Search results for L-Arginine

596 hits were found for L-Arginine

# Family MCID Name MIFTS Score
1
CRB148 Cerebral Creatine Deficiency Syndrome 3 41 11.299
2
LRG010 L-Arginine:glycine Amidinotransferase Deficiency 12 6.612
3
c PRC016 Pre-Eclampsia 63 0.429
4
c HYP836 Hypercholesterolemia, Familial, 1 74 0.418
5
c HYP595 Hypertension, Essential 87 0.374
6
P KDN018 Kidney Disease 73 0.374
7
P PLM037 Pulmonary Hypertension 69 0.371
8
ISC004 Ischemia 62 0.371
9
c ACT027 Acute Pancreatitis 60 0.368
10
P PNC044 Pancreatitis 61 0.339
11
TXC005 Toxic Shock Syndrome 63 0.311
12
IMP005 Impotence 53 0.271
13
ATH013 Atherosclerosis Susceptibility 68 0.267
14
P VSC007 Vascular Disease 65 0.262
15
c ACT071 Acute Kidney Failure 60 0.262
16
P ECL001 Eclampsia 53 0.254
17
P HRT032 Heart Disease 78 0.249
18
CNG034 Congestive Heart Failure 69 0.249
19
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.235
20
P CRN018 Coronary Artery Anomaly 67 0.235
21
PRP027 Peripheral Vascular Disease 72 0.225
22
ART140 Arteries, Anomalies of 60 0.209
23
P SZR006 Seizure Disorder 59 0.209
24
VSL002 Visual Epilepsy 58 0.209
25
HYP266 Hypoxia 58 0.209
26
ANG054 Angina Pectoris 66 0.203
27
c CHR684 Chronic Kidney Disease 68 0.198
28
END030 End Stage Renal Failure 60 0.198
29
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 58 0.198
30
P LCT001 Lactic Acidosis 52 0.198
31
CYS001 Cystic Fibrosis 84 0.192
32
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.192
33
P MSC005 Muscular Dystrophy 68 0.192
34
P GLM007 Glomerulonephritis 58 0.192
35
CRB039 Cerebrovascular Disease 71 0.186
36
HYP066 Hyperglycemia 63 0.186
37
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.186
38
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.173
39
STR067 Stroke, Ischemic 82 0.173
40
P MYP004 Myopathy 63 0.173
41
P CRN300 Coronary Heart Disease 1 59 0.173
42
URM002 Uremia 50 0.173
43
P DBT009 Diabetes Mellitus 66 0.166
44
P MTC133 Mitochondrial Myopathy 53 0.166
45
ENT011 Enterocolitis 51 0.166
46
MSC157 Muscular Dystrophy, Duchenne Type 70 0.159
47
CLT003 Colitis 63 0.159
48
GLC003 Glucose Intolerance 55 0.159
49
PRN019 Perinatal Necrotizing Enterocolitis 55 0.159
50
INS024 Insulin-Like Growth Factor I 79 0.152
51
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.152
52
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.152
53
LPD008 Lipid Metabolism Disorder 64 0.152
54
P CYS018 Cystitis 59 0.152
55
c ACT210 Acute Respiratory Distress Syndrome 59 0.152
56
TRM010 Traumatic Brain Injury 54 0.152
57
P SCK005 Sickle Cell Disease 53 0.152
58
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.152
59
LMB062 Limb Ischemia 50 0.152
60
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.152
61
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.152
62
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.152
63
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.152
64
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.152
65
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.152
66
CYT002 Cytokine Deficiency 46 0.152
67
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.152
68
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.152
69
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.152
70
CRB004 Cerebral Artery Occlusion 38 0.152
71
MLR004 Malaria 82 0.144
72
P MYC007 Myocardial Infarction 74 0.144
73
LVR012 Liver Cirrhosis 67 0.144
74
P ENC018 Encephalopathy 64 0.144
75
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.144
76
SPN186 Spinal Cord Injury 63 0.144
77
P INT143 Interstitial Cystitis 62 0.144
78
GST033 Gestational Diabetes 58 0.144
79
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.144
80
HLX001 Helix Syndrome 46 0.144
81
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.144
82
48X005 48,xyyy 37 0.144
83
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 36 0.144
84
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.136
85
c MGR028 Migraine with or Without Aura 1 70 0.136
86
PRT036 Peritonitis 66 0.136
87
LSH001 Leishmaniasis 64 0.136
88
LNG099 Lung Disease 62 0.136
89
INT002 Intermittent Claudication 60 0.136
90
PLM033 Pulmonary Embolism 60 0.136
91
AGN016 Aging 58 0.136
92
HYP060 Hyperinsulinism 55 0.136
93
P DRR001 Diarrhea 55 0.136
94
PNG002 Pain Agnosia 52 0.136
95
P RNV001 Renovascular Hypertension 49 0.136
96
P KLZ004 Kala-Azar 1 43 0.136
97
AST005 Asthma 80 0.127
98
SCK003 Sickle Cell Anemia 74 0.127
99
P CRD119 Cardiac Arrest 71 0.127
100
P MCR115 Microvascular Complications of Diabetes 5 67 0.127
101
P BRS044 Breast Adenocarcinoma 59 0.127
102
c ACT075 Acute Myocardial Infarction 59 0.127
103
c MCR113 Microvascular Complications of Diabetes 3 55 0.127
104
PRP080 Peripheral Artery Disease 51 0.127
105
BRN071 Brain Injury 51 0.127
106
c MCR120 Microvascular Complications of Diabetes 7 48 0.127
107
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.127
108
P PRC031 Preeclampsia/eclampsia 1 42 0.127
109
c MCR130 Microvascular Complications of Diabetes 6 42 0.127
110
c MCR133 Microvascular Complications of Diabetes 4 42 0.127
111
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.127
112
P CLR023 Colorectal Cancer 100 0.117
113
DFC004 Deficiency Anemia 77 0.117
114
c ATR087 Atrial Standstill 1 76 0.117
115
ULC004 Ulcerative Colitis 75 0.117
116
P LVR013 Liver Disease 71 0.117
117
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.117
118
PRT037 Pertussis 66 0.117
119
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.117
120
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.117
121
ALL026 Allergic Hypersensitivity Disease 65 0.117
122
DPR016 Depression 64 0.117
123
ADL002 Adult Syndrome 62 0.117
124
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.117
125
c SCL052 Scleroderma, Familial Progressive 62 0.117
126
MNT002 Mental Depression 60 0.117
127
P NRP001 Neuropathy 57 0.117
128
ALL006 Allergic Asthma 56 0.117
129
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.117
130
HMC014 Homocysteinemia 54 0.117
131
BNR002 Bone Resorption Disease 51 0.117
132
URT010 Ureteral Obstruction 46 0.117
133
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.117
134
P SCH015 Schizophrenia 76 0.107
135
P BCL017 B-Cell Lymphoma 61 0.107
136
P OPT006 Optic Nerve Disease 59 0.107
137
BRN004 Brain Edema 57 0.107
138
P ART021 Arteriosclerosis 56 0.107
139
RYN005 Raynaud Phenomenon 50 0.107
140
BWN001 Bowen-Conradi Syndrome 49 0.107
141
OBS082 Obstructive Nephropathy 44 0.107
142
c HMG029 Hemoglobin Se Disease 40 0.107
143
SPR126 Superior Semicircular Canal Dehiscence 39 0.107
144
CRT055 Creatine Deficiency Syndromes 39 0.107
145
P ALZ034 Alzheimer Disease 90 0.096
146
PLM001 Pulmonary Tuberculosis 72 0.096
147
P MJR001 Major Depressive Disorder 69 0.096
148
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.096
149
P NRB010 Neuroblastoma 1 66 0.096
150
CLN015 Colon Adenocarcinoma 65 0.096
151
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.096
152
c BRN108 Branchiootic Syndrome 1 62 0.096
153
P ESP024 Esophagitis 62 0.096
154
CHL068 Cholestasis 61 0.096
155
PRT013 Portal Hypertension 61 0.096
156
P MYC008 Myocarditis 60 0.096
157
P INF032 Infertility 60 0.096
158
P HDC001 Headache 59 0.096
159
P MTC069 Mitochondrial Disorders 57 0.096
160
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.096
161
DBT010 Diabetic Neuropathy 56 0.096
162
PLM010 Pulmonary Edema 56 0.096
163
ARG007 Argininemia 55 0.096
164
LYS003 Lysinuric Protein Intolerance 54 0.096
165
PLS007 Plasmodium Falciparum Malaria 53 0.096
166
GST023 Gastric Ulcer 53 0.096
167
RNL077 Renal Fibrosis 49 0.096
168
HPT014 Hepatorenal Syndrome 49 0.096
169
MTB004 Metabolic Acidosis 48 0.096
170
WTH001 Withdrawal Disorder 47 0.096
171
P RNL015 Renal Hypertension 47 0.096
172
ART004 Aortic Atherosclerosis 47 0.096
173
NPH010 Nephrosclerosis 46 0.096
174
ATX019 Ataxia with Vitamin E Deficiency 46 0.096
175
HPT004 Hepatic Coma 42 0.096
176
P BRS047 Breast Cancer 99 0.083
177
P GST053 Gastric Cancer 85 0.083
178
OST012 Osteoarthritis 80 0.083
179
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.083
180
c THR092 Thrombophilia Due to Thrombin Defect 74 0.083
181
HMN044 Human Immunodeficiency Virus Type 1 73 0.083
182
c BTT014 Beta-Thalassemia 73 0.083
183
P CNR004 Cone-Rod Dystrophy 2 72 0.083
184
P SLP006 Sleep Apnea 71 0.083
185
RCK004 Rickets 70 0.083
186
P MYC084 Mycobacterium Tuberculosis 1 69 0.083
187
HYP056 Hypoglycemia 68 0.083
188
PSY004 Psychotic Disorder 68 0.083
189
P PLM036 Pulmonary Fibrosis 66 0.083
190
CHG001 Chagas Disease 66 0.083
191
P DYS154 Dystonia 65 0.083
192
P ADN016 Adenocarcinoma 65 0.083
193
IDP011 Idiopathic Interstitial Pneumonia 65 0.083
194
ANR007 Anorexia Nervosa 64 0.083
195
c RHB024 Rhabdomyosarcoma 2 64 0.083
196
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.083
197
c ALP101 Alpha-Thalassemia 63 0.083
198
MDD011 Mood Disorder 62 0.083
199
P HYP750 Hypertriglyceridemia, Familial 62 0.083
200
P THL005 Thalassemia 62 0.083
201
TRN015 Transient Cerebral Ischemia 62 0.083
202
STT001 Status Epilepticus 61 0.083
203
P PLY014 Polycystic Kidney Disease 61 0.083
204
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.083
205
PRT058 Pure Autonomic Failure 60 0.083
206
CHL123 Chlamydia 60 0.083
207
MSC152 Muscular Dystrophy, Becker Type 60 0.083
208
HPT019 Hepatic Encephalopathy 60 0.083
209
P INT070 Intestinal Obstruction 60 0.083
210
THR024 Thrombosis 58 0.083
211
P FBR017 Fibrosarcoma 57 0.083
212
P MLN007 Male Infertility 57 0.083
213
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.083
214
c ACT134 Acute Liver Failure 53 0.083
215
DNT012 Dental Caries 52 0.083
216
P CHR345 Chronic Pain 52 0.083
217
CRB151 Cerebral Creatine Deficiency Syndrome 1 51 0.083
218
c SVR005 Severe Pre-Eclampsia 50 0.083
219
SCH012 Schizoaffective Disorder 50 0.083
220
SXL003 Sexual Disorder 49 0.083
221
CRN030 Coronary Stenosis 49 0.083
222
SCH003 Schizophreniform Disorder 49 0.083
223
P OBS001 Obstructive Jaundice 49 0.083
224
ART031 Aortic Coarctation 45 0.083
225
ATN011 Autoinflammation with Infantile Enterocolitis 45 0.083
226
MYC005 Myocardial Stunning 45 0.083
227
DYS032 Dystrophinopathies 42 0.083
228
c SCH080 Schizophrenia 3 34 0.083
229
QLT002 Qualitative or Quantitative Defects of Dystrophin 21 0.083
230
IDP022 Idiopathic Spinal Cord Herniation 17 0.083
231
c SYS001 Systemic Lupus Erythematosus 88 0.068
232
P ATX030 Ataxia-Telangiectasia 83 0.068
233
P OST002 Osteoporosis 79 0.068
234
BRN028 Brain Cancer 75 0.068
235
GLB002 Glioblastoma 74 0.068
236
SVR004 Severe Combined Immunodeficiency 74 0.068
237
MLT157 Multiple System Atrophy 1 71 0.068
238
P HYP086 Hypothyroidism 70 0.068
239
P SYS005 Systemic Scleroderma 68 0.068
240
BRK010 Burkitt Lymphoma 68 0.068
241
P ATR011 Atrial Fibrillation 67 0.068
242
P PRM011 Primary Ciliary Dyskinesia 67 0.068
243
P HYP098 Hypereosinophilic Syndrome 67 0.068
244
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 67 0.068
245
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.068
246
c MCR129 Microvascular Complications of Diabetes 1 67 0.068
247
P MNN013 Meningitis 67 0.068
248
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.068
249
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.068
250
P PRD008 Periodontitis 66 0.068
251
CRN036 Craniopharyngioma 65 0.068
252
P PRP019 Peripheral Nervous System Disease 64 0.068
253
P NTR004 Neutropenia 64 0.068
254
APN008 Apnea, Obstructive Sleep 64 0.068
255
FTT001 Fatty Liver Disease 63 0.068
256
P SNS001 Sensorineural Hearing Loss 62 0.068
257
P CTR002 Cataract 62 0.068
258
c PNS012 Paine Syndrome 61 0.068
259
CTN007 Cutaneous Leishmaniasis 61 0.068
260
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.068
261
NTR005 Nutritional Deficiency Disease 61 0.068
262
P ATR010 Atrial Heart Septal Defect 61 0.068
263
P ADL010 Adult Respiratory Distress Syndrome 61 0.068
264
P VNT002 Ventricular Septal Defect 61 0.068
265
GLB015 Glioblastoma Multiforme 60 0.068
266
CHL067 Cholecystitis 60 0.068
267
INS001 Insulinoma 60 0.068
268
c MCL013 Mucolipidosis Iv 60 0.068
269
ARG002 Argininosuccinic Aciduria 59 0.068
270
EYD002 Eye Disease 59 0.068
271
P THR005 Thrombotic Thrombocytopenic Purpura 59 0.068
272
P UVT001 Uveitis 58 0.068
273
P PLY011 Polycystic Ovary Syndrome 58 0.068
274
DSS009 Disseminated Intravascular Coagulation 58 0.068
275
INT007 Intermediate Coronary Syndrome 58 0.068
276
P GST044 Gastritis 58 0.068
277
P INF037 Inflammatory Bowel Disease 57 0.068
278
SCH014 Schistosomiasis 57 0.068
279
GST050 Gastrointestinal System Disease 57 0.068
280
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.068
281
PRP030 Purpura 56 0.068
282
c BCT007 Bacterial Meningitis 56 0.068
283
P PLY018 Polycythemia 56 0.068
284
MCS002 Mucositis 56 0.068
285
VSC003 Visceral Leishmaniasis 55 0.068
286
PLC005 Placental Insufficiency 55 0.068
287
INT075 Intracranial Hypertension 54 0.068
288
TLN003 Telangiectasis 53 0.068
289
P ACT105 Acute Mountain Sickness 53 0.068
290
OCL069 Ocular Motor Apraxia 53 0.068
291
RTN003 Retinal Ischemia 52 0.068
292
GSG001 Gas Gangrene 52 0.068
293
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 52 0.068
294
HRT011 Heart Septal Defect 52 0.068
295
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.068
296
PLC008 Placenta Disease 51 0.068
297
OVR082 Overgrowth Syndrome 51 0.068
298
QDR001 Quadriplegia 51 0.068
299
HYP081 Hypolipoproteinemia 51 0.068
300
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.068
301
GLS018 Glass Syndrome 51 0.068
302
URC002 Urea Cycle Disorder 51 0.068
303
P SHR001 Short Bowel Syndrome 50 0.068
304
CRT013 Carotid Stenosis 50 0.068
305
RTN020 Retinal Vascular Disease 49 0.068
306
HPT009 Hepatopulmonary Syndrome 49 0.068
307
47X002 47,xyy 49 0.068
308
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.068
309
ATN005 Autonomic Dysfunction 48 0.068
310
GRW007 Growth Hormone Deficiency 48 0.068
311
c MLG069 Malignant Hypertension 46 0.068
312
LCK001 Locked-in Syndrome 46 0.068
313
CCC002 Coccidiosis 46 0.068
314
NWC001 Newcastle Disease 45 0.068
315
CRB090 Cerebral Hypoxia 45 0.068
316
CTS005 Catastrophic Antiphospholipid Syndrome 44 0.068
317
c HYP272 Hypercholesterolemia, Familial, 3 44 0.068
318
MTC004 Mitochondrial Encephalomyopathy 44 0.068
319
ANX004 Anoxia 44 0.068
320
CRT015 Carotid Artery Occlusion 44 0.068
321
BCT021 Bacterial Sepsis 44 0.068
322
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.068
323
P CPL003 Capillary Leak Syndrome 42 0.068
324
ACT003 Acute Kidney Tubular Necrosis 42 0.068
325
MRP001 Morphine Dependence 41 0.068
326
c SYS007 Systemic Capillary Leak Syndrome 41 0.068
327
ALL014 Allergic Encephalomyelitis 40 0.068
328
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.068
329
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.068
330
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.068
331
c CHR682 Chronic Bilirubin Encephalopathy 36 0.068
333
PPL052 Papillomatosis, Confluent and Reticulated 34 0.068
334
ART010 Arteriolosclerosis 32 0.068
335
MST020 Mast Cell Activation Syndrome 28 0.068
336
MD2001 Med23 25 0.068
337
P OVR042 Ovarian Cancer 89 0.048
338
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.048
340
MYL069 Myeloma, Multiple 85 0.048
341
P RHM011 Rheumatoid Arthritis 82 0.048
342
c DLT002 Dilated Cardiomyopathy 81 0.048
343
IMM167 Immune Deficiency Disease 79 0.048
344
P RTN008 Retinitis Pigmentosa 77 0.048
345
P NRF023 Neurofibromatosis, Type Ii 77 0.048
346
P RSP003 Respiratory Failure 75 0.048
347
CRH001 Crohn's Disease 75 0.048
348
ANX010 Anxiety 75 0.048
349
ACR006 Aceruloplasminemia 74 0.048
350
c SPN225 Spondyloarthropathy 1 74 0.048
351
P EPL164 Epilepsy 73 0.048
352
LPT014 Leptin Deficiency or Dysfunction 72 0.048
353
P AMY004 Amyloidosis 71 0.048
354
P ART022 Arthritis 71 0.048
355
P PNM007 Pneumonia 71 0.048
356
ACR007 Acromegaly 70 0.048
357
P TTR001 Tetralogy of Fallot 70 0.048
358
BRN024 Bronchitis 70 0.048
359
DWN001 Down Syndrome 70 0.048
360
CRB037 Cerebral Palsy 69 0.048
361
OBS002 Obsessive-Compulsive Disorder 69 0.048
362
P ATS364 Autism 68 0.048
363
P DMN002 Dementia 68 0.048
364
P ORT004 Orthostatic Intolerance 68 0.048
365
GST092 Gastroesophageal Reflux 68 0.048
366
CRT072 Creutzfeldt-Jakob Disease 67 0.048
367
c FML021 Familial Hypercholesterolemia 67 0.048
368
P THR014 Thrombocytopenia 67 0.048
369
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.048
370
c ART101 Aortic Valve Disease 2 67 0.048
371
P SKN015 Skin Carcinoma 67 0.048
372
OST159 Osteogenic Sarcoma 67 0.048
373
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.048
374
P HRP006 Herpes Simplex 66 0.048
375
P TRN020 Turner Syndrome 66 0.048
376
c CNG006 Congenital Hypothyroidism 65 0.048
377
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.048
378
MSC007 Muscle Hypertrophy 65 0.048
379
P NPH012 Nephrotic Syndrome 65 0.048
380
TBC004 Tobacco Addiction 65 0.048
381
CLR108 Colorectal Adenoma 64 0.048
382
c FNC043 Fanconi Anemia, Complementation Group E 64 0.048
383
P GLM045 Glioma 64 0.048
384
P ANR048 Aniridia 1 64 0.048
385
P PSR002 Psoriasis 63 0.048
386
c ACT068 Acute Cystitis 63 0.048
387
c HPT016 Hepatitis B 63 0.048
388
PRP001 Propionic Acidemia 63 0.048
389
PSR001 Psoriatic Arthritis 63 0.048
390
c GLC092 Glaucoma, Primary Open Angle 63 0.048
391
c GLY060 Glycogen Storage Disease Ia 63 0.048
392
P FCL005 Focal Segmental Glomerulosclerosis 63 0.048
393
P MST009 Mastocytosis 62 0.048
394
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 0.048
395
P EPD009 Epidermolysis Bullosa Dystrophica 62 0.048
396
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.048
397
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.048
398
CRC021 Carcinosarcoma 62 0.048
399
ACN002 Acanthosis Nigricans 62 0.048
400
THY029 Thyroid Carcinoma 62 0.048
401
ATM095 Autoimmune Disease 62 0.048
402
TYP007 Typhoid Fever 61 0.048
403
c DNG003 Dengue Disease 61 0.048
404
P URT039 Urticaria 61 0.048
405
P ART023 Arthropathy 61 0.048
406
ACQ007 Acquired Immunodeficiency Syndrome 61 0.048
407
CHR066 Chronic Fatigue Syndrome 61 0.048
408
MSL001 Measles 61 0.048
409
HLC007 Helicobacter Pylori Infection 61 0.048
410
P CRD132 Cardiac Conduction Defect 61 0.048
411
P CND004 Candidiasis 61 0.048
412
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 60 0.048
413
PPT005 Peptic Ulcer Disease 60 0.048
414
P PTN014 Patent Ductus Arteriosus 1 60 0.048
415
P KDN017 Kidney Cancer 60 0.048
416
BND020 Bone Disease 60 0.048
417
ADN018 Adenoma 60 0.048
418
c ACT073 Acute Leukemia 59 0.048
419
P HRD011 Hereditary Spherocytosis 59 0.048
420
P GLY013 Glycogen Storage Disease 59 0.048
421
CNS004 Constipation 59 0.048
422
c GM1007 Gm1 Gangliosidosis 59 0.048
423
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 59 0.048
424
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.048
425
P ALP008 Alopecia 58 0.048
426
P MYP006 Myopia 58 0.048
427
CNT047 Contact Dermatitis 58 0.048
428
LYM027 Lymphopenia 58 0.048
429
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.048
430
CHL014 Cholera 58 0.048
431
P TRC086 Trichohepatoenteric Syndrome 1 57 0.048
432
PLS011 Plasmacytoma 57 0.048
433
P PRN023 Prion Disease 57 0.048
434
BRN056 Bronchopulmonary Dysplasia 57 0.048
435
VSC002 Vascular Dementia 57 0.048
436
PTN001 Patent Foramen Ovale 57 0.048
437
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 56 0.048
438
P RTN016 Retinal Degeneration 56 0.048
439
c PRD040 Periodontitis, Chronic 56 0.048
440
P LTR001 Lateral Sclerosis 56 0.048
441
HRT012 Heart Valve Disease 56 0.048
442
P PLM034 Pulmonary Emphysema 55 0.048
443
AMN003 Amnestic Disorder 55 0.048
444
HYP005 Hypokalemia 55 0.048
445
P HYP076 Hyperthyroidism 55 0.048
446
P TRM003 Tremor 55 0.048
447
P PLY019 Polyneuropathy 55 0.048
448
HMP005 Hemiplegia 55 0.048
449
P EPD016 Epidermolysis Bullosa 54 0.048
450
PRP016 Paraplegia 54 0.048
451
P MMB011 Membranous Nephropathy 54 0.048
452
P RCT021 Rectum Cancer 54 0.048
453
P HML001 Hemolytic-Uremic Syndrome 54 0.048
454
AMN001 Amenorrhea 54 0.048
455
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 54 0.048
456
SPP010 Suppressor of Tumorigenicity 3 54 0.048
457
P SLM003 Salmonellosis 54 0.048
458
CHR100 Chronic Ulcer of Skin 53 0.048
459
P CHL066 Cholangitis 53 0.048
460
OLG003 Oligohydramnios 53 0.048
461
P RTN018 Retinal Disease 53 0.048
462
SPN051 Spondylitis 53 0.048
463
P PTT006 Pituitary Adenoma 53 0.048
464
CRT016 Carotid Artery Disease 53 0.048
465
ALC009 Alcoholic Liver Cirrhosis 53 0.048
466
P MGR003 Migraine with Aura 53 0.048
467
NNL006 Non-Alcoholic Steatohepatitis 53 0.048
468
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.048
469
NPH003 Nephrocalcinosis 52 0.048
470
HYP014 Hyperuricemia 52 0.048
471
ESN011 Eisenmenger Syndrome 52 0.048
472
GST037 Gastroparesis 52 0.048
473
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 52 0.048
474
GNG012 Gingival Overgrowth 52 0.048
475
P RNL017 Renal Oncocytoma 52 0.048
476
P AST007 Astrocytoma 52 0.048
477
ORT008 Orotic Aciduria 51 0.048
478
DYS014 Dyspepsia 51 0.048
479
c INH020 Inherited Metabolic Disorder 51 0.048
480
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.048
481
PNC034 Pancreas Disease 51 0.048
482
CLR109 Colorectal Adenocarcinoma 51 0.048
483
IMM064 Immunodeficiency, Common Variable, 10 51 0.048
484
HYP080 Hypogonadism 51 0.048
485
c PYR010 Peyronie's Disease 51 0.048
486
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 51 0.048
487
PST011 Pustulosis of Palm and Sole 51 0.048
488
OPT003 Opiate Dependence 50 0.048
489
P DDN001 Duodenal Ulcer 50 0.048
490
P RTN022 Retinal Vein Occlusion 50 0.048
491
VCC001 Vaccinia 50 0.048
492
TRY001 Trypanosomiasis 50 0.048
493
ISL003 Isolated Growth Hormone Deficiency 50 0.048
494
c PNC106 Pancreatic Agenesis 1 50 0.048
495
MTC005 Mitochondrial Metabolism Disease 50 0.048
496
P OPN001 Open-Angle Glaucoma 50 0.048
497
P MTH008 Methylmalonic Acidemia 50 0.048
498
PLR008 Pleurisy 50 0.048
499
c INF145 Infantile Liver Failure Syndrome 1 50 0.048
500
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.048
501
TST044 Testicular Torsion 49 0.048
502
NTR046 Neutrophil Migration 49 0.048
503
c BCT013 Bacterial Pneumonia 49 0.048
504
ATS010 Autosomal Recessive Disease 49 0.048
505
PRD004 Prediabetes Syndrome 49 0.048
506
THR013 Thoracic Outlet Syndrome 49 0.048
507
SPL018 Splenomegaly 48 0.048
508
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.048
509
LYM019 Lymphosarcoma 48 0.048
510
GLL048 Glial Tumor 48 0.048
511
P MGR001 Migraine Without Aura 47 0.048
512
CHR074 Choriocarcinoma 47 0.048
513
P MRC003 Mercury Poisoning 47 0.048
514
PPT001 Peptic Esophagitis 47 0.048
515
P MYC033 Myoclonus 47 0.048
516
c ART120 Arthrogryposis, Distal, Type 3 47 0.048
517
EPL131 Epilepsy, Pyridoxine-Dependent 47 0.048
518
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.048
519
PRP007 Priapism 47 0.048
520
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.048
521
RTN023 Retinitis 46 0.048
522
NRR001 Neuroretinitis 46 0.048
523
P HRN001 Horner's Syndrome 46 0.048
524
P SMK004 Smoking As a Quantitative Trait Locus 3 46 0.048
525
LWC001 Low Compliance Bladder 45 0.048
526
P GNG009 Gangliosidosis 45 0.048
527
KHN001 Kuhnt-Junius Degeneration 45 0.048
528
TLR001 Tularemia 44 0.048
529
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 44 0.048
530
P CLS010 Cluster Headache 44 0.048
531
OLG001 Oligospermia 44 0.048
532
P HYP265 Hypotonia 43 0.048
533
FTL021 Fetal Macrosomia 43 0.048
534
SYS003 Systolic Heart Failure 43 0.048
535
DST006 Diastolic Heart Failure 43 0.048
536
GNG003 Gingival Recession 43 0.048
537
GLC086 Glucocorticoid-Induced Osteoporosis 42 0.048
538
DBT008 Diabetic Angiopathy 42 0.048
539
ASP030 Aspirin Resistance 42 0.048
540
CLL021 Collagenous Colitis 42 0.048
541
c MCR112 Microvascular Complications of Diabetes 2 42 0.048
542
c SPR086 Spermatogenic Failure 3 41 0.048
543
P PYR039 Peyronie Disease 41 0.048
544
CRN020 Coronary Restenosis 40 0.048
545
HYP064 Hypogonadotropism 40 0.048
546
HMR023 Hemorrhagic Cystitis 40 0.048
547
IMM001 Immune-Complex Glomerulonephritis 40 0.048
548
GNR003 Generalized Atherosclerosis 39 0.048
549
GNT029 Genetic Hypertension 39 0.048
550
CHL147 Chlamydia Pneumonia 39 0.048
551
P DNT007 Dentin Sensitivity 39 0.048
552
ATX010 Ataxia Neuropathy Spectrum 39 0.048
553
EXT006 Extrahepatic Cholestasis 38 0.048
554
HRN029 Hearing Loss, Noise-Induced 38 0.048
555
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.048
556
HYP008 Hypertensive Retinopathy 38 0.048
557
RTR001 Retrograde Amnesia 38 0.048
558
MNN017 Mononeuropathy 38 0.048
559
BRT043 Bartonellosis 37 0.048
560
SCR011 Scrapie 37 0.048
561
ALC005 Alcoholic Pancreatitis 37 0.048
562
c ATM022 Autoimmune Myocarditis 36 0.048
563
c PRG020 Paragangliomas 3 36 0.048
564
SCR003 Secretory Diarrhea 36 0.048
565
HRW001 Hair Whorl 36 0.048
566
HYP114 Hypertensive Nephropathy 36 0.048
567
ACL001 Acalculous Cholecystitis 35 0.048
568
ANT019 Anterograde Amnesia 35 0.048
569
GGN002 Gigantism 35 0.048
570
P FML187 Familial Hypertension 35 0.048
571
OLG022 Oligoasthenoteratozoospermia 34 0.048
572
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.048
573
CND006 Candida Glabrata 33 0.048
574
RFL002 Reflex Epilepsy 33 0.048
575
PRX097 Paroxysmal Dystonia 31 0.048
576
CRB009 Cerebritis 31 0.048
578
RSP007 Respiratory Distress Syndrome, Infant 31 0.048
579
MYC088 Mycobacterium Avium Complex Infections 30 0.048
580
CRB137 Cerebral Creatine Deficiency Syndrome 30 0.048
581
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.048
582
ISL099 Isolated Methylmalonic Acidemia 30 0.048
583
MTC026 Mitochondrial Myopathy with Lactic Acidosis 29 0.048
584
INF009 Inflammatory Spondylopathy 29 0.048
585
P ACT232 Acute Necrotizing Encephalopathy 28 0.048
586
CHL079 Children's Interstitial Lung Disease 27 0.048
587
ADG002 Audiogenic Seizures 25 0.048
588
NCR014 Necrotizing Soft Tissue Infection 24 0.048
589
P ART034 Aortopulmonary Window 23 0.048
590
VLK001 Volkmann Contracture 22 0.048
591
P RRN010 Rare Neurodegenerative Disease 21 0.048
592
AND005 Androgen Insensitivity Syndrome, Mild 20 0.048
593
SPN092 Spinal Shock 19 0.048
594
ORN004 Ornithinemia 17 0.048
595
BLD137 Blood Group--Ahonen 17 0.048
596
ISP002 Isoproterenol-Mediated Vasodilatation 8 0.048
Content
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