Search results for Oxygen

2386 hits were found for Oxygen

# Family MCID Name MIFTS Score
1
HMG031 Hemoglobin, High Altitude Adaptation 15 2.899
2
P RSP003 Respiratory Failure 75 0.656
3
HYP266 Hypoxia 58 0.534
4
c ACT210 Acute Respiratory Distress Syndrome 59 0.456
5
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.433
6
LNG099 Lung Disease 62 0.411
7
P CRD119 Cardiac Arrest 71 0.408
8
ANX004 Anoxia 44 0.367
9
P PLM037 Pulmonary Hypertension 69 0.366
10
CRD137 Cardiogenic Shock 50 0.339
11
ISC004 Ischemia 62 0.338
12
BRN071 Brain Injury 51 0.316
13
TXC005 Toxic Shock Syndrome 63 0.315
14
TRM010 Traumatic Brain Injury 54 0.304
15
c EXD008 Exudative Vitreoretinopathy 1 69 0.277
16
CNG034 Congestive Heart Failure 69 0.261
17
P HRT032 Heart Disease 78 0.260
18
P ADL010 Adult Respiratory Distress Syndrome 61 0.259
19
P VSC007 Vascular Disease 65 0.251
20
PLM010 Pulmonary Edema 56 0.249
21
P SLP006 Sleep Apnea 71 0.245
22
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.244
23
c DPH024 Diaphragmatic Hernia, Congenital 66 0.234
24
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.233
25
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.228
26
BRN056 Bronchopulmonary Dysplasia 57 0.225
27
OCL069 Ocular Motor Apraxia 53 0.219
28
48X005 48,xyyy 37 0.218
29
BRC085 Brca2 Hereditary Breast and Ovarian Cancer Syndrome 24 0.212
30
CRB039 Cerebrovascular Disease 71 0.210
31
PNG002 Pain Agnosia 52 0.208
32
MTB004 Metabolic Acidosis 48 0.198
33
P PLM036 Pulmonary Fibrosis 66 0.196
34
IDP011 Idiopathic Interstitial Pneumonia 65 0.196
35
CRB004 Cerebral Artery Occlusion 38 0.194
36
P MCR115 Microvascular Complications of Diabetes 5 67 0.193
37
HDN002 Head Injury 47 0.191
38
P PNM007 Pneumonia 71 0.187
39
DFC004 Deficiency Anemia 77 0.185
40
P MYC007 Myocardial Infarction 74 0.185
41
BRN002 Bronchiolitis 60 0.184
42
c ACT075 Acute Myocardial Infarction 59 0.184
43
CRB090 Cerebral Hypoxia 45 0.184
44
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.184
45
RTN020 Retinal Vascular Disease 49 0.184
46
PLM033 Pulmonary Embolism 60 0.181
47
PRP027 Peripheral Vascular Disease 72 0.180
48
STR067 Stroke, Ischemic 82 0.177
49
SPN186 Spinal Cord Injury 63 0.177
50
P MYC008 Myocarditis 60 0.176
51
HYP066 Hyperglycemia 63 0.175
52
BRN024 Bronchitis 70 0.171
53
P GLM045 Glioma 64 0.171
54
LMB062 Limb Ischemia 50 0.171
55
NWB001 Newborn Respiratory Distress Syndrome 58 0.170
56
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.170
57
GLL048 Glial Tumor 48 0.170
58
P CRN018 Coronary Artery Anomaly 67 0.169
59
P NRB010 Neuroblastoma 1 66 0.169
60
P SCK005 Sickle Cell Disease 53 0.169
61
GSG001 Gas Gangrene 52 0.168
62
P KDN018 Kidney Disease 73 0.166
63
P SZR006 Seizure Disorder 59 0.166
64
ART140 Arteries, Anomalies of 60 0.165
65
PNM008 Pneumothorax 56 0.165
66
OST017 Osteomyelitis 65 0.164
67
c ACT071 Acute Kidney Failure 60 0.164
68
CHR100 Chronic Ulcer of Skin 53 0.164
69
CYS001 Cystic Fibrosis 84 0.162
70
P CYS018 Cystitis 59 0.162
71
c PRC016 Pre-Eclampsia 63 0.160
72
P CLR023 Colorectal Cancer 100 0.160
73
VSL002 Visual Epilepsy 58 0.160
74
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.159
75
c FNC043 Fanconi Anemia, Complementation Group E 64 0.159
76
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.157
77
c ACT027 Acute Pancreatitis 60 0.157
78
c HYP595 Hypertension, Essential 87 0.155
79
P ENC018 Encephalopathy 64 0.154
80
PRT036 Peritonitis 66 0.152
81
P LCT001 Lactic Acidosis 52 0.152
82
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.150
83
P SNS001 Sensorineural Hearing Loss 62 0.148
84
INT066 Interstitial Lung Disease 61 0.148
85
GLB002 Glioblastoma 74 0.147
86
GLB015 Glioblastoma Multiforme 60 0.147
87
ADL002 Adult Syndrome 62 0.146
88
P PLY018 Polycythemia 56 0.146
89
P CMP008 Compartment Syndrome 45 0.146
90
MCN007 Meconium Aspiration Syndrome 53 0.142
91
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.142
92
P PTN014 Patent Ductus Arteriosus 1 60 0.142
93
AGN016 Aging 58 0.142
94
CRB037 Cerebral Palsy 69 0.141
95
ATH013 Atherosclerosis Susceptibility 68 0.141
96
P FBR017 Fibrosarcoma 57 0.141
97
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.140
98
ANG054 Angina Pectoris 66 0.140
99
BRN004 Brain Edema 57 0.140
100
HRT011 Heart Septal Defect 52 0.140
101
CYN002 Cyanosis, Transient Neonatal 45 0.139
102
P CRN300 Coronary Heart Disease 1 59 0.138
103
c CHR684 Chronic Kidney Disease 68 0.137
104
CYT002 Cytokine Deficiency 46 0.136
105
ENT011 Enterocolitis 51 0.134
106
LVR012 Liver Cirrhosis 67 0.134
107
P HDC001 Headache 59 0.132
108
c ATR087 Atrial Standstill 1 76 0.132
109
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.132
110
c DLT002 Dilated Cardiomyopathy 81 0.131
111
P CHR012 Chronic Granulomatous Disease 69 0.130
112
P INF032 Infertility 60 0.129
113
47X002 47,xyy 49 0.129
114
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.129
115
RRS014 Rare Surgical Neurologic Disease 33 0.129
116
c MCR113 Microvascular Complications of Diabetes 3 55 0.129
117
P BCL017 B-Cell Lymphoma 61 0.128
118
SDD008 Sudden Sensorineural Hearing Loss 44 0.128
119
P PNC044 Pancreatitis 61 0.127
120
P MLN007 Male Infertility 57 0.127
121
INT075 Intracranial Hypertension 54 0.127
122
c MCR120 Microvascular Complications of Diabetes 7 48 0.127
123
P LNG032 Lung Cancer 99 0.126
124
ATX019 Ataxia with Vitamin E Deficiency 46 0.126
125
c MCR130 Microvascular Complications of Diabetes 6 42 0.126
126
c MCR133 Microvascular Complications of Diabetes 4 42 0.126
127
DWN001 Down Syndrome 70 0.125
128
APN008 Apnea, Obstructive Sleep 64 0.125
129
P DBT009 Diabetes Mellitus 66 0.125
130
SNG003 Single Ventricular Heart 31 0.125
131
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.124
132
HLX001 Helix Syndrome 46 0.124
133
P LVR013 Liver Disease 71 0.123
134
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.122
135
SCK003 Sickle Cell Anemia 74 0.122
136
PRN019 Perinatal Necrotizing Enterocolitis 55 0.121
137
HYP056 Hypoglycemia 68 0.121
138
CRN030 Coronary Stenosis 49 0.121
139
P MLT020 Multiple Sclerosis 73 0.120
140
THR024 Thrombosis 58 0.120
141
P CTR002 Cataract 62 0.119
142
P ACT105 Acute Mountain Sickness 53 0.119
143
FSC004 Fasciitis 47 0.116
144
P BRS047 Breast Cancer 99 0.116
145
P PNC035 Pancreatic Cancer 86 0.116
146
P PHC003 Pheochromocytoma 71 0.116
147
NNT004 Neonatal Respiratory Failure 33 0.116
148
P NRP001 Neuropathy 57 0.115
149
P TTR001 Tetralogy of Fallot 70 0.114
150
ADR040 Adrenal Gland Pheochromocytoma 51 0.114
151
END030 End Stage Renal Failure 60 0.113
152
PPL052 Papillomatosis, Confluent and Reticulated 34 0.113
153
PRT037 Pertussis 66 0.112
154
P RTN018 Retinal Disease 53 0.112
155
CRV035 Cervical Cancer 77 0.111
156
P PRS040 Prostate Cancer 97 0.110
157
ATM095 Autoimmune Disease 62 0.110
158
INT002 Intermittent Claudication 60 0.110
159
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.110
160
P VNT002 Ventricular Septal Defect 61 0.110
161
P INF037 Inflammatory Bowel Disease 57 0.110
162
NCR007 Necrotizing Fasciitis 47 0.110
163
P CLS010 Cluster Headache 44 0.110
164
SBC016 Subacute Delirium 43 0.110
165
HMR023 Hemorrhagic Cystitis 40 0.109
166
P BLD134 Bladder Cancer 79 0.108
167
P PRD008 Periodontitis 66 0.108
168
P HYP055 Hypoplastic Left Heart Syndrome 63 0.108
169
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.108
170
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.108
171
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.108
172
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.108
173
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.108
174
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.108
175
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.108
176
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.108
177
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.108
178
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.108
179
P HPT023 Hepatocellular Carcinoma 99 0.107
180
c MCR129 Microvascular Complications of Diabetes 1 67 0.107
181
PLM001 Pulmonary Tuberculosis 72 0.106
182
P TRN020 Turner Syndrome 66 0.106
183
P ECL001 Eclampsia 53 0.106
184
P THR014 Thrombocytopenia 67 0.105
185
P MYP004 Myopathy 63 0.104
186
OST003 Osteonecrosis 62 0.104
187
P OVR042 Ovarian Cancer 89 0.103
188
c BRN108 Branchiootic Syndrome 1 62 0.103
189
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.103
190
c PCH010 Pachyonychia Congenita 3 43 0.103
191
ART016 Aortic Aneurysm 71 0.102
192
SQM006 Squamous Cell Carcinoma 60 0.102
193
P ART021 Arteriosclerosis 56 0.101
194
c MCR112 Microvascular Complications of Diabetes 2 42 0.101
195
c SYS001 Systemic Lupus Erythematosus 88 0.100
196
AST005 Asthma 80 0.100
197
P MYL006 Myeloid Leukemia 61 0.100
198
P LYM031 Lymphocytic Leukemia 56 0.100
199
BCT022 Bacterial Infectious Disease 57 0.099
201
ULC004 Ulcerative Colitis 75 0.098
202
OST159 Osteogenic Sarcoma 67 0.098
203
CRD001 Cardiac Tamponade 45 0.098
204
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.097
205
P PLM034 Pulmonary Emphysema 55 0.097
206
P MTH007 Methemoglobinemia 47 0.097
207
c MGR028 Migraine with or Without Aura 1 70 0.096
208
P ADN016 Adenocarcinoma 65 0.096
209
P VSC011 Vasculitis 64 0.096
210
TLN003 Telangiectasis 53 0.096
211
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.096
212
ESP021 Esophageal Cancer 90 0.095
213
ALL026 Allergic Hypersensitivity Disease 65 0.095
214
DPR016 Depression 64 0.095
215
TTN003 Tetanus 62 0.095
216
ANR040 Aneurysm 60 0.095
217
P MTR003 Mitral Valve Stenosis 54 0.095
218
P LKM002 Leukemia 69 0.094
219
CLT003 Colitis 63 0.094
220
IRN002 Iron Metabolism Disease 58 0.094
221
PRP080 Peripheral Artery Disease 51 0.094
222
P LNG064 Lung Cancer Susceptibility 3 79 0.093
223
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.093
224
RDT001 Radiation Cystitis 39 0.093
225
HRW001 Hair Whorl 36 0.093
226
HMG005 Hemoglobinopathy 57 0.092
227
P HYP076 Hyperthyroidism 55 0.092
228
P GST053 Gastric Cancer 85 0.091
229
c HYP836 Hypercholesterolemia, Familial, 1 74 0.091
230
FTT001 Fatty Liver Disease 63 0.091
231
HMS001 Hemosiderosis 54 0.091
232
RSP007 Respiratory Distress Syndrome, Infant 31 0.091
233
RTN017 Retinal Detachment 62 0.090
234
P ATR010 Atrial Heart Septal Defect 61 0.090
235
DCB001 Decubitus Ulcer 54 0.090
236
P RTN022 Retinal Vein Occlusion 50 0.090
237
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.089
238
P ALZ034 Alzheimer Disease 90 0.089
239
P ART005 Arteriovenous Malformation 63 0.089
240
BNR002 Bone Resorption Disease 51 0.089
241
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.089
242
ASP004 Asphyxia Neonatorum 44 0.089
243
PRC003 Proctitis 44 0.089
244
TRN044 Transposition of the Great Arteries 44 0.089
245
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.088
246
c LKM061 Leukemia, Acute Myeloid 84 0.088
247
CRH001 Crohn's Disease 75 0.088
248
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.088
249
ORL011 Oral Cancer 62 0.088
250
SPP010 Suppressor of Tumorigenicity 3 54 0.088
251
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 46 0.088
252
P SKN015 Skin Carcinoma 67 0.086
253
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.086
254
c RHB024 Rhabdomyosarcoma 2 64 0.086
255
P LTR001 Lateral Sclerosis 56 0.086
256
IMP005 Impotence 53 0.086
257
RTN003 Retinal Ischemia 52 0.086
258
HPR003 Heparin-Induced Thrombocytopenia 49 0.086
259
c PNS012 Paine Syndrome 61 0.085
260
EYD002 Eye Disease 59 0.085
261
PRP016 Paraplegia 54 0.085
262
P RRH023 Rare Hereditary Hemochromatosis 41 0.085
263
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.085
264
c ERY064 Erythrocytosis, Familial, 6 22 0.085
265
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.084
266
ANX010 Anxiety 75 0.084
267
SVR004 Severe Combined Immunodeficiency 74 0.084
268
P CNR004 Cone-Rod Dystrophy 2 72 0.084
269
P NTR004 Neutropenia 64 0.084
270
DSS009 Disseminated Intravascular Coagulation 58 0.084
271
BLR008 Bilirubin Metabolic Disorder 58 0.084
272
c ACT134 Acute Liver Failure 53 0.084
273
P CHR345 Chronic Pain 52 0.084
274
CRT013 Carotid Stenosis 50 0.084
275
P RTN014 Retinal Artery Occlusion 46 0.084
276
CRT015 Carotid Artery Occlusion 44 0.084
277
RST023 Resting Heart Rate, Variation in 43 0.084
278
BRN026 Branch Retinal Artery Occlusion 41 0.084
279
SKN016 Skin Disease 64 0.083
280
c SCL052 Scleroderma, Familial Progressive 62 0.083
281
PST028 Post-Traumatic Stress Disorder 60 0.083
282
P OPT006 Optic Nerve Disease 59 0.083
283
PRV004 Periventricular Leukomalacia 50 0.083
284
c ATS307 Autosomal Recessive Cerebellar Ataxia 44 0.083
285
ACT084 Acute Stress Disorder 42 0.083
286
c PLM022 Pulmonary Valve Insufficiency 35 0.083
287
P BRN022 Bronchiectasis 60 0.082
288
STT002 Status Asthmaticus 47 0.082
289
c MLG068 Malignant Glioma 46 0.082
290
MYC005 Myocardial Stunning 45 0.082
291
FRN014 Fournier Gangrene 38 0.082
292
FBR047 Fibromyalgia 60 0.081
293
P GLM007 Glomerulonephritis 58 0.081
294
SLC006 Silicosis 55 0.081
295
P VNS003 Venous Insufficiency 55 0.081
296
P TRC005 Tracheal Stenosis 39 0.081
298
OST012 Osteoarthritis 80 0.079
299
P INF038 Influenza 69 0.079
300
P ATS364 Autism 68 0.079
301
MLN008 Melanoma 68 0.079
302
c SML038 Small Cell Cancer of the Lung 67 0.079
303
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.079
304
CYN003 Cyanide Poisoning 24 0.079
305
P HYD006 Hydrocephalus 68 0.078
306
P LPS004 Lupus Erythematosus 62 0.078
307
MNT002 Mental Depression 60 0.078
308
P GST044 Gastritis 58 0.078
309
c CNG216 Congenital Hydrocephalus 55 0.078
310
HMT018 Hematopoietic Stem Cell Transplantation 54 0.078
311
c CNT015 Central Sleep Apnea 48 0.078
312
TRN015 Transient Cerebral Ischemia 62 0.077
313
SDD001 Sudden Infant Death Syndrome 61 0.077
314
PPT005 Peptic Ulcer Disease 60 0.077
315
P OPN001 Open-Angle Glaucoma 50 0.077
316
P ATX030 Ataxia-Telangiectasia 83 0.076
317
P SRC025 Sarcoidosis 1 72 0.076
318
P HML002 Hemolytic Anemia 64 0.076
319
P MYP006 Myopia 58 0.076
320
HPT009 Hepatopulmonary Syndrome 49 0.076
321
SYN036 Syncope 46 0.076
322
CHR466 Chronic Thromboembolic Pulmonary Hypertension 41 0.076
323
MYL069 Myeloma, Multiple 85 0.074
324
CNT097 Central Hypoventilation Syndrome, Congenital 70 0.074
325
P MSC005 Muscular Dystrophy 68 0.074
326
LSH001 Leishmaniasis 64 0.074
327
P THL005 Thalassemia 62 0.074
328
PRS030 Persistent Fetal Circulation Syndrome 50 0.074
329
c ACT076 Acute Myocarditis 45 0.074
330
P KLZ004 Kala-Azar 1 43 0.074
331
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 38 0.074
332
MLR004 Malaria 82 0.073
333
P RTN008 Retinitis Pigmentosa 77 0.073
334
LPT014 Leptin Deficiency or Dysfunction 72 0.073
335
CRD223 Cardiac Arrhythmia 61 0.073
336
RHM027 Rheumatic Disease 56 0.073
337
RTN023 Retinitis 46 0.073
338
NRR001 Neuroretinitis 46 0.073
339
CHL079 Children's Interstitial Lung Disease 27 0.073
340
c THR092 Thrombophilia Due to Thrombin Defect 74 0.071
341
OTT002 Otitis Media 71 0.071
342
P LKM062 Leukemia, Acute Lymphoblastic 68 0.071
343
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.071
344
STT001 Status Epilepticus 61 0.071
345
VRC005 Varicose Veins 61 0.071
346
ATR057 Atrioventricular Block 56 0.071
347
P TRM003 Tremor 55 0.071
348
URM002 Uremia 50 0.071
349
P DDN001 Duodenal Ulcer 50 0.071
350
BCK006 Back Pain 44 0.071
351
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.071
352
P SYS005 Systemic Scleroderma 68 0.070
353
CLN015 Colon Adenocarcinoma 65 0.070
354
P PSR002 Psoriasis 63 0.070
355
P KDN017 Kidney Cancer 60 0.070
356
P BRS044 Breast Adenocarcinoma 59 0.070
357
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.070
358
PTN001 Patent Foramen Ovale 57 0.070
359
DBT010 Diabetic Neuropathy 56 0.070
360
P MYM013 Moyamoya Disease 1 53 0.070
361
MCL006 Macular Retinal Edema 52 0.070
362
P HYP086 Hypothyroidism 70 0.069
363
P NSP012 Nasopharyngeal Carcinoma 67 0.069
364
P INT070 Intestinal Obstruction 60 0.069
365
INT007 Intermediate Coronary Syndrome 58 0.069
366
PST011 Pustulosis of Palm and Sole 51 0.069
367
c BCT013 Bacterial Pneumonia 49 0.069
368
ANP008 Anaplastic Oligoastrocytoma 31 0.069
369
OST173 Osteoradionecrosis of the Mandible 18 0.069
370
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.067
371
MYL009 Myelodysplastic Syndrome 72 0.067
372
P LYM118 Lymphoma 70 0.067
373
P DMN002 Dementia 68 0.067
374
ALC007 Alcohol Dependence 68 0.067
375
ACT119 Acute Promyelocytic Leukemia 63 0.067
376
BRN012 Bronchiolitis Obliterans 55 0.067
377
PLC005 Placental Insufficiency 55 0.067
378
VRC001 Varicocele 51 0.067
379
c MTR002 Mitral Valve Insufficiency 49 0.067
380
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.067
381
BRN028 Brain Cancer 75 0.066
382
P ATR011 Atrial Fibrillation 67 0.066
383
MSC007 Muscle Hypertrophy 65 0.066
384
c GLC092 Glaucoma, Primary Open Angle 63 0.066
385
THY029 Thyroid Carcinoma 62 0.066
386
PRT013 Portal Hypertension 61 0.066
387
CHL123 Chlamydia 60 0.066
388
c VRL010 Viral Hepatitis 56 0.066
389
P RTN016 Retinal Degeneration 56 0.066
390
HYP060 Hyperinsulinism 55 0.066
391
HYP005 Hypokalemia 55 0.066
392
MCR141 Mucormycosis 48 0.066
393
RDT013 Radiation Proctitis 48 0.066
394
ENT004 Enthesopathy 46 0.066
395
SRC014 Sarcoma 67 0.064
396
NRM005 Neuromuscular Disease 62 0.064
397
PNM010 Pneumothorax, Primary Spontaneous 60 0.064
398
VSC002 Vascular Dementia 57 0.064
399
SPN035 Spindle Cell Sarcoma 57 0.064
400
GLS001 Gliosarcoma 56 0.064
401
PYD001 Pyoderma Gangrenosum 53 0.064
402
P AST007 Astrocytoma 52 0.064
403
PYD002 Pyoderma 51 0.064
404
c CNT016 Central Retinal Vein Occlusion 48 0.064
405
ORL015 Oral Squamous Cell Carcinoma 44 0.064
406
P CRN026 Corneal Edema 44 0.064
407
NCR014 Necrotizing Soft Tissue Infection 24 0.064
408
P RHM011 Rheumatoid Arthritis 82 0.063
409
P OST002 Osteoporosis 79 0.063
410
PLY001 Polycythemia Vera 70 0.063
411
P ASP006 Aspergillosis 67 0.063
412
P PRP019 Peripheral Nervous System Disease 64 0.063
413
P RHB003 Rhabdomyosarcoma 62 0.063
414
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.063
415
P END033 Endocarditis 58 0.063
416
PLM031 Poliomyelitis 58 0.063
417
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.063
418
PLM017 Pulmonary Alveolar Microlithiasis 54 0.063
419
CLC001 Calciphylaxis 49 0.063
420
c CHR431 Chronic Venous Insufficiency 48 0.063
421
P BNG032 Benign Mesothelioma 47 0.063
422
HPT004 Hepatic Coma 42 0.063
423
c VRL005 Viral Pneumonia 42 0.063
424
c TRC022 Tricuspid Valve Insufficiency 41 0.063
425
c CNT028 Central Retinal Artery Occlusion 40 0.063
426
P CLL020 Collagenopathy Type 2 Alpha 1 25 0.063
427
c LKM071 Leukemia, Chronic Lymphocytic 81 0.061
428
P PRK057 Parkinson Disease, Late-Onset 77 0.061
429
c HPT073 Hepatitis C Virus 74 0.061
430
P HYP061 Hypertrophic Cardiomyopathy 68 0.061
431
P INT143 Interstitial Cystitis 62 0.061
432
P CRD132 Cardiac Conduction Defect 61 0.061
433
P PYL005 Pyelonephritis 58 0.061
434
P MTC069 Mitochondrial Disorders 57 0.061
435
GST023 Gastric Ulcer 53 0.061
436
P MSC003 Muscular Atrophy 52 0.061
437
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.061
438
P PLM006 Pulmonary Alveolar Proteinosis 50 0.061
439
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.061
440
CRB086 Cerebral Aneurysms 41 0.061
441
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.061
442
c LKM004 Leukemia, B-Cell, Chronic 35 0.061
443
INS024 Insulin-Like Growth Factor I 79 0.059
444
P HNT016 Huntington Disease 72 0.059
445
P DRM053 Dermatitis, Atopic 68 0.059
446
P LPR021 Leprosy 3 67 0.059
447
DRM006 Dermatitis 63 0.059
448
P END044 Endometriosis 63 0.059
449
P ART023 Arthropathy 61 0.059
450
P PNM006 Pneumoconiosis 55 0.059
451
P DRR001 Diarrhea 55 0.059
452
ILS001 Ileus 51 0.059
453
ANT018 Anthracosis 46 0.059
454
ACT003 Acute Kidney Tubular Necrosis 42 0.059
455
HNS001 Hansen's Disease 35 0.059
456
P NRF023 Neurofibromatosis, Type Ii 77 0.058
457
c BTT014 Beta-Thalassemia 73 0.058
458
c ACT068 Acute Cystitis 63 0.058
459
ACQ007 Acquired Immunodeficiency Syndrome 61 0.058
460
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.058
461
HMP005 Hemiplegia 55 0.058
462
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.058
463
P MTC133 Mitochondrial Myopathy 53 0.058
464
QDR001 Quadriplegia 51 0.058
465
CHR074 Choriocarcinoma 47 0.058
466
ACT017 Acute Chest Syndrome 47 0.058
467
ASP007 Aspiration Pneumonia 46 0.058
468
ATN011 Autoinflammation with Infantile Enterocolitis 45 0.058
469
MDS022 Mediastinitis 42 0.058
470
PRM329 Premature Aging 41 0.058
471
c FNC027 Fanconi Anemia, Complementation Group a 81 0.056
472
P GRF003 Graft-Versus-Host Disease 71 0.056
473
LYM133 Lymphoma, Hodgkin, Classic 70 0.056
474
P ENC004 Encephalitis 64 0.056
475
P SCL018 Scoliosis 61 0.056
476
INS001 Insulinoma 60 0.056
477
P ERY058 Erythrocytosis, Familial, 1 60 0.056
478
P SLP005 Sleep Disorder 58 0.056
479
RHM028 Rheumatic Heart Disease 54 0.056
480
P RCT021 Rectum Cancer 54 0.056
481
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.056
482
SYS003 Systolic Heart Failure 43 0.056
483
ALL014 Allergic Encephalomyelitis 40 0.056
484
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.056
485
MTH071 Methane Production 26 0.056
486
c LKM063 Leukemia, Chronic Myeloid 74 0.054
487
P EPL164 Epilepsy 73 0.054
488
HMN044 Human Immunodeficiency Virus Type 1 73 0.054
489
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.054
490
LPD008 Lipid Metabolism Disorder 64 0.054
491
CRC021 Carcinosarcoma 62 0.054
492
NTR005 Nutritional Deficiency Disease 61 0.054
493
CMP010 Complex Regional Pain Syndrome 57 0.054
494
SFT003 Soft Tissue Sarcoma 57 0.054
495
PRS047 Prostatitis 57 0.054
496
ENH001 Enhanced S-Cone Syndrome 56 0.054
497
AMN003 Amnestic Disorder 55 0.054
498
c GRV008 Graves Disease 1 55 0.054
499
INF034 Infective Endocarditis 53 0.054
500
c PRM012 Primary Polycythemia 52 0.054
502
ATN005 Autonomic Dysfunction 48 0.054
503
ART031 Aortic Coarctation 45 0.054
504
RDN001 Reading Disorder 42 0.054
505
OST115 Osteonecrosis of the Jaw 40 0.054
506
P RTN024 Retinoblastoma 74 0.052
507
CNN005 Connective Tissue Disease 68 0.052
508
KWS002 Kawasaki Disease 65 0.052
509
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.052
510
CHR066 Chronic Fatigue Syndrome 61 0.052
511
CHL014 Cholera 58 0.052
512
PRP030 Purpura 56 0.052
513
P MYS005 Myositis 54 0.052
514
CRT016 Carotid Artery Disease 53 0.052
515
DYS073 Dysphagia 52 0.052
516
ESN011 Eisenmenger Syndrome 52 0.052
517
OVR082 Overgrowth Syndrome 51 0.052
518
c FML008 Familial Retinoblastoma 46 0.052
519
P CRB088 Cerebral Atrophy 43 0.052
520
GGN002 Gigantism 35 0.052
521
c ERY065 Erythrocytosis, Familial, 7 32 0.052
522
PLY150 Polykaryocytosis Inducer 31 0.052
523
DFF031 Diffuse Alveolar Hemorrhage 28 0.052
524
ERY007 Erythropoietin Polycythemia 16 0.052
525
NRL016 Neural Tube Defects 83 0.051
526
P ART022 Arthritis 71 0.051
527
KRT019 Keratitis, Hereditary 69 0.051
528
BRK010 Burkitt Lymphoma 68 0.051
529
c ART101 Aortic Valve Disease 2 67 0.051
530
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.051
531
CHG001 Chagas Disease 66 0.051
532
CHL068 Cholestasis 61 0.051
533
BND020 Bone Disease 60 0.051
534
LPT001 Leptospirosis 60 0.051
535
HPT019 Hepatic Encephalopathy 60 0.051
536
P PRP029 Porphyria 58 0.051
537
APH002 Aphasia 56 0.051
538
CLL003 Cellulitis 56 0.051
539
HRT012 Heart Valve Disease 56 0.051
540
GLC003 Glucose Intolerance 55 0.051
541
NNL006 Non-Alcoholic Steatohepatitis 53 0.051
542
RYN005 Raynaud Phenomenon 50 0.051
543
RNL077 Renal Fibrosis 49 0.051
544
ACT029 Acute Interstitial Pneumonia 46 0.051
545
HRN029 Hearing Loss, Noise-Induced 38 0.051
546
CHR178 Chromosomal Triplication 36 0.051
547
PNM003 Pneumatosis Cystoides Intestinalis 33 0.051
548
RRD056 Rare Disease in Surgical Orthopedic 29 0.051
549
IMM167 Immune Deficiency Disease 79 0.049
550
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.049
551
P AMY004 Amyloidosis 71 0.049
552
P MNN013 Meningitis 67 0.049
553
P NPH012 Nephrotic Syndrome 65 0.049
554
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.049
555
c HPT001 Hepatitis C 62 0.049
556
HLC007 Helicobacter Pylori Infection 61 0.049
557
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.049
558
GNG013 Gingivitis 60 0.049
559
P RHN004 Rhinitis 59 0.049
560
RSP006 Respiratory System Disease 57 0.049
561
LNG031 Lung Benign Neoplasm 52 0.049
562
CLR109 Colorectal Adenocarcinoma 51 0.049
563
MTC005 Mitochondrial Metabolism Disease 50 0.049
564
P ART018 Aortic Valve Insufficiency 47 0.049
565
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.049
566
RFR003 Refractive Error 44 0.049
567
P AVS003 Avascular Necrosis 43 0.049
568
DBT008 Diabetic Angiopathy 42 0.049
569
ART008 Arteriosclerosis Obliterans 40 0.049
570
SPS057 Spasticity 38 0.049
571
BCK003 Background Diabetic Retinopathy 37 0.049
572
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.049
573
URT049 Urate Oxidase, Pseudogene 26 0.049
574
c ADL080 Adult Acute Respiratory Distress Syndrome 24 0.049
575
CRT057 Critical Congenital Heart Disease 21 0.049
576
MSC157 Muscular Dystrophy, Duchenne Type 70 0.047
577
P MYC084 Mycobacterium Tuberculosis 1 69 0.047
578
P HYP098 Hypereosinophilic Syndrome 67 0.047
579
PPL049 Papillon-Lefevre Syndrome 63 0.047
580
P DRM010 Dermatomyositis 62 0.047
581
P CND004 Candidiasis 61 0.047
582
HMR039 Hemorrhage, Intracerebral 59 0.047
583
P LRY044 Larynx Cancer 59 0.047
584
HPT022 Hepatoblastoma 58 0.047
585
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.047
586
INT030 Intracranial Aneurysm 57 0.047
587
ALL006 Allergic Asthma 56 0.047
588
c BCT007 Bacterial Meningitis 56 0.047
589
c PRD040 Periodontitis, Chronic 56 0.047
590
AVN001 Avian Influenza 56 0.047
591
MST005 Mastitis 55 0.047
592
RSC001 Rosacea 55 0.047
593
GTR002 Goiter 54 0.047
594
SPS003 Spastic Diplegia 53 0.047
595
DNT012 Dental Caries 52 0.047
596
ASC010 Ascaris Lumbricoides Infection 51 0.047
597
DGN001 Degenerative Disc Disease 49 0.047
598
P OBS001 Obstructive Jaundice 49 0.047
599
CRN027 Corneal Neovascularization 48 0.047
600
LPT006 Leptin Receptor Deficiency 47 0.047
601
KLD004 Keloid Disorder 41 0.047
602
P OTT001 Otitis Externa 41 0.047
603
OVR094 Ovarian Epithelial Cancer 39 0.047
604
ASC001 Ascaridiasis 36 0.047
605
VRS002 Virus-Associated Trichodysplasia Spinulosa 33 0.047
606
P TBR001 Tuberous Sclerosis 72 0.044
607
c ATS007 Autism Spectrum Disorder 69 0.044
608
CHL065 Cholangiocarcinoma 68 0.044
609
GST092 Gastroesophageal Reflux 68 0.044
610
P HRP006 Herpes Simplex 66 0.044
611
ING001 Inguinal Hernia 61 0.044
612
PRT058 Pure Autonomic Failure 60 0.044
613
P UVT001 Uveitis 58 0.044
614
GST033 Gestational Diabetes 58 0.044
615
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.044
616
SYN007 Synovitis 55 0.044
617
LST001 Listeriosis 55 0.044
618
VSC003 Visceral Leishmaniasis 55 0.044
619
PLM012 Pulmonary Sarcoidosis 54 0.044
620
INT079 Intrahepatic Cholangiocarcinoma 54 0.044
621
HMC014 Homocysteinemia 54 0.044
622
CHC001 Chickenpox 53 0.044
623
NRT004 Neuritis 52 0.044
624
P PRC012 Pericardial Effusion 51 0.044
625
CHR005 Chorioamnionitis 51 0.044
626
IMM064 Immunodeficiency, Common Variable, 10 51 0.044
627
P CLB034 Coloboma, Ocular, Autosomal Dominant 50 0.044
628
TST044 Testicular Torsion 49 0.044
629
MTN003 Motion Sickness 48 0.044
630
HYP017 Hypophosphatemia 48 0.044
631
ANR004 Anuria 47 0.044
632
HMP009 Haemophilus Influenzae 46 0.044
633
OBS037 Obesity-Hypoventilation Syndrome 46 0.044
634
LCK001 Locked-in Syndrome 46 0.044
635
PLR007 Pleural Empyema 44 0.044
636
HMP001 Hemopericardium 44 0.044
637
ATN004 Autonomic Neuropathy 43 0.044
638
P GLM044 Glomerular Disease 42 0.044
639
PST092 Posttransplant Acute Limbic Encephalitis 29 0.044
640
c MLG042 Malignant Otitis Externa 29 0.044
641
KPS004 Kaposi Sarcoma 75 0.042
642
END057 Endometrial Cancer 74 0.042
643
c MNN043 Meningioma, Familial 74 0.042
644
LYM007 Lymphangioleiomyomatosis 67 0.042
645
ACR008 Acrocallosal Syndrome 66 0.042
646
P OCL013 Oculodentodigital Dysplasia 65 0.042
647
MNN042 Meningioma, Radiation-Induced 64 0.042
648
CTN007 Cutaneous Leishmaniasis 61 0.042
649
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.042
650
CHL067 Cholecystitis 60 0.042
651
IRN001 Iron Deficiency Anemia 59 0.042
652
P PLY011 Polycystic Ovary Syndrome 58 0.042
653
P EXN002 Exanthem 58 0.042
654
MCS002 Mucositis 56 0.042
655
PPL022 Papilloma 56 0.042
656
P SBS003 Substance Abuse 56 0.042
657
P TRT010 Teratoma 52 0.042
658
PLC008 Placenta Disease 51 0.042
659
P KRT007 Keratoconus 51 0.042
660
c SVR005 Severe Pre-Eclampsia 50 0.042
661
NTR046 Neutrophil Migration 49 0.042
662
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.042
663
SPL018 Splenomegaly 48 0.042
664
BRN014 Bronchopneumonia 47 0.042
665
PRP009 Peripartum Cardiomyopathy 47 0.042
666
DBT006 Diabetic Macular Edema 46 0.042
667
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.042
668
P PRP034 Purpura Fulminans 42 0.042
669
SPN021 Spinal Meningioma 40 0.042
670
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.042
671
MYF002 Myofascial Pain Syndrome 39 0.042
672
SCR001 Secretory Meningioma 38 0.042
673
CRP002 Croup 38 0.042
674
ALV006 Alveolar Capillary Dysplasia 33 0.042
675
MTH047 Methanol Poisoning 31 0.042
676
P APL001 Aplastic Anemia 76 0.040
677
c HMC039 Hemochromatosis, Type 1 73 0.040
678
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.040
679
P MJR001 Major Depressive Disorder 69 0.040
680
P GLM040 Glioma Susceptibility 1 68 0.040
681
GST040 Gastric Adenocarcinoma 67 0.040
682
P MTR014 Motor Neuron Disease 66 0.040
683
KRN002 Kearns-Sayre Syndrome 64 0.040
684
P HYP750 Hypertriglyceridemia, Familial 62 0.040
685
GST045 Gastroenteritis 60 0.040
686
P MLG056 Malignant Hyperthermia 60 0.040
687
c ACT073 Acute Leukemia 59 0.040
688
c MST023 Mesothelioma, Malignant 59 0.040
689
EXT034 Extrinsic Allergic Alveolitis 58 0.040
690
P ALC033 Alcohol Use Disorder 58 0.040
691
P DNG005 Dengue Virus 57 0.040
692
c SVR001 Severe Acute Respiratory Syndrome 56 0.040
693
PNM001 Pneumocystosis 53 0.040
694
OLG003 Oligohydramnios 53 0.040
695
SPN051 Spondylitis 53 0.040
696
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.040
697
HYD061 Hydrocephalus, Normal-Pressure 49 0.040
698
SQM002 Squamous Cell Papilloma 49 0.040
699
c INV001 Invasive Aspergillosis 48 0.040
700
VTR007 Vitreoretinopathy 48 0.040
701
MYL001 Myelitis 48 0.040
702
TRC040 Tracheoesophageal Fistula 47 0.040
703
P RNL015 Renal Hypertension 47 0.040
704
URT010 Ureteral Obstruction 46 0.040
705
P HRN001 Horner's Syndrome 46 0.040
706
PRS063 Paresthesia 46 0.040
707
CMP034 Complete Androgen Insensitivity Syndrome 46 0.040
708
TND005 Tendinitis 45 0.040
709
TND004 Tendinopathy 44 0.040
710
BCT021 Bacterial Sepsis 44 0.040
711
c HMG001 Hemoglobin C Disease 43 0.040
712
c ACQ010 Acquired Polycythemia 43 0.040
713
c HMG029 Hemoglobin Se Disease 40 0.040
714
HYP264 Hypertonia 39 0.040
715
LVD003 Livedoid Vasculitis 39 0.040
716
c PRS136 Prostate Cancer, Hereditary, 6 34 0.040
717
c PRS130 Prostate Cancer, Hereditary, 8 33 0.040
718
INF009 Inflammatory Spondylopathy 29 0.040
719
PRQ002 Paraquat Poisoning 25 0.040
720
APN006 Apnea of Prematurity 24 0.040
721
P RTT002 Rett Syndrome 81 0.037
722
c TBR025 Tuberous Sclerosis 1 74 0.037
723
c BSL007 Basal Cell Carcinoma 68 0.037
724
BRR014 Barrett Esophagus 67 0.037
725
c ALP101 Alpha-Thalassemia 63 0.037
726
ALP103 Alpha-1-Antitrypsin Deficiency 63 0.037
727
GRN037 Granulomatosis with Polyangiitis 62 0.037
728
VRL011 Viral Infectious Disease 62 0.037
729
P ART067 Aortic Aneurysm, Familial Thoracic 1 62 0.037
730
TYP007 Typhoid Fever 61 0.037
731
HDR002 Hidradenitis Suppurativa 58 0.037
732
TRG002 Trigeminal Neuralgia 58 0.037
733
GST050 Gastrointestinal System Disease 57 0.037
734
ORL004 Oral Submucous Fibrosis 55 0.037
735
P LYM025 Lymphedema 54 0.037
736
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.037
737
c ERY048 Erythrocytosis, Familial, 2 53 0.037
738
P CHL066 Cholangitis 53 0.037
739
GST009 Gastroschisis 52 0.037
740
CRV040 Cervix Carcinoma 52 0.037
741
PRS021 Prostatic Adenoma 52 0.037
742
MCR088 Microscopic Polyangiitis 51 0.037
743
STM007 Stomatitis 51 0.037
744
ACR041 Acromelic Frontonasal Dysostosis 50 0.037
745
P BLR006 Biliary Tract Disease 49 0.037
746
ATS010 Autosomal Recessive Disease 49 0.037
747
TRC062 Tricuspid Atresia 49 0.037
748
P END046 Endometritis 49 0.037
749
P TCL004 T-Cell Leukemia 48 0.037
750
HDR003 Hidradenitis 48 0.037
751
NVS001 Neovascular Glaucoma 46 0.037
752
DYS015 Dysentery 45 0.037
753
MCL003 Macular Holes 44 0.037
754
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 42 0.037
755
49X002 49,xxxxy Syndrome 39 0.037
756
SPR126 Superior Semicircular Canal Dehiscence 39 0.037
757
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.037
758
c LKM005 Leukemia, T-Cell, Chronic 35 0.037
759
EPD005 Epidural Abscess 35 0.037
760
CND006 Candida Glabrata 33 0.037
761
HND015 Hand Skill, Relative 33 0.037
762
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 32 0.037
763
UNV002 Univentricular Heart 29 0.037
764
PLM186 Pulmonary Arterial Hypertension Associated with Portal Hypertension 26 0.037
765
c ATM006 Autoimmune Lymphoproliferative Syndrome 73 0.034
766
VNH007 Von Hippel-Lindau Syndrome 73 0.034
767
MNT001 Mantle Cell Lymphoma 69 0.034
768
P HPT021 Hepatitis 69 0.034
769
MYL005 Myelofibrosis 69 0.034
770
ALL003 Allergic Rhinitis 69 0.034
771
PNC129 Pancreatic Adenocarcinoma 69 0.034
772
SKN019 Skin Melanoma 68 0.034
773
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.034
774
P DYS154 Dystonia 65 0.034
775
LYM017 Lyme Disease 64 0.034
776
P HYP069 Hyperparathyroidism 64 0.034
777
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 64 0.034
778
c HPT016 Hepatitis B 63 0.034
779
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.034
780
ADN018 Adenoma 60 0.034
781
c DWL002 Dowling-Degos Disease 1 59 0.034
782
GRD007 Grade Iii Astrocytoma 59 0.034
783
P MTR012 Mitral Valve Disease 59 0.034
784
CNT047 Contact Dermatitis 58 0.034
785
BRG013 Buerger Disease 58 0.034
786
SCH014 Schistosomiasis 57 0.034
787
P GRV001 Graves' Disease 57 0.034
788
ANT024 Anthrax Disease 56 0.034
789
FLR002 Filariasis 56 0.034
790
FCL014 Focal Epilepsy 56 0.034
791
P FTL001 Fetal Alcohol Syndrome 56 0.034
792
PHR003 Pharyngitis 56 0.034
793
P PLY019 Polyneuropathy 55 0.034
794
P OPT009 Optic Neuritis 55 0.034
795
P ATR001 Atrioventricular Septal Defect 55 0.034
796
PRS045 Prostatic Hypertrophy 55 0.034
797
P INS002 in Situ Carcinoma 55 0.034
798
PRC013 Pericarditis 54 0.034
799
DMY004 Demyelinating Disease 54 0.034
800
P PRG013 Paraganglioma 53 0.034
801
P TMP001 Temporal Lobe Epilepsy 53 0.034
802
c GLL024 Gallbladder Disease 1 53 0.034
803
AST006 Astigmatism 53 0.034
804
P MNC007 Monocytic Leukemia 52 0.034
805
AZS001 Azoospermia 51 0.034
806
DYS014 Dyspepsia 51 0.034
807
LRN003 Learning Disability 51 0.034
808
IGG001 Iga Glomerulonephritis 50 0.034
809
SXL003 Sexual Disorder 49 0.034
810
PRS129 Prostatic Hyperplasia, Benign 49 0.034
811
HMG002 Hemoglobinuria 49 0.034
812
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 0.034
813
P RNV001 Renovascular Hypertension 49 0.034
814
HYP781 Hypoascorbemia 48 0.034
815
LYM019 Lymphosarcoma 48 0.034
816
WTH001 Withdrawal Disorder 47 0.034
817
c HYD064 Hydrocephalus, Congenital, 1 47 0.034
818
EPD015 Epidemic Typhus 47 0.034
819
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 46 0.034
820
INT276 Interatrial Communication 46 0.034
821
INT071 Intestinal Perforation 45 0.034
822
CRN017 Coronary Thrombosis 45 0.034
823
SPS007 Spastic Cerebral Palsy 45 0.034
824
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.034
825
DMP001 Dumping Syndrome 44 0.034
826
c CHR546 Chronic Mountain Sickness 43 0.034
827
P HYP265 Hypotonia 43 0.034
828
P CPL003 Capillary Leak Syndrome 42 0.034
829
P CRN024 Corneal Disease 42 0.034
830
P PLM025 Pulmonary Venoocclusive Disease 42 0.034
831
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.034
832
SNL007 Senile Cataract 41 0.034
833
c SYS007 Systemic Capillary Leak Syndrome 41 0.034
834
CHP002 Chops Syndrome 41 0.034
835
c CHR096 Chronic Pulmonary Heart Disease 40 0.034
836
BLS002 Blastomycosis 40 0.034
837
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.034
838
LPD014 Lipodermatosclerosis 40 0.034
839
CHL147 Chlamydia Pneumonia 39 0.034
840
ANM001 Anemia of Prematurity 38 0.034
841
c CHR098 Chronic Pyelonephritis 38 0.034
842
ABD010 Abdominal Wall Defect 37 0.034
843
SRF006 Surfactant Dysfunction 36 0.034
844
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 36 0.034
846
STN013 Stenotrophomonas Maltophilia Infection 26 0.034
847
HVY002 Heavy Metal Poisoning 23 0.034
848
RDT014 Radiation Myelitis 15 0.034
849
P SCH015 Schizophrenia 76 0.031
850
RCK004 Rickets 70 0.031
851
P NRV007 Nervous System Disease 68 0.031
852
c FML001 Familial Atrial Fibrillation 67 0.031
853
c JVN010 Juvenile Rheumatoid Arthritis 67 0.031
854
CLF027 Cleft Palate, Isolated 67 0.031
855
INC002 Inclusion Body Myositis 66 0.031
856
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.031
857
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 65 0.031
858
ANR007 Anorexia Nervosa 64 0.031
859
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.031
860
KHL003 Kohlschutter-Tonz Syndrome 63 0.031
861
GT001 Gout 63 0.031
862
P MVM001 Movement Disease 63 0.031
863
c PRG042 Progressive Familial Heart Block, Type Ia 62 0.031
864
APP008 Appendicitis 61 0.031
865
P PLY014 Polycystic Kidney Disease 61 0.031
866
URN010 Urinary Tract Obstruction 59 0.031
867
SPN027 Spinal Stenosis 58 0.031
868
P ALP008 Alopecia 58 0.031
869
ERY051 Erythroleukemia, Familial 58 0.031
870
RHM001 Rheumatic Fever 56 0.031
871
P INT068 Intestinal Disease 56 0.031
872
ORP003 Oropharynx Cancer 55 0.031
873
MSS001 Masa Syndrome 55 0.031
874
PRM042 Primary Effusion Lymphoma 55 0.031
875
CCC001 Coccidioidomycosis 54 0.031
876
PLS007 Plasmodium Falciparum Malaria 53 0.031
877
P MGR003 Migraine with Aura 53 0.031
878
BRN038 Bronchial Disease 53 0.031
879
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.031
880
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.031
881
P THY032 Thyroiditis 52 0.031
882
P PLY017 Polyarteritis Nodosa 52 0.031
883
FLR001 Filarial Elephantiasis 51 0.031
884
APL002 Aplasia of Lacrimal and Salivary Glands 51 0.031
885
AMB002 Amblyopia 51 0.031
886
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 51 0.031
887
RFL001 Reflex Sympathetic Dystrophy 50 0.031
888
P ESN008 Eosinophilic Pneumonia 50 0.031
889
MNN009 Meningoencephalitis 50 0.031
890
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 48 0.031
891
CRN019 Coronary Artery Vasospasm 48 0.031
892
SCH038 Schopf-Schulz-Passarge Syndrome 48 0.031
893
INT010 Intracranial Embolism 47 0.031
894
HYP025 Hyperphosphatemia 47 0.031
895
P MYC033 Myoclonus 47 0.031
896
KRT008 Keratopathy 46 0.031
897
KRT013 Keratolytic Winter Erythema 45 0.031
898
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 44 0.031
899
BNS003 Binswanger's Disease 43 0.031
900
ANC002 Anca-Associated Vasculitis 43 0.031
901
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 43 0.031
902
c MLG079 Malignant Pleural Mesothelioma 43 0.031
903
LKS001 Leukostasis 43 0.031
904
DST006 Diastolic Heart Failure 43 0.031
905
P MYG005 Myoglobinuria 43 0.031
906
c ACQ017 Acquired Von Willebrand Syndrome 42 0.031
907
P SBR004 Seborrheic Dermatitis 41 0.031
908
VTR003 Vitreous Detachment 41 0.031
909
c HYP543 Hypoplastic Left Heart Syndrome 1 41 0.031
910
JWD001 Jawad Syndrome 41 0.031
911
MST004 Mast Cell Neoplasm 40 0.031
912
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 40 0.031
913
PLX004 Plexopathy 39 0.031
914
EXT007 Extracutaneous Mastocytoma 39 0.031
915
ACT056 Acute Cor Pulmonale 38 0.031
916
AML001 Amelanotic Melanoma 38 0.031
917
SPP007 Suppression Amblyopia 37 0.031
918
P MXL015 Maxillary Sinusitis 37 0.031
919
CHN040 Choanal Atresia and Lymphedema 36 0.031
920
MXD026 Mixed Glioma 36 0.031
921
MDD003 Middle Cerebral Artery Infarction 35 0.031
922
c HMG004 Hemoglobin D Disease 34 0.031
923
TRC020 Tracheitis 32 0.031
924
HMG010 Hemoglobinemia 29 0.031
925
TRC110 Tracheobronchial Stenosis, Congenital 25 0.031
926
CLS032 Clostridium Perfringens Infection 17 0.031
927
c CNG370 Congenital Tracheal Stenosis 16 0.031
928
ACR006 Aceruloplasminemia 74 0.028
929
ADR007 Adrenoleukodystrophy 72 0.028
930
ADN011 Adenoid Cystic Carcinoma 71 0.028
931
LGH007 Leigh Syndrome 69 0.028
932
FBR012 Fabry Disease 68 0.028
933
P ORT004 Orthostatic Intolerance 68 0.028
934
WRN001 Werner Syndrome 68 0.028
935
MYL031 Myeloproliferative Neoplasm 66 0.028
936
c INF071 Inflammatory Bowel Disease 1 66 0.028
937
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.028
938
TBC004 Tobacco Addiction 65 0.028
939
INT146 Intervertebral Disc Disease 64 0.028
940
P LMY004 Leiomyosarcoma 63 0.028
941
MDD011 Mood Disorder 62 0.028
942
MCR013 Microphthalmia 62 0.028
943
P HMN010 Hemangioma 62 0.028
944
P ESP024 Esophagitis 62 0.028
945
BRC012 Brucellosis 62 0.028
946
PTT048 Pituitary Adenoma, Prolactin-Secreting 61 0.028
947
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.028
948
c ANM038 Anemia, Autoimmune Hemolytic 61 0.028
949
ART001 Arterial Tortuosity Syndrome 60 0.028
950
ALC006 Alcoholic Hepatitis 60 0.028
951
P PRD006 Prader-Willi Syndrome 60 0.028
952
ART141 Arteriovenous Malformations of the Brain 60 0.028
953
LNG108 Langerhans Cell Histiocytosis 60 0.028
954
MSC152 Muscular Dystrophy, Becker Type 60 0.028
955
P BPL003 Bipolar Disorder 59 0.028
956
TRD006 Tardive Dyskinesia 58 0.028
957
P HMP007 Hemophilia 58 0.028
958
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 58 0.028
959
LYM027 Lymphopenia 58 0.028
960
ALK013 Alkaptonuria 57 0.028
961
P STR020 Strabismus 57 0.028
962
TNG003 Tongue Cancer 57 0.028
963
PRM236 Primary Biliary Cholangitis 57 0.028
964
P PLY041 Polymyositis 57 0.028
965
EMB004 Embryonal Carcinoma 57 0.028
966
P CHN012 Chondrosarcoma 57 0.028
967
CRH005 Crohn's Colitis 56 0.028
968
P RBL001 Rubella 56 0.028
969
JPN002 Japanese Encephalitis 56 0.028
970
P ANT006 Antiphospholipid Syndrome 56 0.028
971
SNS003 Sensory Peripheral Neuropathy 56 0.028
972
P PTT014 Pitt-Hopkins Syndrome 55 0.028
973
DBL002 Double Outlet Right Ventricle 55 0.028
974
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.028
975
CLF004 Cleft Lip/palate 55 0.028
976
P NRV006 Nervous System Cancer 55 0.028
977
SPT004 Septic Arthritis 55 0.028
978
P PRM006 Primary Biliary Cirrhosis 54 0.028
979
P HST010 Histiocytosis 54 0.028
980
GDP001 Goodpasture Syndrome 54 0.028
981
OVR059 Ovary Adenocarcinoma 54 0.028
982
PLG002 Plague 54 0.028
983
P ANG015 Angioedema 54 0.028
984
LYM040 Lymphoblastic Lymphoma 54 0.028
985
MCN017 Meconium Ileus 54 0.028
986
CRT017 Cartilage Disease 54 0.028
987
P HMR003 Hemorrhagic Disease 54 0.028
988
PTH003 Pathologic Nystagmus 53 0.028
989
EBS001 Ebstein Anomaly 53 0.028
990
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.028
991
HMN009 Hemangioblastoma 53 0.028
992
P LRY019 Laryngitis 53 0.028
993
FCL012 Facial Paralysis 53 0.028
994
c LRG017 Large Intestine Cancer 53 0.028
995
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 53 0.028
996
CLF001 Cleft Lip 53 0.028
997
NRT001 Neurotic Disorder 53 0.028
998
CHR073 Choreatic Disease 52 0.028
999
HYP014 Hyperuricemia 52 0.028
1000
P CTN015 Cutaneous T Cell Lymphoma 52 0.028
1001
KRT009 Keratosis 52 0.028
1002
c CNT033 Central Nervous System Cancer 51 0.028
1003
BLR001 Biliary Atresia 51 0.028
1004
c OPT053 Optic Atrophy 1 51 0.028
1005
BNN003 Bone Inflammation Disease 51 0.028
1006
CHL004 Cholelithiasis 50 0.028
1007
LPR001 Lepromatous Leprosy 50 0.028
1008
END021 Endomyocardial Fibrosis 50 0.028
1009
c MLG074 Malignant Mesenchymoma 50 0.028
1010
ESP020 Esophageal Atresia 49 0.028
1011
BRX001 Bruxism 49 0.028
1012
ART017 Aortic Disease 49 0.028
1013
DRM011 Dermatophytosis 49 0.028
1014
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 49 0.028
1015
CHL061 Childhood Leukemia 49 0.028
1016
GRW007 Growth Hormone Deficiency 48 0.028
1017
PLP001 Pulpitis 48 0.028
1018
OVR063 Overnutrition 47 0.028
1019
KRT002 Keratomalacia 47 0.028
1020
LFT001 Left Bundle Branch Hemiblock 47 0.028
1021
MLR002 Miliary Tuberculosis 47 0.028
1022
PRP007 Priapism 47 0.028
1023
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.028
1024
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.028
1025
LRY022 Laryngoonychocutaneous Syndrome 45 0.028
1026
c PRM038 Primary Agammaglobulinemia 45 0.028
1027
DBT002 Diabetic Autonomic Neuropathy 45 0.028
1028
c FTL006 Fetal Alcohol Spectrum Disorder 45 0.028
1029
LYM009 Lymphocytic Choriomeningitis 45 0.028
1030
TLR001 Tularemia 44 0.028
1031
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.028
1032
BRN032 Brain Glioma 44 0.028
1033
MTC004 Mitochondrial Encephalomyopathy 44 0.028
1034
ASB001 Asbestosis 44 0.028
1035
PRL008 Paralytic Ileus 43 0.028
1036
c PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 43 0.028
1037
ISC015 Ischemic Colitis 43 0.028
1038
c PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 43 0.028
1039
c HYP072 Hypersensitivity Reaction Type Iii Disease 42 0.028
1040
c MJR024 Major Affective Disorder 9 42 0.028
1041
THR123 Thrombotic Microangiopathy 41 0.028
1042
PLY100 Polyploidy 41 0.028
1043
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 40 0.028
1045
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 40 0.028
1046
IDP070 Idiopathic Scoliosis 39 0.028
1047
INT011 Interstitial Emphysema 39 0.028
1048
c MJR022 Major Affective Disorder 8 39 0.028
1049
ALG001 Algoneurodystrophy 38 0.028
1050
RBS002 Rubeosis Iridis 38 0.028
1051
PNB004 Panbronchiolitis, Diffuse 37 0.028
1052
SCR011 Scrapie 37 0.028
1053
CRT012 Cortical Blindness 37 0.028
1054
DVL001 Developmental Coordination Disorder 36 0.028
1055
ART110 Arteritic Anterior Ischemic Optic Neuropathy 36 0.028
1056
NCR002 Necrobiosis Lipoidica 36 0.028
1057
BRK012 Broken Heart Syndrome 36 0.028
1058
HYP114 Hypertensive Nephropathy 36 0.028
1059
VSC004 Vasculogenic Impotence 33 0.028
1060
VRT003 Vertebrobasilar Insufficiency 33 0.028
1061
CRD016 Cardiac Rupture 33 0.028
1062
INT009 Intracranial Abscess 32 0.028
1063
DYS013 Dysbaric Osteonecrosis 32 0.028
1064
MCH006 Mechanical Strabismus 31 0.028
1065
GNT019 Giant Cell Myocarditis 30 0.028
1066
DSC004 Discitis 30 0.028
1067
ARG004 Argyria 28 0.028
1068
MST020 Mast Cell Activation Syndrome 28 0.028
1069
ACT162 Acute Sensory Ataxic Neuropathy 27 0.028
1070
HDG004 Hodgkin's Granuloma 27 0.028
1071
FTL073 Fetal Anticonvulsant Syndrome 26 0.028
1072
ASB003 Asbestos Intoxication 26 0.028
1073
P PLM069 Pulmonary Venous Return Anomaly 26 0.028
1074
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.028
1075
DVL005 Developmental Dyspraxia 24 0.028
1076
CNG092 Congenital Extrahepatic Portosystemic Shunt 24 0.028
1077
P PLM064 Pulmonary Sequestration 23 0.028
1078
CRB087 Cerebral Arteriosclerosis 23 0.028
1079
HDG006 Hodgkin's Paragranuloma 23 0.028
1080
VLK001 Volkmann Contracture 22 0.028
1081
MRF001 Marfan Syndrome 75 0.024
1082
c SPN225 Spondyloarthropathy 1 74 0.024
1083
MLT157 Multiple System Atrophy 1 71 0.024
1084
P BRG001 Brugada Syndrome 70 0.024
1085
c PRM196 Premature Ovarian Failure 1 70 0.024
1086
P OST001 Osteopetrosis 70 0.024
1087
c WLM013 Wilms Tumor 1 69 0.024
1088
P LNG028