Search results for Emtricitabine

443 hits were found for Emtricitabine

# Family MCID Name MIFTS Score
1
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.321
2
ACQ007 Acquired Immunodeficiency Syndrome 60 0.316
3
HV1006 Hiv-1 80 0.278
4
PRM097 Primary Immunodeficiency Disease 60 0.277
5
IMM142 Immunodeficiency 50 20 0.213
6
CSY001 C Syndrome 50 0.199
7
CD4004 Cd4 Deficiency 14 0.187
8
IMM076 Immunodeficiency 24 27 0.174
9
VRL011 Viral Infectious Disease 55 0.169
10
P HPT021 Hepatitis 69 0.164
11
IMM065 Immunodeficiency 10 36 0.164
12
IMM071 Immunodeficiency 12 26 0.164
13
IMM066 Immunodeficiency 9 30 0.155
14
c VRL010 Viral Hepatitis 60 0.152
15
c HPT003 Hepatitis a 59 0.152
16
ADM013 Adamantinoma of Long Bones 57 0.152
17
NTR005 Nutritional Deficiency Disease 36 0.152
18
IMM081 Immunodeficiency 19 29 0.149
19
c HPT016 Hepatitis B 64 0.146
20
ART002 Arts Syndrome 51 0.142
21
C9D001 C9 Deficiency 29 0.142
22
WST001 West Syndrome 57 0.139
23
BCL002 B Cell Deficiency 49 0.136
24
SXL003 Sexual Disorder 42 0.136
25
P LVR013 Liver Disease 75 0.121
26
KND001 Kindler Syndrome 57 0.121
27
IMM068 Immunodeficiency 8 30 0.121
28
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.118
29
HPD002 Hepadnavirus Infection 22 0.118
30
c RNL016 Renal Infectious Disease 20 0.118
31
CNT098 Central Core Disease 65 0.114
32
WRT001 Worth's Syndrome 34 0.114
33
SVR004 Severe Combined Immunodeficiency 69 0.109
34
SXD001 Sex Differentiation Disease 38 0.109
35
SVR077 Severe Combined Immune Deficiency 36 0.109
36
ADL002 Adult Syndrome 52 0.105
37
GDS001 Good Syndrome 44 0.105
38
IMM102 Immunodeficiency 14 31 0.105
39
IMM085 Immunodeficiency 25 23 0.105
40
WLL006 Wells Syndrome 59 0.101
41
c ART120 Arthrogryposis, Distal, Type 3 42 0.101
42
MLL015 Mills Syndrome 17 0.101
43
c HPT073 Hepatitis C Virus 73 0.096
44
c HPT001 Hepatitis C 68 0.096
45
CHL071 Child Syndrome 58 0.096
46
PLN006 Poland Syndrome 54 0.096
47
KDS001 Kid Syndrome 53 0.096
48
MYC002 Mycobacterium Avium Complex Disease 52 0.096
49
TCL003 T Cell Deficiency 45 0.096
50
NSY001 N Syndrome 36 0.096
51
P WGN003 Wagner Syndrome 36 0.096
52
c WGN005 Wagner Syndrome 1 28 0.096
53
IMM096 Immunodeficiency 30 27 0.096
54
HRP008 Herpes Simiae 12 0.096
55
HRP012 Herpesvirus Simiae B Virus 10 0.096
56
OLV001 Olivopontocerebellar Atrophy 53 0.091
57
SBS006 Sebastian Syndrome 35 0.091
58
IMM074 Immunodeficiency 16 26 0.091
59
c HPT007 Hepatitis E 54 0.086
60
c HPT015 Hepatitis D 52 0.086
61
ACR041 Acromelic Frontonasal Dysostosis 45 0.086
62
BRT030 Birth Defects 43 0.086
63
IMM063 Immunodeficiency 15 26 0.086
64
IMM120 Immunodeficiency 40 24 0.086
65
GRM003 German Syndrome 22 0.086
66
C3D001 C3 Deficiency 53 0.080
67
IMM136 Immune System Disease 51 0.080
68
IMM082 Immunodeficiency 18 31 0.080
69
IMM101 Immunodeficiency 38 28 0.080
70
WSC001 Wisconsin Syndrome 14 0.080
71
TCL006 T Cell Immunodeficiency Primary 12 0.080
72
PRT011 Protein C Deficiency 52 0.074
73
P SPS003 Spastic Diplegia 52 0.074
74
STM006 Stomach Disease 50 0.074
75
CMB003 Combined T Cell and B Cell Immunodeficiency 42 0.074
76
PRM025 Primary Bacterial Infectious Disease 41 0.074
77
BND014 Bone Development Disease 40 0.074
78
ACR002 Acrocapitofemoral Dysplasia 33 0.074
79
c TRC078 Trichohepatoenteric Syndrome 2 29 0.074
80
IMM070 Immunodeficiency 13 27 0.074
81
BNM008 Bone Mineral Density, Low 16 0.074
82
NVD002 Nevada Syndrome 14 0.074
83
RLT001 Raltegravir Toxicity 9 0.074
84
TBR010 Tuberculosis 70 0.068
85
P ADD001 Addison's Disease 62 0.068
86
FCT003 Factor X Deficiency 61 0.068
87
RBR001 Roberts Syndrome 60 0.068
88
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.068
89
LPD008 Lipid Metabolism Disorder 58 0.068
90
EXF001 Exfoliation Syndrome 57 0.068
91
DSS008 Disease of Mental Health 52 0.068
92
PLS009 Plasma Cell Neoplasm 48 0.068
93
MSS002 Mass Syndrome 48 0.068
94
BLD053 Blood Platelet Disease 46 0.068
95
P PLN008 Peeling Skin Syndrome 45 0.068
96
ALN001 Aland Island Eye Disease 45 0.068
97
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.068
98
ADJ001 Adjustment Disorder 38 0.068
99
P ACQ009 Acquired Metabolic Disease 38 0.068
100
BNR001 Bone Remodeling Disease 37 0.068
101
WTH001 Withdrawal Disorder 37 0.068
102
BNS002 Bone Structure Disease 37 0.068
103
c PLN017 Peeling Skin Syndrome 1 34 0.068
104
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.068
105
ANS012 Anus Disease 32 0.068
106
IRS003 Iris Disease 31 0.068
107
RMN002 Ramon Syndrome 30 0.068
108
BRW006 Brown Syndrome 29 0.068
109
c PLN021 Peeling Skin Syndrome 3 29 0.068
110
IMM080 Immunodeficiency 23 27 0.068
111
IMM075 Immunodeficiency 22 26 0.068
112
TYL001 Taylor's Syndrome 26 0.068
113
IMM088 Immunodeficiency 36 22 0.068
114
c MYC055 Mycobacterium Tuberculosis 3 15 0.068
115
P MYC054 Mycobacterium Tuberculosis 2 14 0.068
116
MNT045 Montefiore Syndrome 10 0.068
117
PCK002 Pick Disease 68 0.061
118
ANX002 Anxiety Disorder 67 0.061
119
PLM001 Pulmonary Tuberculosis 67 0.061
120
CHG001 Chagas Disease 67 0.061
121
P KDN018 Kidney Disease 66 0.061
122
DWN001 Down Syndrome 66 0.061
123
PTR006 Peters Anomaly 65 0.061
124
P OST002 Osteoporosis 64 0.061
125
P RCK004 Rickets 61 0.061
126
CTS003 Coats Disease 57 0.061
127
P EXN002 Exanthem 57 0.061
128
P LPD010 Lipodystrophy 55 0.061
129
CHN016 Cohen Syndrome 54 0.061
130
NWC001 Newcastle Disease 54 0.061
131
FDL002 Food Allergy 53 0.061
132
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.061
133
KRT002 Keratomalacia 52 0.061
134
TXC002 Toxic Encephalopathy 51 0.061
135
LPD004 Lipoid Nephrosis 48 0.061
136
FML039 Female Reproductive System Disease 48 0.061
137
P TRC086 Trichohepatoenteric Syndrome 1 48 0.061
138
NLS001 Nelson Syndrome 47 0.061
139
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.061
140
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.061
141
PRD011 Proud Syndrome 42 0.061
142
RPR002 Reproductive System Disease 41 0.061
143
RCT017 Rectal Disease 40 0.061
144
c PLN018 Peeling Skin Syndrome 2 40 0.061
145
ORL003 Oral Tuberculosis 39 0.061
146
MNR003 Mineral Metabolism Disease 38 0.061
147
ALR002 Al-Raqad Syndrome 36 0.061
148
MLR007 Male Reproductive System Disease 34 0.061
149
ACD004 Acdc 33 0.061
150
GRN016 Grant Syndrome 29 0.061
151
PRM243 Primary Bone Cancer 29 0.061
152
IMM095 Immunodeficiency 35 28 0.061
153
IMM077 Immunodeficiency 20 27 0.061
154
c VRL008 Viral Exanthem 26 0.061
155
FNT003 Fountain Syndrome 26 0.061
156
MND006 Mondor Disease 21 0.061
157
NGY001 Nguyen Syndrome 11 0.061
158
PRT056 Protein R Deficiency 10 0.061
159
ABC017 Abacavir Toxicity 9 0.061
160
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.053
161
P NRV007 Nervous System Disease 71 0.053
162
PRP027 Peripheral Vascular Disease 68 0.053
163
PSY004 Psychotic Disorder 67 0.053
164
LVR012 Liver Cirrhosis 67 0.053
165
KPS004 Kaposi Sarcoma 67 0.053
166
P MYL005 Myelofibrosis 67 0.053
167
BRC012 Brucellosis 66 0.053
168
ATP002 Atopy 66 0.053
169
SRC014 Sarcoma 66 0.053
170
DMN002 Dementia 65 0.053
171
LPP001 Lipoprotein Lipase Deficiency 63 0.053
172
LPM004 Lipoma 60 0.053
173
c CNT035 Central Nervous System Disease 60 0.053
174
OCL009 Ocular Cancer 59 0.053
175
P NRP001 Neuropathy 59 0.053
176
ETN001 Eating Disorder 58 0.053
177
SFT003 Soft Tissue Sarcoma 57 0.053
178
HRP004 Herpes Zoster 56 0.053
179
PRP019 Peripheral Nervous System Disease 55 0.053
180
END030 End Stage Renal Failure 55 0.053
181
RCT018 Rectal Neoplasm 54 0.053
182
SLP005 Sleep Disorder 53 0.053
183
P SYP003 Syphilis 53 0.053
184
BLT006 Bilateral Breast Cancer 53 0.053
185
MNT002 Mental Depression 53 0.053
186
TTH006 Tooth Disease 52 0.053
187
ALL026 Allergic Hypersensitivity Disease 52 0.053
188
VSC006 Vascular Cancer 51 0.053
189
P RNL028 Renal Tubular Dysgenesis 51 0.053
190
MLL012 Miller Syndrome 49 0.053
191
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.053
192
QBC001 Quebec Platelet Disorder 48 0.053
193
HRT007 Heart Cancer 46 0.053
194
HMN032 Human Herpesvirus 8 46 0.053
195
URT004 Urethral Syndrome 45 0.053
196
CCN007 Cocoon Syndrome 45 0.053
197
EXT033 Extrapulmonary Tuberculosis 44 0.053
198
c MTR002 Mitral Valve Insufficiency 44 0.053
199
BNN003 Bone Inflammation Disease 44 0.053
200
LKC003 Leukocyte Disease 43 0.053
201
VGN020 Vaginal Disease 41 0.053
202
P CNN004 Connective Tissue Cancer 40 0.053
203
TRP009 Triple X Syndrome 40 0.053
204
GST078 Gastrointestinal Allergy 40 0.053
205
ADS004 Aids Dementia Complex 39 0.053
206
DRG001 Drug Psychosis 38 0.053
207
IMM003 Immunoglobulin Alpha Deficiency 36 0.053
208
PYR016 Pyridoxine Deficiency 36 0.053
209
NTR006 Neutrophil Immunodeficiency Syndrome 35 0.053
210
IMM078 Immunodeficiency 21 35 0.053
211
RDN001 Reading Disorder 34 0.053
212
IMP003 Impaired Renal Function Disease 34 0.053
213
c PRM022 Primary Syphilis 33 0.053
214
FNC006 Functional Gastric Disease 32 0.053
215
c CNN010 Connective Tissue Benign Neoplasm 32 0.053
216
LPS020 Lipase Deficiency, Combined 32 0.053
217
P HRT017 Heart Tumor 32 0.053
218
ADP002 Adiponectin Deficiency 30 0.053
219
VTM003 Vitamin Metabolic Disorder 30 0.053
220
IMM099 Immunodeficiency 33 29 0.053
221
WTS001 Watson Syndrome 28 0.053
222
WDS002 Woods Syndrome 27 0.053
223
TYP027 Type 1 Diabetes Mellitus 10 27 0.053
224
CRT055 Creatine Deficiency Syndromes 27 0.053
225
IMM036 Immunodeficiency, Isolated 27 0.053
226
IMM062 Immunodeficiency 11 26 0.053
227
YNG002 Young Syndrome 26 0.053
228
NTR042 Neutrophilic Dermatosis, Acute Febrile 25 0.053
229
P SML002 Small Cell Sarcoma 25 0.053
230
IMM025 Immunoglobulin a Deficiency 2 24 0.053
231
P GNR027 Generalized Peeling Skin Syndrome 19 0.053
232
CNG101 Congenital Human Immunodeficiency Virus 19 0.053
233
IMM103 Immunodeficiency 37 19 0.053
234
c CRN176 Coronary Heart Disease 9 18 0.053
235
PYR009 Pyridoxine Deficiency Anemia 18 0.053
236
IMM118 Immunodeficiency 42 17 0.053
237
LCT008 Lactate Dehydrogenase Deficiency 17 0.053
238
c ADL079 Adult Heart Tumor 16 0.053
239
FMR002 Femoral Cancer 16 0.053
240
WHT007 White Platelet Syndrome 15 0.053
241
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 13 0.053
242
NVS004 Nova Syndrome 13 0.053
243
c DLT001 Delta Chain Disease 13 0.053
244
SSC050 Susceptibility/resistance to Hiv Infection 10 0.053
245
MLR004 Malaria 83 0.043
246
P MYC007 Myocardial Infarction 79 0.043
247
P HRT032 Heart Disease 75 0.043
248
P CRN211 Coronary Artery Disease 74 0.043
249
CNG034 Congestive Heart Failure 72 0.043
250
ISC006 Ischemic Heart Disease 68 0.043
251
c CHR089 Chronic Kidney Failure 66 0.043
252
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.043
253
ATH003 Atherosclerosis 65 0.043
254
P KDN017 Kidney Cancer 65 0.043
255
P HRP006 Herpes Simplex 65 0.043
256
DFC004 Deficiency Anemia 64 0.043
257
CRB039 Cerebrovascular Disease 63 0.043
258
CHR103 Charge Syndrome 62 0.043
259
P CRN015 Cornelia De Lange Syndrome 62 0.043
260
HYP056 Hypoglycemia 61 0.043
261
HYP066 Hyperglycemia 61 0.043
262
MTH009 Mouth Disease 61 0.043
263
TTN003 Tetanus 61 0.043
264
CHL123 Chlamydia 60 0.043
265
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.043
266
P ENC018 Encephalopathy 59 0.043
267
DPH001 Diphtheria 59 0.043
268
P GLL020 Gallbladder Disease 59 0.043
269
P INF032 Infertility 59 0.043
270
P INT001 Intrahepatic Cholestasis 59 0.043
271
CHL068 Cholestasis 59 0.043
272
P SHR029 Short Syndrome 58 0.043
273
P HYP060 Hyperinsulinism 58 0.043
274
BNC003 Bone Cancer 58 0.043
275
CRT016 Carotid Artery Disease 57 0.043
276
STR026 Star Syndrome 57 0.043
277
P LYM033 Lymphoproliferative Syndrome 56 0.043
278
HPT019 Hepatic Encephalopathy 56 0.043
279
GLC003 Glucose Intolerance 55 0.043
280
P TMT001 Timothy Syndrome 55 0.043
281
MLN007 Male Infertility 55 0.043
282
c CRD093 Cardiomyopathy, Dilated, 1a 55 0.043
283
PLS007 Plasmodium Falciparum Malaria 55 0.043
284
CNC002 Cinca Syndrome 55 0.043
285
SBS003 Substance Abuse 54 0.043
286
CND002 Conduct Disorder 54 0.043
287
PRT014 Protein S Deficiency 53 0.043
288
GNT003 Genital Herpes 53 0.043
289
SCT005 Scott Syndrome 53 0.043
290
END040 Endogenous Depression 53 0.043
291
BLR006 Biliary Tract Disease 52 0.043
292
RYS001 Reye Syndrome 52 0.043
293
P PRM006 Primary Biliary Cirrhosis 51 0.043
294
DRG011 Drug Addiction 51 0.043
295
P HRD018 Hair Disease 51 0.043
296
GRW007 Growth Hormone Deficiency 50 0.043
297
INT007 Intermediate Coronary Syndrome 50 0.043
298
BNF002 Bone Fracture 50 0.043
299
c LYM107 Lymphoproliferative Syndrome 2 50 0.043
300
NNL002 Nonalcoholic Steatohepatitis 50 0.043
301
RNL024 Renal Glucosuria 50 0.043
302
LPD009 Lipid Storage Disease 49 0.043
303
LRN003 Learning Disability 49 0.043
304
MRS002 Marshall Syndrome 49 0.043
305
c DWL002 Dowling-Degos Disease 1 49 0.043
306
ATN002 Autonomic Nervous System Disease 48 0.043
307
P CMP008 Compartment Syndrome 48 0.043
308
CCN002 Cocaine Abuse 48 0.043
309
DYS073 Dysphagia 48 0.043
310
BLD036 Bile Duct Disease 48 0.043
311
PRT030 Parathyroid Gland Disease 47 0.043
312
RNL077 Renal Fibrosis 47 0.043
313
PRM236 Primary Biliary Cholangitis 47 0.043
314
MLK006 Milk Allergy 47 0.043
315
CRB025 Carbohydrate Metabolic Disorder 46 0.043
316
INC022 Inclusion-Cell Disease 46 0.043
317
INT088 Intrinsic Factor Deficiency 45 0.043
318
CRD118 Cardiovascular Cancer 44 0.043
319
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.043
320
GND002 Gender Identity Disorder 42 0.043
321
GLC008 Glucose Metabolism Disease 42 0.043
322
HPT008 Hepatic Tuberculosis 42 0.043
323
P BLD051 Blood Coagulation Disease 42 0.043
324
BLR008 Bilirubin Metabolic Disorder 42 0.043
325
FCT008 Factitious Disorder 41 0.043
326
SPC010 Speech and Communication Disorders 41 0.043
327
TRC003 Trichomoniasis 41 0.043
328
CWM001 Cow Milk Allergy 40 0.043
329
RNL012 Renal Tuberculosis 40 0.043
330
c ART106 Arterial Calcification, Generalized, of Infancy, 1 39 0.043
331
PHS001 Phosphorus Metabolism Disease 38 0.043
332
SPC003 Specific Developmental Disorder 38 0.043
333
P OCY001 Oocyte Maturation Defect 38 0.043
334
TMP012 Temple Syndrome 38 0.043
335
BLD054 Blood Protein Disease 37 0.043
336
GNR003 Generalized Atherosclerosis 37 0.043
337
AMP007 Amphetamine Abuse 35 0.043
338
PNL013 Penile Disease 34 0.043
339
MSC004 Muscle Tissue Disease 34 0.043
340
GLS018 Glass Syndrome 34 0.043
341
ANG049 Angioedema Induced by Ace Inhibitors 34 0.043
342
PLS010 Plasma Protein Metabolism Disease 34 0.043
343
PLC008 Placenta Disease 33 0.043
344
SWL001 Swallowing Disorders 33 0.043
345
IMM044 Immunoglobulin G Deficiency 33 0.043
346
c LYM106 Lymphoproliferative Syndrome 1 32 0.043
347
SCL013 Scleral Disease 32 0.043
348
c HMG004 Hemoglobin D Disease 31 0.043
349
CYT002 Cytokine Deficiency 30 0.043
350
FWL001 Fowler's Syndrome 25 0.043
351
TMT006 Timothy Grass Allergy 23 0.043
352
NPH064 Nipah Virus Disease 22 0.043
353
SNG003 Single Ventricular Heart 22 0.043
354
P INT103 Intrauterine Infections 22 0.043
355
P CRN178 Coronary Heart Disease 6 21 0.043
356
OPP001 Opportunistic Bacterial Infectious Disease 21 0.043
357
TNR001 Tenorio Syndrome 21 0.043
358
PRT110 Prieto Syndrome 20 0.043
359
c CRN175 Coronary Heart Disease 4 19 0.043
360
c CRN172 Coronary Heart Disease 3 19 0.043
361
SPC022 Specific Antibody Deficiency 18 0.043
362
c CRN173 Coronary Heart Disease 8 18 0.043
363
IMM141 Immunodeficiency 49 17 0.043
364
c BLR024 Biliary Cirrhosis, Primary, 1 16 0.043
365
IMM140 Immunodeficiency 47 16 0.043
366
c GLL026 Gallbladder Disease 3 16 0.043
367
c BLR017 Biliary Cirrhosis, Primary, 3 15 0.043
368
SPR028 Spirochetes Disease 14 0.043
369
TRP010 Treponema Infection 13 0.043
370
YCH003 Y Chromosome Detection 12 0.043
371
SGM003 Segmentation Syndrome 1 12 0.043
372
CYT003 Cytokine Receptor Deficiency 10 0.043
373
PLL007 Pillay Syndrome 9 0.043
374
P HPT023 Hepatocellular Carcinoma 92 0.030
375
GST053 Gastric Cancer 78 0.030
376
P HYP607 Hypercholesterolemia, Familial 76 0.030
377
P RSP003 Respiratory Failure 71 0.030
378
P PNM007 Pneumonia 68 0.030
379
GLC006 Galactosemia 64 0.030
380
P INF037 Inflammatory Bowel Disease 63 0.030
381
P ALX003 Alexander Disease 63 0.030
382
P ENC004 Encephalitis 63 0.030
383
P HYP117 Hypertriglyceridemia 61 0.030
384
P GST049 Gastrointestinal System Cancer 60 0.030
385
WLL001 Williams-Beuren Syndrome 60 0.030
386
P DRR001 Diarrhea 60 0.030
387
IRR002 Irritable Bowel Syndrome 58 0.030
388
PHR003 Pharyngitis 56 0.030
389
EXT034 Extrinsic Allergic Alveolitis 54 0.030
390
c VRL007 Viral Encephalitis 54 0.030
391
P MTC069 Mitochondrial Disorders 53 0.030
392
DMY004 Demyelinating Disease 53 0.030
393
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.030
394
CLL003 Cellulitis 51 0.030
395
CLN019 Colonic Disease 51 0.030
396
URN009 Urinary System Disease 50 0.030
397
P URF003 Urofacial Syndrome 1 50 0.030
398
MVM001 Movement Disease 49 0.030
399
P SHR001 Short Bowel Syndrome 49 0.030
400
c INF067 Inflammatory Bowel Disease 10 49 0.030
401
c THN010 Thanatophoric Dysplasia, Type Ii 49 0.030
402
SLP001 Sleeping Sickness 48 0.030
403
c HMG001 Hemoglobin C Disease 47 0.030
404
GNG011 Gingival Disease 46 0.030
405
VCC001 Vaccinia 46 0.030
406
SPL012 Splenic Disease 46 0.030
407
SHH001 Sheehan Syndrome 44 0.030
408
PHY002 Physical Disorder 43 0.030
409
c VRL005 Viral Pneumonia 42 0.030
410
GLC011 Galactose Epimerase Deficiency 41 0.030
411
c INF087 Inflammatory Bowel Disease 4 40 0.030
412
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.030
413
SPN369 Spinal Disease 39 0.030
414
EPS006 Epstein Syndrome 38 0.030
415
GLC010 Galactokinase Deficiency with Cataracts 37 0.030
416
P ADV001 Advanced Sleep Phase Syndrome 37 0.030
417
PRP056 Porphyria, Acute Hepatic 37 0.030
418
CPL005 Capillary Disease 36 0.030
419
MTC005 Mitochondrial Metabolism Disease 36 0.030
420
LNG095 Lung Abscess 34 0.030
421
TXC007 Toxic Pneumonitis 33 0.030
422
CRV069 Cervix Disease 32 0.030
423
c DRR007 Diarrhea 7 31 0.030
424
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.030
425
EPM005 Epimerase Deficiency Galactosemia 27 0.030
426
FNC005 Functional Colonic Disease 27 0.030
427
INF036 Inflammatory and Toxic Neuropathy 27 0.030
428
c INF093 Inflammatory Bowel Disease 14 23 0.030
429
NTH002 Nathalie Syndrome 23 0.030
430
INS009 Insulin-Resistance Type B 22 0.030
431
c CRN214 Coronary Heart Disease 5 22 0.030
432
c INF079 Inflammatory Bowel Disease 20 21 0.030
433
IMM123 Immunodeficiency 39 16 0.030
434
c ADV005 Advanced Sleep Phase Syndrome 3 15 0.030
435
GNR029 Generalized Galactose Epimerase Deficiency 15 0.030
436
HVS002 Hiv-Associated Cancer 13 0.030
437
HNR001 Heiner Syndrome 13 0.030
438
SGM001 Sigmoid Disease 12 0.030
439
BDS001 Bd Syndrome 12 0.030
440
c SCN046 Secondary Short Bowel Syndrome 12 0.030
441
c FML078 Familial Myelofibrosis 11 0.030
442
SLT010 Solitary Necrotic Tumor of the Liver 11 0.030
443
TSY001 Tau Syndrome 10 0.030
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