Search results for Carbon dioxide

1146 hits were found for Carbon dioxide

# Family MCID Name MIFTS Score
1
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.324
2
P RSP003 Respiratory Failure 74 0.317
3
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.316
4
P CRD119 Cardiac Arrest 67 0.301
5
HYP266 Hypoxia 56 0.263
6
LNG099 Lung Disease 61 0.243
7
P PNC025 Panic Disorder 53 0.234
8
MTB004 Metabolic Acidosis 50 0.233
9
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.226
10
P KDN018 Kidney Disease 70 0.215
11
HRW001 Hair Whorl 36 0.211
12
P NRF023 Neurofibromatosis, Type Ii 76 0.205
13
OCL069 Ocular Motor Apraxia 51 0.204
14
c DWL002 Dowling-Degos Disease 1 58 0.202
15
MTH071 Methane Production 26 0.197
16
LVR012 Liver Cirrhosis 63 0.195
17
c CHR684 Chronic Kidney Disease 66 0.183
18
P ENC018 Encephalopathy 61 0.182
19
TXC005 Toxic Shock Syndrome 61 0.178
20
ANX004 Anoxia 42 0.178
21
ALL026 Allergic Hypersensitivity Disease 64 0.175
22
ISC004 Ischemia 60 0.166
23
P LVR013 Liver Disease 68 0.166
24
P SLP006 Sleep Apnea 69 0.165
25
P PLM037 Pulmonary Hypertension 68 0.164
26
ANX010 Anxiety 72 0.160
27
48X005 48,xyyy 39 0.160
28
BRN024 Bronchitis 68 0.155
29
P RHN004 Rhinitis 57 0.154
30
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.152
31
PLM010 Pulmonary Edema 55 0.148
32
P VSC007 Vascular Disease 63 0.147
33
47X002 47,xyy 49 0.146
34
CRB039 Cerebrovascular Disease 69 0.145
35
CNG034 Congestive Heart Failure 70 0.144
36
P PLM036 Pulmonary Fibrosis 61 0.143
37
PPL052 Papillomatosis, Confluent and Reticulated 34 0.143
38
ADN018 Adenoma 58 0.143
39
IDP011 Idiopathic Interstitial Pneumonia 63 0.143
40
P CLR023 Colorectal Cancer 98 0.142
41
PNM008 Pneumothorax 56 0.141
42
ALL003 Allergic Rhinitis 67 0.140
43
BNR002 Bone Resorption Disease 48 0.140
44
HLX001 Helix Syndrome 47 0.138
45
c CRV002 Cervix Uteri Carcinoma in Situ 44 0.136
46
CRV045 Cervical Intraepithelial Neoplasia 39 0.136
47
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.134
48
P HDC001 Headache 57 0.133
49
P HPT023 Hepatocellular Carcinoma 100 0.133
50
END030 End Stage Renal Failure 58 0.130
51
P LNG032 Lung Cancer 97 0.128
52
P HMN010 Hemangioma 61 0.127
53
P RNL007 Renal Tubular Acidosis 50 0.126
54
BRN071 Brain Injury 49 0.123
55
PLM033 Pulmonary Embolism 59 0.123
56
SQM006 Squamous Cell Carcinoma 60 0.122
57
P SZR006 Seizure Disorder 58 0.121
58
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.121
59
PPL022 Papilloma 54 0.121
60
P PNC035 Pancreatic Cancer 84 0.121
61
P ADN016 Adenocarcinoma 64 0.121
62
P ADL010 Adult Respiratory Distress Syndrome 63 0.120
63
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.119
64
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.119
65
INT075 Intracranial Hypertension 53 0.119
66
PRT036 Peritonitis 65 0.118
67
VSL002 Visual Epilepsy 58 0.118
68
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.117
69
FTT001 Fatty Liver Disease 61 0.117
70
DPR016 Depression 63 0.117
71
P PLM034 Pulmonary Emphysema 56 0.116
72
RRS014 Rare Surgical Neurologic Disease 32 0.116
73
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.116
74
P NRB001 Neuroblastoma 71 0.116
75
ART016 Aortic Aneurysm 68 0.115
76
P END044 Endometriosis 62 0.114
77
AST005 Asthma 77 0.113
78
PNG002 Pain Agnosia 51 0.113
79
CYT002 Cytokine Deficiency 44 0.111
80
LKP003 Leukoplakia 39 0.110
81
ANR040 Aneurysm 58 0.109
82
P BPL003 Bipolar Disorder 56 0.109
83
P INS002 in Situ Carcinoma 52 0.109
84
SLC006 Silicosis 56 0.108
85
LMB062 Limb Ischemia 55 0.108
86
c MGR028 Migraine with or Without Aura 1 69 0.107
87
HYP457 Hypertrophic Scars 43 0.107
88
c MJR024 Major Affective Disorder 9 41 0.106
89
c MJR022 Major Affective Disorder 8 38 0.106
90
c FNC043 Fanconi Anemia, Complementation Group E 62 0.106
91
P PNM007 Pneumonia 68 0.105
92
P HRT032 Heart Disease 75 0.105
93
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.104
94
P GLM045 Glioma 63 0.103
95
GLL048 Glial Tumor 45 0.101
96
P CRN300 Coronary Heart Disease 1 63 0.101
97
STR067 Stroke, Ischemic 80 0.101
98
APN008 Apnea, Obstructive Sleep 65 0.101
99
P HYP076 Hyperthyroidism 55 0.100
100
KLD004 Keloid Disorder 40 0.100
101
c ACT071 Acute Kidney Failure 59 0.100
102
P DRR001 Diarrhea 57 0.099
103
ART140 Arteries, Anomalies of 53 0.099
104
DNT012 Dental Caries 51 0.099
105
P PRS040 Prostate Cancer 97 0.099
106
MNT002 Mental Depression 57 0.099
107
P BNG032 Benign Mesothelioma 45 0.099
108
TRM010 Traumatic Brain Injury 53 0.098
109
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.097
110
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.097
111
SDD001 Sudden Infant Death Syndrome 61 0.097
112
DYS073 Dysphagia 50 0.097
113
SQM002 Squamous Cell Papilloma 42 0.096
114
ADL002 Adult Syndrome 69 0.096
115
P CRN018 Coronary Artery Anomaly 63 0.096
116
P NTR004 Neutropenia 63 0.096
117
DRM006 Dermatitis 61 0.095
118
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.095
119
OST159 Osteogenic Sarcoma 66 0.095
120
NRL016 Neural Tube Defects 82 0.094
121
HDR002 Hidradenitis Suppurativa 53 0.094
122
LYM022 Lymphangioma 53 0.094
123
HDR003 Hidradenitis 49 0.094
124
P RRL003 Rare Lymphatic Malformation 31 0.094
125
P BLD134 Bladder Cancer 78 0.094
126
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.094
127
MLN008 Melanoma 69 0.094
128
ATH013 Atherosclerosis Susceptibility 66 0.093
129
c BSL007 Basal Cell Carcinoma 68 0.093
130
CYS001 Cystic Fibrosis 80 0.092
131
P TRM003 Tremor 53 0.092
132
BRN002 Bronchiolitis 59 0.091
133
AMN003 Amnestic Disorder 54 0.090
134
BCT022 Bacterial Infectious Disease 56 0.090
135
CNS004 Constipation 57 0.090
136
THY029 Thyroid Carcinoma 59 0.090
137
NWB001 Newborn Respiratory Distress Syndrome 58 0.089
138
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.089
139
P LTR001 Lateral Sclerosis 53 0.089
140
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.088
141
PLM031 Poliomyelitis 57 0.088
142
P HYP086 Hypothyroidism 68 0.088
143
OST012 Osteoarthritis 78 0.088
144
P MYC007 Myocardial Infarction 70 0.087
145
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.087
146
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.087
147
CNT097 Central Hypoventilation Syndrome, Congenital 70 0.087
148
KRT009 Keratosis 53 0.087
149
P TRN020 Turner Syndrome 65 0.087
150
SPN186 Spinal Cord Injury 60 0.086
151
P KDN017 Kidney Cancer 61 0.086
152
P INF032 Infertility 57 0.086
153
ATX019 Ataxia with Vitamin E Deficiency 48 0.086
154
P NRP001 Neuropathy 56 0.086
155
c BNG091 Benign Chronic Pemphigus 59 0.085
156
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.085
157
STM007 Stomatitis 49 0.085
158
P GST053 Gastric Cancer 83 0.085
159
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.085
160
P SKN015 Skin Carcinoma 67 0.085
161
LSH001 Leishmaniasis 63 0.085
162
P KLZ004 Kala-Azar 1 41 0.085
163
ANT018 Anthracosis 48 0.084
164
HMP009 Haemophilus Influenzae 42 0.084
165
HYP056 Hypoglycemia 66 0.084
166
RCK004 Rickets 69 0.084
167
RSC001 Rosacea 55 0.084
168
CHL056 Cheilitis 48 0.084
169
ACT093 Actinic Cheilitis 40 0.084
170
TLN003 Telangiectasis 51 0.084
171
PRP027 Peripheral Vascular Disease 71 0.084
172
P PNM006 Pneumoconiosis 55 0.084
173
HMN044 Human Immunodeficiency Virus Type 1 71 0.083
174
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.083
175
HRT011 Heart Septal Defect 50 0.083
176
HDN002 Head Injury 45 0.083
177
c SCL052 Scleroderma, Familial Progressive 62 0.083
178
c SML038 Small Cell Cancer of the Lung 65 0.083
179
P LCT001 Lactic Acidosis 51 0.083
180
AGN016 Aging 56 0.083
181
P HYP098 Hypereosinophilic Syndrome 66 0.082
182
IRN002 Iron Metabolism Disease 57 0.082
183
P OPN001 Open-Angle Glaucoma 49 0.082
184
AGR002 Agoraphobia 44 0.082
185
ORL012 Oral Leukoplakia 39 0.082
186
CLT003 Colitis 62 0.082
187
P RCT021 Rectum Cancer 53 0.082
188
c RHB024 Rhabdomyosarcoma 2 65 0.081
189
GST023 Gastric Ulcer 53 0.081
190
P PRD008 Periodontitis 62 0.081
191
ESP021 Esophageal Cancer 90 0.080
192
DFC004 Deficiency Anemia 75 0.080
193
P CRD246 Cardiovascular System Disease 56 0.080
194
ORL015 Oral Squamous Cell Carcinoma 43 0.080
195
PST092 Posttransplant Acute Limbic Encephalitis 29 0.080
196
P OVR042 Ovarian Cancer 89 0.080
197
c HYP595 Hypertension, Essential 84 0.080
198
c PRC016 Pre-Eclampsia 63 0.080
199
c GLL024 Gallbladder Disease 1 52 0.080
200
SYN036 Syncope 45 0.079
201
CRB086 Cerebral Aneurysms 40 0.078
202
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.078
203
ALC007 Alcohol Dependence 66 0.078
204
MCS002 Mucositis 55 0.078
205
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.077
206
P SYR003 Syringoma 37 0.077
207
ORL011 Oral Cancer 60 0.077
208
GST045 Gastroenteritis 59 0.076
209
ADN011 Adenoid Cystic Carcinoma 70 0.076
210
SKN016 Skin Disease 63 0.076
211
ILS001 Ileus 51 0.076
212
MDD011 Mood Disorder 62 0.075
213
END040 Endogenous Depression 54 0.075
214
P ALZ034 Alzheimer Disease 88 0.075
215
RTN020 Retinal Vascular Disease 48 0.075
216
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.075
217
P HYD006 Hydrocephalus 65 0.075
218
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.075
219
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.075
220
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.075
221
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.075
222
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.075
223
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.075
224
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.075
225
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.075
226
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.075
227
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.075
228
P TBR001 Tuberous Sclerosis 70 0.074
229
OBS037 Obesity-Hypoventilation Syndrome 45 0.074
230
HYP005 Hypokalemia 55 0.074
231
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.074
232
P VNT002 Ventricular Septal Defect 60 0.074
233
P SYS005 Systemic Scleroderma 70 0.073
234
c PNS012 Paine Syndrome 61 0.073
235
PRT013 Portal Hypertension 60 0.073
236
c EXD008 Exudative Vitreoretinopathy 1 69 0.073
237
P PMP001 Pemphigus 55 0.073
238
P CND004 Candidiasis 57 0.072
239
P ACT105 Acute Mountain Sickness 52 0.072
240
ANG054 Angina Pectoris 66 0.072
241
HYP066 Hyperglycemia 61 0.072
242
BRN028 Brain Cancer 73 0.072
243
c PCH010 Pachyonychia Congenita 3 43 0.072
244
ANP008 Anaplastic Oligoastrocytoma 30 0.072
245
P LNG064 Lung Cancer Susceptibility 3 77 0.072
246
BRN012 Bronchiolitis Obliterans 56 0.072
247
P DST107 Distal Renal Tubular Acidosis 41 0.072
248
c ACT075 Acute Myocardial Infarction 56 0.071
249
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.071
250
NRT001 Neurotic Disorder 52 0.071
251
BRN056 Bronchopulmonary Dysplasia 57 0.071
252
ING001 Inguinal Hernia 60 0.071
253
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.070
255
c CNT015 Central Sleep Apnea 46 0.070
256
LNT004 Lentigines 46 0.070
257
TRC005 Tracheal Stenosis 38 0.070
258
TNP004 Tn Polyagglutination Syndrome 40 0.070
259
CRB090 Cerebral Hypoxia 43 0.070
260
URT049 Urate Oxidase, Pseudogene 25 0.070
261
P INF037 Inflammatory Bowel Disease 56 0.069
262
CHL014 Cholera 55 0.069
263
P ART021 Arteriosclerosis 54 0.069
264
CTN007 Cutaneous Leishmaniasis 61 0.069
265
ALL006 Allergic Asthma 56 0.069
266
PPL001 Papillary Adenoma 45 0.069
267
INT002 Intermittent Claudication 61 0.069
268
P HML002 Hemolytic Anemia 62 0.069
269
P CTR002 Cataract 60 0.069
270
P RTN008 Retinitis Pigmentosa 77 0.069
271
ATM095 Autoimmune Disease 61 0.069
272
P ALP008 Alopecia 56 0.069
273
VRR004 Verrucous Carcinoma 49 0.069
274
LCH016 Lichen Sclerosus Et Atrophicus 41 0.069
275
ERY023 Erythroplakia 24 0.069
276
P PHC003 Pheochromocytoma 71 0.069
277
GTR002 Goiter 52 0.069
278
ADR040 Adrenal Gland Pheochromocytoma 46 0.069
279
P MCR115 Microvascular Complications of Diabetes 5 66 0.068
280
P FBR017 Fibrosarcoma 56 0.068
281
RTN023 Retinitis 46 0.068
282
NRR001 Neuroretinitis 43 0.068
283
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.068
284
TRN018 Transitional Cell Carcinoma 56 0.068
285
DMP001 Dumping Syndrome 44 0.068
286
P SCH015 Schizophrenia 75 0.068
287
RSP007 Respiratory Distress Syndrome, Infant 30 0.068
288
OBS532 Obsolete: Ehlers-Danlos Syndrome, Fibronectinemic Type 15 0.068
289
P PNC044 Pancreatitis 61 0.068
290
VRC005 Varicose Veins 60 0.068
291
DWN001 Down Syndrome 70 0.067
292
P PLY019 Polyneuropathy 56 0.067
293
INT066 Interstitial Lung Disease 59 0.067
294
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.066
295
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.066
296
CLN015 Colon Adenocarcinoma 63 0.066
297
MYL020 Myelomeningocele 51 0.066
298
c GLC092 Glaucoma, Primary Open Angle 62 0.066
299
c ACT134 Acute Liver Failure 51 0.066
300
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.066
301
P OVR082 Overgrowth Syndrome 50 0.066
302
P MLG056 Malignant Hyperthermia 67 0.066
303
MST005 Mastitis 53 0.066
304
P PRP019 Peripheral Nervous System Disease 57 0.065
305
CNT047 Contact Dermatitis 57 0.065
306
BRN004 Brain Edema 55 0.065
307
ANT024 Anthrax Disease 58 0.065
308
P PSR002 Psoriasis 62 0.065
309
PST011 Pustulosis of Palm and Sole 52 0.065
310
c ART068 Aortic Aneurysm, Familial Thoracic 2 34 0.065
311
SKN019 Skin Melanoma 67 0.065
312
P ENC004 Encephalitis 61 0.065
313
RTN017 Retinal Detachment 60 0.065
314
CRD137 Cardiogenic Shock 48 0.065
315
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 22 0.065
316
c ACT068 Acute Cystitis 63 0.064
317
ANG005 Anogenital Venereal Wart 56 0.064
318
STT002 Status Asthmaticus 49 0.064
319
MDS022 Mediastinitis 47 0.064
320
BWN006 Bowen's Disease 32 0.064
321
P MYP004 Myopathy 64 0.064
322
NRM005 Neuromuscular Disease 63 0.064
323
CHL079 Children's Interstitial Lung Disease 27 0.064
324
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.064
325
P BRS044 Breast Adenocarcinoma 59 0.064
326
P CNR004 Cone-Rod Dystrophy 2 71 0.064
327
P SCK005 Sickle Cell Disease 50 0.064
328
CYN002 Cyanosis, Transient Neonatal 45 0.063
329
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.063
330
NRF007 Neurofibroma 64 0.063
331
CHL004 Cholelithiasis 49 0.063
332
P ART022 Arthritis 70 0.063
333
P MYS003 Myasthenia Gravis 68 0.063
334
c BRN108 Branchiootic Syndrome 1 61 0.063
335
c ACT027 Acute Pancreatitis 59 0.063
336
RRD056 Rare Disease in Surgical Orthopedic 28 0.063
337
ULC004 Ulcerative Colitis 73 0.063
338
P LKM002 Leukemia 66 0.063
339
NNL006 Non-Alcoholic Steatohepatitis 51 0.063
340
P GST044 Gastritis 55 0.063
341
SPP010 Suppressor of Tumorigenicity 3 51 0.063
342
P AST007 Astrocytoma 50 0.063
343
PLM001 Pulmonary Tuberculosis 70 0.062
344
P BRN022 Bronchiectasis 59 0.062
345
CHL067 Cholecystitis 58 0.062
346
P CHN012 Chondrosarcoma 56 0.062
347
P PRM006 Primary Biliary Cirrhosis 61 0.061
348
URM002 Uremia 49 0.061
349
OST003 Osteonecrosis 61 0.061
350
CHR100 Chronic Ulcer of Skin 53 0.061
351
CLC006 Calcinosis 48 0.061
352
c GRV008 Graves Disease 1 55 0.061
353
P DBT005 Diabetes Insipidus 55 0.061
354
CHG001 Chagas Disease 66 0.060
355
SRC014 Sarcoma 65 0.060
356
P BCL017 B-Cell Lymphoma 58 0.060
357
P SJG008 Sjogren Syndrome 56 0.060
358
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.060
359
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.060
360
c HYP836 Hypercholesterolemia, Familial, 1 72 0.060
361
P HRP006 Herpes Simplex 65 0.060
362
TTN003 Tetanus 64 0.060
363
SYN007 Synovitis 55 0.060
364
P ATR010 Atrial Heart Septal Defect 60 0.060
365
P PYL005 Pyelonephritis 56 0.060
366
PST028 Post-Traumatic Stress Disorder 58 0.060
367
P FBR031 Febrile Seizures 51 0.060
368
P MTR003 Mitral Valve Stenosis 50 0.060
369
ACT084 Acute Stress Disorder 48 0.060
370
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.060
371
HPT004 Hepatic Coma 43 0.060
372
P PRK001 Porokeratosis 53 0.059
373
P ECT005 Ectropion 41 0.059
374
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.059
375
SNG003 Single Ventricular Heart 30 0.059
376
MLR004 Malaria 80 0.059
377
NTR005 Nutritional Deficiency Disease 61 0.059
378
PPT005 Peptic Ulcer Disease 58 0.059
379
P LYM031 Lymphocytic Leukemia 55 0.059
380
c CHR682 Chronic Bilirubin Encephalopathy 38 0.059
381
P SNS001 Sensorineural Hearing Loss 61 0.059
382
SBC016 Subacute Delirium 44 0.059
383
CHL068 Cholestasis 60 0.059
384
P PRC012 Pericardial Effusion 51 0.058
385
HMP001 Hemopericardium 46 0.058
386
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.058
387
c MNN043 Meningioma, Familial 74 0.058
388
MNN042 Meningioma, Radiation-Induced 62 0.058
389
TRG002 Trigeminal Neuralgia 60 0.058
390
SPN035 Spindle Cell Sarcoma 51 0.058
391
SPN021 Spinal Meningioma 47 0.058
392
SCR001 Secretory Meningioma 37 0.058
393
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.058
394
c ATR087 Atrial Standstill 1 74 0.058
395
P LYM118 Lymphoma 68 0.058
396
P DMN002 Dementia 67 0.058
397
OTT002 Otitis Media 71 0.057
398
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.057
399
P SLP005 Sleep Disorder 59 0.057
400
RHM027 Rheumatic Disease 56 0.057
401
P DRM053 Dermatitis, Atopic 66 0.057
402
BRR014 Barrett Esophagus 64 0.057
403
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.057
404
RDN001 Reading Disorder 40 0.057
405
c HPT073 Hepatitis C Virus 70 0.056
406
PLR007 Pleural Empyema 49 0.056
407
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.056
408
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.056
409
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.055
410
LYM133 Lymphoma, Hodgkin, Classic 69 0.055
411
P NSP012 Nasopharyngeal Carcinoma 67 0.055
412
P MSC005 Muscular Dystrophy 66 0.055
413
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.055
414
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.055
415
P AMY004 Amyloidosis 70 0.055
416
CHL065 Cholangiocarcinoma 67 0.055
417
INT079 Intrahepatic Cholangiocarcinoma 50 0.055
418
RYN005 Raynaud Phenomenon 46 0.055
419
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.055
420
NVS017 Nevus, Epidermal 68 0.054
421
P INF038 Influenza 68 0.054
422
GNG013 Gingivitis 59 0.054
423
CRT013 Carotid Stenosis 50 0.054
424
ECT026 Ectopic Pregnancy 49 0.054
425
BLN010 Balanitis 36 0.054
426
IMM167 Immune Deficiency Disease 78 0.054
427
c ATS007 Autism Spectrum Disorder 67 0.054
428
P SCL018 Scoliosis 60 0.054
429
P MJR001 Major Depressive Disorder 68 0.054
430
LPD008 Lipid Metabolism Disorder 62 0.054
431
HPT019 Hepatic Encephalopathy 60 0.054
432
CRD223 Cardiac Arrhythmia 60 0.054
433
P SRC025 Sarcoidosis 1 70 0.053
434
c MCR113 Microvascular Complications of Diabetes 3 52 0.053
435
THY124 Thyroid Gland Papillary Carcinoma 52 0.053
436
c MCR120 Microvascular Complications of Diabetes 7 47 0.053
437
c MLG068 Malignant Glioma 45 0.053
438
c MCR130 Microvascular Complications of Diabetes 6 41 0.053
439
c MCR133 Microvascular Complications of Diabetes 4 41 0.053
440
PRP030 Purpura 55 0.053
441
CRP002 Croup 42 0.053
442
SCK001 Sick Building Syndrome 35 0.053
443
LPT014 Leptin Deficiency or Dysfunction 73 0.053
444
DPH001 Diphtheria 60 0.053
445
DYS015 Dysentery 50 0.053
446
P CLS010 Cluster Headache 43 0.053
447
ARG004 Argyria 28 0.053
448
c LKM061 Leukemia, Acute Myeloid 83 0.053
449
CRH001 Crohn's Disease 74 0.053
450
c LRG017 Large Intestine Cancer 47 0.053
451
DNT008 Denture Stomatitis 35 0.052
452
P URT039 Urticaria 58 0.052
453
END057 Endometrial Cancer 74 0.051
454
P ATS364 Autism 65 0.051
455
OST017 Osteomyelitis 64 0.051
456
ENT004 Enthesopathy 48 0.051
457
P OBS001 Obstructive Jaundice 48 0.051
458
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.051
459
YLL002 Yellow Fever 60 0.051
460
PNM010 Pneumothorax, Primary Spontaneous 60 0.051
461
STT041 Stuttering 52 0.051
462
NTR046 Neutrophil Migration 50 0.051
463
KRT013 Keratolytic Winter Erythema 46 0.051
464
RTR001 Retrograde Amnesia 45 0.051
465
P RHM011 Rheumatoid Arthritis 80 0.051
466
c THR092 Thrombophilia Due to Thrombin Defect 73 0.051
467
P MNN013 Meningitis 65 0.051
468
P MYC008 Myocarditis 59 0.051
469
P EXN002 Exanthem 57 0.051
470
CHP002 Chops Syndrome 42 0.051
471
BCK006 Back Pain 42 0.051
472
P APL001 Aplastic Anemia 74 0.051
473
SCK003 Sickle Cell Anemia 72 0.051
474
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.051
475
PTH003 Pathologic Nystagmus 51 0.051
476
THY030 Thyroid Gland Disease 51 0.051
477
P MLT020 Multiple Sclerosis 72 0.050
478
PLG002 Plague 57 0.050
479
CLF001 Cleft Lip 53 0.050
480
LNG031 Lung Benign Neoplasm 50 0.050
481
CRN030 Coronary Stenosis 50 0.050
482
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.049
483
P LKM062 Leukemia, Acute Lymphoblastic 68 0.049
484
P DYS154 Dystonia 65 0.049
485
P ECL001 Eclampsia 51 0.049
486
c PRS136 Prostate Cancer, Hereditary, 6 33 0.049
487
c PRS130 Prostate Cancer, Hereditary, 8 32 0.049
488
P CYS018 Cystitis 59 0.049
489
PRP080 Peripheral Artery Disease 53 0.049
490
BTN004 Biotin Deficiency 38 0.049
491
IRR002 Irritable Bowel Syndrome 63 0.049
492
P ALP009 Alopecia Areata 60 0.049
493
GNR004 Generalized Anxiety Disorder 56 0.049
494
MMM001 Mammary Paget's Disease 53 0.049
495
P ACT008 Actinic Keratosis 52 0.049
496
LGN006 Legionnaire Disease 50 0.049
497
P OTS001 Otosclerosis 50 0.049
498
CVR006 Cavernous Hemangioma 49 0.049
499
RCR004 Recurrent Respiratory Papillomatosis 48 0.049
500
VLV044 Vulvar Intraepithelial Neoplasia 44 0.049
501
PYG006 Pyogenic Granuloma 40 0.049
502
SPR012 Separation Anxiety Disorder 37 0.049
503
INF057 Inflammatory Linear Verrucous Epidermal Nevus 34 0.049
504
c PST106 Post-Cardiac Arrest Syndrome 34 0.049
505
SBG002 Subglottic Angioma 13 0.049
506
OBS002 Obsessive-Compulsive Disorder 68 0.048
507
P OPT006 Optic Nerve Disease 57 0.048
508
HRD005 Hard Palate Cancer 46 0.048
509
P BRB001 Beriberi 44 0.048
510
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.048
511
c MCR129 Microvascular Complications of Diabetes 1 66 0.048
512
STT001 Status Epilepticus 59 0.048
513
HLC007 Helicobacter Pylori Infection 59 0.048
514
HMS001 Hemosiderosis 54 0.048
515
PLY150 Polykaryocytosis Inducer 31 0.048
516
P ART005 Arteriovenous Malformation 65 0.047
517
P THY023 Thymoma 65 0.047
518
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.047
519
PSR001 Psoriatic Arthritis 62 0.047
520
ACN002 Acanthosis Nigricans 60 0.047
521
P LCH002 Lichen Planus 54 0.047
522
c THY107 Thymoma, Familial 54 0.047
523
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.047
524
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.047
525
P GLM040 Glioma Susceptibility 1 81 0.046
526
PNC129 Pancreatic Adenocarcinoma 67 0.046
527
GST050 Gastrointestinal System Disease 56 0.046
528
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.046
529
HRN029 Hearing Loss, Noise-Induced 37 0.046
530
BNG077 Benign Idiopathic Neonatal Seizures 26 0.046
531
IGR001 Ige Responsiveness, Atopic 59 0.046
532
P PLY011 Polycystic Ovary Syndrome 56 0.046
533
GNG003 Gingival Recession 44 0.046
534
MCR011 Microinvasive Gastric Cancer 43 0.046
535
FNT004 Fainting 31 0.046
536
ENM002 Enamel Erosion 27 0.046
537
NWC001 Newcastle Disease 44 0.046
538
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.045
539
CLR108 Colorectal Adenoma 64 0.045
540
MSC007 Muscle Hypertrophy 63 0.045
541
P RHB003 Rhabdomyosarcoma 62 0.045
542
P ALC033 Alcohol Use Disorder 58 0.045
543
THR024 Thrombosis 56 0.045
544
HYP060 Hyperinsulinism 54 0.045
545
P TCD001 Tic Disorder 54 0.045
546
c MCR112 Microvascular Complications of Diabetes 2 41 0.045
547
c RNG015 Ring Chromosome 2 26 0.045
548
KRT019 Keratitis, Hereditary 67 0.045
549
TRN015 Transient Cerebral Ischemia 62 0.045
550
HYD002 Hydronephrosis 59 0.045
551
LYM027 Lymphopenia 57 0.045
552
VSC002 Vascular Dementia 57 0.045
553
CHK001 Chikungunya 53 0.045
554
P INT068 Intestinal Disease 52 0.045
555
MCN007 Meconium Aspiration Syndrome 52 0.045
556
CRT015 Carotid Artery Occlusion 44 0.045
557
c PLM022 Pulmonary Valve Insufficiency 40 0.045
558
ENT001 Enterocele 39 0.045
559
c HPT003 Hepatitis a 63 0.044
560
P VSC011 Vasculitis 62 0.044
561
P MYP006 Myopia 55 0.044
562
NVS001 Neovascular Glaucoma 52 0.044
563
CLR109 Colorectal Adenocarcinoma 50 0.044
564
LMY002 Leiomyoma 50 0.044
565
OVR094 Ovarian Epithelial Cancer 38 0.044
566
c SPN225 Spondyloarthropathy 1 73 0.043
567
P EPL164 Epilepsy 71 0.043
568
c LKM063 Leukemia, Chronic Myeloid 71 0.043
569
GT001 Gout 63 0.043
570
TYP007 Typhoid Fever 63 0.043
571
APH002 Aphasia 57 0.043
572
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.043
573
P CHR345 Chronic Pain 50 0.043
574
SPL018 Splenomegaly 48 0.043
575
CLL003 Cellulitis 54 0.042
576
SVR097 Severe Cutaneous Adverse Reaction 67 0.042
577
ERY003 Erythema Multiforme 57 0.042
578
AVN001 Avian Influenza 56 0.042
579
c BCT007 Bacterial Meningitis 55 0.042
580
TNG003 Tongue Cancer 55 0.042
581
c PRD040 Periodontitis, Chronic 54 0.042
582
ASP007 Aspiration Pneumonia 48 0.042
583
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.042
584
IDP070 Idiopathic Scoliosis 37 0.042
585
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.042
586
ERY066 Erythema Multiforme Major 28 0.042
587
P HYP055 Hypoplastic Left Heart Syndrome 62 0.042
588
c LCL006 Localized Scleroderma 62 0.042
589
P PRP029 Porphyria 62 0.042
590
NRL005 Neurilemmoma 60 0.042
591
P PTN014 Patent Ductus Arteriosus 1 60 0.042
592
c LPM012 Lipomatosis, Multiple 59 0.042
593
FDB001 Foodborne Botulism 56 0.042
594
WST005 West Nile Virus 55 0.042
595
MYM001 Myoma 53 0.042
596
ECH003 Echinococcosis 53 0.042
597
CRT016 Carotid Artery Disease 52 0.042
598
PYD002 Pyoderma 51 0.042
599
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 0.042
600
TRT001 Teratocarcinoma 46 0.042
601
P OVR046 Ovarian Cyst 45 0.042
602
SPR005 Superficial Basal Cell Carcinoma 45 0.042
603
LRY017 Laryngeal Disease 42 0.042
604
PLM005 Pleomorphic Lipoma 39 0.042
605
BLN002 Balanitis Xerotica Obliterans 30 0.042
606
MCC003 Mucocele of Salivary Gland 29 0.042
607
P EPL003 Epulis 29 0.042
608
LKP001 Leukoplakia of Penis 18 0.042
609
P ATX030 Ataxia-Telangiectasia 83 0.042
610
P HPT021 Hepatitis 67 0.042
611
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.042
612
P LPS004 Lupus Erythematosus 61 0.042
613
ERY051 Erythroleukemia, Familial 56 0.042
614
HST009 Histiocytoma 46 0.042
615
P HYP733 Hypercalciuria, Absorptive, 2 46 0.042
616
FBR003 Fibrous Histiocytoma 41 0.042
617
CNN005 Connective Tissue Disease 66 0.040
618
P DNG005 Dengue Virus 57 0.040
619
P PLY041 Polymyositis 57 0.040
620
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.040
621
ALL010 Allergic Contact Dermatitis 55 0.040
622
NPH003 Nephrocalcinosis 51 0.040
623
CRB004 Cerebral Artery Occlusion 44 0.040
624
ADG002 Audiogenic Seizures 26 0.040
625
APP008 Appendicitis 60 0.040
626
ETN001 Eating Disorder 59 0.040
627
CHL123 Chlamydia 59 0.040
628
P LRY044 Larynx Cancer 54 0.040
629
P MNC007 Monocytic Leukemia 54 0.040
630
PRS045 Prostatic Hypertrophy 52 0.040
631
c BCT013 Bacterial Pneumonia 47 0.040
632
VSM001 Vasomotor Rhinitis 37 0.040
633
CHR178 Chromosomal Triplication 35 0.040
634
P RNL115 Renal Tubular Acidosis, Proximal 31 0.040
635
EXT062 Extracranial Carotid Artery Aneurysm 21 0.040
636
c SVR005 Severe Pre-Eclampsia 49 0.039
637
MLN073 Melanosis, Neurocutaneous 45 0.039
638
c ACT042 Acute Pyelonephritis 44 0.039
640
ANG020 Angiosarcoma 58 0.039
641
c JVN010 Juvenile Rheumatoid Arthritis 67 0.038
642
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.038
643
MYC006 Mycosis Fungoides 66 0.038
644
P MTR014 Motor Neuron Disease 64 0.038
645
P ART023 Arthropathy 62 0.038
646
P UVT001 Uveitis 57 0.038
647
SCH014 Schistosomiasis 56 0.038
648
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.038
649
P RTN016 Retinal Degeneration 53 0.038
650
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.038
651
P MSC003 Muscular Atrophy 52 0.038
652
P MYT002 Myotonic Dystrophy 49 0.038
653
PLC008 Placenta Disease 49 0.038
654
VCC001 Vaccinia 49 0.038
655
BHR001 Behr Syndrome 49 0.038
656
MXD026 Mixed Glioma 45 0.038
657
ACT003 Acute Kidney Tubular Necrosis 45 0.038
658
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.038
659
P PRC031 Preeclampsia/eclampsia 1 37 0.038
660
c RNG019 Ring Chromosome 3 21 0.038
661
P MYC084 Mycobacterium Tuberculosis 1 68 0.037
662
c DPH024 Diaphragmatic Hernia, Congenital 64 0.037
663
DCB001 Decubitus Ulcer 60 0.037
664
c VSC019 Vesicoureteral Reflux 1 59 0.037
665
P SYP003 Syphilis 59 0.037
666
GST033 Gestational Diabetes 57 0.037
667
P MLN007 Male Infertility 56 0.037
668
P VNS003 Venous Insufficiency 55 0.037
669
PRC013 Pericarditis 54 0.037
670
P PTS002 Ptosis 52 0.037
671
MTN003 Motion Sickness 52 0.037
672
PRS021 Prostatic Adenoma 51 0.037
673
ACH005 Achalasia 50 0.037
674
RSP006 Respiratory System Disease 50 0.037
675
SYS003 Systolic Heart Failure 50 0.037
676
PRS129 Prostatic Hyperplasia, Benign 49 0.037
677
SCL003 Social Phobia 48 0.037
678
PYL006 Pyloric Stenosis 48 0.037
679
URT010 Ureteral Obstruction 46 0.037
680
RSP021 Respiratory Allergy 45 0.037
681
CRS005 Crest Syndrome 44 0.037
682
P HYP009 Hypertrophic Pyloric Stenosis 42 0.037
683
CHN011 Chondromalacia 37 0.037
684
MYC014 Mycobacterium Chelonae 32 0.037
685
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.036
686
INS024 Insulin-Like Growth Factor I 79 0.036
687
MYL009 Myelodysplastic Syndrome 70 0.036
688
MYL005 Myelofibrosis 67 0.036
689
P SPN046 Spinal Muscular Atrophy 64 0.036
690
c HPT001 Hepatitis C 63 0.036
691
VRL011 Viral Infectious Disease 61 0.036
692
P END033 Endocarditis 57 0.036
693
INT303 Intracranial Hypertension, Idiopathic 56 0.036
694
HMP005 Hemiplegia 54 0.036
695
PRP016 Paraplegia 53 0.036
696
OST016 Osteochondrosis 53 0.036
697
P RTN018 Retinal Disease 52 0.036
698
P HMR003 Hemorrhagic Disease 52 0.036
699
P TRT010 Teratoma 51 0.036
700
CND002 Conduct Disorder 51 0.036
701
HYP781 Hypoascorbemia 50 0.036
702
PRT029 Parathyroid Adenoma 50 0.036
703
CLN045 Colonic Benign Neoplasm 49 0.036
704
PPL021 Papilledema 48 0.036
705
LCK001 Locked-in Syndrome 46 0.036
706
MYX004 Myxedema 44 0.036
707
PLR022 Pleural Disease 44 0.036
708
MLG065 Malignant Fibroxanthoma 44 0.036
709
PRS063 Paresthesia 43 0.036
710
c ADN012 Adenocarcinoma in Situ 42 0.036
711
PRM020 Premenstrual Tension 39 0.036
712
P LRY019 Laryngitis 51 0.035
713
HMN016 Hemangioendothelioma 34 0.035
714
BSL036 Basal Cell Nevus Syndrome 72 0.034
715
c INF071 Inflammatory Bowel Disease 1 68 0.034
716
P MST009 Mastocytosis 63 0.034
717
P GLL020 Gallbladder Disease 58 0.034
718
ORL005 Oral Candidiasis 56 0.034
719
PTN001 Patent Foramen Ovale 56 0.034
720
CMM005 Common Cold 56 0.034
721
MTH009 Mouth Disease 56 0.034
722
PLV003 Pelvic Inflammatory Disease 55 0.034
723
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.034
724
P NLD001 Nail Disease 54 0.034
725
FML037 Female Breast Cancer 52 0.034
726
PRV004 Periventricular Leukomalacia 51 0.034
727
VGN020 Vaginal Disease 50 0.034
728
FDL002 Food Allergy 49 0.034
729
P MTC133 Mitochondrial Myopathy 49 0.034
730
PRN014 Paronychia 49 0.034
731
BLS002 Blastomycosis 49 0.034
732
c BSL024 Basal Cell Carcinoma 1 47 0.034
733
CRB008 Cerebral Atherosclerosis 44 0.034
734
VGN019 Vaginal Discharge 44 0.034
735
STT007 Steatocystoma Multiplex 44 0.034
736
FBR054 Fibroma 44 0.034
737
ANL017 Anal Squamous Cell Carcinoma 43 0.034
738
MGS001 Megaesophagus 43 0.034
739
c PRK082 Porokeratosis 1, Multiple Types 41 0.034
740
DSS010 Dissociative Disorder 38 0.034
741
ANG016 Angiokeratoma 38 0.034
742
CHL013 Cholecystolithiasis 37 0.034
743
KLD003 Keloid Formation 37 0.034
744
EPD070 Epidermoid Cysts 37 0.034
745
LCR004 La Crosse Encephalitis 36 0.034
746
ANG007 Angiokeratoma Circumscriptum 34 0.034
747
BWN003 Bowenoid Papulosis 34 0.034
748
DRM003 Dermatosis Papulosa Nigra 34 0.034
749
P CLR001 Clear Cell Acanthoma 34 0.034
750
ACN010 Acanthoma 33 0.034
751
HDR001 Hidrocystoma 33 0.034
752
CMM003 Common Wart 31 0.034
753
ELS002 Elastosis Perforans Serpiginosa 31 0.034
754
LRY027 Laryngeal Papillomatosis 23 0.034
755
P SPN237 Spina Bifida Aperta 20 0.034
756
APN007 Apnea, Central Sleep 18 0.034
757
RSP020 Respiratory Underresponsiveness to Hypoxia and Hypercapnia 9 0.034
758
KPS004 Kaposi Sarcoma 75 0.034
759
MLT157 Multiple System Atrophy 1 70 0.034
760
P CHR012 Chronic Granulomatous Disease 67 0.034
761
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.034
762
P HYP061 Hypertrophic Cardiomyopathy 66 0.034
763
P ORT004 Orthostatic Intolerance 63 0.034
764
P DRM010 Dermatomyositis 61 0.034
765
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.034
766
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.034
767
DSS009 Disseminated Intravascular Coagulation 57 0.034
768
P GLM007 Glomerulonephritis 57 0.034
769
P MYS005 Myositis 56 0.034
770
INT007 Intermediate Coronary Syndrome 55 0.034
771
INT051 Intussusception 53 0.034
772
DRM011 Dermatophytosis 52 0.034
773
KRT002 Keratomalacia 48 0.034
774
QDR001 Quadriplegia 48 0.034
775
DYS009 Dysthymic Disorder 48 0.034
776
NRN001 Neuroendocrine Carcinoma 47 0.034
777
RNL077 Renal Fibrosis 47 0.034
778
EXS001 Exostosis 46 0.034
779
P MYC033 Myoclonus 46 0.034
780
GST010 Gestational Trophoblastic Neoplasm 46 0.034
781
P CRB088 Cerebral Atrophy 38 0.034
782
GRM010 Germ Cells Tumors 34 0.034
783
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.034
784
MST020 Mast Cell Activation Syndrome 27 0.034
785
LTH043 Lithium Transport 18 0.034
786
P RTT002 Rett Syndrome 80 0.031
787
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.031
788
P FML011 Familial Adenomatous Polyposis 72 0.031
789
c HMP029 Hemophilia a 65 0.031
790
P CNJ013 Conjunctivitis 65 0.031
791
DSM004 Desmoid Tumor 64 0.031
792
c ART101 Aortic Valve Disease 2 63 0.031
793
BDD001 Budd-Chiari Syndrome 62 0.031
794
BLD131 Bladder Urothelial Carcinoma 61 0.031
795
URN010 Urinary Tract Obstruction 57 0.031
796
BLM002 Bulimia Nervosa 57 0.031
797
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 57 0.031
798
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.031
799
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.031
800
FCT001 Factor Viii Deficiency 55 0.031
801
VGN023 Vaginitis 55 0.031
802
CLF004 Cleft Lip/palate 54 0.031
803
GNT003 Genital Herpes 54 0.031
804
AMN001 Amenorrhea 54 0.031
805
RHM028 Rheumatic Heart Disease 53 0.031
806
GLS018 Glass Syndrome 53 0.031
807
THR013 Thoracic Outlet Syndrome 53 0.031
808
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.031
809
P HMP007 Hemophilia 51 0.031
810
CHL122 Cholesteatoma of Middle Ear 51 0.031
811
ESP002 Esophageal Varix 51 0.031
812
NRM004 Neuroma 51 0.031
813
HPT014 Hepatorenal Syndrome 50 0.031
814
BRX001 Bruxism 50 0.031
815
P FNC004 Fanconi Syndrome 50 0.031
816
CHL061 Childhood Leukemia 50 0.031
817
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.031
818
HMG002 Hemoglobinuria 49 0.031
819
TBR011 Tuberculous Meningitis 48 0.031
820
c CNT033 Central Nervous System Cancer 46 0.031
821
KRT008 Keratopathy 46 0.031
822
P PRD037 Periodontal Ehlers-Danlos Syndrome 46 0.031
823
ISC015 Ischemic Colitis 44 0.031
824
TNG009 Tongue Squamous Cell Carcinoma 44 0.031
825
P MYG005 Myoglobinuria 43 0.031
826
P CRN024 Corneal Disease 43 0.031
827
c ACT004 Acute Diarrhea 39 0.031
828
OST115 Osteonecrosis of the Jaw 39 0.031
829
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.031
830
P DNT007 Dentin Sensitivity 35 0.031
831
ABD010 Abdominal Wall Defect 35 0.031
832
TBL029 Tubulin, Beta 28 0.031
833
P HRM021 Hair Morphology 2 21 0.031
834
P BLD062 Bile Duct Cancer 65 0.030
835
APH001 Aphthous Stomatitis 57 0.030
836
LST001 Listeriosis 54 0.030
837
P LYM025 Lymphedema 53 0.030
838
P OVR049 Ovarian Disease 53 0.030
839
c HYD064 Hydrocephalus, Congenital, 1 47 0.030
840
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.030
841
SCR011 Scrapie 38 0.030
842
ADR007 Adrenoleukodystrophy 74 0.028
843
c NRF024 Neurofibromatosis, Type I 71 0.028
844
P TTR001 Tetralogy of Fallot 69 0.028
845
P MPL001 Maple Syrup Urine Disease 69 0.028
846
ACR008 Acrocallosal Syndrome 68 0.028
847
P PRP003 Porphyria Cutanea Tarda 67 0.028
848
P PSD087 Pseudoxanthoma Elasticum 67 0.028
849
FML089 Familial Thoracic Aortic Aneurysm and Dissection 66 0.028
850
FCT007 Factor Vii Deficiency 66 0.028
851
LNG039 Lung Squamous Cell Carcinoma 65 0.028
852
P HRS035 Hirschsprung Disease 1 65 0.028
853
ART002 Arts Syndrome 63 0.028
854
P FRD001 Friedreich Ataxia 63 0.028
855
BLL006 Bullous Pemphigoid 62 0.028
856
DRR014 Darier-White Disease 61 0.028
857
CHC001 Chickenpox 60 0.028
858
P GLL022 Guillain-Barre Syndrome 59 0.028
859
P PRD006 Prader-Willi Syndrome 59 0.028
860
P INT070 Intestinal Obstruction 58 0.028
861
RBS001 Rabies 58 0.028
862
EXT034 Extrinsic Allergic Alveolitis 58 0.028
863
P MTR012 Mitral Valve Disease 57 0.028
864
PRS047 Prostatitis 56 0.028
865
P PNL012 Penile Cancer 56 0.028
866
KRT071 Keratosis, Seborrheic 56 0.028
867
HPT022 Hepatoblastoma 56 0.028
868
VSC003 Visceral Leishmaniasis 55 0.028
869
GLS001 Gliosarcoma 54 0.028
870
P SLM003 Salmonellosis 54 0.028
871
HMN009 Hemangioblastoma 54 0.028
872
GST009 Gastroschisis 54 0.028
873
P HST010 Histiocytosis 53 0.028
874
HYP063 Hypersplenism 53 0.028
875
P END047 Endophthalmitis 52 0.028
876
P NRC002 Narcolepsy 51 0.028
877
AZS001 Azoospermia 50 0.028
878
BRN014 Bronchopneumonia 50 0.028
879
c CNG216 Congenital Hydrocephalus 50 0.028
880
KRT001 Keratoconjunctivitis Sicca 50 0.028
881
RYN001 Raynaud Disease 49 0.028
882
ADN009 Adenosquamous Carcinoma 49 0.028
883
SKN013 Skin Benign Neoplasm 49 0.028
884
DFF035 Diffuse Cutaneous Systemic Sclerosis 48 0.028
885
PLP001 Pulpitis 48 0.028
886
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 48 0.028
887
HPR003 Heparin-Induced Thrombocytopenia 47 0.028
888
INT017 Intestinal Schistosomiasis 47 0.028
889
NDL007 Nodular Goiter 47 0.028
890
P TCL004 T-Cell Leukemia 47 0.028
891
ANL022 Anal Fistula 47 0.028
892
HYP082 Hypopharynx Cancer 47 0.028
893
CMP002 Campylobacteriosis 46 0.028
894
EXS017 Exstrophy of Bladder 46 0.028
895
ANG018 Angiomyolipoma 45 0.028
896
SPN032 Spindle Cell Carcinoma 45 0.028
897
ASP026 Asplenia, Isolated Congenital 44 0.028
898
CRB025 Carbohydrate Metabolic Disorder 44 0.028
899
CHR031 Chromoblastomycosis 44 0.028
900
DBT008 Diabetic Angiopathy 44 0.028
901
ANK020 Ankyloglossia with or Without Tooth Anomalies 44 0.028
902
RTC009 Reticulum Cell Sarcoma 43 0.028
903
c PRG001 Progressive Muscular Atrophy 42 0.028
904
P CYS017 Cystic Teratoma 42 0.028
905
LCR013 Lacrimal Duct Defect 41 0.028
906
ELP001 Elephantiasis 40 0.028
907
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.028
908
P DYS021 Dysautonomia 39 0.028
909
BLP006 Blepharoconjunctivitis 38 0.028
910
ENC005 Encephalomalacia 38 0.028
911
RTN002 Retinal Perforation 38 0.028
912
CRD016 Cardiac Rupture 38 0.028
913
MLN011 Malonyl-Coa Decarboxylase Deficiency 37 0.028
914
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 37 0.028
915
HMM004 Hamamy Syndrome 37 0.028
916
SHW001 Shwartzman Phenomenon 36 0.028
917
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.028
918
c CHR098 Chronic Pyelonephritis 35 0.028
919
SLL001 Sialolithiasis 35 0.028
920
PTL009 Patella, Chondromalacia of 35 0.028
921
PLR005 Pleuropneumonia 32 0.028
922
INV005 Inverted Follicular Keratosis 32 0.028
923
CRT069 Cortical Malformations, Occipital 30 0.028
925
MLG163 Malignant Tumor of Penis 29 0.028
926
MYC088 Mycobacterium Avium Complex Infections 29 0.028
927
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.028
928
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.028
929
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 20 0.028
930
c ART115 Aortic Valve Disease 1 75 0.024
931
ACR007 Acromegaly 71 0.024
932
PTZ001 Peutz-Jeghers Syndrome 69 0.024
933
P CRN037 Craniosynostosis 68 0.024
934
STH001 Saethre-Chotzen Syndrome 67 0.024
935
P CWD010 Cowden Syndrome 66 0.024
936
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 0.024
937
P ART067 Aortic Aneurysm, Familial Thoracic 1 62 0.024
938
c ANM038 Anemia, Autoimmune Hemolytic 61 0.024
939
TKY002 Takayasu Arteritis 61 0.024
940
P INT143 Interstitial Cystitis 61 0.024
941
LYM012 Lymphoplasmacytic Lymphoma 61 0.024
942
BRK001 Brooke-Spiegler Syndrome 60 0.024
943
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.024
944
KLP010 Klippel-Trenaunay-Weber Syndrome 60 0.024
945
P PLV020 Pelvic Organ Prolapse 59 0.024
946
PLM026 Pilomatrixoma 59 0.024
947
P HMN036 Hemangiopericytoma, Malignant 58 0.024
948
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 58 0.024
949
PMP006 Pemphigus Vulgaris, Familial 58 0.024
950
TNS005 Tonsillitis 57 0.024
951
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.024
952
CYT008 Cytomegalovirus Infection 56 0.024
953
PHR003 Pharyngitis 56 0.024
954
ACS001 Acoustic Neuroma 56 0.024
955
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.024
956
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.024
957
CRC006 Carcinoid Syndrome 55 0.024
958
DBT010 Diabetic Neuropathy 55 0.024
959
PYD001 Pyoderma Gangrenosum 54 0.024
960
NRG002 Neurogenic Bladder 54 0.024
961
P MYM013 Moyamoya Disease 1 54 0.024
962
TRC008 Trachoma 53 0.024
963
FRZ001 Frozen Shoulder 53 0.024
964
MYP139 Myopathy, Proximal, and Ophthalmoplegia 53 0.024
965
ALC009 Alcoholic Liver Cirrhosis 53 0.024
966
KRT006 Keratoconjunctivitis 53 0.024
967
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.024
968
ERD001 Erdheim-Chester Disease 52 0.024
969
c PSR017 Psoriasis 2 52 0.024
970
TRC003 Trichomoniasis 52 0.024
971
OVR059 Ovary Adenocarcinoma 51 0.024
972
P HRD012 Hereditary Elliptocytosis 51 0.024
973
CHR005 Chorioamnionitis 51 0.024
974
P CPL006 Capillary Hemangioma 51 0.024
975
VLV011 Vulvovaginal Candidiasis 51 0.024
976
c PYR010 Peyronie's Disease 50 0.024
977
P MGR003 Migraine with Aura 50 0.024
978
CHN065 Choanal Atresia, Posterior 50 0.024
979
P OMP004 Omphalocele 50 0.024
980
PTS001 Patau Syndrome 49 0.024
981
ART017 Aortic Disease 49 0.024
982
c PSR023 Psoriasis 1 49 0.024
983
BLL004 Bullous Keratopathy 49 0.024
984
P GND004 Gonadal Dysgenesis 49 0.024
985
LPD016 Lipoid Proteinosis of Urbach and Wiethe 49 0.024
986
NRL018 Neural Tube Defects, Folate-Sensitive 49 0.024
987
GST049 Gastrointestinal System Cancer 49 0.024
988
SLP001 Sleeping Sickness 48 0.024
989
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 48 0.024
990
FCL012 Facial Paralysis 48 0.024
991
P RNL015 Renal Hypertension 48 0.024
992
PCT003 Pectus Excavatum 48 0.024
993
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.024
994
P UTR058 Uterine Anomalies 48 0.024
995
P CRN028 Corneal Ulcer 47 0.024
996
BRS064 Bursitis 47 0.024
997
CRN027 Corneal Neovascularization 47 0.024
998
CRD001 Cardiac Tamponade 46 0.024
999
PPL018 Papillary Adenocarcinoma 46 0.024
1000
VLV036 Vulvar Disease 46 0.024
1001
c ACT076 Acute Myocarditis 46 0.024
1002
CLN019 Colonic Disease 46 0.024
1003
MGC001 Megacolon 46 0.024
1004
c HYP575 Hypotrichosis 7 46 0.024
1005
KDN015 Kidney Angiomyolipoma 46 0.024
1006
MCR037 Macroglossia 45 0.024
1007
PLL012 Pollen Allergy 45 0.024
1008
GST071 Gastrointestinal Carcinoma 45 0.024
1009
TWN001 Twin-to-Twin Transfusion Syndrome 45 0.024
1010
RTR008 Root Resorption 45 0.024
1011
BLC012 Bile Acid Malabsorption, Primary 45 0.024
1012
P DCR003 Dacryoadenitis 45 0.024
1013
ASP004 Asphyxia Neonatorum 45 0.024
1014
LRY029 Laryngomalacia 45 0.024
1015
INF058 Inflammatory Myofibroblastic Tumor 45 0.024
1016
DVR002 Diverticulitis 44 0.024
1017
DST006 Diastolic Heart Failure 44 0.024
1018
c JVN003 Juvenile Xanthogranuloma 44 0.024
1019
FBR019 Fibromatosis 44 0.024
1020
MTR010 Mature Teratoma 43 0.024
1021
P CMM008 Communicating Hydrocephalus 43 0.024
1022
RNL097 Renal Artery Disease 43 0.024
1023
P PRM001 Primary Cutaneous Amyloidosis 43 0.024
1024
P PLM085 Pulmonary Hemosiderosis 43 0.024
1025
ANG011 Angiodysplasia 43 0.024
1026
ARC002 Arachnoiditis 42 0.024
1027
CLN044 Colon Adenoma 42 0.024
1028
NDL009 Nodular Basal Cell Carcinoma 42 0.024
1029
DSC009 Discoid Lupus Erythematosus 42 0.024
1030
P GRN010 Granular Cell Tumor 42 0.024
1031
P DWL001 Dowling-Degos Disease 42 0.024
1032
MCR103 Microtia 42 0.024
1033
P HYP087 Hypotrichosis 42 0.024
1034
c BNG093 Benign Teratoma 42 0.024
1035
DFF003 Diffuse Scleroderma 42 0.024
1036
GST020 Gastric Antral Vascular Ectasia 41 0.024
1037
VST004 Vestibular Disease 41 0.024
1038
c NLD016 Nail Disorder, Nonsyndromic Congenital, 10 41 0.024
1039
CTN004 Cutaneous Fibrous Histiocytoma 41 0.024
1040
P HRD018 Hair Disease 41 0.024
1041
HYP540 Hypertension, Diastolic 40 0.024
1042
PHB003 Phobia, Specific 40 0.024
1043
P CHR342 Chiari Malformation 40 0.024
1044
c AMY060 Amyloidosis, Primary Localized Cutaneous, 1 40 0.024
1045
SCR015 Scarlet Fever 40 0.024
1046
END011 Endometriosis of Ovary 40 0.024
1047
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.024
1048
ART008 Arteriosclerosis Obliterans 40 0.024
1049
MLT016 Multicentric Reticulohistiocytosis 40 0.024
1050
CNS002 Constrictive Pericarditis 40 0.024
1051
TRC026 Tracheal Disease 39 0.024
1052
NVS015 Nevus Comedonicus 39 0.024
1053
ADP007 Adie Pupil 39 0.024
1054
c PSR028 Psoriasis 7 39 0.024
1055
c PSR032 Psoriasis 11 38 0.024
1056
c PSR018 Psoriasis 13 38 0.024
1057
NCR002 Necrobiosis Lipoidica 38 0.024
1058
NM001 Noma 38 0.024
1059
URT004 Urethral Syndrome 38 0.024
1060
CHL070 Cholesterol Embolism 37 0.024
1061
OCH001 Ochronosis 37 0.024
1062
P SLP003 Salpingitis 37 0.024
1063
WST002 Western Equine Encephalitis 37 0.024
1064
BLR004 Biliary Dyskinesia 37 0.024
1065
HPT082 Hepatic Adenomas, Familial 37 0.024
1066
PHM001 Phimosis 37 0.024
1067
TNN002 Tinea Unguium 36 0.024
1069
LYM010 Lymph Node Tuberculosis 36 0.024
1070
SPN354 Spinal Arachnoiditis 36 0.024
1071
c ELL005 Elliptocytosis 2 36 0.024
1072
RHM008 Rheumatic Myocarditis 36 0.024
1073
RHN002 Rhinoscleroma 36 0.024
1074
ACL001 Acalculous Cholecystitis 35 0.024
1075
PLN001 Plantar Wart 35 0.024
1076
P DCR004 Dacryocystitis 35 0.024
1077
MLG141 Malignant Atrophic Papulosis 35 0.024
1078
PCT001 Pectus Carinatum 35 0.024
1079
LNR004 Linear Porokeratosis 35 0.024
1080
STL001 St. Louis Encephalitis 35 0.024
1081
OVL001 Ovalocytosis, Southeast Asian 35 0.024
1082
ATY012 Atypical Mycobacteriosis, Familial 34 0.024
1083
NND010 Nondisjunction 34 0.024
1084
PPC001 Pepck 1 Deficiency 34 0.024
1085
c NLD006 Nail Disorder, Nonsyndromic Congenital, 9 34 0.024