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"

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

# Family MCID Name MIFTS Score
1
HV1006 Hiv-1 80 1.439
2
ACQ007 Acquired Immunodeficiency Syndrome 60 0.507
3
HMN014 Human Immunodeficiency Virus Infectious Disease 46 0.485
4
IMM102 Immunodeficiency 14 33 0.457
5
P LKM002 Leukemia 70 0.413
6
P BRS047 Breast Cancer 100 0.409
7
P HPT021 Hepatitis 74 0.389
8
NTR005 Nutritional Deficiency Disease 51 0.364
9
TBR010 Tuberculosis 70 0.351
10
ADM013 Adamantinoma of Long Bones 57 0.348
11
SXL003 Sexual Disorder 45 0.339
12
VRL011 Viral Infectious Disease 56 0.339
13
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.330
14
END072 Endotheliitis 41 0.314
15
P PRS040 Prostate Cancer 89 0.312
16
CD4004 Cd4 Deficiency 15 0.281
17
PRS047 Prostatitis 56 0.277
18
CSY001 C Syndrome 49 0.271
19
NRN002 Neuronitis 40 0.269
20
P LYM118 Lymphoma 68 0.266
21
C3D001 C3 Deficiency 50 0.247
22
c HPT001 Hepatitis C 68 0.246
23
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.233
24
P THY032 Thyroiditis 57 0.227
25
ART002 Arts Syndrome 53 0.227
26
IMM071 Immunodeficiency 12 27 0.224
27
ALL026 Allergic Hypersensitivity Disease 53 0.221
28
RPR002 Reproductive System Disease 45 0.219
29
P MYL006 Myeloid Leukemia 67 0.215
30
MLR007 Male Reproductive System Disease 36 0.215
31
IMM076 Immunodeficiency 24 27 0.212
32
P PNM007 Pneumonia 67 0.212
33
IMM068 Immunodeficiency 8 32 0.212
34
IMM065 Immunodeficiency 10 39 0.212
35
CHL071 Child Syndrome 58 0.211
36
KDS001 Kid Syndrome 53 0.211
37
c HPT003 Hepatitis a 55 0.211
38
P ART022 Arthritis 73 0.210
39
c HPT016 Hepatitis B 61 0.209
40
P INF038 Influenza 71 0.208
41
MLN008 Melanoma 61 0.207
42
c VRL010 Viral Hepatitis 60 0.206
43
c HPT073 Hepatitis C Virus 72 0.206
44
TCL003 T Cell Deficiency 44 0.205
45
SRC014 Sarcoma 66 0.202
46
GDS001 Good Syndrome 46 0.202
47
P PNC044 Pancreatitis 62 0.201
48
WLL006 Wells Syndrome 57 0.201
49
ADL002 Adult Syndrome 53 0.199
50
P LVR013 Liver Disease 76 0.199
51
MLR004 Malaria 80 0.198
52
BRT030 Birth Defects 44 0.196
53
ACR041 Acromelic Frontonasal Dysostosis 45 0.195
54
P CLR023 Colorectal Cancer 96 0.191
55
PCK002 Pick Disease 66 0.190
56
DMN002 Dementia 62 0.189
57
PRS042 Prostate Disease 50 0.189
58
FML039 Female Reproductive System Disease 49 0.185
59
HPT023 Hepatocellular Carcinoma 90 0.185
60
SXD001 Sex Differentiation Disease 39 0.183
61
P CRV039 Cervicitis 45 0.182
62
P SPS003 Spastic Diplegia 49 0.182
63
SKN016 Skin Disease 69 0.178
64
P KDN018 Kidney Disease 64 0.178
65
RTN023 Retinitis 49 0.176
66
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.176
67
P ENC018 Encephalopathy 59 0.174
68
P NRB001 Neuroblastoma 70 0.173
69
INC022 Inclusion-Cell Disease 46 0.173
70
PRM025 Primary Bacterial Infectious Disease 42 0.171
71
DSS008 Disease of Mental Health 48 0.170
72
BCL002 B Cell Deficiency 50 0.169
73
P EPL164 Epilepsy 60 0.169
74
WST001 West Syndrome 61 0.169
75
WTH001 Withdrawal Disorder 36 0.168
76
BLD054 Blood Protein Disease 38 0.167
77
P RHM011 Rheumatoid Arthritis 87 0.166
78
P GLM045 Glioma 53 0.164
79
P MYP004 Myopathy 67 0.163
80
ALN001 Aland Island Eye Disease 45 0.162
81
SKN027 Skin Conditions 44 0.162
82
ATH003 Atherosclerosis 63 0.161
83
SPN041 Spinal Cord Disease 50 0.161
84
HYP266 Hypoxia 55 0.160
85
c CNG401 Congenital Heart Disease 67 0.159
86
VCC001 Vaccinia 46 0.158
87
CRB009 Cerebritis 36 0.158
88
IMM066 Immunodeficiency 9 30 0.158
89
P HRP006 Herpes Simplex 65 0.157
90
LPD008 Lipid Metabolism Disorder 42 0.157
91
P MNN013 Meningitis 66 0.157
92
P ENC004 Encephalitis 60 0.157
93
MDD011 Mood Disorder 60 0.156
94
BNS002 Bone Structure Disease 37 0.155
95
NSY001 N Syndrome 42 0.155
96
P HRT032 Heart Disease 64 0.154
97
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.153
98
END040 Endogenous Depression 51 0.152
99
MNT002 Mental Depression 52 0.151
100
TCL006 T Cell Immunodeficiency Primary 13 0.151
101
MSC004 Muscle Tissue Disease 35 0.150
102
c PRS116 Prostate Cancer 1 39 0.148
103
IMM077 Immunodeficiency 20 28 0.148
104
VND001 Vein Disease 51 0.147
105
LRN003 Learning Disability 49 0.146
106
P GLB002 Glioblastoma 65 0.146
107
PRP027 Peripheral Vascular Disease 69 0.142
108
P INF032 Infertility 61 0.140
109
BNC003 Bone Cancer 44 0.139
110
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.138
111
ADJ001 Adjustment Disorder 38 0.138
112
P NRV007 Nervous System Disease 71 0.138
113
BLD053 Blood Platelet Disease 44 0.138
114
P MSC033 Muscle Disorders 52 0.137
115
c RNL016 Renal Infectious Disease 22 0.137
116
P LPD010 Lipodystrophy 51 0.136
117
P LPS004 Lupus Erythematosus 63 0.136
118
SKN023 Skin Tag 48 0.135
119
IMM074 Immunodeficiency 16 28 0.135
120
P NRP001 Neuropathy 57 0.135
121
DRG001 Drug Psychosis 39 0.134
122
BCT015 Bacteremia 50 0.134
123
RSP006 Respiratory System Disease 61 0.134
124
c CNT035 Central Nervous System Disease 60 0.134
125
P NRV006 Nervous System Cancer 62 0.133
126
ACD009 Acid-Labile Subunit, Deficiency of 37 0.132
127
c PND001 Pain Disorder 53 0.132
128
LPD004 Lipoid Nephrosis 49 0.132
129
IMP003 Impaired Renal Function Disease 36 0.131
130
ATP002 Atopy 62 0.129
131
P TCL004 T-Cell Leukemia 44 0.129
132
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 56 0.129
133
MTH009 Mouth Disease 63 0.129
134
P URF003 Urofacial Syndrome 1 51 0.128
135
IMM096 Immunodeficiency 30 30 0.127
136
VGN023 Vaginitis 41 0.127
137
P BCL006 B-Cell Lymphomas 64 0.126
138
c ACT073 Acute Leukemia 61 0.126
139
HYP066 Hyperglycemia 61 0.126
140
c SYS001 Systemic Lupus Erythematosus 87 0.125
141
LKC003 Leukocyte Disease 45 0.125
142
PLM001 Pulmonary Tuberculosis 69 0.125
143
P DRR001 Diarrhea 60 0.125
144
BNM001 Bone Marrow Cancer 56 0.125
145
IMM081 Immunodeficiency 19 28 0.125
146
VSC007 Vascular Disease 51 0.124
147
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.124
148
HYP005 Hypokalemia 52 0.123
149
ANX002 Anxiety Disorder 67 0.123
150
PRP019 Peripheral Nervous System Disease 52 0.122
151
P CRN178 Coronary Heart Disease 6 22 0.122
152
RHM027 Rheumatic Disease 55 0.121
153
IMM082 Immunodeficiency 18 31 0.121
154
PRT036 Peritonitis 65 0.121
155
EXF001 Exfoliation Syndrome 56 0.120
156
LNG099 Lung Disease 63 0.120
157
P CLL015 Collagen Disease 49 0.119
158
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.119
159
P PLN008 Peeling Skin Syndrome 45 0.119
160
c CRN214 Coronary Heart Disease 5 22 0.119
161
SPC003 Specific Developmental Disorder 39 0.118
162
FTT001 Fatty Liver Disease 60 0.118
163
c MTB001 Metabolic Syndrome X 61 0.117
164
c CHR089 Chronic Kidney Failure 67 0.117
165
P RCK004 Rickets 59 0.116
166
ATN002 Autonomic Nervous System Disease 46 0.116
167
SVR004 Severe Combined Immunodeficiency 71 0.116
168
RCT017 Rectal Disease 35 0.116
169
P PLM037 Pulmonary Hypertension 78 0.116
170
GLC003 Glucose Intolerance 56 0.115
171
PLS007 Plasmodium Falciparum Malaria 56 0.115
172
c CRN175 Coronary Heart Disease 4 19 0.115
173
PHY002 Physical Disorder 43 0.114
174
c TRC078 Trichohepatoenteric Syndrome 2 30 0.114
175
BRN038 Bronchial Disease 54 0.114
176
IMM085 Immunodeficiency 25 25 0.114
177
PLC008 Placenta Disease 33 0.114
178
END030 End Stage Renal Failure 53 0.113
179
ART021 Arteriosclerosis 59 0.113
180
PLS009 Plasma Cell Neoplasm 47 0.112
181
URN009 Urinary System Disease 52 0.111
182
MYC002 Mycobacterium Avium Complex Disease 52 0.111
183
ATM052 Autoimmune Disease 1 26 0.111
184
CRB039 Cerebrovascular Disease 49 0.110
185
NWC001 Newcastle Disease 51 0.110
186
P CND004 Candidiasis 58 0.110
187
RDN001 Reading Disorder 39 0.110
188
IMM063 Immunodeficiency 15 27 0.110
189
ATM053 Autoimmune Disease 2 16 0.110
190
ALR002 Al-Raqad Syndrome 36 0.109
191
THR013 Thoracic Outlet Syndrome 48 0.109
192
P HYP086 Hypothyroidism 63 0.108
193
GST050 Gastrointestinal System Disease 58 0.108
194
GNR004 Generalized Anxiety Disorder 49 0.108
195
STR067 Stroke, Ischemic 74 0.107
196
IMM120 Immunodeficiency 40 24 0.107
197
P SHR029 Short Syndrome 60 0.107
198
GST078 Gastrointestinal Allergy 41 0.107
199
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.107
200
CND002 Conduct Disorder 54 0.106
201
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 60 0.106
202
LSH001 Leishmaniasis 63 0.106
203
HMT018 Hematopoietic Stem Cell Transplantation 39 0.106
204
STM007 Stomatitis 50 0.106
205
C9D001 C9 Deficiency 31 0.105
206
URT001 Urethritis 39 0.105
207
STM006 Stomach Disease 48 0.105
208
CTS003 Coats Disease 57 0.104
209
DFC004 Deficiency Anemia 64 0.104
210
P EXN002 Exanthem 57 0.104
211
NSD001 Nose Disease 51 0.103
212
PRT037 Pertussis 63 0.103
213
CNT098 Central Core Disease 68 0.102
214
P BLD051 Blood Coagulation Disease 44 0.102
215
ATM054 Autoimmune Disease 3 16 0.102
216
P THR014 Thrombocytopenia 63 0.101
217
P INT068 Intestinal Disease 60 0.101
218
P OST002 Osteoporosis 63 0.101
219
c CRN173 Coronary Heart Disease 8 19 0.101
220
MRC001 Marchiafava Bignami Disease 33 0.100
221
ETH011 Ethylmalonic Encephalopathy 57 0.100
222
P AST007 Astrocytoma 66 0.100
223
c PLN017 Peeling Skin Syndrome 1 32 0.100
224
FCT003 Factor X Deficiency 62 0.100
225
WRT001 Worth's Syndrome 37 0.099
226
SPS057 Spasticity 41 0.099
227
SVR077 Severe Combined Immune Deficiency 36 0.098
228
P CNJ013 Conjunctivitis 65 0.098
229
c PLN018 Peeling Skin Syndrome 2 36 0.098
230
HYP056 Hypoglycemia 60 0.098
231
CYT002 Cytokine Deficiency 30 0.098
232
TTH006 Tooth Disease 52 0.098
233
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.097
234
IMM062 Immunodeficiency 11 27 0.096
235
ETN001 Eating Disorder 59 0.096
236
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.096
237
OLV001 Olivopontocerebellar Atrophy 53 0.096
238
PHR003 Pharyngitis 58 0.096
239
ACN011 Acne 63 0.095
240
P LRY019 Laryngitis 55 0.095
241
SBS003 Substance Abuse 54 0.095
242
PLM129 Pulmonary Disease, Chronic Obstructive 61 0.094
243
P LPR003 Leprosy 70 0.094
244
GNT003 Genital Herpes 55 0.094
245
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.094
246
WSC001 Wisconsin Syndrome 16 0.094
247
IMM078 Immunodeficiency 21 35 0.093
248
c CHR418 Chronic Leukemia 48 0.092
249
P RTN024 Retinoblastoma 75 0.092
250
P ATX004 Ataxia 53 0.092
251
MST005 Mastitis 53 0.092
252
P HMP007 Hemophilia 55 0.092
253
P SYP003 Syphilis 51 0.091
254
ATM055 Autoimmune Disease 4 16 0.091
255
FDL002 Food Allergy 56 0.091
256
PRT011 Protein C Deficiency 52 0.090
257
VSC008 Vascular Hemostatic Disease 30 0.090
258
VGN020 Vaginal Disease 42 0.090
259
FCT006 Factor V Deficiency 62 0.090
260
PRT014 Protein S Deficiency 54 0.089
261
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 0.089
262
c HPT015 Hepatitis D 51 0.089
263
RBS001 Rabies 55 0.088
264
DRG003 Drug Dependence 53 0.088
265
DPH001 Diphtheria 55 0.088
266
c MLG068 Malignant Glioma 49 0.088
267
LVR012 Liver Cirrhosis 71 0.088
268
P PRS038 Personality Disorder 60 0.088
269
HDC001 Headache 52 0.088
270
c CRN177 Coronary Heart Disease 7 21 0.087
271
MSL001 Measles 61 0.087
272
BRN071 Brain Injury 51 0.087
273
BRN028 Brain Cancer 69 0.086
274
TTN003 Tetanus 62 0.086
275
BNF002 Bone Fracture 46 0.086
276
ATR060 Atrial Standstill, Digenic 51 0.085
277
PMP001 Pemphigus 49 0.084
278
HDG012 Hodgkin Lymphoma 75 0.084
279
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.084
280
IMM070 Immunodeficiency 13 30 0.084
281
OCY001 Oocyte Maturation Defect 31 0.083
282
c PLN021 Peeling Skin Syndrome 3 30 0.083
283
SSC050 Susceptibility/resistance to Hiv Infection 10 0.083
284
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 35 0.082
285
SPT004 Septic Arthritis 60 0.082
286
VSC003 Visceral Leishmaniasis 56 0.082
287
P ACT135 Acute Graft Versus Host Disease 52 0.082
288
PRS036 Parasitic Protozoa Infectious Disease 45 0.081
289
ANG049 Angioedema Induced by Ace Inhibitors 35 0.080
290
CHL123 Chlamydia 60 0.080
291
CHL014 Cholera 56 0.080
292
IMM088 Immunodeficiency 36 21 0.080
293
DRG011 Drug Addiction 55 0.080
294
NNL002 Nonalcoholic Steatohepatitis 49 0.079
295
TBR011 Tuberculous Meningitis 46 0.079
296
c THR092 Thrombophilia Due to Thrombin Defect 56 0.079
297
PRT056 Protein R Deficiency 12 0.078
298
ATM059 Autoimmune Disease 6 23 0.078
299
ATM012 Autoimmune Disease of Blood 36 0.078
300
PLM033 Pulmonary Embolism 59 0.078
301
BCT002 Bacterial Vaginosis 53 0.078
302
P THL005 Thalassemia 61 0.078
303
VSC011 Vasculitis 62 0.078
304
WLS001 Wilson Disease 72 0.078
305
P TRC086 Trichohepatoenteric Syndrome 1 46 0.077
306
TYP011 Typhus 57 0.077
307
ORL005 Oral Candidiasis 47 0.077
308
PLY023 Polycystic Liver Disease 57 0.077
309
c ADL017 Adult T-Cell Leukemia 59 0.076
310
P MYS005 Myositis 57 0.076
311
ALL006 Allergic Asthma 59 0.076
312
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.076
313
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.075
314
GRM003 German Syndrome 24 0.075
315
P MYL005 Myelofibrosis 67 0.075
316
SPC010 Speech and Communication Disorders 42 0.074
317
CHG001 Chagas Disease 62 0.074
318
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.074
319
GRW007 Growth Hormone Deficiency 49 0.074
320
HRP004 Herpes Zoster 56 0.074
321
CYT005 Cytomegalovirus Retinitis 48 0.074
322
PLG002 Plague 49 0.074
323
ALL003 Allergic Rhinitis 67 0.074
324
BNN003 Bone Inflammation Disease 46 0.073
325
RBR001 Roberts Syndrome 61 0.073
326
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.073
327
SCH014 Schistosomiasis 59 0.073
328
CRV045 Cervical Intraepithelial Neoplasia 41 0.072
329
CRY004 Cryoglobulinemia 47 0.072
330
MSS002 Mass Syndrome 49 0.072
331
MVD001 Moved to 60 0.072
332
MNT045 Montefiore Syndrome 11 0.072
333
BND014 Bone Development Disease 40 0.072
334
CYT008 Cytomegalovirus Infection 51 0.072
335
NVD002 Nevada Syndrome 15 0.072
336
ACR002 Acrocapitofemoral Dysplasia 35 0.072
337
DMY004 Demyelinating Disease 52 0.072
338
IMP005 Impotence 49 0.072
339
IMP004 Impetigo 41 0.072
340
HML018 Homologous Wasting Disease 14 0.071
341
IMM075 Immunodeficiency 22 26 0.071
342
ADT003 Auditory System Disease 49 0.071
343
NVS004 Nova Syndrome 18 0.071
344
P DRM010 Dermatomyositis 59 0.071
345
BCT004 Bacteriuria 48 0.071
346
ACD004 Acdc 35 0.071
347
LYM116 Lymph Node Disease 42 0.071
348
c ACT004 Acute Diarrhea 38 0.070
349
P UTR038 Uterine Disease 38 0.070
350
SCR008 Scrub Typhus 55 0.070
351
P ATX030 Ataxia-Telangiectasia 78 0.070
352
MTB004 Metabolic Acidosis 49 0.070
353
SBS004 Substance Dependence 48 0.070
354
c HMN021 Human T-Cell Leukemia Virus Type 1 51 0.069
355
BRW006 Brown Syndrome 31 0.069
356
WRN001 Werner Syndrome 69 0.069
357
LYM027 Lymphopenia 54 0.069
358
c SVR001 Severe Acute Respiratory Syndrome 56 0.069
359
P ALC004 Alcohol Abuse 57 0.069
360
c ATM003 Autoimmune Thyroiditis 59 0.068
361
ALC007 Alcohol Dependence 66 0.068
362
P MTC069 Mitochondrial Disorders 51 0.068
363
IMM044 Immunoglobulin G Deficiency 22 0.067
364
TNG009 Tongue Squamous Cell Carcinoma 73 0.067
365
SML019 Smallpox 49 0.067
366
FXF002 Fox-Fordyce Disease 37 0.067
367
PTT037 Pituitary Tumors 45 0.067
368
CRD001 Cardiac Tamponade 43 0.067
369
DYS073 Dysphagia 51 0.067
370
c CHR417 Chronic Graft Versus Host Disease 50 0.067
371
c HPT007 Hepatitis E 51 0.067
372
MYC017 Mycobacterium Kansasii 40 0.066
373
FNT003 Fountain Syndrome 26 0.066
374
IMM095 Immunodeficiency 35 30 0.066
375
c MYC055 Mycobacterium Tuberculosis 3 16 0.066
376
PPL022 Papilloma 54 0.066
377
TRY001 Trypanosomiasis 51 0.066
378
DRM011 Dermatophytosis 44 0.066
379
P ANT006 Antiphospholipid Syndrome 60 0.065
380
SPN186 Spinal Cord Injury 62 0.065
381
KRT002 Keratomalacia 50 0.065
382
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.065
383
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.065
384
CRB037 Cerebral Palsy 54 0.065
385
CCN007 Cocoon Syndrome 32 0.065
386
KRT006 Keratoconjunctivitis 51 0.065
387
PRD011 Proud Syndrome 42 0.065
388
BRN002 Bronchiolitis 56 0.064
389
c HMP004 Hemophilia B 61 0.064
390
THY030 Thyroid Gland Disease 52 0.064
391
OPD001 Opioid Abuse 38 0.064
392
TRC003 Trichomoniasis 41 0.063
393
IMM036 Immunodeficiency, Isolated 26 0.063
394
WST005 West Nile Virus 50 0.063
395
EVN001 Evans' Syndrome 39 0.063
396
BRK010 Burkitt Lymphoma 66 0.063
397
VLV010 Vulvovaginitis 41 0.063
398
INT067 Interstitial Nephritis 48 0.063
399
WLL001 Williams-Beuren Syndrome 61 0.063
400
TNS005 Tonsillitis 58 0.062
401
INT007 Intermediate Coronary Syndrome 52 0.062
402
VSC018 Visceral Steatosis 37 0.062
403
P LCT001 Lactic Acidosis 52 0.062
404
P HMC003 Hemochromatosis 71 0.062
405
HPT022 Hepatoblastoma 57 0.061
406
DWN001 Down Syndrome 65 0.061
407
TYL001 Taylor's Syndrome 28 0.061
408
LPM004 Lipoma 59 0.061
409
ORC001 Orchitis 35 0.061
410
AND015 Androgen Insensitivity 64 0.061
411
PRC002 Paracoccidioidomycosis 57 0.061
412
P GNR027 Generalized Peeling Skin Syndrome 21 0.060
413
SWN001 Swine Influenza 42 0.060
414
P CNT005 Central Nervous System Lymphoma 51 0.060
415
ECH003 Echinococcosis 53 0.060
416
IMM118 Immunodeficiency 42 17 0.060
417
P MMP001 Mumps 56 0.060
418
CHR005 Chorioamnionitis 47 0.060
419
SWL001 Swallowing Disorders 33 0.060
420
c PRM023 Pre-Malignant Neoplasm 42 0.060
421
c HMP029 Hemophilia a 61 0.060
422
CMR002 Coumarin Resistance 49 0.059
423
P TXP001 Toxoplasmosis 61 0.059
424
LKP003 Leukoplakia 44 0.059
425
MNN009 Meningoencephalitis 42 0.059
426
CMM004 Common Variable Immunodeficiency 68 0.059
427
MND006 Mondor Disease 20 0.059
428
P FBR017 Fibrosarcoma 55 0.059
429
SCT005 Scott Syndrome 51 0.059
430
CHL004 Cholelithiasis 48 0.059
431
PLN006 Poland Syndrome 48 0.059
432
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.058
433
HPT074 Hepatic Adenoma, Somatic 35 0.058
434
MYC033 Myoclonus 41 0.058
435
TXC002 Toxic Encephalopathy 52 0.058
436
c PRM226 Primary Central Nervous System Lymphoma 51 0.058
437
P NPH009 Nephrolithiasis 59 0.058
438
CRY005 Cryptococcosis 50 0.057
439
INC002 Inclusion Body Myositis 64 0.057
440
MYC019 Mycobacterium Marinum 30 0.057
441
c DLT001 Delta Chain Disease 14 0.057
442
TSY001 Tau Syndrome 11 0.057
443
RSC001 Rosacea 54 0.057
444
CMM005 Common Cold 58 0.057
445
LPR001 Lepromatous Leprosy 50 0.056
446
FLL008 Folliculitis 47 0.056
447
P MMB011 Membranous Nephropathy 53 0.056
448
SPS019 Spastic Paraparesis 34 0.056
449
YNG002 Young Syndrome 25 0.056
450
DVL001 Developmental Coordination Disorder 36 0.056
451
YLL002 Yellow Fever 58 0.056
452
c MTR002 Mitral Valve Insufficiency 42 0.055
453
RLT001 Raltegravir Toxicity 10 0.055
454
SNS001 Sensorineural Hearing Loss 52 0.055
455
SPC005 Speech Disorder 41 0.055
456
CCN002 Cocaine Abuse 47 0.054
457
VNZ002 Venezuelan Equine Encephalitis 43 0.054
458
CGL001 Coagulation Protein Disease 14 0.054
459
c ACT020 Acute T Cell Leukemia 38 0.054
460
c VRL008 Viral Exanthem 29 0.054
461
IRS003 Iris Disease 32 0.054
462
SPL004 Splenic Marginal Zone Lymphoma 43 0.054
463
AVN001 Avian Influenza 52 0.054
464
EXT033 Extrapulmonary Tuberculosis 45 0.054
465
CCC001 Coccidioidomycosis 55 0.054
466
CHN016 Cohen Syndrome 55 0.054
467
BNM008 Bone Mineral Density, Low 28 0.053
468
PMP004 Pemphigus Foliaceus 42 0.053
469
IMM099 Immunodeficiency 33 28 0.053
470
ALC006 Alcoholic Hepatitis 60 0.053
471
P CMP008 Compartment Syndrome 46 0.053
472
PRG004 Progeria 54 0.053
473
ORL014 Oral Pharyngeal Disorders 13 0.053
474
HNS001 Hansen's Disease 30 0.053
475
VGN019 Vaginal Discharge 32 0.052
476
MTC005 Mitochondrial Metabolism Disease 37 0.052
477
c LKM005 Leukemia, T-Cell, Chronic 21 0.051
478
SBS006 Sebastian Syndrome 36 0.051
479
P HRP009 Herpes Simplex Encephalitis 46 0.051
480
HND003 Hand-Foot-Uterus Syndrome 46 0.051
481
NRS003 Neurosyphilis 41 0.051
482
P FTT008 Fatty Liver Disease, Nonalcoholic 1 31 0.051
483
P LBY004 Labyrinthitis 39 0.050
484
CYS005 Cysticercosis 52 0.050
485
c INH004 Inherited Blood Coagulation Disease 38 0.050
486
FCT001 Factor Viii Deficiency 41 0.049
487
HYP017 Hypophosphatemia 43 0.049
488
NCR004 Nocardiosis 44 0.049
489
PLS025 Plasmablastic Lymphoma 46 0.049
490
ANS012 Anus Disease 32 0.048
491
TRP002 Tropical Spastic Paraparesis 55 0.048
492
c DRR009 Diarrhea 6 30 0.048
493
IMM135 Immunodeficiency 46 13 0.048
494
FBR012 Fabry Disease 68 0.048
495
TCK001 Tick-Borne Encephalitis 49 0.048
496
MTR014 Motor Neuron Disease 57 0.047
497
c LYM107 Lymphoproliferative Syndrome 2 32 0.047
498
P RTT002 Rett Syndrome 77 0.047
499
c CRD093 Cardiomyopathy, Dilated, 1a 30 0.047
500
c BRN108 Branchiootic Syndrome 1 36 0.047
501
CHC001 Chickenpox 50 0.047
502
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.047
503
LMB010 Lambert Syndrome 35 0.046
504
P ACQ009 Acquired Metabolic Disease 42 0.046
505
CHY002 Chylomicron Retention Disease 54 0.046
506
P NJM001 Nijmegen Breakage Syndrome 68 0.046
507
CWP001 Cowpox 45 0.046
508
WDS002 Woods Syndrome 30 0.045
509
c LYM106 Lymphoproliferative Syndrome 1 33 0.045
510
IMM080 Immunodeficiency 23 29 0.045
511
HMN032 Human Herpesvirus 8 42 0.045
512
HTC002 Hutchinson-Gilford Progeria 51 0.045
513
P CMR001 Camurati-Engelmann Disease 63 0.045
514
CST005 Castleman Disease 42 0.045
515
c HYP072 Hypersensitivity Reaction Type Iii Disease 39 0.045
516
BHR001 Behr Syndrome 43 0.045
517
BRD001 Brody Myopathy 49 0.044
518
P SHR001 Short Bowel Syndrome 51 0.044
519
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 30 0.044
520
NTR040 Neutropenia, Cyclic 51 0.043
521
P ACR001 Aicardi-Goutieres Syndrome 54 0.043
522
OPS006 Opsoclonus-Myoclonus Syndrome 47 0.043
523
MMB002 Membranous Glomerulonephritis 47 0.043
524
MYC021 Mycobacterium Xenopi 26 0.043
525
P CRN015 Cornelia De Lange Syndrome 65 0.043
526
HRP005 Herpetic Whitlow 31 0.043
527
WHT007 White Platelet Syndrome 17 0.043
528
P ADD001 Addison's Disease 60 0.042
529
HRN022 Hearing Loss/deafness 23 0.042
530
PRM042 Primary Effusion Lymphoma 55 0.042
531
HYP458 Hyper Ige Syndrome 43 0.042
532
NLL002 Null Syndrome 21 0.042
533
FNC006 Functional Gastric Disease 33 0.042
534
P SJG001 Sjogren's Syndrome 55 0.042
535
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 36 0.041
536
GNT002 Giant Cell Glioblastoma 51 0.041
537
TRP009 Triple X Syndrome 40 0.041
538
P PFF001 Pfeiffer Syndrome 73 0.041
539
ORL019 Oral Hairy Leukoplakia 33 0.041
540
GLC006 Galactosemia 64 0.041
541
WRT002 Writing Disorder 26 0.041
542
NTR006 Neutrophil Immunodeficiency Syndrome 36 0.041
543
BLL012 Bullous Impetigo 28 0.041
544
LYM041 Lymphocytes Absent 15 0.041
545
MTR007 Motor Peripheral Neuropathy 44 0.040
546
CRZ001 Crouzon Syndrome 70 0.040
547
c SCN036 Secondary Progressive Multiple Sclerosis 50 0.040
548
OTP003 Oto-Palatal-Digital Syndrome 14 0.040
549
PTY004 Pityriasis Lichenoides 25 0.040
550
P SPR013 Spiradenoma 37 0.039
551
P IGN003 Iga Nephropathy 1 31 0.039
552
CNT067 Central Cord Syndrome 22 0.039
553
ESN015 Eosinophilic Fasciitis 46 0.039
554
GST020 Gastric Antral Vascular Ectasia 33 0.039
555
VHW001 Vohwinkel Syndrome 47 0.039
556
BRG013 Buerger Disease 54 0.038
557
c HYP507 Hypotrichosis 1 30 0.038
558
PTY006 Pityriasis Lichenoides Et Varioliformis Acuta 22 0.038
559
CYT004 Cytomegalic Inclusion Disease 29 0.038
560
EPT021 Epithelial Recurrent Erosion Dystrophy 32 0.038
561
RYS001 Reye Syndrome 51 0.037
562
c INF002 Inflammatory Diarrhea 31 0.037
563
MN1001 Mn1 28 0.036
564
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.036
565
BRL010 Buruli Ulcer 47 0.036
566
P ATX010 Ataxia Neuropathy Spectrum 24 0.036
567
ADP007 Adie Pupil 33 0.035
568
LCH011 Lichen Planopilaris 40 0.035
569
DRR010 Darier Disease 60 0.035
570
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 50 0.035
571
CRB159 Cerebral Visual Impairment 34 0.035
572
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 43 0.035
573
c RBN008 Rubinstein-Taybi Syndrome 2 34 0.035
574
c PRD030 Periodontitis 1, Juvenile 34 0.035
575
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 21 0.035
576
PSD029 Pseudocholinesterase Deficiency 40 0.034
577
c NNN010 Noonan Syndrome 3 37 0.034
578
HMF008 Hemifacial Atrophy, Progressive 31 0.034
579
HNM002 Hinman Syndrome 22 0.034
580
TMR010 Tumor Predisposition Syndrome 58 0.034
581
P MWT001 Mowat-Wilson Syndrome 50 0.034
582
ENG004 Engraftment Syndrome 34 0.034
583
ADP002 Adiponectin Deficiency 30 0.033
584
P RFS001 Refsum Disease 60 0.033
585
c PCH015 Pachyonychia Congenita 1 35 0.033
586
SML020 Small Patella Syndrome 36 0.033
587
SVN001 Sveinsson Choreoretinal Atrophy 28 0.033
588
c BNG076 Benign Exophthalmos Syndrome 15 0.033
589
CRT055 Creatine Deficiency Syndromes 26 0.033
590
AMS002 Amish Infantile Epilepsy Syndrome 34 0.032
591
P IDP049 Idiopathic Anterior Uveitis 22 0.032
592
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 54 0.032
593
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 50 0.032
594
INT046 Intestinal Tuberculosis 35 0.032
595
CHR103 Charge Syndrome 64 0.031
596
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 16 0.031
597
GRN016 Grant Syndrome 30 0.030
598
NTR018 Neutrophilia, Hereditary 32 0.030
599
SRN001 Serine Deficiency 31 0.029
600
IMM003 Immunoglobulin Alpha Deficiency 36 0.029
601
EPS006 Epstein Syndrome 40 0.029
602
TRC012 Trichuriasis 42 0.028
603
MYL013 Myeloperoxidase Deficiency 46 0.028
604
TMP012 Temple Syndrome 39 0.028
605
MRS002 Marshall Syndrome 51 0.027
606
CYT003 Cytokine Receptor Deficiency 10 0.024