 0.045
150
HMR023 Hemorrhagic Cystitis 45 0.045
151
CRB004 Cerebral Artery Occlusion 45 0.045
152
SPS007 Spastic Cerebral Palsy 45 0.045
153
BCT021 Bacterial Sepsis 44 0.045
154
LWC001 Low Compliance Bladder 43 0.045
155
SPN050 Spinocerebellar Degeneration 42 0.045
156
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 41 0.045
157
ANX004 Anoxia 40 0.045
158
ADR022 Adrenomyeloneuropathy 38 0.045
159
DTR001 Detrusor Sphincter Dyssynergia 38 0.045
160
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.045
161
SCR039 Scorpion Envenomation 38 0.045
162
MTH086 Methotrexate Toxicity 33 0.045
163
THY001 Thyroid Crisis 31 0.045
164
DYS001 Dyskinetic Cerebral Palsy 31 0.045
165
ASC003 Ascending Cholangitis 29 0.045
166
c MLG148 Malignant Hyperthermia 2 24 0.045
167
c MLG149 Malignant Hyperthermia 3 22 0.045
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