Search results for "pulmonary disease"

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

3997 hits were found for 'pulmonary disease'

# Family MCID Name MIFTS Score
1
PLM129 Pulmonary Disease, Chronic Obstructive 62 3.792
2
P PLM025 Pulmonary Venoocclusive Disease 46 3.780
3
PLM134 Pulmonary Fibrosis, Idiopathic 61 3.636
4
c PLM132 Pulmonary Venoocclusive Disease 2 32 3.001
5
c PLM130 Pulmonary Venoocclusive Disease 1 30 2.630
6
c SRF003 Surfactant Metabolism Dysfunction, Pulmonary, 2 29 2.114
7
c SRF005 Surfactant Metabolism Dysfunction, Pulmonary, 3 28 2.109
8
c SRF004 Surfactant Metabolism Dysfunction, Pulmonary, 1 29 2.032
9
RHM002 Rheumatic Pulmonary Valve Disease 16 2.007
10
GDP001 Goodpasture Syndrome 49 1.989
11
P ACT080 Acute Pulmonary Heart Disease 32 1.980
12
P PLM040 Pulmonary Valve Disease 45 1.961
13
INT271 Interstitial Lung and Liver Disease 34 1.920
14
c CHR096 Chronic Pulmonary Heart Disease 40 1.853
15
P PLZ001 Pelizaeus-Merzbacher Disease 64 1.752
16
P PLM071 Pulmonary Surfactant Metabolism Dysfunction 36 1.732
17
NWB001 Newborn Respiratory Distress Syndrome 47 1.635
18
c SCN005 Secondary Hypertrophic Osteoarthropathy 40 1.524
19
INH001 Inhalation Anthrax 39 1.457
20
c CHR037 Chronic Eosinophilic Pneumonia 44 1.441
21
NNT049 Nontuberculous Mycobacterial Lung Disease 41 1.425
22
c ABC006 Abca3-Related Pulmonary Surfactant Metabolism Dysfunction 9 1.424
23
c SFT005 Sftpb-Related Pulmonary Surfactant Metabolism Dysfunction 9 1.424
24
INT224 Interstitial Lung Disease, Nephrotic Syndrome, and Epidermolysis Bullosa, Congenital 23 1.377
25
ECH003 Echinococcosis 53 1.366
26
PLM015 Pulmonary Systemic Sclerosis 24 1.277
27
ACT029 Acute Interstitial Pneumonia 43 1.270
28
c SFT007 Sftpc-Related Pulmonary Surfactant Metabolism Dysfunction 9 1.213
29
KPS004 Kaposi Sarcoma 66 1.142
30
P ALL008 Allergic Bronchopulmonary Aspergillosis 49 1.099
31
P BRY005 Beryllium Disease 38 1.054
32
PRG008 Paragonimiasis 39 1.049
33
CCC001 Coccidioidomycosis 55 1.031
34
P CNG390 Congenital Pulmonary Airway Malformation 41 1.029
35
SRF006 Surfactant Dysfunction 33 0.963
36
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 21 0.953
37
c CNG396 Congenital Pulmonary Airway Malformation Type 2 16 0.937
38
c CNG397 Congenital Pulmonary Airway Malformation Type 3 14 0.937
39
c CNG398 Congenital Pulmonary Airway Malformation Type 1 14 0.930
40
HNR001 Heiner Syndrome 14 0.924
41
P PLM037 Pulmonary Hypertension 79 0.473
42
LNG099 Lung Disease 62 0.399
43
RSP006 Respiratory System Disease 62 0.346
44
P PLM036 Pulmonary Fibrosis 68 0.345
45
TBR010 Tuberculosis 69 0.318
46
PLM033 Pulmonary Embolism 59 0.296
47
PLM001 Pulmonary Tuberculosis 68 0.284
48
P HRT032 Heart Disease 76 0.247
49
PLM010 Pulmonary Edema 56 0.227
50
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 47 0.221
51
P AST005 Asthma 82 0.218
52
PLM034 Pulmonary Emphysema 54 0.214
53
c HYP595 Hypertension, Essential 69 0.209
54
P PNM007 Pneumonia 66 0.207
55
CHR466 Chronic Thromboembolic Pulmonary Hypertension 37 0.207
56
PLM012 Pulmonary Sarcoidosis 54 0.200
57
END072 Endotheliitis 42 0.200
58
P PLM006 Pulmonary Alveolar Proteinosis 48 0.198
59
P PLM064 Pulmonary Sequestration 26 0.186
60
INT066 Interstitial Lung Disease 58 0.176
61
P PRP019 Peripheral Nervous System Disease 54 0.173
62
ATN002 Autonomic Nervous System Disease 47 0.170
63
VSC007 Vascular Disease 67 0.161
64
c AST037 Asthma 1 31 0.161
65
P ADN016 Adenocarcinoma 69 0.159
66
c AST039 Asthma 2 31 0.159
67
P RSP003 Respiratory Failure 70 0.159
68
P ASP006 Aspergillosis 60 0.156
69
HRT015 Heritable Pulmonary Arterial Hypertension 45 0.154
70
P LNG032 Lung Cancer 94 0.153
71
PHY002 Physical Disorder 44 0.152
72
CNN005 Connective Tissue Disease 61 0.151
73
P VNT002 Ventricular Septal Defect 59 0.149
74
P ESN007 Eosinophilia 61 0.148
75
ART005 Arteriovenous Malformation 65 0.144
76
c PLM128 Pulmonary Hypertension, Primary, 2 30 0.143
77
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.143
78
CYS001 Cystic Fibrosis 86 0.141
79
P CRN178 Coronary Heart Disease 6 24 0.141
80
ANR040 Aneurysm 57 0.140
81
P LYM118 Lymphoma 70 0.138
82
PLM052 Pulmonary Arteriovenous Malformation 34 0.137
83
P CRN211 Coronary Artery Disease 75 0.137
84
P FML187 Familial Hypertension 41 0.136
85
PLM035 Pulmonary Eosinophilia 46 0.135
86
HYP266 Hypoxia 55 0.134
87
ART111 Artery Disease 57 0.133
88
PLM068 Pulmonary Vein Stenosis 39 0.133
89
TTR001 Tetralogy of Fallot 71 0.132
90
HNT002 Hantavirus Pulmonary Syndrome 51 0.131
91
P ATR011 Atrial Fibrillation 64 0.131
92
MTH009 Mouth Disease 63 0.130
93
VND001 Vein Disease 52 0.129
94
HMS001 Hemosiderosis 45 0.129
95
P PLM085 Pulmonary Hemosiderosis 44 0.128
96
PLM017 Pulmonary Alveolar Microlithiasis 46 0.128
97
c PLM127 Pulmonary Hypertension, Primary, 3 30 0.126
98
P HPT021 Hepatitis 70 0.125
99
P MYP004 Myopathy 67 0.124
100
PRP027 Peripheral Vascular Disease 69 0.124
101
c CRN214 Coronary Heart Disease 5 23 0.124
102
SRC014 Sarcoma 66 0.122
103
PLM041 Pulmonary Valve Stenosis 48 0.120
104
CNG034 Congestive Heart Failure 71 0.119
105
MSC004 Muscle Tissue Disease 36 0.119
106
P MSC033 Muscle Disorders 52 0.116
107
IDP011 Idiopathic Interstitial Pneumonia 57 0.116
108
P LKM002 Leukemia 70 0.116
109
BLS003 Blastoma 37 0.114
110
PLM032 Pulmonary Blastoma 49 0.114
111
PLM058 Pulmonary Atresia with Intact Ventricular Septum 24 0.113
112
P LVR013 Liver Disease 72 0.113
113
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.112
114
c CRN175 Coronary Heart Disease 4 21 0.112
115
c PLM121 Pulmonary Hypertension, Primary, 4 29 0.112
116
P LYM007 Lymphangioleiomyomatosis 65 0.111
117
P ART022 Arthritis 75 0.111
118
BRN038 Bronchial Disease 54 0.110
119
PCK002 Pick Disease 67 0.109
120
P THY032 Thyroiditis 54 0.108
121
BRN024 Bronchitis 63 0.107
122
PLM007 Pulmonary Aspergilloma 27 0.106
123
c CRN172 Coronary Heart Disease 3 21 0.103
124
LRN003 Learning Disability 51 0.102
125
PLM059 Pulmonary Atresia with Ventricular Septal Defect 21 0.101
126
SCK005 Sickle Cell Disease 49 0.101
127
NCR004 Nocardiosis 42 0.101
128
CRB009 Cerebritis 38 0.100
129
BLD053 Blood Platelet Disease 46 0.100
130
P HST010 Histiocytosis 55 0.099
131
CRH001 Crohn's Disease 76 0.099
132
PNM008 Pneumothorax 52 0.098
133
P RHM011 Rheumatoid Arthritis 88 0.097
134
INT011 Interstitial Emphysema 38 0.097
135
CRY005 Cryptococcosis 50 0.096
136
PRP080 Peripheral Artery Disease 36 0.095
137
P MYC007 Myocardial Infarction 79 0.095
138
UPP004 Upper Respiratory Tract Disease 48 0.095
139
P CRD011 Cardiomyopathy 67 0.093
140
SLP005 Sleep Disorder 53 0.093
141
P BRS047 Breast Cancer 100 0.093
142
BRT030 Birth Defects 43 0.092
143
c CRN174 Coronary Heart Disease 2 22 0.091
144
ACR041 Acromelic Frontonasal Dysostosis 46 0.091
145
c THR092 Thrombophilia Due to Thrombin Defect 56 0.091
146
ALL006 Allergic Asthma 58 0.091
147
P OBS005 Obesity 93 0.090
148
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.089
149
NTR005 Nutritional Deficiency Disease 39 0.088
150
PRM025 Primary Bacterial Infectious Disease 43 0.088
151
P LPS004 Lupus Erythematosus 63 0.088
152
MDS022 Mediastinitis 41 0.088
153
c SYS001 Systemic Lupus Erythematosus 87 0.087
154
BRN022 Bronchiectasis 47 0.086
155
P PLR004 Pleuropulmonary Blastoma 64 0.086
156
DRF001 Dirofilariasis 37 0.086
157
c ACT210 Acute Respiratory Distress Syndrome 57 0.086
158
ALR002 Al-Raqad Syndrome 36 0.085
159
ADJ001 Adjustment Disorder 38 0.084
160
ISC004 Ischemia 59 0.084
161
BRN056 Bronchopulmonary Dysplasia 49 0.083
162
P MTR012 Mitral Valve Disease 59 0.083
163
ATR060 Atrial Standstill, Digenic 53 0.083
164
NRM005 Neuromuscular Disease 57 0.082
165
SNG003 Single Ventricular Heart 24 0.082
166
MVM001 Movement Disease 54 0.082
167
TRN044 Transposition of the Great Arteries 47 0.081
168
P INF038 Influenza 74 0.081
169
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 0.081
170
ALN001 Aland Island Eye Disease 45 0.080
171
P ESP024 Esophagitis 62 0.080
172
P HMN010 Hemangioma 60 0.079
173
c CRN173 Coronary Heart Disease 8 20 0.079
174
VSC011 Vasculitis 62 0.079
175
ISC006 Ischemic Heart Disease 68 0.079
176
c FML001 Familial Atrial Fibrillation 59 0.078
177
P CNG015 Congenital Diaphragmatic Hernia 58 0.078
178
ATH003 Atherosclerosis 62 0.078
179
DFC004 Deficiency Anemia 65 0.078
180
c PLM022 Pulmonary Valve Insufficiency 38 0.077
181
BLD054 Blood Protein Disease 40 0.077
182
RHM027 Rheumatic Disease 57 0.077
183
BRN002 Bronchiolitis 56 0.076
184
BNS002 Bone Structure Disease 36 0.076
185
P CLC005 Celiac Disease 67 0.076
186
NWC001 Newcastle Disease 54 0.076
187
P ADL010 Adult Respiratory Distress Syndrome 60 0.076
188
CHR012 Chronic Granulomatous Disease 65 0.076
189
VSC047 Vascular Malformation 45 0.076
190
CND002 Conduct Disorder 56 0.075
191
NRN002 Neuronitis 42 0.075
192
P AMY004 Amyloidosis 64 0.075
193
KWS002 Kawasaki Disease 70 0.074
194
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.074
195
ALL026 Allergic Hypersensitivity Disease 53 0.074
196
CRT028 Cor Triatriatum 21 0.074
197
ASB001 Asbestosis 42 0.073
198
ART016 Aortic Aneurysm 67 0.073
199
CHL071 Child Syndrome 58 0.073
200
ESN011 Eisenmenger Syndrome 44 0.073
201
NSD001 Nose Disease 52 0.073
202
P PNC044 Pancreatitis 60 0.072
203
KDS001 Kid Syndrome 53 0.072
204
P PTN002 Patent Ductus Arteriosus 52 0.072
205
MYC002 Mycobacterium Avium Complex Disease 51 0.072
206
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.071
207
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.071
208
BLS002 Blastomycosis 42 0.071
209
HRT012 Heart Valve Disease 41 0.071
210
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 45 0.071
211
SCK003 Sickle Cell Anemia 68 0.071
212
P GLM007 Glomerulonephritis 56 0.071
213
STR067 Stroke, Ischemic 77 0.071
214
GST092 Gastroesophageal Reflux 61 0.071
215
ATP002 Atopy 63 0.071
216
P HYP055 Hypoplastic Left Heart Syndrome 60 0.071
217
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.071
218
P ALZ034 Alzheimer Disease 93 0.071
219
TTH006 Tooth Disease 52 0.070
220
RTN023 Retinitis 49 0.070
221
P HML002 Hemolytic Anemia 60 0.070
222
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.069
223
LYM024 Lymphatic System Disease 50 0.069
224
MRF001 Marfan Syndrome 73 0.069
225
CRN017 Coronary Thrombosis 48 0.069
226
P ENC018 Encephalopathy 59 0.069
227
C3D001 C3 Deficiency 53 0.069
228
IMM136 Immune System Disease 50 0.069
229
P LMY004 Leiomyosarcoma 53 0.069
230
CLT003 Colitis 59 0.068
231
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.068
232
P SPS003 Spastic Diplegia 53 0.068
233
CRD118 Cardiovascular Cancer 47 0.068
234
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.068
235
P SML001 Small Cell Carcinoma 57 0.068
236
VSC006 Vascular Cancer 54 0.068
237
SKN016 Skin Disease 68 0.068
238
HMT018 Hematopoietic Stem Cell Transplantation 41 0.067
239
P SLP006 Sleep Apnea 61 0.067
240
DMN002 Dementia 64 0.067
241
PLM070 Pulmonic Stenosis 59 0.067
242
P ART084 Arteriovenous Fistula 44 0.066
243
TRC062 Tricuspid Atresia 34 0.066
244
HMN016 Hemangioendothelioma 38 0.066
245
ACT055 Actinomycosis 41 0.066
246
SCL017 Sclerosing Hemangioma 41 0.066
247
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 43 0.066
248
ZYG002 Zygomycosis 33 0.066
249
P END033 Endocarditis 52 0.066
250
SLC006 Silicosis 53 0.066
251
FBR012 Fabry Disease 69 0.066
252
CRB031 Cerebral Arterial Disease 31 0.065
253
DFF002 Diffuse Pulmonary Fibrosis 33 0.065
254
HST011 Histoplasmosis 54 0.065
255
PRC002 Paracoccidioidomycosis 55 0.065
256
PLM053 Pulmonary Artery Agenesis 12 0.065
257
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.064
258
PLM018 Pulmonary Sclerosing Hemangioma 39 0.064
259
PTN001 Patent Foramen Ovale 54 0.064
260
MYC017 Mycobacterium Kansasii 40 0.064
261
LPD004 Lipoid Nephrosis 48 0.063
262
IMP003 Impaired Renal Function Disease 37 0.063
263
P SYS005 Systemic Scleroderma 58 0.063
264
P THL005 Thalassemia 61 0.063
265
OBS061 Obstructive Sleep Apnea 66 0.063
266
P LYM033 Lymphoproliferative Syndrome 53 0.063
267
c CHR417 Chronic Graft Versus Host Disease 50 0.062
268
P INT068 Intestinal Disease 61 0.062
269
P GRV001 Graves' Disease 61 0.062
270
WTH001 Withdrawal Disorder 41 0.062
271
BRN012 Bronchiolitis Obliterans 58 0.062
272
LKC003 Leukocyte Disease 47 0.062
273
P PRD008 Periodontitis 46 0.062
274
c CHR089 Chronic Kidney Failure 66 0.062
275
P MYC054 Mycobacterium Tuberculosis 2 17 0.062
276
CPL005 Capillary Disease 40 0.062
277
ART021 Arteriosclerosis 59 0.062
278
GST050 Gastrointestinal System Disease 54 0.062
279
HV1006 Hiv-1 82 0.061
280
ADM013 Adamantinoma of Long Bones 59 0.061
281
EXT034 Extrinsic Allergic Alveolitis 56 0.061
282
EPT020 Epithelioid Hemangioendothelioma 45 0.061
283
TTL010 Total Anomalous Pulmonary Venous Return 35 0.061
284
P NMN002 Niemann-Pick Disease 63 0.061
285
P ART034 Aortopulmonary Window 23 0.061
286
ADL030 Adult-Onset Still's Disease 57 0.061
287
HRT007 Heart Cancer 50 0.061
288
WLS001 Wilson Disease 72 0.061
289
ACT017 Acute Chest Syndrome 48 0.060
290
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.060
291
P HRT017 Heart Tumor 35 0.060
292
c ADL079 Adult Heart Tumor 19 0.060
293
ESP023 Esophageal Disease 53 0.060
294
PRD007 Periodontal Disease 43 0.060
295
IDP075 Idiopathic and/or Familial Pulmonary Arterial Hypertension 13 0.060
296
VNT001 Ventilation Pneumonitis 37 0.060
297
P MYL006 Myeloid Leukemia 67 0.060
298
CRN030 Coronary Stenosis 50 0.060
299
ART017 Aortic Disease 58 0.059
300
ANX002 Anxiety Disorder 69 0.059
301
ULC004 Ulcerative Colitis 75 0.059
302
c CRN177 Coronary Heart Disease 7 22 0.059
303
GLC008 Glucose Metabolism Disease 47 0.059
304
P RNL014 Renal Cell Carcinoma 81 0.059
305
P CRV039 Cervicitis 44 0.059
306
NRN004 Neuroendocrine Tumor 54 0.059
307
P THR014 Thrombocytopenia 64 0.059
308
PLM027 Pulmonary Embolism and Infarction 26 0.059
309
P BCL006 B-Cell Lymphomas 64 0.058
310
HMG005 Hemoglobinopathy 50 0.058
311
c PND001 Pain Disorder 55 0.058
312
PRM133 Primary Pulmonary Lymphoma 24 0.058
313
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 41 0.058
314
PNC034 Pancreas Disease 57 0.058
315
ALV006 Alveolar Capillary Dysplasia 30 0.058
316
ACD009 Acid-Labile Subunit, Deficiency of 48 0.058
317
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.058
318
HPT023 Hepatocellular Carcinoma 91 0.058
319
FTT001 Fatty Liver Disease 60 0.058
320
ADL002 Adult Syndrome 53 0.058
321
c CRN176 Coronary Heart Disease 9 20 0.058
322
CRN073 Coronary Arteries Congenital Malformation 13 0.058
323
LYM051 Lymphomatoid Granulomatosis 46 0.058
324
EXT033 Extrapulmonary Tuberculosis 44 0.057
325
HYP540 Hypertension, Diastolic 41 0.057
326
ADN018 Adenoma 59 0.057
327
P NRP001 Neuropathy 60 0.057
328
PLM151 Pulmonary Arteriovenous Fistulas 26 0.057
329
P GLY013 Glycogen Storage Disease 59 0.057
330
END030 End Stage Renal Failure 52 0.057
331
CHR074 Choriocarcinoma 46 0.057
332
P CLR023 Colorectal Cancer 97 0.057
333
P MLT019 Multiple Myeloma 80 0.057
334
DFF003 Diffuse Scleroderma 41 0.057
335
HPT009 Hepatopulmonary Syndrome 48 0.057
336
DXT001 Dextrocardia 44 0.057
337
SYS003 Systolic Heart Failure 43 0.057
338
P LRY019 Laryngitis 55 0.057
339
PLM062 Pulmonary Hyalinizing Granuloma 12 0.057
340
LYM035 Lymphangiectasis 28 0.056
341
P DRM010 Dermatomyositis 58 0.056
342
P PNM006 Pneumoconiosis 51 0.056
343
c INF067 Inflammatory Bowel Disease 10 51 0.056
344
PRS047 Prostatitis 56 0.056
345
MCR088 Microscopic Polyangiitis 48 0.056
346
P CLL015 Collagen Disease 49 0.056
347
P MNN013 Meningitis 65 0.056
348
VSC008 Vascular Hemostatic Disease 33 0.056
349
DFF020 Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia 12 0.056
350
c ADL080 Adult Acute Respiratory Distress Syndrome 23 0.055
351
LPT001 Leptospirosis 63 0.055
352
MYC021 Mycobacterium Xenopi 26 0.055
353
VSC009 Vascular Skin Disease 22 0.055
354
c INV001 Invasive Aspergillosis 47 0.055
355
P HMR003 Hemorrhagic Disease 57 0.055
356
c SRC025 Sarcoidosis 1 58 0.055
357
PRD011 Proud Syndrome 42 0.055
358
c CNT035 Central Nervous System Disease 59 0.055
359
MYL009 Myelodysplastic Syndrome 74 0.054
360
MLT006 Multidrug-Resistant Tuberculosis 46 0.054
361
PRM097 Primary Immunodeficiency Disease 61 0.054
362
c GCH015 Gaucher Disease, Type I 66 0.054
363
HYP006 Hypertensive Heart Disease 50 0.054
364
c PNC106 Pancreatic Agenesis 1 40 0.054
365
URN009 Urinary System Disease 53 0.054
366
c TRC078 Trichohepatoenteric Syndrome 2 31 0.054
367
P ANT006 Antiphospholipid Syndrome 58 0.054
368
c ACT075 Acute Myocardial Infarction 60 0.054
369
c HPT001 Hepatitis C 68 0.054
370
CSY001 C Syndrome 49 0.054
371
P ALX003 Alexander Disease 64 0.054
372
P URF003 Urofacial Syndrome 1 52 0.054
373
SXL003 Sexual Disorder 47 0.054
374
P LRG014 Large Cell Neuroendocrine Carcinoma 41 0.054
375
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.054
376
c MYC055 Mycobacterium Tuberculosis 3 18 0.054
377
PRT011 Protein C Deficiency 51 0.054
378
ANG018 Angiomyolipoma 46 0.054
379
SPN051 Spondylitis 50 0.053
380
P HNT016 Huntington Disease 80 0.053
381
MYC012 Mycetoma 43 0.053
382
RSP007 Respiratory Distress Syndrome, Infant 26 0.053
383
GST045 Gastroenteritis 60 0.053
384
FBR028 Fibrosing Mediastinitis 24 0.053
385
P BRN120 Bronchus Cancer 46 0.053
386
P MSC003 Muscular Atrophy 51 0.053
387
AND005 Androgen Insensitivity Syndrome, Mild 16 0.053
388
SCH014 Schistosomiasis 58 0.053
389
P PRK057 Parkinson Disease, Late-Onset 72 0.052
390
WLL006 Wells Syndrome 56 0.052
391
P TRC086 Trichohepatoenteric Syndrome 1 46 0.052
392
ORL003 Oral Tuberculosis 41 0.052
393
LKS001 Leukostasis 39 0.052
394
PRC013 Pericarditis 52 0.052
395
c CNG027 Congenital Hemolytic Anemia 48 0.052
396
LMY002 Leiomyoma 42 0.052
397
MYC013 Mycobacterium Abscessus 40 0.052
398
EYD002 Eye Disease 63 0.051
399
ERD001 Erdheim-Chester Disease 51 0.051
400
P NRV007 Nervous System Disease 71 0.051
401
P MYM002 Moyamoya Disease 60 0.051
402
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.051
403
RNL097 Renal Artery Disease 45 0.051
404
GDS001 Good Syndrome 45 0.051
405
P RNL015 Renal Hypertension 47 0.051
406
P ATR001 Atrioventricular Septal Defect 52 0.051
407
c HMP029 Hemophilia a 64 0.051
408
MRG013 Mirage Syndrome 26 0.051
409
ATM053 Autoimmune Disease 2 19 0.051
410
c DLT002 Dilated Cardiomyopathy 75 0.051
411
DSS008 Disease of Mental Health 55 0.050
412
ANG049 Angioedema Induced by Ace Inhibitors 35 0.050
413
PLM016 Pleomorphic Carcinoma 36 0.050
414
P ALG002 Alagille Syndrome 72 0.050
415
PLM038 Pulmonary Large Cell Neuroendocrine Carcinoma 36 0.050
416
c INH020 Inherited Metabolic Disorder 49 0.050
417
P ACT135 Acute Graft Versus Host Disease 53 0.050
418
PLM028 Pulmonary Coin Lesion 26 0.050
419
DST006 Diastolic Heart Failure 46 0.050
420
MLR002 Miliary Tuberculosis 42 0.050
421
NPH064 Nipah Virus Disease 25 0.050
422
P BLD051 Blood Coagulation Disease 45 0.050
423
NNS002 Nonspecific Interstitial Pneumonia 44 0.049
424
CNV002 Conversion Disorder 42 0.049
425
GLT021 Glutaricaciduria, Type I 48 0.049
426
P THR015 Thrombophilia 59 0.049
427
PLM039 Pulmonary Neuroendocrine Tumor 42 0.049
428
c INF071 Inflammatory Bowel Disease 1 51 0.049
429
PDT040 Pediatric Hypertension 31 0.049
430
BSL008 Basal Ganglia Disease 43 0.049
431
CTS003 Coats Disease 57 0.049
432
ATM052 Autoimmune Disease 1 28 0.048
433
PLR022 Pleural Disease 52 0.048
434
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.048
435
DPH021 Diaphragm Disease 45 0.048
436
DYS073 Dysphagia 49 0.048
437
PRP030 Purpura 59 0.048
438
DRM006 Dermatitis 61 0.048
439
MRC001 Marchiafava Bignami Disease 50 0.048
440
LPD008 Lipid Metabolism Disorder 58 0.048
441
AYM001 Ayme-Gripp Syndrome 45 0.048
442
ATN005 Autonomic Dysfunction 45 0.048
443
LYM017 Lyme Disease 63 0.048
444
P CHR071 Charcot-Marie-Tooth Disease 66 0.048
445
HPT074 Hepatic Adenoma, Somatic 51 0.047
446
SPC003 Specific Developmental Disorder 40 0.047
447
PLM124 Pulmonary Hypertension, Neonatal 27 0.047
448
LMY003 Leiomyomatosis 41 0.047
449
SPC010 Speech and Communication Disorders 46 0.047
450
CHG001 Chagas Disease 62 0.047
451
P ESN008 Eosinophilic Pneumonia 49 0.047
452
GLB003 Globe Disease 35 0.047
453
HYD012 Hydrops Fetalis 44 0.047
454
HMN014 Human Immunodeficiency Virus Infectious Disease 49 0.047
455
PRT036 Peritonitis 62 0.047
456
P LPR003 Leprosy 68 0.047
457
LVR012 Liver Cirrhosis 67 0.047
458
CHR028 Chronic Wasting Disease 34 0.047
459
STR008 Strongyloidiasis 50 0.047
460
c SRC023 Sarcoidosis 2 33 0.047
461
P PRT013 Portal Hypertension 59 0.046
462
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 57 0.046
463
CRT016 Carotid Artery Disease 55 0.046
464
RSP019 Respiratory Distress Syndrome in Premature Infants 44 0.046
465
CRD001 Cardiac Tamponade 44 0.046
466
MNT002 Mental Depression 54 0.046
467
c PNC108 Pancreatitis, Hereditary 67 0.046
468
UNV002 Univentricular Heart 26 0.046
469
BRC012 Brucellosis 65 0.046
470
P PLY041 Polymyositis 51 0.046
471
P CHR345 Chronic Pain 49 0.046
472
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.046
473
HTR003 Heterotaxy 42 0.046
474
UNL013 Unilateral Absence of a Pulmonary Artery 18 0.046
475
P OST002 Osteoporosis 64 0.046
476
P PLY018 Polycythemia 57 0.046
477
ABS016 Absence of the Pulmonary Artery 19 0.046
478
CRD119 Cardiac Arrest 63 0.045
479
P HMR012 Hemorrhagic Fever 55 0.045
480
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 23 0.045
481
P HYP086 Hypothyroidism 65 0.045
482
P KDN017 Kidney Cancer 67 0.045
483
STM006 Stomach Disease 50 0.045
484
HNS001 Hansen's Disease 29 0.045
485
P NRV006 Nervous System Cancer 62 0.045
486
P THR003 Thoracic Aortic Aneurysm 57 0.045
487
THR016 Thrombophlebitis 52 0.045
488
P TRC005 Tracheal Stenosis 38 0.045
489
ANG020 Angiosarcoma 52 0.045
490
PRT014 Protein S Deficiency 52 0.045
491
SPR010 Sporotrichosis 48 0.045
492
c RNL016 Renal Infectious Disease 24 0.045
493
RSD004 Rosai-Dorfman Disease 39 0.045
494
BRN055 Bronchogenic Cyst 27 0.045
495
c LRG001 Large Cell Carcinoma 51 0.045
496
OCL009 Ocular Cancer 62 0.045
497
P ATX004 Ataxia 53 0.045
498
PNM001 Pneumocystosis 50 0.045
499
CCN007 Cocoon Syndrome 35 0.044
500
MLD001 Melioidosis 67 0.044
501
MSS002 Mass Syndrome 59 0.044
502
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.044
503
P CRD194 Cardiomyopathy, Familial Hypertrophic 64 0.044
504
RGH006 Right Aortic Arch 26 0.044
505
OLG003 Oligohydramnios 52 0.044
506
PMS001 Poems Syndrome 55 0.044
507
BRN106 Burns 52 0.044
508
RHM028 Rheumatic Heart Disease 51 0.044
509
DFF031 Diffuse Alveolar Hemorrhage 24 0.044
510
PRC012 Pericardial Effusion 50 0.044
511
THR004 Thrombocytosis 55 0.044
512
P MSC005 Muscular Dystrophy 64 0.044
513
PLS011 Plasmacytoma 56 0.044
514
P PSR002 Psoriasis 63 0.044
515
P ACT105 Acute Mountain Sickness 53 0.043
516
ANM031 Anomalous Left Coronary Artery from the Pulmonary Artery 16 0.043
517
ASP007 Aspiration Pneumonia 46 0.043
518
c HMG004 Hemoglobin D Disease 33 0.043
519
HYP037 Hyperhomocysteinemia 50 0.043
520
BNC003 Bone Cancer 45 0.043
521
OCL006 Ocular Hypertension 48 0.043
522
c SVR001 Severe Acute Respiratory Syndrome 57 0.043
523
BNG041 Benign Metastasizing Leiomyoma 31 0.043
524
IRN001 Iron Deficiency Anemia 51 0.043
525
CYT008 Cytomegalovirus Infection 51 0.043
526
LYM006 Lymphoepithelioma-Like Carcinoma 42 0.043
527
RTN018 Retinal Disease 56 0.043
528
INT046 Intestinal Tuberculosis 38 0.043
529
P LNG064 Lung Cancer Susceptibility 3 62 0.043
530
c SCN051 Secondary Pulmonary Alveolar Proteinosis 18 0.043
531
CMM004 Common Variable Immunodeficiency 67 0.043
532
P DRR001 Diarrhea 51 0.043
533
MCN007 Meconium Aspiration Syndrome 51 0.042
534
HNM002 Hinman Syndrome 25 0.042
535
FRM003 Farmer's Lung 47 0.042
536
c SML023 Small Cell Lung Cancer, Adult 17 0.042
537
P INF032 Infertility 61 0.042
538
CTS002 Cat-Scratch Disease 45 0.042
539
SKN023 Skin Tag 46 0.042
540
ANG054 Angina Pectoris 51 0.042
541
DWN001 Down Syndrome 65 0.042
542
LYS002 Lysosomal Storage Disease 52 0.042
543
BRS051 Breast Disease 62 0.042
544
c PLM044 Pulmonary Fibrosis, Familial 30 0.042
545
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.042
546
P NTR004 Neutropenia 59 0.042
547
SPN369 Spinal Disease 41 0.041
548
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.041
549
P LYM026 Lymphoblastic Leukemia 60 0.041
550
HDG012 Hodgkin Lymphoma 73 0.041
551
P UVT001 Uveitis 59 0.041
552
ANT018 Anthracosis 42 0.041
553
P ALP004 Alport Syndrome 68 0.041
554
VNW001 Von Willebrand's Disease 61 0.041
555
CLN019 Colonic Disease 50 0.041
556
PRP021 Peripheral Nervous System Neoplasm 50 0.041
557
LYM023 Lymphatic System Cancer 35 0.041
558
LGH004 Light Chain Deposition Disease 42 0.041
559
ATM054 Autoimmune Disease 3 18 0.041
560
LYM021 Lymphadenitis 58 0.041
561
CHL079 Children's Interstitial Lung Disease 19 0.041
562
HGH021 Hughes-Stovin Syndrome 18 0.041
563
BRN071 Brain Injury 52 0.041
564
PLM108 Pulmonary Interstitial Glycogenosis 14 0.041
565
VRL011 Viral Infectious Disease 59 0.041
566
CRB025 Carbohydrate Metabolic Disorder 47 0.041
567
P LGH007 Leigh Syndrome 70 0.041
568
P SYP003 Syphilis 53 0.041
569
SFT003 Soft Tissue Sarcoma 56 0.041
570
PLM116 Pulmonary Artery Hypoplasia 18 0.041
571
FRB001 Farber Lipogranulomatosis 51 0.041
572
RDN001 Reading Disorder 39 0.041
573
c SRF008 Surfactant Metabolism Dysfunction, Pulmonary, 4 26 0.041
574
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.041
575
PLM004 Pulmonary Artery Leiomyosarcoma 17 0.041
576
c HRD171 Hereditary Pulmonary Alveolar Proteinosis 23 0.041
577
MDD011 Mood Disorder 61 0.040
578
SCR035 Sacral Agenesis with Vertebral Anomalies 33 0.040
579
P APL001 Aplastic Anemia 73 0.040
580
P CNT061 Conotruncal Heart Malformations 62 0.040
581
SYN036 Syncope 47 0.040
582
INF058 Inflammatory Myofibroblastic Tumor 46 0.040
583
CHN010 Chondroma 41 0.040
584
c ACT073 Acute Leukemia 62 0.040
585
P CRN074 Coronary Artery Aneurysm 44 0.040
586
HST009 Histiocytoma 47 0.040
587
WLL001 Williams-Beuren Syndrome 61 0.040
588
c HMG001 Hemoglobin C Disease 47 0.040
589
MRG003 Marginal Zone B-Cell Lymphoma 50 0.040
590
P HYP069 Hyperparathyroidism 57 0.040
591
P PHC003 Pheochromocytoma 71 0.040
592
P PRS040 Prostate Cancer 89 0.040
593
P CTS001 Cutis Laxa 59 0.040
594
c MYC058 Myocardial Infarction 2 29 0.040
595
P HYP076 Hyperthyroidism 56 0.040
596
P CSH001 Cushing's Syndrome 64 0.039
597
MLR004 Malaria 79 0.039
598
LYM019 Lymphosarcoma 53 0.039
599
SPN186 Spinal Cord Injury 62 0.039
600
BRN014 Bronchopneumonia 45 0.039
601
OST017 Osteomyelitis 59 0.039
602
PYR010 Peyronie's Disease 53 0.039
603
c CNG121 Congenital Pulmonary Alveolar Proteinosis 13 0.039
604
CNS002 Constrictive Pericarditis 34 0.039
605
RGH009 Right Atrial Isomerism 32 0.039
606
PLV003 Pelvic Inflammatory Disease 53 0.039
607
CRY001 Cryptogenic Organizing Pneumonia 44 0.039
608
INF034 Infective Endocarditis 50 0.039
609
ADR007 Adrenoleukodystrophy 71 0.039
610
P SCL018 Scoliosis 56 0.039
611
P CHN012 Chondrosarcoma 57 0.039
612
PHR003 Pharyngitis 58 0.039
613
ART031 Aortic Coarctation 42 0.039
614
CNG134 Congenitally Corrected Transposition of the Great Arteries 23 0.039
615
NNT004 Neonatal Respiratory Failure 41 0.039
616
BNM001 Bone Marrow Cancer 52 0.039
617
P MTC069 Mitochondrial Disorders 52 0.039
618
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 55 0.039
619
P PRM011 Primary Ciliary Dyskinesia 58 0.039
620
RHM009 Rheumatoid Lung Disease 40 0.039
621
LYM095 Lymphangiomatosis 33 0.039
622
c MCP009 Mucopolysaccharidosis Ii 62 0.039
623
MCN001 Mucinous Adenocarcinoma 50 0.039
624
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.039
625
P TRT010 Teratoma 52 0.038
626
END031 Endometrial Stromal Sarcoma 49 0.038
627
CNT098 Central Core Disease 66 0.038
628
BRY001 Berylliosis 38 0.038
629
INT007 Intermediate Coronary Syndrome 52 0.038
630
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.038
631
PRN023 Prion Disease 48 0.038
632
PLC008 Placenta Disease 36 0.038
633
HPR003 Heparin-Induced Thrombocytopenia 46 0.038
634
P ABD003 Abdominal Aortic Aneurysm 43 0.038
635
PRS030 Persistent Fetal Circulation Syndrome 40 0.038
636
c INF078 Inflammatory Bowel Disease 2 24 0.038
637
LYM122 Lymphangiectasia, Pulmonary, Congenital 21 0.038
638
MSC072 Muscle Cancer 51 0.038
639
P MYS005 Myositis 56 0.038
640
NCT008 Nicotine Dependence, Protection Against 52 0.038
641
MYC015 Mycobacterium Fortuitum 27 0.038
642
c NMN015 Niemann-Pick Disease, Type C1 64 0.038
643
GST053 Gastric Cancer 77 0.038
644
TRC026 Tracheal Disease 35 0.038
645
PRQ002 Paraquat Poisoning 24 0.038
646
P MYC008 Myocarditis 54 0.038
647
P MSC007 Muscle Hypertrophy 59 0.038
648
LPD009 Lipid Storage Disease 49 0.038
649
c NMN016 Niemann-Pick Disease, Type B 45 0.038
650
GNR004 Generalized Anxiety Disorder 51 0.038
651
P MYL005 Myelofibrosis 67 0.038
652
P ART023 Arthropathy 63 0.037
653
SML033 Small Cell Cancer of the Lung, Somatic 53 0.037
654
P DYS007 Dyskeratosis Congenita 63 0.037
655
JNT002 Joint Disorders 56 0.037
656
HMT002 Hematologic Cancer 64 0.037
657
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.037
658
c TRC022 Tricuspid Valve Insufficiency 34 0.037
659
MCP006 Mucoepidermoid Carcinoma 47 0.037
660
BRN018 Borna Disease 42 0.037
661
c LNG031 Lung Benign Neoplasm 44 0.037
662
BRN028 Brain Cancer 70 0.037
663
CRT057 Critical Congenital Heart Disease 20 0.037
664
STC004 Stachybotrys Chartarum 37 0.037
665
PLY022 Polycystic Kidney and Hepatic Disease 66 0.037
666
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.037
667
EMP007 Emphysema Due to Aat Deficiency 56 0.037
668
IMP006 Impulse Control Disorder 40 0.037
669
HND002 Hand, Foot and Mouth Disease 48 0.037
670
RLP001 Relapsing Polychondritis 49 0.036
671
DDN006 Duodenitis 44 0.036
672
ATR076 Atrophic Muscular Disease 18 0.036
673
P EXN002 Exanthem 57 0.036
674
P PRM006 Primary Biliary Cirrhosis 52 0.036
675
P CPL003 Capillary Leak Syndrome 43 0.036
676
RHM001 Rheumatic Fever 50 0.036
677
P SJG001 Sjogren's Syndrome 53 0.036
678
SWL001 Swallowing Disorders 34 0.036
679
LSH001 Leishmaniasis 62 0.036
680
ATM012 Autoimmune Disease of Blood 37 0.036
681
SKN027 Skin Conditions 45 0.036
682
PPT005 Peptic Ulcer Disease 56 0.036
683
FLR002 Filariasis 55 0.036
684
CMP005 Campomelic Dysplasia 72 0.036
685
PMP001 Pemphigus 49 0.036
686
LTT002 Letterer-Siwe Disease 54 0.036
687
c CNT015 Central Sleep Apnea 44 0.036
688
LYM014 Lymphangitis 36 0.036
689
ATM059 Autoimmune Disease 6 26 0.036
690
WGN006 Wegener Granulomatosis 62 0.035
691
CRR007 Cirrhosis, Cryptogenic 44 0.035
692
P GNT008 Giant Cell Tumor 49 0.035
693
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.035
694
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.035
695
CHL123 Chlamydia 59 0.035
696
c VRL005 Viral Pneumonia 42 0.035
697
c HPT073 Hepatitis C Virus 72 0.035
698
ATM005 Autoimmune Disease of Musculoskeletal System 16 0.035
699
PLR008 Pleurisy 50 0.035
700
MNK001 Menkes Disease 61 0.035
701
HMR004 Hemorrhagic Fever with Renal Syndrome 57 0.035
702
ATM013 Autoimmune Disease of Cardiovascular System 15 0.035
703
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 34 0.035
704
HRT011 Heart Septal Defect 41 0.035
705
MRB003 Morbid Obesity 58 0.035
706
CHR413 Chronic Myocardial Ischemia 40 0.035
707
RGH001 Right Bundle Branch Block 43 0.035
708
PYD001 Pyoderma Gangrenosum 49 0.035
709
CHR005 Chorioamnionitis 48 0.035
710
DMY004 Demyelinating Disease 55 0.035
711
P TXP001 Toxoplasmosis 60 0.035
712
FBR003 Fibrous Histiocytoma 42 0.035
713
CMP035 Complete Atrioventricular Canal 29 0.035
714
P ATX030 Ataxia-Telangiectasia 76 0.035
715
BNN003 Bone Inflammation Disease 46 0.035
716
DRM009 Dermatomycosis 36 0.035
717
P RCK004 Rickets 59 0.034
718
P CND004 Candidiasis 57 0.034
719
ANT039 Antisynthetase Syndrome 37 0.034
720
c HPT016 Hepatitis B 64 0.034
721
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 41 0.034
722
EWN003 Ewing Sarcoma 64 0.034
723
RHB003 Rhabdomyosarcoma 58 0.034
724
P ENC004 Encephalitis 61 0.034
725
P EPL164 Epilepsy 66 0.034
726
MXD023 Mixed Cell Type Cancer 47 0.034
727
CRB085 Cerebral Hemorrhage 43 0.034
728
PYD002 Pyoderma 49 0.034
729
P PTN008 Patent Arterial Duct 29 0.034
730
PKL002 Poikiloderma, Hereditary Fibrosing, with Tendon Contractures, Myopathy, and Pulmonary Fibrosis 22 0.034
731
P HRT035 Heart Block, Congenital 39 0.034
732
NSY001 N Syndrome 39 0.034
733
LYM004 Lymphoid Interstitial Pneumonia 40 0.034
734
MDY003 Mody, Type Ii 38 0.034
735
CRD137 Cardiogenic Shock 46 0.034
736
LMB062 Limb Ischemia 48 0.034
737
P ATP001 Atopic Dermatitis 62 0.034
738
PLR001 Pleural Tuberculosis 47 0.034
739
c PRM023 Pre-Malignant Neoplasm 43 0.034
740
TRC040 Tracheoesophageal Fistula 41 0.034
741
ADL082 Adult Pulmonary Langerhans Cell Histiocytosis 22 0.034
742
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.034
743
CHR001 Churg-Strauss Syndrome 49 0.034
744
P CTR002 Cataract 57 0.034
745
PLM139 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 1 27 0.034
746
IMM090 Immunodeficiency 27a, Mycobacteriosis, Ar 28 0.034
747
TST021 Testicular Germ Cell Tumor 70 0.034
748
P GST049 Gastrointestinal System Cancer 60 0.034
749
BNF002 Bone Fracture 47 0.034
750
MYC018 Mycobacterium Malmoense 28 0.034
751
HDC001 Headache 54 0.034
752
SXD001 Sex Differentiation Disease 40 0.034
753
LNG095 Lung Abscess 34 0.033
754
RSP004 Respiratory System Benign Neoplasm 28 0.033
755
PRN021 Paranasal Sinus Disease 50 0.033
756
LMT001 Limited Scleroderma 45 0.033
757
ESP021 Esophageal Cancer 75 0.033
758
c HPT003 Hepatitis a 59 0.033
759
P HYP098 Hypereosinophilic Syndrome 51 0.033
760
c ATR075 Atrial Fibrillation 15 25 0.033
761
WBR001 Weber Syndrome 37 0.033
762
LYS003 Lysinuric Protein Intolerance 50 0.033
763
c MTR002 Mitral Valve Insufficiency 44 0.033
764
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 0.033
765
THL018 Thalassemia Major 42 0.033
766
CRC006 Carcinoid Syndrome 51 0.033
767
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.033
768
c TLN011 Telangiectasia, Hereditary Hemorrhagic, Type 2 36 0.033
769
GNG013 Gingivitis 60 0.033
770
INS024 Insulin-Like Growth Factor I 74 0.033
771
THR011 Thoracic Benign Neoplasm 32 0.033
772
c SRF007 Surfactant Metabolism Dysfunction, Pulmonary, 5 21 0.033
773
ETH011 Ethylmalonic Encephalopathy 59 0.033
774
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.033
775
SPL018 Splenomegaly 44 0.033
776
GLC077 Glucocorticoid Therapy, Response to 19 0.033
777
CRH005 Crohn's Colitis 52 0.033
778
CHR008 Choroiditis 43 0.033
779
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.033
780
GLM008 Glomus Tumor 42 0.033
781
P LTR001 Lateral Sclerosis 52 0.033
782
HYP056 Hypoglycemia 61 0.033
783
QFV001 Q Fever 60 0.033
784
PSR001 Psoriatic Arthritis 64 0.033
785
APH001 Aphthous Stomatitis 62 0.033
786
P HRD011 Hereditary Spherocytosis 53 0.033
787
TLN003 Telangiectasis 52 0.033
788
BHC003 Behcet Syndrome 61 0.033
789
c MCR256 Microphthalmia, Syndromic 9 42 0.033
790
P MCP010 Mucopolysaccharidosis 58 0.033
791
ADS001 Adiaspiromycosis 21 0.033
792
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.033
793
DSS009 Disseminated Intravascular Coagulation 51 0.033
794
CNG063 Congenital Cardiovascular Shunt 12 0.033
795
MTR003 Mitral Valve Stenosis 45 0.033
796
GRN017 Granulocytopenia 42 0.033
797
PRT019 Protein-Losing Enteropathy 41 0.032
798
ATM055 Autoimmune Disease 4 18 0.032
799
LNG054 Lung Agenesis 33 0.032
800
HML018 Homologous Wasting Disease 17 0.032
801
P CNJ013 Conjunctivitis 65 0.032
802
HRT029 Heart Tumor of the Child 17 0.032
803
PHN003 Phenylketonuria 73 0.032
804
P HVY001 Heavy Chain Disease 41 0.032
805
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 35 0.032
806
P TCL004 T-Cell Leukemia 46 0.032
807
LBR003 Labrador Lung 15 0.032
808
SPR035 Superior Vena Cava Syndrome 32 0.032
809
P CNN004 Connective Tissue Cancer 45 0.032
810
TLR001 Tularemia 42 0.032
811
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 24 0.032
812
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.032
813
CYT004 Cytomegalic Inclusion Disease 30 0.032
814
CRN019 Coronary Artery Vasospasm 42 0.032
815
TKY002 Takayasu Arteritis 60 0.032
816
NRR001 Neuroretinitis 42 0.032
817
VNH007 Von Hippel-Lindau Syndrome 69 0.032
818
c INF086 Inflammatory Bowel Disease 3 21 0.032
819
c SCN006 Secondary Syphilis 41 0.032
820
INF013 Inferior Myocardial Infarction 37 0.032
821
DCH001 Duchenne Muscular Dystrophy 80 0.032
822
KRT002 Keratomalacia 54 0.032
823
ART012 Aortitis 31 0.032
824
MYC016 Mycobacterium Gordonae 21 0.032
825
P PLY017 Polyarteritis Nodosa 55 0.032
826
ACR002 Acrocapitofemoral Dysplasia 36 0.032
827
GTR002 Goiter 54 0.032
828
c NRF018 Neurofibromatosis, Type 1 68 0.032
829
BND014 Bone Development Disease 42 0.032
830
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.032
831
CRD003 Cardiac Sarcoidosis 43 0.032
832
INT020 Intravenous Leiomyomatosis 31 0.032
833
PLM061 Pulmonary Edema of Mountaineers 14 0.032
834
CST005 Castleman Disease 38 0.032
835
IMM127 Immune System Cancer 42 0.032
836
TXC020 Toxic Oil Syndrome 39 0.032
837
GLC037 Glucocorticoid Resistance 62 0.032
838
NDL013 Nodular Regenerative Hyperplasia 49 0.032
839
VGN023 Vaginitis 42 0.032
840
P TRM003 Tremor 54 0.032
841
CLC006 Calcinosis 49 0.031
842
LPD027 Lip Disease 36 0.031
843
c KNN009 Kenny-Caffey Syndrome, Type 1 62 0.031
844
ASP008 Aspiration Pneumonitis 38 0.031
845
APP008 Appendicitis 60 0.031
846
SVR004 Severe Combined Immunodeficiency 68 0.031
847
c ATM010 Autoimmune Hemolytic Anemia 60 0.031
848
ADR038 Adermatoglyphia 48 0.031
849
ACT056 Acute Cor Pulmonale 31 0.031
850
CRN197 Coronary Arterial Fistulas 24 0.031
851
c GLY008 Glycogen Storage Disease Ii 61 0.031
852
c SRC024 Sarcoidosis 3 19 0.031
853
P TRC087 Tricuspid Valve Disease 44 0.031
854
DYS011 Dyskinesia of Esophagus 33 0.031
855
SPT004 Septic Arthritis 59 0.031
856
c ACT068 Acute Cystitis 50 0.031
857
P ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 60 0.031
858
NNL002 Nonalcoholic Steatohepatitis 53 0.031
859
P THY023 Thymoma 53 0.031
860
c ACT071 Acute Kidney Failure 50 0.031
861
P HMC003 Hemochromatosis 72 0.031
862
LNG037 Lung Sarcoma 43 0.031
863
P HYP014 Hyperuricemia 50 0.031
864
PLS009 Plasma Cell Neoplasm 48 0.031
865
MND006 Mondor Disease 21 0.031
866
c SCL052 Scleroderma, Familial Progressive 27 0.031
867
c ADL017 Adult T-Cell Leukemia 58 0.031
868
CRY004 Cryoglobulinemia 47 0.031
869
AND015 Androgen Insensitivity 63 0.031
870
INT040 Intrinsic Asthma 40 0.031
871
TXC011 Toxocariasis 37 0.031
872
PYR013 Pyruvate Kinase Deficiency 58 0.031
873
RNL077 Renal Fibrosis 47 0.031
874
CLC001 Calciphylaxis 40 0.031
875
c PRK030 Parkinson Disease 4 39 0.031
876
c CNN010 Connective Tissue Benign Neoplasm 35 0.031
877
P XLN007 X-Linked Disease 34 0.031
878
PLM002 Pulmonary Plasma Cell Granuloma 15 0.030
879
PPL018 Papillary Adenocarcinoma 48 0.030
880
ANX004 Anoxia 44 0.030
881
RCR004 Recurrent Respiratory Papillomatosis 40 0.030
882
CYS008 Cystic Echinococcosis 50 0.030
883
KRT004 Keratitis 70 0.030
884
PLG002 Plague 49 0.030
885
P KRB001 Krabbe Disease 69 0.030
886
c ART101 Aortic Valve Disease 2 55 0.030
887
ANG011 Angiodysplasia 44 0.030
888
NSL022 Nasal Cavity Disease 42 0.030
889
c ATM011 Autoimmune Hepatitis 58 0.030
890
c INF089 Inflammatory Bowel Disease 6 20 0.030
891
P SPN046 Spinal Muscular Atrophy 63 0.030
892
P SNS014 Sinusitis 60 0.030
893
HMP009 Haemophilus Influenzae 45 0.030
894
P GT001 Gout 58 0.030
895
c ACT134 Acute Liver Failure 50 0.030
896
P ALC004 Alcohol Abuse 60 0.030
897
c LCL006 Localized Scleroderma 59 0.030
898
HPT020 Hepatic Vascular Disease 44 0.030
899
SPH010 Sphingolipidosis 45 0.030
900
P MDL005 Medulloblastoma 77 0.030
901
ATR024 Atrial Fibrillation and Stroke 22 0.030
902
CRY003 Cryptosporidiosis 46 0.030
903
NRR002 Norrie Disease 61 0.030
904
P SDR002 Siderosis 44 0.030
905
CNT047 Contact Dermatitis 62 0.030
906
CNT097 Central Hypoventilation Syndrome, Congenital 60 0.030
907
P GRN010 Granular Cell Tumor 47 0.030
908
c CNG031 Congenital Nervous System Abnormality 39 0.030
909
SPN041 Spinal Cord Disease 48 0.030
910
CRT060 Cor Triatriatum Sinister 17 0.030
911
P SHR029 Short Syndrome 60 0.030
912
BRN080 Brain Ischemia 41 0.030
913
CLV009 Clove Syndrome, Somatic 42 0.030
914
P SDD001 Sudden Infant Death Syndrome 61 0.030
915
P RBL001 Rubella 56 0.030
916
PRP009 Peripartum Cardiomyopathy 41 0.030
917
MNT001 Mantle Cell Lymphoma 70 0.030
918
P DGR001 Digeorge Syndrome 52 0.030
919
CYS039 Cystic Kidney Disease 52 0.030
920
c LKM061 Leukemia, Acute Myeloid 71 0.030
921
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 26 0.030
922
VGT001 Vogt-Koyanagi-Harada Disease 52 0.030
923
ETN001 Eating Disorder 60 0.029
924
ALB002 Albinism 43 0.029
925
INT253 Intestinal Benign Neoplasm 50 0.029
926
P TRN020 Turner Syndrome 64 0.029
927
P END044 Endometriosis 53 0.029
928
HLY001 Hailey-Hailey Disease 53 0.029
929
ACH005 Achalasia 54 0.029
930
FXF002 Fox-Fordyce Disease 39 0.029
931
OTT002 Otitis Media 66 0.029
932
c CHR090 Chronic Lymphocytic Leukemia 74 0.029
933
P ADM011 Adams-Oliver Syndrome 48 0.029
934
c CHR064 Chronic Monocytic Leukemia 43 0.029
935
SMT004 Smith-Lemli-Opitz Syndrome 67 0.029
936
CHC001 Chickenpox 52 0.029
937
P OST001 Osteopetrosis 62 0.029
938
BCK006 Back Pain 42 0.029
939
FCT022 Factor Xi Deficiency, Autosomal Recessive 56 0.029
940
P LPS002 Liposarcoma 50 0.029
941
CYS014 Cystadenocarcinoma 46 0.029
942
ADP007 Adie Pupil 34 0.029
943
P GLM045 Glioma 58 0.029
944
PST046 Post-Transplant Lymphoproliferative Disease 53 0.029
945
WRN001 Werner Syndrome 67 0.029
946
CRB037 Cerebral Palsy 54 0.029
947
YLL001 Yellow Nail Syndrome 47 0.029
948
LYM040 Lymphoblastic Lymphoma 54 0.029
949
ART002 Arts Syndrome 53 0.029
950
HRP004 Herpes Zoster 56 0.029
951
ALV010 Alveolar Soft-Part Sarcoma 53 0.029
952
PPL022 Papilloma 55 0.029
953
BYS001 Byssinosis 31 0.029
954
c INF073 Inflammatory Bowel Disease 12 21 0.029
955
CYN002 Cyanosis, Transient Neonatal 31 0.029
956
c CLL013 Cell Type Cancer 48 0.029
957
P RHN004 Rhinitis 61 0.029
958
c ADL001 Adult Lymphoma 41 0.029
959
LMR001 Lemierre's Syndrome 41 0.029
960
ADN002 Adenoiditis 40 0.029
961
CRS005 Crest Syndrome 47 0.029
962
P OCL002 Oculocutaneous Albinism 51 0.029
963
OVR063 Overnutrition 49 0.029
964
ATM016 Autoimmune Disease of Skin and Connective Tissue 31 0.029
965
BCT015 Bacteremia 48 0.029
966
P OST005 Osteogenesis Imperfecta 67 0.029
967
c ATM024 Autoimmune Pancreatitis 46 0.029
968
THL017 Thalassemia Intermedia 40 0.029
969
ACT084 Acute Stress Disorder 40 0.029
970
P CHL066 Cholangitis 49 0.029
971
MLK004 Malakoplakia 27 0.029
972
ACR007 Acromegaly 65 0.029
973
P VNS003 Venous Insufficiency 53 0.029
974
TRC037 Tracheobronchomalacia 22 0.029
975
TRN018 Transitional Cell Carcinoma 54 0.029
976
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 33 0.029
977
MCR004 Macroglobulinemia 50 0.029
978
P ESS003 Essential Thrombocythemia 68 0.029
979
DFF005 Diffuse Large B-Cell Lymphoma 56 0.029
980
LNG013 Lung Lymphoma 40 0.029
981
P HMP007 Hemophilia 56 0.028
982
CNG048 Congenital Hepatic Fibrosis 45 0.028
983
HPT022 Hepatoblastoma 53 0.028
984
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 50 0.028
985
P RTN008 Retinitis Pigmentosa 79 0.028
986
P PLY019 Polyneuropathy 54 0.028
987
MLG097 Malignant Mesenchymal Tumor 37 0.028
988
P PRT010 Parathyroid Carcinoma 62 0.028
989
P HRD018 Hair Disease 50 0.028
990
c SPN225 Spondyloarthropathy 1 63 0.028
991
SML020 Small Patella Syndrome 36 0.028
992
P NNN008 Noonan Syndrome 1 67 0.028
993
P HRP006 Herpes Simplex 65 0.028
994
CLD007 Cold Agglutinin Disease 43 0.028
995
PNN001 Panniculitis 50 0.028
996
MCN008 Mucinous Cystadenocarcinoma 40 0.028
997
c NPH055 Nephrotic Syndrome, Type 1 59 0.028
998
CRB018 Cerebral Lipidosis 30 0.028
999
P FML056 Familial Deafness 20 0.028
1000
RPR002 Reproductive System Disease 46 0.028
1001
LYM116 Lymph Node Disease 44 0.028
1002
P FTL009 Fetal Akinesia Deformation Sequence 49 0.028
1003
LFT009 Left Ventricular Outflow Tract Obstruction 44 0.028
1004
SPN032 Spindle Cell Carcinoma 43 0.028
1005
MDD010 Middle Ear Disease 46 0.028
1006
BLR006 Biliary Tract Disease 51 0.028
1007
SNS023 Sensory System Cancer 46 0.028
1008
FNC006 Functional Gastric Disease 34 0.028
1009
PLM013 Pulmonary Immaturity 37 0.028
1010
MTR027 Mitral Atresia 16 0.028
1011
WLS002 Wilson-Mikity Syndrome 14 0.028
1012
ORL011 Oral Cancer 55 0.028
1013
UND007 Undifferentiated Connective Tissue Disease 29 0.028
1014
CHL068 Cholestasis 58 0.028
1015
P CYS018 Cystitis 53 0.028
1016
ATN003 Autonomic Nervous System Neoplasm 43 0.028
1017
DBT088 Diabetes Insipidus, Nephrogenic 59 0.028
1018
c ACT027 Acute Pancreatitis 56 0.028
1019
c ALP005 Alpha Chain Disease 37 0.028
1020
SLV003 Salivary Gland Disease 49 0.028
1021
WHP001 Whipple Disease 48 0.028
1022
PRS042 Prostate Disease 52 0.028
1023
PLS010 Plasma Protein Metabolism Disease 38 0.028
1024
PTR006 Peters Anomaly 64 0.028
1025
CTN007 Cutaneous Leishmaniasis 62 0.028
1026
TST014 Testicular Cancer 52 0.028
1027
c PRK045 Parkinson Disease 5 44 0.028
1028
KTL001 Keutel Syndrome 35 0.028
1029
URT001 Urethritis 40 0.028
1030
ASC002 Ascariasis 38 0.028
1031
c MLG079 Malignant Pleural Mesothelioma 50 0.028
1032
c AST050 Asthma, Phf11-Related 22 0.028
1033
WLM001 Wolman Disease 56 0.028
1034
LYM067 Lymphoid Leukemia 43 0.028
1035
FCT007 Factor Vii Deficiency 62 0.028
1036
P TMP003 Temporal Arteritis 60 0.028
1037
ESN017 Eosinophilic Granuloma 34 0.028
1038
c GCH017 Gaucher Disease, Type Iii 45 0.028
1039
DNG002 Dengue Hemorrhagic Fever 62 0.028
1040
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 18 0.028
1041
P GST044 Gastritis 58 0.028
1042
RDT005 Radiation Induced Cancer 28 0.028
1043
PNC032 Pancoast Tumor 34 0.028
1044
PLM069 Pulmonary Venous Return Anomaly 17 0.028
1045
PRT037 Pertussis 64 0.027
1046
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy