Search results for chloroquine

665 hits were found for chloroquine

# Family MCID Name MIFTS Score
1
MLR004 Malaria 81 0.711
2
PLS007 Plasmodium Falciparum Malaria 52 0.541
3
CVD001 Covid-19 44 0.355
4
PLS006 Plasmodium Vivax Malaria 51 0.341
5
c SVR001 Severe Acute Respiratory Syndrome 62 0.273
6
P LPS004 Lupus Erythematosus 61 0.245
7
P PRP029 Porphyria 62 0.233
8
P RHM011 Rheumatoid Arthritis 80 0.220
9
P PRP003 Porphyria Cutanea Tarda 67 0.205
10
P ART022 Arthritis 69 0.202
11
c SYS001 Systemic Lupus Erythematosus 86 0.193
12
P MYP004 Myopathy 70 0.191
13
DFC004 Deficiency Anemia 70 0.166
14
ATM095 Autoimmune Disease 62 0.158
15
GLB015 Glioblastoma Multiforme 75 0.155
16
48X005 48,xyyy 39 0.151
17
CMR002 Coumarin Resistance 56 0.149
18
c RHB024 Rhabdomyosarcoma 2 67 0.146
19
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.139
20
P SRC025 Sarcoidosis 1 70 0.131
21
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.131
22
DSC009 Discoid Lupus Erythematosus 42 0.131
23
c ATR087 Atrial Standstill 1 75 0.129
24
P PNM007 Pneumonia 68 0.129
25
KRT008 Keratopathy 47 0.123
26
CNN005 Connective Tissue Disease 68 0.120
27
P GLM045 Glioma 63 0.120
28
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.120
29
GLL048 Glial Tumor 45 0.120
30
IMM167 Immune Deficiency Disease 78 0.114
31
HMN044 Human Immunodeficiency Virus Type 1 71 0.114
32
P DRR001 Diarrhea 55 0.111
33
ENT004 Enthesopathy 49 0.111
34
SPL018 Splenomegaly 48 0.111
35
ATX019 Ataxia with Vitamin E Deficiency 42 0.111
36
ACQ007 Acquired Immunodeficiency Syndrome 60 0.108
37
AMB001 Amebiasis 55 0.108
38
CHL079 Children's Interstitial Lung Disease 26 0.108
39
P CRD119 Cardiac Arrest 67 0.105
40
ALL026 Allergic Hypersensitivity Disease 62 0.105
41
CYT002 Cytokine Deficiency 42 0.105
42
P GLM040 Glioma Susceptibility 1 81 0.102
43
P HPT021 Hepatitis 67 0.102
44
P SZR006 Seizure Disorder 56 0.102
45
P LNG032 Lung Cancer 98 0.098
46
P HDC001 Headache 57 0.098
47
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.098
48
c PRM038 Primary Agammaglobulinemia 44 0.098
49
c INC015 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 2 37 0.098
50
P INC033 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 2 30 0.098
51
P ATX030 Ataxia-Telangiectasia 82 0.095
52
DWN001 Down Syndrome 70 0.095
53
DRM006 Dermatitis 61 0.095
54
c DWL002 Dowling-Degos Disease 1 58 0.095
55
CHK001 Chikungunya 57 0.095
56
HYP005 Hypokalemia 55 0.095
57
TLN003 Telangiectasis 52 0.095
58
ADL002 Adult Syndrome 70 0.091
59
VRL011 Viral Infectious Disease 61 0.091
60
VSL002 Visual Epilepsy 59 0.091
61
49X006 49, Xxxxy Syndrome 41 0.091
62
PLS032 Plasmodium Falciparum Blood Infection Level 22 0.091
64
P PNC035 Pancreatic Cancer 84 0.087
65
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.087
66
HYP056 Hypoglycemia 66 0.087
67
c HPT016 Hepatitis B 59 0.087
68
HYP266 Hypoxia 57 0.087
69
CRN322 Coronavirus Infectious Disease 40 0.087
70
P CLR023 Colorectal Cancer 99 0.083
71
P BRS047 Breast Cancer 97 0.083
72
P RSP003 Respiratory Failure 74 0.083
73
c SML038 Small Cell Cancer of the Lung 65 0.083
74
P PSR002 Psoriasis 62 0.083
75
c ACT071 Acute Kidney Failure 60 0.083
76
P NRP001 Neuropathy 56 0.083
77
ATR057 Atrioventricular Block 55 0.083
78
PST011 Pustulosis of Palm and Sole 52 0.083
79
c SYS043 Systemic Lupus Erythematosus 1 38 0.083
80
P HPT023 Hepatocellular Carcinoma 100 0.079
81
AST005 Asthma 76 0.079
82
P CNR004 Cone-Rod Dystrophy 2 73 0.079
83
P KDN018 Kidney Disease 72 0.079
84
CNG034 Congestive Heart Failure 69 0.079
85
P LVR013 Liver Disease 68 0.079
86
CHL065 Cholangiocarcinoma 68 0.079
87
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.079
88
P TRN020 Turner Syndrome 67 0.079
89
SKN016 Skin Disease 63 0.079
90
c ATM011 Autoimmune Hepatitis 63 0.079
91
NTR005 Nutritional Deficiency Disease 62 0.079
92
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.079
93
IRN002 Iron Metabolism Disease 57 0.079
94
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.079
95
c VRL005 Viral Pneumonia 52 0.079
96
OCL069 Ocular Motor Apraxia 51 0.079
97
INT079 Intrahepatic Cholangiocarcinoma 51 0.079
98
c MLG068 Malignant Glioma 46 0.079
99
HRW001 Hair Whorl 36 0.079
100
P TXC009 Toxic Maculopathy 22 0.079
101
STR067 Stroke, Ischemic 81 0.074
102
BRN028 Brain Cancer 74 0.074
103
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.074
104
P HML002 Hemolytic Anemia 63 0.074
105
c FNC043 Fanconi Anemia, Complementation Group E 62 0.074
106
c HPT003 Hepatitis a 62 0.074
107
c ACT027 Acute Pancreatitis 60 0.074
108
RBS001 Rabies 58 0.074
109
BCT022 Bacterial Infectious Disease 56 0.074
110
P RST002 Restrictive Cardiomyopathy 56 0.074
111
P SCK005 Sickle Cell Disease 50 0.074
112
47X002 47,xyy 49 0.074
113
c FML324 Familial Porphyria Cutanea Tarda 31 0.074
114
c LKM061 Leukemia, Acute Myeloid 84 0.069
115
PFF001 Pfeiffer Syndrome 79 0.069
116
P MLN008 Melanoma 69 0.069
117
P THR014 Thrombocytopenia 67 0.069
118
CRB039 Cerebrovascular Disease 67 0.069
119
TTN003 Tetanus 65 0.069
120
NRM005 Neuromuscular Disease 64 0.069
121
P VSC007 Vascular Disease 63 0.069
122
LPD008 Lipid Metabolism Disorder 62 0.069
123
c HPT001 Hepatitis C 62 0.069
124
MSL001 Measles 62 0.069
125
P ENC018 Encephalopathy 61 0.069
126
P PNC044 Pancreatitis 61 0.069
127
P MYL006 Myeloid Leukemia 60 0.069
128
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.069
129
ANT024 Anthrax Disease 58 0.069
130
P RTN018 Retinal Disease 53 0.069
131
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.069
132
MXD026 Mixed Glioma 45 0.069
133
GRD001 Giardiasis 45 0.069
134
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.069
135
OST012 Osteoarthritis 78 0.064
136
c HPT073 Hepatitis C Virus 72 0.064
137
P GRF003 Graft-Versus-Host Disease 72 0.064
138
P LKM062 Leukemia, Acute Lymphoblastic 69 0.064
139
P SYS005 Systemic Scleroderma 68 0.064
140
P ATR011 Atrial Fibrillation 66 0.064
141
ATH013 Atherosclerosis Susceptibility 65 0.064
142
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.064
143
LSH001 Leishmaniasis 63 0.064
144
LVR012 Liver Cirrhosis 62 0.064
145
HPT019 Hepatic Encephalopathy 60 0.064
146
LNG099 Lung Disease 60 0.064
147
SQM006 Squamous Cell Carcinoma 60 0.064
148
P OPT006 Optic Nerve Disease 60 0.064
149
c DNG003 Dengue Disease 59 0.064
150
P DNG005 Dengue Virus 59 0.064
151
CNS004 Constipation 58 0.064
152
P EXN002 Exanthem 57 0.064
153
GLC003 Glucose Intolerance 54 0.064
154
P LCH002 Lichen Planus 53 0.064
155
P RTN016 Retinal Degeneration 53 0.064
156
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.064
157
LNG031 Lung Benign Neoplasm 51 0.064
158
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.064
159
VLV047 Volvulus of Midgut 49 0.064
160
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.064
161
PRD004 Prediabetes Syndrome 47 0.064
162
c DRR009 Diarrhea 6 46 0.064
163
HPT004 Hepatic Coma 45 0.064
164
P KLZ004 Kala-Azar 1 41 0.064
165
PRG008 Paragonimiasis 38 0.064
166
PLS005 Plasmodium Ovale Malaria 26 0.064
167
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.064
168
P ALZ034 Alzheimer Disease 88 0.059
169
MYL069 Myeloma, Multiple 85 0.059
170
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.059
171
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.059
172
SCK003 Sickle Cell Anemia 74 0.059
173
P NRB001 Neuroblastoma 72 0.059
174
FBR012 Fabry Disease 72 0.059
175
P LYM118 Lymphoma 68 0.059
176
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.059
177
OST159 Osteogenic Sarcoma 66 0.059
178
P HRP006 Herpes Simplex 65 0.059
179
DPR016 Depression 63 0.059
180
BRS099 Breast Ductal Carcinoma 62 0.059
181
MDD011 Mood Disorder 62 0.059
182
P DRM010 Dermatomyositis 61 0.059
183
DPH001 Diphtheria 60 0.059
184
DCT002 Ductal Carcinoma in Situ 59 0.059
185
CRY005 Cryptococcosis 58 0.059
186
ERY003 Erythema Multiforme 58 0.059
187
P PRP019 Peripheral Nervous System Disease 58 0.059
188
P CHN012 Chondrosarcoma 56 0.059
189
P PMP001 Pemphigus 54 0.059
190
GLS001 Gliosarcoma 54 0.059
191
HMS001 Hemosiderosis 54 0.059
192
P INS002 in Situ Carcinoma 53 0.059
193
LYS002 Lysosomal Storage Disease 52 0.059
194
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.059
195
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.059
196
ONC002 Onchocerciasis 52 0.059
197
P AST007 Astrocytoma 51 0.059
198
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.059
199
P CLL015 Collagen Disease 47 0.059
200
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.059
201
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.059
202
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.059
203
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.059
204
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.059
205
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.059
206
SBC016 Subacute Delirium 44 0.059
207
SCT002 Scotoma 44 0.059
208
CLN003 Clonorchiasis 44 0.059
209
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.059
210
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.059
211
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.059
212
c HYP595 Hypertension, Essential 84 0.053
213
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.053
214
ANX010 Anxiety 73 0.053
215
OTT002 Otitis Media 72 0.053
216
SVR097 Severe Cutaneous Adverse Reaction 69 0.053
217
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.053
218
P LKM002 Leukemia 68 0.053
219
SKN019 Skin Melanoma 68 0.053
220
P INF038 Influenza 68 0.053
221
PNC129 Pancreatic Adenocarcinoma 68 0.053
222
P PLM037 Pulmonary Hypertension 67 0.053
223
c FML001 Familial Atrial Fibrillation 65 0.053
224
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.053
225
c JVN010 Juvenile Rheumatoid Arthritis 64 0.053
226
P NTR004 Neutropenia 63 0.053
227
CTN007 Cutaneous Leishmaniasis 62 0.053
228
PSR001 Psoriatic Arthritis 61 0.053
229
YLL002 Yellow Fever 61 0.053
230
P ENC004 Encephalitis 61 0.053
231
P KDN017 Kidney Cancer 60 0.053
232
HRP004 Herpes Zoster 60 0.053
233
P ALP009 Alopecia Areata 60 0.053
234
QFV001 Q Fever 60 0.053
235
STT001 Status Epilepticus 60 0.053
236
P MCR010 Microcephaly 59 0.053
237
CHL014 Cholera 59 0.053
238
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.053
239
ISC004 Ischemia 58 0.053
240
P URT039 Urticaria 58 0.053
241
LYM027 Lymphopenia 58 0.053
242
GLS018 Glass Syndrome 57 0.053
243
TNS005 Tonsillitis 57 0.053
244
P PLY019 Polyneuropathy 56 0.053
245
P ALP008 Alopecia 54 0.053
246
PLM012 Pulmonary Sarcoidosis 53 0.053
247
P CTN003 Cutaneous Lupus Erythematosus 53 0.053
248
ACR041 Acromelic Frontonasal Dysostosis 52 0.053
249
P SML001 Small Cell Carcinoma 52 0.053
250
DYS015 Dysentery 52 0.053
251
PLS009 Plasma Cell Neoplasm 51 0.053
252
STM007 Stomatitis 50 0.053
253
P INC029 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 1 47 0.053
254
LNG020 Lung Oat Cell Carcinoma 47 0.053
255
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.053
256
c SHR030 Short Qt Syndrome 46 0.053
257
LYM019 Lymphosarcoma 46 0.053
258
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.053
259
INT304 Interstitial Pneumonitis, Desquamative, Familial 45 0.053
260
PLN005 Palindromic Rheumatism 45 0.053
261
P SDR002 Siderosis 44 0.053
262
KWS001 Kwashiorkor 44 0.053
263
MDD018 Middle East Respiratory Syndrome 43 0.053
264
TRP009 Triple X Syndrome 42 0.053
265
DRG024 Drug Allergy 42 0.053
266
GST020 Gastric Antral Vascular Ectasia 41 0.053
267
SKN006 Skin Sarcoidosis 41 0.053
268
RDN001 Reading Disorder 40 0.053
269
SPR126 Superior Semicircular Canal Dehiscence 40 0.053
270
c HMG029 Hemoglobin Se Disease 39 0.053
271
MNT252 Mental Retardation, Skeletal Dysplasia, and Abducens Palsy 38 0.053
272
ATM052 Autoimmune Disease 1 37 0.053
273
UPP004 Upper Respiratory Tract Disease 37 0.053
274
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.053
275
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.053
276
ERY066 Erythema Multiforme Major 30 0.053
277
c SHR033 Short Qt Syndrome 3 29 0.053
278
c INC034 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 1 22 0.053
279
P GST053 Gastric Cancer 83 0.045
280
CYS001 Cystic Fibrosis 81 0.045
281
P BLD134 Bladder Cancer 79 0.045
282
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.045
283
P HRT032 Heart Disease 75 0.045
284
ADR007 Adrenoleukodystrophy 75 0.045
285
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.045
286
c EXD008 Exudative Vitreoretinopathy 1 71 0.045
287
c CHR684 Chronic Kidney Disease 70 0.045
288
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.045
289
RCK004 Rickets 68 0.045
290
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.045
291
P HYP098 Hypereosinophilic Syndrome 67 0.045
292
P LNG028 Long Qt Syndrome 66 0.045
293
P NSP012 Nasopharyngeal Carcinoma 66 0.045
294
P DRM053 Dermatitis, Atopic 66 0.045
295
P ADN016 Adenocarcinoma 64 0.045
296
TYP007 Typhoid Fever 63 0.045
297
P CRN300 Coronary Heart Disease 1 63 0.045
298
c ACT068 Acute Cystitis 63 0.045
299
c SCL052 Scleroderma, Familial Progressive 61 0.045
300
P PTN014 Patent Ductus Arteriosus 1 60 0.045
301
CHL123 Chlamydia 59 0.045
302
P BRS044 Breast Adenocarcinoma 59 0.045
303
GRD007 Grade Iii Astrocytoma 59 0.045
304
CRD132 Cardiac Conduction Defect 58 0.045
305
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.045
306
EYD002 Eye Disease 58 0.045
307
MNT002 Mental Depression 58 0.045
308
P UVT001 Uveitis 57 0.045
309
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.045
310
P MYS005 Myositis 56 0.045
311
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 56 0.045
312
P EXD001 Exudative Vitreoretinopathy 55 0.045
313
SYN007 Synovitis 54 0.045
314
P INF037 Inflammatory Bowel Disease 54 0.045
315
P TCD001 Tic Disorder 53 0.045
316
GLM004 Gliomatosis Cerebri 52 0.045
317
BWN001 Bowen-Conradi Syndrome 52 0.045
318
HYP781 Hypoascorbemia 51 0.045
319
P HYP077 Hypertrichosis 50 0.045
320
PLR008 Pleurisy 50 0.045
321
BNR002 Bone Resorption Disease 48 0.045
322
KRT002 Keratomalacia 47 0.045
323
ZKF001 Zika Fever 47 0.045
324
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.045
325
CRD137 Cardiogenic Shock 47 0.045
326
KRT013 Keratolytic Winter Erythema 46 0.045
327
c FML294 Familial Short Qt Syndrome 41 0.045
328
DFF003 Diffuse Scleroderma 41 0.045
329
ALL014 Allergic Encephalomyelitis 38 0.045
330
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 36 0.045
331
PLC002 Plica Syndrome 36 0.045
332
CLC008 Colchicine Resistance 34 0.045
333
ANN011 Annular Erythema 32 0.045
334
PLY150 Polykaryocytosis Inducer 31 0.045
335
c RNG015 Ring Chromosome 2 26 0.045
336
PLS008 Plasmodium Malariae Malaria 25 0.045
337
P CRT085 Carotid Intimal Medial Thickness 2 24 0.045
338
KR001 Koro 24 0.045
339
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.037
340
P OVR042 Ovarian Cancer 88 0.037
341
CNN003 Conn's Syndrome 79 0.037
342
P LNG064 Lung Cancer Susceptibility 3 78 0.037
343
c SPN225 Spondyloarthropathy 1 73 0.037
344
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.037
345
P MLT020 Multiple Sclerosis 72 0.037
346
PRP027 Peripheral Vascular Disease 71 0.037
347
P HYP061 Hypertrophic Cardiomyopathy 70 0.037
348
P LPR021 Leprosy 3 69 0.037
349
P MYC084 Mycobacterium Tuberculosis 1 68 0.037
350
P MYS003 Myasthenia Gravis 68 0.037
351
MLD001 Melioidosis 68 0.037
352
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.037
353
BRK010 Burkitt Lymphoma 67 0.037
354
PSY004 Psychotic Disorder 67 0.037
355
KRT019 Keratitis, Hereditary 65 0.037
356
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.037
357
P ADL010 Adult Respiratory Distress Syndrome 65 0.037
358
P THY023 Thymoma 65 0.037
359
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.037
360
PRP083 Porphyria, Acute Intermittent 64 0.037
361
PLM031 Poliomyelitis 64 0.037
362
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.037
363
ACT119 Acute Promyelocytic Leukemia 63 0.037
364
LPP008 Lipoprotein Quantitative Trait Locus 62 0.037
365
BLL006 Bullous Pemphigoid 62 0.037
366
P ART023 Arthropathy 62 0.037
367
P VSC011 Vasculitis 62 0.037
368
INT066 Interstitial Lung Disease 60 0.037
369
CRD223 Cardiac Arrhythmia 60 0.037
370
P SNS001 Sensorineural Hearing Loss 60 0.037
371
CHC001 Chickenpox 60 0.037
372
SPP011 Suppression of Tumorigenicity 12 59 0.037
373
AVN001 Avian Influenza 59 0.037
374
P SYP003 Syphilis 58 0.037
375
NWB001 Newborn Respiratory Distress Syndrome 58 0.037
376
MXD005 Mixed Connective Tissue Disease 58 0.037
377
BRN056 Bronchopulmonary Dysplasia 57 0.037
378
P PLY041 Polymyositis 57 0.037
379
DSS009 Disseminated Intravascular Coagulation 57 0.037
380
P CRD246 Cardiovascular System Disease 57 0.037
381
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.037
382
MTH009 Mouth Disease 56 0.037
383
GST050 Gastrointestinal System Disease 56 0.037
384
LMB062 Limb Ischemia 55 0.037
385
VSC003 Visceral Leishmaniasis 55 0.037
386
P ANT006 Antiphospholipid Syndrome 55 0.037
387
P MYP006 Myopia 55 0.037
388
PRP030 Purpura 54 0.037
389
AMN003 Amnestic Disorder 54 0.037
390
PRT038 Protein-Energy Malnutrition 54 0.037
391
PLM010 Pulmonary Edema 54 0.037
392
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.037
393
P TRM003 Tremor 54 0.037
394
PRC002 Paracoccidioidomycosis 54 0.037
395
GTR002 Goiter 53 0.037
396
IRD001 Iridocyclitis 53 0.037
397
c THY107 Thymoma, Familial 52 0.037
398
P THY032 Thyroiditis 52 0.037
399
PNN001 Panniculitis 51 0.037
400
END086 End Stage Renal Disease 51 0.037
401
RSP006 Respiratory System Disease 50 0.037
402
P MYS079 Miyoshi Muscular Dystrophy 50 0.037
403
MNN009 Meningoencephalitis 49 0.037
404
VTM033 Vitamin K Deficiency Bleeding 48 0.037
405
HYP025 Hyperphosphatemia 48 0.037
406
HLX001 Helix Syndrome 47 0.037
407
ASP004 Asphyxia Neonatorum 46 0.037
408
SYN036 Syncope 45 0.037
409
CYN002 Cyanosis, Transient Neonatal 45 0.037
410
CRB004 Cerebral Artery Occlusion 45 0.037
411
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.037
412
THR099 Third-Degree Atrioventricular Block 45 0.037
413
GRN017 Granulocytopenia 44 0.037
414
P PLM085 Pulmonary Hemosiderosis 44 0.037
415
ORL015 Oral Squamous Cell Carcinoma 43 0.037
416
P RRH023 Rare Hereditary Hemochromatosis 41 0.037
417
c CHR682 Chronic Bilirubin Encephalopathy 39 0.037
418
CTN011 Cutaneous Porphyria 38 0.037
419
HRN029 Hearing Loss, Noise-Induced 37 0.037
420
NRS005 Neurosarcoidosis 36 0.037
421
HNS001 Hansen's Disease 34 0.037
422
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.037
423
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.037
424
c PRP091 Porphyria Cutanea Tarda, Type I 29 0.037
425
PST092 Posttransplant Acute Limbic Encephalitis 29 0.037
426
PHS025 Phosphatase, Acid, of Tissues 28 0.037
427
ARG004 Argyria 27 0.037
428
EXF003 Exfoliative Dermatitis 27 0.037
429
CPG001 Capgras Syndrome 24 0.037
430
P PRS040 Prostate Cancer 97 0.026
431
ESP021 Esophageal Cancer 90 0.026
432
c TBR025 Tuberous Sclerosis 1 77 0.026
433
KPS004 Kaposi Sarcoma 75 0.026
434
P APL001 Aplastic Anemia 74 0.026
435
END057 Endometrial Cancer 74 0.026
436
P SCH015 Schizophrenia 74 0.026
437
c HMC039 Hemochromatosis, Type 1 74 0.026
438
P OST002 Osteoporosis 74 0.026
439
CRH001 Crohn's Disease 74 0.026
440
SVR004 Severe Combined Immunodeficiency 73 0.026
441
c HYP836 Hypercholesterolemia, Familial, 1 73 0.026
442
ULC004 Ulcerative Colitis 73 0.026
443
P RTN024 Retinoblastoma 73 0.026
444
SCH036 Scheie Syndrome 72 0.026
445
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.026
446
P HNT016 Huntington Disease 72 0.026
447
ACR007 Acromegaly 71 0.026
448
P EPL164 Epilepsy 71 0.026
449
P AMY004 Amyloidosis 70 0.026
450
P TBR001 Tuberous Sclerosis 70 0.026
451
P ASP006 Aspergillosis 69 0.026
452
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 68 0.026
453
P FRN006 Frontotemporal Dementia 68 0.026
454
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.026
455
P CHR012 Chronic Granulomatous Disease 67 0.026
456
ANG054 Angina Pectoris 66 0.026
457
P MSC005 Muscular Dystrophy 66 0.026
458
P SKN015 Skin Carcinoma 66 0.026
459
P MCR115 Microvascular Complications of Diabetes 5 66 0.026
460
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.026
461
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.026
462
P NRV007 Nervous System Disease 66 0.026
463
P PLM036 Pulmonary Fibrosis 65 0.026
464
P DYS154 Dystonia 65 0.026
465
SRC014 Sarcoma 65 0.026
466
P LPS002 Liposarcoma 65 0.026
467
PRT037 Pertussis 65 0.026
468
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.026
469
PRT036 Peritonitis 64 0.026
470
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.026
471
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.026
472
CLF027 Cleft Palate, Isolated 64 0.026
473
BRC012 Brucellosis 64 0.026
474
P PLZ001 Pelizaeus-Merzbacher Disease 64 0.026
475
P PRD008 Periodontitis 64 0.026
476
P RHB003 Rhabdomyosarcoma 63 0.026
477
P MVM001 Movement Disease 63 0.026
478
P END044 Endometriosis 63 0.026
479
CLT003 Colitis 62 0.026
480
c BRN108 Branchiootic Syndrome 1 62 0.026
481
c ANM038 Anemia, Autoimmune Hemolytic 62 0.026
482
HSH003 Hashimoto Thyroiditis 62 0.026
483
P INT143 Interstitial Cystitis 61 0.026
484
HYP066 Hyperglycemia 61 0.026
485
FTT001 Fatty Liver Disease 61 0.026
486
RCT015 Reactive Arthritis 61 0.026
487
SPN186 Spinal Cord Injury 60 0.026
488
P NPH012 Nephrotic Syndrome 60 0.026
489
c JVN061 Juvenile Arthritis 60 0.026
490
P TXP001 Toxoplasmosis 60 0.026
491
DNG002 Dengue Hemorrhagic Fever 60 0.026
492
RHM001 Rheumatic Fever 60 0.026
493
P CTR002 Cataract 60 0.026
494
PRT013 Portal Hypertension 59 0.026
495
P BND020 Bone Disease 59 0.026
496
P CYS018 Cystitis 59 0.026
497
BRN002 Bronchiolitis 59 0.026
498
P NMN002 Niemann-Pick Disease 59 0.026
499
ADN018 Adenoma 59 0.026
500
CYS010 Cystinosis 59 0.026
501
ANR040 Aneurysm 59 0.026
502
INC002 Inclusion Body Myositis 58 0.026
503
c ACT073 Acute Leukemia 58 0.026
504
P PGT001 Paget's Disease of Bone 58 0.026
505
FBR047 Fibromyalgia 58 0.026
506
SCR008 Scrub Typhus 58 0.026
507
P STR022 Stargardt Disease 58 0.026
508
SPT004 Septic Arthritis 58 0.026
509
ADL030 Adult-Onset Still's Disease 58 0.026
510
DSS008 Disease of Mental Health 58 0.026
511
EXT034 Extrinsic Allergic Alveolitis 58 0.026
512
P GLL018 Gallbladder Cancer 57 0.026
513
P GLM007 Glomerulonephritis 57 0.026
514
c CHR417 Chronic Graft Versus Host Disease 57 0.026
515
P PRN023 Prion Disease 57 0.026
516
c MST023 Mesothelioma, Malignant 57 0.026
517
P END033 Endocarditis 57 0.026
518
BLR008 Bilirubin Metabolic Disorder 57 0.026
519
SCH014 Schistosomiasis 57 0.026
520
P BPL003 Bipolar Disorder 56 0.026
521
P FBR017 Fibrosarcoma 56 0.026
522
PLS011 Plasmacytoma 56 0.026
523
HMG005 Hemoglobinopathy 56 0.026
524
SLC006 Silicosis 56 0.026
525
BRN004 Brain Edema 56 0.026
526
HST011 Histoplasmosis 55 0.026
527
NRN004 Neuroendocrine Tumor 55 0.026
528
P SCK002 Sick Sinus Syndrome 55 0.026
529
P GRV001 Graves' Disease 55 0.026
530
FLR002 Filariasis 55 0.026
531
c ATM024 Autoimmune Pancreatitis 55 0.026
532
P DBT005 Diabetes Insipidus 55 0.026
533
END040 Endogenous Depression 55 0.026
534
RSC001 Rosacea 54 0.026
535
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.026
536
BRN014 Bronchopneumonia 54 0.026
537
PRC013 Pericarditis 54 0.026
538
SNS003 Sensory Peripheral Neuropathy 54 0.026
539
PNC001 Pancytopenia 54 0.026
540
CRM001 Crimean-Congo Hemorrhagic Fever 53 0.026
541
P MNC007 Monocytic Leukemia 53 0.026
542
P EMB005 Embryonal Rhabdomyosarcoma 53 0.026
543
OCL006 Ocular Hypertension 53 0.026
544
P PTS002 Ptosis 53 0.026
545
HYP063 Hypersplenism 53 0.026
546
SPN035 Spindle Cell Sarcoma 53 0.026
547
c FML008 Familial Retinoblastoma 53 0.026
548
TRC008 Trachoma 53 0.026
549
EXP004 Exophthalmos 52 0.026
550
CHR073 Choreatic Disease 52 0.026
551
c VRL010 Viral Hepatitis 52 0.026
552
NRT004 Neuritis 52 0.026
553
IMP005 Impotence 52 0.026
554
PTH003 Pathologic Nystagmus 52 0.026
555
c ACT135 Acute Graft Versus Host Disease 52 0.026
556
LYM004 Lymphoid Interstitial Pneumonia 51 0.026
558
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.026
559
c PRM108 Primary Progressive Multiple Sclerosis 51 0.026
560
CCC002 Coccidiosis 51 0.026
561
TRM010 Traumatic Brain Injury 51 0.026
562
HND002 Hand, Foot and Mouth Disease 51 0.026
563
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.026
564
c ACT078 Acute Porphyria 51 0.026
565
SCB001 Scabies 50 0.026
566
WLL006 Wells Syndrome 50 0.026
567
P ESN008 Eosinophilic Pneumonia 50 0.026
568
P MTR003 Mitral Valve Stenosis 50 0.026
569
FSC004 Fasciitis 50 0.026
570
ASC010 Ascaris Lumbricoides Infection 50 0.026
571
TRY001 Trypanosomiasis 50 0.026
572
DYS073 Dysphagia 50 0.026
573
c PSR021 Psoriasis 14, Pustular 50 0.026
574
P MYT002 Myotonic Dystrophy 49 0.026
575
AMB002 Amblyopia 49 0.026
576
LFT001 Left Bundle Branch Hemiblock 49 0.026
577
BRN071 Brain Injury 49 0.026
578
P SDR003 Sideroblastic Anemia 49 0.026
579
c INV001 Invasive Aspergillosis 49 0.026
580
ADR016 Adrenal Cortical Carcinoma 48 0.026
581
RFR010 Refractory Anemia 48 0.026
582
RGH001 Right Bundle Branch Block 48 0.026
583
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.026
584
BBS001 Babesiosis 48 0.026
585
BNN003 Bone Inflammation Disease 48 0.026
586
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.026
587
P PLY020 Polyradiculoneuropathy 48 0.026
588
ESN015 Eosinophilic Fasciitis 48 0.026
589
SXL003 Sexual Disorder 47 0.026
590
P PRR002 Pure Red-Cell Aplasia 47 0.026
591
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.026
592
c STR084 Stargardt Disease 1 47 0.026
593
ORC001 Orchitis 46 0.026
594
P BNG032 Benign Mesothelioma 46 0.026
595
P MTH007 Methemoglobinemia 46 0.026
596
EPD015 Epidemic Typhus 45 0.026
597
ORL013 Oral Lichen Planus 45 0.026
598
ACT003 Acute Kidney Tubular Necrosis 45 0.026
600
MCR225 Macrophage Activation Syndrome 44 0.026
601
PTT037 Pituitary Tumors 44 0.026
602
c PCH010 Pachyonychia Congenita 3 44 0.026
603
IRT001 Iritis 44 0.026
604
P GNG009 Gangliosidosis 44 0.026
605
GRN007 Granuloma Annulare 44 0.026
606
DPR002 Depersonalization Disorder 43 0.026
607
RDC006 Red Cell Aplasia 43 0.026
608
P CRN026 Corneal Edema 43 0.026
609
c RTN047 Retinitis Pigmentosa 18 42 0.026
610
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.026
611
BCK006 Back Pain 42 0.026
612
FSC002 Fascioliasis 42 0.026
613
LCH016 Lichen Sclerosus Et Atrophicus 41 0.026
614
c MJR024 Major Affective Disorder 9 41 0.026
615
PRS063 Paresthesia 41 0.026
616
PST053 Postherpetic Neuralgia 40 0.026
617
ANX004 Anoxia 40 0.026
618
TRN012 Transient Global Amnesia 39 0.026
619
NDL003 Nodular Nonsuppurative Panniculitis 39 0.026
620
RTC012 Reticuloendotheliosis, X-Linked 39 0.026
621
ADR004 Adrenal Cortical Adenocarcinoma 39 0.026
622
SPP007 Suppression Amblyopia 39 0.026
623
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.026
624
NTR042 Neutrophilic Dermatosis, Acute Febrile 38 0.026
625
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.026
626
ERY017 Erythema Elevatum Diutinum 38 0.026
627
ORF044 Orofacial Granulomatosis 38 0.026
628
NCR002 Necrobiosis Lipoidica 38 0.026
629
PRP005 Parapsoriasis 38 0.026
630
c MJR022 Major Affective Disorder 8 38 0.026
631
ACR005 Acrodermatitis 38 0.026
632
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.026
633
P PST059 Pustular Psoriasis 37 0.026
634
SYS071 Systemic Autoimmune Disease 37 0.026
635
ASC001 Ascaridiasis 35 0.026
636
c ATM112 Autoimmune Hepatitis Type 1 35 0.026
637
GLN002 Glanders 35 0.026
638
MYT011 Myotonia 34 0.026
640
c PRG106 Progressive Muscular Dystrophy 33 0.026
641
GRN009 Granulomatous Hepatitis 33 0.026
642
CND006 Candida Glabrata 32 0.026
643
c INC031 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 3 32 0.026
644
DGN002 Degenerative Myopia 32 0.026
645
GST039 Gastroduodenitis 31 0.026
646
ACN019 Acanthamoeba Keratitis 31 0.026
647
MLT177 Multisystem Proteinopathy 30 0.026
648
BLC004 Blackwater Fever 30 0.026
649
PYR016 Pyridoxine Deficiency 30 0.026
650
ACR097 Acrodermatitis Chronica Atrophicans 27 0.026
651
PRM004 Primary Amebic Meningoencephalitis 27 0.026
652
c INC035 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 3 27 0.026
653
c ACQ016 Acquired Pure Red Cell Aplasia 27 0.026
654
c SYS038 Systemic Lupus Erythematosus 2 26 0.026
655
PRQ002 Paraquat Poisoning 26 0.026
656
CRB018 Cerebral Lipidosis 25 0.026
657
VSC052 Vasculitis, Lymphocytic, Nodular 25 0.026
658
MXD019 Mixed Malaria 24 0.026
659
ANT078 Antipyrine Metabolism 24 0.026
660
c RNG021 Ring Chromosome 5 23 0.026
661
c TYP034 Type 1 Diabetes Mellitus 8 20 0.026
662
MLN071 Melanoma Tumor Antigen Gp90 17 0.026
663
LTH004 Lathyrism 16 0.026
664
CNG400 Congenital Hereditary Endothelial Dystrophy Type I 13 0.026
665
HND011 Hendra Virus Infection 12 0.026
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