Search results for Insulin (human) recombinant

1866 hits were found for Insulin (human) recombinant

# Family MCID Name MIFTS Score
1
INS024 Insulin-Like Growth Factor I 79 0.938
2
HYP056 Hypoglycemia 66 0.913
3
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.855
4
P DBT009 Diabetes Mellitus 64 0.752
5
HYP060 Hyperinsulinism 54 0.656
6
c DBT099 Diabetes Mellitus, Type I 65 0.645
7
HYP066 Hyperglycemia 61 0.630
8
IMM167 Immune Deficiency Disease 78 0.603
9
HMN044 Human Immunodeficiency Virus Type 1 71 0.579
10
P BRS047 Breast Cancer 97 0.499
11
P CLR023 Colorectal Cancer 99 0.455
12
GLC003 Glucose Intolerance 54 0.441
13
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.431
14
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.427
15
P PLY011 Polycystic Ovary Syndrome 56 0.426
16
VCC001 Vaccinia 49 0.425
17
ATM095 Autoimmune Disease 62 0.410
18
P KDN018 Kidney Disease 72 0.399
19
SVR004 Severe Combined Immunodeficiency 73 0.397
20
P LVR013 Liver Disease 68 0.384
21
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.383
22
CYT002 Cytokine Deficiency 42 0.381
23
P NRB001 Neuroblastoma 72 0.376
24
LPD008 Lipid Metabolism Disorder 62 0.368
25
P HPT023 Hepatocellular Carcinoma 100 0.366
26
48X005 48,xyyy 39 0.365
27
FTT001 Fatty Liver Disease 61 0.363
28
P OVR042 Ovarian Cancer 88 0.363
29
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.363
30
PRT037 Pertussis 65 0.361
31
P ADN016 Adenocarcinoma 64 0.357
32
P PRS040 Prostate Cancer 97 0.348
33
c HPT073 Hepatitis C Virus 72 0.348
34
P LKM002 Leukemia 68 0.345
35
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.345
36
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.344
37
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.344
38
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.344
39
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.344
40
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.344
41
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.344
42
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.344
43
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.344
44
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.344
45
P GLM045 Glioma 63 0.343
46
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.341
47
GLL048 Glial Tumor 45 0.335
48
ATH013 Atherosclerosis Susceptibility 65 0.332
49
P LNG032 Lung Cancer 98 0.331
50
ACQ007 Acquired Immunodeficiency Syndrome 60 0.329
51
OST159 Osteogenic Sarcoma 66 0.326
52
GLB015 Glioblastoma Multiforme 75 0.326
53
P PNC035 Pancreatic Cancer 84 0.324
54
P HRP006 Herpes Simplex 65 0.322
55
c HPT016 Hepatitis B 59 0.319
56
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.318
57
c HYP595 Hypertension, Essential 84 0.314
58
P INF032 Infertility 57 0.311
59
P NTR004 Neutropenia 63 0.311
60
c HPT001 Hepatitis C 62 0.309
61
LVR012 Liver Cirrhosis 62 0.308
62
P VSC007 Vascular Disease 63 0.308
63
THY029 Thyroid Carcinoma 59 0.307
64
CRV035 Cervical Cancer 76 0.306
65
P HMP007 Hemophilia 51 0.306
66
INS001 Insulinoma 60 0.306
67
GST033 Gestational Diabetes 61 0.303
68
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.303
69
CHL014 Cholera 59 0.300
70
END086 End Stage Renal Disease 51 0.298
71
P MLN008 Melanoma 69 0.296
72
ADN018 Adenoma 59 0.294
73
P HYP086 Hypothyroidism 69 0.294
74
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.294
75
c PRM038 Primary Agammaglobulinemia 44 0.291
76
ALL026 Allergic Hypersensitivity Disease 62 0.290
77
P ALZ034 Alzheimer Disease 88 0.288
78
P BLD134 Bladder Cancer 79 0.284
79
c MCR113 Microvascular Complications of Diabetes 3 52 0.282
80
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.281
81
c MCR120 Microvascular Complications of Diabetes 7 47 0.281
82
c MCR130 Microvascular Complications of Diabetes 6 41 0.281
83
c MCR133 Microvascular Complications of Diabetes 4 41 0.281
84
c CHR684 Chronic Kidney Disease 70 0.281
85
P DRR001 Diarrhea 55 0.279
86
P HYP750 Hypertriglyceridemia, Familial 62 0.278
87
P LYM118 Lymphoma 68 0.278
88
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.272
89
OCL069 Ocular Motor Apraxia 51 0.272
90
PPL022 Papilloma 54 0.270
91
HLX001 Helix Syndrome 47 0.265
92
CYS001 Cystic Fibrosis 81 0.265
93
P MYL006 Myeloid Leukemia 60 0.265
94
ISC004 Ischemia 58 0.261
95
P MCR115 Microvascular Complications of Diabetes 5 66 0.261
96
DWN001 Down Syndrome 70 0.261
97
c PRC016 Pre-Eclampsia 63 0.257
98
BNR002 Bone Resorption Disease 48 0.256
99
P CRN300 Coronary Heart Disease 1 63 0.256
100
GRW007 Growth Hormone Deficiency 46 0.256
101
P TRN020 Turner Syndrome 67 0.254
102
HYP266 Hypoxia 57 0.254
103
SQM006 Squamous Cell Carcinoma 60 0.254
104
SQM002 Squamous Cell Papilloma 46 0.253
105
P GST053 Gastric Cancer 83 0.253
106
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.253
107
P THR014 Thrombocytopenia 67 0.251
108
c LKM005 Leukemia, T-Cell, Chronic 34 0.251
109
P NRP001 Neuropathy 56 0.250
110
P INF038 Influenza 68 0.250
111
CNG034 Congestive Heart Failure 69 0.246
112
DFC004 Deficiency Anemia 70 0.246
113
TTN003 Tetanus 65 0.246
114
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.245
115
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.244
116
P HRT032 Heart Disease 75 0.244
117
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.243
118
c ACT075 Acute Myocardial Infarction 57 0.242
119
GST045 Gastroenteritis 59 0.241
120
P HPT021 Hepatitis 67 0.241
121
47X002 47,xyy 49 0.238
122
P CRD246 Cardiovascular System Disease 57 0.237
123
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.237
124
P KLZ004 Kala-Azar 1 41 0.234
125
LSH001 Leishmaniasis 63 0.234
126
P PRD008 Periodontitis 64 0.234
127
TXC005 Toxic Shock Syndrome 62 0.231
128
END057 Endometrial Cancer 74 0.231
129
STM007 Stomatitis 50 0.231
130
P LKM062 Leukemia, Acute Lymphoblastic 69 0.231
131
c SML038 Small Cell Cancer of the Lung 65 0.230
132
c LKM061 Leukemia, Acute Myeloid 84 0.230
133
P LNG064 Lung Cancer Susceptibility 3 78 0.229
134
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.228
135
P ENC004 Encephalitis 61 0.228
136
P RTN024 Retinoblastoma 73 0.226
137
LNG099 Lung Disease 60 0.226
138
c FML008 Familial Retinoblastoma 53 0.226
139
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.226
140
MYL069 Myeloma, Multiple 85 0.225
141
c HYP836 Hypercholesterolemia, Familial, 1 73 0.225
142
P BCL017 B-Cell Lymphoma 58 0.225
143
ADL002 Adult Syndrome 70 0.225
144
P GRV001 Graves' Disease 55 0.221
145
AGN016 Aging 56 0.221
146
KPS004 Kaposi Sarcoma 75 0.221
147
P HYP076 Hyperthyroidism 55 0.217
148
P MYC007 Myocardial Infarction 70 0.216
149
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.216
150
ACR007 Acromegaly 71 0.215
151
c RHB024 Rhabdomyosarcoma 2 67 0.214
152
c PCH010 Pachyonychia Congenita 3 44 0.212
153
c SYS001 Systemic Lupus Erythematosus 86 0.210
154
LPP008 Lipoprotein Quantitative Trait Locus 62 0.210
155
ACT088 Acute Insulin Response 41 0.208
156
P MSC005 Muscular Dystrophy 66 0.207
157
P FBR017 Fibrosarcoma 56 0.207
158
P SPP010 Suppressor of Tumorigenicity 3 51 0.206
159
P GRF003 Graft-Versus-Host Disease 72 0.204
160
CHL123 Chlamydia 59 0.204
161
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.202
162
P AST007 Astrocytoma 51 0.202
163
P ENC018 Encephalopathy 61 0.202
164
HYP043 Hyperandrogenism 48 0.202
165
P OST002 Osteoporosis 74 0.201
166
MSL001 Measles 62 0.201
167
SRC014 Sarcoma 65 0.199
168
DPH001 Diphtheria 60 0.199
169
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.199
170
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.198
171
CRV045 Cervical Intraepithelial Neoplasia 39 0.198
172
NTR005 Nutritional Deficiency Disease 62 0.198
173
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.197
174
MYL009 Myelodysplastic Syndrome 70 0.197
175
NNL006 Non-Alcoholic Steatohepatitis 54 0.197
176
HYP080 Hypogonadism 50 0.196
177
P EXN002 Exanthem 57 0.196
178
P LTR001 Lateral Sclerosis 54 0.195
179
P RHM011 Rheumatoid Arthritis 80 0.195
180
SKN016 Skin Disease 63 0.195
181
P ATX030 Ataxia-Telangiectasia 82 0.194
182
RCK004 Rickets 68 0.194
183
STR067 Stroke, Ischemic 81 0.192
184
CRB039 Cerebrovascular Disease 67 0.192
185
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.191
186
TLN003 Telangiectasis 52 0.190
187
SPN186 Spinal Cord Injury 60 0.190
188
URM002 Uremia 49 0.189
189
OST012 Osteoarthritis 78 0.189
190
c HPT003 Hepatitis a 62 0.189
191
SCH014 Schistosomiasis 57 0.188
192
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.188
193
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.188
194
P CTR002 Cataract 60 0.188
195
ACN002 Acanthosis Nigricans 60 0.188
196
CLN015 Colon Adenocarcinoma 65 0.187
197
c SVR001 Severe Acute Respiratory Syndrome 62 0.187
198
PRS045 Prostatic Hypertrophy 53 0.187
199
BCT022 Bacterial Infectious Disease 56 0.185
200
IRN002 Iron Metabolism Disease 57 0.185
201
HRW001 Hair Whorl 36 0.184
202
P INF037 Inflammatory Bowel Disease 54 0.184
203
SPN035 Spindle Cell Sarcoma 53 0.183
204
VRL011 Viral Infectious Disease 61 0.183
205
BRK010 Burkitt Lymphoma 67 0.181
206
P GLM007 Glomerulonephritis 57 0.180
207
P AMY004 Amyloidosis 70 0.180
208
P NSP012 Nasopharyngeal Carcinoma 66 0.180
209
ART140 Arteries, Anomalies of 52 0.179
210
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.179
211
P DNG005 Dengue Virus 59 0.179
212
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.179
213
CHC001 Chickenpox 60 0.179
214
ATX019 Ataxia with Vitamin E Deficiency 42 0.179
215
P LKM071 Leukemia, Chronic Lymphocytic 79 0.178
216
CHR074 Choriocarcinoma 47 0.178
217
P OVR082 Overgrowth Syndrome 50 0.178
218
MLR004 Malaria 81 0.178
219
P HYP098 Hypereosinophilic Syndrome 67 0.178
220
PRS021 Prostatic Adenoma 51 0.177
221
PRS129 Prostatic Hyperplasia, Benign 49 0.177
222
GTR002 Goiter 53 0.177
223
ESP021 Esophageal Cancer 90 0.176
224
P THY032 Thyroiditis 52 0.175
225
P RHB003 Rhabdomyosarcoma 63 0.175
226
P PSR002 Psoriasis 62 0.174
227
P TXP001 Toxoplasmosis 60 0.173
228
LPT014 Leptin Deficiency or Dysfunction 74 0.172
229
PRP030 Purpura 54 0.172
230
P THL005 Thalassemia 60 0.171
231
DWR001 Dwarfism 44 0.171
232
BRC012 Brucellosis 64 0.171
233
PLY150 Polykaryocytosis Inducer 31 0.171
234
P MSC003 Muscular Atrophy 52 0.170
235
P PRP019 Peripheral Nervous System Disease 58 0.170
236
c VRL010 Viral Hepatitis 52 0.170
237
c MLG068 Malignant Glioma 46 0.170
238
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.170
239
CHR178 Chromosomal Triplication 35 0.169
240
PST011 Pustulosis of Palm and Sole 52 0.169
241
P MYP004 Myopathy 70 0.169
242
VSC003 Visceral Leishmaniasis 55 0.169
243
NWC001 Newcastle Disease 45 0.168
244
P SKN015 Skin Carcinoma 66 0.168
245
ERY051 Erythroleukemia, Familial 56 0.168
246
P MLN007 Male Infertility 55 0.167
247
MTH009 Mouth Disease 56 0.167
248
c ACT027 Acute Pancreatitis 60 0.167
249
ANV001 Anovulation 47 0.167
251
HMS001 Hemosiderosis 54 0.166
252
P HMN032 Human Herpesvirus 8 47 0.166
253
c ACT071 Acute Kidney Failure 60 0.166
254
BRN071 Brain Injury 49 0.166
255
P HYP069 Hyperparathyroidism 63 0.165
256
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.165
257
P KDN017 Kidney Cancer 60 0.165
258
P LPS004 Lupus Erythematosus 61 0.165
259
P PNC044 Pancreatitis 61 0.164
260
P BNG032 Benign Mesothelioma 46 0.164
261
CYT008 Cytomegalovirus Infection 57 0.164
262
P END044 Endometriosis 63 0.163
263
P ART022 Arthritis 69 0.163
264
c ACT073 Acute Leukemia 58 0.162
265
CHG001 Chagas Disease 66 0.162
266
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.161
267
TRM010 Traumatic Brain Injury 51 0.160
268
P RRH023 Rare Hereditary Hemochromatosis 41 0.160
269
ECH003 Echinococcosis 53 0.160
270
BRN024 Bronchitis 68 0.160
271
OVR094 Ovarian Epithelial Cancer 38 0.159
272
DSS009 Disseminated Intravascular Coagulation 57 0.159
273
PPL052 Papillomatosis, Confluent and Reticulated 33 0.159
274
P HNT016 Huntington Disease 72 0.159
275
OVR029 Ovarian Hyperstimulation Syndrome 64 0.159
276
P PHC003 Pheochromocytoma 71 0.158
277
DRM006 Dermatitis 61 0.157
278
P PRN023 Prion Disease 57 0.157
279
P DRM053 Dermatitis, Atopic 66 0.157
280
c DLT002 Dilated Cardiomyopathy 79 0.156
281
c ATR087 Atrial Standstill 1 75 0.156
282
P ART021 Arteriosclerosis 54 0.155
283
PRT036 Peritonitis 64 0.155
284
PLM031 Poliomyelitis 64 0.155
285
LYM017 Lyme Disease 64 0.155
286
P PLM036 Pulmonary Fibrosis 65 0.154
287
ADR040 Adrenal Gland Pheochromocytoma 46 0.153
288
AST005 Asthma 76 0.153
289
c HMP004 Hemophilia B 68 0.153
290
P RHN004 Rhinitis 57 0.153
291
PNC129 Pancreatic Adenocarcinoma 68 0.152
292
ARG004 Argyria 27 0.152
293
P SYP003 Syphilis 58 0.152
294
PLG002 Plague 63 0.152
295
P TRT010 Teratoma 52 0.152
296
P SLP006 Sleep Apnea 69 0.152
297
LYM133 Lymphoma, Hodgkin, Classic 69 0.151
298
c LKM063 Leukemia, Chronic Myeloid 72 0.151
299
P BND020 Bone Disease 59 0.150
300
c NRF023 Neurofibromatosis, Type Ii 80 0.150
301
CRH001 Crohn's Disease 74 0.149
302
PRP027 Peripheral Vascular Disease 71 0.149
303
LYM027 Lymphopenia 58 0.149
304
P PLY019 Polyneuropathy 56 0.149
305
HYP005 Hypokalemia 55 0.148
306
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.148
307
P ECL001 Eclampsia 50 0.148
308
P RSP003 Respiratory Failure 74 0.147
309
P LPR021 Leprosy 3 69 0.147
310
P GST044 Gastritis 56 0.147
311
HNS001 Hansen's Disease 34 0.147
312
CRB004 Cerebral Artery Occlusion 45 0.147
313
P BRS044 Breast Adenocarcinoma 59 0.146
314
THR024 Thrombosis 57 0.145
315
PTT037 Pituitary Tumors 44 0.145
316
P APL001 Aplastic Anemia 74 0.145
317
c MCR129 Microvascular Complications of Diabetes 1 66 0.145
318
P GLM040 Glioma Susceptibility 1 81 0.145
319
HMP009 Haemophilus Influenzae 43 0.144
320
ALL014 Allergic Encephalomyelitis 38 0.144
321
ATN004 Autonomic Neuropathy 45 0.144
322
ATS010 Autosomal Recessive Disease 48 0.144
323
P GND004 Gonadal Dysgenesis 48 0.143
324
ANG005 Anogenital Venereal Wart 55 0.143
325
ALC007 Alcohol Dependence 66 0.142
326
DBT010 Diabetic Neuropathy 54 0.142
328
ORL015 Oral Squamous Cell Carcinoma 43 0.141
329
P CRD119 Cardiac Arrest 67 0.140
330
DPR016 Depression 63 0.140
331
NRR001 Neuroretinitis 42 0.140
332
RTN023 Retinitis 46 0.139
333
SKN019 Skin Melanoma 68 0.139
334
P CND004 Candidiasis 58 0.139
335
P DDN001 Duodenal Ulcer 52 0.139
336
c WLM018 Wilms Tumor 5 61 0.139
337
P MYT002 Myotonic Dystrophy 49 0.138
338
c THR092 Thrombophilia Due to Thrombin Defect 73 0.138
339
MTB004 Metabolic Acidosis 50 0.138
340
ANT024 Anthrax Disease 58 0.138
341
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.138
342
c HNT011 Huntington Disease-Like 3 38 0.138
343
LYM019 Lymphosarcoma 46 0.138
344
DNH001 Donohue Syndrome 62 0.138
345
IMP005 Impotence 52 0.138
346
P ALP008 Alopecia 54 0.137
347
P HYP730 Hypogonadotropic Hypogonadism 52 0.137
348
P PNM007 Pneumonia 68 0.137
349
FCT001 Factor Viii Deficiency 51 0.136
350
EYD002 Eye Disease 58 0.136
351
P ALC033 Alcohol Use Disorder 58 0.136
352
HPT022 Hepatoblastoma 56 0.136
353
P MTR004 Maturity-Onset Diabetes of the Young 65 0.136
354
P INS002 in Situ Carcinoma 53 0.136
355
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.135
356
ANX010 Anxiety 73 0.135
357
ANR007 Anorexia Nervosa 63 0.135
358
P MLT020 Multiple Sclerosis 72 0.135
359
P PTT006 Pituitary Adenoma 55 0.135
360
P THY023 Thymoma 65 0.135
361
P HYP083 Hypopituitarism 53 0.134
362
ORL011 Oral Cancer 60 0.134
363
MSC157 Muscular Dystrophy, Duchenne Type 72 0.134
364
c THY107 Thymoma, Familial 52 0.134
365
PLM001 Pulmonary Tuberculosis 69 0.134
366
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.133
367
EMB004 Embryonal Carcinoma 56 0.133
368
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.133
369
HYP014 Hyperuricemia 52 0.133
370
LRN002 Laron Syndrome 62 0.133
371
MSC007 Muscle Hypertrophy 64 0.133
372
ENT011 Enterocolitis 51 0.133
373
P NPH012 Nephrotic Syndrome 60 0.132
374
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.132
375
P SZR006 Seizure Disorder 56 0.132
376
MDD018 Middle East Respiratory Syndrome 43 0.132
377
AMN001 Amenorrhea 54 0.131
378
TRY001 Trypanosomiasis 50 0.131
379
c HPT007 Hepatitis E 53 0.130
380
P PRK057 Parkinson Disease, Late-Onset 78 0.130
381
TRN018 Transitional Cell Carcinoma 56 0.130
382
WST005 West Nile Virus 54 0.130
383
P RBL001 Rubella 59 0.130
384
P SCH015 Schizophrenia 74 0.130
385
P RTN018 Retinal Disease 53 0.130
386
SPL018 Splenomegaly 48 0.129
387
P VSC011 Vasculitis 62 0.129
388
ANG054 Angina Pectoris 66 0.129
389
c HNT004 Huntington Disease-Like 2 50 0.128
390
P MDL005 Medulloblastoma 77 0.128
391
c SCL052 Scleroderma, Familial Progressive 61 0.127
392
c BRN108 Branchiootic Syndrome 1 62 0.127
393
MNT002 Mental Depression 58 0.127
394
c FNC027 Fanconi Anemia, Complementation Group a 81 0.126
395
ULC004 Ulcerative Colitis 73 0.126
396
P MMP001 Mumps 58 0.126
397
MST005 Mastitis 53 0.126
398
CLT003 Colitis 62 0.125
399
YLL002 Yellow Fever 61 0.125
400
GRN017 Granulocytopenia 44 0.124
401
MCS002 Mucositis 56 0.124
402
P URT039 Urticaria 58 0.124
403
AZS001 Azoospermia 50 0.124
404
FLR002 Filariasis 55 0.123
405
WRN001 Werner Syndrome 69 0.123
406
SFT003 Soft Tissue Sarcoma 56 0.123
407
P CLC063 Celiac Disease 1 66 0.123
408
P OVR049 Ovarian Disease 52 0.123
409
VSL002 Visual Epilepsy 59 0.123
410
HLC007 Helicobacter Pylori Infection 59 0.123
411
P MYS003 Myasthenia Gravis 68 0.123
412
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.123
413
PLM033 Pulmonary Embolism 59 0.123
414
c ACT134 Acute Liver Failure 56 0.123
415
P CHN012 Chondrosarcoma 56 0.122
416
CYS005 Cysticercosis 53 0.122
417
DFF036 Differentiated Thyroid Carcinoma 52 0.122
418
BRN028 Brain Cancer 74 0.122
419
P ART023 Arthropathy 62 0.121
420
P DMN002 Dementia 66 0.121
421
P UVT001 Uveitis 57 0.121
422
P SYS005 Systemic Scleroderma 68 0.121
423
P BPL003 Bipolar Disorder 56 0.121
424
P MYC084 Mycobacterium Tuberculosis 1 68 0.121
425
P ANG015 Angioedema 57 0.120
426
ALL006 Allergic Asthma 56 0.120
427
GST040 Gastric Adenocarcinoma 70 0.120
428
c MJR024 Major Affective Disorder 9 41 0.120
429
c MJR022 Major Affective Disorder 8 38 0.120
430
BRN002 Bronchiolitis 59 0.120
431
DNT012 Dental Caries 53 0.120
432
P GLY013 Glycogen Storage Disease 60 0.120
433
c MCR112 Microvascular Complications of Diabetes 2 41 0.119
434
P PLM037 Pulmonary Hypertension 67 0.119
435
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.119
436
CHL079 Children's Interstitial Lung Disease 26 0.119
437
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.119
438
P MYC008 Myocarditis 59 0.119
439
c MST023 Mesothelioma, Malignant 57 0.119
440
CTN007 Cutaneous Leishmaniasis 62 0.118
441
PRN019 Perinatal Necrotizing Enterocolitis 59 0.118
442
c ACT135 Acute Graft Versus Host Disease 52 0.118
443
c GRV008 Graves Disease 1 56 0.118
444
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.118
445
CHL065 Cholangiocarcinoma 68 0.117
446
P MCR010 Microcephaly 59 0.117
447
P TRM003 Tremor 54 0.117
448
ALL003 Allergic Rhinitis 67 0.117
449
INT007 Intermediate Coronary Syndrome 55 0.116
450
LMY002 Leiomyoma 52 0.116
452
c HMC039 Hemochromatosis, Type 1 74 0.115
453
MNN042 Meningioma, Radiation-Induced 62 0.115
454
DMY004 Demyelinating Disease 52 0.115
455
P SCK005 Sickle Cell Disease 50 0.115
456
c PLY105 Polycystic Ovary Syndrome 1 38 0.114
457
HRP004 Herpes Zoster 60 0.114
458
P CHR345 Chronic Pain 44 0.114
459
ISL003 Isolated Growth Hormone Deficiency 49 0.114
460
THY030 Thyroid Gland Disease 52 0.114
461
CLR109 Colorectal Adenocarcinoma 51 0.114
462
P HYP061 Hypertrophic Cardiomyopathy 70 0.114
463
VRL003 Variola Major 42 0.114
464
PPT005 Peptic Ulcer Disease 59 0.114
465
INT079 Intrahepatic Cholangiocarcinoma 51 0.113
466
P HML002 Hemolytic Anemia 63 0.113
467
P RTN008 Retinitis Pigmentosa 79 0.113
468
P CNR004 Cone-Rod Dystrophy 2 73 0.113
469
PLC008 Placenta Disease 50 0.113
470
c ACT068 Acute Cystitis 63 0.113
471
P GCH001 Gaucher's Disease 63 0.112
472
P ASP006 Aspergillosis 69 0.112
473
P PRD006 Prader-Willi Syndrome 59 0.112
474
TRT001 Teratocarcinoma 45 0.112
475
LNG031 Lung Benign Neoplasm 51 0.112
476
P PLY018 Polycythemia 56 0.111
477
FCT007 Factor Vii Deficiency 67 0.111
478
LYS002 Lysosomal Storage Disease 52 0.111
479
GT001 Gout 64 0.111
480
ART016 Aortic Aneurysm 69 0.111
481
ANR040 Aneurysm 59 0.111
482
P LCT001 Lactic Acidosis 51 0.111
483
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.110
484
P PRM006 Primary Biliary Cirrhosis 62 0.110
485
ACD008 Acid-Labile Subunit Deficiency 54 0.110
486
P MNN013 Meningitis 66 0.109
487
HSH003 Hashimoto Thyroiditis 62 0.109
488
HYP020 Hyperprolactinemia 64 0.109
489
PLM010 Pulmonary Edema 54 0.109
490
P RCT021 Rectum Cancer 52 0.109
491
ATN005 Autonomic Dysfunction 46 0.109
492
CVD001 Covid-19 44 0.108
493
CRT072 Creutzfeldt-Jakob Disease 70 0.108
494
SCR011 Scrapie 39 0.108
495
CHR100 Chronic Ulcer of Skin 55 0.108
496
CNN005 Connective Tissue Disease 68 0.108
497
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.107
498
BLR008 Bilirubin Metabolic Disorder 57 0.107
499
NRL016 Neural Tube Defects 82 0.107
500
P RTN016 Retinal Degeneration 53 0.107
501
P ADL010 Adult Respiratory Distress Syndrome 65 0.107
502
PRT013 Portal Hypertension 59 0.107
503
PRM329 Premature Aging 35 0.107
504
P MJR001 Major Depressive Disorder 68 0.106
505
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.106
506
c BTT014 Beta-Thalassemia 74 0.106
507
MDD011 Mood Disorder 62 0.106
508
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 0.106
509
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.105
510
c SPN225 Spondyloarthropathy 1 73 0.105
511
c FML035 Familial Hyperlipidemia 55 0.105
512
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.105
513
P ATS364 Autism 70 0.105
514
ETN001 Eating Disorder 60 0.105
515
DGN001 Degenerative Disc Disease 48 0.104
516
GNG013 Gingivitis 59 0.104
517
ACT119 Acute Promyelocytic Leukemia 63 0.104
518
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.104
519
P HML001 Hemolytic-Uremic Syndrome 53 0.104
520
KRT019 Keratitis, Hereditary 65 0.104
521
c MNN043 Meningioma, Familial 74 0.104
522
c GCH015 Gaucher Disease, Type I 70 0.103
523
HDN002 Head Injury 46 0.103
524
ANX004 Anoxia 40 0.102
525
END041 Endometrial Adenocarcinoma 63 0.102
526
SPN021 Spinal Meningioma 50 0.102
527
P END033 Endocarditis 57 0.102
528
EWN003 Ewing Sarcoma 69 0.101
529
c MGR028 Migraine with or Without Aura 1 67 0.101
530
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.101
531
c ATS007 Autism Spectrum Disorder 67 0.101
532
P SRC025 Sarcoidosis 1 70 0.101
533
c EXD008 Exudative Vitreoretinopathy 1 71 0.101
534
P NRF002 Neurofibromatosis 56 0.101
535
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.100
536
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.100
537
SCR001 Secretory Meningioma 41 0.100
538
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.100
539
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 57 0.100
540
VLV047 Volvulus of Midgut 49 0.100
541
ISL001 Islet Cell Tumor 56 0.100
542
NRM005 Neuromuscular Disease 64 0.100
543
P HYP024 Hypoparathyroidism 56 0.100
544
TCK001 Tick-Borne Encephalitis 56 0.100
545
CCC001 Coccidioidomycosis 58 0.099
546
OTT002 Otitis Media 72 0.099
547
PLS011 Plasmacytoma 56 0.099
548
BCL014 B-Cell Growth Factor 35 0.099
549
KRT009 Keratosis 51 0.099
550
c DNG003 Dengue Disease 59 0.099
551
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.099
552
c PRD040 Periodontitis, Chronic 53 0.098
553
CHL068 Cholestasis 61 0.098
554
BRN056 Bronchopulmonary Dysplasia 57 0.098
555
P MTR014 Motor Neuron Disease 65 0.098
556
HMC014 Homocysteinemia 53 0.098
557
P MNC007 Monocytic Leukemia 53 0.098
558
P HYD006 Hydrocephalus 66 0.098
559
NTR046 Neutrophil Migration 50 0.097
560
P SLM003 Salmonellosis 55 0.097
561
BRS051 Breast Disease 58 0.097
562
HYP081 Hypolipoproteinemia 51 0.097
563
c FML021 Familial Hypercholesterolemia 66 0.097
564
PNC001 Pancytopenia 54 0.097
565
ONC002 Onchocerciasis 52 0.097
566
P LMY004 Leiomyosarcoma 63 0.096
567
49X006 49, Xxxxy Syndrome 41 0.096
568
SPN051 Spondylitis 51 0.096
569
CRD137 Cardiogenic Shock 47 0.096
570
P TMP001 Temporal Lobe Epilepsy 50 0.096
571
SYN007 Synovitis 54 0.096
572
PLC002 Plica Syndrome 36 0.096
573
IGR001 Ige Responsiveness, Atopic 59 0.095
574
TRP002 Tropical Spastic Paraparesis 50 0.095
575
c SCN007 Secondary Hyperparathyroidism 51 0.095
576
CRY003 Cryptosporidiosis 54 0.095
577
LMB062 Limb Ischemia 55 0.095
578
INF009 Inflammatory Spondylopathy 31 0.095
579
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.095
580
P CNJ013 Conjunctivitis 65 0.095
581
RFR010 Refractory Anemia 48 0.094
582
P HDC001 Headache 57 0.094
583
P PLY014 Polycystic Kidney Disease 62 0.094
584
IGG001 Iga Glomerulonephritis 48 0.094
585
CNS004 Constipation 58 0.094
586
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.094
587
PLY100 Polyploidy 40 0.094
588
P EPL164 Epilepsy 71 0.094
589
P THR117 Three M Syndrome 1 63 0.093
590
c JVN010 Juvenile Rheumatoid Arthritis 64 0.093
591
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.093
592
c GLL024 Gallbladder Disease 1 53 0.093
593
P LRY044 Larynx Cancer 55 0.093
594
BRN004 Brain Edema 56 0.093
595
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.092
596
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.092
597
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.092
598
c PRM005 Primary Hyperparathyroidism 58 0.092
599
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.092
600
P SCL018 Scoliosis 60 0.092
601
OST017 Osteomyelitis 64 0.092
602
SPP011 Suppression of Tumorigenicity 12 59 0.092
603
CHL147 Chlamydia Pneumonia 48 0.091
604
GST023 Gastric Ulcer 53 0.091
605
IRN001 Iron Deficiency Anemia 59 0.091
606
NRT004 Neuritis 52 0.091
607
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.090
608
RDC006 Red Cell Aplasia 43 0.090
609
P SNS001 Sensorineural Hearing Loss 60 0.090
610
P TBR001 Tuberous Sclerosis 70 0.090
611
RTN020 Retinal Vascular Disease 46 0.090
612
DFF005 Diffuse Large B-Cell Lymphoma 55 0.089
613
PST092 Posttransplant Acute Limbic Encephalitis 29 0.089
614
PLS007 Plasmodium Falciparum Malaria 52 0.089
615
P SML001 Small Cell Carcinoma 52 0.089
616
P PMP001 Pemphigus 54 0.089
617
THR004 Thrombocytosis 51 0.089
618
c FNC043 Fanconi Anemia, Complementation Group E 62 0.089
619
NDL007 Nodular Goiter 47 0.089
620
P MTC069 Mitochondrial Disorders 56 0.088
621
c BSL007 Basal Cell Carcinoma 68 0.088
622
P PRC019 Precocious Puberty 46 0.088
623
PHN003 Phenylketonuria 75 0.088
624
ORP003 Oropharynx Cancer 55 0.088
625
ALV002 Alveolar Echinococcosis 49 0.088
626
LST001 Listeriosis 56 0.088
627
RNL077 Renal Fibrosis 47 0.088
628
LYM009 Lymphocytic Choriomeningitis 47 0.088
629
SCK003 Sickle Cell Anemia 74 0.088
630
LMY014 Leiomyoma, Uterine 56 0.088
631
HYP017 Hypophosphatemia 50 0.088
632
c GLY008 Glycogen Storage Disease Ii 70 0.088
633
MYL005 Myelofibrosis 70 0.087
634
FST010 Fasting Hypoglycemia 35 0.087
635
RTN017 Retinal Detachment 61 0.087
636
PNG002 Pain Agnosia 51 0.087
637
CNT047 Contact Dermatitis 58 0.087
638
THY111 Thyroid Carcinoma, Familial Medullary 67 0.087
639
NPH009 Nephrolithiasis 55 0.087
640
NRN004 Neuroendocrine Tumor 55 0.086
641
FLR001 Filarial Elephantiasis 55 0.086
642
SWN001 Swine Influenza 45 0.086
643
c DWL002 Dowling-Degos Disease 1 58 0.086
644
KLD004 Keloid Disorder 40 0.086
645
c PRS136 Prostate Cancer, Hereditary, 6 33 0.086
646
c PRS130 Prostate Cancer, Hereditary, 8 32 0.086
647
P CYS018 Cystitis 59 0.086
648
CRN017 Coronary Thrombosis 47 0.086
649
P PRR002 Pure Red-Cell Aplasia 47 0.085
650
P FML011 Familial Adenomatous Polyposis 72 0.085
651
PRT058 Pure Autonomic Failure 59 0.085
652
THY125 Thyroid Gland Medullary Carcinoma 50 0.085
653
DYS073 Dysphagia 50 0.085
654
VRC005 Varicose Veins 60 0.085
655
BNG077 Benign Idiopathic Neonatal Seizures 26 0.085
656
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.085
657
P MLT008 Multinodular Goiter 42 0.085
658
KRT006 Keratoconjunctivitis 53 0.085
659
NWB001 Newborn Respiratory Distress Syndrome 58 0.085
660
P FRG001 Fragile X Syndrome 70 0.085
661
BBS001 Babesiosis 48 0.084
662
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.084
663
TST014 Testicular Cancer 46 0.084
664
P CTN015 Cutaneous T Cell Lymphoma 49 0.084
665
OST003 Osteonecrosis 61 0.084
666
FDL002 Food Allergy 51 0.084
667
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.083
668
EPD015 Epidemic Typhus 45 0.083
669
P HMN010 Hemangioma 61 0.083
670
ART002 Arts Syndrome 64 0.083
671
TRC023 Trichinosis 53 0.083
672
P NRV007 Nervous System Disease 66 0.083
673
P SLP005 Sleep Disorder 59 0.083
674
ADR016 Adrenal Cortical Carcinoma 48 0.082
675
BLM001 Bloom Syndrome 67 0.082
676
ECT026 Ectopic Pregnancy 50 0.082
677
LYM040 Lymphoblastic Lymphoma 54 0.082
678
c WLM013 Wilms Tumor 1 65 0.082
679
P HYP265 Hypotonia 43 0.082
680
FBR012 Fabry Disease 72 0.082
681
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.082
682
P PRP029 Porphyria 62 0.082
683
PLY001 Polycythemia Vera 69 0.082
684
MNN009 Meningoencephalitis 49 0.082
685
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.082
686
DYS015 Dysentery 52 0.082
687
P OPT006 Optic Nerve Disease 60 0.082
688
PLC005 Placental Insufficiency 57 0.081
689
ADR004 Adrenal Cortical Adenocarcinoma 39 0.081
690
MCL006 Macular Retinal Edema 55 0.081
691
CRB037 Cerebral Palsy 69 0.081
692
NSS002 Neisseria Meningitidis Infection 47 0.081
693
MYC006 Mycosis Fungoides 66 0.081
695
P END084 Endocrine System Disease 45 0.081
696
P MLN069 Melanoma, Uveal 59 0.080
697
CMM005 Common Cold 57 0.080
698
AMN003 Amnestic Disorder 54 0.080
699
P OPN001 Open-Angle Glaucoma 49 0.080
700
HPT004 Hepatic Coma 45 0.080
701
BRT037 Brittle Diabetes 25 0.079
702
CMM004 Common Variable Immunodeficiency 68 0.079
703
RST023 Resting Heart Rate, Variation in 41 0.079
704
P LKD001 Leukodystrophy 59 0.079
705
PPL002 Papillary Carcinoma 47 0.079
706
P OLG002 Oligodendroglioma 67 0.079
707
CLF027 Cleft Palate, Isolated 64 0.079
708
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.079
709
P MYS005 Myositis 56 0.079
710
P MYP006 Myopia 55 0.079
711
THY122 Thyroid Gland Cancer 57 0.079
712
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.079
713
c SVR005 Severe Pre-Eclampsia 50 0.078
714
GNT003 Genital Herpes 54 0.078
715
CRN030 Coronary Stenosis 50 0.078
716
P EPD016 Epidermolysis Bullosa 53 0.078
717
c ATM011 Autoimmune Hepatitis 63 0.078
718
INT017 Intestinal Schistosomiasis 48 0.078
719
P SHR001 Short Bowel Syndrome 53 0.078
720
PSR001 Psoriatic Arthritis 61 0.078
721
ANS011 Anus Cancer 56 0.078
722
P SBS003 Substance Abuse 55 0.078
723
P LPS002 Liposarcoma 65 0.078
724
P MLT074 Multiple Endocrine Neoplasia 56 0.077
725
GST019 Gastrointestinal Stromal Tumor 78 0.077
726
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.077
727
HMG005 Hemoglobinopathy 56 0.077
728
PRP080 Peripheral Artery Disease 53 0.077
729
P INT068 Intestinal Disease 53 0.077
730
CRD132 Cardiac Conduction Defect 58 0.077
731
SMN007 Seminoma 43 0.077
732
CNN003 Conn's Syndrome 79 0.077
733
GLM044 Glomerular Disease 37 0.076
734
SNS003 Sensory Peripheral Neuropathy 54 0.076
735
ATM052 Autoimmune Disease 1 37 0.076
736
P HMR003 Hemorrhagic Disease 53 0.076
737
GRD007 Grade Iii Astrocytoma 59 0.076
738
P MLG074 Malignant Mesenchymoma 40 0.076
739
TRN015 Transient Cerebral Ischemia 63 0.076
740
P GLL022 Guillain-Barre Syndrome 59 0.076
741
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.076
742
HRT012 Heart Valve Disease 53 0.076
743
NRL005 Neurilemmoma 60 0.076
744
INF034 Infective Endocarditis 53 0.076
745
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.075
746
P LYM033 Lymphoproliferative Syndrome 59 0.075
747
P BCK002 Beckwith-Wiedemann Syndrome 62 0.075
748
P DYS154 Dystonia 65 0.075
749
P DBT005 Diabetes Insipidus 55 0.075
750
P RTT002 Rett Syndrome 80 0.075
751
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.075
752
MTC005 Mitochondrial Metabolism Disease 49 0.075
753
P LNG028 Long Qt Syndrome 66 0.074
754
KRT008 Keratopathy 47 0.074
755
TND005 Tendinitis 54 0.074
756
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 44 0.074
757
HMR039 Hemorrhage, Intracerebral 57 0.074
758
P CCK001 Cockayne Syndrome 66 0.074
759
P AGM001 Agammaglobulinemia 65 0.074
760
CCC002 Coccidiosis 51 0.074
761
c DRR009 Diarrhea 6 46 0.074
762
P LCH002 Lichen Planus 53 0.074
763
PMP006 Pemphigus Vulgaris, Familial 57 0.074
764
PRT038 Protein-Energy Malnutrition 54 0.073
765
P OBS001 Obstructive Jaundice 50 0.073
766
DNG002 Dengue Hemorrhagic Fever 60 0.073
767
DSS008 Disease of Mental Health 58 0.073
768
GST071 Gastrointestinal Carcinoma 47 0.073
769
GST010 Gestational Trophoblastic Neoplasm 46 0.073
770
c PRG020 Paragangliomas 3 39 0.073
771
c TBR025 Tuberous Sclerosis 1 77 0.072
772
BRS099 Breast Ductal Carcinoma 62 0.072
773
DCT002 Ductal Carcinoma in Situ 59 0.072
774
P CHL066 Cholangitis 51 0.072
775
PNC034 Pancreas Disease 48 0.072
776
CRN027 Corneal Neovascularization 47 0.072
777
CHR066 Chronic Fatigue Syndrome 61 0.072
778
c PNC106 Pancreatic Agenesis 1 51 0.072
779
SCH036 Scheie Syndrome 72 0.072
780
HMT002 Hematologic Cancer 62 0.072
781
HPT019 Hepatic Encephalopathy 60 0.072
783
PTT009 Pituitary Gland Disease 54 0.072
784
APH002 Aphasia 57 0.072
785
P PYL005 Pyelonephritis 56 0.072
786
PRP016 Paraplegia 52 0.072
787
c OVR114 Ovarian Cancer 1 38 0.072
788
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.072
789
CRY005 Cryptococcosis 58 0.071
790
GLS018 Glass Syndrome 57 0.071
791
GNG003 Gingival Recession 44 0.071
792
LPR001 Lepromatous Leprosy 50 0.071
793
SYN036 Syncope 45 0.071
794
c LRG001 Large Cell Carcinoma 50 0.071
795
P SPN046 Spinal Muscular Atrophy 62 0.071
796
P MMB011 Membranous Nephropathy 50 0.071
797
FNG017 Fungal Infectious Disease 53 0.071
798
P ANP001 Anaplastic Large Cell Lymphoma 58 0.071
799
HYP457 Hypertrophic Scars 42 0.071
800
c JVN061 Juvenile Arthritis 60 0.071
801
PLS009 Plasma Cell Neoplasm 51 0.071
802
CHL004 Cholelithiasis 49 0.071
803
HST011 Histoplasmosis 55 0.071
804
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.071
805
P PLM034 Pulmonary Emphysema 55 0.071
806
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.071
807
AMB001 Amebiasis 55 0.071
808
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.070
809
MST004 Mast Cell Neoplasm 42 0.070
810
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.070
811
ALL010 Allergic Contact Dermatitis 56 0.070
812
P ANT006 Antiphospholipid Syndrome 55 0.070
813
P SJG008 Sjogren Syndrome 61 0.070
814
HRT011 Heart Septal Defect 50 0.070
815
SRC027 Sarcoma, Synovial 58 0.070
816
C1N001 C1 Inhibitor Deficiency 39 0.070
817
RTR008 Root Resorption 45 0.070
818
c PRM196 Premature Ovarian Failure 1 67 0.070
819
SPS057 Spasticity 45 0.070
820
c ACT004 Acute Diarrhea 39 0.070
821
GST050 Gastrointestinal System Disease 56 0.069
822
RDN001 Reading Disorder 40 0.069
823
CRH005 Crohn's Colitis 53 0.069
824
MLD001 Melioidosis 68 0.069
825
P PLY041 Polymyositis 57 0.069
826
c INH020 Inherited Metabolic Disorder 47 0.069
827
P FCL005 Focal Segmental Glomerulosclerosis 57 0.069
828
CLL003 Cellulitis 54 0.069
829
CLF001 Cleft Lip 53 0.068
830
P CHR071 Charcot-Marie-Tooth Disease 65 0.068
831
CRN322 Coronavirus Infectious Disease 40 0.068
832
PRC002 Paracoccidioidomycosis 54 0.068
833
TND004 Tendinopathy 43 0.068
834
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.068
835
P VTR007 Vitreoretinopathy 46 0.068
836
FBR047 Fibromyalgia 58 0.068
837
INT075 Intracranial Hypertension 53 0.068
838
P FRN006 Frontotemporal Dementia 68 0.068
839
MMM001 Mammary Paget's Disease 53 0.067
840
c PSR023 Psoriasis 1 52 0.067
841
APN008 Apnea, Obstructive Sleep 64 0.067
842
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.067
843
P ANR048 Aniridia 1 63 0.067
844
PTH003 Pathologic Nystagmus 52 0.067
845
MCP033 Mucopolysaccharidoses 38 0.067
846
ANG020 Angiosarcoma 64 0.067
847
ORL005 Oral Candidiasis 56 0.067
848
BRR014 Barrett Esophagus 65 0.067
849
IDP033 Idiopathic Edema 44 0.067
850
GST092 Gastroesophageal Reflux 67 0.067
851
c CHR682 Chronic Bilirubin Encephalopathy 39 0.067
852
P OVR046 Ovarian Cyst 47 0.067
853
c GLC092 Glaucoma, Primary Open Angle 62 0.067
854
CRT013 Carotid Stenosis 50 0.067
855
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.066
856
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.066
857
P ANG001 Angelman Syndrome 69 0.066
858
CRN036 Craniopharyngioma 65 0.066
859
SXL003 Sexual Disorder 47 0.066
860
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 53 0.066
861
LNG039 Lung Squamous Cell Carcinoma 66 0.066
862
KHL003 Kohlschutter-Tonz Syndrome 65 0.066
863
ACT200 Acute Monoblastic Leukemia 52 0.066
864
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.066
865
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.066
866
TNG007 Tongue Carcinoma 51 0.065
867
INT002 Intermittent Claudication 61 0.065
868
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.065
869
CRD223 Cardiac Arrhythmia 60 0.065
870
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.065
871
P GLL018 Gallbladder Cancer 57 0.065
872
P NJM001 Nijmegen Breakage Syndrome 74 0.065
873
DBT004 Diabetic Polyneuropathy 49 0.065
874
c PSR017 Psoriasis 2 53 0.065
875
c CNG006 Congenital Hypothyroidism 64 0.065
876
BLD131 Bladder Urothelial Carcinoma 62 0.065
877
MNT001 Mantle Cell Lymphoma 69 0.065
878
INT066 Interstitial Lung Disease 60 0.065
879
P ALP009 Alopecia Areata 60 0.065
880
CHL067 Cholecystitis 57 0.065
881
c PSR032 Psoriasis 11 47 0.065
882
c PSR028 Psoriasis 7 42 0.065
883
c PSR018 Psoriasis 13 41 0.065
884
c ALP101 Alpha-Thalassemia 62 0.064
885
MNK002 Monkeypox 39 0.064
886
AND002 Androgen Insensitivity Syndrome 66 0.064
887
MLT157 Multiple System Atrophy 1 70 0.064
888
TTH006 Tooth Disease 46 0.064
889
URT049 Urate Oxidase, Pseudogene 25 0.064
890
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.063
891
P BLD062 Bile Duct Cancer 67 0.063
892
OST011 Osteomalacia 52 0.063
893
END062 Endometrial Hyperplasia 48 0.063
894
c CNT035 Central Nervous System Disease 52 0.063
895
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.063
896
c CNG012 Congenital Generalized Lipodystrophy 52 0.063
897
ALB002 Albinism 46 0.063
898
HST010 Histiocytosis 48 0.063
899
BRT054 Brittle Bone Disorder 72 0.063
900
ASP026 Asplenia, Isolated Congenital 44 0.063
901
c LKM070 Leukemia, Acute Monocytic 57 0.063
902
P CRV031 Cervical Adenocarcinoma 49 0.063
903
FBR054 Fibroma 44 0.063
904
IRR002 Irritable Bowel Syndrome 65 0.063
905
c PNC108 Pancreatitis, Hereditary 70 0.063
906
MCR013 Microphthalmia 57 0.063
907
OVR059 Ovary Adenocarcinoma 53 0.063
908
ASP003 Aseptic Meningitis 51 0.063
909
CRC006 Carcinoid Syndrome 55 0.062
910
P ESP024 Esophagitis 62 0.062
911
P TRC086 Trichohepatoenteric Syndrome 1 62 0.062
912
P CRV039 Cervicitis 49 0.062
913
ACT003 Acute Kidney Tubular Necrosis 45 0.062
914
P FML187 Familial Hypertension 37 0.062
915
CND006 Candida Glabrata 32 0.062
916
ADR007 Adrenoleukodystrophy 75 0.062
917
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.062
918
P ICH004 Ichthyosis 54 0.062
919
END040 Endogenous Depression 55 0.062
920
P NMN002 Niemann-Pick Disease 59 0.062
921
c BCT013 Bacterial Pneumonia 48 0.062
922
P BNG030 Benign Ependymoma 60 0.062
923
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 50 0.061
924
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.061
925
CRP001 Carpal Tunnel Syndrome 67 0.061
926
GRM010 Germ Cells Tumors 34 0.061
927
MXD026 Mixed Glioma 45 0.061
928
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.061
929
CRC014 Carcinoid Tumors, Intestinal 47 0.061
930
c HYP272 Hypercholesterolemia, Familial, 3 44 0.061
931
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.060
932
c MLG079 Malignant Pleural Mesothelioma 42 0.060
933
P CRN037 Craniosynostosis 68 0.060
934
P MYC033 Myoclonus 46 0.060
935
SBC016 Subacute Delirium 44 0.060
936
ANK001 Ankylosis 51 0.060
937
CLL010 Cellular Ependymoma 54 0.060
938
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.060
939
BCK006 Back Pain 42 0.060
940
c LPM012 Lipomatosis, Multiple 60 0.060
941
P FML012 Familial Partial Lipodystrophy 54 0.060
942
CHR005 Chorioamnionitis 51 0.060
943
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.060
944
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.060
945
INT029 Interleukin-7 Receptor Alpha Deficiency 22 0.060
946
P DRM010 Dermatomyositis 61 0.060
947
P ATR005 Atrophic Gastritis 50 0.060
948
c CHR417 Chronic Graft Versus Host Disease 57 0.059
949
GYN001 Gynecomastia 49 0.059
950
P SCL009 Sclerosing Cholangitis 48 0.059
951
CCN002 Cocaine Abuse 49 0.059
952
TLR001 Tularemia 51 0.059
953
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.059
954
SRS001 Serous Cystadenocarcinoma 52 0.059
955
P OCY003 Oocyte Maturation Defect 1 45 0.059
956
PST028 Post-Traumatic Stress Disorder 58 0.059
957
THR013 Thoracic Outlet Syndrome 54 0.059
958
P HMC002 Homocystinuria 53 0.059
959
MSN004 Mesenchymal Cell Neoplasm 41 0.059
960
NRF007 Neurofibroma 64 0.059
961
INT067 Interstitial Nephritis 48 0.059
962
P RNL015 Renal Hypertension 47 0.059
963
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.058
964
NRN001 Neuroendocrine Carcinoma 47 0.058
965
ENT004 Enthesopathy 49 0.058
966
c VRL007 Viral Encephalitis 51 0.058
967
ACT228 Acute Radiation Syndrome 29 0.058
968
INF021 Infant Gynecomastia 31 0.058
969
OBS002 Obsessive-Compulsive Disorder 68 0.058
970
CLF004 Cleft Lip/palate 54 0.058
971
c HRD202 Hereditary Lymphedema I 50 0.058
972
c THY102 Thyroid Cancer, Nonmedullary, 2 58 0.058
973
ADN011 Adenoid Cystic Carcinoma 70 0.058
974
NSP002 Nasopharyngitis 43 0.058
975
GSG001 Gas Gangrene 53 0.058
976
HMR023 Hemorrhagic Cystitis 45 0.058
977
SBC001 Subacute Sclerosing Panencephalitis 56 0.058
978
AND020 Androgen Insensitivity, Partial 56 0.058
979
P MTC003 Metachromatic Leukodystrophy 70 0.058
980
TNS007 Taeniasis 45 0.058
981
CHL131 Chlorpropamide-Alcohol Flushing 22 0.058
982
MCR004 Macroglobulinemia 49 0.058
983
CRC021 Carcinosarcoma 62 0.057
984
PNM001 Pneumocystosis 59 0.057
985
CHR073 Choreatic Disease 52 0.057
986
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.057
987
TNS005 Tonsillitis 57 0.057
988
HMP005 Hemiplegia 55 0.057
989
GRD001 Giardiasis 45 0.057
990
MXD005 Mixed Connective Tissue Disease 58 0.057
991
P PRS038 Personality Disorder 65 0.057
992
IMM003 Immunoglobulin Alpha Deficiency 45 0.057
993
P RNG032 Ring Chromosome 42 0.057
994
HMP001 Hemopericardium 48 0.057
995
STT001 Status Epilepticus 60 0.056
996
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.056
997
P CRB059 Cerebellar Degeneration 37 0.056
998
MMB001 Membranoproliferative Glomerulonephritis 55 0.056
999
MYX004 Myxedema 43 0.056
1000
P WSK001 Wiskott-Aldrich Syndrome 72 0.056
1001
RHM001 Rheumatic Fever 60 0.056
1002
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.056
1003
DBT006 Diabetic Macular Edema 48 0.056
1004
HRP008 Herpes Simiae 25 0.056
1005
P MLG056 Malignant Hyperthermia 67 0.056
1006
TTR011 Tetraploidy 47 0.056
1007
SHG001 Shigellosis 60 0.056
1008
MYL031 Myeloproliferative Neoplasm 66 0.056
1009
c HYP768 Hyperlipoproteinemia, Type I 67 0.056
1010
MLG164 Malignant Epithelial Tumor of Ovary 26 0.056
1011
HYD038 Hydrops Fetalis, Nonimmune 62 0.056
1012
P BNC003 Bone Cancer 58 0.056
1013
SYS003 Systolic Heart Failure 49 0.056
1014
THR016 Thrombophlebitis 51 0.056
1015
BCT002 Bacterial Vaginosis 53 0.056
1016
c CHL119 Cholangitis, Primary Sclerosing 57 0.055
1017
P NNN008 Noonan Syndrome 1 76 0.055
1018
EXS001 Exostosis 46 0.055
1019
RYN005 Raynaud Phenomenon 47 0.055
1020
ZLL002 Zollinger-Ellison Syndrome 55 0.055
1021
OLG001 Oligospermia 45 0.055
1022
P CRN024 Corneal Disease 44 0.055
1023
c INF071 Inflammatory Bowel Disease 1 67 0.055
1024
P VNT002 Ventricular Septal Defect 60 0.055
1025
P END047 Endophthalmitis 53 0.055
1026
BRN032 Brain Glioma 45 0.055
1027
BLL003 Bell's Palsy 51 0.055
1028
c SYS043 Systemic Lupus Erythematosus 1 38 0.055
1029
VRC001 Varicocele 49 0.055
1030
c MLG084 Malignant Fibrous Histiocytoma 63 0.055
1031
P ART005 Arteriovenous Malformation 65 0.055
1032
c INF145 Infantile Liver Failure Syndrome 1 50 0.055
1033
P TTR001 Tetralogy of Fallot 70 0.054
1034
OMN001 Omenn Syndrome 67 0.054
1035
P PLY006 Polydactyly 59 0.054
1036
ACT084 Acute Stress Disorder 47 0.054
1037
DRM011 Dermatophytosis 52 0.054
1038
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.054
1039
PRS042 Prostate Disease 43 0.054
1040
KHN001 Kuhnt-Junius Degeneration 47 0.054
1041
BRN018 Borna Disease 36 0.054
1042
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.054
1043
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.054
1044
P FRD001 Friedreich Ataxia 64 0.053
1045
KRT002 Keratomalacia 47 0.053
1046
P KRT007 Keratoconus 50 0.053
1047
DNG001 Dengue Shock Syndrome 43 0.053
1048
P HRD011 Hereditary Spherocytosis 60 0.053
1049
P GNG009 Gangliosidosis 44 0.053
1050
P PRC012 Pericardial Effusion 51 0.053
1051
P NRC002 Narcolepsy 52 0.053
1052
MSC152 Muscular Dystrophy, Becker Type 63 0.053
1053
c MYT021 Myotonic Dystrophy 1 69 0.053
1054
P HYP040 Hypospadias 51 0.053
1055
PPL049 Papillon-Lefevre Syndrome 65 0.053
1056
P BRD002 Bardet-Biedl Syndrome 66 0.053
1057
c LPD032 Lipodystrophy, Congenital Generalized, Type 1 57 0.053
1058
P LYN001 Lynch Syndrome 77 0.053
1059
URT001 Urethritis 49 0.053
1060
P ECT006 Ectodermal Dysplasia 62 0.053
1061