Search results for emphysema

398 hits were found for emphysema

# Family MCID Name MIFTS Score
1
EMP007 Emphysema Due to Aat Deficiency 58 6.800
2
PLM034 Pulmonary Emphysema 55 6.541
3
EMP011 Emphysema, Congenital Lobar 27 5.040
4
INT011 Interstitial Emphysema 38 4.657
5
CMP003 Compensatory Emphysema 11 3.919
6
BRR006 Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification 6 3.196
7
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 7 2.299
8
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 30 2.250
9
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.352
10
LNG099 Lung Disease 64 0.277
11
PNM008 Pneumothorax 53 0.256
12
P PLM036 Pulmonary Fibrosis 71 0.242
13
BRN024 Bronchitis 64 0.206
14
RSP006 Respiratory System Disease 58 0.197
15
P PLM040 Pulmonary Valve Disease 43 0.155
16
P LNG032 Lung Cancer 95 0.151
17
P AST005 Asthma 82 0.151
18
P PNM007 Pneumonia 68 0.151
19
MDS022 Mediastinitis 41 0.144
20
BRN038 Bronchial Disease 51 0.140
21
P PLM037 Pulmonary Hypertension 79 0.131
22
UPP004 Upper Respiratory Tract Disease 46 0.131
23
NTR005 Nutritional Deficiency Disease 36 0.127
24
P CTS001 Cutis Laxa 58 0.122
25
BRN002 Bronchiolitis 56 0.112
26
c CHR096 Chronic Pulmonary Heart Disease 40 0.112
27
BRN055 Bronchogenic Cyst 28 0.112
28
TBR010 Tuberculosis 70 0.107
29
END072 Endotheliitis 42 0.107
30
SRN001 Serine Deficiency 32 0.107
31
MRF001 Marfan Syndrome 73 0.102
32
PRT011 Protein C Deficiency 52 0.096
33
INT066 Interstitial Lung Disease 59 0.090
34
c AST037 Asthma 1 28 0.090
35
P HRT032 Heart Disease 75 0.083
36
ATH003 Atherosclerosis 65 0.083
37
BRN022 Bronchiectasis 50 0.083
38
CRB009 Cerebritis 39 0.083
39
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.083
40
PNM003 Pneumatosis Cystoides Intestinalis 29 0.083
41
c AST039 Asthma 2 28 0.083
42
NNT039 Neonatal Marfan Syndrome 27 0.083
43
CYS001 Cystic Fibrosis 83 0.076
44
P INF038 Influenza 72 0.076
45
P OST002 Osteoporosis 64 0.076
46
VSC011 Vasculitis 62 0.076
47
P DRM010 Dermatomyositis 62 0.076
48
ANR040 Aneurysm 57 0.076
49
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.076
50
P PNM006 Pneumoconiosis 51 0.076
51
STT002 Status Asthmaticus 42 0.076
52
DFF002 Diffuse Pulmonary Fibrosis 33 0.076
53
HYP193 Hypocomplementemic Urticarial Vasculitis 31 0.076
54
P RSP003 Respiratory Failure 71 0.068
55
PLM001 Pulmonary Tuberculosis 67 0.068
56
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.068
57
SLC006 Silicosis 53 0.068
58
SLP005 Sleep Disorder 53 0.068
59
FSC004 Fasciitis 48 0.068
60
BRN056 Bronchopulmonary Dysplasia 48 0.068
61
NCR007 Necrotizing Fasciitis 46 0.068
62
DPH021 Diaphragm Disease 41 0.068
63
MLR002 Miliary Tuberculosis 41 0.068
64
MRG013 Mirage Syndrome 29 0.068
65
P LVR013 Liver Disease 75 0.059
66
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.059
67
CNN005 Connective Tissue Disease 62 0.059
68
MSL001 Measles 61 0.059
69
P CNG015 Congenital Diaphragmatic Hernia 60 0.059
70
CHL123 Chlamydia 60 0.059
71
ALL006 Allergic Asthma 58 0.059
72
ELL001 Ellis-Van Creveld Syndrome 58 0.059
73
c ACT210 Acute Respiratory Distress Syndrome 57 0.059
74
HYP266 Hypoxia 56 0.059
75
IDP011 Idiopathic Interstitial Pneumonia 56 0.059
76
PRP019 Peripheral Nervous System Disease 55 0.059
77
P CYS018 Cystitis 52 0.059
78
BRT002 Birt-Hogg-Dube Syndrome 52 0.059
79
GSG001 Gas Gangrene 49 0.059
80
ATN002 Autonomic Nervous System Disease 48 0.059
81
NNS002 Nonspecific Interstitial Pneumonia 45 0.059
82
CRR007 Cirrhosis, Cryptogenic 43 0.059
83
DDN006 Duodenitis 42 0.059
84
BNS002 Bone Structure Disease 37 0.059
85
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 33 0.059
86
c CTS019 Cutis Laxa, Ad 31 0.059
87
LYM035 Lymphangiectasis 28 0.059
88
P PLM064 Pulmonary Sequestration 27 0.059
89
SBS002 Substernal Goiter 24 0.059
90
TRC037 Tracheobronchomalacia 23 0.059
91
c AST050 Asthma, Phf11-Related 22 0.059
92
c CTS037 Cutis Laxa, Autosomal Recessive, Type Ib 20 0.059
93
AND005 Androgen Insensitivity Syndrome, Mild 16 0.059
94
CTS042 Cutis Laxa, Neonatal, with Marfanoid Phenotype 12 0.059
95
SPN014 Spontaneous Tension Pneumothorax 12 0.059
96
P MYC007 Myocardial Infarction 79 0.048
97
P LKM002 Leukemia 71 0.048
98
P NRF002 Neurofibromatosis 71 0.048
99
FBR012 Fabry Disease 69 0.048
100
c HYP595 Hypertension, Essential 69 0.048
101
ART016 Aortic Aneurysm 69 0.048
102
CMM004 Common Variable Immunodeficiency 68 0.048
103
PCK002 Pick Disease 68 0.048
104
DRM006 Dermatitis 66 0.048
105
P LYM007 Lymphangioleiomyomatosis 66 0.048
106
SRC014 Sarcoma 66 0.048
107
PRT037 Pertussis 64 0.048
108
P PRD008 Periodontitis 63 0.048
109
c TBR024 Tuberous Sclerosis-1 63 0.048
110
P HML002 Hemolytic Anemia 62 0.048
111
P ATP001 Atopic Dermatitis 62 0.048
112
c SRC025 Sarcoidosis 1 61 0.048
113
P ADL010 Adult Respiratory Distress Syndrome 61 0.048
114
ACQ007 Acquired Immunodeficiency Syndrome 60 0.048
115
P SNS014 Sinusitis 60 0.048
116
CLT003 Colitis 60 0.048
117
APP008 Appendicitis 60 0.048
118
PRM097 Primary Immunodeficiency Disease 60 0.048
119
PRD007 Periodontal Disease 60 0.048
120
P VNT002 Ventricular Septal Defect 60 0.048
121
c GLY008 Glycogen Storage Disease Ii 59 0.048
122
BRN012 Bronchiolitis Obliterans 58 0.048
123
P HST010 Histiocytosis 58 0.048
124
P HYP035 Hypophosphatasia 57 0.048
125
NRM005 Neuromuscular Disease 56 0.048
126
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.048
127
c EHL033 Ehlers-Danlos Syndrome, Classic Type 55 0.048
128
EXT034 Extrinsic Allergic Alveolitis 54 0.048
129
GST037 Gastroparesis 54 0.048
130
NTH001 Netherton Syndrome 54 0.048
131
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.048
132
GTR002 Goiter 52 0.048
133
CYT008 Cytomegalovirus Infection 52 0.048
134
CLL003 Cellulitis 51 0.048
135
P DDN001 Duodenal Ulcer 50 0.048
136
RTN023 Retinitis 50 0.048
137
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.048
138
MCR088 Microscopic Polyangiitis 49 0.048
139
NCT008 Nicotine Dependence, Protection Against 49 0.048
140
LPD004 Lipoid Nephrosis 48 0.048
141
PPL021 Papilledema 47 0.048
142
BRN014 Bronchopneumonia 45 0.048
143
P CRV039 Cervicitis 45 0.048
144
P BRN120 Bronchus Cancer 44 0.048
145
BNN003 Bone Inflammation Disease 44 0.048
146
P SLL003 Salla Disease 43 0.048
147
INT071 Intestinal Perforation 42 0.048
148
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.048
149
P LRG014 Large Cell Neuroendocrine Carcinoma 41 0.048
150
HMT018 Hematopoietic Stem Cell Transplantation 41 0.048
151
SPC003 Specific Developmental Disorder 38 0.048
152
CPL005 Capillary Disease 36 0.048
153
CNJ007 Conjunctivochalasis 36 0.048
154
ALR002 Al-Raqad Syndrome 36 0.048
155
LYM014 Lymphangitis 35 0.048
156
PNM010 Pneumothorax, Primary Spontaneous 33 0.048
157
c CTS008 Cutis Laxa, Autosomal Dominant 28 0.048
158
ANT005 Anteroseptal Myocardial Infarction 22 0.048
159
LRY028 Laryngocele 20 0.048
160
ANT017 Anthracosilicosis 19 0.048
161
LMN005 Lmna-Related Cardiocutaneous Progeria Syndrome 15 0.048
162
P BRS047 Breast Cancer 100 0.034
163
P RHM011 Rheumatoid Arthritis 89 0.034
164
P PNC035 Pancreatic Cancer 87 0.034
165
ULC004 Ulcerative Colitis 76 0.034
166
P ART022 Arthritis 75 0.034
167
STR067 Stroke, Ischemic 75 0.034
168
P APL001 Aplastic Anemia 75 0.034
169
KWS002 Kawasaki Disease 70 0.034
170
P ADN016 Adenocarcinoma 69 0.034
171
P LYM118 Lymphoma 69 0.034
172
PSY004 Psychotic Disorder 67 0.034
173
P MYP004 Myopathy 67 0.034
174
P MNN013 Meningitis 67 0.034
175
OBS002 Obsessive-Compulsive Disorder 66 0.034
176
P NMN002 Niemann-Pick Disease 65 0.034
177
P PLR004 Pleuropulmonary Blastoma 65 0.034
178
CRB039 Cerebrovascular Disease 63 0.034
179
P ALX003 Alexander Disease 63 0.034
180
OST085 Osteosarcoma, Somatic 63 0.034
181
P PRS038 Personality Disorder 62 0.034
182
FCT003 Factor X Deficiency 61 0.034
183
CRD119 Cardiac Arrest 61 0.034
184
MTH009 Mouth Disease 61 0.034
185
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.034
186
P PNC044 Pancreatitis 61 0.034
187
P SYS005 Systemic Scleroderma 61 0.034
188
MNK001 Menkes Disease 60 0.034
189
PLM033 Pulmonary Embolism 60 0.034
190
WLL001 Williams-Beuren Syndrome 60 0.034
191
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.034
192
P HRM001 Hermansky-Pudlak Syndrome 59 0.034
193
P INF032 Infertility 59 0.034
194
P SHR029 Short Syndrome 58 0.034
195
ETN001 Eating Disorder 58 0.034
196
P MSC007 Muscle Hypertrophy 58 0.034
197
FCT006 Factor V Deficiency 57 0.034
198
URT039 Urticaria 57 0.034
199
P EPS003 Episodic Ataxia 57 0.034
200
EXF001 Exfoliation Syndrome 57 0.034
201
P ANP001 Anaplastic Large Cell Lymphoma 57 0.034
202
RTN017 Retinal Detachment 56 0.034
203
LKN001 Leukoencephalopathy with Vanishing White Matter 56 0.034
204
P CDS001 Cadasil 55 0.034
205
P MNC007 Monocytic Leukemia 55 0.034
206
PLM012 Pulmonary Sarcoidosis 54 0.034
207
HDC001 Headache 54 0.034
208
VSC002 Vascular Dementia 54 0.034
209
SBS003 Substance Abuse 54 0.034
210
PRT014 Protein S Deficiency 53 0.034
211
ADL002 Adult Syndrome 52 0.034
212
BLM002 Bulimia Nervosa 52 0.034
213
BRN106 Burns 52 0.034
214
QDR001 Quadriplegia 52 0.034
215
P PYL005 Pyelonephritis 52 0.034
216
P PNC001 Pancytopenia 52 0.034
217
P MGR003 Migraine with Aura 52 0.034
218
P MSC033 Muscle Disorders 52 0.034
219
P ALL008 Allergic Bronchopulmonary Aspergillosis 51 0.034
220
PLR022 Pleural Disease 51 0.034
221
HNT002 Hantavirus Pulmonary Syndrome 51 0.034
222
PNN001 Panniculitis 51 0.034
223
c FML023 Familial Hemiplegic Migraine 51 0.034
224
RTC002 Reticular Dysgenesis 50 0.034
225
BNF002 Bone Fracture 50 0.034
226
RLP001 Relapsing Polychondritis 50 0.034
227
THR013 Thoracic Outlet Syndrome 50 0.034
228
PNM001 Pneumocystosis 50 0.034
229
HPT074 Hepatic Adenoma, Somatic 50 0.034
230
CSY001 C Syndrome 50 0.034
231
BRX001 Bruxism 49 0.034
232
MVM001 Movement Disease 49 0.034
233
LRN003 Learning Disability 49 0.034
234
CCN001 Cocaine Dependence 49 0.034
235
ACT017 Acute Chest Syndrome 48 0.034
236
c ATS308 Autosomal Dominant Cerebellar Ataxia 48 0.034
237
P CMP008 Compartment Syndrome 48 0.034
238
CCN002 Cocaine Abuse 48 0.034
239
STT041 Stuttering 48 0.034
240
GLC012 Galactosialidosis 47 0.034
241
ANT011 Antisocial Personality Disorder 47 0.034
242
LYM116 Lymph Node Disease 47 0.034
243
c ERL020 Early-Onset Schizophrenia 47 0.034
244
FRM003 Farmer's Lung 47 0.034
245
ASP007 Aspiration Pneumonia 47 0.034
246
HMS001 Hemosiderosis 46 0.034
247
RSP002 Respiratory Syncytial Virus Infectious Disease 46 0.034
248
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 0.034
249
BLD053 Blood Platelet Disease 46 0.034
250
SCL003 Social Phobia 46 0.034
251
PYL006 Pyloric Stenosis 46 0.034
252
BRN045 Brunner Syndrome 46 0.034
253
MGC001 Megacolon 45 0.034
254
ACR041 Acromelic Frontonasal Dysostosis 45 0.034
255
DVR002 Diverticulitis 45 0.034
256
PRM003 Premature Ejaculation 45 0.034
257
ALN001 Aland Island Eye Disease 45 0.034
258
P HMP006 Hemiplegic Migraine 45 0.034
259
CRY001 Cryptogenic Organizing Pneumonia 44 0.034
260
RGH009 Right Atrial Isomerism 44 0.034
261
P RTN014 Retinal Artery Occlusion 44 0.034
262
c NMN016 Niemann-Pick Disease, Type B 43 0.034
263
NCR004 Nocardiosis 43 0.034
264
PHY002 Physical Disorder 43 0.034
265
ANX004 Anoxia 43 0.034
266
BRT030 Birth Defects 43 0.034
267
SKN027 Skin Conditions 43 0.034
268
RSP019 Respiratory Distress Syndrome in Premature Infants 43 0.034
269
OPP004 Oppositional Defiant Disorder 43 0.034
270
CRP017 Carpal Tunnel Syndrome, Familial 43 0.034
271
CRB008 Cerebral Atherosclerosis 43 0.034
272
SXL003 Sexual Disorder 42 0.034
273
P HYP009 Hypertrophic Pyloric Stenosis 42 0.034
274
c VRL005 Viral Pneumonia 42 0.034
275
EXS001 Exostosis 42 0.034
276
P RST011 Restrictive Dermopathy, Lethal 41 0.034
277
SPR007 Superior Mesenteric Artery Syndrome 41 0.034
278
SPC010 Speech and Communication Disorders 41 0.034
279
TRC003 Trichomoniasis 41 0.034
280
URT001 Urethritis 41 0.034
281
c SCN006 Secondary Syphilis 41 0.034
282
DFF003 Diffuse Scleroderma 41 0.034
283
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.034
284
c CHR530 Charcot-Marie-Tooth Disease, Type 2b 40 0.034
285
ALX001 Alexia 40 0.034
286
HRT012 Heart Valve Disease 40 0.034
287
CRL004 Caroli Disease 40 0.034
288
PRD002 Periodic Limb Movement Disorder 40 0.034
289
PYM001 Pyomyositis 40 0.034
290
BND014 Bone Development Disease 40 0.034
291
CHR078 Chorioretinitis 40 0.034
292
CRB086 Cerebral Aneurysms 39 0.034
293
ANT039 Antisynthetase Syndrome 39 0.034
294
ISC015 Ischemic Colitis 39 0.034
295
c CNG033 Congenital Syphilis 39 0.034
296
c BNG023 Benign Familial Infantile Epilepsy 39 0.034
297
P FML187 Familial Hypertension 38 0.034
298
ADJ001 Adjustment Disorder 38 0.034
299
GST007 Gastric Dilatation 38 0.034
300
IMM015 Immune Defect Due to Absence of Thymus 38 0.034
301
SXD001 Sex Differentiation Disease 38 0.034
302
BLD054 Blood Protein Disease 37 0.034
303
ALX002 Alexithymia 37 0.034
304
WTH001 Withdrawal Disorder 37 0.034
305
ISC002 Ischemic Optic Neuropathy 37 0.034
306
c CNT028 Central Retinal Artery Occlusion 37 0.034
307
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 37 0.034
308
DYS016 Dysgammaglobulinemia 37 0.034
309
BRL011 Bare Lymphocyte Syndrome, Type I 37 0.034
310
CNG069 Congenital Cytomegalovirus 36 0.034
311
ASY002 Asymptomatic Neurosyphilis 36 0.034
312
TTR016 Tetra-Amelia Syndrome 36 0.034
313
BLS003 Blastoma 36 0.034
314
LYS017 Loeys-Dietz Syndrome 4 36 0.034
315
HYP015 Hyperlucent Lung 36 0.034
316
TRC026 Tracheal Disease 35 0.034
317
NTR006 Neutrophil Immunodeficiency Syndrome 35 0.034
318
ADP007 Adie Pupil 34 0.034
319
ACT216 Acute Leukemia of Ambiguous Lineage 34 0.034
320
MSC004 Muscle Tissue Disease 34 0.034
321
ERL004 Early Yaws 34 0.034
322
PLS010 Plasma Protein Metabolism Disease 34 0.034
323
RHN002 Rhinoscleroma 34 0.034
324
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.034
325
ACR002 Acrocapitofemoral Dysplasia 33 0.034
326
c PRM022 Primary Syphilis 33 0.034
327
EPG003 Epiglottitis 33 0.034
328
HRS011 Horseshoe Kidney 33 0.034
329
ALC003 Alcoholic Psychosis 33 0.034
330
ANT013 Anterior Spinal Artery Syndrome 33 0.034
331
GNC003 Geniculate Herpes Zoster 32 0.034
332
TBS001 Tabes Dorsalis 32 0.034
333
LNG054 Lung Agenesis 32 0.034
334
TRT003 Tertiary Syphilis 31 0.034
335
BYS001 Byssinosis 31 0.034
336
c PLM044 Pulmonary Fibrosis, Familial 31 0.034
337
TRC020 Tracheitis 31 0.034
338
c FRN011 Frontal Sinusitis 31 0.034
339
c ADL027 Adult Dermatomyositis 31 0.034
340
c SPR083 Sporadic Hemiplegic Migraine 30 0.034
341
IMM068 Immunodeficiency 8 30 0.034
342
LRY004 Laryngotracheitis 30 0.034
343
BRW004 Brown-Sequard Syndrome 29 0.034
344
c CHR094 Chronic Polyneuropathy 29 0.034
345
CRB142 Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant 29 0.034
346
CRB005 Cerebral Arteritis 29 0.034
347
PSY003 Psychosexual Disorder 28 0.034
348
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.034
349
CYN002 Cyanosis, Transient Neonatal 28 0.034
350
TXC001 Toxic Megacolon 28 0.034
351
SPN331 Spondyloocular Syndrome 27 0.034
352
ALC013 Alcohol-Induced Mental Disorder 27 0.034
353
OCL003 Oculomotor Nerve Paralysis 27 0.034
354
TRT002 Tertiary Neurosyphilis 27 0.034
355
LTN001 Latent Syphilis 27 0.034
356
LGP001 Lagophthalmos 27 0.034
357
APC001 Apical Myocardial Infarction 27 0.034
358
c ACQ027 Acquired Cutis Laxa 26 0.034
359
SVN001 Sveinsson Choreoretinal Atrophy 26 0.034
360
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 26 0.034
361
ORB006 Orbital Cellulitis 26 0.034
362
THR010 Third Cranial Nerve Disease 26 0.034
363
HNM002 Hinman Syndrome 25 0.034
364
TRC038 Tracheobronchomegaly 25 0.034
365
c FML306 Familial or Sporadic Hemiplegic Migraine 24 0.034
366
MNN005 Meningovascular Neurosyphilis 24 0.034
367
P ACQ041 Acquired Amegakaryocytic Thrombocytopenia 23 0.034
368
c LTC001 Late Congenital Syphilis 23 0.034
369
PLM015 Pulmonary Systemic Sclerosis 23 0.034
370
NPH064 Nipah Virus Disease 22 0.034
371
c CTS041 Cutis Laxa, Autosomal Dominant 3 22 0.034
372
c CTS031 Cutis Laxa, Autosomal Dominant 2 22 0.034
373
c CRN214 Coronary Heart Disease 5 22 0.034
374
P CRN178 Coronary Heart Disease 6 21 0.034
375
c MRG011 Meier-Gorlin Syndrome 4 20 0.034
376
c ALL027 Allergic Bronchopulmonary Aspergillosis, Familial 20 0.034
377
c ACT035 Acute Frontal Sinusitis 20 0.034
378
CYS040 Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Mental Retardation 20 0.034
379
SHK001 Shaken Baby Syndrome 19 0.034
380
P AST022 Asthma Susceptibility 5 19 0.034
381
VSC009 Vascular Skin Disease 19 0.034
382
SLP002 Salpingitis Isthmica Nodosa 18 0.034
383
PLY135 Polydactyly, Postaxial, with Progressive Myopia 18 0.034
384
PLM116 Pulmonary Artery Hypoplasia 17 0.034
385
CCT003 Cicatricial Entropion 16 0.034
386
GLC077 Glucocorticoid Therapy, Response to 16 0.034
387
c ALX006 Alexander Disease Type Ii 15 0.034
388
CHT006 Chitayat Syndrome 15 0.034
389
c INF136 Influenza, Severe 15 0.034
390
CD4004 Cd4 Deficiency 14 0.034
391
PRN006 Parenchymatous Neurosyphilis 14 0.034
392
WLS002 Wilson-Mikity Syndrome 14 0.034
393
PLM053 Pulmonary Artery Agenesis 12 0.034
394
ORL014 Oral Pharyngeal Disorders 11 0.034
395
PRM053 Primary Release Disorder of Platelets 11 0.034
396
IDP075 Idiopathic and/or Familial Pulmonary Arterial Hypertension 11 0.034
397
MNT045 Montefiore Syndrome 10 0.034
398
ALM002 Aluminium Lung 9 0.034
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