Search results for Allopurinol

616 hits were found for Allopurinol

# Family MCID Name MIFTS Score
1
ALL025 Allopurinol Toxicity 11 2.900
2
P OBS331 Obsolete: Susceptibility to Toxic Epidermal Necrolysis Due to Allopurinol Treatment 3 2.772
3
GT001 Gout 63 0.675
4
HYP014 Hyperuricemia 51 0.533
5
ALL026 Allergic Hypersensitivity Disease 64 0.337
6
P KDN018 Kidney Disease 70 0.294
7
P EXN002 Exanthem 57 0.254
8
c CHR684 Chronic Kidney Disease 66 0.249
9
LSH001 Leishmaniasis 63 0.246
10
P KLZ004 Kala-Azar 1 41 0.246
11
P HYP098 Hypereosinophilic Syndrome 66 0.236
12
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.231
13
ISC004 Ischemia 60 0.216
14
ERY003 Erythema Multiforme 57 0.216
15
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.207
16
SVR097 Severe Cutaneous Adverse Reaction 67 0.205
17
ERY066 Erythema Multiforme Major 28 0.205
18
P HRT032 Heart Disease 75 0.199
19
CNG034 Congestive Heart Failure 70 0.186
20
c HYP595 Hypertension, Essential 84 0.180
21
P INF037 Inflammatory Bowel Disease 56 0.177
22
P LYM118 Lymphoma 68 0.163
23
ADL002 Adult Syndrome 69 0.161
24
P LKM002 Leukemia 66 0.161
25
P LYM031 Lymphocytic Leukemia 55 0.158
26
LYM019 Lymphosarcoma 47 0.156
27
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.153
28
P ART022 Arthritis 70 0.145
29
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.145
30
CTN007 Cutaneous Leishmaniasis 61 0.145
31
P PNC044 Pancreatitis 61 0.145
32
P CRD246 Cardiovascular System Disease 56 0.145
33
VSC003 Visceral Leishmaniasis 55 0.145
34
P LKM062 Leukemia, Acute Lymphoblastic 68 0.142
35
CHG001 Chagas Disease 66 0.142
36
DWN001 Down Syndrome 70 0.133
37
ANG054 Angina Pectoris 66 0.133
38
P VSC011 Vasculitis 62 0.133
39
48X005 48,xyyy 39 0.133
40
c ACT071 Acute Kidney Failure 59 0.130
41
P MSC005 Muscular Dystrophy 66 0.127
42
P PSR002 Psoriasis 62 0.127
43
END030 End Stage Renal Failure 58 0.127
44
CHL079 Children's Interstitial Lung Disease 27 0.127
45
P NTR004 Neutropenia 63 0.124
46
HYP266 Hypoxia 56 0.124
47
MCS002 Mucositis 55 0.124
48
PST011 Pustulosis of Palm and Sole 52 0.124
49
P BPL003 Bipolar Disorder 56 0.121
50
c MJR024 Major Affective Disorder 9 41 0.121
51
c MJR022 Major Affective Disorder 8 38 0.121
52
P MYC007 Myocardial Infarction 70 0.117
53
P CRN018 Coronary Artery Anomaly 63 0.117
54
P CRN300 Coronary Heart Disease 1 63 0.117
55
LYM040 Lymphoblastic Lymphoma 54 0.117
56
ADN024 Adenine Phosphoribosyltransferase Deficiency 52 0.117
57
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.117
58
CRB039 Cerebrovascular Disease 69 0.114
59
P DBT009 Diabetes Mellitus 64 0.114
60
LSC001 Lesch-Nyhan Syndrome 62 0.114
61
c ACT027 Acute Pancreatitis 59 0.114
62
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.110
63
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.110
64
P ART023 Arthropathy 62 0.110
65
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 35 0.110
66
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.106
67
P UVT001 Uveitis 57 0.106
68
c PSR017 Psoriasis 2 52 0.106
69
STM007 Stomatitis 49 0.106
70
c PSR023 Psoriasis 1 49 0.106
71
INT067 Interstitial Nephritis 46 0.106
72
c PSR028 Psoriasis 7 39 0.106
73
c PSR032 Psoriasis 11 38 0.106
74
c PSR018 Psoriasis 13 38 0.106
75
STR067 Stroke, Ischemic 80 0.102
76
c ATR087 Atrial Standstill 1 74 0.102
77
ULC004 Ulcerative Colitis 73 0.102
78
ATH013 Atherosclerosis Susceptibility 66 0.102
79
c RHB024 Rhabdomyosarcoma 2 65 0.102
80
PNC001 Pancytopenia 54 0.102
81
P XNT004 Xanthinuria 41 0.102
82
c HRD142 Hereditary Xanthinuria 32 0.102
83
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.102
84
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.098
85
MSC157 Muscular Dystrophy, Duchenne Type 71 0.098
86
P VSC007 Vascular Disease 63 0.098
87
c ACT075 Acute Myocardial Infarction 56 0.098
88
ART140 Arteries, Anomalies of 53 0.098
89
c MCR113 Microvascular Complications of Diabetes 3 52 0.098
90
EXF003 Exfoliative Dermatitis 27 0.098
91
P SRC025 Sarcoidosis 1 70 0.094
92
P CTR002 Cataract 60 0.094
93
P SZR006 Seizure Disorder 58 0.094
94
VSL002 Visual Epilepsy 58 0.094
95
RHM027 Rheumatic Disease 56 0.094
96
P MJR007 Major Affective Disorder 1 43 0.094
97
c DLT002 Dilated Cardiomyopathy 79 0.090
98
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.090
99
MYL009 Myelodysplastic Syndrome 70 0.090
100
MSC007 Muscle Hypertrophy 63 0.090
101
HMT002 Hematologic Cancer 62 0.090
102
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.090
103
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.090
104
ENT004 Enthesopathy 48 0.090
105
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.090
106
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.090
107
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.090
108
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.090
109
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.090
110
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.090
111
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.090
112
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.090
113
c MJR008 Major Affective Disorder 2 34 0.090
114
c MJR003 Major Affective Disorder 6 33 0.090
115
c MJR006 Major Affective Disorder 5 33 0.090
116
c MJR023 Major Affective Disorder 7 33 0.090
117
c MJR004 Major Affective Disorder 4 28 0.090
118
P EPL164 Epilepsy 71 0.085
119
PRP027 Peripheral Vascular Disease 71 0.085
120
P TRN020 Turner Syndrome 65 0.085
121
HYP066 Hyperglycemia 61 0.085
122
P ENC018 Encephalopathy 61 0.085
123
P MYL006 Myeloid Leukemia 60 0.085
124
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 59 0.085
125
c MCR120 Microvascular Complications of Diabetes 7 47 0.085
126
c MCR130 Microvascular Complications of Diabetes 6 41 0.085
127
c MCR133 Microvascular Complications of Diabetes 4 41 0.085
128
FXD003 Fixed Drug Eruption 35 0.085
129
GRN009 Granulomatous Hepatitis 31 0.085
130
URT049 Urate Oxidase, Pseudogene 25 0.085
131
c LKM061 Leukemia, Acute Myeloid 83 0.080
132
P SCH015 Schizophrenia 75 0.080
133
P APL001 Aplastic Anemia 74 0.080
134
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.080
135
BRK010 Burkitt Lymphoma 67 0.080
136
CLT003 Colitis 62 0.080
137
P NRP001 Neuropathy 56 0.080
139
ASP004 Asphyxia Neonatorum 45 0.080
140
CRB090 Cerebral Hypoxia 43 0.080
141
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.080
142
OST012 Osteoarthritis 78 0.075
143
CRH001 Crohn's Disease 74 0.075
144
LYM133 Lymphoma, Hodgkin, Classic 69 0.075
145
P LVR013 Liver Disease 68 0.075
146
P CRD119 Cardiac Arrest 67 0.075
147
MDD011 Mood Disorder 62 0.075
148
FTT001 Fatty Liver Disease 61 0.075
149
CHL068 Cholestasis 60 0.075
150
PRS047 Prostatitis 56 0.075
151
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.075
152
c XNT010 Xanthinuria, Type I 50 0.075
153
TST044 Testicular Torsion 47 0.075
154
GRN017 Granulocytopenia 44 0.075
155
c ATM099 Autoimmune Uveitis 44 0.075
156
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.075
157
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.075
158
PHC015 Phacoanaphylactic Uveitis 19 0.075
159
MYL069 Myeloma, Multiple 85 0.070
160
P RHM011 Rheumatoid Arthritis 80 0.070
161
c LKM071 Leukemia, Chronic Lymphocytic 79 0.070
162
DFC004 Deficiency Anemia 75 0.070
163
P GRF003 Graft-Versus-Host Disease 71 0.070
164
c LKM063 Leukemia, Chronic Myeloid 71 0.070
165
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.070
166
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.070
167
DPR016 Depression 63 0.070
168
SKN016 Skin Disease 63 0.070
169
LPD008 Lipid Metabolism Disorder 62 0.070
170
c ATM011 Autoimmune Hepatitis 62 0.070
171
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.070
172
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.070
173
P DRR001 Diarrhea 57 0.070
174
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.070
175
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.070
176
ORT008 Orotic Aciduria 54 0.070
177
PLS009 Plasma Cell Neoplasm 51 0.070
178
NPH078 Nephrolithiasis, Uric Acid 40 0.070
179
SVR004 Severe Combined Immunodeficiency 73 0.064
180
c HYP836 Hypercholesterolemia, Familial, 1 72 0.064
181
P THR014 Thrombocytopenia 68 0.064
182
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.064
183
P MCR115 Microvascular Complications of Diabetes 5 66 0.064
184
c MCR129 Microvascular Complications of Diabetes 1 66 0.064
185
P CNJ013 Conjunctivitis 65 0.064
186
c ACT073 Acute Leukemia 58 0.064
187
P BCL017 B-Cell Lymphoma 58 0.064
188
MNT002 Mental Depression 57 0.064
189
P GLM007 Glomerulonephritis 57 0.064
190
c ACT134 Acute Liver Failure 51 0.064
191
TRY001 Trypanosomiasis 50 0.064
192
BRN071 Brain Injury 49 0.064
193
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.064
194
MCC002 Mucocutaneous Leishmaniasis 47 0.064
195
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.064
196
c INH020 Inherited Metabolic Disorder 46 0.064
197
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.064
198
c CHR064 Chronic Monocytic Leukemia 34 0.064
199
P CLR023 Colorectal Cancer 98 0.057
200
c SYS001 Systemic Lupus Erythematosus 86 0.057
201
P CNR004 Cone-Rod Dystrophy 2 71 0.057
202
HMN044 Human Immunodeficiency Virus Type 1 71 0.057
203
RCK004 Rickets 69 0.057
204
P SLP006 Sleep Apnea 69 0.057
205
P HPT021 Hepatitis 67 0.057
206
PSY004 Psychotic Disorder 67 0.057
207
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.057
208
P ADN016 Adenocarcinoma 64 0.057
209
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.057
210
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.057
211
INT002 Intermittent Claudication 61 0.057
212
DRM006 Dermatitis 61 0.057
213
P LPS004 Lupus Erythematosus 61 0.057
214
ATM095 Autoimmune Disease 61 0.057
215
HYD002 Hydronephrosis 59 0.057
216
P CYS018 Cystitis 59 0.057
217
P HDC001 Headache 57 0.057
218
P PRP019 Peripheral Nervous System Disease 57 0.057
219
PLC005 Placental Insufficiency 57 0.057
220
SCH003 Schizophreniform Disorder 56 0.057
221
AGN016 Aging 56 0.057
222
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.057
223
INT007 Intermediate Coronary Syndrome 55 0.057
224
CRT017 Cartilage Disease 54 0.057
225
PRP080 Peripheral Artery Disease 53 0.057
226
P INT068 Intestinal Disease 52 0.057
227
SYS003 Systolic Heart Failure 50 0.057
228
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.057
229
P OBS001 Obstructive Jaundice 48 0.057
230
ATX019 Ataxia with Vitamin E Deficiency 48 0.057
231
SPL018 Splenomegaly 48 0.057
232
PRL017 Prolymphocytic Leukemia 47 0.057
233
FLL008 Folliculitis 46 0.057
234
GRN007 Granuloma Annulare 45 0.057
235
CHL152 Childhood Acute Lymphocytic Leukemia 43 0.057
236
c PRM038 Primary Agammaglobulinemia 43 0.057
237
RDC006 Red Cell Aplasia 42 0.057
238
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 36 0.057
239
DSR074 Disorder of Purine Metabolism 29 0.057
240
DHY008 Dihydroxyadeninuria 19 0.057
241
P PRS040 Prostate Cancer 97 0.049
242
ESP021 Esophageal Cancer 90 0.049
243
IMM167 Immune Deficiency Disease 78 0.049
244
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.049
245
LPT014 Leptin Deficiency or Dysfunction 73 0.049
246
P MYC084 Mycobacterium Tuberculosis 1 68 0.049
247
c INF071 Inflammatory Bowel Disease 1 68 0.049
248
MNT001 Mantle Cell Lymphoma 66 0.049
249
P FLL037 Follicular Lymphoma 66 0.049
250
P MNN013 Meningitis 65 0.049
251
P ATS364 Autism 65 0.049
252
MYL031 Myeloproliferative Neoplasm 65 0.049
253
APN008 Apnea, Obstructive Sleep 65 0.049
254
CLR108 Colorectal Adenoma 64 0.049
255
NTR005 Nutritional Deficiency Disease 61 0.049
256
P HYP750 Hypertriglyceridemia, Familial 61 0.049
257
P ANP001 Anaplastic Large Cell Lymphoma 61 0.049
258
LYM012 Lymphoplasmacytic Lymphoma 61 0.049
259
PRT013 Portal Hypertension 60 0.049
260
HPT019 Hepatic Encephalopathy 60 0.049
261
ACQ007 Acquired Immunodeficiency Syndrome 60 0.049
262
P MYC008 Myocarditis 59 0.049
263
ADN018 Adenoma 58 0.049
264
IRN002 Iron Metabolism Disease 57 0.049
265
BLR008 Bilirubin Metabolic Disorder 57 0.049
266
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.049
267
c ADL017 Adult T-Cell Leukemia 57 0.049
268
P ALP008 Alopecia 56 0.049
269
HYP005 Hypokalemia 55 0.049
270
HRY003 Hairy Cell Leukemia 55 0.049
271
GLC003 Glucose Intolerance 54 0.049
272
GLS018 Glass Syndrome 53 0.049
273
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.049
274
c ACT135 Acute Graft Versus Host Disease 51 0.049
275
HYP074 Hypersensitivity Vasculitis 51 0.049
276
BWN001 Bowen-Conradi Syndrome 51 0.049
277
P CHL066 Cholangitis 50 0.049
278
MCR004 Macroglobulinemia 50 0.049
279
P CHR345 Chronic Pain 50 0.049
280
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.049
281
c FLL041 Follicular Lymphoma 1 49 0.049
282
ATY042 Atypical Chronic Myeloid Leukemia 49 0.049
283
STP011 Stapes Ankylosis with Broad Thumbs and Toes 48 0.049
284
P PRR002 Pure Red-Cell Aplasia 48 0.049
285
PRD004 Prediabetes Syndrome 47 0.049
286
P TCL004 T-Cell Leukemia 47 0.049
287
PLS025 Plasmablastic Lymphoma 47 0.049
288
CLL014 Cll/sll 45 0.049
289
CRB004 Cerebral Artery Occlusion 44 0.049
290
DST006 Diastolic Heart Failure 44 0.049
291
CYT002 Cytokine Deficiency 44 0.049
292
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.049
293
HPT004 Hepatic Coma 43 0.049
294
ADN022 Adenylosuccinase Deficiency 43 0.049
295
ANX004 Anoxia 42 0.049
296
GST020 Gastric Antral Vascular Ectasia 41 0.049
297
c MCR112 Microvascular Complications of Diabetes 2 41 0.049
298
c ADL052 Adult Acute Lymphocytic Leukemia 40 0.049
299
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 39 0.049
300
SKN006 Skin Sarcoidosis 39 0.049
301
KLL014 Kelley-Seegmiller Syndrome 38 0.049
302
c SYS043 Systemic Lupus Erythematosus 1 38 0.049
303
PSD088 Pseudobulbar Affect 36 0.049
304
c XNT011 Xanthinuria, Type Ii 36 0.049
305
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 35 0.049
306
c PRG106 Progressive Muscular Dystrophy 33 0.049
307
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.049
308
ESN016 Eosinophilic Pustular Folliculitis 25 0.049
309
HML018 Homologous Wasting Disease 22 0.049
310
P OVR042 Ovarian Cancer 89 0.040
311
MLR004 Malaria 80 0.040
312
P BLD134 Bladder Cancer 78 0.040
313
BRN028 Brain Cancer 73 0.040
314
P TTR001 Tetralogy of Fallot 69 0.040
315
P OCL013 Oculodentodigital Dysplasia 69 0.040
316
P INF038 Influenza 68 0.040
317
CRB037 Cerebral Palsy 68 0.040
318
P PNM007 Pneumonia 68 0.040
319
MYL005 Myelofibrosis 67 0.040
320
P DMN002 Dementia 67 0.040
321
HYP056 Hypoglycemia 66 0.040
322
MYC006 Mycosis Fungoides 66 0.040
323
PRT037 Pertussis 65 0.040
324
PRT036 Peritonitis 65 0.040
325
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.040
326
KHL003 Kohlschutter-Tonz Syndrome 64 0.040
327
c PRC016 Pre-Eclampsia 63 0.040
328
LVR012 Liver Cirrhosis 63 0.040
329
c HPT003 Hepatitis a 63 0.040
330
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.040
331
P HYP055 Hypoplastic Left Heart Syndrome 62 0.040
332
OST003 Osteonecrosis 61 0.040
333
VRL011 Viral Infectious Disease 61 0.040
334
SZR001 Sezary's Disease 60 0.040
335
SPN186 Spinal Cord Injury 60 0.040
336
MCR013 Microphthalmia 60 0.040
337
STT001 Status Epilepticus 59 0.040
338
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.040
339
PPT005 Peptic Ulcer Disease 58 0.040
340
CHL067 Cholecystitis 58 0.040
341
P URT039 Urticaria 58 0.040
342
LYM027 Lymphopenia 57 0.040
343
c CHR417 Chronic Graft Versus Host Disease 56 0.040
344
THR024 Thrombosis 56 0.040
345
PLS011 Plasmacytoma 56 0.040
346
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.040
347
c FML035 Familial Hyperlipidemia 55 0.040
348
LMB062 Limb Ischemia 55 0.040
349
DBT010 Diabetic Neuropathy 55 0.040
350
CLF004 Cleft Lip/palate 54 0.040
351
HYP060 Hyperinsulinism 54 0.040
352
P ART021 Arteriosclerosis 54 0.040
353
P ICH004 Ichthyosis 54 0.040
354
PNM001 Pneumocystosis 54 0.040
355
PRP016 Paraplegia 53 0.040
356
MRG003 Marginal Zone B-Cell Lymphoma 53 0.040
357
KRT009 Keratosis 53 0.040
358
GST023 Gastric Ulcer 53 0.040
359
CLF001 Cleft Lip 53 0.040
360
THR013 Thoracic Outlet Syndrome 53 0.040
361
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.040
362
PRS045 Prostatic Hypertrophy 52 0.040
363
P MSC003 Muscular Atrophy 52 0.040
364
TXC002 Toxic Encephalopathy 52 0.040
365
NPH003 Nephrocalcinosis 51 0.040
366
PRS021 Prostatic Adenoma 51 0.040
367
P ECL001 Eclampsia 51 0.040
368
SPL004 Splenic Marginal Zone Lymphoma 51 0.040
369
SCH012 Schizoaffective Disorder 50 0.040
370
HYP781 Hypoascorbemia 50 0.040
371
P DDN001 Duodenal Ulcer 50 0.040
372
MTB004 Metabolic Acidosis 50 0.040
373
P IGN003 Iga Nephropathy 1 49 0.040
374
BLP005 Blepharitis 49 0.040
375
47X002 47,xyy 49 0.040
376
PRS129 Prostatic Hyperplasia, Benign 49 0.040
377
KRT002 Keratomalacia 48 0.040
378
IGG001 Iga Glomerulonephritis 48 0.040
379
P RNL015 Renal Hypertension 48 0.040
380
ATN005 Autonomic Dysfunction 47 0.040
381
NDL013 Nodular Regenerative Hyperplasia 47 0.040
382
URT010 Ureteral Obstruction 46 0.040
383
PLS016 Plasma Cell Leukemia 46 0.040
384
P PRD037 Periodontal Ehlers-Danlos Syndrome 46 0.040
385
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.040
386
ACT003 Acute Kidney Tubular Necrosis 45 0.040
387
P HYP758 Hyperuricemic Nephropathy, Familial Juvenile, 1 44 0.040
388
TST015 Testicular Disease 43 0.040
389
BNM001 Bone Marrow Cancer 43 0.040
390
NSP002 Nasopharyngitis 41 0.040
391
GLM044 Glomerular Disease 39 0.040
392
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.040
393
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.040
394
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.040
395
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.040
396
ACT216 Acute Leukemia of Ambiguous Lineage 32 0.040
397
RFR002 Refractory Hairy Cell Leukemia 32 0.040
398
CLS052 Classic Hairy Cell Leukemia 27 0.040
399
KYR001 Kyrle Disease 23 0.040
400
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 22 0.040
402
P HPT023 Hepatocellular Carcinoma 100 0.028
403
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.028
405
P RTT002 Rett Syndrome 80 0.028
406
P LNG064 Lung Cancer Susceptibility 3 77 0.028
407
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.028
408
GLB015 Glioblastoma Multiforme 75 0.028
409
ADR007 Adrenoleukodystrophy 74 0.028
410
c SPN225 Spondyloarthropathy 1 73 0.028
411
P MLT020 Multiple Sclerosis 72 0.028
412
c EXD008 Exudative Vitreoretinopathy 1 69 0.028
413
P HYP086 Hypothyroidism 68 0.028
414
P ALP004 Alport Syndrome 68 0.028
415
P MJR001 Major Depressive Disorder 68 0.028
416
KRT019 Keratitis, Hereditary 67 0.028
417
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.028
418
P PRP003 Porphyria Cutanea Tarda 67 0.028
419
P LPR021 Leprosy 3 67 0.028
420
P ANG001 Angelman Syndrome 67 0.028
421
P SKN015 Skin Carcinoma 67 0.028
422
FLL027 Fallopian Tube Carcinoma 67 0.028
423
ALC007 Alcohol Dependence 66 0.028
424
FCT007 Factor Vii Deficiency 66 0.028
425
P ATR011 Atrial Fibrillation 66 0.028
426
P NRV007 Nervous System Disease 66 0.028
427
SRC014 Sarcoma 65 0.028
428
P HRP006 Herpes Simplex 65 0.028
429
P EPD009 Epidermolysis Bullosa Dystrophica 64 0.028
430
P MYP004 Myopathy 64 0.028
431
P MTR014 Motor Neuron Disease 64 0.028
432
TTN003 Tetanus 64 0.028
433
CTR172 Citrullinemia, Classic 64 0.028
434
CLN015 Colon Adenocarcinoma 63 0.028
435
NRM005 Neuromuscular Disease 63 0.028
436
P ADL010 Adult Respiratory Distress Syndrome 63 0.028
437
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.028
438
c ACT068 Acute Cystitis 63 0.028
439
P HYP069 Hyperparathyroidism 62 0.028
440
CYS013 Cystinuria 62 0.028
441
c FNC043 Fanconi Anemia, Complementation Group E 62 0.028
442
BDD001 Budd-Chiari Syndrome 62 0.028
443
PSR001 Psoriatic Arthritis 62 0.028
444
P PRP029 Porphyria 62 0.028
445
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.028
446
P ENC004 Encephalitis 61 0.028
447
ALV005 Alveolar Soft Part Sarcoma 61 0.028
448
P SNS001 Sensorineural Hearing Loss 61 0.028
449
ERL001 Early Myoclonic Encephalopathy 61 0.028
450
P ALP009 Alopecia Areata 60 0.028
451
HRP004 Herpes Zoster 60 0.028
452
WST001 West Syndrome 60 0.028
453
P PTN014 Patent Ductus Arteriosus 1 60 0.028
454
P GLL022 Guillain-Barre Syndrome 59 0.028
455
P SLP005 Sleep Disorder 59 0.028
456
P PLY014 Polycystic Kidney Disease 59 0.028
457
P TRC086 Trichohepatoenteric Syndrome 1 59 0.028
458
P SYP003 Syphilis 59 0.028
459
BRN002 Bronchiolitis 59 0.028
460
P CHR285 Chronic Myelomonocytic Leukemia 59 0.028
461
CRD132 Cardiac Conduction Defect 59 0.028
462
CRY005 Cryptococcosis 58 0.028
463
P ALC033 Alcohol Use Disorder 58 0.028
464
QFV001 Q Fever 58 0.028
465
c CHL119 Cholangitis, Primary Sclerosing 57 0.028
466
URN010 Urinary Tract Obstruction 57 0.028
467
GST033 Gestational Diabetes 57 0.028
468
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.028
469
BRN056 Bronchopulmonary Dysplasia 57 0.028
470
P PYL005 Pyelonephritis 56 0.028
471
CYT008 Cytomegalovirus Infection 56 0.028
472
P CHN012 Chondrosarcoma 56 0.028
473
SFT003 Soft Tissue Sarcoma 56 0.028
474
BCT022 Bacterial Infectious Disease 56 0.028
475
P MYS005 Myositis 56 0.028
476
HPT022 Hepatoblastoma 56 0.028
477
BRN012 Bronchiolitis Obliterans 56 0.028
478
DFF005 Diffuse Large B-Cell Lymphoma 56 0.028
479
PRP030 Purpura 55 0.028
480
BRN004 Brain Edema 55 0.028
481
GRN034 Grange Syndrome 55 0.028
482
c GRV008 Graves Disease 1 55 0.028
483
P HYP076 Hyperthyroidism 55 0.028
484
PLM010 Pulmonary Edema 55 0.028
485
VGN023 Vaginitis 55 0.028
486
PRN019 Perinatal Necrotizing Enterocolitis 54 0.028
487
ESN011 Eisenmenger Syndrome 54 0.028
488
END040 Endogenous Depression 54 0.028
489
GNT003 Genital Herpes 54 0.028
490
P ANG015 Angioedema 54 0.028
491
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.028
492
c CNT035 Central Nervous System Disease 54 0.028
493
P EPD016 Epidermolysis Bullosa 53 0.028
494
P LTR001 Lateral Sclerosis 53 0.028
495
RCS002 Recessive Dystrophic Epidermolysis Bullosa 53 0.028
496
HRT012 Heart Valve Disease 53 0.028
497
P HYP730 Hypogonadotropic Hypogonadism 53 0.028
498
MMB001 Membranoproliferative Glomerulonephritis 53 0.028
499
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 53 0.028
500
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 0.028
501
NRT001 Neurotic Disorder 52 0.028
502
CRH005 Crohn's Colitis 52 0.028
503
ACR041 Acromelic Frontonasal Dysostosis 52 0.028
504
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.028
505
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.028
506
c GLL024 Gallbladder Disease 1 52 0.028
507
OCL069 Ocular Motor Apraxia 51 0.028
508
URC002 Urea Cycle Disorder 51 0.028
509
THR016 Thrombophlebitis 51 0.028
510
THR004 Thrombocytosis 51 0.028
511
ASP003 Aseptic Meningitis 51 0.028
512
NNL006 Non-Alcoholic Steatohepatitis 51 0.028
513
SPN035 Spindle Cell Sarcoma 51 0.028
514
c SCN007 Secondary Hyperparathyroidism 50 0.028
515
P THR015 Thrombophilia 50 0.028
516
ENT011 Enterocolitis 50 0.028
517
DYS073 Dysphagia 50 0.028
518
P SCK005 Sickle Cell Disease 50 0.028
519
VLV047 Volvulus of Midgut 50 0.028
520
c INF145 Infantile Liver Failure Syndrome 1 50 0.028
521
LPR001 Lepromatous Leprosy 50 0.028
522
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.028
523
c BPL002 Bipolar I Disorder 49 0.028
524
MLR002 Miliary Tuberculosis 49 0.028
525
RTC005 Reticulosarcoma 49 0.028
526
HMG002 Hemoglobinuria 49 0.028
527
MNN009 Meningoencephalitis 49 0.028
528
P RNV001 Renovascular Hypertension 49 0.028
529
URM002 Uremia 49 0.028
530
P CMP008 Compartment Syndrome 48 0.028
531
RFR010 Refractory Anemia 48 0.028
532
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.028
533
CHR563 Chronic Eosinophilic Leukemia 48 0.028
534
CRD137 Cardiogenic Shock 48 0.028
535
SXL003 Sexual Disorder 48 0.028
536
c VRL012 Viral Meningitis 48 0.028
537
OPT070 Optic Nerve Hypoplasia, Bilateral 48 0.028
538
ADR038 Adermatoglyphia 48 0.028
539
PRP007 Priapism 48 0.028
540
HYP025 Hyperphosphatemia 47 0.028
541
P SCL009 Sclerosing Cholangitis 47 0.028
542
TST014 Testicular Cancer 46 0.028
543
ANR004 Anuria 46 0.028
544
DRG013 Drug-Induced Lupus Erythematosus 46 0.028
545
TWN001 Twin-to-Twin Transfusion Syndrome 45 0.028
546
SCL002 Scleredema Adultorum 45 0.028
547
MLY008 Molybdenum Cofactor Deficiency, Complementation Group a 45 0.028
548
HRP001 Herpangina 45 0.028
549
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.028
551
PTY001 Pityriasis Rosea 44 0.028
552
ATN004 Autonomic Neuropathy 44 0.028
553
c CLR085 Colorectal Cancer 1 44 0.028
554
P MYG005 Myoglobinuria 43 0.028
555
c PCH010 Pachyonychia Congenita 3 43 0.028
556
PNM013 Pneumococcal Meningitis 43 0.028
557
DRG024 Drug Allergy 43 0.028
558
c HYP272 Hypercholesterolemia, Familial, 3 43 0.028
559
IDP073 Idiopathic Hypercalciuria 43 0.028
560
OVR112 Ovarian Germ Cell Cancer 43 0.028
561
RNL025 Renal Hypoplasia 43 0.028
562
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 42 0.028
563
DSC009 Discoid Lupus Erythematosus 42 0.028
564
P HYP761 Hypouricemia, Renal, 1 42 0.028
565
PRS036 Parasitic Protozoa Infectious Disease 42 0.028
566
P CLL015 Collagen Disease 42 0.028
567
EHR002 Ehrlichiosis 42 0.028
568
ALC010 Alcoholic Cardiomyopathy 42 0.028
569
MCR103 Microtia 42 0.028
570
MLY001 Molybdenum Cofactor Deficiency 42 0.028
571
TND006 Tendinosis 42 0.028
572
DBT002 Diabetic Autonomic Neuropathy 41 0.028
573
EPC002 Epicondylitis 41 0.028
574
SLF014 Sulfite Oxidase Deficiency, Isolated 40 0.028
575
JWD001 Jawad Syndrome 40 0.028
576
UTR043 Uterine Sarcoma 40 0.028
577
ULC007 Ulcerative Stomatitis 39 0.028
578
c MLG074 Malignant Mesenchymoma 39 0.028
579
PCH007 Pouchitis 39 0.028
580
PLY010 Polyclonal Hypergammaglobulinemia 39 0.028
581
c OVR114 Ovarian Cancer 1 38 0.028
582
ADR022 Adrenomyeloneuropathy 38 0.028
583
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.028
584
OVR094 Ovarian Epithelial Cancer 38 0.028
585
HRN029 Hearing Loss, Noise-Induced 37 0.028
586
ACL001 Acalculous Cholecystitis 35 0.028
587
FST010 Fasting Hypoglycemia 35 0.028
588
c ACT036 Acute Cholangitis 35 0.028
589
GRN003 Granulomatous Dermatitis 35 0.028
590
c CHR087 Chronic Cystitis 35 0.028
591
HNS001 Hansen's Disease 34 0.028
592
GRM010 Germ Cells Tumors 34 0.028
593
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.028
594
HYP114 Hypertensive Nephropathy 34 0.028
595
MTC037 Mitochondrial Phosphate Carrier Deficiency 33 0.028
596
INF013 Inferior Myocardial Infarction 33 0.028
597
P PLM182 Pulmonary Hypoplasia, Primary 32 0.028
598
HPT085 Hepatitis, Fulminant Viral 32 0.028
599
c DRR009 Diarrhea 6 32 0.028
600
P ATS382 Autosomal Dominant Tubulointerstitial Kidney Disease 31 0.028
601
c THR048 Thrombocytopenia 4 31 0.028
602
ELS002 Elastosis Perforans Serpiginosa 31 0.028
603
PLY150 Polykaryocytosis Inducer 31 0.028
604
c BLD140 Blood Group, I System 30 0.028
605
PST092 Posttransplant Acute Limbic Encephalitis 29 0.028
606
PDT027 Pediatric Ulcerative Colitis 28 0.028
607
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.028
608
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.028
609
PRC008 Pericholangitis 26 0.028
610
DFF031 Diffuse Alveolar Hemorrhage 26 0.028
611
MLG164 Malignant Epithelial Tumor of Ovary 26 0.028
612
GRW027 Growth Restriction, Severe, with Distinctive Facies 25 0.028
613
PSD004 Pseudomembranous Conjunctivitis 25 0.028
614
c CHR465 Chronic Diarrhea Due to Guanylate Cyclase 2c Overactivity 20 0.028
615
CRY024 Crystal Arthropathies 20 0.028
616
OBS860 Obsolete: Familial Juvenile Hyperuricemic Nephropathy Type 1 13 0.028
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