Search results for "emphysema"

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

646 hits were found for 'emphysema'

# Family MCID Name MIFTS Score
1
EMP007 Emphysema Due to Aat Deficiency 57 6.707
2
PLM034 Pulmonary Emphysema 55 6.186
3
EMP011 Emphysema, Congenital Lobar 26 4.966
4
INT011 Interstitial Emphysema 37 4.466
5
CMP003 Compensatory Emphysema 9 3.870
6
BRR006 Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification 6 3.156
7
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 5 2.252
8
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 30 2.224
9
LNG099 Lung Disease 63 0.293
10
PLM129 Pulmonary Disease, Chronic Obstructive 61 0.282
11
PNM008 Pneumothorax 51 0.207
12
P PLM036 Pulmonary Fibrosis 69 0.197
13
BRN024 Bronchitis 67 0.171
14
RSP006 Respiratory System Disease 61 0.142
15
P PNM007 Pneumonia 67 0.139
16
P AST005 Asthma 80 0.125
17
P PLM040 Pulmonary Valve Disease 45 0.119
18
MDS022 Mediastinitis 37 0.119
19
P LNG032 Lung Cancer 92 0.116
20
P PLM037 Pulmonary Hypertension 78 0.109
21
BRN038 Bronchial Disease 54 0.109
22
UPP004 Upper Respiratory Tract Disease 48 0.106
23
TBR010 Tuberculosis 70 0.102
24
P CTS001 Cutis Laxa 57 0.102
25
BRN002 Bronchiolitis 56 0.099
26
NTR005 Nutritional Deficiency Disease 51 0.095
27
BRN055 Bronchogenic Cyst 27 0.095
28
INT066 Interstitial Lung Disease 60 0.091
29
END072 Endotheliitis 41 0.091
30
P LVR013 Liver Disease 76 0.087
31
c CHR096 Chronic Pulmonary Heart Disease 40 0.087
32
MRF001 Marfan Syndrome 73 0.082
33
ATH003 Atherosclerosis 63 0.082
34
CRB009 Cerebritis 36 0.082
35
SRN001 Serine Deficiency 31 0.082
36
VSC011 Vasculitis 62 0.077
37
CHL123 Chlamydia 60 0.077
38
P HRT032 Heart Disease 64 0.077
39
P DRM010 Dermatomyositis 59 0.072
40
BRN022 Bronchiectasis 55 0.072
41
P INF038 Influenza 71 0.072
42
PLM001 Pulmonary Tuberculosis 69 0.072
43
PRT011 Protein C Deficiency 52 0.072
44
ANR040 Aneurysm 56 0.072
45
PNM003 Pneumatosis Cystoides Intestinalis 32 0.072
46
CYS001 Cystic Fibrosis 87 0.067
47
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 57 0.067
48
P OST002 Osteoporosis 63 0.067
49
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.067
50
SPN041 Spinal Cord Disease 50 0.067
51
P CYS018 Cystitis 54 0.067
52
c AST050 Asthma, Phf11-Related 23 0.067
53
DFF002 Diffuse Pulmonary Fibrosis 32 0.067
54
P RSP003 Respiratory Failure 68 0.061
55
KWS002 Kawasaki Disease 70 0.061
56
P SYS005 Systemic Scleroderma 60 0.061
57
c CNG401 Congenital Heart Disease 67 0.061
58
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.061
59
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.061
60
APP008 Appendicitis 61 0.061
61
P MNN013 Meningitis 66 0.061
62
STT002 Status Asthmaticus 43 0.061
63
CNN005 Connective Tissue Disease 60 0.061
64
c AST037 Asthma 1 35 0.061
65
c AST039 Asthma 2 28 0.061
66
DVR002 Diverticulitis 47 0.061
67
BRN056 Bronchopulmonary Dysplasia 56 0.061
68
CNJ007 Conjunctivochalasis 38 0.061
69
P PYL005 Pyelonephritis 52 0.061
70
SBS002 Substernal Goiter 24 0.061
71
NNT039 Neonatal Marfan Syndrome 27 0.061
72
OST085 Osteosarcoma, Somatic 63 0.055
73
KRT004 Keratitis 70 0.055
74
P LPR003 Leprosy 70 0.055
75
GLL022 Guillain-Barre Syndrome 58 0.055
76
LNG024 Langerhans-Cell Histiocytosis 64 0.055
77
P TMP003 Temporal Arteritis 61 0.055
78
LPT001 Leptospirosis 65 0.055
79
OTT002 Otitis Media 66 0.055
80
c JVN010 Juvenile Rheumatoid Arthritis 65 0.055
81
c ACT210 Acute Respiratory Distress Syndrome 55 0.055
82
HST011 Histoplasmosis 54 0.055
83
P CNG015 Congenital Diaphragmatic Hernia 58 0.055
84
LSH001 Leishmaniasis 63 0.055
85
BRC012 Brucellosis 66 0.055
86
CRR007 Cirrhosis, Cryptogenic 38 0.055
87
PRT036 Peritonitis 65 0.055
88
TKY002 Takayasu Arteritis 60 0.055
89
SLP005 Sleep Disorder 52 0.055
90
MSL001 Measles 61 0.055
91
TYP007 Typhoid Fever 61 0.055
92
PLS007 Plasmodium Falciparum Malaria 56 0.055
93
CHG001 Chagas Disease 62 0.055
94
LYM017 Lyme Disease 64 0.055
95
P TXP001 Toxoplasmosis 61 0.055
96
IDP011 Idiopathic Interstitial Pneumonia 57 0.055
97
ACQ007 Acquired Immunodeficiency Syndrome 60 0.055
98
SLC006 Silicosis 53 0.055
99
CLL003 Cellulitis 49 0.055
100
CRT016 Carotid Artery Disease 54 0.055
101
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 36 0.055
102
MXD005 Mixed Connective Tissue Disease 63 0.055
103
FLR002 Filariasis 55 0.055
104
PRN019 Perinatal Necrotizing Enterocolitis 47 0.055
105
BRN012 Bronchiolitis Obliterans 58 0.055
106
DPH021 Diaphragm Disease 45 0.055
107
MLR002 Miliary Tuberculosis 39 0.055
108
ALR002 Al-Raqad Syndrome 36 0.055
109
c BCT007 Bacterial Meningitis 55 0.055
110
P MYC008 Myocarditis 56 0.055
111
URT001 Urethritis 39 0.055
112
NCR007 Necrotizing Fasciitis 43 0.055
113
MCR088 Microscopic Polyangiitis 47 0.055
114
PLV003 Pelvic Inflammatory Disease 52 0.055
115
HMN014 Human Immunodeficiency Virus Infectious Disease 46 0.055
116
INF034 Infective Endocarditis 50 0.055
117
P SCL015 Scleritis 49 0.055
118
SPP008 Suppurative Otitis Media 45 0.055
119
CYT008 Cytomegalovirus Infection 51 0.055
120
AFR002 African Tick-Bite Fever 35 0.055
121
c ANT034 Anterior Uveitis 49 0.055
122
PLR008 Pleurisy 51 0.055
123
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 28 0.055
124
FSC004 Fasciitis 47 0.055
125
BNN003 Bone Inflammation Disease 46 0.055
126
ACL001 Acalculous Cholecystitis 35 0.055
127
PRD003 Periodontosis 40 0.055
128
TRC037 Tracheobronchomalacia 20 0.055
129
P PNM006 Pneumoconiosis 51 0.055
130
MNN002 Mononeuritis Multiplex 26 0.055
131
LYM035 Lymphangiectasis 28 0.055
132
CRD137 Cardiogenic Shock 44 0.055
133
c CHR091 Chronic Meningitis 40 0.055
134
SPN014 Spontaneous Tension Pneumothorax 13 0.055
135
EXT035 Extrinsic Cardiomyopathy 38 0.055
136
CHR005 Chorioamnionitis 47 0.055
137
MNN014 Mononeuritis 24 0.055
138
PRM025 Primary Bacterial Infectious Disease 42 0.055
139
P RHM011 Rheumatoid Arthritis 87 0.047
140
PLM033 Pulmonary Embolism 59 0.047
141
P ATP001 Atopic Dermatitis 60 0.047
142
P NRF002 Neurofibromatosis 66 0.047
143
PCK002 Pick Disease 66 0.047
144
ART016 Aortic Aneurysm 67 0.047
145
ELL001 Ellis-Van Creveld Syndrome 56 0.047
146
DRM006 Dermatitis 58 0.047
147
P SLL003 Salla Disease 44 0.047
148
P ART022 Arthritis 73 0.047
149
PRP019 Peripheral Nervous System Disease 52 0.047
150
PRT037 Pertussis 63 0.047
151
BRT002 Birt-Hogg-Dube Syndrome 51 0.047
152
P HML002 Hemolytic Anemia 60 0.047
153
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 34 0.047
154
ATN002 Autonomic Nervous System Disease 46 0.047
155
GTR002 Goiter 54 0.047
156
PPL021 Papilledema 47 0.047
157
SRC014 Sarcoma 66 0.047
158
P ADL010 Adult Respiratory Distress Syndrome 60 0.047
159
EXT034 Extrinsic Allergic Alveolitis 58 0.047
160
NRM005 Neuromuscular Disease 56 0.047
161
P HST010 Histiocytosis 56 0.047
162
GSG001 Gas Gangrene 49 0.047
163
PRD007 Periodontal Disease 42 0.047
164
RLP001 Relapsing Polychondritis 52 0.047
165
P PRD008 Periodontitis 46 0.047
166
SKN027 Skin Conditions 44 0.047
167
ALL006 Allergic Asthma 59 0.047
168
c CTS037 Cutis Laxa, Autosomal Recessive, Type Ib 21 0.047
169
DDN006 Duodenitis 44 0.047
170
FRM003 Farmer's Lung 47 0.047
171
P CRN178 Coronary Heart Disease 6 22 0.047
172
c CTS019 Cutis Laxa, Ad 26 0.047
173
BYS001 Byssinosis 32 0.047
174
LYM014 Lymphangitis 35 0.047
175
NNS002 Nonspecific Interstitial Pneumonia 43 0.047
176
CTS042 Cutis Laxa, Neonatal, with Marfanoid Phenotype 13 0.047
177
HYP266 Hypoxia 55 0.047
178
LYM116 Lymph Node Disease 42 0.047
179
P PLM064 Pulmonary Sequestration 26 0.047
180
P ORG009 Organ System Cancer 45 0.047
181
P LRG014 Large Cell Neuroendocrine Carcinoma 41 0.047
182
c HYP595 Hypertension, Essential 69 0.039
183
STR067 Stroke, Ischemic 74 0.039
184
FBR012 Fabry Disease 68 0.039
185
P MYC007 Myocardial Infarction 80 0.039
186
LKN001 Leukoencephalopathy with Vanishing White Matter 56 0.039
187
SCK003 Sickle Cell Anemia 72 0.039
188
c GLY008 Glycogen Storage Disease Ii 59 0.039
189
P EHL033 Ehlers-Danlos Syndrome, Classic Type 55 0.039
190
P CRN211 Coronary Artery Disease 74 0.039
191
c SPN225 Spondyloarthropathy 1 62 0.039
192
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.039
193
P ADD001 Addison's Disease 60 0.039
194
P HYP035 Hypophosphatasia 56 0.039
195
CNG034 Congestive Heart Failure 72 0.039
196
LGG001 Legg-Calve-Perthes Disease 58 0.039
197
P ESS003 Essential Thrombocythemia 66 0.039
198
MLN008 Melanoma 61 0.039
199
P MYS003 Myasthenia Gravis 64 0.039
200
PSR001 Psoriatic Arthritis 64 0.039
201
GST050 Gastrointestinal System Disease 58 0.039
202
P FND001 Fundus Albipunctatus 52 0.039
203
DFC004 Deficiency Anemia 64 0.039
204
NTH001 Netherton Syndrome 52 0.039
205
P LYM007 Lymphangioleiomyomatosis 65 0.039
206
PNM010 Pneumothorax, Primary Spontaneous 34 0.039
207
P RST011 Restrictive Dermopathy, Lethal 38 0.039
208
VRL011 Viral Infectious Disease 56 0.039
209
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.039
210
WGN006 Wegener Granulomatosis 63 0.039
211
P DGR001 Digeorge Syndrome 52 0.039
212
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 35 0.039
213
CCC001 Coccidioidomycosis 55 0.039
214
ART001 Arterial Tortuosity Syndrome 51 0.039
215
RTC002 Reticular Dysgenesis 50 0.039
216
CRB142 Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant 31 0.039
217
GNC003 Geniculate Herpes Zoster 34 0.039
218
MLD001 Melioidosis 67 0.039
219
TYP011 Typhus 57 0.039
220
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.039
221
CMM004 Common Variable Immunodeficiency 68 0.039
222
BHC003 Behcet Syndrome 60 0.039
223
P ASP006 Aspergillosis 61 0.039
224
CHR063 Chronic Mucocutaneous Candidiasis 61 0.039
225
P MYP004 Myopathy 67 0.039
226
URN009 Urinary System Disease 52 0.039
227
CHR066 Chronic Fatigue Syndrome 63 0.039
228
P ALP009 Alopecia Areata 62 0.039
229
TTN003 Tetanus 62 0.039
230
P ART023 Arthropathy 63 0.039
231
THR013 Thoracic Outlet Syndrome 48 0.039
232
PRC002 Paracoccidioidomycosis 57 0.039
233
BRG013 Buerger Disease 54 0.039
234
NCT008 Nicotine Dependence, Protection Against 51 0.039
235
APH001 Aphthous Stomatitis 62 0.039
236
P LKM002 Leukemia 70 0.039
237
PRP027 Peripheral Vascular Disease 69 0.039
238
ART005 Arteriovenous Malformation 63 0.039
239
RSP019 Respiratory Distress Syndrome in Premature Infants 43 0.039
240
IRK001 Irak4 Deficiency 46 0.039
241
HRY003 Hairy Cell Leukemia 56 0.039
242
P GRV001 Graves' Disease 62 0.039
243
DNG003 Dengue Disease 60 0.039
244
CNT047 Contact Dermatitis 62 0.039
245
P PLY017 Polyarteritis Nodosa 54 0.039
246
INT007 Intermediate Coronary Syndrome 52 0.039
247
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.039
248
PLY135 Polydactyly, Postaxial, with Progressive Myopia 23 0.039
249
IDP024 Idiopathic Inflammatory Myopathy 50 0.039
250
RSC001 Rosacea 54 0.039
251
P RBL001 Rubella 54 0.039
252
SPT004 Septic Arthritis 60 0.039
253
TRC008 Trachoma 50 0.039
254
QFV001 Q Fever 62 0.039
255
GNG013 Gingivitis 61 0.039
256
IMM102 Immunodeficiency 14 33 0.039
257
c ATM003 Autoimmune Thyroiditis 59 0.039
258
SCH014 Schistosomiasis 59 0.039
259
CYS005 Cysticercosis 52 0.039
260
PRS034 Parasitic Helminthiasis Infectious Disease 47 0.039
261
P VNT002 Ventricular Septal Defect 59 0.039
262
CMP010 Complex Regional Pain Syndrome 59 0.039
263
SCR008 Scrub Typhus 55 0.039
264
RHM001 Rheumatic Fever 50 0.039
265
RCT015 Reactive Arthritis 65 0.039
266
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.039
267
c LCL006 Localized Scleroderma 60 0.039
268
RHM027 Rheumatic Disease 55 0.039
269
HPT074 Hepatic Adenoma, Somatic 35 0.039
270
PRP030 Purpura 60 0.039
271
SPT005 Spotted Fever 56 0.039
272
HYP074 Hypersensitivity Vasculitis 49 0.039
273
GST037 Gastroparesis 54 0.039
274
GGR001 Geographic Tongue 45 0.039
275
RSP007 Respiratory Distress Syndrome, Infant 26 0.039
276
HNC001 Henoch-Schoenlein Purpura 45 0.039
277
TRP002 Tropical Spastic Paraparesis 55 0.039
278
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 43 0.039
279
SVN001 Sveinsson Choreoretinal Atrophy 28 0.039
280
P NRM001 Neuromyelitis Optica 55 0.039
281
P DDN001 Duodenal Ulcer 51 0.039
282
ALN001 Aland Island Eye Disease 45 0.039
283
VGT001 Vogt-Koyanagi-Harada Disease 54 0.039
284
LGN002 Legionellosis 61 0.039
285
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.039
286
c SVR001 Severe Acute Respiratory Syndrome 56 0.039
287
PLS006 Plasmodium Vivax Malaria 52 0.039
288
ESN002 Eosinophilia-Myalgia Syndrome 45 0.039
289
TXC005 Toxic Shock Syndrome 61 0.039
290
P MMP001 Mumps 56 0.039
291
P BRN009 Burning Mouth Syndrome 54 0.039
292
c ATM011 Autoimmune Hepatitis 62 0.039
293
CHR031 Chromoblastomycosis 43 0.039
294
MLL002 Miller Fisher Syndrome 43 0.039
295
CYS008 Cystic Echinococcosis 48 0.039
296
MYD002 Myd88 Deficiency 47 0.039
297
ECH003 Echinococcosis 53 0.039
298
HMR004 Hemorrhagic Fever with Renal Syndrome 52 0.039
299
CYN002 Cyanosis, Transient Neonatal 29 0.039
300
BRW004 Brown-Sequard Syndrome 32 0.039
301
TRN004 Trench Fever 38 0.039
302
ADL030 Adult-Onset Still's Disease 57 0.039
303
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.039
304
c CTS008 Cutis Laxa, Autosomal Dominant 33 0.039
305
VSC003 Visceral Leishmaniasis 56 0.039
306
c NRP033 Neuropathy, Hereditary Sensory and Autonomic, Type Ia 27 0.039
307
OBS061 Obstructive Sleep Apnea 61 0.039
308
BTN002 Boutonneuse Fever 37 0.039
309
DFF021 Diffuse Mesangial Sclerosis 40 0.039
310
P INT068 Intestinal Disease 60 0.039
311
P VNS003 Venous Insufficiency 53 0.039
312
INT051 Intussusception 50 0.039
313
IRD001 Iridocyclitis 40 0.039
314
c VRL010 Viral Hepatitis 60 0.039
315
P LCH002 Lichen Planus 61 0.039
316
DSS009 Disseminated Intravascular Coagulation 52 0.039
317
GST045 Gastroenteritis 59 0.039
318
INT002 Intermittent Claudication 56 0.039
319
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.039
320
P SYP003 Syphilis 51 0.039
321
TNS005 Tonsillitis 58 0.039
322
TRC003 Trichomoniasis 41 0.039
323
CMP002 Campylobacteriosis 47 0.039
324
P SLP006 Sleep Apnea 60 0.039
325
DPH001 Diphtheria 55 0.039
326
ART021 Arteriosclerosis 59 0.039
327
ACT216 Acute Leukemia of Ambiguous Lineage 30 0.039
328
END030 End Stage Renal Failure 53 0.039
329
FCH002 Fuchs' Heterochromic Uveitis 41 0.039
330
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.039
331
PRR002 Pure Red-Cell Aplasia 47 0.039
332
PLN005 Palindromic Rheumatism 43 0.039
333
PRS012 Pars Planitis 43 0.039
334
ALX001 Alexia 42 0.039
335
P HMR012 Hemorrhagic Fever 55 0.039
336
P SPN052 Spondyloarthropathy 58 0.039
337
TBR008 Tuberculous Peritonitis 37 0.039
338
P MSC033 Muscle Disorders 52 0.039
339
ALV002 Alveolar Echinococcosis 50 0.039
340
RCR004 Recurrent Respiratory Papillomatosis 42 0.039
341
TBS001 Tabes Dorsalis 32 0.039
342
PRC013 Pericarditis 52 0.039
343
CTN007 Cutaneous Leishmaniasis 62 0.039
344
CLD007 Cold Agglutinin Disease 44 0.039
345
SPN331 Spondyloocular Syndrome 27 0.039
346
SYN007 Synovitis 56 0.039
347
DNG002 Dengue Hemorrhagic Fever 60 0.039
348
MLT075 Multifocal Motor Neuropathy 40 0.039
349
PNN001 Panniculitis 47 0.039
350
TRS001 Tarsal Tunnel Syndrome 33 0.039
351
c ALL027 Allergic Bronchopulmonary Aspergillosis, Familial 20 0.039
352
c HPT007 Hepatitis E 51 0.039
353
P UVT001 Uveitis 60 0.039
354
RLP003 Relapsing Fever 40 0.039
355
GLC003 Glucose Intolerance 56 0.039
356
P AST032 Asthma-Related Traits 7 16 0.039
357
BCT004 Bacteriuria 48 0.039
358
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 45 0.039
359
BRN014 Bronchopneumonia 45 0.039
360
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 50 0.039
361
c CNG033 Congenital Syphilis 39 0.039
362
IRT001 Iritis 36 0.039
363
DRS001 Dressler's Syndrome 34 0.039
364
ARB001 Ariboflavinosis 30 0.039
365
BLP001 Blepharochalasis 35 0.039
366
CYT005 Cytomegalovirus Retinitis 48 0.039
367
P PNV001 Panuveitis 50 0.039
368
c ACT027 Acute Pancreatitis 59 0.039
369
CPL005 Capillary Disease 39 0.039
370
ERY004 Erysipelas 39 0.039
371
THR010 Third Cranial Nerve Disease 27 0.039
372
OBS001 Obstructive Jaundice 47 0.039
373
DMY004 Demyelinating Disease 52 0.039
374
LSB001 Louse-Borne Relapsing Fever 42 0.039
375
HYP458 Hyper Ige Syndrome 43 0.039
376
RSP002 Respiratory Syncytial Virus Infectious Disease 31 0.039
377
VRL003 Variola Major 41 0.039
378
BCT015 Bacteremia 50 0.039
379
NPH004 Nephropathia Epidemica 39 0.039
380
TRT003 Tertiary Syphilis 33 0.039
381
c VRL012 Viral Meningitis 48 0.039
382
P BRY005 Beryllium Disease 39 0.039
383
ALC009 Alcoholic Liver Cirrhosis 53 0.039
384
PTY001 Pityriasis Rosea 42 0.039
385
PRL014 Paralytic Squint 25 0.039
386
ASY002 Asymptomatic Neurosyphilis 35 0.039
387
c ATM024 Autoimmune Pancreatitis 46 0.039
388
AGR018 Agraphia 38 0.039
389
P END033 Endocarditis 52 0.039
390
ORL013 Oral Lichen Planus 53 0.039
391
MNC006 Monoclonal Gammopathy of Uncertain Significance 45 0.039
392
TRY001 Trypanosomiasis 51 0.039
393
JNT002 Joint Disorders 55 0.039
394
OCL003 Oculomotor Nerve Paralysis 26 0.039
395
P EXN002 Exanthem 57 0.039
396
ALC006 Alcoholic Hepatitis 60 0.039
397
CLT003 Colitis 56 0.039
398
BRY001 Berylliosis 38 0.039
399
DYS016 Dysgammaglobulinemia 37 0.039
400
INT042 Internuclear Ophthalmoplegia 36 0.039
401
ORL003 Oral Tuberculosis 40 0.039
402
JPN001 Japanese Spotted Fever 31 0.039
403
PRS047 Prostatitis 56 0.039
404
QLT001 Qualitative Platelet Defect 30 0.039
405
ANG002 Angiostrongyliasis 40 0.039
406
c SVR005 Severe Pre-Eclampsia 48 0.039
407
TRT002 Tertiary Neurosyphilis 28 0.039
408
DBT062 Diabetic Foot Ulcers 55 0.039
409
PRS115 Prosthetic Joint Infection 45 0.039
410
ANT013 Anterior Spinal Artery Syndrome 27 0.039
411
P ACQ041 Acquired Amegakaryocytic Thrombocytopenia 22 0.039
412
P ACT135 Acute Graft Versus Host Disease 52 0.039
413
MNN005 Meningovascular Neurosyphilis 24 0.039
414
NNT049 Nontuberculous Mycobacterial Lung Disease 41 0.039
415
c SCN036 Secondary Progressive Multiple Sclerosis 50 0.039
416
ACT164 Actinic Prurigo 40 0.039
417
c CHR576 Chronic Beryllium Disease 39 0.039
418
LWN001 Lown-Ganong-Levine Syndrome 28 0.039
419
RHM009 Rheumatoid Lung Disease 41 0.039
420
IND004 Indeterminate Leprosy 32 0.039
421
UNL013 Unilateral Absence of a Pulmonary Artery 22 0.039
422
CRY008 Cryopyrin-Associated Periodic Syndrome 31 0.039
423
HDN004 Head and Neck Carcinoma 54 0.039
424
P PRM108 Primary Progressive Multiple Sclerosis 47 0.039
425
PRS036 Parasitic Protozoa Infectious Disease 45 0.039
426
MYS002 Myositis Fibrosa 35 0.039
427
CCC002 Coccidiosis 49 0.039
428
LRY028 Laryngocele 20 0.039
429
HMN032 Human Herpesvirus 8 42 0.039
430
c INT064 Intermediate Uveitis 47 0.039
431
PST053 Postherpetic Neuralgia 41 0.039
432
NRS003 Neurosyphilis 41 0.039
433
P CHL066 Cholangitis 48 0.039
434
PNC005 Penicilliosis 38 0.039
435
ANC002 Anca-Associated Vasculitis 43 0.039
436
c ACT059 Acute Maxillary Sinusitis 38 0.039
437
CHR276 Chronic Active Epstein-Barr Virus Infection 45 0.039
438
P BLD051 Blood Coagulation Disease 44 0.039
439
PYL004 Pyelitis 39 0.039
440
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.039
441
BRN039 Bronchial Neoplasm 35 0.039
442
DNG001 Dengue Shock Syndrome 41 0.039
443
FLL029 Fallopian Tube Disease 33 0.039
444
PRN006 Parenchymatous Neurosyphilis 14 0.039
445
HTR001 Heterophyiasis 31 0.039
446
MCR191 Microscopic Colitis 46 0.039
447
P SCL009 Sclerosing Cholangitis 47 0.039
448
c SCN006 Secondary Syphilis 41 0.039
449
P CRV039 Cervicitis 45 0.039
450
END074 Endocardium Disease 26 0.039
451
ABD004 Abdominal Tuberculosis 37 0.039
452
INT071 Intestinal Perforation 40 0.039
453
PLY010 Polyclonal Hypergammaglobulinemia 31 0.039
454
SHW001 Shwartzman Phenomenon 38 0.039
455
P SLP003 Salpingitis 32 0.039
456
SPN186 Spinal Cord Injury 62 0.039
457
CRT009 Critical Illness Polyneuropathy 38 0.039
458
CRB005 Cerebral Arteritis 27 0.039
459
SPN051 Spondylitis 50 0.039
460
CRN030 Coronary Stenosis 50 0.039
461
PLS010 Plasma Protein Metabolism Disease 37 0.039
462
MRN002 Mooren's Ulcer 34 0.039
463
PRN049 Paraneoplastic Pemphigus 40 0.039
464
c HYP072 Hypersensitivity Reaction Type Iii Disease 39 0.039
465
NRS001 Neuroschistosomiasis 30 0.039
466
MDD010 Middle Ear Disease 47 0.039
467
SYS003 Systolic Heart Failure 42 0.039
468
TBL007 Tibial Neuropathy 28 0.039
469
RTN023 Retinitis 49 0.039
470
CNT046 Central Nervous System Vasculitis 44 0.039
471
EXT033 Extrapulmonary Tuberculosis 45 0.039
472
LYM045 Lymphocytic Vasculitis 35 0.039
473
OTP003 Oto-Palatal-Digital Syndrome 14 0.039
474
RHM014 Rheumatoid Vasculitis 42 0.039
475
PRN039 Paraneoplastic Syndromes 42 0.039
476
OCL025 Ocular Toxoplasmosis 40 0.039
477
MLN003 Melancholia 36 0.039
478
MNC004 Monoclonal Paraproteinemia 35 0.039
479
GLC001 Glaucomatocyclitic Crisis 28 0.039
480
GNG006 Gingival Hypertrophy 29 0.039
481
c CHR098 Chronic Pyelonephritis 38 0.039
482
OVR063 Overnutrition 49 0.039
483
PLY020 Polyradiculoneuropathy 42 0.039
484
IDP064 Idiopathic Neutropenia 43 0.039
485
SLP002 Salpingitis Isthmica Nodosa 19 0.039
486
STR077 Streptococcal Toxic-Shock Syndrome 38 0.039
487
ANT017 Anthracosilicosis 19 0.039
488
CRB086 Cerebral Aneurysms 39 0.039
489
ANG054 Angina Pectoris 48 0.039
490
c CHR099 Chronic Salpingitis 28 0.039
491
HMT018 Hematopoietic Stem Cell Transplantation 39 0.039
492
c INV001 Invasive Aspergillosis 44 0.039
493
SPP004 Suppurative Cholangitis 35 0.039
494
URM005 Uremic Pruritus 38 0.039
495
ANT005 Anteroseptal Myocardial Infarction 23 0.039
496
END016 Endocervicitis 27 0.039
497
c ACT036 Acute Cholangitis 31 0.039
498
c ACT066 Acute Cervicitis 31 0.039
499
CCT003 Cicatricial Entropion 16 0.039
500
c CHR094 Chronic Polyneuropathy 29 0.039
501
IDP074 Idiopathic Bronchiectasis 34 0.039
502
SPS002 Spastic Entropion 29 0.039
503
THY003 Thymic Dysplasia 35 0.039
504
DSS024 Disease of Anatomical Entity 40 0.039
505
CMM006 Commensal Bacterial Infectious Disease 30 0.039
506
P ACQ009 Acquired Metabolic Disease 42 0.039
507
BNS002 Bone Structure Disease 37 0.039
508
OST008 Osteosclerotic Myeloma 37 0.039
509
RHM013 Rheumatoid Nodulosis 27 0.039
510
LMB062 Limb Ischemia 48 0.039
511
P PSD086 Pseudoarthrosis 23 0.039
512
MSC004 Muscle Tissue Disease 35 0.039
513
CHR415 Chronic Venous Leg Ulcers 31 0.039
514
P BRS047 Breast Cancer 100 0.027
515
P PNC035 Pancreatic Cancer 86 0.027
516
SKN016 Skin Disease 69 0.027
517
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.027
518
P APL001 Aplastic Anemia 74 0.027
519
MNK001 Menkes Disease 61 0.027
520
c TBR024 Tuberous Sclerosis-1 50 0.027
521
WLL001 Williams-Beuren Syndrome 61 0.027
522
P TBR001 Tuberous Sclerosis 68 0.027
523
P ALX003 Alexander Disease 64 0.027
524
P NMN002 Niemann-Pick Disease 63 0.027
525
P PLR004 Pleuropulmonary Blastoma 63 0.027
526
URT039 Urticaria 58 0.027
527
CRD119 Cardiac Arrest 63 0.027
528
CSY001 C Syndrome 49 0.027
529
ULC004 Ulcerative Colitis 74 0.027
530
FCT003 Factor X Deficiency 62 0.027
531
P SHR029 Short Syndrome 60 0.027
532
c NMN016 Niemann-Pick Disease, Type B 43 0.027
533
FCT006 Factor V Deficiency 62 0.027
534
c ATS308 Autosomal Dominant Cerebellar Ataxia 51 0.027
535
ACR041 Acromelic Frontonasal Dysostosis 45 0.027
536
P INF032 Infertility 61 0.027
537
ADL002 Adult Syndrome 53 0.027
538
LYS017 Loeys-Dietz Syndrome 4 37 0.027
539
MTH009 Mouth Disease 63 0.027
540
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 27 0.027
541
P HRM001 Hermansky-Pudlak Syndrome 56 0.027
542
ALL026 Allergic Hypersensitivity Disease 53 0.027
543
PNM001 Pneumocystosis 50 0.027
544
P LYM118 Lymphoma 68 0.027
545
NCR004 Nocardiosis 44 0.027
546
GLC012 Galactosialidosis 46 0.027
547
P IGN003 Iga Nephropathy 1 31 0.027
548
BRL011 Bare Lymphocyte Syndrome, Type I 40 0.027
549
C3D001 C3 Deficiency 50 0.027
550
QDR001 Quadriplegia 51 0.027
551
SPC010 Speech and Communication Disorders 42 0.027
552
P ANP001 Anaplastic Large Cell Lymphoma 58 0.027
553
P SNS014 Sinusitis 66 0.027
554
IMM068 Immunodeficiency 8 32 0.027
555
ACR002 Acrocapitofemoral Dysplasia 35 0.027
556
CYS040 Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Mental Retardation 20 0.027
557
MVM001 Movement Disease 45 0.027
558
c CTS031 Cutis Laxa, Autosomal Dominant 2 23 0.027
559
c MRG011 Meier-Gorlin Syndrome 4 21 0.027
560
DBT001 Diabetic Ketoacidosis 45 0.027
561
LNG054 Lung Agenesis 33 0.027
562
P PNC044 Pancreatitis 62 0.027
563
IMM015 Immune Defect Due to Absence of Thymus 38 0.027
564
P MSC007 Muscle Hypertrophy 55 0.027
565
CRY001 Cryptogenic Organizing Pneumonia 44 0.027
566
NTR006 Neutrophil Immunodeficiency Syndrome 36 0.027
567
P ADN016 Adenocarcinoma 69 0.027
568
PRT014 Protein S Deficiency 54 0.027
569
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.027
570
RTN017 Retinal Detachment 58 0.027
571
LPD004 Lipoid Nephrosis 49 0.027
572
TRT015 Torticollis, Keloids, Cryptorchidism, and Renal Dysplasia 19 0.027
573
DFF003 Diffuse Scleroderma 39 0.027
574
CRL004 Caroli Disease 40 0.027
575
BLM002 Bulimia Nervosa 54 0.027
576
LRN003 Learning Disability 49 0.027
577
EXS001 Exostosis 42 0.027
578
MGC001 Megacolon 50 0.027
579
PYM001 Pyomyositis 39 0.027
580
SPR007 Superior Mesenteric Artery Syndrome 37 0.027
581
c CTS041 Cutis Laxa, Autosomal Dominant 3 22 0.027
582
P CMP008 Compartment Syndrome 46 0.027
583
TRC038 Tracheobronchomegaly 24 0.027
584
MCH010 Michels Syndrome 24 0.027
585
ASP007 Aspiration Pneumonia 46 0.027
586
P AST022 Asthma Susceptibility 5 18 0.027
587
c CRN214 Coronary Heart Disease 5 22 0.027
588
ACT017 Acute Chest Syndrome 50 0.027
589
TRC020 Tracheitis 30 0.027
590
P PNC001 Pancytopenia 53 0.027
591
HMS001 Hemosiderosis 42 0.027
592
SXL003 Sexual Disorder 45 0.027
593
LGP001 Lagophthalmos 27 0.027
594
ANT039 Antisynthetase Syndrome 36 0.027
595
EPG003 Epiglottitis 32 0.027
596
BRT030 Birth Defects 44 0.027
597
ADJ001 Adjustment Disorder 38 0.027
598
PYL006 Pyloric Stenosis 46 0.027
599
PLM012 Pulmonary Sarcoidosis 54 0.027
600
P HYP009 Hypertrophic Pyloric Stenosis 40 0.027
601
TRC026 Tracheal Disease 33 0.027
602
BLD053 Blood Platelet Disease 44 0.027
603
VSC009 Vascular Skin Disease 21 0.027
604
c VRL005 Viral Pneumonia 44 0.027
605
P MNC007 Monocytic Leukemia 52 0.027
606
ISC015 Ischemic Colitis 38 0.027
607
PHY002 Physical Disorder 43 0.027
608
ANX004 Anoxia 45 0.027
609
c CNT028 Central Retinal Artery Occlusion 34 0.027
610
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.027
611
HRS011 Horseshoe Kidney 34 0.027
612
HRT012 Heart Valve Disease 39 0.027
613
SPC003 Specific Developmental Disorder 39 0.027
614
GLC077 Glucocorticoid Therapy, Response to 17 0.027
615
c INF136 Influenza, Severe 17 0.027
616
ORB006 Orbital Cellulitis 27 0.027
617
SXD001 Sex Differentiation Disease 39 0.027
618
WLS002 Wilson-Mikity Syndrome 15 0.027
619
LRY004 Laryngotracheitis 29 0.027
620
PLM015 Pulmonary Systemic Sclerosis 23 0.027
621
RHN002 Rhinoscleroma 34 0.027
622
TXC001 Toxic Megacolon 26 0.027
623
BLD054 Blood Protein Disease 38 0.027
624
GST007 Gastric Dilatation 38 0.027
625
HYP015 Hyperlucent Lung 35 0.027
626
c ACQ027 Acquired Cutis Laxa 27 0.027
627
P RTN014 Retinal Artery Occlusion 32 0.027
628
ALM002 Aluminium Lung 8 0.027
629
c ALX006 Alexander Disease Type Ii 17 0.027
630
c ADL027 Adult Dermatomyositis 31 0.027
631
BLS003 Blastoma 37 0.027
632
BND014 Bone Development Disease 40 0.027
633
LMN005 Lmna-Related Cardiocutaneous Progeria Syndrome 15 0.027
634
c PLM044 Pulmonary Fibrosis, Familial 28 0.027
635
PRM053 Primary Release Disorder of Platelets 13 0.027
636
WTH001 Withdrawal Disorder 36 0.027
637
CNG069 Congenital Cytomegalovirus 34 0.027
638
PLM116 Pulmonary Artery Hypoplasia 16 0.027
639
IDP075 Idiopathic and/or Familial Pulmonary Arterial Hypertension 11 0.027
640
P FML187 Familial Hypertension 35 0.027
641
CD4004 Cd4 Deficiency 15 0.027
642
BNF002 Bone Fracture 46 0.027
643
PLM053 Pulmonary Artery Agenesis 12 0.027
644
ORL014 Oral Pharyngeal Disorders 13 0.027
645
MNT045 Montefiore Syndrome 11 0.027
646
SHK001 Shaken Baby Syndrome 17 0.027