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

386 hits were found for 'emphysema'

# Family MCID Name MIFTS Score
1
PLM034 Pulmonary Emphysema 60 6.790
2
ALP007 Alpha 1-Antitrypsin Deficiency 61 6.743
3
CNG105 Congenital Lobar Emphysema 29 5.179
4
INT011 Interstitial Emphysema 26 4.505
5
CMP003 Compensatory Emphysema 8 3.687
6
BRR006 Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification 1 3.634
7
EMP007 Emphysema Due to Aat Deficiency 28 3.126
8
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 7 2.979
9
EMP008 Emphysema-Cirrhosis, Due to Aat Deficiency 6 2.979
10
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 31 2.128
11
c FBL003 Fbln5-Related Cutis Laxa 18 2.078
12
c XP2001 Xp22.3 Microdeletion Syndrome 21 0.263
13
PNM008 Pneumothorax 55 0.244
14
P PLM036 Pulmonary Fibrosis 66 0.215
15
BRN056 Bronchopulmonary Dysplasia 47 0.213
16
BRN024 Bronchitis 76 0.207
17
END072 Endotheliitis 47 0.198
18
IDP042 Idiopathic Recurrent Stupor 15 0.183
19
LNT002 Lentigo Maligna Melanoma 28 0.154
20
P STR035 Streptococcal Group a Invasive Disease 14 0.154
21
P LNG032 Lung Cancer 74 0.150
22
MDS022 Mediastinitis 56 0.150
23
P RSP003 Respiratory Failure 70 0.146
24
c RSP007 Respiratory Distress Syndrome, Infant 15 0.146
25
c SPN183 Spontaneous Pneumothorax 31 0.138
26
ANK002 Ankylosing Spondylitis 75 0.134
27
THR013 Thoracic Outlet Syndrome 54 0.134
28
P SRC025 Sarcoidosis 1 32 0.134
29
CRK001 Cork-Handlers' Disease 32 0.134
30
FTL044 Fetal Cytomegalovirus Syndrome 28 0.134
31
CRB009 Cerebritis 56 0.129
32
c ACQ027 Acquired Cutis Laxa 29 0.129
33
P AST005 Asthma 88 0.124
34
P ATX002 Ataxia Telangiectasia 93 0.120
35
P PNM007 Pneumonia 79 0.120
36
P CTS001 Cutis Laxa 63 0.120
37
MLR002 Miliary Tuberculosis 55 0.114
38
TRC037 Tracheobronchomalacia 11 0.114
39
SRS007 Sorsby Fundus Dystrophy 38 0.109
40
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 36 0.109
41
P HYP075 Hypertension 86 0.104
42
LYM014 Lymphangitis 46 0.104
43
DFF002 Diffuse Pulmonary Fibrosis 19 0.104
44
ACN002 Acanthosis Nigricans 73 0.098
45
c LCL006 Localized Scleroderma 68 0.098
46
RTC002 Reticular Dysgenesis 58 0.098
47
APP008 Appendicitis 57 0.098
48
OBS006 Obstructive Lung Disease 57 0.098
49
SCN006 Secondary Syphilis 55 0.098
50
INT066 Interstitial Lung Disease 53 0.098
51
P JBR004 Joubert Syndrome 2 52 0.098
52
VND002 Van Der Woude Syndrome 43 0.098
53
DDF001 Dedifferentiated Liposarcoma 42 0.098
54
CLL021 Collagenous Colitis 41 0.098
55
PNM003 Pneumatosis Cystoides Intestinalis 26 0.098
56
NNS006 Non-Suppurative Otitis Media 26 0.098
57
SPN014 Spontaneous Tension Pneumothorax 14 0.098
58
HSL001 House Allergic Alveolitis 11 0.098
59
TBR010 Tuberculosis 84 0.091
60
P ADL010 Adult Respiratory Distress Syndrome 71 0.091
61
P INF038 Influenza 69 0.091
62
IDP003 Idiopathic Pulmonary Fibrosis 69 0.091
63
BRN002 Bronchiolitis 61 0.091
64
P PST022 Posterior Uveal Melanoma 49 0.091
65
LNG017 Lung Giant Cell Carcinoma 47 0.091
66
CYT008 Cytomegalovirus Infection 34 0.091
67
c MLG033 Malignant Ovarian Cyst 31 0.091
68
ACQ007 Acquired Immunodeficiency Syndrome 63 0.085
69
WLL003 Williams Syndrome 58 0.085
70
MYC002 Mycobacterium Avium Complex Disease 57 0.085
71
c CNG015 Congenital Diaphragmatic Hernia 55 0.085
72
ENT015 Enthesitis-Related Arthritis 48 0.085
73
P ATM029 Autoimmune Lymphoproliferative Syndrome, Type Ib 46 0.085
74
CHL079 Children's Interstitial Lung Disease 46 0.085
75
SYN053 Syndromic Diarrhea 42 0.085
76
FCL041 Focal Myositis 40 0.085
77
P DPH016 Diaphragmatic Hernia 3 36 0.085
78
INT103 Intrauterine Infections 36 0.085
79
ADM001 Adamantinous Craniopharyngioma 25 0.085
80
RHM009 Rheumatoid Lung Disease 23 0.085
81
c EXT037 Extragonadal Germ Cell Tumor 20 0.085
82
CYS001 Cystic Fibrosis 103 0.077
83
MRF001 Marfan Syndrome 92 0.077
84
P DRM010 Dermatomyositis 70 0.077
85
RLP001 Relapsing Polychondritis 69 0.077
86
PLM033 Pulmonary Embolism 68 0.077
87
EXT034 Extrinsic Allergic Alveolitis 65 0.077
88
ALL006 Allergic Asthma 60 0.077
89
SLC006 Silicosis 58 0.077
90
STT002 Status Asthmaticus 57 0.077
91
NCR004 Nocardiosis 54 0.077
92
BRN038 Bronchial Disease 42 0.077
93
PRL042 Proliferating Trichilemmal Cyst 38 0.077
94
TFT003 Tufting Enteropathy 21 0.077
95
RSP016 Respiratory Bronchiolitis - Interstitial Lung Disease 13 0.077
96
P ALZ001 Alzheimer's Disease 103 0.069
97
P NRF002 Neurofibromatosis 100 0.069
98
HPT023 Hepatocellular Carcinoma 89 0.069
99
P OST002 Osteoporosis 77 0.069
100
LVR012 Liver Cirrhosis 75 0.069
101
ATH003 Atherosclerosis 71 0.069
102
WST001 West Syndrome 64 0.069
103
BRN022 Bronchiectasis 64 0.069
104
P PNM006 Pneumoconiosis 59 0.069
105
ATX019 Ataxia with Vitamin E Deficiency 55 0.069
106
DST006 Diastolic Heart Failure 52 0.069
107
c JBR001 Joubert Syndrome 51 0.069
108
FSC004 Fasciitis 50 0.069
109
P HYP172 Hyperphosphatemic Familial Tumoral Calcinosis 50 0.069
110
c ACR001 Aicardi-Goutieres Syndrome 49 0.069
111
P ATX010 Ataxia Neuropathy Spectrum 44 0.069
112
VLV044 Vulvar Intraepithelial Neoplasia 42 0.069
113
NCR007 Necrotizing Fasciitis 41 0.069
114
PRT082 Preterm Premature Rupture of the Membranes 38 0.069
115
FCT013 Factor V Leiden Thrombophilia 35 0.069
116
P SLP004 Salpingo-Oophoritis 31 0.069
117
PRT015 Partial Third-Nerve Palsy 26 0.069
118
NNT039 Neonatal Marfan Syndrome 24 0.069
119
HNM002 Hinman Syndrome 24 0.069
120
HSB001 His Bundle Tachycardia 18 0.069
121
AMY016 Amyopathic Dermatomyositis 17 0.069
122
PLM108 Pulmonary Interstitial Glycogenosis 14 0.069
123
c THR041 Thrombocytopenia, Acquired Amegakaryocytic 12 0.069
124
PLM116 Pulmonary Artery Hypoplasia 12 0.069
125
c PLM064 Pulmonary Sequestration 11 0.069
126
P PRM021 Primary Pulmonary Hypertension 82 0.060
127
P HMP004 Hemophilia B 80 0.060
128
c MCP002 Mucopolysaccharidosis I 80 0.060
129
P ANG001 Angelman Syndrome 70 0.060
130
ART019 Aortic Valve Stenosis 68 0.060
131
VSC011 Vasculitis 67 0.060
132
MSL001 Measles 66 0.060
133
GSG001 Gas Gangrene 66 0.060
134
c NPH012 Nephrotic Syndrome 66 0.060
135
PLM001 Pulmonary Tuberculosis 63 0.060
136
SRC014 Sarcoma 63 0.060
137
ART001 Arterial Tortuosity Syndrome 62 0.060
138
P GTR002 Goiter 61 0.060
139
BRN012 Bronchiolitis Obliterans 59 0.060
140
P RNV001 Renovascular Hypertension 58 0.060
141
NRN001 Neuroendocrine Carcinoma 57 0.060
142
CNN005 Connective Tissue Disease 57 0.060
143
BCT002 Bacterial Vaginosis 56 0.060
144
NNS002 Nonspecific Interstitial Pneumonia 55 0.060
145
NRM005 Neuromuscular Disease 55 0.060
146
EVN001 Evans' Syndrome 54 0.060
147
P CYS018 Cystitis 54 0.060
148
WLL001 Williams-Beuren Syndrome 52 0.060
149
SYN006 Synovial Sarcoma 51 0.060
150
MNN014 Mononeuritis 48 0.060
151
P PRM100 Primary Spontaneous Pneumothorax 46 0.060
152
P PLM129 Pulmonary Disease, Chronic Obstructive 45 0.060
153
AND003 Andersen-Tawil Syndrome 43 0.060
154
ENT001 Enterocele 42 0.060
155
P SLL003 Salla Disease 38 0.060
156
ERL004 Early Yaws 33 0.060
157
c PLM071 Pulmonary Surfactant Metabolism Dysfunction 28 0.060
158
NSL006 Nasal Cavity Squamous Cell Carcinoma 28 0.060
159
DFN039 Deafness-Infertility Syndrome 27 0.060
160
P KRN003 Kernicterus Due to Isoimmunization 21 0.060
161
c MNS010 Monosomy Xp21 20 0.060
162
ANT017 Anthracosilicosis 19 0.060
163
AND005 Androgen Insensitivity Syndrome, Mild 18 0.060
164
c TTL001 Total Internal Ophthalmoplegia 17 0.060
165
c PRM041 Primary Cortisol Resistance 13 0.060
166
P LFR001 Li-Fraumeni Syndrome 93 0.049
167
P RHM011 Rheumatoid Arthritis 91 0.049
168
P MYC007 Myocardial Infarction 88 0.049
169
P WSK001 Wiskott-Aldrich Syndrome 87 0.049
170
CRH001 Crohn's Disease 83 0.049
171
MNK001 Menkes Disease 81 0.049
172
P LKM002 Leukemia 79 0.049
173
P ART022 Arthritis 75 0.049
174
THR006 Thromboangiitis Obliterans 75 0.049
175
P CNG026 Congenital Heart Defect 73 0.049
176
c MNN013 Meningitis 71 0.049
177
P LVR013 Liver Disease 70 0.049
178
c SRC013 Sarcoidosis 69 0.049
179
c ATM006 Autoimmune Lymphoproliferative Syndrome 68 0.049
180
BRR003 Barrett's Esophagus 68 0.049
181
P HML002 Hemolytic Anemia 68 0.049
182
DSS009 Disseminated Intravascular Coagulation 66 0.049
183
P PRD008 Periodontitis 66 0.049
184
HYP458 Hyper Ige Syndrome 65 0.049
185
PRT037 Pertussis 64 0.049
186
ELL001 Ellis-Van Creveld Syndrome 64 0.049
187
GST009 Gastroschisis 63 0.049
188
ART016 Aortic Aneurysm 62 0.049
189
RTN023 Retinitis 61 0.049
190
PRD007 Periodontal Disease 61 0.049
191
ANR008 Aneurysm Disease 57 0.049
192
GST037 Gastroparesis 57 0.049
193
RSC001 Rosacea 57 0.049
194
P PRT008 Proteus Syndrome 56 0.049
195
CLL003 Cellulitis 56 0.049
196
PLM012 Pulmonary Sarcoidosis 55 0.049
197
ACT017 Acute Chest Syndrome 55 0.049
198
LPC002 Lip Cancer 55 0.049
199
SPN020 Spondylosis 54 0.049
200
RFR003 Refractive Error 53 0.049
201
c VNT002 Ventricular Septal Defect 53 0.049
202
MCR088 Microscopic Polyangiitis 53 0.049
203
INT007 Intermediate Coronary Syndrome 53 0.049
204
P CRV039 Cervicitis 52 0.049
205
HMS001 Hemosiderosis 52 0.049
206
PPL021 Papilledema 52 0.049
207
P LCT002 Lactose Intolerance 50 0.049
208
SCH016 Schimke Immunoosseous Dysplasia 49 0.049
209
NWB001 Newborn Respiratory Distress Syndrome 48 0.049
210
ACT095 Acute Biphenotypic Leukemia 47 0.049
211
BTN002 Boutonneuse Fever 47 0.049
212
RCR001 Recurrent Corneal Erosion 44 0.049
213
BRN014 Bronchopneumonia 44 0.049
214
TTR016 Tetra-Amelia Syndrome 43 0.049
215
PLM038 Pulmonary Large Cell Neuroendocrine Carcinoma 43 0.049
216
WTH001 Withdrawal Disorder 40 0.049
217
INT071 Intestinal Perforation 39 0.049
218
IPX001 Ipex Syndrome 39 0.049
219
CRB086 Cerebral Aneurysms 37 0.049
220
CRP018 Cor Pulmonale 36 0.049
221
LMB051 Lumbar Disc Disease 36 0.049
222
LRY004 Laryngotracheitis 36 0.049
223
GNG006 Gingival Hypertrophy 35 0.049
224
P INF131 Infant Acute Respiratory Distress Syndrome 35 0.049
225
GST007 Gastric Dilatation 34 0.049
226
ALP044 Alpha-1-Antichymotrypsin Deficiency 33 0.049
227
c CTS019 Cutis Laxa, Ad 29 0.049
228
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.049
229
P HYP078 Hypertrophy of Breast 26 0.049
230
PLM074 Pulmonary Function 24 0.049
231
SBS002 Substernal Goiter 22 0.049
232
c BNG076 Benign Exophthalmos Syndrome 21 0.049
233
c PDT025 Pediatric Multiple Sclerosis 21 0.049
234
ANT005 Anteroseptal Myocardial Infarction 17 0.049
235
LYM035 Lymphangiectasis 16 0.049
236
CMV001 Cmv Antenatal Infection 13 0.049
237
CYS021 Cystic Adenomatoid Malformation of Lung 10 0.049
238
P BRS047 Breast Cancer 105 0.035
239
P PNC035 Pancreatic Cancer 95 0.035
240
GLC006 Galactosemia 93 0.035
241
P TBR001 Tuberous Sclerosis 91 0.035
242
FBR012 Fabry Disease 88 0.035
243
AND002 Androgen Insensitivity Syndrome 88 0.035
244
P NMN002 Niemann-Pick Disease 87 0.035
245
SVR004 Severe Combined Immunodeficiency 85 0.035
246
c DBT009 Diabetes Mellitus 80 0.035
247
P ACT074 Acute Lymphocytic Leukemia 77 0.035
248
LNG024 Langerhans-Cell Histiocytosis 75 0.035
249
P WGN002 Wegener's Granulomatosis 75 0.035
250
c HPT021 Hepatitis 75 0.035
251
P FML018 Familial Mediterranean Fever 74 0.035
252
P LYM007 Lymphangioleiomyomatosis 74 0.035
253
P GLY008 Glycogen Storage Disease Ii 73 0.035
254
ASP006 Aspergillosis 73 0.035
255
P HYP035 Hypophosphatasia 73 0.035
256
ULC004 Ulcerative Colitis 72 0.035
257
P ABD003 Abdominal Aortic Aneurysm 71 0.035
258
P SYS005 Systemic Scleroderma 69 0.035
259
DBT001 Diabetic Ketoacidosis 69 0.035
260
P DDN001 Duodenal Ulcer 68 0.035
261
P MTB001 Metabolic Syndrome X 67 0.035
262
c PNC044 Pancreatitis 67 0.035
263
GNG013 Gingivitis 67 0.035
264
P FBR017 Fibrosarcoma 66 0.035
265
DFC004 Deficiency Anemia 66 0.035
266
ARS001 Aarskog-Scott Syndrome 65 0.035
267
c SML001 Small Cell Carcinoma 64 0.035
268
ALL008 Allergic Bronchopulmonary Aspergillosis 64 0.035
269
CHL068 Cholestasis 63 0.035
270
c ACT027 Acute Pancreatitis 63 0.035
271
NTH001 Netherton Syndrome 63 0.035
272
TYP007 Typhoid Fever 63 0.035
273
CRN036 Craniopharyngioma 62 0.035
274
BLM002 Bulimia Nervosa 62 0.035
275
DDN006 Duodenitis 62 0.035
276
SMT015 Smith Magenis Syndrome 62 0.035
277
P ALP009 Alopecia Areata 61 0.035
278
P ANP001 Anaplastic Large Cell Lymphoma 61 0.035
279
NRN004 Neuroendocrine Tumor 61 0.035
280
RTN017 Retinal Detachment 60 0.035
281
c AXN002 Axenfeld-Rieger Syndrome 60 0.035
282
P ADN016 Adenocarcinoma 60 0.035
283
ACT049 Acute Disseminated Encephalomyelitis 60 0.035
284
P CLL015 Collagen Disease 59 0.035
285
BRT002 Birt-Hogg-Dube Syndrome 59 0.035
286
INT051 Intussusception 59 0.035
287
c MNC007 Monocytic Leukemia 59 0.035
288
CMP002 Campylobacteriosis 59 0.035
289
CRT016 Carotid Artery Disease 58 0.035
290
ORL004 Oral Submucous Fibrosis 57 0.035
291
P PYL005 Pyelonephritis 57 0.035
292
MGC001 Megacolon 56 0.035
293
P INT030 Intracranial Aneurysm 56 0.035
294
P END047 Endophthalmitis 56 0.035
295
HYP006 Hypertensive Heart Disease 56 0.035
296
CHR005 Chorioamnionitis 56 0.035
297
P PNC001 Pancytopenia 55 0.035
298
PRP007 Priapism 55 0.035
299
CRN027 Corneal Neovascularization 55 0.035
300
ENC006 Encephalomyelitis 55 0.035
301
BNF002 Bone Fracture 55 0.035
302
BRN016 Bronchogenic Carcinoma 55 0.035
303
P ESN008 Eosinophilic Pneumonia 54 0.035
304
c BCT007 Bacterial Meningitis 54 0.035
305
EXS001 Exostosis 54 0.035
306
c DNT011 Dentinogenesis Imperfecta 54 0.035
307
ART017 Aortic Disease 54 0.035
308
CRV038 Cervical Squamous Cell Carcinoma 54 0.035
309
c LRG001 Large Cell Carcinoma 53 0.035
310
c RTN014 Retinal Artery Occlusion 53 0.035
311
ADL002 Adult Syndrome 52 0.035
312
MCN007 Meconium Aspiration Syndrome 52 0.035
313
EXF001 Exfoliation Syndrome 51 0.035
314
FRM003 Farmer's Lung 51 0.035
315
P PLR004 Pleuropulmonary Blastoma 51 0.035
316
P CMP008 Compartment Syndrome 51 0.035
317
PLM035 Pulmonary Eosinophilia 51 0.035
318
c KRT007 Keratoconus 50 0.035
319
BLS003 Blastoma 50 0.035
320
IDP064 Idiopathic Neutropenia 50 0.035
321
KLT001 Klatskin's Tumor 50 0.035
322
HYP009 Hypertrophic Pyloric Stenosis 50 0.035
323
P CNT028 Central Retinal Artery Occlusion 49 0.035
324
PYL006 Pyloric Stenosis 49 0.035
325
LNG029 Lung Adenocarcinoma 49 0.035
326
STV001 Stevens-Johnson Syndrome 49 0.035
327
SCR002 Scurvy 49 0.035
328
TND004 Tendinopathy 48 0.035
329
c TYP003 Type I Ehlers-Danlos Syndrome 48 0.035
330
c ART084 Arteriovenous Fistula 47 0.035
331
PYM001 Pyomyositis 47 0.035
332
IMM060 Immunodeficiency, Common Variable, 9 46 0.035
333
ASP007 Aspiration Pneumonia 45 0.035
334
DVR002 Diverticulitis 45 0.035
335
CRY001 Cryptogenic Organizing Pneumonia 44 0.035
336
ACT100 Acute Febrile Neutrophilic Dermatosis 43 0.035
337
PST062 Pustulosis Palmaris Et Plantaris 43 0.035
338
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 43 0.035
339
BRL002 Buruli Ulcer Disease 43 0.035
340
CNJ007 Conjunctivochalasis 43 0.035
341
QDR001 Quadriplegia 43 0.035
342
INT052 Intestinal Volvulus 42 0.035
343
c HYP057 Hypervitaminosis D 42 0.035
344
BLP005 Blepharitis 42 0.035
345
GRN022 Granulosa Cell Tumor of the Ovary 41 0.035
346
c ADL027 Adult Dermatomyositis 41 0.035
347
EPG003 Epiglottitis 40 0.035
348
MCR001 Microcystic Meningioma 40 0.035
349
HYP030 Hypoactive Sexual Desire Disorder 39 0.035
350
PRL008 Paralytic Ileus 39 0.035
351
ORP003 Oropharynx Cancer 38 0.035
352
USL001 Usual Interstitial Pneumonia 38 0.035
353
VRL011 Viral Infectious Disease 37 0.035
354
THY042 Thymic Epithelial Tumor 36 0.035
355
ELP001 Elephantiasis 36 0.035
356
MTR001 Mature Cataract 34 0.035
357
BYS001 Byssinosis 33 0.035
358
ADS002 Adie Syndrome 33 0.035
359
TRC020 Tracheitis 33 0.035
360
ODN005 Odontogenic Myxoma 33 0.035
361
c CTS009 Cutis Laxa, Autosomal Recessive Type 2a 33 0.035
362
ANG004 Angioid Streaks 33 0.035
363
SLL001 Sialolithiasis 33 0.035
364
LGP001 Lagophthalmos 31 0.035
365
c FRT001 Fourth Cranial Nerve Palsy 30 0.035
366
ORB006 Orbital Cellulitis 29 0.035
367
TXC001 Toxic Megacolon 29 0.035
368
RHN002 Rhinoscleroma 29 0.035
369
HMT018 Hematopoietic Stem Cell Transplantation 29 0.035
370
NTR005 Nutritional Deficiency Disease 28 0.035
371
c PLM044 Pulmonary Fibrosis, Familial 27 0.035
372
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 27 0.035
373
RPT003 Ruptured Aortic Aneurysm 27 0.035
374
BRN055 Bronchogenic Cyst 24 0.035
375
c TMR002 Tumoral Calcinosis, Hyperphosphatemic 22 0.035
376
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 22 0.035
377
c EFM001 Efemp2-Related Cutis Laxa 21 0.035
378
c HMP017 Hemophilia a, Congenital 21 0.035
379
OPT010 Optic Papillitis 20 0.035
380
CPD002 Copd, Rate of Decline of Lung Function in 18 0.035
381
PLM015 Pulmonary Systemic Sclerosis 18 0.035
382
HYP015 Hyperlucent Lung 17 0.035
383
PSD089 Pseudomonas Aeruginosa Chronic Infection by, in Cystic Fibrosis 15 0.035
384
P ISC010 Isochromosome Yp 14 0.035
385
RPT001 Ruptured Thoracoabdominal Aortic Aneurysm 13 0.035
386
CTS024 Cutis Laxa-Marfanoid Syndrome 11 0.035