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"

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

# Family MCID Name MIFTS Score
1
HV1006 Hiv-1 80 1.472
2
ACQ007 Acquired Immunodeficiency Syndrome 60 0.517
3
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.516
4
PRM097 Primary Immunodeficiency Disease 60 0.464
5
P LKM002 Leukemia 71 0.416
6
P BRS047 Breast Cancer 100 0.411
7
P HPT021 Hepatitis 69 0.391
8
TBR010 Tuberculosis 70 0.357
9
ADM013 Adamantinoma of Long Bones 57 0.336
10
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.333
11
VRL011 Viral Infectious Disease 55 0.331
12
END072 Endotheliitis 42 0.316
13
P PRS040 Prostate Cancer 90 0.315
14
SXL003 Sexual Disorder 42 0.313
15
NTR005 Nutritional Deficiency Disease 36 0.309
16
CD4004 Cd4 Deficiency 14 0.287
17
CSY001 C Syndrome 50 0.278
18
PRS047 Prostatitis 56 0.277
19
NRN002 Neuronitis 41 0.270
20
P LYM118 Lymphoma 69 0.265
21
c HPT001 Hepatitis C 68 0.248
22
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.235
23
ART002 Arts Syndrome 51 0.235
24
IMM142 Immunodeficiency 50 20 0.234
25
IMM071 Immunodeficiency 12 26 0.232
26
ALL026 Allergic Hypersensitivity Disease 52 0.226
27
MLR007 Male Reproductive System Disease 34 0.223
28
P THY032 Thyroiditis 54 0.222
29
IMM076 Immunodeficiency 24 27 0.221
30
IMM065 Immunodeficiency 10 36 0.220
31
IMM068 Immunodeficiency 8 30 0.218
32
P MYL006 Myeloid Leukemia 66 0.214
33
c HPT003 Hepatitis a 59 0.213
34
c HPT016 Hepatitis B 65 0.211
35
P PNM007 Pneumonia 68 0.210
36
GDS001 Good Syndrome 44 0.209
37
TCL003 T Cell Deficiency 45 0.208
38
P LVR013 Liver Disease 75 0.208
39
c HPT073 Hepatitis C Virus 73 0.208
40
c VRL010 Viral Hepatitis 60 0.208
41
P INF038 Influenza 72 0.208
42
WLL006 Wells Syndrome 59 0.208
43
RPR002 Reproductive System Disease 41 0.206
44
P ART022 Arthritis 75 0.206
45
SRC014 Sarcoma 66 0.205
46
MLN008 Melanoma 62 0.204
47
P PNC044 Pancreatitis 61 0.201
48
MLR004 Malaria 83 0.198
49
INC022 Inclusion-Cell Disease 46 0.196
50
SXD001 Sex Differentiation Disease 38 0.194
51
PRS042 Prostate Disease 52 0.194
52
P CLR023 Colorectal Cancer 97 0.192
53
DMN002 Dementia 65 0.191
54
CHL071 Child Syndrome 58 0.191
55
KDS001 Kid Syndrome 53 0.191
56
P HPT023 Hepatocellular Carcinoma 92 0.188
57
P HRT032 Heart Disease 75 0.187
58
FML039 Female Reproductive System Disease 48 0.186
59
C3D001 C3 Deficiency 53 0.183
60
P CRV039 Cervicitis 45 0.182
61
IMM136 Immune System Disease 51 0.182
62
PRM025 Primary Bacterial Infectious Disease 41 0.178
63
P SPS003 Spastic Diplegia 52 0.178
64
WTH001 Withdrawal Disorder 37 0.177
65
P KDN018 Kidney Disease 66 0.177
66
BCL002 B Cell Deficiency 49 0.176
67
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.175
68
RTN023 Retinitis 50 0.175
69
THR024 Thrombosis 57 0.173
70
PCK002 Pick Disease 68 0.172
71
WST001 West Syndrome 57 0.172
72
P NRB001 Neuroblastoma 70 0.172
73
SQM006 Squamous Cell Carcinoma 70 0.172
74
ADL002 Adult Syndrome 52 0.170
75
P EPL164 Epilepsy 66 0.169
76
BLD054 Blood Protein Disease 37 0.169
77
P RHM011 Rheumatoid Arthritis 89 0.162
78
DSS008 Disease of Mental Health 52 0.162
79
P MYP004 Myopathy 67 0.162
80
ATH003 Atherosclerosis 65 0.162
81
P GLM045 Glioma 60 0.161
82
P ENC018 Encephalopathy 59 0.161
83
VCC001 Vaccinia 46 0.160
84
LPD008 Lipid Metabolism Disorder 58 0.159
85
NSY001 N Syndrome 36 0.159
86
IMM066 Immunodeficiency 9 30 0.159
87
BRT030 Birth Defects 43 0.158
88
MDD011 Mood Disorder 61 0.158
89
HYP266 Hypoxia 56 0.157
90
ACR041 Acromelic Frontonasal Dysostosis 45 0.157
91
P HRP006 Herpes Simplex 65 0.157
92
ALN001 Aland Island Eye Disease 45 0.156
93
P ENC004 Encephalitis 63 0.156
94
TCL006 T Cell Immunodeficiency Primary 12 0.155
95
c PRS116 Prostate Cancer 1 37 0.153
96
BNC003 Bone Cancer 58 0.153
97
CRB009 Cerebritis 39 0.153
98
P MNN013 Meningitis 67 0.152
99
IMM077 Immunodeficiency 20 27 0.150
100
SKN016 Skin Disease 66 0.149
101
BNS002 Bone Structure Disease 37 0.149
102
MSC004 Muscle Tissue Disease 34 0.149
103
P INF032 Infertility 59 0.146
104
PRP027 Peripheral Vascular Disease 69 0.146
105
P NRV007 Nervous System Disease 71 0.146
106
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.145
107
c RNL016 Renal Infectious Disease 20 0.144
108
ADJ001 Adjustment Disorder 38 0.144
109
P GLB002 Glioblastoma 68 0.143
110
VND001 Vein Disease 47 0.143
111
c CNT035 Central Nervous System Disease 60 0.142
112
PRM243 Primary Bone Cancer 29 0.141
113
BLD053 Blood Platelet Disease 46 0.141
114
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.140
115
MRG013 Mirage Syndrome 29 0.140
116
P MSC033 Muscle Disorders 52 0.139
117
LRN003 Learning Disability 49 0.139
118
IMM074 Immunodeficiency 16 26 0.138
119
RSP006 Respiratory System Disease 58 0.138
120
SKN023 Skin Tag 44 0.136
121
P LPD010 Lipodystrophy 55 0.136
122
P NRV006 Nervous System Cancer 60 0.135
123
LPD004 Lipoid Nephrosis 48 0.134
124
IMP003 Impaired Renal Function Disease 34 0.133
125
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.133
126
ATP002 Atopy 66 0.132
127
P LPS004 Lupus Erythematosus 64 0.132
128
IMM096 Immunodeficiency 30 27 0.131
129
BCT015 Bacteremia 48 0.131
130
P NRP001 Neuropathy 59 0.131
131
ACD009 Acid-Labile Subunit, Deficiency of 45 0.130
132
LKC003 Leukocyte Disease 43 0.130
133
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.130
134
EXF001 Exfoliation Syndrome 57 0.129
135
P TCL004 T-Cell Leukemia 47 0.128
136
P PLN008 Peeling Skin Syndrome 45 0.127
137
VGN023 Vaginitis 42 0.127
138
HYP066 Hyperglycemia 61 0.127
139
BNM001 Bone Marrow Cancer 51 0.127
140
PLM001 Pulmonary Tuberculosis 67 0.127
141
c ACT073 Acute Leukemia 60 0.126
142
MCS002 Mucositis 55 0.126
143
c PND001 Pain Disorder 54 0.126
144
IMM025 Immunoglobulin a Deficiency 2 24 0.125
145
IMM081 Immunodeficiency 19 29 0.125
146
MTH009 Mouth Disease 61 0.124
147
RCT017 Rectal Disease 40 0.123
148
P BCL006 B-Cell Lymphomas 65 0.123
149
P DRR001 Diarrhea 60 0.123
150
IMM082 Immunodeficiency 18 31 0.122
151
SPC003 Specific Developmental Disorder 38 0.122
152
c SYS001 Systemic Lupus Erythematosus 86 0.121
153
LNG099 Lung Disease 64 0.121
154
P CRN178 Coronary Heart Disease 6 21 0.121
155
IMM085 Immunodeficiency 25 23 0.121
156
IMM102 Immunodeficiency 14 31 0.120
157
RHM027 Rheumatic Disease 58 0.120
158
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.120
159
c CRN214 Coronary Heart Disease 5 22 0.120
160
FTT001 Fatty Liver Disease 59 0.120
161
ANX002 Anxiety Disorder 67 0.120
162
PLS009 Plasma Cell Neoplasm 48 0.119
163
PRP019 Peripheral Nervous System Disease 55 0.119
164
P RCK004 Rickets 61 0.119
165
P CLL015 Collagen Disease 50 0.118
166
c CHR089 Chronic Kidney Failure 66 0.118
167
c TRC078 Trichohepatoenteric Syndrome 2 29 0.118
168
SVR004 Severe Combined Immunodeficiency 69 0.118
169
GLC003 Glucose Intolerance 55 0.117
170
KND001 Kindler Syndrome 57 0.116
171
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.116
172
PLC008 Placenta Disease 33 0.116
173
PRT036 Peritonitis 63 0.116
174
MYC002 Mycobacterium Avium Complex Disease 52 0.114
175
ATN002 Autonomic Nervous System Disease 48 0.114
176
IMM063 Immunodeficiency 15 26 0.114
177
END030 End Stage Renal Failure 55 0.114
178
CTS003 Coats Disease 57 0.113
179
PLS007 Plasmodium Falciparum Malaria 55 0.113
180
BRN038 Bronchial Disease 51 0.112
181
c CRN175 Coronary Heart Disease 4 19 0.112
182
PHY002 Physical Disorder 43 0.112
183
P PLM037 Pulmonary Hypertension 79 0.112
184
RDN001 Reading Disorder 34 0.112
185
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.112
186
ATM052 Autoimmune Disease 1 25 0.111
187
GST078 Gastrointestinal Allergy 40 0.111
188
ATM053 Autoimmune Disease 2 16 0.111
189
NWC001 Newcastle Disease 54 0.110
190
STR067 Stroke, Ischemic 75 0.110
191
IMM120 Immunodeficiency 40 24 0.110
192
GNR004 Generalized Anxiety Disorder 51 0.110
193
CRB039 Cerebrovascular Disease 63 0.110
194
STM006 Stomach Disease 50 0.110
195
c PLN017 Peeling Skin Syndrome 1 34 0.108
196
STM007 Stomatitis 50 0.108
197
P CND004 Candidiasis 57 0.108
198
P SHR029 Short Syndrome 58 0.108
199
ALR002 Al-Raqad Syndrome 36 0.107
200
P HYP086 Hypothyroidism 64 0.107
201
DFC004 Deficiency Anemia 64 0.107
202
NSD001 Nose Disease 48 0.106
203
CNT098 Central Core Disease 65 0.105
204
P EXN002 Exanthem 57 0.105
205
P BLD051 Blood Coagulation Disease 42 0.105
206
C9D001 C9 Deficiency 29 0.105
207
LSH001 Leishmaniasis 66 0.104
208
WRT001 Worth's Syndrome 34 0.104
209
HMT018 Hematopoietic Stem Cell Transplantation 41 0.104
210
c CRN173 Coronary Heart Disease 8 18 0.104
211
URT001 Urethritis 41 0.104
212
P INT068 Intestinal Disease 60 0.104
213
ATM054 Autoimmune Disease 3 15 0.103
214
c PLN018 Peeling Skin Syndrome 2 40 0.101
215
P LYM033 Lymphoproliferative Syndrome 56 0.101
216
SVR077 Severe Combined Immune Deficiency 36 0.101
217
IMM062 Immunodeficiency 11 26 0.101
218
CYT002 Cytokine Deficiency 30 0.101
219
ETN001 Eating Disorder 58 0.100
220
TTH006 Tooth Disease 52 0.100
221
PRT037 Pertussis 64 0.099
222
SPN369 Spinal Disease 39 0.099
223
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.099
224
PHR003 Pharyngitis 56 0.098
225
FCT003 Factor X Deficiency 61 0.098
226
P THR014 Thrombocytopenia 64 0.098
227
HYP056 Hypoglycemia 61 0.097
228
P OST002 Osteoporosis 64 0.097
229
P AST007 Astrocytoma 65 0.097
230
OLV001 Olivopontocerebellar Atrophy 53 0.097
231
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.096
232
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.096
233
P CNJ013 Conjunctivitis 64 0.096
234
SPS057 Spasticity 42 0.096
235
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.095
236
WSC001 Wisconsin Syndrome 14 0.095
237
IMM078 Immunodeficiency 21 35 0.094
238
FDL002 Food Allergy 53 0.094
239
GNT003 Genital Herpes 53 0.093
240
ACN011 Acne 62 0.092
241
ETH011 Ethylmalonic Encephalopathy 56 0.092
242
PRT011 Protein C Deficiency 52 0.092
243
VSC008 Vascular Hemostatic Disease 30 0.092
244
c CHR418 Chronic Leukemia 47 0.092
245
VGN020 Vaginal Disease 41 0.092
246
ATM055 Autoimmune Disease 4 15 0.091
247
c PLN021 Peeling Skin Syndrome 3 29 0.091
248
IMM070 Immunodeficiency 13 27 0.091
249
P HMR003 Hemorrhagic Disease 57 0.090
250
c HPT015 Hepatitis D 52 0.090
251
c CRN177 Coronary Heart Disease 7 20 0.090
252
P LPR003 Leprosy 69 0.090
253
P LRY019 Laryngitis 54 0.090
254
BRN071 Brain Injury 52 0.089
255
MST005 Mastitis 51 0.089
256
HDC001 Headache 54 0.089
257
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.089
258
SBS003 Substance Abuse 54 0.089
259
BRN028 Brain Cancer 70 0.089
260
LVR012 Liver Cirrhosis 67 0.089
261
P SYP003 Syphilis 53 0.088
262
FCT006 Factor V Deficiency 57 0.088
263
P HMP007 Hemophilia 57 0.088
264
P ATX004 Ataxia 53 0.088
265
RBS001 Rabies 56 0.088
266
P RTN024 Retinoblastoma 74 0.088
267
NNL002 Nonalcoholic Steatohepatitis 50 0.088
268
ATR060 Atrial Standstill, Digenic 51 0.087
269
MSL001 Measles 61 0.087
270
DRG003 Drug Dependence 50 0.086
271
TTN003 Tetanus 61 0.085
272
PRT014 Protein S Deficiency 53 0.085
273
AYM001 Ayme-Gripp Syndrome 41 0.085
274
IMM088 Immunodeficiency 36 22 0.085
275
DPH001 Diphtheria 59 0.085
276
P OCY001 Oocyte Maturation Defect 38 0.085
277
SSC050 Susceptibility/resistance to Hiv Infection 10 0.084
278
P PYL005 Pyelonephritis 52 0.084
279
P PRS038 Personality Disorder 62 0.084
280
c MLG068 Malignant Glioma 51 0.083
281
P ACT135 Acute Graft Versus Host Disease 53 0.083
282
ANG049 Angioedema Induced by Ace Inhibitors 34 0.082
283
BNF002 Bone Fracture 50 0.082
284
PRS036 Parasitic Protozoa Infectious Disease 41 0.081
285
DRG011 Drug Addiction 51 0.081
286
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.081
287
PRT056 Protein R Deficiency 10 0.081
288
SPC010 Speech and Communication Disorders 41 0.081
289
ATM059 Autoimmune Disease 6 22 0.080
290
MSS002 Mass Syndrome 48 0.080
291
HDG012 Hodgkin Lymphoma 77 0.080
292
PMP001 Pemphigus 50 0.080
293
VSC003 Visceral Leishmaniasis 56 0.079
294
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.079
295
SLM003 Salmonellosis 52 0.079
296
SPN041 Spinal Cord Disease 51 0.079
297
SPT004 Septic Arthritis 60 0.079
298
PLY023 Polycystic Liver Disease 56 0.078
299
ATM012 Autoimmune Disease of Blood 35 0.078
300
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.078
301
BCT002 Bacterial Vaginosis 52 0.077
302
GRF001 Graft-Versus-Host Disease, Protection Against 52 0.077
303
c ADL017 Adult T-Cell Leukemia 60 0.077
304
CHL123 Chlamydia 60 0.076
305
HML018 Homologous Wasting Disease 13 0.076
306
TBR011 Tuberculous Meningitis 47 0.076
307
P MYL005 Myelofibrosis 67 0.075
308
GRM003 German Syndrome 22 0.075
309
CHL014 Cholera 53 0.075
310
NVD002 Nevada Syndrome 14 0.075
311
CHG001 Chagas Disease 67 0.075
312
LYM116 Lymph Node Disease 47 0.075
313
ORL005 Oral Candidiasis 48 0.074
314
P TRC086 Trichohepatoenteric Syndrome 1 48 0.074
315
DMY004 Demyelinating Disease 53 0.074
316
BNN003 Bone Inflammation Disease 44 0.074
317
CYT008 Cytomegalovirus Infection 52 0.074
318
VSC011 Vasculitis 62 0.073
319
P THL005 Thalassemia 64 0.073
320
GRW007 Growth Hormone Deficiency 50 0.073
321
P MYS005 Myositis 57 0.073
322
RBR001 Roberts Syndrome 60 0.073
323
P UTR038 Uterine Disease 37 0.073
324
ACD004 Acdc 33 0.072
325
ADT003 Auditory System Disease 40 0.072
326
BND014 Bone Development Disease 40 0.072
327
ACR002 Acrocapitofemoral Dysplasia 33 0.072
328
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.072
329
PLM033 Pulmonary Embolism 60 0.072
330
IMM075 Immunodeficiency 22 26 0.072
331
NVS004 Nova Syndrome 13 0.072
332
HRP004 Herpes Zoster 56 0.072
333
P ALC004 Alcohol Abuse 59 0.071
334
MNT045 Montefiore Syndrome 10 0.071
335
PLG002 Plague 51 0.070
336
FXF002 Fox-Fordyce Disease 36 0.070
337
SCH014 Schistosomiasis 58 0.070
338
BRW006 Brown Syndrome 29 0.070
339
WLS001 Wilson Disease 72 0.070
340
c THR092 Thrombophilia Due to Thrombin Defect 54 0.070
341
CRV045 Cervical Intraepithelial Neoplasia 38 0.070
342
ALC007 Alcohol Dependence 63 0.070
343
P MTC069 Mitochondrial Disorders 53 0.070
344
CRY004 Cryoglobulinemia 46 0.069
345
SCR008 Scrub Typhus 55 0.069
346
IMM044 Immunoglobulin G Deficiency 33 0.069
347
c HPT007 Hepatitis E 54 0.068
348
BCT004 Bacteriuria 45 0.068
349
IMP005 Impotence 51 0.068
350
IMP004 Impetigo 42 0.068
351
CRB037 Cerebral Palsy 66 0.068
352
P ATX030 Ataxia-Telangiectasia 77 0.068
353
SPN186 Spinal Cord Injury 63 0.067
354
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.067
355
c CHR417 Chronic Graft Versus Host Disease 51 0.067
356
FNT003 Fountain Syndrome 26 0.067
357
P DRM010 Dermatomyositis 62 0.067
358
c ACT004 Acute Diarrhea 39 0.067
359
MTB004 Metabolic Acidosis 48 0.067
360
DYS073 Dysphagia 48 0.067
361
CCN007 Cocoon Syndrome 45 0.067
362
IMM095 Immunodeficiency 35 28 0.066
363
c MYC055 Mycobacterium Tuberculosis 3 15 0.066
364
KRT002 Keratomalacia 52 0.066
365
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.066
366
SWL001 Swallowing Disorders 33 0.066
367
SBS004 Substance Dependence 47 0.066
368
PRD011 Proud Syndrome 42 0.065
369
c ACT042 Acute Pyelonephritis 45 0.065
370
IMM036 Immunodeficiency, Isolated 27 0.065
371
WLL001 Williams-Beuren Syndrome 60 0.065
372
WRN001 Werner Syndrome 67 0.065
373
c CNT068 Central Pain Syndrome 29 0.065
374
P ANT006 Antiphospholipid Syndrome 56 0.064
375
THY030 Thyroid Gland Disease 48 0.064
376
c SVR001 Severe Acute Respiratory Syndrome 57 0.064
377
SML019 Smallpox 54 0.064
378
P GNR027 Generalized Peeling Skin Syndrome 19 0.063
379
LYM027 Lymphopenia 56 0.063
380
IMM118 Immunodeficiency 42 17 0.063
381
VSC018 Visceral Steatosis 37 0.063
382
PPL022 Papilloma 55 0.063
383
MYC017 Mycobacterium Kansasii 40 0.063
384
PLN006 Poland Syndrome 54 0.062
385
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.062
386
EVN001 Evans' Syndrome 43 0.062
387
TYL001 Taylor's Syndrome 26 0.062
388
TRY001 Trypanosomiasis 51 0.062
389
DRM011 Dermatophytosis 46 0.062
390
KRT006 Keratoconjunctivitis 52 0.062
391
YNG002 Young Syndrome 26 0.062
392
BRK010 Burkitt Lymphoma 69 0.062
393
P ALX003 Alexander Disease 63 0.062
394
DVL001 Developmental Coordination Disorder 36 0.061
395
MND006 Mondor Disease 21 0.061
396
P CSH001 Cushing's Syndrome 65 0.061
397
TSY001 Tau Syndrome 10 0.061
398
DWN001 Down Syndrome 66 0.061
399
INT007 Intermediate Coronary Syndrome 50 0.061
400
SWN001 Swine Influenza 44 0.060
401
ERY003 Erythema Multiforme 55 0.060
402
c DLT001 Delta Chain Disease 13 0.060
403
c PRM023 Pre-Malignant Neoplasm 41 0.060
404
OPD001 Opioid Abuse 40 0.060
405
PLM031 Poliomyelitis 60 0.060
406
CRD001 Cardiac Tamponade 44 0.060
407
TNS005 Tonsillitis 57 0.059
408
TRC003 Trichomoniasis 41 0.059
409
c HMP004 Hemophilia B 62 0.059
410
c HMP029 Hemophilia a 63 0.059
411
INT067 Interstitial Nephritis 46 0.059
412
WST005 West Nile Virus 53 0.058
413
CMM005 Common Cold 59 0.058
414
c VRL008 Viral Exanthem 26 0.058
415
PRC002 Paracoccidioidomycosis 55 0.057
416
c MTR002 Mitral Valve Insufficiency 44 0.057
417
HPT022 Hepatoblastoma 55 0.057
418
CGL001 Coagulation Protein Disease 14 0.057
419
P HMC003 Hemochromatosis 72 0.057
420
c ACT020 Acute T Cell Leukemia 35 0.057
421
IMM099 Immunodeficiency 33 29 0.057
422
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.057
423
SPC005 Speech Disorder 41 0.056
424
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.056
425
CHR005 Chorioamnionitis 48 0.056
426
ORC001 Orchitis 31 0.056
427
P CNT005 Central Nervous System Lymphoma 53 0.056
428
ECH003 Echinococcosis 54 0.056
429
RLT001 Raltegravir Toxicity 9 0.056
430
LKP003 Leukoplakia 38 0.056
431
HND003 Hand-Foot-Uterus Syndrome 50 0.055
432
SBS006 Sebastian Syndrome 35 0.055
433
P LCT001 Lactic Acidosis 51 0.055
434
P MMP001 Mumps 58 0.055
435
P TXP001 Toxoplasmosis 61 0.055
436
CMM004 Common Variable Immunodeficiency 68 0.055
437
MNN009 Meningoencephalitis 47 0.055
438
CHN016 Cohen Syndrome 54 0.055
439
TXC002 Toxic Encephalopathy 51 0.055
440
IRS003 Iris Disease 31 0.054
441
FLL008 Folliculitis 46 0.054
442
CHL004 Cholelithiasis 48 0.054
443
SNS001 Sensorineural Hearing Loss 57 0.054
444
P MMB011 Membranous Nephropathy 54 0.054
445
P NPH009 Nephrolithiasis 60 0.054
446
MTC005 Mitochondrial Metabolism Disease 36 0.054
447
MYC019 Mycobacterium Marinum 28 0.054
448
AND015 Androgen Insensitivity 64 0.054
449
BNM008 Bone Mineral Density, Low 16 0.054
450
AVN001 Avian Influenza 54 0.054
451
MYC033 Myoclonus 42 0.054
452
c PRM226 Primary Central Nervous System Lymphoma 49 0.054
453
CMR002 Coumarin Resistance 48 0.053
454
ORL014 Oral Pharyngeal Disorders 11 0.053
455
CRY005 Cryptococcosis 50 0.053
456
P CMP008 Compartment Syndrome 48 0.053
457
INC002 Inclusion Body Myositis 66 0.053
458
RSC001 Rosacea 52 0.052
459
SPS019 Spastic Paraparesis 41 0.052
460
LPR001 Lepromatous Leprosy 50 0.052
461
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.051
462
c LKM005 Leukemia, T-Cell, Chronic 20 0.051
463
KRT001 Keratoconjunctivitis Sicca 59 0.051
464
KPS004 Kaposi Sarcoma 67 0.051
465
YLL002 Yellow Fever 58 0.051
466
P FTT008 Fatty Liver Disease, Nonalcoholic 1 30 0.051
467
HYP017 Hypophosphatemia 43 0.050
468
CCC001 Coccidioidomycosis 55 0.050
469
SPL004 Splenic Marginal Zone Lymphoma 44 0.050
470
c INH004 Inherited Blood Coagulation Disease 36 0.050
471
VNZ002 Venezuelan Equine Encephalitis 45 0.050
472
CCN002 Cocaine Abuse 48 0.049
473
c DRR009 Diarrhea 6 29 0.049
474
PRG004 Progeria 44 0.049
475
EXT033 Extrapulmonary Tuberculosis 44 0.049
476
ALC006 Alcoholic Hepatitis 59 0.049
477
ANS012 Anus Disease 32 0.049
478
MTR014 Motor Neuron Disease 58 0.049
479
P CMR001 Camurati-Engelmann Disease 58 0.048
480
IMM135 Immunodeficiency 46 14 0.048
481
PMP004 Pemphigus Foliaceus 42 0.048
482
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.048
483
VGN019 Vaginal Discharge 33 0.048
484
c CRD093 Cardiomyopathy, Dilated, 1a 55 0.048
485
c LYM107 Lymphoproliferative Syndrome 2 50 0.047
486
CHC001 Chickenpox 51 0.047
487
LMB010 Lambert Syndrome 36 0.047
488
NRS003 Neurosyphilis 41 0.047
489
c LYM106 Lymphoproliferative Syndrome 1 32 0.047
490
P HRP009 Herpes Simplex Encephalitis 47 0.047
491
P LBY004 Labyrinthitis 40 0.046
492
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.046
493
WDS002 Woods Syndrome 27 0.046
494
HNS001 Hansen's Disease 30 0.046
495
CYS005 Cysticercosis 54 0.046
496
TRP002 Tropical Spastic Paraparesis 55 0.046
497
P ACQ009 Acquired Metabolic Disease 38 0.045
498
IMM080 Immunodeficiency 23 27 0.045
499
FNC006 Functional Gastric Disease 32 0.045
500
BHR001 Behr Syndrome 42 0.045
501
NCR004 Nocardiosis 43 0.045
502
BRD001 Brody Myopathy 47 0.044
503
c VRL005 Viral Pneumonia 42 0.044
504
HTC002 Hutchinson-Gilford Progeria 57 0.044
505
PRS034 Parasitic Helminthiasis Infectious Disease 38 0.044
506
P SHR001 Short Bowel Syndrome 49 0.044
507
P NJM001 Nijmegen Breakage Syndrome 67 0.044
508
P CRN015 Cornelia De Lange Syndrome 62 0.043
509
c VRL007 Viral Encephalitis 54 0.043
510
c BRN108 Branchiootic Syndrome 1 34 0.043
511
WHT007 White Platelet Syndrome 15 0.043
512
HPT074 Hepatic Adenoma, Somatic 50 0.043
513
P ADD001 Addison's Disease 62 0.043
514
HRN022 Hearing Loss/deafness 26 0.042
515
P FNC043 Fanconi Anemia, Complementation Group E 55 0.042
516
NLL002 Null Syndrome 20 0.042
517
FBR012 Fabry Disease 69 0.042
518
P RTT002 Rett Syndrome 77 0.042
519
GLC006 Galactosemia 64 0.042
520
WRT002 Writing Disorder 27 0.042
521
NTR006 Neutrophil Immunodeficiency Syndrome 35 0.041
522
CWP001 Cowpox 45 0.041
523
C2D001 C2 Deficiency 45 0.041
524
MTR007 Motor Peripheral Neuropathy 37 0.041
525
HYP458 Hyper Ige Syndrome 42 0.041
526
TRP009 Triple X Syndrome 40 0.041
527
CHY002 Chylomicron Retention Disease 57 0.041
528
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.041
529
HMN032 Human Herpesvirus 8 46 0.040
530
RYS001 Reye Syndrome 52 0.040
531
HNM002 Hinman Syndrome 25 0.040
532
PLS025 Plasmablastic Lymphoma 46 0.040
533
AND005 Androgen Insensitivity Syndrome, Mild 16 0.040
534
CNT067 Central Cord Syndrome 23 0.040
535
LYM041 Lymphocytes Absent 13 0.040
536
OPS006 Opsoclonus-Myoclonus Syndrome 46 0.040
537
HRP005 Herpetic Whitlow 29 0.039
538
NTR040 Neutropenia, Cyclic 51 0.039
539
BDS001 Bd Syndrome 12 0.039
540
MYC021 Mycobacterium Xenopi 26 0.038
541
CYT004 Cytomegalic Inclusion Disease 31 0.038
542
PRM042 Primary Effusion Lymphoma 53 0.038
543
c INF002 Inflammatory Diarrhea 27 0.038
544
ORL019 Oral Hairy Leukoplakia 34 0.037
545
P ATX010 Ataxia Neuropathy Spectrum 30 0.037
546
GNT002 Giant Cell Glioblastoma 51 0.037
547
BLL012 Bullous Impetigo 35 0.036
548
PTY004 Pityriasis Lichenoides 23 0.036
549
ADP002 Adiponectin Deficiency 30 0.036
550
CHR103 Charge Syndrome 62 0.035
551
P PFF001 Pfeiffer Syndrome 73 0.035
552
GRN016 Grant Syndrome 29 0.035
553
CRB159 Cerebral Visual Impairment 33 0.035
554
TMR010 Tumor Predisposition Syndrome 47 0.035
555
PSD029 Pseudocholinesterase Deficiency 40 0.034
556
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 37 0.034
557
ENG004 Engraftment Syndrome 32 0.034
558
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 49 0.033
559
CRT055 Creatine Deficiency Syndromes 27 0.033
560
PTY006 Pityriasis Lichenoides Et Varioliformis Acuta 21 0.033
561
GST020 Gastric Antral Vascular Ectasia 33 0.033
562
c HYP507 Hypotrichosis 1 38 0.033
563
INT046 Intestinal Tuberculosis 37 0.032
564
c CRN159 Craniosynostosis, Type 1 33 0.032
565
ATM021 Autoimmune Inner Ear Disease 31 0.032
566
c EHL032 Ehlers-Danlos Syndrome, Type Viib 49 0.032
567
BRL010 Buruli Ulcer 48 0.031
568
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 13 0.031
569
P SPR013 Spiradenoma 36 0.031
570
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.030
571
ADP007 Adie Pupil 34 0.030
572
P PCH015 Pachyonychia Congenita 1 49 0.030
573
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 44 0.030
574
NTR018 Neutrophilia, Hereditary 42 0.030
575
INT017 Intestinal Schistosomiasis 45 0.030
576
IMM003 Immunoglobulin Alpha Deficiency 36 0.029
577
SRN001 Serine Deficiency 32 0.029
578
TRC012 Trichuriasis 45 0.029
579
c NNN010 Noonan Syndrome 3 35 0.029
580
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 21 0.029
581
MYL013 Myeloperoxidase Deficiency 46 0.028
582
EPS006 Epstein Syndrome 39 0.028
583
TMP012 Temple Syndrome 38 0.028
584
P RFS001 Refsum Disease 63 0.028
585
P MWT001 Mowat-Wilson Syndrome 46 0.028
586
P MYS033 Miyoshi Muscular Dystrophy 1 42 0.028
587
EPT021 Epithelial Recurrent Erosion Dystrophy 33 0.028
588
HMF008 Hemifacial Atrophy, Progressive 36 0.027
589
MRS002 Marshall Syndrome 49 0.027
590
AMS002 Amish Infantile Epilepsy Syndrome 35 0.027
591
IMM140 Immunodeficiency 47 16 0.026
592
c BNG076 Benign Exophthalmos Syndrome 15 0.026
593
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.026
594
c PRD030 Periodontitis 1, Juvenile 33 0.026
595
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 51 0.026
596
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 17 0.026
597
c HYP293 Hypophosphatasia, Adult 47 0.025
598
SML020 Small Patella Syndrome 36 0.024
599
CYT003 Cytokine Receptor Deficiency 10 0.024
600
P FNG005 Feingold Syndrome 42 0.024
601
SVN001 Sveinsson Choreoretinal Atrophy 26 0.024