Search results for emphysema

389 hits were found for emphysema

# Family MCID Name MIFTS Score
1
P PLM034 Pulmonary Emphysema 59 6.405
2
ALP103 Alpha-1-Antitrypsin Deficiency 60 6.301
3
EMP011 Emphysema, Congenital Lobar 35 5.980
4
INT011 Interstitial Emphysema 40 4.526
5
CMP003 Compensatory Emphysema 11 3.764
6
BRR006 Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification 12 3.753
7
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 9 2.229
8
c EMP012 Emphysema, Hereditary Pulmonary 9 2.201
9
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 32 2.167
10
EMP013 Emphysema, Congenital, with Deafness, Penoscrotal Web, and Mental Retardation 6 2.167
11
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.399
12
LNG099 Lung Disease 67 0.377
13
RSP006 Respiratory System Disease 63 0.321
14
PNM008 Pneumothorax 57 0.266
15
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.262
16
P PLM036 Pulmonary Fibrosis 68 0.248
17
BRN024 Bronchitis 67 0.212
18
P LNG032 Lung Cancer 99 0.168
19
AST005 Asthma 83 0.165
20
P PNM007 Pneumonia 70 0.161
21
MDS022 Mediastinitis 44 0.150
22
P PLM037 Pulmonary Hypertension 79 0.142
23
P CTS001 Cutis Laxa 62 0.124
24
BRN002 Bronchiolitis 59 0.119
25
BRN055 Bronchogenic Cyst 28 0.119
26
PNM010 Pneumothorax, Primary Spontaneous 41 0.114
27
MRF001 Marfan Syndrome 75 0.109
28
END072 Endotheliitis 46 0.109
29
P STR035 Streptococcal Group a Invasive Disease 28 0.109
30
P LVR013 Liver Disease 76 0.103
31
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.097
32
INT066 Interstitial Lung Disease 63 0.097
33
BRN038 Bronchial Disease 58 0.097
34
P HRT032 Heart Disease 80 0.091
35
P MYC084 Mycobacterium Tuberculosis 1 69 0.091
36
NWB001 Newborn Respiratory Distress Syndrome 56 0.091
37
BRN022 Bronchiectasis 55 0.091
38
VSC011 Vasculitis 66 0.084
39
AGN016 Aging 65 0.084
40
BRN056 Bronchopulmonary Dysplasia 61 0.084
41
ANR040 Aneurysm 61 0.084
42
CRB009 Cerebritis 41 0.084
43
c CTS045 Cutis Laxa, Autosomal Dominant 1 36 0.084
44
NNT039 Neonatal Marfan Syndrome 33 0.084
45
PNM003 Pneumatosis Cystoides Intestinalis 31 0.084
46
CYS001 Cystic Fibrosis 85 0.077
47
P INF038 Influenza 77 0.077
48
P OST002 Osteoporosis 75 0.077
49
P DRM010 Dermatomyositis 65 0.077
50
BRR014 Barrett Esophagus 64 0.077
51
P PNM006 Pneumoconiosis 55 0.077
52
STT002 Status Asthmaticus 46 0.077
53
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.077
54
HYP193 Hypocomplementemic Urticarial Vasculitis 38 0.077
55
c BLD140 Blood Group, I System 37 0.077
56
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.077
57
P PLM064 Pulmonary Sequestration 25 0.077
58
P RSP003 Respiratory Failure 71 0.069
59
WLL001 Williams-Beuren Syndrome 63 0.069
60
SLC006 Silicosis 57 0.069
61
NCR007 Necrotizing Fasciitis 49 0.069
62
FSC004 Fasciitis 48 0.069
63
MLR002 Miliary Tuberculosis 40 0.069
64
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 36 0.069
65
LYM035 Lymphangiectasis 31 0.069
66
DFF002 Diffuse Pulmonary Fibrosis 29 0.069
67
c CTS037 Cutis Laxa, Autosomal Recessive, Type Ib 25 0.069
68
CTS042 Cutis Laxa, Neonatal, with Marfanoid Phenotype 16 0.069
69
SQM006 Squamous Cell Carcinoma 74 0.060
70
P ANR048 Aniridia 1 68 0.060
71
CNN005 Connective Tissue Disease 65 0.060
72
MSL001 Measles 64 0.060
73
APP008 Appendicitis 64 0.060
74
CHL123 Chlamydia 64 0.060
75
HYP266 Hypoxia 61 0.060
76
ELL001 Ellis-Van Creveld Syndrome 61 0.060
77
c SCL052 Scleroderma, Familial Progressive 60 0.060
78
IDP011 Idiopathic Interstitial Pneumonia 60 0.060
79
BRN012 Bronchiolitis Obliterans 60 0.060
80
P VNT002 Ventricular Septal Defect 59 0.060
81
MCR088 Microscopic Polyangiitis 58 0.060
82
P CYS018 Cystitis 57 0.060
83
CYT008 Cytomegalovirus Infection 57 0.060
84
BRT002 Birt-Hogg-Dube Syndrome 54 0.060
85
GSG001 Gas Gangrene 51 0.060
86
NNS002 Nonspecific Interstitial Pneumonia 46 0.060
87
DDN006 Duodenitis 46 0.060
88
INT071 Intestinal Perforation 44 0.060
89
TRC037 Tracheobronchomalacia 26 0.060
90
BLD163 Blood Group, Dombrock System 23 0.060
91
ANR038 Anorexia Nervosa 1 21 0.060
92
BLD137 Blood Group--Ahonen 17 0.060
93
SPN014 Spontaneous Tension Pneumothorax 15 0.060
94
P RHM011 Rheumatoid Arthritis 91 0.049
95
P MYC007 Myocardial Infarction 81 0.049
96
P ART022 Arthritis 77 0.049
97
P LKM002 Leukemia 75 0.049
98
APL001 Aplastic Anemia 74 0.049
99
PLM001 Pulmonary Tuberculosis 72 0.049
100
FBR012 Fabry Disease 72 0.049
101
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.049
102
CMM004 Common Variable Immunodeficiency 71 0.049
103
WGN006 Wegener Granulomatosis 71 0.049
104
ART016 Aortic Aneurysm 70 0.049
105
PRT037 Pertussis 70 0.049
106
LYM007 Lymphangioleiomyomatosis 68 0.049
107
SRC014 Sarcoma 68 0.049
108
P NMN002 Niemann-Pick Disease 68 0.049
109
P ADL010 Adult Respiratory Distress Syndrome 67 0.049
110
P PRD008 Periodontitis 67 0.049
111
c SML038 Small Cell Cancer of the Lung 67 0.049
112
DRM006 Dermatitis 67 0.049
113
ACQ007 Acquired Immunodeficiency Syndrome 65 0.049
114
c GLY008 Glycogen Storage Disease Ii 64 0.049
115
PRD007 Periodontal Disease 64 0.049
116
P SRC025 Sarcoidosis 1 63 0.049
117
c DPH024 Diaphragmatic Hernia, Congenital 63 0.049
118
LNG108 Langerhans Cell Histiocytosis 63 0.049
119
c ACT210 Acute Respiratory Distress Syndrome 63 0.049
120
c TBR025 Tuberous Sclerosis 1 63 0.049
121
CLT003 Colitis 63 0.049
122
P SNS014 Sinusitis 62 0.049
123
P HML002 Hemolytic Anemia 62 0.049
124
P PLR004 Pleuropulmonary Blastoma 62 0.049
125
NRM005 Neuromuscular Disease 60 0.049
126
NTH001 Netherton Syndrome 60 0.049
127
P HST010 Histiocytosis 60 0.049
128
P HYP035 Hypophosphatasia 58 0.049
129
HMT018 Hematopoietic Stem Cell Transplantation 58 0.049
130
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.049
131
EXT034 Extrinsic Allergic Alveolitis 57 0.049
132
GST037 Gastroparesis 56 0.049
133
c EHL073 Ehlers-Danlos Syndrome, Classic Type, 1 54 0.049
134
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.049
135
GTR002 Goiter 53 0.049
136
RSP002 Respiratory Syncytial Virus Infectious Disease 53 0.049
137
CLL003 Cellulitis 53 0.049
138
P DDN001 Duodenal Ulcer 53 0.049
139
RTN023 Retinitis 52 0.049
140
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.049
141
PPL021 Papilledema 50 0.049
142
P CRV039 Cervicitis 49 0.049
143
ANX004 Anoxia 49 0.049
144
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.049
145
CRY001 Cryptogenic Organizing Pneumonia 45 0.049
146
BRN014 Bronchopneumonia 45 0.049
147
BRL011 Bare Lymphocyte Syndrome, Type I 44 0.049
148
ACT088 Acute Insulin Response 43 0.049
149
P SLL003 Salla Disease 43 0.049
150
IMM015 Immune Defect Due to Absence of Thymus 42 0.049
151
CRB086 Cerebral Aneurysms 42 0.049
152
c NMN016 Niemann-Pick Disease, Type B 42 0.049
153
FRM003 Farmer's Lung 41 0.049
154
BLS003 Blastoma 40 0.049
155
CNG069 Congenital Cytomegalovirus 40 0.049
156
CNJ007 Conjunctivochalasis 39 0.049
157
LYS017 Loeys-Dietz Syndrome 4 38 0.049
158
P LRG014 Large Cell Neuroendocrine Carcinoma 37 0.049
159
ESN017 Eosinophilic Granuloma 37 0.049
160
HRS011 Horseshoe Kidney 35 0.049
161
LRY004 Laryngotracheitis 35 0.049
162
SPN331 Spondyloocular Syndrome 34 0.049
163
LYM014 Lymphangitis 32 0.049
164
LCR013 Lacrimal Duct Defect 31 0.049
165
PLY135 Polydactyly, Postaxial, with Progressive Myopia 30 0.049
166
P RNG031 Ring Chromosome Y Syndrome 29 0.049
167
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 28 0.049
168
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 28 0.049
169
P SCL057 Scoliosis, Isolated 1 28 0.049
170
SBS002 Substernal Goiter 25 0.049
171
ANT005 Anteroseptal Myocardial Infarction 24 0.049
172
RDN004 Radin Blood Group Antigen 23 0.049
173
LMN005 Lmna-Related Cardiocutaneous Progeria Syndrome 23 0.049
174
LRY028 Laryngocele 22 0.049
175
BRN133 Bronchomalacia 22 0.049
176
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.049
177
c MRG014 Meier-Gorlin Syndrome 6 21 0.049
178
ANT017 Anthracosilicosis 20 0.049
179
c MRG011 Meier-Gorlin Syndrome 4 20 0.049
180
P BRS047 Breast Cancer 100 0.034
181
P PNC035 Pancreatic Cancer 89 0.034
182
ULC004 Ulcerative Colitis 80 0.034
183
SQM013 Squamous Cell Carcinoma, Head and Neck 79 0.034
184
ALP046 Alport Syndrome, X-Linked 74 0.034
185
P DBT009 Diabetes Mellitus 72 0.034
186
KWS002 Kawasaki Disease 72 0.034
187
VSC007 Vascular Disease 71 0.034
188
P MNN013 Meningitis 71 0.034
189
P LYM118 Lymphoma 71 0.034
190
P ADN016 Adenocarcinoma 71 0.034
191
P DRM053 Dermatitis, Atopic 68 0.034
192
P SYS005 Systemic Scleroderma 67 0.034
193
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.034
194
PCK003 Pick Disease of Brain 66 0.034
195
P ART067 Aortic Aneurysm, Familial Thoracic 1 65 0.034
196
VRC005 Varicose Veins 64 0.034
197
CRP001 Carpal Tunnel Syndrome 64 0.034
198
SVR097 Severe Cutaneous Adverse Reaction 64 0.034
199
GNG013 Gingivitis 64 0.034
200
P PNC044 Pancreatitis 64 0.034
201
MNK001 Menkes Disease 64 0.034
202
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.034
203
P PLV020 Pelvic Organ Prolapse 63 0.034
204
P LYM025 Lymphedema 63 0.034
205
CRD119 Cardiac Arrest 63 0.034
206
P HRM001 Hermansky-Pudlak Syndrome 62 0.034
207
PLM033 Pulmonary Embolism 62 0.034
208
P HMN010 Hemangioma 61 0.034
209
P FBR017 Fibrosarcoma 61 0.034
210
ALL006 Allergic Asthma 60 0.034
211
P ANP001 Anaplastic Large Cell Lymphoma 60 0.034
212
ATH013 Atherosclerosis Susceptibility 59 0.034
213
P INF032 Infertility 59 0.034
214
SLP005 Sleep Disorder 59 0.034
215
RTN017 Retinal Detachment 59 0.034
216
ING001 Inguinal Hernia 59 0.034
217
URT039 Urticaria 59 0.034
218
P MNC007 Monocytic Leukemia 59 0.034
219
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.034
220
SRC027 Sarcoma, Synovial 58 0.034
221
CRT016 Carotid Artery Disease 58 0.034
222
PLM012 Pulmonary Sarcoidosis 58 0.034
223
ANG020 Angiosarcoma 57 0.034
224
ADN027 Adenomyosis 57 0.034
225
IMM136 Immune System Disease 57 0.034
226
BRN106 Burns 57 0.034
227
P ALL008 Allergic Bronchopulmonary Aspergillosis 56 0.034
228
P CPL006 Capillary Hemangioma 56 0.034
229
P PYL005 Pyelonephritis 56 0.034
230
BNF002 Bone Fracture 56 0.034
231
LKN001 Leukoencephalopathy with Vanishing White Matter 56 0.034
232
RLP001 Relapsing Polychondritis 55 0.034
233
PNM001 Pneumocystosis 55 0.034
234
SPR004 Supravalvular Aortic Stenosis 54 0.034
235
PLR022 Pleural Disease 54 0.034
236
QDR001 Quadriplegia 54 0.034
237
LYM022 Lymphangioma 53 0.034
238
GLC012 Galactosialidosis 53 0.034
239
P BLM007 Bulimia Nervosa 1 53 0.034
240
RTC002 Reticular Dysgenesis 53 0.034
241
c BLM008 Bulimia Nervosa 2 53 0.034
242
CHR005 Chorioamnionitis 52 0.034
243
P PRC012 Pericardial Effusion 52 0.034
244
LYM008 Lymphangiosarcoma 51 0.034
245
NTR046 Neutrophil Migration 51 0.034
246
PRT082 Preterm Premature Rupture of the Membranes 51 0.034
247
HNN001 Hennekam Syndrome 50 0.034
248
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.034
249
GNG011 Gingival Disease 50 0.034
250
PNC001 Pancytopenia 50 0.034
251
HMS001 Hemosiderosis 50 0.034
252
MGC001 Megacolon 50 0.034
253
c PRD040 Periodontitis, Chronic 49 0.034
254
c PRD039 Periodontitis, Aggressive, 1 49 0.034
255
ASP007 Aspiration Pneumonia 49 0.034
256
SRS007 Sorsby Fundus Dystrophy 49 0.034
257
P SDR002 Siderosis 48 0.034
258
P CMP008 Compartment Syndrome 48 0.034
259
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.034
260
c BRN108 Branchiootic Syndrome 1 47 0.034
261
MLL018 Miller-Dieker Lissencephaly Syndrome 47 0.034
262
PYL006 Pyloric Stenosis 47 0.034
263
LGH004 Light Chain Deposition Disease 47 0.034
264
MYC012 Mycetoma 46 0.034
265
CHR100 Chronic Ulcer of Skin 46 0.034
266
KPS002 Kaposiform Hemangioendothelioma 46 0.034
267
EXS001 Exostosis 46 0.034
268
ANT039 Antisynthetase Syndrome 46 0.034
269
CNT007 Central Nervous System Tuberculosis 46 0.034
270
LYM127 Lymphatic Malformations 45 0.034
271
P HYP009 Hypertrophic Pyloric Stenosis 45 0.034
272
P RTN014 Retinal Artery Occlusion 45 0.034
273
CHR031 Chromoblastomycosis 45 0.034
274
TND004 Tendinopathy 45 0.034
275
RST011 Restrictive Dermopathy, Lethal 45 0.034
276
RSP019 Respiratory Distress Syndrome in Premature Infants 45 0.034
277
DFF003 Diffuse Scleroderma 44 0.034
278
DVR002 Diverticulitis 44 0.034
279
LYM116 Lymph Node Disease 43 0.034
280
NCR004 Nocardiosis 43 0.034
281
ERY004 Erysipelas 43 0.034
282
VSC006 Vascular Cancer 43 0.034
283
NDL001 Nodular Malignant Melanoma 42 0.034
284
PYM001 Pyomyositis 42 0.034
285
P MRG008 Meier-Gorlin Syndrome 1 42 0.034
286
SPR007 Superior Mesenteric Artery Syndrome 42 0.034
287
SQM021 Squamous Cell Carcinoma of the Hypopharynx 42 0.034
288
c RBN009 Robinow Syndrome, Autosomal Recessive 42 0.034
289
c ALZ056 Alzheimer Disease 3 41 0.034
290
c ADL027 Adult Dermatomyositis 41 0.034
291
ELP001 Elephantiasis 40 0.034
292
SKN018 Skin Hemangioma 40 0.034
293
c CNT028 Central Retinal Artery Occlusion 40 0.034
294
ANT018 Anthracosis 39 0.034
295
KTL001 Keutel Syndrome 39 0.034
296
ISC015 Ischemic Colitis 39 0.034
297
c INT059 Internal Hemorrhoid 39 0.034
298
RHN002 Rhinoscleroma 39 0.034
299
DBR002 De Barsy Syndrome 38 0.034
300
CHR415 Chronic Venous Leg Ulcers 38 0.034
301
P EXT032 Extraosseous Osteosarcoma 38 0.034
302
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.034
303
GRH001 Gorham's Disease 37 0.034
304
AMR003 Amaurosis Fugax 37 0.034
305
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 37 0.034
306
c CNG004 Congenital Epulis 37 0.034
307
P ANX007 Anauxetic Dysplasia 1 36 0.034
308
TST043 Testicular Seminoma 36 0.034
309
MCR001 Microcystic Meningioma 36 0.034
310
BRS004 Breast Angiosarcoma 36 0.034
311
HYP015 Hyperlucent Lung 36 0.034
312
CHR010 Chorioangioma 35 0.034
313
TRC026 Tracheal Disease 35 0.034
314
WRN004 Wrinkly Skin Syndrome 35 0.034
315
CRL004 Caroli Disease 35 0.034
316
GNG006 Gingival Hypertrophy 35 0.034
317
MSN004 Mesenchymal Cell Neoplasm 35 0.034
318
NSL006 Nasal Cavity Squamous Cell Carcinoma 35 0.034
319
EPG003 Epiglottitis 35 0.034
320
TXC001 Toxic Megacolon 34 0.034
321
LNG054 Lung Agenesis 34 0.034
322
HMP001 Hemopericardium 34 0.034
323
CHR463 Chronic Actinic Dermatitis 34 0.034
324
TRC020 Tracheitis 33 0.034
325
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.034
326
ALK003 Aleukemic Leukemia Cutis 33 0.034
327
BYS001 Byssinosis 33 0.034
328
ATS238 Autosomal Recessive Cutis Laxa Type 2, Classic Type 32 0.034
329
CYN002 Cyanosis, Transient Neonatal 32 0.034
330
VNS002 Venous Hemangioma 32 0.034
331
GST007 Gastric Dilatation 32 0.034
332
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.034
333
MDD015 Mid-Dermal Elastolysis 31 0.034
334
ALR002 Al-Raqad Syndrome 30 0.034
335
NRG003 Neurogenic Arthropathy 30 0.034
336
SPL011 Spleen Cancer 30 0.034
337
ACT216 Acute Leukemia of Ambiguous Lineage 30 0.034
338
HMN004 Hemangioma of Liver 30 0.034
339
c FRN011 Frontal Sinusitis 30 0.034
340
NRG001 Neurogenic Bowel 29 0.034
341
PRM008 Parametritis 29 0.034
342
ANG019 Angiomyoma 29 0.034
343
CYS021 Cystic Adenomatoid Malformation of Lung 29 0.034
344
GLM001 Glomeruloid Hemangioma 29 0.034
345
c ACQ027 Acquired Cutis Laxa 29 0.034
346
SPS002 Spastic Entropion 29 0.034
347
IMP001 Impetigo Herpetiformis 29 0.034
348
ORB006 Orbital Cellulitis 29 0.034
349
SPN017 Spindle Cell Liposarcoma 29 0.034
350
LGP001 Lagophthalmos 29 0.034
351
SVN002 Sveinsson Chorioretinal Atrophy 29 0.034
352
INF005 Infiltrating Lipoma 28 0.034
353
TRC038 Tracheobronchomegaly 28 0.034
354
PDT004 Pediatric Angiosarcoma 27 0.034
355
SNL004 Senile Ectropion 27 0.034
356
VLV038 Vulvar Sarcoma 25 0.034
357
MXD006 Mixed Liposarcoma 25 0.034
358
c CTS041 Cutis Laxa, Autosomal Dominant 3 25 0.034
359
CRD007 Cardiovascular Organ Benign Neoplasm 24 0.034
360
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 24 0.034
361
BNG033 Benign Perivascular Tumor 24 0.034
362
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.034
363
c ALL027 Allergic Bronchopulmonary Aspergillosis, Familial 23 0.034
364
ANG014 Angiokeratoma of Fordyce 22 0.034
365
OVR003 Ovarian Angiosarcoma 21 0.034
366
CRL006 Caroli Disease, Isolated 21 0.034
367
CYS040 Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Mental Retardation 21 0.034
368
THY031 Thyroid Sarcoma 21 0.034
369
SHK001 Shaken Baby Syndrome 21 0.034
370
c ACT035 Acute Frontal Sinusitis 21 0.034
371
c INT282 Integumentary System Benign Neoplasm 20 0.034
372
HMN011 Hemangioma of Intra-Abdominal Structure 20 0.034
373
HBN001 Hobnail Hemangioma 20 0.034
374
CLF050 Cleft Palate, Cardiac Defects, and Mental Retardation 20 0.034
375
BNP002 Bone Epithelioid Hemangioma 20 0.034
376
OVR061 Ovary Sarcoma 20 0.034
377
CPL002 Capillary Lymphangioma 19 0.034
378
c CTS031 Cutis Laxa, Autosomal Dominant 2 19 0.034
379
SPL001 Spleen Angiosarcoma 19 0.034
380
BLD138 Blood Group--Diego System 18 0.034
381
THY004 Thyroid Angiosarcoma 18 0.034
382
c WLM017 Wilms Tumor 4 17 0.034
383
INT055 Intravascular Fasciitis 17 0.034
384
WLS002 Wilson-Mikity Syndrome 16 0.034
385
c WLM015 Wilms Tumor 3 16 0.034
386
CNV001 Conventional Angiosarcoma 15 0.034
387
PLM116 Pulmonary Artery Hypoplasia 15 0.034
388
c ACQ004 Acquired Hemangioma 15 0.034
389
PLM053 Pulmonary Artery Agenesis 14 0.034
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