Search results for "hiv-1, resistance to"

The MalaCard for "hiv-1, resistance to" has been retired.
Searching MalaCards for entries containing "hiv-1, resistance to"

594 hits were found for 'hiv-1, resistance to'

# Family MCID Name MIFTS Score
1
HV1006 Hiv-1 82 1.483
2
HMN014 Human Immunodeficiency Virus Infectious Disease 49 0.490
3
PRM097 Primary Immunodeficiency Disease 61 0.465
4
P LKM002 Leukemia 70 0.418
5
P BRS047 Breast Cancer 100 0.412
6
P HPT021 Hepatitis 70 0.394
7
TBR010 Tuberculosis 69 0.358
8
NTR005 Nutritional Deficiency Disease 39 0.345
9
ADM013 Adamantinoma of Long Bones 59 0.343
10
VRL011 Viral Infectious Disease 59 0.334
11
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.333
12
END072 Endotheliitis 42 0.317
13
SXL003 Sexual Disorder 47 0.317
14
P PRS040 Prostate Cancer 89 0.315
15
CD4004 Cd4 Deficiency 17 0.286
16
PRS047 Prostatitis 56 0.277
17
CSY001 C Syndrome 49 0.272
18
NRN002 Neuronitis 42 0.272
19
P LYM118 Lymphoma 70 0.267
20
c HPT001 Hepatitis C 68 0.249
21
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.235
22
ART002 Arts Syndrome 53 0.231
23
IMM071 Immunodeficiency 12 28 0.230
24
ALL026 Allergic Hypersensitivity Disease 53 0.229
25
P THY032 Thyroiditis 54 0.225
26
MLR007 Male Reproductive System Disease 37 0.224
27
IMM065 Immunodeficiency 10 40 0.217
28
IMM068 Immunodeficiency 8 32 0.217
29
IMM076 Immunodeficiency 24 27 0.217
30
c HPT003 Hepatitis a 59 0.214
31
P MYL006 Myeloid Leukemia 67 0.214
32
P LVR013 Liver Disease 72 0.214
33
c HPT016 Hepatitis B 64 0.212
34
P PNM007 Pneumonia 66 0.211
35
P INF038 Influenza 74 0.210
36
P ART022 Arthritis 75 0.209
37
c VRL010 Viral Hepatitis 61 0.209
38
c HPT073 Hepatitis C Virus 72 0.209
39
RPR002 Reproductive System Disease 46 0.208
40
TCL003 T Cell Deficiency 45 0.207
41
GDS001 Good Syndrome 45 0.206
42
WLL006 Wells Syndrome 56 0.204
43
SRC014 Sarcoma 66 0.203
44
P PNC044 Pancreatitis 60 0.201
45
MLR004 Malaria 79 0.198
46
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.196
47
CHL071 Child Syndrome 58 0.195
48
KDS001 Kid Syndrome 53 0.195
49
PRS042 Prostate Disease 52 0.194
50
DMN002 Dementia 64 0.191
51
P CLR023 Colorectal Cancer 97 0.190
52
SXD001 Sex Differentiation Disease 40 0.190
53
P HRT032 Heart Disease 76 0.188
54
C3D001 C3 Deficiency 53 0.186
55
FML039 Female Reproductive System Disease 48 0.186
56
HPT023 Hepatocellular Carcinoma 91 0.185
57
IMM136 Immune System Disease 50 0.184
58
P CRV039 Cervicitis 44 0.182
59
P SPS003 Spastic Diplegia 53 0.181
60
WTH001 Withdrawal Disorder 41 0.178
61
PRM025 Primary Bacterial Infectious Disease 43 0.177
62
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.177
63
RTN023 Retinitis 49 0.177
64
PCK002 Pick Disease 67 0.175
65
BCL002 B Cell Deficiency 50 0.174
66
P NRB001 Neuroblastoma 69 0.172
67
WST001 West Syndrome 61 0.170
68
P EPL164 Epilepsy 66 0.169
69
BLD054 Blood Protein Disease 40 0.169
70
ACR041 Acromelic Frontonasal Dysostosis 46 0.168
71
ADL002 Adult Syndrome 53 0.167
72
BRT030 Birth Defects 43 0.166
73
DSS008 Disease of Mental Health 55 0.165
74
P MYP004 Myopathy 67 0.165
75
P ENC018 Encephalopathy 59 0.164
76
P RHM011 Rheumatoid Arthritis 88 0.163
77
ATH003 Atherosclerosis 62 0.163
78
P GLM045 Glioma 58 0.162
79
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.160
80
LPD008 Lipid Metabolism Disorder 58 0.159
81
ALN001 Aland Island Eye Disease 45 0.159
82
VCC001 Vaccinia 46 0.159
83
IMM066 Immunodeficiency 9 32 0.159
84
MDD011 Mood Disorder 61 0.158
85
P HRP006 Herpes Simplex 65 0.158
86
HYP266 Hypoxia 55 0.158
87
P ENC004 Encephalitis 61 0.157
88
NSY001 N Syndrome 39 0.157
89
CRB009 Cerebritis 38 0.156
90
TCL006 T Cell Immunodeficiency Primary 15 0.155
91
P MNN013 Meningitis 65 0.154
92
BNC003 Bone Cancer 45 0.153
93
c PRS116 Prostate Cancer 1 41 0.153
94
SKN016 Skin Disease 68 0.153
95
BNS002 Bone Structure Disease 36 0.150
96
MSC004 Muscle Tissue Disease 36 0.150
97
IMM077 Immunodeficiency 20 29 0.149
98
VND001 Vein Disease 52 0.147
99
P NRV007 Nervous System Disease 71 0.147
100
PRP027 Peripheral Vascular Disease 69 0.147
101
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.147
102
ADJ001 Adjustment Disorder 38 0.144
103
P GLB002 Glioblastoma 66 0.144
104
c CNT035 Central Nervous System Disease 59 0.143
105
P INF032 Infertility 61 0.143
106
P MSC033 Muscle Disorders 52 0.143
107
MRG013 Mirage Syndrome 26 0.141
108
c RNL016 Renal Infectious Disease 24 0.141
109
RSP006 Respiratory System Disease 62 0.141
110
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.140
111
BLD053 Blood Platelet Disease 46 0.140
112
LRN003 Learning Disability 51 0.140
113
IMM074 Immunodeficiency 16 29 0.138
114
P LPD010 Lipodystrophy 52 0.136
115
P NRV006 Nervous System Cancer 62 0.135
116
IMP003 Impaired Renal Function Disease 37 0.133
117
LPD004 Lipoid Nephrosis 48 0.133
118
P LPS004 Lupus Erythematosus 63 0.133
119
P NRP001 Neuropathy 60 0.133
120
ATP002 Atopy 63 0.132
121
ACD009 Acid-Labile Subunit, Deficiency of 48 0.132
122
IMM096 Immunodeficiency 30 30 0.131
123
BCT015 Bacteremia 48 0.131
124
SKN023 Skin Tag 46 0.131
125
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.131
126
P TCL004 T-Cell Leukemia 46 0.129
127
MTH009 Mouth Disease 63 0.128
128
LKC003 Leukocyte Disease 47 0.128
129
PLM001 Pulmonary Tuberculosis 68 0.128
130
VGN023 Vaginitis 42 0.127
131
c PND001 Pain Disorder 55 0.127
132
c ACT073 Acute Leukemia 62 0.127
133
BNM001 Bone Marrow Cancer 52 0.127
134
HYP066 Hyperglycemia 60 0.127
135
HYP005 Hypokalemia 51 0.125
136
LNG099 Lung Disease 62 0.125
137
IMM081 Immunodeficiency 19 29 0.125
138
EXF001 Exfoliation Syndrome 57 0.124
139
P BCL006 B-Cell Lymphomas 64 0.124
140
P CRN178 Coronary Heart Disease 6 24 0.123
141
RCT017 Rectal Disease 39 0.123
142
P DRR001 Diarrhea 51 0.123
143
c CRN214 Coronary Heart Disease 5 23 0.123
144
P PLN008 Peeling Skin Syndrome 47 0.123
145
RHM027 Rheumatic Disease 57 0.123
146
ANX002 Anxiety Disorder 69 0.123
147
c SYS001 Systemic Lupus Erythematosus 87 0.122
148
IMM082 Immunodeficiency 18 31 0.122
149
P PRP019 Peripheral Nervous System Disease 54 0.122
150
P CLL015 Collagen Disease 49 0.122
151
STR067 Stroke, Ischemic 77 0.122
152
c CRN175 Coronary Heart Disease 4 21 0.121
153
SPC003 Specific Developmental Disorder 40 0.121
154
IMM102 Immunodeficiency 14 31 0.121
155
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.120
156
PHY002 Physical Disorder 44 0.120
157
IMM085 Immunodeficiency 25 25 0.119
158
c CHR089 Chronic Kidney Failure 66 0.119
159
FTT001 Fatty Liver Disease 60 0.118
160
P RCK004 Rickets 59 0.118
161
GLC003 Glucose Intolerance 55 0.117
162
PRT036 Peritonitis 62 0.117
163
c TRC078 Trichohepatoenteric Syndrome 2 31 0.117
164
SVR004 Severe Combined Immunodeficiency 68 0.117
165
ATN002 Autonomic Nervous System Disease 47 0.117
166
PLC008 Placenta Disease 36 0.115
167
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 0.115
168
ART021 Arteriosclerosis 59 0.115
169
BRN038 Bronchial Disease 54 0.115
170
PLS009 Plasma Cell Neoplasm 48 0.114
171
END030 End Stage Renal Failure 52 0.114
172
MYC002 Mycobacterium Avium Complex Disease 51 0.114
173
PLS007 Plasmodium Falciparum Malaria 54 0.113
174
IMM063 Immunodeficiency 15 28 0.113
175
P PLM037 Pulmonary Hypertension 79 0.113
176
CTS003 Coats Disease 57 0.112
177
RDN001 Reading Disorder 39 0.112
178
ATM052 Autoimmune Disease 1 28 0.112
179
ATM053 Autoimmune Disease 2 19 0.112
180
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.110
181
IMM127 Immune System Cancer 42 0.110
182
NWC001 Newcastle Disease 54 0.110
183
GNR004 Generalized Anxiety Disorder 51 0.110
184
GST078 Gastrointestinal Allergy 41 0.109
185
STM007 Stomatitis 50 0.109
186
P CND004 Candidiasis 57 0.108
187
P SHR029 Short Syndrome 60 0.108
188
STM006 Stomach Disease 50 0.107
189
P HYP086 Hypothyroidism 65 0.107
190
IMM120 Immunodeficiency 40 26 0.107
191
P INT068 Intestinal Disease 61 0.105
192
DFC004 Deficiency Anemia 65 0.105
193
c PLN017 Peeling Skin Syndrome 1 33 0.105
194
NSD001 Nose Disease 52 0.105
195
C9D001 C9 Deficiency 32 0.105
196
URT001 Urethritis 40 0.105
197
HMT018 Hematopoietic Stem Cell Transplantation 41 0.105
198
LSH001 Leishmaniasis 62 0.104
199
CNT098 Central Core Disease 66 0.104
200
P BLD051 Blood Coagulation Disease 45 0.104
201
ATM054 Autoimmune Disease 3 18 0.103
202
c CRN173 Coronary Heart Disease 8 20 0.103
203
P EXN002 Exanthem 57 0.103
204
ALR002 Al-Raqad Syndrome 36 0.102
205
P LYM033 Lymphoproliferative Syndrome 53 0.102
206
c PLN018 Peeling Skin Syndrome 2 35 0.102
207
MRC001 Marchiafava Bignami Disease 50 0.102
208
PRT037 Pertussis 64 0.101
209
SPN369 Spinal Disease 41 0.100
210
SCR035 Sacral Agenesis with Vertebral Anomalies 33 0.099
211
SVR077 Severe Combined Immune Deficiency 36 0.099
212
ETN001 Eating Disorder 60 0.099
213
HYP056 Hypoglycemia 61 0.099
214
CYT002 Cytokine Deficiency 31 0.099
215
FCT003 Factor X Deficiency 62 0.098
216
PHR003 Pharyngitis 58 0.098
217
P AST007 Astrocytoma 65 0.098
218
P SPN301 Spinocerebellar Ataxia 2 63 0.098
219
P THR014 Thrombocytopenia 64 0.097
220
P OST002 Osteoporosis 64 0.097
221
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.097
222
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.097
223
IMM062 Immunodeficiency 11 27 0.097
224
SPS057 Spasticity 42 0.097
225
P CNJ013 Conjunctivitis 65 0.096
226
TTH006 Tooth Disease 52 0.096
227
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.096
228
ETH011 Ethylmalonic Encephalopathy 59 0.095
229
WSC001 Wisconsin Syndrome 17 0.095
230
IMM078 Immunodeficiency 21 35 0.094
231
c HPT015 Hepatitis D 52 0.093
232
GNT003 Genital Herpes 54 0.093
233
c CHR418 Chronic Leukemia 48 0.093
234
VSC008 Vascular Hemostatic Disease 33 0.092
235
ACN011 Acne 63 0.092
236
FDL002 Food Allergy 54 0.092
237
ATM055 Autoimmune Disease 4 18 0.091
238
P LRY019 Laryngitis 55 0.091
239
VGN020 Vaginal Disease 45 0.091
240
P HMR003 Hemorrhagic Disease 57 0.091
241
P LPR003 Leprosy 68 0.091
242
HDC001 Headache 54 0.090
243
PRT011 Protein C Deficiency 51 0.090
244
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.090
245
LVR012 Liver Cirrhosis 67 0.090
246
SBS003 Substance Abuse 56 0.090
247
MST005 Mastitis 52 0.089
248
P SYP003 Syphilis 53 0.089
249
P ATX004 Ataxia 53 0.089
250
c CRN177 Coronary Heart Disease 7 22 0.089
251
IMM070 Immunodeficiency 13 29 0.089
252
P HMP007 Hemophilia 56 0.089
253
P RTN024 Retinoblastoma 75 0.089
254
FCT006 Factor V Deficiency 60 0.088
255
BRN071 Brain Injury 52 0.088
256
MSL001 Measles 61 0.088
257
NNL002 Nonalcoholic Steatohepatitis 53 0.088
258
RBS001 Rabies 56 0.088
259
BRN028 Brain Cancer 70 0.088
260
ATR060 Atrial Standstill, Digenic 53 0.087
261
c PLN021 Peeling Skin Syndrome 3 31 0.087
262
DRG003 Drug Dependence 53 0.087
263
DPH001 Diphtheria 58 0.086
264
P ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 60 0.086
265
PRT014 Protein S Deficiency 52 0.085
266
P PYL005 Pyelonephritis 52 0.085
267
P PRS038 Personality Disorder 61 0.085
268
P OCY001 Oocyte Maturation Defect 39 0.084
269
c MLG068 Malignant Glioma 50 0.084
270
TTN003 Tetanus 61 0.084
271
SSC050 Susceptibility/resistance to Hiv Infection 12 0.083
272
P ACT135 Acute Graft Versus Host Disease 53 0.083
273
BNF002 Bone Fracture 47 0.083
274
MSS002 Mass Syndrome 59 0.083
275
AYM001 Ayme-Gripp Syndrome 45 0.083
276
IMM088 Immunodeficiency 36 21 0.083
277
ANG049 Angioedema Induced by Ace Inhibitors 35 0.082
278
PRS036 Parasitic Protozoa Infectious Disease 45 0.082
279
ATM059 Autoimmune Disease 6 26 0.081
280
PMP001 Pemphigus 49 0.081
281
HDG012 Hodgkin Lymphoma 73 0.081
282
VSC003 Visceral Leishmaniasis 55 0.080
283
PRT056 Protein R Deficiency 14 0.079
284
SPN041 Spinal Cord Disease 48 0.079
285
ATM012 Autoimmune Disease of Blood 37 0.079
286
SPT004 Septic Arthritis 59 0.078
287
SPC010 Speech and Communication Disorders 46 0.078
288
PLY023 Polycystic Liver Disease 57 0.078
289
DRG011 Drug Addiction 51 0.078
290
c ADL017 Adult T-Cell Leukemia 58 0.077
291
CHL123 Chlamydia 59 0.077
292
P MYL005 Myelofibrosis 67 0.077
293
CHL014 Cholera 55 0.076
294
RBR001 Roberts Syndrome 59 0.076
295
TBR011 Tuberculous Meningitis 46 0.076
296
BCT002 Bacterial Vaginosis 51 0.076
297
GRM003 German Syndrome 24 0.076
298
VSC011 Vasculitis 62 0.075
299
NVD002 Nevada Syndrome 16 0.075
300
BNN003 Bone Inflammation Disease 46 0.074
301
BND014 Bone Development Disease 42 0.074
302
ACR002 Acrocapitofemoral Dysplasia 36 0.074
303
ORL005 Oral Candidiasis 47 0.074
304
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.074
305
DMY004 Demyelinating Disease 55 0.074
306
GRW007 Growth Hormone Deficiency 48 0.074
307
CYT008 Cytomegalovirus Infection 51 0.074
308
P THL005 Thalassemia 61 0.073
309
HML018 Homologous Wasting Disease 17 0.073
310
P MYS005 Myositis 56 0.073
311
LYM116 Lymph Node Disease 44 0.073
312
MNT045 Montefiore Syndrome 13 0.073
313
PLM033 Pulmonary Embolism 59 0.073
314
P TRC086 Trichohepatoenteric Syndrome 1 46 0.072
315
ACD004 Acdc 34 0.072
316
CHG001 Chagas Disease 62 0.072
317
IMM075 Immunodeficiency 22 27 0.072
318
NVS004 Nova Syndrome 19 0.072
319
HRP004 Herpes Zoster 56 0.072
320
P UTR038 Uterine Disease 40 0.071
321
ADT003 Auditory System Disease 51 0.071
322
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.071
323
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.071
324
c THR092 Thrombophilia Due to Thrombin Defect 56 0.071
325
ALL006 Allergic Asthma 58 0.071
326
ALC007 Alcohol Dependence 65 0.070
327
CRV045 Cervical Intraepithelial Neoplasia 38 0.070
328
PLG002 Plague 49 0.070
329
CRY004 Cryoglobulinemia 47 0.070
330
BRW006 Brown Syndrome 26 0.070
331
SCH014 Schistosomiasis 58 0.069
332
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.069
333
WLS001 Wilson Disease 72 0.069
334
P MTC069 Mitochondrial Disorders 52 0.069
335
IMP005 Impotence 50 0.069
336
CYT005 Cytomegalovirus Retinitis 49 0.069
337
BCT004 Bacteriuria 47 0.068
338
IMM044 Immunoglobulin G Deficiency 35 0.068
339
IMP004 Impetigo 42 0.068
340
c CHR417 Chronic Graft Versus Host Disease 50 0.068
341
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 29 0.068
342
DYS073 Dysphagia 49 0.068
343
c HPT007 Hepatitis E 54 0.068
344
SPN186 Spinal Cord Injury 62 0.068
345
SCR008 Scrub Typhus 54 0.068
346
TNG009 Tongue Squamous Cell Carcinoma 74 0.068
347
MTB004 Metabolic Acidosis 48 0.068
348
c ACT004 Acute Diarrhea 38 0.067
349
WLL001 Williams-Beuren Syndrome 61 0.067
350
FXF002 Fox-Fordyce Disease 39 0.067
351
P DRM010 Dermatomyositis 58 0.067
352
SWL001 Swallowing Disorders 34 0.067
353
P ATX030 Ataxia-Telangiectasia 76 0.067
354
CRB037 Cerebral Palsy 54 0.067
355
FNT003 Fountain Syndrome 27 0.067
356
c MYC055 Mycobacterium Tuberculosis 3 18 0.067
357
c HMN021 Human T-Cell Leukemia Virus Type 1 51 0.067
358
IMM095 Immunodeficiency 35 31 0.066
359
CCN007 Cocoon Syndrome 35 0.066
360
KRT002 Keratomalacia 54 0.066
361
SBS004 Substance Dependence 50 0.066
362
c ACT042 Acute Pyelonephritis 46 0.066
363
P ALC004 Alcohol Abuse 60 0.065
364
LYM027 Lymphopenia 54 0.065
365
c SVR001 Severe Acute Respiratory Syndrome 57 0.065
366
P ANT006 Antiphospholipid Syndrome 58 0.065
367
PRD011 Proud Syndrome 42 0.064
368
SML019 Smallpox 53 0.064
369
THY030 Thyroid Gland Disease 51 0.064
370
IMM036 Immunodeficiency, Isolated 27 0.064
371
PPL022 Papilloma 55 0.064
372
ATT013 Attention Deficit-Hyperactivity Disorder 68 0.063
373
WRN001 Werner Syndrome 67 0.063
374
MYC017 Mycobacterium Kansasii 40 0.063
375
VSC018 Visceral Steatosis 37 0.063
376
DRM011 Dermatophytosis 45 0.062
377
CRD001 Cardiac Tamponade 44 0.062
378
TRY001 Trypanosomiasis 52 0.062
379
INT007 Intermediate Coronary Syndrome 52 0.062
380
EVN001 Evans' Syndrome 43 0.062
381
TYL001 Taylor's Syndrome 29 0.061
382
P GNR027 Generalized Peeling Skin Syndrome 22 0.061
383
DVL001 Developmental Coordination Disorder 37 0.061
384
DWN001 Down Syndrome 65 0.061
385
KRT006 Keratoconjunctivitis 52 0.061
386
c PRM023 Pre-Malignant Neoplasm 43 0.061
387
SWN001 Swine Influenza 37 0.061
388
OPD001 Opioid Abuse 41 0.060
389
IMM118 Immunodeficiency 42 18 0.060
390
BRK010 Burkitt Lymphoma 66 0.060
391
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.060
392
P CSH001 Cushing's Syndrome 64 0.060
393
MND006 Mondor Disease 21 0.060
394
c HMP029 Hemophilia a 64 0.059
395
INT067 Interstitial Nephritis 47 0.059
396
WST005 West Nile Virus 53 0.059
397
c DLT001 Delta Chain Disease 16 0.059
398
PLN006 Poland Syndrome 48 0.059
399
TRC003 Trichomoniasis 41 0.059
400
MLL012 Miller Syndrome 49 0.059
401
c HMP004 Hemophilia B 62 0.059
402
BRN002 Bronchiolitis 56 0.059
403
VLV010 Vulvovaginitis 42 0.059
404
PLM031 Poliomyelitis 59 0.058
405
TNS005 Tonsillitis 58 0.058
406
c MTR002 Mitral Valve Insufficiency 44 0.058
407
TSY001 Tau Syndrome 12 0.058
408
HPT022 Hepatoblastoma 53 0.057
409
P HMC003 Hemochromatosis 72 0.057
410
CMM005 Common Cold 58 0.057
411
CGL001 Coagulation Protein Disease 16 0.057
412
c ACT020 Acute T Cell Leukemia 39 0.057
413
ORC001 Orchitis 34 0.057
414
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 34 0.057
415
CHR005 Chorioamnionitis 48 0.057
416
P CNT005 Central Nervous System Lymphoma 53 0.056
417
PRC002 Paracoccidioidomycosis 55 0.056
418
ECH003 Echinococcosis 53 0.056
419
P LCT001 Lactic Acidosis 52 0.056
420
P MMB011 Membranous Nephropathy 56 0.056
421
LKP003 Leukoplakia 41 0.056
422
RLT001 Raltegravir Toxicity 11 0.056
423
P MMP001 Mumps 56 0.056
424
SBS006 Sebastian Syndrome 37 0.055
425
SPC005 Speech Disorder 43 0.055
426
P TXP001 Toxoplasmosis 60 0.055
427
MNN009 Meningoencephalitis 45 0.055
428
CMM004 Common Variable Immunodeficiency 67 0.055
429
CHN016 Cohen Syndrome 55 0.055
430
IMM099 Immunodeficiency 33 28 0.055
431
TXC002 Toxic Encephalopathy 51 0.055
432
CHL004 Cholelithiasis 48 0.055
433
SNS001 Sensorineural Hearing Loss 57 0.054
434
IRS003 Iris Disease 32 0.054
435
HND003 Hand-Foot-Uterus Syndrome 47 0.054
436
AVN001 Avian Influenza 53 0.054
437
AND015 Androgen Insensitivity 63 0.054
438
BNM008 Bone Mineral Density, Low 19 0.054
439
c VRL008 Viral Exanthem 30 0.054
440
MYC033 Myoclonus 41 0.054
441
P NPH009 Nephrolithiasis 60 0.054
442
c PRM226 Primary Central Nervous System Lymphoma 49 0.054
443
P CMP008 Compartment Syndrome 48 0.054
444
ORL014 Oral Pharyngeal Disorders 14 0.054
445
CRY005 Cryptococcosis 50 0.054
446
CMR002 Coumarin Resistance 48 0.053
447
YNG002 Young Syndrome 26 0.053
448
INC002 Inclusion Body Myositis 63 0.053
449
FLL008 Folliculitis 47 0.053
450
MYC019 Mycobacterium Marinum 28 0.053
451
MTC005 Mitochondrial Metabolism Disease 38 0.053
452
RSC001 Rosacea 53 0.053
453
SPS019 Spastic Paraparesis 34 0.052
454
LPR001 Lepromatous Leprosy 49 0.052
455
c STR089 Striatal Degeneration, Autosomal Dominant 2 30 0.052
456
c LKM005 Leukemia, T-Cell, Chronic 22 0.052
457
YLL002 Yellow Fever 57 0.051
458
HYP017 Hypophosphatemia 42 0.051
459
c INH004 Inherited Blood Coagulation Disease 39 0.051
460
SPL004 Splenic Marginal Zone Lymphoma 43 0.050
461
P FTT008 Fatty Liver Disease, Nonalcoholic 1 33 0.050
462
CCC001 Coccidioidomycosis 55 0.050
463
CCN002 Cocaine Abuse 47 0.050
464
VNZ002 Venezuelan Equine Encephalitis 44 0.050
465
EXT033 Extrapulmonary Tuberculosis 44 0.049
466
ALC006 Alcoholic Hepatitis 59 0.049
467
c DRR009 Diarrhea 6 31 0.049
468
PMP004 Pemphigus Foliaceus 39 0.049
469
ANS012 Anus Disease 32 0.049
470
MTR014 Motor Neuron Disease 59 0.048
471
VGN019 Vaginal Discharge 33 0.048
472
IMM135 Immunodeficiency 46 15 0.048
473
c LYM107 Lymphoproliferative Syndrome 2 34 0.048
474
SCT005 Scott Syndrome 50 0.048
475
c CRD093 Cardiomyopathy, Dilated, 1a 38 0.048
476
c HYP072 Hypersensitivity Reaction Type Iii Disease 41 0.047
477
c LYM106 Lymphoproliferative Syndrome 1 34 0.047
478
CHC001 Chickenpox 52 0.047
479
NRS003 Neurosyphilis 41 0.047
480
LMB010 Lambert Syndrome 35 0.047
481
P HRP009 Herpes Simplex Encephalitis 46 0.047
482
P LBY004 Labyrinthitis 40 0.046
483
P CMR001 Camurati-Engelmann Disease 59 0.046
484
P ACQ009 Acquired Metabolic Disease 41 0.046
485
WDS002 Woods Syndrome 30 0.046
486
TRP002 Tropical Spastic Paraparesis 57 0.046
487
CYS005 Cysticercosis 52 0.046
488
IMM080 Immunodeficiency 23 30 0.045
489
BHR001 Behr Syndrome 44 0.045
490
c BRN108 Branchiootic Syndrome 1 36 0.045
491
HNS001 Hansen's Disease 29 0.045
492
BRD001 Brody Myopathy 49 0.045
493
NCR004 Nocardiosis 42 0.045
494
P SHR001 Short Bowel Syndrome 48 0.044
495
CHK001 Chikungunya 50 0.044
496
c VRL007 Viral Encephalitis 54 0.044
497
c VRL005 Viral Pneumonia 42 0.043
498
FNC006 Functional Gastric Disease 34 0.043
499
P ADD001 Addison's Disease 62 0.043
500
JPN002 Japanese Encephalitis 54 0.043
501
WHT007 White Platelet Syndrome 18 0.043
502
HRN022 Hearing Loss/deafness 25 0.043
503
HTC002 Hutchinson-Gilford Progeria 62 0.043
504
NLL002 Null Syndrome 22 0.043
505
HPT074 Hepatic Adenoma, Somatic 51 0.042
506
FBR012 Fabry Disease 69 0.042
507
TCK001 Tick-Borne Encephalitis 49 0.042
508
P RTT002 Rett Syndrome 78 0.042
509
WRT002 Writing Disorder 29 0.042
510
PLS025 Plasmablastic Lymphoma 45 0.042
511
NTR006 Neutrophil Immunodeficiency Syndrome 36 0.042
512
GLC006 Galactosemia 67 0.042
513
P NJM001 Nijmegen Breakage Syndrome 66 0.042
514
CWP001 Cowpox 46 0.041
515
AND005 Androgen Insensitivity Syndrome, Mild 16 0.041
516
LYM041 Lymphocytes Absent 16 0.041
517
TRP009 Triple X Syndrome 40 0.041
518
HMN032 Human Herpesvirus 8 46 0.041
519
CHY002 Chylomicron Retention Disease 59 0.041
520
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.041
521
MTR007 Motor Peripheral Neuropathy 43 0.041
522
HNM002 Hinman Syndrome 25 0.040
523
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.040
524
CNT067 Central Cord Syndrome 24 0.040
525
HRP005 Herpetic Whitlow 30 0.039
526
BDS001 Bd Syndrome 14 0.039
527
MYC021 Mycobacterium Xenopi 26 0.039
528
CYT004 Cytomegalic Inclusion Disease 30 0.038
529
OPS006 Opsoclonus-Myoclonus Syndrome 46 0.038
530
P CRN139 Cornelia De Lange Syndrome 1 60 0.038
531
PRM042 Primary Effusion Lymphoma 53 0.038
532
HYP458 Hyper Ige Syndrome 41 0.038
533
RYS001 Reye Syndrome 51 0.038
534
ORL019 Oral Hairy Leukoplakia 33 0.037
535
c INF002 Inflammatory Diarrhea 31 0.037
536
CST005 Castleman Disease 38 0.037
537
GNT002 Giant Cell Glioblastoma 51 0.037
538
INT054 Intraocular Lymphoma 45 0.037
539
BLL012 Bullous Impetigo 35 0.036
540
ADP002 Adiponectin Deficiency 31 0.036
541
P PFF001 Pfeiffer Syndrome 73 0.036
542
CRB159 Cerebral Visual Impairment 40 0.035
543
CHR103 Charge Syndrome 64 0.035
544
PTY004 Pityriasis Lichenoides 24 0.035
545
TMR010 Tumor Predisposition Syndrome 52 0.035
546
c PNC108 Pancreatitis, Hereditary 67 0.035
547
c SCN036 Secondary Progressive Multiple Sclerosis 50 0.034
548
TRN066 Transmitted_by 24 0.034
549
ENG004 Engraftment Syndrome 35 0.034
550
BRC085 Brca2 Hereditary Breast and Ovarian Cancer Syndrome 44 0.034
551
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 35 0.034
552
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 50 0.034
553
PSD029 Pseudocholinesterase Deficiency 40 0.033
554
CRT055 Creatine Deficiency Syndromes 27 0.033
555
c HYP507 Hypotrichosis 1 29 0.033
556
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 44 0.033
557
INT046 Intestinal Tuberculosis 38 0.032
558
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.032
559
GST020 Gastric Antral Vascular Ectasia 32 0.032
560
ADP007 Adie Pupil 34 0.032
561
PTY006 Pityriasis Lichenoides Et Varioliformis Acuta 20 0.032
562
P ATX010 Ataxia Neuropathy Spectrum 28 0.032
563
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 17 0.031
564
P SPR013 Spiradenoma 36 0.031
565
CRZ001 Crouzon Syndrome 70 0.030
566
BRL010 Buruli Ulcer 47 0.030
567
GRN016 Grant Syndrome 30 0.030
568
P PCH015 Pachyonychia Congenita 1 49 0.030
569
NTR018 Neutrophilia, Hereditary 45 0.030
570
SRN001 Serine Deficiency 32 0.030
571
DRR010 Darier Disease 61 0.029
572
IMM003 Immunoglobulin Alpha Deficiency 38 0.029
573
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 51 0.029
574
EPS006 Epstein Syndrome 40 0.029
575
c RBN008 Rubinstein-Taybi Syndrome 2 35 0.029
576
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 21 0.029
577
MYL013 Myeloperoxidase Deficiency 46 0.029
578
TRC012 Trichuriasis 45 0.029
579
TMP012 Temple Syndrome 40 0.029
580
HMF008 Hemifacial Atrophy, Progressive 38 0.029
581
c NNN010 Noonan Syndrome 3 36 0.028
582
P MWT001 Mowat-Wilson Syndrome 46 0.028
583
EPT021 Epithelial Recurrent Erosion Dystrophy 33 0.028
584
c PRD030 Periodontitis 1, Juvenile 35 0.028
585
P RFS001 Refsum Disease 62 0.027
586
MRS002 Marshall Syndrome 50 0.027
587
AMS002 Amish Infantile Epilepsy Syndrome 35 0.026
588
IMM139 Immunodeficiency 47 16 0.026
589
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 53 0.026
590
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.026
591
SML020 Small Patella Syndrome 36 0.024
592
CYT003 Cytokine Receptor Deficiency 10 0.024
593
SVN001 Sveinsson Choreoretinal Atrophy 26 0.023
594
P IDP049 Idiopathic Anterior Uveitis 23 0.023