Search results for Efavirenz

487 hits were found for Efavirenz

# Family MCID Name MIFTS Score
1
EFV001 Efavirenz, Poor Metabolism of 12 6.651
2
c CYP005 Cyp2b6-Related Altered Drug Metabolism 5 2.708
3
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.344
4
ACQ007 Acquired Immunodeficiency Syndrome 60 0.313
5
PRM097 Primary Immunodeficiency Disease 60 0.310
6
CSY001 C Syndrome 50 0.310
7
IMM066 Immunodeficiency 9 30 0.309
8
IMM081 Immunodeficiency 19 29 0.309
9
C9D001 C9 Deficiency 29 0.305
10
HV1006 Hiv-1 80 0.259
11
CD4004 Cd4 Deficiency 14 0.198
12
ART002 Arts Syndrome 51 0.193
13
IMM142 Immunodeficiency 50 20 0.193
14
SXL003 Sexual Disorder 42 0.173
15
BCL002 B Cell Deficiency 49 0.168
16
NTR005 Nutritional Deficiency Disease 36 0.162
17
IMM076 Immunodeficiency 24 27 0.162
18
ADM013 Adamantinoma of Long Bones 57 0.154
19
VRL011 Viral Infectious Disease 55 0.151
20
IMM068 Immunodeficiency 8 30 0.148
21
IMM065 Immunodeficiency 10 36 0.145
22
IMM071 Immunodeficiency 12 26 0.145
23
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.141
24
TBR010 Tuberculosis 70 0.138
25
c MYC055 Mycobacterium Tuberculosis 3 15 0.121
26
P MYC054 Mycobacterium Tuberculosis 2 14 0.121
27
P HPT021 Hepatitis 69 0.117
28
SXD001 Sex Differentiation Disease 38 0.117
29
WST001 West Syndrome 57 0.113
30
NSY001 N Syndrome 36 0.113
31
TCL003 T Cell Deficiency 45 0.109
32
c HPT073 Hepatitis C Virus 73 0.104
33
c HPT001 Hepatitis C 68 0.104
34
c HPT016 Hepatitis B 64 0.104
35
c VRL010 Viral Hepatitis 60 0.104
36
c HPT003 Hepatitis a 59 0.104
37
PRM025 Primary Bacterial Infectious Disease 41 0.104
38
IMM077 Immunodeficiency 20 27 0.100
39
IMM074 Immunodeficiency 16 26 0.100
40
SVR004 Severe Combined Immunodeficiency 69 0.095
41
LPD008 Lipid Metabolism Disorder 58 0.095
42
KND001 Kindler Syndrome 57 0.095
43
SVR077 Severe Combined Immune Deficiency 36 0.095
44
IMM102 Immunodeficiency 14 31 0.095
45
TCL006 T Cell Immunodeficiency Primary 12 0.095
46
P LVR013 Liver Disease 75 0.090
47
c TRC078 Trichohepatoenteric Syndrome 2 29 0.090
48
IMM096 Immunodeficiency 30 27 0.090
49
IMM085 Immunodeficiency 25 23 0.090
50
CHL071 Child Syndrome 58 0.085
51
KDS001 Kid Syndrome 53 0.085
52
SLP005 Sleep Disorder 53 0.085
53
CNT098 Central Core Disease 65 0.080
54
WLL006 Wells Syndrome 59 0.080
55
P SPS003 Spastic Diplegia 52 0.080
56
GDS001 Good Syndrome 44 0.080
57
CMB003 Combined T Cell and B Cell Immunodeficiency 42 0.080
58
BRW006 Brown Syndrome 29 0.080
59
IMM120 Immunodeficiency 40 24 0.080
60
P LPD010 Lipodystrophy 55 0.074
61
MYC002 Mycobacterium Avium Complex Disease 52 0.074
62
STM006 Stomach Disease 50 0.074
63
ORL003 Oral Tuberculosis 39 0.074
64
ADJ001 Adjustment Disorder 38 0.074
65
ALR002 Al-Raqad Syndrome 36 0.074
66
SBS006 Sebastian Syndrome 35 0.074
67
IMM082 Immunodeficiency 18 31 0.074
68
IMM080 Immunodeficiency 23 27 0.074
69
IMM088 Immunodeficiency 36 22 0.074
70
ANX002 Anxiety Disorder 67 0.067
71
c CNT035 Central Nervous System Disease 60 0.067
72
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.067
73
P EXN002 Exanthem 57 0.067
74
C3D001 C3 Deficiency 53 0.067
75
OLV001 Olivopontocerebellar Atrophy 53 0.067
76
END040 Endogenous Depression 53 0.067
77
MNT002 Mental Depression 53 0.067
78
IMM136 Immune System Disease 51 0.067
79
ACR041 Acromelic Frontonasal Dysostosis 45 0.067
80
ALN001 Aland Island Eye Disease 45 0.067
81
BRT030 Birth Defects 43 0.067
82
WRT001 Worth's Syndrome 34 0.067
83
SWL001 Swallowing Disorders 33 0.067
84
RMN002 Ramon Syndrome 30 0.067
85
FNT003 Fountain Syndrome 26 0.067
86
WSC001 Wisconsin Syndrome 14 0.067
87
P HRT032 Heart Disease 75 0.060
88
P NRV007 Nervous System Disease 71 0.060
89
PCK002 Pick Disease 68 0.060
90
PLM001 Pulmonary Tuberculosis 67 0.060
91
RBR001 Roberts Syndrome 60 0.060
92
EXF001 Exfoliation Syndrome 57 0.060
93
FDL002 Food Allergy 53 0.060
94
DSS008 Disease of Mental Health 52 0.060
95
ALL026 Allergic Hypersensitivity Disease 52 0.060
96
PRT011 Protein C Deficiency 52 0.060
97
TXC002 Toxic Encephalopathy 51 0.060
98
MSS002 Mass Syndrome 48 0.060
99
BLD053 Blood Platelet Disease 46 0.060
100
P PLN008 Peeling Skin Syndrome 45 0.060
101
c MTR002 Mitral Valve Insufficiency 44 0.060
102
PRD011 Proud Syndrome 42 0.060
103
c PLN018 Peeling Skin Syndrome 2 40 0.060
104
DRG001 Drug Psychosis 38 0.060
105
c PLN017 Peeling Skin Syndrome 1 34 0.060
106
ANG049 Angioedema Induced by Ace Inhibitors 34 0.060
107
IRS003 Iris Disease 31 0.060
108
c PLN021 Peeling Skin Syndrome 3 29 0.060
109
GRM003 German Syndrome 22 0.060
110
c RNL016 Renal Infectious Disease 20 0.060
111
IMM141 Immunodeficiency 49 17 0.060
112
MLL015 Mills Syndrome 17 0.060
113
NVD002 Nevada Syndrome 14 0.060
114
TSY001 Tau Syndrome 10 0.060
115
ABC017 Abacavir Toxicity 9 0.060
116
P PRS040 Prostate Cancer 90 0.052
117
P PNC035 Pancreatic Cancer 87 0.052
118
MLR004 Malaria 83 0.052
119
LVR012 Liver Cirrhosis 67 0.052
120
CHG001 Chagas Disease 67 0.052
121
P MNN013 Meningitis 67 0.052
122
P KDN018 Kidney Disease 66 0.052
123
BRC012 Brucellosis 66 0.052
124
DWN001 Down Syndrome 66 0.052
125
P ALX003 Alexander Disease 63 0.052
126
P ADD001 Addison's Disease 62 0.052
127
FCT003 Factor X Deficiency 61 0.052
128
P RCK004 Rickets 61 0.052
129
TTN003 Tetanus 61 0.052
130
OCL009 Ocular Cancer 59 0.052
131
DPH001 Diphtheria 59 0.052
132
PNC034 Pancreas Disease 58 0.052
133
CTS003 Coats Disease 57 0.052
134
c CRD093 Cardiomyopathy, Dilated, 1a 55 0.052
135
CHN016 Cohen Syndrome 54 0.052
136
NWC001 Newcastle Disease 54 0.052
137
P MTC069 Mitochondrial Disorders 53 0.052
138
SCT005 Scott Syndrome 53 0.052
139
TTH006 Tooth Disease 52 0.052
140
KRT002 Keratomalacia 52 0.052
141
c HPT015 Hepatitis D 52 0.052
142
PRS042 Prostate Disease 52 0.052
143
P FML035 Familial Hyperlipidemia 48 0.052
144
P CMP008 Compartment Syndrome 48 0.052
145
GYN001 Gynecomastia 48 0.052
146
TBR011 Tuberculous Meningitis 47 0.052
147
NLS001 Nelson Syndrome 47 0.052
148
INC022 Inclusion-Cell Disease 46 0.052
149
CCN007 Cocoon Syndrome 45 0.052
150
EPS006 Epstein Syndrome 38 0.052
151
c PRS116 Prostate Cancer 1 37 0.052
152
c PNC106 Pancreatic Agenesis 1 37 0.052
153
P ADV001 Advanced Sleep Phase Syndrome 37 0.052
154
PRP056 Porphyria, Acute Hepatic 37 0.052
155
BNS002 Bone Structure Disease 37 0.052
156
MTC005 Mitochondrial Metabolism Disease 36 0.052
157
c PNC095 Pancreatic Cancer 3 30 0.052
158
IMM101 Immunodeficiency 38 28 0.052
159
c PNC111 Pancreatic Cancer 2 28 0.052
160
WDS002 Woods Syndrome 27 0.052
161
IMM070 Immunodeficiency 13 27 0.052
162
c VRL008 Viral Exanthem 26 0.052
163
IMM062 Immunodeficiency 11 26 0.052
164
YNG002 Young Syndrome 26 0.052
165
CNT017 Central Nervous System Origin Vertigo 24 0.052
166
P CRN178 Coronary Heart Disease 6 21 0.052
167
TNR001 Tenorio Syndrome 21 0.052
168
CNG101 Congenital Human Immunodeficiency Virus 19 0.052
169
c CRN175 Coronary Heart Disease 4 19 0.052
170
c CRN172 Coronary Heart Disease 3 19 0.052
171
IMM103 Immunodeficiency 37 19 0.052
172
c CRN176 Coronary Heart Disease 9 18 0.052
173
IMM118 Immunodeficiency 42 17 0.052
174
IMM123 Immunodeficiency 39 16 0.052
175
c ADV005 Advanced Sleep Phase Syndrome 3 15 0.052
176
c BCT003 Bacterial Exanthem 11 0.052
177
NGY001 Nguyen Syndrome 11 0.052
178
MNT045 Montefiore Syndrome 10 0.052
179
RLT001 Raltegravir Toxicity 9 0.052
180
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.043
181
P HYP607 Hypercholesterolemia, Familial 76 0.043
182
P CRN211 Coronary Artery Disease 74 0.043
183
P ADN016 Adenocarcinoma 69 0.043
184
P LYM118 Lymphoma 69 0.043
185
PRP027 Peripheral Vascular Disease 68 0.043
186
ISC006 Ischemic Heart Disease 68 0.043
187
P PNM007 Pneumonia 68 0.043
188
PSY004 Psychotic Disorder 67 0.043
189
WRN001 Werner Syndrome 67 0.043
190
KPS004 Kaposi Sarcoma 67 0.043
191
P MYL005 Myelofibrosis 67 0.043
192
c CHR089 Chronic Kidney Failure 66 0.043
193
DRM006 Dermatitis 66 0.043
194
ATP002 Atopy 66 0.043
195
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.043
196
SRC014 Sarcoma 66 0.043
197
DMN002 Dementia 65 0.043
198
P OST002 Osteoporosis 64 0.043
199
LYM115 Lymphoma, Non-Hodgkin 63 0.043
200
c HMP004 Hemophilia B 62 0.043
201
CHR103 Charge Syndrome 62 0.043
202
P ALP009 Alopecia Areata 62 0.043
203
P NPH009 Nephrolithiasis 60 0.043
204
WLL001 Williams-Beuren Syndrome 60 0.043
205
P ENC018 Encephalopathy 59 0.043
206
P NRP001 Neuropathy 59 0.043
207
ETN001 Eating Disorder 58 0.043
208
P HMP007 Hemophilia 57 0.043
209
ALP008 Alopecia 57 0.043
210
SFT003 Soft Tissue Sarcoma 57 0.043
211
PNC033 Pancreas Adenocarcinoma 57 0.043
212
P LYM033 Lymphoproliferative Syndrome 56 0.043
213
PRP019 Peripheral Nervous System Disease 55 0.043
214
END030 End Stage Renal Failure 55 0.043
215
RCT018 Rectal Neoplasm 54 0.043
216
c BCT007 Bacterial Meningitis 54 0.043
217
c HPT007 Hepatitis E 54 0.043
218
PLN006 Poland Syndrome 54 0.043
219
LYM019 Lymphosarcoma 53 0.043
220
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.043
221
LYM024 Lymphatic System Disease 52 0.043
222
VSC006 Vascular Cancer 51 0.043
223
MYL020 Myelomeningocele 51 0.043
224
P RNL028 Renal Tubular Dysgenesis 51 0.043
225
CRY005 Cryptococcosis 50 0.043
226
c VRL012 Viral Meningitis 50 0.043
227
INT007 Intermediate Coronary Syndrome 50 0.043
228
HND003 Hand-Foot-Uterus Syndrome 50 0.043
229
c ACT134 Acute Liver Failure 50 0.043
230
CRN239 Carnitine Deficiency, Systemic Primary 50 0.043
231
END035 Endocrine Gland Cancer 49 0.043
232
MVM001 Movement Disease 49 0.043
233
MLL012 Miller Syndrome 49 0.043
234
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.043
235
LPD004 Lipoid Nephrosis 48 0.043
236
PLS009 Plasma Cell Neoplasm 48 0.043
237
CRB025 Carbohydrate Metabolic Disorder 46 0.043
238
GNG011 Gingival Disease 46 0.043
239
HMN032 Human Herpesvirus 8 46 0.043
240
EXT033 Extrapulmonary Tuberculosis 44 0.043
241
c SVR056 Severe Hemophilia a 43 0.043
242
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.043
243
MLR006 Male Reproductive Organ Cancer 43 0.043
244
LKC003 Leukocyte Disease 43 0.043
245
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.043
246
c ART120 Arthrogryposis, Distal, Type 3 42 0.043
247
GLC008 Glucose Metabolism Disease 42 0.043
248
BLR008 Bilirubin Metabolic Disorder 42 0.043
249
VGN020 Vaginal Disease 41 0.043
250
END038 Endocrine Pancreas Disease 41 0.043
251
P CNN004 Connective Tissue Cancer 40 0.043
252
TRP009 Triple X Syndrome 40 0.043
253
GST078 Gastrointestinal Allergy 40 0.043
254
DRG002 Drug-Induced Hepatitis 40 0.043
255
SPN369 Spinal Disease 39 0.043
256
ADS004 Aids Dementia Complex 39 0.043
257
c ADL001 Adult Lymphoma 39 0.043
258
P ACQ009 Acquired Metabolic Disease 38 0.043
259
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.043
260
P WGN003 Wagner Syndrome 36 0.043
261
PYR016 Pyridoxine Deficiency 36 0.043
262
IMM078 Immunodeficiency 21 35 0.043
263
RDN001 Reading Disorder 34 0.043
264
MLR007 Male Reproductive System Disease 34 0.043
265
PLC008 Placenta Disease 33 0.043
266
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.043
267
LYM023 Lymphatic System Cancer 33 0.043
268
FNC006 Functional Gastric Disease 32 0.043
269
c CNN010 Connective Tissue Benign Neoplasm 32 0.043
270
c SVR057 Severe Hemophilia B 32 0.043
271
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.043
272
c PNC103 Pancreatic Cancer 4 29 0.043
273
PRS002 Prostate Lymphoma 29 0.043
274
IMM099 Immunodeficiency 33 29 0.043
275
IMM095 Immunodeficiency 35 28 0.043
276
c WGN005 Wagner Syndrome 1 28 0.043
277
c PNC094 Pancreatic Cancer 1 27 0.043
278
INF036 Inflammatory and Toxic Neuropathy 27 0.043
279
IMM075 Immunodeficiency 22 26 0.043
280
TYL001 Taylor's Syndrome 26 0.043
281
NTR042 Neutrophilic Dermatosis, Acute Febrile 25 0.043
282
P SML002 Small Cell Sarcoma 25 0.043
283
NTH002 Nathalie Syndrome 23 0.043
284
HPD002 Hepadnavirus Infection 22 0.043
285
ISN001 Isoniazid Toxicity 21 0.043
286
c CRN174 Coronary Heart Disease 2 20 0.043
287
C8D002 C8 Deficiency, Type I 20 0.043
288
P GNR027 Generalized Peeling Skin Syndrome 19 0.043
289
c ALP039 Alopecia Areata 1 18 0.043
290
PYR009 Pyridoxine Deficiency Anemia 18 0.043
291
PNC007 Pancreas Lymphoma 17 0.043
292
BNM008 Bone Mineral Density, Low 16 0.043
293
WHT007 White Platelet Syndrome 15 0.043
294
c ALP040 Alopecia Areata 2 15 0.043
295
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 14 0.043
296
IMM135 Immunodeficiency 46 14 0.043
297
NVS004 Nova Syndrome 13 0.043
298
SGM003 Segmentation Syndrome 1 12 0.043
299
PRS069 Prostate Cancer, Progression and Metastasis of 12 0.043
300
SSC050 Susceptibility/resistance to Hiv Infection 10 0.043
301
PRT056 Protein R Deficiency 10 0.043
302
PLL007 Pillay Syndrome 9 0.043
303
P RHM011 Rheumatoid Arthritis 89 0.030
304
P ART022 Arthritis 75 0.030
305
CRH001 Crohn's Disease 75 0.030
306
P RSP003 Respiratory Failure 71 0.030
307
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.030
308
P BCL006 B-Cell Lymphomas 65 0.030
309
P KDN017 Kidney Cancer 65 0.030
310
GLC006 Galactosemia 64 0.030
311
DFC004 Deficiency Anemia 64 0.030
312
LNG099 Lung Disease 64 0.030
313
CRB039 Cerebrovascular Disease 63 0.030
314
ALC007 Alcohol Dependence 63 0.030
315
P ENC004 Encephalitis 63 0.030
316
P CRN015 Cornelia De Lange Syndrome 62 0.030
317
P TXP001 Toxoplasmosis 61 0.030
318
P HYP117 Hypertriglyceridemia 61 0.030
319
P DRR001 Diarrhea 60 0.030
320
SPT004 Septic Arthritis 60 0.030
321
FTT001 Fatty Liver Disease 59 0.030
322
STT001 Status Epilepticus 59 0.030
323
P ALC004 Alcohol Abuse 59 0.030
324
DFF005 Diffuse Large B-Cell Lymphoma 59 0.030
325
P PRP029 Porphyria 59 0.030
326
P SHR029 Short Syndrome 58 0.030
327
P HYP060 Hyperinsulinism 58 0.030
328
RHM027 Rheumatic Disease 58 0.030
329
P MYS005 Myositis 57 0.030
330
P INT070 Intestinal Obstruction 57 0.030
331
c PRC016 Pre-Eclampsia 56 0.030
332
PHR003 Pharyngitis 56 0.030
333
RBS001 Rabies 56 0.030
334
CCC001 Coccidioidomycosis 55 0.030
335
P TMT001 Timothy Syndrome 55 0.030
336
P FNC043 Fanconi Anemia, Complementation Group E 55 0.030
337
PLS007 Plasmodium Falciparum Malaria 55 0.030
338
EXT034 Extrinsic Allergic Alveolitis 54 0.030
339
c VRL007 Viral Encephalitis 54 0.030
340
SBS003 Substance Abuse 54 0.030
341
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.030
342
P ECL001 Eclampsia 54 0.030
343
P BRN009 Burning Mouth Syndrome 54 0.030
344
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.030
345
CPR001 Coproporphyria 53 0.030
346
PRT014 Protein S Deficiency 53 0.030
347
PRM042 Primary Effusion Lymphoma 53 0.030
348
ADL002 Adult Syndrome 52 0.030
349
BRN106 Burns 52 0.030
350
HST011 Histoplasmosis 52 0.030
351
IRN001 Iron Deficiency Anemia 52 0.030
352
RYS001 Reye Syndrome 52 0.030
353
P LCT001 Lactic Acidosis 51 0.030
354
c INF071 Inflammatory Bowel Disease 1 51 0.030
355
DRG011 Drug Addiction 51 0.030
356
GNR004 Generalized Anxiety Disorder 51 0.030
357
P HRD018 Hair Disease 51 0.030
358
P PRC031 Preeclampsia/eclampsia 1 51 0.030
359
CCC002 Coccidiosis 51 0.030
360
P STS008 Sotos Syndrome 1 51 0.030
361
IMG001 Image Syndrome 50 0.030
362
c LYM107 Lymphoproliferative Syndrome 2 50 0.030
363
NNL002 Nonalcoholic Steatohepatitis 50 0.030
364
P CLL015 Collagen Disease 50 0.030
365
PNM001 Pneumocystosis 50 0.030
366
DRG003 Drug Dependence 50 0.030
367
HPT074 Hepatic Adenoma, Somatic 50 0.030
368
LPD009 Lipid Storage Disease 49 0.030
369
c SVR005 Severe Pre-Eclampsia 49 0.030
370
LRN003 Learning Disability 49 0.030
371
OST011 Osteomalacia 49 0.030
372
NCT008 Nicotine Dependence, Protection Against 49 0.030
373
CCN001 Cocaine Dependence 49 0.030
374
CNT007 Central Nervous System Tuberculosis 48 0.030
375
P ENC008 Encephalocele 48 0.030
376
CCN002 Cocaine Abuse 48 0.030
377
FML039 Female Reproductive System Disease 48 0.030
378
MTC057 Mitochondrial Recessive Ataxia Syndrome 48 0.030
379
c HMG001 Hemoglobin C Disease 47 0.030
380
SBS004 Substance Dependence 47 0.030
381
VND001 Vein Disease 47 0.030
382
LYM116 Lymph Node Disease 47 0.030
383
ASP007 Aspiration Pneumonia 47 0.030
384
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.030
385
c ACT078 Acute Porphyria 46 0.030
386
ADR038 Adermatoglyphia 46 0.030
387
EST007 Estrogen Resistance 46 0.030
388
INT088 Intrinsic Factor Deficiency 45 0.030
389
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.030
390
SHH001 Sheehan Syndrome 44 0.030
391
CRD118 Cardiovascular Cancer 44 0.030
392
OCL069 Ocular Motor Apraxia 44 0.030
393
SKN023 Skin Tag 44 0.030
394
EVN001 Evans' Syndrome 43 0.030
395
HPT008 Hepatic Tuberculosis 42 0.030
396
HRT008 Heart Conduction Disease 42 0.030
397
CRY014 Cryptococcal Meningitis 42 0.030
398
c VRL005 Viral Pneumonia 42 0.030
399
HMT008 Hematuria, Benign Familial 42 0.030
400
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.030
401
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.030
402
AYM001 Ayme-Gripp Syndrome 41 0.030
403
RPR002 Reproductive System Disease 41 0.030
404
EGG001 Egg Allergy 41 0.030
405
ANM001 Anemia of Prematurity 41 0.030
406
GLC011 Galactose Epimerase Deficiency 41 0.030
407
PRS036 Parasitic Protozoa Infectious Disease 41 0.030
408
OCL025 Ocular Toxoplasmosis 40 0.030
409
RCT017 Rectal Disease 40 0.030
410
RNL012 Renal Tuberculosis 40 0.030
411
BND014 Bone Development Disease 40 0.030
412
MHC001 Mhc Class Ii Deficiency 39 0.030
413
MNR003 Mineral Metabolism Disease 38 0.030
414
P HYP265 Hypotonia 38 0.030
415
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.030
416
LTX001 Latex Allergy 38 0.030
417
SPC003 Specific Developmental Disorder 38 0.030
418
P CRN276 Corneal Endothelial Dystrophy 37 0.030
419
BLD054 Blood Protein Disease 37 0.030
420
GLC010 Galactokinase Deficiency with Cataracts 37 0.030
421
WTH001 Withdrawal Disorder 37 0.030
422
VSC018 Visceral Steatosis 37 0.030
423
CPL005 Capillary Disease 36 0.030
424
NTR006 Neutrophil Immunodeficiency Syndrome 35 0.030
425
CD4001 Cd45 Deficiency 35 0.030
426
c NNN010 Noonan Syndrome 3 35 0.030
427
INT259 Interleukin 1 Receptor Antagonist Deficiency 34 0.030
428
IMP003 Impaired Renal Function Disease 34 0.030
429
FLC001 Folic Acid Deficiency Anemia 34 0.030
430
PLS010 Plasma Protein Metabolism Disease 34 0.030
431
NNT011 Neonatal Anemia 33 0.030
432
ACR002 Acrocapitofemoral Dysplasia 33 0.030
433
BWN006 Bowen's Disease 33 0.030
434
IMM044 Immunoglobulin G Deficiency 33 0.030
435
TXC007 Toxic Pneumonitis 33 0.030
436
DDN007 Duodenal Disease 33 0.030
437
DDN009 Duodenal Obstruction 32 0.030
438
GLB003 Globe Disease 32 0.030
439
c LYM106 Lymphoproliferative Syndrome 1 32 0.030
440
c HMG004 Hemoglobin D Disease 31 0.030
441
CYT002 Cytokine Deficiency 30 0.030
442
P ATX010 Ataxia Neuropathy Spectrum 30 0.030
443
FNG004 Fungal Meningitis 30 0.030
444
c CNT068 Central Pain Syndrome 29 0.030
445
c DRR009 Diarrhea 6 29 0.030
446
GRN016 Grant Syndrome 29 0.030
447
c STS007 Sotos Syndrome 2 29 0.030
448
c AST037 Asthma 1 28 0.030
449
c AST039 Asthma 2 28 0.030
450
PHT004 Photoallergic Dermatitis 28 0.030
451
INT093 Interferon Gamma, Receptor 1, Deficiency 28 0.030
452
EPM005 Epimerase Deficiency Galactosemia 27 0.030
453
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.030
454
IMM063 Immunodeficiency 15 26 0.030
455
SKN021 Skin Sarcoma 25 0.030
456
HNM002 Hinman Syndrome 25 0.030
457
EXF003 Exfoliative Dermatitis 25 0.030
458
IMM025 Immunoglobulin a Deficiency 2 24 0.030
459
CNT067 Central Cord Syndrome 23 0.030
460
TMT006 Timothy Grass Allergy 23 0.030
461
c PRC034 Preeclampsia/eclampsia 4 23 0.030
462
FCL001 Facial Dermatosis 23 0.030
463
NPH064 Nipah Virus Disease 22 0.030
464
P INT103 Intrauterine Infections 22 0.030
465
OPP001 Opportunistic Bacterial Infectious Disease 21 0.030
466
MND006 Mondor Disease 21 0.030
467
PRT110 Prieto Syndrome 20 0.030
468
APD001 Apo a-I Deficiency 20 0.030
469
TCR004 Tacrolimus Dose Selection 20 0.030
470
NVK001 Novak Syndrome 20 0.030
471
C8D003 C8 Deficiency, Type Ii 19 0.030
472
CYT018 Cytochrome P450 2d6 Variant 19 0.030
473
VSC009 Vascular Skin Disease 19 0.030
474
c CRN173 Coronary Heart Disease 8 18 0.030
475
AND005 Androgen Insensitivity Syndrome, Mild 16 0.030
476
LGD001 Leg Dermatosis 16 0.030
477
c PRC032 Preeclampsia/eclampsia 2 16 0.030
478
c PRC033 Preeclampsia/eclampsia 3 16 0.030
479
c HYP333 Hyperlipidemia, Combined, 2 15 0.030
480
LYM126 Lymphoma Aids Related 15 0.030
481
STT044 Statin Toxicity 14 0.030
482
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 13 0.030
483
c DLT001 Delta Chain Disease 13 0.030
484
HRP008 Herpes Simiae 12 0.030
485
BDS001 Bd Syndrome 12 0.030
486
c FML078 Familial Myelofibrosis 11 0.030
487
HRP012 Herpesvirus Simiae B Virus 10 0.030
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