Search results for Insulin aspart

948 hits were found for Insulin aspart

# Family MCID Name MIFTS Score
1
HYP056 Hypoglycemia 66 1.229
2
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 1.215
3
P DBT009 Diabetes Mellitus 64 1.165
4
c DBT099 Diabetes Mellitus, Type I 65 0.918
5
INS024 Insulin-Like Growth Factor I 79 0.853
6
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.769
7
HYP066 Hyperglycemia 61 0.722
8
HYP060 Hyperinsulinism 54 0.700
9
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.518
10
GLC003 Glucose Intolerance 54 0.462
11
FTT001 Fatty Liver Disease 61 0.405
12
P ENC004 Encephalitis 61 0.392
13
P LVR013 Liver Disease 68 0.388
14
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.387
15
LPD008 Lipid Metabolism Disorder 62 0.379
16
GST033 Gestational Diabetes 61 0.349
17
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.343
18
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.315
19
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.309
20
OCL069 Ocular Motor Apraxia 51 0.308
21
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.308
22
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.308
23
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.307
24
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.307
25
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.307
26
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.307
27
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.307
28
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.307
29
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.307
30
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.307
31
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.304
32
LVR012 Liver Cirrhosis 62 0.298
33
INS001 Insulinoma 60 0.290
34
c HYP595 Hypertension, Essential 84 0.284
35
P KDN018 Kidney Disease 72 0.279
36
P ALZ034 Alzheimer Disease 88 0.270
37
48X005 48,xyyy 39 0.266
38
ATM095 Autoimmune Disease 62 0.264
39
ATH013 Atherosclerosis Susceptibility 65 0.255
40
P MCR115 Microvascular Complications of Diabetes 5 66 0.252
41
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.250
42
P HYP750 Hypertriglyceridemia, Familial 62 0.248
43
P CRN300 Coronary Heart Disease 1 63 0.242
44
HLX001 Helix Syndrome 47 0.240
45
P BRS047 Breast Cancer 97 0.240
46
P VSC007 Vascular Disease 63 0.236
47
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.235
48
P TRT010 Teratoma 52 0.232
49
ALL026 Allergic Hypersensitivity Disease 62 0.230
50
P ENC018 Encephalopathy 61 0.230
51
PRT037 Pertussis 65 0.227
52
P NRP001 Neuropathy 56 0.221
53
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.221
54
P TRN020 Turner Syndrome 67 0.218
55
NNL006 Non-Alcoholic Steatohepatitis 54 0.218
56
c RHB024 Rhabdomyosarcoma 2 67 0.210
57
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.209
58
ACN002 Acanthosis Nigricans 60 0.208
59
c HPT001 Hepatitis C 62 0.208
60
P CRD246 Cardiovascular System Disease 57 0.206
61
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.202
62
ISC004 Ischemia 58 0.201
63
P NRB001 Neuroblastoma 72 0.198
64
P SZR006 Seizure Disorder 56 0.197
65
c ACT075 Acute Myocardial Infarction 57 0.196
66
P CLR023 Colorectal Cancer 99 0.194
67
P HPT023 Hepatocellular Carcinoma 100 0.192
68
c CHR684 Chronic Kidney Disease 70 0.192
69
P HYP086 Hypothyroidism 69 0.190
70
DPR016 Depression 63 0.187
71
VSL002 Visual Epilepsy 59 0.187
72
LPP008 Lipoprotein Quantitative Trait Locus 62 0.186
73
HPT004 Hepatic Coma 45 0.184
74
P MYC007 Myocardial Infarction 70 0.183
75
c HPT073 Hepatitis C Virus 72 0.182
76
HPT019 Hepatic Encephalopathy 60 0.178
77
DWN001 Down Syndrome 70 0.178
78
MNT002 Mental Depression 58 0.177
79
P SCH015 Schizophrenia 74 0.176
80
P PRS040 Prostate Cancer 97 0.176
81
ATX019 Ataxia with Vitamin E Deficiency 42 0.176
82
P HRT032 Heart Disease 75 0.175
83
c PRC016 Pre-Eclampsia 63 0.175
84
c HYP836 Hypercholesterolemia, Familial, 1 73 0.173
85
P PNC035 Pancreatic Cancer 84 0.171
86
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.170
87
END086 End Stage Renal Disease 51 0.169
88
ADL002 Adult Syndrome 70 0.167
89
NTR005 Nutritional Deficiency Disease 62 0.167
90
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.164
91
DBT010 Diabetic Neuropathy 54 0.163
92
CYT002 Cytokine Deficiency 42 0.162
93
c ATM075 Autoimmune Encephalitis 38 0.161
94
ART140 Arteries, Anomalies of 52 0.160
95
CNG034 Congestive Heart Failure 69 0.159
96
P PRD008 Periodontitis 64 0.159
97
CRB039 Cerebrovascular Disease 67 0.159
98
ATN005 Autonomic Dysfunction 46 0.157
99
HYP005 Hypokalemia 55 0.156
100
P HYP076 Hyperthyroidism 55 0.156
101
P MJR001 Major Depressive Disorder 68 0.155
102
CYS001 Cystic Fibrosis 81 0.155
103
HYP266 Hypoxia 57 0.155
104
c PRM038 Primary Agammaglobulinemia 44 0.155
105
ADN018 Adenoma 59 0.154
106
ATN004 Autonomic Neuropathy 45 0.152
107
OST159 Osteogenic Sarcoma 66 0.152
108
P LTR001 Lateral Sclerosis 54 0.149
109
P HPT021 Hepatitis 67 0.149
110
P PRP019 Peripheral Nervous System Disease 58 0.148
111
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.148
112
P BPL003 Bipolar Disorder 56 0.145
113
47X002 47,xyy 49 0.144
114
c MJR024 Major Affective Disorder 9 41 0.144
115
c MJR022 Major Affective Disorder 8 38 0.144
116
P MTR004 Maturity-Onset Diabetes of the Young 65 0.143
117
CHL014 Cholera 59 0.143
118
P GLM045 Glioma 63 0.143
119
RCK004 Rickets 68 0.143
120
STR067 Stroke, Ischemic 81 0.143
121
P ADN016 Adenocarcinoma 64 0.142
122
LPT014 Leptin Deficiency or Dysfunction 74 0.142
123
ALC007 Alcohol Dependence 66 0.141
124
GLL048 Glial Tumor 45 0.140
125
CRB004 Cerebral Artery Occlusion 45 0.140
126
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.140
127
BRN071 Brain Injury 49 0.140
128
P PHC003 Pheochromocytoma 71 0.140
129
P HNT016 Huntington Disease 72 0.139
130
PRD004 Prediabetes Syndrome 47 0.138
131
TTN003 Tetanus 65 0.137
132
ADR040 Adrenal Gland Pheochromocytoma 46 0.137
133
TRM010 Traumatic Brain Injury 51 0.136
134
P LNG032 Lung Cancer 98 0.136
135
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.136
136
HMN044 Human Immunodeficiency Virus Type 1 71 0.135
137
OST012 Osteoarthritis 78 0.134
138
PNG002 Pain Agnosia 51 0.134
139
P SLP006 Sleep Apnea 69 0.134
140
c VRL010 Viral Hepatitis 52 0.133
141
AGN016 Aging 56 0.132
142
P AMY004 Amyloidosis 70 0.132
143
PPL052 Papillomatosis, Confluent and Reticulated 33 0.131
144
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.130
145
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.130
146
SPN186 Spinal Cord Injury 60 0.129
147
c SYS001 Systemic Lupus Erythematosus 86 0.129
148
c MCR129 Microvascular Complications of Diabetes 1 66 0.127
149
P ART021 Arteriosclerosis 54 0.127
150
ANX004 Anoxia 40 0.127
151
URM002 Uremia 49 0.125
152
P GRV001 Graves' Disease 55 0.125
153
BNR002 Bone Resorption Disease 48 0.124
154
MDD011 Mood Disorder 62 0.124
155
PRP027 Peripheral Vascular Disease 71 0.124
156
P PNC044 Pancreatitis 61 0.123
157
P OVR042 Ovarian Cancer 88 0.122
158
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.122
159
P TRM003 Tremor 54 0.122
160
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.120
161
P ALC033 Alcohol Use Disorder 58 0.120
162
P DMN002 Dementia 66 0.120
163
P DRR001 Diarrhea 55 0.120
164
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.120
165
GLB015 Glioblastoma Multiforme 75 0.120
166
HYP080 Hypogonadism 50 0.119
167
HRW001 Hair Whorl 36 0.118
168
P HRP006 Herpes Simplex 65 0.117
169
MTB004 Metabolic Acidosis 50 0.117
170
P MSC003 Muscular Atrophy 52 0.116
171
P OVR082 Overgrowth Syndrome 50 0.114
172
P CHR345 Chronic Pain 44 0.113
173
P CRD119 Cardiac Arrest 67 0.113
174
LNG099 Lung Disease 60 0.112
175
IMM167 Immune Deficiency Disease 78 0.111
176
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.110
177
P CTR002 Cataract 60 0.110
178
ANR007 Anorexia Nervosa 63 0.109
179
P MSC005 Muscular Dystrophy 66 0.108
180
P ECL001 Eclampsia 50 0.108
181
LRN002 Laron Syndrome 62 0.107
182
P ATS364 Autism 70 0.106
183
P MYP004 Myopathy 70 0.106
184
ANX010 Anxiety 73 0.106
185
THY029 Thyroid Carcinoma 59 0.105
186
c ACT027 Acute Pancreatitis 60 0.105
187
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.105
188
P INF032 Infertility 57 0.105
189
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.105
190
c HPT016 Hepatitis B 59 0.104
191
DWR001 Dwarfism 44 0.104
192
c MGR028 Migraine with or Without Aura 1 67 0.104
193
PRS045 Prostatic Hypertrophy 53 0.104
194
PRS021 Prostatic Adenoma 51 0.104
195
PRS129 Prostatic Hyperplasia, Benign 49 0.104
196
P HYP069 Hyperparathyroidism 63 0.103
197
P OVR049 Ovarian Disease 52 0.103
198
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.103
199
CHL079 Children's Interstitial Lung Disease 26 0.102
200
HYP014 Hyperuricemia 52 0.102
201
P PSR002 Psoriasis 62 0.102
202
PRT013 Portal Hypertension 59 0.101
203
P LCT001 Lactic Acidosis 51 0.101
204
PST011 Pustulosis of Palm and Sole 52 0.101
205
HMS001 Hemosiderosis 54 0.101
206
BRT037 Brittle Diabetes 25 0.101
207
P LPS004 Lupus Erythematosus 61 0.101
208
P PLY019 Polyneuropathy 56 0.100
209
P RRH023 Rare Hereditary Hemochromatosis 41 0.100
210
P LKM002 Leukemia 68 0.100
211
SBC016 Subacute Delirium 44 0.100
212
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.100
213
c FML035 Familial Hyperlipidemia 55 0.100
214
P RTN018 Retinal Disease 53 0.100
215
P LKM062 Leukemia, Acute Lymphoblastic 69 0.099
216
ACQ007 Acquired Immunodeficiency Syndrome 60 0.099
217
P TMP001 Temporal Lobe Epilepsy 50 0.099
218
AMN003 Amnestic Disorder 54 0.099
219
STT001 Status Epilepticus 60 0.099
220
HDN002 Head Injury 46 0.099
221
P LNG064 Lung Cancer Susceptibility 3 78 0.099
222
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.099
223
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.098
224
ANG054 Angina Pectoris 66 0.098
225
c ATS007 Autism Spectrum Disorder 67 0.097
226
P CND004 Candidiasis 58 0.096
227
HYP081 Hypolipoproteinemia 51 0.096
228
c ACT071 Acute Kidney Failure 60 0.096
229
SVR004 Severe Combined Immunodeficiency 73 0.095
230
IMP005 Impotence 52 0.095
231
GLC008 Glucose Metabolism Disease 40 0.094
232
DFC004 Deficiency Anemia 70 0.093
233
PSY004 Psychotic Disorder 67 0.093
234
STM007 Stomatitis 50 0.093
235
TXC005 Toxic Shock Syndrome 62 0.092
236
ETN001 Eating Disorder 60 0.092
237
IRN002 Iron Metabolism Disease 57 0.092
238
BLR008 Bilirubin Metabolic Disorder 57 0.092
239
VSC002 Vascular Dementia 57 0.091
240
c HPT003 Hepatitis a 62 0.091
241
FBR047 Fibromyalgia 58 0.091
242
c ATR087 Atrial Standstill 1 75 0.091
243
P RTN024 Retinoblastoma 73 0.090
244
c FML008 Familial Retinoblastoma 53 0.090
245
END040 Endogenous Depression 55 0.090
246
CHL068 Cholestasis 61 0.090
247
HYP026 Hypoglycemic Coma 36 0.090
248
PTT037 Pituitary Tumors 44 0.089
249
P MLT020 Multiple Sclerosis 72 0.089
250
PPT005 Peptic Ulcer Disease 59 0.089
251
HMC014 Homocysteinemia 53 0.089
252
TRN015 Transient Cerebral Ischemia 63 0.088
253
CLR108 Colorectal Adenoma 64 0.088
254
c SML038 Small Cell Cancer of the Lung 65 0.088
255
VRC005 Varicose Veins 60 0.087
257
ALL014 Allergic Encephalomyelitis 38 0.087
258
FTL021 Fetal Macrosomia 42 0.087
259
c WLM018 Wilms Tumor 5 61 0.087
260
P SLP005 Sleep Disorder 59 0.086
261
c GRV008 Graves Disease 1 56 0.086
262
c PCH010 Pachyonychia Congenita 3 44 0.086
263
c HMC039 Hemochromatosis, Type 1 74 0.086
264
SRC014 Sarcoma 65 0.086
265
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.085
266
SQM006 Squamous Cell Carcinoma 60 0.085
267
PLC008 Placenta Disease 50 0.085
268
c ACT134 Acute Liver Failure 56 0.085
269
P END084 Endocrine System Disease 45 0.084
270
HYP110 Hyperproinsulinemia 37 0.084
271
P PRK057 Parkinson Disease, Late-Onset 78 0.084
272
MYL069 Myeloma, Multiple 85 0.084
273
HYP020 Hyperprolactinemia 64 0.084
274
P RSP003 Respiratory Failure 74 0.083
275
P AST007 Astrocytoma 51 0.083
276
ATS010 Autosomal Recessive Disease 48 0.083
277
BRN004 Brain Edema 56 0.083
278
P GST053 Gastric Cancer 83 0.083
279
AST005 Asthma 76 0.083
280
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.082
281
49X006 49, Xxxxy Syndrome 41 0.082
282
PLY150 Polykaryocytosis Inducer 31 0.082
283
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.081
284
P ALP008 Alopecia 54 0.081
285
P DYS154 Dystonia 65 0.081
286
P BND020 Bone Disease 59 0.081
287
KHL003 Kohlschutter-Tonz Syndrome 65 0.081
288
P EXN002 Exanthem 57 0.080
289
NRT001 Neurotic Disorder 53 0.080
290
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.080
291
c PRD040 Periodontitis, Chronic 53 0.080
292
MCS002 Mucositis 56 0.080
293
ADG002 Audiogenic Seizures 25 0.080
294
P URT039 Urticaria 58 0.079
295
P THL005 Thalassemia 60 0.079
296
P INF037 Inflammatory Bowel Disease 54 0.079
297
GNG013 Gingivitis 59 0.079
298
ATM052 Autoimmune Disease 1 37 0.078
299
P CLC063 Celiac Disease 1 66 0.078
300
P NTR004 Neutropenia 63 0.078
301
P BCL017 B-Cell Lymphoma 58 0.077
302
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.077
303
P EPL164 Epilepsy 71 0.077
304
APH002 Aphasia 57 0.077
305
DBT002 Diabetic Autonomic Neuropathy 41 0.076
306
PRT036 Peritonitis 64 0.076
307
P CHN012 Chondrosarcoma 56 0.076
308
HPT022 Hepatoblastoma 56 0.076
309
P GLM007 Glomerulonephritis 57 0.076
310
PRT038 Protein-Energy Malnutrition 54 0.076
311
GTR002 Goiter 53 0.076
312
P HDC001 Headache 57 0.076
313
P MTR014 Motor Neuron Disease 65 0.076
314
c BRN108 Branchiootic Syndrome 1 62 0.075
315
P FBR017 Fibrosarcoma 56 0.075
316
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.075
317
PLM010 Pulmonary Edema 54 0.075
318
CHC001 Chickenpox 60 0.075
319
OBS002 Obsessive-Compulsive Disorder 68 0.074
320
SPN035 Spindle Cell Sarcoma 53 0.074
321
CNS004 Constipation 58 0.074
322
DMY004 Demyelinating Disease 52 0.074
323
PRP016 Paraplegia 52 0.073
324
P MYL006 Myeloid Leukemia 60 0.073
325
RTN003 Retinal Ischemia 50 0.073
326
P DYS021 Dysautonomia 39 0.073
327
P ATX030 Ataxia-Telangiectasia 82 0.073
328
P RTT002 Rett Syndrome 80 0.073
329
P BRS044 Breast Adenocarcinoma 59 0.073
330
c HYP272 Hypercholesterolemia, Familial, 3 44 0.072
331
DPH001 Diphtheria 60 0.072
332
P ART022 Arthritis 69 0.072
333
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 53 0.072
334
PNC129 Pancreatic Adenocarcinoma 68 0.072
335
P PLM036 Pulmonary Fibrosis 65 0.072
336
PLM001 Pulmonary Tuberculosis 69 0.072
337
P LYM118 Lymphoma 68 0.072
338
RTN020 Retinal Vascular Disease 46 0.072
339
VCC001 Vaccinia 49 0.072
340
P MLN008 Melanoma 69 0.071
341
APN008 Apnea, Obstructive Sleep 64 0.071
342
P BLD134 Bladder Cancer 79 0.070
343
ANR040 Aneurysm 59 0.070
344
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 55 0.070
345
CRD137 Cardiogenic Shock 47 0.070
346
P SBS003 Substance Abuse 55 0.070
347
P MJR007 Major Affective Disorder 1 43 0.070
348
ALC006 Alcoholic Hepatitis 61 0.069
349
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.069
350
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.068
351
c LKM061 Leukemia, Acute Myeloid 84 0.068
352
GST020 Gastric Antral Vascular Ectasia 41 0.068
353
GST037 Gastroparesis 54 0.068
354
c SCN007 Secondary Hyperparathyroidism 51 0.068
355
EYD002 Eye Disease 58 0.068
356
P RCT021 Rectum Cancer 52 0.068
357
HYP017 Hypophosphatemia 50 0.068
358
ARG004 Argyria 27 0.068
359
P KDN017 Kidney Cancer 60 0.067
360
P TBR001 Tuberous Sclerosis 70 0.067
361
c FNC043 Fanconi Anemia, Complementation Group E 62 0.067
362
DRM006 Dermatitis 61 0.067
363
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 50 0.067
364
SPS057 Spasticity 45 0.067
365
NRT004 Neuritis 52 0.066
366
ERY051 Erythroleukemia, Familial 56 0.066
367
RDN001 Reading Disorder 40 0.066
368
c DLT002 Dilated Cardiomyopathy 79 0.066
369
P MYP006 Myopia 55 0.065
370
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.065
371
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.065
372
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.065
373
SCH012 Schizoaffective Disorder 50 0.065
374
P CNR004 Cone-Rod Dystrophy 2 73 0.064
375
c SVR005 Severe Pre-Eclampsia 50 0.064
376
THY030 Thyroid Gland Disease 52 0.064
377
MNG006 Monogenic Diabetes 46 0.064
378
ESP002 Esophageal Varix 51 0.064
379
VRL011 Viral Infectious Disease 61 0.064
380
TLN003 Telangiectasis 52 0.064
381
P MYC033 Myoclonus 46 0.063
382
LYM019 Lymphosarcoma 46 0.063
383
c DRR009 Diarrhea 6 46 0.063
384
ART016 Aortic Aneurysm 69 0.063
385
DSS008 Disease of Mental Health 58 0.063
386
P ATR011 Atrial Fibrillation 66 0.063
387
MCL006 Macular Retinal Edema 55 0.063
388
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.063
389
PTT009 Pituitary Gland Disease 54 0.063
390
PTH003 Pathologic Nystagmus 52 0.062
391
CRT015 Carotid Artery Occlusion 45 0.062
392
P MDL005 Medulloblastoma 77 0.062
393
CRH001 Crohn's Disease 74 0.062
394
PRT058 Pure Autonomic Failure 59 0.062
395
c ACT073 Acute Leukemia 58 0.062
396
P FTL001 Fetal Alcohol Syndrome 57 0.062
397
ESP021 Esophageal Cancer 90 0.062
398
c MJR008 Major Affective Disorder 2 35 0.062
399
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.062
400
c GLL024 Gallbladder Disease 1 53 0.061
401
P PRC019 Precocious Puberty 46 0.061
402
BCT022 Bacterial Infectious Disease 56 0.061
403
P GLM040 Glioma Susceptibility 1 81 0.061
404
P PLY018 Polycythemia 56 0.061
405
PPL022 Papilloma 54 0.061
406
CHL004 Cholelithiasis 49 0.061
407
MLR004 Malaria 81 0.061
408
CHR073 Choreatic Disease 52 0.061
409
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.061
410
c MJR023 Major Affective Disorder 7 33 0.061
411
c MJR003 Major Affective Disorder 6 33 0.061
412
c MJR006 Major Affective Disorder 5 33 0.061
413
c MJR004 Major Affective Disorder 4 28 0.061
414
P BNG032 Benign Mesothelioma 46 0.061
415
c LKM005 Leukemia, T-Cell, Chronic 34 0.060
416
BRK010 Burkitt Lymphoma 67 0.060
417
P HYP098 Hypereosinophilic Syndrome 67 0.060
418
GLS018 Glass Syndrome 57 0.060
419
SFT003 Soft Tissue Sarcoma 56 0.060
420
MST005 Mastitis 53 0.060
421
c SCL052 Scleroderma, Familial Progressive 61 0.060
422
HLC007 Helicobacter Pylori Infection 59 0.060
423
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.060
424
WST001 West Syndrome 61 0.060
425
P RTN016 Retinal Degeneration 53 0.059
426
P PRS038 Personality Disorder 65 0.059
427
SPL018 Splenomegaly 48 0.059
428
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.059
429
P RBL001 Rubella 59 0.059
430
P MCR010 Microcephaly 59 0.059
431
THR024 Thrombosis 57 0.059
432
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.059
433
ORL015 Oral Squamous Cell Carcinoma 43 0.059
434
P MLN007 Male Infertility 55 0.059
435
P DBT005 Diabetes Insipidus 55 0.059
436
P LKD001 Leukodystrophy 59 0.059
437
NRL016 Neural Tube Defects 82 0.059
438
P PRM006 Primary Biliary Cirrhosis 62 0.059
439
JVN026 Jeavons Syndrome 24 0.059
440
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.058
441
PST021 Postpartum Depression 50 0.058
442
P OBS001 Obstructive Jaundice 50 0.058
443
SKN016 Skin Disease 63 0.058
444
THR013 Thoracic Outlet Syndrome 54 0.058
446
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.058
447
CRD223 Cardiac Arrhythmia 60 0.058
449
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.058
450
c ATM011 Autoimmune Hepatitis 63 0.058
451
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.058
452
WTH001 Withdrawal Disorder 48 0.057
453
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.057
454
P VSC018 Visceral Steatosis 33 0.057
455
CHG001 Chagas Disease 66 0.057
456
LSH001 Leishmaniasis 63 0.057
457
P KLZ004 Kala-Azar 1 41 0.057
458
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.057
459
IRN001 Iron Deficiency Anemia 59 0.057
460
KRT008 Keratopathy 47 0.057
461
P HYP265 Hypotonia 43 0.057
462
c PRG106 Progressive Muscular Dystrophy 33 0.057
463
P MLT074 Multiple Endocrine Neoplasia 56 0.056
464
SNS003 Sensory Peripheral Neuropathy 54 0.056
465
BCK003 Background Diabetic Retinopathy 46 0.056
466
P CTR177 Citrullinemia, Type Ii, Adult-Onset 57 0.056
467
c VRL007 Viral Encephalitis 51 0.056
468
CRT013 Carotid Stenosis 50 0.056
469
CHL065 Cholangiocarcinoma 68 0.056
470
INT079 Intrahepatic Cholangiocarcinoma 51 0.056
471
P ANR048 Aniridia 1 63 0.056
472
EMB004 Embryonal Carcinoma 56 0.056
473
HYP781 Hypoascorbemia 51 0.056
474
c SVR001 Severe Acute Respiratory Syndrome 62 0.056
475
ALV005 Alveolar Soft Part Sarcoma 61 0.056
476
P RHN004 Rhinitis 57 0.056
477
GST040 Gastric Adenocarcinoma 70 0.055
478
P CRB088 Cerebral Atrophy 37 0.055
479
MYL009 Myelodysplastic Syndrome 70 0.055
480
P PNM007 Pneumonia 68 0.055
481
P SHR001 Short Bowel Syndrome 53 0.055
482
P OVR046 Ovarian Cyst 47 0.055
483
P LMY004 Leiomyosarcoma 63 0.055
484
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.055
485
c INF145 Infantile Liver Failure Syndrome 1 50 0.054
486
P NSP012 Nasopharyngeal Carcinoma 66 0.054
487
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.054
488
ULC004 Ulcerative Colitis 73 0.054
489
NSP002 Nasopharyngitis 43 0.054
490
c CHR682 Chronic Bilirubin Encephalopathy 39 0.054
491
INT002 Intermittent Claudication 61 0.054
492
DNT012 Dental Caries 53 0.054
493
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.054
494
P VSC011 Vasculitis 62 0.053
495
MSL001 Measles 62 0.053
496
KRT009 Keratosis 51 0.053
497
SQM002 Squamous Cell Papilloma 46 0.053
498
c THR092 Thrombophilia Due to Thrombin Defect 73 0.053
499
LRN003 Learning Disability 49 0.053
500
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.053
501
P PLM037 Pulmonary Hypertension 67 0.053
502
P PLY014 Polycystic Kidney Disease 62 0.053
503
NRN004 Neuroendocrine Tumor 55 0.052
504
PRP030 Purpura 54 0.052
505
DBT006 Diabetic Macular Edema 48 0.052
506
P THR014 Thrombocytopenia 67 0.052
507
P ADL010 Adult Respiratory Distress Syndrome 65 0.052
508
CHL123 Chlamydia 59 0.052
509
ALC009 Alcoholic Liver Cirrhosis 53 0.052
510
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.052
511
c MLG068 Malignant Glioma 46 0.052
512
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.051
513
P SKN015 Skin Carcinoma 66 0.051
514
c WLM013 Wilms Tumor 1 65 0.051
515
NRM005 Neuromuscular Disease 64 0.051
516
HRT012 Heart Valve Disease 53 0.051
517
SXL003 Sexual Disorder 47 0.051
518
P GLC113 Galactosemia I 64 0.051
519
TRD006 Tardive Dyskinesia 54 0.051
520
c BTT014 Beta-Thalassemia 74 0.051
521
OST017 Osteomyelitis 64 0.051
522
P ALP009 Alopecia Areata 60 0.051
523
NRN001 Neuroendocrine Carcinoma 47 0.051
524
PST028 Post-Traumatic Stress Disorder 58 0.050
525
HMP005 Hemiplegia 55 0.050
526
ORL011 Oral Cancer 60 0.050
527
DMP001 Dumping Syndrome 44 0.050
528
P MYS003 Myasthenia Gravis 68 0.049
529
GST092 Gastroesophageal Reflux 67 0.049
530
CHL067 Cholecystitis 57 0.049
531
PRL032 Perlman Syndrome 57 0.049
532
BRT054 Brittle Bone Disorder 72 0.049
533
PYR009 Pyridoxine Deficiency Anemia 34 0.049
534
P GRF003 Graft-Versus-Host Disease 72 0.049
535
BRR014 Barrett Esophagus 65 0.049
536
STF001 Stiff-Person Syndrome 60 0.049
537
LYM027 Lymphopenia 58 0.049
538
ENT011 Enterocolitis 51 0.049
539
IGG001 Iga Glomerulonephritis 48 0.049
540
RTN023 Retinitis 46 0.049
541
NRR001 Neuroretinitis 42 0.049
542
ATX010 Ataxia Neuropathy Spectrum 34 0.049
543
ACT064 Acute Necrotizing Encephalitis 33 0.049
544
PST092 Posttransplant Acute Limbic Encephalitis 29 0.049
545
BLD137 Blood Group--Ahonen 16 0.049
546
P OPT006 Optic Nerve Disease 60 0.048
547
LYM040 Lymphoblastic Lymphoma 54 0.048
548
CVD001 Covid-19 44 0.048
549
HMP009 Haemophilus Influenzae 43 0.048
550
IRR002 Irritable Bowel Syndrome 65 0.048
551
THY111 Thyroid Carcinoma, Familial Medullary 67 0.048
552
SCH014 Schistosomiasis 57 0.048
553
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.048
554
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.048
555
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.048
556
CLT003 Colitis 62 0.048
557
BLR001 Biliary Atresia 50 0.047
558
P HML002 Hemolytic Anemia 63 0.047
559
P BNC003 Bone Cancer 58 0.047
560
TXC002 Toxic Encephalopathy 53 0.047
561
CRB037 Cerebral Palsy 69 0.047
562
P HYD006 Hydrocephalus 66 0.047
563
c OPT053 Optic Atrophy 1 63 0.047
564
RTN017 Retinal Detachment 61 0.047
565
P ANT006 Antiphospholipid Syndrome 55 0.047
566
TRT001 Teratocarcinoma 45 0.047
567
LWC001 Low Compliance Bladder 43 0.047
568
WLL004 Wallerian Degeneration 39 0.047
569
BRN028 Brain Cancer 74 0.047
570
c JVN010 Juvenile Rheumatoid Arthritis 64 0.047
571
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 61 0.047
572
CRD132 Cardiac Conduction Defect 58 0.047
573
NWB001 Newborn Respiratory Distress Syndrome 58 0.047
574
NNT012 Neonatal Jaundice 53 0.047
575
CRB090 Cerebral Hypoxia 44 0.046
576
c CNG006 Congenital Hypothyroidism 64 0.046
577
P SCK005 Sickle Cell Disease 50 0.046
578
c OST080 Osteogenesis Imperfecta, Type Ii 54 0.045
579
P MYC084 Mycobacterium Tuberculosis 1 68 0.045
580
P FRN006 Frontotemporal Dementia 68 0.045
581
P PRN023 Prion Disease 57 0.045
582
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.045
583
LNG031 Lung Benign Neoplasm 51 0.045
584
P CHL066 Cholangitis 51 0.045
585
P END046 Endometritis 49 0.045
586
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.045
587
P MLG074 Malignant Mesenchymoma 40 0.045
588
OCL006 Ocular Hypertension 53 0.045
589
BCK006 Back Pain 42 0.045
590
HND015 Hand Skill, Relative 33 0.045
591
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.045
592
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.045
593
P OCL013 Oculodentodigital Dysplasia 69 0.044
594
PLM031 Poliomyelitis 64 0.044
595
PRN019 Perinatal Necrotizing Enterocolitis 59 0.044
596
TND005 Tendinitis 54 0.044
597
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 52 0.044
598
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.044
599
TRP009 Triple X Syndrome 42 0.044
600
P LPR021 Leprosy 3 69 0.044
601
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.044
602
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.044
603
c DWL002 Dowling-Degos Disease 1 58 0.043
604
CLL003 Cellulitis 54 0.043
605
P ATM019 Autoimmune Polyendocrine Syndrome 46 0.043
606
SYN036 Syncope 45 0.043
607
IMM064 Immunodeficiency, Common Variable, 10 44 0.043
608
CRY036 Cryptogenic Cirrhosis 36 0.043
609
PRT082 Preterm Premature Rupture of the Membranes 54 0.043
610
MNN009 Meningoencephalitis 49 0.042
611
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.042
612
P CNJ013 Conjunctivitis 65 0.042
613
FLR002 Filariasis 55 0.042
614
FCL014 Focal Epilepsy 54 0.042
615
P MGR003 Migraine with Aura 52 0.042
616
VLV047 Volvulus of Midgut 49 0.042
617
CCN002 Cocaine Abuse 49 0.042
618
TBC004 Tobacco Addiction 64 0.042
619
CRC021 Carcinosarcoma 62 0.042
620
P PYL005 Pyelonephritis 56 0.042
621
GST050 Gastrointestinal System Disease 56 0.042
622
c ATM024 Autoimmune Pancreatitis 55 0.042
623
SYN007 Synovitis 54 0.042
624
P HMC002 Homocystinuria 53 0.042
625
CRT016 Carotid Artery Disease 52 0.042
626
KRT002 Keratomalacia 47 0.042
627
PLC002 Plica Syndrome 36 0.042
628
HNS001 Hansen's Disease 34 0.042
629
c LKM063 Leukemia, Chronic Myeloid 72 0.042
630
P NRV007 Nervous System Disease 66 0.042
631
P GLL020 Gallbladder Disease 57 0.042
632
CYT008 Cytomegalovirus Infection 57 0.042
633
CLR030 Clear Cell Renal Cell Carcinoma 53 0.042
634
THY125 Thyroid Gland Medullary Carcinoma 50 0.042
635
MYT011 Myotonia 34 0.042
636
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.041
637
P CYS018 Cystitis 59 0.041
638
P DNG005 Dengue Virus 59 0.041
639
VGN023 Vaginitis 54 0.041
640
P CLS010 Cluster Headache 42 0.041
641
PSD088 Pseudobulbar Affect 36 0.041
642
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.040
643
P RTN008 Retinitis Pigmentosa 79 0.040
644
P FRG001 Fragile X Syndrome 70 0.040
645
P LPS002 Liposarcoma 65 0.040
646
PSR001 Psoriatic Arthritis 61 0.040
647
c JVN061 Juvenile Arthritis 60 0.040
648
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.040
649
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.040
650
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.040
651
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.040
652
TST014 Testicular Cancer 46 0.040
653
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.040
654
GST045 Gastroenteritis 59 0.040
655
P PLY041 Polymyositis 57 0.040
656
P LRY044 Larynx Cancer 55 0.040
657
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.040
658
P PNC025 Panic Disorder 53 0.040
659
DYS073 Dysphagia 50 0.040
660
ACT084 Acute Stress Disorder 47 0.040
661
CYS009 Cystadenoma 44 0.040
662
SCR011 Scrapie 39 0.040
663
c PNC108 Pancreatitis, Hereditary 70 0.039
664
CMM004 Common Variable Immunodeficiency 68 0.039
665
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.039
666
PLM033 Pulmonary Embolism 59 0.039
667
THY122 Thyroid Gland Cancer 57 0.039
668
P MTC069 Mitochondrial Disorders 56 0.039
669
MCR141 Mucormycosis 56 0.039
670
INT075 Intracranial Hypertension 53 0.039
671
ENT004 Enthesopathy 49 0.039
672
MDS022 Mediastinitis 46 0.039
673
TND004 Tendinopathy 43 0.039
674
DNC004 Diencephalic Syndrome 36 0.039
675
c RNL113 Renal Failure, Progressive, with Hypertension 34 0.039
676
c PRS136 Prostate Cancer, Hereditary, 6 33 0.039
677
c PRS130 Prostate Cancer, Hereditary, 8 32 0.039
678
P ASP006 Aspergillosis 69 0.039
679
P TXP001 Toxoplasmosis 60 0.039
680
CMP010 Complex Regional Pain Syndrome 58 0.039
681
MTH009 Mouth Disease 56 0.039
682
MYL001 Myelitis 51 0.039
683
c BSL007 Basal Cell Carcinoma 68 0.038
684
P ESP024 Esophagitis 62 0.038
685
P SCK002 Sick Sinus Syndrome 55 0.038
686
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.038
687
INF034 Infective Endocarditis 53 0.038
688
P PTS002 Ptosis 53 0.038
689
P SML001 Small Cell Carcinoma 52 0.038
690
APR001 Apraxia 52 0.038
691
TNG007 Tongue Carcinoma 51 0.038
692
CLN045 Colonic Benign Neoplasm 46 0.038
693
MDD018 Middle East Respiratory Syndrome 43 0.038
694
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 35 0.038
695
c SCK038 Seckel Syndrome 10 23 0.038
696
ANT019 Anterograde Amnesia 38 0.038
697
PRN039 Paraneoplastic Syndromes 38 0.038
698
PHN003 Phenylketonuria 75 0.037
699
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.037
700
P DRM010 Dermatomyositis 61 0.037
701
c PNS012 Paine Syndrome 61 0.037
702
P MYS005 Myositis 56 0.037
703
P FNC004 Fanconi Syndrome 50 0.037
704
AZS001 Azoospermia 50 0.037
705
MTC005 Mitochondrial Metabolism Disease 49 0.037
706
P SCL009 Sclerosing Cholangitis 48 0.037
707
P PRC031 Preeclampsia/eclampsia 1 38 0.037
708
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.037
709
CRT072 Creutzfeldt-Jakob Disease 70 0.036
710
P MNN013 Meningitis 66 0.036
711
P SYP003 Syphilis 58 0.036
712
HMG005 Hemoglobinopathy 56 0.036
713
P NRC002 Narcolepsy 52 0.036
714
PTT041 Pituitary Stalk Interruption Syndrome 50 0.036
715
c BPL002 Bipolar I Disorder 49 0.036
716
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.036
718
AMN006 Aminoaciduria 38 0.036
719
HRP008 Herpes Simiae 25 0.036
720
SKN019 Skin Melanoma 68 0.036
721
c PRM196 Premature Ovarian Failure 1 67 0.036
722
P LNG028 Long Qt Syndrome 66 0.036
723
ERY029 Erythermalgia, Primary 58 0.036
724
c CHL119 Cholangitis, Primary Sclerosing 57 0.036
725
P END033 Endocarditis 57 0.036
726
INT030 Intracranial Aneurysm 56 0.036
727
P PLM034 Pulmonary Emphysema 55 0.036
728
BRN014 Bronchopneumonia 54 0.036
729
CRH005 Crohn's Colitis 53 0.036
730
CRN027 Corneal Neovascularization 47 0.036
731
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.036
732
PLY100 Polyploidy 40 0.036
733
c PRG020 Paragangliomas 3 39 0.036
734
ADN011 Adenoid Cystic Carcinoma 70 0.035
735
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.035
736
OPT003 Opiate Dependence 50 0.035
737
P MGR001 Migraine Without Aura 49 0.035
738
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 42 0.035
739
MNN017 Mononeuropathy 42 0.035
740
SCK003 Sickle Cell Anemia 74 0.034
741
P OLG002 Oligodendroglioma 67 0.034
742
c MCL013 Mucolipidosis Iv 66 0.034
744
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.034
745
P INT068 Intestinal Disease 53 0.034
746
BWN001 Bowen-Conradi Syndrome 52 0.034
747
ILS001 Ileus 51 0.034
748
PRN009 Paranoid Schizophrenia 50 0.034
749
P BRB001 Beriberi 46 0.034
750
MXD026 Mixed Glioma 45 0.034
751
TST015 Testicular Disease 43 0.034
752
P FNC034 Fanconi Renotubular Syndrome 2 40 0.034
753
CRB086 Cerebral Aneurysms 40 0.034
754
ACT228 Acute Radiation Syndrome 29 0.034
755
MST020 Mast Cell Activation Syndrome 26 0.034
756
ALL003 Allergic Rhinitis 67 0.033
757
KRT019 Keratitis, Hereditary 65 0.033
758
KWS002 Kawasaki Disease 65 0.033
759
P EHL001 Ehlers-Danlos Syndrome 58 0.033
760
c BSL024 Basal Cell Carcinoma 1 56 0.033
761
SPN041 Spinal Cord Disease 56 0.033
762
c HPT007 Hepatitis E 53 0.033
763
P OLV001 Olivopontocerebellar Atrophy 51 0.033
764
ACT049 Acute Disseminated Encephalomyelitis 51 0.033
765
BLL004 Bullous Keratopathy 49 0.033
766
OLF005 Olfactory Neuroblastoma 48 0.033
767
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.033
768
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.032
769
PNM008 Pneumothorax 56 0.032
770
DFF005 Diffuse Large B-Cell Lymphoma 55 0.032
771
c SPN294 Spinocerebellar Ataxia 1 53 0.032
772
ACR041 Acromelic Frontonasal Dysostosis 52 0.032
773
TRY001 Trypanosomiasis 50 0.032
774
P MTC133 Mitochondrial Myopathy 49 0.032
775
SLD003 Sialadenitis 49 0.032
776
TST044 Testicular Torsion 47 0.032
777
OLG001 Oligospermia 45 0.032
778
IMM003 Immunoglobulin Alpha Deficiency 45 0.032
779
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.032
780
MYF002 Myofascial Pain Syndrome 42 0.032
781
c HYP841 Hypoalphalipoproteinemia, Primary, 1 41 0.032
782
GRM004 Germinoma 40 0.032
783
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.032
784
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.032
785
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.032
786
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.032
787
CYT018 Cytochrome P450 2d6 Variant 27 0.032
788
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.032
789
VLK001 Volkmann Contracture 25 0.032
790
INT146 Intervertebral Disc Disease 63 0.030
791
ORL005 Oral Candidiasis 56 0.030
792
BRD004 Borderline Personality Disorder 53 0.030
793
FNG017 Fungal Infectious Disease 53 0.030
794
P FBR031 Febrile Seizures 53 0.030
795
P RNL007 Renal Tubular Acidosis 51 0.030
796
MCP006 Mucoepidermoid Carcinoma 50 0.030
797
SNT005 Sinoatrial Node Disease 49 0.030
798
MLT006 Multidrug-Resistant Tuberculosis 48 0.030
799
CRD043 Ceroid Storage Disease 44 0.030
800
c ART028 Aortic Aneurysm, Familial Thoracic 4 38 0.030
801
MTB016 Metabolic Myopathy 32 0.030
802
PRN071 Parenteral Nutrition-Associated Cholestasis 25 0.030
803
MYL005 Myelofibrosis 70 0.030
804
c INF071 Inflammatory Bowel Disease 1 67 0.030
805
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.030
806
P TST021 Testicular Germ Cell Tumor 60 0.030
807
RHM001 Rheumatic Fever 60 0.030
808
P CHR285 Chronic Myelomonocytic Leukemia 60 0.030
809
GRD007 Grade Iii Astrocytoma 59 0.030
810
INC002 Inclusion Body Myositis 58 0.030
811
TNS005 Tonsillitis 57 0.030
812
CMR002 Coumarin Resistance 56 0.030
813
GNR004 Generalized Anxiety Disorder 56 0.030
814
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.030
815
DNT005 Dentatorubral-Pallidoluysian Atrophy 54 0.030
816
MMM001 Mammary Paget's Disease 53 0.030
817
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.030
818
PLM014 Pleomorphic Adenoma 52 0.030
819
CND002 Conduct Disorder 51 0.030
820
PLS009 Plasma Cell Neoplasm 51 0.030
821
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 51 0.030
822
URC002 Urea Cycle Disorder 51 0.030
823
RFR010 Refractory Anemia 48 0.030
824
THY128 Thyroid Tumor 47 0.030
825
P CRC039 Coarctation of Aorta 47 0.030
826
TTH006 Tooth Disease 46 0.030
827
BRN032 Brain Glioma 45 0.030
828
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.030
829
NRF003 Neurofibrosarcoma 43 0.030
830
MLN003 Melancholia 38 0.030
831
SCR039 Scorpion Envenomation 38 0.030
832
P EXT030 Extraosseous Chondrosarcoma 35 0.030
833
LGH007 Leigh Syndrome 70 0.027
834
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.027
835
c LNG044 Long Qt Syndrome 1 66 0.027
836
DMN031 Dementia, Lewy Body 65 0.027
837
DGR001 Digeorge Syndrome 64 0.027
838
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 0.027
839
P SPN046 Spinal Muscular Atrophy 62 0.027
840
SDD001 Sudden Infant Death Syndrome 61 0.027
841
PNM010 Pneumothorax, Primary Spontaneous 60 0.027
842
c DNG003 Dengue Disease 59 0.027
843
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 59 0.027
844
P GLL022 Guillain-Barre Syndrome 59 0.027
845
MNR012 Meniere Disease 57 0.027
846
P ICH004 Ichthyosis 54 0.027
847
CYS005 Cysticercosis 53 0.027
848
MTN003 Motion Sickness 53 0.027
849
c ACT135 Acute Graft Versus Host Disease 52 0.027
850
P HMP007 Hemophilia 51 0.027
851
THR004 Thrombocytosis 51 0.027
852
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.027
853
TLR001 Tularemia 51 0.027
854
HPT014 Hepatorenal Syndrome 50 0.027
855
c DYS119 Dystonia 9 50 0.027
856
CCN001 Cocaine Dependence 48 0.027
857
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.027
858
P BLR006 Biliary Tract Disease 47 0.027
859
MYC005 Myocardial Stunning 46 0.027
860
GRN017 Granulocytopenia 44 0.027
861
P GNG009 Gangliosidosis 44 0.027
862
P CRN024 Corneal Disease 44 0.027
863
ANP009 Anaplastic Oligodendroglioma 43 0.027
864
RFR003 Refractive Error 43 0.027
865
c MLG079 Malignant Pleural Mesothelioma 42 0.027
866
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.027
867
c HMG001 Hemoglobin C Disease 40 0.027
868
CHL039 Choledocholithiasis 38 0.027
869
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.027
870
ANG061 Angular Cheilitis 26 0.027
871
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.027
872
MRF001 Marfan Syndrome 77 0.024
873
WLS001 Wilson Disease 71 0.024
874
P TYS001 Tay-Sachs Disease 69 0.024
875
WLF001 Wolff-Parkinson-White Syndrome 66 0.024
876
P CNG001 Congenital Myasthenic Syndrome 66 0.024
877
MYL031 Myeloproliferative Neoplasm 66 0.024
878
BRK001 Brooke-Spiegler Syndrome 64 0.024
879
CYS013 Cystinuria 63 0.024
880
HMT002 Hematologic Cancer 62 0.024
881
ERL001 Early Myoclonic Encephalopathy 62 0.024
882
BLD131 Bladder Urothelial Carcinoma 62 0.024
883
WHM001 Whim Syndrome 61 0.024
884
TRG002 Trigeminal Neuralgia 60 0.024
885
DNG002 Dengue Hemorrhagic Fever 60 0.024
886
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 59 0.024
887
c CHL140 Chilblain Lupus 1 58 0.024
888
P MYM013 Moyamoya Disease 1 57 0.024
889
CHR105 Choreoacanthocytosis 57 0.024
890
c LKM070 Leukemia, Acute Monocytic 57 0.024
891
c ESS001 Essential Tremor 56 0.024
892
PRS047 Prostatitis 56 0.024
893
ACS001 Acoustic Neuroma 56 0.024
894
P PNM006 Pneumoconiosis 56 0.024
895
FLR001 Filarial Elephantiasis 55 0.024
896
PLV003 Pelvic Inflammatory Disease 55 0.024
897
WST005 West Nile Virus 54 0.024
898
BRN038 Bronchial Disease 53 0.024
899
ONC002 Onchocerciasis 52 0.024
900
RYS001 Reye Syndrome 51 0.024
901
VSC006 Vascular Cancer 51 0.024
902
NRM004 Neuroma 51 0.024
903
TRP002 Tropical Spastic Paraparesis 50 0.024
904
LPR001 Lepromatous Leprosy 50 0.024
905
P MST002 Mast-Cell Leukemia 49 0.024
906
MYL003 Myeloid Sarcoma 49 0.024
907
ACT098 Acute Erythroid Leukemia 48 0.024
908
ANT018 Anthracosis 48 0.024
909
CRN017 Coronary Thrombosis 47 0.024
910
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.024
911
P RTN014 Retinal Artery Occlusion 47 0.024
912
OPS006 Opsoclonus-Myoclonus Syndrome 47 0.024
913
NSS002 Neisseria Meningitidis Infection 47 0.024
914
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.024
915
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.024
916
P TRN034 Transverse Myelitis 45 0.024
917
c HRD039 Hereditary Amyloidosis 45 0.024
918
NRS003 Neurosyphilis 45 0.024
919
HRN003 Heroin Dependence 44 0.024
920
PRM003 Premature Ejaculation 44 0.024
921
c SPR086 Spermatogenic Failure 3 44 0.024
922
ICH002 Ichthyosis Bullosa of Siemens 43 0.024
923
DRG002 Drug-Induced Hepatitis 43 0.024
924
MST004 Mast Cell Neoplasm 42 0.024
925
SPN050 Spinocerebellar Degeneration 42 0.024
926
c PRG001 Progressive Muscular Atrophy 42 0.024
927
ASY002 Asymptomatic Neurosyphilis 41 0.024
928
BRN026 Branch Retinal Artery Occlusion 40 0.024
929
EXT006 Extrahepatic Cholestasis 39 0.024
930
HNZ004 Heinz Body Anemias 39 0.024
931
SCR015 Scarlet Fever 39 0.024
932
CVT001 Cavitary Optic Disc Anomalies 38 0.024
933
c CHR098 Chronic Pyelonephritis 38 0.024
934
HRN029 Hearing Loss, Noise-Induced 37 0.024
935
c WLM011 Wilms Tumor 6 37 0.024
936
CHL013 Cholecystolithiasis 37 0.024
937
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 35 0.024
938
CND006 Candida Glabrata 32 0.024
939
PHS025 Phosphatase, Acid, of Tissues 28 0.024
940
c ART105 Aortic Aneurysm, Familial Thoracic 7 28 0.024
941
MTH071 Methane Production 26 0.024
942
c DMN005 Diamond-Blackfan Anemia 2 25 0.024
943
SRN001 Serine Deficiency 24 0.024
944
CHR176 Chromophil Renal Cell Carcinoma 23 0.024
945
c SCH086 Schizophrenia 11 22 0.024
946
c RNG019 Ring Chromosome 3 22 0.024
947
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 17 0.024
948
NRM021 Neurometabolic Disorder Due to Serine Deficiency 15 0.024
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