Search results for myo-Inositol 1,4,5-trisphosphate

269 hits were found for myo-Inositol 1,4,5-trisphosphate

# Family MCID Name MIFTS Score
1
P PLY011 Polycystic Ovary Syndrome 57 19.315
2
P NRB001 Neuroblastoma 66 15.121
3
PRT037 Pertussis 49 14.551
4
c MJR022 Major Affective Disorder 8 37 11.004
5
c MJR024 Major Affective Disorder 9 40 11.004
6
P BPL003 Bipolar Disorder 56 11.004
7
P INF032 Infertility 60 8.958
8
DWN001 Down Syndrome 70 8.262
9
c TYP009 Type 2 Diabetes Mellitus 91 8.048
10
GLM045 Glioma 62 7.828
11
GLL048 Glial Tumor 51 7.812
12
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 7.587
13
DBT010 Diabetic Neuropathy 54 7.520
14
P DBT009 Diabetes Mellitus 67 6.954
15
P ALZ034 Alzheimer Disease 87 6.794
16
FTT001 Fatty Liver Disease 61 6.325
17
P GLM040 Glioma Susceptibility 1 70 6.255
18
MLG169 Malignant Astrocytoma 57 6.255
19
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 6.010
20
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 6.010
21
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 6.010
22
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 6.010
23
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 6.010
24
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 6.010
25
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 6.010
26
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 6.010
27
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 6.010
28
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 6.010
29
PPL052 Papillomatosis, Confluent and Reticulated 34 5.641
30
HYP066 Hyperglycemia 60 5.593
31
HLX001 Helix Syndrome 47 5.499
32
GLC003 Glucose Intolerance 53 5.292
33
P HNT016 Huntington Disease 73 5.210
34
CHR178 Chromosomal Triplication 33 5.184
35
c MCR133 Microvascular Complications of Diabetes 4 41 5.049
36
c MCR113 Microvascular Complications of Diabetes 3 52 5.049
37
c MCR130 Microvascular Complications of Diabetes 6 41 5.049
38
c MCR120 Microvascular Complications of Diabetes 7 47 5.049
39
CHL014 Cholera 62 4.994
40
CHG001 Chagas Disease 65 4.760
41
TTN003 Tetanus 64 4.721
42
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 4.489
43
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 4.470
44
P PRP019 Peripheral Nervous System Disease 57 4.410
45
MLD018 Mild Cognitive Impairment 48 4.377
46
GLB002 Glioblastoma 67 4.376
47
P KDN018 Kidney Disease 71 4.376
48
MNT002 Mental Depression 56 4.320
49
c DNT047 Dentinogenesis Imperfecta Type 2 35 4.277
50
P MLN007 Male Infertility 56 4.227
51
P SZR006 Seizure Disorder 69 4.137
52
P PLY014 Polycystic Kidney Disease 71 4.100
53
P BCL017 B-Cell Lymphoma 57 4.003
54
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 3.993
55
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 3.944
56
P NRP001 Neuropathy 59 3.942
57
P LNG032 Lung Cancer 98 3.925
58
P PHC003 Pheochromocytoma 70 3.921
59
ADR040 Adrenal Gland Pheochromocytoma 45 3.921
60
48X005 48,xyyy 39 3.913
61
WHP001 Whipple Disease 45 3.774
62
CHL068 Cholestasis 61 3.770
63
P MJR001 Major Depressive Disorder 68 3.734
64
P LNG064 Lung Cancer Susceptibility 3 69 3.709
65
HYP056 Hypoglycemia 65 3.598
66
P PLY019 Polyneuropathy 52 3.580
67
P PRD008 Periodontitis 63 3.503
68
HYP266 Hypoxia 56 3.501
69
P HYP086 Hypothyroidism 68 3.486
70
P MSC005 Muscular Dystrophy 66 3.462
71
MDD011 Mood Disorder 61 3.458
72
DPR016 Depression 64 3.449
73
P ATX030 Ataxia-Telangiectasia 80 3.446
74
TLN003 Telangiectasis 51 3.446
75
OST159 Osteogenic Sarcoma 66 3.370
76
MSC157 Muscular Dystrophy, Duchenne Type 78 3.275
77
OBS002 Obsessive-Compulsive Disorder 67 3.272
78
CYT002 Cytokine Deficiency 43 3.237
79
P MJR007 Major Affective Disorder 1 42 3.172
80
ORL015 Oral Squamous Cell Carcinoma 43 3.148
81
P LVR013 Liver Disease 68 3.133
82
c SML038 Small Cell Cancer of the Lung 68 2.938
83
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.924
84
STT001 Status Epilepticus 58 2.911
85
P SCH015 Schizophrenia 74 2.906
86
P FBR017 Fibrosarcoma 55 2.838
87
PTT037 Pituitary Tumors 44 2.809
88
P PNC025 Panic Disorder 52 2.770
89
P MCH002 Machado-Joseph Disease 62 2.768
90
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.722
91
P VSC007 Vascular Disease 62 2.713
92
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.712
93
CLT003 Colitis 63 2.655
94
ULC004 Ulcerative Colitis 74 2.655
95
INS024 Insulin-Like Growth Factor I 77 2.649
96
ANX010 Anxiety 70 2.612
97
P MSC003 Muscular Atrophy 52 2.587
98
P BLD134 Bladder Cancer 79 2.554
99
OLV001 Olivopontocerebellar Atrophy 50 2.542
100
ACT098 Acute Erythroid Leukemia 55 2.542
101
CRB004 Cerebral Artery Occlusion 45 2.447
102
BRN056 Bronchopulmonary Dysplasia 57 2.439
103
c ACT134 Acute Liver Failure 57 2.396
104
47X002 47,xyy 47 2.327
105
CHL065 Cholangiocarcinoma 57 2.316
106
INT079 Intrahepatic Cholangiocarcinoma 51 2.316
107
CYS001 Cystic Fibrosis 77 2.296
108
P MLT020 Multiple Sclerosis 79 2.281
109
AGN016 Aging 53 2.190
110
BRN071 Brain Injury 50 2.152
111
NNL006 Non-Alcoholic Steatohepatitis 54 2.134
112
LPD008 Lipid Metabolism Disorder 61 2.123
113
c MCR115 Microvascular Complications of Diabetes 5 65 2.100
114
TRM010 Traumatic Brain Injury 50 2.086
115
c ACT071 Acute Kidney Failure 60 2.067
116
ISC004 Ischemia 61 2.066
117
ARG004 Argyria 26 2.061
118
PRP016 Paraplegia 52 2.039
119
P FCL005 Focal Segmental Glomerulosclerosis 57 2.010
120
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.993
121
ANX004 Anoxia 40 1.993
122
c HRD010 Hereditary Spastic Paraplegia 65 1.975
123
NPH009 Nephrolithiasis 54 1.973
124
c HYP836 Hypercholesterolemia, Familial, 1 73 1.958
125
P RTN024 Retinoblastoma 72 1.927
126
ADN018 Adenoma 58 1.905
127
PRM329 Premature Aging 36 1.905
128
P TMP001 Temporal Lobe Epilepsy 49 1.881
129
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.820
130
DPH001 Diphtheria 59 1.801
131
P PRK057 Parkinson Disease, Late-Onset 79 1.796
132
BNR002 Bone Resorption Disease 47 1.795
133
THY029 Thyroid Carcinoma 55 1.788
134
TRT001 Teratocarcinoma 41 1.775
135
P BRS047 Breast Cancer 97 1.774
136
PMP014 Pemphigoid 48 1.774
137
BLL006 Bullous Pemphigoid 61 1.774
138
c SPN294 Spinocerebellar Ataxia 1 53 1.768
139
CLN015 Colon Adenocarcinoma 64 1.766
140
P EPL164 Epilepsy 70 1.690
141
P GLM007 Glomerulonephritis 59 1.690
142
IMM167 Immune Deficiency Disease 76 1.677
144
DSS032 Disease by Infectious Agent 55 1.671
145
c KNN009 Kenny-Caffey Syndrome, Type 1 35 1.666
146
SVR004 Severe Combined Immunodeficiency 70 1.666
147
P MYL006 Myeloid Leukemia 60 1.666
148
P KLZ004 Kala-Azar 1 41 1.661
149
LSH001 Leishmaniasis 63 1.661
150
PNC129 Pancreatic Adenocarcinoma 64 1.653
151
CHL123 Chlamydia 58 1.639
152
c TBR025 Tuberous Sclerosis 1 84 1.599
153
P AGM001 Agammaglobulinemia 67 1.598
154
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.595
155
P PNC035 Pancreatic Cancer 87 1.595
156
ALL014 Allergic Encephalomyelitis 34 1.594
157
PRT251 Proteinuria, Chronic Benign 58 1.573
158
SQM006 Squamous Cell Carcinoma 59 1.538
159
ATS010 Autosomal Recessive Disease 42 1.526
160
TRY001 Trypanosomiasis 50 1.526
161
LNG039 Lung Squamous Cell Carcinoma 57 1.526
162
ATN005 Autonomic Dysfunction 45 1.526
163
P TRM003 Tremor 50 1.526
164
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.523
165
P LTR001 Lateral Sclerosis 57 1.523
166
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.509
167
IMP005 Impotence 52 1.509
168
MST004 Mast Cell Neoplasm 41 1.509
169
EXT007 Extracutaneous Mastocytoma 38 1.509
170
AMN003 Amnestic Disorder 53 1.509
171
PNG002 Pain Agnosia 51 1.469
172
ADS004 Aids Dementia Complex 39 1.424
173
P CLR023 Colorectal Cancer 100 1.396
174
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.380
175
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.307
176
P RHB003 Rhabdomyosarcoma 66 1.307
177
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 1.294
178
P ANR048 Aniridia 1 66 1.239
179
CRH001 Crohn's Disease 80 1.239
180
LVR012 Liver Cirrhosis 62 1.221
181
c ATS007 Autism Spectrum Disorder 71 0.989
182
P VSC011 Vasculitis 61 0.986
183
ALC007 Alcohol Dependence 65 0.985
184
CHR177 Chromophobe Renal Cell Carcinoma 54 0.927
185
P ATS364 Autism 72 0.873
186
P PLM037 Pulmonary Hypertension 69 0.787
187
P HYP265 Hypotonia 42 0.783
188
CRT015 Carotid Artery Occlusion 45 0.745
189
ATM095 Autoimmune Disease 61 0.736
190
P SLP006 Sleep Apnea 69 0.726
191
P TBR001 Tuberous Sclerosis 69 0.726
192
P MYP004 Myopathy 67 0.726
193
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.703
194
c HYP595 Hypertension, Essential 84 0.703
195
PST028 Post-Traumatic Stress Disorder 58 0.683
196
c PRC016 Pre-Eclampsia 64 0.683
197
P DMN002 Dementia 65 0.683
198
P MLN008 Melanoma 75 0.683
199
c HPT001 Hepatitis C 61 0.658
200
ORL011 Oral Cancer 60 0.657
201
ALX003 Alexander Disease 61 0.648
202
P HPT021 Hepatitis 68 0.622
203
ANR040 Aneurysm 60 0.611
204
SPN186 Spinal Cord Injury 60 0.611
205
P AST005 Asthma 75 0.610
206
P HRT032 Heart Disease 84 0.610
207
PRT013 Portal Hypertension 59 0.610
208
P ADN016 Adenocarcinoma 63 0.606
209
P SPP010 Suppressor of Tumorigenicity 3 50 0.569
210
PRS129 Prostatic Hyperplasia, Benign 48 0.569
211
P FTL001 Fetal Alcohol Syndrome 55 0.569
212
PRS021 Prostatic Adenoma 43 0.569
213
PLM010 Pulmonary Edema 54 0.569
214
PRS045 Prostatic Hypertrophy 53 0.569
215
P OVR042 Ovarian Cancer 88 0.554
216
P PRS040 Prostate Cancer 95 0.554
217
PLY150 Polykaryocytosis Inducer 29 0.554
218
P CHL066 Cholangitis 51 0.554
219
P OVR082 Overgrowth Syndrome 41 0.554
220
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 0.549
221
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.549
222
P HYP069 Hyperparathyroidism 62 0.549
223
P LKM002 Leukemia 65 0.549
224
PRM236 Primary Biliary Cholangitis 62 0.549
225
P CHR071 Charcot-Marie-Tooth Disease 64 0.549
226
P GCH001 Gaucher's Disease 69 0.521
227
P DRR001 Diarrhea 55 0.521
228
P SBS003 Substance Abuse 54 0.521
229
LNG099 Lung Disease 62 0.521
230
c HNT011 Huntington Disease-Like 3 33 0.481
231
P FRG001 Fragile X Syndrome 70 0.481
232
SKN016 Skin Disease 63 0.481
233
P AMY004 Amyloidosis 69 0.481
234
P RTT002 Rett Syndrome 79 0.465
235
THR024 Thrombosis 56 0.465
236
P BNG032 Benign Mesothelioma 53 0.465
237
CRV038 Cervical Squamous Cell Carcinoma 56 0.465
238
P EYD002 Eye Disease 57 0.465
239
END041 Endometrial Adenocarcinoma 63 0.465
240
LRN003 Learning Disability 49 0.465
241
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.465
242
c LKM005 Leukemia, T-Cell, Chronic 33 0.465
243
IRR002 Irritable Bowel Syndrome 64 0.465
244
P FML023 Familial Hemiplegic Migraine 53 0.392
245
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.392
246
ATH013 Atherosclerosis Susceptibility 63 0.392
247
AGM019 Agammaglobulinemia, X-Linked 71 0.392
248
c CHL119 Cholangitis, Primary Sclerosing 57 0.392
249
P MYC007 Myocardial Infarction 69 0.392
250
END057 Endometrial Cancer 76 0.392
251
CMB007 Combined Immunodeficiency 56 0.392
252
P SPN046 Spinal Muscular Atrophy 62 0.392
253
CNG034 Congestive Heart Failure 69 0.392
254
P SCL009 Sclerosing Cholangitis 46 0.392
255
P ANT006 Antiphospholipid Syndrome 55 0.392
256
P KDN017 Kidney Cancer 60 0.392
257
CNS004 Constipation 56 0.392
258
MNN009 Meningoencephalitis 47 0.392
259
LMY002 Leiomyoma 51 0.392
260
SCH014 Schistosomiasis 56 0.392
261
P CRD246 Cardiovascular System Disease 55 0.392
262
OVR059 Ovary Adenocarcinoma 49 0.392
263
GST040 Gastric Adenocarcinoma 66 0.392
264
HPT022 Hepatoblastoma 54 0.392
265
PTH003 Pathologic Nystagmus 52 0.392
266
P HRP006 Herpes Simplex 65 0.392
267
CHL078 Childhood-Onset Schizophrenia 29 0.392
268
RYN005 Raynaud Phenomenon 45 0.392
269
CRB090 Cerebral Hypoxia 42 0.392
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