Search results for "sepsis"

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

880 hits were found for 'sepsis'

# Family MCID Name MIFTS Score
1
LMR001 Lemierre's Syndrome 43 4.734
2
SPS090 Sepsis in Premature Infants 21 2.922
3
TXC005 Toxic Shock Syndrome 60 0.335
4
DSS009 Disseminated Intravascular Coagulation 51 0.214
5
c RNL016 Renal Infectious Disease 20 0.201
6
P PNM007 Pneumonia 68 0.200
7
CSY001 C Syndrome 50 0.193
8
PRM025 Primary Bacterial Infectious Disease 41 0.186
9
END072 Endotheliitis 42 0.166
10
PRP030 Purpura 58 0.155
11
c ACT210 Acute Respiratory Distress Syndrome 57 0.148
12
BCT015 Bacteremia 48 0.148
13
P PRP034 Purpura Fulminans 41 0.148
14
CHL071 Child Syndrome 58 0.146
15
KDS001 Kid Syndrome 53 0.146
16
BRN106 Burns 52 0.146
17
GDS001 Good Syndrome 44 0.146
18
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.144
19
P MNN013 Meningitis 67 0.142
20
WLL006 Wells Syndrome 59 0.142
21
P ADL010 Adult Respiratory Distress Syndrome 61 0.138
22
P HPT021 Hepatitis 69 0.134
23
PRT036 Peritonitis 63 0.128
24
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.128
25
P NTR004 Neutropenia 59 0.122
26
P RSP003 Respiratory Failure 71 0.117
27
c ACT071 Acute Kidney Failure 49 0.117
28
NSY001 N Syndrome 36 0.117
29
RSP006 Respiratory System Disease 58 0.115
30
CHR005 Chorioamnionitis 48 0.115
31
WST001 West Syndrome 57 0.113
32
P PLY019 Polyneuropathy 56 0.108
33
ADM013 Adamantinoma of Long Bones 57 0.106
34
MLD001 Melioidosis 67 0.100
35
P BLD051 Blood Coagulation Disease 42 0.100
36
OLV001 Olivopontocerebellar Atrophy 53 0.098
37
LKC003 Leukocyte Disease 43 0.098
38
CRT009 Critical Illness Polyneuropathy 40 0.098
39
ISC004 Ischemia 61 0.095
40
P PNC044 Pancreatitis 61 0.095
41
ADL002 Adult Syndrome 52 0.092
42
c SVR001 Severe Acute Respiratory Syndrome 57 0.089
43
BLD054 Blood Protein Disease 37 0.089
44
VSC008 Vascular Hemostatic Disease 30 0.089
45
c ADL080 Adult Acute Respiratory Distress Syndrome 19 0.089
46
P LKM002 Leukemia 71 0.086
47
HYP066 Hyperglycemia 61 0.086
48
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.086
49
ECT004 Ecthyma 35 0.086
50
IMP003 Impaired Renal Function Disease 34 0.086
51
P ART022 Arthritis 75 0.083
52
P THR014 Thrombocytopenia 64 0.083
53
THR024 Thrombosis 57 0.083
54
HYP266 Hypoxia 56 0.083
55
NWB001 Newborn Respiratory Distress Syndrome 45 0.083
56
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 40 0.083
57
RSP007 Respiratory Distress Syndrome, Infant 22 0.083
58
P LVR013 Liver Disease 75 0.080
59
LVR012 Liver Cirrhosis 67 0.080
60
P KDN018 Kidney Disease 66 0.080
61
P INF037 Inflammatory Bowel Disease 63 0.080
62
P ENC018 Encephalopathy 59 0.080
63
EXF001 Exfoliation Syndrome 57 0.080
64
P PLN008 Peeling Skin Syndrome 45 0.080
65
MLR004 Malaria 83 0.076
66
P INF038 Influenza 72 0.076
67
ACT017 Acute Chest Syndrome 48 0.076
68
c HYP595 Hypertension, Essential 69 0.073
69
P MYP004 Myopathy 67 0.073
70
MCR225 Macrophage Activation Syndrome 41 0.073
71
NTR005 Nutritional Deficiency Disease 36 0.073
72
NVS004 Nova Syndrome 13 0.073
73
P AST005 Asthma 82 0.069
74
PRP027 Peripheral Vascular Disease 69 0.069
75
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.069
76
C3D001 C3 Deficiency 53 0.069
77
CLL003 Cellulitis 51 0.069
78
INT007 Intermediate Coronary Syndrome 50 0.069
79
VND001 Vein Disease 47 0.069
80
BLD053 Blood Platelet Disease 46 0.069
81
GRN017 Granulocytopenia 44 0.069
82
RNL097 Renal Artery Disease 43 0.069
83
HYP017 Hypophosphatemia 43 0.069
84
PRN019 Perinatal Necrotizing Enterocolitis 42 0.069
85
GLC006 Galactosemia 64 0.065
86
P THR015 Thrombophilia 59 0.065
87
P SHR029 Short Syndrome 58 0.065
88
LYM027 Lymphopenia 56 0.065
89
c BCT007 Bacterial Meningitis 54 0.065
90
P MTC069 Mitochondrial Disorders 53 0.065
91
P SPS003 Spastic Diplegia 52 0.065
92
IMM136 Immune System Disease 51 0.065
93
MTB004 Metabolic Acidosis 48 0.065
94
CRB009 Cerebritis 39 0.065
95
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.065
96
NNT021 Neonatal Meningitis 28 0.065
97
GRM003 German Syndrome 22 0.065
98
P HRT032 Heart Disease 75 0.061
99
c CHR089 Chronic Kidney Failure 66 0.061
100
SPT004 Septic Arthritis 60 0.061
101
GST045 Gastroenteritis 59 0.061
102
P HMR003 Hemorrhagic Disease 57 0.061
103
END030 End Stage Renal Failure 55 0.061
104
PLM010 Pulmonary Edema 54 0.061
105
P PYL005 Pyelonephritis 52 0.061
106
PRT011 Protein C Deficiency 52 0.061
107
INT071 Intestinal Perforation 42 0.061
108
c PLN018 Peeling Skin Syndrome 2 40 0.061
109
PYM001 Pyomyositis 40 0.061
110
SPC003 Specific Developmental Disorder 38 0.061
111
SPL007 Splenic Abscess 30 0.061
112
TBR010 Tuberculosis 70 0.056
113
PCK002 Pick Disease 68 0.056
114
DWN001 Down Syndrome 66 0.056
115
P KDN017 Kidney Cancer 65 0.056
116
HYP056 Hypoglycemia 61 0.056
117
OST017 Osteomyelitis 61 0.056
118
c ACT027 Acute Pancreatitis 57 0.056
119
THR016 Thrombophlebitis 53 0.056
120
P MSC033 Muscle Disorders 52 0.056
121
c ACT068 Acute Cystitis 50 0.056
122
GSG001 Gas Gangrene 49 0.056
123
MSS002 Mass Syndrome 48 0.056
124
PRV004 Periventricular Leukomalacia 48 0.056
125
MNN009 Meningoencephalitis 47 0.056
126
ANL022 Anal Fistula 43 0.056
127
RSP019 Respiratory Distress Syndrome in Premature Infants 43 0.056
128
LKM006 Leukomalacia 43 0.056
129
P CHL066 Cholangitis 42 0.056
130
PRP080 Peripheral Artery Disease 37 0.056
131
PRM026 Primary Systemic Mycosis 37 0.056
132
c PLN017 Peeling Skin Syndrome 1 34 0.056
133
BRW006 Brown Syndrome 29 0.056
134
GRN016 Grant Syndrome 29 0.056
135
SBC016 Subacute Delirium 24 0.056
136
c CRN177 Coronary Heart Disease 7 20 0.056
137
WSC001 Wisconsin Syndrome 14 0.056
138
P LYM118 Lymphoma 69 0.052
139
P CRD011 Cardiomyopathy 68 0.052
140
WLL001 Williams-Beuren Syndrome 60 0.052
141
P DRR001 Diarrhea 60 0.052
142
P INF032 Infertility 59 0.052
143
LPD008 Lipid Metabolism Disorder 58 0.052
144
CHL067 Cholecystitis 57 0.052
145
P ANT006 Antiphospholipid Syndrome 56 0.052
146
VRL011 Viral Infectious Disease 55 0.052
147
MCS002 Mucositis 55 0.052
148
SLP005 Sleep Disorder 53 0.052
149
ALL026 Allergic Hypersensitivity Disease 52 0.052
150
P MSC003 Muscular Atrophy 50 0.052
151
FSC004 Fasciitis 48 0.052
152
P RNL015 Renal Hypertension 48 0.052
153
AMN002 Amino Acid Metabolic Disorder 47 0.052
154
NCR007 Necrotizing Fasciitis 46 0.052
155
ACR041 Acromelic Frontonasal Dysostosis 45 0.052
156
MNN020 Meningococcal Infection 43 0.052
157
BRT030 Birth Defects 43 0.052
158
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.052
159
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.052
160
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.052
161
TMP012 Temple Syndrome 38 0.052
162
HYP189 Hypoadrenalism 37 0.052
163
VNT001 Ventilation Pneumonitis 35 0.052
164
WRT001 Worth's Syndrome 34 0.052
165
MSC004 Muscle Tissue Disease 34 0.052
166
c INF078 Inflammatory Bowel Disease 2 31 0.052
167
WTR001 Waterhouse-Friderichsen Syndrome 28 0.052
168
SHP003 Shapiro Syndrome 26 0.052
169
c CRN214 Coronary Heart Disease 5 22 0.052
170
BNJ001 Benjamin Syndrome 9 0.052
171
P OBS005 Obesity 92 0.046
172
P RHM011 Rheumatoid Arthritis 89 0.046
173
c SYS001 Systemic Lupus Erythematosus 86 0.046
174
STR067 Stroke, Ischemic 75 0.046
175
P LPS004 Lupus Erythematosus 64 0.046
176
DFC004 Deficiency Anemia 64 0.046
177
LNG099 Lung Disease 64 0.046
178
P INT068 Intestinal Disease 60 0.046
179
RBR001 Roberts Syndrome 60 0.046
180
P GLM007 Glomerulonephritis 59 0.046
181
CHL068 Cholestasis 59 0.046
182
P CND004 Candidiasis 57 0.046
183
P MYS005 Myositis 57 0.046
184
PHR003 Pharyngitis 56 0.046
185
SCR008 Scrub Typhus 55 0.046
186
P END033 Endocarditis 54 0.046
187
SCT005 Scott Syndrome 53 0.046
188
KRT002 Keratomalacia 52 0.046
189
BRN071 Brain Injury 52 0.046
190
c INF071 Inflammatory Bowel Disease 1 51 0.046
191
SCK005 Sickle Cell Disease 51 0.046
192
URN009 Urinary System Disease 50 0.046
193
DRG003 Drug Dependence 50 0.046
194
c ACT134 Acute Liver Failure 50 0.046
195
P URF003 Urofacial Syndrome 1 50 0.046
196
ATN005 Autonomic Dysfunction 49 0.046
197
LPD004 Lipoid Nephrosis 48 0.046
198
ADR012 Adrenal Gland Disease 48 0.046
199
BRN056 Bronchopulmonary Dysplasia 48 0.046
200
UPP004 Upper Respiratory Tract Disease 46 0.046
201
HPT014 Hepatorenal Syndrome 46 0.046
202
CRD137 Cardiogenic Shock 46 0.046
203
c ACT042 Acute Pyelonephritis 45 0.046
204
HMP009 Haemophilus Influenzae 45 0.046
205
ACH037 Achalasia-Addisonianism-Alacrimia Syndrome 45 0.046
206
OCL069 Ocular Motor Apraxia 44 0.046
207
BNN003 Bone Inflammation Disease 44 0.046
208
HMT018 Hematopoietic Stem Cell Transplantation 41 0.046
209
NRN002 Neuronitis 41 0.046
210
MNN021 Meningococcemia 39 0.046
211
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.046
212
CPL005 Capillary Disease 36 0.046
213
ADR010 Adrenal Cortical Hypofunction 36 0.046
214
c PLM022 Pulmonary Valve Insufficiency 34 0.046
215
CND006 Candida Glabrata 34 0.046
216
P ACT080 Acute Pulmonary Heart Disease 31 0.046
217
ADP002 Adiponectin Deficiency 30 0.046
218
P MLT027 Multiple Mitochondrial Dysfunctions Syndrome 27 0.046
219
YNG002 Young Syndrome 26 0.046
220
P CRN178 Coronary Heart Disease 6 21 0.046
221
NLL002 Null Syndrome 20 0.046
222
P LNG032 Lung Cancer 95 0.040
223
P HPT023 Hepatocellular Carcinoma 92 0.040
224
P MYC007 Myocardial Infarction 79 0.040
225
CNG034 Congestive Heart Failure 72 0.040
226
SRC014 Sarcoma 66 0.040
227
P AGM001 Agammaglobulinemia 64 0.040
228
HMT002 Hematologic Cancer 64 0.040
229
LPT001 Leptospirosis 62 0.040
230
P HML002 Hemolytic Anemia 62 0.040
231
P RCK004 Rickets 61 0.040
232
c ACT075 Acute Myocardial Infarction 60 0.040
233
ACQ007 Acquired Immunodeficiency Syndrome 60 0.040
234
CLT003 Colitis 60 0.040
235
c ACT073 Acute Leukemia 60 0.040
236
ALC006 Alcoholic Hepatitis 59 0.040
237
P ALC004 Alcohol Abuse 59 0.040
238
P NPH012 Nephrotic Syndrome 59 0.040
239
ADL030 Adult-Onset Still's Disease 59 0.040
240
P AGM005 Agammaglobulinemia, X-Linked 1 57 0.040
241
NRM005 Neuromuscular Disease 56 0.040
242
c SVR003 Severe Congenital Neutropenia 56 0.040
243
GST050 Gastrointestinal System Disease 56 0.040
244
c THR092 Thrombophilia Due to Thrombin Defect 54 0.040
245
SHG001 Shigellosis 54 0.040
246
PLN006 Poland Syndrome 54 0.040
247
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.040
248
P PNC001 Pancytopenia 52 0.040
249
MYM001 Myoma 52 0.040
250
P PRM006 Primary Biliary Cirrhosis 51 0.040
251
ART002 Arts Syndrome 51 0.040
252
P PMP005 Pemphigus Vulgaris 51 0.040
253
GNR004 Generalized Anxiety Disorder 51 0.040
254
CRS005 Crest Syndrome 51 0.040
255
PMP001 Pemphigus 50 0.040
256
NNT012 Neonatal Jaundice 50 0.040
257
c INF067 Inflammatory Bowel Disease 10 49 0.040
258
MLL012 Miller Syndrome 49 0.040
259
P CMP008 Compartment Syndrome 48 0.040
260
ASP007 Aspiration Pneumonia 47 0.040
261
PRP021 Peripheral Nervous System Neoplasm 46 0.040
262
HRT007 Heart Cancer 46 0.040
263
CLC001 Calciphylaxis 46 0.040
264
P END047 Endophthalmitis 45 0.040
265
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.040
266
c ART120 Arthrogryposis, Distal, Type 3 42 0.040
267
INH001 Inhalation Anthrax 42 0.040
268
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.040
269
PNM013 Pneumococcal Meningitis 41 0.040
270
c PRM225 Primary Thrombocytopenia 39 0.040
271
ACT088 Acute Insulin Response 39 0.040
272
STR002 Streptococcal Meningitis 38 0.040
273
c INF086 Inflammatory Bowel Disease 3 38 0.040
274
ADJ001 Adjustment Disorder 38 0.040
275
WTH001 Withdrawal Disorder 37 0.040
276
FNS001 Funisitis 37 0.040
277
ACL001 Acalculous Cholecystitis 35 0.040
278
PLC008 Placenta Disease 33 0.040
279
P TRN016 Transient Hypogammaglobulinemia 33 0.040
280
MYS004 Myiasis 33 0.040
281
P END046 Endometritis 32 0.040
282
MYC014 Mycobacterium Chelonae 32 0.040
283
P HRT017 Heart Tumor 32 0.040
284
PDT040 Pediatric Hypertension 30 0.040
285
VTM003 Vitamin Metabolic Disorder 30 0.040
286
MRG013 Mirage Syndrome 29 0.040
287
c PLN021 Peeling Skin Syndrome 3 29 0.040
288
c INF002 Inflammatory Diarrhea 27 0.040
289
FWL001 Fowler's Syndrome 25 0.040
290
c CRN175 Coronary Heart Disease 4 19 0.040
291
c CRN173 Coronary Heart Disease 8 18 0.040
292
c ADL079 Adult Heart Tumor 16 0.040
293
ATR076 Atrophic Muscular Disease 15 0.040
294
GRP002 Group B Strep Disease in Newborns 8 0.040
295
CYS001 Cystic Fibrosis 83 0.033
296
P MLT019 Multiple Myeloma 83 0.033
297
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.033
298
P PLM037 Pulmonary Hypertension 79 0.033
299
CRH001 Crohn's Disease 75 0.033
300
P WSK001 Wiskott-Aldrich Syndrome 73 0.033
301
WLS001 Wilson Disease 72 0.033
302
SCK003 Sickle Cell Anemia 71 0.033
303
OMN001 Omenn Syndrome 67 0.033
304
P ATR011 Atrial Fibrillation 66 0.033
305
OBS061 Obstructive Sleep Apnea 66 0.033
306
ATP002 Atopy 66 0.033
307
CHR012 Chronic Granulomatous Disease 65 0.033
308
P HRP006 Herpes Simplex 65 0.033
309
CNT098 Central Core Disease 65 0.033
310
P THL005 Thalassemia 64 0.033
311
P HYP086 Hypothyroidism 64 0.033
312
P ALX003 Alexander Disease 63 0.033
313
P LYM026 Lymphoblastic Leukemia 62 0.033
314
P SLP006 Sleep Apnea 61 0.033
315
P ASP006 Aspergillosis 61 0.033
316
P ESP024 Esophagitis 61 0.033
317
CRD119 Cardiac Arrest 61 0.033
318
FCT007 Factor Vii Deficiency 61 0.033
319
TTN003 Tetanus 61 0.033
320
P NPH009 Nephrolithiasis 60 0.033
321
MNK001 Menkes Disease 60 0.033
322
PLM033 Pulmonary Embolism 60 0.033
323
APP008 Appendicitis 60 0.033
324
P GST049 Gastrointestinal System Cancer 60 0.033
325
P CNG015 Congenital Diaphragmatic Hernia 60 0.033
326
c CNT035 Central Nervous System Disease 60 0.033
327
c HPT003 Hepatitis a 59 0.033
328
CNT097 Central Hypoventilation Syndrome, Congenital 59 0.033
329
STT001 Status Epilepticus 59 0.033
330
LGN002 Legionellosis 59 0.033
331
P NRP001 Neuropathy 59 0.033
332
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.033
333
c EXD008 Exudative Vitreoretinopathy 1 59 0.033
334
BNC003 Bone Cancer 58 0.033
335
P HRS035 Hirschsprung Disease 1 58 0.033
336
PST028 Post-Traumatic Stress Disorder 57 0.033
337
CRT016 Carotid Artery Disease 57 0.033
338
ANR040 Aneurysm 57 0.033
339
CNG008 Congenital Ichthyosiform Erythroderma 56 0.033
340
c PRC016 Pre-Eclampsia 56 0.033
341
PRS047 Prostatitis 56 0.033
342
PRP019 Peripheral Nervous System Disease 55 0.033
343
P TMT001 Timothy Syndrome 55 0.033
344
P FNC043 Fanconi Anemia, Complementation Group E 55 0.033
345
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.033
346
EXT034 Extrinsic Allergic Alveolitis 55 0.033
347
P HRD011 Hereditary Spherocytosis 54 0.033
348
P MYC008 Myocarditis 54 0.033
349
P THY032 Thyroiditis 54 0.033
350
CHN016 Cohen Syndrome 54 0.033
351
LMY002 Leiomyoma 54 0.033
352
P ECL001 Eclampsia 54 0.033
353
PLV003 Pelvic Inflammatory Disease 54 0.033
354
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.033
355
LST001 Listeriosis 53 0.033
356
RTN018 Retinal Disease 53 0.033
357
CHL014 Cholera 53 0.033
358
P NNT009 Neonatal Diabetes Mellitus 52 0.033
359
TRM010 Traumatic Brain Injury 52 0.033
360
QDR001 Quadriplegia 52 0.033
361
HYP542 Hypersensitivity Syndrome, Carbamazepine-Induced 52 0.033
362
P PTN002 Patent Ductus Arteriosus 52 0.033
363
P LCT001 Lactic Acidosis 51 0.033
364
ANK001 Ankylosis 51 0.033
365
ASP003 Aseptic Meningitis 51 0.033
366
DRG011 Drug Addiction 51 0.033
367
STR008 Strongyloidiasis 51 0.033
368
VSC044 Visceral Myopathy 51 0.033
369
INF034 Infective Endocarditis 51 0.033
370
PRC012 Pericardial Effusion 51 0.033
371
GRW007 Growth Hormone Deficiency 50 0.033
372
RTC002 Reticular Dysgenesis 50 0.033
373
MSC072 Muscle Cancer 49 0.033
374
P SHR001 Short Bowel Syndrome 49 0.033
375
PRN021 Paranasal Sinus Disease 49 0.033
376
ALC009 Alcoholic Liver Cirrhosis 49 0.033
377
CHL061 Childhood Leukemia 49 0.033
378
BCL002 B Cell Deficiency 49 0.033
379
PRT018 Portal Vein Thrombosis 49 0.033
380
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.033
381
PLS009 Plasma Cell Neoplasm 48 0.033
382
P SCL009 Sclerosing Cholangitis 48 0.033
383
ATN002 Autonomic Nervous System Disease 48 0.033
384
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.033
385
c INV001 Invasive Aspergillosis 47 0.033
386
SCB001 Scabies 47 0.033
387
HYD005 Hydrocele 46 0.033
388
MYL013 Myeloperoxidase Deficiency 46 0.033
389
INC022 Inclusion-Cell Disease 46 0.033
390
FLT011 Felty Syndrome 46 0.033
391
ADN027 Adenomyosis 46 0.033
392
P KRN004 Kernicterus 46 0.033
393
MGC001 Megacolon 45 0.033
394
ANR004 Anuria 45 0.033
395
BCT004 Bacteriuria 45 0.033
396
URT010 Ureteral Obstruction 45 0.033
397
P MTH007 Methemoglobinemia 45 0.033
398
ALN001 Aland Island Eye Disease 45 0.033
399
c PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 44 0.033
400
SYS003 Systolic Heart Failure 43 0.033
401
PHY002 Physical Disorder 43 0.033
402
SNS023 Sensory System Cancer 43 0.033
403
MLT001 Multiple Chemical Sensitivity 43 0.033
404
NRW001 Norwegian Scabies 42 0.033
405
VGN023 Vaginitis 42 0.033
406
SXL003 Sexual Disorder 42 0.033
407
CRS001 Crescentic Glomerulonephritis 42 0.033
408
AYM001 Ayme-Gripp Syndrome 41 0.033
409
URT001 Urethritis 41 0.033
410
P CPL003 Capillary Leak Syndrome 41 0.033
411
MDS022 Mediastinitis 41 0.033
412
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.033
413
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.033
414
ACT084 Acute Stress Disorder 40 0.033
415
STR077 Streptococcal Toxic-Shock Syndrome 40 0.033
416
BND014 Bone Development Disease 40 0.033
417
c INF087 Inflammatory Bowel Disease 4 40 0.033
418
GRN009 Granulomatous Hepatitis 39 0.033
419
ADR009 Adrenal Cortex Disease 39 0.033
420
NSL022 Nasal Cavity Disease 38 0.033
421
OCL010 Ocular Hypotension 38 0.033
422
EMN001 Emanuel Syndrome 36 0.033
423
c TRN009 Transient Hypogammaglobulinemia of Infancy 36 0.033
424
c CNG413 Congenital Short Bowel Syndrome 36 0.033
425
MTC005 Mitochondrial Metabolism Disease 36 0.033
426
ALR002 Al-Raqad Syndrome 36 0.033
427
LMB010 Lambert Syndrome 36 0.033
428
c THR037 Thrombocytopenia 2 35 0.033
429
BLL012 Bullous Impetigo 35 0.033
430
SPL006 Splenic Infarction 35 0.033
431
LYM014 Lymphangitis 35 0.033
432
c ACT036 Acute Cholangitis 34 0.033
433
MTH039 Methylmalonic Aciduria, Mut(0) Type 34 0.033
434
LNG095 Lung Abscess 34 0.033
435
ACR002 Acrocapitofemoral Dysplasia 33 0.033
436
SPP004 Suppurative Cholangitis 33 0.033
437
EPD005 Epidural Abscess 33 0.033
438
IMM064 Immunodeficiency, Common Variable, 10 32 0.033
439
AGM004 Agammaglobulinemia, Non-Bruton Type 31 0.033
440
EPD040 Epidermolysis Bullosa Simplex with Pyloric Atresia 30 0.033
441
c INF075 Inflammatory Bowel Disease 16 30 0.033
442
c CNT068 Central Pain Syndrome 29 0.033
443
PRM243 Primary Bone Cancer 29 0.033
444
c AST039 Asthma 2 28 0.033
445
WDS002 Woods Syndrome 27 0.033
446
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.033
447
ORB006 Orbital Cellulitis 26 0.033
448
c MLT069 Multiple Mitochondrial Dysfunctions Syndrome 2 26 0.033
449
c MLT068 Multiple Mitochondrial Dysfunctions Syndrome 1 25 0.033
450
SNT004 Sinoatrial Node Dysfunction and Deafness 25 0.033
451
ASP026 Asplenia, Isolated Congenital 24 0.033
452
VBR003 Vibrio Vulnificus Infection 23 0.033
453
c MLT139 Multiple Mitochondrial Dysfunctions Syndrome 4 22 0.033
454
MND006 Mondor Disease 21 0.033
455
c THR110 Thrombocytopenia 6 20 0.033
456
ACT228 Acute Radiation Syndrome 20 0.033
457
P GNR027 Generalized Peeling Skin Syndrome 19 0.033
458
c INF083 Inflammatory Bowel Disease 24 19 0.033
459
LDW001 Ludwig's Angina 17 0.033
460
ADS015 Aids Wasting Syndrome 17 0.033
461
c BLR024 Biliary Cirrhosis, Primary, 1 16 0.033
462
GLC077 Glucocorticoid Therapy, Response to 16 0.033
463
BNM008 Bone Mineral Density, Low 16 0.033
464
ISL085 Isolated Agammaglobulinemia 15 0.033
465
LTN011 Late-Onset Isolated Acth Deficiency 14 0.033
466
CGL001 Coagulation Protein Disease 14 0.033
467
DSS023 Disease_ontology 12 0.033
468
CMB055 Combined Immunodeficiency Due to Crac Channel Dysfunction 11 0.033
469
TSY001 Tau Syndrome 10 0.033
470
PRS125 Pura Syndrome 10 0.033
471
IDP055 Idiopathic Severe Pneumococcemia 3 0.033
472
P BRS047 Breast Cancer 100 0.023
473
P CLR023 Colorectal Cancer 97 0.023
474
P PNC035 Pancreatic Cancer 87 0.023
475
P RNL014 Renal Cell Carcinoma 82 0.023
476
HDG012 Hodgkin Lymphoma 77 0.023
477
c CHR090 Chronic Lymphocytic Leukemia 76 0.023
478
ULC004 Ulcerative Colitis 76 0.023
479
P APL001 Aplastic Anemia 75 0.023
480
INS024 Insulin-Like Growth Factor I 75 0.023
481
P CRN211 Coronary Artery Disease 74 0.023
482
c LKM061 Leukemia, Acute Myeloid 73 0.023
483
MYL009 Myelodysplastic Syndrome 73 0.023
484
MNT001 Mantle Cell Lymphoma 72 0.023
485
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.023
486
P PLM036 Pulmonary Fibrosis 71 0.023
487
P PHC003 Pheochromocytoma 71 0.023
488
SQM006 Squamous Cell Carcinoma 70 0.023
489
SVR004 Severe Combined Immunodeficiency 69 0.023
490
P LPR003 Leprosy 69 0.023
491
ART016 Aortic Aneurysm 69 0.023
492
c HPT001 Hepatitis C 68 0.023
493
P CLC005 Celiac Disease 68 0.023
494
ANX002 Anxiety Disorder 67 0.023
495
P HYD006 Hydrocephalus 66 0.023
496
MYC006 Mycosis Fungoides 66 0.023
497
P MYL006 Myeloid Leukemia 66 0.023
498
LSH001 Leishmaniasis 66 0.023
499
DRM006 Dermatitis 66 0.023
500
BRC012 Brucellosis 66 0.023
501
P CSH001 Cushing's Syndrome 65 0.023
502
P TRN020 Turner Syndrome 65 0.023
503
PTR006 Peters Anomaly 65 0.023
504
P AMY004 Amyloidosis 65 0.023
505
P PLR004 Pleuropulmonary Blastoma 65 0.023
506
c HPT016 Hepatitis B 65 0.023
507
P LNG028 Long Qt Syndrome 64 0.023
508
CRB039 Cerebrovascular Disease 63 0.023
509
ALC007 Alcohol Dependence 63 0.023
510
P ENC004 Encephalitis 63 0.023
511
SPN186 Spinal Cord Injury 63 0.023
512
CHR103 Charge Syndrome 62 0.023
513
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.023
514
P CRN015 Cornelia De Lange Syndrome 62 0.023
515
VSC011 Vasculitis 62 0.023
516
GST092 Gastroesophageal Reflux 62 0.023
517
GLC037 Glucocorticoid Resistance 62 0.023
518
TNG002 Tangier Disease 62 0.023
519
P TXP001 Toxoplasmosis 61 0.023
520
P ANR007 Anorexia Nervosa 61 0.023
521
OVR029 Ovarian Hyperstimulation Syndrome 61 0.023
522
c ATM010 Autoimmune Hemolytic Anemia 61 0.023
523
P SNS014 Sinusitis 60 0.023
524
P PRT013 Portal Hypertension 60 0.023
525
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.023
526
PRM097 Primary Immunodeficiency Disease 60 0.023
527
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.023
528
P ORL007 Oral Cavity Cancer 59 0.023
529
OCL009 Ocular Cancer 59 0.023
530
BLL006 Bullous Pemphigoid 59 0.023
531
CMM005 Common Cold 59 0.023
532
c FML001 Familial Atrial Fibrillation 58 0.023
533
P MTR012 Mitral Valve Disease 58 0.023
534
P HST010 Histiocytosis 58 0.023
535
PNC034 Pancreas Disease 58 0.023
536
DBT087 Diabetes Insipidus, Neurohypophyseal 58 0.023
537
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.023
538
ART017 Aortic Disease 57 0.023
539
P EXN002 Exanthem 57 0.023
540
HRY003 Hairy Cell Leukemia 57 0.023
541
SFT003 Soft Tissue Sarcoma 57 0.023
542
UTR039 Uterine Fibroid 57 0.023
543
P ANP001 Anaplastic Large Cell Lymphoma 57 0.023
544
BTN003 Biotinidase Deficiency 57 0.023
545
STR026 Star Syndrome 57 0.023
546
ORL011 Oral Cancer 56 0.023
547
P SZR006 Seizure Disorder 56 0.023
548
P GST044 Gastritis 56 0.023
549
DSM004 Desmoid Tumor 56 0.023
550
P HMR012 Hemorrhagic Fever 56 0.023
551
HPT019 Hepatic Encephalopathy 56 0.023
552
DBT010 Diabetic Neuropathy 55 0.023
553
P HYP076 Hyperthyroidism 55 0.023
554
LKC001 Leukocyte Adhesion Deficiency 55 0.023
555
PLS007 Plasmodium Falciparum Malaria 55 0.023
556
ECH003 Echinococcosis 54 0.023
557
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.023
558
P HYP083 Hypopituitarism 54 0.023
559
c PND001 Pain Disorder 54 0.023
560
P MMB011 Membranous Nephropathy 54 0.023
561
SBS003 Substance Abuse 54 0.023
562
NTH001 Netherton Syndrome 54 0.023
563
NWC001 Newcastle Disease 54 0.023
564
VRR004 Verrucous Carcinoma 54 0.023
565
PRT014 Protein S Deficiency 53 0.023
566
THL016 Thalassemias, Alpha- 53 0.023
567
P PLY014 Polycystic Kidney Disease 53 0.023
568
SPT005 Spotted Fever 53 0.023
569
P SYP003 Syphilis 53 0.023
570
P DBT005 Diabetes Insipidus 53 0.023
571
PLS006 Plasmodium Vivax Malaria 53 0.023
572
LYM019 Lymphosarcoma 53 0.023
573
PRV006 Pervasive Developmental Disorder 53 0.023
574
BRT005 Barth Syndrome 52 0.023
575
CYT008 Cytomegalovirus Infection 52 0.023
576
HMG005 Hemoglobinopathy 52 0.023
577
OPT006 Optic Nerve Disease 52 0.023
578
MCN007 Meconium Aspiration Syndrome 52 0.023
579
MYC002 Mycobacterium Avium Complex Disease 52 0.023
580
BLR001 Biliary Atresia 52 0.023
581
PRC013 Pericarditis 51 0.023
582
BLD044 Bladder Disease 51 0.023
583
HDR002 Hidradenitis Suppurativa 51 0.023
584
PLR022 Pleural Disease 51 0.023
585
P HML001 Hemolytic-Uremic Syndrome 51 0.023
586
P GND004 Gonadal Dysgenesis 51 0.023
587
VSC006 Vascular Cancer 51 0.023
588
PTH002 Pathological Gambling 51 0.023
589
ATR060 Atrial Standstill, Digenic 51 0.023
590
P LRS001 Larsen Syndrome 51 0.023
591
NTR040 Neutropenia, Cyclic 51 0.023
592
BNM001 Bone Marrow Cancer 51 0.023
593
PLG002 Plague 51 0.023
594
c VRL012 Viral Meningitis 50 0.023
595
P LFT003 Left Ventricular Noncompaction 50 0.023
596
END031 Endometrial Stromal Sarcoma 50 0.023
597
P EPD002 Epidermolytic Hyperkeratosis 50 0.023
598
INT051 Intussusception 50 0.023
599
BNF002 Bone Fracture 50 0.023
600
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.023
601
HLL004 Hellp Syndrome 50 0.023
602
P SCK002 Sick Sinus Syndrome 50 0.023
603
PRP016 Paraplegia 49 0.023
604
SRT004 Serotonin Syndrome 49 0.023
605
c SVR005 Severe Pre-Eclampsia 49 0.023
606
LRN003 Learning Disability 49 0.023
607
ACR003 Acrodermatitis Enteropathica 49 0.023
608
PRT038 Protein-Energy Malnutrition 49 0.023
609
NCT008 Nicotine Dependence, Protection Against 49 0.023
610
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.023
611
HMG002 Hemoglobinuria 48 0.023
612
MTN003 Motion Sickness 48 0.023
613
PSD007 Pseudomyxoma Peritonei 48 0.023
614
URM002 Uremia 48 0.023
615
THL018 Thalassemia Major 48 0.023
616
P NGH001 Night Blindness 48 0.023
617
FML039 Female Reproductive System Disease 48 0.023
618
TWN001 Twin-to-Twin Transfusion Syndrome 48 0.023
619
P TRC086 Trichohepatoenteric Syndrome 1 48 0.023
620
c CNG027 Congenital Hemolytic Anemia 48 0.023
621
ACT098 Acute Erythroid Leukemia 47 0.023
622
P HMR005 Hemorrhoid 47 0.023
623
c XNT010 Xanthinuria, Type I 47 0.023
624
PTT009 Pituitary Gland Disease 47 0.023
625
RNL077 Renal Fibrosis 47 0.023
626
PRM236 Primary Biliary Cholangitis 47 0.023
627
HYD002 Hydronephrosis 47 0.023
628
CMP004 Complement Factor I Deficiency 47 0.023
629
PLC007 Placental Abruption 47 0.023
630
c ATM024 Autoimmune Pancreatitis 47 0.023
631
HYP025 Hyperphosphatemia 47 0.023
632
CRB025 Carbohydrate Metabolic Disorder 46 0.023
633
GLT021 Glutaricaciduria, Type I 46 0.023
634
ICH054 Ichthyosis, X-Linked 46 0.023
635
SCR002 Scurvy 46 0.023
636
DNT012 Dental Caries 46 0.023
637
CHR074 Choriocarcinoma 46 0.023
638
c CLL013 Cell Type Cancer 46 0.023
639
PRT082 Preterm Premature Rupture of the Membranes 46 0.023
640
CYS008 Cystic Echinococcosis 46 0.023
641
DST006 Diastolic Heart Failure 46 0.023
642
IDP024 Idiopathic Inflammatory Myopathy 46 0.023
643
HPR003 Heparin-Induced Thrombocytopenia 45 0.023
644
RLP003 Relapsing Fever 45 0.023
645
BRN014 Bronchopneumonia 45 0.023
646
CRB090 Cerebral Hypoxia 45 0.023
647
HDN002 Head Injury 45 0.023
648
P CRV039 Cervicitis 45 0.023
649
VSC047 Vascular Malformation 45 0.023
650
HDR003 Hidradenitis 45 0.023
651
P ABD003 Abdominal Aortic Aneurysm 45 0.023
652
CCN007 Cocoon Syndrome 45 0.023
653
C2D001 C2 Deficiency 45 0.023
654
P RPD001 Rapidly Progressive Glomerulonephritis 45 0.023
655
P ANL018 Analbuminemia 44 0.023
656
P SDR002 Siderosis 44 0.023
657
PLC001 Placenta Accreta 44 0.023
658
CRD001 Cardiac Tamponade 44 0.023
659
CRD118 Cardiovascular Cancer 44 0.023
660
P BRN120 Bronchus Cancer 44 0.023
661
CLD007 Cold Agglutinin Disease 44 0.023
662
SKN023 Skin Tag 44 0.023
663
c CHL119 Cholangitis, Primary Sclerosing 44 0.023
664
SPL018 Splenomegaly 44 0.023
665
URT031 Ureteral Disease 44 0.023
666
DSM003 Desmoid Disease, Hereditary 44 0.023
667
P DMY001 Demyelinating Polyneuropathy 43 0.023
668
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.023
669
CRR007 Cirrhosis, Cryptogenic 43 0.023
670
DXT001 Dextrocardia 43 0.023
671
PLR007 Pleural Empyema 43 0.023
672
CTY001 Cat Eye Syndrome 43 0.023
673
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.023
674
EVN001 Evans' Syndrome 43 0.023
675
NSS002 Neisseria Meningitidis Infection 43 0.023
676
ACT087 Acth Deficiency 43 0.023
677
BCK006 Back Pain 43 0.023
678
PRT026 Parotitis 42 0.023
679
CLS016 Clostridium Difficile Colitis 42 0.023
680
NM001 Noma 42 0.023
681
PLS016 Plasma Cell Leukemia 42 0.023
682
HPT008 Hepatic Tuberculosis 42 0.023
683
MNN032 Meningococcal Meningitis 42 0.023
684
HYP458 Hyper Ige Syndrome 42 0.023
685
c VRL005 Viral Pneumonia 42 0.023
686
BLR008 Bilirubin Metabolic Disorder 42 0.023
687
PRD011 Proud Syndrome 42 0.023
688
c CHR064 Chronic Monocytic Leukemia 42 0.023
689
ERY004 Erysipelas 41 0.023
690
FCT008 Factitious Disorder 41 0.023
691
P HVY001 Heavy Chain Disease 41 0.023
692
GLC009 Glucosephosphate Dehydrogenase Deficiency 41 0.023
693
VGN020 Vaginal Disease 41 0.023
694
BRB001 Beriberi 41 0.023
695
CHL052 Choledochal Cyst 41 0.023
696
SPC010 Speech and Communication Disorders 41 0.023
697
MYC013 Mycobacterium Abscessus 41 0.023
698
DPH021 Diaphragm Disease 41 0.023
699
RPR002 Reproductive System Disease 41 0.023
700
TBR008 Tuberculous Peritonitis 41 0.023
701
c SCN006 Secondary Syphilis 41 0.023
702
CNV002 Conversion Disorder 41 0.023
703
MLR002 Miliary Tuberculosis 41 0.023
704
PNC085 Penicillin Allergy 40 0.023
705
GST078 Gastrointestinal Allergy 40 0.023
706
ATX003 Ataxia with Isolated Vitamin E Deficiency 40 0.023
707
ACT055 Actinomycosis 40 0.023
708
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.023
709
MYC012 Mycetoma 40 0.023
710
CHR078 Chorioretinitis 40 0.023
711
TLR001 Tularemia 39 0.023
712
SKL003 Skeletal Muscle Cancer 39 0.023
713
ILC002 Ileocolitis 39 0.023
714
PRS023 Pearson Syndrome 39 0.023
715
TXC020 Toxic Oil Syndrome 39 0.023
716
BBN001 Bubonic Plague 39 0.023
717
ISC015 Ischemic Colitis 39 0.023
718
RCK002 Rocky Mountain Spotted Fever 39 0.023
719
HMG025 Hemoglobin H Disease, Nondeletional 39 0.023
720
THL010 Thalassemia Minor 39 0.023
721
EST003 Eastern Equine Encephalitis 39 0.023
722
c ADL001 Adult Lymphoma 39 0.023
723
HYP391 Hyperammonemia 38 0.023
724
PCH007 Pouchitis 38 0.023
725
MNR003 Mineral Metabolism Disease 38 0.023
726
P HYP265 Hypotonia 38 0.023
727
ABD010 Abdominal Wall Defect 38 0.023
728
EHR002 Ehrlichiosis 38 0.023
729
c ICH041 Ichthyosis, Autosomal Recessive 4b 38 0.023
730
P ACQ009 Acquired Metabolic Disease 38 0.023
731
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.023
732
SXD001 Sex Differentiation Disease 38 0.023
733
P OCY001 Oocyte Maturation Defect 38 0.023
734
P UTR038 Uterine Disease 37 0.023
735
ACT113 Acute Myeloblastic Leukemia with Maturation 37 0.023
736
MYS001 Myositis Ossificans 37 0.023
737
c PNC106 Pancreatic Agenesis 1 37 0.023
738
c CNG031 Congenital Nervous System Abnormality 37 0.023
739
ANG037 Angiomatosis 37 0.023
740
CLD014 Cole Disease 37 0.023
741
PRP056 Porphyria, Acute Hepatic 37 0.023
742
c SCN052 Secondary Adrenal Insufficiency 37 0.023
743
BNS002 Bone Structure Disease 37 0.023
744
ETH004 Euthyroid Sick Syndrome 36 0.023
745
URT014 Ureterolithiasis 36 0.023
746
ACR005 Acrodermatitis 36 0.023
747
CHP002 Chops Syndrome 35 0.023
748
VRS001 Virus Associated Hemophagocytic Syndrome 35 0.023
749
ATM012 Autoimmune Disease of Blood 35 0.023
750
INF013 Inferior Myocardial Infarction 35 0.023
751
MNK002 Monkeypox 35 0.023
752
c ACT081 Acute Salpingitis 35 0.023
753
FRN014 Fournier Gangrene 35 0.023
754
CRT012 Cortical Blindness 35 0.023
755
RDN001 Reading Disorder 34 0.023
756
GLS018 Glass Syndrome 34 0.023
757
CHL039 Choledocholithiasis 34 0.023
758
PLM013 Pulmonary Immaturity 34 0.023
759
ANG049 Angioedema Induced by Ace Inhibitors 34 0.023
760
PLS010 Plasma Protein Metabolism Disease 34 0.023
761
CHR028 Chronic Wasting Disease 34 0.023
762
FHR001 Fuhrmann Syndrome 34 0.023
763
GST020 Gastric Antral Vascular Ectasia 33 0.023
764
P SLP003 Salpingitis 33 0.023
765
TXC007 Toxic Pneumonitis 33 0.023
766
BLK001 Balkan Nephropathy 33 0.023
767
P FTL033 Fetal Hemoglobin Quantitative Trait Locus 1 33 0.023
768
GLB003 Globe Disease 32 0.023
769
BNM005 Bone Marrow Necrosis 32 0.023
770
BRS102 Breast Abscess 32 0.023
771
c INF088 Inflammatory Bowel Disease 5 31 0.023
772
SPR035 Superior Vena Cava Syndrome 31 0.023
773
FSR001 Fusariosis 31 0.023
774
FST001 Foster-Kennedy Syndrome 31 0.023
775
3MT013 3-Methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome 31 0.023
776
STL007 Steel Syndrome 31 0.023
777
HYP084 Hypopyon 31 0.023
778
IMM082 Immunodeficiency 18 31 0.023
779
ENT007 Enteropathica 31 0.023
780
IRS003 Iris Disease 31 0.023
781
CYT002 Cytokine Deficiency 30 0.023
782
ART012 Aortitis 30 0.023
783
HNS001 Hansen's Disease 30 0.023
784
ACT118 Acute Non Lymphoblastic Leukemia 30 0.023
785
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 30 0.023
786
c VRL017 Viral Hemorrhagic Fever 30 0.023
787
RMN002 Ramon Syndrome 30 0.023
788
c SCK017 Sick Sinus Syndrome 1 29 0.023
789
c TRC078 Trichohepatoenteric Syndrome 2 29 0.023
790
ACT114 Acute Myeloblastic Leukemia Without Maturation 29 0.023
791
CCL002 Cecal Disease 29 0.023
792
PNM003 Pneumatosis Cystoides Intestinalis 29 0.023
793
c AST037 Asthma 1 29 0.023
794
WTS001 Watson Syndrome 28 0.023
795
XNT001 Xanthogranulomatous Pyelonephritis 28 0.023
796
MYC015 Mycobacterium Fortuitum 28 0.023
797
GLC043 Glucocorticoid Deficiency 2 28 0.023
798
TXC001 Toxic Megacolon 28 0.023
799
GLC073 Glucocorticoid Deficiency 4 28 0.023
800
SPL009 Splenic Sequestration 28 0.023
801
c MYC058 Myocardial Infarction 2 28 0.023
802
c NTR039 Neutropenia, Severe Congenital 4, Autosomal Recessive 27 0.023
803
CRB031 Cerebral Arterial Disease 27 0.023
804
IMM076 Immunodeficiency 24 27 0.023
805
c PNC094 Pancreatic Cancer 1 27 0.023
806
HST007 Histidine Metabolism Disease 27 0.023
807
c SCK014 Sick Sinus Syndrome 2 27 0.023
808
c THR048 Thrombocytopenia 4 27 0.023
809
CMP041 Complement Factor D Deficiency 26 0.023
810
c CHR036 Chronic Cholangitis 26 0.023
811
DSC004 Discitis 26 0.023
812
c INF090 Inflammatory Bowel Disease 7 26 0.023
813
NSP003 Nasopharyngeal Disease 26 0.023
814
NTR042 Neutrophilic Dermatosis, Acute Febrile 25 0.023
815
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.023
816
ATM052 Autoimmune Disease 1 25 0.023
817
ILM001 Ileum Cancer 25 0.023
818
MND023 Mend Syndrome 24 0.023
819
c INF093 Inflammatory Bowel Disease 14 23 0.023
820
c SCK022 Sick Sinus Syndrome 3 22 0.023
821
PLM124 Pulmonary Hypertension, Neonatal 22 0.023
822
ATM059 Autoimmune Disease 6 22 0.023
823
c HRD192 Hereditary Spherocytosis Type 2 22 0.023
824
GST046 Gastrointestinal Anthrax 22 0.023
825
KLB004 Klebsiella Infection 22 0.023
826
HRD183 Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome 21 0.023
827
OPP001 Opportunistic Bacterial Infectious Disease 21 0.023
828
WND002 Wandering Spleen 21 0.023
829
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.023
830
PNT023 Pontine Hemorrhage 21 0.023
831
c INF079 Inflammatory Bowel Disease 20 21 0.023
832
JMP001 Jmp Syndrome 21 0.023
833
c CRN174 Coronary Heart Disease 2 20 0.023
834
PRT110 Prieto Syndrome 20 0.023
835
CRT057 Critical Congenital Heart Disease 20 0.023
836
INT062 Interstitial Myocarditis 20 0.023
837
PRL018 Purulent Endophthalmitis 19 0.023
838
NCR014 Necrotizing Soft Tissue Infection 19 0.023
839
PRC021 Parc Syndrome 19 0.023
840
ANT040 Anton's Syndrome 19 0.023
841
c CRN172 Coronary Heart Disease 3 19 0.023
842
VSC009 Vascular Skin Disease 19 0.023
843
IMM103 Immunodeficiency 37 19 0.023
844
CML001 Cumulative Trauma Disorders 18 0.023
845
c CRN176 Coronary Heart Disease 9 18 0.023
846
CHT005 Chitotriosidase Deficiency 18 0.023
847
P STR035 Streptococcal Group a Invasive Disease 17 0.023
848
PST037 Pasteurella Multocida Infection 17 0.023
849
MLL015 Mills Syndrome 17 0.023
850
STR033 Storm Syndrome 17 0.023
851
IMM118 Immunodeficiency 42 17 0.023
852
ZNC006 Zinc, Elevated Plasma 17 0.023
853
HRD180 Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome 16 0.023
854
MGC006 Magic Syndrome 15 0.023
855
ATM055 Autoimmune Disease 4 15 0.023
856
c BLR017 Biliary Cirrhosis, Primary, 3 15 0.023
857
WHT007 White Platelet Syndrome 15 0.023
858
c UTR006 Uterine Inflammatory Disease 15 0.023
859
LYM126 Lymphoma Aids Related 15 0.023
860
STT044 Statin Toxicity 14 0.023
861
MYC003 Myocardium Cancer 14 0.023
862
GLC053 Glucocorticoid Deficiency 3 14 0.023
863
AMN012 Aminoacidopathies 14 0.023
864
NVD002 Nevada Syndrome 14 0.023
865
c BLR026 Biliary Cirrhosis, Primary, 5 14 0.023
866
P MYC054 Mycobacterium Tuberculosis 2 14 0.023
867
ACQ011 Acquired Agranulocytosis 13 0.023
868
RCT033 Rectal Duplication 13 0.023
869
c DLT001 Delta Chain Disease 13 0.023
870
INB001 Inborn Amino Acid Metabolism Disorder 12 0.023
871
MLR020 Malaria, Mild 12 0.023
872
c ACQ039 Acquired Purpura Fulminans 12 0.023
873
BDS001 Bd Syndrome 12 0.023
874
BLT017 Bilateral Massive Adrenal Hemorrhage 12 0.023
875
ORL014 Oral Pharyngeal Disorders 11 0.023
876
P ANT062 Anterior Urethral Valve 11 0.023
877
NGY001 Nguyen Syndrome 11 0.023
878
RDR001 Radio Renal Syndrome 9 0.023
879
INV015 Invasive Non-Typhoidal Salmonellosis 8 0.023
880
c STR036 Streptococcal Group B Invasive Disease 7 0.023