Search results for "emphysema"

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

608 hits were found for 'emphysema'

# Family MCID Name MIFTS Score
1
EMP007 Emphysema Due to Aat Deficiency 56 6.714
2
PLM034 Pulmonary Emphysema 54 6.227
3
EMP011 Emphysema, Congenital Lobar 27 4.985
4
INT011 Interstitial Emphysema 38 4.486
5
CMP003 Compensatory Emphysema 11 3.873
6
BRR006 Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification 6 3.159
7
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 7 2.266
8
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 29 2.226
9
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.291
10
LNG099 Lung Disease 62 0.284
11
PNM008 Pneumothorax 52 0.210
12
P PLM036 Pulmonary Fibrosis 68 0.199
13
BRN024 Bronchitis 63 0.171
14
RSP006 Respiratory System Disease 62 0.169
15
P PNM007 Pneumonia 66 0.132
16
P LNG032 Lung Cancer 94 0.129
17
P AST005 Asthma 82 0.129
18
P PLM040 Pulmonary Valve Disease 45 0.126
19
MDS022 Mediastinitis 41 0.119
20
BRN038 Bronchial Disease 54 0.116
21
P PLM037 Pulmonary Hypertension 79 0.109
22
UPP004 Upper Respiratory Tract Disease 48 0.109
23
P CTS001 Cutis Laxa 59 0.101
24
BRN002 Bronchiolitis 56 0.101
25
NTR005 Nutritional Deficiency Disease 39 0.101
26
c CHR096 Chronic Pulmonary Heart Disease 40 0.093
27
BRN055 Bronchogenic Cyst 27 0.093
28
TBR010 Tuberculosis 69 0.089
29
END072 Endotheliitis 42 0.089
30
SRN001 Serine Deficiency 32 0.084
31
MRF001 Marfan Syndrome 73 0.079
32
ATH003 Atherosclerosis 62 0.079
33
INT066 Interstitial Lung Disease 58 0.074
34
PRT011 Protein C Deficiency 51 0.074
35
P HRT032 Heart Disease 76 0.069
36
VSC011 Vasculitis 62 0.069
37
BRN022 Bronchiectasis 47 0.069
38
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.069
39
CRB009 Cerebritis 38 0.069
40
PNM003 Pneumatosis Cystoides Intestinalis 31 0.069
41
c AST037 Asthma 1 31 0.069
42
c AST039 Asthma 2 31 0.069
43
CYS001 Cystic Fibrosis 86 0.063
44
P INF038 Influenza 74 0.063
45
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.063
46
P OST002 Osteoporosis 64 0.063
47
CHL123 Chlamydia 59 0.063
48
P DRM010 Dermatomyositis 58 0.063
49
ANR040 Aneurysm 57 0.063
50
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.063
51
P PNM006 Pneumoconiosis 51 0.063
52
STT002 Status Asthmaticus 43 0.063
53
DFF002 Diffuse Pulmonary Fibrosis 33 0.063
54
P RSP003 Respiratory Failure 70 0.056
55
PLM001 Pulmonary Tuberculosis 68 0.056
56
CNN005 Connective Tissue Disease 61 0.056
57
MSL001 Measles 61 0.056
58
c ACT210 Acute Respiratory Distress Syndrome 57 0.056
59
SLP005 Sleep Disorder 53 0.056
60
SLC006 Silicosis 53 0.056
61
P CYS018 Cystitis 53 0.056
62
BRN056 Bronchopulmonary Dysplasia 49 0.056
63
FSC004 Fasciitis 46 0.056
64
DPH021 Diaphragm Disease 45 0.056
65
NCR007 Necrotizing Fasciitis 45 0.056
66
NNS002 Nonspecific Interstitial Pneumonia 44 0.056
67
MLR002 Miliary Tuberculosis 42 0.056
68
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 29 0.056
69
MRG013 Mirage Syndrome 26 0.056
70
NNT039 Neonatal Marfan Syndrome 26 0.056
71
P LVR013 Liver Disease 72 0.049
72
KWS002 Kawasaki Disease 70 0.049
73
PCK002 Pick Disease 67 0.049
74
P MNN013 Meningitis 65 0.049
75
APP008 Appendicitis 60 0.049
76
P CNG015 Congenital Diaphragmatic Hernia 58 0.049
77
P SYS005 Systemic Scleroderma 58 0.049
78
ALL006 Allergic Asthma 58 0.049
79
BRN012 Bronchiolitis Obliterans 58 0.049
80
ELL001 Ellis-Van Creveld Syndrome 57 0.049
81
IDP011 Idiopathic Interstitial Pneumonia 57 0.049
82
HYP266 Hypoxia 55 0.049
83
P PRP019 Peripheral Nervous System Disease 54 0.049
84
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.049
85
P PYL005 Pyelonephritis 52 0.049
86
BRT002 Birt-Hogg-Dube Syndrome 51 0.049
87
CYT008 Cytomegalovirus Infection 51 0.049
88
GSG001 Gas Gangrene 49 0.049
89
HMN014 Human Immunodeficiency Virus Infectious Disease 49 0.049
90
MCR088 Microscopic Polyangiitis 48 0.049
91
ATN002 Autonomic Nervous System Disease 47 0.049
92
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 47 0.049
93
BNN003 Bone Inflammation Disease 46 0.049
94
CRR007 Cirrhosis, Cryptogenic 44 0.049
95
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.049
96
DDN006 Duodenitis 44 0.049
97
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 33 0.049
98
LYM035 Lymphangiectasis 28 0.049
99
P PLM064 Pulmonary Sequestration 26 0.049
100
c CTS019 Cutis Laxa, Ad 26 0.049
101
SBS002 Substernal Goiter 24 0.049
102
TRC037 Tracheobronchomalacia 22 0.049
103
c CTS037 Cutis Laxa, Autosomal Recessive, Type Ib 20 0.049
104
AND005 Androgen Insensitivity Syndrome, Mild 16 0.049
105
CTS042 Cutis Laxa, Neonatal, with Marfanoid Phenotype 13 0.049
106
SPN014 Spontaneous Tension Pneumothorax 12 0.049
107
P RHM011 Rheumatoid Arthritis 88 0.040
108
HV1006 Hiv-1 82 0.040
109
P MYC007 Myocardial Infarction 79 0.040
110
P ART022 Arthritis 75 0.040
111
ULC004 Ulcerative Colitis 75 0.040
112
KRT004 Keratitis 70 0.040
113
P LKM002 Leukemia 70 0.040
114
FBR012 Fabry Disease 69 0.040
115
c HYP595 Hypertension, Essential 69 0.040
116
P LPR003 Leprosy 68 0.040
117
CMM004 Common Variable Immunodeficiency 67 0.040
118
ART016 Aortic Aneurysm 67 0.040
119
SRC014 Sarcoma 66 0.040
120
OTT002 Otitis Media 66 0.040
121
P LYM007 Lymphangioleiomyomatosis 65 0.040
122
BRC012 Brucellosis 65 0.040
123
TBR024 Tuberous Sclerosis-1 65 0.040
124
PRT037 Pertussis 64 0.040
125
LPT001 Leptospirosis 63 0.040
126
LYM017 Lyme Disease 63 0.040
127
P ATP001 Atopic Dermatitis 62 0.040
128
PRT036 Peritonitis 62 0.040
129
CHG001 Chagas Disease 62 0.040
130
PRM097 Primary Immunodeficiency Disease 61 0.040
131
DRM006 Dermatitis 61 0.040
132
c GLY008 Glycogen Storage Disease Ii 61 0.040
133
TYP007 Typhoid Fever 61 0.040
134
P HML002 Hemolytic Anemia 60 0.040
135
P TMP003 Temporal Arteritis 60 0.040
136
P TXP001 Toxoplasmosis 60 0.040
137
P ADL010 Adult Respiratory Distress Syndrome 60 0.040
138
TKY002 Takayasu Arteritis 60 0.040
139
P SNS014 Sinusitis 60 0.040
140
P VNT002 Ventricular Septal Defect 59 0.040
141
CLT003 Colitis 59 0.040
142
RHM027 Rheumatic Disease 57 0.040
143
HMR004 Hemorrhagic Fever with Renal Syndrome 57 0.040
144
NRM005 Neuromuscular Disease 57 0.040
145
EXT034 Extrinsic Allergic Alveolitis 56 0.040
146
CRT016 Carotid Artery Disease 55 0.040
147
DMY004 Demyelinating Disease 55 0.040
148
FLR002 Filariasis 55 0.040
149
P HST010 Histiocytosis 55 0.040
150
c BCT007 Bacterial Meningitis 54 0.040
151
P EHL033 Ehlers-Danlos Syndrome, Classic Type 54 0.040
152
GTR002 Goiter 54 0.040
153
GST037 Gastroparesis 53 0.040
154
PLV003 Pelvic Inflammatory Disease 53 0.040
155
NTH001 Netherton Syndrome 52 0.040
156
DBT062 Diabetic Foot Ulcers 52 0.040
157
HYP596 Hypophosphatasia, Childhood 52 0.040
158
NCT008 Nicotine Dependence, Protection Against 52 0.040
159
P DDN001 Duodenal Ulcer 51 0.040
160
SPN051 Spondylitis 50 0.040
161
PLR008 Pleurisy 50 0.040
162
INF034 Infective Endocarditis 50 0.040
163
CYS008 Cystic Echinococcosis 50 0.040
164
P SCL015 Scleritis 49 0.040
165
RLP001 Relapsing Polychondritis 49 0.040
166
RTN023 Retinitis 49 0.040
167
c ANT034 Anterior Uveitis 49 0.040
168
CLL003 Cellulitis 49 0.040
169
PPL021 Papilledema 48 0.040
170
CHR005 Chorioamnionitis 48 0.040
171
DVR002 Diverticulitis 47 0.040
172
FRM003 Farmer's Lung 47 0.040
173
P BRN120 Bronchus Cancer 46 0.040
174
P PRD008 Periodontitis 46 0.040
175
SPP008 Suppurative Otitis Media 45 0.040
176
BRN014 Bronchopneumonia 45 0.040
177
P CRV039 Cervicitis 44 0.040
178
LYM116 Lymph Node Disease 44 0.040
179
P SLL003 Salla Disease 43 0.040
180
PRD007 Periodontal Disease 43 0.040
181
PRM025 Primary Bacterial Infectious Disease 43 0.040
182
P LRG014 Large Cell Neuroendocrine Carcinoma 41 0.040
183
INT071 Intestinal Perforation 41 0.040
184
PRD003 Periodontosis 41 0.040
185
HMT018 Hematopoietic Stem Cell Transplantation 41 0.040
186
CPL005 Capillary Disease 40 0.040
187
c CHR091 Chronic Meningitis 40 0.040
188
URT001 Urethritis 40 0.040
189
CRB086 Cerebral Aneurysms 39 0.040
190
CNJ007 Conjunctivochalasis 37 0.040
191
BNS002 Bone Structure Disease 36 0.040
192
ALR002 Al-Raqad Syndrome 36 0.040
193
ACL001 Acalculous Cholecystitis 36 0.040
194
LYM014 Lymphangitis 36 0.040
195
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 35 0.040
196
PNM010 Pneumothorax, Primary Spontaneous 33 0.040
197
AFR002 African Tick-Bite Fever 33 0.040
198
c CTS008 Cutis Laxa, Autosomal Dominant 32 0.040
199
BYS001 Byssinosis 31 0.040
200
MNN002 Mononeuritis Multiplex 25 0.040
201
P CRN178 Coronary Heart Disease 6 24 0.040
202
c CRN214 Coronary Heart Disease 5 23 0.040
203
c AST050 Asthma, Phf11-Related 22 0.040
204
ANT005 Anteroseptal Myocardial Infarction 22 0.040
205
c ALL027 Allergic Bronchopulmonary Aspergillosis, Familial 20 0.040
206
LRY028 Laryngocele 20 0.040
207
ANT017 Anthracosilicosis 18 0.040
208
P BRS047 Breast Cancer 100 0.028
209
P PNC035 Pancreatic Cancer 85 0.028
210
P CRN211 Coronary Artery Disease 75 0.028
211
P APL001 Aplastic Anemia 73 0.028
212
P LYM118 Lymphoma 70 0.028
213
P ADN016 Adenocarcinoma 69 0.028
214
PRP027 Peripheral Vascular Disease 69 0.028
215
SCK003 Sickle Cell Anemia 68 0.028
216
ISC006 Ischemic Heart Disease 68 0.028
217
VSC007 Vascular Disease 67 0.028
218
P MYP004 Myopathy 67 0.028
219
MLD001 Melioidosis 67 0.028
220
OBS061 Obstructive Sleep Apnea 66 0.028
221
c MLT024 Multiple Endocrine Neoplasia Iia 65 0.028
222
ART005 Arteriovenous Malformation 65 0.028
223
P PLR004 Pleuropulmonary Blastoma 64 0.028
224
PSR001 Psoriatic Arthritis 64 0.028
225
P ALX003 Alexander Disease 64 0.028
226
CHR066 Chronic Fatigue Syndrome 64 0.028
227
MTH009 Mouth Disease 63 0.028
228
P ART023 Arthropathy 63 0.028
229
OST085 Osteosarcoma, Somatic 63 0.028
230
CRD119 Cardiac Arrest 63 0.028
231
P NMN002 Niemann-Pick Disease 63 0.028
232
c SPN225 Spondyloarthropathy 1 63 0.028
233
RCT015 Reactive Arthritis 62 0.028
234
SPN186 Spinal Cord Injury 62 0.028
235
DNG002 Dengue Hemorrhagic Fever 62 0.028
236
LSH001 Leishmaniasis 62 0.028
237
CNT047 Contact Dermatitis 62 0.028
238
APH001 Aphthous Stomatitis 62 0.028
239
CTN007 Cutaneous Leishmaniasis 62 0.028
240
FCT003 Factor X Deficiency 62 0.028
241
WGN006 Wegener Granulomatosis 62 0.028
242
INT146 Intervertebral Disc Disease 62 0.028
243
TXC005 Toxic Shock Syndrome 61 0.028
244
MNK001 Menkes Disease 61 0.028
245
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.028
246
WLL001 Williams-Beuren Syndrome 61 0.028
247
P INT068 Intestinal Disease 61 0.028
248
P ALP009 Alopecia Areata 61 0.028
249
P INF032 Infertility 61 0.028
250
P SLP006 Sleep Apnea 61 0.028
251
c ACT075 Acute Myocardial Infarction 60 0.028
252
P ASP006 Aspergillosis 60 0.028
253
GNG013 Gingivitis 60 0.028
254
P PNC044 Pancreatitis 60 0.028
255
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.028
256
P SPN052 Spondyloarthropathy 60 0.028
257
P SHR029 Short Syndrome 60 0.028
258
GST045 Gastroenteritis 60 0.028
259
FCT006 Factor V Deficiency 60 0.028
260
QFV001 Q Fever 60 0.028
261
PLM033 Pulmonary Embolism 59 0.028
262
SPT004 Septic Arthritis 59 0.028
263
c LCL006 Localized Scleroderma 59 0.028
264
P MSC007 Muscle Hypertrophy 59 0.028
265
VRL011 Viral Infectious Disease 59 0.028
266
ALC006 Alcoholic Hepatitis 59 0.028
267
PRP030 Purpura 59 0.028
268
URT039 Urticaria 59 0.028
269
LGN002 Legionellosis 59 0.028
270
ART021 Arteriosclerosis 59 0.028
271
P NRM001 Neuromyelitis Optica 59 0.028
272
P ANT006 Antiphospholipid Syndrome 58 0.028
273
c ATM011 Autoimmune Hepatitis 58 0.028
274
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 58 0.028
275
P ANP001 Anaplastic Large Cell Lymphoma 58 0.028
276
SCH014 Schistosomiasis 58 0.028
277
TNS005 Tonsillitis 58 0.028
278
RTN017 Retinal Detachment 57 0.028
279
P NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 57 0.028
280
P EXN002 Exanthem 57 0.028
281
ADL030 Adult-Onset Still's Disease 57 0.028
282
c SVR001 Severe Acute Respiratory Syndrome 57 0.028
283
P BRN009 Burning Mouth Syndrome 57 0.028
284
LGG001 Legg-Calve-Perthes Disease 57 0.028
285
TRP002 Tropical Spastic Paraparesis 57 0.028
286
P MMP001 Mumps 56 0.028
287
P RBL001 Rubella 56 0.028
288
SPT005 Spotted Fever 56 0.028
289
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.028
290
GLL022 Guillain-Barre Syndrome 56 0.028
291
JNT002 Joint Disorders 56 0.028
292
INT002 Intermittent Claudication 56 0.028
293
VSC003 Visceral Leishmaniasis 55 0.028
294
PRC002 Paracoccidioidomycosis 55 0.028
295
P PLY017 Polyarteritis Nodosa 55 0.028
296
P MNC007 Monocytic Leukemia 55 0.028
297
CCC001 Coccidioidomycosis 55 0.028
298
P HMR012 Hemorrhagic Fever 55 0.028
299
LKN001 Leukoencephalopathy with Vanishing White Matter 54 0.028
300
SCR008 Scrub Typhus 54 0.028
301
MVM001 Movement Disease 54 0.028
302
c VRL007 Viral Encephalitis 54 0.028
303
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.028
304
HST011 Histoplasmosis 54 0.028
305
PLM012 Pulmonary Sarcoidosis 54 0.028
306
c HPT007 Hepatitis E 54 0.028
307
P MYC008 Myocarditis 54 0.028
308
BLM002 Bulimia Nervosa 54 0.028
309
P VNS003 Venous Insufficiency 53 0.028
310
RSC001 Rosacea 53 0.028
311
ADL002 Adult Syndrome 53 0.028
312
BRG013 Buerger Disease 53 0.028
313
ECH003 Echinococcosis 53 0.028
314
P SYP003 Syphilis 53 0.028
315
PLS006 Plasmodium Vivax Malaria 53 0.028
316
INT007 Intermediate Coronary Syndrome 52 0.028
317
END030 End Stage Renal Failure 52 0.028
318
P MSC033 Muscle Disorders 52 0.028
319
PRT014 Protein S Deficiency 52 0.028
320
P END033 Endocarditis 52 0.028
321
QDR001 Quadriplegia 52 0.028
322
P PNC001 Pancytopenia 52 0.028
323
VGT001 Vogt-Koyanagi-Harada Disease 52 0.028
324
BRN106 Burns 52 0.028
325
c INT064 Intermediate Uveitis 52 0.028
326
TRY001 Trypanosomiasis 52 0.028
327
CYS005 Cysticercosis 52 0.028
328
PRC013 Pericarditis 52 0.028
329
ALV002 Alveolar Echinococcosis 51 0.028
330
ANG054 Angina Pectoris 51 0.028
331
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.028
332
CRT049 Critical Limb Ischemia 51 0.028
333
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 51 0.028
334
LRN003 Learning Disability 51 0.028
335
HPT074 Hepatic Adenoma, Somatic 51 0.028
336
RHM028 Rheumatic Heart Disease 51 0.028
337
CRN030 Coronary Stenosis 50 0.028
338
c VRL012 Viral Meningitis 50 0.028
339
INT051 Intussusception 50 0.028
340
PRG009 Progressive Multifocal Leukoencephalopathy 50 0.028
341
PNM001 Pneumocystosis 50 0.028
342
c SCN036 Secondary Progressive Multiple Sclerosis 50 0.028
343
P CTN003 Cutaneous Lupus Erythematosus 50 0.028
344
P HML001 Hemolytic-Uremic Syndrome 50 0.028
345
MGC001 Megacolon 50 0.028
346
RHM001 Rheumatic Fever 50 0.028
347
OVR063 Overnutrition 49 0.028
348
RTC002 Reticular Dysgenesis 49 0.028
349
CSY001 C Syndrome 49 0.028
350
CYT005 Cytomegalovirus Retinitis 49 0.028
351
CCC002 Coccidiosis 49 0.028
352
CHR001 Churg-Strauss Syndrome 49 0.028
353
c ATS308 Autosomal Dominant Cerebellar Ataxia 49 0.028
354
P PNV001 Panuveitis 49 0.028
355
THR013 Thoracic Outlet Syndrome 49 0.028
356
P CHL066 Cholangitis 49 0.028
357
LMB062 Limb Ischemia 48 0.028
358
P CMP008 Compartment Syndrome 48 0.028
359
ACT017 Acute Chest Syndrome 48 0.028
360
SPN041 Spinal Cord Disease 48 0.028
361
P TRN034 Transverse Myelitis 48 0.028
362
RSP002 Respiratory Syncytial Virus Infectious Disease 48 0.028
363
BCT015 Bacteremia 48 0.028
364
LPD004 Lipoid Nephrosis 48 0.028
365
MYL001 Myelitis 48 0.028
366
CMP002 Campylobacteriosis 47 0.028
367
BNF002 Bone Fracture 47 0.028
368
c INV001 Invasive Aspergillosis 47 0.028
369
P PRM108 Primary Progressive Multiple Sclerosis 47 0.028
370
HYP074 Hypersensitivity Vasculitis 47 0.028
371
BCT004 Bacteriuria 47 0.028
372
PST062 Pustulosis Palmaris Et Plantaris 47 0.028
373
SXL003 Sexual Disorder 47 0.028
374
P SCL009 Sclerosing Cholangitis 47 0.028
375
GLC008 Glucose Metabolism Disease 47 0.028
376
GLC012 Galactosialidosis 47 0.028
377
MCR191 Microscopic Colitis 47 0.028
378
CNT046 Central Nervous System Vasculitis 47 0.028
379
MDD010 Middle Ear Disease 46 0.028
380
ASP007 Aspiration Pneumonia 46 0.028
381
SPC010 Speech and Communication Disorders 46 0.028
382
ACR041 Acromelic Frontonasal Dysostosis 46 0.028
383
PRR002 Pure Red-Cell Aplasia 46 0.028
384
BLD053 Blood Platelet Disease 46 0.028
385
HMN032 Human Herpesvirus 8 46 0.028
386
c ATM024 Autoimmune Pancreatitis 46 0.028
387
MYD002 Myd88 Deficiency 46 0.028
388
PYL006 Pyloric Stenosis 46 0.028
389
CRD137 Cardiogenic Shock 46 0.028
390
ALN001 Aland Island Eye Disease 45 0.028
391
MNN009 Meningoencephalitis 45 0.028
392
P BLD051 Blood Coagulation Disease 45 0.028
393
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 45 0.028
394
HDN002 Head Injury 45 0.028
395
NTR018 Neutrophilia, Hereditary 45 0.028
396
DBT008 Diabetic Angiopathy 45 0.028
397
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 45 0.028
398
c NMN016 Niemann-Pick Disease, Type B 45 0.028
399
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.028
400
HMS001 Hemosiderosis 45 0.028
401
IDP064 Idiopathic Neutropenia 45 0.028
402
IDP024 Idiopathic Inflammatory Myopathy 45 0.028
403
ALX001 Alexia 45 0.028
404
PRS036 Parasitic Protozoa Infectious Disease 45 0.028
405
PHY002 Physical Disorder 44 0.028
406
RSP019 Respiratory Distress Syndrome in Premature Infants 44 0.028
407
MNC006 Monoclonal Gammopathy of Uncertain Significance 44 0.028
408
GGR001 Geographic Tongue 44 0.028
409
IRK001 Irak4 Deficiency 44 0.028
410
CRP017 Carpal Tunnel Syndrome, Familial 44 0.028
411
P ART084 Arteriovenous Fistula 44 0.028
412
ANX004 Anoxia 44 0.028
413
CRY001 Cryptogenic Organizing Pneumonia 44 0.028
414
PRN019 Perinatal Necrotizing Enterocolitis 44 0.028
415
EXT033 Extrapulmonary Tuberculosis 44 0.028
416
PLY020 Polyradiculoneuropathy 44 0.028
417
RYN001 Raynaud Disease 44 0.028
418
EXS001 Exostosis 44 0.028
419
VRL003 Variola Major 43 0.028
420
P RTN014 Retinal Artery Occlusion 43 0.028
421
DNG001 Dengue Shock Syndrome 43 0.028
422
CHR276 Chronic Active Epstein-Barr Virus Infection 43 0.028
423
PLN005 Palindromic Rheumatism 43 0.028
424
SYS003 Systolic Heart Failure 43 0.028
425
PRS115 Prosthetic Joint Infection 43 0.028
426
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 43 0.028
427
RHM014 Rheumatoid Vasculitis 43 0.028
428
BRT030 Birth Defects 43 0.028
429
CLD007 Cold Agglutinin Disease 43 0.028
430
MLL002 Miller Fisher Syndrome 43 0.028
431
URM005 Uremic Pruritus 42 0.028
432
GNT001 Giant Cell Reparative Granuloma 42 0.028
433
c VRL005 Viral Pneumonia 42 0.028
434
PRS012 Pars Planitis 42 0.028
435
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.028
436
BND014 Bone Development Disease 42 0.028
437
LSB001 Louse-Borne Relapsing Fever 42 0.028
438
NCR004 Nocardiosis 42 0.028
439
CHR031 Chromoblastomycosis 42 0.028
440
IRD001 Iridocyclitis 42 0.028
441
STR077 Streptococcal Toxic-Shock Syndrome 41 0.028
442
ESN002 Eosinophilia-Myalgia Syndrome 41 0.028
443
PTY001 Pityriasis Rosea 41 0.028
444
c CHR576 Chronic Beryllium Disease 41 0.028
445
PST053 Postherpetic Neuralgia 41 0.028
446
c ATM022 Autoimmune Myocarditis 41 0.028
447
NNT049 Nontuberculous Mycobacterial Lung Disease 41 0.028
448
MLT075 Multifocal Motor Neuropathy 41 0.028
449
NRS003 Neurosyphilis 41 0.028
450
c SCN006 Secondary Syphilis 41 0.028
451
SPN369 Spinal Disease 41 0.028
452
DFF003 Diffuse Scleroderma 41 0.028
453
P ACQ009 Acquired Metabolic Disease 41 0.028
454
P HYP009 Hypertrophic Pyloric Stenosis 41 0.028
455
TCL002 T-Cell Large Granular Lymphocyte Leukemia 41 0.028
456
P FML187 Familial Hypertension 41 0.028
457
ANC002 Anca-Associated Vasculitis 41 0.028
458
c HYP072 Hypersensitivity Reaction Type Iii Disease 41 0.028
459
HRT012 Heart Valve Disease 41 0.028
460
BRL011 Bare Lymphocyte Syndrome, Type I 41 0.028
461
ORL003 Oral Tuberculosis 41 0.028
462
WTH001 Withdrawal Disorder 41 0.028
463
TRC003 Trichomoniasis 41 0.028
464
RCR004 Recurrent Respiratory Papillomatosis 40 0.028
465
OCL025 Ocular Toxoplasmosis 40 0.028
466
ISC015 Ischemic Colitis 40 0.028
467
SXD001 Sex Differentiation Disease 40 0.028
468
NPH004 Nephropathia Epidemica 40 0.028
469
BLD054 Blood Protein Disease 40 0.028
470
RHM009 Rheumatoid Lung Disease 40 0.028
471
SPC003 Specific Developmental Disorder 40 0.028
472
c SBC007 Subacute Thyroiditis 39 0.028
473
SPR007 Superior Mesenteric Artery Syndrome 39 0.028
474
TRN004 Trench Fever 39 0.028
475
ANG002 Angiostrongyliasis 39 0.028
476
CRT009 Critical Illness Polyneuropathy 39 0.028
477
BTN002 Boutonneuse Fever 39 0.028
478
EXT035 Extrinsic Cardiomyopathy 39 0.028
479
GST007 Gastric Dilatation 39 0.028
480
AGR018 Agraphia 39 0.028
481
PRN049 Paraneoplastic Pemphigus 39 0.028
482
PYM001 Pyomyositis 39 0.028
483
c CNG033 Congenital Syphilis 39 0.028
484
CRL004 Caroli Disease 39 0.028
485
ADJ001 Adjustment Disorder 38 0.028
486
BRY001 Berylliosis 38 0.028
487
STR002 Streptococcal Meningitis 38 0.028
488
PYL004 Pyelitis 38 0.028
489
P BRY005 Beryllium Disease 38 0.028
490
c ACT059 Acute Maxillary Sinusitis 38 0.028
491
c CHR098 Chronic Pyelonephritis 38 0.028
492
P RST011 Restrictive Dermopathy, Lethal 38 0.028
493
PLS010 Plasma Protein Metabolism Disease 38 0.028
494
DYS016 Dysgammaglobulinemia 37 0.028
495
IMM015 Immune Defect Due to Absence of Thymus 37 0.028
496
SHW001 Shwartzman Phenomenon 37 0.028
497
BLS003 Blastoma 37 0.028
498
P PSD086 Pseudoarthrosis 37 0.028
499
ANT039 Antisynthetase Syndrome 37 0.028
500
IDP074 Idiopathic Bronchiectasis 37 0.028
501
ACT216 Acute Leukemia of Ambiguous Lineage 36 0.028
502
MSC004 Muscle Tissue Disease 36 0.028
503
PNC005 Penicilliosis 36 0.028
504
INT042 Internuclear Ophthalmoplegia 36 0.028
505
TTR016 Tetra-Amelia Syndrome 36 0.028
506
LYS017 Loeys-Dietz Syndrome 4 36 0.028
507
NTR006 Neutrophil Immunodeficiency Syndrome 36 0.028
508
ACR002 Acrocapitofemoral Dysplasia 36 0.028
509
OST008 Osteosclerotic Myeloma 36 0.028
510
MRN002 Mooren's Ulcer 36 0.028
511
BLP001 Blepharochalasis 36 0.028
512
IRT001 Iritis 35 0.028
513
c CNT028 Central Retinal Artery Occlusion 35 0.028
514
THY003 Thymic Dysplasia 35 0.028
515
c ATM093 Autoimmune Disease of Peripheral Nervous System 35 0.028
516
HRS011 Horseshoe Kidney 35 0.028
517
TRC026 Tracheal Disease 35 0.028
518
CNG069 Congenital Cytomegalovirus 34 0.028
519
HYP015 Hyperlucent Lung 34 0.028
520
CRY008 Cryopyrin-Associated Periodic Syndrome 34 0.028
521
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.028
522
RHN002 Rhinoscleroma 34 0.028
523
ESN017 Eosinophilic Granuloma 34 0.028
524
FLL029 Fallopian Tube Disease 34 0.028
525
ADP007 Adie Pupil 34 0.028
526
MYS002 Myositis Fibrosa 33 0.028
527
SPP004 Suppurative Cholangitis 33 0.028
528
ASY002 Asymptomatic Neurosyphilis 33 0.028
529
EPG003 Epiglottitis 33 0.028
530
DRS001 Dressler's Syndrome 33 0.028
531
IND004 Indeterminate Leprosy 33 0.028
532
LNG054 Lung Agenesis 33 0.028
533
QLT001 Qualitative Platelet Defect 32 0.028
534
IMM068 Immunodeficiency 8 32 0.028
535
LYM045 Lymphocytic Vasculitis 32 0.028
536
TRC020 Tracheitis 32 0.028
537
BRW004 Brown-Sequard Syndrome 32 0.028
538
c ACT036 Acute Cholangitis 32 0.028
539
P SLP003 Salpingitis 32 0.028
540
GNC003 Geniculate Herpes Zoster 32 0.028
541
TBS001 Tabes Dorsalis 32 0.028
542
GNG006 Gingival Hypertrophy 32 0.028
543
c ADL027 Adult Dermatomyositis 31 0.028
544
c MLT009 Multiple Cranial Nerve Palsy 31 0.028
545
SCR039 Scorpion Envenomation 31 0.028
546
CYN002 Cyanosis, Transient Neonatal 31 0.028
547
CRB142 Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant 31 0.028
548
c PLM044 Pulmonary Fibrosis, Familial 30 0.028
549
JPN001 Japanese Spotted Fever 30 0.028
550
ARB001 Ariboflavinosis 30 0.028
551
c CHR094 Chronic Polyneuropathy 30 0.028
552
c FRN011 Frontal Sinusitis 30 0.028
553
c ATM078 Autoimmune Addison Disease 30 0.028
554
c ACT066 Acute Cervicitis 30 0.028
555
HTR001 Heterophyiasis 29 0.028
556
CRB005 Cerebral Arteritis 29 0.028
557
LGP001 Lagophthalmos 29 0.028
558
c PLM121 Pulmonary Hypertension, Primary, 4 29 0.028
559
ANT013 Anterior Spinal Artery Syndrome 29 0.028
560
LRY004 Laryngotracheitis 28 0.028
561
ORB006 Orbital Cellulitis 28 0.028
562
TXC001 Toxic Megacolon 28 0.028
563
SPS002 Spastic Entropion 28 0.028
564
THR010 Third Cranial Nerve Disease 28 0.028
565
OCL003 Oculomotor Nerve Paralysis 27 0.028
566
GLC001 Glaucomatocyclitic Crisis 27 0.028
567
SPN331 Spondyloocular Syndrome 27 0.028
568
ATR048 Atrial Tachyarrhythmia with Short Pr Interval 27 0.028
569
c ACQ027 Acquired Cutis Laxa 26 0.028
570
END074 Endocardium Disease 26 0.028
571
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 26 0.028
572
SVN001 Sveinsson Choreoretinal Atrophy 26 0.028
573
NPH064 Nipah Virus Disease 25 0.028
574
RHM013 Rheumatoid Nodulosis 25 0.028
575
HNM002 Hinman Syndrome 25 0.028
576
PLM015 Pulmonary Systemic Sclerosis 24 0.028
577
MNN005 Meningovascular Neurosyphilis 24 0.028
578
TRC038 Tracheobronchomegaly 23 0.028
579
PRL014 Paralytic Squint 23 0.028
580
VSC009 Vascular Skin Disease 22 0.028
581
c CTS031 Cutis Laxa, Autosomal Dominant 2 22 0.028
582
PLY135 Polydactyly, Postaxial, with Progressive Myopia 22 0.028
583
c CTS041 Cutis Laxa, Autosomal Dominant 3 22 0.028
584
TRT002 Tertiary Neurosyphilis 21 0.028
585
P ACQ041 Acquired Amegakaryocytic Thrombocytopenia 21 0.028
586
c MRG011 Meier-Gorlin Syndrome 4 20 0.028
587
CYS040 Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Mental Retardation 19 0.028
588
c ACT035 Acute Frontal Sinusitis 19 0.028
589
P AST022 Asthma Susceptibility 5 19 0.028
590
c INF136 Influenza, Severe 19 0.028
591
GLC077 Glucocorticoid Therapy, Response to 19 0.028
592
SLP002 Salpingitis Isthmica Nodosa 18 0.028
593
UNL013 Unilateral Absence of a Pulmonary Artery 18 0.028
594
c ALX006 Alexander Disease Type Ii 18 0.028
595
TRT015 Torticollis, Keloids, Cryptorchidism, and Renal Dysplasia 18 0.028
596
SHK001 Shaken Baby Syndrome 18 0.028
597
PLM116 Pulmonary Artery Hypoplasia 18 0.028
598
CD4004 Cd4 Deficiency 17 0.028
599
CCT003 Cicatricial Entropion 16 0.028
600
ORL014 Oral Pharyngeal Disorders 14 0.028
601
LMN005 Lmna-Related Cardiocutaneous Progeria Syndrome 14 0.028
602
PRM053 Primary Release Disorder of Platelets 14 0.028
603
WLS002 Wilson-Mikity Syndrome 14 0.028
604
PRN006 Parenchymatous Neurosyphilis 14 0.028
605
IDP075 Idiopathic and/or Familial Pulmonary Arterial Hypertension 13 0.028
606
MNT045 Montefiore Syndrome 13 0.028
607
PLM053 Pulmonary Artery Agenesis 12 0.028
608
ALM002 Aluminium Lung 10 0.028