Search results for "emphysema"

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

331 hits were found for 'emphysema'

# Family MCID Name MIFTS Score
1
EMP007 Emphysema Due to Aat Deficiency 48 7.692
2
PLM034 Pulmonary Emphysema 55 6.883
3
CNG105 Congenital Lobar Emphysema 39 5.706
4
INT011 Interstitial Emphysema 22 4.666
5
CMP003 Compensatory Emphysema 7 3.881
6
BRR006 Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification 6 3.853
7
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 36 3.146
8
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 5 3.104
9
PNM008 Pneumothorax 48 0.255
10
P PLM036 Pulmonary Fibrosis 67 0.216
11
BRN024 Bronchitis 66 0.201
12
PLM074 Pulmonary Function 35 0.173
13
MDS022 Mediastinitis 45 0.144
14
CRP018 Cor Pulmonale 43 0.144
15
P PNM007 Pneumonia 76 0.135
16
P AST005 Asthma 91 0.130
17
P LNG032 Lung Cancer 95 0.125
18
P PLM037 Pulmonary Hypertension 92 0.125
19
P CTS001 Cutis Laxa 57 0.125
20
P SPN183 Spontaneous Pneumothorax 52 0.125
21
END072 Endotheliitis 51 0.114
22
BRN055 Bronchogenic Cyst 38 0.114
23
BRN002 Bronchiolitis 59 0.108
24
P RSP003 Respiratory Failure 68 0.102
25
TBR010 Tuberculosis 84 0.095
26
CYS001 Cystic Fibrosis 100 0.088
27
MRF001 Marfan Syndrome 86 0.088
28
P CNG401 Congenital Heart Disease 70 0.088
29
P TRC086 Trichohepatoenteric Syndrome 1 45 0.088
30
PNM003 Pneumatosis Cystoides Intestinalis 23 0.088
31
P DRM010 Dermatomyositis 71 0.081
32
ATH003 Atherosclerosis 65 0.081
33
BRN022 Bronchiectasis 61 0.081
34
INT066 Interstitial Lung Disease 51 0.081
35
CRB009 Cerebritis 37 0.081
36
P ATX030 Ataxia-Telangiectasia 86 0.072
37
P OST002 Osteoporosis 81 0.072
38
ACN002 Acanthosis Nigricans 63 0.072
39
P AND016 Andersen Syndrome 61 0.072
40
STT002 Status Asthmaticus 60 0.072
41
MLR002 Miliary Tuberculosis 58 0.072
42
LNG024 Langerhans-Cell Histiocytosis 57 0.072
43
SLC006 Silicosis 57 0.072
44
BRN056 Bronchopulmonary Dysplasia 57 0.072
45
ART001 Arterial Tortuosity Syndrome 56 0.072
46
PLM129 Pulmonary Disease, Chronic Obstructive 54 0.072
47
THR013 Thoracic Outlet Syndrome 52 0.072
48
P PNM006 Pneumoconiosis 49 0.072
49
ANR040 Aneurysm 45 0.072
50
FSC004 Fasciitis 45 0.072
51
NCR007 Necrotizing Fasciitis 44 0.072
52
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 42 0.072
53
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 35 0.072
54
PLM064 Pulmonary Sequestration 33 0.072
55
c PNM010 Pneumothorax, Primary Spontaneous 33 0.072
56
P ATX010 Ataxia Neuropathy Spectrum 29 0.072
57
CRK001 Cork-Handlers' Disease 28 0.072
58
LYM035 Lymphangiectasis 24 0.072
59
DFF002 Diffuse Pulmonary Fibrosis 18 0.072
60
P ANG001 Angelman Syndrome 76 0.062
61
LVR012 Liver Cirrhosis 75 0.062
62
MSL001 Measles 67 0.062
63
GSG001 Gas Gangrene 66 0.062
64
VSC011 Vasculitis 65 0.062
65
P CNG015 Congenital Diaphragmatic Hernia 65 0.062
66
c HYP595 Hypertension, Essential 62 0.062
67
ELL001 Ellis-Van Creveld Syndrome 61 0.062
68
MYC002 Mycobacterium Avium Complex Disease 59 0.062
69
NNS002 Nonspecific Interstitial Pneumonia 57 0.062
70
P VNT002 Ventricular Septal Defect 55 0.062
71
SCH016 Schimke Immunoosseous Dysplasia 53 0.062
72
c SPN225 Spondyloarthropathy 1 52 0.062
73
P CYS018 Cystitis 50 0.062
74
CYT008 Cytomegalovirus Infection 43 0.062
75
c ACQ027 Acquired Cutis Laxa 42 0.062
76
TTR016 Tetra-Amelia Syndrome 42 0.062
77
CRB086 Cerebral Aneurysms 39 0.062
78
c ART101 Aortic Valve Disease 2 37 0.062
79
UND005 Undifferentiated Pleomorphic Sarcoma 30 0.062
80
TRC037 Tracheobronchomalacia 22 0.062
81
c BNG076 Benign Exophthalmos Syndrome 21 0.062
82
AND005 Androgen Insensitivity Syndrome, Mild 19 0.062
83
SPN014 Spontaneous Tension Pneumothorax 14 0.062
84
HPT023 Hepatocellular Carcinoma 100 0.051
85
P ALZ034 Alzheimer Disease 99 0.051
86
P MYC007 Myocardial Infarction 93 0.051
87
FBR012 Fabry Disease 86 0.051
88
P NRF002 Neurofibromatosis 79 0.051
89
HV1006 Hiv-1 79 0.051
90
AND015 Androgen Insensitivity 78 0.051
91
P TBR001 Tuberous Sclerosis 78 0.051
92
CMM004 Common Variable Immunodeficiency 77 0.051
93
P LKM002 Leukemia 76 0.051
94
P LYM007 Lymphangioleiomyomatosis 75 0.051
95
P ART022 Arthritis 74 0.051
96
P HYP035 Hypophosphatasia 74 0.051
97
PCK002 Pick Disease 72 0.051
98
P NMN002 Niemann-Pick Disease 72 0.051
99
ART016 Aortic Aneurysm 71 0.051
100
P LVR013 Liver Disease 71 0.051
101
P PRD008 Periodontitis 68 0.051
102
P PNC044 Pancreatitis 68 0.051
103
SRC014 Sarcoma 68 0.051
104
P INF038 Influenza 68 0.051
105
P ABD003 Abdominal Aortic Aneurysm 67 0.051
106
ALL008 Allergic Bronchopulmonary Aspergillosis 66 0.051
107
ACT049 Acute Disseminated Encephalomyelitis 66 0.051
108
P HML002 Hemolytic Anemia 65 0.051
109
P HPT021 Hepatitis 63 0.051
110
c GLY008 Glycogen Storage Disease Ii 62 0.051
111
P ACR001 Aicardi-Goutieres Syndrome 62 0.051
112
EXT034 Extrinsic Allergic Alveolitis 62 0.051
113
P HST010 Histiocytosis 62 0.051
114
P EHL049 Ehlers-Danlos Syndrome Classical Type 62 0.051
115
PRT037 Pertussis 61 0.051
116
GTR002 Goiter 61 0.051
117
P ADL010 Adult Respiratory Distress Syndrome 59 0.051
118
MLL005 Miller-Dieker Syndrome 58 0.051
119
BRN012 Bronchiolitis Obliterans 58 0.051
120
CNN005 Connective Tissue Disease 58 0.051
121
NRN001 Neuroendocrine Carcinoma 57 0.051
122
BRT002 Birt-Hogg-Dube Syndrome 57 0.051
123
NTH001 Netherton Syndrome 57 0.051
124
CLL003 Cellulitis 57 0.051
125
P AXN010 Axenfeld-Rieger Syndrome, Type 3 57 0.051
126
P CRV039 Cervicitis 56 0.051
127
ACT100 Acute Febrile Neutrophilic Dermatosis 56 0.051
128
P PLR004 Pleuropulmonary Blastoma 55 0.051
129
P INT030 Intracranial Aneurysm 55 0.051
130
APP008 Appendicitis 55 0.051
131
GST037 Gastroparesis 55 0.051
132
PRD007 Periodontal Disease 54 0.051
133
P SLL003 Salla Disease 53 0.051
134
c ACT210 Acute Respiratory Distress Syndrome 53 0.051
135
PPL021 Papilledema 53 0.051
136
BLS003 Blastoma 52 0.051
137
PLM012 Pulmonary Sarcoidosis 52 0.051
138
ACQ007 Acquired Immunodeficiency Syndrome 51 0.051
139
RTN023 Retinitis 51 0.051
140
OBS006 Obstructive Lung Disease 51 0.051
141
NRM005 Neuromuscular Disease 50 0.051
142
MNN014 Mononeuritis 49 0.051
143
CNG069 Congenital Cytomegalovirus 48 0.051
144
DVR002 Diverticulitis 48 0.051
145
BRN014 Bronchopneumonia 46 0.051
146
CNJ007 Conjunctivochalasis 45 0.051
147
c LRG014 Large Cell Neuroendocrine Carcinoma 45 0.051
148
HRS011 Horseshoe Kidney 44 0.051
149
HMT018 Hematopoietic Stem Cell Transplantation 41 0.051
150
INT071 Intestinal Perforation 40 0.051
151
BRN038 Bronchial Disease 40 0.051
152
c CTS008 Cutis Laxa, Autosomal Dominant 38 0.051
153
c NMN016 Niemann-Pick Disease, Type B 38 0.051
154
LRY004 Laryngotracheitis 36 0.051
155
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 34 0.051
156
NNT039 Neonatal Marfan Syndrome 32 0.051
157
TFT003 Tufting Enteropathy 31 0.051
158
c CTS019 Cutis Laxa, Ad 31 0.051
159
AMY016 Amyopathic Dermatomyositis 30 0.051
160
LRY028 Laryngocele 27 0.051
161
SBS002 Substernal Goiter 22 0.051
162
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 20 0.051
163
c CTS037 Cutis Laxa, Autosomal Recessive, Type Ib 19 0.051
164
ANT017 Anthracosilicosis 18 0.051
165
ANT005 Anteroseptal Myocardial Infarction 16 0.051
166
CTS024 Cutis Laxa-Marfanoid Syndrome 12 0.051
167
P RHM011 Rheumatoid Arthritis 96 0.036
168
P PNC035 Pancreatic Cancer 95 0.036
169
P BRS047 Breast Cancer 91 0.036
170
P LFR001 Li-Fraumeni Syndrome 90 0.036
171
GLC006 Galactosemia 85 0.036
172
c FNC027 Fanconi Anemia, Complementation Group a 78 0.036
173
THR006 Thromboangiitis Obliterans 77 0.036
174
SVR004 Severe Combined Immunodeficiency 77 0.036
175
KWS002 Kawasaki Disease 75 0.036
176
CRH001 Crohn's Disease 75 0.036
177
MNK001 Menkes Disease 74 0.036
178
RLP001 Relapsing Polychondritis 72 0.036
179
P FRD001 Friedreich Ataxia 71 0.036
180
PRT036 Peritonitis 71 0.036
181
P VLC001 Velocardiofacial Syndrome 70 0.036
182
PLY017 Polyarteritis Nodosa 69 0.036
183
P NPH012 Nephrotic Syndrome 68 0.036
184
c MTB001 Metabolic Syndrome X 67 0.036
185
P MNN013 Meningitis 67 0.036
186
WLL001 Williams-Beuren Syndrome 66 0.036
187
P PRT013 Portal Hypertension 66 0.036
188
PLM033 Pulmonary Embolism 66 0.036
189
ARS001 Aarskog-Scott Syndrome 65 0.036
190
ULC004 Ulcerative Colitis 63 0.036
191
SMT008 Smith-Magenis Syndrome 63 0.036
192
P ALP009 Alopecia Areata 63 0.036
193
c ACT027 Acute Pancreatitis 63 0.036
194
CLT003 Colitis 62 0.036
195
CMP002 Campylobacteriosis 62 0.036
196
P ANP001 Anaplastic Large Cell Lymphoma 62 0.036
197
P FTL001 Fetal Alcohol Syndrome 62 0.036
198
TYP007 Typhoid Fever 61 0.036
199
WGN006 Wegener Granulomatosis 61 0.036
200
HPT022 Hepatoblastoma 61 0.036
201
DFC004 Deficiency Anemia 61 0.036
202
FBR032 Fibromuscular Dysplasia 60 0.036
203
OST085 Osteosarcoma, Somatic 60 0.036
204
PGM001 Pigmented Villonodular Synovitis 60 0.036
205
GNG013 Gingivitis 60 0.036
206
GLC012 Galactosialidosis 60 0.036
207
P DDN001 Duodenal Ulcer 60 0.036
208
EXF001 Exfoliation Syndrome 59 0.036
209
SCR002 Scurvy 59 0.036
210
PLM001 Pulmonary Tuberculosis 59 0.036
211
P MYM002 Moyamoya Disease 59 0.036
212
MGC001 Megacolon 59 0.036
213
SPN020 Spondylosis 58 0.036
214
SYN007 Synovitis 58 0.036
215
P SZR006 Seizure Disorder 58 0.036
216
PRT093 Proteus Syndrome, Somatic 58 0.036
217
CHL068 Cholestasis 58 0.036
218
CLL021 Collagenous Colitis 57 0.036
219
P ADN016 Adenocarcinoma 57 0.036
220
P DGR001 Digeorge Syndrome 57 0.036
221
ACT095 Acute Biphenotypic Leukemia 57 0.036
222
HYP266 Hypoxia 57 0.036
223
DBT001 Diabetic Ketoacidosis 57 0.036
224
MCN007 Meconium Aspiration Syndrome 56 0.036
225
BLM002 Bulimia Nervosa 56 0.036
226
MCR088 Microscopic Polyangiitis 56 0.036
227
VLV044 Vulvar Intraepithelial Neoplasia 56 0.036
228
P RPD001 Rapidly Progressive Glomerulonephritis 56 0.036
229
P SNS014 Sinusitis 56 0.036
230
P SDR002 Siderosis 56 0.036
231
HMS001 Hemosiderosis 56 0.036
232
P FML161 Familial Mediterranean Fever, Ar 55 0.036
233
RTN017 Retinal Detachment 55 0.036
234
P MNC007 Monocytic Leukemia 55 0.036
235
INT007 Intermediate Coronary Syndrome 55 0.036
236
DDN006 Duodenitis 55 0.036
237
ORL004 Oral Submucous Fibrosis 55 0.036
238
PPL049 Papillon-Lefevre Syndrome 55 0.036
239
P RTN014 Retinal Artery Occlusion 55 0.036
240
P CMP008 Compartment Syndrome 54 0.036
241
NCR004 Nocardiosis 54 0.036
242
PLM134 Pulmonary Fibrosis, Idiopathic 54 0.036
243
PRT082 Preterm Premature Rupture of the Membranes 54 0.036
244
DST006 Diastolic Heart Failure 54 0.036
245
ART017 Aortic Disease 53 0.036
246
RTC002 Reticular Dysgenesis 53 0.036
247
ALL006 Allergic Asthma 53 0.036
248
FRM003 Farmer's Lung 53 0.036
249
STT004 Steatorrhea 52 0.036
250
IMP005 Impotence 52 0.036
251
VLL003 Villonodular Synovitis 52 0.036
252
PLY013 Polymyalgia Rheumatica 52 0.036
253
P KRT007 Keratoconus 52 0.036
254
ISC015 Ischemic Colitis 52 0.036
255
c CNT028 Central Retinal Artery Occlusion 51 0.036
256
CLC006 Calcinosis 51 0.036
257
P PYL005 Pyelonephritis 50 0.036
258
EXS001 Exostosis 50 0.036
259
MYC013 Mycobacterium Abscessus 49 0.036
260
FML091 Familial Tumoral Calcinosis 49 0.036
261
P HYP009 Hypertrophic Pyloric Stenosis 49 0.036
262
ART006 Arthus Reaction 49 0.036
263
PYL006 Pyloric Stenosis 49 0.036
264
CHR005 Chorioamnionitis 49 0.036
265
DFF021 Diffuse Mesangial Sclerosis 48 0.036
266
PYM001 Pyomyositis 48 0.036
267
EXC002 Exocrine Pancreatic Insufficiency 48 0.036
268
PST010 Pasteurellosis 48 0.036
269
ASP007 Aspiration Pneumonia 47 0.036
270
P PNC001 Pancytopenia 47 0.036
271
CRY001 Cryptogenic Organizing Pneumonia 47 0.036
272
P ART084 Arteriovenous Fistula 46 0.036
273
P TMR011 Tumoral Calcinosis, Hyperphosphatemic, Familial 46 0.036
274
CRT013 Carotid Stenosis 46 0.036
275
c ADL027 Adult Dermatomyositis 46 0.036
276
EVN001 Evans' Syndrome 45 0.036
277
FND002 Fundus Dystrophy 45 0.036
278
BNF002 Bone Fracture 45 0.036
279
P OVR046 Ovarian Cyst 45 0.036
280
ANT039 Antisynthetase Syndrome 45 0.036
281
ODN005 Odontogenic Myxoma 44 0.036
282
c OPT055 Optic Atrophy Plus Syndrome 44 0.036
283
c OPT053 Optic Atrophy 1 44 0.036
284
QDR001 Quadriplegia 42 0.036
285
MCR001 Microcystic Meningioma 42 0.036
286
SRC027 Sarcoma, Synovial 41 0.036
287
c HYP057 Hypervitaminosis D 41 0.036
288
EPG003 Epiglottitis 40 0.036
289
SKN005 Skin Atrophy 39 0.036
290
NCT008 Nicotine Dependence, Protection Against 39 0.036
291
GST064 Gastric Outlet Obstruction 39 0.036
292
GNG006 Gingival Hypertrophy 37 0.036
293
BRN016 Bronchogenic Carcinoma 37 0.036
294
IPX001 Ipex Syndrome 36 0.036
295
NWB001 Newborn Respiratory Distress Syndrome 36 0.036
296
CHL028 Childhood Type Dermatomyositis 36 0.036
297
VRL011 Viral Infectious Disease 35 0.036
298
BRL011 Bare Lymphocyte Syndrome, Type I 34 0.036
299
ADS002 Adie Syndrome 34 0.036
300
SHK001 Shaken Baby Syndrome 34 0.036
301
c INF131 Infant Acute Respiratory Distress Syndrome 33 0.036
302
HPT012 Hepatocellular Fibrolamellar Carcinoma 33 0.036
303
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 32 0.036
304
TRC020 Tracheitis 32 0.036
305
NTR005 Nutritional Deficiency Disease 31 0.036
306
LGP001 Lagophthalmos 30 0.036
307
BYS001 Byssinosis 30 0.036
308
HNM002 Hinman Syndrome 29 0.036
309
PNG002 Pain Agnosia 29 0.036
310
ORB006 Orbital Cellulitis 29 0.036
311
c MLG033 Malignant Ovarian Cyst 28 0.036
312
TXC001 Toxic Megacolon 28 0.036
313
CRL004 Caroli Disease 27 0.036
314
RHN002 Rhinoscleroma 27 0.036
315
GST007 Gastric Dilatation 27 0.036
316
HRT011 Heart Septal Defect 27 0.036
317
ALP044 Alpha-1-Antichymotrypsin Deficiency 25 0.036
318
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 25 0.036
319
ARM003 Aromatic Amino Acid Decarboxylase Deficiency 23 0.036
320
LYS013 Loeys-Dietz Syndrome, Type 4 22 0.036
321
c MRG011 Meier-Gorlin Syndrome 4 22 0.036
322
IMM015 Immune Defect Due to Absence of Thymus 20 0.036
323
P RSP007 Respiratory Distress Syndrome, Infant 18 0.036
324
HYP015 Hyperlucent Lung 18 0.036
325
FML066 Familial Hypersensitivity Pneumonitis 18 0.036
326
WLS002 Wilson-Mikity Syndrome 17 0.036
327
ATS053 Autosomal Dominant Optic Atrophy, Hearing Loss, and Peripheral Neuropathy 15 0.036
328
P THR041 Thrombocytopenia, Acquired Amegakaryocytic 15 0.036
329
CYS021 Cystic Adenomatoid Malformation of Lung 15 0.036
330
PLM116 Pulmonary Artery Hypoplasia 15 0.036
331
PLS010 Plasma Protein Metabolism Disease 8 0.036