Search results for "emphysema"

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

509 hits were found for 'emphysema'

# Family MCID Name MIFTS Score
1
PLM034 Pulmonary Emphysema 49 6.693
2
ALP007 Alpha 1-Antitrypsin Deficiency 55 6.300
3
CNG105 Congenital Lobar Emphysema 36 5.020
4
INT011 Interstitial Emphysema 32 4.479
5
EMP007 Emphysema Due to Aat Deficiency 36 4.461
6
CMP003 Compensatory Emphysema 8 3.820
7
BRR006 Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification 6 3.123
8
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 9 2.231
9
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 32 2.200
10
PLM129 Pulmonary Disease, Chronic Obstructive 51 0.297
11
OBS006 Obstructive Lung Disease 45 0.294
12
CRK001 Cork-Handlers' Disease 40 0.292
13
PNM008 Pneumothorax 41 0.220
14
P PLM036 Pulmonary Fibrosis 59 0.202
15
BRN024 Bronchitis 56 0.182
16
RSP006 Respiratory System Disease 36 0.166
17
P AST005 Asthma 77 0.134
18
P LNG032 Lung Cancer 91 0.131
19
P PLM040 Pulmonary Valve Disease 28 0.131
20
MDS022 Mediastinitis 33 0.127
21
P PNM007 Pneumonia 56 0.123
22
BRN038 Bronchial Disease 41 0.119
23
P PLM037 Pulmonary Hypertension 78 0.115
24
UPP004 Upper Respiratory Tract Disease 34 0.115
25
P CTS001 Cutis Laxa 51 0.111
26
NTR005 Nutritional Deficiency Disease 41 0.107
27
c CHR096 Chronic Pulmonary Heart Disease 30 0.102
28
BRN055 Bronchogenic Cyst 26 0.102
29
P LVR013 Liver Disease 59 0.097
30
BRN002 Bronchiolitis 48 0.097
31
END072 Endotheliitis 39 0.097
32
GLC006 Galactosemia 76 0.092
33
TBR010 Tuberculosis 64 0.092
34
P RSP003 Respiratory Failure 58 0.092
35
SPN020 Spondylosis 46 0.092
36
NNS006 Non-Suppurative Otitis Media 36 0.092
37
SRN001 Serine Deficiency 25 0.092
38
PRT011 Protein C Deficiency 46 0.087
39
MRF001 Marfan Syndrome 72 0.082
40
SLP005 Sleep Disorder 47 0.082
41
P CNG401 Congenital Heart Disease 68 0.075
42
P DRM010 Dermatomyositis 57 0.075
43
BRN022 Bronchiectasis 49 0.075
44
P INT066 Interstitial Lung Disease 46 0.075
45
P TRC086 Trichohepatoenteric Syndrome 1 42 0.075
46
CRB009 Cerebritis 37 0.075
47
PNM003 Pneumatosis Cystoides Intestinalis 32 0.075
48
CYS001 Cystic Fibrosis 90 0.069
49
P OST002 Osteoporosis 75 0.069
50
P APL001 Aplastic Anemia 70 0.069
51
VSC011 Vasculitis 50 0.069
52
ATH003 Atherosclerosis 50 0.069
53
ANR040 Aneurysm 43 0.069
54
PNM010 Pneumothorax, Primary Spontaneous 35 0.069
55
DFF002 Diffuse Pulmonary Fibrosis 28 0.069
56
c AST037 Asthma 1 20 0.069
57
c CRN178 Coronary Heart Disease 6 10 0.069
58
P ATX030 Ataxia-Telangiectasia 76 0.062
59
ANR002 Aniridia 72 0.062
60
c HYP595 Hypertension, Essential 68 0.062
61
LNG024 Langerhans-Cell Histiocytosis 63 0.062
62
PCK002 Pick Disease 61 0.062
63
ART001 Arterial Tortuosity Syndrome 59 0.062
64
P AND016 Andersen Syndrome 58 0.062
65
ACQ007 Acquired Immunodeficiency Syndrome 55 0.062
66
ACN002 Acanthosis Nigricans 53 0.062
67
c ACT210 Acute Respiratory Distress Syndrome 52 0.062
68
SLC006 Silicosis 47 0.062
69
THR013 Thoracic Outlet Syndrome 47 0.062
70
P PNM006 Pneumoconiosis 45 0.062
71
STT002 Status Asthmaticus 44 0.062
72
BRN056 Bronchopulmonary Dysplasia 43 0.062
73
HYP266 Hypoxia 42 0.062
74
FSC004 Fasciitis 40 0.062
75
MLR002 Miliary Tuberculosis 40 0.062
76
NCR007 Necrotizing Fasciitis 39 0.062
77
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.062
78
DPH021 Diaphragm Disease 33 0.062
79
P ATX010 Ataxia Neuropathy Spectrum 31 0.062
80
HYP461 Hypocomplementemic Urticarial Vasculitis Syndrome 30 0.062
81
LYM035 Lymphangiectasis 26 0.062
82
P PLM064 Pulmonary Sequestration 24 0.062
83
c AST039 Asthma 2 23 0.062
84
c SPN225 Spondyloarthropathy 1 66 0.053
85
P ANG001 Angelman Syndrome 66 0.053
86
P HRM001 Hermansky-Pudlak Syndrome 62 0.053
87
PLL001 Pallister-Hall Syndrome 60 0.053
88
PLM001 Pulmonary Tuberculosis 60 0.053
89
c PNC108 Pancreatitis, Hereditary 59 0.053
90
LVR012 Liver Cirrhosis 59 0.053
91
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.053
92
P CNG015 Congenital Diaphragmatic Hernia 58 0.053
93
ELL001 Ellis-Van Creveld Syndrome 57 0.053
94
IMG001 Image Syndrome 56 0.053
95
P PTT014 Pitt-Hopkins Syndrome 55 0.053
96
MSL001 Measles 52 0.053
97
HNT002 Hantavirus Pulmonary Syndrome 52 0.053
98
GSG001 Gas Gangrene 51 0.053
99
SCH016 Schimke Immunoosseous Dysplasia 51 0.053
100
P VNT002 Ventricular Septal Defect 50 0.053
101
P SHR029 Short Syndrome 49 0.053
102
BRN012 Bronchiolitis Obliterans 49 0.053
103
CNN005 Connective Tissue Disease 49 0.053
104
THR100 Thrombocytopenic Purpura, Autoimmune 47 0.053
105
CYT008 Cytomegalovirus Infection 47 0.053
106
P CYS018 Cystitis 47 0.053
107
ALL006 Allergic Asthma 46 0.053
108
IDP011 Idiopathic Interstitial Pneumonia 46 0.053
109
c ART101 Aortic Valve Disease 2 46 0.053
110
MYC002 Mycobacterium Avium Complex Disease 46 0.053
111
P THR012 Thoracic Cancer 44 0.053
112
BRN014 Bronchopneumonia 40 0.053
113
DDN006 Duodenitis 40 0.053
114
CRP017 Carpal Tunnel Syndrome, Familial 39 0.053
115
NCT008 Nicotine Dependence, Protection Against 39 0.053
116
TTR016 Tetra-Amelia Syndrome 38 0.053
117
CRR007 Cirrhosis, Cryptogenic 36 0.053
118
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 35 0.053
119
PRP019 Peripheral Nervous System Disease 31 0.053
120
UND005 Undifferentiated Pleomorphic Sarcoma 31 0.053
121
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 29 0.053
122
USL001 Usual Interstitial Pneumonia 28 0.053
123
c CTS019 Cutis Laxa, Ad 27 0.053
124
ATN002 Autonomic Nervous System Disease 27 0.053
125
AMY016 Amyopathic Dermatomyositis 25 0.053
126
c CTS037 Cutis Laxa, Autosomal Recessive, Type Ib 24 0.053
127
BNS002 Bone Structure Disease 24 0.053
128
P ACQ041 Acquired Amegakaryocytic Thrombocytopenia 20 0.053
129
TRC037 Tracheobronchomalacia 19 0.053
130
AND005 Androgen Insensitivity Syndrome, Mild 19 0.053
131
SPN014 Spontaneous Tension Pneumothorax 13 0.053
132
HPT023 Hepatocellular Carcinoma 90 0.044
133
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 0.044
134
HV1006 Hiv-1 77 0.044
135
P MYC007 Myocardial Infarction 76 0.044
136
FBR012 Fabry Disease 75 0.044
137
P BRD002 Bardet-Biedl Syndrome 68 0.044
138
P NRF002 Neurofibromatosis 66 0.044
139
P TBR001 Tuberous Sclerosis 65 0.044
140
P RFS001 Refsum Disease 65 0.044
141
CMM004 Common Variable Immunodeficiency 64 0.044
142
c SYS005 Systemic Scleroderma 62 0.044
143
P LKM002 Leukemia 61 0.044
144
P LYM007 Lymphangioleiomyomatosis 61 0.044
145
P EHL033 Ehlers-Danlos Syndrome, Classic Type 60 0.044
146
c BRD010 Bardet-Biedl Syndrome 1 59 0.044
147
P NMN002 Niemann-Pick Disease 59 0.044
148
P HPT021 Hepatitis 58 0.044
149
P HYP035 Hypophosphatasia 58 0.044
150
SRC014 Sarcoma 57 0.044
151
OST085 Osteosarcoma, Somatic 56 0.044
152
P ADL010 Adult Respiratory Distress Syndrome 55 0.044
153
PRT037 Pertussis 55 0.044
154
ART016 Aortic Aneurysm 55 0.044
155
VSC007 Vascular Disease 55 0.044
156
SMT008 Smith-Magenis Syndrome 54 0.044
157
PLM134 Pulmonary Fibrosis, Idiopathic 54 0.044
158
P ACR001 Aicardi-Goutieres Syndrome 53 0.044
159
P MCP010 Mucopolysaccharidosis 53 0.044
160
P PLR004 Pleuropulmonary Blastoma 53 0.044
161
P HML002 Hemolytic Anemia 52 0.044
162
P PRD008 Periodontitis 52 0.044
163
APP008 Appendicitis 52 0.044
164
NTH001 Netherton Syndrome 51 0.044
165
P HST010 Histiocytosis 51 0.044
166
P MYP004 Myopathy 50 0.044
167
MLL005 Miller-Dieker Syndrome 50 0.044
168
BRT002 Birt-Hogg-Dube Syndrome 50 0.044
169
MCR088 Microscopic Polyangiitis 49 0.044
170
c OPT053 Optic Atrophy 1 49 0.044
171
RTC002 Reticular Dysgenesis 49 0.044
172
PRD007 Periodontal Disease 49 0.044
173
P FNG005 Feingold Syndrome 48 0.044
174
c SCN006 Secondary Syphilis 48 0.044
175
ALL008 Allergic Bronchopulmonary Aspergillosis 47 0.044
176
GTR002 Goiter 47 0.044
177
PTN002 Patent Ductus Arteriosus 46 0.044
178
P SLL003 Salla Disease 46 0.044
179
GST037 Gastroparesis 46 0.044
180
EVN001 Evans' Syndrome 46 0.044
181
P DDN001 Duodenal Ulcer 46 0.044
182
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.044
183
NRM005 Neuromuscular Disease 45 0.044
184
HMT018 Hematopoietic Stem Cell Transplantation 45 0.044
185
EXT034 Extrinsic Allergic Alveolitis 44 0.044
186
c NMN016 Niemann-Pick Disease, Type B 44 0.044
187
c OPT055 Optic Atrophy Plus Syndrome 43 0.044
188
P CLL015 Collagen Disease 43 0.044
189
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.044
190
RTN023 Retinitis 43 0.044
191
NRN001 Neuroendocrine Carcinoma 42 0.044
192
P CRV039 Cervicitis 42 0.044
193
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 42 0.044
194
CLL003 Cellulitis 41 0.044
195
HRT012 Heart Valve Disease 40 0.044
196
NNS002 Nonspecific Interstitial Pneumonia 40 0.044
197
P RST011 Restrictive Dermopathy, Lethal 39 0.044
198
MNN014 Mononeuritis 39 0.044
199
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 39 0.044
200
P MSC033 Muscle Disorders 38 0.044
201
PPL021 Papilledema 38 0.044
202
BYS001 Byssinosis 38 0.044
203
P LRG014 Large Cell Neuroendocrine Carcinoma 36 0.044
204
INT071 Intestinal Perforation 35 0.044
205
BLS003 Blastoma 33 0.044
206
RHN002 Rhinoscleroma 33 0.044
207
BNN003 Bone Inflammation Disease 33 0.044
208
HMN014 Human Immunodeficiency Virus Infectious Disease 33 0.044
209
LYM014 Lymphangitis 33 0.044
210
c CTS008 Cutis Laxa, Autosomal Dominant 32 0.044
211
LRY004 Laryngotracheitis 32 0.044
212
CNJ007 Conjunctivochalasis 31 0.044
213
SPN331 Spondyloocular Syndrome 30 0.044
214
BRN039 Bronchial Neoplasm 29 0.044
215
MYL015 Myeloproliferative Disorder with Eosinophilia 29 0.044
216
HRS011 Horseshoe Kidney 29 0.044
217
CNG069 Congenital Cytomegalovirus 28 0.044
218
ORB006 Orbital Cellulitis 28 0.044
219
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 28 0.044
220
SBS002 Substernal Goiter 27 0.044
221
TFT003 Tufting Enteropathy 27 0.044
222
CPL005 Capillary Disease 26 0.044
223
BLD054 Blood Protein Disease 24 0.044
224
ANT005 Anteroseptal Myocardial Infarction 24 0.044
225
MSC004 Muscle Tissue Disease 23 0.044
226
LRY028 Laryngocele 22 0.044
227
c BNG076 Benign Exophthalmos Syndrome 21 0.044
228
NNT039 Neonatal Marfan Syndrome 21 0.044
229
ANT017 Anthracosilicosis 19 0.044
230
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 18 0.044
231
c ATS069 Autosomal Dominant Optic Atrophy Plus Syndrome 16 0.044
232
P BRS047 Breast Cancer 100 0.031
233
P ALZ034 Alzheimer Disease 98 0.031
234
P RHM011 Rheumatoid Arthritis 88 0.031
235
CRH001 Crohn's Disease 80 0.031
236
P LFR001 Li-Fraumeni Syndrome 79 0.031
237
P PNC035 Pancreatic Cancer 78 0.031
238
ULC004 Ulcerative Colitis 75 0.031
239
P HMC003 Hemochromatosis 75 0.031
240
P PFF001 Pfeiffer Syndrome 71 0.031
241
c FNC027 Fanconi Anemia, Complementation Group a 71 0.031
242
PRP003 Porphyria Cutanea Tarda 69 0.031
243
P SCL016 Scleroderma 69 0.031
244
P FML161 Familial Mediterranean Fever, Ar 67 0.031
245
AND015 Androgen Insensitivity 65 0.031
246
MNK001 Menkes Disease 65 0.031
247
CNG034 Congestive Heart Failure 65 0.031
248
SVR004 Severe Combined Immunodeficiency 65 0.031
249
P INF038 Influenza 64 0.031
250
KWS002 Kawasaki Disease 62 0.031
251
P VLC001 Velocardiofacial Syndrome 61 0.031
252
P FRD001 Friedreich Ataxia 61 0.031
253
P ALX003 Alexander Disease 61 0.031
254
SKN016 Skin Disease 61 0.031
255
c GLY008 Glycogen Storage Disease Ii 61 0.031
256
P ART022 Arthritis 61 0.031
257
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.031
258
c SRC025 Sarcoidosis 1 60 0.031
259
THR006 Thromboangiitis Obliterans 60 0.031
260
WGN006 Wegener Granulomatosis 59 0.031
261
TYP007 Typhoid Fever 59 0.031
262
WLL001 Williams-Beuren Syndrome 59 0.031
263
LKN001 Leukoencephalopathy with Vanishing White Matter 59 0.031
264
INC021 Incontinentia Pigmenti 58 0.031
265
FCT003 Factor X Deficiency 58 0.031
266
c MYT021 Myotonic Dystrophy 1 58 0.031
267
P ADN016 Adenocarcinoma 56 0.031
268
ARS001 Aarskog-Scott Syndrome 55 0.031
269
HJD001 Hajdu-Cheney Syndrome 55 0.031
270
FCT006 Factor V Deficiency 54 0.031
271
P PRM011 Primary Ciliary Dyskinesia 54 0.031
272
GLL022 Guillain-Barre Syndrome 54 0.031
273
P FND001 Fundus Albipunctatus 54 0.031
274
P NRM001 Neuromyelitis Optica 54 0.031
275
P LDD002 Liddle Syndrome 54 0.031
276
MLN008 Melanoma 54 0.031
277
MLK003 Melkersson-Rosenthal Syndrome 53 0.031
278
PLM033 Pulmonary Embolism 53 0.031
279
CHR020 Chronic Interstitial Cystitis 53 0.031
280
PRT093 Proteus Syndrome, Somatic 52 0.031
281
P INF032 Infertility 52 0.031
282
DFC004 Deficiency Anemia 52 0.031
283
P ALP009 Alopecia Areata 52 0.031
284
P NPH012 Nephrotic Syndrome 52 0.031
285
RLP001 Relapsing Polychondritis 52 0.031
286
SCR002 Scurvy 51 0.031
287
P DGR001 Digeorge Syndrome 51 0.031
288
P PNC044 Pancreatitis 51 0.031
289
P MNN013 Meningitis 51 0.031
290
P FTL001 Fetal Alcohol Syndrome 50 0.031
291
DBT001 Diabetic Ketoacidosis 50 0.031
292
VRL011 Viral Infectious Disease 50 0.031
293
URT039 Urticaria 50 0.031
294
P SNS014 Sinusitis 49 0.031
295
CMP002 Campylobacteriosis 49 0.031
296
ACT049 Acute Disseminated Encephalomyelitis 49 0.031
297
ATX019 Ataxia with Vitamin E Deficiency 49 0.031
298
CHC001 Chickenpox 49 0.031
299
PNM001 Pneumocystosis 49 0.031
300
P SZR006 Seizure Disorder 48 0.031
301
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 48 0.031
302
GLC012 Galactosialidosis 48 0.031
303
CLT003 Colitis 47 0.031
304
P PTT050 Pituitary Adenoma, Growth Hormone-Secreting 47 0.031
305
c PSD095 Pseudohypoaldosteronism, Type I 47 0.031
306
LRN003 Learning Disability 47 0.031
307
P ANP001 Anaplastic Large Cell Lymphoma 47 0.031
308
CGN006 Cogan Syndrome 46 0.031
309
PLS011 Plasmacytoma 46 0.031
310
PLM012 Pulmonary Sarcoidosis 46 0.031
311
ACH005 Achalasia 46 0.031
312
c INF069 Infantile Neuroaxonal Dystrophy 1 46 0.031
313
c LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 46 0.031
314
P ACT105 Acute Mountain Sickness 46 0.031
315
PRT014 Protein S Deficiency 46 0.031
316
P PRT013 Portal Hypertension 45 0.031
317
P MNC007 Monocytic Leukemia 45 0.031
318
INT007 Intermediate Coronary Syndrome 45 0.031
319
MGC001 Megacolon 45 0.031
320
CRD119 Cardiac Arrest 45 0.031
321
PLS009 Plasma Cell Neoplasm 45 0.031
322
NCR004 Nocardiosis 44 0.031
323
c GMM003 Gamma Heavy Chain Disease 44 0.031
324
BLM002 Bulimia Nervosa 44 0.031
325
RTN017 Retinal Detachment 44 0.031
326
MTH009 Mouth Disease 44 0.031
327
WHP001 Whipple Disease 44 0.031
328
CSY001 C Syndrome 44 0.031
329
SML033 Small Cell Cancer of the Lung, Somatic 43 0.031
330
IPX001 Ipex Syndrome 43 0.031
331
ADL002 Adult Syndrome 43 0.031
332
MCN007 Meconium Aspiration Syndrome 43 0.031
333
MSM001 Meesmann Corneal Dystrophy 42 0.031
334
P PYL005 Pyelonephritis 42 0.031
335
PYM001 Pyomyositis 41 0.031
336
CHR078 Chorioretinitis 41 0.031
337
P EXN002 Exanthem 41 0.031
338
P PNC001 Pancytopenia 41 0.031
339
SPN035 Spindle Cell Sarcoma 41 0.031
340
SBC012 Subcorneal Pustular Dermatosis 41 0.031
341
HMS001 Hemosiderosis 40 0.031
342
FRM003 Farmer's Lung 40 0.031
343
P PSD003 Pseudohypoaldosteronism 40 0.031
344
DVR002 Diverticulitis 40 0.031
345
PRT019 Protein-Losing Enteropathy 40 0.031
346
c BRT042 Bartter Syndrome, Type 3 40 0.031
347
NWB001 Newborn Respiratory Distress Syndrome 40 0.031
348
ICH020 Ichthyosis Prematurity Syndrome 40 0.031
349
DFF021 Diffuse Mesangial Sclerosis 40 0.031
350
MNT002 Mental Depression 39 0.031
351
ULC007 Ulcerative Stomatitis 39 0.031
352
EXS001 Exostosis 39 0.031
353
BNF002 Bone Fracture 39 0.031
354
ACT032 Acute Hemorrhagic Leukoencephalitis 39 0.031
355
P HYP009 Hypertrophic Pyloric Stenosis 39 0.031
356
BCL002 B Cell Deficiency 39 0.031
357
DFF003 Diffuse Scleroderma 39 0.031
358
c PSD092 Pseudohypoaldosteronism, Type Iie 39 0.031
359
QDR001 Quadriplegia 39 0.031
360
CRL004 Caroli Disease 39 0.031
361
HTR003 Heterotaxy 38 0.031
362
P RTN014 Retinal Artery Occlusion 38 0.031
363
INC003 Inclusion Conjunctivitis 37 0.031
364
PYL006 Pyloric Stenosis 37 0.031
365
SRC027 Sarcoma, Synovial 37 0.031
366
c ART120 Arthrogryposis, Distal, Type 3 37 0.031
367
PNN001 Panniculitis 37 0.031
368
MNC006 Monoclonal Gammopathy of Uncertain Significance 37 0.031
369
ASP007 Aspiration Pneumonia 37 0.031
370
SPR007 Superior Mesenteric Artery Syndrome 37 0.031
371
ANT039 Antisynthetase Syndrome 36 0.031
372
P CMP008 Compartment Syndrome 36 0.031
373
PLR007 Pleural Empyema 36 0.031
374
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 36 0.031
375
IRN002 Iron Metabolism Disease 36 0.031
376
RGH009 Right Atrial Isomerism 36 0.031
377
HRT011 Heart Septal Defect 35 0.031
378
SKN027 Skin Conditions 34 0.031
379
SPL007 Splenic Abscess 34 0.031
380
LCH003 Lichen Nitidus 34 0.031
381
SLV003 Salivary Gland Disease 34 0.031
382
CRY001 Cryptogenic Organizing Pneumonia 34 0.031
383
ENT001 Enterocele 34 0.031
384
EPG003 Epiglottitis 34 0.031
385
c CNT028 Central Retinal Artery Occlusion 34 0.031
386
URN009 Urinary System Disease 33 0.031
387
PHY002 Physical Disorder 33 0.031
388
RHN003 Rhinosporidiosis 33 0.031
389
SML008 Small Intestine Lymphoma 33 0.031
390
c CHR093 Chronic Orbital Inflammation 33 0.031
391
BLP001 Blepharochalasis 33 0.031
392
GNC003 Geniculate Herpes Zoster 33 0.031
393
ASY002 Asymptomatic Neurosyphilis 33 0.031
394
BLD053 Blood Platelet Disease 32 0.031
395
ILL001 Ileal Neoplasm 32 0.031
396
ADN067 Adenoid Hypertrophy 32 0.031
397
c CHR546 Chronic Mountain Sickness 32 0.031
398
CRB086 Cerebral Aneurysms 32 0.031
399
XNT001 Xanthogranulomatous Pyelonephritis 32 0.031
400
GST007 Gastric Dilatation 31 0.031
401
LYM116 Lymph Node Disease 31 0.031
402
DYN001 Doyne Honeycomb Degeneration of Retina 31 0.031
403
c ANT023 Anterior Scleritis 31 0.031
404
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 31 0.031
405
MVM001 Movement Disease 31 0.031
406
IDP074 Idiopathic Bronchiectasis 31 0.031
407
SPC010 Speech and Communication Disorders 31 0.031
408
PRC001 Pericoronitis 31 0.031
409
VSL002 Visual Epilepsy 31 0.031
410
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 30 0.031
411
P DCR004 Dacryocystitis 30 0.031
412
ALK003 Aleukemic Leukemia Cutis 30 0.031
413
ADJ001 Adjustment Disorder 30 0.031
414
CYS015 Cystadenofibroma 30 0.031
415
GST039 Gastroduodenitis 30 0.031
416
c CNG020 Congenital Hypogammaglobulinemia 30 0.031
417
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.031
418
XNT002 Xanthogranulomatous Cholecystitis 30 0.031
419
RTC001 Reticulohistiocytic Granuloma 30 0.031
420
ETH009 Ethmoid Sinusitis 30 0.031
421
BRL011 Bare Lymphocyte Syndrome, Type I 30 0.031
422
TRC020 Tracheitis 30 0.031
423
HYP347 Hypotonia-Cystinuria Syndrome 29 0.031
424
ENC003 Encephalitozoonosis 29 0.031
425
LGP001 Lagophthalmos 29 0.031
426
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 29 0.031
427
MLG065 Malignant Fibroxanthoma 29 0.031
428
c INV003 Invasive Malignant Thymoma 28 0.031
429
MCL014 Mcleod Neuroacanthocytosis Syndrome 28 0.031
430
PLY010 Polyclonal Hypergammaglobulinemia 28 0.031
431
LNG013 Lung Lymphoma 28 0.031
432
BND014 Bone Development Disease 28 0.031
433
HYP015 Hyperlucent Lung 28 0.031
434
CYC008 Cyclic Vomiting Syndrome 28 0.031
435
c ACQ027 Acquired Cutis Laxa 28 0.031
436
c HYP073 Hypersensitivity Reaction Type Iv Disease 28 0.031
437
ATR003 Atrophic Rhinitis 28 0.031
438
P PLM071 Pulmonary Surfactant Metabolism Dysfunction 28 0.031
439
TRC026 Tracheal Disease 27 0.031
440
c FRN011 Frontal Sinusitis 27 0.031
441
c ADL027 Adult Dermatomyositis 27 0.031
442
c SRC023 Sarcoidosis 2 27 0.031
443
SLT001 Solitary Osseous Plasmacytoma 27 0.031
444
ACT216 Acute Leukemia of Ambiguous Lineage 27 0.031
445
MCL055 Mcleod Syndrome with or Without Chronic Granulomatous Disease 26 0.031
446
PNG002 Pain Agnosia 26 0.031
447
LYS017 Loeys-Dietz Syndrome 4 26 0.031
448
CHR068 Chronic Nk-Cell Lymphocytosis 26 0.031
449
RPR002 Reproductive System Disease 26 0.031
450
P ACT077 Acute Orbital Inflammation 26 0.031
451
LYM002 Lymphoplasmacyte-Rich Meningioma 26 0.031
452
c INF131 Infant Acute Respiratory Distress Syndrome 25 0.031
453
RNL021 Renal Tubular Transport Disease 25 0.031
454
TXC001 Toxic Megacolon 25 0.031
455
GRN036 Granulomatous Myositis 25 0.031
456
c PSD090 Pseudohypoaldosteronism, Type Iia 25 0.031
457
SPC003 Specific Developmental Disorder 25 0.031
458
SVN001 Sveinsson Choreoretinal Atrophy 25 0.031
459
SHR073 Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, Skeletal Abnormalities 24 0.031
460
GLY075 Glycogen Storage Disease Due to Acid Maltase Deficiency 24 0.031
461
ATM012 Autoimmune Disease of Blood 24 0.031
462
END059 Endocrine-Cerebroosteodysplasia 24 0.031
463
MDN008 Median Arcuate Ligament Syndrome 24 0.031
464
P IGN003 Iga Nephropathy 1 24 0.031
465
c CTS031 Cutis Laxa, Autosomal Dominant 2 24 0.031
466
ALR002 Al-Raqad Syndrome 23 0.031
467
LNG054 Lung Agenesis 23 0.031
468
PLS010 Plasma Protein Metabolism Disease 23 0.031
469
c MRG011 Meier-Gorlin Syndrome 4 23 0.031
470
c CTS041 Cutis Laxa, Autosomal Dominant 3 22 0.031
471
P ADL037 Adult Xanthogranuloma 22 0.031
472
P FML187 Familial Hypertension 21 0.031
473
OPT010 Optic Papillitis 21 0.031
474
P ACT070 Acute Inflammation of Lacrimal Passage 21 0.031
475
c VRL006 Viral Esophagitis 21 0.031
476
P RSP007 Respiratory Distress Syndrome, Infant 20 0.031
477
c PLM121 Pulmonary Hypertension, Primary, 4 20 0.031
478
c PLM044 Pulmonary Fibrosis, Familial 19 0.031
479
LCR013 Lacrimal Duct Defect 19 0.031
480
PLL005 Pallister-Killian Mosaic Syndrome 18 0.031
481
PHC001 Phacolytic Glaucoma 18 0.031
482
IMM015 Immune Defect Due to Absence of Thymus 18 0.031
483
INF026 Inflammatory Mfh 18 0.031
484
PLM028 Pulmonary Coin Lesion 18 0.031
485
PLM015 Pulmonary Systemic Sclerosis 17 0.031
486
SHK001 Shaken Baby Syndrome 17 0.031
487
CNG452 Congenital Factor V Deficiency 17 0.031
488
PRS035 Parasitic Ichthyosporea Infectious Disease 17 0.031
489
IDP075 Idiopathic and/or Familial Pulmonary Arterial Hypertension 16 0.031
490
TRC038 Tracheobronchomegaly 16 0.031
491
PLM116 Pulmonary Artery Hypoplasia 15 0.031
492
CYT018 Cytochrome P450 2d6 Variant 15 0.031
493
MCH010 Michels Syndrome 14 0.031
494
WLS002 Wilson-Mikity Syndrome 14 0.031
495
CYS021 Cystic Adenomatoid Malformation of Lung 13 0.031
496
PLM053 Pulmonary Artery Agenesis 13 0.031
497
CD3001 Cd3zeta Deficiency 12 0.031
498
AST022 Asthma Susceptibility 5 10 0.031
499
P CRN214 Coronary Heart Disease 5 10 0.031
500
c INF136 Influenza, Severe 9 0.031
501
c ALX006 Alexander Disease Type Ii 9 0.031
502
CTS024 Cutis Laxa-Marfanoid Syndrome 9 0.031
503
c CRN175 Coronary Heart Disease 4 9 0.031
504
VSC009 Vascular Skin Disease 9 0.031
505
FCT015 Factor 2 Deficiency 7 0.031
506
GLC077 Glucocorticoid Therapy, Response to 6 0.031
507
ALM002 Aluminium Lung 4 0.031
508
PRM053 Primary Release Disorder of Platelets 3 0.031
509
ORL014 Oral Pharyngeal Disorders 2 0.031