Search results for Inositol 1,4,5-trisphosphate

137 hits were found for Inositol 1,4,5-trisphosphate

# Family MCID Name MIFTS Score
1
PRT037 Pertussis 65 0.491
2
P NRB001 Neuroblastoma 72 0.391
3
P BPL003 Bipolar Disorder 56 0.225
4
c MJR024 Major Affective Disorder 9 41 0.225
5
c MJR022 Major Affective Disorder 8 38 0.225
6
P GLM045 Glioma 63 0.222
7
GLL048 Glial Tumor 45 0.220
8
CHL014 Cholera 59 0.210
9
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.205
10
P HNT016 Huntington Disease 72 0.174
11
INS001 Insulinoma 60 0.155
12
P PHC003 Pheochromocytoma 71 0.153
13
ADR040 Adrenal Gland Pheochromocytoma 46 0.153
14
P ALZ034 Alzheimer Disease 88 0.147
15
P INF032 Infertility 57 0.146
16
HLX001 Helix Syndrome 47 0.145
17
P AST007 Astrocytoma 51 0.145
18
P CLR023 Colorectal Cancer 99 0.141
19
OST159 Osteogenic Sarcoma 66 0.140
20
FTT001 Fatty Liver Disease 61 0.138
21
PPL052 Papillomatosis, Confluent and Reticulated 33 0.137
22
CHG001 Chagas Disease 66 0.137
23
HYP066 Hyperglycemia 61 0.137
24
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.133
25
CHL068 Cholestasis 61 0.131
26
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.130
27
P MLG056 Malignant Hyperthermia 67 0.125
28
DWN001 Down Syndrome 70 0.120
29
P MSC005 Muscular Dystrophy 66 0.120
30
P PLY014 Polycystic Kidney Disease 62 0.120
31
c KNN009 Kenny-Caffey Syndrome, Type 1 34 0.118
32
GLC003 Glucose Intolerance 54 0.116
33
MSC157 Muscular Dystrophy, Duchenne Type 72 0.116
34
ERY051 Erythroleukemia, Familial 56 0.113
35
GLB015 Glioblastoma Multiforme 75 0.110
36
P KDN018 Kidney Disease 72 0.110
37
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.109
38
VSL002 Visual Epilepsy 59 0.108
39
P NRP001 Neuropathy 56 0.108
40
P SZR006 Seizure Disorder 56 0.108
41
P BRS047 Breast Cancer 97 0.107
42
TTN003 Tetanus 65 0.106
43
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.104
44
P LVR013 Liver Disease 68 0.103
45
INS024 Insulin-Like Growth Factor I 79 0.101
46
c ACT027 Acute Pancreatitis 60 0.099
47
c SPN290 Spinocerebellar Ataxia 15 40 0.099
48
P BCL017 B-Cell Lymphoma 58 0.099
49
CHR178 Chromosomal Triplication 35 0.099
50
48X005 48,xyyy 39 0.092
51
P MCH002 Machado-Joseph Disease 62 0.090
52
P OLV001 Olivopontocerebellar Atrophy 51 0.090
53
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.088
54
SQM006 Squamous Cell Carcinoma 60 0.088
55
ADN018 Adenoma 59 0.088
56
CYT002 Cytokine Deficiency 42 0.088
57
P OVR042 Ovarian Cancer 88 0.085
58
LVR012 Liver Cirrhosis 62 0.085
59
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.085
60
P LKM071 Leukemia, Chronic Lymphocytic 79 0.084
61
PTT037 Pituitary Tumors 44 0.081
62
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.081
63
CHL065 Cholangiocarcinoma 68 0.079
64
INT079 Intrahepatic Cholangiocarcinoma 51 0.079
65
c LKM061 Leukemia, Acute Myeloid 84 0.078
66
P BLD134 Bladder Cancer 79 0.078
67
P AGM001 Agammaglobulinemia 65 0.078
68
47X002 47,xyy 49 0.078
69
SVR004 Severe Combined Immunodeficiency 73 0.074
70
P PRP019 Peripheral Nervous System Disease 58 0.074
71
P FBR017 Fibrosarcoma 56 0.074
72
ORL015 Oral Squamous Cell Carcinoma 43 0.074
73
c CHL142 Cholestasis, Intrahepatic, of Pregnancy 3 38 0.074
74
P HRT032 Heart Disease 75 0.073
75
CNT061 Conotruncal Heart Malformations 63 0.073
76
c SCL052 Scleroderma, Familial Progressive 61 0.073
77
ARG004 Argyria 27 0.073
78
CLN015 Colon Adenocarcinoma 65 0.070
79
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.070
80
BCT022 Bacterial Infectious Disease 56 0.070
81
P PLY019 Polyneuropathy 56 0.070
82
NNL006 Non-Alcoholic Steatohepatitis 54 0.070
83
HPT014 Hepatorenal Syndrome 50 0.070
84
P LYM118 Lymphoma 68 0.065
85
ALC007 Alcohol Dependence 66 0.065
86
c BRN108 Branchiootic Syndrome 1 62 0.065
87
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.065
88
P MYL006 Myeloid Leukemia 60 0.065
89
DPH001 Diphtheria 60 0.065
90
P DRR001 Diarrhea 55 0.065
91
P GST053 Gastric Cancer 83 0.059
92
P GLM040 Glioma Susceptibility 1 81 0.059
93
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.059
94
BRK010 Burkitt Lymphoma 67 0.059
95
BLL006 Bullous Pemphigoid 62 0.059
96
P PMP001 Pemphigus 54 0.059
97
AMN003 Amnestic Disorder 54 0.059
98
P MSC003 Muscular Atrophy 52 0.059
99
c SPN101 Spinocerebellar Ataxia 29 42 0.059
100
ANX004 Anoxia 40 0.059
101
EPD052 Epidermolysis Bullosa Simplex Superficialis 24 0.059
102
c DLT002 Dilated Cardiomyopathy 79 0.052
103
P PRK057 Parkinson Disease, Late-Onset 78 0.052
104
c ATR087 Atrial Standstill 1 75 0.052
105
P TTR001 Tetralogy of Fallot 70 0.052
106
CNG034 Congestive Heart Failure 69 0.052
107
CMM004 Common Variable Immunodeficiency 68 0.052
108
CNN005 Connective Tissue Disease 68 0.052
109
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.052
110
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.052
111
c HRD010 Hereditary Spastic Paraplegia 66 0.052
112
P KLL001 Kallmann Syndrome 61 0.052
113
ALC006 Alcoholic Hepatitis 61 0.052
114
P ACH003 Achromatopsia 61 0.052
115
P PNC044 Pancreatitis 61 0.052
116
P MYC008 Myocarditis 59 0.052
117
CHL123 Chlamydia 59 0.052
118
P GLL022 Guillain-Barre Syndrome 59 0.052
119
EMB004 Embryonal Carcinoma 56 0.052
120
CLR030 Clear Cell Renal Cell Carcinoma 53 0.052
121
CHR073 Choreatic Disease 52 0.052
122
PRP016 Paraplegia 52 0.052
123
IMP005 Impotence 52 0.052
124
HYP025 Hyperphosphatemia 48 0.052
125
DRG003 Drug Dependence 47 0.052
126
ANH002 Anhidrosis 47 0.052
127
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.052
128
c MLG147 Malignant Hyperthermia 1 43 0.052
129
MST004 Mast Cell Neoplasm 42 0.052
130
SPN050 Spinocerebellar Degeneration 42 0.052
131
ADS004 Aids Dementia Complex 40 0.052
132
EXT007 Extracutaneous Mastocytoma 38 0.052
133
ATX023 Ataxia, Sensory, 1, Autosomal Dominant 38 0.052
134
P FML187 Familial Hypertension 37 0.052
135
P CRB059 Cerebellar Degeneration 37 0.052
136
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 33 0.052
137
c RNL034 Renal Cell Carcinoma 4 16 0.052
Content
Loading form....