Search results for Insulin human

2988 hits were found for Insulin human

# Family MCID Name MIFTS Score
1
HYP056 Hypoglycemia 66 1.059
2
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 1.004
3
INS024 Insulin-Like Growth Factor I 79 0.998
4
P DBT009 Diabetes Mellitus 64 0.880
5
HYP060 Hyperinsulinism 54 0.775
6
c DBT099 Diabetes Mellitus, Type I 65 0.733
7
HYP066 Hyperglycemia 61 0.726
8
IMM167 Immune Deficiency Disease 78 0.590
9
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.523
10
GLC003 Glucose Intolerance 54 0.513
11
P BRS047 Breast Cancer 97 0.502
12
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.493
13
HMN044 Human Immunodeficiency Virus Type 1 71 0.488
14
P PLY011 Polycystic Ovary Syndrome 56 0.457
15
P CLR023 Colorectal Cancer 99 0.454
16
LPD008 Lipid Metabolism Disorder 62 0.426
17
FTT001 Fatty Liver Disease 61 0.420
18
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.396
19
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.395
20
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.395
21
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.395
22
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.394
23
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.394
24
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.394
25
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.394
26
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.394
27
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.394
28
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.394
29
P LVR013 Liver Disease 68 0.393
30
P NRB001 Neuroblastoma 72 0.386
31
ATM095 Autoimmune Disease 62 0.376
32
ATH013 Atherosclerosis Susceptibility 65 0.365
33
GST033 Gestational Diabetes 61 0.362
34
c HYP595 Hypertension, Essential 84 0.356
35
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.355
36
P HPT023 Hepatocellular Carcinoma 100 0.353
37
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.353
38
SVR004 Severe Combined Immunodeficiency 73 0.352
39
P PRS040 Prostate Cancer 97 0.351
40
INS001 Insulinoma 60 0.351
41
P ADN016 Adenocarcinoma 64 0.350
42
CYT002 Cytokine Deficiency 42 0.350
43
P KDN018 Kidney Disease 72 0.345
44
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.337
45
P VSC007 Vascular Disease 63 0.333
46
ADN018 Adenoma 59 0.333
47
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.330
48
PRT037 Pertussis 65 0.330
49
P OVR042 Ovarian Cancer 88 0.330
50
48X005 48,xyyy 39 0.329
51
OST159 Osteogenic Sarcoma 66 0.329
52
P GLM045 Glioma 63 0.328
53
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.324
54
GLL048 Glial Tumor 45 0.320
55
P PNC035 Pancreatic Cancer 84 0.317
56
GLB015 Glioblastoma Multiforme 75 0.315
57
c MCR113 Microvascular Complications of Diabetes 3 52 0.315
58
c MCR120 Microvascular Complications of Diabetes 7 47 0.313
59
c MCR130 Microvascular Complications of Diabetes 6 41 0.312
60
c MCR133 Microvascular Complications of Diabetes 4 41 0.312
61
CRV035 Cervical Cancer 76 0.308
62
P LNG032 Lung Cancer 98 0.306
63
P HYP750 Hypertriglyceridemia, Familial 62 0.305
64
P ALZ034 Alzheimer Disease 88 0.305
65
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.305
66
LVR012 Liver Cirrhosis 62 0.299
67
P LKM002 Leukemia 68 0.295
68
OCL069 Ocular Motor Apraxia 51 0.290
69
P CRN300 Coronary Heart Disease 1 63 0.288
70
P MCR115 Microvascular Complications of Diabetes 5 66 0.286
71
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.285
72
c HPT073 Hepatitis C Virus 72 0.277
73
ACQ007 Acquired Immunodeficiency Syndrome 60 0.277
74
c PRC016 Pre-Eclampsia 63 0.276
75
ALL026 Allergic Hypersensitivity Disease 62 0.269
76
PPL022 Papilloma 54 0.263
77
SQM006 Squamous Cell Carcinoma 60 0.263
78
P NRP001 Neuropathy 56 0.263
79
HYP266 Hypoxia 57 0.259
80
P CRD246 Cardiovascular System Disease 57 0.257
81
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.256
82
P INF032 Infertility 57 0.255
83
P MLN008 Melanoma 69 0.254
84
P BLD134 Bladder Cancer 79 0.254
85
ACT088 Acute Insulin Response 41 0.253
86
c HPT001 Hepatitis C 62 0.251
87
P GST053 Gastric Cancer 83 0.249
88
P HYP086 Hypothyroidism 69 0.248
89
END057 Endometrial Cancer 74 0.248
90
SQM002 Squamous Cell Papilloma 46 0.247
91
AGN016 Aging 56 0.247
92
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.245
93
ACR007 Acromegaly 71 0.244
94
c LKM005 Leukemia, T-Cell, Chronic 34 0.244
95
c CHR684 Chronic Kidney Disease 70 0.243
96
P HRT032 Heart Disease 75 0.240
97
END086 End Stage Renal Disease 51 0.239
98
c HYP836 Hypercholesterolemia, Familial, 1 73 0.238
99
P RTN024 Retinoblastoma 73 0.238
100
c FML008 Familial Retinoblastoma 53 0.238
101
HLX001 Helix Syndrome 47 0.236
102
HYP043 Hyperandrogenism 48 0.233
103
BNR002 Bone Resorption Disease 48 0.233
104
CHL014 Cholera 59 0.233
105
CNG034 Congestive Heart Failure 69 0.233
106
ISC004 Ischemia 58 0.232
107
P PRD008 Periodontitis 64 0.230
108
LPP008 Lipoprotein Quantitative Trait Locus 62 0.227
109
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.226
110
CYS001 Cystic Fibrosis 81 0.225
111
P LNG064 Lung Cancer Susceptibility 3 78 0.222
112
THY029 Thyroid Carcinoma 59 0.221
113
P DRR001 Diarrhea 55 0.221
114
c PCH010 Pachyonychia Congenita 3 44 0.220
115
NNL006 Non-Alcoholic Steatohepatitis 54 0.219
116
ACN002 Acanthosis Nigricans 60 0.218
117
P LYM118 Lymphoma 68 0.217
118
DWN001 Down Syndrome 70 0.216
119
P TRN020 Turner Syndrome 67 0.215
120
P MYL006 Myeloid Leukemia 60 0.212
121
c PRM038 Primary Agammaglobulinemia 44 0.211
122
PRS045 Prostatic Hypertrophy 53 0.211
123
47X002 47,xyy 49 0.210
124
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.209
125
LNG099 Lung Disease 60 0.209
126
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.209
127
CRV045 Cervical Intraepithelial Neoplasia 39 0.209
128
P HRP006 Herpes Simplex 65 0.208
129
P HYP076 Hyperthyroidism 55 0.207
130
P SPP010 Suppressor of Tumorigenicity 3 51 0.206
131
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.205
132
P MYC007 Myocardial Infarction 70 0.203
133
GRW007 Growth Hormone Deficiency 46 0.202
134
PRS021 Prostatic Adenoma 51 0.201
135
P GRV001 Graves' Disease 55 0.200
136
P BCL017 B-Cell Lymphoma 58 0.199
137
PRS129 Prostatic Hyperplasia, Benign 49 0.199
138
P AST007 Astrocytoma 51 0.198
139
RCK004 Rickets 68 0.198
140
P CTR002 Cataract 60 0.197
141
NTR005 Nutritional Deficiency Disease 62 0.197
142
TTN003 Tetanus 65 0.196
143
ART140 Arteries, Anomalies of 52 0.196
144
c SML038 Small Cell Cancer of the Lung 65 0.194
145
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.194
146
c ACT075 Acute Myocardial Infarction 57 0.193
147
OST012 Osteoarthritis 78 0.193
148
ADL002 Adult Syndrome 70 0.193
149
CHR074 Choriocarcinoma 47 0.192
150
KPS004 Kaposi Sarcoma 75 0.190
151
c SYS001 Systemic Lupus Erythematosus 86 0.189
152
P LKM062 Leukemia, Acute Lymphoblastic 69 0.189
153
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.188
154
P LTR001 Lateral Sclerosis 54 0.188
155
c LKM061 Leukemia, Acute Myeloid 84 0.186
156
HRW001 Hair Whorl 36 0.185
157
MYL069 Myeloma, Multiple 85 0.185
158
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.184
159
P ENC018 Encephalopathy 61 0.184
160
P AMY004 Amyloidosis 70 0.184
161
c RHB024 Rhabdomyosarcoma 2 67 0.184
162
TXC005 Toxic Shock Syndrome 62 0.184
163
P MSC005 Muscular Dystrophy 66 0.184
164
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.182
165
SPN186 Spinal Cord Injury 60 0.182
166
P OVR082 Overgrowth Syndrome 50 0.179
167
c HPT016 Hepatitis B 59 0.179
168
SKN016 Skin Disease 63 0.177
169
P PRP019 Peripheral Nervous System Disease 58 0.177
170
CRB039 Cerebrovascular Disease 67 0.176
171
LPT014 Leptin Deficiency or Dysfunction 74 0.176
172
P HPT021 Hepatitis 67 0.176
173
CLN015 Colon Adenocarcinoma 65 0.174
174
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.174
175
P RHB003 Rhabdomyosarcoma 63 0.174
176
P OST002 Osteoporosis 74 0.174
177
P FBR017 Fibrosarcoma 56 0.173
178
HYP080 Hypogonadism 50 0.173
179
SRC014 Sarcoma 65 0.172
180
VCC001 Vaccinia 49 0.171
181
P SKN015 Skin Carcinoma 66 0.171
182
STR067 Stroke, Ischemic 81 0.171
183
P RHM011 Rheumatoid Arthritis 80 0.171
184
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.170
185
P NTR004 Neutropenia 63 0.169
186
DBT010 Diabetic Neuropathy 54 0.169
187
P SLP006 Sleep Apnea 69 0.169
188
ESP021 Esophageal Cancer 90 0.169
189
P MSC003 Muscular Atrophy 52 0.168
190
P MYP004 Myopathy 70 0.168
191
ATN004 Autonomic Neuropathy 45 0.168
192
GST045 Gastroenteritis 59 0.168
193
P GRF003 Graft-Versus-Host Disease 72 0.167
194
P INF037 Inflammatory Bowel Disease 54 0.167
195
P GLM007 Glomerulonephritis 57 0.167
196
URM002 Uremia 49 0.166
197
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.165
198
P HMN032 Human Herpesvirus 8 47 0.164
199
P PSR002 Psoriasis 62 0.163
200
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.163
201
P ART021 Arteriosclerosis 54 0.163
202
c NRF023 Neurofibromatosis, Type Ii 80 0.163
203
P ENC004 Encephalitis 61 0.161
204
P PHC003 Pheochromocytoma 71 0.160
205
P THY032 Thyroiditis 52 0.160
206
HYP005 Hypokalemia 55 0.160
207
P TRT010 Teratoma 52 0.160
208
P HYP069 Hyperparathyroidism 63 0.160
209
P ECL001 Eclampsia 50 0.159
210
P END044 Endometriosis 63 0.159
211
c ATR087 Atrial Standstill 1 75 0.158
212
BRK010 Burkitt Lymphoma 67 0.158
213
P MTR004 Maturity-Onset Diabetes of the Young 65 0.158
214
P PNC044 Pancreatitis 61 0.157
215
PTT037 Pituitary Tumors 44 0.157
216
PST011 Pustulosis of Palm and Sole 52 0.157
217
PRP027 Peripheral Vascular Disease 71 0.157
218
LSH001 Leishmaniasis 63 0.156
219
P KLZ004 Kala-Azar 1 41 0.156
220
P INF038 Influenza 68 0.156
221
DPR016 Depression 63 0.156
222
c ACT027 Acute Pancreatitis 60 0.155
223
c HNT011 Huntington Disease-Like 3 38 0.155
224
DNH001 Donohue Syndrome 62 0.155
225
ADR040 Adrenal Gland Pheochromocytoma 46 0.155
226
P EXN002 Exanthem 57 0.155
227
ERY051 Erythroleukemia, Familial 56 0.154
228
CHL123 Chlamydia 59 0.154
229
P MLN007 Male Infertility 55 0.154
230
c DLT002 Dilated Cardiomyopathy 79 0.153
231
c MCR129 Microvascular Complications of Diabetes 1 66 0.153
232
CYT008 Cytomegalovirus Infection 57 0.153
233
P LPS004 Lupus Erythematosus 61 0.153
234
BCT022 Bacterial Infectious Disease 56 0.152
235
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.152
236
c HNT004 Huntington Disease-Like 2 50 0.152
237
SPN035 Spindle Cell Sarcoma 53 0.152
238
ATX019 Ataxia with Vitamin E Deficiency 42 0.152
239
P ATX030 Ataxia-Telangiectasia 82 0.152
240
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.151
241
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.151
242
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.151
243
ORL015 Oral Squamous Cell Carcinoma 43 0.150
244
ANX010 Anxiety 73 0.150
245
ANV001 Anovulation 47 0.149
246
DFC004 Deficiency Anemia 70 0.149
247
MLR004 Malaria 81 0.148
248
P BNG032 Benign Mesothelioma 46 0.148
249
DWR001 Dwarfism 44 0.148
250
P PTT006 Pituitary Adenoma 55 0.147
251
P DDN001 Duodenal Ulcer 52 0.147
252
HMS001 Hemosiderosis 54 0.147
253
HRT040 Hirata Disease 38 0.147
254
P HNT016 Huntington Disease 72 0.146
255
ALC007 Alcohol Dependence 66 0.146
256
PRD004 Prediabetes Syndrome 47 0.146
257
IMP005 Impotence 52 0.146
258
TLN003 Telangiectasis 52 0.146
260
c MLG068 Malignant Glioma 46 0.145
261
P SCH015 Schizophrenia 74 0.145
262
MSC007 Muscle Hypertrophy 64 0.145
263
P BRS044 Breast Adenocarcinoma 59 0.145
264
ORL011 Oral Cancer 60 0.145
265
OVR094 Ovarian Epithelial Cancer 38 0.145
266
P PLY019 Polyneuropathy 56 0.144
267
PLY150 Polykaryocytosis Inducer 31 0.144
268
P THR014 Thrombocytopenia 67 0.144
269
P THL005 Thalassemia 60 0.144
270
P RRH023 Rare Hereditary Hemochromatosis 41 0.144
271
c ACT071 Acute Kidney Failure 60 0.144
272
P PLM036 Pulmonary Fibrosis 65 0.143
273
PNC129 Pancreatic Adenocarcinoma 68 0.143
274
P INS002 in Situ Carcinoma 53 0.143
275
DRM006 Dermatitis 61 0.143
276
MTB004 Metabolic Acidosis 50 0.143
277
P ALC033 Alcohol Use Disorder 58 0.143
278
SCH014 Schistosomiasis 57 0.142
279
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.142
280
P GLM040 Glioma Susceptibility 1 81 0.142
281
P NSP012 Nasopharyngeal Carcinoma 66 0.141
282
AST005 Asthma 76 0.141
283
P LKM071 Leukemia, Chronic Lymphocytic 79 0.141
284
c WLM018 Wilms Tumor 5 61 0.141
285
P MYT002 Myotonic Dystrophy 49 0.140
286
TRM010 Traumatic Brain Injury 51 0.140
287
c VRL010 Viral Hepatitis 52 0.140
288
MSL001 Measles 62 0.140
289
GTR002 Goiter 53 0.139
290
P ART022 Arthritis 69 0.139
291
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.138
292
CHC001 Chickenpox 60 0.137
293
P KDN017 Kidney Cancer 60 0.137
294
DPH001 Diphtheria 60 0.137
295
MNT002 Mental Depression 58 0.137
296
ARG004 Argyria 27 0.137
297
STM007 Stomatitis 50 0.137
298
P MDL005 Medulloblastoma 77 0.136
299
VRL011 Viral Infectious Disease 61 0.136
300
BRN071 Brain Injury 49 0.135
301
c ACT073 Acute Leukemia 58 0.135
302
P HYP098 Hypereosinophilic Syndrome 67 0.135
303
P ALP008 Alopecia 54 0.135
304
BRC012 Brucellosis 64 0.135
305
ANR007 Anorexia Nervosa 63 0.135
306
c BRN108 Branchiootic Syndrome 1 62 0.135
307
P BND020 Bone Disease 59 0.134
308
EMB004 Embryonal Carcinoma 56 0.134
309
c HPT003 Hepatitis a 62 0.134
310
P GST044 Gastritis 56 0.133
311
HPT022 Hepatoblastoma 56 0.133
312
TRY001 Trypanosomiasis 50 0.133
313
P DMN002 Dementia 66 0.132
314
c SVR001 Severe Acute Respiratory Syndrome 62 0.132
315
NRR001 Neuroretinitis 42 0.132
316
CHR178 Chromosomal Triplication 35 0.131
317
RTN023 Retinitis 46 0.131
318
P DRM053 Dermatitis, Atopic 66 0.131
319
LMY002 Leiomyoma 52 0.130
320
AMN001 Amenorrhea 54 0.130
321
P BPL003 Bipolar Disorder 56 0.130
322
CRH001 Crohn's Disease 74 0.130
323
IRN002 Iron Metabolism Disease 57 0.129
324
c MJR024 Major Affective Disorder 9 41 0.129
325
c MJR022 Major Affective Disorder 8 38 0.129
326
ANG054 Angina Pectoris 66 0.127
327
MNN042 Meningioma, Radiation-Induced 62 0.127
328
P OVR049 Ovarian Disease 52 0.126
329
PLC008 Placenta Disease 50 0.126
330
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.126
331
CLR108 Colorectal Adenoma 64 0.126
332
P CRD119 Cardiac Arrest 67 0.126
333
ANG005 Anogenital Venereal Wart 55 0.125
334
HYP014 Hyperuricemia 52 0.125
335
P HYP083 Hypopituitarism 53 0.125
336
P NPH012 Nephrotic Syndrome 60 0.124
337
EYD002 Eye Disease 58 0.124
338
c MCR112 Microvascular Complications of Diabetes 2 41 0.123
339
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.123
340
PRP030 Purpura 54 0.123
341
P CHN012 Chondrosarcoma 56 0.123
342
ATS010 Autosomal Recessive Disease 48 0.123
343
P THY023 Thymoma 65 0.123
344
c THY107 Thymoma, Familial 52 0.122
345
ECH003 Echinococcosis 53 0.121
346
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.121
347
P SZR006 Seizure Disorder 56 0.121
348
GST040 Gastric Adenocarcinoma 70 0.121
349
P LCT001 Lactic Acidosis 51 0.121
350
PRT036 Peritonitis 64 0.121
351
P TRM003 Tremor 54 0.120
352
P PRK057 Parkinson Disease, Late-Onset 78 0.120
353
LRN002 Laron Syndrome 62 0.120
354
P SYP003 Syphilis 58 0.120
355
P RSP003 Respiratory Failure 74 0.120
356
PLM001 Pulmonary Tuberculosis 69 0.119
357
P HMP007 Hemophilia 51 0.119
358
c LKM063 Leukemia, Chronic Myeloid 72 0.119
359
P RTN018 Retinal Disease 53 0.119
360
MYL009 Myelodysplastic Syndrome 70 0.119
361
PPL052 Papillomatosis, Confluent and Reticulated 33 0.118
362
P MJR001 Major Depressive Disorder 68 0.118
363
P PRN023 Prion Disease 57 0.118
364
P CLC063 Celiac Disease 1 66 0.118
365
ULC004 Ulcerative Colitis 73 0.117
366
P URT039 Urticaria 58 0.117
367
ATN005 Autonomic Dysfunction 46 0.116
368
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.116
369
OVR063 Overnutrition 44 0.116
370
ETN001 Eating Disorder 60 0.116
371
LYM133 Lymphoma, Hodgkin, Classic 69 0.116
372
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.115
373
CHG001 Chagas Disease 66 0.115
374
P ATR011 Atrial Fibrillation 66 0.115
375
BRN028 Brain Cancer 74 0.115
377
PLM031 Poliomyelitis 64 0.115
378
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.114
379
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.114
380
P DNG005 Dengue Virus 59 0.114
381
CHL065 Cholangiocarcinoma 68 0.114
382
c FML035 Familial Hyperlipidemia 55 0.114
383
CHL079 Children's Interstitial Lung Disease 26 0.114
384
P CND004 Candidiasis 58 0.114
385
P MLT020 Multiple Sclerosis 72 0.114
386
END041 Endometrial Adenocarcinoma 63 0.113
387
P MMP001 Mumps 58 0.113
388
P RHN004 Rhinitis 57 0.113
389
PPT005 Peptic Ulcer Disease 59 0.113
390
INT079 Intrahepatic Cholangiocarcinoma 51 0.113
391
MDD011 Mood Disorder 62 0.113
392
P HYP730 Hypogonadotropic Hypogonadism 52 0.112
393
ANR040 Aneurysm 59 0.112
394
P HYP061 Hypertrophic Cardiomyopathy 70 0.112
395
CRB004 Cerebral Artery Occlusion 45 0.112
396
c GRV008 Graves Disease 1 56 0.111
397
VSL002 Visual Epilepsy 59 0.111
398
MSC157 Muscular Dystrophy, Duchenne Type 72 0.111
399
P TMP001 Temporal Lobe Epilepsy 50 0.111
400
ENT011 Enterocolitis 51 0.111
401
CHL068 Cholestasis 61 0.111
402
TRT001 Teratocarcinoma 45 0.110
403
DNT012 Dental Caries 53 0.110
404
c MNN043 Meningioma, Familial 74 0.110
405
SPN021 Spinal Meningioma 50 0.110
406
P PLM037 Pulmonary Hypertension 67 0.110
407
P TXP001 Toxoplasmosis 60 0.110
408
P LPR021 Leprosy 3 69 0.110
409
P ATS364 Autism 70 0.110
410
HLC007 Helicobacter Pylori Infection 59 0.110
411
c MGR028 Migraine with or Without Aura 1 67 0.109
412
c ACT068 Acute Cystitis 63 0.109
413
c ATS007 Autism Spectrum Disorder 67 0.109
414
HYP020 Hyperprolactinemia 64 0.109
415
ANX004 Anoxia 40 0.109
416
P RBL001 Rubella 59 0.109
417
CLR109 Colorectal Adenocarcinoma 51 0.109
418
LYM027 Lymphopenia 58 0.109
419
HNS001 Hansen's Disease 34 0.108
420
WRN001 Werner Syndrome 69 0.108
421
SCR001 Secretory Meningioma 41 0.108
422
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.108
423
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.108
424
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 57 0.108
425
TRN018 Transitional Cell Carcinoma 56 0.108
426
c SCL052 Scleroderma, Familial Progressive 61 0.108
427
c GLL024 Gallbladder Disease 1 53 0.108
428
P VSC011 Vasculitis 62 0.107
429
AZS001 Azoospermia 50 0.107
430
TRP002 Tropical Spastic Paraparesis 50 0.107
431
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.107
432
GNG013 Gingivitis 59 0.107
433
VSC003 Visceral Leishmaniasis 55 0.107
434
c PRM005 Primary Hyperparathyroidism 58 0.107
435
BRS051 Breast Disease 58 0.107
436
NRL016 Neural Tube Defects 82 0.106
437
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.106
438
GT001 Gout 64 0.106
439
c HMC039 Hemochromatosis, Type 1 74 0.106
440
DMY004 Demyelinating Disease 52 0.106
441
P SYS005 Systemic Scleroderma 68 0.106
442
EWN003 Ewing Sarcoma 69 0.106
443
P GND004 Gonadal Dysgenesis 48 0.106
444
ISL001 Islet Cell Tumor 56 0.106
445
P MCR010 Microcephaly 59 0.105
446
c MST023 Mesothelioma, Malignant 57 0.105
447
P CNR004 Cone-Rod Dystrophy 2 73 0.105
448
HMC014 Homocysteinemia 53 0.105
449
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.105
450
DBT020 Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 39 0.105
451
HYP081 Hypolipoproteinemia 51 0.104
452
P UVT001 Uveitis 57 0.104
453
P PNM007 Pneumonia 68 0.103
454
c PLY105 Polycystic Ovary Syndrome 1 38 0.103
455
PLG002 Plague 63 0.103
456
HSH003 Hashimoto Thyroiditis 62 0.103
457
P MYS003 Myasthenia Gravis 68 0.102
458
KRT009 Keratosis 51 0.102
459
ORP003 Oropharynx Cancer 55 0.102
460
P EPL164 Epilepsy 71 0.102
461
c ACT134 Acute Liver Failure 56 0.102
462
c PRD040 Periodontitis, Chronic 53 0.102
463
P CHR345 Chronic Pain 44 0.102
464
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.102
465
ART016 Aortic Aneurysm 69 0.102
466
THY030 Thyroid Gland Disease 52 0.101
467
P ART023 Arthropathy 62 0.101
468
BLR008 Bilirubin Metabolic Disorder 57 0.101
469
P RTN008 Retinitis Pigmentosa 79 0.101
470
P RCT021 Rectum Cancer 52 0.101
471
CRT072 Creutzfeldt-Jakob Disease 70 0.100
472
INT007 Intermediate Coronary Syndrome 55 0.100
473
CHR100 Chronic Ulcer of Skin 55 0.100
474
ALL014 Allergic Encephalomyelitis 38 0.100
475
P SCK005 Sickle Cell Disease 50 0.100
476
SKN019 Skin Melanoma 68 0.099
477
BRN024 Bronchitis 68 0.099
478
ACD008 Acid-Labile Subunit Deficiency 54 0.099
479
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.099
480
CLT003 Colitis 62 0.099
481
P SRC025 Sarcoidosis 1 70 0.099
482
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.098
483
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.098
484
PRN019 Perinatal Necrotizing Enterocolitis 59 0.098
485
LMY014 Leiomyoma, Uterine 56 0.098
486
P RTN016 Retinal Degeneration 53 0.098
487
c SPN225 Spondyloarthropathy 1 73 0.097
488
P LMY004 Leiomyosarcoma 63 0.097
489
P MYC084 Mycobacterium Tuberculosis 1 68 0.097
490
PRT013 Portal Hypertension 59 0.097
491
HDN002 Head Injury 46 0.097
492
FST010 Fasting Hypoglycemia 35 0.097
493
CNT047 Contact Dermatitis 58 0.097
494
BRN002 Bronchiolitis 59 0.097
495
P GLY013 Glycogen Storage Disease 60 0.097
496
SFT003 Soft Tissue Sarcoma 56 0.096
497
P SNS001 Sensorineural Hearing Loss 60 0.095
498
P TBR001 Tuberous Sclerosis 70 0.095
499
P PRD006 Prader-Willi Syndrome 59 0.095
500
P MYC008 Myocarditis 59 0.095
501
ADR016 Adrenal Cortical Carcinoma 48 0.095
502
OVR029 Ovarian Hyperstimulation Syndrome 64 0.094
503
PRM329 Premature Aging 35 0.094
504
PLM010 Pulmonary Edema 54 0.094
505
HMP009 Haemophilus Influenzae 43 0.094
506
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.094
507
ISL003 Isolated Growth Hormone Deficiency 49 0.094
508
ACT119 Acute Promyelocytic Leukemia 63 0.094
509
THR024 Thrombosis 57 0.094
510
PLC005 Placental Insufficiency 57 0.093
511
P NNT009 Neonatal Diabetes Mellitus 50 0.093
512
ADR004 Adrenal Cortical Adenocarcinoma 39 0.093
513
NRM005 Neuromuscular Disease 64 0.093
514
RTN020 Retinal Vascular Disease 46 0.093
515
ALL006 Allergic Asthma 56 0.093
516
P PLY014 Polycystic Kidney Disease 62 0.093
517
IGG001 Iga Glomerulonephritis 48 0.093
518
FLR002 Filariasis 55 0.092
519
P MTR014 Motor Neuron Disease 65 0.092
520
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.092
521
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.092
522
PNG002 Pain Agnosia 51 0.092
523
P PRM006 Primary Biliary Cirrhosis 62 0.092
524
LYM019 Lymphosarcoma 46 0.091
525
c SCN007 Secondary Hyperparathyroidism 51 0.091
526
P SLP005 Sleep Disorder 59 0.091
527
CNS004 Constipation 58 0.091
528
c BSL007 Basal Cell Carcinoma 68 0.091
529
P APL001 Aplastic Anemia 74 0.091
530
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.091
531
BRT037 Brittle Diabetes 25 0.091
532
c FML021 Familial Hypercholesterolemia 66 0.091
533
RST023 Resting Heart Rate, Variation in 41 0.091
534
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.090
535
MDD018 Middle East Respiratory Syndrome 43 0.090
536
PST092 Posttransplant Acute Limbic Encephalitis 29 0.090
537
SPP011 Suppression of Tumorigenicity 12 59 0.090
539
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.089
540
P SBS003 Substance Abuse 55 0.089
541
NPH009 Nephrolithiasis 55 0.089
542
LYM017 Lyme Disease 64 0.089
543
P MNC007 Monocytic Leukemia 53 0.088
544
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.088
545
P OPN001 Open-Angle Glaucoma 49 0.088
546
TST014 Testicular Cancer 46 0.088
547
P SLM003 Salmonellosis 55 0.088
548
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.088
549
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.088
550
YLL002 Yellow Fever 61 0.088
551
SMN007 Seminoma 43 0.088
552
HPT004 Hepatic Coma 45 0.087
553
CTN007 Cutaneous Leishmaniasis 62 0.087
554
P HML002 Hemolytic Anemia 63 0.087
555
CYS005 Cysticercosis 53 0.087
556
SPN051 Spondylitis 51 0.087
557
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 30 0.087
558
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.087
559
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.087
560
P END033 Endocarditis 57 0.087
561
KRT019 Keratitis, Hereditary 65 0.087
562
c EXD008 Exudative Vitreoretinopathy 1 71 0.087
563
P SML001 Small Cell Carcinoma 52 0.086
564
HYP026 Hypoglycemic Coma 36 0.086
565
GST023 Gastric Ulcer 53 0.086
566
HYP110 Hyperproinsulinemia 37 0.086
567
MST005 Mastitis 53 0.086
568
c FNC043 Fanconi Anemia, Complementation Group E 62 0.086
569
P MTC069 Mitochondrial Disorders 56 0.086
570
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.086
571
INF009 Inflammatory Spondylopathy 31 0.086
572
ECT026 Ectopic Pregnancy 50 0.086
573
P PLY018 Polycythemia 56 0.086
574
P MLN069 Melanoma, Uveal 59 0.086
575
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.086
576
P LRY044 Larynx Cancer 55 0.085
577
THY111 Thyroid Carcinoma, Familial Medullary 67 0.085
578
P FML011 Familial Adenomatous Polyposis 72 0.085
579
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.085
580
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.085
581
CNN005 Connective Tissue Disease 68 0.085
582
P HYD006 Hydrocephalus 66 0.085
583
c BTT014 Beta-Thalassemia 74 0.085
584
ALL003 Allergic Rhinitis 67 0.085
585
c ACT135 Acute Graft Versus Host Disease 52 0.085
586
P MLT074 Multiple Endocrine Neoplasia 56 0.085
587
P PRC019 Precocious Puberty 46 0.084
588
IGR001 Ige Responsiveness, Atopic 59 0.084
589
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.084
590
CRD132 Cardiac Conduction Defect 58 0.084
591
CNN003 Conn's Syndrome 79 0.084
592
P MNN013 Meningitis 66 0.084
593
CHL147 Chlamydia Pneumonia 48 0.084
594
WST005 West Nile Virus 54 0.084
595
NTR046 Neutrophil Migration 50 0.084
596
P NRF002 Neurofibromatosis 56 0.084
597
P MYP006 Myopia 55 0.083
598
THY125 Thyroid Gland Medullary Carcinoma 50 0.083
599
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.083
600
SPL018 Splenomegaly 48 0.083
601
OST017 Osteomyelitis 64 0.083
602
VRC005 Varicose Veins 60 0.083
603
DSS008 Disease of Mental Health 58 0.083
604
CVD001 Covid-19 44 0.083
605
LMB062 Limb Ischemia 55 0.083
606
DGN001 Degenerative Disc Disease 48 0.083
607
GST010 Gestational Trophoblastic Neoplasm 46 0.083
608
DCT002 Ductal Carcinoma in Situ 59 0.082
609
NRN004 Neuroendocrine Tumor 55 0.082
610
NRT004 Neuritis 52 0.082
611
RTN017 Retinal Detachment 61 0.081
612
RNL077 Renal Fibrosis 47 0.081
613
VSC002 Vascular Dementia 57 0.081
614
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.081
615
PLY100 Polyploidy 40 0.081
616
P ADL010 Adult Respiratory Distress Syndrome 65 0.081
617
AND014 Androgenic Alopecia 46 0.081
618
CRN030 Coronary Stenosis 50 0.081
619
BRN056 Bronchopulmonary Dysplasia 57 0.080
620
ART002 Arts Syndrome 64 0.080
621
MCL006 Macular Retinal Edema 55 0.080
622
OTT002 Otitis Media 72 0.080
623
LNG031 Lung Benign Neoplasm 51 0.080
624
PRT058 Pure Autonomic Failure 59 0.080
625
ANS011 Anus Cancer 56 0.080
626
ANT024 Anthrax Disease 58 0.080
627
CHL004 Cholelithiasis 49 0.080
628
NRL005 Neurilemmoma 60 0.080
629
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.080
630
FTL021 Fetal Macrosomia 42 0.079
631
CRD137 Cardiogenic Shock 47 0.079
632
P HDC001 Headache 57 0.079
633
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.079
634
GST019 Gastrointestinal Stromal Tumor 78 0.079
635
PRP080 Peripheral Artery Disease 53 0.079
636
P DBT005 Diabetes Insipidus 55 0.079
637
BRR012 Berardinelli-Seip Congenital Lipodystrophy 49 0.079
638
c SVR005 Severe Pre-Eclampsia 50 0.079
639
GST037 Gastroparesis 54 0.079
640
GLC008 Glucose Metabolism Disease 40 0.078
641
HYP017 Hypophosphatemia 50 0.078
642
c WLM013 Wilms Tumor 1 65 0.078
643
GLM044 Glomerular Disease 37 0.078
644
49X006 49, Xxxxy Syndrome 41 0.078
645
DFF005 Diffuse Large B-Cell Lymphoma 55 0.078
646
HPT019 Hepatic Encephalopathy 60 0.078
647
P OLG002 Oligodendroglioma 67 0.078
648
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.077
649
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.077
650
AMN003 Amnestic Disorder 54 0.077
651
c THR092 Thrombophilia Due to Thrombin Defect 73 0.077
652
c DBT103 Diabetes Mellitus, Permanent Neonatal 4 46 0.077
653
P CNJ013 Conjunctivitis 65 0.077
654
P HML001 Hemolytic-Uremic Syndrome 53 0.077
655
P BCK002 Beckwith-Wiedemann Syndrome 62 0.077
656
P DYS154 Dystonia 65 0.077
657
c FNC027 Fanconi Anemia, Complementation Group a 81 0.077
658
SYN007 Synovitis 54 0.076
659
PLC002 Plica Syndrome 36 0.076
661
KLD004 Keloid Disorder 40 0.076
662
HND015 Hand Skill, Relative 33 0.076
663
PPL002 Papillary Carcinoma 47 0.076
664
SNS003 Sensory Peripheral Neuropathy 54 0.076
665
APN008 Apnea, Obstructive Sleep 64 0.076
666
P LPS002 Liposarcoma 65 0.076
667
ALL010 Allergic Contact Dermatitis 56 0.076
668
P GCH001 Gaucher's Disease 63 0.076
669
c TBR025 Tuberous Sclerosis 1 77 0.076
670
PTH003 Pathologic Nystagmus 52 0.075
671
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 0.075
672
CHR066 Chronic Fatigue Syndrome 61 0.075
673
BRR014 Barrett Esophagus 65 0.075
674
P MYS005 Myositis 56 0.075
675
c JVN010 Juvenile Rheumatoid Arthritis 64 0.075
676
MCS002 Mucositis 56 0.075
677
SCR011 Scrapie 39 0.075
678
P OVR046 Ovarian Cyst 47 0.075
679
DBT002 Diabetic Autonomic Neuropathy 41 0.075
680
c DWL002 Dowling-Degos Disease 1 58 0.075
681
CRY003 Cryptosporidiosis 54 0.075
683
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.075
684
PRT038 Protein-Energy Malnutrition 54 0.074
685
BCL014 B-Cell Growth Factor 35 0.074
686
P SCL018 Scoliosis 60 0.074
687
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.074
688
c HPT007 Hepatitis E 53 0.074
689
P FRG001 Fragile X Syndrome 70 0.074
690
HRP004 Herpes Zoster 60 0.074
691
MTC005 Mitochondrial Metabolism Disease 49 0.074
692
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 53 0.074
693
PSY004 Psychotic Disorder 67 0.074
694
P LNG028 Long Qt Syndrome 66 0.074
695
DSS009 Disseminated Intravascular Coagulation 57 0.073
696
P ALP061 Alopecia, Androgenetic, 1 49 0.073
697
P PRP029 Porphyria 62 0.073
698
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.073
699
BRS099 Breast Ductal Carcinoma 62 0.073
700
TND005 Tendinitis 54 0.073
701
P CHL066 Cholangitis 51 0.073
702
P END084 Endocrine System Disease 45 0.073
703
TRC023 Trichinosis 53 0.073
704
MTH009 Mouth Disease 56 0.073
705
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.073
706
c PNC106 Pancreatic Agenesis 1 51 0.073
707
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.073
708
CMM005 Common Cold 57 0.073
709
P LCH002 Lichen Planus 53 0.073
710
PLS011 Plasmacytoma 56 0.073
711
FBR047 Fibromyalgia 58 0.073
712
NWC001 Newcastle Disease 45 0.072
713
P RTT002 Rett Syndrome 80 0.072
714
CHL067 Cholecystitis 57 0.072
715
ATM052 Autoimmune Disease 1 37 0.072
716
LST001 Listeriosis 56 0.072
717
TRN015 Transient Cerebral Ischemia 63 0.072
718
P HYP024 Hypoparathyroidism 56 0.072
719
SCK003 Sickle Cell Anemia 74 0.072
720
HYP781 Hypoascorbemia 51 0.072
721
MNN009 Meningoencephalitis 49 0.072
722
P NRV007 Nervous System Disease 66 0.072
723
c LRG001 Large Cell Carcinoma 50 0.071
724
IRN001 Iron Deficiency Anemia 59 0.071
725
P ASP006 Aspergillosis 69 0.071
726
c GLC092 Glaucoma, Primary Open Angle 62 0.071
727
PLS007 Plasmodium Falciparum Malaria 52 0.071
728
ONC002 Onchocerciasis 52 0.071
729
P CYS018 Cystitis 59 0.071
730
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.071
731
END062 Endometrial Hyperplasia 48 0.071
732
DBT008 Diabetic Angiopathy 44 0.070
733
GRD007 Grade Iii Astrocytoma 59 0.070
734
P OPT006 Optic Nerve Disease 60 0.070
735
CLR030 Clear Cell Renal Cell Carcinoma 53 0.070
736
P OBS001 Obstructive Jaundice 50 0.070
737
ASP026 Asplenia, Isolated Congenital 44 0.070
738
P INT068 Intestinal Disease 53 0.070
739
PRP016 Paraplegia 52 0.070
740
SRC027 Sarcoma, Synovial 58 0.070
741
HRT012 Heart Valve Disease 53 0.070
742
P ANG015 Angioedema 57 0.070
743
KHL003 Kohlschutter-Tonz Syndrome 65 0.070
744
TNG007 Tongue Carcinoma 51 0.069
745
CRD223 Cardiac Arrhythmia 60 0.069
746
GST050 Gastrointestinal System Disease 56 0.069
747
P FRN006 Frontotemporal Dementia 68 0.069
748
P MMB011 Membranous Nephropathy 50 0.069
749
VRL003 Variola Major 42 0.069
750
P ANR048 Aniridia 1 63 0.069
751
P FTL001 Fetal Alcohol Syndrome 57 0.069
752
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.069
753
P PMP001 Pemphigus 54 0.069
754
P PLY041 Polymyositis 57 0.069
755
CRB037 Cerebral Palsy 69 0.069
756
P FCL005 Focal Segmental Glomerulosclerosis 57 0.069
757
END040 Endogenous Depression 55 0.069
758
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 55 0.069
759
CLF027 Cleft Palate, Isolated 64 0.068
760
GST092 Gastroesophageal Reflux 67 0.068
761
PSR001 Psoriatic Arthritis 61 0.068
762
CRT013 Carotid Stenosis 50 0.068
763
KRT008 Keratopathy 47 0.068
764
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 50 0.068
765
AND002 Androgen Insensitivity Syndrome 66 0.068
766
c GCH015 Gaucher Disease, Type I 70 0.068
767
LYS002 Lysosomal Storage Disease 52 0.068
768
OST003 Osteonecrosis 61 0.068
769
P HYP265 Hypotonia 43 0.067
770
CRN036 Craniopharyngioma 65 0.067
771
SYN036 Syncope 45 0.067
772
SPS057 Spasticity 45 0.067
773
P VTR007 Vitreoretinopathy 46 0.067
774
PHN003 Phenylketonuria 75 0.067
775
LWC001 Low Compliance Bladder 43 0.067
776
PNC034 Pancreas Disease 48 0.067
777
VLV047 Volvulus of Midgut 49 0.067
778
c HMP004 Hemophilia B 68 0.067
779
SBC016 Subacute Delirium 44 0.067
780
LNG039 Lung Squamous Cell Carcinoma 66 0.067
781
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.067
782
DYS015 Dysentery 52 0.067
783
BRN004 Brain Edema 56 0.067
784
THY122 Thyroid Gland Cancer 57 0.067
785
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.067
786
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.066
787
P PYL005 Pyelonephritis 56 0.066
788
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 55 0.066
789
IRR002 Irritable Bowel Syndrome 65 0.066
790
c PRG020 Paragangliomas 3 39 0.066
791
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.066
792
c DNG003 Dengue Disease 59 0.066
793
P DBT100 Diabetes Mellitus, Permanent Neonatal 1 59 0.066
794
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.066
795
DYS073 Dysphagia 50 0.066
796
INT066 Interstitial Lung Disease 60 0.066
797
GLS018 Glass Syndrome 57 0.066
798
P ALP009 Alopecia Areata 60 0.066
799
TND004 Tendinopathy 43 0.065
800
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.065
801
NWB001 Newborn Respiratory Distress Syndrome 58 0.065
802
ACT003 Acute Kidney Tubular Necrosis 45 0.065
803
GLC036 Glucagonoma 45 0.065
804
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.065
805
P HMN010 Hemangioma 61 0.065
806
MLT157 Multiple System Atrophy 1 70 0.065
807
NDL007 Nodular Goiter 47 0.065
808
MNG006 Monogenic Diabetes 46 0.065
809
SXL003 Sexual Disorder 47 0.065
810
BLM002 Bulimia Nervosa 57 0.065
811
c ATM011 Autoimmune Hepatitis 63 0.065
812
PTT009 Pituitary Gland Disease 54 0.065
813
P SHR001 Short Bowel Syndrome 53 0.065
814
P ANT006 Antiphospholipid Syndrome 55 0.065
815
NRN001 Neuroendocrine Carcinoma 47 0.064
816
ORL005 Oral Candidiasis 56 0.064
817
INT002 Intermittent Claudication 61 0.064
818
OBS002 Obsessive-Compulsive Disorder 68 0.064
819
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.064
820
BBS001 Babesiosis 48 0.064
821
GRM010 Germ Cells Tumors 34 0.064
822
DFF036 Differentiated Thyroid Carcinoma 52 0.064
823
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.064
824
c CNG012 Congenital Generalized Lipodystrophy 52 0.064
825
CCC001 Coccidioidomycosis 58 0.064
826
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.064
827
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.064
828
TCK001 Tick-Borne Encephalitis 56 0.063
829
c HYP272 Hypercholesterolemia, Familial, 3 44 0.063
830
P ANG001 Angelman Syndrome 69 0.063
831
MCR013 Microphthalmia 57 0.063
832
ALC006 Alcoholic Hepatitis 61 0.063
833
P TRC086 Trichohepatoenteric Syndrome 1 62 0.063
834
FLR001 Filarial Elephantiasis 55 0.063
835
FCL014 Focal Epilepsy 54 0.063
836
P CRV039 Cervicitis 49 0.063
837
P LKD001 Leukodystrophy 59 0.063
838
INF034 Infective Endocarditis 53 0.063
839
CLL003 Cellulitis 54 0.063
840
c LPM012 Lipomatosis, Multiple 60 0.063
841
P FML012 Familial Partial Lipodystrophy 54 0.063
842
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.063
843
GNT167 Genetic Obesity 33 0.063
844
P LYM033 Lymphoproliferative Syndrome 59 0.063
845
P FML187 Familial Hypertension 37 0.062
846
HMG005 Hemoglobinopathy 56 0.062
847
P THR117 Three M Syndrome 1 63 0.062
848
P MJR007 Major Affective Disorder 1 43 0.062
849
HYP457 Hypertrophic Scars 42 0.062
850
P ATR005 Atrophic Gastritis 50 0.062
851
P GLL018 Gallbladder Cancer 57 0.062
852
P AGM001 Agammaglobulinemia 65 0.062
853
P GLL022 Guillain-Barre Syndrome 59 0.062
854
GRN017 Granulocytopenia 44 0.062
855
DBT004 Diabetic Polyneuropathy 49 0.062
856
P BNG030 Benign Ependymoma 60 0.062
857
KRT006 Keratoconjunctivitis 53 0.062
858
c DRR009 Diarrhea 6 46 0.062
859
CRH005 Crohn's Colitis 53 0.062
860
P EPD016 Epidermolysis Bullosa 53 0.062
861
PST028 Post-Traumatic Stress Disorder 58 0.061
862
HST010 Histiocytosis 48 0.061
863
c WLF013 Wolfram Syndrome 1 60 0.061
864
PLM033 Pulmonary Embolism 59 0.061
865
P CRV031 Cervical Adenocarcinoma 49 0.061
866
SWN001 Swine Influenza 45 0.061
867
PNC001 Pancytopenia 54 0.061
868
BCT002 Bacterial Vaginosis 53 0.061
869
P CCK001 Cockayne Syndrome 66 0.061
870
CMM004 Common Variable Immunodeficiency 68 0.061
871
ENT004 Enthesopathy 49 0.061
872
GST071 Gastrointestinal Carcinoma 47 0.061
873
P ESP024 Esophagitis 62 0.061
874
DMP001 Dumping Syndrome 44 0.061
875
LYM040 Lymphoblastic Lymphoma 54 0.060
876
ALV002 Alveolar Echinococcosis 49 0.060
877
ZLL002 Zollinger-Ellison Syndrome 55 0.060
878
P PLM034 Pulmonary Emphysema 55 0.060
879
RDN001 Reading Disorder 40 0.060
880
TNG009 Tongue Squamous Cell Carcinoma 44 0.060
881
CLL010 Cellular Ependymoma 54 0.060
882
CRY005 Cryptococcosis 58 0.060
883
c LPD015 Lipodystrophy, Familial Partial, Type 2 64 0.060
884
BCK006 Back Pain 42 0.060
886
CHR005 Chorioamnionitis 51 0.060
887
GNG003 Gingival Recession 44 0.060
888
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.060
889
MCH006 Mechanical Strabismus 42 0.060
890
MMM001 Mammary Paget's Disease 53 0.060
891
P SCL009 Sclerosing Cholangitis 48 0.059
892
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.059
893
PRS042 Prostate Disease 43 0.059
894
PLY001 Polycythemia Vera 69 0.059
895
SRS001 Serous Cystadenocarcinoma 52 0.059
896
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 68 0.059
897
OVR059 Ovary Adenocarcinoma 53 0.059
898
THR013 Thoracic Outlet Syndrome 54 0.059
899
c CHR682 Chronic Bilirubin Encephalopathy 39 0.059
900
P PRD021 Periodic Paralysis 45 0.059
901
LYM009 Lymphocytic Choriomeningitis 47 0.059
902
c HRN019 Hair-an Syndrome 17 0.059
903
MYT011 Myotonia 34 0.058
904
P SJG008 Sjogren Syndrome 61 0.058
905
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.058
906
HRT011 Heart Septal Defect 50 0.058
907
c INH020 Inherited Metabolic Disorder 47 0.058
908
KRT002 Keratomalacia 47 0.058
909
FLL031 Follicular Adenoma 39 0.058
910
P SPN046 Spinal Muscular Atrophy 62 0.058
911
P KRT007 Keratoconus 50 0.058
912
P RNL015 Renal Hypertension 47 0.058
913
P WSK001 Wiskott-Aldrich Syndrome 72 0.058
914
P STR020 Strabismus 55 0.058
915
P MYC033 Myoclonus 46 0.058
916
P NRC002 Narcolepsy 52 0.058
917
c CNG006 Congenital Hypothyroidism 64 0.058
918
c JVN061 Juvenile Arthritis 60 0.058
919
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.058
920
DBT006 Diabetic Macular Edema 48 0.058
921
P BRD002 Bardet-Biedl Syndrome 66 0.058
922
ADR007 Adrenoleukodystrophy 75 0.058
923
c ACT004 Acute Diarrhea 39 0.058
924
P CTN015 Cutaneous T Cell Lymphoma 49 0.058
925
BNG077 Benign Idiopathic Neonatal Seizures 26 0.058
926
c CNT035 Central Nervous System Disease 52 0.058
927
c HYP768 Hyperlipoproteinemia, Type I 67 0.058
928
ADN011 Adenoid Cystic Carcinoma 70 0.058
929
P BNC003 Bone Cancer 58 0.057
930
c BCT013 Bacterial Pneumonia 48 0.057
931
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.057
932
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.057
933
EPD015 Epidemic Typhus 45 0.057
934
P DRM010 Dermatomyositis 61 0.057
935
MYF001 Myofibroma 45 0.057
936
P CRB088 Cerebral Atrophy 37 0.057
937
PST021 Postpartum Depression 50 0.057
938
NRT001 Neurotic Disorder 53 0.057
939
EXS001 Exostosis 46 0.057
941
ADN009 Adenosquamous Carcinoma 47 0.057
942
GYN001 Gynecomastia 49 0.057
943
OLG001 Oligospermia 45 0.057
944
CHR073 Choreatic Disease 52 0.057
945
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.057
946
TLR001 Tularemia 51 0.057
947
TNS005 Tonsillitis 57 0.057
948
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.056
949
c DPH024 Diaphragmatic Hernia, Congenital 63 0.056
950
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.056
951
P SMP003 Simpson-Golabi-Behmel Syndrome 50 0.056
952
P BRS053 Breast Fibroadenoma 49 0.056
953
c MLG084 Malignant Fibrous Histiocytoma 63 0.056
954
MSN004 Mesenchymal Cell Neoplasm 41 0.056
955
IDP033 Idiopathic Edema 44 0.056
956
P PRS038 Personality Disorder 65 0.056
957
PRN011 Pernicious Anemia 53 0.056
958
MYL005 Myelofibrosis 70 0.056
959
P ANP001 Anaplastic Large Cell Lymphoma 58 0.056
960
MMM006 Mammographic Density 41 0.056
961
c PRS136 Prostate Cancer, Hereditary, 6 33 0.056
962
c PRS130 Prostate Cancer, Hereditary, 8 32 0.056
963
RTR008 Root Resorption 45 0.055
964
CYT005 Cytomegalovirus Retinitis 50 0.055
965
ALD013 Aldosterone-Producing Adenoma 39 0.055
966
ACT084 Acute Stress Disorder 47 0.055
967
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 60 0.055
968
HST011 Histoplasmosis 55 0.055
969
INF021 Infant Gynecomastia 31 0.055
970
TBC004 Tobacco Addiction 64 0.055
971
c PNC108 Pancreatitis, Hereditary 70 0.055
972
P GLC113 Galactosemia I 64 0.055
973
CLF001 Cleft Lip 53 0.055
974
HYP835 Hypothalamic Obesity 38 0.055
975
c OPT053 Optic Atrophy 1 63 0.055
976
CRP001 Carpal Tunnel Syndrome 67 0.055
977
TTR011 Tetraploidy 47 0.055
978
BLD131 Bladder Urothelial Carcinoma 62 0.055
979
PMP006 Pemphigus Vulgaris, Familial 57 0.055
980
CHL131 Chlorpropamide-Alcohol Flushing 22 0.055
981
P TCD001 Tic Disorder 53 0.054
982
FNG017 Fungal Infectious Disease 53 0.054
983
FCL012 Facial Paralysis 46 0.054
984
CHL122 Cholesteatoma of Middle Ear 50 0.054
985
BCK003 Background Diabetic Retinopathy 46 0.054
986
ADS004 Aids Dementia Complex 40 0.054
987
c CHL119 Cholangitis, Primary Sclerosing 57 0.054
988
INT075 Intracranial Hypertension 53 0.054
989
MYC006 Mycosis Fungoides 66 0.054
990
MNK002 Monkeypox 39 0.054
991
ADR041 Adrenal Cortical Adenoma 43 0.054
992
c LPD032 Lipodystrophy, Congenital Generalized, Type 1 57 0.054
993
c MLG079 Malignant Pleural Mesothelioma 42 0.054
994
ANN002 Anencephaly 56 0.054
995
URT001 Urethritis 49 0.054
996
ALB002 Albinism 46 0.054
997
GRD001 Giardiasis 45 0.054
998
CLP005 Ciliopathy 43 0.054
999
P EMB005 Embryonal Rhabdomyosarcoma 53 0.054
1000
P SHR029 Short Syndrome 63 0.054
1001
BRT054 Brittle Bone Disorder 72 0.054
1002
P RNV001 Renovascular Hypertension 48 0.054
1003
BRS050 Breast Cyst 40 0.054
1004
c PNS012 Paine Syndrome 61 0.054
1005
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.054
1006
PLC006 Placental Choriocarcinoma 36 0.054
1007
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.054
1008
NNT012 Neonatal Jaundice 53 0.054
1009
MLD001 Melioidosis 68 0.053
1010
OCL006 Ocular Hypertension 53 0.053
1011
BLL003 Bell's Palsy 51 0.053
1012
GST020 Gastric Antral Vascular Ectasia 41 0.053
1013
VRC001 Varicocele 49 0.053
1014
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.053
1015
c HRD202 Hereditary Lymphedema I 50 0.053
1016
NSP002 Nasopharyngitis 43 0.053
1017
P FBR003 Fibrous Histiocytoma 44 0.053
1018
c PRM196 Premature Ovarian Failure 1 67 0.053
1019
BRN014 Bronchopneumonia 54 0.053
1020
CRN027 Corneal Neovascularization 47 0.053
1021
c SPR086 Spermatogenic Failure 3 44 0.053
1022
P BLD062 Bile Duct Cancer 67 0.053
1023
ACT200 Acute Monoblastic Leukemia 52 0.053
1024
SCH036 Scheie Syndrome 72 0.053
1025
P MLG074 Malignant Mesenchymoma 40 0.053
1026
WLL004 Wallerian Degeneration 39 0.053
1027
CCN002 Cocaine Abuse 49 0.053
1028
DRM011 Dermatophytosis 52 0.053
1029
PLM014 Pleomorphic Adenoma 52 0.053
1030
SDD001 Sudden Infant Death Syndrome 61 0.052
1031
P CHR071 Charcot-Marie-Tooth Disease 65 0.052
1032
CRN322 Coronavirus Infectious Disease 40 0.052
1033
PLM005 Pleomorphic Lipoma 40 0.052
1034
P ICH004 Ichthyosis 54 0.052
1035
CRC021 Carcinosarcoma 62 0.052
1036
APH002 Aphasia 57 0.052
1037
P MLT008 Multinodular Goiter 42 0.052
1038
P HMC002 Homocystinuria 53 0.052
1039
c INS009 Insulin-Resistance Type B 24 0.052
1040
RFR003 Refractive Error 43 0.052
1041
DNG002 Dengue Hemorrhagic Fever 60 0.052
1042
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.052
1043
PRT029 Parathyroid Adenoma 50 0.052
1044
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.052
1045
STF001 Stiff-Person Syndrome 60 0.052
1046
HYP784 Hypogonadism, Male 40 0.052
1047
P PLY188 Polyendocrinopathy 32 0.052
1048
P GNG009 Gangliosidosis 44 0.051
1049
P CRN024 Corneal Disease 44 0.051
1050
P PNL012 Penile Cancer 56 0.051
1051
P SCL048 Sclerosteosis 55 0.051
1052
PNM008 Pneumothorax 56 0.051
1053
c MYT021 Myotonic Dystrophy 1 69 0.051
1054
ADR022 Adrenomyeloneuropathy 38 0.051
1055
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.051
1056
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 26 0.051
1057
P PNC025 Panic Disorder 53 0.051
1058
P PRL003 Proliferative Glomerulonephritis 44 0.051
1059
c ART101 Aortic Valve Disease 2 65 0.051
1060
P MTC133 Mitochondrial Myopathy 49 0.051
1061
ANG020 Angiosarcoma 64 0.051
1062
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.051
1063
c LKM070 Leukemia, Acute Monocytic 57 0.051
1064
TNS007 Taeniasis 45 0.051
1065
MMB001 Membranoproliferative Glomerulonephritis 55 0.051
1066
KWS001 Kwashiorkor 44 0.051
1067
DCB001 Decubitus Ulcer 61 0.051
1068
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.051
1069
HYP068 Hyperostosis 48 0.051
1070
P WLF004 Wolfram Syndrome 60 0.051
1071
ING001 Inguinal Hernia 60 0.051
1072
RHM001 Rheumatic Fever 60 0.051
1073
P CRN037 Craniosynostosis 68 0.051
1074
MLG163 Malignant Tumor of Penis 29 0.051
1075
c ATM006