Search results for "emphysema"

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

324 hits were found for 'emphysema'

# Family MCID Name MIFTS Score
1
ALP007 Alpha 1-Antitrypsin Deficiency 64 6.891
2
PLM034 Pulmonary Emphysema 57 6.739
3
CNG105 Congenital Lobar Emphysema 40 5.996
4
INT011 Interstitial Emphysema 23 4.569
5
CMP003 Compensatory Emphysema 8 3.761
6
BRR006 Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification 6 3.733
7
EMP007 Emphysema Due to Aat Deficiency 31 3.134
8
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 7 3.048
9
EMP008 Emphysema-Cirrhosis, Due to Aat Deficiency 4 3.005
10
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 36 2.216
11
PNM008 Pneumothorax 49 0.262
12
P PLM036 Pulmonary Fibrosis 68 0.223
13
BRN024 Bronchitis 66 0.203
14
PLM074 Pulmonary Function 34 0.182
15
P CHR409 Chronic Obstructive Pulmonary Disease 54 0.170
16
MDS022 Mediastinitis 45 0.148
17
CRP018 Cor Pulmonale 44 0.144
18
P PNM007 Pneumonia 77 0.139
19
P AST005 Asthma 87 0.134
20
c CTS001 Cutis Laxa 57 0.128
21
c SPN183 Spontaneous Pneumothorax 52 0.128
22
P LNG032 Lung Cancer 78 0.123
23
P HYP075 Hypertension 85 0.117
24
c PLM037 Pulmonary Hypertension 73 0.117
25
END072 Endotheliitis 50 0.117
26
BRN055 Bronchogenic Cyst 37 0.117
27
BRN002 Bronchiolitis 60 0.111
28
P RSP003 Respiratory Failure 68 0.105
29
IDP003 Idiopathic Pulmonary Fibrosis 68 0.105
30
TBR010 Tuberculosis 85 0.098
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 96 0.083
37
ATH003 Atherosclerosis 68 0.083
38
INT066 Interstitial Lung Disease 52 0.083
39
THR013 Thoracic Outlet Syndrome 52 0.083
40
CRB009 Cerebritis 38 0.083
41
P ATX002 Ataxia Telangiectasia 87 0.074
42
P OST002 Osteoporosis 76 0.074
43
LVR012 Liver Cirrhosis 76 0.074
44
P DRM010 Dermatomyositis 71 0.074
45
ACN002 Acanthosis Nigricans 64 0.074
46
STT002 Status Asthmaticus 63 0.074
47
BRN022 Bronchiectasis 61 0.074
48
MLR002 Miliary Tuberculosis 59 0.074
49
SLC006 Silicosis 57 0.074
50
LNG024 Langerhans-Cell Histiocytosis 57 0.074
51
BRN056 Bronchopulmonary Dysplasia 56 0.074
52
ART001 Arterial Tortuosity Syndrome 55 0.074
53
AND003 Andersen-Tawil Syndrome 53 0.074
54
P PNM006 Pneumoconiosis 49 0.074
55
P ATX010 Ataxia Neuropathy Spectrum 47 0.074
56
ANR040 Aneurysm 45 0.074
57
FSC004 Fasciitis 45 0.074
58
NCR007 Necrotizing Fasciitis 43 0.074
59
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.074
60
c CTS019 Cutis Laxa, Ad 35 0.074
61
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 34 0.074
62
P PLM064 Pulmonary Sequestration 29 0.074
63
CRK001 Cork-Handlers' Disease 28 0.074
64
LYM035 Lymphangiectasis 24 0.074
65
DFF002 Diffuse Pulmonary Fibrosis 19 0.074
66
P PRM021 Primary Pulmonary Hypertension 80 0.064
67
ANK002 Ankylosing Spondylitis 76 0.064
68
P ANG001 Angelman Syndrome 71 0.064
69
MSL001 Measles 67 0.064
70
GSG001 Gas Gangrene 67 0.064
71
VSC011 Vasculitis 65 0.064
72
ART019 Aortic Valve Stenosis 63 0.064
73
ELL001 Ellis-Van Creveld Syndrome 61 0.064
74
MYC002 Mycobacterium Avium Complex Disease 58 0.064
75
c CNG015 Congenital Diaphragmatic Hernia 58 0.064
76
P VNT002 Ventricular Septal Defect 53 0.064
77
OBS006 Obstructive Lung Disease 52 0.064
78
P CYS018 Cystitis 51 0.064
79
CYT008 Cytomegalovirus Infection 43 0.064
80
c ACQ027 Acquired Cutis Laxa 41 0.064
81
CRB086 Cerebral Aneurysms 38 0.064
82
TRC037 Tracheobronchomalacia 22 0.064
83
AND005 Androgen Insensitivity Syndrome, Mild 21 0.064
84
SPN014 Spontaneous Tension Pneumothorax 15 0.064
85
CTS024 Cutis Laxa-Marfanoid Syndrome 12 0.064
86
P NRF002 Neurofibromatosis 94 0.052
87
P MYC007 Myocardial Infarction 92 0.052
88
P TBR001 Tuberous Sclerosis 86 0.052
89
FBR012 Fabry Disease 85 0.052
90
P NMN002 Niemann-Pick Disease 83 0.052
91
AND002 Androgen Insensitivity Syndrome 80 0.052
92
P LKM002 Leukemia 76 0.052
93
P ART022 Arthritis 74 0.052
94
P LYM007 Lymphangioleiomyomatosis 74 0.052
95
ACQ007 Acquired Immunodeficiency Syndrome 70 0.052
96
ART016 Aortic Aneurysm 70 0.052
97
c AXN002 Axenfeld-Rieger Syndrome 69 0.052
98
SRC014 Sarcoma 68 0.052
99
P PRD008 Periodontitis 68 0.052
100
c PNC044 Pancreatitis 68 0.052
101
P LVR013 Liver Disease 68 0.052
102
P ABD003 Abdominal Aortic Aneurysm 67 0.052
103
P INF038 Influenza 67 0.052
104
ALL008 Allergic Bronchopulmonary Aspergillosis 67 0.052
105
c HML002 Hemolytic Anemia 65 0.052
106
BRR003 Barrett's Esophagus 63 0.052
107
EXT034 Extrinsic Allergic Alveolitis 63 0.052
108
P ADL010 Adult Respiratory Distress Syndrome 63 0.052
109
P HST010 Histiocytosis 63 0.052
110
P GLY008 Glycogen Storage Disease Ii 62 0.052
111
MLL005 Miller-Dieker Syndrome 62 0.052
112
PRT037 Pertussis 61 0.052
113
P GTR002 Goiter 61 0.052
114
BRN012 Bronchiolitis Obliterans 59 0.052
115
NTH001 Netherton Syndrome 59 0.052
116
NRN001 Neuroendocrine Carcinoma 58 0.052
117
P PLR004 Pleuropulmonary Blastoma 58 0.052
118
CLL003 Cellulitis 58 0.052
119
CNN005 Connective Tissue Disease 58 0.052
120
BRT002 Birt-Hogg-Dube Syndrome 57 0.052
121
NNS002 Nonspecific Interstitial Pneumonia 57 0.052
122
P CRV039 Cervicitis 57 0.052
123
ACT100 Acute Febrile Neutrophilic Dermatosis 57 0.052
124
PRD007 Periodontal Disease 56 0.052
125
P INT030 Intracranial Aneurysm 56 0.052
126
GST037 Gastroparesis 55 0.052
127
APP008 Appendicitis 55 0.052
128
c ACR001 Aicardi-Goutieres Syndrome 54 0.052
129
BLS003 Blastoma 53 0.052
130
PPL021 Papilledema 53 0.052
131
RTN023 Retinitis 53 0.052
132
PLM012 Pulmonary Sarcoidosis 53 0.052
133
P SLL003 Salla Disease 51 0.052
134
USL001 Usual Interstitial Pneumonia 51 0.052
135
NRM005 Neuromuscular Disease 50 0.052
136
SYN006 Synovial Sarcoma 50 0.052
137
DVR002 Diverticulitis 48 0.052
138
SCH016 Schimke Immunoosseous Dysplasia 48 0.052
139
IMM030 Immunodeficiency, Common Variable, 3 48 0.052
140
BRN014 Bronchopneumonia 47 0.052
141
CNJ007 Conjunctivochalasis 46 0.052
142
c LRG014 Large Cell Neuroendocrine Carcinoma 45 0.052
143
HRS011 Horseshoe Kidney 44 0.052
144
TTR016 Tetra-Amelia Syndrome 43 0.052
145
INT071 Intestinal Perforation 42 0.052
146
BRN038 Bronchial Disease 41 0.052
147
HMT018 Hematopoietic Stem Cell Transplantation 40 0.052
148
c TYP003 Type I Ehlers-Danlos Syndrome 40 0.052
149
ODN002 Odontohypophosphatasia 38 0.052
150
LRY004 Laryngotracheitis 37 0.052
151
CNG069 Congenital Cytomegalovirus 36 0.052
152
LYM014 Lymphangitis 33 0.052
153
NNT039 Neonatal Marfan Syndrome 31 0.052
154
AMY016 Amyopathic Dermatomyositis 30 0.052
155
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 29 0.052
156
TFT003 Tufting Enteropathy 28 0.052
157
c EFM001 Efemp2-Related Cutis Laxa 27 0.052
158
LRY028 Laryngocele 26 0.052
159
SBS002 Substernal Goiter 22 0.052
160
c BNG076 Benign Exophthalmos Syndrome 22 0.052
161
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 22 0.052
162
ANT017 Anthracosilicosis 19 0.052
163
ANT005 Anteroseptal Myocardial Infarction 17 0.052
164
c THR041 Thrombocytopenia, Acquired Amegakaryocytic 15 0.052
165
P ALZ001 Alzheimer's Disease 98 0.037
166
P RHM011 Rheumatoid Arthritis 94 0.037
167
P PNC035 Pancreatic Cancer 92 0.037
168
P LVR011 Liver Cancer 90 0.037
169
P LFR001 Li-Fraumeni Syndrome 88 0.037
170
GLC006 Galactosemia 85 0.037
171
P BRS047 Breast Cancer 85 0.037
172
THR006 Thromboangiitis Obliterans 79 0.037
173
SVR004 Severe Combined Immunodeficiency 78 0.037
174
KWS002 Kawasaki Disease 75 0.037
175
CRH001 Crohn's Disease 75 0.037
176
P FML018 Familial Mediterranean Fever 75 0.037
177
MNK001 Menkes Disease 74 0.037
178
P SRC013 Sarcoidosis 73 0.037
179
P WGN002 Wegener's Granulomatosis 73 0.037
180
c DBT009 Diabetes Mellitus 73 0.037
181
RLP001 Relapsing Polychondritis 72 0.037
182
PCK001 Pick's Disease 71 0.037
183
PRT036 Peritonitis 71 0.037
184
P MTB001 Metabolic Syndrome X 69 0.037
185
PLY017 Polyarteritis Nodosa 69 0.037
186
c MNN013 Meningitis 67 0.037
187
DBT001 Diabetic Ketoacidosis 67 0.037
188
c NPH012 Nephrotic Syndrome 67 0.037
189
ACT049 Acute Disseminated Encephalomyelitis 66 0.037
190
ARS001 Aarskog-Scott Syndrome 65 0.037
191
PLM033 Pulmonary Embolism 65 0.037
192
ULC004 Ulcerative Colitis 64 0.037
193
XLN002 X-Linked Hypophosphatemia 64 0.037
194
P ALP009 Alopecia Areata 64 0.037
195
CLT003 Colitis 64 0.037
196
c HPT021 Hepatitis 63 0.037
197
c ACT027 Acute Pancreatitis 63 0.037
198
CMP002 Campylobacteriosis 62 0.037
199
DFC004 Deficiency Anemia 62 0.037
200
TYP007 Typhoid Fever 62 0.037
201
P ANP001 Anaplastic Large Cell Lymphoma 62 0.037
202
P DDN001 Duodenal Ulcer 61 0.037
203
FBR032 Fibromuscular Dysplasia 61 0.037
204
GNG013 Gingivitis 60 0.037
205
PLM001 Pulmonary Tuberculosis 60 0.037
206
P PRT008 Proteus Syndrome 60 0.037
207
PGM001 Pigmented Villonodular Synovitis 60 0.037
208
P PRM054 Primary Sclerosing Cholangitis 60 0.037
209
NRN004 Neuroendocrine Tumor 59 0.037
210
P SYN007 Synovitis 59 0.037
211
SPN020 Spondylosis 59 0.037
212
GLC012 Galactosialidosis 59 0.037
213
SCR002 Scurvy 59 0.037
214
MGC001 Megacolon 59 0.037
215
EXF001 Exfoliation Syndrome 59 0.037
216
P ADN016 Adenocarcinoma 58 0.037
217
CHL068 Cholestasis 58 0.037
218
BLM002 Bulimia Nervosa 58 0.037
219
SMT015 Smith Magenis Syndrome 58 0.037
220
CLL021 Collagenous Colitis 58 0.037
221
P SNS014 Sinusitis 57 0.037
222
P MYM002 Moyamoya Disease 57 0.037
223
P SDR002 Siderosis 57 0.037
224
HYP266 Hypoxia 57 0.037
225
c RTN014 Retinal Artery Occlusion 57 0.037
226
HMS001 Hemosiderosis 57 0.037
227
MCN007 Meconium Aspiration Syndrome 56 0.037
228
P RPD001 Rapidly Progressive Glomerulonephritis 56 0.037
229
c MNC007 Monocytic Leukemia 56 0.037
230
INT007 Intermediate Coronary Syndrome 56 0.037
231
RTN017 Retinal Detachment 56 0.037
232
MCR088 Microscopic Polyangiitis 56 0.037
233
P CMP008 Compartment Syndrome 55 0.037
234
DDN006 Duodenitis 55 0.037
235
ART017 Aortic Disease 55 0.037
236
STV001 Stevens-Johnson Syndrome 55 0.037
237
ORL004 Oral Submucous Fibrosis 55 0.037
238
VLV044 Vulvar Intraepithelial Neoplasia 55 0.037
239
NCR004 Nocardiosis 55 0.037
240
DST006 Diastolic Heart Failure 55 0.037
241
ACT095 Acute Biphenotypic Leukemia 54 0.037
242
IMP005 Impotence 54 0.037
243
ALL006 Allergic Asthma 54 0.037
244
P PYL005 Pyelonephritis 54 0.037
245
WLL001 Williams-Beuren Syndrome 54 0.037
246
P HYP172 Hyperphosphatemic Familial Tumoral Calcinosis 53 0.037
247
STT004 Steatorrhea 53 0.037
248
VLL003 Villonodular Synovitis 53 0.037
249
RTC002 Reticular Dysgenesis 53 0.037
250
FRM003 Farmer's Lung 53 0.037
251
P KRT007 Keratoconus 53 0.037
252
P CNT028 Central Retinal Artery Occlusion 52 0.037
253
CLC006 Calcinosis 52 0.037
254
ISC015 Ischemic Colitis 52 0.037
255
ART006 Arthus Reaction 51 0.037
256
EXS001 Exostosis 51 0.037
257
MNN014 Mononeuritis 51 0.037
258
CHR005 Chorioamnionitis 50 0.037
259
PYL006 Pyloric Stenosis 49 0.037
260
MYC013 Mycobacterium Abscessus 49 0.037
261
HYP009 Hypertrophic Pyloric Stenosis 49 0.037
262
CRT013 Carotid Stenosis 49 0.037
263
PRT082 Preterm Premature Rupture of the Membranes 49 0.037
264
PST010 Pasteurellosis 49 0.037
265
EXC002 Exocrine Pancreatic Insufficiency 48 0.037
266
ASP007 Aspiration Pneumonia 48 0.037
267
PYM001 Pyomyositis 48 0.037
268
LMB051 Lumbar Disc Disease 48 0.037
269
P PNC001 Pancytopenia 48 0.037
270
CRY001 Cryptogenic Organizing Pneumonia 47 0.037
271
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 47 0.037
272
P OVR046 Ovarian Cyst 47 0.037
273
P ART084 Arteriovenous Fistula 46 0.037
274
FND002 Fundus Dystrophy 46 0.037
275
c ADL027 Adult Dermatomyositis 46 0.037
276
EVN001 Evans' Syndrome 45 0.037
277
BNF002 Bone Fracture 45 0.037
278
ODN005 Odontogenic Myxoma 44 0.037
279
ANT039 Antisynthetase Syndrome 44 0.037
280
MHC002 Mhc Class I Deficiency 44 0.037
281
MCR001 Microcystic Meningioma 43 0.037
282
QDR001 Quadriplegia 43 0.037
283
c HYP057 Hypervitaminosis D 42 0.037
284
EPG003 Epiglottitis 41 0.037
285
P DPH016 Diaphragmatic Hernia 3 40 0.037
286
SKN005 Skin Atrophy 40 0.037
287
GNG006 Gingival Hypertrophy 39 0.037
288
P INF131 Infant Acute Respiratory Distress Syndrome 39 0.037
289
GST064 Gastric Outlet Obstruction 39 0.037
290
VRL011 Viral Infectious Disease 38 0.037
291
NWB001 Newborn Respiratory Distress Syndrome 37 0.037
292
BRN016 Bronchogenic Carcinoma 37 0.037
293
PSD089 Pseudomonas Aeruginosa Chronic Infection by, in Cystic Fibrosis 36 0.037
294
IPX001 Ipex Syndrome 36 0.037
295
SHK001 Shaken Baby Syndrome 34 0.037
296
FML091 Familial Tumoral Calcinosis 33 0.037
297
NTR005 Nutritional Deficiency Disease 33 0.037
298
TRC020 Tracheitis 33 0.037
299
CRL004 Caroli Disease 32 0.037
300
LGP001 Lagophthalmos 31 0.037
301
c MLG033 Malignant Ovarian Cyst 31 0.037
302
BYS001 Byssinosis 31 0.037
303
PNG002 Pain Agnosia 30 0.037
304
ORB006 Orbital Cellulitis 30 0.037
305
TXC001 Toxic Megacolon 29 0.037
306
RHN002 Rhinoscleroma 28 0.037
307
GST007 Gastric Dilatation 28 0.037
308
HRT011 Heart Septal Defect 27 0.037
309
ALP044 Alpha-1-Antichymotrypsin Deficiency 27 0.037
310
c TMR002 Tumoral Calcinosis, Hyperphosphatemic 25 0.037
311
ART007 Aorta Atresia 22 0.037
312
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 22 0.037
313
IMM015 Immune Defect Due to Absence of Thymus 21 0.037
314
PRM041 Primary Cortisol Resistance 21 0.037
315
HYP015 Hyperlucent Lung 19 0.037
316
c RSP007 Respiratory Distress Syndrome, Infant 18 0.037
317
LBN002 Lubani Al Saleh Teebi Syndrome 18 0.037
318
c MRG011 Meier-Gorlin Syndrome 4 18 0.037
319
WLS002 Wilson-Mikity Syndrome 17 0.037
320
CYS021 Cystic Adenomatoid Malformation of Lung 15 0.037
321
PLM116 Pulmonary Artery Hypoplasia 14 0.037
322
LYS013 Loeys-Dietz Syndrome, Type 4 13 0.037
323
TRC038 Tracheobronchomegaly 13 0.037
324
CPD002 Copd, Rate of Decline of Lung Function in 8 0.037