Search results for "sepsis"

The MalaCard for "sepsis" has been retired.
Searching MalaCards for entries containing "sepsis"

832 hits were found for 'sepsis'

# Family MCID Name MIFTS Score
1
LMR001 Lemierre's Syndrome 41 4.730
2
SPS090 Sepsis in Premature Infants 23 2.924
3
TXC005 Toxic Shock Syndrome 61 0.334
4
DSS009 Disseminated Intravascular Coagulation 51 0.218
5
P PNM007 Pneumonia 66 0.200
6
c RNL016 Renal Infectious Disease 24 0.197
7
CSY001 C Syndrome 49 0.194
8
PRM025 Primary Bacterial Infectious Disease 43 0.187
9
END072 Endotheliitis 42 0.170
10
CHL071 Child Syndrome 58 0.166
11
KDS001 Kid Syndrome 53 0.160
12
PRP030 Purpura 59 0.158
13
P PRP034 Purpura Fulminans 42 0.151
14
c ACT210 Acute Respiratory Distress Syndrome 57 0.149
15
BRN106 Burns 52 0.149
16
BCT015 Bacteremia 48 0.149
17
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.145
18
P MNN013 Meningitis 65 0.145
19
GDS001 Good Syndrome 45 0.145
20
P ADL010 Adult Respiratory Distress Syndrome 60 0.141
21
WLL006 Wells Syndrome 56 0.141
22
P HPT021 Hepatitis 70 0.137
23
PRT036 Peritonitis 62 0.129
24
P NTR004 Neutropenia 59 0.125
25
RSP006 Respiratory System Disease 62 0.122
26
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.122
27
P RSP003 Respiratory Failure 70 0.118
28
CHR005 Chorioamnionitis 48 0.118
29
WST001 West Syndrome 61 0.115
30
c ACT071 Acute Kidney Failure 50 0.115
31
P PLY019 Polyneuropathy 54 0.110
32
NSY001 N Syndrome 39 0.110
33
MLD001 Melioidosis 67 0.103
34
ADM013 Adamantinoma of Long Bones 59 0.103
35
CRT009 Critical Illness Polyneuropathy 39 0.100
36
LKC003 Leukocyte Disease 47 0.097
37
P BLD051 Blood Coagulation Disease 45 0.097
38
P SPN301 Spinocerebellar Ataxia 2 63 0.094
39
P PNC044 Pancreatitis 60 0.094
40
c SVR001 Severe Acute Respiratory Syndrome 57 0.091
41
c ADL080 Adult Acute Respiratory Distress Syndrome 23 0.091
42
P LKM002 Leukemia 70 0.088
43
HYP066 Hyperglycemia 60 0.088
44
ADL002 Adult Syndrome 53 0.088
45
BLD054 Blood Protein Disease 40 0.088
46
ECT004 Ecthyma 35 0.088
47
VSC008 Vascular Hemostatic Disease 33 0.088
48
P ART022 Arthritis 75 0.085
49
NWB001 Newborn Respiratory Distress Syndrome 47 0.085
50
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 41 0.085
51
IMP003 Impaired Renal Function Disease 37 0.085
52
RSP007 Respiratory Distress Syndrome, Infant 26 0.085
53
P LVR013 Liver Disease 72 0.082
54
LVR012 Liver Cirrhosis 67 0.082
55
P THR014 Thrombocytopenia 64 0.082
56
HYP266 Hypoxia 55 0.082
57
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.082
58
MLR004 Malaria 79 0.078
59
P INF038 Influenza 74 0.078
60
VND001 Vein Disease 52 0.078
61
P HRT032 Heart Disease 76 0.074
62
P MYP004 Myopathy 67 0.074
63
P ENC018 Encephalopathy 59 0.074
64
EXF001 Exfoliation Syndrome 57 0.074
65
P SPS003 Spastic Diplegia 53 0.074
66
c INF067 Inflammatory Bowel Disease 10 51 0.074
67
ACT017 Acute Chest Syndrome 48 0.074
68
P PLN008 Peeling Skin Syndrome 47 0.074
69
MCR225 Macrophage Activation Syndrome 40 0.074
70
NVS004 Nova Syndrome 19 0.074
71
c HYP595 Hypertension, Essential 69 0.071
72
PRP027 Peripheral Vascular Disease 69 0.071
73
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.071
74
C3D001 C3 Deficiency 53 0.071
75
INT007 Intermediate Coronary Syndrome 52 0.071
76
CLL003 Cellulitis 49 0.071
77
RNL097 Renal Artery Disease 45 0.071
78
HYP017 Hypophosphatemia 42 0.071
79
GRN017 Granulocytopenia 42 0.071
80
GLC006 Galactosemia 67 0.067
81
P SHR029 Short Syndrome 60 0.067
82
P THR015 Thrombophilia 59 0.067
83
ISC004 Ischemia 59 0.067
84
c BCT007 Bacterial Meningitis 54 0.067
85
LYM027 Lymphopenia 54 0.067
86
IMM136 Immune System Disease 50 0.067
87
BLD053 Blood Platelet Disease 46 0.067
88
PRN019 Perinatal Necrotizing Enterocolitis 44 0.067
89
ATN011 Autoinflammation with Infantile Enterocolitis 41 0.067
90
NTR005 Nutritional Deficiency Disease 39 0.067
91
CRB009 Cerebritis 38 0.067
92
NNT021 Neonatal Meningitis 24 0.067
93
GRM003 German Syndrome 24 0.067
94
P AST005 Asthma 82 0.062
95
c CHR089 Chronic Kidney Failure 66 0.062
96
GST045 Gastroenteritis 60 0.062
97
SPT004 Septic Arthritis 59 0.062
98
P HMR003 Hemorrhagic Disease 57 0.062
99
P PYL005 Pyelonephritis 52 0.062
100
END030 End Stage Renal Failure 52 0.062
101
P MTC069 Mitochondrial Disorders 52 0.062
102
P CHL066 Cholangitis 49 0.062
103
INT071 Intestinal Perforation 41 0.062
104
PYM001 Pyomyositis 39 0.062
105
SPL007 Splenic Abscess 31 0.062
106
STR067 Stroke, Ischemic 77 0.058
107
TBR010 Tuberculosis 69 0.058
108
P KDN017 Kidney Cancer 67 0.058
109
DWN001 Down Syndrome 65 0.058
110
HYP056 Hypoglycemia 61 0.058
111
VRL011 Viral Infectious Disease 59 0.058
112
MSS002 Mass Syndrome 59 0.058
113
OST017 Osteomyelitis 59 0.058
114
c ACT027 Acute Pancreatitis 56 0.058
115
THR016 Thrombophlebitis 52 0.058
116
P MSC033 Muscle Disorders 52 0.058
117
PRT011 Protein C Deficiency 51 0.058
118
GSG001 Gas Gangrene 49 0.058
119
MTB004 Metabolic Acidosis 48 0.058
120
PRV004 Periventricular Leukomalacia 48 0.058
121
ACR041 Acromelic Frontonasal Dysostosis 46 0.058
122
MNN009 Meningoencephalitis 45 0.058
123
RSP019 Respiratory Distress Syndrome in Premature Infants 44 0.058
124
BRT030 Birth Defects 43 0.058
125
ANL022 Anal Fistula 42 0.058
126
LKM006 Leukomalacia 42 0.058
127
PRM026 Primary Systemic Mycosis 41 0.058
128
SPC003 Specific Developmental Disorder 40 0.058
129
MSC004 Muscle Tissue Disease 36 0.058
130
PRP080 Peripheral Artery Disease 36 0.058
131
GRN016 Grant Syndrome 30 0.058
132
c CRN177 Coronary Heart Disease 7 22 0.058
133
WSC001 Wisconsin Syndrome 17 0.058
134
CNG034 Congestive Heart Failure 71 0.053
135
P LYM118 Lymphoma 70 0.053
136
PCK002 Pick Disease 67 0.053
137
P CRD011 Cardiomyopathy 67 0.053
138
P ANT006 Antiphospholipid Syndrome 58 0.053
139
LPD008 Lipid Metabolism Disorder 58 0.053
140
CHL067 Cholecystitis 56 0.053
141
PLM010 Pulmonary Edema 56 0.053
142
SLP005 Sleep Disorder 53 0.053
143
P MSC003 Muscular Atrophy 51 0.053
144
P DRR001 Diarrhea 51 0.053
145
AMN002 Amino Acid Metabolic Disorder 48 0.053
146
P RNL015 Renal Hypertension 47 0.053
147
FSC004 Fasciitis 46 0.053
148
NCR007 Necrotizing Fasciitis 45 0.053
149
MNN020 Meningococcal Infection 43 0.053
150
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.053
151
CTS005 Catastrophic Antiphospholipid Syndrome 41 0.053
152
TMP012 Temple Syndrome 40 0.053
153
HYP189 Hypoadrenalism 40 0.053
154
VNT001 Ventilation Pneumonitis 37 0.053
155
c PLN018 Peeling Skin Syndrome 2 35 0.053
156
c PLN017 Peeling Skin Syndrome 1 33 0.053
157
SBC016 Subacute Delirium 27 0.053
158
BRW006 Brown Syndrome 26 0.053
159
SHP003 Shapiro Syndrome 25 0.053
160
c INF078 Inflammatory Bowel Disease 2 24 0.053
161
c CRN214 Coronary Heart Disease 5 23 0.053
162
BNJ001 Benjamin Syndrome 12 0.053
163
P OBS005 Obesity 93 0.047
164
P RHM011 Rheumatoid Arthritis 88 0.047
165
c SYS001 Systemic Lupus Erythematosus 87 0.047
166
DFC004 Deficiency Anemia 65 0.047
167
P LPS004 Lupus Erythematosus 63 0.047
168
LNG099 Lung Disease 62 0.047
169
P INT068 Intestinal Disease 61 0.047
170
P INF032 Infertility 61 0.047
171
RBR001 Roberts Syndrome 59 0.047
172
CHL068 Cholestasis 58 0.047
173
PHR003 Pharyngitis 58 0.047
174
P CND004 Candidiasis 57 0.047
175
P GLM007 Glomerulonephritis 56 0.047
176
P MYS005 Myositis 56 0.047
177
SCR008 Scrub Typhus 54 0.047
178
GST050 Gastrointestinal System Disease 54 0.047
179
ALL026 Allergic Hypersensitivity Disease 53 0.047
180
DRG003 Drug Dependence 53 0.047
181
P END033 Endocarditis 52 0.047
182
c INF071 Inflammatory Bowel Disease 1 51 0.047
183
c ACT068 Acute Cystitis 50 0.047
184
c ACT134 Acute Liver Failure 50 0.047
185
BRN056 Bronchopulmonary Dysplasia 49 0.047
186
UPP004 Upper Respiratory Tract Disease 48 0.047
187
LPD004 Lipoid Nephrosis 48 0.047
188
BNN003 Bone Inflammation Disease 46 0.047
189
HPT014 Hepatorenal Syndrome 46 0.047
190
CRD137 Cardiogenic Shock 46 0.047
191
c ACT042 Acute Pyelonephritis 46 0.047
192
ATN005 Autonomic Dysfunction 45 0.047
193
ACH037 Achalasia-Addisonianism-Alacrimia Syndrome 45 0.047
194
HMP009 Haemophilus Influenzae 45 0.047
195
NRN002 Neuronitis 42 0.047
196
HMT018 Hematopoietic Stem Cell Transplantation 41 0.047
197
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.047
198
CPL005 Capillary Disease 40 0.047
199
MNN021 Meningococcemia 38 0.047
200
c PLM022 Pulmonary Valve Insufficiency 38 0.047
201
ADR010 Adrenal Cortical Hypofunction 38 0.047
202
CND006 Candida Glabrata 34 0.047
203
P ACT080 Acute Pulmonary Heart Disease 32 0.047
204
ADP002 Adiponectin Deficiency 31 0.047
205
P MLT027 Multiple Mitochondrial Dysfunctions Syndrome 26 0.047
206
YNG002 Young Syndrome 26 0.047
207
P CRN178 Coronary Heart Disease 6 24 0.047
208
NLL002 Null Syndrome 22 0.047
209
P LNG032 Lung Cancer 94 0.041
210
HPT023 Hepatocellular Carcinoma 91 0.041
211
P MYC007 Myocardial Infarction 79 0.041
212
SRC014 Sarcoma 66 0.041
213
P AGM001 Agammaglobulinemia 64 0.041
214
LPT001 Leptospirosis 63 0.041
215
c ACT073 Acute Leukemia 62 0.041
216
WLL001 Williams-Beuren Syndrome 61 0.041
217
c ACT075 Acute Myocardial Infarction 60 0.041
218
P HML002 Hemolytic Anemia 60 0.041
219
P RCK004 Rickets 59 0.041
220
ALC006 Alcoholic Hepatitis 59 0.041
221
CLT003 Colitis 59 0.041
222
NRM005 Neuromuscular Disease 57 0.041
223
P AGM005 Agammaglobulinemia, X-Linked 1 57 0.041
224
ADL030 Adult-Onset Still's Disease 57 0.041
225
c SVR003 Severe Congenital Neutropenia 56 0.041
226
c THR092 Thrombophilia Due to Thrombin Defect 56 0.041
227
KRT002 Keratomalacia 54 0.041
228
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.041
229
URN009 Urinary System Disease 53 0.041
230
ART002 Arts Syndrome 53 0.041
231
BRN071 Brain Injury 52 0.041
232
P PNC001 Pancytopenia 52 0.041
233
P URF003 Urofacial Syndrome 1 52 0.041
234
P PRM006 Primary Biliary Cirrhosis 52 0.041
235
MYM001 Myoma 51 0.041
236
GNR004 Generalized Anxiety Disorder 51 0.041
237
NNT012 Neonatal Jaundice 51 0.041
238
SCT005 Scott Syndrome 50 0.041
239
PRP021 Peripheral Nervous System Neoplasm 50 0.041
240
HRT007 Heart Cancer 50 0.041
241
PMP001 Pemphigus 49 0.041
242
ADR012 Adrenal Gland Disease 49 0.041
243
MLL012 Miller Syndrome 49 0.041
244
SCK005 Sickle Cell Disease 49 0.041
245
P CMP008 Compartment Syndrome 48 0.041
246
PLN006 Poland Syndrome 48 0.041
247
CRS005 Crest Syndrome 47 0.041
248
ASP007 Aspiration Pneumonia 46 0.041
249
P END047 Endophthalmitis 46 0.041
250
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.041
251
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.041
252
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.041
253
OCL069 Ocular Motor Apraxia 44 0.041
254
P PMP005 Pemphigus Vulgaris 43 0.041
255
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.041
256
PNM013 Pneumococcal Meningitis 41 0.041
257
WTH001 Withdrawal Disorder 41 0.041
258
ACT088 Acute Insulin Response 39 0.041
259
FNS001 Funisitis 38 0.041
260
STR002 Streptococcal Meningitis 38 0.041
261
PLC008 Placenta Disease 36 0.041
262
ACL001 Acalculous Cholecystitis 36 0.041
263
P HRT017 Heart Tumor 35 0.041
264
VTM003 Vitamin Metabolic Disorder 33 0.041
265
P END046 Endometritis 32 0.041
266
P TRN016 Transient Hypogammaglobulinemia 32 0.041
267
MYC014 Mycobacterium Chelonae 32 0.041
268
c INF002 Inflammatory Diarrhea 31 0.041
269
MYS004 Myiasis 31 0.041
270
PDT040 Pediatric Hypertension 31 0.041
271
MRG013 Mirage Syndrome 26 0.041
272
FWL001 Fowler's Syndrome 25 0.041
273
c INF086 Inflammatory Bowel Disease 3 21 0.041
274
c CRN175 Coronary Heart Disease 4 21 0.041
275
c CRN173 Coronary Heart Disease 8 20 0.041
276
c ADL079 Adult Heart Tumor 19 0.041
277
ATR076 Atrophic Muscular Disease 18 0.041
278
GRP002 Group B Strep Disease in Newborns 9 0.041
279
CYS001 Cystic Fibrosis 86 0.033
280
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.033
281
P MLT019 Multiple Myeloma 80 0.033
282
P PLM037 Pulmonary Hypertension 79 0.033
283
CRH001 Crohn's Disease 76 0.033
284
P WSK001 Wiskott-Aldrich Syndrome 72 0.033
285
WLS001 Wilson Disease 72 0.033
286
CNT098 Central Core Disease 66 0.033
287
OBS061 Obstructive Sleep Apnea 66 0.033
288
CHR012 Chronic Granulomatous Disease 65 0.033
289
P HYP086 Hypothyroidism 65 0.033
290
P HRP006 Herpes Simplex 65 0.033
291
P ATR011 Atrial Fibrillation 64 0.033
292
P PLR004 Pleuropulmonary Blastoma 64 0.033
293
HMT002 Hematologic Cancer 64 0.033
294
CRD119 Cardiac Arrest 63 0.033
295
P ESP024 Esophagitis 62 0.033
296
FCT007 Factor Vii Deficiency 62 0.033
297
TTN003 Tetanus 61 0.033
298
OMN001 Omenn Syndrome 61 0.033
299
MNK001 Menkes Disease 61 0.033
300
P SLP006 Sleep Apnea 61 0.033
301
P NPH009 Nephrolithiasis 60 0.033
302
P ASP006 Aspergillosis 60 0.033
303
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.033
304
P LYM026 Lymphoblastic Leukemia 60 0.033
305
P GST049 Gastrointestinal System Cancer 60 0.033
306
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.033
307
CNT097 Central Hypoventilation Syndrome, Congenital 60 0.033
308
APP008 Appendicitis 60 0.033
309
P NRP001 Neuropathy 60 0.033
310
c EXD008 Exudative Vitreoretinopathy 1 60 0.033
311
P ALC004 Alcohol Abuse 60 0.033
312
PLM033 Pulmonary Embolism 59 0.033
313
c CNT035 Central Nervous System Disease 59 0.033
314
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.033
315
P HRS035 Hirschsprung Disease 1 59 0.033
316
c HPT003 Hepatitis a 59 0.033
317
LGN002 Legionellosis 59 0.033
318
STT001 Status Epilepticus 59 0.033
319
PST028 Post-Traumatic Stress Disorder 57 0.033
320
ANR040 Aneurysm 57 0.033
321
RTN018 Retinal Disease 56 0.033
322
PRS047 Prostatitis 56 0.033
323
EXT034 Extrinsic Allergic Alveolitis 56 0.033
324
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.033
325
CRT016 Carotid Artery Disease 55 0.033
326
CHL014 Cholera 55 0.033
327
CHN016 Cohen Syndrome 55 0.033
328
LST001 Listeriosis 54 0.033
329
P ECL001 Eclampsia 54 0.033
330
P THY032 Thyroiditis 54 0.033
331
P PRP019 Peripheral Nervous System Disease 54 0.033
332
P MYC008 Myocarditis 54 0.033
333
P HRD011 Hereditary Spherocytosis 53 0.033
334
SHG001 Shigellosis 53 0.033
335
CNG008 Congenital Ichthyosiform Erythroderma 53 0.033
336
PLV003 Pelvic Inflammatory Disease 53 0.033
337
TRM010 Traumatic Brain Injury 52 0.033
338
ANK001 Ankylosis 52 0.033
339
P LCT001 Lactic Acidosis 52 0.033
340
P PTN002 Patent Ductus Arteriosus 52 0.033
341
QDR001 Quadriplegia 52 0.033
342
P NNT009 Neonatal Diabetes Mellitus 52 0.033
343
MSC072 Muscle Cancer 51 0.033
344
ASP003 Aseptic Meningitis 51 0.033
345
DRG011 Drug Addiction 51 0.033
346
MRC001 Marchiafava Bignami Disease 50 0.033
347
HYP542 Hypersensitivity Syndrome, Carbamazepine-Induced 50 0.033
348
PRC012 Pericardial Effusion 50 0.033
349
PRN021 Paranasal Sinus Disease 50 0.033
350
INF034 Infective Endocarditis 50 0.033
351
STR008 Strongyloidiasis 50 0.033
352
MGC001 Megacolon 50 0.033
353
CYS008 Cystic Echinococcosis 50 0.033
354
BCL002 B Cell Deficiency 50 0.033
355
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.033
356
RTC002 Reticular Dysgenesis 49 0.033
357
PRT018 Portal Vein Thrombosis 49 0.033
358
P SHR001 Short Bowel Syndrome 48 0.033
359
ALC009 Alcoholic Liver Cirrhosis 48 0.033
360
c CLL013 Cell Type Cancer 48 0.033
361
PLS009 Plasma Cell Neoplasm 48 0.033
362
CHL061 Childhood Leukemia 48 0.033
363
c INV001 Invasive Aspergillosis 47 0.033
364
BCT004 Bacteriuria 47 0.033
365
SXL003 Sexual Disorder 47 0.033
366
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.033
367
P SCL009 Sclerosing Cholangitis 47 0.033
368
HYD005 Hydrocele 47 0.033
369
ATN002 Autonomic Nervous System Disease 47 0.033
370
P KRN004 Kernicterus 46 0.033
371
ANR004 Anuria 46 0.033
372
MYL013 Myeloperoxidase Deficiency 46 0.033
373
SNS023 Sensory System Cancer 46 0.033
374
ADN027 Adenomyosis 46 0.033
375
SCB001 Scabies 45 0.033
376
BNC003 Bone Cancer 45 0.033
377
URT010 Ureteral Obstruction 45 0.033
378
FLT011 Felty Syndrome 45 0.033
379
AYM001 Ayme-Gripp Syndrome 45 0.033
380
DSM003 Desmoid Disease, Hereditary 44 0.033
381
PHY002 Physical Disorder 44 0.033
382
P CPL003 Capillary Leak Syndrome 43 0.033
383
SYS003 Systolic Heart Failure 43 0.033
384
LMY002 Leiomyoma 42 0.033
385
c PRM225 Primary Thrombocytopenia 42 0.033
386
VGN023 Vaginitis 42 0.033
387
OCL010 Ocular Hypotension 42 0.033
388
NSL022 Nasal Cavity Disease 42 0.033
389
MDS022 Mediastinitis 41 0.033
390
STR077 Streptococcal Toxic-Shock Syndrome 41 0.033
391
CRS001 Crescentic Glomerulonephritis 41 0.033
392
URT001 Urethritis 40 0.033
393
ACT084 Acute Stress Disorder 40 0.033
394
INH001 Inhalation Anthrax 39 0.033
395
GRN009 Granulomatous Hepatitis 38 0.033
396
ADJ001 Adjustment Disorder 38 0.033
397
MTC005 Mitochondrial Metabolism Disease 38 0.033
398
c TRN009 Transient Hypogammaglobulinemia of Infancy 37 0.033
399
ALR002 Al-Raqad Syndrome 36 0.033
400
c CNG413 Congenital Short Bowel Syndrome 36 0.033
401
LYM014 Lymphangitis 36 0.033
402
SPL006 Splenic Infarction 35 0.033
403
LMB010 Lambert Syndrome 35 0.033
404
BLL012 Bullous Impetigo 35 0.033
405
MTH039 Methylmalonic Aciduria, Mut(0) Type 34 0.033
406
LNG095 Lung Abscess 34 0.033
407
SPP004 Suppurative Cholangitis 33 0.033
408
EMN001 Emanuel Syndrome 33 0.033
409
c ACT036 Acute Cholangitis 32 0.033
410
EPD005 Epidural Abscess 32 0.033
411
c PLN021 Peeling Skin Syndrome 3 31 0.033
412
c AST039 Asthma 2 31 0.033
413
NRW001 Norwegian Scabies 30 0.033
414
WDS002 Woods Syndrome 30 0.033
415
AGM004 Agammaglobulinemia, Non-Bruton Type 30 0.033
416
EPD040 Epidermolysis Bullosa Simplex with Pyloric Atresia 29 0.033
417
c MLT068 Multiple Mitochondrial Dysfunctions Syndrome 1 28 0.033
418
ORB006 Orbital Cellulitis 28 0.033
419
c INF087 Inflammatory Bowel Disease 4 27 0.033
420
SNT004 Sinoatrial Node Dysfunction and Deafness 27 0.033
421
c MLT069 Multiple Mitochondrial Dysfunctions Syndrome 2 26 0.033
422
ASP026 Asplenia, Isolated Congenital 24 0.033
423
VBR003 Vibrio Vulnificus Infection 23 0.033
424
c MLT139 Multiple Mitochondrial Dysfunctions Syndrome 4 22 0.033
425
MND006 Mondor Disease 21 0.033
426
c INF075 Inflammatory Bowel Disease 16 20 0.033
427
c INF083 Inflammatory Bowel Disease 24 19 0.033
428
BNM008 Bone Mineral Density, Low 19 0.033
429
ADS015 Aids Wasting Syndrome 18 0.033
430
c BLR024 Biliary Cirrhosis, Primary, 1 18 0.033
431
LDW001 Ludwig's Angina 17 0.033
432
CGL001 Coagulation Protein Disease 16 0.033
433
ISL085 Isolated Agammaglobulinemia 15 0.033
434
DSS023 Disease_ontology 11 0.033
435
CMB055 Combined Immunodeficiency Due to Crac Channel Dysfunction 11 0.033
436
PRS125 Pura Syndrome 8 0.033
437
IDP055 Idiopathic Severe Pneumococcemia 3 0.033
438
P BRS047 Breast Cancer 100 0.024
439
P CLR023 Colorectal Cancer 97 0.024
440
P PNC035 Pancreatic Cancer 85 0.024
441
HV1006 Hiv-1 82 0.024
442
P RNL014 Renal Cell Carcinoma 81 0.024
443
P CRN211 Coronary Artery Disease 75 0.024
444
ULC004 Ulcerative Colitis 75 0.024
445
INS024 Insulin-Like Growth Factor I 74 0.024
446
c CHR090 Chronic Lymphocytic Leukemia 74 0.024
447
MYL009 Myelodysplastic Syndrome 74 0.024
448
P APL001 Aplastic Anemia 73 0.024
449
HDG012 Hodgkin Lymphoma 73 0.024
450
c LKM061 Leukemia, Acute Myeloid 71 0.024
451
P PHC003 Pheochromocytoma 71 0.024
452
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 0.024
453
MNT001 Mantle Cell Lymphoma 70 0.024
454
ANX002 Anxiety Disorder 69 0.024
455
SCK003 Sickle Cell Anemia 68 0.024
456
P LPR003 Leprosy 68 0.024
457
ISC006 Ischemic Heart Disease 68 0.024
458
P PLM036 Pulmonary Fibrosis 68 0.024
459
c HPT001 Hepatitis C 68 0.024
460
SVR004 Severe Combined Immunodeficiency 68 0.024
461
ART016 Aortic Aneurysm 67 0.024
462
P MYL006 Myeloid Leukemia 67 0.024
463
P CLC005 Celiac Disease 67 0.024
464
P HYD006 Hydrocephalus 67 0.024
465
MYC006 Mycosis Fungoides 66 0.024
466
ALC007 Alcohol Dependence 65 0.024
467
LKC001 Leukocyte Adhesion Deficiency 65 0.024
468
BRC012 Brucellosis 65 0.024
469
c HPT016 Hepatitis B 64 0.024
470
P AMY004 Amyloidosis 64 0.024
471
CHR103 Charge Syndrome 64 0.024
472
P ALX003 Alexander Disease 64 0.024
473
PTR006 Peters Anomaly 64 0.024
474
P CSH001 Cushing's Syndrome 64 0.024
475
ATP002 Atopy 63 0.024
476
P ANR007 Anorexia Nervosa 63 0.024
477
SPN186 Spinal Cord Injury 62 0.024
478
LSH001 Leishmaniasis 62 0.024
479
VSC011 Vasculitis 62 0.024
480
OCL009 Ocular Cancer 62 0.024
481
GST092 Gastroesophageal Reflux 61 0.024
482
PRM097 Primary Immunodeficiency Disease 61 0.024
483
P ESN007 Eosinophilia 61 0.024
484
DRM006 Dermatitis 61 0.024
485
P ENC004 Encephalitis 61 0.024
486
P THL005 Thalassemia 61 0.024
487
TNG002 Tangier Disease 61 0.024
488
P TXP001 Toxoplasmosis 60 0.024
489
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.024
490
OVR029 Ovarian Hyperstimulation Syndrome 60 0.024
491
P SNS014 Sinusitis 60 0.024
492
HRY003 Hairy Cell Leukemia 60 0.024
493
c ATM010 Autoimmune Hemolytic Anemia 60 0.024
494
P CRN139 Cornelia De Lange Syndrome 1 60 0.024
495
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.024
496
P PRT013 Portal Hypertension 59 0.024
497
P MTR012 Mitral Valve Disease 59 0.024
498
c FML001 Familial Atrial Fibrillation 59 0.024
499
DBT087 Diabetes Insipidus, Neurohypophyseal 59 0.024
500
P CNG015 Congenital Diaphragmatic Hernia 58 0.024
501
CMM005 Common Cold 58 0.024
502
P GST044 Gastritis 58 0.024
503
P ANP001 Anaplastic Large Cell Lymphoma 58 0.024
504
ART017 Aortic Disease 58 0.024
505
BLL006 Bullous Pemphigoid 58 0.024
506
P ORL007 Oral Cavity Cancer 58 0.024
507
PNC034 Pancreas Disease 57 0.024
508
P EXN002 Exanthem 57 0.024
509
P SZR006 Seizure Disorder 57 0.024
510
BTN003 Biotinidase Deficiency 56 0.024
511
STR026 Star Syndrome 56 0.024
512
SPT005 Spotted Fever 56 0.024
513
SBS003 Substance Abuse 56 0.024
514
HPT019 Hepatic Encephalopathy 56 0.024
515
SFT003 Soft Tissue Sarcoma 56 0.024
516
P TMT001 Timothy Syndrome 56 0.024
517
P HYP076 Hyperthyroidism 56 0.024
518
P MMB011 Membranous Nephropathy 56 0.024
519
ORL011 Oral Cancer 55 0.024
520
DBT010 Diabetic Neuropathy 55 0.024
521
c PND001 Pain Disorder 55 0.024
522
P HST010 Histiocytosis 55 0.024
523
P HMR012 Hemorrhagic Fever 55 0.024
524
PLS007 Plasmodium Falciparum Malaria 54 0.024
525
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.024
526
NWC001 Newcastle Disease 54 0.024
527
VSC006 Vascular Cancer 54 0.024
528
VRR004 Verrucous Carcinoma 53 0.024
529
LYM019 Lymphosarcoma 53 0.024
530
ECH003 Echinococcosis 53 0.024
531
P SYP003 Syphilis 53 0.024
532
P DBT005 Diabetes Insipidus 53 0.024
533
PLS006 Plasmodium Vivax Malaria 53 0.024
534
ATR060 Atrial Standstill, Digenic 53 0.024
535
P GND004 Gonadal Dysgenesis 53 0.024
536
BNM001 Bone Marrow Cancer 52 0.024
537
NTH001 Netherton Syndrome 52 0.024
538
PRT014 Protein S Deficiency 52 0.024
539
P HYP083 Hypopituitarism 52 0.024
540
NCT008 Nicotine Dependence, Protection Against 52 0.024
541
PLR022 Pleural Disease 52 0.024
542
PRC013 Pericarditis 52 0.024
543
ALV002 Alveolar Echinococcosis 51 0.024
544
BLR001 Biliary Atresia 51 0.024
545
MCN007 Meconium Aspiration Syndrome 51 0.024
546
P LRS001 Larsen Syndrome 51 0.024
547
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.024
548
CYT008 Cytomegalovirus Infection 51 0.024
549
VSC044 Visceral Myopathy 51 0.024
550
MYC002 Mycobacterium Avium Complex Disease 51 0.024
551
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 51 0.024
552
LRN003 Learning Disability 51 0.024
553
OPT006 Optic Nerve Disease 51 0.024
554
BLD044 Bladder Disease 51 0.024
555
PTH002 Pathological Gambling 51 0.024
556
NTR040 Neutropenia, Cyclic 50 0.024
557
c VRL012 Viral Meningitis 50 0.024
558
INT051 Intussusception 50 0.024
559
URM002 Uremia 50 0.024
560
P HML001 Hemolytic-Uremic Syndrome 50 0.024
561
P SCK002 Sick Sinus Syndrome 50 0.024
562
PRV006 Pervasive Developmental Disorder 50 0.024
563
PRP016 Paraplegia 49 0.024
564
END031 Endometrial Stromal Sarcoma 49 0.024
565
SRT004 Serotonin Syndrome 49 0.024
566
HMN014 Human Immunodeficiency Virus Infectious Disease 49 0.024
567
P EPD002 Epidermolytic Hyperkeratosis 49 0.024
568
HMG002 Hemoglobinuria 49 0.024
569
PRT038 Protein-Energy Malnutrition 49 0.024
570
HLL004 Hellp Syndrome 49 0.024
571
PLG002 Plague 49 0.024
572
P LFT003 Left Ventricular Noncompaction 49 0.024
573
ICH054 Ichthyosis, X-Linked 48 0.024
574
GRW007 Growth Hormone Deficiency 48 0.024
575
PTT009 Pituitary Gland Disease 48 0.024
576
FML039 Female Reproductive System Disease 48 0.024
577
ACR003 Acrodermatitis Enteropathica 48 0.024
578
c SVR005 Severe Pre-Eclampsia 48 0.024
579
MTN003 Motion Sickness 48 0.024
580
P HMR005 Hemorrhoid 48 0.024
581
c XNT010 Xanthinuria, Type I 48 0.024
582
BNF002 Bone Fracture 47 0.024
583
HYD002 Hydronephrosis 47 0.024
584
CRB025 Carbohydrate Metabolic Disorder 47 0.024
585
URT031 Ureteral Disease 47 0.024
586
CRD118 Cardiovascular Cancer 47 0.024
587
PLC007 Placental Abruption 47 0.024
588
BLR008 Bilirubin Metabolic Disorder 47 0.024
589
PSD007 Pseudomyxoma Peritonei 47 0.024
590
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 47 0.024
591
RNL077 Renal Fibrosis 47 0.024
592
PRT082 Preterm Premature Rupture of the Membranes 47 0.024
593
P BRN120 Bronchus Cancer 46 0.024
594
RLP003 Relapsing Fever 46 0.024
595
SPC010 Speech and Communication Disorders 46 0.024
596
RPR002 Reproductive System Disease 46 0.024
597
TWN001 Twin-to-Twin Transfusion Syndrome 46 0.024
598
CHR074 Choriocarcinoma 46 0.024
599
P TRC086 Trichohepatoenteric Syndrome 1 46 0.024
600
HDR003 Hidradenitis 46 0.024
601
DNT012 Dental Caries 46 0.024
602
HYP025 Hyperphosphatemia 46 0.024
603
DST006 Diastolic Heart Failure 46 0.024
604
c ATM024 Autoimmune Pancreatitis 46 0.024
605
HPR003 Heparin-Induced Thrombocytopenia 46 0.024
606
SKN023 Skin Tag 46 0.024
607
P ANL018 Analbuminemia 46 0.024
608
ALN001 Aland Island Eye Disease 45 0.024
609
SCR002 Scurvy 45 0.024
610
DPH021 Diaphragm Disease 45 0.024
611
VSC047 Vascular Malformation 45 0.024
612
VGN020 Vaginal Disease 45 0.024
613
BRN014 Bronchopneumonia 45 0.024
614
c PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 45 0.024
615
IDP024 Idiopathic Inflammatory Myopathy 45 0.024
616
P MTH007 Methemoglobinemia 45 0.024
617
CRR007 Cirrhosis, Cryptogenic 44 0.024
618
C2D001 C2 Deficiency 44 0.024
619
P SDR002 Siderosis 44 0.024
620
PLR007 Pleural Empyema 44 0.024
621
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.024
622
P CRV039 Cervicitis 44 0.024
623
SPL018 Splenomegaly 44 0.024
624
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.024
625
CRD001 Cardiac Tamponade 44 0.024
626
DXT001 Dextrocardia 44 0.024
627
ATX003 Ataxia with Isolated Vitamin E Deficiency 44 0.024
628
P DMY001 Demyelinating Polyneuropathy 43 0.024
629
P ABD003 Abdominal Aortic Aneurysm 43 0.024
630
MLT001 Multiple Chemical Sensitivity 43 0.024
631
NSS002 Neisseria Meningitidis Infection 43 0.024
632
c CHR064 Chronic Monocytic Leukemia 43 0.024
633
PRM236 Primary Biliary Cholangitis 43 0.024
634
MYC012 Mycetoma 43 0.024
635
CMP004 Complement Factor I Deficiency 43 0.024
636
FCT008 Factitious Disorder 43 0.024
637
CLD007 Cold Agglutinin Disease 43 0.024
638
PLC001 Placenta Accreta 43 0.024
639
RCK002 Rocky Mountain Spotted Fever 43 0.024
640
CLS016 Clostridium Difficile Colitis 42 0.024
641
PRD011 Proud Syndrome 42 0.024
642
THL018 Thalassemia Major 42 0.024
643
CTY001 Cat Eye Syndrome 42 0.024
644
MLR002 Miliary Tuberculosis 42 0.024
645
PRT026 Parotitis 42 0.024
646
HPT008 Hepatic Tuberculosis 42 0.024
647
BCK006 Back Pain 42 0.024
648
IMM127 Immune System Cancer 42 0.024
649
c VRL005 Viral Pneumonia 42 0.024
650
CNV002 Conversion Disorder 42 0.024
651
TLR001 Tularemia 42 0.024
652
BND014 Bone Development Disease 42 0.024
653
PLS016 Plasma Cell Leukemia 42 0.024
654
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.024
655
ACT055 Actinomycosis 41 0.024
656
CHR078 Chorioretinitis 41 0.024
657
GST078 Gastrointestinal Allergy 41 0.024
658
HYP458 Hyper Ige Syndrome 41 0.024
659
TBR008 Tuberculous Peritonitis 41 0.024
660
SKL003 Skeletal Muscle Cancer 41 0.024
661
PNC085 Penicillin Allergy 41 0.024
662
c SCN006 Secondary Syphilis 41 0.024
663
c ADL001 Adult Lymphoma 41 0.024
664
P ACQ009 Acquired Metabolic Disease 41 0.024
665
EHR002 Ehrlichiosis 41 0.024
666
ADR009 Adrenal Cortex Disease 41 0.024
667
MYS001 Myositis Ossificans 41 0.024
668
MNR003 Mineral Metabolism Disease 41 0.024
669
NM001 Noma 41 0.024
670
PCH007 Pouchitis 40 0.024
671
ERY004 Erysipelas 40 0.024
672
MYC013 Mycobacterium Abscessus 40 0.024
673
ISC015 Ischemic Colitis 40 0.024
674
ACT167 Acute Generalized Exanthematous Pustulosis 40 0.024
675
BRB001 Beriberi 40 0.024
676
SXD001 Sex Differentiation Disease 40 0.024
677
CHL052 Choledochal Cyst 40 0.024
678
c PNC106 Pancreatic Agenesis 1 40 0.024
679
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.024
680
P UTR038 Uterine Disease 40 0.024
681
RDN001 Reading Disorder 39 0.024
682
c CNG031 Congenital Nervous System Abnormality 39 0.024
683
P HYP265 Hypotonia 39 0.024
684
TXC020 Toxic Oil Syndrome 39 0.024
685
CLD014 Cole Disease 39 0.024
686
P OCY001 Oocyte Maturation Defect 39 0.024
687
HYP391 Hyperammonemia 39 0.024
688
EST003 Eastern Equine Encephalitis 39 0.024
689
ILC002 Ileocolitis 38 0.024
690
ABD010 Abdominal Wall Defect 38 0.024
691
MNN032 Meningococcal Meningitis 38 0.024
692
ETH004 Euthyroid Sick Syndrome 38 0.024
693
PLS010 Plasma Protein Metabolism Disease 38 0.024
694
ATM012 Autoimmune Disease of Blood 37 0.024
695
PRP056 Porphyria, Acute Hepatic 37 0.024
696
BBN001 Bubonic Plague 37 0.024
697
PLM013 Pulmonary Immaturity 37 0.024
698
INF013 Inferior Myocardial Infarction 37 0.024
699
c THR037 Thrombocytopenia 2 37 0.024
700
BNS002 Bone Structure Disease 36 0.024
701
PRS023 Pearson Syndrome 36 0.024
702
c SCN052 Secondary Adrenal Insufficiency 36 0.024
703
URT014 Ureterolithiasis 36 0.024
704
ACR002 Acrocapitofemoral Dysplasia 36 0.024
705
TXC007 Toxic Pneumonitis 36 0.024
706
MNK002 Monkeypox 36 0.024
707
ANG049 Angioedema Induced by Ace Inhibitors 35 0.024
708
GLS018 Glass Syndrome 35 0.024
709
GLB003 Globe Disease 35 0.024
710
CCN007 Cocoon Syndrome 35 0.024
711
c ICH041 Ichthyosis, Autosomal Recessive 4b 35 0.024
712
c ACT081 Acute Salpingitis 35 0.024
713
FST001 Foster-Kennedy Syndrome 34 0.024
714
VRS001 Virus Associated Hemophagocytic Syndrome 34 0.024
715
CHR028 Chronic Wasting Disease 34 0.024
716
ANG037 Angiomatosis 34 0.024
717
ACR005 Acrodermatitis 34 0.024
718
FHR001 Fuhrmann Syndrome 34 0.024
719
FRN014 Fournier Gangrene 34 0.024
720
CHL039 Choledocholithiasis 34 0.024
721
BLK001 Balkan Nephropathy 33 0.024
722
BRS102 Breast Abscess 33 0.024
723
c CHL119 Cholangitis, Primary Sclerosing 33 0.024
724
FSR001 Fusariosis 33 0.024
725
IRS003 Iris Disease 32 0.024
726
SPR035 Superior Vena Cava Syndrome 32 0.024
727
P SLP003 Salpingitis 32 0.024
728
GST020 Gastric Antral Vascular Ectasia 32 0.024
729
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 32 0.024
730
c VRL017 Viral Hemorrhagic Fever 32 0.024
731
ART012 Aortitis 31 0.024
732
c TRC078 Trichohepatoenteric Syndrome 2 31 0.024
733
CYT002 Cytokine Deficiency 31 0.024
734
PNM003 Pneumatosis Cystoides Intestinalis 31 0.024
735
IMM082 Immunodeficiency 18 31 0.024
736
CCL002 Cecal Disease 31 0.024
737
RMN002 Ramon Syndrome 31 0.024
738
c AST037 Asthma 1 31 0.024
739
NTR042 Neutrophilic Dermatosis, Acute Febrile 30 0.024
740
IMM064 Immunodeficiency, Common Variable, 10 30 0.024
741
XNT001 Xanthogranulomatous Pyelonephritis 30 0.024
742
HYP084 Hypopyon 30 0.024
743
ACT114 Acute Myeloblastic Leukemia Without Maturation 30 0.024
744
NSP003 Nasopharyngeal Disease 30 0.024
745
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 29 0.024
746
c THR048 Thrombocytopenia 4 29 0.024
747
WTS001 Watson Syndrome 29 0.024
748
HNS001 Hansen's Disease 29 0.024
749
ACT118 Acute Non Lymphoblastic Leukemia 29 0.024
750
c MYC058 Myocardial Infarction 2 29 0.024
751
c SCK017 Sick Sinus Syndrome 1 29 0.024
752
c PNC094 Pancreatic Cancer 1 29 0.024
753
SPL009 Splenic Sequestration 28 0.024
754
c NTR039 Neutropenia, Severe Congenital 4, Autosomal Recessive 28 0.024
755
TXC001 Toxic Megacolon 28 0.024
756
ATM052 Autoimmune Disease 1 28 0.024
757
HST007 Histidine Metabolism Disease 28 0.024
758
GST095 Gastritis, Familial Giant Hypertrophic 27 0.024
759
ILM001 Ileum Cancer 27 0.024
760
IMM076 Immunodeficiency 24 27 0.024
761
c SCK014 Sick Sinus Syndrome 2 27 0.024
762
CMP041 Complement Factor D Deficiency 27 0.024
763
PLM124 Pulmonary Hypertension, Neonatal 27 0.024
764
c CHR036 Chronic Cholangitis 27 0.024
765
MYC015 Mycobacterium Fortuitum 27 0.024
766
3MT013 3-Methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome 27 0.024
767
DSC004 Discitis 27 0.024
768
ENT007 Enteropathica 26 0.024
769
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.024
770
ATM059 Autoimmune Disease 6 26 0.024
771
OPP001 Opportunistic Bacterial Infectious Disease 25 0.024
772
MND023 Mend Syndrome 24 0.024
773
GST046 Gastrointestinal Anthrax 23 0.024
774
c INF093 Inflammatory Bowel Disease 14 23 0.024
775
c SCK022 Sick Sinus Syndrome 3 22 0.024
776
PRC021 Parc Syndrome 22 0.024
777
VSC009 Vascular Skin Disease 22 0.024
778
INT062 Interstitial Myocarditis 22 0.024
779
c THR110 Thrombocytopenia 6 22 0.024
780
KLB004 Klebsiella Infection 22 0.024
781
c CRN174 Coronary Heart Disease 2 22 0.024
782
P GNR027 Generalized Peeling Skin Syndrome 22 0.024
783
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.024
784
PRL018 Purulent Endophthalmitis 21 0.024
785
CML001 Cumulative Trauma Disorders 21 0.024
786
ACT228 Acute Radiation Syndrome 21 0.024
787
c CRN172 Coronary Heart Disease 3 21 0.024
788
c INF088 Inflammatory Bowel Disease 5 21 0.024
789
PRT110 Prieto Syndrome 21 0.024
790
PNT023 Pontine Hemorrhage 20 0.024
791
CRT057 Critical Congenital Heart Disease 20 0.024
792
WND002 Wandering Spleen 20 0.024
793
c INF079 Inflammatory Bowel Disease 20 20 0.024
794
c CRN176 Coronary Heart Disease 9 20 0.024
795
ZNC006 Zinc, Elevated Plasma 20 0.024
796
MLL015 Mills Syndrome 19 0.024
797
c INF090 Inflammatory Bowel Disease 7 19 0.024
798
NCR014 Necrotizing Soft Tissue Infection 19 0.024
799
ANT040 Anton's Syndrome 19 0.024
800
GLC077 Glucocorticoid Therapy, Response to 19 0.024
801
IMM103 Immunodeficiency 37 19 0.024
802
LYM126 Lymphoma Aids Related 18 0.024
803
ATM055 Autoimmune Disease 4 18 0.024
804
WHT007 White Platelet Syndrome 18 0.024
805
IMM118 Immunodeficiency 42 18 0.024
806
P STR035 Streptococcal Group a Invasive Disease 18 0.024
807
c UTR006 Uterine Inflammatory Disease 18 0.024
808
STR033 Storm Syndrome 18 0.024
809
STT044 Statin Toxicity 17 0.024
810
MYC003 Myocardium Cancer 17 0.024
811
CHT005 Chitotriosidase Deficiency 17 0.024
812
P MYC054 Mycobacterium Tuberculosis 2 17 0.024
813
c BLR017 Biliary Cirrhosis, Primary, 3 16 0.024
814
PST037 Pasteurella Multocida Infection 16 0.024
815
NVD002 Nevada Syndrome 16 0.024
816
INB001 Inborn Amino Acid Metabolism Disorder 15 0.024
817
MGC006 Magic Syndrome 15 0.024
818
c BLR026 Biliary Cirrhosis, Primary, 5 15 0.024
819
ORL014 Oral Pharyngeal Disorders 14 0.024
820
BDS001 Bd Syndrome 14 0.024
821
MLR020 Malaria, Mild 14 0.024
822
AMN012 Aminoacidopathies 14 0.024
823
ACQ011 Acquired Agranulocytosis 14 0.024
824
NGY001 Nguyen Syndrome 13 0.024
825
RCT033 Rectal Duplication 12 0.024
826
c ACQ039 Acquired Purpura Fulminans 12 0.024
827
TSY001 Tau Syndrome 12 0.024
828
BLT017 Bilateral Massive Adrenal Hemorrhage 11 0.024
829
P ANT062 Anterior Urethral Valve 11 0.024
830
RDR001 Radio Renal Syndrome 10 0.024
831
c STR036 Streptococcal Group B Invasive Disease 9 0.024
832
INV015 Invasive Non-Typhoidal Salmonellosis 7 0.024