Search results for Carbon dioxide

1160 hits were found for Carbon dioxide

# Family MCID Name MIFTS Score
1
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.319
2
P RSP003 Respiratory Failure 74 0.316
3
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.315
4
P CRD119 Cardiac Arrest 67 0.301
5
HYP266 Hypoxia 57 0.257
6
LNG099 Lung Disease 60 0.240
7
MTB004 Metabolic Acidosis 50 0.231
8
P PNC025 Panic Disorder 53 0.229
9
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.220
10
P KDN018 Kidney Disease 72 0.213
11
HRW001 Hair Whorl 36 0.209
12
c NRF023 Neurofibromatosis, Type Ii 80 0.203
13
MTH071 Methane Production 26 0.198
14
OCL069 Ocular Motor Apraxia 51 0.198
15
c DWL002 Dowling-Degos Disease 1 58 0.197
16
LVR012 Liver Cirrhosis 62 0.193
17
P ENC018 Encephalopathy 61 0.181
18
c CHR684 Chronic Kidney Disease 70 0.180
19
TXC005 Toxic Shock Syndrome 62 0.179
20
ANX004 Anoxia 40 0.174
21
P LVR013 Liver Disease 68 0.163
22
ISC004 Ischemia 58 0.162
23
P SLP006 Sleep Apnea 69 0.160
24
P PLM037 Pulmonary Hypertension 67 0.157
25
ANX010 Anxiety 73 0.156
26
48X005 48,xyyy 39 0.156
27
ALL026 Allergic Hypersensitivity Disease 62 0.152
28
BRN024 Bronchitis 68 0.151
29
P RHN004 Rhinitis 57 0.150
30
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.149
31
PLM010 Pulmonary Edema 54 0.146
32
P VSC007 Vascular Disease 63 0.145
33
47X002 47,xyy 49 0.144
34
CNG034 Congestive Heart Failure 69 0.142
35
P CLR023 Colorectal Cancer 99 0.142
36
P PLM036 Pulmonary Fibrosis 65 0.141
37
PPL052 Papillomatosis, Confluent and Reticulated 33 0.140
38
ADN018 Adenoma 59 0.139
39
PNM008 Pneumothorax 56 0.138
40
CRB039 Cerebrovascular Disease 67 0.137
41
ALL003 Allergic Rhinitis 67 0.137
42
BNR002 Bone Resorption Disease 48 0.137
43
HLX001 Helix Syndrome 47 0.135
44
P HPT023 Hepatocellular Carcinoma 100 0.134
45
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.132
46
CRV045 Cervical Intraepithelial Neoplasia 39 0.132
47
P HDC001 Headache 57 0.129
48
PLM033 Pulmonary Embolism 59 0.129
49
P HMN010 Hemangioma 61 0.124
50
P LNG032 Lung Cancer 98 0.124
51
P RNL007 Renal Tubular Acidosis 51 0.123
52
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.121
53
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.121
54
P ADL010 Adult Respiratory Distress Syndrome 65 0.121
55
PRT036 Peritonitis 64 0.121
56
INT075 Intracranial Hypertension 53 0.119
57
P PNC035 Pancreatic Cancer 84 0.118
58
PPL022 Papilloma 54 0.118
59
P ADN016 Adenocarcinoma 64 0.118
60
P SZR006 Seizure Disorder 56 0.118
61
SQM006 Squamous Cell Carcinoma 60 0.117
62
BRN071 Brain Injury 49 0.117
63
FTT001 Fatty Liver Disease 61 0.116
64
END086 End Stage Renal Disease 51 0.116
65
VSL002 Visual Epilepsy 59 0.115
66
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.115
67
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.114
68
P PLM034 Pulmonary Emphysema 55 0.114
69
CYT002 Cytokine Deficiency 42 0.113
70
ART016 Aortic Aneurysm 69 0.113
71
P NRB001 Neuroblastoma 72 0.112
72
P END044 Endometriosis 63 0.111
73
LMB062 Limb Ischemia 55 0.111
74
PNG002 Pain Agnosia 51 0.111
75
AST005 Asthma 76 0.110
76
HYP457 Hypertrophic Scars 42 0.110
77
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.110
78
DPR016 Depression 63 0.109
79
P PNM007 Pneumonia 68 0.108
80
LKP003 Leukoplakia 39 0.107
81
P BPL003 Bipolar Disorder 56 0.107
82
P INS002 in Situ Carcinoma 53 0.106
83
SLC006 Silicosis 56 0.105
84
c ACT071 Acute Kidney Failure 60 0.105
85
c MGR028 Migraine with or Without Aura 1 67 0.104
86
c FNC043 Fanconi Anemia, Complementation Group E 62 0.104
87
c MJR024 Major Affective Disorder 9 41 0.104
88
c MJR022 Major Affective Disorder 8 38 0.104
89
ANR040 Aneurysm 59 0.104
90
P HRT032 Heart Disease 75 0.103
91
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.102
92
STR067 Stroke, Ischemic 81 0.102
93
DNT012 Dental Caries 53 0.100
94
P DRR001 Diarrhea 55 0.100
95
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.100
96
P GLM045 Glioma 63 0.100
97
GLL048 Glial Tumor 45 0.098
98
APN008 Apnea, Obstructive Sleep 64 0.098
99
P HYP076 Hyperthyroidism 55 0.098
100
KLD004 Keloid Disorder 40 0.098
101
P PRS040 Prostate Cancer 97 0.098
102
P NTR004 Neutropenia 63 0.098
103
P BNG032 Benign Mesothelioma 46 0.097
104
NRL016 Neural Tube Defects 82 0.097
105
ADL002 Adult Syndrome 70 0.097
106
P CRN300 Coronary Heart Disease 1 63 0.097
107
DYS073 Dysphagia 50 0.096
108
SDD001 Sudden Infant Death Syndrome 61 0.096
109
ART140 Arteries, Anomalies of 52 0.095
110
MNT002 Mental Depression 58 0.095
111
OST159 Osteogenic Sarcoma 66 0.095
112
TRM010 Traumatic Brain Injury 51 0.094
113
SQM002 Squamous Cell Papilloma 46 0.094
114
LPP008 Lipoprotein Quantitative Trait Locus 62 0.093
115
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.093
116
NWB001 Newborn Respiratory Distress Syndrome 58 0.093
117
HDR002 Hidradenitis Suppurativa 55 0.092
118
LYM022 Lymphangioma 54 0.092
119
HDR003 Hidradenitis 49 0.092
120
P RRL003 Rare Lymphatic Malformation 31 0.092
121
BCT022 Bacterial Infectious Disease 56 0.092
122
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.092
123
CNS004 Constipation 58 0.091
124
DRM006 Dermatitis 61 0.091
125
c BSL007 Basal Cell Carcinoma 68 0.090
126
CYS001 Cystic Fibrosis 81 0.090
127
P TRM003 Tremor 54 0.090
128
IRN002 Iron Metabolism Disease 57 0.090
129
THY029 Thyroid Carcinoma 59 0.090
130
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.089
131
BRN002 Bronchiolitis 59 0.089
132
AGN016 Aging 56 0.088
133
AMN003 Amnestic Disorder 54 0.088
134
P MLN008 Melanoma 69 0.087
135
DFC004 Deficiency Anemia 70 0.087
136
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.087
137
P MYC007 Myocardial Infarction 70 0.087
138
P TRN020 Turner Syndrome 67 0.087
139
HYP056 Hypoglycemia 66 0.087
140
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.087
141
P LTR001 Lateral Sclerosis 54 0.087
142
P PRD008 Periodontitis 64 0.086
143
P BLD134 Bladder Cancer 79 0.086
144
PLM031 Poliomyelitis 64 0.086
145
P KDN017 Kidney Cancer 60 0.086
146
ATH013 Atherosclerosis Susceptibility 65 0.085
147
PRP027 Peripheral Vascular Disease 71 0.085
148
HMN044 Human Immunodeficiency Virus Type 1 71 0.085
149
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.085
150
KRT009 Keratosis 51 0.085
151
HRT011 Heart Septal Defect 50 0.085
152
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.085
153
OST012 Osteoarthritis 78 0.085
154
P HYP086 Hypothyroidism 69 0.084
155
P NRP001 Neuropathy 56 0.084
156
SPN186 Spinal Cord Injury 60 0.084
157
c RHB024 Rhabdomyosarcoma 2 67 0.084
158
LSH001 Leishmaniasis 63 0.084
159
P KLZ004 Kala-Azar 1 41 0.084
160
c BNG091 Benign Chronic Pemphigus 58 0.084
161
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.084
162
STM007 Stomatitis 50 0.083
163
ANT018 Anthracosis 48 0.083
164
P HYP098 Hypereosinophilic Syndrome 67 0.083
165
P SKN015 Skin Carcinoma 66 0.083
166
TLN003 Telangiectasis 52 0.083
167
P INF032 Infertility 57 0.083
168
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.082
169
HMP009 Haemophilus Influenzae 43 0.082
170
P PNM006 Pneumoconiosis 56 0.082
171
RCK004 Rickets 68 0.082
172
RSC001 Rosacea 54 0.082
173
CHL056 Cheilitis 48 0.082
174
ACT093 Actinic Cheilitis 40 0.082
175
P GST053 Gastric Cancer 83 0.082
176
P RCT021 Rectum Cancer 52 0.082
177
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.081
178
HDN002 Head Injury 46 0.081
179
c SCL052 Scleroderma, Familial Progressive 61 0.081
180
P LCT001 Lactic Acidosis 51 0.081
181
ATX019 Ataxia with Vitamin E Deficiency 42 0.081
182
P OPN001 Open-Angle Glaucoma 49 0.080
183
AGR002 Agoraphobia 45 0.080
184
ORL012 Oral Leukoplakia 39 0.080
185
CLT003 Colitis 62 0.080
186
ORL015 Oral Squamous Cell Carcinoma 43 0.080
187
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.080
188
c SML038 Small Cell Cancer of the Lung 65 0.079
189
CVD001 Covid-19 44 0.079
190
SKN016 Skin Disease 63 0.079
191
GST023 Gastric Ulcer 53 0.079
192
ESP021 Esophageal Cancer 90 0.079
193
c PRC016 Pre-Eclampsia 63 0.079
194
c GLL024 Gallbladder Disease 1 53 0.079
195
P CRD246 Cardiovascular System Disease 57 0.078
196
PST092 Posttransplant Acute Limbic Encephalitis 29 0.078
197
c HYP595 Hypertension, Essential 84 0.078
198
HYP066 Hyperglycemia 61 0.078
199
ORL011 Oral Cancer 60 0.077
200
MCS002 Mucositis 56 0.077
201
SYN036 Syncope 45 0.077
202
ALL006 Allergic Asthma 56 0.077
203
GST045 Gastroenteritis 59 0.077
204
CRB086 Cerebral Aneurysms 40 0.076
205
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.076
206
ALC007 Alcohol Dependence 66 0.076
207
P INF037 Inflammatory Bowel Disease 54 0.076
208
P VNT002 Ventricular Septal Defect 60 0.076
209
ADN011 Adenoid Cystic Carcinoma 70 0.076
210
P OVR042 Ovarian Cancer 88 0.075
211
P ALP008 Alopecia 54 0.075
212
P SYR003 Syringoma 37 0.075
213
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.075
214
MDD011 Mood Disorder 62 0.074
215
P ALZ034 Alzheimer Disease 88 0.074
216
ILS001 Ileus 51 0.074
217
P ANP001 Anaplastic Large Cell Lymphoma 58 0.073
218
END040 Endogenous Depression 55 0.073
219
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.073
220
RTN020 Retinal Vascular Disease 46 0.073
221
DWN001 Down Syndrome 70 0.073
222
P HYD006 Hydrocephalus 66 0.073
223
P TBR001 Tuberous Sclerosis 70 0.073
224
OBS037 Obesity-Hypoventilation Syndrome 46 0.073
225
ANP008 Anaplastic Oligoastrocytoma 30 0.073
226
TNP004 Tn Polyagglutination Syndrome 39 0.073
227
HYP005 Hypokalemia 55 0.073
228
P LNG064 Lung Cancer Susceptibility 3 78 0.072
229
P ACT105 Acute Mountain Sickness 52 0.072
230
P SYS005 Systemic Scleroderma 68 0.072
231
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.072
232
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.072
233
c PCH010 Pachyonychia Congenita 3 44 0.072
234
PRT013 Portal Hypertension 59 0.071
235
URL001 Urolithiasis 45 0.071
236
c EXD008 Exudative Vitreoretinopathy 1 71 0.071
237
P PMP001 Pemphigus 54 0.071
238
P CND004 Candidiasis 58 0.071
239
RSP007 Respiratory Distress Syndrome, Infant 30 0.071
240
CHL014 Cholera 59 0.071
241
ANG054 Angina Pectoris 66 0.071
242
BRN028 Brain Cancer 74 0.071
243
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.070
244
BRN012 Bronchiolitis Obliterans 55 0.070
245
P DST107 Distal Renal Tubular Acidosis 42 0.070
246
c ACT075 Acute Myocardial Infarction 57 0.070
247
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.070
248
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.070
249
c CHR682 Chronic Bilirubin Encephalopathy 39 0.070
250
NRT001 Neurotic Disorder 53 0.069
251
BRN056 Bronchopulmonary Dysplasia 57 0.069
252
ING001 Inguinal Hernia 60 0.069
253
CRD137 Cardiogenic Shock 47 0.069
254
P PHC003 Pheochromocytoma 71 0.069
255
ADR040 Adrenal Gland Pheochromocytoma 46 0.069
256
ATM095 Autoimmune Disease 62 0.069
257
LNT004 Lentigines 50 0.069
258
c CNT015 Central Sleep Apnea 45 0.069
259
TRC005 Tracheal Stenosis 38 0.069
260
P PSR002 Psoriasis 62 0.069
261
PST011 Pustulosis of Palm and Sole 52 0.069
263
CRB090 Cerebral Hypoxia 44 0.068
264
URT049 Urate Oxidase, Pseudogene 25 0.068
265
P ART021 Arteriosclerosis 54 0.068
266
P SCK005 Sickle Cell Disease 50 0.068
267
CTN007 Cutaneous Leishmaniasis 62 0.068
268
PPL001 Papillary Adenoma 44 0.068
269
INT002 Intermittent Claudication 61 0.068
270
c PNS012 Paine Syndrome 61 0.068
271
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.067
272
P HML002 Hemolytic Anemia 63 0.067
273
P CTR002 Cataract 60 0.067
274
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.067
275
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.067
276
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.067
277
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.067
278
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.067
279
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.067
280
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.067
281
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.067
282
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.067
283
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.067
284
P RTN008 Retinitis Pigmentosa 79 0.067
285
ANG005 Anogenital Venereal Wart 55 0.067
286
STT002 Status Asthmaticus 50 0.067
287
VRR004 Verrucous Carcinoma 49 0.067
288
LCH016 Lichen Sclerosus Et Atrophicus 41 0.067
289
ERY023 Erythroplakia 24 0.067
290
CHL079 Children's Interstitial Lung Disease 26 0.067
291
GTR002 Goiter 53 0.067
292
c ART068 Aortic Aneurysm, Familial Thoracic 2 34 0.067
293
P MCR115 Microvascular Complications of Diabetes 5 66 0.067
294
P FBR017 Fibrosarcoma 56 0.067
295
RTN023 Retinitis 46 0.066
296
NRR001 Neuroretinitis 42 0.066
297
TRN018 Transitional Cell Carcinoma 56 0.066
298
DMP001 Dumping Syndrome 44 0.066
299
VRC005 Varicose Veins 60 0.066
300
P PNC044 Pancreatitis 61 0.066
301
SRC014 Sarcoma 65 0.066
302
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.066
303
P BRS044 Breast Adenocarcinoma 59 0.066
304
P OVR082 Overgrowth Syndrome 50 0.066
305
c ACT134 Acute Liver Failure 56 0.066
306
P PLY019 Polyneuropathy 56 0.066
307
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.065
308
INT066 Interstitial Lung Disease 60 0.065
309
P SCH015 Schizophrenia 74 0.065
310
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.065
311
CLN015 Colon Adenocarcinoma 65 0.065
312
MYL020 Myelomeningocele 51 0.065
313
CYN002 Cyanosis, Transient Neonatal 45 0.065
314
c GLC092 Glaucoma, Primary Open Angle 62 0.065
315
CHR100 Chronic Ulcer of Skin 55 0.065
316
P MLG056 Malignant Hyperthermia 67 0.065
317
c ACT068 Acute Cystitis 63 0.065
318
c SVR001 Severe Acute Respiratory Syndrome 62 0.065
319
MST005 Mastitis 53 0.064
320
P PRP019 Peripheral Nervous System Disease 58 0.064
321
CNT047 Contact Dermatitis 58 0.064
322
BRN004 Brain Edema 56 0.064
323
MLR004 Malaria 81 0.063
324
ANT024 Anthrax Disease 58 0.063
325
SPN035 Spindle Cell Sarcoma 53 0.063
326
SKN019 Skin Melanoma 68 0.063
327
P ENC004 Encephalitis 61 0.063
328
RTN017 Retinal Detachment 61 0.063
329
P FBR031 Febrile Seizures 53 0.063
330
NPH009 Nephrolithiasis 55 0.063
331
MDS022 Mediastinitis 46 0.063
332
BWN006 Bowen's Disease 32 0.063
333
P MYP004 Myopathy 70 0.062
334
NRM005 Neuromuscular Disease 64 0.062
335
c ACT027 Acute Pancreatitis 60 0.062
336
P CNR004 Cone-Rod Dystrophy 2 73 0.062
337
P AST007 Astrocytoma 51 0.062
338
P CHN012 Chondrosarcoma 56 0.062
339
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.062
340
NRF007 Neurofibroma 64 0.062
341
CHL004 Cholelithiasis 49 0.062
342
P INF038 Influenza 68 0.062
343
P ART022 Arthritis 69 0.061
344
P MYS003 Myasthenia Gravis 68 0.061
345
c BRN108 Branchiootic Syndrome 1 62 0.061
346
ULC004 Ulcerative Colitis 73 0.061
347
P DBT005 Diabetes Insipidus 55 0.061
348
P BCL017 B-Cell Lymphoma 58 0.061
349
P GST044 Gastritis 56 0.061
350
P SPP010 Suppressor of Tumorigenicity 3 51 0.061
351
P MLT020 Multiple Sclerosis 72 0.060
352
PLM001 Pulmonary Tuberculosis 69 0.060
353
P BRN022 Bronchiectasis 59 0.060
354
CHL067 Cholecystitis 57 0.060
355
P PYL005 Pyelonephritis 56 0.060
356
P PRM006 Primary Biliary Cirrhosis 62 0.060
357
URM002 Uremia 49 0.060
358
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.060
359
P LKM002 Leukemia 68 0.060
360
OST003 Osteonecrosis 61 0.060
361
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.060
362
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.060
363
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.060
364
CLC006 Calcinosis 48 0.060
365
c GRV008 Graves Disease 1 56 0.059
366
HPT004 Hepatic Coma 45 0.059
367
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.059
368
CHG001 Chagas Disease 66 0.059
369
P SJG008 Sjogren Syndrome 61 0.059
370
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.059
371
P ATR010 Atrial Heart Septal Defect 60 0.059
372
c HYP836 Hypercholesterolemia, Familial, 1 73 0.059
373
TTN003 Tetanus 65 0.059
374
SYN007 Synovitis 54 0.059
375
PLC002 Plica Syndrome 36 0.059
376
PST028 Post-Traumatic Stress Disorder 58 0.058
377
P MTR003 Mitral Valve Stenosis 50 0.058
378
ACT084 Acute Stress Disorder 47 0.058
379
P PRK001 Porokeratosis 55 0.058
380
P ECT005 Ectropion 42 0.058
381
SNG003 Single Ventricular Heart 30 0.058
382
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.058
383
NTR005 Nutritional Deficiency Disease 62 0.058
384
PPT005 Peptic Ulcer Disease 59 0.058
385
P SNS001 Sensorineural Hearing Loss 60 0.057
386
SBC016 Subacute Delirium 44 0.057
387
c ATR087 Atrial Standstill 1 75 0.057
388
CHL068 Cholestasis 61 0.057
389
P PRC012 Pericardial Effusion 51 0.057
390
HMP001 Hemopericardium 48 0.057
391
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.057
392
SCK003 Sickle Cell Anemia 74 0.057
393
c MNN043 Meningioma, Familial 74 0.057
394
MNN042 Meningioma, Radiation-Induced 62 0.057
395
TRG002 Trigeminal Neuralgia 60 0.057
396
SPN021 Spinal Meningioma 50 0.057
397
SCR001 Secretory Meningioma 41 0.057
398
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.057
399
P DMN002 Dementia 66 0.056
400
OTT002 Otitis Media 72 0.056
401
P SLP005 Sleep Disorder 59 0.056
402
P AMY004 Amyloidosis 70 0.055
403
P HPT021 Hepatitis 67 0.055
404
P DRM053 Dermatitis, Atopic 66 0.055
405
BRR014 Barrett Esophagus 65 0.055
406
P EXN002 Exanthem 57 0.055
407
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.055
408
PRP080 Peripheral Artery Disease 53 0.055
409
RDN001 Reading Disorder 40 0.055
410
P NSP012 Nasopharyngeal Carcinoma 66 0.055
411
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.055
412
IMP005 Impotence 52 0.055
413
c HPT073 Hepatitis C Virus 72 0.055
414
GNG013 Gingivitis 59 0.055
415
PLR007 Pleural Empyema 50 0.055
416
KRT013 Keratolytic Winter Erythema 46 0.055
417
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.055
418
P HRP006 Herpes Simplex 65 0.054
419
LYM133 Lymphoma, Hodgkin, Classic 69 0.054
420
P MSC005 Muscular Dystrophy 66 0.054
421
HPT019 Hepatic Encephalopathy 60 0.054
422
CHL065 Cholangiocarcinoma 68 0.053
423
INT079 Intrahepatic Cholangiocarcinoma 51 0.053
424
RYN005 Raynaud Phenomenon 47 0.053
425
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.053
426
NVS017 Nevus, Epidermal 68 0.053
427
P ALP009 Alopecia Areata 60 0.053
428
AVN001 Avian Influenza 59 0.053
429
CRT013 Carotid Stenosis 50 0.053
430
ECT026 Ectopic Pregnancy 50 0.053
431
BLN010 Balanitis 37 0.053
432
IMM167 Immune Deficiency Disease 78 0.053
433
c ATS007 Autism Spectrum Disorder 67 0.053
434
P SCL018 Scoliosis 60 0.053
435
ARG004 Argyria 27 0.053
436
P SRC025 Sarcoidosis 1 70 0.053
437
P MJR001 Major Depressive Disorder 68 0.053
438
LPD008 Lipid Metabolism Disorder 62 0.053
439
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.053
440
CRD223 Cardiac Arrhythmia 60 0.053
441
c MCR113 Microvascular Complications of Diabetes 3 52 0.052
442
c MCR120 Microvascular Complications of Diabetes 7 47 0.052
443
c MLG068 Malignant Glioma 46 0.052
444
c MCR130 Microvascular Complications of Diabetes 6 41 0.052
445
c MCR133 Microvascular Complications of Diabetes 4 41 0.052
446
PRP030 Purpura 54 0.052
447
CRP002 Croup 44 0.051
448
SCK001 Sick Building Syndrome 34 0.051
449
LPT014 Leptin Deficiency or Dysfunction 74 0.051
450
c THR092 Thrombophilia Due to Thrombin Defect 73 0.051
451
DPH001 Diphtheria 60 0.051
452
DYS015 Dysentery 52 0.051
453
P CLS010 Cluster Headache 42 0.051
454
MSC007 Muscle Hypertrophy 64 0.051
455
P OBS001 Obstructive Jaundice 50 0.051
456
DNT008 Denture Stomatitis 35 0.051
457
P URT039 Urticaria 58 0.051
458
c LKM061 Leukemia, Acute Myeloid 84 0.050
459
END057 Endometrial Cancer 74 0.050
460
CRH001 Crohn's Disease 74 0.050
461
P ATS364 Autism 70 0.050
462
OST017 Osteomyelitis 64 0.050
463
ENT004 Enthesopathy 49 0.050
464
c HPT001 Hepatitis C 62 0.050
465
YLL002 Yellow Fever 61 0.050
466
VRL011 Viral Infectious Disease 61 0.050
467
PNM010 Pneumothorax, Primary Spontaneous 60 0.050
468
P NRF002 Neurofibromatosis 56 0.050
469
c PRD040 Periodontitis, Chronic 53 0.050
470
STT041 Stuttering 52 0.050
471
NTR046 Neutrophil Migration 50 0.050
472
RTR001 Retrograde Amnesia 44 0.050
473
P RHM011 Rheumatoid Arthritis 80 0.050
474
P MNN013 Meningitis 66 0.050
475
P MYC008 Myocarditis 59 0.050
476
CHP002 Chops Syndrome 44 0.050
477
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.049
478
P APL001 Aplastic Anemia 74 0.049
479
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.049
480
P THR014 Thrombocytopenia 67 0.049
481
THY030 Thyroid Gland Disease 52 0.049
482
PTH003 Pathologic Nystagmus 52 0.049
483
OBS002 Obsessive-Compulsive Disorder 68 0.048
484
PLG002 Plague 63 0.048
485
P OPT006 Optic Nerve Disease 60 0.048
486
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.048
487
CLF001 Cleft Lip 53 0.048
488
LNG031 Lung Benign Neoplasm 51 0.048
489
CRN030 Coronary Stenosis 50 0.048
490
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.048
491
P LKM062 Leukemia, Acute Lymphoblastic 69 0.048
492
P DYS154 Dystonia 65 0.048
493
P ECL001 Eclampsia 50 0.048
494
c PRS136 Prostate Cancer, Hereditary, 6 33 0.048
495
c PRS130 Prostate Cancer, Hereditary, 8 32 0.048
496
P CYS018 Cystitis 59 0.048
497
BCK006 Back Pain 42 0.048
498
BTN004 Biotin Deficiency 38 0.048
499
IRR002 Irritable Bowel Syndrome 65 0.047
500
GNR004 Generalized Anxiety Disorder 56 0.047
501
MMM001 Mammary Paget's Disease 53 0.047
502
P ACT008 Actinic Keratosis 53 0.047
503
LGN006 Legionnaire Disease 52 0.047
504
HYP781 Hypoascorbemia 51 0.047
505
P OTS001 Otosclerosis 49 0.047
506
CVR006 Cavernous Hemangioma 49 0.047
507
P RCR004 Recurrent Respiratory Papillomatosis 49 0.047
508
NWC001 Newcastle Disease 45 0.047
509
VLV044 Vulvar Intraepithelial Neoplasia 44 0.047
510
PYG006 Pyogenic Granuloma 41 0.047
511
SPR012 Separation Anxiety Disorder 38 0.047
512
c PST106 Post-Cardiac Arrest Syndrome 35 0.047
513
INF057 Inflammatory Linear Verrucous Epidermal Nevus 34 0.047
514
SBG002 Subglottic Angioma 13 0.047
515
P BRB001 Beriberi 46 0.047
516
c MCR129 Microvascular Complications of Diabetes 1 66 0.047
517
STT001 Status Epilepticus 60 0.047
518
HLC007 Helicobacter Pylori Infection 59 0.047
519
HMS001 Hemosiderosis 54 0.047
520
PLY150 Polykaryocytosis Inducer 31 0.047
521
BNG077 Benign Idiopathic Neonatal Seizures 26 0.047
522
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.046
523
P ART005 Arteriovenous Malformation 65 0.046
524
KRT019 Keratitis, Hereditary 65 0.046
525
P THY023 Thymoma 65 0.046
526
PSR001 Psoriatic Arthritis 61 0.046
527
ACN002 Acanthosis Nigricans 60 0.046
528
P LCH002 Lichen Planus 53 0.046
529
c THY107 Thymoma, Familial 52 0.046
530
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.046
531
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.046
532
IGR001 Ige Responsiveness, Atopic 59 0.045
533
P GLM040 Glioma Susceptibility 1 81 0.045
534
PNC129 Pancreatic Adenocarcinoma 68 0.045
535
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.045
536
THR024 Thrombosis 57 0.045
537
GST050 Gastrointestinal System Disease 56 0.045
538
HYP060 Hyperinsulinism 54 0.045
539
NNL006 Non-Alcoholic Steatohepatitis 54 0.045
540
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.045
541
HRN029 Hearing Loss, Noise-Induced 37 0.045
542
P PLY011 Polycystic Ovary Syndrome 56 0.045
543
CLR109 Colorectal Adenocarcinoma 51 0.045
544
GNG003 Gingival Recession 44 0.045
545
MCR011 Microinvasive Gastric Cancer 43 0.045
546
MDD018 Middle East Respiratory Syndrome 43 0.045
547
FNT004 Fainting 30 0.045
548
ENM002 Enamel Erosion 26 0.045
549
GT001 Gout 64 0.044
550
CLR108 Colorectal Adenoma 64 0.044
551
P RHB003 Rhabdomyosarcoma 63 0.044
552
TYP007 Typhoid Fever 63 0.044
553
P ALC033 Alcohol Use Disorder 58 0.044
554
P TCD001 Tic Disorder 53 0.044
555
SPL018 Splenomegaly 48 0.044
556
c MCR112 Microvascular Complications of Diabetes 2 41 0.044
557
c RNG015 Ring Chromosome 2 26 0.044
558
TRN015 Transient Cerebral Ischemia 63 0.044
559
HYD002 Hydronephrosis 60 0.044
560
LYM027 Lymphopenia 58 0.044
561
CHK001 Chikungunya 57 0.044
562
VSC002 Vascular Dementia 57 0.044
563
MCN007 Meconium Aspiration Syndrome 55 0.044
564
P INT068 Intestinal Disease 53 0.044
565
CRT015 Carotid Artery Occlusion 45 0.044
566
ENT001 Enterocele 39 0.044
567
c PLM022 Pulmonary Valve Insufficiency 39 0.044
568
c HPT003 Hepatitis a 62 0.043
569
P VSC011 Vasculitis 62 0.043
570
P MYP006 Myopia 55 0.043
571
NVS001 Neovascular Glaucoma 53 0.043
572
LMY002 Leiomyoma 52 0.043
573
c DRR009 Diarrhea 6 46 0.043
574
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.043
575
OVR094 Ovarian Epithelial Cancer 38 0.043
576
P ATX030 Ataxia-Telangiectasia 82 0.042
577
c SPN225 Spondyloarthropathy 1 73 0.042
578
P EPL164 Epilepsy 71 0.042
579
APH002 Aphasia 57 0.042
580
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.042
581
P CHR345 Chronic Pain 44 0.042
582
ANG020 Angiosarcoma 64 0.042
583
CLL003 Cellulitis 54 0.042
584
SVR097 Severe Cutaneous Adverse Reaction 69 0.041
585
ETN001 Eating Disorder 60 0.041
586
ERY003 Erythema Multiforme 58 0.041
587
c BCT007 Bacterial Meningitis 55 0.041
588
TNG007 Tongue Carcinoma 51 0.041
589
ASP007 Aspiration Pneumonia 48 0.041
590
RNL077 Renal Fibrosis 47 0.041
591
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.041
592
IDP070 Idiopathic Scoliosis 42 0.041
593
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.041
594
ERY066 Erythema Multiforme Major 30 0.041
595
P HYP055 Hypoplastic Left Heart Syndrome 63 0.041
596
c LCL006 Localized Scleroderma 62 0.041
597
P PRP029 Porphyria 62 0.041
598
DCB001 Decubitus Ulcer 61 0.041
599
NRL005 Neurilemmoma 60 0.041
600
c LPM012 Lipomatosis, Multiple 60 0.041
601
P PTN014 Patent Ductus Arteriosus 1 60 0.041
602
FDB001 Foodborne Botulism 55 0.041
603
WST005 West Nile Virus 54 0.041
604
MYM001 Myoma 54 0.041
605
ECH003 Echinococcosis 53 0.041
606
CRT016 Carotid Artery Disease 52 0.041
607
PYD002 Pyoderma 50 0.041
608
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 0.041
609
P OVR046 Ovarian Cyst 47 0.041
610
STT007 Steatocystoma Multiplex 46 0.041
611
SPR005 Superficial Basal Cell Carcinoma 46 0.041
612
TRT001 Teratocarcinoma 45 0.041
613
c PRM038 Primary Agammaglobulinemia 44 0.041
614
LRY017 Laryngeal Disease 42 0.041
615
PLM005 Pleomorphic Lipoma 40 0.041
616
P EPL003 Epulis 30 0.041
617
BLN002 Balanitis Xerotica Obliterans 29 0.041
618
MCC003 Mucocele of Salivary Gland 28 0.041
619
LKP001 Leukoplakia of Penis 25 0.041
620
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.041
621
P LPS004 Lupus Erythematosus 61 0.041
622
P DNG005 Dengue Virus 59 0.041
623
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.041
624
ERY051 Erythroleukemia, Familial 56 0.041
625
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.041
626
P HYP733 Hypercalciuria, Absorptive, 2 45 0.041
627
P FBR003 Fibrous Histiocytoma 44 0.041
628
SPR126 Superior Semicircular Canal Dehiscence 40 0.041
629
c HMG029 Hemoglobin Se Disease 39 0.041
630
c LKM063 Leukemia, Chronic Myeloid 72 0.039
631
CNN005 Connective Tissue Disease 68 0.039
632
P ART023 Arthropathy 62 0.039
633
P PLY041 Polymyositis 57 0.039
634
SCH014 Schistosomiasis 57 0.039
635
ALL010 Allergic Contact Dermatitis 56 0.039
636
NPH003 Nephrocalcinosis 51 0.039
637
CRB004 Cerebral Artery Occlusion 45 0.039
638
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.039
639
ADG002 Audiogenic Seizures 25 0.039
640
APP008 Appendicitis 61 0.039
641
CHL123 Chlamydia 59 0.039
642
AYM001 Ayme-Gripp Syndrome 57 0.039
643
P LRY044 Larynx Cancer 55 0.039
644
PRS045 Prostatic Hypertrophy 53 0.039
645
P MNC007 Monocytic Leukemia 53 0.039
646
c BCT013 Bacterial Pneumonia 48 0.039
647
VSM001 Vasomotor Rhinitis 38 0.039
648
CHR178 Chromosomal Triplication 35 0.039
649
P RNL115 Renal Tubular Acidosis, Proximal 31 0.039
650
EXT062 Extracranial Carotid Artery Aneurysm 21 0.039
651
c SVR005 Severe Pre-Eclampsia 50 0.038
652
PLP001 Pulpitis 49 0.038
653
c ACT042 Acute Pyelonephritis 46 0.038
654
MLN073 Melanosis, Neurocutaneous 45 0.038
656
P HYP061 Hypertrophic Cardiomyopathy 70 0.037
657
MYC006 Mycosis Fungoides 66 0.037
658
P MTR014 Motor Neuron Disease 65 0.037
659
c JVN010 Juvenile Rheumatoid Arthritis 64 0.037
660
c MLG084 Malignant Fibrous Histiocytoma 63 0.037
661
P UVT001 Uveitis 57 0.037
662
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.037
663
P RTN016 Retinal Degeneration 53 0.037
664
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.037
665
P MSC003 Muscular Atrophy 52 0.037
666
BHR001 Behr Syndrome 51 0.037
667
PLC008 Placenta Disease 50 0.037
668
P MYT002 Myotonic Dystrophy 49 0.037
669
VCC001 Vaccinia 49 0.037
670
SXL003 Sexual Disorder 47 0.037
671
MXD026 Mixed Glioma 45 0.037
672
ACT003 Acute Kidney Tubular Necrosis 45 0.037
673
P PRC031 Preeclampsia/eclampsia 1 38 0.037
674
c RNG019 Ring Chromosome 3 22 0.037
675
P MYC084 Mycobacterium Tuberculosis 1 68 0.037
676
c DPH024 Diaphragmatic Hernia, Congenital 63 0.037
677
GST033 Gestational Diabetes 61 0.037
678
P SYP003 Syphilis 58 0.037
679
GLS018 Glass Syndrome 57 0.037
680
c VSC019 Vesicoureteral Reflux 1 57 0.037
681
c BSL024 Basal Cell Carcinoma 1 56 0.037
682
P MLN007 Male Infertility 55 0.037
683
P VNS003 Venous Insufficiency 55 0.037
684
PRC013 Pericarditis 54 0.037
685
MTN003 Motion Sickness 53 0.037
686
P PTS002 Ptosis 53 0.037
687
PRS021 Prostatic Adenoma 51 0.037
688
ACH005 Achalasia 51 0.037
689
RSP006 Respiratory System Disease 50 0.037
690
SYS003 Systolic Heart Failure 49 0.037
691
PRS129 Prostatic Hyperplasia, Benign 49 0.037
692
SCL003 Social Phobia 48 0.037
693
PYL006 Pyloric Stenosis 48 0.037
694
RSP021 Respiratory Allergy 45 0.037
695
URT010 Ureteral Obstruction 45 0.037
696
CRS005 Crest Syndrome 43 0.037
697
P HYP009 Hypertrophic Pyloric Stenosis 41 0.037
698
c ACT004 Acute Diarrhea 39 0.037
699
CHN011 Chondromalacia 38 0.037
700
MYC014 Mycobacterium Chelonae 31 0.037
701
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.035
702
INS024 Insulin-Like Growth Factor I 79 0.035
703
MYL005 Myelofibrosis 70 0.035
704
P OCL013 Oculodentodigital Dysplasia 69 0.035
705
P SPN046 Spinal Muscular Atrophy 62 0.035
706
P END033 Endocarditis 57 0.035
707
INT303 Intracranial Hypertension, Idiopathic 57 0.035
708
HMP005 Hemiplegia 55 0.035
709
OST016 Osteochondrosis 53 0.035
710
P HMR003 Hemorrhagic Disease 53 0.035
711
P RTN018 Retinal Disease 53 0.035
712
PRP016 Paraplegia 52 0.035
713
P TRT010 Teratoma 52 0.035
714
CND002 Conduct Disorder 51 0.035
715
PRT029 Parathyroid Adenoma 50 0.035
716
PPL021 Papilledema 49 0.035
717
CLN045 Colonic Benign Neoplasm 46 0.035
718
PLR022 Pleural Disease 45 0.035
719
MYX004 Myxedema 43 0.035
720
c ADN012 Adenocarcinoma in Situ 42 0.035
721
PRS063 Paresthesia 41 0.035
722
PRM020 Premenstrual Tension 40 0.035
723
P LRY019 Laryngitis 52 0.034
724
HMN016 Hemangioendothelioma 34 0.034
725
BSL036 Basal Cell Nevus Syndrome 73 0.034
726
P MST009 Mastocytosis 64 0.034
727
PTN001 Patent Foramen Ovale 60 0.034
728
P GLL020 Gallbladder Disease 57 0.034
729
CMM005 Common Cold 57 0.034
730
MTH009 Mouth Disease 56 0.034
731
ORL005 Oral Candidiasis 56 0.034
732
PLV003 Pelvic Inflammatory Disease 55 0.034
733
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.034
734
P NLD001 Nail Disease 54 0.034
735
c PSR017 Psoriasis 2 53 0.034
736
c PSR023 Psoriasis 1 52 0.034
737
FML037 Female Breast Cancer 52 0.034
738
PRV004 Periventricular Leukomalacia 52 0.034
739
FDL002 Food Allergy 51 0.034
740
c PYR010 Peyronie's Disease 50 0.034
741
BLS002 Blastomycosis 50 0.034
742
VGN020 Vaginal Disease 49 0.034
743
P MTC133 Mitochondrial Myopathy 49 0.034
744
PRN014 Paronychia 49 0.034
745
c PSR032 Psoriasis 11 47 0.034
746
VGN019 Vaginal Discharge 46 0.034
747
CRB008 Cerebral Atherosclerosis 44 0.034
748
ANL017 Anal Squamous Cell Carcinoma 44 0.034
749
FBR054 Fibroma 44 0.034
750
MGS001 Megaesophagus 43 0.034
751
c PSR028 Psoriasis 7 42 0.034
752
c PRK082 Porokeratosis 1, Multiple Types 41 0.034
753
c PSR018 Psoriasis 13 41 0.034
754
HYP344 Hyperthyroidism, Familial Gestational 39 0.034
755
DSS010 Dissociative Disorder 39 0.034
756
ANG016 Angiokeratoma 38 0.034
757
ACN010 Acanthoma 38 0.034
758
KLD003 Keloid Formation 38 0.034
759
LCR004 La Crosse Encephalitis 37 0.034
760
EPD070 Epidermoid Cysts 37 0.034
761
CHL013 Cholecystolithiasis 37 0.034
762
BWN003 Bowenoid Papulosis 34 0.034
763
P CLR001 Clear Cell Acanthoma 34 0.034
764
ANG007 Angiokeratoma Circumscriptum 34 0.034
765
DRM003 Dermatosis Papulosa Nigra 33 0.034
766
CMM003 Common Wart 32 0.034
767
HDR001 Hidrocystoma 31 0.034
768
ELS002 Elastosis Perforans Serpiginosa 30 0.034
769
LRY027 Laryngeal Papillomatosis 23 0.034
770
P SPN237 Spina Bifida Aperta 20 0.034
771
APN007 Apnea, Central Sleep 18 0.034
772
RSP020 Respiratory Underresponsiveness to Hypoxia and Hypercapnia 9 0.034
773
KPS004 Kaposi Sarcoma 75 0.033
774
MYL009 Myelodysplastic Syndrome 70 0.033
775
MLT157 Multiple System Atrophy 1 70 0.033
776
P CHR012 Chronic Granulomatous Disease 67 0.033
777
c DBT099 Diabetes Mellitus, Type I 65 0.033
778
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.033
779
P ORT004 Orthostatic Intolerance 62 0.033
780
P DRM010 Dermatomyositis 61 0.033
781
c HPT016 Hepatitis B 59 0.033
782
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.033
783
P GLM007 Glomerulonephritis 57 0.033
784
DSS009 Disseminated Intravascular Coagulation 57 0.033
785
P MYS005 Myositis 56 0.033
786
INT007 Intermediate Coronary Syndrome 55 0.033
787
VGN023 Vaginitis 54 0.033
788
INT051 Intussusception 53 0.033
789
DRM011 Dermatophytosis 52 0.033
790
DYS009 Dysthymic Disorder 49 0.033
791
QDR001 Quadriplegia 48 0.033
792
NRN001 Neuroendocrine Carcinoma 47 0.033
793
KRT002 Keratomalacia 47 0.033
794
EXS001 Exostosis 46 0.033
795
GST010 Gestational Trophoblastic Neoplasm 46 0.033
796
P MYC033 Myoclonus 46 0.033
797
P CRB088 Cerebral Atrophy 37 0.033
798
GRM010 Germ Cells Tumors 34 0.033
799
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.033
800
MST020 Mast Cell Activation Syndrome 26 0.033
801
LTH043 Lithium Transport 18 0.033
802
P RTT002 Rett Syndrome 80 0.031
803
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.031
804
P FML011 Familial Adenomatous Polyposis 72 0.031
805
c HMP029 Hemophilia a 67 0.031
806
P CNJ013 Conjunctivitis 65 0.031
807
c ART101 Aortic Valve Disease 2 65 0.031
808
DSM004 Desmoid Tumor 64 0.031
809
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.031
810
BDD001 Budd-Chiari Syndrome 63 0.031
811
BLD131 Bladder Urothelial Carcinoma 62 0.031
812
BLM002 Bulimia Nervosa 57 0.031
813
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.031
814
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.031
815
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.031
816
URN010 Urinary Tract Obstruction 55 0.031
817
CLF004 Cleft Lip/palate 54 0.031
818
GNT003 Genital Herpes 54 0.031
819
THR013 Thoracic Outlet Syndrome 54 0.031
820
AMN001 Amenorrhea 54 0.031
821
RHM028 Rheumatic Heart Disease 53 0.031
822
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.031
823
P HMP007 Hemophilia 51 0.031
824
ESP002 Esophageal Varix 51 0.031
825
NRM004 Neuroma 51 0.031
826
P FNC004 Fanconi Syndrome 50 0.031
827
BRX001 Bruxism 50 0.031
828
HPT014 Hepatorenal Syndrome 50 0.031
829
CHL122 Cholesteatoma of Middle Ear 50 0.031
830
HMG002 Hemoglobinuria 50 0.031
831
CHL061 Childhood Leukemia 48 0.031
832
INT017 Intestinal Schistosomiasis 48 0.031
833
TBR011 Tuberculous Meningitis 48 0.031
834
KRT008 Keratopathy 47 0.031
835
CNT033 Central Nervous System Cancer 47 0.031
836
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.031
837
ISC015 Ischemic Colitis 44 0.031
838
TNG009 Tongue Squamous Cell Carcinoma 44 0.031
839
P CRN024 Corneal Disease 44 0.031
840
P MYG005 Myoglobinuria 44 0.031
841
OST115 Osteonecrosis of the Jaw 40 0.031
842
P FNC034 Fanconi Renotubular Syndrome 2 40 0.031
843
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.031
844
P DNT007 Dentin Sensitivity 36 0.031
845
ABD010 Abdominal Wall Defect 36 0.031
846
TBL029 Tubulin, Beta 28 0.031
847
P HRM021 Hair Morphology 2 22 0.031
848
c INF071 Inflammatory Bowel Disease 1 67 0.030
849
P BLD062 Bile Duct Cancer 67 0.030
850
APH001 Aphthous Stomatitis 57 0.030
851
PHR003 Pharyngitis 57 0.030
852
LST001 Listeriosis 56 0.030
853
P OVR049 Ovarian Disease 52 0.030
854
c HRD202 Hereditary Lymphedema I 50 0.030
855
c HYD064 Hydrocephalus, Congenital, 1 48 0.030
856
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.030
857
SCR011 Scrapie 39 0.030
858
c NRF024 Neurofibromatosis, Type I 77 0.028
859
ADR007 Adrenoleukodystrophy 75 0.028
860
P TTR001 Tetralogy of Fallot 70 0.028
861
ACR008 Acrocallosal Syndrome 69 0.028
862
P MPL001 Maple Syrup Urine Disease 69 0.028
863
FCT007 Factor Vii Deficiency 67 0.028
864
P PRP003 Porphyria Cutanea Tarda 67 0.028
865
LNG039 Lung Squamous Cell Carcinoma 66 0.028
866
P HRS035 Hirschsprung Disease 1 65 0.028
867
P PSD087 Pseudoxanthoma Elasticum 65 0.028
868
ART002 Arts Syndrome 64 0.028
869
BLL006 Bullous Pemphigoid 62 0.028
870
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.028
871
CHC001 Chickenpox 60 0.028
872
DRR014 Darier-White Disease 60 0.028
873
P PRD006 Prader-Willi Syndrome 59 0.028
874
P GLL022 Guillain-Barre Syndrome 59 0.028
875
KRT071 Keratosis, Seborrheic 58 0.028
876
P INT070 Intestinal Obstruction 58 0.028
877
RBS001 Rabies 58 0.028
878
P MTR012 Mitral Valve Disease 58 0.028
879
EXT034 Extrinsic Allergic Alveolitis 58 0.028
880
P PNL012 Penile Cancer 56 0.028
881
PRS047 Prostatitis 56 0.028
882
HPT022 Hepatoblastoma 56 0.028
883
VSC003 Visceral Leishmaniasis 55 0.028
884
P SLM003 Salmonellosis 55 0.028
885
GLS001 Gliosarcoma 54 0.028
886
HMN009 Hemangioblastoma 54 0.028
887
BRN014 Bronchopneumonia 54 0.028
888
GST009 Gastroschisis 53 0.028
889
P END047 Endophthalmitis 53 0.028
890
HYP063 Hypersplenism 53 0.028
891
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 53 0.028
892
TRC003 Trichomoniasis 53 0.028
893
P NRC002 Narcolepsy 52 0.028
894
SKN013 Skin Benign Neoplasm 51 0.028
895
AZS001 Azoospermia 50 0.028
896
RBF001 Riboflavin Deficiency 49 0.028
897
KRT001 Keratoconjunctivitis Sicca 49 0.028
898
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.028
899
HST010 Histiocytosis 48 0.028
900
RYN001 Raynaud Disease 48 0.028
901
HPR003 Heparin-Induced Thrombocytopenia 48 0.028
902
ADN009 Adenosquamous Carcinoma 47 0.028
903
CHR031 Chromoblastomycosis 47 0.028
904
NDL007 Nodular Goiter 47 0.028
905
c CNG216 Congenital Hydrocephalus 47 0.028
906
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.028
907
HYP082 Hypopharynx Cancer 47 0.028
908
CMP002 Campylobacteriosis 46 0.028
909
ANL022 Anal Fistula 46 0.028
910
ANG018 Angiomyolipoma 46 0.028
911
EXS017 Exstrophy of Bladder 45 0.028
912
ASP026 Asplenia, Isolated Congenital 44 0.028
913
DBT008 Diabetic Angiopathy 44 0.028
914
ANK020 Ankyloglossia with or Without Tooth Anomalies 44 0.028
915
SPN032 Spindle Cell Carcinoma 44 0.028
916
DVR002 Diverticulitis 43 0.028
917
ENC005 Encephalomalacia 43 0.028
918
RTC009 Reticulum Cell Sarcoma 43 0.028
919
c PRG001 Progressive Muscular Atrophy 42 0.028
920
CRB025 Carbohydrate Metabolic Disorder 41 0.028
921
P CYS017 Cystic Teratoma 41 0.028
922
ELP001 Elephantiasis 41 0.028
923
LCR013 Lacrimal Duct Defect 41 0.028
924
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.028
925
P DYS021 Dysautonomia 39 0.028
926
RTN002 Retinal Perforation 38 0.028
927
MLN011 Malonyl-Coa Decarboxylase Deficiency 38 0.028
928
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.028
929
c CHR098 Chronic Pyelonephritis 38 0.028
930
SHW001 Shwartzman Phenomenon 37 0.028
931
CRD016 Cardiac Rupture 37 0.028
932
HMM004 Hamamy Syndrome 37 0.028
933
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.028
934
SLL001 Sialolithiasis 35 0.028
935
c LKM005 Leukemia, T-Cell, Chronic 34 0.028
936
PTL009 Patella, Chondromalacia of 33 0.028
937
P VSC018 Visceral Steatosis 33 0.028
938
INV005 Inverted Follicular Keratosis 32 0.028
939
BLP006 Blepharoconjunctivitis 31 0.028
940
PLR005 Pleuropneumonia 31 0.028
941
CRT069 Cortical Malformations, Occipital 30 0.028
943
MLG163 Malignant Tumor of Penis 29 0.028
944
MYC088 Mycobacterium Avium Complex Infections 29 0.028
945
CYT018 Cytochrome P450 2d6 Variant 27 0.028
946
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.028
947
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.028
948
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 20 0.028
949
c ART115 Aortic Valve Disease 1 75 0.024
950
ACR007 Acromegaly 71 0.024
951
PTZ001 Peutz-Jeghers Syndrome 70 0.024
952
P CRN037 Craniosynostosis 68 0.024
953
P CWD010 Cowden Syndrome 67 0.024
954
STH001 Saethre-Chotzen Syndrome 67 0.024
955
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 67 0.024
956
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 66 0.024
957
BRK001 Brooke-Spiegler Syndrome 64 0.024
958
P FRD001 Friedreich Ataxia 64 0.024
959
TKY002 Takayasu Arteritis 62 0.024
960
c ANM038 Anemia, Autoimmune Hemolytic 62 0.024
961
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 62 0.024
962
P INT143 Interstitial Cystitis 61 0.024
963
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.024
964
KLP010 Klippel-Trenaunay-Weber Syndrome 59 0.024
965
P HMN036 Hemangiopericytoma, Malignant 59 0.024
966
PLM026 Pilomatrixoma 58 0.024
967
PMP006 Pemphigus Vulgaris, Familial 57 0.024
968
P PLV020 Pelvic Organ Prolapse 57 0.024
969
P MYM013 Moyamoya Disease 1 57 0.024
970
TNS005 Tonsillitis 57 0.024
971
CYT008 Cytomegalovirus Infection 57 0.024
972
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.024
973
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.024
974
ACS001 Acoustic Neuroma 56 0.024
975
PTS001 Patau Syndrome 55 0.024
976
NRG002 Neurogenic Bladder 55 0.024
977
CRC006 Carcinoid Syndrome 55 0.024
978
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.024
979
PYD001 Pyoderma Gangrenosum 54 0.024
980
DBT010 Diabetic Neuropathy 54 0.024
981
SLP001 Sleeping Sickness 54 0.024
982
FRZ001 Frozen Shoulder 53 0.024
983
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 53 0.024
984
KRT006 Keratoconjunctivitis 53 0.024
985
ERD001 Erdheim-Chester Disease 53 0.024
986
ALC009 Alcoholic Liver Cirrhosis 53 0.024
987
TRC008 Trachoma 53 0.024
988
OVR059 Ovary Adenocarcinoma 53 0.024
989
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.024
990
ART074 Aortic Dissection 52 0.024
991
P MGR003 Migraine with Aura 52 0.024
992
P CPL006 Capillary Hemangioma 51 0.024
993
P HRD012 Hereditary Elliptocytosis 51 0.024
994
CHR005 Chorioamnionitis 51 0.024
995
LPD016 Lipoid Proteinosis of Urbach and Wiethe 50 0.024
996
P OMP004 Omphalocele 50 0.024
997
BLL004 Bullous Keratopathy 49 0.024
998
VLV011 Vulvovaginal Candidiasis 49 0.024
999
PCT003 Pectus Excavatum 49 0.024
1000
ART017 Aortic Disease 49 0.024
1001
GST049 Gastrointestinal System Cancer 49 0.024
1002
CHN065 Choanal Atresia, Posterior 49 0.024
1003
P ALP061 Alopecia, Androgenetic, 1 49 0.024
1004
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.024
1005
BRS064 Bursitis 48 0.024
1006
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.024
1007
P GND004 Gonadal Dysgenesis 48 0.024
1008
P UTR058 Uterine Anomalies 47 0.024
1009
LRY029 Laryngomalacia 47 0.024
1010
CLN019 Colonic Disease 47 0.024
1011
P CRN028 Corneal Ulcer 47 0.024
1012
CRD001 Cardiac Tamponade 47 0.024
1013
P RNL015 Renal Hypertension 47 0.024
1014
CRN027 Corneal Neovascularization 47 0.024
1015
LYM012 Lymphoplasmacytic Lymphoma 47 0.024
1016
GST071 Gastrointestinal Carcinoma 47 0.024
1017
ASP004 Asphyxia Neonatorum 46 0.024
1018
c ACT076 Acute Myocarditis 46 0.024
1019
FCL012 Facial Paralysis 46 0.024
1020
PLL012 Pollen Allergy 46 0.024
1021
AND014 Androgenic Alopecia 46 0.024
1022
MGC001 Megacolon 46 0.024
1023
VLV036 Vulvar Disease 46 0.024
1024
RTR008 Root Resorption 45 0.024
1025
c NLD009 Nail Disorder, Nonsyndromic Congenital, 1 45 0.024
1026
PPL018 Papillary Adenocarcinoma 45 0.024
1027
DST006 Diastolic Heart Failure 45 0.024
1028
P CMM008 Communicating Hydrocephalus 45 0.024
1029
KDN015 Kidney Angiomyolipoma 45 0.024
1030
MCR037 Macroglossia 45 0.024
1031
P DCR003 Dacryoadenitis 45 0.024
1032
TWN001 Twin-to-Twin Transfusion Syndrome 45 0.024
1033
BLC012 Bile Acid Malabsorption, Primary 45 0.024
1034
INF058 Inflammatory Myofibroblastic Tumor 45 0.024
1035
c JVN003 Juvenile Xanthogranuloma 44 0.024
1036
HPT082 Hepatic Adenomas, Familial 44 0.024
1037
MTR010 Mature Teratoma 44 0.024
1038
P PRM001 Primary Cutaneous Amyloidosis 44 0.024
1039
CLN044 Colon Adenoma 44 0.024
1040
P PLM085 Pulmonary Hemosiderosis 44 0.024
1041
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.024
1042
c HYP575 Hypotrichosis 7 43 0.024
1043
NDL009 Nodular Basal Cell Carcinoma 43 0.024
1044
ANG011 Angiodysplasia 43 0.024
1045
P HRD018 Hair Disease 43 0.024
1046
MCR103 Microtia 43 0.024
1047
DSC009 Discoid Lupus Erythematosus 42 0.024
1048
P GRN010 Granular Cell Tumor 42 0.024
1049
RNL097 Renal Artery Disease 42 0.024
1050
P DWL001 Dowling-Degos Disease 42 0.024
1051
P HYP087 Hypotrichosis 42 0.024
1052
ARC002 Arachnoiditis 42 0.024
1053
FBR019 Fibromatosis 41 0.024
1054
GST020 Gastric Antral Vascular Ectasia 41 0.024
1055
P CHR342 Chiari Malformation 41 0.024
1056
LYM010 Lymph Node Tuberculosis 41 0.024
1057
DFF003 Diffuse Scleroderma 41 0.024
1058
PHB003 Phobia, Specific 41 0.024
1059
VST004 Vestibular Disease 41 0.024
1060
c FBR072 Febrile Seizures, Familial, 11 41 0.024
1061
c AMY060 Amyloidosis, Primary Localized Cutaneous, 1 41 0.024
1062
CNS002 Constrictive Pericarditis 40 0.024
1063
CLD014 Cole Disease 40 0.024
1064
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.024
1065
HYP540 Hypertension, Diastolic 40 0.024
1066
ART008 Arteriosclerosis Obliterans 40 0.024
1067
WST002 Western Equine Encephalitis 40 0.024
1068
SCR015 Scarlet Fever 39 0.024
1069
NVS015 Nevus Comedonicus 39 0.024
1070
CTN004 Cutaneous Fibrous Histiocytoma 39 0.024
1071
END011 Endometriosis of Ovary 39 0.024
1072
MLT016 Multicentric Reticulohistiocytosis 39 0.024
1073
CHL070 Cholesterol Embolism 39 0.024
1074
ADP007 Adie Pupil 39 0.024
1075
NM001 Noma 38 0.024
1076
OCH001 Ochronosis 38 0.024
1077
URT004 Urethral Syndrome 38 0.024
1078
TRC026 Tracheal Disease 38 0.024
1079
NCR002 Necrobiosis Lipoidica 38 0.024
1080
c ELL005 Elliptocytosis 2 38 0.024
1081
BLR004 Biliary Dyskinesia 38 0.024
1082
P SLP003 Salpingitis 38 0.024
1083
STL001 St. Louis Encephalitis 37 0.024
1084