Search results for L-Arginine

405 hits were found for L-Arginine

# Family MCID Name MIFTS Score
1
LRG010 L-Arginine:glycine Amidinotransferase Deficiency 12 11.176
2
CRB148 Cerebral Creatine Deficiency Syndrome 3 36 11.091
3
END072 Endotheliitis 42 0.359
4
NRN002 Neuronitis 41 0.240
5
ISC004 Ischemia 61 0.185
6
P PNC044 Pancreatitis 61 0.185
7
c PRC016 Pre-Eclampsia 56 0.178
8
c ACT027 Acute Pancreatitis 57 0.170
9
P ECL001 Eclampsia 54 0.162
10
c HYP595 Hypertension, Essential 69 0.154
11
ART111 Artery Disease 55 0.145
12
P PRC031 Preeclampsia/eclampsia 1 51 0.145
13
PLC008 Placenta Disease 33 0.145
14
P CRN211 Coronary Artery Disease 74 0.136
15
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.136
16
P HPT021 Hepatitis 69 0.126
17
VSC007 Vascular Disease 67 0.126
18
ATH003 Atherosclerosis 65 0.126
19
CRB009 Cerebritis 39 0.126
20
P PLM037 Pulmonary Hypertension 79 0.115
21
P RNV001 Renovascular Hypertension 47 0.115
22
CCN007 Cocoon Syndrome 45 0.115
23
c PRC033 Preeclampsia/eclampsia 3 16 0.115
24
P CLR023 Colorectal Cancer 97 0.103
25
P HRT032 Heart Disease 75 0.103
26
ISC006 Ischemic Heart Disease 68 0.103
27
P MYP004 Myopathy 67 0.103
28
END030 End Stage Renal Failure 55 0.103
29
P MSC033 Muscle Disorders 52 0.103
30
SXL003 Sexual Disorder 42 0.103
31
c PRC032 Preeclampsia/eclampsia 2 16 0.103
32
P BRS047 Breast Cancer 100 0.089
33
MLR004 Malaria 83 0.089
34
P AST005 Asthma 82 0.089
35
DCH001 Duchenne Muscular Dystrophy 79 0.089
36
SCK003 Sickle Cell Anemia 71 0.089
37
PRP027 Peripheral Vascular Disease 68 0.089
38
P CRD011 Cardiomyopathy 68 0.089
39
P EPL164 Epilepsy 66 0.089
40
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.089
41
P MSC005 Muscular Dystrophy 65 0.089
42
HYP066 Hyperglycemia 61 0.089
43
P ORL007 Oral Cavity Cancer 59 0.089
44
ORL011 Oral Cancer 56 0.089
45
NRM005 Neuromuscular Disease 56 0.089
46
HYP266 Hypoxia 56 0.089
47
P MTC069 Mitochondrial Disorders 53 0.089
48
ADL002 Adult Syndrome 52 0.089
49
LYS003 Lysinuric Protein Intolerance 52 0.089
50
BRN038 Bronchial Disease 51 0.089
51
URN009 Urinary System Disease 50 0.089
52
P URF003 Urofacial Syndrome 1 50 0.089
53
c SVR005 Severe Pre-Eclampsia 49 0.089
54
c ACT071 Acute Kidney Failure 49 0.089
55
URM002 Uremia 48 0.089
56
P RNL015 Renal Hypertension 48 0.089
57
ACD009 Acid-Labile Subunit, Deficiency of 45 0.089
58
MYC005 Myocardial Stunning 44 0.089
59
BWN001 Bowen-Conradi Syndrome 44 0.089
60
BLD054 Blood Protein Disease 37 0.089
61
IMP003 Impaired Renal Function Disease 34 0.089
62
VSC008 Vascular Hemostatic Disease 30 0.089
63
c AST037 Asthma 1 28 0.089
64
c AST039 Asthma 2 28 0.089
65
P OBS005 Obesity 92 0.072
66
CYS001 Cystic Fibrosis 83 0.072
67
P MYC007 Myocardial Infarction 79 0.072
68
P SCH015 Schizophrenia 77 0.072
69
P PLM036 Pulmonary Fibrosis 71 0.072
70
P RSP003 Respiratory Failure 71 0.072
71
TBR010 Tuberculosis 70 0.072
72
BCK001 Becker Muscular Dystrophy 69 0.072
73
PSY004 Psychotic Disorder 67 0.072
74
PLM001 Pulmonary Tuberculosis 67 0.072
75
P KDN018 Kidney Disease 66 0.072
76
c CHR089 Chronic Kidney Failure 66 0.072
77
ATP002 Atopy 66 0.072
78
P KDN017 Kidney Cancer 65 0.072
79
DFC004 Deficiency Anemia 64 0.072
80
PRT036 Peritonitis 63 0.072
81
P HML002 Hemolytic Anemia 62 0.072
82
P ANR007 Anorexia Nervosa 61 0.072
83
c ACT075 Acute Myocardial Infarction 60 0.072
84
CLT003 Colitis 60 0.072
85
P ENC018 Encephalopathy 59 0.072
86
P NRP001 Neuropathy 59 0.072
87
P INF032 Infertility 59 0.072
88
CHL068 Cholestasis 59 0.072
89
ART021 Arteriosclerosis 58 0.072
90
CHL071 Child Syndrome 58 0.072
91
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.072
92
GST033 Gestational Diabetes 57 0.072
93
INT002 Intermittent Claudication 56 0.072
94
GST023 Gastric Ulcer 56 0.072
95
GLC003 Glucose Intolerance 55 0.072
96
KDS001 Kid Syndrome 53 0.072
97
DSS008 Disease of Mental Health 52 0.072
98
HMG005 Hemoglobinopathy 52 0.072
99
ALL026 Allergic Hypersensitivity Disease 52 0.072
100
IMP005 Impotence 51 0.072
101
VSC006 Vascular Cancer 51 0.072
102
SCK005 Sickle Cell Disease 51 0.072
103
P MSC003 Muscular Atrophy 50 0.072
104
c ACT134 Acute Liver Failure 50 0.072
105
CSY001 C Syndrome 50 0.072
106
HYP037 Hyperhomocysteinemia 50 0.072
107
LRN003 Learning Disability 49 0.072
108
c INH020 Inherited Metabolic Disorder 49 0.072
109
LMB062 Limb Ischemia 48 0.072
110
NSD001 Nose Disease 48 0.072
111
HPT009 Hepatopulmonary Syndrome 48 0.072
112
c CNG027 Congenital Hemolytic Anemia 48 0.072
113
RNL077 Renal Fibrosis 47 0.072
114
ACR041 Acromelic Frontonasal Dysostosis 45 0.072
115
URT010 Ureteral Obstruction 45 0.072
116
BRT030 Birth Defects 43 0.072
117
RNL097 Renal Artery Disease 43 0.072
118
NPH010 Nephrosclerosis 43 0.072
119
GLC008 Glucose Metabolism Disease 42 0.072
120
P MTC004 Mitochondrial Encephalomyopathy 42 0.072
121
PRD011 Proud Syndrome 42 0.072
122
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.072
123
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.072
124
c PRG106 Progressive Muscular Dystrophy 40 0.072
125
HYP030 Hypoactive Sexual Desire Disorder 39 0.072
126
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.072
127
P UTR038 Uterine Disease 37 0.072
128
P ENC011 Encephalomyopathy 37 0.072
129
MTC005 Mitochondrial Metabolism Disease 36 0.072
130
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.072
131
MSC004 Muscle Tissue Disease 34 0.072
132
MLR007 Male Reproductive System Disease 34 0.072
133
P XLN007 X-Linked Disease 34 0.072
134
c CRD187 Cardiomyopathy, Dilated, 3b 33 0.072
135
MTC028 Mitochondrial Cardiomyopathy 32 0.072
136
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.072
137
c SCH051 Schizophrenia 4 28 0.072
138
c CRN214 Coronary Heart Disease 5 22 0.072
139
MSC012 Muscular Dystrophy, Duchenne and Becker Type 22 0.072
140
c CRN174 Coronary Heart Disease 2 20 0.072
141
c CRN175 Coronary Heart Disease 4 19 0.072
142
c CRN172 Coronary Heart Disease 3 19 0.072
143
c HYP454 Hypertension, Essential 8 16 0.072
144
ATR076 Atrophic Muscular Disease 15 0.072
145
FTL016 Fetal Edema 15 0.072
146
P PRS040 Prostate Cancer 90 0.051
147
c SYS001 Systemic Lupus Erythematosus 86 0.051
148
P OST012 Osteoarthritis 83 0.051
149
P MLT019 Multiple Myeloma 83 0.051
150
P RNL014 Renal Cell Carcinoma 82 0.051
151
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.051
152
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.051
153
c DLT002 Dilated Cardiomyopathy 76 0.051
154
P HYP607 Hypercholesterolemia, Familial 76 0.051
155
ULC004 Ulcerative Colitis 76 0.051
156
P LVR013 Liver Disease 75 0.051
157
STR067 Stroke, Ischemic 75 0.051
158
WLS001 Wilson Disease 72 0.051
159
P NRV007 Nervous System Disease 71 0.051
160
MLT021 Multiple System Atrophy 70 0.051
161
P NRB001 Neuroblastoma 70 0.051
162
BRN028 Brain Cancer 70 0.051
163
P ADN016 Adenocarcinoma 69 0.051
164
P LYM118 Lymphoma 69 0.051
165
SVR004 Severe Combined Immunodeficiency 69 0.051
166
LVR012 Liver Cirrhosis 67 0.051
167
CRB037 Cerebral Palsy 66 0.051
168
LSH001 Leishmaniasis 66 0.051
169
P DYS154 Dystonia 65 0.051
170
P AST007 Astrocytoma 65 0.051
171
PRT037 Pertussis 64 0.051
172
P THL005 Thalassemia 64 0.051
173
HMT002 Hematologic Cancer 64 0.051
174
P THR014 Thrombocytopenia 64 0.051
175
LNG099 Lung Disease 64 0.051
176
P HYP086 Hypothyroidism 64 0.051
177
PNC041 Pancreatic Ductal Adenocarcinoma 64 0.051
178
P INF037 Inflammatory Bowel Disease 63 0.051
179
P PRD008 Periodontitis 63 0.051
180
CRB039 Cerebrovascular Disease 63 0.051
181
P ESP024 Esophagitis 61 0.051
182
P ADL010 Adult Respiratory Distress Syndrome 61 0.051
183
MTH009 Mouth Disease 61 0.051
184
P INT068 Intestinal Disease 60 0.051
185
PLM033 Pulmonary Embolism 60 0.051
186
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.051
187
P NRV006 Nervous System Cancer 60 0.051
188
P GST049 Gastrointestinal System Cancer 60 0.051
189
PRD007 Periodontal Disease 60 0.051
190
P CLR108 Colorectal Adenoma 60 0.051
191
P GLY013 Glycogen Storage Disease 60 0.051
192
P DRR001 Diarrhea 60 0.051
193
OCL009 Ocular Cancer 59 0.051
194
c HPT003 Hepatitis a 59 0.051
195
GST045 Gastroenteritis 59 0.051
196
P GRV001 Graves' Disease 59 0.051
197
STT001 Status Epilepticus 59 0.051
198
P GLM007 Glomerulonephritis 59 0.051
199
LPD008 Lipid Metabolism Disorder 58 0.051
200
P HYP060 Hyperinsulinism 58 0.051
201
ADN018 Adenoma 58 0.051
202
PNC034 Pancreas Disease 58 0.051
203
CTS003 Coats Disease 57 0.051
204
ABL002 Ablepharon-Macrostomia Syndrome 57 0.051
205
ART017 Aortic Disease 57 0.051
206
CHY002 Chylomicron Retention Disease 57 0.051
207
CRT016 Carotid Artery Disease 57 0.051
208
P PRM011 Primary Ciliary Dyskinesia 57 0.051
209
c ACT210 Acute Respiratory Distress Syndrome 57 0.051
210
c SVR001 Severe Acute Respiratory Syndrome 57 0.051
211
EXF001 Exfoliation Syndrome 57 0.051
212
SNS001 Sensorineural Hearing Loss 57 0.051
213
EPD016 Epidermolysis Bullosa 57 0.051
214
PLS011 Plasmacytoma 56 0.051
215
TRN015 Transient Cerebral Ischemia 56 0.051
216
P PLY019 Polyneuropathy 56 0.051
217
DBT010 Diabetic Neuropathy 55 0.051
218
P CDS001 Cadasil 55 0.051
219
PLS007 Plasmodium Falciparum Malaria 55 0.051
220
P HRD011 Hereditary Spherocytosis 54 0.051
221
HDC001 Headache 54 0.051
222
P MYC008 Myocarditis 54 0.051
223
P THY032 Thyroiditis 54 0.051
224
GST037 Gastroparesis 54 0.051
225
c RNL003 Renal Clear Cell Carcinoma 54 0.051
226
PLM010 Pulmonary Edema 54 0.051
227
C3D001 C3 Deficiency 53 0.051
228
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 53 0.051
229
P PLY014 Polycystic Kidney Disease 53 0.051
230
OLG003 Oligohydramnios 53 0.051
231
END040 Endogenous Depression 53 0.051
232
RTN018 Retinal Disease 53 0.051
233
MNT002 Mental Depression 53 0.051
234
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.051
235
TTH006 Tooth Disease 52 0.051
236
BRN106 Burns 52 0.051
237
KRT002 Keratomalacia 52 0.051
238
BRN004 Brain Edema 52 0.051
239
P SPS003 Spastic Diplegia 52 0.051
240
PRS042 Prostate Disease 52 0.051
241
RYS001 Reye Syndrome 52 0.051
242
P LCT001 Lactic Acidosis 51 0.051
243
CRT049 Critical Limb Ischemia 51 0.051
244
c INF071 Inflammatory Bowel Disease 1 51 0.051
245
DBT062 Diabetic Foot Ulcers 51 0.051
246
IMM136 Immune System Disease 51 0.051
247
SPN041 Spinal Cord Disease 51 0.051
248
CLN019 Colonic Disease 51 0.051
249
CRN030 Coronary Stenosis 51 0.051
250
CRB152 Carbamoylphosphate Synthetase I Deficiency 50 0.051
251
P HYP014 Hyperuricemia 50 0.051
252
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 50 0.051
253
RTN023 Retinitis 50 0.051
254
P CHR345 Chronic Pain 50 0.051
255
ANG054 Angina Pectoris 50 0.051
256
MVM001 Movement Disease 49 0.051
257
P SHR001 Short Bowel Syndrome 49 0.051
258
ALC009 Alcoholic Liver Cirrhosis 49 0.051
259
P INT063 Intellectual Disability 49 0.051
260
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.051
261
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.051
262
P FML035 Familial Hyperlipidemia 48 0.051
263
OBS001 Obstructive Jaundice 48 0.051
264
BCT015 Bacteremia 48 0.051
265
PLS009 Plasma Cell Neoplasm 48 0.051
266
ATN002 Autonomic Nervous System Disease 48 0.051
267
THL018 Thalassemia Major 48 0.051
268
NPH003 Nephrocalcinosis 48 0.051
269
THY030 Thyroid Gland Disease 48 0.051
270
RTN020 Retinal Vascular Disease 48 0.051
271
c HMG001 Hemoglobin C Disease 47 0.051
272
P RNL017 Renal Oncocytoma 47 0.051
273
VND001 Vein Disease 47 0.051
274
P HYP237 Hypercalcemia, Infantile 47 0.051
275
INT253 Intestinal Benign Neoplasm 47 0.051
276
SDD007 Sudden Cardiac Death 47 0.051
277
c MLG069 Malignant Hypertension 47 0.051
278
AMN002 Amino Acid Metabolic Disorder 47 0.051
279
GNG011 Gingival Disease 46 0.051
280
ART004 Aortic Atherosclerosis 46 0.051
281
BLD053 Blood Platelet Disease 46 0.051
282
GLT021 Glutaricaciduria, Type I 46 0.051
283
HPT014 Hepatorenal Syndrome 46 0.051
284
PRT082 Preterm Premature Rupture of the Membranes 46 0.051
285
DST006 Diastolic Heart Failure 46 0.051
286
CRB151 Cerebral Creatine Deficiency Syndrome 1 46 0.051
287
NWB001 Newborn Respiratory Distress Syndrome 45 0.051
288
P PLN008 Peeling Skin Syndrome 45 0.051
289
ESN011 Eisenmenger Syndrome 45 0.051
290
CRB090 Cerebral Hypoxia 45 0.051
291
c CLR085 Colorectal Cancer 1 45 0.051
292
VSC047 Vascular Malformation 45 0.051
293
HRT015 Heritable Pulmonary Arterial Hypertension 45 0.051
294
ALN001 Aland Island Eye Disease 45 0.051
295
VTM002 Vitamin B12 Deficiency 44 0.051
296
GDS001 Good Syndrome 44 0.051
297
c PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 44 0.051
298
DYS032 Dystrophinopathies 44 0.051
299
CRD118 Cardiovascular Cancer 44 0.051
300
c MTR002 Mitral Valve Insufficiency 44 0.051
301
SYS003 Systolic Heart Failure 43 0.051
302
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.051
303
ANX004 Anoxia 43 0.051
304
MLR006 Male Reproductive Organ Cancer 43 0.051
305
PRD004 Prediabetes Syndrome 43 0.051
306
P CRD132 Cardiac Conduction Defect 43 0.051
307
MRP001 Morphine Dependence 43 0.051
308
IDP033 Idiopathic Edema 42 0.051
309
c ATM022 Autoimmune Myocarditis 42 0.051
310
PRN019 Perinatal Necrotizing Enterocolitis 42 0.051
311
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.051
312
P BLD051 Blood Coagulation Disease 42 0.051
313
PRM025 Primary Bacterial Infectious Disease 41 0.051
314
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.051
315
RPR002 Reproductive System Disease 41 0.051
316
CNV002 Conversion Disorder 41 0.051
317
P CPL003 Capillary Leak Syndrome 41 0.051
318
PRS036 Parasitic Protozoa Infectious Disease 41 0.051
319
THL017 Thalassemia Intermedia 40 0.051
320
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 40 0.051
321
GST078 Gastrointestinal Allergy 40 0.051
322
PDT035 Pediatric Systemic Lupus Erythematosus 40 0.051
323
c PLN018 Peeling Skin Syndrome 2 40 0.051
324
BND014 Bone Development Disease 40 0.051
325
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.051
326
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.051
327
SPN040 Spinal Cancer 39 0.051
328
SPN369 Spinal Disease 39 0.051
329
ORL003 Oral Tuberculosis 39 0.051
330
THL010 Thalassemia Minor 39 0.051
331
HYP540 Hypertension, Diastolic 39 0.051
332
CLL021 Collagenous Colitis 39 0.051
333
HPT004 Hepatic Coma 39 0.051
334
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.051
335
SCR011 Scrapie 38 0.051
336
c INF086 Inflammatory Bowel Disease 3 38 0.051
337
GNG003 Gingival Recession 38 0.051
338
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 38 0.051
339
P RTN022 Retinal Vein Occlusion 38 0.051
340
SXD001 Sex Differentiation Disease 38 0.051
341
DRG001 Drug Psychosis 38 0.051
342
EXT006 Extrahepatic Cholestasis 37 0.051
343
PRP080 Peripheral Artery Disease 37 0.051
344
c PNC106 Pancreatic Agenesis 1 37 0.051
345
c CNG031 Congenital Nervous System Abnormality 37 0.051
346
ISC002 Ischemic Optic Neuropathy 37 0.051
347
MDY003 Mody, Type Ii 36 0.051
348
NTR005 Nutritional Deficiency Disease 36 0.051
349
SCR003 Secretory Diarrhea 36 0.051
350
PYR016 Pyridoxine Deficiency 36 0.051
351
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.051
352
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.051
353
DNT007 Dentin Sensitivity 35 0.051
354
c BRN108 Branchiootic Syndrome 1 34 0.051
355
VTM001 Vitamin K Deficiency Hemorrhagic Disease 34 0.051
356
GST051 Gastrointestinal Tuberculosis 34 0.051
357
ACR002 Acrocapitofemoral Dysplasia 33 0.051
358
HYP114 Hypertensive Nephropathy 33 0.051
359
CRB159 Cerebral Visual Impairment 33 0.051
360
c SYS043 Systemic Lupus Erythematosus 1 33 0.051
361
TTH007 Tooth Erosion 33 0.051
362
ALL014 Allergic Encephalomyelitis 32 0.051
363
GLB003 Globe Disease 32 0.051
364
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 32 0.051
365
CVT001 Cavitary Optic Disc Anomalies 31 0.051
366
c HMG004 Hemoglobin D Disease 31 0.051
367
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 31 0.051
368
P SCK034 Sickle Beta Thalassemia 30 0.051
369
VTM003 Vitamin Metabolic Disorder 30 0.051
370
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.051
371
c PLN021 Peeling Skin Syndrome 3 29 0.051
372
c TRC078 Trichohepatoenteric Syndrome 2 29 0.051
373
c CLR075 Colorectal Cancer 3 28 0.051
374
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.051
375
c MYC058 Myocardial Infarction 2 28 0.051
376
CRB031 Cerebral Arterial Disease 27 0.051
377
RFL002 Reflex Epilepsy 27 0.051
378
c SYS038 Systemic Lupus Erythematosus 2 27 0.051
379
CRT055 Creatine Deficiency Syndromes 27 0.051
380
HRN022 Hearing Loss/deafness 26 0.051
381
c PRC045 Preeclampsia/eclampsia 5 26 0.051
382
HMN031 Human Venous Malformation 25 0.051
383
RSP007 Respiratory Distress Syndrome, Infant 22 0.051
384
SCK020 Sickle Cell - Hemoglobin D Disease 22 0.051
385
DNT002 Dentine Erosion 22 0.051
386
P CRN178 Coronary Heart Disease 6 21 0.051
387
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.051
388
P GNR027 Generalized Peeling Skin Syndrome 19 0.051
389
c ADL080 Adult Acute Respiratory Distress Syndrome 19 0.051
390
c CRN173 Coronary Heart Disease 8 18 0.051
391
c CRN176 Coronary Heart Disease 9 18 0.051
392
PYR009 Pyridoxine Deficiency Anemia 18 0.051
393
AND005 Androgen Insensitivity Syndrome, Mild 16 0.051
394
c GRV009 Graves Disease 2 16 0.051
395
c HYP333 Hyperlipidemia, Combined, 2 15 0.051
396
PLM069 Pulmonary Venous Return Anomaly 15 0.051
397
c MYC055 Mycobacterium Tuberculosis 3 15 0.051
398
MTC024 Mitochondrial Genetic Disorders 14 0.051
399
HMG015 Hemoglobin S Beta-Thalassemia 14 0.051
400
P MYC054 Mycobacterium Tuberculosis 2 14 0.051
401
OCL023 Ocular Muscular Dystrophy 13 0.051
402
CMP052 Complication in Hemodialysis 13 0.051
403
INB001 Inborn Amino Acid Metabolism Disorder 12 0.051
404
BRN069 Brain and Spinal Tumors 12 0.051
405
c SCK008 Sickle Delta Beta Thalassemia 9 0.051
Content
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