Search results for Oxygen

2420 hits were found for Oxygen

# Family MCID Name MIFTS Score
1
HMG031 Hemoglobin, High Altitude Adaptation 15 2.891
2
P RSP003 Respiratory Failure 74 0.663
3
HYP266 Hypoxia 57 0.524
4
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.423
5
P CRD119 Cardiac Arrest 67 0.402
6
LNG099 Lung Disease 60 0.396
7
ANX004 Anoxia 40 0.359
8
CRD137 Cardiogenic Shock 47 0.357
9
P PLM037 Pulmonary Hypertension 67 0.347
10
ISC004 Ischemia 58 0.323
11
TXC005 Toxic Shock Syndrome 62 0.312
12
BRN071 Brain Injury 49 0.293
13
TRM010 Traumatic Brain Injury 51 0.288
14
c EXD008 Exudative Vitreoretinopathy 1 71 0.275
15
P ADL010 Adult Respiratory Distress Syndrome 65 0.269
16
PLM010 Pulmonary Edema 54 0.246
17
P SLP006 Sleep Apnea 69 0.246
18
CNG034 Congestive Heart Failure 69 0.245
19
P VSC007 Vascular Disease 63 0.243
20
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.241
21
P HRT032 Heart Disease 75 0.236
22
c DPH024 Diaphragmatic Hernia, Congenital 63 0.230
23
BRN056 Bronchopulmonary Dysplasia 57 0.222
24
48X005 48,xyyy 39 0.211
25
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.209
26
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.208
27
OCL069 Ocular Motor Apraxia 51 0.208
28
PNG002 Pain Agnosia 51 0.203
29
P PLM036 Pulmonary Fibrosis 65 0.196
30
P PNM007 Pneumonia 68 0.194
31
MTB004 Metabolic Acidosis 50 0.193
32
CRB039 Cerebrovascular Disease 67 0.192
33
P MCR115 Microvascular Complications of Diabetes 5 66 0.190
34
CRB004 Cerebral Artery Occlusion 45 0.189
35
BRN002 Bronchiolitis 59 0.186
36
HDN002 Head Injury 46 0.185
37
PLM033 Pulmonary Embolism 59 0.184
38
RTN020 Retinal Vascular Disease 46 0.183
39
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.181
40
c ACT075 Acute Myocardial Infarction 57 0.181
41
P MYC007 Myocardial Infarction 70 0.181
42
CRB090 Cerebral Hypoxia 44 0.181
43
P MYC008 Myocarditis 59 0.178
44
STR067 Stroke, Ischemic 81 0.178
45
PRP027 Peripheral Vascular Disease 71 0.176
46
LMB062 Limb Ischemia 55 0.174
47
DFC004 Deficiency Anemia 70 0.173
48
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.173
49
NWB001 Newborn Respiratory Distress Syndrome 58 0.172
50
P SCK005 Sickle Cell Disease 50 0.171
51
P KDN018 Kidney Disease 72 0.168
52
P NRB001 Neuroblastoma 72 0.168
53
SPN186 Spinal Cord Injury 60 0.168
54
BRN024 Bronchitis 68 0.167
55
P GLM045 Glioma 63 0.167
56
HYP066 Hyperglycemia 61 0.167
57
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.166
58
LPP008 Lipoprotein Quantitative Trait Locus 62 0.166
59
GLL048 Glial Tumor 45 0.166
60
PNM008 Pneumothorax 56 0.163
61
CHR100 Chronic Ulcer of Skin 55 0.163
62
GSG001 Gas Gangrene 53 0.163
63
ART140 Arteries, Anomalies of 52 0.163
64
c ACT071 Acute Kidney Failure 60 0.162
65
P SZR006 Seizure Disorder 56 0.162
66
P CYS018 Cystitis 59 0.161
67
OST017 Osteomyelitis 64 0.160
68
c FNC043 Fanconi Anemia, Complementation Group E 62 0.160
69
CYS001 Cystic Fibrosis 81 0.159
70
c PRC016 Pre-Eclampsia 63 0.159
71
CVD001 Covid-19 44 0.158
72
P CLR023 Colorectal Cancer 99 0.157
73
VSL002 Visual Epilepsy 59 0.156
74
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.156
75
c ACT027 Acute Pancreatitis 60 0.153
76
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.152
77
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.152
78
c HYP595 Hypertension, Essential 84 0.150
79
P SNS001 Sensorineural Hearing Loss 60 0.150
80
P ENC018 Encephalopathy 61 0.150
81
INT066 Interstitial Lung Disease 60 0.149
82
PRT036 Peritonitis 64 0.147
83
P LCT001 Lactic Acidosis 51 0.147
84
P PLY018 Polycythemia 56 0.144
85
P CMP008 Compartment Syndrome 49 0.144
86
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.143
87
GLB015 Glioblastoma Multiforme 75 0.142
88
P PTN014 Patent Ductus Arteriosus 1 60 0.140
89
MCN007 Meconium Aspiration Syndrome 55 0.140
90
CRB037 Cerebral Palsy 69 0.139
91
HRT011 Heart Septal Defect 50 0.138
92
c CHR684 Chronic Kidney Disease 70 0.138
93
ATH013 Atherosclerosis Susceptibility 65 0.138
94
P FBR017 Fibrosarcoma 56 0.138
95
BRN004 Brain Edema 56 0.138
96
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.136
97
ENT011 Enterocolitis 51 0.136
98
ADL002 Adult Syndrome 70 0.136
99
ANG054 Angina Pectoris 66 0.136
100
CYN002 Cyanosis, Transient Neonatal 45 0.136
101
P CRN300 Coronary Heart Disease 1 63 0.134
102
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.134
103
CYT002 Cytokine Deficiency 42 0.134
104
AGN016 Aging 56 0.132
105
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.132
106
SDD008 Sudden Sensorineural Hearing Loss 43 0.131
107
P BCL017 B-Cell Lymphoma 58 0.129
108
P HDC001 Headache 57 0.129
109
LVR012 Liver Cirrhosis 62 0.129
110
INT075 Intracranial Hypertension 53 0.128
111
c DLT002 Dilated Cardiomyopathy 79 0.127
112
DWN001 Down Syndrome 70 0.127
113
P CHR012 Chronic Granulomatous Disease 67 0.127
114
c MCR113 Microvascular Complications of Diabetes 3 52 0.127
115
SNG003 Single Ventricular Heart 30 0.126
116
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.125
117
c ATR087 Atrial Standstill 1 75 0.125
118
P MLN007 Male Infertility 55 0.125
119
SCK003 Sickle Cell Anemia 74 0.124
120
HYP056 Hypoglycemia 66 0.124
121
APN008 Apnea, Obstructive Sleep 64 0.124
122
PRN019 Perinatal Necrotizing Enterocolitis 59 0.124
123
c MCR120 Microvascular Complications of Diabetes 7 47 0.124
124
ATX019 Ataxia with Vitamin E Deficiency 42 0.124
125
P LNG032 Lung Cancer 98 0.124
126
P INF032 Infertility 57 0.124
127
c MCR130 Microvascular Complications of Diabetes 6 41 0.124
128
c MCR133 Microvascular Complications of Diabetes 4 41 0.124
129
47X002 47,xyy 49 0.122
130
P LVR013 Liver Disease 68 0.121
131
P PNC044 Pancreatitis 61 0.120
132
P PHC003 Pheochromocytoma 71 0.119
133
CRN030 Coronary Stenosis 50 0.118
134
HLX001 Helix Syndrome 47 0.118
135
ADR040 Adrenal Gland Pheochromocytoma 46 0.117
136
P CTR002 Cataract 60 0.117
137
P ACT105 Acute Mountain Sickness 52 0.117
138
P DBT009 Diabetes Mellitus 64 0.116
139
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.116
140
THR024 Thrombosis 57 0.116
141
P NRP001 Neuropathy 56 0.115
142
FSC004 Fasciitis 50 0.115
143
P TTR001 Tetralogy of Fallot 70 0.114
144
SBC016 Subacute Delirium 44 0.114
145
NNT004 Neonatal Respiratory Failure 36 0.113
146
P MLT020 Multiple Sclerosis 72 0.112
147
P BRS047 Breast Cancer 97 0.111
148
P PNC035 Pancreatic Cancer 84 0.111
149
PRT037 Pertussis 65 0.110
150
P VNT002 Ventricular Septal Defect 60 0.110
151
P RTN018 Retinal Disease 53 0.110
152
PPL052 Papillomatosis, Confluent and Reticulated 33 0.110
153
P HPT023 Hepatocellular Carcinoma 100 0.109
154
ATM095 Autoimmune Disease 62 0.109
155
P INF037 Inflammatory Bowel Disease 54 0.109
156
END086 End Stage Renal Disease 51 0.108
157
NCR007 Necrotizing Fasciitis 48 0.108
158
P BLD134 Bladder Cancer 79 0.107
159
P THR014 Thrombocytopenia 67 0.107
160
P PRD008 Periodontitis 64 0.107
161
P HYP055 Hypoplastic Left Heart Syndrome 63 0.107
162
INT002 Intermittent Claudication 61 0.107
163
P MYL006 Myeloid Leukemia 60 0.107
164
HMR023 Hemorrhagic Cystitis 45 0.107
165
P CLS010 Cluster Headache 42 0.107
166
P PRS040 Prostate Cancer 97 0.106
167
c MCR129 Microvascular Complications of Diabetes 1 66 0.106
168
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.105
169
CRV035 Cervical Cancer 76 0.105
170
OST003 Osteonecrosis 61 0.105
171
P TRN020 Turner Syndrome 67 0.104
172
AST005 Asthma 76 0.103
173
PLM001 Pulmonary Tuberculosis 69 0.103
174
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.103
175
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.103
176
P ECL001 Eclampsia 50 0.103
177
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.103
178
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.103
179
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.103
180
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.103
181
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.103
182
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.103
183
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.103
184
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.103
185
P OVR042 Ovarian Cancer 88 0.102
186
P MYP004 Myopathy 70 0.102
187
c PCH010 Pachyonychia Congenita 3 44 0.102
188
c SVR001 Severe Acute Respiratory Syndrome 62 0.102
189
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.102
190
BCT022 Bacterial Infectious Disease 56 0.102
191
c BRN108 Branchiootic Syndrome 1 62 0.101
193
ART016 Aortic Aneurysm 69 0.100
194
c MCR112 Microvascular Complications of Diabetes 2 41 0.100
195
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.099
196
P ART021 Arteriosclerosis 54 0.099
197
OST159 Osteogenic Sarcoma 66 0.098
198
ESP021 Esophageal Cancer 90 0.097
199
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.097
200
P LNG064 Lung Cancer Susceptibility 3 78 0.096
201
SQM006 Squamous Cell Carcinoma 60 0.096
202
CRD001 Cardiac Tamponade 47 0.096
203
HRW001 Hair Whorl 36 0.096
204
RSP007 Respiratory Distress Syndrome, Infant 30 0.096
205
c SYS001 Systemic Lupus Erythematosus 86 0.095
206
P ADN016 Adenocarcinoma 64 0.095
207
P PLM034 Pulmonary Emphysema 55 0.095
208
PRP080 Peripheral Artery Disease 53 0.095
209
P VSC011 Vasculitis 62 0.094
210
TLN003 Telangiectasis 52 0.094
211
TTN003 Tetanus 65 0.093
212
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.093
213
P MTR003 Mitral Valve Stenosis 50 0.093
214
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.093
215
HPR003 Heparin-Induced Thrombocytopenia 48 0.093
216
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.093
217
RDT001 Radiation Cystitis 32 0.093
218
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.092
219
ULC004 Ulcerative Colitis 73 0.092
220
c MGR028 Migraine with or Without Aura 1 67 0.092
221
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.092
222
FTT001 Fatty Liver Disease 61 0.092
223
IRN002 Iron Metabolism Disease 57 0.092
224
HMG005 Hemoglobinopathy 56 0.092
225
c HYP836 Hypercholesterolemia, Familial, 1 73 0.091
226
P LKM002 Leukemia 68 0.091
227
BNR002 Bone Resorption Disease 48 0.091
228
c LKM061 Leukemia, Acute Myeloid 84 0.090
229
P HYP076 Hyperthyroidism 55 0.090
230
ASP004 Asphyxia Neonatorum 46 0.090
231
CLT003 Colitis 62 0.089
232
EYD002 Eye Disease 58 0.089
233
HMS001 Hemosiderosis 54 0.089
234
ART074 Aortic Dissection 52 0.089
235
P MTH007 Methemoglobinemia 46 0.089
236
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.088
237
CRH001 Crohn's Disease 74 0.088
238
ANX010 Anxiety 73 0.088
239
P SKN015 Skin Carcinoma 66 0.088
240
P ART005 Arteriovenous Malformation 65 0.088
241
RTN017 Retinal Detachment 61 0.088
242
P ATR010 Atrial Heart Septal Defect 60 0.088
243
P RTN022 Retinal Vein Occlusion 53 0.088
244
IMP005 Impotence 52 0.088
245
P RTN014 Retinal Artery Occlusion 47 0.088
246
BRN026 Branch Retinal Artery Occlusion 40 0.088
247
DCB001 Decubitus Ulcer 61 0.087
248
ORL011 Oral Cancer 60 0.087
249
P LTR001 Lateral Sclerosis 54 0.087
250
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.087
251
P ALZ034 Alzheimer Disease 88 0.086
252
DPR016 Depression 63 0.086
253
ANR040 Aneurysm 59 0.086
254
P SPP010 Suppressor of Tumorigenicity 3 51 0.086
255
RTN003 Retinal Ischemia 50 0.086
256
PRC003 Proctitis 47 0.086
257
c PLM022 Pulmonary Valve Insufficiency 39 0.086
258
P GST053 Gastric Cancer 83 0.085
259
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.085
260
c SCL052 Scleroderma, Familial Progressive 61 0.085
261
P OPT006 Optic Nerve Disease 60 0.085
262
P CRD246 Cardiovascular System Disease 57 0.085
263
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.085
264
RST023 Resting Heart Rate, Variation in 41 0.085
265
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.085
266
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.084
267
P CNR004 Cone-Rod Dystrophy 2 73 0.084
268
ALL026 Allergic Hypersensitivity Disease 62 0.084
269
PRP016 Paraplegia 52 0.084
270
PRV004 Periventricular Leukomalacia 52 0.084
271
P RRH023 Rare Hereditary Hemochromatosis 41 0.084
272
c ERY064 Erythrocytosis, Familial, 6 23 0.084
273
SVR004 Severe Combined Immunodeficiency 73 0.083
274
P NTR004 Neutropenia 63 0.083
275
IDP011 Idiopathic Interstitial Pneumonia 59 0.083
276
P BRN022 Bronchiectasis 59 0.083
277
PST028 Post-Traumatic Stress Disorder 58 0.083
278
FBR047 Fibromyalgia 58 0.083
279
DSS009 Disseminated Intravascular Coagulation 57 0.083
280
c ACT134 Acute Liver Failure 56 0.083
281
CRT013 Carotid Stenosis 50 0.083
282
ACT084 Acute Stress Disorder 47 0.083
283
CRT015 Carotid Artery Occlusion 45 0.083
284
P CHR345 Chronic Pain 44 0.083
285
SKN016 Skin Disease 63 0.081
286
BLR008 Bilirubin Metabolic Disorder 57 0.081
287
STT002 Status Asthmaticus 50 0.081
288
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.081
289
c RHB024 Rhabdomyosarcoma 2 67 0.080
290
c PNS012 Paine Syndrome 61 0.080
291
c MLG068 Malignant Glioma 46 0.080
292
FRN014 Fournier Gangrene 37 0.080
293
LPT014 Leptin Deficiency or Dysfunction 74 0.079
294
P HYD006 Hydrocephalus 66 0.079
295
P GLM007 Glomerulonephritis 57 0.079
296
MYC005 Myocardial Stunning 46 0.079
298
SLC006 Silicosis 56 0.078
299
P VNS003 Venous Insufficiency 55 0.078
300
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.078
301
TRC005 Tracheal Stenosis 38 0.078
302
CHL079 Children's Interstitial Lung Disease 26 0.078
303
OST012 Osteoarthritis 78 0.077
304
P ATS364 Autism 70 0.077
305
TRN015 Transient Cerebral Ischemia 63 0.077
306
c CNT015 Central Sleep Apnea 45 0.077
307
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.077
308
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.077
309
CYN003 Cyanide Poisoning 24 0.077
310
P GST044 Gastritis 56 0.076
311
SYN036 Syncope 45 0.076
312
P ATX030 Ataxia-Telangiectasia 82 0.074
313
P MLN008 Melanoma 69 0.074
314
P HML002 Hemolytic Anemia 63 0.074
315
SDD001 Sudden Infant Death Syndrome 61 0.074
316
PPT005 Peptic Ulcer Disease 59 0.074
317
P MYP006 Myopia 55 0.074
318
c VRL005 Viral Pneumonia 52 0.074
319
P OPN001 Open-Angle Glaucoma 49 0.074
320
c ACT076 Acute Myocarditis 46 0.074
321
P SRC025 Sarcoidosis 1 70 0.073
322
P LPS004 Lupus Erythematosus 61 0.073
323
PTN001 Patent Foramen Ovale 60 0.073
324
HPT009 Hepatopulmonary Syndrome 48 0.073
325
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.073
326
c THR092 Thrombophilia Due to Thrombin Defect 73 0.072
327
P MSC005 Muscular Dystrophy 66 0.072
328
LSH001 Leishmaniasis 63 0.072
329
STT001 Status Epilepticus 60 0.072
330
P THL005 Thalassemia 60 0.072
331
MNT002 Mental Depression 58 0.072
332
PRS030 Persistent Fetal Circulation Syndrome 52 0.072
333
c BCT013 Bacterial Pneumonia 48 0.072
334
c MTR002 Mitral Valve Insufficiency 48 0.072
335
P KLZ004 Kala-Azar 1 41 0.072
336
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.072
337
P RTN008 Retinitis Pigmentosa 79 0.070
338
OTT002 Otitis Media 72 0.070
339
P LKM062 Leukemia, Acute Lymphoblastic 69 0.070
340
P INF038 Influenza 68 0.070
341
CRD223 Cardiac Arrhythmia 60 0.070
342
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.070
343
MCL006 Macular Retinal Edema 55 0.070
344
P TRM003 Tremor 54 0.070
345
RTN023 Retinitis 46 0.070
346
NRR001 Neuroretinitis 42 0.070
347
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.070
348
ANP008 Anaplastic Oligoastrocytoma 30 0.070
349
MLR004 Malaria 81 0.069
350
P HYP086 Hypothyroidism 69 0.069
351
P NSP012 Nasopharyngeal Carcinoma 66 0.069
352
P KDN017 Kidney Cancer 60 0.069
353
VRC005 Varicose Veins 60 0.069
354
P BRS044 Breast Adenocarcinoma 59 0.069
355
P PRP019 Peripheral Nervous System Disease 58 0.069
356
ATR057 Atrioventricular Block 55 0.069
357
DBT010 Diabetic Neuropathy 54 0.069
358
P DDN001 Duodenal Ulcer 52 0.069
359
URM002 Uremia 49 0.069
360
BCK006 Back Pain 42 0.069
361
MYL069 Myeloma, Multiple 85 0.068
362
P SYS005 Systemic Scleroderma 68 0.068
363
P ATR011 Atrial Fibrillation 66 0.068
364
ACT119 Acute Promyelocytic Leukemia 63 0.068
365
THY029 Thyroid Carcinoma 59 0.068
366
P MYM013 Moyamoya Disease 1 57 0.068
367
PLC005 Placental Insufficiency 57 0.068
368
P RTN016 Retinal Degeneration 53 0.068
369
c CNT028 Central Retinal Artery Occlusion 43 0.068
370
c LKM063 Leukemia, Chronic Myeloid 72 0.066
371
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.066
372
MYL009 Myelodysplastic Syndrome 70 0.066
373
c SML038 Small Cell Cancer of the Lung 65 0.066
374
MSC007 Muscle Hypertrophy 64 0.066
375
P INT070 Intestinal Obstruction 58 0.066
376
BRN012 Bronchiolitis Obliterans 55 0.066
377
INT007 Intermediate Coronary Syndrome 55 0.066
378
OST173 Osteoradionecrosis of the Mandible 17 0.066
379
ALC007 Alcohol Dependence 66 0.065
380
CLN015 Colon Adenocarcinoma 65 0.065
381
NRM005 Neuromuscular Disease 64 0.065
382
P PSR002 Psoriasis 62 0.065
383
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.065
384
P END033 Endocarditis 57 0.065
385
MCR141 Mucormycosis 56 0.065
386
VRC001 Varicocele 49 0.065
387
c TRC022 Tricuspid Valve Insufficiency 45 0.065
388
BRN028 Brain Cancer 74 0.064
389
P LYM118 Lymphoma 68 0.064
390
c GLC092 Glaucoma, Primary Open Angle 62 0.064
391
PNM010 Pneumothorax, Primary Spontaneous 60 0.064
392
PRT013 Portal Hypertension 59 0.064
393
CHL123 Chlamydia 59 0.064
394
VSC002 Vascular Dementia 57 0.064
395
P DRR001 Diarrhea 55 0.064
396
HYP060 Hyperinsulinism 54 0.064
397
PYD001 Pyoderma Gangrenosum 54 0.064
398
c CNT016 Central Retinal Vein Occlusion 53 0.064
399
c VRL010 Viral Hepatitis 52 0.064
400
PYD002 Pyoderma 50 0.064
401
ENT004 Enthesopathy 49 0.064
402
RDT013 Radiation Proctitis 47 0.064
403
P BNG032 Benign Mesothelioma 46 0.064
404
P RHM011 Rheumatoid Arthritis 80 0.062
405
P OST002 Osteoporosis 74 0.062
406
P HNT016 Huntington Disease 72 0.062
407
PLM031 Poliomyelitis 64 0.062
408
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.062
409
GLS001 Gliosarcoma 54 0.062
410
PST011 Pustulosis of Palm and Sole 52 0.062
411
CLC001 Calciphylaxis 51 0.062
412
P AST007 Astrocytoma 51 0.062
413
ASP007 Aspiration Pneumonia 48 0.062
414
ACT003 Acute Kidney Tubular Necrosis 45 0.062
415
P CRN026 Corneal Edema 43 0.062
416
ORL015 Oral Squamous Cell Carcinoma 43 0.062
417
NCR014 Necrotizing Soft Tissue Infection 23 0.062
418
P PRK057 Parkinson Disease, Late-Onset 78 0.061
419
P HYP061 Hypertrophic Cardiomyopathy 70 0.061
420
P ASP006 Aspergillosis 69 0.061
421
PLY001 Polycythemia Vera 69 0.061
422
SRC014 Sarcoma 65 0.061
423
c DBT099 Diabetes Mellitus, Type I 65 0.061
424
P RHB003 Rhabdomyosarcoma 63 0.061
425
P END044 Endometriosis 63 0.061
426
P INT143 Interstitial Cystitis 61 0.061
427
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.061
428
P MTC069 Mitochondrial Disorders 56 0.061
429
SPN035 Spindle Cell Sarcoma 53 0.061
430
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.061
431
c CHR431 Chronic Venous Insufficiency 49 0.061
432
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.061
433
HPT004 Hepatic Coma 45 0.061
434
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.061
435
P LKM071 Leukemia, Chronic Lymphocytic 79 0.059
436
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.059
437
c ACT068 Acute Cystitis 63 0.059
438
CRD132 Cardiac Conduction Defect 58 0.059
439
P PYL005 Pyelonephritis 56 0.059
440
P PNM006 Pneumoconiosis 56 0.059
441
HYP005 Hypokalemia 55 0.059
442
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.059
443
P PLM006 Pulmonary Alveolar Proteinosis 53 0.059
444
GST023 Gastric Ulcer 53 0.059
445
P MSC003 Muscular Atrophy 52 0.059
446
ACT017 Acute Chest Syndrome 51 0.059
447
QDR001 Quadriplegia 48 0.059
448
ANT018 Anthracosis 48 0.059
449
CRB086 Cerebral Aneurysms 40 0.059
450
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.059
451
INS024 Insulin-Like Growth Factor I 79 0.058
452
c HPT073 Hepatitis C Virus 72 0.058
453
P LPR021 Leprosy 3 69 0.058
454
P DMN002 Dementia 66 0.058
455
P DRM053 Dermatitis, Atopic 66 0.058
456
P ART023 Arthropathy 62 0.058
457
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.058
458
DRM006 Dermatitis 61 0.058
459
ACQ007 Acquired Immunodeficiency Syndrome 60 0.058
460
INF034 Infective Endocarditis 53 0.058
461
ILS001 Ileus 51 0.058
462
CHR074 Choriocarcinoma 47 0.058
463
HNS001 Hansen's Disease 34 0.058
464
MTH071 Methane Production 26 0.058
465
P GLM040 Glioma Susceptibility 1 81 0.056
466
c NRF023 Neurofibromatosis, Type Ii 80 0.056
467
c BTT014 Beta-Thalassemia 74 0.056
468
P GRF003 Graft-Versus-Host Disease 72 0.056
469
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.056
470
c ART101 Aortic Valve Disease 2 65 0.056
471
P SLP005 Sleep Disorder 59 0.056
472
CMP010 Complex Regional Pain Syndrome 58 0.056
473
HMP005 Hemiplegia 55 0.056
474
P RCT021 Rectum Cancer 52 0.056
475
SYS003 Systolic Heart Failure 49 0.056
476
P MTC133 Mitochondrial Myopathy 49 0.056
477
MDS022 Mediastinitis 46 0.056
478
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.056
479
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.056
480
RDN001 Reading Disorder 40 0.056
481
OST115 Osteonecrosis of the Jaw 40 0.056
482
ALL014 Allergic Encephalomyelitis 38 0.056
483
PRM329 Premature Aging 35 0.056
484
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.056
485
DFF031 Diffuse Alveolar Hemorrhage 30 0.056
486
c FNC027 Fanconi Anemia, Complementation Group a 81 0.054
487
P EPL164 Epilepsy 71 0.054
488
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.054
489
LPD008 Lipid Metabolism Disorder 62 0.054
490
P ENC004 Encephalitis 61 0.054
491
P SCL018 Scoliosis 60 0.054
492
INS001 Insulinoma 60 0.054
493
P ERY058 Erythrocytosis, Familial, 1 59 0.054
494
ESN011 Eisenmenger Syndrome 55 0.054
495
PRP030 Purpura 54 0.054
496
RHM028 Rheumatic Heart Disease 53 0.054
497
ATN005 Autonomic Dysfunction 46 0.054
498
c ERY065 Erythrocytosis, Familial, 7 33 0.054
499
HMN044 Human Immunodeficiency Virus Type 1 71 0.053
500
P ART022 Arthritis 69 0.053
501
LYM133 Lymphoma, Hodgkin, Classic 69 0.053
502
CHG001 Chagas Disease 66 0.053
503
KWS002 Kawasaki Disease 65 0.053
504
CRC021 Carcinosarcoma 62 0.053
505
NTR005 Nutritional Deficiency Disease 62 0.053
506
CHR066 Chronic Fatigue Syndrome 61 0.053
507
CHL014 Cholera 59 0.053
508
P MYS005 Myositis 56 0.053
509
SFT003 Soft Tissue Sarcoma 56 0.053
510
PRS047 Prostatitis 56 0.053
511
c GRV008 Graves Disease 1 56 0.053
512
AMN003 Amnestic Disorder 54 0.053
514
c PRM012 Primary Polycythemia 50 0.053
515
P OVR082 Overgrowth Syndrome 50 0.053
516
DYS073 Dysphagia 50 0.053
517
RNL077 Renal Fibrosis 47 0.053
518
RYN005 Raynaud Phenomenon 47 0.053
519
GGN002 Gigantism 33 0.053
520
PLY150 Polykaryocytosis Inducer 31 0.053
521
CRT057 Critical Congenital Heart Disease 21 0.053
522
NRL016 Neural Tube Defects 82 0.051
523
P RTN024 Retinoblastoma 73 0.051
524
CNN005 Connective Tissue Disease 68 0.051
525
BRK010 Burkitt Lymphoma 67 0.051
526
c ATS007 Autism Spectrum Disorder 67 0.051
527
LPT001 Leptospirosis 66 0.051
528
KRT019 Keratitis, Hereditary 65 0.051
529
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.051
530
CHL068 Cholestasis 61 0.051
531
P BND020 Bone Disease 59 0.051
532
P RHN004 Rhinitis 57 0.051
533
GLC003 Glucose Intolerance 54 0.051
534
HRT012 Heart Valve Disease 53 0.051
535
MST005 Mastitis 53 0.051
536
c FML008 Familial Retinoblastoma 53 0.051
537
CRT016 Carotid Artery Disease 52 0.051
538
P CRB088 Cerebral Atrophy 37 0.051
539
HRN029 Hearing Loss, Noise-Induced 37 0.051
540
ERY007 Erythropoietin Polycythemia 16 0.051
541
IMM167 Immune Deficiency Disease 78 0.049
542
PPL049 Papillon-Lefevre Syndrome 65 0.049
543
P PRP029 Porphyria 62 0.049
544
HPT019 Hepatic Encephalopathy 60 0.049
545
APH002 Aphasia 57 0.049
546
CLL003 Cellulitis 54 0.049
547
GTR002 Goiter 53 0.049
548
SPS003 Spastic Diplegia 51 0.049
549
CLR109 Colorectal Adenocarcinoma 51 0.049
550
P ART018 Aortic Valve Insufficiency 49 0.049
551
MTC005 Mitochondrial Metabolism Disease 49 0.049
552
ACT029 Acute Interstitial Pneumonia 49 0.049
553
DGN001 Degenerative Disc Disease 48 0.049
554
BCK003 Background Diabetic Retinopathy 46 0.049
555
OBS037 Obesity-Hypoventilation Syndrome 46 0.049
556
SPS057 Spasticity 45 0.049
557
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.049
558
RFR003 Refractive Error 43 0.049
559
P AVS003 Avascular Necrosis 42 0.049
560
KLD004 Keloid Disorder 40 0.049
561
ART008 Arteriosclerosis Obliterans 40 0.049
562
CHR178 Chromosomal Triplication 35 0.049
563
PNM003 Pneumatosis Cystoides Intestinalis 32 0.049
564
P AMY004 Amyloidosis 70 0.047
565
CHL065 Cholangiocarcinoma 68 0.047
566
RCK004 Rickets 68 0.047
567
P HYP098 Hypereosinophilic Syndrome 67 0.047
568
P MNN013 Meningitis 66 0.047
569
c HPT001 Hepatitis C 62 0.047
570
P DRM010 Dermatomyositis 61 0.047
571
P NPH012 Nephrotic Syndrome 60 0.047
572
GNG013 Gingivitis 59 0.047
573
HLC007 Helicobacter Pylori Infection 59 0.047
574
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.047
575
LST001 Listeriosis 56 0.047
576
ALL006 Allergic Asthma 56 0.047
577
PRP009 Peripartum Cardiomyopathy 55 0.047
578
P LRY044 Larynx Cancer 55 0.047
579
INT079 Intrahepatic Cholangiocarcinoma 51 0.047
580
LNG031 Lung Benign Neoplasm 51 0.047
581
RSP006 Respiratory System Disease 50 0.047
582
PLC008 Placenta Disease 50 0.047
583
LPT006 Leptin Receptor Deficiency 48 0.047
584
DBT008 Diabetic Angiopathy 44 0.047
585
c HMG029 Hemoglobin Se Disease 39 0.047
586
MTH047 Methanol Poisoning 34 0.047
587
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.047
588
c ADL080 Adult Acute Respiratory Distress Syndrome 26 0.047
589
URT049 Urate Oxidase, Pseudogene 25 0.047
590
MSC157 Muscular Dystrophy, Duchenne Type 72 0.045
591
GST040 Gastric Adenocarcinoma 70 0.045
592
P TBR001 Tuberous Sclerosis 70 0.045
593
P MYC084 Mycobacterium Tuberculosis 1 68 0.045
594
GST033 Gestational Diabetes 61 0.045
595
PRT058 Pure Autonomic Failure 59 0.045
596
AVN001 Avian Influenza 59 0.045
597
P CND004 Candidiasis 58 0.045
598
P UVT001 Uveitis 57 0.045
599
INT030 Intracranial Aneurysm 56 0.045
600
HPT022 Hepatoblastoma 56 0.045
601
c BCT007 Bacterial Meningitis 55 0.045
602
RSC001 Rosacea 54 0.045
603
c PRD040 Periodontitis, Chronic 53 0.045
604
DNT012 Dental Caries 53 0.045
605
ASC010 Ascaris Lumbricoides Infection 50 0.045
606
P OBS001 Obstructive Jaundice 50 0.045
607
DBT006 Diabetic Macular Edema 48 0.045
608
CRN027 Corneal Neovascularization 47 0.045
609
P CRC039 Coarctation of Aorta 47 0.045
610
TST044 Testicular Torsion 47 0.045
611
ANR004 Anuria 46 0.045
612
P PRP034 Purpura Fulminans 43 0.045
613
PRS063 Paresthesia 41 0.045
614
P OTT001 Otitis Externa 39 0.045
615
OVR094 Ovarian Epithelial Cancer 38 0.045
616
ASC001 Ascaridiasis 35 0.045
617
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.045
618
APN006 Apnea of Prematurity 24 0.045
619
END057 Endometrial Cancer 74 0.043
620
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.043
621
P OCL013 Oculodentodigital Dysplasia 69 0.043
622
P MJR001 Major Depressive Disorder 68 0.043
623
GST092 Gastroesophageal Reflux 67 0.043
624
P HRP006 Herpes Simplex 65 0.043
625
CHC001 Chickenpox 60 0.043
626
ING001 Inguinal Hernia 60 0.043
627
PNM001 Pneumocystosis 59 0.043
628
IRN001 Iron Deficiency Anemia 59 0.043
629
P EXN002 Exanthem 57 0.043
630
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.043
631
HMR039 Hemorrhage, Intracerebral 57 0.043
632
P PLY011 Polycystic Ovary Syndrome 56 0.043
633
VSC003 Visceral Leishmaniasis 55 0.043
634
SYN007 Synovitis 54 0.043
635
PPL022 Papilloma 54 0.043
636
PLM012 Pulmonary Sarcoidosis 53 0.043
637
MTN003 Motion Sickness 53 0.043
638
HMC014 Homocysteinemia 53 0.043
639
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 53 0.043
640
P PRC012 Pericardial Effusion 51 0.043
641
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.043
642
CHR005 Chorioamnionitis 51 0.043
643
PLR007 Pleural Empyema 50 0.043
644
P KRT007 Keratoconus 50 0.043
645
HYP017 Hypophosphatemia 50 0.043
646
SPL018 Splenomegaly 48 0.043
647
HMP001 Hemopericardium 48 0.043
648
P CLB034 Coloboma, Ocular, Autosomal Dominant 47 0.043
649
ATN004 Autonomic Neuropathy 45 0.043
650
HMP009 Haemophilus Influenzae 43 0.043
651
MYF002 Myofascial Pain Syndrome 42 0.043
652
SPR126 Superior Semicircular Canal Dehiscence 40 0.043
653
GLM044 Glomerular Disease 37 0.043
654
PLC002 Plica Syndrome 36 0.043
655
PST092 Posttransplant Acute Limbic Encephalitis 29 0.043
656
c MLG042 Malignant Otitis Externa 25 0.043
657
KPS004 Kaposi Sarcoma 75 0.041
658
c MNN043 Meningioma, Familial 74 0.041
659
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.041
660
ACR008 Acrocallosal Syndrome 69 0.041
661
LYM007 Lymphangioleiomyomatosis 69 0.041
662
P MTR014 Motor Neuron Disease 65 0.041
663
P HYP750 Hypertriglyceridemia, Familial 62 0.041
664
MNN042 Meningioma, Radiation-Induced 62 0.041
665
CTN007 Cutaneous Leishmaniasis 62 0.041
666
VRL011 Viral Infectious Disease 61 0.041
667
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.041
668
CHL067 Cholecystitis 57 0.041
669
MCS002 Mucositis 56 0.041
670
P SBS003 Substance Abuse 55 0.041
671
BRN014 Bronchopneumonia 54 0.041
672
NNL006 Non-Alcoholic Steatohepatitis 54 0.041
673
NRT004 Neuritis 52 0.041
674
P TRT010 Teratoma 52 0.041
675
SPN021 Spinal Meningioma 50 0.041
676
c SVR005 Severe Pre-Eclampsia 50 0.041
677
NTR046 Neutrophil Migration 50 0.041
678
P RNL015 Renal Hypertension 47 0.041
679
c ACQ010 Acquired Polycythemia 46 0.041
680
SQM002 Squamous Cell Papilloma 46 0.041
681
URT010 Ureteral Obstruction 45 0.041
682
CRP002 Croup 44 0.041
683
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.041
684
SCR001 Secretory Meningioma 41 0.041
685
LVD003 Livedoid Vasculitis 36 0.041
686
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.041
687
c PRS136 Prostate Cancer, Hereditary, 6 33 0.041
688
c PRS130 Prostate Cancer, Hereditary, 8 32 0.041
689
c TBR025 Tuberous Sclerosis 1 77 0.038
690
P APL001 Aplastic Anemia 74 0.038
691
c HMC039 Hemochromatosis, Type 1 74 0.038
692
c BSL007 Basal Cell Carcinoma 68 0.038
693
PNC129 Pancreatic Adenocarcinoma 68 0.038
694
P MLG056 Malignant Hyperthermia 67 0.038
695
KRN002 Kearns-Sayre Syndrome 63 0.038
696
c ALP101 Alpha-Thalassemia 62 0.038
697
P DNG005 Dengue Virus 59 0.038
698
ADN018 Adenoma 59 0.038
699
GST045 Gastroenteritis 59 0.038
700
c ACT073 Acute Leukemia 58 0.038
701
P ALC033 Alcohol Use Disorder 58 0.038
702
EXT034 Extrinsic Allergic Alveolitis 58 0.038
703
c MST023 Mesothelioma, Malignant 57 0.038
704
NPH009 Nephrolithiasis 55 0.038
705
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.038
706
P NRM002 Normal Pressure Hydrocephalus 54 0.038
707
TND005 Tendinitis 54 0.038
708
TRC062 Tricuspid Atresia 54 0.038
709
GST009 Gastroschisis 53 0.038
710
ACR041 Acromelic Frontonasal Dysostosis 52 0.038
711
SPN051 Spondylitis 51 0.038
712
OLG003 Oligohydramnios 51 0.038
713
MYL001 Myelitis 51 0.038
714
HYP781 Hypoascorbemia 51 0.038
715
c HRD202 Hereditary Lymphedema I 50 0.038
716
c ACQ017 Acquired Von Willebrand Syndrome 49 0.038
717
c INV001 Invasive Aspergillosis 49 0.038
718
P VTR007 Vitreoretinopathy 46 0.038
719
CMP034 Complete Androgen Insensitivity Syndrome 46 0.038
720
P HRN001 Horner's Syndrome 45 0.038
721
BCT021 Bacterial Sepsis 44 0.038
722
TND004 Tendinopathy 43 0.038
723
MDD018 Middle East Respiratory Syndrome 43 0.038
724
c HMG001 Hemoglobin C Disease 40 0.038
725
HYP264 Hypertonia 38 0.038
726
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.038
727
INF009 Inflammatory Spondylopathy 31 0.038
728
UNV002 Univentricular Heart 28 0.038
729
PRQ002 Paraquat Poisoning 26 0.038
730
P RTT002 Rett Syndrome 80 0.036
731
P DYS154 Dystonia 65 0.036
732
BRR014 Barrett Esophagus 65 0.036
733
GRN037 Granulomatosis with Polyangiitis 65 0.036
734
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.036
735
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.036
736
TYP007 Typhoid Fever 63 0.036
737
P HYP069 Hyperparathyroidism 63 0.036
738
P PLY014 Polycystic Kidney Disease 62 0.036
739
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.036
740
TRG002 Trigeminal Neuralgia 60 0.036
741
SPN027 Spinal Stenosis 59 0.036
742
c DWL002 Dowling-Degos Disease 1 58 0.036
743
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.036
744
P BPL003 Bipolar Disorder 56 0.036
745
GST050 Gastrointestinal System Disease 56 0.036
746
c ERY071 Erythrocytosis, Familial, 2, Autosomal Recessive 55 0.036
747
ORL004 Oral Submucous Fibrosis 55 0.036
748
CPL003 Capillary Leak Syndrome 55 0.036
749
HDR002 Hidradenitis Suppurativa 55 0.036
750
NVS001 Neovascular Glaucoma 53 0.036
751
P PRG013 Paraganglioma 52 0.036
752
DYS015 Dysentery 52 0.036
753
MCR088 Microscopic Polyangiitis 51 0.036
754
PRS021 Prostatic Adenoma 51 0.036
755
P HYP040 Hypospadias 51 0.036
756
CRV040 Cervix Carcinoma 51 0.036
757
P CHL066 Cholangitis 51 0.036
758
STM007 Stomatitis 50 0.036
759
P TMP001 Temporal Lobe Epilepsy 50 0.036
760
BLS002 Blastomycosis 50 0.036
761
P END046 Endometritis 49 0.036
762
HDR003 Hidradenitis 49 0.036
763
ATS010 Autosomal Recessive Disease 48 0.036
764
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 0.036
765
P BLR006 Biliary Tract Disease 47 0.036
766
AST006 Astigmatism 47 0.036
767
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.036
768
EPD015 Epidemic Typhus 45 0.036
769
49X006 49, Xxxxy Syndrome 41 0.036
770
c MJR024 Major Affective Disorder 9 41 0.036
771
MCL003 Macular Holes 40 0.036
772
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.036
773
c MJR022 Major Affective Disorder 8 38 0.036
774
ABD010 Abdominal Wall Defect 36 0.036
775
EPD005 Epidural Abscess 35 0.036
776
c LKM005 Leukemia, T-Cell, Chronic 34 0.036
777
HND015 Hand Skill, Relative 33 0.036
778
CND006 Candida Glabrata 32 0.036
779
ANM001 Anemia of Prematurity 31 0.036
780
PLM186 Pulmonary Arterial Hypertension Associated with Portal Hypertension 24 0.036
781
P SCH015 Schizophrenia 74 0.033
782
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.033
783
VNH007 Von Hippel-Lindau Syndrome 73 0.033
784
MNT001 Mantle Cell Lymphoma 69 0.033
785
SKN019 Skin Melanoma 68 0.033
786
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.033
787
P HPT021 Hepatitis 67 0.033
788
ALL003 Allergic Rhinitis 67 0.033
789
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 0.033
790
P NRV007 Nervous System Disease 66 0.033
791
KHL003 Kohlschutter-Tonz Syndrome 65 0.033
792
CLF027 Cleft Palate, Isolated 64 0.033
793
LYM017 Lyme Disease 64 0.033
794
c OPT053 Optic Atrophy 1 63 0.033
795
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.033
796
c HPT016 Hepatitis B 59 0.033
797
GRD007 Grade Iii Astrocytoma 59 0.033
798
P PLY017 Polyarteritis Nodosa 58 0.033
799
ANT024 Anthrax Disease 58 0.033
800
CNT047 Contact Dermatitis 58 0.033
801
P MTR012 Mitral Valve Disease 58 0.033
802
BRG013 Buerger Disease 58 0.033
803
P FTL001 Fetal Alcohol Syndrome 57 0.033
804
SCH014 Schistosomiasis 57 0.033
805
PHR003 Pharyngitis 57 0.033
806
AYM001 Ayme-Gripp Syndrome 57 0.033
807
P PLY019 Polyneuropathy 56 0.033
808
P ATR001 Atrioventricular Septal Defect 55 0.033
809
P ANT006 Antiphospholipid Syndrome 55 0.033
810
P GRV001 Graves' Disease 55 0.033
811
FLR002 Filariasis 55 0.033
812
FCL014 Focal Epilepsy 54 0.033
813
PRC013 Pericarditis 54 0.033
814
PRS045 Prostatic Hypertrophy 53 0.033
815
P INS002 in Situ Carcinoma 53 0.033
816
P MNC007 Monocytic Leukemia 53 0.033
817
BRN038 Bronchial Disease 53 0.033
818
NRT001 Neurotic Disorder 53 0.033
819
c GLL024 Gallbladder Disease 1 53 0.033
820
DMY004 Demyelinating Disease 52 0.033
821
P MGR003 Migraine with Aura 52 0.033
822
INT071 Intestinal Perforation 51 0.033
823
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.033
824
P ESN008 Eosinophilic Pneumonia 50 0.033
825
AZS001 Azoospermia 50 0.033
826
HMG002 Hemoglobinuria 50 0.033
827
PRS129 Prostatic Hyperplasia, Benign 49 0.033
828
LRN003 Learning Disability 49 0.033
829
WTH001 Withdrawal Disorder 48 0.033
830
P RNV001 Renovascular Hypertension 48 0.033
831
IGG001 Iga Glomerulonephritis 48 0.033
832
CHL147 Chlamydia Pneumonia 48 0.033
833
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.033
834
c HYD064 Hydrocephalus, Congenital, 1 48 0.033
835
SXL003 Sexual Disorder 47 0.033
836
CRN017 Coronary Thrombosis 47 0.033
837
LYM019 Lymphosarcoma 46 0.033
838
LKS001 Leukostasis 46 0.033
839
DST006 Diastolic Heart Failure 45 0.033
840
SPS007 Spastic Cerebral Palsy 45 0.033
841
CHP002 Chops Syndrome 44 0.033
842
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.033
843
DMP001 Dumping Syndrome 44 0.033
844
c PRM038 Primary Agammaglobulinemia 44 0.033
845
P CRN024 Corneal Disease 44 0.033
846
P MYG005 Myoglobinuria 44 0.033
847
c CHR096 Chronic Pulmonary Heart Disease 43 0.033
848
c CHR546 Chronic Mountain Sickness 43 0.033
849
P HYP265 Hypotonia 43 0.033
850
P PLM025 Pulmonary Venoocclusive Disease 42 0.033
851
SNL007 Senile Cataract 42 0.033
852
INT276 Interatrial Communication 42 0.033
853
c MLG079 Malignant Pleural Mesothelioma 42 0.033
854
ANC002 Anca-Associated Vasculitis 41 0.033
855
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.033
856
c HYP543 Hypoplastic Left Heart Syndrome 1 40 0.033
857
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.033
858
LPD014 Lipodermatosclerosis 38 0.033
859
c CHR098 Chronic Pyelonephritis 38 0.033
861
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 36 0.033
862
SRF006 Surfactant Dysfunction 35 0.033
863
PLX004 Plexopathy 30 0.033
864
STN013 Stenotrophomonas Maltophilia Infection 25 0.033
865
HVY002 Heavy Metal Poisoning 22 0.033
866
RDT014 Radiation Myelitis 16 0.033
867
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.030
868
PSY004 Psychotic Disorder 67 0.030
869
MYL031 Myeloproliferative Neoplasm 66 0.030
870
c FML001 Familial Atrial Fibrillation 65 0.030
871
TBC004 Tobacco Addiction 64 0.030
872
c JVN010 Juvenile Rheumatoid Arthritis 64 0.030
873
GT001 Gout 64 0.030
874
PLG002 Plague 63 0.030
875
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.030
876
P MVM001 Movement Disease 63 0.030
877
ANR007 Anorexia Nervosa 63 0.030
878
MSS001 Masa Syndrome 62 0.030
879
APP008 Appendicitis 61 0.030
880
RHM001 Rheumatic Fever 60 0.030
881
INC002 Inclusion Body Myositis 58 0.030
882
SPT004 Septic Arthritis 58 0.030
883
CCC001 Coccidioidomycosis 58 0.030
884
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.030
885
P OPT009 Optic Neuritis 57 0.030
886
ERY051 Erythroleukemia, Familial 56 0.030
887
FLR001 Filarial Elephantiasis 55 0.030
888
ORP003 Oropharynx Cancer 55 0.030
889
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.030
890
URN010 Urinary Tract Obstruction 55 0.030
891
END040 Endogenous Depression 55 0.030
892
CRT017 Cartilage Disease 54 0.030
893
RFL001 Reflex Sympathetic Dystrophy 54 0.030
894
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.030
895
P ALP008 Alopecia 54 0.030
896
FNG017 Fungal Infectious Disease 53 0.030
897
CLF001 Cleft Lip 53 0.030
898
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.030
899
P INT068 Intestinal Disease 53 0.030
900
PLS007 Plasmodium Falciparum Malaria 52 0.030
901
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.030
902
P THY032 Thyroiditis 52 0.030
903
HYP014 Hyperuricemia 52 0.030
904
KRT009 Keratosis 51 0.030
905
PLS009 Plasma Cell Neoplasm 51 0.030
906
AMB002 Amblyopia 49 0.030
907
MNN009 Meningoencephalitis 49 0.030
908
CHL061 Childhood Leukemia 48 0.030
909
HYP025 Hyperphosphatemia 48 0.030
910
INT010 Intracranial Embolism 48 0.030
911
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 47 0.030
912
KRT008 Keratopathy 47 0.030
913
KHN001 Kuhnt-Junius Degeneration 47 0.030
914
FCL012 Facial Paralysis 46 0.030
915
KRT013 Keratolytic Winter Erythema 46 0.030
916
CRN019 Coronary Artery Vasospasm 46 0.030
917
P MYC033 Myoclonus 46 0.030
918
MXD026 Mixed Glioma 45 0.030
919
P SBR004 Seborrheic Dermatitis 45 0.030
921
LRY022 Laryngoonychocutaneous Syndrome 44 0.030
922
OVR063 Overnutrition 44 0.030
923
MST004 Mast Cell Neoplasm 42 0.030
924
BNS003 Binswanger's Disease 42 0.030
925
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.030
926
CRN322 Coronavirus Infectious Disease 40 0.030
927
JWD001 Jawad Syndrome 40 0.030
928
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 39 0.030
929
VTR003 Vitreous Detachment 39 0.030
930
SPP007 Suppression Amblyopia 39 0.030
931
AML001 Amelanotic Melanoma 39 0.030
932
EXT007 Extracutaneous Mastocytoma 38 0.030
933
MDD003 Middle Cerebral Artery Infarction 36 0.030
934
TRC020 Tracheitis 36 0.030
935
P MXL015 Maxillary Sinusitis 36 0.030
936
c HMG004 Hemoglobin D Disease 36 0.030
937
ACT056 Acute Cor Pulmonale 36 0.030
938
BRK012 Broken Heart Syndrome 35 0.030
939
TRC110 Tracheobronchial Stenosis, Congenital 28 0.030
940
SPN185 Spinal Cord Infarction 28 0.030
941
P PLM069 Pulmonary Venous Return Anomaly 26 0.030
942
HRL002 Harlequin Syndrome 23 0.030
943
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 20 0.030
944
CLS032 Clostridium Perfringens Infection 17 0.030
945
ADR007 Adrenoleukodystrophy 75 0.027
946
FBR012 Fabry Disease 72 0.027
947
MYL005 Myelofibrosis 70 0.027
948
LGH007 Leigh Syndrome 70 0.027
949
ADN011 Adenoid Cystic Carcinoma 70 0.027
950
WRN001 Werner Syndrome 69 0.027
951
c INF071 Inflammatory Bowel Disease 1 67 0.027
952
ART001 Arterial Tortuosity Syndrome 66 0.027
953
P CNJ013 Conjunctivitis 65 0.027
954
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.027
955
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.027
956
BRC012 Brucellosis 64 0.027
957
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.027
958
MSC152 Muscular Dystrophy, Becker Type 63 0.027
959
INT146 Intervertebral Disc Disease 63 0.027
960
P PTT014 Pitt-Hopkins Syndrome 63 0.027
961
P LMY004 Leiomyosarcoma 63 0.027
962
P ORT004 Orthostatic Intolerance 62 0.027
963
c ANM038 Anemia, Autoimmune Hemolytic 62 0.027
964
MDD011 Mood Disorder 62 0.027
965
P PRM006 Primary Biliary Cirrhosis 62 0.027
966
ESP020 Esophageal Atresia 62 0.027
967
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.027
968
ALC006 Alcoholic Hepatitis 61 0.027
969
ART141 Arteriovenous Malformations of the Brain 61 0.027
970
P HMN010 Hemangioma 61 0.027
971
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.027
972
ANT009 Antithrombin Iii Deficiency 59 0.027
973
P RBL001 Rubella 59 0.027
974
P PRD006 Prader-Willi Syndrome 59 0.027
975
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.027
976
P ANP001 Anaplastic Large Cell Lymphoma 58 0.027
977
ALK013 Alkaptonuria 58 0.027
978
DSS008 Disease of Mental Health 58 0.027
979
LYM027 Lymphopenia 58 0.027
980
LNG108 Langerhans Cell Histiocytosis 58 0.027
981
MCR013 Microphthalmia 57 0.027
982
P PLY041 Polymyositis 57 0.027
983
JPN002 Japanese Encephalitis 57 0.027
984
P ANG015 Angioedema 57 0.027
985
P CHN012 Chondrosarcoma 56 0.027
986
DBL002 Double Outlet Right Ventricle 56 0.027
987
EMB004 Embryonal Carcinoma 56 0.027
988
GDP001 Goodpasture Syndrome 55 0.027
989
EBS001 Ebstein Anomaly 55 0.027
990
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.027
991
P STR020 Strabismus 55 0.027
992
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.027
993
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 55 0.027
994
CLF004 Cleft Lip/palate 54 0.027
995
TRD006 Tardive Dyskinesia 54 0.027
996
HMN009 Hemangioblastoma 54 0.027
997
LYM040 Lymphoblastic Lymphoma 54 0.027
998
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.027
999
SNS003 Sensory Peripheral Neuropathy 54 0.027
1000
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 54 0.027
1001
MMM001 Mammary Paget's Disease 53 0.027
1002
CRH005 Crohn's Colitis 53 0.027
1003
P HMR003 Hemorrhagic Disease 53 0.027
1004
OVR059 Ovary Adenocarcinoma 53 0.027
1005
CHR073 Choreatic Disease 52 0.027
1006
P LRY019 Laryngitis 52 0.027
1007
DRM011 Dermatophytosis 52 0.027
1008
MCN017 Meconium Ileus 52 0.027
1009
PTH003 Pathologic Nystagmus 52 0.027
1010
P HMP007 Hemophilia 51 0.027
1011
TNG007 Tongue Carcinoma 51 0.027
1012
TLR001 Tularemia 51 0.027
1013
PLR008 Pleurisy 50 0.027
1014
BRX001 Bruxism 50 0.027
1015
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 50 0.027
1016
BLR001 Biliary Atresia 50 0.027
1017
LPR001 Lepromatous Leprosy 50 0.027
1018
VLV047 Volvulus of Midgut 49 0.027
1019
PLP001 Pulpitis 49 0.027
1020
LFT001 Left Bundle Branch Hemiblock 49 0.027
1021
END021 Endomyocardial Fibrosis 49 0.027
1022
ART017 Aortic Disease 49 0.027
1023
CHL004 Cholelithiasis 49 0.027
1024
P CTN015 Cutaneous T Cell Lymphoma 49 0.027
1025
MLR002 Miliary Tuberculosis 49 0.027
1026
HST010 Histiocytosis 48 0.027
1027
BNN003 Bone Inflammation Disease 48 0.027
1028
PRP007 Priapism 47 0.027
1029
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.027
1030
ASB001 Asbestosis 47 0.027
1031
LYM009 Lymphocytic Choriomeningitis 47 0.027
1032
KRT002 Keratomalacia 47 0.027
1033
CNT033 Central Nervous System Cancer 47 0.027
1034
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.027
1035
MTS001 Mutism 46 0.027
1036
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.027
1037
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.027
1038
GRW007 Growth Hormone Deficiency 46 0.027
1039
PRL008 Paralytic Ileus 45 0.027
1040
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.027
1041
BRN032 Brain Glioma 45 0.027
1042
ASP026 Asplenia, Isolated Congenital 44 0.027
1043
P MTC004 Mitochondrial Encephalomyopathy 44 0.027
1044
ISC015 Ischemic Colitis 44 0.027
1045
c SPR086 Spermatogenic Failure 3 44 0.027
1046
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.027
1048
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.027
1049
IDP070 Idiopathic Scoliosis 42 0.027
1050
MCH006 Mechanical Strabismus 42 0.027
1051
GST020 Gastric Antral Vascular Ectasia 41 0.027
1052
DBT002 Diabetic Autonomic Neuropathy 41 0.027
1053
P MLG074 Malignant Mesenchymoma 40 0.027
1054
c HYP072 Hypersensitivity Reaction Type Iii Disease 40 0.027
1055
PLY100 Polyploidy 40 0.027
1056
ALG001 Algoneurodystrophy 39 0.027
1057
SCR011 Scrapie 39 0.027
1058
NCR002 Necrobiosis Lipoidica 38 0.027
1059
CRD016 Cardiac Rupture 37 0.027
1060
CRT012 Cortical Blindness 37 0.027
1061
PNB004 Panbronchiolitis, Diffuse 37 0.027
1062
INT011 Interstitial Emphysema 36 0.027
1063
THR123 Thrombotic Microangiopathy 36 0.027
1064
HYP114 Hypertensive Nephropathy 36 0.027
1065
c PST106 Post-Cardiac Arrest Syndrome 35 0.027
1066
DVL001 Developmental Coordination Disorder 34 0.027
1067
NNT024 Neonatal Stroke 34 0.027
1068
ART110 Arteritic Anterior Ischemic Optic Neuropathy 33 0.027
1069
RBS002 Rubeosis Iridis 33 0.027
1070
VRT003 Vertebrobasilar Insufficiency 30 0.027
1071
GNT019 Giant Cell Myocarditis 30 0.027
1072
DSC004 Discitis 29 0.027
1073
VSC004 Vasculogenic Impotence 28 0.027
1074
ARG004 Argyria 27 0.027
1075
INT009 Intracranial Abscess 27 0.027
1076
MST020 Mast Cell Activation Syndrome 26 0.027
1077
ACT162 Acute Sensory Ataxic Neuropathy 26 0.027
1078
ASB003 Asbestos Intoxication 26 0.027
1079
FTL073 Fetal Anticonvulsant Syndrome 26 0.027
1080
VLK001 Volkmann Contracture 25 0.027
1081
ADG002 Audiogenic Seizures 25 0.027
1082
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 23 0.027
1083
DVL005 Developmental Dyspraxia 23 0.027
1084
CNG092 Congenital Extrahepatic Portosystemic Shunt 23 0.027
1085
P PLM064 Pulmonary Sequestration 22 0.027
1086
CRB087 Cerebral Arteriosclerosis 22 0.027
1087
DYS013 Dysbaric Osteonecrosis 20 0.027
1088
RDT004 Radiation Induced Brachial Plexopathy 17 0.027