Search results for Guanosine monophosphate

266 hits were found for Guanosine monophosphate

# Family MCID Name MIFTS Score
1
CHL014 Cholera 59 0.408
2
PRT037 Pertussis 65 0.377
3
P NRB001 Neuroblastoma 72 0.271
4
IMP005 Impotence 52 0.187
5
P HRP006 Herpes Simplex 65 0.186
6
CNG034 Congestive Heart Failure 69 0.185
7
HLX001 Helix Syndrome 47 0.182
8
GLL048 Glial Tumor 45 0.168
9
P PLM037 Pulmonary Hypertension 67 0.161
10
P GLM045 Glioma 63 0.161
11
P PHC003 Pheochromocytoma 71 0.153
12
ADR040 Adrenal Gland Pheochromocytoma 46 0.153
13
P HRT032 Heart Disease 75 0.146
14
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.137
15
48X005 48,xyyy 39 0.136
16
P LKM002 Leukemia 68 0.136
17
HMN044 Human Immunodeficiency Virus Type 1 71 0.134
18
P LKM071 Leukemia, Chronic Lymphocytic 79 0.133
19
c HPT016 Hepatitis B 59 0.130
20
LVR012 Liver Cirrhosis 62 0.130
21
INS024 Insulin-Like Growth Factor I 79 0.128
22
c HPT073 Hepatitis C Virus 72 0.125
23
OST159 Osteogenic Sarcoma 66 0.123
24
P RHN004 Rhinitis 57 0.123
25
P TRM003 Tremor 54 0.122
26
ALL003 Allergic Rhinitis 67 0.121
27
P DYS154 Dystonia 65 0.120
28
c HYP595 Hypertension, Essential 84 0.120
29
HYP056 Hypoglycemia 66 0.119
30
ADN018 Adenoma 59 0.119
31
c PRC016 Pre-Eclampsia 63 0.117
32
VSL002 Visual Epilepsy 59 0.117
33
P SZR006 Seizure Disorder 56 0.117
34
P CLR023 Colorectal Cancer 99 0.116
35
P HYP076 Hyperthyroidism 55 0.114
36
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.114
37
VCC001 Vaccinia 49 0.112
38
RTN023 Retinitis 46 0.111
39
NRR001 Neuroretinitis 42 0.111
40
ADR016 Adrenal Cortical Carcinoma 48 0.108
41
ADR004 Adrenal Cortical Adenocarcinoma 39 0.108
42
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.108
43
BNR002 Bone Resorption Disease 48 0.106
44
ANX004 Anoxia 40 0.105
45
TXC005 Toxic Shock Syndrome 62 0.105
46
P LKM062 Leukemia, Acute Lymphoblastic 69 0.104
47
c ACT073 Acute Leukemia 58 0.104
48
SPN186 Spinal Cord Injury 60 0.104
49
CHC001 Chickenpox 60 0.102
50
P GRV001 Graves' Disease 55 0.102
51
IMM167 Immune Deficiency Disease 78 0.101
52
HYP060 Hyperinsulinism 54 0.101
53
c MCR113 Microvascular Complications of Diabetes 3 52 0.101
54
c MCR120 Microvascular Complications of Diabetes 7 47 0.101
55
c MCR130 Microvascular Complications of Diabetes 6 41 0.101
56
c MCR133 Microvascular Complications of Diabetes 4 41 0.101
57
P LVR013 Liver Disease 68 0.101
58
P AST007 Astrocytoma 51 0.101
59
P KDN018 Kidney Disease 72 0.099
60
P MYL006 Myeloid Leukemia 60 0.099
61
P RTN008 Retinitis Pigmentosa 79 0.099
62
P ALZ034 Alzheimer Disease 88 0.098
63
c SYS001 Systemic Lupus Erythematosus 86 0.096
64
P LYM118 Lymphoma 68 0.096
65
P VSC007 Vascular Disease 63 0.095
66
ALL006 Allergic Asthma 56 0.095
67
HYP266 Hypoxia 57 0.093
68
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.092
69
CRB004 Cerebral Artery Occlusion 45 0.092
70
CYS001 Cystic Fibrosis 81 0.091
71
FTT001 Fatty Liver Disease 61 0.091
72
IGR001 Ige Responsiveness, Atopic 59 0.091
73
GLB015 Glioblastoma Multiforme 75 0.090
74
PPT005 Peptic Ulcer Disease 59 0.090
75
BRN071 Brain Injury 49 0.089
76
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.089
77
STM007 Stomatitis 50 0.089
78
P BRS047 Breast Cancer 97 0.087
79
c LKM061 Leukemia, Acute Myeloid 84 0.087
80
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.085
81
P ADN016 Adenocarcinoma 64 0.084
82
PRS045 Prostatic Hypertrophy 53 0.081
83
P PSR002 Psoriasis 62 0.080
84
ISC004 Ischemia 58 0.080
85
c GRV008 Graves Disease 1 56 0.080
86
PST011 Pustulosis of Palm and Sole 52 0.080
87
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.080
88
OCL069 Ocular Motor Apraxia 51 0.080
89
MST004 Mast Cell Neoplasm 42 0.080
90
EXT007 Extracutaneous Mastocytoma 38 0.080
91
P OVR042 Ovarian Cancer 88 0.077
92
P GLM007 Glomerulonephritis 57 0.077
93
P BPL003 Bipolar Disorder 56 0.077
94
c VRL010 Viral Hepatitis 52 0.077
95
PNG002 Pain Agnosia 51 0.077
96
c MJR024 Major Affective Disorder 9 41 0.077
97
c MJR022 Major Affective Disorder 8 38 0.077
98
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.077
99
P MLN008 Melanoma 69 0.076
100
MDD011 Mood Disorder 62 0.076
101
PRT013 Portal Hypertension 59 0.076
102
P GST053 Gastric Cancer 83 0.072
103
c DLT002 Dilated Cardiomyopathy 79 0.072
104
TTN003 Tetanus 65 0.072
105
P ADL010 Adult Respiratory Distress Syndrome 65 0.072
106
DPH001 Diphtheria 60 0.072
107
BRN004 Brain Edema 56 0.072
108
P HPT023 Hepatocellular Carcinoma 100 0.070
109
CHG001 Chagas Disease 66 0.070
110
47X002 47,xyy 49 0.070
111
HPT004 Hepatic Coma 45 0.070
112
P PRS040 Prostate Cancer 97 0.070
113
DFC004 Deficiency Anemia 70 0.070
114
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.070
115
INS001 Insulinoma 60 0.070
116
CYT002 Cytokine Deficiency 42 0.070
117
P ENC018 Encephalopathy 61 0.070
118
TRM010 Traumatic Brain Injury 51 0.070
119
MDD018 Middle East Respiratory Syndrome 43 0.070
120
P LNG032 Lung Cancer 98 0.068
121
P ATR011 Atrial Fibrillation 66 0.068
122
P DBT009 Diabetes Mellitus 64 0.068
123
GST033 Gestational Diabetes 61 0.068
124
P NPH012 Nephrotic Syndrome 60 0.068
125
BRN056 Bronchopulmonary Dysplasia 57 0.068
126
P INF037 Inflammatory Bowel Disease 54 0.068
127
PRS021 Prostatic Adenoma 51 0.068
128
END086 End Stage Renal Disease 51 0.068
129
PRS129 Prostatic Hyperplasia, Benign 49 0.068
130
SXL003 Sexual Disorder 47 0.068
131
PPL002 Papillary Carcinoma 47 0.068
132
OVR094 Ovarian Epithelial Cancer 38 0.068
133
c CHR684 Chronic Kidney Disease 70 0.066
134
P HYP098 Hypereosinophilic Syndrome 67 0.066
135
DPR016 Depression 63 0.066
136
LNG099 Lung Disease 60 0.066
137
P SCK005 Sickle Cell Disease 50 0.066
138
PPL052 Papillomatosis, Confluent and Reticulated 33 0.066
139
HND015 Hand Skill, Relative 33 0.066
140
CLT003 Colitis 62 0.063
141
HPT019 Hepatic Encephalopathy 60 0.063
142
P MYP004 Myopathy 70 0.062
143
IRR002 Irritable Bowel Syndrome 65 0.062
144
LSC001 Lesch-Nyhan Syndrome 62 0.062
145
P RTN016 Retinal Degeneration 53 0.062
146
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.062
147
ILT001 Ileitis 50 0.062
148
CHL004 Cholelithiasis 49 0.062
149
RSP007 Respiratory Distress Syndrome, Infant 30 0.062
150
P BLD134 Bladder Cancer 79 0.062
151
ANX010 Anxiety 73 0.062
152
P MJR001 Major Depressive Disorder 68 0.062
153
CLN015 Colon Adenocarcinoma 65 0.062
154
LPD008 Lipid Metabolism Disorder 62 0.062
155
ATM095 Autoimmune Disease 62 0.062
156
P LPS004 Lupus Erythematosus 61 0.062
157
MNT002 Mental Depression 58 0.062
158
c ACT075 Acute Myocardial Infarction 57 0.062
159
ERY051 Erythroleukemia, Familial 56 0.062
160
WTH001 Withdrawal Disorder 48 0.062
161
SPL018 Splenomegaly 48 0.062
162
ESP021 Esophageal Cancer 90 0.057
163
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.057
164
P RHM011 Rheumatoid Arthritis 80 0.057
165
P HPT021 Hepatitis 67 0.057
166
P MCR115 Microvascular Complications of Diabetes 5 66 0.057
167
P MNN013 Meningitis 66 0.057
168
NRM005 Neuromuscular Disease 64 0.057
169
GT001 Gout 64 0.057
170
LYM017 Lyme Disease 64 0.057
171
P CRN300 Coronary Heart Disease 1 63 0.057
172
ACT119 Acute Promyelocytic Leukemia 63 0.057
173
c HPT001 Hepatitis C 62 0.057
174
MSL001 Measles 62 0.057
175
c BCT007 Bacterial Meningitis 55 0.057
176
P MYP006 Myopia 55 0.057
177
P ECL001 Eclampsia 50 0.057
178
RNL077 Renal Fibrosis 47 0.057
179
c MLG068 Malignant Glioma 46 0.057
180
URT010 Ureteral Obstruction 45 0.057
181
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.057
182
DWR001 Dwarfism 44 0.057
183
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.057
184
ULC004 Ulcerative Colitis 73 0.054
185
GNT003 Genital Herpes 54 0.054
186
DMY004 Demyelinating Disease 52 0.054
187
HYP014 Hyperuricemia 52 0.054
188
P CTN015 Cutaneous T Cell Lymphoma 49 0.054
189
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.054
190
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.054
191
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.054
192
CRT015 Carotid Artery Occlusion 45 0.054
193
P PRL003 Proliferative Glomerulonephritis 44 0.054
194
P HYP265 Hypotonia 43 0.054
195
HRW001 Hair Whorl 36 0.054
196
c LKM005 Leukemia, T-Cell, Chronic 34 0.054
197
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.051
198
P MLT020 Multiple Sclerosis 72 0.051
199
BRN024 Bronchitis 68 0.051
200
CHD001 Chediak-Higashi Syndrome 66 0.051
201
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.051
202
P PRD008 Periodontitis 64 0.051
203
P NTR004 Neutropenia 63 0.051
204
P MYC008 Myocarditis 59 0.051
205
P BND020 Bone Disease 59 0.051
206
P GLL022 Guillain-Barre Syndrome 59 0.051
207
HYP005 Hypokalemia 55 0.051
208
HRY003 Hairy Cell Leukemia 55 0.051
209
GLC003 Glucose Intolerance 54 0.051
210
SLP001 Sleeping Sickness 54 0.051
211
GST023 Gastric Ulcer 53 0.051
212
TRY001 Trypanosomiasis 50 0.051
213
LWC001 Low Compliance Bladder 43 0.051
214
SCR003 Secretory Diarrhea 37 0.051
215
P LNG064 Lung Cancer Susceptibility 3 78 0.044
216
P SCH015 Schizophrenia 74 0.044
217
P FML011 Familial Adenomatous Polyposis 72 0.044
218
P TTR001 Tetralogy of Fallot 70 0.044
219
ALC007 Alcohol Dependence 66 0.044
220
P SKN015 Skin Carcinoma 66 0.044
221
KRN002 Kearns-Sayre Syndrome 63 0.044
222
DNH001 Donohue Syndrome 62 0.044
223
SDD001 Sudden Infant Death Syndrome 61 0.044
224
P SCL018 Scoliosis 60 0.044
225
P MTR012 Mitral Valve Disease 58 0.044
226
CNS004 Constipation 58 0.044
227
P UVT001 Uveitis 57 0.044
228
P EXN002 Exanthem 57 0.044
229
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.044
230
PLS011 Plasmacytoma 56 0.044
231
P NRF002 Neurofibromatosis 56 0.044
232
AGN016 Aging 56 0.044
233
ACT058 Active Peptic Ulcer Disease 55 0.044
234
P SLM003 Salmonellosis 55 0.044
235
NNL006 Non-Alcoholic Steatohepatitis 54 0.044
236
P INS002 in Situ Carcinoma 53 0.044
237
P PTS002 Ptosis 53 0.044
238
ALC009 Alcoholic Liver Cirrhosis 53 0.044
239
P BRT004 Bartter Disease 52 0.044
240
c INH030 Inherited Retinal Disorder 51 0.044
241
P LCT001 Lactic Acidosis 51 0.044
242
ASP003 Aseptic Meningitis 51 0.044
243
SGW002 Segawa Syndrome, Autosomal Recessive 51 0.044
244
c PYR010 Peyronie's Disease 50 0.044
245
c SVR005 Severe Pre-Eclampsia 50 0.044
246
P PNV001 Panuveitis 50 0.044
247
NTR046 Neutrophil Migration 50 0.044
248
P OBS001 Obstructive Jaundice 50 0.044
249
RYN005 Raynaud Phenomenon 47 0.044
250
ASP004 Asphyxia Neonatorum 46 0.044
251
RTN020 Retinal Vascular Disease 46 0.044
252
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.044
253
GRW007 Growth Hormone Deficiency 46 0.044
254
ANR004 Anuria 46 0.044
255
CRB090 Cerebral Hypoxia 44 0.044
256
ORL015 Oral Squamous Cell Carcinoma 43 0.044
257
ACR011 Acromesomelic Dysplasia, Maroteaux Type 42 0.044
258
IDP070 Idiopathic Scoliosis 42 0.044
259
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 40 0.044
260
WLL004 Wallerian Degeneration 39 0.044
261
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.044
262
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.044
263
ACR016 Acromesomelic Dysplasia 37 0.044
264
P RTN034 Retinal Cone Dystrophy 3a 30 0.044
265
ADG002 Audiogenic Seizures 25 0.044
266
APC001 Apical Myocardial Infarction 15 0.044
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