Search results for Carbonic acid

2340 hits were found for Carbonic acid

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.460
2
P LVR013 Liver Disease 68 0.370
3
LVR012 Liver Cirrhosis 62 0.359
4
P KDN018 Kidney Disease 72 0.354
5
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.328
6
FTT001 Fatty Liver Disease 61 0.312
7
MTB004 Metabolic Acidosis 50 0.308
8
P CLR023 Colorectal Cancer 99 0.290
9
HLX001 Helix Syndrome 47 0.286
10
P ENC018 Encephalopathy 61 0.281
11
c CHR684 Chronic Kidney Disease 70 0.271
12
HYP266 Hypoxia 57 0.258
13
CHL068 Cholestasis 61 0.256
14
48X005 48,xyyy 39 0.255
15
P NRB001 Neuroblastoma 72 0.255
16
NRL016 Neural Tube Defects 82 0.253
17
BNR002 Bone Resorption Disease 48 0.253
18
ISC004 Ischemia 58 0.250
19
HRW001 Hair Whorl 36 0.247
20
P SZR006 Seizure Disorder 56 0.245
21
OCL069 Ocular Motor Apraxia 51 0.239
22
VSL002 Visual Epilepsy 59 0.239
23
c NRF023 Neurofibromatosis, Type Ii 80 0.238
24
P BRS047 Breast Cancer 97 0.235
25
P HPT023 Hepatocellular Carcinoma 100 0.234
26
P GLM045 Glioma 63 0.229
27
P DRR001 Diarrhea 55 0.228
28
GLL048 Glial Tumor 45 0.226
29
HYP014 Hyperuricemia 52 0.224
30
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.224
31
GLB015 Glioblastoma Multiforme 75 0.223
32
P DDN001 Duodenal Ulcer 52 0.221
33
P PRS040 Prostate Cancer 97 0.220
34
P RSP003 Respiratory Failure 74 0.220
35
LNG099 Lung Disease 60 0.216
36
P CRN300 Coronary Heart Disease 1 63 0.215
37
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.215
38
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.215
39
OST012 Osteoarthritis 78 0.214
40
ALL026 Allergic Hypersensitivity Disease 62 0.213
41
P VSC007 Vascular Disease 63 0.213
42
P PNC035 Pancreatic Cancer 84 0.212
43
LPD008 Lipid Metabolism Disorder 62 0.211
44
ATH013 Atherosclerosis Susceptibility 65 0.210
45
P ADN016 Adenocarcinoma 64 0.209
46
GST092 Gastroesophageal Reflux 67 0.209
47
ACT119 Acute Promyelocytic Leukemia 63 0.209
48
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.205
49
P CRD119 Cardiac Arrest 67 0.203
50
MTH071 Methane Production 26 0.203
51
END086 End Stage Renal Disease 51 0.202
52
CLT003 Colitis 62 0.201
53
P LNG032 Lung Cancer 98 0.198
54
P BPL003 Bipolar Disorder 56 0.198
55
HYP066 Hyperglycemia 61 0.197
56
HYP056 Hypoglycemia 66 0.196
57
c GLL024 Gallbladder Disease 1 53 0.196
58
P OST002 Osteoporosis 74 0.194
59
c MJR024 Major Affective Disorder 9 41 0.194
60
c MJR022 Major Affective Disorder 8 38 0.194
61
47X002 47,xyy 49 0.194
62
LPP008 Lipoprotein Quantitative Trait Locus 62 0.190
63
HYP025 Hyperphosphatemia 48 0.190
64
GT001 Gout 64 0.189
65
PPL052 Papillomatosis, Confluent and Reticulated 33 0.187
66
ADN018 Adenoma 59 0.187
67
DFC004 Deficiency Anemia 70 0.187
68
P PRM006 Primary Biliary Cirrhosis 62 0.185
69
ATM095 Autoimmune Disease 62 0.185
70
ANX004 Anoxia 40 0.184
71
DPR016 Depression 63 0.184
72
P INF037 Inflammatory Bowel Disease 54 0.183
73
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.182
74
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.182
75
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.181
76
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.181
77
P BND020 Bone Disease 59 0.181
78
DRM006 Dermatitis 61 0.180
79
c PRC016 Pre-Eclampsia 63 0.179
80
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.179
81
P PSR002 Psoriasis 62 0.179
82
P HRT032 Heart Disease 75 0.179
83
P NRP001 Neuropathy 56 0.179
84
ULC004 Ulcerative Colitis 73 0.178
85
PPT005 Peptic Ulcer Disease 59 0.178
86
ART140 Arteries, Anomalies of 52 0.178
87
P LKM002 Leukemia 68 0.177
88
OST159 Osteogenic Sarcoma 66 0.177
89
PST011 Pustulosis of Palm and Sole 52 0.177
90
P NTR004 Neutropenia 63 0.177
91
CNG034 Congestive Heart Failure 69 0.175
92
CYS001 Cystic Fibrosis 81 0.175
93
c ACT071 Acute Kidney Failure 60 0.175
94
PRT037 Pertussis 65 0.173
95
CYT002 Cytokine Deficiency 42 0.173
96
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.173
97
P MYC007 Myocardial Infarction 70 0.172
98
P ALZ034 Alzheimer Disease 88 0.170
99
c HYP836 Hypercholesterolemia, Familial, 1 73 0.170
100
c DWL002 Dowling-Degos Disease 1 58 0.169
101
IRN002 Iron Metabolism Disease 57 0.169
102
P OVR042 Ovarian Cancer 88 0.168
103
P GST044 Gastritis 56 0.168
104
CRB039 Cerebrovascular Disease 67 0.166
105
RCK004 Rickets 68 0.166
106
MNT002 Mental Depression 58 0.166
107
P HYP750 Hypertriglyceridemia, Familial 62 0.165
108
P BLD134 Bladder Cancer 79 0.165
109
BRN071 Brain Injury 49 0.164
110
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.163
111
HPT004 Hepatic Coma 45 0.163
112
GST023 Gastric Ulcer 53 0.163
113
HMN044 Human Immunodeficiency Virus Type 1 71 0.162
114
P HYP086 Hypothyroidism 69 0.162
115
URT049 Urate Oxidase, Pseudogene 25 0.161
116
SQM006 Squamous Cell Carcinoma 60 0.161
117
P GST053 Gastric Cancer 83 0.160
118
c HYP595 Hypertension, Essential 84 0.160
119
P PLM036 Pulmonary Fibrosis 65 0.159
120
PLM001 Pulmonary Tuberculosis 69 0.159
121
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.159
122
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.159
123
TXC005 Toxic Shock Syndrome 62 0.158
124
P HYP069 Hyperparathyroidism 63 0.158
125
HMC014 Homocysteinemia 53 0.157
126
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.157
127
NNL006 Non-Alcoholic Steatohepatitis 54 0.157
128
PLM010 Pulmonary Edema 54 0.157
129
P CRD246 Cardiovascular System Disease 57 0.156
130
P MYL006 Myeloid Leukemia 60 0.156
131
HYP060 Hyperinsulinism 54 0.156
132
P TRN020 Turner Syndrome 67 0.156
133
THY029 Thyroid Carcinoma 59 0.155
134
CRV035 Cervical Cancer 76 0.154
135
P DBT009 Diabetes Mellitus 64 0.153
136
CHL014 Cholera 59 0.152
137
P HNT016 Huntington Disease 72 0.152
138
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.152
139
ALC007 Alcohol Dependence 66 0.151
140
STR067 Stroke, Ischemic 81 0.149
141
BCT022 Bacterial Infectious Disease 56 0.149
142
HPT019 Hepatic Encephalopathy 60 0.149
143
SPN186 Spinal Cord Injury 60 0.149
144
CMP034 Complete Androgen Insensitivity Syndrome 46 0.149
145
PLM033 Pulmonary Embolism 59 0.148
146
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.148
147
P LTR001 Lateral Sclerosis 54 0.147
148
c PCH010 Pachyonychia Congenita 3 44 0.146
149
MYL069 Myeloma, Multiple 85 0.145
150
P PRD008 Periodontitis 64 0.145
151
c ACT075 Acute Myocardial Infarction 57 0.144
152
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.144
153
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.144
154
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.144
155
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.144
156
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.144
157
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.144
158
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.144
159
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.144
160
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.144
161
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.144
162
P BNG032 Benign Mesothelioma 46 0.144
163
TRM010 Traumatic Brain Injury 51 0.143
164
STT001 Status Epilepticus 60 0.143
165
P ESP024 Esophagitis 62 0.143
166
c LKM061 Leukemia, Acute Myeloid 84 0.142
167
c MGR028 Migraine with or Without Aura 1 67 0.141
168
NPH009 Nephrolithiasis 55 0.141
169
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.141
170
c SML038 Small Cell Cancer of the Lung 65 0.141
171
NTR005 Nutritional Deficiency Disease 62 0.141
172
PRT036 Peritonitis 64 0.141
173
P CHL066 Cholangitis 51 0.140
174
ANX010 Anxiety 73 0.140
175
P HDC001 Headache 57 0.140
176
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.140
177
P PLM037 Pulmonary Hypertension 67 0.139
178
URM002 Uremia 49 0.139
179
DNT012 Dental Caries 53 0.139
180
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.138
181
ADL002 Adult Syndrome 70 0.138
182
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.138
183
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.137
184
P PRP019 Peripheral Nervous System Disease 58 0.137
185
P HYP076 Hyperthyroidism 55 0.137
186
SKN016 Skin Disease 63 0.137
187
BRN024 Bronchitis 68 0.137
188
P HRP006 Herpes Simplex 65 0.137
189
P MLN008 Melanoma 69 0.136
190
AGN016 Aging 56 0.136
191
P ATS364 Autism 70 0.136
192
DWN001 Down Syndrome 70 0.136
193
c RHB024 Rhabdomyosarcoma 2 67 0.135
194
P RNL007 Renal Tubular Acidosis 51 0.135
195
P RHN004 Rhinitis 57 0.135
196
HMP009 Haemophilus Influenzae 43 0.134
197
c MCR120 Microvascular Complications of Diabetes 7 47 0.134
198
P MYP004 Myopathy 70 0.134
199
c MCR113 Microvascular Complications of Diabetes 3 52 0.134
200
CRH001 Crohn's Disease 74 0.134
201
URL001 Urolithiasis 45 0.133
202
P PNC025 Panic Disorder 53 0.133
203
c MCR130 Microvascular Complications of Diabetes 6 41 0.133
204
c MCR133 Microvascular Complications of Diabetes 4 41 0.133
205
CNS004 Constipation 58 0.133
206
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.132
207
ESP021 Esophageal Cancer 90 0.132
208
MDD011 Mood Disorder 62 0.132
209
HYP005 Hypokalemia 55 0.132
210
P LCT001 Lactic Acidosis 51 0.131
211
P TRM003 Tremor 54 0.130
212
c HPT073 Hepatitis C Virus 72 0.130
213
P MJR001 Major Depressive Disorder 68 0.130
214
P LNG064 Lung Cancer Susceptibility 3 78 0.130
215
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.130
216
MCS002 Mucositis 56 0.129
217
P CTR002 Cataract 60 0.129
218
PPL022 Papilloma 54 0.129
219
P ART021 Arteriosclerosis 54 0.128
220
P PHC003 Pheochromocytoma 71 0.128
221
ANG054 Angina Pectoris 66 0.128
222
ADR040 Adrenal Gland Pheochromocytoma 46 0.128
223
P RCT021 Rectum Cancer 52 0.127
224
EMB004 Embryonal Carcinoma 56 0.127
225
P SKN015 Skin Carcinoma 66 0.127
226
P ART022 Arthritis 69 0.127
227
P DRM053 Dermatitis, Atopic 66 0.127
228
ATX019 Ataxia with Vitamin E Deficiency 42 0.127
229
P OVR082 Overgrowth Syndrome 50 0.126
230
P PLY019 Polyneuropathy 56 0.126
231
INS024 Insulin-Like Growth Factor I 79 0.126
232
P PNC044 Pancreatitis 61 0.126
233
KRT009 Keratosis 51 0.126
234
P BCL017 B-Cell Lymphoma 58 0.126
235
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.126
236
STM007 Stomatitis 50 0.125
237
HYP781 Hypoascorbemia 51 0.125
238
c ATS007 Autism Spectrum Disorder 67 0.125
239
c ACT027 Acute Pancreatitis 60 0.124
240
GLC003 Glucose Intolerance 54 0.124
241
OST003 Osteonecrosis 61 0.124
242
THR024 Thrombosis 57 0.123
243
VTM002 Vitamin B12 Deficiency 48 0.123
244
BRR014 Barrett Esophagus 65 0.123
245
P SCH015 Schizophrenia 74 0.123
246
P PNM007 Pneumonia 68 0.123
247
P AST007 Astrocytoma 51 0.123
248
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.123
249
CRV045 Cervical Intraepithelial Neoplasia 39 0.123
250
P SLP006 Sleep Apnea 69 0.122
251
PNG002 Pain Agnosia 51 0.122
252
P MSC005 Muscular Dystrophy 66 0.122
253
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.121
254
c FNC043 Fanconi Anemia, Complementation Group E 62 0.121
255
P MCR115 Microvascular Complications of Diabetes 5 66 0.120
256
c ACT134 Acute Liver Failure 56 0.120
257
P THR014 Thrombocytopenia 67 0.120
258
P LYM118 Lymphoma 68 0.119
259
SRC014 Sarcoma 65 0.119
260
ALL003 Allergic Rhinitis 67 0.119
261
P FBR017 Fibrosarcoma 56 0.119
262
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.118
263
c MLG068 Malignant Glioma 46 0.118
264
c SYS001 Systemic Lupus Erythematosus 86 0.118
265
AST005 Asthma 76 0.118
266
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.117
267
PHN003 Phenylketonuria 75 0.117
268
HLC007 Helicobacter Pylori Infection 59 0.117
269
SPN035 Spindle Cell Sarcoma 53 0.117
270
RTN023 Retinitis 46 0.116
271
NRR001 Neuroretinitis 42 0.116
272
c SCN007 Secondary Hyperparathyroidism 51 0.116
273
SQM002 Squamous Cell Papilloma 46 0.115
274
P RHM011 Rheumatoid Arthritis 80 0.115
275
P EPL164 Epilepsy 71 0.115
276
P KDN017 Kidney Cancer 60 0.115
277
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.115
278
P RTN008 Retinitis Pigmentosa 79 0.115
279
c ACT068 Acute Cystitis 63 0.115
280
CRB004 Cerebral Artery Occlusion 45 0.115
281
P ENC004 Encephalitis 61 0.115
282
P SPP010 Suppressor of Tumorigenicity 3 51 0.114
283
P INS002 in Situ Carcinoma 53 0.114
284
c DBT099 Diabetes Mellitus, Type I 65 0.114
285
PRT013 Portal Hypertension 59 0.114
286
c THR092 Thrombophilia Due to Thrombin Defect 73 0.113
287
P BRS044 Breast Adenocarcinoma 59 0.113
288
CNT047 Contact Dermatitis 58 0.112
289
P CNR004 Cone-Rod Dystrophy 2 73 0.112
290
P MJR007 Major Affective Disorder 1 43 0.112
291
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.111
292
SVR004 Severe Combined Immunodeficiency 73 0.111
293
ORL011 Oral Cancer 60 0.111
294
P ADL010 Adult Respiratory Distress Syndrome 65 0.111
295
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.111
296
IMM167 Immune Deficiency Disease 78 0.110
297
P END044 Endometriosis 63 0.110
298
P INF032 Infertility 57 0.110
299
P DMN002 Dementia 66 0.110
300
c INH020 Inherited Metabolic Disorder 47 0.109
301
VCC001 Vaccinia 49 0.109
302
P RTN024 Retinoblastoma 73 0.109
303
c FML008 Familial Retinoblastoma 53 0.109
304
TTN003 Tetanus 65 0.109
305
DYS073 Dysphagia 50 0.109
306
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.108
307
ADR007 Adrenoleukodystrophy 75 0.108
308
P ECL001 Eclampsia 50 0.108
309
CLN015 Colon Adenocarcinoma 65 0.108
310
GST045 Gastroenteritis 59 0.108
311
CHL079 Children's Interstitial Lung Disease 26 0.108
312
P LPS004 Lupus Erythematosus 61 0.108
313
ALL014 Allergic Encephalomyelitis 38 0.108
314
P HPT021 Hepatitis 67 0.108
315
PPT001 Peptic Esophagitis 52 0.108
316
ORL015 Oral Squamous Cell Carcinoma 43 0.108
317
CHL123 Chlamydia 59 0.108
318
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.107
319
c ATR087 Atrial Standstill 1 75 0.107
320
P MLT020 Multiple Sclerosis 72 0.107
321
P MNN013 Meningitis 66 0.107
322
BLR008 Bilirubin Metabolic Disorder 57 0.107
323
P NSP012 Nasopharyngeal Carcinoma 66 0.106
324
LSH001 Leishmaniasis 63 0.106
325
P KLZ004 Kala-Azar 1 41 0.106
326
P OPN001 Open-Angle Glaucoma 49 0.106
327
AMN003 Amnestic Disorder 54 0.105
328
P ANP001 Anaplastic Large Cell Lymphoma 58 0.105
329
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.105
330
P ALP008 Alopecia 54 0.105
331
CHR073 Choreatic Disease 52 0.104
332
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.104
333
PRP027 Peripheral Vascular Disease 71 0.104
334
ACQ007 Acquired Immunodeficiency Syndrome 60 0.104
335
CRD132 Cardiac Conduction Defect 58 0.104
336
c PRS136 Prostate Cancer, Hereditary, 6 33 0.104
337
c PRS130 Prostate Cancer, Hereditary, 8 32 0.104
338
BRN028 Brain Cancer 74 0.104
339
CHL004 Cholelithiasis 49 0.104
340
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.104
341
GTR002 Goiter 53 0.103
342
P MSC003 Muscular Atrophy 52 0.103
343
c VRL010 Viral Hepatitis 52 0.103
344
P MPL001 Maple Syrup Urine Disease 69 0.103
345
P LKM062 Leukemia, Acute Lymphoblastic 69 0.103
346
c MJR003 Major Affective Disorder 6 33 0.103
347
c MJR006 Major Affective Disorder 5 33 0.103
348
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.103
349
END040 Endogenous Depression 55 0.103
350
c MJR008 Major Affective Disorder 2 35 0.103
351
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.103
352
CLF027 Cleft Palate, Isolated 64 0.102
353
c MJR023 Major Affective Disorder 7 33 0.102
354
c MJR004 Major Affective Disorder 4 28 0.102
355
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.102
356
P ALC033 Alcohol Use Disorder 58 0.102
358
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.102
359
BRN004 Brain Edema 56 0.102
360
ADR022 Adrenomyeloneuropathy 38 0.102
361
P ATR011 Atrial Fibrillation 66 0.101
362
P HYP098 Hypereosinophilic Syndrome 67 0.101
363
c ACT073 Acute Leukemia 58 0.101
364
c HPT001 Hepatitis C 62 0.101
365
GST050 Gastrointestinal System Disease 56 0.101
366
ATS010 Autosomal Recessive Disease 48 0.101
367
c BSL007 Basal Cell Carcinoma 68 0.100
368
P SCK005 Sickle Cell Disease 50 0.100
369
P CND004 Candidiasis 58 0.100
370
HNS001 Hansen's Disease 34 0.100
371
P LPR021 Leprosy 3 69 0.100
372
P CYS018 Cystitis 59 0.099
373
HND015 Hand Skill, Relative 33 0.099
374
MLR004 Malaria 81 0.099
375
c SCL052 Scleroderma, Familial Progressive 61 0.099
376
MYL009 Myelodysplastic Syndrome 70 0.099
377
RSC001 Rosacea 54 0.099
378
PRS045 Prostatic Hypertrophy 53 0.099
379
c SVR001 Severe Acute Respiratory Syndrome 62 0.098
380
P PRP029 Porphyria 62 0.098
381
P GLM007 Glomerulonephritis 57 0.098
382
ENT004 Enthesopathy 49 0.098
383
P EXN002 Exanthem 57 0.097
384
PLM031 Poliomyelitis 64 0.097
385
P INF038 Influenza 68 0.097
386
KRT002 Keratomalacia 47 0.097
387
TRT001 Teratocarcinoma 45 0.096
388
PST092 Posttransplant Acute Limbic Encephalitis 29 0.096
389
TLN003 Telangiectasis 52 0.095
390
GST033 Gestational Diabetes 61 0.095
391
AVN001 Avian Influenza 59 0.095
392
P GLM040 Glioma Susceptibility 1 81 0.095
393
EYD002 Eye Disease 58 0.095
394
CHG001 Chagas Disease 66 0.095
395
OCL006 Ocular Hypertension 53 0.094
396
SFT003 Soft Tissue Sarcoma 56 0.094
397
P GLY013 Glycogen Storage Disease 60 0.094
398
PLY150 Polykaryocytosis Inducer 31 0.094
399
P OBS001 Obstructive Jaundice 50 0.094
400
P PRK057 Parkinson Disease, Late-Onset 78 0.093
401
P SCL009 Sclerosing Cholangitis 48 0.093
402
HMS001 Hemosiderosis 54 0.093
403
c GRV008 Graves Disease 1 56 0.093
404
P CHR345 Chronic Pain 44 0.093
405
P PLY011 Polycystic Ovary Syndrome 56 0.093
406
LPT014 Leptin Deficiency or Dysfunction 74 0.092
407
DPH001 Diphtheria 60 0.092
408
P OST001 Osteopetrosis 70 0.092
409
P HYD006 Hydrocephalus 66 0.092
410
P PYL005 Pyelonephritis 56 0.092
411
P HML002 Hemolytic Anemia 63 0.092
412
CLR030 Clear Cell Renal Cell Carcinoma 53 0.092
413
P ART023 Arthropathy 62 0.092
414
P SYS005 Systemic Scleroderma 68 0.092
415
INT075 Intracranial Hypertension 53 0.092
416
P TMP001 Temporal Lobe Epilepsy 50 0.092
417
END057 Endometrial Cancer 74 0.091
418
P CHN012 Chondrosarcoma 56 0.091
419
NRT001 Neurotic Disorder 53 0.091
420
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.091
421
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.091
422
CHL065 Cholangiocarcinoma 68 0.091
423
ANR040 Aneurysm 59 0.091
424
PNM008 Pneumothorax 56 0.091
425
CLR108 Colorectal Adenoma 64 0.091
426
P AMY004 Amyloidosis 70 0.090
427
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.090
428
ALL006 Allergic Asthma 56 0.090
429
LYM133 Lymphoma, Hodgkin, Classic 69 0.090
430
LYM019 Lymphosarcoma 46 0.090
431
ADN011 Adenoid Cystic Carcinoma 70 0.090
432
c LKM063 Leukemia, Chronic Myeloid 72 0.090
433
c VSC019 Vesicoureteral Reflux 1 57 0.090
434
CHR072 Chordoma 58 0.090
435
INT079 Intrahepatic Cholangiocarcinoma 51 0.089
436
DBT010 Diabetic Neuropathy 54 0.089
437
c CHL119 Cholangitis, Primary Sclerosing 57 0.089
438
P SRC025 Sarcoidosis 1 70 0.089
439
MNN042 Meningioma, Radiation-Induced 62 0.089
440
PRX001 Peroxisomal Disease 46 0.089
441
ART016 Aortic Aneurysm 69 0.089
442
c MNN043 Meningioma, Familial 74 0.089
443
SYN007 Synovitis 54 0.089
444
PLC002 Plica Syndrome 36 0.089
445
SPN021 Spinal Meningioma 50 0.088
446
SCR001 Secretory Meningioma 41 0.088
447
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.088
448
IRR002 Irritable Bowel Syndrome 65 0.088
449
c HPT016 Hepatitis B 59 0.088
450
P THL005 Thalassemia 60 0.088
451
P RRH023 Rare Hereditary Hemochromatosis 41 0.088
452
PRN011 Pernicious Anemia 53 0.088
453
RNL077 Renal Fibrosis 47 0.088
454
OST115 Osteonecrosis of the Jaw 40 0.088
455
c GLC092 Glaucoma, Primary Open Angle 62 0.088
456
P DYS154 Dystonia 65 0.088
457
CND006 Candida Glabrata 32 0.087
459
PSY004 Psychotic Disorder 67 0.087
460
ILS001 Ileus 51 0.087
461
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.087
462
PRS021 Prostatic Adenoma 51 0.087
463
P NPH012 Nephrotic Syndrome 60 0.087
464
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.086
465
ANT024 Anthrax Disease 58 0.086
466
HDN002 Head Injury 46 0.086
467
LKP003 Leukoplakia 39 0.086
468
ARG004 Argyria 27 0.086
469
NWC001 Newcastle Disease 45 0.086
470
P RTN016 Retinal Degeneration 53 0.086
471
c PNS012 Paine Syndrome 61 0.086
472
IMP005 Impotence 52 0.085
473
P HMN010 Hemangioma 61 0.085
474
MTH009 Mouth Disease 56 0.085
475
SBC016 Subacute Delirium 44 0.085
476
MST005 Mastitis 53 0.085
477
P GRF003 Graft-Versus-Host Disease 72 0.085
478
P NMN002 Niemann-Pick Disease 59 0.085
479
ENT011 Enterocolitis 51 0.085
480
SDD001 Sudden Infant Death Syndrome 61 0.085
481
PNC129 Pancreatic Adenocarcinoma 68 0.085
482
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.084
483
PRS129 Prostatic Hyperplasia, Benign 49 0.084
484
P ACT008 Actinic Keratosis 53 0.084
485
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.084
486
HYP081 Hypolipoproteinemia 51 0.084
487
PRP030 Purpura 54 0.084
488
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.084
489
LNG031 Lung Benign Neoplasm 51 0.084
490
P PLM034 Pulmonary Emphysema 55 0.084
491
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.084
492
INT007 Intermediate Coronary Syndrome 55 0.084
493
c MCR129 Microvascular Complications of Diabetes 1 66 0.084
494
ALL010 Allergic Contact Dermatitis 56 0.083
495
SCK003 Sickle Cell Anemia 74 0.083
496
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.083
497
P MYC084 Mycobacterium Tuberculosis 1 68 0.083
498
LMB062 Limb Ischemia 55 0.083
499
ERY051 Erythroleukemia, Familial 56 0.083
500
ANP008 Anaplastic Oligoastrocytoma 30 0.083
501
P HYP024 Hypoparathyroidism 56 0.083
502
c BRN108 Branchiootic Syndrome 1 62 0.083
503
MSC007 Muscle Hypertrophy 64 0.082
504
P LKM071 Leukemia, Chronic Lymphocytic 79 0.082
505
c HPT003 Hepatitis a 62 0.082
506
P GCH001 Gaucher's Disease 63 0.082
507
GRN017 Granulocytopenia 44 0.082
508
P PLY018 Polycythemia 56 0.082
509
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.082
510
NWB001 Newborn Respiratory Distress Syndrome 58 0.082
511
SCH014 Schistosomiasis 57 0.081
512
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.081
513
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.081
514
TRN018 Transitional Cell Carcinoma 56 0.081
515
P DNG005 Dengue Virus 59 0.081
516
PLS009 Plasma Cell Neoplasm 51 0.081
517
MCL006 Macular Retinal Edema 55 0.081
518
INS001 Insulinoma 60 0.081
519
P GRV001 Graves' Disease 55 0.081
520
P SCL018 Scoliosis 60 0.080
521
CHL067 Cholecystitis 57 0.080
522
CHR100 Chronic Ulcer of Skin 55 0.080
523
VRC005 Varicose Veins 60 0.080
524
RNL011 Renal Osteodystrophy 50 0.080
525
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.080
526
RTN017 Retinal Detachment 61 0.079
527
HYP457 Hypertrophic Scars 42 0.079
528
SPL018 Splenomegaly 48 0.079
529
CYS013 Cystinuria 63 0.079
530
PLG002 Plague 63 0.079
531
MSC157 Muscular Dystrophy, Duchenne Type 72 0.078
532
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.078
533
DYS015 Dysentery 52 0.078
534
P RHB003 Rhabdomyosarcoma 63 0.078
535
TYP007 Typhoid Fever 63 0.078
536
CVD001 Covid-19 44 0.078
537
P MVM001 Movement Disease 63 0.078
538
SYN036 Syncope 45 0.078
539
P URT039 Urticaria 58 0.078
540
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.078
541
P HMC002 Homocystinuria 53 0.078
542
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.078
543
THY030 Thyroid Gland Disease 52 0.078
544
P DBT005 Diabetes Insipidus 55 0.078
545
ZLL002 Zollinger-Ellison Syndrome 55 0.078
546
c SPN225 Spondyloarthropathy 1 73 0.077
547
PHS025 Phosphatase, Acid, of Tissues 28 0.077
548
SLC006 Silicosis 56 0.077
549
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.077
550
INT066 Interstitial Lung Disease 60 0.077
551
OST017 Osteomyelitis 64 0.077
552
c MST023 Mesothelioma, Malignant 57 0.077
553
GNG013 Gingivitis 59 0.077
554
P HYP265 Hypotonia 43 0.076
555
MGL001 Megaloblastic Anemia 51 0.076
556
c DRR009 Diarrhea 6 46 0.076
557
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.076
558
P INT068 Intestinal Disease 53 0.076
559
c CHR682 Chronic Bilirubin Encephalopathy 39 0.076
560
OTT002 Otitis Media 72 0.076
561
MMM001 Mammary Paget's Disease 53 0.076
562
MDD018 Middle East Respiratory Syndrome 43 0.076
563
SKN019 Skin Melanoma 68 0.075
564
TRN015 Transient Cerebral Ischemia 63 0.075
565
CLF001 Cleft Lip 53 0.075
566
GST040 Gastric Adenocarcinoma 70 0.075
567
CHL056 Cheilitis 48 0.075
568
PRP080 Peripheral Artery Disease 53 0.075
569
CRB037 Cerebral Palsy 69 0.075
570
ANT018 Anthracosis 48 0.075
571
P MLN007 Male Infertility 55 0.075
572
IRN001 Iron Deficiency Anemia 59 0.074
573
ANR007 Anorexia Nervosa 63 0.074
574
P ATR005 Atrophic Gastritis 50 0.074
575
CRD223 Cardiac Arrhythmia 60 0.074
576
c PRD040 Periodontitis, Chronic 53 0.074
577
c ATM011 Autoimmune Hepatitis 63 0.074
578
P HYP061 Hypertrophic Cardiomyopathy 70 0.074
579
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.074
580
RYS001 Reye Syndrome 51 0.074
581
CHR074 Choriocarcinoma 47 0.073
582
KLD004 Keloid Disorder 40 0.073
583
PLC008 Placenta Disease 50 0.073
584
ADG002 Audiogenic Seizures 25 0.073
585
DSS009 Disseminated Intravascular Coagulation 57 0.073
586
CLR109 Colorectal Adenocarcinoma 51 0.073
587
P SJG008 Sjogren Syndrome 61 0.073
588
P UVT001 Uveitis 57 0.073
589
c GCH015 Gaucher Disease, Type I 70 0.073
590
INT002 Intermittent Claudication 61 0.073
591
DSS008 Disease of Mental Health 58 0.072
592
TBR011 Tuberculous Meningitis 48 0.072
593
P PNM006 Pneumoconiosis 56 0.072
594
PTH003 Pathologic Nystagmus 52 0.072
595
P END033 Endocarditis 57 0.072
596
CRN030 Coronary Stenosis 50 0.072
597
P MYC008 Myocarditis 59 0.072
598
P SLP005 Sleep Disorder 59 0.072
599
APN008 Apnea, Obstructive Sleep 64 0.072
600
P VSC011 Vasculitis 62 0.071
601
MXD026 Mixed Glioma 45 0.071
602
SPN051 Spondylitis 51 0.071
603
INF009 Inflammatory Spondylopathy 31 0.071
604
BRN056 Bronchopulmonary Dysplasia 57 0.071
605
P CNJ013 Conjunctivitis 65 0.071
606
TBC004 Tobacco Addiction 64 0.071
607
P MYS003 Myasthenia Gravis 68 0.071
608
PRN019 Perinatal Necrotizing Enterocolitis 59 0.071
609
c DLT002 Dilated Cardiomyopathy 79 0.070
610
P MTH008 Methylmalonic Acidemia 50 0.070
611
IGR001 Ige Responsiveness, Atopic 59 0.070
612
c LKM005 Leukemia, T-Cell, Chronic 34 0.070
613
P ATX030 Ataxia-Telangiectasia 82 0.070
614
c CHR064 Chronic Monocytic Leukemia 33 0.070
615
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.070
616
CRB090 Cerebral Hypoxia 44 0.070
617
RTN020 Retinal Vascular Disease 46 0.070
618
P THY032 Thyroiditis 52 0.070
619
P MDL005 Medulloblastoma 77 0.070
620
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.070
621
P RTN018 Retinal Disease 53 0.070
622
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.070
623
HRT011 Heart Septal Defect 50 0.069
624
OVR094 Ovarian Epithelial Cancer 38 0.069
625
P BRB001 Beriberi 46 0.069
626
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.069
627
P FBR031 Febrile Seizures 53 0.069
628
c PRM038 Primary Agammaglobulinemia 44 0.069
629
49X006 49, Xxxxy Syndrome 41 0.069
630
AMN006 Aminoaciduria 38 0.069
631
LYS002 Lysosomal Storage Disease 52 0.069
632
FDL002 Food Allergy 51 0.069
633
BRK010 Burkitt Lymphoma 67 0.068
634
ACT058 Active Peptic Ulcer Disease 55 0.068
635
NRM005 Neuromuscular Disease 64 0.068
636
P TBR001 Tuberous Sclerosis 70 0.068
637
P PLY014 Polycystic Kidney Disease 62 0.068
638
LNT004 Lentigines 50 0.068
639
XNT003 Xanthomatosis 49 0.068
640
HRY003 Hairy Cell Leukemia 55 0.068
641
c MCR112 Microvascular Complications of Diabetes 2 41 0.067
642
ANN002 Anencephaly 56 0.067
643
P SNS001 Sensorineural Hearing Loss 60 0.067
644
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.067
645
P ALP009 Alopecia Areata 60 0.067
646
P MYC033 Myoclonus 46 0.067
647
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.067
648
TRD006 Tardive Dyskinesia 54 0.067
650
KPS004 Kaposi Sarcoma 75 0.067
651
P CLC063 Celiac Disease 1 66 0.067
652
NRN004 Neuroendocrine Tumor 55 0.067
653
ACT084 Acute Stress Disorder 47 0.067
654
HYP017 Hypophosphatemia 50 0.067
655
KRT013 Keratolytic Winter Erythema 46 0.067
656
c EXD008 Exudative Vitreoretinopathy 1 71 0.067
657
STN013 Stenotrophomonas Maltophilia Infection 25 0.067
658
P NRV007 Nervous System Disease 66 0.066
659
PPL001 Papillary Adenoma 44 0.066
660
CHD004 Chudley-Mccullough Syndrome 46 0.066
661
P BNC003 Bone Cancer 58 0.066
662
VSC002 Vascular Dementia 57 0.066
663
PST028 Post-Traumatic Stress Disorder 58 0.066
664
CNN005 Connective Tissue Disease 68 0.066
665
P SPN046 Spinal Muscular Atrophy 62 0.066
666
P FML011 Familial Adenomatous Polyposis 72 0.066
667
P HMP007 Hemophilia 51 0.066
668
c OST163 Osteopetrosis, Autosomal Recessive 3 55 0.066
669
CRB011 Cerebrotendinous Xanthomatosis 65 0.066
670
BRN002 Bronchiolitis 59 0.065
671
KRT019 Keratitis, Hereditary 65 0.065
672
VRL011 Viral Infectious Disease 61 0.065
673
P OPT006 Optic Nerve Disease 60 0.065
674
CMM005 Common Cold 57 0.065
675
LMY002 Leiomyoma 52 0.065
676
LYM027 Lymphopenia 58 0.065
677
SPP011 Suppression of Tumorigenicity 12 59 0.065
678
P PRS038 Personality Disorder 65 0.065
679
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.065
680
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.065
681
P APL001 Aplastic Anemia 74 0.065
682
P OLG002 Oligodendroglioma 67 0.065
683
BTN004 Biotin Deficiency 38 0.065
684
P PRN023 Prion Disease 57 0.065
685
P CTN015 Cutaneous T Cell Lymphoma 49 0.065
686
MYL020 Myelomeningocele 51 0.064
687
ORL012 Oral Leukoplakia 39 0.064
688
P MTR014 Motor Neuron Disease 65 0.064
689
P DST107 Distal Renal Tubular Acidosis 42 0.064
690
URT010 Ureteral Obstruction 45 0.064
691
ACD003 Acid Sphingomyelinase Deficiency 32 0.064
692
P TYR004 Tyrosinemia 58 0.064
693
CTN007 Cutaneous Leishmaniasis 62 0.064
694
ANR004 Anuria 46 0.064
695
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.064
696
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.064
697
c BCT007 Bacterial Meningitis 55 0.064
698
c PRM005 Primary Hyperparathyroidism 58 0.063
699
c ACT135 Acute Graft Versus Host Disease 52 0.063
700
P INT143 Interstitial Cystitis 61 0.063
701
TXC002 Toxic Encephalopathy 53 0.063
702
c RNG015 Ring Chromosome 2 26 0.063
703
DMY004 Demyelinating Disease 52 0.063
704
P SHR001 Short Bowel Syndrome 53 0.063
705
KHL003 Kohlschutter-Tonz Syndrome 65 0.063
706
c NMN013 Niemann-Pick Disease, Type a 62 0.063
707
P LCH002 Lichen Planus 53 0.063
708
PRP001 Propionic Acidemia 65 0.063
709
HYD002 Hydronephrosis 60 0.062
710
P VNT002 Ventricular Septal Defect 60 0.062
711
RDN001 Reading Disorder 40 0.062
712
THY122 Thyroid Gland Cancer 57 0.062
713
P MNC007 Monocytic Leukemia 53 0.062
714
YLL002 Yellow Fever 61 0.062
715
c FML035 Familial Hyperlipidemia 55 0.061
716
PRT038 Protein-Energy Malnutrition 54 0.061
717
ING001 Inguinal Hernia 60 0.061
718
P FNC004 Fanconi Syndrome 50 0.061
719
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.061
720
ACT003 Acute Kidney Tubular Necrosis 45 0.061
721
OBS002 Obsessive-Compulsive Disorder 68 0.061
722
WLL004 Wallerian Degeneration 39 0.061
723
c FML021 Familial Hypercholesterolemia 66 0.061
724
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.061
725
PTT037 Pituitary Tumors 44 0.061
726
CRD137 Cardiogenic Shock 47 0.061
727
MYC006 Mycosis Fungoides 66 0.061
728
TRG002 Trigeminal Neuralgia 60 0.061
729
WTH001 Withdrawal Disorder 48 0.061
730
OST011 Osteomalacia 52 0.061
731
DMP001 Dumping Syndrome 44 0.061
732
P MLG074 Malignant Mesenchymoma 40 0.061
733
BRC012 Brucellosis 64 0.060
734
SCH003 Schizophreniform Disorder 56 0.060
735
CRH005 Crohn's Colitis 53 0.060
736
EXN003 Exencephaly 31 0.060
737
P FNC034 Fanconi Renotubular Syndrome 2 40 0.060
738
NTR046 Neutrophil Migration 50 0.060
739
P BRN022 Bronchiectasis 59 0.060
740
BCK006 Back Pain 42 0.060
741
P HYP726 Hypercalcemia, Infantile, 1 58 0.060
742
c WLM018 Wilms Tumor 5 61 0.060
743
ACN002 Acanthosis Nigricans 60 0.059
744
P TRT010 Teratoma 52 0.059
745
SCH012 Schizoaffective Disorder 50 0.059
746
SCR011 Scrapie 39 0.059
747
PRP016 Paraplegia 52 0.059
748
P MYP006 Myopia 55 0.059
749
P PMP001 Pemphigus 54 0.059
750
CRT015 Carotid Artery Occlusion 45 0.059
751
GNG003 Gingival Recession 44 0.059
752
HRN026 Hernia, Hiatus 47 0.059
753
ETN001 Eating Disorder 60 0.059
754
P MTC069 Mitochondrial Disorders 56 0.059
755
HRN029 Hearing Loss, Noise-Induced 37 0.059
756
CYN002 Cyanosis, Transient Neonatal 45 0.059
757
CHC001 Chickenpox 60 0.059
758
PST021 Postpartum Depression 50 0.059
759
RSP007 Respiratory Distress Syndrome, Infant 30 0.059
760
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.059
761
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.058
762
ENM002 Enamel Erosion 26 0.058
763
P FLL037 Follicular Lymphoma 67 0.058
764
GLS001 Gliosarcoma 54 0.058
765
BRT054 Brittle Bone Disorder 72 0.058
766
c JVN010 Juvenile Rheumatoid Arthritis 64 0.058
767
HPT022 Hepatoblastoma 56 0.058
768
BWN006 Bowen's Disease 32 0.058
769
WST005 West Nile Virus 54 0.058
770
HDR003 Hidradenitis 49 0.058
771
ATR057 Atrioventricular Block 55 0.058
772
VGN023 Vaginitis 54 0.057
773
c BTT014 Beta-Thalassemia 74 0.057
774
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.057
775
P PRC031 Preeclampsia/eclampsia 1 38 0.057
776
GRD007 Grade Iii Astrocytoma 59 0.057
777
P THY023 Thymoma 65 0.057
778
c THY107 Thymoma, Familial 52 0.057
779
CHP002 Chops Syndrome 44 0.057
780
c INF145 Infantile Liver Failure Syndrome 1 50 0.057
781
PRS047 Prostatitis 56 0.057
782
CYN003 Cyanide Poisoning 24 0.057
783
DFF005 Diffuse Large B-Cell Lymphoma 55 0.057
784
LYM040 Lymphoblastic Lymphoma 54 0.057
785
NRT004 Neuritis 52 0.057
786
GLS018 Glass Syndrome 57 0.057
787
DWR001 Dwarfism 44 0.057
788
P ACT105 Acute Mountain Sickness 52 0.056
789
MCR013 Microphthalmia 57 0.056
790
CHR178 Chromosomal Triplication 35 0.056
791
CRB155 Carbonic Anhydrase Va Deficiency 20 0.056
792
GSG001 Gas Gangrene 53 0.056
793
ISL099 Isolated Methylmalonic Acidemia 29 0.056
794
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.056
795
PLR007 Pleural Empyema 50 0.056
796
HDR002 Hidradenitis Suppurativa 55 0.056
797
PLS011 Plasmacytoma 56 0.056
798
PSR001 Psoriatic Arthritis 61 0.056
799
ASP007 Aspiration Pneumonia 48 0.056
800
P TXP001 Toxoplasmosis 60 0.056
801
HMG005 Hemoglobinopathy 56 0.056
802
c BPL002 Bipolar I Disorder 49 0.056
803
PRP083 Porphyria, Acute Intermittent 64 0.056
804
P HYP733 Hypercalciuria, Absorptive, 2 45 0.056
805
PPL049 Papillon-Lefevre Syndrome 65 0.056
806
P LRY044 Larynx Cancer 55 0.056
807
APR001 Apraxia 52 0.056
808
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.056
809
RBS001 Rabies 58 0.055
810
c SVR005 Severe Pre-Eclampsia 50 0.055
811
MLK006 Milk Allergy 48 0.055
812
CRB086 Cerebral Aneurysms 40 0.055
813
IDP070 Idiopathic Scoliosis 42 0.055
814
P TCD001 Tic Disorder 53 0.055
815
VSC003 Visceral Leishmaniasis 55 0.055
816
DRY001 Dry Eye Syndrome 47 0.055
817
MCR011 Microinvasive Gastric Cancer 43 0.054
818
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.054
819
FCL014 Focal Epilepsy 54 0.054
820
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.054
821
SPS057 Spasticity 45 0.054
822
ATN004 Autonomic Neuropathy 45 0.054
823
P MYS005 Myositis 56 0.054
824
ATN005 Autonomic Dysfunction 46 0.054
825
PYR009 Pyridoxine Deficiency Anemia 34 0.054
826
P CMP008 Compartment Syndrome 49 0.054
827
P MTH007 Methemoglobinemia 46 0.054
828
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.054
829
P LKD001 Leukodystrophy 59 0.054
830
JPN002 Japanese Encephalitis 57 0.054
831
SPR126 Superior Semicircular Canal Dehiscence 40 0.054
832
c HMG029 Hemoglobin Se Disease 39 0.054
833
MNT001 Mantle Cell Lymphoma 69 0.054
834
MNN009 Meningoencephalitis 49 0.054
835
MLT157 Multiple System Atrophy 1 70 0.054
836
P OCL013 Oculodentodigital Dysplasia 69 0.054
837
RST023 Resting Heart Rate, Variation in 41 0.054
838
P PRC012 Pericardial Effusion 51 0.054
839
HMP001 Hemopericardium 48 0.054
840
P MYT002 Myotonic Dystrophy 49 0.053
841
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.053
842
GLB001 Gilbert Syndrome 58 0.053
843
HPT014 Hepatorenal Syndrome 50 0.053
844
MTS001 Mutism 46 0.053
845
P ICH004 Ichthyosis 54 0.053
846
P MLG056 Malignant Hyperthermia 67 0.053
847
P HMR003 Hemorrhagic Disease 53 0.053
848
P SBS003 Substance Abuse 55 0.053
849
P VSC018 Visceral Steatosis 33 0.053
850
NPH003 Nephrocalcinosis 51 0.053
851
P TRC086 Trichohepatoenteric Syndrome 1 62 0.053
852
HVY002 Heavy Metal Poisoning 22 0.053
853
MLN073 Melanosis, Neurocutaneous 45 0.053
854
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.053
855
ANG005 Anogenital Venereal Wart 55 0.053
856
PRS063 Paresthesia 41 0.053
857
KRT006 Keratoconjunctivitis 53 0.053
858
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.053
859
c MLG079 Malignant Pleural Mesothelioma 42 0.053
860
APP008 Appendicitis 61 0.053
861
c XNT010 Xanthinuria, Type I 53 0.053
862
c PSR017 Psoriasis 2 53 0.052
863
c PSR023 Psoriasis 1 52 0.052
864
c PSR032 Psoriasis 11 47 0.052
865
c PSR028 Psoriasis 7 42 0.052
866
c PSR018 Psoriasis 13 41 0.052
867
RHM001 Rheumatic Fever 60 0.052
868
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.052
869
DRM011 Dermatophytosis 52 0.052
870
P SLM003 Salmonellosis 55 0.052
871
PNC001 Pancytopenia 54 0.052
872
DDN004 Duodenogastric Reflux 33 0.052
873
P MTR003 Mitral Valve Stenosis 50 0.052
874
FNG017 Fungal Infectious Disease 53 0.052
875
PYL006 Pyloric Stenosis 48 0.052
876
MYL005 Myelofibrosis 70 0.052
877
P NRF002 Neurofibromatosis 56 0.052
878
RTN003 Retinal Ischemia 50 0.052
879
CLN045 Colonic Benign Neoplasm 46 0.052
880
CHL045 Choline Deficiency Disease 39 0.052
881
FCT007 Factor Vii Deficiency 67 0.052
882
KRT001 Keratoconjunctivitis Sicca 49 0.052
883
c ACT042 Acute Pyelonephritis 46 0.052
884
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 33 0.052
885
P PRM002 Primary Hyperoxaluria 62 0.052
886
NRF007 Neurofibroma 64 0.052
887
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.052
888
P PLY041 Polymyositis 57 0.051
889
BRN012 Bronchiolitis Obliterans 55 0.051
890
WLS001 Wilson Disease 71 0.051
891
LYS003 Lysinuric Protein Intolerance 57 0.051
892
CLC006 Calcinosis 48 0.051
893
P NRC002 Narcolepsy 52 0.051
894
ACT093 Actinic Cheilitis 40 0.051
895
ESP002 Esophageal Varix 51 0.051
896
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.051
897
c PNC108 Pancreatitis, Hereditary 70 0.051
898
LYM022 Lymphangioma 54 0.051
899
P RRL003 Rare Lymphatic Malformation 31 0.051
900
TRP009 Triple X Syndrome 42 0.051
901
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 68 0.051
902
FBR047 Fibromyalgia 58 0.051
903
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.051
904
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.051
905
BRN032 Brain Glioma 45 0.051
906
BNG077 Benign Idiopathic Neonatal Seizures 26 0.051
907
DCT002 Ductal Carcinoma in Situ 59 0.050
908
INT303 Intracranial Hypertension, Idiopathic 57 0.050
909
P CHR071 Charcot-Marie-Tooth Disease 65 0.050
910
DGN001 Degenerative Disc Disease 48 0.050
911
MLD001 Melioidosis 68 0.050
912
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.050
913
c DPH024 Diaphragmatic Hernia, Congenital 63 0.050
914
P SYP003 Syphilis 58 0.050
915
GST037 Gastroparesis 54 0.050
916
TRY001 Trypanosomiasis 50 0.050
917
ERY003 Erythema Multiforme 58 0.050
918
P CHR285 Chronic Myelomonocytic Leukemia 60 0.050
919
P SBR004 Seborrheic Dermatitis 45 0.050
920
ALC006 Alcoholic Hepatitis 61 0.050
921
THY111 Thyroid Carcinoma, Familial Medullary 67 0.050
922
MCP006 Mucoepidermoid Carcinoma 50 0.050
923
P MCH002 Machado-Joseph Disease 62 0.050
924
RYN005 Raynaud Phenomenon 47 0.050
925
MTH047 Methanol Poisoning 34 0.050
926
c INF071 Inflammatory Bowel Disease 1 67 0.050
927
TNS005 Tonsillitis 57 0.050
928
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.050
929
P MCR010 Microcephaly 59 0.050
930
PLY100 Polyploidy 40 0.049
931
c HMP029 Hemophilia a 67 0.049
932
P PTS002 Ptosis 53 0.049
933
P ADL017 Adult T-Cell Leukemia 56 0.049
934
P ATR010 Atrial Heart Septal Defect 60 0.049
935
P ASP006 Aspergillosis 69 0.049
936
SPN041 Spinal Cord Disease 56 0.049
937
PRD004 Prediabetes Syndrome 47 0.049
938
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.049
939
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.049
940
P CRN037 Craniosynostosis 68 0.049
941
SLP001 Sleeping Sickness 54 0.049
942
DFF036 Differentiated Thyroid Carcinoma 52 0.049
943
PRM020 Premenstrual Tension 40 0.049
944
APH002 Aphasia 57 0.049
945
AZS001 Azoospermia 50 0.049
947
PYR016 Pyridoxine Deficiency 30 0.049
948
c NMN016 Niemann-Pick Disease, Type B 58 0.049
949
AMN001 Amenorrhea 54 0.049
950
HYP080 Hypogonadism 50 0.049
951
LCH016 Lichen Sclerosus Et Atrophicus 41 0.049
952
P DRM010 Dermatomyositis 61 0.049
953
P THR015 Thrombophilia 51 0.048
954
ERL001 Early Myoclonic Encephalopathy 62 0.048
955
c CNT035 Central Nervous System Disease 52 0.048
956
PHR003 Pharyngitis 57 0.048
957
THR013 Thoracic Outlet Syndrome 54 0.048
958
MYM001 Myoma 54 0.048
959
PLY001 Polycythemia Vera 69 0.048
960
MST020 Mast Cell Activation Syndrome 26 0.048
961
CYT008 Cytomegalovirus Infection 57 0.048
962
SVR097 Severe Cutaneous Adverse Reaction 69 0.048
963
P MRC003 Mercury Poisoning 48 0.048
964
SXL003 Sexual Disorder 47 0.048
965
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.048
966
URN010 Urinary Tract Obstruction 55 0.048
967
P CHR012 Chronic Granulomatous Disease 67 0.048
968
c WLM013 Wilms Tumor 1 65 0.048
969
CHK001 Chikungunya 57 0.048
970
P CRB088 Cerebral Atrophy 37 0.048
971
ISV001 Isovaleric Acidemia 55 0.048
972
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.048
973
P INT070 Intestinal Obstruction 58 0.048
974
MYC005 Myocardial Stunning 46 0.048
975
HMP005 Hemiplegia 55 0.047
976
CRT013 Carotid Stenosis 50 0.047
977
ERY066 Erythema Multiforme Major 30 0.047
978
c ATM024 Autoimmune Pancreatitis 55 0.047
979
PCK003 Pick Disease of Brain 68 0.047
980
c MLG084 Malignant Fibrous Histiocytoma 63 0.047
981
MYL031 Myeloproliferative Neoplasm 66 0.047
982
P ANR048 Aniridia 1 63 0.047
983
SPR005 Superficial Basal Cell Carcinoma 46 0.047
984
ILT001 Ileitis 50 0.047
985
P BNG030 Benign Ependymoma 60 0.047
986
PRC003 Proctitis 47 0.047
987
c BNG091 Benign Chronic Pemphigus 58 0.047
988
ECT026 Ectopic Pregnancy 50 0.047
989
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.047
990
c FLL041 Follicular Lymphoma 1 49 0.047
991
TND005 Tendinitis 54 0.047
992
RFR010 Refractory Anemia 48 0.047
993
TRC005 Tracheal Stenosis 38 0.047
994
AVD001 Avoidant Personality Disorder 51 0.047
995
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.047
996
STT002 Status Asthmaticus 50 0.047
997
EXT006 Extrahepatic Cholestasis 39 0.047
998
c NMN015 Niemann-Pick Disease, Type C1 68 0.046
999
c ALP101 Alpha-Thalassemia 62 0.046
1000
BLD131 Bladder Urothelial Carcinoma 62 0.046
1001
DBT006 Diabetic Macular Edema 48 0.046
1002
P GLL020 Gallbladder Disease 57 0.046
1003
CLL010 Cellular Ependymoma 54 0.046
1004
c HMC039 Hemochromatosis, Type 1 74 0.046
1005
TRP004 Tropical Sprue 41 0.046
1006
P FRN006 Frontotemporal Dementia 68 0.046
1007
TST014 Testicular Cancer 46 0.046
1008
BNG036 Bone Giant Cell Tumor 49 0.046
1009
LPT006 Leptin Receptor Deficiency 48 0.046
1010
P AGN002 Agnosia 55 0.046
1011
CHR066 Chronic Fatigue Syndrome 61 0.046
1012
BLC012 Bile Acid Malabsorption, Primary 45 0.046
1013
MCN017 Meconium Ileus 52 0.046
1014
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.046
1015
CLF056 Cleft Lip with or Without Cleft Palate 47 0.046
1016
WST001 West Syndrome 61 0.045
1017
P PRV006 Pervasive Developmental Disorder 57 0.045
1018
P RTT002 Rett Syndrome 80 0.045
1019
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.045
1020
ACR007 Acromegaly 71 0.045
1021
P SML001 Small Cell Carcinoma 52 0.045
1022
c JVN061 Juvenile Arthritis 60 0.045
1023
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.045
1024
P FBR003 Fibrous Histiocytoma 44 0.045
1025
P CLS010 Cluster Headache 42 0.045
1026
SPT004 Septic Arthritis 58 0.045
1027
ORG002 Organic Acidemia 44 0.045
1028
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.045
1029
CNT033 Central Nervous System Cancer 47 0.045
1030
ABD010 Abdominal Wall Defect 36 0.045
1031
SPN050 Spinocerebellar Degeneration 42 0.045
1032
MDS022 Mediastinitis 46 0.045
1033
LST001 Listeriosis 56 0.045
1034
ORT008 Orotic Aciduria 55 0.045
1035
IMP004 Impetigo 49 0.045
1036
INT067 Interstitial Nephritis 48 0.045
1037
PLC007 Placental Abruption 48 0.045
1038
P CLL015 Collagen Disease 47 0.045
1039
ACT228 Acute Radiation Syndrome 29 0.045
1040
AND002 Androgen Insensitivity Syndrome 66 0.045
1041
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 65 0.045
1042
P MST009 Mastocytosis 64 0.045
1043
c DNG003 Dengue Disease 59 0.045
1044
SNS003 Sensory Peripheral Neuropathy 54 0.045
1045
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.045
1046
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.045
1047
c BCT013 Bacterial Pneumonia 48 0.045
1048
CLF004 Cleft Lip/palate 54 0.045
1049
BHR001 Behr Syndrome 51 0.044
1050
INC002 Inclusion Body Myositis 58 0.044
1051
INF034 Infective Endocarditis 53 0.044
1052
TTH006 Tooth Disease 46 0.044
1053
CHL013 Cholecystolithiasis 37 0.044
1054
c PRG106 Progressive Muscular Dystrophy 33 0.044
1055
c LKM070 Leukemia, Acute Monocytic 57 0.044
1056
AMB002 Amblyopia 49 0.044
1057
SPP007 Suppression Amblyopia 39 0.044
1058
PSD088 Pseudobulbar Affect 36 0.044
1059
IRR003 Irritant Dermatitis 49 0.044
1060
P ANG001 Angelman Syndrome 69 0.044
1061
P GLL022 Guillain-Barre Syndrome 59 0.044
1062
HYP043 Hyperandrogenism 48 0.044
1063
CRN017 Coronary Thrombosis 47 0.044
1064
c PLY105 Polycystic Ovary Syndrome 1 38 0.044
1065
ACR006 Aceruloplasminemia 65 0.044
1066
DNT001 Dental Fluorosis 43 0.044
1067
HMG002 Hemoglobinuria 50 0.044
1068
RTC005 Reticulosarcoma 47 0.044
1069
c ACT004 Acute Diarrhea 39 0.044
1070
P LMY004 Leiomyosarcoma 63 0.043
1071
P STR020 Strabismus 55 0.043
1072
MCH006 Mechanical Strabismus 42 0.043
1073
BNN003 Bone Inflammation Disease 48 0.043
1074
ARG002 Argininosuccinic Aciduria 61 0.043
1075
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 58 0.043
1076
P RHZ001 Rhizomelic Chondrodysplasia Punctata 53 0.043
1077
THR004 Thrombocytosis 51 0.043
1078
MYT011