Search results for "emphysema"

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

320 hits were found for 'emphysema'

# Family MCID Name MIFTS Score
1
ALP007 Alpha 1-Antitrypsin Deficiency 62 6.886
2
PLM034 Pulmonary Emphysema 58 6.747
3
CNG105 Congenital Lobar Emphysema 39 5.998
4
INT011 Interstitial Emphysema 23 4.574
5
CMP003 Compensatory Emphysema 9 3.762
6
BRR006 Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification 2 3.718
7
EMP007 Emphysema Due to Aat Deficiency 31 3.124
8
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 7 3.049
9
EMP008 Emphysema-Cirrhosis, Due to Aat Deficiency 4 3.005
10
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 34 2.180
11
PNM008 Pneumothorax 50 0.264
12
P PLM036 Pulmonary Fibrosis 69 0.224
13
BRN024 Bronchitis 67 0.204
14
PLM074 Pulmonary Function 34 0.183
15
P CHR409 Chronic Obstructive Pulmonary Disease 54 0.171
16
MDS022 Mediastinitis 46 0.149
17
CRP018 Cor Pulmonale 45 0.144
18
P PNM007 Pneumonia 78 0.139
19
P AST005 Asthma 89 0.134
20
c SPN183 Spontaneous Pneumothorax 52 0.129
21
P LNG032 Lung Cancer 79 0.124
22
c CTS001 Cutis Laxa 49 0.124
23
P HYP075 Hypertension 87 0.118
24
c PLM037 Pulmonary Hypertension 73 0.118
25
END072 Endotheliitis 51 0.118
26
BRN055 Bronchogenic Cyst 38 0.118
27
BRN002 Bronchiolitis 61 0.112
28
P RSP003 Respiratory Failure 70 0.105
29
IDP003 Idiopathic Pulmonary Fibrosis 67 0.105
30
TBR010 Tuberculosis 87 0.099
31
MRF001 Marfan Syndrome 85 0.091
32
P CNG401 Congenital Heart Disease 69 0.091
33
P PRM100 Primary Spontaneous Pneumothorax 58 0.091
34
SYN053 Syndromic Diarrhea 34 0.091
35
PNM003 Pneumatosis Cystoides Intestinalis 25 0.091
36
CYS001 Cystic Fibrosis 97 0.083
37
ATH003 Atherosclerosis 69 0.083
38
INT066 Interstitial Lung Disease 53 0.083
39
THR013 Thoracic Outlet Syndrome 52 0.083
40
CRB009 Cerebritis 39 0.083
41
P ATX002 Ataxia Telangiectasia 87 0.075
42
LVR012 Liver Cirrhosis 77 0.075
43
P OST002 Osteoporosis 76 0.075
44
P DRM010 Dermatomyositis 71 0.075
45
STT002 Status Asthmaticus 64 0.075
46
ACN002 Acanthosis Nigricans 63 0.075
47
BRN022 Bronchiectasis 62 0.075
48
MLR002 Miliary Tuberculosis 60 0.075
49
SLC006 Silicosis 58 0.075
50
LNG024 Langerhans-Cell Histiocytosis 57 0.075
51
BRN056 Bronchopulmonary Dysplasia 57 0.075
52
ART001 Arterial Tortuosity Syndrome 55 0.075
53
AND003 Andersen-Tawil Syndrome 54 0.075
54
P PNM006 Pneumoconiosis 50 0.075
55
ANR040 Aneurysm 46 0.075
56
FSC004 Fasciitis 46 0.075
57
NCR007 Necrotizing Fasciitis 44 0.075
58
P ATX010 Ataxia Neuropathy Spectrum 43 0.075
59
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.075
60
P PLM064 Pulmonary Sequestration 29 0.075
61
CRK001 Cork-Handlers' Disease 29 0.075
62
LYM035 Lymphangiectasis 24 0.075
63
DFF002 Diffuse Pulmonary Fibrosis 19 0.075
64
ANK002 Ankylosing Spondylitis 77 0.065
65
P PRM021 Primary Pulmonary Hypertension 77 0.065
66
P ANG001 Angelman Syndrome 70 0.065
67
MSL001 Measles 68 0.065
68
GSG001 Gas Gangrene 68 0.065
69
VSC011 Vasculitis 66 0.065
70
ART019 Aortic Valve Stenosis 64 0.065
71
MYC002 Mycobacterium Avium Complex Disease 59 0.065
72
c CNG015 Congenital Diaphragmatic Hernia 59 0.065
73
P VNT002 Ventricular Septal Defect 54 0.065
74
OBS006 Obstructive Lung Disease 53 0.065
75
P CYS018 Cystitis 51 0.065
76
CYT008 Cytomegalovirus Infection 44 0.065
77
c ACQ027 Acquired Cutis Laxa 41 0.065
78
CRB086 Cerebral Aneurysms 39 0.065
79
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 33 0.065
80
TRC037 Tracheobronchomalacia 23 0.065
81
AND005 Androgen Insensitivity Syndrome, Mild 21 0.065
82
SPN014 Spontaneous Tension Pneumothorax 15 0.065
83
P NRF002 Neurofibromatosis 94 0.053
84
P MYC007 Myocardial Infarction 93 0.053
85
FBR012 Fabry Disease 86 0.053
86
P TBR001 Tuberous Sclerosis 86 0.053
87
P NMN002 Niemann-Pick Disease 80 0.053
88
AND002 Androgen Insensitivity Syndrome 80 0.053
89
P LKM002 Leukemia 77 0.053
90
P ART022 Arthritis 75 0.053
91
ACQ007 Acquired Immunodeficiency Syndrome 71 0.053
92
ART016 Aortic Aneurysm 71 0.053
93
SRC014 Sarcoma 70 0.053
94
c PNC044 Pancreatitis 69 0.053
95
P LVR013 Liver Disease 69 0.053
96
P INF038 Influenza 68 0.053
97
P ABD003 Abdominal Aortic Aneurysm 68 0.053
98
c AXN002 Axenfeld-Rieger Syndrome 67 0.053
99
P PRD008 Periodontitis 67 0.053
100
c HML002 Hemolytic Anemia 66 0.053
101
BRR003 Barrett's Esophagus 64 0.053
102
EXT034 Extrinsic Allergic Alveolitis 64 0.053
103
P ADL010 Adult Respiratory Distress Syndrome 64 0.053
104
P HST010 Histiocytosis 64 0.053
105
PRT037 Pertussis 62 0.053
106
P GTR002 Goiter 62 0.053
107
P GLY008 Glycogen Storage Disease Ii 62 0.053
108
ELL001 Ellis-Van Creveld Syndrome 61 0.053
109
MLL005 Miller-Dieker Syndrome 60 0.053
110
BRN012 Bronchiolitis Obliterans 60 0.053
111
NRN001 Neuroendocrine Carcinoma 59 0.053
112
CLL003 Cellulitis 59 0.053
113
CNN005 Connective Tissue Disease 58 0.053
114
NNS002 Nonspecific Interstitial Pneumonia 58 0.053
115
P CRV039 Cervicitis 58 0.053
116
ACT100 Acute Febrile Neutrophilic Dermatosis 57 0.053
117
P PLR004 Pleuropulmonary Blastoma 57 0.053
118
PRD007 Periodontal Disease 56 0.053
119
P INT030 Intracranial Aneurysm 56 0.053
120
GST037 Gastroparesis 56 0.053
121
APP008 Appendicitis 56 0.053
122
c ACR001 Aicardi-Goutieres Syndrome 54 0.053
123
BLS003 Blastoma 54 0.053
124
PPL021 Papilledema 54 0.053
125
RTN023 Retinitis 54 0.053
126
PLM012 Pulmonary Sarcoidosis 53 0.053
127
USL001 Usual Interstitial Pneumonia 52 0.053
128
NRM005 Neuromuscular Disease 51 0.053
129
SYN006 Synovial Sarcoma 50 0.053
130
DVR002 Diverticulitis 49 0.053
131
P SLL003 Salla Disease 49 0.053
132
BRN014 Bronchopneumonia 48 0.053
133
SCH016 Schimke Immunoosseous Dysplasia 47 0.053
134
CNJ007 Conjunctivochalasis 47 0.053
135
c LRG014 Large Cell Neuroendocrine Carcinoma 46 0.053
136
HRS011 Horseshoe Kidney 45 0.053
137
INT071 Intestinal Perforation 42 0.053
138
BRN038 Bronchial Disease 42 0.053
139
TTR016 Tetra-Amelia Syndrome 42 0.053
140
HMT018 Hematopoietic Stem Cell Transplantation 41 0.053
141
c TYP003 Type I Ehlers-Danlos Syndrome 39 0.053
142
LRY004 Laryngotracheitis 37 0.053
143
CNG069 Congenital Cytomegalovirus 36 0.053
144
c CTS019 Cutis Laxa, Ad 34 0.053
145
LYM014 Lymphangitis 33 0.053
146
NNT039 Neonatal Marfan Syndrome 32 0.053
147
AMY016 Amyopathic Dermatomyositis 31 0.053
148
TFT003 Tufting Enteropathy 28 0.053
149
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.053
150
LRY028 Laryngocele 27 0.053
151
SBS002 Substernal Goiter 23 0.053
152
c BNG076 Benign Exophthalmos Syndrome 22 0.053
153
ANT017 Anthracosilicosis 20 0.053
154
ANT005 Anteroseptal Myocardial Infarction 17 0.053
155
c THR041 Thrombocytopenia, Acquired Amegakaryocytic 15 0.053
156
P ALZ001 Alzheimer's Disease 100 0.037
157
P RHM011 Rheumatoid Arthritis 94 0.037
158
P PNC035 Pancreatic Cancer 93 0.037
159
P LVR011 Liver Cancer 91 0.037
160
P LFR001 Li-Fraumeni Syndrome 88 0.037
161
GLC006 Galactosemia 86 0.037
162
P BRS047 Breast Cancer 86 0.037
163
THR006 Thromboangiitis Obliterans 79 0.037
164
CRH001 Crohn's Disease 76 0.037
165
P FML018 Familial Mediterranean Fever 76 0.037
166
KWS002 Kawasaki Disease 76 0.037
167
P SRC013 Sarcoidosis 75 0.037
168
P LYM007 Lymphangioleiomyomatosis 74 0.037
169
c DBT009 Diabetes Mellitus 74 0.037
170
MNK001 Menkes Disease 74 0.037
171
SVR004 Severe Combined Immunodeficiency 74 0.037
172
P WGN002 Wegener's Granulomatosis 74 0.037
173
RLP001 Relapsing Polychondritis 72 0.037
174
PRT036 Peritonitis 72 0.037
175
P MTB001 Metabolic Syndrome X 70 0.037
176
PLY017 Polyarteritis Nodosa 69 0.037
177
PCK001 Pick's Disease 69 0.037
178
c MNN013 Meningitis 68 0.037
179
c NPH012 Nephrotic Syndrome 67 0.037
180
ALL008 Allergic Bronchopulmonary Aspergillosis 67 0.037
181
ACT049 Acute Disseminated Encephalomyelitis 67 0.037
182
DBT001 Diabetic Ketoacidosis 66 0.037
183
PLM033 Pulmonary Embolism 66 0.037
184
ULC004 Ulcerative Colitis 65 0.037
185
P ALP009 Alopecia Areata 65 0.037
186
ARS001 Aarskog-Scott Syndrome 64 0.037
187
c HPT021 Hepatitis 64 0.037
188
c ACT027 Acute Pancreatitis 64 0.037
189
CLT003 Colitis 64 0.037
190
CMP002 Campylobacteriosis 63 0.037
191
DFC004 Deficiency Anemia 63 0.037
192
XLN002 X-Linked Hypophosphatemia 63 0.037
193
P ANP001 Anaplastic Large Cell Lymphoma 63 0.037
194
HPT022 Hepatoblastoma 62 0.037
195
P DDN001 Duodenal Ulcer 62 0.037
196
TYP007 Typhoid Fever 62 0.037
197
GNG013 Gingivitis 61 0.037
198
PLM001 Pulmonary Tuberculosis 61 0.037
199
P PRT008 Proteus Syndrome 61 0.037
200
PGM001 Pigmented Villonodular Synovitis 61 0.037
201
NRN004 Neuroendocrine Tumor 60 0.037
202
P SYN007 Synovitis 60 0.037
203
SPN020 Spondylosis 60 0.037
204
MGC001 Megacolon 60 0.037
205
P PRM054 Primary Sclerosing Cholangitis 60 0.037
206
FBR032 Fibromuscular Dysplasia 60 0.037
207
P ADN016 Adenocarcinoma 59 0.037
208
CHL068 Cholestasis 59 0.037
209
BLM002 Bulimia Nervosa 59 0.037
210
CLL021 Collagenous Colitis 58 0.037
211
NTH001 Netherton Syndrome 58 0.037
212
GLC012 Galactosialidosis 58 0.037
213
SCR002 Scurvy 58 0.037
214
P MYM002 Moyamoya Disease 58 0.037
215
P SNS014 Sinusitis 58 0.037
216
P SDR002 Siderosis 58 0.037
217
HYP266 Hypoxia 58 0.037
218
c RTN014 Retinal Artery Occlusion 58 0.037
219
HMS001 Hemosiderosis 57 0.037
220
MCN007 Meconium Aspiration Syndrome 57 0.037
221
SMT015 Smith Magenis Syndrome 57 0.037
222
EXF001 Exfoliation Syndrome 57 0.037
223
c MNC007 Monocytic Leukemia 57 0.037
224
P RPD001 Rapidly Progressive Glomerulonephritis 57 0.037
225
BRT002 Birt-Hogg-Dube Syndrome 57 0.037
226
INT007 Intermediate Coronary Syndrome 57 0.037
227
P CMP008 Compartment Syndrome 56 0.037
228
DDN006 Duodenitis 56 0.037
229
ART017 Aortic Disease 56 0.037
230
STV001 Stevens-Johnson Syndrome 56 0.037
231
RTN017 Retinal Detachment 56 0.037
232
VLV044 Vulvar Intraepithelial Neoplasia 56 0.037
233
NCR004 Nocardiosis 56 0.037
234
MCR088 Microscopic Polyangiitis 56 0.037
235
DST006 Diastolic Heart Failure 55 0.037
236
ACT095 Acute Biphenotypic Leukemia 55 0.037
237
IMP005 Impotence 55 0.037
238
ORL004 Oral Submucous Fibrosis 55 0.037
239
ALL006 Allergic Asthma 55 0.037
240
P PYL005 Pyelonephritis 55 0.037
241
STT004 Steatorrhea 54 0.037
242
VLL003 Villonodular Synovitis 54 0.037
243
FRM003 Farmer's Lung 54 0.037
244
WLL001 Williams-Beuren Syndrome 54 0.037
245
P KRT007 Keratoconus 53 0.037
246
P CNT028 Central Retinal Artery Occlusion 53 0.037
247
PLY013 Polymyalgia Rheumatica 53 0.037
248
CLC006 Calcinosis 53 0.037
249
P HYP172 Hyperphosphatemic Familial Tumoral Calcinosis 53 0.037
250
RTC002 Reticular Dysgenesis 53 0.037
251
ISC015 Ischemic Colitis 52 0.037
252
ART006 Arthus Reaction 52 0.037
253
EXS001 Exostosis 52 0.037
254
MNN014 Mononeuritis 51 0.037
255
CHR005 Chorioamnionitis 50 0.037
256
PYL006 Pyloric Stenosis 50 0.037
257
MYC013 Mycobacterium Abscessus 50 0.037
258
HYP009 Hypertrophic Pyloric Stenosis 50 0.037
259
CRT013 Carotid Stenosis 49 0.037
260
PST010 Pasteurellosis 49 0.037
261
EXC002 Exocrine Pancreatic Insufficiency 49 0.037
262
ASP007 Aspiration Pneumonia 49 0.037
263
LMB051 Lumbar Disc Disease 49 0.037
264
P PNC001 Pancytopenia 48 0.037
265
PYM001 Pyomyositis 48 0.037
266
PRT082 Preterm Premature Rupture of the Membranes 48 0.037
267
CRY001 Cryptogenic Organizing Pneumonia 48 0.037
268
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 48 0.037
269
IMM030 Immunodeficiency, Common Variable, 3 48 0.037
270
P OVR046 Ovarian Cyst 47 0.037
271
P ART084 Arteriovenous Fistula 47 0.037
272
FND002 Fundus Dystrophy 47 0.037
273
c ADL027 Adult Dermatomyositis 46 0.037
274
EVN001 Evans' Syndrome 46 0.037
275
BNF002 Bone Fracture 45 0.037
276
ODN005 Odontogenic Myxoma 45 0.037
277
ANT039 Antisynthetase Syndrome 44 0.037
278
MCR001 Microcystic Meningioma 44 0.037
279
QDR001 Quadriplegia 44 0.037
280
c HYP057 Hypervitaminosis D 43 0.037
281
EPG003 Epiglottitis 41 0.037
282
SKN005 Skin Atrophy 41 0.037
283
GNG006 Gingival Hypertrophy 40 0.037
284
P DPH016 Diaphragmatic Hernia 3 40 0.037
285
GST064 Gastric Outlet Obstruction 39 0.037
286
VRL011 Viral Infectious Disease 39 0.037
287
NWB001 Newborn Respiratory Distress Syndrome 38 0.037
288
BRN016 Bronchogenic Carcinoma 38 0.037
289
ODN002 Odontohypophosphatasia 37 0.037
290
IPX001 Ipex Syndrome 37 0.037
291
P INF131 Infant Acute Respiratory Distress Syndrome 37 0.037
292
SHK001 Shaken Baby Syndrome 34 0.037
293
FML091 Familial Tumoral Calcinosis 34 0.037
294
PSD089 Pseudomonas Aeruginosa Chronic Infection by, in Cystic Fibrosis 34 0.037
295
NTR005 Nutritional Deficiency Disease 33 0.037
296
TRC020 Tracheitis 33 0.037
297
LGP001 Lagophthalmos 32 0.037
298
c MLG033 Malignant Ovarian Cyst 31 0.037
299
BYS001 Byssinosis 31 0.037
300
PNG002 Pain Agnosia 30 0.037
301
ORB006 Orbital Cellulitis 30 0.037
302
CRL004 Caroli Disease 30 0.037
303
TXC001 Toxic Megacolon 30 0.037
304
RHN002 Rhinoscleroma 28 0.037
305
GST007 Gastric Dilatation 28 0.037
306
HRT011 Heart Septal Defect 28 0.037
307
ALP044 Alpha-1-Antichymotrypsin Deficiency 27 0.037
308
c TMR002 Tumoral Calcinosis, Hyperphosphatemic 26 0.037
309
ART007 Aorta Atresia 23 0.037
310
c EFM001 Efemp2-Related Cutis Laxa 22 0.037
311
PRM041 Primary Cortisol Resistance 21 0.037
312
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 21 0.037
313
HYP015 Hyperlucent Lung 19 0.037
314
c RSP007 Respiratory Distress Syndrome, Infant 18 0.037
315
WLS002 Wilson-Mikity Syndrome 17 0.037
316
CYS021 Cystic Adenomatoid Malformation of Lung 15 0.037
317
PLM116 Pulmonary Artery Hypoplasia 14 0.037
318
TRC038 Tracheobronchomegaly 13 0.037
319
CTS024 Cutis Laxa-Marfanoid Syndrome 11 0.037
320
CPD002 Copd, Rate of Decline of Lung Function in 7 0.037