Search results for Tenofovir

422 hits were found for Tenofovir

# Family MCID Name MIFTS Score
1
c HPT016 Hepatitis B 59 0.824
2
HMN044 Human Immunodeficiency Virus Type 1 71 0.816
3
48X005 48,xyyy 39 0.744
4
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.723
5
P HPT021 Hepatitis 67 0.692
6
IMM167 Immune Deficiency Disease 78 0.557
7
c HPT003 Hepatitis a 62 0.549
8
ACQ007 Acquired Immunodeficiency Syndrome 60 0.522
9
HRP008 Herpes Simiae 25 0.455
10
LVR012 Liver Cirrhosis 62 0.337
11
P FNC004 Fanconi Syndrome 50 0.304
12
P FNC034 Fanconi Renotubular Syndrome 2 40 0.304
13
c RHB024 Rhabdomyosarcoma 2 67 0.301
14
P LVR013 Liver Disease 68 0.299
15
CHL079 Children's Interstitial Lung Disease 26 0.299
16
P HPT023 Hepatocellular Carcinoma 100 0.276
17
P KDN018 Kidney Disease 72 0.265
18
CMR002 Coumarin Resistance 56 0.257
19
VRL011 Viral Infectious Disease 61 0.223
20
c HPT001 Hepatitis C 62 0.211
21
c ACT071 Acute Kidney Failure 60 0.207
22
HYP017 Hypophosphatemia 50 0.207
23
RCK004 Rickets 68 0.204
24
c HPT073 Hepatitis C Virus 72 0.194
25
c CHR684 Chronic Kidney Disease 70 0.194
26
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.189
27
c VRL010 Viral Hepatitis 52 0.189
28
P CRD246 Cardiovascular System Disease 57 0.186
29
P MYC084 Mycobacterium Tuberculosis 1 68 0.183
30
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.177
31
ATX019 Ataxia with Vitamin E Deficiency 42 0.177
32
OST011 Osteomalacia 52 0.175
33
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.169
34
P BND020 Bone Disease 59 0.166
35
49X006 49, Xxxxy Syndrome 41 0.166
36
ADL002 Adult Syndrome 70 0.163
37
P HRP006 Herpes Simplex 65 0.163
38
P LCT001 Lactic Acidosis 51 0.159
39
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.159
40
c PRM038 Primary Agammaglobulinemia 44 0.156
41
LPD008 Lipid Metabolism Disorder 62 0.153
42
c HPT015 Hepatitis D 49 0.153
43
P OST002 Osteoporosis 74 0.146
44
P EXN002 Exanthem 57 0.146
45
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.146
46
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.146
47
DWN001 Down Syndrome 70 0.143
48
c INF145 Infantile Liver Failure Syndrome 1 50 0.143
49
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.135
50
P DRR001 Diarrhea 55 0.135
51
BNR002 Bone Resorption Disease 48 0.135
52
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.135
53
HYP005 Hypokalemia 55 0.131
54
P CNR004 Cone-Rod Dystrophy 2 73 0.127
55
P NRP001 Neuropathy 56 0.127
56
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.119
57
ANX010 Anxiety 73 0.115
58
c MCL013 Mucolipidosis Iv 66 0.115
59
NTR005 Nutritional Deficiency Disease 62 0.115
60
P PRP019 Peripheral Nervous System Disease 58 0.110
61
ACT003 Acute Kidney Tubular Necrosis 45 0.110
62
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.110
63
DPR016 Depression 63 0.106
64
MNT002 Mental Depression 58 0.106
65
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.106
66
c HYP836 Hypercholesterolemia, Familial, 1 73 0.101
67
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.101
68
P MYP004 Myopathy 70 0.101
69
P TRN020 Turner Syndrome 67 0.101
70
P HYP069 Hyperparathyroidism 63 0.101
71
AGN016 Aging 56 0.101
72
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.101
73
P LYM118 Lymphoma 68 0.096
74
LYM019 Lymphosarcoma 46 0.096
75
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.090
76
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.090
77
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.090
78
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.090
79
END086 End Stage Renal Disease 51 0.090
80
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.090
81
CVD001 Covid-19 44 0.090
82
NSP002 Nasopharyngitis 43 0.090
83
STR067 Stroke, Ischemic 81 0.084
84
KPS004 Kaposi Sarcoma 75 0.084
85
P HRT032 Heart Disease 75 0.084
86
LYM133 Lymphoma, Hodgkin, Classic 69 0.084
87
CRB039 Cerebrovascular Disease 67 0.084
88
SRC014 Sarcoma 65 0.084
89
ART002 Arts Syndrome 64 0.084
90
c SVR001 Severe Acute Respiratory Syndrome 62 0.084
91
SFT003 Soft Tissue Sarcoma 56 0.084
92
SPN035 Spindle Cell Sarcoma 53 0.084
93
TXC002 Toxic Encephalopathy 53 0.084
94
P MLG074 Malignant Mesenchymoma 40 0.084
95
ANG049 Angioedema Induced by Ace Inhibitors 40 0.084
96
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.078
97
MLR004 Malaria 81 0.078
98
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.078
99
P MYC007 Myocardial Infarction 70 0.078
100
P CRN300 Coronary Heart Disease 1 63 0.078
101
LPP008 Lipoprotein Quantitative Trait Locus 62 0.078
102
ALL026 Allergic Hypersensitivity Disease 62 0.078
103
P PNC044 Pancreatitis 61 0.078
104
c ACT027 Acute Pancreatitis 60 0.078
105
P SLP005 Sleep Disorder 59 0.078
106
c ACT134 Acute Liver Failure 56 0.078
107
P DBT005 Diabetes Insipidus 55 0.078
108
GNT003 Genital Herpes 54 0.078
109
c HPT007 Hepatitis E 53 0.078
110
HYP081 Hypolipoproteinemia 51 0.078
111
47X002 47,xyy 49 0.078
112
P HMN032 Human Herpesvirus 8 47 0.078
113
CYT018 Cytochrome P450 2d6 Variant 27 0.078
114
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.078
115
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.078
116
P LKM071 Leukemia, Chronic Lymphocytic 79 0.071
117
P OCL013 Oculodentodigital Dysplasia 69 0.071
118
P LKM002 Leukemia 68 0.071
119
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.071
120
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.071
121
P HYP750 Hypertriglyceridemia, Familial 62 0.071
122
P PRM006 Primary Biliary Cirrhosis 62 0.071
123
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.071
124
HPT019 Hepatic Encephalopathy 60 0.071
125
CHL123 Chlamydia 59 0.071
126
BLR008 Bilirubin Metabolic Disorder 57 0.071
127
c FML035 Familial Hyperlipidemia 55 0.071
128
DFF005 Diffuse Large B-Cell Lymphoma 55 0.071
129
NPH009 Nephrolithiasis 55 0.071
130
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.071
131
AMN001 Amenorrhea 54 0.071
132
ART140 Arteries, Anomalies of 52 0.071
133
MTB004 Metabolic Acidosis 50 0.071
134
INT067 Interstitial Nephritis 48 0.071
135
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.071
136
HPT004 Hepatic Coma 45 0.071
137
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.071
138
c FML363 Familial Adult Myoclonic Epilepsy 41 0.071
139
CRN322 Coronavirus Infectious Disease 40 0.071
140
c HYP595 Hypertension, Essential 84 0.064
141
LPT014 Leptin Deficiency or Dysfunction 74 0.064
142
PRP027 Peripheral Vascular Disease 71 0.064
143
DFC004 Deficiency Anemia 70 0.064
144
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.064
145
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.064
146
ATH013 Atherosclerosis Susceptibility 65 0.064
147
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.064
148
FTT001 Fatty Liver Disease 61 0.064
149
P ENC018 Encephalopathy 61 0.064
150
VSL002 Visual Epilepsy 59 0.064
151
P SYP003 Syphilis 58 0.064
152
P BCL017 B-Cell Lymphoma 58 0.064
153
P SZR006 Seizure Disorder 56 0.064
154
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.064
155
P RNL007 Renal Tubular Acidosis 51 0.064
156
RTC005 Reticulosarcoma 47 0.064
157
TRP009 Triple X Syndrome 42 0.064
158
CYT002 Cytokine Deficiency 42 0.064
160
OST012 Osteoarthritis 78 0.055
161
c ATR087 Atrial Standstill 1 75 0.055
162
PLM001 Pulmonary Tuberculosis 69 0.055
163
P THR014 Thrombocytopenia 67 0.055
164
BRK010 Burkitt Lymphoma 67 0.055
165
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.055
166
LPT001 Leptospirosis 66 0.055
167
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.055
168
P MNN013 Meningitis 66 0.055
169
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.055
170
P VSC007 Vascular Disease 63 0.055
171
c ACT068 Acute Cystitis 63 0.055
172
c FNC043 Fanconi Anemia, Complementation Group E 62 0.055
173
HYP066 Hyperglycemia 61 0.055
174
P NPH012 Nephrotic Syndrome 60 0.055
175
VRC005 Varicose Veins 60 0.055
176
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.055
177
INC002 Inclusion Body Myositis 58 0.055
178
DSS008 Disease of Mental Health 58 0.055
179
P GLM007 Glomerulonephritis 57 0.055
180
IRN002 Iron Metabolism Disease 57 0.055
181
P HDC001 Headache 57 0.055
182
HMR039 Hemorrhage, Intracerebral 57 0.055
183
HYP266 Hypoxia 57 0.055
184
P MYS005 Myositis 56 0.055
185
BCT022 Bacterial Infectious Disease 56 0.055
186
PTS001 Patau Syndrome 55 0.055
187
HMF006 Hemifacial Microsomia 55 0.055
188
P SBS003 Substance Abuse 55 0.055
189
VGN023 Vaginitis 54 0.055
190
NNL006 Non-Alcoholic Steatohepatitis 54 0.055
191
HRT012 Heart Valve Disease 53 0.055
192
ACR041 Acromelic Frontonasal Dysostosis 52 0.055
193
PNG002 Pain Agnosia 51 0.055
194
c SCN007 Secondary Hyperparathyroidism 51 0.055
195
P CHL066 Cholangitis 51 0.055
196
c ORF040 Orofaciodigital Syndrome Viii 50 0.055
197
OPT003 Opiate Dependence 50 0.055
198
CRY014 Cryptococcal Meningitis 48 0.055
199
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.055
200
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.055
201
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.055
202
OPD001 Opioid Abuse 46 0.055
203
c DRR009 Diarrhea 6 46 0.055
204
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.055
205
IMM136 Immune System Disease 45 0.055
206
URL001 Urolithiasis 45 0.055
207
CLL014 Cll/sll 45 0.055
208
IMM064 Immunodeficiency, Common Variable, 10 44 0.055
209
c HYP272 Hypercholesterolemia, Familial, 3 44 0.055
210
DRG024 Drug Allergy 42 0.055
211
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.055
212
CRD017 Cardiac Valvular Dysplasia, X-Linked 40 0.055
213
c FNC026 Fanconi Renotubular Syndrome 1 39 0.055
214
MCL069 Macular Dystrophy, Retinal, 1, North Carolina Type 39 0.055
215
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.055
216
c CHR682 Chronic Bilirubin Encephalopathy 39 0.055
217
AMN006 Aminoaciduria 38 0.055
218
CHR178 Chromosomal Triplication 35 0.055
219
c FNC059 Fanconi-Like Syndrome 35 0.055
220
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.055
221
HPT085 Hepatitis, Fulminant Viral 32 0.055
222
CRN051 Craniofacial Microsomia 28 0.055
223
P OVR096 Overlap Myositis 27 0.055
224
c DRR021 Diarrhea 11, Malabsorptive, Congenital 25 0.055
225
HMS005 Homosexuality 1 23 0.055
226
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.045
227
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.045
228
GST040 Gastric Adenocarcinoma 70 0.045
229
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.045
230
BRN024 Bronchitis 68 0.045
231
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.045
232
P DMN002 Dementia 66 0.045
233
P NRV007 Nervous System Disease 66 0.045
234
KHL003 Kohlschutter-Tonz Syndrome 65 0.045
235
P PLM036 Pulmonary Fibrosis 65 0.045
236
TTN003 Tetanus 65 0.045
237
P MTR014 Motor Neuron Disease 65 0.045
238
LYM017 Lyme Disease 64 0.045
239
OST017 Osteomyelitis 64 0.045
240
P NTR004 Neutropenia 63 0.045
241
CLT003 Colitis 62 0.045
242
P PSR002 Psoriasis 62 0.045
243
ATM095 Autoimmune Disease 62 0.045
244
P ACR001 Aicardi-Goutieres Syndrome 62 0.045
245
TXC005 Toxic Shock Syndrome 62 0.045
246
INT002 Intermittent Claudication 61 0.045
247
DPH001 Diphtheria 60 0.045
248
P TXP001 Toxoplasmosis 60 0.045
249
P LKD001 Leukodystrophy 59 0.045
250
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.045
251
P HYP726 Hypercalcemia, Infantile, 1 58 0.045
252
ISC004 Ischemia 58 0.045
253
P ALC033 Alcohol Use Disorder 58 0.045
254
LYM027 Lymphopenia 58 0.045
255
P CND004 Candidiasis 58 0.045
256
CYT008 Cytomegalovirus Infection 57 0.045
257
HPT022 Hepatoblastoma 56 0.045
258
P PLM034 Pulmonary Emphysema 55 0.045
259
P ALP008 Alopecia 54 0.045
260
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.045
261
P LTR001 Lateral Sclerosis 54 0.045
262
BCT002 Bacterial Vaginosis 53 0.045
263
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.045
264
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.045
265
c CNT035 Central Nervous System Disease 52 0.045
266
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.045
267
PST011 Pustulosis of Palm and Sole 52 0.045
268
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.045
269
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.045
270
HPT014 Hepatorenal Syndrome 50 0.045
271
PLC008 Placenta Disease 50 0.045
272
DYS073 Dysphagia 50 0.045
273
HYP006 Hypertensive Heart Disease 49 0.045
274
VCC001 Vaccinia 49 0.045
275
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.045
276
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.045
277
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.045
278
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.045
279
ANR004 Anuria 46 0.045
280
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.045
281
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.045
282
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.045
283
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.045
284
P DST107 Distal Renal Tubular Acidosis 42 0.045
285
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.045
286
HYP540 Hypertension, Diastolic 40 0.045
287
CRP033 Corpus Callosum, Agenesis of, with Abnormal Genitalia 39 0.045
288
ATM052 Autoimmune Disease 1 37 0.045
289
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.045
290
CYS021 Cystic Adenomatoid Malformation of Lung 33 0.045
291
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.045
292
JVN026 Jeavons Syndrome 24 0.045
293
P BRS047 Breast Cancer 97 0.032
294
ESP021 Esophageal Cancer 90 0.032
295
MYL069 Myeloma, Multiple 85 0.032
296
NRL016 Neural Tube Defects 82 0.032
297
CNN003 Conn's Syndrome 79 0.032
298
c NRF024 Neurofibromatosis, Type I 77 0.032
299
CRH001 Crohn's Disease 74 0.032
300
ULC004 Ulcerative Colitis 73 0.032
301
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.032
302
P PHC003 Pheochromocytoma 71 0.032
303
CNG034 Congestive Heart Failure 69 0.032
304
P ASP006 Aspergillosis 69 0.032
305
P HYP086 Hypothyroidism 69 0.032
306
P PNM007 Pneumonia 68 0.032
307
P MJR001 Major Depressive Disorder 68 0.032
308
P CRD119 Cardiac Arrest 67 0.032
309
c INF071 Inflammatory Bowel Disease 1 67 0.032
310
P HYP098 Hypereosinophilic Syndrome 67 0.032
311
P LNG028 Long Qt Syndrome 66 0.032
312
P MCR115 Microvascular Complications of Diabetes 5 66 0.032
313
c MCR129 Microvascular Complications of Diabetes 1 66 0.032
314
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.032
315
P PRS038 Personality Disorder 65 0.032
316
P DBT009 Diabetes Mellitus 64 0.032
317
P ADN016 Adenocarcinoma 64 0.032
318
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.032
319
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.032
320
P ESP024 Esophagitis 62 0.032
321
P VSC011 Vasculitis 62 0.032
322
MSL001 Measles 62 0.032
323
CHL068 Cholestasis 61 0.032
324
OST003 Osteonecrosis 61 0.032
325
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 61 0.032
326
c WLM018 Wilms Tumor 5 61 0.032
327
TRG002 Trigeminal Neuralgia 60 0.032
328
INT066 Interstitial Lung Disease 60 0.032
329
LNG099 Lung Disease 60 0.032
330
CHC001 Chickenpox 60 0.032
331
HYD002 Hydronephrosis 60 0.032
332
P OPT006 Optic Nerve Disease 60 0.032
333
PRT013 Portal Hypertension 59 0.032
334
IDP011 Idiopathic Interstitial Pneumonia 59 0.032
335
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 59 0.032
336
GST045 Gastroenteritis 59 0.032
337
GLB001 Gilbert Syndrome 58 0.032
338
P URT039 Urticaria 58 0.032
339
EYD002 Eye Disease 58 0.032
340
P UVT001 Uveitis 57 0.032
341
P ESP035 Esophagitis, Eosinophilic, 1 57 0.032
342
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.032
343
P END033 Endocarditis 57 0.032
344
P FCL005 Focal Segmental Glomerulosclerosis 57 0.032
345
PHR003 Pharyngitis 57 0.032
346
P BPL003 Bipolar Disorder 56 0.032
347
PLS011 Plasmacytoma 56 0.032
348
P NRF002 Neurofibromatosis 56 0.032
349
ORL005 Oral Candidiasis 56 0.032
350
SML019 Smallpox 56 0.032
351
P PLY019 Polyneuropathy 56 0.032
352
MMB001 Membranoproliferative Glomerulonephritis 55 0.032
353
c INT064 Intermediate Uveitis 55 0.032
354
PRN001 Purine Nucleoside Phosphorylase Deficiency 55 0.032
355
ESN005 Eosinophilic Gastroenteritis 55 0.032
356
PRP030 Purpura 54 0.032
357
PPL022 Papilloma 54 0.032
358
SNS003 Sensory Peripheral Neuropathy 54 0.032
359
P TRM003 Tremor 54 0.032
360
CRH005 Crohn's Colitis 53 0.032
361
INF034 Infective Endocarditis 53 0.032
362
ALC009 Alcoholic Liver Cirrhosis 53 0.032
363
c PSR017 Psoriasis 2 53 0.032
364
c MCR113 Microvascular Complications of Diabetes 3 52 0.032
365
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.032
366
c PSR023 Psoriasis 1 52 0.032
367
LNG095 Lung Abscess 51 0.032
368
CYS036 Cystinosis, Nephropathic 51 0.032
369
ESP002 Esophageal Varix 51 0.032
370
P MMB011 Membranous Nephropathy 50 0.032
371
CYT005 Cytomegalovirus Retinitis 50 0.032
372
MLL001 Molluscum Contagiosum 50 0.032
373
HYP080 Hypogonadism 50 0.032
374
VLV011 Vulvovaginal Candidiasis 49 0.032
375
GYN001 Gynecomastia 49 0.032
376
c BCT013 Bacterial Pneumonia 48 0.032
377
c PSR032 Psoriasis 11 47 0.032
378
c MCR120 Microvascular Complications of Diabetes 7 47 0.032
379
GLS007 Glossitis 47 0.032
380
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.032
381
RYN005 Raynaud Phenomenon 47 0.032
382
RTN023 Retinitis 46 0.032
383
ADR040 Adrenal Gland Pheochromocytoma 46 0.032
384
VGN019 Vaginal Discharge 46 0.032
385
CWP001 Cowpox 46 0.032
386
SQM002 Squamous Cell Papilloma 46 0.032
387
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.032
388
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.032
389
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.032
390
P PRD021 Periodic Paralysis 45 0.032
391
RTN179 Retinal Arteries, Tortuosity of 44 0.032
392
URT037 Urethral Stricture 43 0.032
393
P DMY001 Demyelinating Polyneuropathy 43 0.032
394
MDD018 Middle East Respiratory Syndrome 43 0.032
395
c RTN047 Retinitis Pigmentosa 18 42 0.032
396
P CLS010 Cluster Headache 42 0.032
397
c PSR028 Psoriasis 7 42 0.032
398
NRR001 Neuroretinitis 42 0.032
399
c MCR130 Microvascular Complications of Diabetes 6 41 0.032
400
c MCR133 Microvascular Complications of Diabetes 4 41 0.032
401
c PSR018 Psoriasis 13 41 0.032
402
c MJR024 Major Affective Disorder 9 41 0.032
403
c MCR112 Microvascular Complications of Diabetes 2 41 0.032
404
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.032
405
IMM001 Immune-Complex Glomerulonephritis 40 0.032
406
FML039 Female Reproductive System Disease 39 0.032
407
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.032
408
c MJR022 Major Affective Disorder 8 38 0.032
409
GLM044 Glomerular Disease 37 0.032
410
GGR001 Geographic Tongue 37 0.032
411
HRW001 Hair Whorl 36 0.032
412
LYM011 Lymphogranuloma Venereum 36 0.032
413
c LKM005 Leukemia, T-Cell, Chronic 34 0.032
414
SCL025 Scleromyxedema 32 0.032
415
CYT004 Cytomegalic Inclusion Disease 31 0.032
416
c CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 31 0.032
417
P RNL115 Renal Tubular Acidosis, Proximal 31 0.032
418
c MYP088 Myopathy, Tubular Aggregate, 2 31 0.032
419
INF021 Infant Gynecomastia 31 0.032
420
PHT004 Photoallergic Dermatitis 28 0.032
421
ESN022 Eosinophilic Colitis 25 0.032
422
CD4008 Cd4/cd8 T-Cell Ratio 20 0.032
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