Search results for arachidonic acid

211 hits were found for arachidonic acid

# Family MCID Name MIFTS Score
1
PRS047 Prostatitis 59 0.315
2
c BLD140 Blood Group, I System 37 0.285
3
P PRS040 Prostate Cancer 88 0.282
4
END072 Endotheliitis 46 0.280
5
P BRS047 Breast Cancer 100 0.257
6
P LKM002 Leukemia 75 0.254
7
NRN002 Neuronitis 43 0.248
8
P HPT021 Hepatitis 75 0.214
9
ISC004 Ischemia 66 0.208
10
P ADN016 Adenocarcinoma 71 0.205
11
AGN016 Aging 65 0.192
12
P NRB001 Neuroblastoma 73 0.192
13
AST005 Asthma 83 0.188
14
P DBT009 Diabetes Mellitus 72 0.188
15
P PNC044 Pancreatitis 64 0.186
16
P LNG032 Lung Cancer 99 0.181
17
P HRT032 Heart Disease 80 0.181
18
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.181
19
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.181
20
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.181
21
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.181
22
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.181
23
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.181
24
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.181
25
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.181
26
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.181
27
P ART022 Arthritis 77 0.175
28
P GLM045 Glioma 61 0.172
29
P MYC007 Myocardial Infarction 81 0.167
30
P CLR023 Colorectal Cancer 98 0.164
31
P CRN018 Coronary Artery Anomaly 69 0.161
32
P CRN300 Coronary Heart Disease 1 57 0.158
33
ART140 Arteries, Anomalies of 51 0.157
34
CRB009 Cerebritis 41 0.152
35
P SCH015 Schizophrenia 71 0.151
36
VSC007 Vascular Disease 71 0.149
37
ISC006 Ischemic Heart Disease 73 0.146
38
P ESP024 Esophagitis 64 0.143
39
P MYL006 Myeloid Leukemia 69 0.140
40
P THY032 Thyroiditis 56 0.138
41
P ART021 Arteriosclerosis 62 0.138
42
GLC008 Glucose Metabolism Disease 38 0.137
43
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.137
44
P ALZ034 Alzheimer Disease 95 0.135
45
THR024 Thrombosis 61 0.133
46
P ENC018 Encephalopathy 58 0.130
47
HYP266 Hypoxia 61 0.130
48
OST012 Osteoarthritis 88 0.127
49
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.126
50
PSY004 Psychotic Disorder 72 0.126
51
SQM006 Squamous Cell Carcinoma 74 0.125
52
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.124
53
DRM006 Dermatitis 67 0.124
54
LPD008 Lipid Metabolism Disorder 59 0.119
55
P RHM011 Rheumatoid Arthritis 91 0.119
56
BRR014 Barrett Esophagus 64 0.117
57
c CNT035 Central Nervous System Disease 65 0.117
58
HYP060 Hyperinsulinism 56 0.116
59
P LYM118 Lymphoma 71 0.115
60
MLN008 Melanoma 72 0.114
61
LNG099 Lung Disease 67 0.111
62
P INF032 Infertility 59 0.110
63
RTN023 Retinitis 52 0.109
64
P NRV007 Nervous System Disease 75 0.109
65
P BPL003 Bipolar Disorder 61 0.109
66
SPS003 Spastic Diplegia 55 0.109
67
P BLD051 Blood Coagulation Disease 38 0.108
68
PLC008 Placenta Disease 48 0.108
69
P AST007 Astrocytoma 66 0.107
70
RSP006 Respiratory System Disease 63 0.107
71
CLT003 Colitis 63 0.106
72
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.106
73
ADN018 Adenoma 63 0.106
74
P HMR003 Hemorrhagic Disease 61 0.105
75
CRB039 Cerebrovascular Disease 68 0.104
76
PRT036 Peritonitis 67 0.103
77
ACQ007 Acquired Immunodeficiency Syndrome 65 0.102
78
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.101
79
CYS001 Cystic Fibrosis 85 0.100
80
VSC008 Vascular Hemostatic Disease 36 0.100
81
CLN015 Colon Adenocarcinoma 53 0.100
82
HMN044 Human Immunodeficiency Virus Type 1 71 0.099
83
OVR063 Overnutrition 53 0.099
84
P INF038 Influenza 77 0.099
85
BRN071 Brain Injury 54 0.098
86
c TRC078 Trichohepatoenteric Syndrome 2 34 0.098
87
P PRD008 Periodontitis 67 0.098
88
P INF037 Inflammatory Bowel Disease 52 0.098
89
PHN003 Phenylketonuria 73 0.097
90
TRN015 Transient Cerebral Ischemia 58 0.096
91
P RNG031 Ring Chromosome Y Syndrome 29 0.096
92
VRL011 Viral Infectious Disease 64 0.095
93
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.094
94
ADR007 Adrenoleukodystrophy 72 0.093
95
P MLT020 Multiple Sclerosis 85 0.091
96
P PNM007 Pneumonia 70 0.091
97
P STR035 Streptococcal Group a Invasive Disease 28 0.091
98
DMN002 Dementia 68 0.089
99
TRM010 Traumatic Brain Injury 54 0.089
100
INS024 Insulin-Like Growth Factor I 83 0.088
101
P GLM007 Glomerulonephritis 61 0.088
102
P ZLL001 Zellweger Syndrome 56 0.087
103
P NMN002 Niemann-Pick Disease 68 0.087
104
CHR074 Choriocarcinoma 49 0.086
105
c LKM063 Leukemia, Chronic Myeloid 80 0.085
106
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.083
107
MCS002 Mucositis 61 0.082
108
HDC001 Headache 55 0.082
109
STR067 Stroke, Ischemic 84 0.082
110
RTN018 Retinal Disease 56 0.082
111
PRT037 Pertussis 70 0.081
112
ULC004 Ulcerative Colitis 80 0.080
113
P ATS364 Autism 70 0.080
114
AMN002 Amino Acid Metabolic Disorder 38 0.080
115
GNG013 Gingivitis 64 0.077
116
HDN002 Head Injury 48 0.077
117
P DRM053 Dermatitis, Atopic 68 0.077
118
ENC005 Encephalomalacia 36 0.077
119
ASP030 Aspirin Resistance 44 0.076
120
SPP011 Suppression of Tumorigenicity 12 41 0.076
121
PLR008 Pleurisy 52 0.075
122
PLC006 Placental Choriocarcinoma 35 0.074
123
c HPT016 Hepatitis B 68 0.074
124
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.073
125
INB001 Inborn Amino Acid Metabolism Disorder 16 0.073
126
AMN012 Aminoacidopathies 15 0.073
127
c ACT071 Acute Kidney Failure 54 0.073
128
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.072
129
HYP056 Hypoglycemia 62 0.072
130
URT039 Urticaria 59 0.072
131
P RTN024 Retinoblastoma 76 0.071
132
c ATS007 Autism Spectrum Disorder 68 0.071
133
P MSC005 Muscular Dystrophy 66 0.071
134
P FBR017 Fibrosarcoma 61 0.070
135
CLR108 Colorectal Adenoma 60 0.070
136
BRN080 Brain Ischemia 45 0.070
137
HMG005 Hemoglobinopathy 53 0.068
138
SCH014 Schistosomiasis 62 0.068
139
PRP027 Peripheral Vascular Disease 71 0.068
140
PRX034 Peroxisome Disorders 20 0.068
141
GST033 Gestational Diabetes 62 0.064
142
PRV006 Pervasive Developmental Disorder 56 0.064
143
c BLD154 Bleeding Disorder, Platelet-Type, 12 20 0.064
144
P UVT001 Uveitis 61 0.064
145
SCK003 Sickle Cell Anemia 73 0.063
146
P HYP607 Hypercholesterolemia, Familial 81 0.062
147
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.062
148
CRN027 Corneal Neovascularization 51 0.062
149
c PCH010 Pachyonychia Congenita 3 38 0.062
150
SCK005 Sickle Cell Disease 54 0.062
151
P END046 Endometritis 51 0.061
152
CRT016 Carotid Artery Disease 58 0.060
153
P FML011 Familial Adenomatous Polyposis 71 0.060
154
HMS001 Hemosiderosis 50 0.060
155
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.060
156
MNG003 Mungan Syndrome 34 0.060
157
ALL006 Allergic Asthma 60 0.059
158
MSC157 Muscular Dystrophy, Duchenne Type 74 0.058
159
P HYP726 Hypercalcemia, Infantile, 1 57 0.057
160
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.057
161
CRT013 Carotid Stenosis 52 0.057
162
CNN002 Cannabis Abuse 40 0.057
163
CHL014 Cholera 56 0.057
164
P DBT005 Diabetes Insipidus 54 0.057
165
c EXD008 Exudative Vitreoretinopathy 1 65 0.055
166
P DLT002 Dilated Cardiomyopathy 76 0.054
167
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.054
168
c SCN036 Secondary Progressive Multiple Sclerosis 52 0.054
169
ART006 Arthus Reaction 39 0.054
170
DST016 Distomatosis 23 0.054
171
MTG001 Metagonimiasis 21 0.054
172
GLC036 Glucagonoma 52 0.053
173
APL001 Aplastic Anemia 74 0.053
174
P THY109 Thyroid Cancer, Nonmedullary, 1 64 0.053
175
c WLM011 Wilms Tumor 6 44 0.053
176
VSC002 Vascular Dementia 58 0.052
177
ALL014 Allergic Encephalomyelitis 37 0.052
178
CLS049 Classic Phenylketonuria 43 0.051
179
P PHC003 Pheochromocytoma 72 0.050
180
TST014 Testicular Cancer 54 0.050
181
CRV038 Cervical Squamous Cell Carcinoma 61 0.048
182
P DNG005 Dengue Virus 56 0.048
183
HPT022 Hepatoblastoma 55 0.048
184
CRN017 Coronary Thrombosis 48 0.048
185
BRN014 Bronchopneumonia 45 0.048
186
ART008 Arteriosclerosis Obliterans 45 0.047
187
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 59 0.045
188
ONC002 Onchocerciasis 53 0.045
189
NTR046 Neutrophil Migration 51 0.045
190
DFF012 Differentiating Neuroblastoma 34 0.045
191
INT066 Interstitial Lung Disease 63 0.043
192
SDD001 Sudden Infant Death Syndrome 61 0.043
193
ACH005 Achalasia 52 0.043
194
CRB045 Cerebellar Hypoplasia 48 0.043
195
MRP001 Morphine Dependence 43 0.043
196
IMM001 Immune-Complex Glomerulonephritis 39 0.043
197
CRB004 Cerebral Artery Occlusion 46 0.041
198
IRR003 Irritant Dermatitis 45 0.041
199
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 43 0.041
200
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.039
201
MGS001 Megaesophagus 42 0.039
202
KSH001 Keshan Disease 33 0.039
203
OST006 Osteoblastoma 32 0.039
204
GRY002 Gray Platelet Syndrome 56 0.037
205
QBC001 Quebec Platelet Disorder 44 0.037
206
FCH003 Fechtner Syndrome 38 0.037
207
IMM078 Immunodeficiency 21 38 0.037
208
SBS006 Sebastian Syndrome 30 0.037
209
GHS005 Ghosal Hematodiaphyseal Dysplasia 28 0.037
210
c BLD156 Bleeding Disorder, Platelet-Type, 14 21 0.037
211
c BLD123 Bleeding Disorder, Platelet-Type, 13 20 0.037
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