Search results for Miglustat hydrochloride

132 hits were found for Miglustat hydrochloride

# Family MCID Name MIFTS Score
1
P NMN002 Niemann-Pick Disease 60 10.921
2
P GCH001 Gaucher's Disease 69 10.288
3
ADL002 Adult Syndrome 69 10.279
4
c NMN015 Niemann-Pick Disease, Type C1 68 10.006
5
P DRR001 Diarrhea 55 8.539
6
AGN016 Aging 54 8.317
7
CYS001 Cystic Fibrosis 77 7.794
8
P ANR048 Aniridia 1 66 7.753
9
P TRN020 Turner Syndrome 67 7.294
10
P TRM003 Tremor 50 7.230
11
RHB024 Rhabdomyosarcoma 2 65 7.221
12
48X005 48,xyyy 39 6.903
13
P DMN002 Dementia 65 6.726
14
P NRP001 Neuropathy 59 6.710
15
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 6.487
16
P PRK039 Parkinsonism 55 6.250
17
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 6.225
18
P PRP019 Peripheral Nervous System Disease 57 5.511
19
P SZR006 Seizure Disorder 69 5.472
20
P NTR004 Neutropenia 62 5.390
21
LYS002 Lysosomal Storage Disease 51 5.330
22
DYS073 Dysphagia 53 5.254
23
SPS057 Spasticity 43 5.090
24
AND005 Androgen Insensitivity Syndrome, Mild 21 4.936
25
ALL029 Allergic Disease 61 4.910
26
ANT039 Antisynthetase Syndrome 55 4.902
27
P ALZ034 Alzheimer Disease 87 4.860
28
P KHL003 Kohlschutter-Tonz Syndrome 57 4.551
29
P BND020 Bone Disease 60 4.439
30
HMN044 Human Immunodeficiency Virus Type 1 76 4.436
31
ACQ007 Acquired Immunodeficiency Syndrome 58 4.265
32
P PRK057 Parkinson Disease, Late-Onset 79 3.976
33
P TYS001 Tay-Sachs Disease 69 3.966
34
P NRB001 Neuroblastoma 66 3.924
35
CRH001 Crohn's Disease 80 3.820
36
P DYS154 Dystonia 64 3.816
37
P EPL164 Epilepsy 70 3.813
38
APH002 Aphasia 55 3.787
39
SPL018 Splenomegaly 47 3.668
40
c MCL013 Mucolipidosis Iv 64 3.495
41
P PTS002 Ptosis 52 3.494
42
HMN014 Human Immunodeficiency Virus Infectious Disease 54 3.385
43
P LVR013 Liver Disease 68 3.335
44
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 3.326
45
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 52 3.294
46
P NRC002 Narcolepsy 55 3.212
47
SBC016 Subacute Delirium 42 3.211
48
ATS010 Autosomal Recessive Disease 42 3.164
49
c HPT003 Hepatitis a 63 3.144
50
FRN006 Frontotemporal Dementia 68 3.140
51
c DRR009 Diarrhea 6 46 3.133
52
P ALC033 Alcohol Use Disorder 67 3.122
53
P NRV007 Nervous System Disease 66 3.008
54
P CRD119 Cardiac Arrest 68 2.977
55
ERL001 Early Myoclonic Encephalopathy 63 2.961
56
SVR001 Severe Acute Respiratory Syndrome 68 2.917
57
47X002 47,xyy 48 2.884
58
PCK003 Pick Disease of Brain 69 2.838
59
P BPL003 Bipolar Disorder 56 2.807
60
IMM167 Immune Deficiency Disease 77 2.805
61
c DYS119 Dystonia 9 54 2.766
62
MDD011 Mood Disorder 62 2.688
63
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 2.629
64
PRP016 Paraplegia 52 2.551
65
CVD001 Covid-19 58 2.516
66
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.485
67
ASP007 Aspiration Pneumonia 49 2.478
68
P VSC011 Vasculitis 61 2.449
69
P HYP265 Hypotonia 42 2.440
70
c GLY008 Glycogen Storage Disease Ii 72 2.373
71
P INF032 Infertility 60 2.251
72
FBR012 Fabry Disease 71 2.238
73
PRS063 Paresthesia 39 2.222
74
c MJR024 Major Affective Disorder 9 40 2.219
75
c MJR022 Major Affective Disorder 8 37 2.219
76
P THR014 Thrombocytopenia 66 2.191
77
P SLP005 Sleep Disorder 62 2.042
78
BNR002 Bone Resorption Disease 47 2.031
79
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 2.016
80
P GLY013 Glycogen Storage Disease 59 2.005
81
c INH020 Inherited Metabolic Disorder 47 1.987
82
P MSC003 Muscular Atrophy 52 1.964
84
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 1.922
86
P MVM001 Movement Disease 61 1.911
87
NNT012 Neonatal Jaundice 53 1.851
88
SPS019 Spastic Paraparesis 38 1.805
89
PNC001 Pancytopenia 52 1.769
90
SCH036 Scheie Syndrome 73 1.769
91
P MYT002 Myotonic Dystrophy 51 1.735
92
CHL068 Cholestasis 61 1.724
93
KRN002 Kearns-Sayre Syndrome 63 1.619
94
P MYP004 Myopathy 67 1.611
95
P HYP061 Hypertrophic Cardiomyopathy 69 1.610
96
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 1.541
97
CHR073 Choreatic Disease 53 1.541
98
BRN014 Bronchopneumonia 52 1.539
99
PRR013 Prurigo Nodularis 37 1.521
100
P SPN046 Spinal Muscular Atrophy 62 1.448
101
c DRR018 Diarrhea 9 25 1.398
102
ATM095 Autoimmune Disease 61 1.386
103
PTH003 Pathologic Nystagmus 52 1.304
104
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 1.281
105
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.223
106
P DNG005 Dengue Virus 55 1.213
107
P PLY014 Polycystic Kidney Disease 71 1.166
108
TNG002 Tangier Disease 64 1.148
109
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 1.125
110
CRB037 Cerebral Palsy 67 1.117
111
c HRD202 Hereditary Lymphedema I 55 1.083
112
P HYP263 Hypersomnia 40 1.065
113
IDP031 Idiopathic Hypersomnia 39 0.988
114
PHN003 Phenylketonuria 76 0.965
115
P HML001 Hemolytic-Uremic Syndrome 52 0.958
116
P CRB088 Cerebral Atrophy 33 0.948
117
ALL014 Allergic Encephalomyelitis 34 0.875
118
P SCL018 Scoliosis 57 0.848
119
c VRL010 Viral Hepatitis 52 0.789
120
P MYC033 Myoclonus 46 0.757
121
P AGN002 Agnosia 53 0.566
122
DSS009 Disseminated Intravascular Coagulation 56 0.514
123
EBL001 Ebola Hemorrhagic Fever 56 0.507
124
c CNT035 Central Nervous System Disease 53 0.505
125
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.475
126
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.395
127
OST003 Osteonecrosis 61 0.361
128
CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 29 0.349
129
TYP007 Typhoid Fever 63 0.334
130
INT042 Internuclear Ophthalmoplegia 32 0.255
131
MTC005 Mitochondrial Metabolism Disease 45 0.255
132
P GLC113 Galactosemia I 65 0.223
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