Search results for "emphysema"

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

330 hits were found for 'emphysema'

# Family MCID Name MIFTS Score
1
EMP007 Emphysema Due to Aat Deficiency 50 8.008
2
PLM034 Pulmonary Emphysema 53 6.887
3
CNG105 Congenital Lobar Emphysema 34 5.710
4
INT011 Interstitial Emphysema 19 4.669
5
CMP003 Compensatory Emphysema 7 3.893
6
BRR006 Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification 6 3.868
7
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 32 3.146
8
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 4 3.127
9
PNM008 Pneumothorax 43 0.255
10
P PLM036 Pulmonary Fibrosis 64 0.217
11
BRN024 Bronchitis 62 0.201
12
PLM074 Pulmonary Function 30 0.173
13
MDS022 Mediastinitis 39 0.144
14
CRP018 Cor Pulmonale 37 0.144
15
P PNM007 Pneumonia 64 0.135
16
P AST005 Asthma 84 0.130
17
P LNG032 Lung Cancer 94 0.125
18
P PLM037 Pulmonary Hypertension 85 0.125
19
P CTS001 Cutis Laxa 50 0.125
20
P SPN183 Spontaneous Pneumothorax 45 0.125
21
END072 Endotheliitis 44 0.114
22
BRN055 Bronchogenic Cyst 32 0.114
23
BRN002 Bronchiolitis 52 0.108
24
P RSP003 Respiratory Failure 62 0.102
25
TBR010 Tuberculosis 73 0.095
26
CYS001 Cystic Fibrosis 92 0.088
27
MRF001 Marfan Syndrome 75 0.088
28
P CNG401 Congenital Heart Disease 62 0.088
29
P TRC086 Trichohepatoenteric Syndrome 1 39 0.088
30
PNM003 Pneumatosis Cystoides Intestinalis 21 0.088
31
ATH003 Atherosclerosis 56 0.081
32
BRN022 Bronchiectasis 54 0.081
33
INT066 Interstitial Lung Disease 44 0.081
34
CRB009 Cerebritis 33 0.081
35
P ATX030 Ataxia-Telangiectasia 76 0.072
36
P OST002 Osteoporosis 71 0.072
37
P DRM010 Dermatomyositis 62 0.072
38
ACN002 Acanthosis Nigricans 55 0.072
39
P AND016 Andersen Syndrome 54 0.072
40
STT002 Status Asthmaticus 52 0.072
41
LNG024 Langerhans-Cell Histiocytosis 51 0.072
42
MLR002 Miliary Tuberculosis 50 0.072
43
SLC006 Silicosis 49 0.072
44
BRN056 Bronchopulmonary Dysplasia 49 0.072
45
ART001 Arterial Tortuosity Syndrome 48 0.072
46
PLM129 Pulmonary Disease, Chronic Obstructive 53 0.072
47
THR013 Thoracic Outlet Syndrome 45 0.072
48
P PNM006 Pneumoconiosis 43 0.072
49
FSC004 Fasciitis 39 0.072
50
NCR007 Necrotizing Fasciitis 38 0.072
51
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.072
52
ANR040 Aneurysm 35 0.072
53
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 30 0.072
54
c PNM010 Pneumothorax, Primary Spontaneous 31 0.072
55
P ATX010 Ataxia Neuropathy Spectrum 29 0.072
56
PLM064 Pulmonary Sequestration 28 0.072
57
CRK001 Cork-Handlers' Disease 22 0.072
58
LYM035 Lymphangiectasis 21 0.072
59
DFF002 Diffuse Pulmonary Fibrosis 15 0.072
60
P LKM002 Leukemia 66 0.063
61
P ANG001 Angelman Syndrome 66 0.063
62
LVR012 Liver Cirrhosis 66 0.063
63
c HYP595 Hypertension, Essential 66 0.063
64
MSL001 Measles 58 0.063
65
GSG001 Gas Gangrene 58 0.063
66
VSC011 Vasculitis 57 0.063
67
P CNG015 Congenital Diaphragmatic Hernia 56 0.063
68
ELL001 Ellis-Van Creveld Syndrome 53 0.063
69
MYC002 Mycobacterium Avium Complex Disease 51 0.063
70
NNS002 Nonspecific Interstitial Pneumonia 49 0.063
71
c SPN225 Spondyloarthropathy 1 48 0.063
72
P VNT002 Ventricular Septal Defect 47 0.063
73
SCH016 Schimke Immunoosseous Dysplasia 46 0.063
74
P CYS018 Cystitis 43 0.063
75
CYT008 Cytomegalovirus Infection 39 0.063
76
c ACQ027 Acquired Cutis Laxa 37 0.063
77
TTR016 Tetra-Amelia Syndrome 36 0.063
78
CRB086 Cerebral Aneurysms 33 0.063
79
c ART101 Aortic Valve Disease 2 32 0.063
80
UND005 Undifferentiated Pleomorphic Sarcoma 28 0.063
81
TFT003 Tufting Enteropathy 26 0.063
82
TRC037 Tracheobronchomalacia 19 0.063
83
c BNG076 Benign Exophthalmos Syndrome 19 0.063
84
AND005 Androgen Insensitivity Syndrome, Mild 17 0.063
85
SPN014 Spontaneous Tension Pneumothorax 12 0.063
86
P ALZ034 Alzheimer Disease 100 0.051
87
HPT023 Hepatocellular Carcinoma 95 0.051
88
P RHM011 Rheumatoid Arthritis 94 0.051
89
P MYC007 Myocardial Infarction 81 0.051
90
FBR012 Fabry Disease 76 0.051
91
HV1006 Hiv-1 83 0.051
92
P NRF002 Neurofibromatosis 69 0.051
93
AND015 Androgen Insensitivity 69 0.051
94
P TBR001 Tuberous Sclerosis 68 0.051
95
CMM004 Common Variable Immunodeficiency 67 0.051
96
P LYM007 Lymphangioleiomyomatosis 65 0.051
97
P ART022 Arthritis 65 0.051
98
P HYP035 Hypophosphatasia 64 0.051
99
PCK002 Pick Disease 64 0.051
100
P NMN002 Niemann-Pick Disease 63 0.051
101
ART016 Aortic Aneurysm 62 0.051
102
P LVR013 Liver Disease 62 0.051
103
SRC014 Sarcoma 61 0.051
104
P PRD008 Periodontitis 59 0.051
105
P PNC044 Pancreatitis 59 0.051
106
P INF038 Influenza 67 0.051
107
P ABD003 Abdominal Aortic Aneurysm 58 0.051
108
ALL008 Allergic Bronchopulmonary Aspergillosis 57 0.051
109
ACT049 Acute Disseminated Encephalomyelitis 57 0.051
110
P HML002 Hemolytic Anemia 56 0.051
111
P SZR006 Seizure Disorder 56 0.051
112
P HST010 Histiocytosis 55 0.051
113
P HPT021 Hepatitis 55 0.051
114
c GLY008 Glycogen Storage Disease Ii 54 0.051
115
PRT037 Pertussis 54 0.051
116
P ACR001 Aicardi-Goutieres Syndrome 54 0.051
117
EXT034 Extrinsic Allergic Alveolitis 54 0.051
118
P EHL049 Ehlers-Danlos Syndrome Classical Type 53 0.051
119
P ADL010 Adult Respiratory Distress Syndrome 53 0.051
120
GTR002 Goiter 53 0.051
121
c ACT210 Acute Respiratory Distress Syndrome 52 0.051
122
MLL005 Miller-Dieker Syndrome 50 0.051
123
BRN012 Bronchiolitis Obliterans 50 0.051
124
CNN005 Connective Tissue Disease 50 0.051
125
NRN001 Neuroendocrine Carcinoma 50 0.051
126
BRT002 Birt-Hogg-Dube Syndrome 50 0.051
127
CLL003 Cellulitis 50 0.051
128
NTH001 Netherton Syndrome 49 0.051
129
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.051
130
P CRV039 Cervicitis 49 0.051
131
ACT100 Acute Febrile Neutrophilic Dermatosis 48 0.051
132
P PLR004 Pleuropulmonary Blastoma 48 0.051
133
P INT030 Intracranial Aneurysm 48 0.051
134
APP008 Appendicitis 48 0.051
135
PRD007 Periodontal Disease 47 0.051
136
P SLL003 Salla Disease 46 0.051
137
GST037 Gastroparesis 46 0.051
138
PPL021 Papilledema 46 0.051
139
ACQ007 Acquired Immunodeficiency Syndrome 46 0.051
140
BLS003 Blastoma 45 0.051
141
PLM012 Pulmonary Sarcoidosis 45 0.051
142
RTN023 Retinitis 44 0.051
143
OBS006 Obstructive Lung Disease 43 0.051
144
NRM005 Neuromuscular Disease 43 0.051
145
MNN014 Mononeuritis 43 0.051
146
CNG069 Congenital Cytomegalovirus 42 0.051
147
DVR002 Diverticulitis 41 0.051
148
BRN014 Bronchopneumonia 40 0.051
149
CNJ007 Conjunctivochalasis 39 0.051
150
c LRG014 Large Cell Neuroendocrine Carcinoma 39 0.051
151
HRS011 Horseshoe Kidney 38 0.051
152
HMT018 Hematopoietic Stem Cell Transplantation 36 0.051
153
INT071 Intestinal Perforation 35 0.051
154
BRN038 Bronchial Disease 34 0.051
155
c CTS008 Cutis Laxa, Autosomal Dominant 33 0.051
156
c NMN016 Niemann-Pick Disease, Type B 34 0.051
157
LRY004 Laryngotracheitis 31 0.051
158
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 28 0.051
159
NNT039 Neonatal Marfan Syndrome 28 0.051
160
AMY016 Amyopathic Dermatomyositis 26 0.051
161
c CTS019 Cutis Laxa, Ad 25 0.051
162
LRY028 Laryngocele 23 0.051
163
SBS002 Substernal Goiter 19 0.051
164
c CTS037 Cutis Laxa, Autosomal Recessive, Type Ib 17 0.051
165
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 17 0.051
166
ANT017 Anthracosilicosis 15 0.051
167
ANT005 Anteroseptal Myocardial Infarction 13 0.051
168
CTS024 Cutis Laxa-Marfanoid Syndrome 11 0.051
169
P PNC035 Pancreatic Cancer 82 0.036
170
P BRS047 Breast Cancer 90 0.036
171
P LFR001 Li-Fraumeni Syndrome 81 0.036
172
GLC006 Galactosemia 75 0.036
173
P RTN024 Retinoblastoma 75 0.036
174
THR006 Thromboangiitis Obliterans 68 0.036
175
SVR004 Severe Combined Immunodeficiency 68 0.036
176
KWS002 Kawasaki Disease 66 0.036
177
CRH001 Crohn's Disease 71 0.036
178
MNK001 Menkes Disease 65 0.036
179
RLP001 Relapsing Polychondritis 63 0.036
180
PRT036 Peritonitis 61 0.036
181
PLY017 Polyarteritis Nodosa 60 0.036
182
P NPH012 Nephrotic Syndrome 60 0.036
183
c MTB001 Metabolic Syndrome X 58 0.036
184
P MNN013 Meningitis 58 0.036
185
WLL001 Williams-Beuren Syndrome 58 0.036
186
PLM033 Pulmonary Embolism 56 0.036
187
ARS001 Aarskog-Scott Syndrome 56 0.036
188
ULC004 Ulcerative Colitis 63 0.036
189
WGN006 Wegener Granulomatosis 57 0.036
190
P ALP009 Alopecia Areata 56 0.036
191
SMT008 Smith-Magenis Syndrome 56 0.036
192
c ACT027 Acute Pancreatitis 55 0.036
193
CLT003 Colitis 54 0.036
194
CMP002 Campylobacteriosis 54 0.036
195
DFC004 Deficiency Anemia 54 0.036
196
P ANP001 Anaplastic Large Cell Lymphoma 53 0.036
197
TYP007 Typhoid Fever 53 0.036
198
FBR032 Fibromuscular Dysplasia 53 0.036
199
RBR001 Roberts Syndrome 53 0.036
200
HPT022 Hepatoblastoma 53 0.036
201
P DDN001 Duodenal Ulcer 53 0.036
202
PGM001 Pigmented Villonodular Synovitis 53 0.036
203
ESN015 Eosinophilic Fasciitis 52 0.036
204
GNG013 Gingivitis 52 0.036
205
GLC012 Galactosialidosis 52 0.036
206
DBT001 Diabetic Ketoacidosis 52 0.036
207
PLM001 Pulmonary Tuberculosis 60 0.036
208
P FML161 Familial Mediterranean Fever, Ar 51 0.036
209
EXF001 Exfoliation Syndrome 51 0.036
210
P MYM002 Moyamoya Disease 51 0.036
211
SCR002 Scurvy 51 0.036
212
SPN020 Spondylosis 51 0.036
213
MGC001 Megacolon 51 0.036
214
SYN007 Synovitis 51 0.036
215
PRT093 Proteus Syndrome, Somatic 50 0.036
216
CHL068 Cholestasis 50 0.036
217
CLL021 Collagenous Colitis 50 0.036
218
ACT095 Acute Biphenotypic Leukemia 49 0.036
219
P SDR002 Siderosis 49 0.036
220
HYP266 Hypoxia 49 0.036
221
P ADN016 Adenocarcinoma 49 0.036
222
P RPD001 Rapidly Progressive Glomerulonephritis 49 0.036
223
P MNC007 Monocytic Leukemia 49 0.036
224
BLM002 Bulimia Nervosa 49 0.036
225
P PRT013 Portal Hypertension 49 0.036
226
MCR088 Microscopic Polyangiitis 49 0.036
227
VLV044 Vulvar Intraepithelial Neoplasia 48 0.036
228
P SNS014 Sinusitis 56 0.036
229
RTN017 Retinal Detachment 48 0.036
230
ORL004 Oral Submucous Fibrosis 48 0.036
231
DDN006 Duodenitis 48 0.036
232
PRT082 Preterm Premature Rupture of the Membranes 47 0.036
233
P RTN014 Retinal Artery Occlusion 47 0.036
234
NCR004 Nocardiosis 47 0.036
235
PPL049 Papillon-Lefevre Syndrome 48 0.036
236
HMS001 Hemosiderosis 47 0.036
237
P CMP008 Compartment Syndrome 47 0.036
238
INT007 Intermediate Coronary Syndrome 47 0.036
239
MCN007 Meconium Aspiration Syndrome 47 0.036
240
PLM134 Pulmonary Fibrosis, Idiopathic 48 0.036
241
DST006 Diastolic Heart Failure 46 0.036
242
ART017 Aortic Disease 46 0.036
243
RTC002 Reticular Dysgenesis 46 0.036
244
ALL006 Allergic Asthma 46 0.036
245
FRM003 Farmer's Lung 46 0.036
246
PLY013 Polymyalgia Rheumatica 45 0.036
247
STT004 Steatorrhea 45 0.036
248
IMP005 Impotence 45 0.036
249
VLL003 Villonodular Synovitis 45 0.036
250
P KRT007 Keratoconus 45 0.036
251
ISC015 Ischemic Colitis 45 0.036
252
c CNT028 Central Retinal Artery Occlusion 45 0.036
253
CLC006 Calcinosis 44 0.036
254
P PYL005 Pyelonephritis 43 0.036
255
EXS001 Exostosis 43 0.036
256
MYC013 Mycobacterium Abscessus 43 0.036
257
FML091 Familial Tumoral Calcinosis 43 0.036
258
P HYP009 Hypertrophic Pyloric Stenosis 43 0.036
259
ART006 Arthus Reaction 42 0.036
260
CHR005 Chorioamnionitis 42 0.036
261
PYM001 Pyomyositis 42 0.036
262
EXC002 Exocrine Pancreatic Insufficiency 41 0.036
263
PYL006 Pyloric Stenosis 41 0.036
264
PST010 Pasteurellosis 41 0.036
265
ASP007 Aspiration Pneumonia 41 0.036
266
P PNC001 Pancytopenia 41 0.036
267
CRY001 Cryptogenic Organizing Pneumonia 40 0.036
268
P ART084 Arteriovenous Fistula 40 0.036
269
P TMR011 Tumoral Calcinosis, Hyperphosphatemic, Familial 41 0.036
270
CRT013 Carotid Stenosis 39 0.036
271
c ADL027 Adult Dermatomyositis 39 0.036
272
EVN001 Evans' Syndrome 39 0.036
273
FND002 Fundus Dystrophy 39 0.036
274
BNF002 Bone Fracture 39 0.036
275
P OVR046 Ovarian Cyst 39 0.036
276
ANT039 Antisynthetase Syndrome 39 0.036
277
ODN005 Odontogenic Myxoma 38 0.036
278
QDR001 Quadriplegia 37 0.036
279
MCR001 Microcystic Meningioma 36 0.036
280
NRN002 Neuronitis 36 0.036
281
SRC027 Sarcoma, Synovial 36 0.036
282
c HYP057 Hypervitaminosis D 35 0.036
283
HPT012 Hepatocellular Fibrolamellar Carcinoma 34 0.036
284
EPG003 Epiglottitis 34 0.036
285
P MLT028 Multiminicore Disease 34 0.036
286
SKN005 Skin Atrophy 34 0.036
287
NCT008 Nicotine Dependence, Protection Against 33 0.036
288
GST064 Gastric Outlet Obstruction 33 0.036
289
GNG006 Gingival Hypertrophy 32 0.036
290
P MYS033 Miyoshi Muscular Dystrophy 1 32 0.036
291
BRN016 Bronchogenic Carcinoma 32 0.036
292
NWB001 Newborn Respiratory Distress Syndrome 32 0.036
293
IPX001 Ipex Syndrome 32 0.036
294
VRL011 Viral Infectious Disease 31 0.036
295
ANT024 Anthrax Disease 31 0.036
296
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 31 0.036
297
BRL011 Bare Lymphocyte Syndrome, Type I 30 0.036
298
ADS002 Adie Syndrome 30 0.036
299
c INF131 Infant Acute Respiratory Distress Syndrome 29 0.036
300
SHK001 Shaken Baby Syndrome 29 0.036
301
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 27 0.036
302
NTR005 Nutritional Deficiency Disease 28 0.036
303
TRC020 Tracheitis 27 0.036
304
LGP001 Lagophthalmos 26 0.036
305
BYS001 Byssinosis 26 0.036
306
HNM002 Hinman Syndrome 26 0.036
307
PNG002 Pain Agnosia 25 0.036
308
ORB006 Orbital Cellulitis 25 0.036
309
c MLG033 Malignant Ovarian Cyst 24 0.036
310
TXC001 Toxic Megacolon 24 0.036
311
CRL004 Caroli Disease 24 0.036
312
RHN002 Rhinoscleroma 23 0.036
313
GST007 Gastric Dilatation 23 0.036
314
HRT011 Heart Septal Defect 23 0.036
315
ALP044 Alpha-1-Antichymotrypsin Deficiency 22 0.036
316
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 22 0.036
317
ARM003 Aromatic Amino Acid Decarboxylase Deficiency 19 0.036
318
LYS013 Loeys-Dietz Syndrome, Type 4 19 0.036
319
c MRG011 Meier-Gorlin Syndrome 4 18 0.036
320
c ADL014 Adult Mesoblastic Nephroma 18 0.036
321
IMM015 Immune Defect Due to Absence of Thymus 17 0.036
322
P RSP007 Respiratory Distress Syndrome, Infant 17 0.036
323
HYP015 Hyperlucent Lung 16 0.036
324
FML066 Familial Hypersensitivity Pneumonitis 16 0.036
325
CYT018 Cytochrome P450 2d6 Variant 15 0.036
326
WLS002 Wilson-Mikity Syndrome 14 0.036
327
PLM116 Pulmonary Artery Hypoplasia 14 0.036
328
P THR041 Thrombocytopenia, Acquired Amegakaryocytic 13 0.036
329
CYS021 Cystic Adenomatoid Malformation of Lung 13 0.036
330
PLS010 Plasma Protein Metabolism Disease 7 0.036