Search results for Hydroxychloroquine

706 hits were found for Hydroxychloroquine

# Family MCID Name MIFTS Score
1
CVD001 Covid-19 44 0.624
2
c SVR001 Severe Acute Respiratory Syndrome 62 0.496
3
P LPS004 Lupus Erythematosus 61 0.447
4
c SYS001 Systemic Lupus Erythematosus 86 0.436
5
P RHM011 Rheumatoid Arthritis 80 0.330
6
P ART022 Arthritis 69 0.297
7
ATM095 Autoimmune Disease 62 0.261
8
P PNM007 Pneumonia 68 0.252
9
MLR004 Malaria 81 0.248
10
c SYS043 Systemic Lupus Erythematosus 1 38 0.206
11
c RHB024 Rhabdomyosarcoma 2 67 0.190
12
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.190
13
P ANT006 Antiphospholipid Syndrome 55 0.190
14
P RSP003 Respiratory Failure 74 0.186
15
VRL011 Viral Infectious Disease 61 0.173
16
ATM052 Autoimmune Disease 1 37 0.172
17
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.168
18
CRN322 Coronavirus Infectious Disease 40 0.164
19
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.162
20
CYT002 Cytokine Deficiency 42 0.149
21
P EXN002 Exanthem 57 0.145
22
48X005 48,xyyy 39 0.145
23
P CTN003 Cutaneous Lupus Erythematosus 53 0.142
24
P INF038 Influenza 68 0.138
25
P TRN020 Turner Syndrome 67 0.138
26
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.138
27
c ATR087 Atrial Standstill 1 75 0.133
28
P SRC025 Sarcoidosis 1 70 0.133
29
CNN005 Connective Tissue Disease 68 0.133
30
LNG099 Lung Disease 60 0.133
31
c VRL005 Viral Pneumonia 52 0.133
32
c PRM038 Primary Agammaglobulinemia 44 0.133
33
P ADL010 Adult Respiratory Distress Syndrome 65 0.130
34
c DWL002 Dowling-Degos Disease 1 58 0.130
35
P SJG008 Sjogren Syndrome 61 0.128
36
P CRD246 Cardiovascular System Disease 57 0.128
37
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.128
38
ADL002 Adult Syndrome 70 0.125
39
DSC009 Discoid Lupus Erythematosus 42 0.125
40
P PNC035 Pancreatic Cancer 84 0.123
41
P ADN016 Adenocarcinoma 64 0.123
42
NWB001 Newborn Respiratory Distress Syndrome 58 0.123
43
DWN001 Down Syndrome 70 0.120
44
P KDN018 Kidney Disease 72 0.117
45
P DRR001 Diarrhea 55 0.117
46
ATX019 Ataxia with Vitamin E Deficiency 42 0.117
47
P LNG032 Lung Cancer 98 0.114
48
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.114
49
LPP008 Lipoprotein Quantitative Trait Locus 62 0.111
50
IMM167 Immune Deficiency Disease 78 0.108
51
c SML038 Small Cell Cancer of the Lung 65 0.108
52
P PSR002 Psoriasis 62 0.108
53
P PRP029 Porphyria 62 0.108
54
PST011 Pustulosis of Palm and Sole 52 0.108
55
P MYP004 Myopathy 70 0.105
56
P MLN008 Melanoma 69 0.105
57
SKN019 Skin Melanoma 68 0.105
58
THR024 Thrombosis 57 0.105
59
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.105
60
MDD018 Middle East Respiratory Syndrome 43 0.105
61
P PRS040 Prostate Cancer 97 0.102
62
OST012 Osteoarthritis 78 0.102
63
HMN044 Human Immunodeficiency Virus Type 1 71 0.102
64
P ALP008 Alopecia 54 0.102
65
ENT004 Enthesopathy 49 0.102
66
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.099
67
P HPT021 Hepatitis 67 0.099
68
P PRP003 Porphyria Cutanea Tarda 67 0.099
69
HYP056 Hypoglycemia 66 0.099
70
P VSC011 Vasculitis 62 0.099
71
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.099
72
c PRS136 Prostate Cancer, Hereditary, 6 33 0.099
73
c PRS130 Prostate Cancer, Hereditary, 8 32 0.099
74
PNC129 Pancreatic Adenocarcinoma 68 0.096
75
ATH013 Atherosclerosis Susceptibility 65 0.096
76
P DBT009 Diabetes Mellitus 64 0.096
77
P DRM010 Dermatomyositis 61 0.096
78
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.096
79
P BRS047 Breast Cancer 97 0.092
80
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.092
81
c CHR684 Chronic Kidney Disease 70 0.092
82
P THR014 Thrombocytopenia 67 0.092
83
SKN016 Skin Disease 63 0.092
84
INT066 Interstitial Lung Disease 60 0.092
85
HYP005 Hypokalemia 55 0.092
86
P LCH002 Lichen Planus 53 0.092
87
ART140 Arteries, Anomalies of 52 0.092
88
CHL079 Children's Interstitial Lung Disease 26 0.092
89
P CLR023 Colorectal Cancer 99 0.089
90
MYL069 Myeloma, Multiple 85 0.089
91
c HYP595 Hypertension, Essential 84 0.089
92
P GRF003 Graft-Versus-Host Disease 72 0.089
93
P CRN300 Coronary Heart Disease 1 63 0.089
94
ISC004 Ischemia 58 0.089
95
LNG031 Lung Benign Neoplasm 51 0.089
96
END086 End Stage Renal Disease 51 0.089
97
IGG001 Iga Glomerulonephritis 48 0.089
98
P LVR013 Liver Disease 68 0.085
99
c PRC016 Pre-Eclampsia 63 0.085
100
c FNC043 Fanconi Anemia, Complementation Group E 62 0.085
101
P GLM007 Glomerulonephritis 57 0.085
102
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.085
103
c DRR009 Diarrhea 6 46 0.085
104
SCT002 Scotoma 44 0.085
105
P PRG092 Pregnancy Loss, Recurrent 1 40 0.085
106
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.081
107
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.081
108
GLB015 Glioblastoma Multiforme 75 0.081
109
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.081
110
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.081
111
c JVN010 Juvenile Rheumatoid Arthritis 64 0.081
112
TXC005 Toxic Shock Syndrome 62 0.081
113
P MYL006 Myeloid Leukemia 60 0.081
114
c DNG003 Dengue Disease 59 0.081
115
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.081
116
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.081
117
PRP030 Purpura 54 0.081
118
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.081
119
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.081
120
HYP781 Hypoascorbemia 51 0.081
121
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.081
122
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.081
123
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.081
124
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.081
125
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.081
126
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.081
127
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.081
128
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.081
129
P CNR004 Cone-Rod Dystrophy 2 73 0.077
130
CNG034 Congestive Heart Failure 69 0.077
131
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.077
132
P NTR004 Neutropenia 63 0.077
133
P KDN017 Kidney Cancer 60 0.077
134
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.077
135
ERY003 Erythema Multiforme 58 0.077
136
HYP266 Hypoxia 57 0.077
137
P RTN018 Retinal Disease 53 0.077
138
PLS009 Plasma Cell Neoplasm 51 0.077
139
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.077
140
RSP007 Respiratory Distress Syndrome, Infant 30 0.077
141
P TXC009 Toxic Maculopathy 22 0.077
142
P GLM040 Glioma Susceptibility 1 81 0.072
143
P LKM002 Leukemia 68 0.072
144
LPD008 Lipid Metabolism Disorder 62 0.072
145
c HPT001 Hepatitis C 62 0.072
146
P ART023 Arthropathy 62 0.072
147
QFV001 Q Fever 60 0.072
148
c CHR417 Chronic Graft Versus Host Disease 57 0.072
149
P HDC001 Headache 57 0.072
150
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.072
151
ORL013 Oral Lichen Planus 45 0.072
152
BRN028 Brain Cancer 74 0.068
153
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.068
154
c THR092 Thrombophilia Due to Thrombin Defect 73 0.068
155
P MLT020 Multiple Sclerosis 72 0.068
156
P MYC007 Myocardial Infarction 70 0.068
157
SVR097 Severe Cutaneous Adverse Reaction 69 0.068
158
RCK004 Rickets 68 0.068
159
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.068
160
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.068
161
P VSC007 Vascular Disease 63 0.068
162
ALL026 Allergic Hypersensitivity Disease 62 0.068
163
ACQ007 Acquired Immunodeficiency Syndrome 60 0.068
164
PLM033 Pulmonary Embolism 59 0.068
165
c CHL140 Chilblain Lupus 1 58 0.068
166
P URT039 Urticaria 58 0.068
167
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.068
168
EYD002 Eye Disease 58 0.068
169
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.068
170
P RTN016 Retinal Degeneration 53 0.068
171
FDL002 Food Allergy 51 0.068
172
KRT001 Keratoconjunctivitis Sicca 49 0.068
173
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.068
174
c SRC023 Sarcoidosis 2 43 0.068
175
P PST059 Pustular Psoriasis 37 0.068
176
P HPT023 Hepatocellular Carcinoma 100 0.063
178
P RTN008 Retinitis Pigmentosa 79 0.063
179
AST005 Asthma 76 0.063
180
P HRT032 Heart Disease 75 0.063
181
CRH001 Crohn's Disease 74 0.063
182
c SPN225 Spondyloarthropathy 1 73 0.063
183
c LKM063 Leukemia, Chronic Myeloid 72 0.063
184
P SYS005 Systemic Scleroderma 68 0.063
185
P MYS003 Myasthenia Gravis 68 0.063
186
P CRD119 Cardiac Arrest 67 0.063
187
CLT003 Colitis 62 0.063
188
DRM006 Dermatitis 61 0.063
189
YLL002 Yellow Fever 61 0.063
190
P ENC004 Encephalitis 61 0.063
191
P MYC008 Myocarditis 59 0.063
192
P DNG005 Dengue Virus 59 0.063
193
CHK001 Chikungunya 57 0.063
194
CMM005 Common Cold 57 0.063
195
MCL006 Macular Retinal Edema 55 0.063
196
SYN007 Synovitis 54 0.063
197
PLM012 Pulmonary Sarcoidosis 53 0.063
198
P IGN003 Iga Nephropathy 1 49 0.063
199
ZKF001 Zika Fever 47 0.063
200
RTN023 Retinitis 46 0.063
201
NRR001 Neuroretinitis 42 0.063
202
SYS071 Systemic Autoimmune Disease 37 0.063
203
PLC002 Plica Syndrome 36 0.063
204
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.063
205
c FML324 Familial Porphyria Cutanea Tarda 31 0.063
206
UND007 Undifferentiated Connective Tissue Disease 29 0.063
207
STR067 Stroke, Ischemic 81 0.057
208
P LKM071 Leukemia, Chronic Lymphocytic 79 0.057
209
P NRB001 Neuroblastoma 72 0.057
210
FBR012 Fabry Disease 72 0.057
211
CRB039 Cerebrovascular Disease 67 0.057
212
SRC014 Sarcoma 65 0.057
213
c DBT099 Diabetes Mellitus, Type I 65 0.057
214
P HML002 Hemolytic Anemia 63 0.057
215
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.057
216
HMT002 Hematologic Cancer 62 0.057
217
c BRN108 Branchiootic Syndrome 1 62 0.057
218
HSH003 Hashimoto Thyroiditis 62 0.057
219
HYP066 Hyperglycemia 61 0.057
220
P ALP009 Alopecia Areata 60 0.057
221
LYM027 Lymphopenia 58 0.057
222
P END033 Endocarditis 57 0.057
223
SFT003 Soft Tissue Sarcoma 56 0.057
224
P RST002 Restrictive Cardiomyopathy 56 0.057
225
WST005 West Nile Virus 54 0.057
226
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.057
227
SPN035 Spindle Cell Sarcoma 53 0.057
228
P RCT021 Rectum Cancer 52 0.057
229
P THY032 Thyroiditis 52 0.057
230
SPN051 Spondylitis 51 0.057
231
P THR015 Thrombophilia 51 0.057
232
RSP006 Respiratory System Disease 50 0.057
233
GST049 Gastrointestinal System Cancer 49 0.057
234
FRN020 Frontal Fibrosing Alopecia 49 0.057
235
DRY001 Dry Eye Syndrome 47 0.057
236
GST071 Gastrointestinal Carcinoma 47 0.057
237
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.057
238
IMM136 Immune System Disease 45 0.057
239
PLN005 Palindromic Rheumatism 45 0.057
240
GRN007 Granuloma Annulare 44 0.057
241
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.057
242
P PHT010 Photoparoxysmal Response 1 42 0.057
243
XRP001 Xerophthalmia 41 0.057
244
P MLG074 Malignant Mesenchymoma 40 0.057
245
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.057
246
ALP048 Alopecia Totalis 32 0.057
247
INF009 Inflammatory Spondylopathy 31 0.057
248
ERY066 Erythema Multiforme Major 30 0.057
249
c RNG015 Ring Chromosome 2 26 0.057
250
P ALZ034 Alzheimer Disease 88 0.051
251
c LKM061 Leukemia, Acute Myeloid 84 0.051
252
P LNG064 Lung Cancer Susceptibility 3 78 0.051
253
c HYP836 Hypercholesterolemia, Familial, 1 73 0.051
254
DFC004 Deficiency Anemia 70 0.051
255
MYL009 Myelodysplastic Syndrome 70 0.051
256
P HYP086 Hypothyroidism 69 0.051
257
LYM007 Lymphangioleiomyomatosis 69 0.051
258
P LYM118 Lymphoma 68 0.051
259
P MCR115 Microvascular Complications of Diabetes 5 66 0.051
260
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.051
261
P PLM036 Pulmonary Fibrosis 65 0.051
262
BRC012 Brucellosis 64 0.051
263
c HPT003 Hepatitis a 62 0.051
264
LVR012 Liver Cirrhosis 62 0.051
265
c SCL052 Scleroderma, Familial Progressive 61 0.051
266
CRD223 Cardiac Arrhythmia 60 0.051
267
P SNS001 Sensorineural Hearing Loss 60 0.051
268
c ACT071 Acute Kidney Failure 60 0.051
269
PNM001 Pneumocystosis 59 0.051
270
c HPT016 Hepatitis B 59 0.051
271
c LTN004 Late-Onset Retinal Degeneration 59 0.051
272
GLS018 Glass Syndrome 57 0.051
273
JPN002 Japanese Encephalitis 57 0.051
274
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.051
275
P LBR014 Leber Congenital Amaurosis 4 56 0.051
276
ATR057 Atrioventricular Block 55 0.051
277
GLC003 Glucose Intolerance 54 0.051
278
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.051
279
PRC013 Pericarditis 54 0.051
280
CLR030 Clear Cell Renal Cell Carcinoma 53 0.051
281
CRH005 Crohn's Colitis 53 0.051
282
LYS002 Lysosomal Storage Disease 52 0.051
283
c PRM108 Primary Progressive Multiple Sclerosis 51 0.051
284
PNN001 Panniculitis 51 0.051
285
P CTN015 Cutaneous T Cell Lymphoma 49 0.051
286
KRT008 Keratopathy 47 0.051
287
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.051
288
P HRT035 Heart Block, Congenital 46 0.051
289
GRN017 Granulocytopenia 44 0.051
290
P MYG005 Myoglobinuria 44 0.051
291
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.051
292
SKN006 Skin Sarcoidosis 41 0.051
293
HPR006 Heparin Cofactor Ii Deficiency 40 0.051
294
c CHR682 Chronic Bilirubin Encephalopathy 39 0.051
295
NCR002 Necrobiosis Lipoidica 38 0.051
296
MNT252 Mental Retardation, Skeletal Dysplasia, and Abducens Palsy 38 0.051
297
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.051
298
MCL018 Macular Dystrophy, Concentric Annular 30 0.051
299
LYM053 Lymphomatous Thyroiditis 22 0.051
300
P OVR042 Ovarian Cancer 88 0.044
301
CYS001 Cystic Fibrosis 81 0.044
302
c NRF024 Neurofibromatosis, Type I 77 0.044
303
P SCH015 Schizophrenia 74 0.044
304
P OST002 Osteoporosis 74 0.044
305
BHC003 Behcet Syndrome 71 0.044
306
c PNC108 Pancreatitis, Hereditary 70 0.044
307
P SLP006 Sleep Apnea 69 0.044
308
P TMP003 Temporal Arteritis 68 0.044
309
CHL065 Cholangiocarcinoma 68 0.044
310
c NMN015 Niemann-Pick Disease, Type C1 68 0.044
311
HYL004 Hyaline Fibromatosis Syndrome 67 0.044
312
c INF071 Inflammatory Bowel Disease 1 67 0.044
313
FCT007 Factor Vii Deficiency 67 0.044
314
P CHR012 Chronic Granulomatous Disease 67 0.044
315
P HYP098 Hypereosinophilic Syndrome 67 0.044
316
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.044
317
OST159 Osteogenic Sarcoma 66 0.044
318
P ATR011 Atrial Fibrillation 66 0.044
319
c FML001 Familial Atrial Fibrillation 65 0.044
320
GRN037 Granulomatosis with Polyangiitis 65 0.044
321
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.044
322
APN008 Apnea, Obstructive Sleep 64 0.044
323
NRF007 Neurofibroma 64 0.044
324
P GLM045 Glioma 63 0.044
325
c LCL006 Localized Scleroderma 62 0.044
326
NTR005 Nutritional Deficiency Disease 62 0.044
327
PSR001 Psoriatic Arthritis 61 0.044
328
CHR001 Churg-Strauss Syndrome 61 0.044
329
c PNS012 Paine Syndrome 61 0.044
330
P PNC044 Pancreatitis 61 0.044
331
c JVN061 Juvenile Arthritis 60 0.044
332
c ACT027 Acute Pancreatitis 60 0.044
333
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.044
334
P CTR002 Cataract 60 0.044
335
c ACT073 Acute Leukemia 58 0.044
336
P INT070 Intestinal Obstruction 58 0.044
337
CNT047 Contact Dermatitis 58 0.044
338
DSS008 Disease of Mental Health 58 0.044
339
P BNC003 Bone Cancer 58 0.044
340
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.044
341
P ZLL001 Zellweger Syndrome 57 0.044
342
IRN002 Iron Metabolism Disease 57 0.044
343
BRD001 Brody Myopathy 57 0.044
344
P URF003 Urofacial Syndrome 1 57 0.044
345
PLS011 Plasmacytoma 56 0.044
346
c PRX059 Peroxisome Biogenesis Disorder 1a 56 0.044
347
SPN041 Spinal Cord Disease 56 0.044
348
MTH009 Mouth Disease 56 0.044
349
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.044
350
P NRF002 Neurofibromatosis 56 0.044
351
GST050 Gastrointestinal System Disease 56 0.044
352
c MCR256 Microphthalmia, Syndromic 9 56 0.044
353
PRP082 Porphyria, Congenital Erythropoietic 56 0.044
354
AMB001 Amebiasis 55 0.044
355
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.044
356
CHR100 Chronic Ulcer of Skin 55 0.044
357
HDR002 Hidradenitis Suppurativa 55 0.044
358
URN010 Urinary Tract Obstruction 55 0.044
359
P SPN052 Spondyloarthropathy 54 0.044
360
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.044
361
GLS001 Gliosarcoma 54 0.044
362
P ART021 Arteriosclerosis 54 0.044
363
P LNG035 Lung Large Cell Carcinoma 54 0.044
364
KRT006 Keratoconjunctivitis 53 0.044
365
c PSR017 Psoriasis 2 53 0.044
366
c PSR023 Psoriasis 1 52 0.044
367
MCR088 Microscopic Polyangiitis 51 0.044
368
c NMN014 Niemann-Pick Disease, Type C2 51 0.044
369
INT079 Intrahepatic Cholangiocarcinoma 51 0.044
370
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.044
371
BHR001 Behr Syndrome 51 0.044
372
SKN013 Skin Benign Neoplasm 51 0.044
373
c ACT078 Acute Porphyria 51 0.044
374
GNT002 Giant Cell Glioblastoma 50 0.044
375
KLT001 Klatskin's Tumor 50 0.044
376
PLC008 Placenta Disease 50 0.044
377
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.044
378
P END046 Endometritis 49 0.044
379
HDR003 Hidradenitis 49 0.044
380
c BCT013 Bacterial Pneumonia 48 0.044
381
ATS010 Autosomal Recessive Disease 48 0.044
382
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.044
383
VTM033 Vitamin K Deficiency Bleeding 48 0.044
384
CLS016 Clostridium Difficile Colitis 48 0.044
385
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.044
386
URN009 Urinary System Disease 48 0.044
387
SXL003 Sexual Disorder 47 0.044
388
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.044
389
PRD004 Prediabetes Syndrome 47 0.044
390
c PSR032 Psoriasis 11 47 0.044
391
VNZ002 Venezuelan Equine Encephalitis 47 0.044
392
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.044
393
CNT033 Central Nervous System Cancer 47 0.044
394
RYN005 Raynaud Phenomenon 47 0.044
395
LYM019 Lymphosarcoma 46 0.044
396
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.044
397
c ACT076 Acute Myocarditis 46 0.044
398
TST014 Testicular Cancer 46 0.044
399
DDN010 Duodenum Cancer 46 0.044
400
c MLG068 Malignant Glioma 46 0.044
401
GLL048 Glial Tumor 45 0.044
402
MXD026 Mixed Glioma 45 0.044
403
c ZLL011 Zellweger Spectrum Disorder 45 0.044
404
CNT017 Central Nervous System Origin Vertigo 45 0.044
405
MRG013 Mirage Syndrome 43 0.044
406
c PSR028 Psoriasis 7 42 0.044
407
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.044
408
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.044
409
ANC002 Anca-Associated Vasculitis 41 0.044
410
c PSR018 Psoriasis 13 41 0.044
411
RDN001 Reading Disorder 40 0.044
412
LWR018 Lower Urinary Tract Obstruction, Congenital 40 0.044
413
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.044
414
c OVR114 Ovarian Cancer 1 38 0.044
415
OVR094 Ovarian Epithelial Cancer 38 0.044
416
CTN011 Cutaneous Porphyria 38 0.044
417
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.044
418
SRF006 Surfactant Dysfunction 35 0.044
420
PRX005 Peroxisomal Biogenesis Disorder 34 0.044
421
c CHR064 Chronic Monocytic Leukemia 33 0.044
422
PLY150 Polykaryocytosis Inducer 31 0.044
423
HYP855 Hyperpigmentation of the Skin 27 0.044
424
CYT018 Cytochrome P450 2d6 Variant 27 0.044
425
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.044
426
ALL012 Allergic Angiitis 24 0.044
427
HML018 Homologous Wasting Disease 22 0.044
428
LPS019 Lupus Erythematosus Tumidus 20 0.044
429
c NNT025 Neonatal Systemic Lupus Erythematosus 20 0.044
430
c DLT002 Dilated Cardiomyopathy 79 0.036
431
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.036
432
LPT014 Leptin Deficiency or Dysfunction 74 0.036
433
ULC004 Ulcerative Colitis 73 0.036
434
P FML018 Familial Mediterranean Fever 73 0.036
435
ANX010 Anxiety 73 0.036
436
P AMY004 Amyloidosis 70 0.036
437
P MYC084 Mycobacterium Tuberculosis 1 68 0.036
438
BRN024 Bronchitis 68 0.036
439
MYC006 Mycosis Fungoides 66 0.036
440
P LNG028 Long Qt Syndrome 66 0.036
441
ANG054 Angina Pectoris 66 0.036
442
P DRM053 Dermatitis, Atopic 66 0.036
443
PND002 Pendred Syndrome 65 0.036
444
PRT036 Peritonitis 64 0.036
445
LYM017 Lyme Disease 64 0.036
446
c EPS035 Episodic Ataxia, Type 2 63 0.036
447
DPR016 Depression 63 0.036
448
c ATM011 Autoimmune Hepatitis 63 0.036
449
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.036
450
MDD011 Mood Disorder 62 0.036
451
RTN017 Retinal Detachment 61 0.036
452
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.036
453
DCB001 Decubitus Ulcer 61 0.036
454
RHM001 Rheumatic Fever 60 0.036
455
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.036
456
CHL123 Chlamydia 59 0.036
457
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.036
458
CRY005 Cryptococcosis 58 0.036
459
P BCL017 B-Cell Lymphoma 58 0.036
460
CRD132 Cardiac Conduction Defect 58 0.036
461
P STR022 Stargardt Disease 58 0.036
462
MNT002 Mental Depression 58 0.036
463
CNS004 Constipation 58 0.036
464
P PRP019 Peripheral Nervous System Disease 58 0.036
465
P INF032 Infertility 57 0.036
466
P UVT001 Uveitis 57 0.036
467
P RHN004 Rhinitis 57 0.036
468
LYM021 Lymphadenitis 57 0.036
469
PLC005 Placental Insufficiency 57 0.036
470
PHR003 Pharyngitis 57 0.036
471
AYM001 Ayme-Gripp Syndrome 57 0.036
472
P MYS005 Myositis 56 0.036
473
c ACT134 Acute Liver Failure 56 0.036
474
P NRP001 Neuropathy 56 0.036
475
P MYP006 Myopia 55 0.036
476
RSC001 Rosacea 54 0.036
477
P PMP001 Pemphigus 54 0.036
478
P MCR240 Microcephalic Osteodysplastic Primordial Dwarfism, Type I 54 0.036
479
PLM010 Pulmonary Edema 54 0.036
480
AMN001 Amenorrhea 54 0.036
481
HMS001 Hemosiderosis 54 0.036
482
P TRM003 Tremor 54 0.036
483
GTR002 Goiter 53 0.036
484
TLN003 Telangiectasis 52 0.036
485
c ACT135 Acute Graft Versus Host Disease 52 0.036
486
KRT009 Keratosis 51 0.036
487
PST021 Postpartum Depression 50 0.036
488
STM007 Stomatitis 50 0.036
489
DYS073 Dysphagia 50 0.036
490
EBL001 Ebola Hemorrhagic Fever 49 0.036
491
BNR002 Bone Resorption Disease 48 0.036
492
P CLL015 Collagen Disease 47 0.036
493
c STR084 Stargardt Disease 1 47 0.036
494
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.036
495
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.036
496
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.036
497
PRT011 Protein C Deficiency 44 0.036
498
CRP002 Croup 44 0.036
499
SPN119 Spondylarthropathy 44 0.036
500
BCK006 Back Pain 42 0.036
501
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.036
502
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.036
503
LCH016 Lichen Sclerosus Et Atrophicus 41 0.036
504
c ACT004 Acute Diarrhea 39 0.036
505
P NNT042 Neonatal Lupus Erythematosus 39 0.036
507
ALL014 Allergic Encephalomyelitis 38 0.036
508
c SRF003 Surfactant Metabolism Dysfunction, Pulmonary, 2 37 0.036
509
NRS005 Neurosarcoidosis 36 0.036
510
HYP193 Hypocomplementemic Urticarial Vasculitis 32 0.036
511
ANN011 Annular Erythema 32 0.036
512
FLL019 Follicular Mucinosis 31 0.036
513
LCH008 Lichen Planus Pigmentosus 24 0.036
514
P GST053 Gastric Cancer 83 0.026
515
P ATX030 Ataxia-Telangiectasia 82 0.026
516
c NRF023 Neurofibromatosis, Type Ii 80 0.026
517
P BLD134 Bladder Cancer 79 0.026
518
CNN003 Conn's Syndrome 79 0.026
519
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.026
520
CRV035 Cervical Cancer 76 0.026
521
ADR007 Adrenoleukodystrophy 75 0.026
522
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.026
523
SVR004 Severe Combined Immunodeficiency 73 0.026
524
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.026
525
c HPT073 Hepatitis C Virus 72 0.026
526
OTT002 Otitis Media 72 0.026
527
PRP027 Peripheral Vascular Disease 71 0.026
528
c GLY008 Glycogen Storage Disease Ii 70 0.026
529
P HYP061 Hypertrophic Cardiomyopathy 70 0.026
530
LYM133 Lymphoma, Hodgkin, Classic 69 0.026
531
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.026
532
MNT001 Mantle Cell Lymphoma 69 0.026
533
GST092 Gastroesophageal Reflux 67 0.026
534
BRK010 Burkitt Lymphoma 67 0.026
535
P PLM037 Pulmonary Hypertension 67 0.026
536
P NRV007 Nervous System Disease 66 0.026
537
TTN003 Tetanus 65 0.026
538
P CNJ013 Conjunctivitis 65 0.026
539
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.026
540
P HRP006 Herpes Simplex 65 0.026
541
P MST009 Mastocytosis 64 0.026
542
PRP083 Porphyria, Acute Intermittent 64 0.026
543
HYP020 Hyperprolactinemia 64 0.026
544
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.026
545
PTR032 Peters-Plus Syndrome 63 0.026
546
P MVM001 Movement Disease 63 0.026
547
c ACT068 Acute Cystitis 63 0.026
548
TRN015 Transient Cerebral Ischemia 63 0.026
549
P END044 Endometriosis 63 0.026
550
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.026
551
P HYP750 Hypertriglyceridemia, Familial 62 0.026
552
P PRM006 Primary Biliary Cirrhosis 62 0.026
553
NRM001 Neuromyelitis Optica 61 0.026
554
FTT001 Fatty Liver Disease 61 0.026
555
INT002 Intermittent Claudication 61 0.026
556
HRP004 Herpes Zoster 60 0.026
557
P NPH012 Nephrotic Syndrome 60 0.026
558
CHC001 Chickenpox 60 0.026
559
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.026
560
STT001 Status Epilepticus 60 0.026
561
IDP011 Idiopathic Interstitial Pneumonia 59 0.026
562
P BRN022 Bronchiectasis 59 0.026
563
P LYM033 Lymphoproliferative Syndrome 59 0.026
564
VSL002 Visual Epilepsy 59 0.026
565
DCT002 Ductal Carcinoma in Situ 59 0.026
566
AVN001 Avian Influenza 59 0.026
567
GST045 Gastroenteritis 59 0.026
568
P PLY017 Polyarteritis Nodosa 58 0.026
569
FBR047 Fibromyalgia 58 0.026
570
CMP010 Complex Regional Pain Syndrome 58 0.026
571
ADL030 Adult-Onset Still's Disease 58 0.026
572
CHL028 Childhood Type Dermatomyositis 58 0.026
573
MXD005 Mixed Connective Tissue Disease 58 0.026
574
P OPT009 Optic Neuritis 57 0.026
575
c CHL119 Cholangitis, Primary Sclerosing 57 0.026
576
BRN056 Bronchopulmonary Dysplasia 57 0.026
577
P PLY041 Polymyositis 57 0.026
578
TNS005 Tonsillitis 57 0.026
579
BLR008 Bilirubin Metabolic Disorder 57 0.026
580
c LKM070 Leukemia, Acute Monocytic 57 0.026
581
P ANG015 Angioedema 57 0.026
582
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.026
583
ERY051 Erythroleukemia, Familial 56 0.026
584
P SZR006 Seizure Disorder 56 0.026
585
SLC006 Silicosis 56 0.026
586
P PLY019 Polyneuropathy 56 0.026
587
P DRM007 Dermatitis Herpetiformis 55 0.026
588
HNC001 Henoch-Schoenlein Purpura 55 0.026
589
END040 Endogenous Depression 55 0.026
590
INT007 Intermediate Coronary Syndrome 55 0.026
591
CRT017 Cartilage Disease 54 0.026
592
CLL003 Cellulitis 54 0.026
593
RHM028 Rheumatic Heart Disease 53 0.026
594
P INS002 in Situ Carcinoma 53 0.026
595
P MNC007 Monocytic Leukemia 53 0.026
596
MST005 Mastitis 53 0.026
597
NRT001 Neurotic Disorder 53 0.026
598
P RTN022 Retinal Vein Occlusion 53 0.026
599
PRP080 Peripheral Artery Disease 53 0.026
600
c CNT035 Central Nervous System Disease 52 0.026
601
EXP004 Exophthalmos 52 0.026
602
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.026
603
c VRL010 Viral Hepatitis 52 0.026
604
NRT004 Neuritis 52 0.026
605
PLS007 Plasmodium Falciparum Malaria 52 0.026
606
FLT011 Felty Syndrome 52 0.026
607
ACT200 Acute Monoblastic Leukemia 52 0.026
608
OCL069 Ocular Motor Apraxia 51 0.026
609
MYL001 Myelitis 51 0.026
610
ILS001 Ileus 51 0.026
611
P PRM018 Primary Hypertrophic Osteoarthropathy 51 0.026
612
PLS006 Plasmodium Vivax Malaria 51 0.026
613
P HYP040 Hypospadias 51 0.026
614
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.026
615
P CHL066 Cholangitis 51 0.026
616
P HYP077 Hypertrichosis 50 0.026
617
P OVR082 Overgrowth Syndrome 50 0.026
618
P ESN008 Eosinophilic Pneumonia 50 0.026
619
c THR071 Thrombocytopenia 1 50 0.026
620
c PSR021 Psoriasis 14, Pustular 50 0.026
621
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.026
622
AMB002 Amblyopia 49 0.026
623
LFT001 Left Bundle Branch Hemiblock 49 0.026
624
IMP004 Impetigo 49 0.026
625
P NGH001 Night Blindness 48 0.026
626
P SCL009 Sclerosing Cholangitis 48 0.026
627
P SCL015 Scleritis 48 0.026
628
CHL056 Cheilitis 48 0.026
629
HYP025 Hyperphosphatemia 48 0.026
630
ART004 Aortic Atherosclerosis 47 0.026
631
AST006 Astigmatism 47 0.026
632
KRT002 Keratomalacia 47 0.026
633
CRD137 Cardiogenic Shock 47 0.026
634
RTN020 Retinal Vascular Disease 46 0.026
635
PDT035 Pediatric Systemic Lupus Erythematosus 46 0.026
636
GLC084 Glaucoma, Normal Tension 46 0.026
637
PLC001 Placenta Accreta 46 0.026
638
P TRN034 Transverse Myelitis 45 0.026
639
PRL008 Paralytic Ileus 45 0.026
640
THR099 Third-Degree Atrioventricular Block 45 0.026
641
GRD001 Giardiasis 45 0.026
642
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.026
643
MCR225 Macrophage Activation Syndrome 44 0.026
644
P SDR002 Siderosis 44 0.026
645
KWS001 Kwashiorkor 44 0.026
646
c HYP272 Hypercholesterolemia, Familial, 3 44 0.026
647
P PLM085 Pulmonary Hemosiderosis 44 0.026
648
SKN005 Skin Atrophy 43 0.026
649
RFR003 Refractive Error 43 0.026
650
SBC012 Subcorneal Pustular Dermatosis 43 0.026
651
c RTN047 Retinitis Pigmentosa 18 42 0.026
652
RST023 Resting Heart Rate, Variation in 41 0.026
653
49X006 49, Xxxxy Syndrome 41 0.026
654
DFF003 Diffuse Scleroderma 41 0.026
655
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.026
656
ANX004 Anoxia 40 0.026
657
C1N001 C1 Inhibitor Deficiency 39 0.026
658
NDL003 Nodular Nonsuppurative Panniculitis 39 0.026
659
HYP008 Hypertensive Retinopathy 39 0.026
660
SPP007 Suppression Amblyopia 39 0.026
661
c PLM022 Pulmonary Valve Insufficiency 39 0.026
662
MLT016 Multicentric Reticulohistiocytosis 39 0.026
663
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.026
664
LPD014 Lipodermatosclerosis 38 0.026
665
OCH001 Ochronosis 38 0.026
666
CRV030 Cervical Adenitis 38 0.026
667
c ATM075 Autoimmune Encephalitis 38 0.026
668
CRB009 Cerebritis 37 0.026
669
P PLY187 Polyarticular Juvenile Idiopathic Arthritis 37 0.026
670
CHR463 Chronic Actinic Dermatitis 37 0.026
671
HYP026 Hypoglycemic Coma 36 0.026
672
NNT004 Neonatal Respiratory Failure 36 0.026
673
GRN003 Granulomatous Dermatitis 35 0.026
674
CMP040 Complement Component 4, Partial Deficiency of 33 0.026
675
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.026
676
PRR001 Periarthritis 32 0.026
677
DGN002 Degenerative Myopia 32 0.026
678
HYD003 Hydrarthrosis 31 0.026
679
SPN011 Spongiotic Dermatitis 31 0.026
680
LCH003 Lichen Nitidus 31 0.026
681
LYM035 Lymphangiectasis 30 0.026
682
GRN033 Granulomatous Mastitis 30 0.026
683
IRR001 Irregular Astigmatism 30 0.026
684
IDP041 Idiopathic Recurrent Pericarditis 30 0.026
685
PRN035 Perniosis 28 0.026
686
PHT004 Photoallergic Dermatitis 28 0.026
687
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.026
688
c PSR024 Psoriasis 3 28 0.026
689
IMP001 Impetigo Herpetiformis 27 0.026
690
c PSR026 Psoriasis 5 27 0.026
691
MST020 Mast Cell Activation Syndrome 26 0.026
692
IGP001 Iga Pemphigus 26 0.026
693
FTL073 Fetal Anticonvulsant Syndrome 26 0.026
694
CHR284 Chronic Lymphocytic Inflammation with Pontine Perivascular Enhancement Responsive to Steroids 25 0.026
695
INT029 Interleukin-7 Receptor Alpha Deficiency 22 0.026
696
c RNG019 Ring Chromosome 3 22 0.026
697
ATR052 Atrophic Lichen Planus 21 0.026
698
P CTS012 Cutis Verticis Gyrata 20 0.026
699
c CHR686 Chronic Cutaneous Lupus Erythematosus 19 0.026
700
CTN031 Cutaneous Pseudolymphoma 18 0.026
701
LPS018 Lupus Erythematosus Panniculitis 18 0.026
702
INT182 Intermittent Hydrarthrosis 18 0.026
703
ATR097 Atrophoderma of Pasini and Pierini 16 0.026
704
ANN013 Annular Atrophic Lichen Planus 14 0.026
705
EXG001 Exogenous Ochronosis 14 0.026
706
RRS004 Rare Systemic Disease 13 0.026
Content
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