Search results for Riluzole

238 hits were found for Riluzole

# Family MCID Name MIFTS Score
1
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.664
2
P LTR001 Lateral Sclerosis 53 0.662
3
P MTR014 Motor Neuron Disease 64 0.310
4
INT002 Intermittent Claudication 61 0.300
5
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.297
6
SPN186 Spinal Cord Injury 60 0.280
7
DPR016 Depression 63 0.223
8
MNT002 Mental Depression 57 0.219
9
OBS002 Obsessive-Compulsive Disorder 68 0.196
10
P HNT016 Huntington Disease 71 0.188
11
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.188
12
P MJR001 Major Depressive Disorder 68 0.170
13
ACR006 Aceruloplasminemia 73 0.165
14
ANX010 Anxiety 72 0.160
15
P CNR004 Cone-Rod Dystrophy 2 71 0.150
16
P BPL003 Bipolar Disorder 56 0.144
17
P ATS364 Autism 65 0.139
18
MDD011 Mood Disorder 62 0.139
19
c MJR024 Major Affective Disorder 9 41 0.139
20
c MJR022 Major Affective Disorder 8 38 0.139
21
ISC004 Ischemia 60 0.133
22
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.133
23
END040 Endogenous Depression 54 0.133
24
c ATS007 Autism Spectrum Disorder 67 0.127
25
NRT001 Neurotic Disorder 52 0.127
26
P MSC003 Muscular Atrophy 52 0.127
27
SPS057 Spasticity 41 0.127
28
MLT157 Multiple System Atrophy 1 70 0.120
29
P SPN046 Spinal Muscular Atrophy 64 0.120
30
DYS073 Dysphagia 50 0.120
31
SPN050 Spinocerebellar Degeneration 41 0.120
32
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.113
33
MLN008 Melanoma 69 0.113
34
PRT037 Pertussis 65 0.113
35
NRM005 Neuromuscular Disease 63 0.113
36
P MCH002 Machado-Joseph Disease 63 0.113
37
P PRV006 Pervasive Developmental Disorder 57 0.113
38
P MJR007 Major Affective Disorder 1 43 0.113
39
c MJR008 Major Affective Disorder 2 34 0.113
40
c MJR003 Major Affective Disorder 6 33 0.113
41
c MJR006 Major Affective Disorder 5 33 0.113
42
c MJR023 Major Affective Disorder 7 33 0.113
43
c MJR004 Major Affective Disorder 4 28 0.113
44
P ALZ034 Alzheimer Disease 88 0.106
45
P MLT020 Multiple Sclerosis 72 0.106
46
SKN019 Skin Melanoma 67 0.106
47
P PRS038 Personality Disorder 65 0.106
48
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.106
49
ALL026 Allergic Hypersensitivity Disease 64 0.106
50
c PRM015 Primary Cerebellar Degeneration 36 0.106
51
SPN187 Spinocerebellar Atrophy 26 0.106
52
P PRK057 Parkinson Disease, Late-Onset 76 0.098
53
P RSP003 Respiratory Failure 74 0.098
54
P DMN002 Dementia 67 0.098
55
PST028 Post-Traumatic Stress Disorder 58 0.098
56
P PRP019 Peripheral Nervous System Disease 57 0.098
57
P NRP001 Neuropathy 56 0.098
58
P TRM003 Tremor 53 0.098
59
ACT084 Acute Stress Disorder 48 0.098
60
OBS003 Obsessive-Compulsive Personality Disorder 44 0.098
61
CHL079 Children's Interstitial Lung Disease 27 0.098
62
P NRB001 Neuroblastoma 71 0.090
63
PSY004 Psychotic Disorder 67 0.090
64
KHL003 Kohlschutter-Tonz Syndrome 64 0.090
65
GNR004 Generalized Anxiety Disorder 56 0.090
66
BRN004 Brain Edema 55 0.090
67
HYP005 Hypokalemia 55 0.090
68
c SPN291 Spinocerebellar Ataxia 7 53 0.090
69
c SPN294 Spinocerebellar Ataxia 1 52 0.090
70
48X005 48,xyyy 39 0.090
71
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.090
72
P BRS047 Breast Cancer 96 0.080
73
P SCH015 Schizophrenia 75 0.080
74
GLB015 Glioblastoma Multiforme 75 0.080
75
P FRG001 Fragile X Syndrome 68 0.080
76
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.080
77
GLL008 Gilles De La Tourette Syndrome 66 0.080
78
P TRN020 Turner Syndrome 65 0.080
79
P DYS154 Dystonia 65 0.080
80
P GLM045 Glioma 63 0.080
81
P NTR004 Neutropenia 63 0.080
82
P PNC044 Pancreatitis 61 0.080
83
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.080
84
c ACT027 Acute Pancreatitis 59 0.080
85
DSS008 Disease of Mental Health 57 0.080
86
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.080
87
BRN071 Brain Injury 49 0.080
88
SCL003 Social Phobia 48 0.080
89
c HRD026 Hereditary Ataxia 48 0.080
90
GLL048 Glial Tumor 45 0.080
91
CRB004 Cerebral Artery Occlusion 44 0.080
92
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.080
93
MNG007 Manganese Poisoning 29 0.080
94
P CLR023 Colorectal Cancer 98 0.069
95
CYS001 Cystic Fibrosis 80 0.069
96
P RHM011 Rheumatoid Arthritis 80 0.069
97
AST005 Asthma 77 0.069
98
HMN044 Human Immunodeficiency Virus Type 1 71 0.069
99
P ART022 Arthritis 70 0.069
100
P OCL013 Oculodentodigital Dysplasia 69 0.069
101
P LYM118 Lymphoma 68 0.069
102
P LKM002 Leukemia 66 0.069
103
OST159 Osteogenic Sarcoma 66 0.069
104
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.069
105
P NRV007 Nervous System Disease 66 0.069
106
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.069
107
P FRD001 Friedreich Ataxia 63 0.069
108
PPL049 Papillon-Lefevre Syndrome 63 0.069
109
P DRM010 Dermatomyositis 61 0.069
110
P MVM001 Movement Disease 61 0.069
111
ACQ007 Acquired Immunodeficiency Syndrome 60 0.069
112
P SPN309 Spinocerebellar Ataxia 6 59 0.069
113
c SPN301 Spinocerebellar Ataxia 2 59 0.069
114
P BCL017 B-Cell Lymphoma 58 0.069
115
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.069
116
DNT005 Dentatorubral-Pallidoluysian Atrophy 57 0.069
117
SPN041 Spinal Cord Disease 56 0.069
118
AGN016 Aging 56 0.069
119
P TCD001 Tic Disorder 54 0.069
120
PRP016 Paraplegia 53 0.069
121
TRM010 Traumatic Brain Injury 53 0.069
122
CHR073 Choreatic Disease 52 0.069
123
P OLV001 Olivopontocerebellar Atrophy 52 0.069
124
c SPN296 Spinocerebellar Ataxia 17 50 0.069
125
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.069
126
SKN013 Skin Benign Neoplasm 49 0.069
127
P ASP001 Asperger Syndrome 48 0.069
128
ATX019 Ataxia with Vitamin E Deficiency 48 0.069
129
LYM019 Lymphosarcoma 47 0.069
130
c SPN395 Spinal Muscular Atrophy, Type Ii 46 0.069
131
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.069
132
CRB027 Cerebellar Disease 45 0.069
133
MRG013 Mirage Syndrome 44 0.069
134
PRS063 Paresthesia 43 0.069
135
c CHR682 Chronic Bilirubin Encephalopathy 38 0.069
136
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 37 0.069
137
CLS047 Classic Progressive Supranuclear Palsy Syndrome 30 0.069
138
ADG002 Audiogenic Seizures 26 0.069
139
DWN001 Down Syndrome 70 0.057
140
ADL002 Adult Syndrome 69 0.057
141
P HPT021 Hepatitis 67 0.057
142
P MCR115 Microvascular Complications of Diabetes 5 66 0.057
143
c RHB024 Rhabdomyosarcoma 2 65 0.057
144
IRR002 Irritable Bowel Syndrome 63 0.057
145
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 63 0.057
146
NTR005 Nutritional Deficiency Disease 61 0.057
147
P SZR006 Seizure Disorder 58 0.057
148
VSL002 Visual Epilepsy 58 0.057
149
P DRR001 Diarrhea 57 0.057
150
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.057
151
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.057
152
CHL014 Cholera 55 0.057
153
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.057
154
AMN003 Amnestic Disorder 54 0.057
155
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 52 0.057
156
c PRM108 Primary Progressive Multiple Sclerosis 51 0.057
157
TRC010 Trichotillomania 50 0.057
158
P MTH007 Methemoglobinemia 46 0.057
159
c PRG001 Progressive Muscular Atrophy 42 0.057
160
P STR001 Striatonigral Degeneration 38 0.057
161
P HPT023 Hepatocellular Carcinoma 100 0.040
163
MYL069 Myeloma, Multiple 85 0.040
164
P PNC035 Pancreatic Cancer 84 0.040
165
P RTT002 Rett Syndrome 80 0.040
166
INS024 Insulin-Like Growth Factor I 79 0.040
167
P PHC003 Pheochromocytoma 71 0.040
168
CNT097 Central Hypoventilation Syndrome, Congenital 70 0.040
169
c EXD008 Exudative Vitreoretinopathy 1 69 0.040
170
P PNM007 Pneumonia 68 0.040
171
P CRD119 Cardiac Arrest 67 0.040
172
ALC007 Alcohol Dependence 66 0.040
173
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.040
174
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.040
175
HYP056 Hypoglycemia 66 0.040
176
c MCR129 Microvascular Complications of Diabetes 1 66 0.040
177
CRB011 Cerebrotendinous Xanthomatosis 63 0.040
178
DGR001 Digeorge Syndrome 63 0.040
179
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.040
180
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.040
181
P VSC011 Vasculitis 62 0.040
182
P ENC018 Encephalopathy 61 0.040
183
c PNS012 Paine Syndrome 61 0.040
184
LNG099 Lung Disease 61 0.040
185
P SCL018 Scoliosis 60 0.040
186
INT066 Interstitial Lung Disease 59 0.040
187
THY029 Thyroid Carcinoma 59 0.040
188
STT001 Status Epilepticus 59 0.040
189
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.040
190
EXT034 Extrinsic Allergic Alveolitis 58 0.040
191
CNS004 Constipation 57 0.040
192
BLR008 Bilirubin Metabolic Disorder 57 0.040
193
P BNC003 Bone Cancer 57 0.040
194
P EXN002 Exanthem 57 0.040
195
c ESS001 Essential Tremor 56 0.040
196
ERY051 Erythroleukemia, Familial 56 0.040
197
c ACT075 Acute Myocardial Infarction 56 0.040
198
c SPS153 Spastic Paraplegia 35, Autosomal Recessive 56 0.040
199
P SBS003 Substance Abuse 54 0.040
200
GLS001 Gliosarcoma 54 0.040
201
PRX015 Paroxysmal Extreme Pain Disorder 53 0.040
202
SNS003 Sensory Peripheral Neuropathy 53 0.040
203
c SPN393 Spinal Muscular Atrophy, Type I 53 0.040
204
BRD004 Borderline Personality Disorder 53 0.040
205
RTN003 Retinal Ischemia 50 0.040
206
P TMP001 Temporal Lobe Epilepsy 50 0.040
207
P AST007 Astrocytoma 50 0.040
208
PRT018 Portal Vein Thrombosis 50 0.040
209
P CHR345 Chronic Pain 50 0.040
210
47X002 47,xyy 49 0.040
211
XNT003 Xanthomatosis 49 0.040
212
RDC002 Radiculopathy 48 0.040
213
CCN001 Cocaine Dependence 48 0.040
214
ASP007 Aspiration Pneumonia 48 0.040
215
FCL012 Facial Paralysis 48 0.040
216
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.040
217
c RCR022 Recurrent Acute Pancreatitis 47 0.040
218
P ERY008 Erythromelalgia 47 0.040
219
P KRN004 Kernicterus 47 0.040
220
CHR074 Choriocarcinoma 46 0.040
221
ADR040 Adrenal Gland Pheochromocytoma 46 0.040
222
P MYC033 Myoclonus 46 0.040
223
CRV043 Cervical Dystonia 45 0.040
224
GRN017 Granulocytopenia 44 0.040
225
CYT002 Cytokine Deficiency 44 0.040
226
ANX004 Anoxia 42 0.040
227
MRP001 Morphine Dependence 41 0.040
228
c MCR112 Microvascular Complications of Diabetes 2 41 0.040
229
ALL014 Allergic Encephalomyelitis 39 0.040
230
HRN029 Hearing Loss, Noise-Induced 37 0.040
231
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.040
232
PLC006 Placental Choriocarcinoma 36 0.040
233
MYT011 Myotonia 35 0.040
234
BRC010 Brachial Plexus Lesion 32 0.040
235
MLT116 Multiple System Atrophy, Parkinsonian Type 31 0.040
236
ARG004 Argyria 28 0.040
237
SHK001 Shaken Baby Syndrome 23 0.040
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