Search results for Aspartic acid

1181 hits were found for Aspartic acid

# Family MCID Name MIFTS Score
1
CTR172 Citrullinemia, Classic 64 3.184
2
P DBT009 Diabetes Mellitus 64 0.529
3
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.485
4
HYP056 Hypoglycemia 66 0.459
5
P ENC004 Encephalitis 61 0.450
6
P LVR013 Liver Disease 68 0.396
7
c DBT099 Diabetes Mellitus, Type I 65 0.388
8
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.373
9
HLX001 Helix Syndrome 47 0.342
10
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.334
11
LVR012 Liver Cirrhosis 62 0.325
12
P SZR006 Seizure Disorder 56 0.325
13
VSL002 Visual Epilepsy 59 0.315
14
FTT001 Fatty Liver Disease 61 0.304
15
P ENC018 Encephalopathy 61 0.297
16
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.280
17
HYP066 Hyperglycemia 61 0.275
18
P NRB001 Neuroblastoma 72 0.263
19
CHL068 Cholestasis 61 0.261
20
48X005 48,xyyy 39 0.258
21
HPT004 Hepatic Coma 45 0.255
22
HPT019 Hepatic Encephalopathy 60 0.246
23
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.244
24
P KDN018 Kidney Disease 72 0.243
25
P CLR023 Colorectal Cancer 99 0.237
26
P TRT010 Teratoma 52 0.229
27
ATM095 Autoimmune Disease 62 0.228
28
ISC004 Ischemia 58 0.225
29
P DRR001 Diarrhea 55 0.223
30
OST012 Osteoarthritis 78 0.222
31
P HNT016 Huntington Disease 72 0.217
32
P GLM045 Glioma 63 0.215
33
P HPT023 Hepatocellular Carcinoma 100 0.214
34
NRL016 Neural Tube Defects 82 0.214
35
LPD008 Lipid Metabolism Disorder 62 0.213
36
DPR016 Depression 63 0.211
37
GLL048 Glial Tumor 45 0.211
38
ALL026 Allergic Hypersensitivity Disease 62 0.211
39
P ALZ034 Alzheimer Disease 88 0.210
40
PRT037 Pertussis 65 0.210
41
HYP014 Hyperuricemia 52 0.210
42
HMN044 Human Immunodeficiency Virus Type 1 71 0.209
43
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.207
44
MTB004 Metabolic Acidosis 50 0.205
45
P BRS047 Breast Cancer 97 0.205
46
MNT002 Mental Depression 58 0.201
47
STT001 Status Epilepticus 60 0.200
48
P BPL003 Bipolar Disorder 56 0.200
49
OCL069 Ocular Motor Apraxia 51 0.200
50
c MJR024 Major Affective Disorder 9 41 0.199
51
c MJR022 Major Affective Disorder 8 38 0.199
52
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.192
53
P CRN300 Coronary Heart Disease 1 63 0.190
54
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.190
55
ATH013 Atherosclerosis Susceptibility 65 0.189
56
P HRP006 Herpes Simplex 65 0.188
57
NNL006 Non-Alcoholic Steatohepatitis 54 0.187
58
ALC007 Alcohol Dependence 66 0.183
59
GST092 Gastroesophageal Reflux 67 0.183
60
BNR002 Bone Resorption Disease 48 0.183
61
GLB015 Glioblastoma Multiforme 75 0.183
62
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.182
63
P MJR001 Major Depressive Disorder 68 0.182
64
P SCH015 Schizophrenia 74 0.181
65
P PNC035 Pancreatic Cancer 84 0.180
66
P LKM002 Leukemia 68 0.180
67
c RHB024 Rhabdomyosarcoma 2 67 0.180
68
P PRD008 Periodontitis 64 0.179
69
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.178
70
P ADN016 Adenocarcinoma 64 0.178
71
CRB004 Cerebral Artery Occlusion 45 0.177
72
BRN071 Brain Injury 49 0.177
73
P PRS040 Prostate Cancer 97 0.177
74
c ATM075 Autoimmune Encephalitis 38 0.176
75
DWN001 Down Syndrome 70 0.175
76
P LTR001 Lateral Sclerosis 54 0.173
77
OVR109 Ovarian Germ Cell Teratoma 32 0.173
78
TRT017 Teratoma, Ovarian 29 0.173
79
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.173
80
c HPT073 Hepatitis C Virus 72 0.172
81
P TRN020 Turner Syndrome 67 0.172
82
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.172
83
P VSC007 Vascular Disease 63 0.171
84
TRM010 Traumatic Brain Injury 51 0.170
85
P PSR002 Psoriasis 62 0.170
86
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.169
87
P PRM006 Primary Biliary Cirrhosis 62 0.169
88
PPT005 Peptic Ulcer Disease 59 0.169
89
CLT003 Colitis 62 0.169
90
PST011 Pustulosis of Palm and Sole 52 0.168
91
c HYP836 Hypercholesterolemia, Familial, 1 73 0.168
92
P ATS364 Autism 70 0.167
93
P INF037 Inflammatory Bowel Disease 54 0.166
94
c CHR684 Chronic Kidney Disease 70 0.166
95
P NRP001 Neuropathy 56 0.166
96
HRW001 Hair Whorl 36 0.165
97
HYP266 Hypoxia 57 0.164
98
SPN186 Spinal Cord Injury 60 0.163
99
HYP060 Hyperinsulinism 54 0.163
100
PNG002 Pain Agnosia 51 0.163
101
DFC004 Deficiency Anemia 70 0.162
102
LPP008 Lipoprotein Quantitative Trait Locus 62 0.162
103
ULC004 Ulcerative Colitis 73 0.162
104
P HYP750 Hypertriglyceridemia, Familial 62 0.160
105
CYS001 Cystic Fibrosis 81 0.160
106
c PRC016 Pre-Eclampsia 63 0.160
107
c ACT075 Acute Myocardial Infarction 57 0.159
108
P MYC007 Myocardial Infarction 70 0.159
109
47X002 47,xyy 49 0.159
110
ANX004 Anoxia 40 0.159
111
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.158
112
TTN003 Tetanus 65 0.158
113
ATX019 Ataxia with Vitamin E Deficiency 42 0.157
114
PPL052 Papillomatosis, Confluent and Reticulated 33 0.157
115
c HYP595 Hypertension, Essential 84 0.157
116
STM007 Stomatitis 50 0.157
117
PLM001 Pulmonary Tuberculosis 69 0.155
118
CYT002 Cytokine Deficiency 42 0.155
119
P HRT032 Heart Disease 75 0.155
120
c HPT001 Hepatitis C 62 0.155
121
P TMP001 Temporal Lobe Epilepsy 50 0.154
122
c GLL024 Gallbladder Disease 1 53 0.154
123
c ATS007 Autism Spectrum Disorder 67 0.154
124
P OVR042 Ovarian Cancer 88 0.153
125
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.152
126
P TRM003 Tremor 54 0.151
127
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.151
128
P MYL006 Myeloid Leukemia 60 0.151
129
MDD011 Mood Disorder 62 0.149
130
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.148
131
IRN002 Iron Metabolism Disease 57 0.148
132
OST159 Osteogenic Sarcoma 66 0.148
133
P CHR345 Chronic Pain 44 0.148
134
DRM006 Dermatitis 61 0.147
135
CHL014 Cholera 59 0.147
136
c VRL010 Viral Hepatitis 52 0.147
137
ART140 Arteries, Anomalies of 52 0.146
138
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.145
139
c MGR028 Migraine with or Without Aura 1 67 0.143
140
CRB039 Cerebrovascular Disease 67 0.143
141
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.142
142
IMM167 Immune Deficiency Disease 78 0.142
143
P PHC003 Pheochromocytoma 71 0.141
144
ADR040 Adrenal Gland Pheochromocytoma 46 0.141
145
P ESP024 Esophagitis 62 0.140
146
P NTR004 Neutropenia 63 0.140
147
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.140
148
c SYS001 Systemic Lupus Erythematosus 86 0.139
149
ADN018 Adenoma 59 0.139
150
P HPT021 Hepatitis 67 0.139
151
P MVM001 Movement Disease 63 0.138
152
NTR005 Nutritional Deficiency Disease 62 0.138
153
P LNG032 Lung Cancer 98 0.138
154
P MYP004 Myopathy 70 0.138
155
INS024 Insulin-Like Growth Factor I 79 0.138
156
P HYP086 Hypothyroidism 69 0.137
157
P CND004 Candidiasis 58 0.137
158
P MCR115 Microvascular Complications of Diabetes 5 66 0.137
159
GST033 Gestational Diabetes 61 0.137
160
c LKM061 Leukemia, Acute Myeloid 84 0.137
161
ADL002 Adult Syndrome 70 0.136
162
STR067 Stroke, Ischemic 81 0.136
163
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.135
164
HMC014 Homocysteinemia 53 0.135
165
P BND020 Bone Disease 59 0.135
166
ALL014 Allergic Encephalomyelitis 38 0.134
167
P CRD246 Cardiovascular System Disease 57 0.134
168
CNG034 Congestive Heart Failure 69 0.131
169
P EPL164 Epilepsy 71 0.131
170
LNG099 Lung Disease 60 0.131
171
P CHL066 Cholangitis 51 0.130
172
HMP009 Haemophilus Influenzae 43 0.130
173
MCS002 Mucositis 56 0.129
174
MYL069 Myeloma, Multiple 85 0.128
175
END086 End Stage Renal Disease 51 0.128
176
P CTR002 Cataract 60 0.128
177
P MLT020 Multiple Sclerosis 72 0.128
178
P BLD134 Bladder Cancer 79 0.126
179
BRN004 Brain Edema 56 0.126
180
P PRP019 Peripheral Nervous System Disease 58 0.125
181
VCC001 Vaccinia 49 0.125
182
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.125
183
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.125
184
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.125
185
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.125
186
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.125
187
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.125
188
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.125
189
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.125
190
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.125
191
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.125
192
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.125
193
ACQ007 Acquired Immunodeficiency Syndrome 60 0.124
194
P ALC033 Alcohol Use Disorder 58 0.123
195
P ART021 Arteriosclerosis 54 0.123
196
c PCH010 Pachyonychia Congenita 3 44 0.123
197
PHN003 Phenylketonuria 75 0.122
198
P CRD119 Cardiac Arrest 67 0.122
199
P GST053 Gastric Cancer 83 0.122
200
HYP005 Hypokalemia 55 0.121
201
BCT022 Bacterial Infectious Disease 56 0.121
202
c HPT016 Hepatitis B 59 0.121
203
HYP781 Hypoascorbemia 51 0.120
204
AMN003 Amnestic Disorder 54 0.120
205
P MSC005 Muscular Dystrophy 66 0.120
206
DBT010 Diabetic Neuropathy 54 0.119
207
P AST007 Astrocytoma 51 0.119
208
PLM010 Pulmonary Edema 54 0.119
209
SQM006 Squamous Cell Carcinoma 60 0.118
210
CRH001 Crohn's Disease 74 0.117
211
P RSP003 Respiratory Failure 74 0.117
212
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.117
213
c ACT134 Acute Liver Failure 56 0.116
214
SKN016 Skin Disease 63 0.116
215
c PRM038 Primary Agammaglobulinemia 44 0.116
216
P LCT001 Lactic Acidosis 51 0.116
217
c ACT071 Acute Kidney Failure 60 0.116
218
EMB004 Embryonal Carcinoma 56 0.116
219
GLC003 Glucose Intolerance 54 0.116
220
THY029 Thyroid Carcinoma 59 0.116
221
ADG002 Audiogenic Seizures 25 0.115
222
LMB024 Limbic Encephalitis 41 0.114
223
P LPS004 Lupus Erythematosus 61 0.114
224
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.113
225
P EXN002 Exanthem 57 0.112
226
URM002 Uremia 49 0.112
227
THR024 Thrombosis 57 0.112
228
ATN005 Autonomic Dysfunction 46 0.112
229
c THR092 Thrombophilia Due to Thrombin Defect 73 0.111
230
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.111
231
P DMN002 Dementia 66 0.111
232
HDN002 Head Injury 46 0.111
233
P DYS154 Dystonia 65 0.111
234
CNS004 Constipation 58 0.111
235
P LKM062 Leukemia, Acute Lymphoblastic 69 0.111
236
KRT009 Keratosis 51 0.110
237
BRR014 Barrett Esophagus 65 0.110
238
c ACT027 Acute Pancreatitis 60 0.110
239
PRT013 Portal Hypertension 59 0.110
240
SBC016 Subacute Delirium 44 0.110
241
ANX010 Anxiety 73 0.110
242
RCK004 Rickets 68 0.110
243
AGN016 Aging 56 0.109
244
P LNG064 Lung Cancer Susceptibility 3 78 0.109
245
CHL123 Chlamydia 59 0.109
246
P BCL017 B-Cell Lymphoma 58 0.109
247
PRT036 Peritonitis 64 0.109
248
P PNC044 Pancreatitis 61 0.108
249
P ART022 Arthritis 69 0.108
250
SRC014 Sarcoma 65 0.106
251
SPN035 Spindle Cell Sarcoma 53 0.106
253
P MLN008 Melanoma 69 0.106
254
PLM033 Pulmonary Embolism 59 0.105
255
c SML038 Small Cell Cancer of the Lung 65 0.105
256
PSY004 Psychotic Disorder 67 0.105
257
P OVR082 Overgrowth Syndrome 50 0.105
258
P THR014 Thrombocytopenia 67 0.104
259
P RTN018 Retinal Disease 53 0.104
260
c HPT003 Hepatitis a 62 0.104
261
P HDC001 Headache 57 0.103
262
P RHN004 Rhinitis 57 0.103
263
P ECL001 Eclampsia 50 0.103
264
P RTN024 Retinoblastoma 73 0.102
265
P MNN013 Meningitis 66 0.102
266
IRR002 Irritable Bowel Syndrome 65 0.102
267
c FML008 Familial Retinoblastoma 53 0.102
268
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.102
269
P PRK057 Parkinson Disease, Late-Onset 78 0.102
270
MTH009 Mouth Disease 56 0.102
271
P LYM118 Lymphoma 68 0.102
272
CHL079 Children's Interstitial Lung Disease 26 0.101
273
P CYS018 Cystitis 59 0.101
274
c ACT073 Acute Leukemia 58 0.101
275
c SVR001 Severe Acute Respiratory Syndrome 62 0.101
276
c DWL002 Dowling-Degos Disease 1 58 0.101
277
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.101
278
P MSC003 Muscular Atrophy 52 0.101
279
TRT001 Teratocarcinoma 45 0.101
280
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.101
281
MYL009 Myelodysplastic Syndrome 70 0.100
282
P SKN015 Skin Carcinoma 66 0.100
283
PRS045 Prostatic Hypertrophy 53 0.100
284
P HYP076 Hyperthyroidism 55 0.100
285
c MLG068 Malignant Glioma 46 0.100
286
PPL022 Papilloma 54 0.100
287
P AMY004 Amyloidosis 70 0.100
288
TXC005 Toxic Shock Syndrome 62 0.100
289
P GLM007 Glomerulonephritis 57 0.100
290
CRD132 Cardiac Conduction Defect 58 0.100
291
BLR008 Bilirubin Metabolic Disorder 57 0.099
292
CHL065 Cholangiocarcinoma 68 0.098
293
KRT002 Keratomalacia 47 0.098
294
HLC007 Helicobacter Pylori Infection 59 0.098
295
CHL004 Cholelithiasis 49 0.097
296
END040 Endogenous Depression 55 0.097
297
c PRD040 Periodontitis, Chronic 53 0.097
298
INT079 Intrahepatic Cholangiocarcinoma 51 0.097
299
ESP021 Esophageal Cancer 90 0.097
300
CNV004 Canavan Disease 61 0.097
301
SQM002 Squamous Cell Papilloma 46 0.096
302
AST005 Asthma 76 0.096
303
VRC005 Varicose Veins 60 0.096
304
LYS012 Lysosomal Acid Lipase Deficiency 65 0.096
305
MLR004 Malaria 81 0.096
306
TRN015 Transient Cerebral Ischemia 63 0.096
307
P ALP008 Alopecia 54 0.095
308
PPT001 Peptic Esophagitis 52 0.095
309
SVR004 Severe Combined Immunodeficiency 73 0.095
310
LYM019 Lymphosarcoma 46 0.094
311
MTH071 Methane Production 26 0.094
312
P SCL009 Sclerosing Cholangitis 48 0.094
313
DNT012 Dental Caries 53 0.094
314
P PLY019 Polyneuropathy 56 0.094
315
LSH001 Leishmaniasis 63 0.093
316
P KLZ004 Kala-Azar 1 41 0.093
317
P PNM007 Pneumonia 68 0.093
318
HNS001 Hansen's Disease 34 0.093
319
P LPR021 Leprosy 3 69 0.093
320
ATS010 Autosomal Recessive Disease 48 0.093
321
GNG013 Gingivitis 59 0.093
322
SPS057 Spasticity 45 0.092
323
CHR073 Choreatic Disease 52 0.092
324
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.092
325
P RTN016 Retinal Degeneration 53 0.092
326
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.092
327
P BRS044 Breast Adenocarcinoma 59 0.092
328
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.091
329
PRP027 Peripheral Vascular Disease 71 0.091
330
NRT001 Neurotic Disorder 53 0.091
331
PRS021 Prostatic Adenoma 51 0.091
332
DPH001 Diphtheria 60 0.091
333
P PLM036 Pulmonary Fibrosis 65 0.091
334
P MYC033 Myoclonus 46 0.090
335
c CHL119 Cholangitis, Primary Sclerosing 57 0.090
336
PLY150 Polykaryocytosis Inducer 31 0.090
337
c LKM005 Leukemia, T-Cell, Chronic 34 0.090
338
ANG054 Angina Pectoris 66 0.090
339
P CNR004 Cone-Rod Dystrophy 2 73 0.090
340
WTH001 Withdrawal Disorder 48 0.090
341
P NSP012 Nasopharyngeal Carcinoma 66 0.090
342
P FBR017 Fibrosarcoma 56 0.090
343
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.090
344
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.090
345
GST050 Gastrointestinal System Disease 56 0.089
346
MST005 Mastitis 53 0.089
347
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.089
348
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.089
349
GST045 Gastroenteritis 59 0.089
350
P ATR011 Atrial Fibrillation 66 0.089
351
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.089
352
PRS129 Prostatic Hyperplasia, Benign 49 0.089
353
BLR001 Biliary Atresia 50 0.088
354
P INF032 Infertility 57 0.088
355
P THL005 Thalassemia 60 0.088
356
P MYC084 Mycobacterium Tuberculosis 1 68 0.088
357
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.088
358
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.087
359
P ZLL001 Zellweger Syndrome 57 0.087
360
VSC002 Vascular Dementia 57 0.087
361
EYD002 Eye Disease 58 0.086
362
FBR047 Fibromyalgia 58 0.086
363
c DRR009 Diarrhea 6 46 0.086
364
P HYP265 Hypotonia 43 0.086
365
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.085
366
CHC001 Chickenpox 60 0.085
367
SPL018 Splenomegaly 48 0.085
368
CHG001 Chagas Disease 66 0.084
369
P CNJ013 Conjunctivitis 65 0.084
370
P PYL005 Pyelonephritis 56 0.084
371
c PRS136 Prostate Cancer, Hereditary, 6 33 0.084
372
c PRS130 Prostate Cancer, Hereditary, 8 32 0.084
373
PTH003 Pathologic Nystagmus 52 0.084
374
DMY004 Demyelinating Disease 52 0.084
375
IRN001 Iron Deficiency Anemia 59 0.084
376
P GLM040 Glioma Susceptibility 1 81 0.083
377
P MJR007 Major Affective Disorder 1 43 0.083
378
P HYP098 Hypereosinophilic Syndrome 67 0.083
379
c FNC043 Fanconi Anemia, Complementation Group E 62 0.083
380
PRP016 Paraplegia 52 0.083
381
P OBS001 Obstructive Jaundice 50 0.083
382
PHS025 Phosphatase, Acid, of Tissues 28 0.082
383
ALL003 Allergic Rhinitis 67 0.082
384
P SLP005 Sleep Disorder 59 0.082
385
ORL015 Oral Squamous Cell Carcinoma 43 0.082
386
ENT004 Enthesopathy 49 0.082
387
P KDN017 Kidney Cancer 60 0.082
388
HYP081 Hypolipoproteinemia 51 0.081
389
ERY051 Erythroleukemia, Familial 56 0.081
390
c BSL007 Basal Cell Carcinoma 68 0.081
391
CLR108 Colorectal Adenoma 64 0.081
392
ENT011 Enterocolitis 51 0.080
393
HMS001 Hemosiderosis 54 0.080
394
P LKD001 Leukodystrophy 59 0.080
395
JPN002 Japanese Encephalitis 57 0.080
396
MSL001 Measles 62 0.080
397
c ATM011 Autoimmune Hepatitis 63 0.080
398
LPT014 Leptin Deficiency or Dysfunction 74 0.080
399
P DNG005 Dengue Virus 59 0.080
400
P URT039 Urticaria 58 0.080
401
OBS002 Obsessive-Compulsive Disorder 68 0.080
402
CRT015 Carotid Artery Occlusion 45 0.079
403
DCR008 Dicarboxylic Aminoaciduria 44 0.079
404
c LKM063 Leukemia, Chronic Myeloid 72 0.079
405
ORL011 Oral Cancer 60 0.079
406
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.079
407
P RRH023 Rare Hereditary Hemochromatosis 41 0.078
408
BRT054 Brittle Bone Disorder 72 0.078
409
P HML002 Hemolytic Anemia 63 0.078
410
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.078
411
RTN003 Retinal Ischemia 50 0.078
412
ARG004 Argyria 27 0.078
413
P RCT021 Rectum Cancer 52 0.078
414
c ATR087 Atrial Standstill 1 75 0.077
415
P MTR014 Motor Neuron Disease 65 0.077
416
P HYP069 Hyperparathyroidism 63 0.077
417
GST040 Gastric Adenocarcinoma 70 0.077
418
SCH014 Schistosomiasis 57 0.077
419
TBR011 Tuberculous Meningitis 48 0.077
420
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.077
421
CYS013 Cystinuria 63 0.077
422
RTN023 Retinitis 46 0.077
423
NRR001 Neuroretinitis 42 0.077
424
P SBS003 Substance Abuse 55 0.076
425
P PLM037 Pulmonary Hypertension 67 0.076
426
ALC006 Alcoholic Hepatitis 61 0.076
427
INS001 Insulinoma 60 0.076
428
P PRS038 Personality Disorder 65 0.076
429
ANR040 Aneurysm 59 0.076
430
LNG031 Lung Benign Neoplasm 51 0.076
431
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.076
432
NRM001 Neuromyelitis Optica 61 0.075
433
BRN028 Brain Cancer 74 0.075
434
P HMC002 Homocystinuria 53 0.075
435
PYR016 Pyridoxine Deficiency 30 0.075
436
PRP030 Purpura 54 0.075
437
RYS001 Reye Syndrome 51 0.075
438
SYN007 Synovitis 54 0.075
439
P SHR001 Short Bowel Syndrome 53 0.075
440
PLC002 Plica Syndrome 36 0.075
441
P RTN008 Retinitis Pigmentosa 79 0.074
442
WST001 West Syndrome 61 0.074
443
DYS073 Dysphagia 50 0.074
444
PLS009 Plasma Cell Neoplasm 51 0.074
445
P ADL010 Adult Respiratory Distress Syndrome 65 0.074
446
PNC129 Pancreatic Adenocarcinoma 68 0.073
447
SFT003 Soft Tissue Sarcoma 56 0.073
448
CVD001 Covid-19 44 0.073
449
c HYP272 Hypercholesterolemia, Familial, 3 44 0.073
450
TRD006 Tardive Dyskinesia 54 0.073
451
c FML035 Familial Hyperlipidemia 55 0.073
452
PRT038 Protein-Energy Malnutrition 54 0.073
453
AMN006 Aminoaciduria 38 0.073
454
c MJR003 Major Affective Disorder 6 33 0.073
455
c MJR006 Major Affective Disorder 5 33 0.073
456
P BNC003 Bone Cancer 58 0.073
457
P MLN007 Male Infertility 55 0.073
458
CHL067 Cholecystitis 57 0.072
459
c MJR008 Major Affective Disorder 2 35 0.072
460
c MJR023 Major Affective Disorder 7 33 0.072
461
c MJR004 Major Affective Disorder 4 28 0.072
462
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.072
463
PRN019 Perinatal Necrotizing Enterocolitis 59 0.072
464
PYR009 Pyridoxine Deficiency Anemia 34 0.072
465
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.072
466
P INT068 Intestinal Disease 53 0.071
467
c INF145 Infantile Liver Failure Syndrome 1 50 0.071
468
MMM001 Mammary Paget's Disease 53 0.071
469
P BNG032 Benign Mesothelioma 46 0.071
470
49X006 49, Xxxxy Syndrome 41 0.071
471
MDD018 Middle East Respiratory Syndrome 43 0.071
472
STF001 Stiff-Person Syndrome 60 0.071
473
P SLP006 Sleep Apnea 69 0.071
474
c MCR129 Microvascular Complications of Diabetes 1 66 0.071
475
P HYD006 Hydrocephalus 66 0.071
476
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.071
477
DSS008 Disease of Mental Health 58 0.071
478
FCL014 Focal Epilepsy 54 0.071
479
P MDL005 Medulloblastoma 77 0.071
480
PLC008 Placenta Disease 50 0.071
481
SCR011 Scrapie 39 0.071
482
MNN009 Meningoencephalitis 49 0.071
483
HND015 Hand Skill, Relative 33 0.071
484
P GRF003 Graft-Versus-Host Disease 72 0.071
485
HRP009 Herpes Simplex Encephalitis 52 0.070
486
c BRN108 Branchiootic Syndrome 1 62 0.070
487
P RNL007 Renal Tubular Acidosis 51 0.070
488
P SCK005 Sickle Cell Disease 50 0.070
489
HPT022 Hepatoblastoma 56 0.070
490
SCH012 Schizoaffective Disorder 50 0.070
491
P DYS021 Dysautonomia 39 0.070
492
APH002 Aphasia 57 0.070
493
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.070
494
VRL011 Viral Infectious Disease 61 0.069
495
GTR002 Goiter 53 0.069
496
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.069
497
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.069
498
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.069
499
P MYP006 Myopia 55 0.069
500
P VSC011 Vasculitis 62 0.069
501
TLN003 Telangiectasis 52 0.069
502
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.068
503
c DLT002 Dilated Cardiomyopathy 79 0.068
504
RTN017 Retinal Detachment 61 0.068
505
ESP002 Esophageal Varix 51 0.068
506
BRK010 Burkitt Lymphoma 67 0.068
507
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.068
508
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.068
509
P FTL001 Fetal Alcohol Syndrome 57 0.067
510
OST017 Osteomyelitis 64 0.067
511
ARG002 Argininosuccinic Aciduria 61 0.067
512
P CHN012 Chondrosarcoma 56 0.067
513
PLM031 Poliomyelitis 64 0.067
514
ART016 Aortic Aneurysm 69 0.067
515
c PNS012 Paine Syndrome 61 0.067
516
c HMC039 Hemochromatosis, Type 1 74 0.067
517
P TXP001 Toxoplasmosis 60 0.067
518
P ALP009 Alopecia Areata 60 0.067
519
P SLL003 Salla Disease 48 0.067
520
P PRN023 Prion Disease 57 0.066
521
P PLY014 Polycystic Kidney Disease 62 0.066
522
PST092 Posttransplant Acute Limbic Encephalitis 29 0.066
523
CRD223 Cardiac Arrhythmia 60 0.066
524
PST021 Postpartum Depression 50 0.066
525
P CTR177 Citrullinemia, Type Ii, Adult-Onset 57 0.066
526
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.066
527
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.066
528
c SCL052 Scleroderma, Familial Progressive 61 0.066
529
P RTT002 Rett Syndrome 80 0.066
530
P ASP006 Aspergillosis 69 0.066
531
GLS001 Gliosarcoma 54 0.065
532
c CHR064 Chronic Monocytic Leukemia 33 0.065
533
c VRL007 Viral Encephalitis 51 0.065
534
P END033 Endocarditis 57 0.065
535
NRT004 Neuritis 52 0.065
536
c BTT014 Beta-Thalassemia 74 0.065
537
KRT019 Keratitis, Hereditary 65 0.065
538
KHL003 Kohlschutter-Tonz Syndrome 65 0.064
539
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.064
540
VGN023 Vaginitis 54 0.064
541
IMP005 Impotence 52 0.064
542
HYP017 Hypophosphatemia 50 0.064
543
P HMP007 Hemophilia 51 0.064
544
CRB037 Cerebral Palsy 69 0.064
545
IGG001 Iga Glomerulonephritis 48 0.064
546
CRC021 Carcinosarcoma 62 0.063
547
ANR007 Anorexia Nervosa 63 0.063
548
MTS001 Mutism 46 0.063
549
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.063
550
RBS001 Rabies 58 0.063
551
c SVR005 Severe Pre-Eclampsia 50 0.063
552
ATM052 Autoimmune Disease 1 37 0.063
553
P GRV001 Graves' Disease 55 0.063
555
P CLC063 Celiac Disease 1 66 0.062
556
MXD026 Mixed Glioma 45 0.062
557
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.062
558
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.062
559
PTT037 Pituitary Tumors 44 0.062
560
CRB090 Cerebral Hypoxia 44 0.062
561
P OPT006 Optic Nerve Disease 60 0.062
562
BCK006 Back Pain 42 0.062
564
CRH005 Crohn's Colitis 53 0.062
565
PST028 Post-Traumatic Stress Disorder 58 0.061
566
LYM040 Lymphoblastic Lymphoma 54 0.061
567
GLS018 Glass Syndrome 57 0.061
568
RDN001 Reading Disorder 40 0.061
569
c GRV008 Graves Disease 1 56 0.061
570
P PLY018 Polycythemia 56 0.061
571
SLP001 Sleeping Sickness 54 0.061
572
P VSC018 Visceral Steatosis 33 0.061
573
HLL004 Hellp Syndrome 54 0.061
574
SCK003 Sickle Cell Anemia 74 0.060
575
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.060
576
LYM027 Lymphopenia 58 0.060
577
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.060
578
P MLG074 Malignant Mesenchymoma 40 0.060
579
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.060
580
c ART068 Aortic Aneurysm, Familial Thoracic 2 34 0.060
581
P NRV007 Nervous System Disease 66 0.059
582
P FNC004 Fanconi Syndrome 50 0.059
583
RTN020 Retinal Vascular Disease 46 0.059
584
P SPN046 Spinal Muscular Atrophy 62 0.059
585
P NRC002 Narcolepsy 52 0.059
586
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.059
587
SNL007 Senile Cataract 42 0.059
588
P ICH004 Ichthyosis 54 0.059
589
CND006 Candida Glabrata 32 0.059
590
TXC002 Toxic Encephalopathy 53 0.058
591
PRS047 Prostatitis 56 0.058
592
ILS001 Ileus 51 0.058
593
NNT017 Neonatal Adrenoleukodystrophy 47 0.058
594
P FNC034 Fanconi Renotubular Syndrome 2 40 0.058
595
P MYS003 Myasthenia Gravis 68 0.058
596
P PNC025 Panic Disorder 53 0.058
597
c CHR682 Chronic Bilirubin Encephalopathy 39 0.058
598
ANP008 Anaplastic Oligoastrocytoma 30 0.058
599
HMG005 Hemoglobinopathy 56 0.058
600
P FBR031 Febrile Seizures 53 0.058
601
SKN019 Skin Melanoma 68 0.058
602
RHM001 Rheumatic Fever 60 0.058
603
LRN003 Learning Disability 49 0.057
604
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.057
605
P LRY044 Larynx Cancer 55 0.057
606
NRL004 Neuroleptic Malignant Syndrome 56 0.057
607
P MCR010 Microcephaly 59 0.057
608
ACT084 Acute Stress Disorder 47 0.057
609
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 33 0.057
610
VLV047 Volvulus of Midgut 49 0.057
611
LYS003 Lysinuric Protein Intolerance 57 0.057
612
c BCT007 Bacterial Meningitis 55 0.057
613
GRN017 Granulocytopenia 44 0.057
614
SPN041 Spinal Cord Disease 56 0.057
615
c PRG106 Progressive Muscular Dystrophy 33 0.057
616
P BRB001 Beriberi 46 0.056
617
GST020 Gastric Antral Vascular Ectasia 41 0.056
618
FNG017 Fungal Infectious Disease 53 0.056
619
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.056
620
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.056
621
THY030 Thyroid Gland Disease 52 0.056
622
P RBL001 Rubella 59 0.056
623
P ATX030 Ataxia-Telangiectasia 82 0.056
624
P OLG002 Oligodendroglioma 67 0.056
625
ACT058 Active Peptic Ulcer Disease 55 0.056
626
WST005 West Nile Virus 54 0.056
627
GRD007 Grade Iii Astrocytoma 59 0.055
628
TRY001 Trypanosomiasis 50 0.055
629
ATN004 Autonomic Neuropathy 45 0.055
630
MST004 Mast Cell Neoplasm 42 0.055
631
EXT007 Extracutaneous Mastocytoma 38 0.055
632
c INF071 Inflammatory Bowel Disease 1 67 0.055
633
c WLM018 Wilms Tumor 5 61 0.055
634
TNS005 Tonsillitis 57 0.055
635
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.055
636
P OPT009 Optic Neuritis 57 0.055
637
CCN002 Cocaine Abuse 49 0.055
638
FSC002 Fascioliasis 42 0.055
639
P SYP003 Syphilis 58 0.055
640
WLL004 Wallerian Degeneration 39 0.055
641
P ADL017 Adult T-Cell Leukemia 56 0.055
642
DWR001 Dwarfism 44 0.055
643
HMT002 Hematologic Cancer 62 0.054
644
c ACT135 Acute Graft Versus Host Disease 52 0.054
645
THY111 Thyroid Carcinoma, Familial Medullary 67 0.054
646
P CRB088 Cerebral Atrophy 37 0.054
647
CMP010 Complex Regional Pain Syndrome 58 0.054
648
MRP001 Morphine Dependence 41 0.054
649
P PTS002 Ptosis 53 0.054
650
OCL006 Ocular Hypertension 53 0.054
651
INT002 Intermittent Claudication 61 0.054
652
SDD001 Sudden Infant Death Syndrome 61 0.054
653
PHR003 Pharyngitis 57 0.054
654
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.054
655
c SCN007 Secondary Hyperparathyroidism 51 0.054
656
ALV005 Alveolar Soft Part Sarcoma 61 0.054
657
PRN071 Parenteral Nutrition-Associated Cholestasis 25 0.053
658
CYT008 Cytomegalovirus Infection 57 0.053
659
HYP080 Hypogonadism 50 0.053
660
INT075 Intracranial Hypertension 53 0.053
661
P CYS017 Cystic Teratoma 41 0.053
662
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.053
663
ALC009 Alcoholic Liver Cirrhosis 53 0.053
664
ACN002 Acanthosis Nigricans 60 0.053
665
FLR002 Filariasis 55 0.052
666
GLC008 Glucose Metabolism Disease 40 0.052
667
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.052
668
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 53 0.052
669
SPS019 Spastic Paraparesis 38 0.052
670
P TBR001 Tuberous Sclerosis 70 0.052
671
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.052
672
ETN001 Eating Disorder 60 0.052
673
P MTC069 Mitochondrial Disorders 56 0.052
674
EXT006 Extrahepatic Cholestasis 39 0.052
675
MTR010 Mature Teratoma 44 0.052
676
ADN011 Adenoid Cystic Carcinoma 70 0.052
677
HMP005 Hemiplegia 55 0.052
678
KRT008 Keratopathy 47 0.052
679
INF034 Infective Endocarditis 53 0.052
680
GLB001 Gilbert Syndrome 58 0.051
681
HPT014 Hepatorenal Syndrome 50 0.051
682
CLN045 Colonic Benign Neoplasm 46 0.051
683
MYL001 Myelitis 51 0.051
684
OCL052 Ocular Dominance 42 0.051
685
NRN004 Neuroendocrine Tumor 55 0.051
686
CRT072 Creutzfeldt-Jakob Disease 70 0.050
687
PRD004 Prediabetes Syndrome 47 0.050
688
DFF005 Diffuse Large B-Cell Lymphoma 55 0.050
689
ORT008 Orotic Aciduria 55 0.050
690
AZS001 Azoospermia 50 0.050
691
P BLR006 Biliary Tract Disease 47 0.050
692
DBT002 Diabetic Autonomic Neuropathy 41 0.050
693
ERL001 Early Myoclonic Encephalopathy 62 0.050
694
NWB001 Newborn Respiratory Distress Syndrome 58 0.050
695
P MYS005 Myositis 56 0.050
696
ORL005 Oral Candidiasis 56 0.049
697
P ANT006 Antiphospholipid Syndrome 55 0.049
698
PSR001 Psoriatic Arthritis 61 0.049
699
THY122 Thyroid Gland Cancer 57 0.049
700
P EHL001 Ehlers-Danlos Syndrome 58 0.049
701
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.049
702
GNT002 Giant Cell Glioblastoma 50 0.049
703
LWC001 Low Compliance Bladder 43 0.049
704
P MGR001 Migraine Without Aura 49 0.049
705
c OST080 Osteogenesis Imperfecta, Type Ii 54 0.049
706
c JVN010 Juvenile Rheumatoid Arthritis 64 0.049
707
P PLM034 Pulmonary Emphysema 55 0.049
708
P END046 Endometritis 49 0.048
709
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 58 0.048
710
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.048
711
THR004 Thrombocytosis 51 0.048
712
P GNG009 Gangliosidosis 44 0.048
713
P PRC031 Preeclampsia/eclampsia 1 38 0.048
714
MYT011 Myotonia 34 0.048
715
P GLC113 Galactosemia I 64 0.048
716
P MGR003 Migraine with Aura 52 0.048
717
PSD088 Pseudobulbar Affect 36 0.048
718
NRM005 Neuromuscular Disease 64 0.048
719
MCL006 Macular Retinal Edema 55 0.048
720
TND005 Tendinitis 54 0.048
721
RFR010 Refractory Anemia 48 0.048
722
P FRN006 Frontotemporal Dementia 68 0.048
723
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.048
724
PRN068 Paraneoplastic Limbic Encephalitis 21 0.048
725
P END084 Endocrine System Disease 45 0.048
726
P FRG001 Fragile X Syndrome 70 0.048
727
P GLL020 Gallbladder Disease 57 0.048
728
PNM008 Pneumothorax 56 0.048
729
OPT003 Opiate Dependence 50 0.047
730
P PLY041 Polymyositis 57 0.047
731
BRD004 Borderline Personality Disorder 53 0.047
732
CRT013 Carotid Stenosis 50 0.047
733
P OCL013 Oculodentodigital Dysplasia 69 0.047
734
LSC001 Lesch-Nyhan Syndrome 62 0.047
735
c BSL024 Basal Cell Carcinoma 1 56 0.046
736
c BPL002 Bipolar I Disorder 49 0.046
737
c INV001 Invasive Aspergillosis 49 0.046
738
MLT006 Multidrug-Resistant Tuberculosis 48 0.046
739
P HYP111 Hyperprolinemia 44 0.046
740
THR013 Thoracic Outlet Syndrome 54 0.046
741
CLL003 Cellulitis 54 0.046
742
TRP009 Triple X Syndrome 42 0.046
743
c DNG003 Dengue Disease 59 0.046
744
SNS003 Sensory Peripheral Neuropathy 54 0.046
745
NNT012 Neonatal Jaundice 53 0.046
746
KWS002 Kawasaki Disease 65 0.046
747
c HPT007 Hepatitis E 53 0.046
748
MYL031 Myeloproliferative Neoplasm 66 0.045
749
P ANR048 Aniridia 1 63 0.045
750
P CHR285 Chronic Myelomonocytic Leukemia 60 0.045
751
INC002 Inclusion Body Myositis 58 0.045
752
THY125 Thyroid Gland Medullary Carcinoma 50 0.045
753
TTH006 Tooth Disease 46 0.045
754
CHL013 Cholecystolithiasis 37 0.045
755
TBC004 Tobacco Addiction 64 0.045
756
P OVR046 Ovarian Cyst 47 0.045
757
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.045
758
MYL005 Myelofibrosis 70 0.045
759
P GLL022 Guillain-Barre Syndrome 59 0.045
760
CRN017 Coronary Thrombosis 47 0.045
761
MNG007 Manganese Poisoning 29 0.045
762
GLY010 Glycine Encephalopathy 62 0.045
763
P SML001 Small Cell Carcinoma 52 0.045
764
MTB016 Metabolic Myopathy 32 0.045
765
WLS001 Wilson Disease 71 0.045
766
BLD131 Bladder Urothelial Carcinoma 62 0.045
767
P HMR005 Hemorrhoid 46 0.045
768
DRG003 Drug Dependence 47 0.044
769
SPC005 Speech Disorder 43 0.044
770
ARG007 Argininemia 57 0.044
771
APN008 Apnea, Obstructive Sleep 64 0.044
772
P DRM010 Dermatomyositis 61 0.044
773
c ESS001 Essential Tremor 56 0.044
774
LPR001 Lepromatous Leprosy 50 0.044
775
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.044
776
c MCL013 Mucolipidosis Iv 66 0.044
777
P DBT005 Diabetes Insipidus 55 0.044
778
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.044
779
c MLG079 Malignant Pleural Mesothelioma 42 0.044
780
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.044
781
MST020 Mast Cell Activation Syndrome 26 0.044
782
P CLS010 Cluster Headache 42 0.044
783
PST053 Postherpetic Neuralgia 40 0.044
784
HGH001 High Pressure Neurological Syndrome 28 0.044
785
HYP020 Hyperprolactinemia 64 0.043
786
MCP006 Mucoepidermoid Carcinoma 50 0.043
788
c WLM013 Wilms Tumor 1 65 0.043
789
CMR002 Coumarin Resistance 56 0.043
790
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.043
791
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.043
792
DMP001 Dumping Syndrome 44 0.043
793
TND004 Tendinopathy 43 0.043
794
ATX010 Ataxia Neuropathy Spectrum 34 0.043
795
ACT064 Acute Necrotizing Encephalitis 33 0.043
796
BLD137 Blood Group--Ahonen 16 0.043
797
PRV004 Periventricular Leukomalacia 52 0.043
798
CLR030 Clear Cell Renal Cell Carcinoma 53 0.043
799
VLV011 Vulvovaginal Candidiasis 49 0.043
800
P DST107 Distal Renal Tubular Acidosis 42 0.043
801
PLY100 Polyploidy 40 0.043
802
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.043
803
TNG007 Tongue Carcinoma 51 0.042
804
FTL021 Fetal Macrosomia 42 0.042
805
HPT085 Hepatitis, Fulminant Viral 32 0.042
806
INT030 Intracranial Aneurysm 56 0.042
807
BRN014 Bronchopneumonia 54 0.042
808
HRT012 Heart Valve Disease 53 0.042
809
TST014 Testicular Cancer 46 0.042
810
OLG001 Oligospermia 45 0.042
811
BRN032 Brain Glioma 45 0.042
812
P MTR004 Maturity-Onset Diabetes of the Young 65 0.042
813
INT146 Intervertebral Disc Disease 63 0.042
814
APR001 Apraxia 52 0.042
815
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.042
816
GST037 Gastroparesis 54 0.041
817
MTC005 Mitochondrial Metabolism Disease 49 0.041
818
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.041
819
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.041
820
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.041
821
HRN029 Hearing Loss, Noise-Induced 37 0.041
822
PRT082 Preterm Premature Rupture of the Membranes 54 0.041
823
ANT019 Anterograde Amnesia 38 0.041
824
NRN001 Neuroendocrine Carcinoma 47 0.041
825
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.041
826
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.041
827
DGR001 Digeorge Syndrome 64 0.041
828
c JVN061 Juvenile Arthritis 60 0.041
829
PLM014 Pleomorphic Adenoma 52 0.041
830
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.041
831
THY128 Thyroid Tumor 47 0.041
832
CRD137 Cardiogenic Shock 47 0.041
833
CHL039 Choledocholithiasis 38 0.041
834
PYR037 Pyruvate Carboxylase Deficiency 43 0.040
835
c PNC108 Pancreatitis, Hereditary 70 0.040
836
c CNG006 Congenital Hypothyroidism 64 0.040
837
c CHR418 Chronic Leukemia 49 0.040
838
CYT018 Cytochrome P450 2d6 Variant 27 0.040
839
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 42 0.040
840
PRN039 Paraneoplastic Syndromes 38 0.040
841
P TYS001 Tay-Sachs Disease 69 0.039
842
c LKM070 Leukemia, Acute Monocytic 57 0.039
843
ACR041 Acromelic Frontonasal Dysostosis 52 0.039
844
URC002 Urea Cycle Disorder 51 0.039
845
DBT006 Diabetic Macular Edema 48 0.039
846
PRM003 Premature Ejaculation 44 0.039
847
BNM001 Bone Marrow Cancer 43 0.039
848
c CHR098 Chronic Pyelonephritis 38 0.039
849
CRY036 Cryptogenic Cirrhosis 36 0.039
850
PRN029 Parainfluenza Virus Type 3 36 0.039
851
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.039
852
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.039
853
MNN017 Mononeuropathy 42 0.039
854
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.039
855
P LMY004 Leiomyosarcoma 63 0.039
856
P MLT074 Multiple Endocrine Neoplasia 56 0.039
857
P MTC133 Mitochondrial Myopathy 49 0.039
858
SXL003 Sexual Disorder 47 0.039
859
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.039
860
CRN027 Corneal Neovascularization 47 0.039
861
ENC005 Encephalomalacia 43 0.039
862
MYF002 Myofascial Pain Syndrome 42 0.039
863
c OPT053 Optic Atrophy 1 63 0.039
864
HYP082 Hypopharynx Cancer 47 0.039
865
HRP008 Herpes Simiae 25 0.039
866
LPT001 Leptospirosis 66 0.038
867
P LNG028 Long Qt Syndrome 66 0.038
868
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 0.038
869
PRT058 Pure Autonomic Failure 59 0.038
870
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.038
871
P SDR003 Sideroblastic Anemia 49 0.038
872
SYN036 Syncope 45 0.038
873
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.038
874
PRL032 Perlman Syndrome 57 0.038
875
LNN001 Lennox-Gastaut Syndrome 57 0.038
876
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.038
877
RTR001 Retrograde Amnesia 44 0.038
878
CYS009 Cystadenoma 44 0.038
879
NSP002 Nasopharyngitis 43 0.038
880
PRR019 Perioral Myoclonia with Absences 27 0.038
881
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.038
882
TRG002 Trigeminal Neuralgia 60 0.038
883
BWN001 Bowen-Conradi Syndrome 52 0.038
884
P ATM019 Autoimmune Polyendocrine Syndrome 46 0.038
885
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.038
886
c SPR086 Spermatogenic Failure 3 44 0.038
887
CRB086 Cerebral Aneurysms 40 0.038
888
ACT228 Acute Radiation Syndrome 29 0.038
889
ASP024 Asparagine Synthetase Deficiency 37 0.038
890
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.037
891
DNG002 Dengue Hemorrhagic Fever 60 0.037
892
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.037
893
LGN006 Legionnaire Disease 52 0.037
894
AMB002 Amblyopia 49 0.037
895
SPP007 Suppression Amblyopia 39 0.037
896
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.037
897
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.037
898
c GLC112 Galactosemia Iii 56 0.037
899
MST024 Mastocytosis, Cutaneous 69 0.037
900
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 59 0.037
901
BRN038 Bronchial Disease 53 0.037
902
CYS005 Cysticercosis 53 0.037
903
P ORL007 Oral Cavity Cancer 53 0.037
904
TLR001 Tularemia 51 0.037
905
P RTN014 Retinal Artery Occlusion 47 0.037
906
BRN026 Branch Retinal Artery Occlusion 40 0.037
907
SCR015 Scarlet Fever 39 0.037
908
c ATM024 Autoimmune Pancreatitis 55 0.036
909
CRT016 Carotid Artery Disease 52 0.036
910
INV006 Inverted Papilloma 52 0.036
911
P OLV001 Olivopontocerebellar Atrophy 51 0.036
912
CRD043 Ceroid Storage Disease 44 0.036
913
OBN001 Ouabain Resistance 18 0.036
914
PNM010 Pneumothorax, Primary Spontaneous 60 0.036
915
GNR004 Generalized Anxiety Disorder 56 0.036
916
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.036
917
PLP001 Pulpitis 49 0.036
918
ANT018 Anthracosis 48 0.036
919
TST015 Testicular Disease 43 0.036
920
SPN050 Spinocerebellar Degeneration 42 0.036
921
GBT001 Gaba-Transaminase Deficiency 40 0.036
922
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.036
923
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.036
924
P OST001 Osteopetrosis 70 0.035
925
PLV003 Pelvic Inflammatory Disease 55 0.035
926
NRM004 Neuroma 51 0.035
927
SCB001 Scabies 50 0.035
928
P CRN024 Corneal Disease 44 0.035
929
OPD006 Opioid Addiction 48 0.035
930
OBS003 Obsessive-Compulsive Personality Disorder 46 0.035
931
MRF001 Marfan Syndrome 77 0.035
932
CMM004 Common Variable Immunodeficiency 68 0.035
933
c HRD010 Hereditary Spastic Paraplegia 66 0.035
934
MGK001 Megakaryocytic Leukemia 64 0.035
935
P PNM006 Pneumoconiosis 56 0.035
936
CCN001 Cocaine Dependence 48 0.035
937
c HRD039 Hereditary Amyloidosis 45 0.035
938
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.035
939
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.035
940
c HYP597 Hyperprolinemia, Type Ii 43 0.035
941
c PRG020 Paragangliomas 3 39 0.035
942
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.035
943
P SCK002 Sick Sinus Syndrome 55 0.034
944
PLS006 Plasmodium Vivax Malaria 51 0.034
945
FLR001 Filarial Elephantiasis 55 0.034
946
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.034
947
STT002 Status Asthmaticus 50 0.034
948
INP001 Inappropriate Adh Syndrome 49 0.034
949
BCK003 Background Diabetic Retinopathy 46 0.034
950
MDS022 Mediastinitis 46 0.034
951
ANP009 Anaplastic Oligodendroglioma 43 0.034
952
RFR003 Refractive Error 43 0.034
953
CHR031 Chromoblastomycosis 47 0.034
954
CHD001 Chediak-Higashi Syndrome 66 0.033
955
DBN001 Dubin-Johnson Syndrome 59 0.033
956
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.033
957
P OVR049 Ovarian Disease 52 0.033
958
FLT009 Folate Malabsorption, Hereditary 50 0.033
959
P ASP001 Asperger Syndrome 48 0.033
960
NSS002 Neisseria Meningitidis Infection 47 0.033
961
MYC005 Myocardial Stunning 46 0.033
962
CVT001 Cavitary Optic Disc Anomalies 38 0.033
963
SPC030 Specific Language Disorder 26 0.033
964
EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.033
965
OLF005 Olfactory Neuroblastoma 48 0.033
966
MCN007 Meconium Aspiration Syndrome 55 0.032
967
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 50 0.032
968
ACT098 Acute Erythroid Leukemia 48 0.032
969
TST044 Testicular Torsion 47 0.032
970
P PRC019 Precocious Puberty 46 0.032
971
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.032
972
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.032
973
SRN001 Serine Deficiency 24 0.032
974
c RNG019 Ring Chromosome 3 22 0.032
975
P AGN002 Agnosia 55 0.032
976
BLL004 Bullous Keratopathy 49 0.032
977
P LPS002 Liposarcoma 65 0.032
978
MNR012 Meniere Disease 57 0.032
979
P NRM002 Normal Pressure Hydrocephalus 54 0.032
980
c DYS119 Dystonia 9 50 0.032
981
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.032
982
DRG002 Drug-Induced Hepatitis 43 0.032
983
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.032
984
c WLM011 Wilms Tumor 6 37 0.032
985
JVN026 Jeavons Syndrome 24 0.032
986
ANS023 Anus, Imperforate 56 0.031
987
c SPN294 Spinocerebellar Ataxia 1 53 0.031
988
CND002 Conduct Disorder 51 0.031
989
MYL003 Myeloid Sarcoma 49 0.031
990
MSC190 Muscular Disease 37 0.031
991
HYP026 Hypoglycemic Coma 36 0.031
992
NNS045 Non-Specific Syndromic Intellectual Disability 31 0.031
993
ATH004 Athetosis 28 0.031
994
ANG061 Angular Cheilitis 26 0.031
995
PTT041 Pituitary Stalk Interruption Syndrome 50 0.030
996
SNT005 Sinoatrial Node Disease 49 0.030
997
c DFN360 Deafness, Autosomal Dominant 69 37 0.030
998
CLM004 Climatic Droplet Keratopathy 16 0.030
999
LGH007 Leigh Syndrome 70 0.030
1000
DMN031 Dementia, Lewy Body 65 0.030
1001
c CHL140 Chilblain Lupus 1 58 0.030
1002
GNG004 Ganglioglioma 54 0.030
1003
PTT009 Pituitary Gland Disease 54 0.030
1004
TRP002 Tropical Spastic Paraparesis 50 0.030
1005
P CRN025 Corneal Dystrophy 49 0.030
1006
c PRG001 Progressive Muscular Atrophy 42 0.030
1007
MYL057 Myelopathy, Htlv-1-Associated 39 0.030
1008
PHT008 Photosensitive Epilepsy 39 0.030
1009
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 35 0.030
1010
NRM021 Neurometabolic Disorder Due to Serine Deficiency 15 0.030
1011
LRN002 Laron Syndrome 62 0.029
1012
P TST021 Testicular Germ Cell Tumor 60 0.029
1013
ACS001 Acoustic Neuroma 56 0.029
1014
P RST002 Restrictive Cardiomyopathy 56 0.029
1015
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.029
1016
ONC002 Onchocerciasis 52 0.029
1017
PRN009 Paranoid Schizophrenia 50 0.029
1018
P MST002 Mast-Cell Leukemia 49 0.029
1019
OPD001 Opioid Abuse 46 0.029
1020
IMM003 Immunoglobulin Alpha Deficiency 45 0.029
1021
LTH001 Lethal Midline Granuloma 44 0.029
1022
CLN003 Clonorchiasis 44 0.029
1023
RFL002 Reflex Epilepsy 40 0.029
1024
DSS010 Dissociative Disorder 39 0.029
1025
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.029
1026
AKN002 Akinetic Mutism 37 0.029
1027
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 35 0.029
1028
c ART112 Arthrogryposis, Distal, Type 10 34 0.029
1029
INT065 Interstitial Keratitis 30 0.029
1030
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.028
1031
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.028
1032
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.028
1033
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.028
1034
P CNG436 Congenital Disorder of Deglycosylation 52 0.028
1035
CRB186 Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to 52 0.028
1036
c STN011 Sting-Associated Vasculopathy with Onset in Infancy 45 0.028
1037
PNT038 Peanut Allergy 45 0.028
1038
IMM064 Immunodeficiency, Common Variable, 10 44 0.028
1039
HRN003 Heroin Dependence 44 0.028
1040
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.028
1041
c HYP841 Hypoalphalipoproteinemia, Primary, 1 41 0.028
1042
c HMG001 Hemoglobin C Disease 40 0.028
1043
MLN003 Melancholia 38 0.028
1044
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.028
1045
TRC123 Trichohepatoneurodevelopmental Syndrome 25 0.028
1047
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.027
1048
ERY029 Erythermalgia, Primary 58 0.027
1049
P AMY084 Amyloidosis, Finnish Type 53 0.027
1050
MTN003 Motion Sickness 53 0.027
1051
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 53 0.027
1052
SLD003 Sialadenitis 49 0.027
1053
c SCH079 Schizophrenia 1 46 0.027
1054
c GM2006 Gm2 Gangliosidosis 45 0.027
1055
DPR002 Depersonalization Disorder 43 0.027
1056
PRS025 Presbyopia 38 0.027
1057
HYP110 Hyperproinsulinemia 37 0.027
1058
HYP041 Hypochondrogenesis 37 0.027
1059
c DMN005 Diamond-Blackfan Anemia 2 25 0.027
1060
c MJR014 Major Depressive Disorder 2 18 0.027
1061
ACT049 Acute Disseminated Encephalomyelitis 51 0.027
1062
c CNG389 Congenital Disorder of Glycosylation, Type Iim 49 0.027
1063
LCR004 La Crosse Encephalitis 37 0.027
1064
c BNG093 Benign Teratoma 37 0.027
1065
CLR012 Clear Cell Adenofibroma 29 0.027
1066
CYS015 Cystadenofibroma 27 0.027
1067
BRT037 Brittle Diabetes 25 0.027
1068
c INF186 Infectious Encephalitis 21 0.027
1069
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.026
1070
c PRM196 Premature Ovarian Failure 1 67 0.026
1071
BDD001 Budd-Chiari Syndrome 63 0.026
1072
EPD002 Epidermolytic Hyperkeratosis 56 0.026
1073
MCR141 Mucormycosis 56 0.026
1074
DNT005 Dentatorubral-Pallidoluysian Atrophy 54 0.026
1075
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 52 0.026
1076
VSC006 Vascular Cancer 51 0.026
1077
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.026
1078
CNT025 Central Pontine Myelinolysis 46 0.026
1079