Search results for AIR

1891 hits were found for AIR

# Family MCID Name MIFTS Score
1
ACT088 Acute Insulin Response 41 10.166
2
MNT256 Mental Retardation, Buenos Aires Type 25 6.163
3
VNT001 Ventilation Pneumonitis 21 4.365
4
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 3.273
5
PNM008 Pneumothorax 56 0.319
6
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.313
7
LNG099 Lung Disease 60 0.313
8
BRN024 Bronchitis 68 0.291
9
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.282
10
P RHN004 Rhinitis 57 0.274
11
AST005 Asthma 76 0.249
12
ALL003 Allergic Rhinitis 67 0.231
13
P CRD119 Cardiac Arrest 67 0.194
14
ATM095 Autoimmune Disease 62 0.187
15
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.185
16
P LNG032 Lung Cancer 98 0.184
17
P CND004 Candidiasis 58 0.177
18
P PLY188 Polyendocrinopathy 32 0.174
19
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.173
20
IGR001 Ige Responsiveness, Atopic 59 0.171
21
P RSP003 Respiratory Failure 74 0.170
22
PNM010 Pneumothorax, Primary Spontaneous 60 0.170
23
SCK001 Sick Building Syndrome 34 0.170
24
DRM006 Dermatitis 61 0.167
25
HYP266 Hypoxia 57 0.153
26
BRN002 Bronchiolitis 59 0.152
27
CVD001 Covid-19 44 0.152
28
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.149
29
P PNM007 Pneumonia 68 0.148
30
OTT002 Otitis Media 72 0.147
31
P MYC007 Myocardial Infarction 70 0.147
32
RTN017 Retinal Detachment 61 0.147
33
INT051 Intussusception 53 0.146
34
P HRT032 Heart Disease 75 0.143
35
c SVR001 Severe Acute Respiratory Syndrome 62 0.143
36
P PLM037 Pulmonary Hypertension 67 0.140
37
CRB039 Cerebrovascular Disease 67 0.139
38
ATH013 Atherosclerosis Susceptibility 65 0.139
39
PTN001 Patent Foramen Ovale 60 0.137
40
OCL069 Ocular Motor Apraxia 51 0.136
41
PLM010 Pulmonary Edema 54 0.135
42
PLM033 Pulmonary Embolism 59 0.134
43
PNG002 Pain Agnosia 51 0.134
44
47X002 47,xyy 49 0.134
45
THR024 Thrombosis 57 0.132
46
P ADN016 Adenocarcinoma 64 0.131
47
CNG034 Congestive Heart Failure 69 0.130
48
48X005 48,xyyy 39 0.130
49
P CRN300 Coronary Heart Disease 1 63 0.129
50
HRW001 Hair Whorl 36 0.129
51
c THR092 Thrombophilia Due to Thrombin Defect 73 0.128
52
ISC004 Ischemia 58 0.128
53
PLL012 Pollen Allergy 46 0.128
54
P LNG064 Lung Cancer Susceptibility 3 78 0.127
55
P SLP006 Sleep Apnea 69 0.127
56
PLM001 Pulmonary Tuberculosis 69 0.126
57
CYS001 Cystic Fibrosis 81 0.125
58
P ASP006 Aspergillosis 69 0.123
59
P INF038 Influenza 68 0.120
60
c ACT075 Acute Myocardial Infarction 57 0.120
61
PLR007 Pleural Empyema 50 0.119
62
HDN002 Head Injury 46 0.119
63
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.118
64
P PLM036 Pulmonary Fibrosis 65 0.118
65
P ATM019 Autoimmune Polyendocrine Syndrome 46 0.118
66
MCL003 Macular Holes 40 0.118
67
STR067 Stroke, Ischemic 81 0.117
68
c ATS007 Autism Spectrum Disorder 67 0.117
69
P ATS364 Autism 70 0.116
70
DCB001 Decubitus Ulcer 61 0.115
71
P DRM053 Dermatitis, Atopic 66 0.113
72
P CTR002 Cataract 60 0.113
73
P BRN022 Bronchiectasis 59 0.113
74
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.112
75
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.111
76
ALL026 Allergic Hypersensitivity Disease 62 0.110
77
c PRC016 Pre-Eclampsia 63 0.107
78
ADN018 Adenoma 59 0.107
79
ALL006 Allergic Asthma 56 0.107
80
P DBT009 Diabetes Mellitus 64 0.106
81
PTH003 Pathologic Nystagmus 52 0.105
82
P HDC001 Headache 57 0.103
83
INT011 Interstitial Emphysema 36 0.103
84
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.101
85
P VSC007 Vascular Disease 63 0.099
86
RSP021 Respiratory Allergy 45 0.099
87
P CNJ013 Conjunctivitis 65 0.098
88
P HYP024 Hypoparathyroidism 56 0.097
89
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.095
90
MSL001 Measles 62 0.094
91
P DRR001 Diarrhea 55 0.094
92
P CLR023 Colorectal Cancer 99 0.092
93
P ATR011 Atrial Fibrillation 66 0.092
94
GST033 Gestational Diabetes 61 0.092
95
CRD223 Cardiac Arrhythmia 60 0.092
96
P INF032 Infertility 57 0.092
97
CYT002 Cytokine Deficiency 42 0.092
98
SPN186 Spinal Cord Injury 60 0.091
99
DYS073 Dysphagia 50 0.091
100
CRP002 Croup 44 0.089
101
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.089
102
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.088
103
ANG054 Angina Pectoris 66 0.088
104
PRT036 Peritonitis 64 0.088
105
P PRD008 Periodontitis 64 0.088
106
CMM005 Common Cold 57 0.088
107
SDD001 Sudden Infant Death Syndrome 61 0.086
108
INT066 Interstitial Lung Disease 60 0.086
109
HRT011 Heart Septal Defect 50 0.086
110
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.084
111
P ADL010 Adult Respiratory Distress Syndrome 65 0.084
112
SKN016 Skin Disease 63 0.084
113
VRC005 Varicose Veins 60 0.084
114
ANR040 Aneurysm 59 0.084
115
SLC006 Silicosis 56 0.084
116
AGN016 Aging 56 0.084
117
P PLM034 Pulmonary Emphysema 55 0.084
118
c INV001 Invasive Aspergillosis 49 0.084
119
P MYC084 Mycobacterium Tuberculosis 1 68 0.083
120
CHR063 Chronic Mucocutaneous Candidiasis 63 0.083
121
c FNC043 Fanconi Anemia, Complementation Group E 62 0.083
122
P SNS001 Sensorineural Hearing Loss 60 0.083
123
BRN012 Bronchiolitis Obliterans 55 0.083
124
HMP005 Hemiplegia 55 0.083
125
ANX010 Anxiety 73 0.081
126
CLF027 Cleft Palate, Isolated 64 0.081
127
CLT003 Colitis 62 0.081
128
EXT034 Extrinsic Allergic Alveolitis 58 0.081
129
ACS001 Acoustic Neuroma 56 0.081
130
P VNS003 Venous Insufficiency 55 0.081
131
P KRT007 Keratoconus 50 0.081
132
ANT018 Anthracosis 48 0.081
133
ANX004 Anoxia 40 0.081
134
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.079
135
APN008 Apnea, Obstructive Sleep 64 0.079
136
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.079
137
LPD008 Lipid Metabolism Disorder 62 0.079
138
c BRN108 Branchiootic Syndrome 1 62 0.079
139
P INF037 Inflammatory Bowel Disease 54 0.079
140
HLX001 Helix Syndrome 47 0.079
141
MLR004 Malaria 81 0.078
142
P BLD134 Bladder Cancer 79 0.078
143
c MGR028 Migraine with or Without Aura 1 67 0.078
144
PRT037 Pertussis 65 0.078
145
LPP008 Lipoprotein Quantitative Trait Locus 62 0.078
146
P SYP003 Syphilis 58 0.078
147
BRN056 Bronchopulmonary Dysplasia 57 0.078
148
P MYP006 Myopia 55 0.078
149
P OTS001 Otosclerosis 49 0.078
150
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.078
151
P KDN018 Kidney Disease 72 0.076
152
P MLT020 Multiple Sclerosis 72 0.076
153
P MYS003 Myasthenia Gravis 68 0.076
154
P DMN002 Dementia 66 0.076
155
DPR016 Depression 63 0.076
156
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.076
157
CHL014 Cholera 59 0.076
158
GST045 Gastroenteritis 59 0.076
159
DSS008 Disease of Mental Health 58 0.076
160
P EXN002 Exanthem 57 0.076
161
ATN005 Autonomic Dysfunction 46 0.076
162
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.074
163
ART016 Aortic Aneurysm 69 0.074
164
RCK004 Rickets 68 0.074
165
HYP056 Hypoglycemia 66 0.074
166
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.074
167
PST028 Post-Traumatic Stress Disorder 58 0.074
168
INT007 Intermediate Coronary Syndrome 55 0.074
169
ACT084 Acute Stress Disorder 47 0.074
170
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.072
171
P SRC025 Sarcoidosis 1 70 0.072
172
DWN001 Down Syndrome 70 0.072
173
P CRD246 Cardiovascular System Disease 57 0.072
174
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.072
175
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.072
176
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.072
177
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.072
178
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.072
179
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.072
180
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.072
181
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.072
182
PPL001 Papillary Adenoma 44 0.072
183
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.072
184
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.072
185
P CRN026 Corneal Edema 43 0.072
186
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 39 0.072
187
HMN044 Human Immunodeficiency Virus Type 1 71 0.070
188
APP008 Appendicitis 61 0.070
189
P VNT002 Ventricular Septal Defect 60 0.070
190
CHL123 Chlamydia 59 0.070
191
NWB001 Newborn Respiratory Distress Syndrome 58 0.070
192
ART140 Arteries, Anomalies of 52 0.070
193
LGN006 Legionnaire Disease 52 0.070
194
TRM010 Traumatic Brain Injury 51 0.070
195
PLC008 Placenta Disease 50 0.070
196
c CHR431 Chronic Venous Insufficiency 49 0.070
197
CHL061 Childhood Leukemia 48 0.070
198
ATS010 Autosomal Recessive Disease 48 0.070
199
AST006 Astigmatism 47 0.070
200
SYN036 Syncope 45 0.070
201
DVR002 Diverticulitis 43 0.070
202
PNM003 Pneumatosis Cystoides Intestinalis 32 0.070
203
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.068
204
P GRF003 Graft-Versus-Host Disease 72 0.068
205
KRT019 Keratitis, Hereditary 65 0.068
206
AVN001 Avian Influenza 59 0.068
207
PPT005 Peptic Ulcer Disease 59 0.068
208
CRD132 Cardiac Conduction Defect 58 0.068
209
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.068
210
P SZR006 Seizure Disorder 56 0.068
211
MTH009 Mouth Disease 56 0.068
212
P GST044 Gastritis 56 0.068
213
P ALP008 Alopecia 54 0.068
214
NRM004 Neuroma 51 0.068
215
CRD137 Cardiogenic Shock 47 0.068
216
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.066
217
P RHM011 Rheumatoid Arthritis 80 0.066
218
P LKM002 Leukemia 68 0.066
219
P HYP098 Hypereosinophilic Syndrome 67 0.066
220
P MCR115 Microvascular Complications of Diabetes 5 66 0.066
221
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.066
222
PHR003 Pharyngitis 57 0.066
223
P PNM006 Pneumoconiosis 56 0.066
224
P LTR001 Lateral Sclerosis 54 0.066
225
c PRD040 Periodontitis, Chronic 53 0.066
226
MTN003 Motion Sickness 53 0.066
227
P CHL066 Cholangitis 51 0.066
228
CHL122 Cholesteatoma of Middle Ear 50 0.066
229
BRN071 Brain Injury 49 0.066
231
ESP021 Esophageal Cancer 90 0.064
232
P LVR013 Liver Disease 68 0.064
233
TXC005 Toxic Shock Syndrome 62 0.064
234
LVR012 Liver Cirrhosis 62 0.064
235
VSL002 Visual Epilepsy 59 0.064
236
CNT047 Contact Dermatitis 58 0.064
237
P PYL005 Pyelonephritis 56 0.064
238
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.064
239
ULC004 Ulcerative Colitis 73 0.062
240
P HYP086 Hypothyroidism 69 0.062
241
P TRN020 Turner Syndrome 67 0.062
242
c RHB024 Rhabdomyosarcoma 2 67 0.062
243
ALC007 Alcohol Dependence 66 0.062
244
CHG001 Chagas Disease 66 0.062
245
P HYD006 Hydrocephalus 66 0.062
246
c HPT003 Hepatitis a 62 0.062
247
MNT002 Mental Depression 58 0.062
248
SML019 Smallpox 56 0.062
249
KRT008 Keratopathy 47 0.062
250
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.062
251
NWC001 Newcastle Disease 45 0.062
252
CHL079 Children's Interstitial Lung Disease 26 0.062
253
c HYP595 Hypertension, Essential 84 0.060
254
P GST053 Gastric Cancer 83 0.060
255
IMM167 Immune Deficiency Disease 78 0.060
256
CRH001 Crohn's Disease 74 0.060
257
c EXD008 Exudative Vitreoretinopathy 1 71 0.060
258
P MJR001 Major Depressive Disorder 68 0.060
259
P NSP012 Nasopharyngeal Carcinoma 66 0.060
260
P MNN013 Meningitis 66 0.060
261
P THY023 Thymoma 65 0.060
262
PLM031 Poliomyelitis 64 0.060
263
P ATR010 Atrial Heart Septal Defect 60 0.060
264
P ALC033 Alcohol Use Disorder 58 0.060
265
EYD002 Eye Disease 58 0.060
266
PRP016 Paraplegia 52 0.060
267
ILS001 Ileus 51 0.060
268
PPL052 Papillomatosis, Confluent and Reticulated 33 0.060
269
ADL002 Adult Syndrome 70 0.057
270
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.057
271
CRB037 Cerebral Palsy 69 0.057
272
P SYS005 Systemic Scleroderma 68 0.057
273
TBC004 Tobacco Addiction 64 0.057
274
c ATM011 Autoimmune Hepatitis 63 0.057
275
P ENC004 Encephalitis 61 0.057
276
P LPS004 Lupus Erythematosus 61 0.057
277
QFV001 Q Fever 60 0.057
278
P URT039 Urticaria 58 0.057
279
BCT022 Bacterial Infectious Disease 56 0.057
280
SYN007 Synovitis 54 0.057
281
CLF001 Cleft Lip 53 0.057
282
P PNC025 Panic Disorder 53 0.057
283
INT071 Intestinal Perforation 51 0.057
284
P ECL001 Eclampsia 50 0.057
285
CYN002 Cyanosis, Transient Neonatal 45 0.057
286
VRL003 Variola Major 42 0.057
287
ATX019 Ataxia with Vitamin E Deficiency 42 0.057
288
PLC002 Plica Syndrome 36 0.057
289
STC004 Stachybotrys Chartarum 34 0.057
290
BRN055 Bronchogenic Cyst 27 0.057
291
P ALZ034 Alzheimer Disease 88 0.055
292
NRL016 Neural Tube Defects 82 0.055
293
c MNN043 Meningioma, Familial 74 0.055
294
LYM133 Lymphoma, Hodgkin, Classic 69 0.055
295
P LKM062 Leukemia, Acute Lymphoblastic 69 0.055
296
GST092 Gastroesophageal Reflux 67 0.055
297
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.055
298
MNN042 Meningioma, Radiation-Induced 62 0.055
299
MDD011 Mood Disorder 62 0.055
300
OST003 Osteonecrosis 61 0.055
301
P KDN017 Kidney Cancer 60 0.055
302
CHC001 Chickenpox 60 0.055
303
P PTN014 Patent Ductus Arteriosus 1 60 0.055
304
c ACT073 Acute Leukemia 58 0.055
305
P UVT001 Uveitis 57 0.055
306
ECH003 Echinococcosis 53 0.055
307
DNT012 Dental Caries 53 0.055
308
P ACT105 Acute Mountain Sickness 52 0.055
309
END086 End Stage Renal Disease 51 0.055
310
P OVR082 Overgrowth Syndrome 50 0.055
311
SPN021 Spinal Meningioma 50 0.055
312
INT010 Intracranial Embolism 48 0.055
313
P VTR007 Vitreoretinopathy 46 0.055
314
SCR001 Secretory Meningioma 41 0.055
315
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.055
316
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.055
317
CRV035 Cervical Cancer 76 0.052
318
c HYP836 Hypercholesterolemia, Familial, 1 73 0.052
319
DFC004 Deficiency Anemia 70 0.052
320
c CHR684 Chronic Kidney Disease 70 0.052
321
P MLN008 Melanoma 69 0.052
322
P MSC005 Muscular Dystrophy 66 0.052
323
c SML038 Small Cell Cancer of the Lung 65 0.052
324
GT001 Gout 64 0.052
325
P VSC011 Vasculitis 62 0.052
326
P ENC018 Encephalopathy 61 0.052
327
P SCL018 Scoliosis 60 0.052
328
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.052
329
P SLP005 Sleep Disorder 59 0.052
330
ANT024 Anthrax Disease 58 0.052
331
IRN002 Iron Metabolism Disease 57 0.052
332
HST011 Histoplasmosis 55 0.052
333
P GRV001 Graves' Disease 55 0.052
334
P END047 Endophthalmitis 53 0.052
335
KRT006 Keratoconjunctivitis 53 0.052
336
P RCT021 Rectum Cancer 52 0.052
337
c THY107 Thymoma, Familial 52 0.052
338
RSP006 Respiratory System Disease 50 0.052
339
FSC004 Fasciitis 50 0.052
340
MLT006 Multidrug-Resistant Tuberculosis 48 0.052
341
CRD001 Cardiac Tamponade 47 0.052
342
P BNG032 Benign Mesothelioma 46 0.052
343
PLR022 Pleural Disease 45 0.052
344
BCK006 Back Pain 42 0.052
345
MLT001 Multiple Chemical Sensitivity 40 0.052
346
SRF006 Surfactant Dysfunction 35 0.052
347
PST092 Posttransplant Acute Limbic Encephalitis 29 0.052
348
P HPT023 Hepatocellular Carcinoma 100 0.050
349
P BRS047 Breast Cancer 97 0.050
350
c SYS001 Systemic Lupus Erythematosus 86 0.050
351
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.050
352
LPT014 Leptin Deficiency or Dysfunction 74 0.050
353
P AMY004 Amyloidosis 70 0.050
354
P TTR001 Tetralogy of Fallot 70 0.050
355
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.050
356
TTN003 Tetanus 65 0.050
357
P ART005 Arteriovenous Malformation 65 0.050
358
IRR002 Irritable Bowel Syndrome 65 0.050
359
NRM005 Neuromuscular Disease 64 0.050
360
PLG002 Plague 63 0.050
361
FTT001 Fatty Liver Disease 61 0.050
362
c PNS012 Paine Syndrome 61 0.050
363
P HMN010 Hemangioma 61 0.050
364
NRL005 Neurilemmoma 60 0.050
365
P DNG005 Dengue Virus 59 0.050
366
P INT070 Intestinal Obstruction 58 0.050
367
P MMP001 Mumps 58 0.050
368
P BPL003 Bipolar Disorder 56 0.050
369
MCS002 Mucositis 56 0.050
370
P SBS003 Substance Abuse 55 0.050
371
P SLM003 Salmonellosis 55 0.050
372
BRN014 Bronchopneumonia 54 0.050
373
P TRM003 Tremor 54 0.050
374
CRY001 Cryptogenic Organizing Pneumonia 53 0.050
375
GST023 Gastric Ulcer 53 0.050
376
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.050
377
P SML001 Small Cell Carcinoma 52 0.050
378
NRT004 Neuritis 52 0.050
379
P DDN001 Duodenal Ulcer 52 0.050
380
P TRT010 Teratoma 52 0.050
381
DFN245 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct 51 0.050
382
P SCK005 Sickle Cell Disease 50 0.050
383
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.050
384
DMP001 Dumping Syndrome 44 0.050
385
HMP009 Haemophilus Influenzae 43 0.050
386
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.050
387
c MJR024 Major Affective Disorder 9 41 0.050
388
c MJR022 Major Affective Disorder 8 38 0.050
389
HRN029 Hearing Loss, Noise-Induced 37 0.050
390
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.050
391
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.050
392
c LKM061 Leukemia, Acute Myeloid 84 0.047
393
BRN028 Brain Cancer 74 0.047
394
MSC157 Muscular Dystrophy, Duchenne Type 72 0.047
395
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.047
396
PRP027 Peripheral Vascular Disease 71 0.047
397
P ART022 Arthritis 69 0.047
398
LYM007 Lymphangioleiomyomatosis 69 0.047
399
P SKN015 Skin Carcinoma 66 0.047
400
P NTR004 Neutropenia 63 0.047
401
HSH003 Hashimoto Thyroiditis 62 0.047
402
P DRM010 Dermatomyositis 61 0.047
403
YLL002 Yellow Fever 61 0.047
404
HRP004 Herpes Zoster 60 0.047
405
c ACT027 Acute Pancreatitis 60 0.047
406
P ALP009 Alopecia Areata 60 0.047
407
STT001 Status Epilepticus 60 0.047
408
P RBL001 Rubella 59 0.047
409
IDP011 Idiopathic Interstitial Pneumonia 59 0.047
410
c DNG003 Dengue Disease 59 0.047
411
CCC001 Coccidioidomycosis 58 0.047
412
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.047
413
CNS004 Constipation 58 0.047
414
LYM027 Lymphopenia 58 0.047
415
CHK001 Chikungunya 57 0.047
416
APH002 Aphasia 57 0.047
417
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.047
418
P ART021 Arteriosclerosis 54 0.047
419
PPL022 Papilloma 54 0.047
420
FNG017 Fungal Infectious Disease 53 0.047
421
P THY032 Thyroiditis 52 0.047
422
ENT011 Enterocolitis 51 0.047
423
LNG031 Lung Benign Neoplasm 51 0.047
424
ACH005 Achalasia 51 0.047
425
BLL004 Bullous Keratopathy 49 0.047
426
QDR001 Quadriplegia 48 0.047
427
BNR002 Bone Resorption Disease 48 0.047
428
CLN019 Colonic Disease 47 0.047
429
RFR003 Refractive Error 43 0.047
430
MDD018 Middle East Respiratory Syndrome 43 0.047
431
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.047
432
VTR003 Vitreous Detachment 39 0.047
434
VST001 Vestibular Neuronitis 34 0.047
435
LRY004 Laryngotracheitis 31 0.047
436
c NRF023 Neurofibromatosis, Type Ii 80 0.044
437
OST012 Osteoarthritis 78 0.044
438
P OST002 Osteoporosis 74 0.044
439
P CNR004 Cone-Rod Dystrophy 2 73 0.044
440
P MYP004 Myopathy 70 0.044
441
P LYM118 Lymphoma 68 0.044
442
P THR014 Thrombocytopenia 67 0.044
443
LPT001 Leptospirosis 66 0.044
444
c MCR129 Microvascular Complications of Diabetes 1 66 0.044
445
c DBT099 Diabetes Mellitus, Type I 65 0.044
446
ART002 Arts Syndrome 64 0.044
447
TRN015 Transient Cerebral Ischemia 63 0.044
448
P ECT006 Ectodermal Dysplasia 62 0.044
449
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.044
450
HYP066 Hyperglycemia 61 0.044
451
c SCL052 Scleroderma, Familial Progressive 61 0.044
452
P MYL006 Myeloid Leukemia 60 0.044
453
DPH001 Diphtheria 60 0.044
454
SQM006 Squamous Cell Carcinoma 60 0.044
455
P MCR010 Microcephaly 59 0.044
456
PNM001 Pneumocystosis 59 0.044
457
THY029 Thyroid Carcinoma 59 0.044
458
GNG013 Gingivitis 59 0.044
459
CRY005 Cryptococcosis 58 0.044
460
RBS001 Rabies 58 0.044
461
LNG108 Langerhans Cell Histiocytosis 58 0.044
462
MNR012 Meniere Disease 57 0.044
463
VSC002 Vascular Dementia 57 0.044
464
SCH014 Schistosomiasis 57 0.044
465
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.044
466
P NRP001 Neuropathy 56 0.044
467
GST050 Gastrointestinal System Disease 56 0.044
468
P MLN007 Male Infertility 55 0.044
469
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.044
470
P LRY044 Larynx Cancer 55 0.044
471
AMN003 Amnestic Disorder 54 0.044
472
GSG001 Gas Gangrene 53 0.044
473
INT075 Intracranial Hypertension 53 0.044
474
EXP004 Exophthalmos 52 0.044
475
c VRL010 Viral Hepatitis 52 0.044
476
LNG095 Lung Abscess 51 0.044
477
P MTR003 Mitral Valve Stenosis 50 0.044
478
MTB004 Metabolic Acidosis 50 0.044
479
HST010 Histiocytosis 48 0.044
480
NCR007 Necrotizing Fasciitis 48 0.044
481
ASP007 Aspiration Pneumonia 48 0.044
482
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.044
483
PLC007 Placental Abruption 48 0.044
484
SQM002 Squamous Cell Papilloma 46 0.044
485
SPS057 Spasticity 45 0.044
486
P CHR345 Chronic Pain 44 0.044
487
FCH001 Fuchs' Endothelial Dystrophy 44 0.044
488
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.044
489
PRS063 Paresthesia 41 0.044
490
c MCR112 Microvascular Complications of Diabetes 2 41 0.044
491
SPR126 Superior Semicircular Canal Dehiscence 40 0.044
492
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.044
493
SYN063 Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction 35 0.044
495
P PRK057 Parkinson Disease, Late-Onset 78 0.041
496
P EPL164 Epilepsy 71 0.041
497
P PRM011 Primary Ciliary Dyskinesia 69 0.041
498
LNG039 Lung Squamous Cell Carcinoma 66 0.041
499
BRC012 Brucellosis 64 0.041
500
P HYP069 Hyperparathyroidism 63 0.041
501
HYP780 Hypoadrenocorticism, Familial 63 0.041
502
NTR005 Nutritional Deficiency Disease 62 0.041
503
ACQ007 Acquired Immunodeficiency Syndrome 60 0.041
504
P MYC008 Myocarditis 59 0.041
505
PRN019 Perinatal Necrotizing Enterocolitis 59 0.041
506
P ANP001 Anaplastic Large Cell Lymphoma 58 0.041
507
P BCL017 B-Cell Lymphoma 58 0.041
508
TNS005 Tonsillitis 57 0.041
509
MCR141 Mucormycosis 56 0.041
510
PRP030 Purpura 54 0.041
511
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.041
512
PRS045 Prostatic Hypertrophy 53 0.041
513
PLM012 Pulmonary Sarcoidosis 53 0.041
514
PRP080 Peripheral Artery Disease 53 0.041
515
P INT068 Intestinal Disease 53 0.041
516
TLN003 Telangiectasis 52 0.041
517
SPN051 Spondylitis 51 0.041
518
P THR015 Thrombophilia 51 0.041
519
P HYP040 Hypospadias 51 0.041
520
c HRD202 Hereditary Lymphedema I 50 0.041
521
ENT004 Enthesopathy 49 0.041
522
P CMP008 Compartment Syndrome 49 0.041
523
HRN026 Hernia, Hiatus 47 0.041
524
ASB001 Asbestosis 47 0.041
525
CLF056 Cleft Lip with or Without Cleft Palate 47 0.041
526
c PRM093 Premature Ovarian Failure 7 47 0.041
527
MDS022 Mediastinitis 46 0.041
528
FCL012 Facial Paralysis 46 0.041
529
MST019 Mastoiditis 43 0.041
530
RST023 Resting Heart Rate, Variation in 41 0.041
531
TRC005 Tracheal Stenosis 38 0.041
532
HMP003 Hemopneumothorax 33 0.041
533
SCL017 Sclerosing Hemangioma 32 0.041
534
INF009 Inflammatory Spondylopathy 31 0.041
535
PLY150 Polykaryocytosis Inducer 31 0.041
537
BNG077 Benign Idiopathic Neonatal Seizures 26 0.041
538
MTH071 Methane Production 26 0.041
539
ASB003 Asbestos Intoxication 26 0.041
540
SDD004 Sudden Arrhythmia Death Syndrome 22 0.041
541
DYS013 Dysbaric Osteonecrosis 20 0.041
542
P PNC035 Pancreatic Cancer 84 0.037
543
END057 Endometrial Cancer 74 0.037
544
P SCH015 Schizophrenia 74 0.037
545
c SPN225 Spondyloarthropathy 1 73 0.037
546
P RTN024 Retinoblastoma 73 0.037
547
c HPT073 Hepatitis C Virus 72 0.037
548
P CRN037 Craniosynostosis 68 0.037
549
CNN005 Connective Tissue Disease 68 0.037
550
P HPT021 Hepatitis 67 0.037
551
OST159 Osteogenic Sarcoma 66 0.037
552
P HRP006 Herpes Simplex 65 0.037
553
P PRS038 Personality Disorder 65 0.037
554
KWS002 Kawasaki Disease 65 0.037
555
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.037
556
c JVN010 Juvenile Rheumatoid Arthritis 64 0.037
557
OST017 Osteomyelitis 64 0.037
558
ANR007 Anorexia Nervosa 63 0.037
559
PSR001 Psoriatic Arthritis 61 0.037
560
LGN002 Legionellosis 60 0.037
561
c JVN061 Juvenile Arthritis 60 0.037
562
RHM001 Rheumatic Fever 60 0.037
563
ETN001 Eating Disorder 60 0.037
564
c ACT071 Acute Kidney Failure 60 0.037
565
ALP097 Alopecia Universalis Congenita 59 0.037
566
c DWL002 Dowling-Degos Disease 1 58 0.037
567
c CHR417 Chronic Graft Versus Host Disease 57 0.037
568
P PLY041 Polymyositis 57 0.037
569
P END033 Endocarditis 57 0.037
570
P ANG015 Angioedema 57 0.037
571
P PLY018 Polycythemia 56 0.037
572
MCL006 Macular Retinal Edema 55 0.037
573
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.037
574
CLL003 Cellulitis 54 0.037
575
GTR002 Goiter 53 0.037
576
c FML008 Familial Retinoblastoma 53 0.037
577
P LRY019 Laryngitis 52 0.037
578
IMP005 Impotence 52 0.037
579
ART074 Aortic Dissection 52 0.037
580
PRS021 Prostatic Adenoma 51 0.037
581
FDL002 Food Allergy 51 0.037
582
MYL001 Myelitis 51 0.037
583
MYL020 Myelomeningocele 51 0.037
584
c SCN007 Secondary Hyperparathyroidism 51 0.037
585
BLP005 Blepharitis 50 0.037
586
P ESN008 Eosinophilic Pneumonia 50 0.037
587
NTR046 Neutrophil Migration 50 0.037
588
c LRG001 Large Cell Carcinoma 50 0.037
589
VLV047 Volvulus of Midgut 49 0.037
590
PRS129 Prostatic Hyperplasia, Benign 49 0.037
591
SPT005 Spotted Fever 49 0.037
592
EBL001 Ebola Hemorrhagic Fever 49 0.037
593
c BCT013 Bacterial Pneumonia 48 0.037
594
MDD010 Middle Ear Disease 48 0.037
595
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 47 0.037
596
P RTN014 Retinal Artery Occlusion 47 0.037
597
RTN020 Retinal Vascular Disease 46 0.037
598
CHD004 Chudley-Mccullough Syndrome 46 0.037
599
P HMR005 Hemorrhoid 46 0.037
600
SWN001 Swine Influenza 45 0.037
601
GRN017 Granulocytopenia 44 0.037
602
SDD008 Sudden Sensorineural Hearing Loss 43 0.037
603
DNT001 Dental Fluorosis 43 0.037
604
BRN026 Branch Retinal Artery Occlusion 40 0.037
605
CRB086 Cerebral Aneurysms 40 0.037
606
RTN002 Retinal Perforation 38 0.037
607
TRC026 Tracheal Disease 38 0.037
608
VSM001 Vasomotor Rhinitis 38 0.037
609
STL001 St. Louis Encephalitis 37 0.037
610
PLM016 Pleomorphic Carcinoma 36 0.037
611
P MTP001 Metaphyseal Dysplasia 36 0.037
612
ARG004 Argyria 27 0.037
613
MNT308 Mental Retardation with Optic Atrophy, Deafness, and Seizures 27 0.037
614
c LNG109 Lung Cancer Susceptibility 1 27 0.037
615
STN013 Stenotrophomonas Maltophilia Infection 25 0.037
616
LRY028 Laryngocele 22 0.037
617
LKC011 Leukocyte Antigen Group Five 9 0.037
618
P PRS040 Prostate Cancer 97 0.033
619
P MDL005 Medulloblastoma 77 0.033
620
PHN003 Phenylketonuria 75 0.033
621
c HMC039 Hemochromatosis, Type 1 74 0.033
622
P LPR021 Leprosy 3 69 0.033
623
CHL065 Cholangiocarcinoma 68 0.033
624
SKN019 Skin Melanoma 68 0.033
625
OMN001 Omenn Syndrome 67 0.033
626
P CLC063 Celiac Disease 1 66 0.033
627
P NRV007 Nervous System Disease 66 0.033
628
LYM017 Lyme Disease 64 0.033
629
P HML002 Hemolytic Anemia 63 0.033
630
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.033
631
TYP007 Typhoid Fever 63 0.033
632
c ACT068 Acute Cystitis 63 0.033
633
P PSR002 Psoriasis 62 0.033
634
P ESP024 Esophagitis 62 0.033
635
P PNC044 Pancreatitis 61 0.033
636
P SJG008 Sjogren Syndrome 61 0.033
637
ORL011 Oral Cancer 60 0.033
638
ING001 Inguinal Hernia 60 0.033
639
c HPT016 Hepatitis B 59 0.033
640
P CYS018 Cystitis 59 0.033
641
HLC007 Helicobacter Pylori Infection 59 0.033
642
CHL067 Cholecystitis 57 0.033
643
P MYS005 Myositis 56 0.033
644
ALL010 Allergic Contact Dermatitis 56 0.033
645
HMG005 Hemoglobinopathy 56 0.033
646
BRN004 Brain Edema 56 0.033
647
P PLY019 Polyneuropathy 56 0.033
648
ATR057 Atrioventricular Block 55 0.033
649
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.033
650
CHR100 Chronic Ulcer of Skin 55 0.033
651
P STR020 Strabismus 55 0.033
652
BRN015 Bronchiolo-Alveolar Adenocarcinoma 54 0.033
653
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.033
654
HMS001 Hemosiderosis 54 0.033
655
P LCT002 Lactose Intolerance 53 0.033
656
P TCD001 Tic Disorder 53 0.033
657
P INS002 in Situ Carcinoma 53 0.033
658
BRN038 Bronchial Disease 53 0.033
659
OCL006 Ocular Hypertension 53 0.033
660
HMC014 Homocysteinemia 53 0.033
661
PRN011 Pernicious Anemia 53 0.033
662
c CNT035 Central Nervous System Disease 52 0.033
663
PST011 Pustulosis of Palm and Sole 52 0.033
664
FML037 Female Breast Cancer 52 0.033
665
c VRL005 Viral Pneumonia 52 0.033
667
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.033
668
c PNC106 Pancreatic Agenesis 1 51 0.033
669
THR016 Thrombophlebitis 51 0.033
670
INT079 Intrahepatic Cholangiocarcinoma 51 0.033
671
HND002 Hand, Foot and Mouth Disease 51 0.033
672
P AST007 Astrocytoma 51 0.033
673
BHR001 Behr Syndrome 51 0.033
674
PLR008 Pleurisy 50 0.033
675
STT002 Status Asthmaticus 50 0.033
676
IRR003 Irritant Dermatitis 49 0.033
677
P OPN001 Open-Angle Glaucoma 49 0.033
678
CHL004 Cholelithiasis 49 0.033
679
PNC034 Pancreas Disease 48 0.033
680
HMP001 Hemopericardium 48 0.033
681
c MTR002 Mitral Valve Insufficiency 48 0.033
682
DRY001 Dry Eye Syndrome 47 0.033
683
PRC003 Proctitis 47 0.033
684
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.033
685
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.033
686
TST014 Testicular Cancer 46 0.033
687
SPN020 Spondylosis 46 0.033
688
PLC001 Placenta Accreta 46 0.033
689
EPD015 Epidemic Typhus 45 0.033
690
SBC016 Subacute Delirium 44 0.033
691
c CNT028 Central Retinal Artery Occlusion 43 0.033
692
MCR103 Microtia 43 0.033
693
TRC097 Tracheomalacia 42 0.033
694
MCH006 Mechanical Strabismus 42 0.033
695
PLC009 Placenta Praevia 39 0.033
696
PLM052 Pulmonary Arteriovenous Malformation 39 0.033
697
c ACT004 Acute Diarrhea 39 0.033
698
MCK029 Meckel Diverticulum 38 0.033
699
SPL006 Splenic Infarction 38 0.033
700
CRT012 Cortical Blindness 37 0.033
701
FRN014 Fournier Gangrene 37 0.033
702
PNB004 Panbronchiolitis, Diffuse 37 0.033
703
c PRM340 Primary Adrenal Insufficiency 36 0.033
704
CHR178 Chromosomal Triplication 35 0.033
705
HNS001 Hansen's Disease 34 0.033
706
PLM151 Pulmonary Arteriovenous Fistulas 34 0.033
707
PLM028 Pulmonary Coin Lesion 33 0.033
708
RSP007 Respiratory Distress Syndrome, Infant 30 0.033
709
ADH006 Adhesive Otitis Media 29 0.033
710
P ATM076 Autoimmune Retinopathy 27 0.033
711
PRL021 Perilymphatic Fistula 22 0.033
712
CGH002 Cough Headache 21 0.033
713
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.033
714
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.029
715
P OVR042 Ovarian Cancer 88 0.029
716
P LKM071 Leukemia, Chronic Lymphocytic 79 0.029
717
PFF001 Pfeiffer Syndrome 79 0.029
718
INS024 Insulin-Like Growth Factor I 79 0.029
719
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.029
720
c ATR087 Atrial Standstill 1 75 0.029
721
c LKM063 Leukemia, Chronic Myeloid 72 0.029
722
ACR008 Acrocallosal Syndrome 69 0.029
723
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.029
724
PSY004 Psychotic Disorder 67 0.029
725
P DYS154 Dystonia 65 0.029
726
PPL049 Papillon-Lefevre Syndrome 65 0.029
727
P MTR014 Motor Neuron Disease 65 0.029
728
DGR001 Digeorge Syndrome 64 0.029
729
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.029
730
c DPH024 Diaphragmatic Hernia, Congenital 63 0.029
731
LSH001 Leishmaniasis 63 0.029
732
BRT002 Birt-Hogg-Dube Syndrome 63 0.029
733
P HYP055 Hypoplastic Left Heart Syndrome 63 0.029
734
c GLC092 Glaucoma, Primary Open Angle 62 0.029
735
P HYP750 Hypertriglyceridemia, Familial 62 0.029
736
BLL006 Bullous Pemphigoid 62 0.029
737
P ART023 Arthropathy 62 0.029
738
P PRP029 Porphyria 62 0.029
739
ESP020 Esophageal Atresia 62 0.029
740
CHL068 Cholestasis 61 0.029
741
ALV005 Alveolar Soft Part Sarcoma 61 0.029
742
SHG001 Shigellosis 60 0.029
743
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.029
744
P TXP001 Toxoplasmosis 60 0.029
745
DNG002 Dengue Hemorrhagic Fever 60 0.029
746
c HRD002 Hereditary Angioedema 60 0.029
747
P BND020 Bone Disease 59 0.029
748
c LTN004 Late-Onset Retinal Degeneration 59 0.029
749
P PRP019 Peripheral Nervous System Disease 58 0.029
750
P GLM007 Glomerulonephritis 57 0.029
751
P PLV020 Pelvic Organ Prolapse 57 0.029
752
c CHL119 Cholangitis, Primary Sclerosing 57 0.029
753
LYM021 Lymphadenitis 57 0.029
754
c MST023 Mesothelioma, Malignant 57 0.029
755
BRT005 Barth Syndrome 57 0.029
756
P FBR017 Fibrosarcoma 56 0.029
757
PLS011 Plasmacytoma 56 0.029
758
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.029
759
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.029
760
P NRF002 Neurofibromatosis 56 0.029
761
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.029
762
AMB001 Amebiasis 55 0.029
763
c BCT007 Bacterial Meningitis 55 0.029
764
P HYP076 Hyperthyroidism 55 0.029
765
END040 Endogenous Depression 55 0.029
766
CLF004 Cleft Lip/palate 54 0.029
767
GNT003 Genital Herpes 54 0.029
768
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.029
769
P PMP001 Pemphigus 54 0.029
770
GLC003 Glucose Intolerance 54 0.029
771
CRY003 Cryptosporidiosis 54 0.029
772
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.029
773
NNL006 Non-Alcoholic Steatohepatitis 54 0.029
774
MMM001 Mammary Paget's Disease 53 0.029
775
RHM028 Rheumatic Heart Disease 53 0.029
776
CRH005 Crohn's Colitis 53 0.029
777
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.029
778
CYS005 Cysticercosis 53 0.029
779
P HML001 Hemolytic-Uremic Syndrome 53 0.029
780
INF034 Infective Endocarditis 53 0.029
781
NRT001 Neurotic Disorder 53 0.029
782
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 53 0.029
783
c HPT007 Hepatitis E 53 0.029
784
c GLL024 Gallbladder Disease 1 53 0.029
785
DRM011 Dermatophytosis 52 0.029
786
DYS015 Dysentery 52 0.029
787
THY030 Thyroid Gland Disease 52 0.029
788
P MSC003 Muscular Atrophy 52 0.029
789
BWN001 Bowen-Conradi Syndrome 52 0.029
790
c ACT135 Acute Graft Versus Host Disease 52 0.029
791
LMY002 Leiomyoma 52 0.029
792
P HMP007 Hemophilia 51 0.029
793
KRT009 Keratosis 51 0.029
794
P LCT001 Lactic Acidosis 51 0.029
795
CYS014 Cystadenocarcinoma 51 0.029
796
BLL003 Bell's Palsy 51 0.029
797
ALL009 Allergic Conjunctivitis 50 0.029
798
PST021 Postpartum Depression 50 0.029
799
HNT002 Hantavirus Pulmonary Syndrome 50 0.029
800
BLS002 Blastomycosis 50 0.029
801
P CRN025 Corneal Dystrophy 49 0.029
802
HYP006 Hypertensive Heart Disease 49 0.029
803
MYC012 Mycetoma 49 0.029
804
PLM041 Pulmonary Valve Stenosis 49 0.029
805
DYS009 Dysthymic Disorder 49 0.029
806
MNN009 Meningoencephalitis 49 0.029
807
ACT029 Acute Interstitial Pneumonia 49 0.029
808
URM002 Uremia 49 0.029
809
ADT003 Auditory System Disease 48 0.029
810
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.029
811
RGH001 Right Bundle Branch Block 48 0.029
812
BLD044 Bladder Disease 48 0.029
813
P CRN028 Corneal Ulcer 47 0.029
814
KRT002 Keratomalacia 47 0.029
815
HYP082 Hypopharynx Cancer 47 0.029
816
NSS002 Neisseria Meningitidis Infection 47 0.029
817
ASP004 Asphyxia Neonatorum 46 0.029
818
c CHR048 Chronic Rhinitis 46 0.029
819
CLN045 Colonic Benign Neoplasm 46 0.029
820
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.029
821
RCT017 Rectal Disease 46 0.029
822
ANR004 Anuria 46 0.029
823
P TRN034 Transverse Myelitis 45 0.029
824
IMM003 Immunoglobulin Alpha Deficiency 45 0.029
825
c CNT015 Central Sleep Apnea 45 0.029
826
P DCR003 Dacryoadenitis 45 0.029
827
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.029
828
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.029
829
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 44 0.029
830
c PCH010 Pachyonychia Congenita 3 44 0.029
831
GNG003 Gingival Recession 44 0.029
832
PRT035 Peritoneum Cancer 44 0.029
833
c PRM038 Primary Agammaglobulinemia 44 0.029
834
P MYG005 Myoglobinuria 44 0.029
835
CRB090 Cerebral Hypoxia 44 0.029
836
P DMY001 Demyelinating Polyneuropathy 43 0.029
837
PHY002 Physical Disorder 42 0.029
838
c ADN012 Adenocarcinoma in Situ 42 0.029
839
c MLG079 Malignant Pleural Mesothelioma 42 0.029
840
ARC002 Arachnoiditis 42 0.029
841
LCN001 Lice Infestation 42 0.029
842
P CHR342 Chiari Malformation 41 0.029
843
P KLZ004 Kala-Azar 1 41 0.029
844
PCD001 Pica Disease 41 0.029
845
VST004 Vestibular Disease 41 0.029
846
CRN322 Coronavirus Infectious Disease 40 0.029
847
FNG016 Fungal Keratitis 40 0.029
848
SCR015 Scarlet Fever 39 0.029
849
ENT001 Enterocele 39 0.029
850
ORN001 Ornithosis 38 0.029
851
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.029
852
TNC002 Tinea Capitis 38 0.029
853
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.029
854
OST160 Osteoid Osteoma 37 0.029
855
PRR004 Preretinal Fibrosis 37 0.029
856
P CRN233 Corneal Dystrophy, Fuchs Endothelial, 1 37 0.029
857
TRC020 Tracheitis 36 0.029
858
SPN354 Spinal Arachnoiditis 36 0.029
859
EPD005 Epidural Abscess 35 0.029
860
ATR003 Atrophic Rhinitis 35 0.029
861
KRN001 Korean Hemorrhagic Fever 35 0.029
862
PRM329 Premature Aging 35 0.029
863
INT040 Intrinsic Asthma 34 0.029
864
DDN009 Duodenal Obstruction 34 0.029
865
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.029
866
HND015 Hand Skill, Relative 33 0.029
867
BWN006 Bowen's Disease 32 0.029
868
c ATM098 Autoimmune Peripheral Neuropathy 32 0.029
869
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.029
870
GST007 Gastric Dilatation 31 0.029
871
MTR001 Mature Cataract 28 0.029
872
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.029
873
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.029
874
SHR097 Short Tarsus with Absence of Lower Eyelashes 26 0.029
875
NCR014 Necrotizing Soft Tissue Infection 23 0.029
876
INF043 Infantile Apnea 22 0.029
877
CHL076 Chilaiditi Syndrome 19 0.029
878
SMC003 Semicircular Canal Dehiscence Syndrome 19 0.029
879
MYL069 Myeloma, Multiple 85 0.023
880
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.023
881
KPS004 Kaposi Sarcoma 75 0.023
882
c ART115 Aortic Valve Disease 1 75 0.023
883
P APL001 Aplastic Anemia 74 0.023
884
SCK003 Sickle Cell Anemia 74 0.023
885
c BTT014 Beta-Thalassemia 74 0.023
886
SVR004 Severe Combined Immunodeficiency 73 0.023
887
P NRB001 Neuroblastoma 72 0.023
888
ACR007 Acromegaly 71 0.023
889
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.023
890
P BRG001 Brugada Syndrome 71 0.023
891
APR006 Apert Syndrome 70 0.023
892
ADN011 Adenoid Cystic Carcinoma 70 0.023
893
P HYP061 Hypertrophic Cardiomyopathy 70 0.023
894
P OCL013 Oculodentodigital Dysplasia 69 0.023
895
c BSL007 Basal Cell Carcinoma 68 0.023
896
MLD001 Melioidosis 68 0.023
897
P FRN006 Frontotemporal Dementia 68 0.023
898
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.023
899
c INF071 Inflammatory Bowel Disease 1 67 0.023
900
P FLL037 Follicular Lymphoma 67 0.023
901
WLF001 Wolff-Parkinson-White Syndrome 66 0.023
902
GLL008 Gilles De La Tourette Syndrome 66 0.023
903
KHL003 Kohlschutter-Tonz Syndrome 65 0.023
904
SRC014 Sarcoma 65 0.023
905
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.023
906
MSC007 Muscle Hypertrophy 64 0.023
907
KRN002 Kearns-Sayre Syndrome 63 0.023
908
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.023
909
P MVM001 Movement Disease 63 0.023
910
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.023
911
HMT002 Hematologic Cancer 62 0.023
912
P SPN046 Spinal Muscular Atrophy 62 0.023
913
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.023
914
WHM001 Whim Syndrome 61 0.023
915
RCT015 Reactive Arthritis 61 0.023
916
c LPM012 Lipomatosis, Multiple 60 0.023
917
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.023
918
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.023
919
P THL005 Thalassemia 60 0.023
920
P OPT006 Optic Nerve Disease 60 0.023
921
PRT013 Portal Hypertension 59 0.023
922
IRN001 Iron Deficiency Anemia 59 0.023
923
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.023
924
P PLY006 Polydactyly 59 0.023
925
ALK013 Alkaptonuria 58 0.023
926
P PGT001 Paget's Disease of Bone 58 0.023
927
SPR004 Supravalvular Aortic Stenosis 58 0.023
928
P MTR012 Mitral Valve Disease 58 0.023
929
CHL028 Childhood Type Dermatomyositis 58 0.023
930
PMP006 Pemphigus Vulgaris, Familial 57 0.023
931
GLS018 Glass Syndrome 57 0.023
932
c VSC019 Vesicoureteral Reflux 1 57 0.023
933
P MYM013 Moyamoya Disease 1 57 0.023
934
TRP006 Tarp Syndrome 57 0.023
935
AYM001 Ayme-Gripp Syndrome 57 0.023
936
c ACT134 Acute Liver Failure 56 0.023
937
c INT072 Intestinal Pseudo-Obstruction 56 0.023
938
GNR004 Generalized Anxiety Disorder 56 0.023
939
PRS047 Prostatitis 56 0.023
940
CYS008 Cystic Echinococcosis 56 0.023
941
MCN007 Meconium Aspiration Syndrome 55 0.023
942
NRN004 Neuroendocrine Tumor 55 0.023
943
P SCK002 Sick Sinus Syndrome 55 0.023
944
NRG002 Neurogenic Bladder 55 0.023
945
DFF005 Diffuse Large B-Cell Lymphoma 55 0.023
946
ACT058 Active Peptic Ulcer Disease 55 0.023
947
P DBT005 Diabetes Insipidus 55 0.023
948
MNN032 Meningococcal Meningitis 54 0.023
949
PRT082 Preterm Premature Rupture of the Membranes 54 0.023
950
VGN023 Vaginitis 54 0.023
951
RFL001 Reflex Sympathetic Dystrophy 54 0.023
952
RLP001 Relapsing Polychondritis 54 0.023
953
PRC013 Pericarditis 54 0.023
954
AMN001 Amenorrhea 54 0.023
955
c CNG021 Congenital Toxoplasmosis 54 0.023
956
WST005 West Nile Virus 54 0.023
957
GST009 Gastroschisis 53 0.023
958
TRC023 Trichinosis 53 0.023
959
P MNC007 Monocytic Leukemia 53 0.023
960
BCT002 Bacterial Vaginosis 53 0.023
961
NVS001 Neovascular Glaucoma 53 0.023
962
MST005 Mastitis 53 0.023
963
P SHR001 Short Bowel Syndrome 53 0.023
964
P PTS002 Ptosis 53 0.023
965
SPN035 Spindle Cell Sarcoma 53 0.023
966
P ACT008 Actinic Keratosis 53 0.023
967
IRD001 Iridocyclitis 53 0.023
968
P RTN022 Retinal Vein Occlusion 53 0.023
969
MCN017 Meconium Ileus 52 0.023
970
PLS007 Plasmodium Falciparum Malaria 52 0.023
971
MRG003 Marginal Zone B-Cell Lymphoma 52 0.023
972
CRT016 Carotid Artery Disease 52 0.023
973
P MGR003 Migraine with Aura 52 0.023
974
NTR018 Neutrophilia, Hereditary 52 0.023
975
SPS003 Spastic Diplegia 51 0.023
976
P SPP010 Suppressor of Tumorigenicity 3 51 0.023
977
AVD001 Avoidant Personality Disorder 51 0.023
978
CND002 Conduct Disorder 51 0.023
979
ACT049 Acute Disseminated Encephalomyelitis 51 0.023
980
CCC002 Coccidiosis 51 0.023
981
P PRC012 Pericardial Effusion 51 0.023
982
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.023
983
c ALM001 Al Amyloidosis 50 0.023
984
P HYP077 Hypertrichosis 50 0.023
985
SCB001 Scabies 50 0.023
986
BRX001 Bruxism 50 0.023
987
CRT013 Carotid Stenosis 50 0.023
988
PLM017 Pulmonary Alveolar Microlithiasis 50 0.023
989
PRT018 Portal Vein Thrombosis 50 0.023
990
ECT026 Ectopic Pregnancy 50 0.023
991
P OBS001 Obstructive Jaundice 50 0.023
992
BLR001 Biliary Atresia 50 0.023
993
TRP002 Tropical Spastic Paraparesis 50 0.023
994
P ATR005 Atrophic Gastritis 50 0.023
995
c DYS119 Dystonia 9 50 0.023
996
KRT001 Keratoconjunctivitis Sicca 49 0.023
997
CHN065 Choanal Atresia, Posterior 49 0.023
998
IMP004 Impetigo 49 0.023
999
P RCR004 Recurrent Respiratory Papillomatosis 49 0.023
1000
VCC001 Vaccinia 49 0.023
1001
MLR002 Miliary Tuberculosis 49 0.023
1002
INT017 Intestinal Schistosomiasis 48 0.023
1003
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 48 0.023
1004
SBS004 Substance Dependence 48 0.023
1005
OLF005 Olfactory Neuroblastoma 48 0.023
1006
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.023
1007
P SCL009 Sclerosing Cholangitis 48 0.023
1008
c HYD064 Hydrocephalus, Congenital, 1 48 0.023
1009
P TRT019 Torticollis 48 0.023
1010
PYL006 Pyloric Stenosis 48 0.023
1011
P MRC003 Mercury Poisoning 48 0.023
1012
LRY029 Laryngomalacia 47 0.023
1013
PRD004 Prediabetes Syndrome 47 0.023
1014
CRN027 Corneal Neovascularization 47 0.023
1015
P CLB034 Coloboma, Ocular, Autosomal Dominant 47 0.023
1016
ZKF001 Zika Fever 47 0.023
1017
P CRC039 Coarctation of Aorta 47 0.023
1018
RYN005 Raynaud Phenomenon 47 0.023
1019
CMP002 Campylobacteriosis 46 0.023
1020
LCK001 Locked-in Syndrome 46 0.023
1021
ORC001 Orchitis 46 0.023
1022
P HRN001 Horner's Syndrome 45 0.023
1023
CRB004 Cerebral Artery Occlusion 45 0.023
1024
P CMM008 Communicating Hydrocephalus 45 0.023
1025
URL001 Urolithiasis 45 0.023
1026
SPP008 Suppurative Otitis Media 45 0.023
1027
CRT015 Carotid Artery Occlusion 45 0.023
1028
c STN011 Sting-Associated Vasculopathy with Onset in Infancy 45 0.023
1029
AGR002 Agoraphobia 45 0.023
1030
GRD001 Giardiasis 45 0.023
1031
CHP002 Chops Syndrome 44 0.023
1032
c CHR579 Chiari Malformation Type Ii 44 0.023
1033
IRT001 Iritis 44 0.023
1034
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.023
1035
P ORF002 Orofacial Cleft 44 0.023
1036
ISC015 Ischemic Colitis 44 0.023
1037
OVR063 Overnutrition 44 0.023
1038
GDS001 Good Syndrome 44 0.023
1039
SCT002 Scotoma 44 0.023
1040
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.023
1041
RDC006 Red Cell Aplasia 43 0.023
1042
ORL015 Oral Squamous Cell Carcinoma 43 0.023
1043
P HRD018 Hair Disease 43 0.023
1044
c RTN047 Retinitis Pigmentosa 18 42 0.023
1046
DRG024 Drug Allergy 42 0.023
1047
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.023
1048
c PRG001 Progressive Muscular Atrophy 42 0.023
1049
ATP013 Atopic Keratoconjunctivitis 42 0.023
1050
EPC002 Epicondylitis 41 0.023
1051
CLR033 Color Vision Deficiency 41 0.023
1052
49X006 49, Xxxxy Syndrome 41 0.023
1053
P HYP263 Hypersomnia 41 0.023
1054
MMM006 Mammographic Density 41 0.023
1055
JWD001 Jawad Syndrome 40 0.023
1056
PLM005 Pleomorphic Lipoma 40 0.023
1057
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 40 0.023
1058
PRM020 Premenstrual Tension 40 0.023
1059
ADJ001 Adjustment Disorder 40 0.023
1060
PYL004 Pyelitis 40 0.023
1061
WST002 Western Equine Encephalitis 40 0.023
1062
c CNG033 Congenital Syphilis 40 0.023
1063
ALG001 Algoneurodystrophy 39 0.023
1064
BLT001 Bilateral Retinoblastoma 39 0.023
1065
MYL057 Myelopathy, Htlv-1-Associated 39 0.023
1066
c PLM022 Pulmonary Valve Insufficiency 39 0.023
1067
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.023
1068
PLM018 Pulmonary Sclerosing Hemangioma 39 0.023
1069
DSS010 Dissociative Disorder 39 0.023
1070
SCR011 Scrapie 39 0.023
1071
ARC025 Arachnoid Cysts, Intracranial 38 0.023
1072
ALL014 Allergic Encephalomyelitis 38 0.023
1073
CVT001 Cavitary Optic Disc Anomalies 38 0.023
1074
P DVL012 Developmental Dysplasia of the Hip 1 38 0.023
1075
SPS019 Spastic Paraparesis 38 0.023
1076
MYS004 Myiasis 38 0.023
1077
CNT060 Central Serous Chorioretinopathy 38 0.023
1078
P HMF004 Hemifacial Spasm 38 0.023
1079
P CRB088 Cerebral Atrophy 37 0.023
1080
MNN021 Meningococcemia 37 0.023
1081
SYS071 Systemic Autoimmune Disease 37 0.023
1082
CGH001 Cough Variant Asthma 37 0.023
1083
BLP004 Blepharophimosis 37 0.023
1084
P DNT007 Dentin Sensitivity 36 0.023
1085
DRM009 Dermatomycosis 36 0.023
1086
ABD010 Abdominal Wall Defect 36 0.023
1087
LYM011 Lymphogranuloma Venereum 36 0.023
1088
PPT002 Peptic Ulcer Perforation 36 0.023
1089
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 35 0.023
1090
c MCR312 Microphthalmia, Syndromic 10 35 0.023
1091
BRK012 Broken Heart Syndrome 35 0.023
1092
CRB079 Cerebrospinal Fluid Leak 35 0.023
1093
LNG013 Lung Lymphoma 35 0.023
1094
GRM010 Germ Cells Tumors 34 0.023
1095
c HMF011 Hemifacial Spasm, Familial 33 0.023
1096
CYS021 Cystic Adenomatoid Malformation of Lung 33 0.023
1097