Search results for L-Arginine

299 hits were found for L-Arginine

# Family MCID Name MIFTS Score
1
CRB148 Cerebral Creatine Deficiency Syndrome 3 38 11.078
2
LRG010 L-Arginine:glycine Amidinotransferase Deficiency 12 9.148
3
END072 Endotheliitis 46 0.437
4
ISC004 Ischemia 66 0.293
5
NRN002 Neuronitis 43 0.293
6
VSC007 Vascular Disease 71 0.286
7
c PRC016 Pre-Eclampsia 65 0.265
8
AST005 Asthma 83 0.257
9
P ECL001 Eclampsia 57 0.250
10
P PRC031 Preeclampsia/eclampsia 1 41 0.234
11
P PNC044 Pancreatitis 64 0.225
12
ART140 Arteries, Anomalies of 51 0.225
13
PLC008 Placenta Disease 48 0.225
14
P CRN018 Coronary Artery Anomaly 69 0.216
15
c ACT027 Acute Pancreatitis 61 0.207
16
ISC006 Ischemic Heart Disease 73 0.187
17
P DBT009 Diabetes Mellitus 72 0.187
18
P KDN018 Kidney Disease 69 0.187
19
P HRT032 Heart Disease 80 0.177
20
c HYP595 Hypertension, Essential 78 0.177
21
P HPT021 Hepatitis 75 0.177
22
HMG005 Hemoglobinopathy 53 0.177
23
c BLD140 Blood Group, I System 37 0.177
24
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.177
25
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.165
26
SCK003 Sickle Cell Anemia 73 0.165
27
P ART021 Arteriosclerosis 62 0.165
28
P CRN300 Coronary Heart Disease 1 57 0.165
29
P MYP004 Myopathy 69 0.153
30
AGN016 Aging 65 0.153
31
NRM005 Neuromuscular Disease 60 0.153
32
URN009 Urinary System Disease 58 0.153
33
SCK005 Sickle Cell Disease 54 0.153
34
MSC033 Muscle Disorders 53 0.153
35
CRB009 Cerebritis 41 0.153
36
MSC004 Muscle Tissue Disease 39 0.153
37
P MYC007 Myocardial Infarction 81 0.140
38
P PLM037 Pulmonary Hypertension 79 0.140
39
MSC157 Muscular Dystrophy, Duchenne Type 74 0.140
40
LNG099 Lung Disease 67 0.140
41
P MSC005 Muscular Dystrophy 66 0.140
42
HYP066 Hyperglycemia 64 0.140
43
GLC003 Glucose Intolerance 58 0.140
44
P RNV001 Renovascular Hypertension 48 0.140
45
P CLR023 Colorectal Cancer 98 0.125
46
MLR004 Malaria 86 0.125
47
CYS001 Cystic Fibrosis 85 0.125
48
PLM001 Pulmonary Tuberculosis 72 0.125
49
c BTT014 Beta-Thalassemia 70 0.125
50
P THL005 Thalassemia 65 0.125
51
MSC152 Muscular Dystrophy, Becker Type 64 0.125
52
P INF032 Infertility 59 0.125
53
END030 End Stage Renal Failure 59 0.125
54
BRN038 Bronchial Disease 58 0.125
55
HYP060 Hyperinsulinism 56 0.125
56
LMB062 Limb Ischemia 52 0.125
57
c CRD187 Cardiomyopathy, Dilated, 3b 46 0.125
58
SXL003 Sexual Disorder 45 0.125
59
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.125
60
GLC008 Glucose Metabolism Disease 38 0.125
61
MSC012 Muscular Dystrophy, Duchenne and Becker Type 35 0.125
62
c TRC078 Trichohepatoenteric Syndrome 2 34 0.125
63
c MYT029 Myotonia Congenita, Autosomal Recessive 32 0.125
64
ATR076 Atrophic Muscular Disease 6 0.125
65
P BRS047 Breast Cancer 100 0.108
66
P LVR013 Liver Disease 76 0.108
67
LVR012 Liver Cirrhosis 73 0.108
68
PSY004 Psychotic Disorder 72 0.108
69
c CHR089 Chronic Kidney Failure 72 0.108
70
PRP027 Peripheral Vascular Disease 71 0.108
71
P SCH015 Schizophrenia 71 0.108
72
P EPL164 Epilepsy 70 0.108
73
P ADL010 Adult Respiratory Distress Syndrome 67 0.108
74
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.108
75
ACQ007 Acquired Immunodeficiency Syndrome 65 0.108
76
c ACT075 Acute Myocardial Infarction 64 0.108
77
P NRP001 Neuropathy 63 0.108
78
c HPT003 Hepatitis a 63 0.108
79
c ACT210 Acute Respiratory Distress Syndrome 63 0.108
80
HYP266 Hypoxia 61 0.108
81
MNT002 Mental Depression 60 0.108
82
PNC034 Pancreas Disease 59 0.108
83
P ENC018 Encephalopathy 58 0.108
84
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.108
85
PLM010 Pulmonary Edema 57 0.108
86
NWB001 Newborn Respiratory Distress Syndrome 56 0.108
87
SPS003 Spastic Diplegia 55 0.108
88
IMP005 Impotence 54 0.108
89
LYS003 Lysinuric Protein Intolerance 53 0.108
90
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.108
91
URM002 Uremia 52 0.108
92
SCH012 Schizoaffective Disorder 51 0.108
93
MYC005 Myocardial Stunning 47 0.108
94
MTC004 Mitochondrial Encephalomyopathy 42 0.108
95
P ENC011 Encephalomyopathy 40 0.108
96
P BLD051 Blood Coagulation Disease 38 0.108
97
RSP007 Respiratory Distress Syndrome, Infant 28 0.108
98
P ALZ034 Alzheimer Disease 95 0.088
99
c SYS001 Systemic Lupus Erythematosus 86 0.088
100
P NRV007 Nervous System Disease 75 0.088
101
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.088
102
CRB039 Cerebrovascular Disease 68 0.088
103
SPN186 Spinal Cord Injury 67 0.088
104
PRT036 Peritonitis 67 0.088
105
GST050 Gastrointestinal System Disease 66 0.088
106
CLT003 Colitis 63 0.088
107
GST033 Gestational Diabetes 62 0.088
108
INT002 Intermittent Claudication 61 0.088
109
P GLM007 Glomerulonephritis 61 0.088
110
P PLY014 Polycystic Kidney Disease 60 0.088
111
PLC005 Placental Insufficiency 59 0.088
112
LPD008 Lipid Metabolism Disorder 59 0.088
113
PLS007 Plasmodium Falciparum Malaria 59 0.088
114
GST023 Gastric Ulcer 57 0.088
115
PRN019 Perinatal Necrotizing Enterocolitis 56 0.088
116
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 55 0.088
117
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.088
118
c ACT071 Acute Kidney Failure 54 0.088
119
PRP080 Peripheral Artery Disease 54 0.088
120
QDR001 Quadriplegia 54 0.088
121
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.088
122
HPT009 Hepatopulmonary Syndrome 53 0.088
123
ANG054 Angina Pectoris 53 0.088
124
P MTC133 Mitochondrial Myopathy 53 0.088
125
c BLM008 Bulimia Nervosa 2 53 0.088
126
ENT011 Enterocolitis 52 0.088
127
c ACT134 Acute Liver Failure 52 0.088
128
CRB151 Cerebral Creatine Deficiency Syndrome 1 50 0.088
129
ACT017 Acute Chest Syndrome 50 0.088
130
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.088
131
MTC069 Mitochondrial Disorders 49 0.088
132
URT010 Ureteral Obstruction 49 0.088
133
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.088
134
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.088
135
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.088
136
NPH010 Nephrosclerosis 46 0.088
137
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.088
138
c MTR002 Mitral Valve Insufficiency 46 0.088
139
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.088
140
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.088
141
DYS032 Dystrophinopathies 43 0.088
142
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.088
143
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.088
144
PST055 Postural Hypotension 40 0.088
145
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.088
146
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.088
147
c INF145 Infantile Liver Failure Syndrome 1 33 0.088
148
P SCK034 Sickle Beta Thalassemia 29 0.088
149
P PRS040 Prostate Cancer 88 0.062
150
OST012 Osteoarthritis 88 0.062
151
MYL069 Myeloma, Multiple 86 0.062
152
INS024 Insulin-Like Growth Factor I 83 0.062
153
P ATX030 Ataxia-Telangiectasia 80 0.062
154
ULC004 Ulcerative Colitis 80 0.062
155
P DLT002 Dilated Cardiomyopathy 76 0.062
156
CNG034 Congestive Heart Failure 74 0.062
157
P NRB001 Neuroblastoma 73 0.062
158
ANX010 Anxiety 72 0.062
159
BRN028 Brain Cancer 72 0.062
160
LSH001 Leishmaniasis 71 0.062
161
SVR004 Severe Combined Immunodeficiency 71 0.062
162
P LYM118 Lymphoma 71 0.062
163
P ADN016 Adenocarcinoma 71 0.062
164
PRT037 Pertussis 70 0.062
165
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.062
166
P MYC084 Mycobacterium Tuberculosis 1 69 0.062
167
P PLM036 Pulmonary Fibrosis 68 0.062
168
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.062
169
P ANR048 Aniridia 1 68 0.062
170
DMN002 Dementia 68 0.062
171
PNC041 Pancreatic Ductal Adenocarcinoma 67 0.062
172
APN008 Apnea, Obstructive Sleep 67 0.062
173
CHR066 Chronic Fatigue Syndrome 67 0.062
174
P PRD008 Periodontitis 67 0.062
175
P AST007 Astrocytoma 66 0.062
176
GST045 Gastroenteritis 65 0.062
177
ACR006 Aceruloplasminemia 65 0.062
178
P SLP006 Sleep Apnea 65 0.062
179
MLT157 Multiple System Atrophy 1 65 0.062
180
P INT068 Intestinal Disease 65 0.062
181
c CNT035 Central Nervous System Disease 65 0.062
182
P THR014 Thrombocytopenia 65 0.062
183
c ART101 Aortic Valve Disease 2 65 0.062
184
PRD007 Periodontal Disease 64 0.062
185
P ESP024 Esophagitis 64 0.062
186
MTH009 Mouth Disease 64 0.062
187
CMB081 Combined Immunodeficiency, X-Linked 64 0.062
188
ADN018 Adenoma 63 0.062
189
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 63 0.062
190
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.062
191
PLM033 Pulmonary Embolism 62 0.062
192
P HYP086 Hypothyroidism 62 0.062
193
NRV006 Nervous System Cancer 61 0.062
194
P DYS154 Dystonia 61 0.062
195
P GLY013 Glycogen Storage Disease 61 0.062
196
ANR040 Aneurysm 61 0.062
197
c SCL052 Scleroderma, Familial Progressive 60 0.062
198
CHL068 Cholestasis 60 0.062
199
P DRR001 Diarrhea 60 0.062
200
STT001 Status Epilepticus 60 0.062
201
CLR108 Colorectal Adenoma 60 0.062
202
PLS011 Plasmacytoma 60 0.062
203
DBT010 Diabetic Neuropathy 60 0.062
204
SLP005 Sleep Disorder 59 0.062
205
DBT062 Diabetic Foot Ulcers 59 0.062
206
TRN015 Transient Cerebral Ischemia 58 0.062
207
P PLY019 Polyneuropathy 58 0.062
208
P MYC008 Myocarditis 58 0.062
209
c GLC092 Glaucoma, Primary Open Angle 58 0.062
210
P RNL003 Renal Clear Cell Carcinoma 58 0.062
211
c GLY060 Glycogen Storage Disease Ia 57 0.062
212
BRN004 Brain Edema 57 0.062
213
EPD016 Epidermolysis Bullosa 57 0.062
214
P PRM011 Primary Ciliary Dyskinesia 57 0.062
215
IMM136 Immune System Disease 57 0.062
216
BRN106 Burns 57 0.062
217
PRS042 Prostate Disease 56 0.062
218
P THY032 Thyroiditis 56 0.062
219
CRT049 Critical Limb Ischemia 56 0.062
220
GST037 Gastroparesis 56 0.062
221
CLN019 Colonic Disease 55 0.062
222
P HRD011 Hereditary Spherocytosis 55 0.062
223
HDC001 Headache 55 0.062
224
c MCR113 Microvascular Complications of Diabetes 3 55 0.062
225
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 55 0.062
226
P HYP014 Hyperuricemia 54 0.062
227
TTH006 Tooth Disease 54 0.062
228
SPN041 Spinal Cord Disease 54 0.062
229
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.062
230
P RTN022 Retinal Vein Occlusion 53 0.062
231
OPT006 Optic Nerve Disease 53 0.062
232
P OBS001 Obstructive Jaundice 53 0.062
233
P CRD132 Cardiac Conduction Defect 53 0.062
234
ALC009 Alcoholic Liver Cirrhosis 53 0.062
235
CRN030 Coronary Stenosis 52 0.062
236
CRB186 Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to 52 0.062
237
P INF037 Inflammatory Bowel Disease 52 0.062
238
RTN023 Retinitis 52 0.062
239
TLN003 Telangiectasis 52 0.062
240
P SHR001 Short Bowel Syndrome 52 0.062
241
THY030 Thyroid Gland Disease 51 0.062
242
P OPN001 Open-Angle Glaucoma 51 0.062
243
P LCT001 Lactic Acidosis 51 0.062
244
PRT082 Preterm Premature Rupture of the Membranes 51 0.062
245
GNG011 Gingival Disease 50 0.062
246
ESN011 Eisenmenger Syndrome 49 0.062
247
c PRD040 Periodontitis, Chronic 49 0.062
248
ANX004 Anoxia 49 0.062
249
HPT014 Hepatorenal Syndrome 49 0.062
250
c MLG069 Malignant Hypertension 49 0.062
251
P RNL017 Renal Oncocytoma 49 0.062
252
NPH003 Nephrocalcinosis 49 0.062
253
RNL077 Renal Fibrosis 49 0.062
254
DBT008 Diabetic Angiopathy 48 0.062
255
CRB027 Cerebellar Disease 48 0.062
256
ISC002 Ischemic Optic Neuropathy 48 0.062
257
ART004 Aortic Atherosclerosis 48 0.062
258
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.062
259
CRB090 Cerebral Hypoxia 47 0.062
260
CHR100 Chronic Ulcer of Skin 46 0.062
261
PRD004 Prediabetes Syndrome 46 0.062
262
HRT012 Heart Valve Disease 45 0.062
263
GNG003 Gingival Recession 45 0.062
264
P CPL003 Capillary Leak Syndrome 44 0.062
265
SYS003 Systolic Heart Failure 44 0.062
266
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.062
267
CLL021 Collagenous Colitis 43 0.062
268
MRP001 Morphine Dependence 43 0.062
269
c MCR130 Microvascular Complications of Diabetes 6 42 0.062
270
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.062
271
SPN050 Spinocerebellar Degeneration 41 0.062
272
OLG003 Oligohydramnios 41 0.062
273
GLC098 Glaucoma-Related Pigment Dispersion Syndrome 40 0.062
274
HPT004 Hepatic Coma 40 0.062
275
c ATM022 Autoimmune Myocarditis 40 0.062
276
SCR011 Scrapie 40 0.062
277
DNT007 Dentin Sensitivity 40 0.062
278
EXT006 Extrahepatic Cholestasis 39 0.062
279
OLG001 Oligospermia 39 0.062
280
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.062
281
AMN002 Amino Acid Metabolic Disorder 38 0.062
282
ALL014 Allergic Encephalomyelitis 37 0.062
283
EPL131 Epilepsy, Pyridoxine-Dependent 37 0.062
284
SCR003 Secretory Diarrhea 36 0.062
285
TTH007 Tooth Erosion 36 0.062
286
P BCT020 Bacteremia 2 34 0.062
287
c MCR120 Microvascular Complications of Diabetes 7 34 0.062
288
c MCR133 Microvascular Complications of Diabetes 4 32 0.062
289
P KLZ004 Kala-Azar 1 31 0.062
290
P STR035 Streptococcal Group a Invasive Disease 28 0.062
291
RFL002 Reflex Epilepsy 27 0.062
292
CRT055 Creatine Deficiency Syndromes 25 0.062
293
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 24 0.062
294
SPN187 Spinocerebellar Atrophy 23 0.062
295
ANR038 Anorexia Nervosa 1 21 0.062
296
BLD137 Blood Group--Ahonen 17 0.062
297
INB001 Inborn Amino Acid Metabolism Disorder 16 0.062
298
AMN012 Aminoacidopathies 15 0.062
299
CMP052 Complication in Hemodialysis 11 0.062
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