Search results for insulin

3247 hits were found for insulin

# Family MCID Name MIFTS Score
1
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 8.657
2
INS024 Insulin-Like Growth Factor I 79 8.535
3
c DBT099 Diabetes Mellitus, Type I 65 7.020
4
DBT020 Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 39 6.837
5
c DBT094 Diabetes Mellitus, Insulin-Dependent, 10 22 4.339
6
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 30 4.232
7
c DBT038 Diabetes Mellitus, Insulin-Dependent, 5 22 3.908
8
P DBT034 Diabetes Mellitus, Insulin-Dependent, 20 38 3.897
9
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 21 3.897
10
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 68 3.666
11
c DBT032 Diabetes Mellitus, Insulin-Dependent, 22 31 3.637
12
DBT060 Diabetes Mellitus, Insulin-Dependent, X-Linked 9 3.363
13
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 57 3.277
14
c DBT077 Diabetes Mellitus, Insulin-Dependent, 19 18 3.080
15
HRT040 Hirata Disease 38 3.070
16
c INS009 Insulin-Resistance Type B 24 2.819
17
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 60 2.807
18
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 18 2.792
19
c DBT059 Diabetes Mellitus, Insulin-Dependent, 8 16 2.780
20
c DBT055 Diabetes Mellitus, Insulin-Dependent, 3 14 2.777
21
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 14 2.774
22
c DBT049 Diabetes Mellitus, Insulin-Dependent, 13 15 2.771
23
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 25 2.756
24
c DBT057 Diabetes Mellitus, Insulin-Dependent, 6 16 2.756
25
c DBT050 Diabetes Mellitus, Insulin-Dependent, 15 15 2.756
26
c DBT053 Diabetes Mellitus, Insulin-Dependent, 23 31 2.752
27
c DBT079 Diabetes Mellitus, Insulin-Dependent, 21 16 2.752
28
c DBT048 Diabetes Mellitus, Insulin-Dependent, 11 13 2.752
29
c DBT051 Diabetes Mellitus, Insulin-Dependent, 17 12 2.752
30
GRW032 Growth Factors, Combined Defect of 20 2.747
31
c DBT052 Diabetes Mellitus, Insulin-Dependent, 18 12 2.747
32
ACT088 Acute Insulin Response 41 2.545
33
PNC050 Pancreatic Beta Cell Agenesis with Neonatal Diabetes Mellitus 17 2.397
34
INS001 Insulinoma 60 2.143
35
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 2.111
36
DBT084 Diabetes Mellitus, Ketosis-Prone 60 2.067
37
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 53 2.063
38
c HRN019 Hair-an Syndrome 17 2.052
39
c TYP030 Type 1 Diabetes Mellitus 4 20 2.001
40
c TYP032 Type 1 Diabetes Mellitus 6 20 1.989
41
c TYP028 Type 1 Diabetes Mellitus 2 28 1.982
42
c TYP036 Type 1 Diabetes Mellitus 12 20 1.982
43
c TYP034 Type 1 Diabetes Mellitus 8 20 1.982
44
c TYP031 Type 1 Diabetes Mellitus 5 18 1.978
45
c TYP037 Type 1 Diabetes Mellitus 13 17 1.978
46
c TYP029 Type 1 Diabetes Mellitus 3 21 1.974
47
c TYP040 Type 1 Diabetes Mellitus 18 22 1.966
48
c TYP027 Type 1 Diabetes Mellitus 10 21 1.966
49
BNG086 Bangstad Syndrome 20 1.966
50
ACN028 Acanthosis Nigricans with Muscle Cramps and Acral Enlargement 16 1.966
51
FST003 Fasting Insulin Level Quantitative Trait Locus 1 6 1.962
52
c TYP033 Type 1 Diabetes Mellitus 7 18 1.957
53
c TYP035 Type 1 Diabetes Mellitus 11 23 1.952
54
c TYP039 Type 1 Diabetes Mellitus 17 20 1.952
55
c TYP038 Type 1 Diabetes Mellitus 15 16 1.952
57
c MTR021 Maturity-Onset Diabetes of the Young, Type 4 44 1.430
58
c LPD021 Lipodystrophy, Familial Partial, Type 3 47 1.415
59
PSD116 Pseudoacromegaly with Severe Insulin Resistance 5 1.415
60
INS028 Insulin Receptors, Familial Increase in 6 1.411
61
MCR279 Microcephalic Primordial Dwarfism-Insulin Resistance Syndrome 18 1.401
62
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 15 1.401
63
RTN071 Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 20 1.396
64
SVR045 Severe Early-Onset Obesity-Insulin Resistance Syndrome Due to Sh2b1 Deficiency 10 1.390
65
SHR095 Short Fifth Metacarpals-Insulin Resistance Syndrome 8 1.390
66
P RRN005 Rare Insulin-Resistance Syndrome 5 1.390
67
c RRD013 Rare Diabetes Mellitus Type 2 31 1.384
68
c RRD012 Rare Diabetes Mellitus Type 1 9 1.366
69
HYP056 Hypoglycemia 66 1.327
70
P DBT009 Diabetes Mellitus 64 1.100
71
HYP060 Hyperinsulinism 54 0.962
72
HYP066 Hyperglycemia 61 0.858
73
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.663
74
GLC003 Glucose Intolerance 54 0.642
75
P PLY011 Polycystic Ovary Syndrome 56 0.539
76
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.520
77
LPD008 Lipid Metabolism Disorder 62 0.490
78
FTT001 Fatty Liver Disease 61 0.469
79
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.460
80
GST033 Gestational Diabetes 61 0.423
81
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.418
82
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.417
83
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.417
84
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.417
85
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.417
86
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.417
87
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.417
88
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.417
89
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.417
90
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.417
91
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.399
92
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.380
93
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.380
94
c HYP595 Hypertension, Essential 84 0.348
95
P LVR013 Liver Disease 68 0.348
96
P HYP750 Hypertriglyceridemia, Familial 62 0.340
97
c MCR113 Microvascular Complications of Diabetes 3 52 0.328
98
c MCR120 Microvascular Complications of Diabetes 7 47 0.326
99
c MCR130 Microvascular Complications of Diabetes 6 41 0.326
100
c MCR133 Microvascular Complications of Diabetes 4 41 0.326
101
P KDN018 Kidney Disease 72 0.324
102
OCL069 Ocular Motor Apraxia 51 0.321
103
ATH013 Atherosclerosis Susceptibility 65 0.310
104
P CRN300 Coronary Heart Disease 1 63 0.299
105
HYP043 Hyperandrogenism 48 0.289
106
P BRS047 Breast Cancer 97 0.284
107
P VSC007 Vascular Disease 63 0.281
108
ACN002 Acanthosis Nigricans 60 0.281
109
P MCR115 Microvascular Complications of Diabetes 5 66 0.279
110
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.264
111
ACR007 Acromegaly 71 0.258
112
P CRD246 Cardiovascular System Disease 57 0.257
113
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.256
114
P ALZ034 Alzheimer Disease 88 0.253
115
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.252
116
LVR012 Liver Cirrhosis 62 0.251
117
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.250
118
48X005 48,xyyy 39 0.250
119
P NRP001 Neuropathy 56 0.243
120
ATM095 Autoimmune Disease 62 0.239
121
NNL006 Non-Alcoholic Steatohepatitis 54 0.227
122
LPP008 Lipoprotein Quantitative Trait Locus 62 0.227
123
c CHR684 Chronic Kidney Disease 70 0.226
124
PRT037 Pertussis 65 0.223
125
P CLR023 Colorectal Cancer 99 0.221
126
ALL026 Allergic Hypersensitivity Disease 62 0.215
127
P HYP086 Hypothyroidism 69 0.214
128
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.212
129
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.210
130
END086 End Stage Renal Disease 51 0.208
131
P PRS040 Prostate Cancer 97 0.208
132
c HYP836 Hypercholesterolemia, Familial, 1 73 0.203
133
P HRT032 Heart Disease 75 0.200
134
c PRC016 Pre-Eclampsia 63 0.200
135
P TRN020 Turner Syndrome 67 0.200
136
ATN004 Autonomic Neuropathy 45 0.200
137
DNH001 Donohue Syndrome 62 0.196
138
c ACT075 Acute Myocardial Infarction 57 0.195
139
ART140 Arteries, Anomalies of 52 0.195
140
ADN018 Adenoma 59 0.193
141
c HPT001 Hepatitis C 62 0.192
142
GRW007 Growth Hormone Deficiency 46 0.191
143
P MYC007 Myocardial Infarction 70 0.190
144
NTR005 Nutritional Deficiency Disease 62 0.190
145
P HYP076 Hyperthyroidism 55 0.189
146
CNG034 Congestive Heart Failure 69 0.188
147
ISC004 Ischemia 58 0.188
148
RCK004 Rickets 68 0.186
149
LPT014 Leptin Deficiency or Dysfunction 74 0.184
150
c RHB024 Rhabdomyosarcoma 2 67 0.181
151
DBT010 Diabetic Neuropathy 54 0.180
152
P NRB001 Neuroblastoma 72 0.179
153
PRD004 Prediabetes Syndrome 47 0.179
154
P MTR004 Maturity-Onset Diabetes of the Young 65 0.178
155
P HPT023 Hepatocellular Carcinoma 100 0.176
156
CYT002 Cytokine Deficiency 42 0.173
157
CYS001 Cystic Fibrosis 81 0.172
158
c HPT073 Hepatitis C Virus 72 0.169
159
HYP005 Hypokalemia 55 0.169
160
CRB039 Cerebrovascular Disease 67 0.166
161
P SLP006 Sleep Apnea 69 0.164
162
OST159 Osteogenic Sarcoma 66 0.163
163
URM002 Uremia 49 0.160
164
END057 Endometrial Cancer 74 0.158
165
P PNC035 Pancreatic Cancer 84 0.158
166
P PRP019 Peripheral Nervous System Disease 58 0.158
167
ADL002 Adult Syndrome 70 0.156
168
ANV001 Anovulation 47 0.155
169
P LNG032 Lung Cancer 98 0.154
170
c MCR129 Microvascular Complications of Diabetes 1 66 0.154
171
AGN016 Aging 56 0.154
172
P GRV001 Graves' Disease 55 0.151
173
STR067 Stroke, Ischemic 81 0.150
174
CHL014 Cholera 59 0.146
175
HYP266 Hypoxia 57 0.146
176
BNR002 Bone Resorption Disease 48 0.143
177
PRP027 Peripheral Vascular Disease 71 0.142
178
HYP080 Hypogonadism 50 0.142
179
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.141
180
DWN001 Down Syndrome 70 0.141
181
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.141
182
c HNT004 Huntington Disease-Like 2 50 0.140
183
P DDN001 Duodenal Ulcer 52 0.140
184
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.139
185
P MSC003 Muscular Atrophy 52 0.139
186
c NRF023 Neurofibromatosis, Type Ii 80 0.138
187
P AMY004 Amyloidosis 70 0.138
188
ATX019 Ataxia with Vitamin E Deficiency 42 0.137
189
ANR007 Anorexia Nervosa 63 0.137
190
P OST002 Osteoporosis 74 0.136
191
OVR063 Overnutrition 44 0.135
192
LRN002 Laron Syndrome 62 0.135
193
P PNC044 Pancreatitis 61 0.135
194
P OVR082 Overgrowth Syndrome 50 0.135
195
MTB004 Metabolic Acidosis 50 0.132
196
c PRM038 Primary Agammaglobulinemia 44 0.132
197
P HPT021 Hepatitis 67 0.131
198
P INF032 Infertility 57 0.131
199
47X002 47,xyy 49 0.131
200
P ADN016 Adenocarcinoma 64 0.131
201
MSC007 Muscle Hypertrophy 64 0.130
202
DWR001 Dwarfism 44 0.130
203
P OVR042 Ovarian Cancer 88 0.129
204
HLX001 Helix Syndrome 47 0.129
205
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.128
206
DPR016 Depression 63 0.128
207
P HYP069 Hyperparathyroidism 63 0.128
208
P OVR049 Ovarian Disease 52 0.128
209
P ART021 Arteriosclerosis 54 0.127
210
HYP014 Hyperuricemia 52 0.127
211
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.125
212
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.124
213
c HNT011 Huntington Disease-Like 3 38 0.124
214
c ACT027 Acute Pancreatitis 60 0.122
215
P MYT002 Myotonic Dystrophy 49 0.122
216
FST010 Fasting Hypoglycemia 35 0.121
217
ANG054 Angina Pectoris 66 0.120
218
PRS045 Prostatic Hypertrophy 53 0.120
219
PRS021 Prostatic Adenoma 51 0.120
220
PRS129 Prostatic Hyperplasia, Benign 49 0.120
221
P HYP083 Hypopituitarism 53 0.119
222
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.119
223
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.119
224
P SCH015 Schizophrenia 74 0.118
225
ISL001 Islet Cell Tumor 56 0.118
226
c ACT071 Acute Kidney Failure 60 0.117
227
P THY032 Thyroiditis 52 0.117
228
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.117
229
c MCR112 Microvascular Complications of Diabetes 2 41 0.117
230
HMS001 Hemosiderosis 54 0.116
231
ATN005 Autonomic Dysfunction 46 0.116
232
c PLY105 Polycystic Ovary Syndrome 1 38 0.116
233
BRT037 Brittle Diabetes 25 0.116
234
P GLM045 Glioma 63 0.115
235
P PLY019 Polyneuropathy 56 0.115
236
P RRH023 Rare Hereditary Hemochromatosis 41 0.115
237
MNT002 Mental Depression 58 0.115
238
c FML035 Familial Hyperlipidemia 55 0.114
239
GLL048 Glial Tumor 45 0.114
240
OST012 Osteoarthritis 78 0.113
241
P ECL001 Eclampsia 50 0.113
242
ETN001 Eating Disorder 60 0.113
243
c SYS001 Systemic Lupus Erythematosus 86 0.111
244
P RHM011 Rheumatoid Arthritis 80 0.111
245
P PRD008 Periodontitis 64 0.111
246
AMN001 Amenorrhea 54 0.111
247
c ATR087 Atrial Standstill 1 75 0.110
248
P PHC003 Pheochromocytoma 71 0.110
249
P RHB003 Rhabdomyosarcoma 63 0.110
250
LNG099 Lung Disease 60 0.110
251
ACD008 Acid-Labile Subunit Deficiency 54 0.110
252
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.109
253
P DMN002 Dementia 66 0.109
254
PPL052 Papillomatosis, Confluent and Reticulated 33 0.109
255
HYP081 Hypolipoproteinemia 51 0.109
256
HYP026 Hypoglycemic Coma 36 0.109
257
SVR004 Severe Combined Immunodeficiency 73 0.108
258
P ENC018 Encephalopathy 61 0.108
259
IMP005 Impotence 52 0.108
260
PTT037 Pituitary Tumors 44 0.108
261
P NNT009 Neonatal Diabetes Mellitus 50 0.106
262
ADR040 Adrenal Gland Pheochromocytoma 46 0.106
263
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.106
264
HRW001 Hair Whorl 36 0.106
265
CHL079 Children's Interstitial Lung Disease 26 0.105
266
c WLM018 Wilms Tumor 5 61 0.104
267
THY029 Thyroid Carcinoma 59 0.104
268
P LTR001 Lateral Sclerosis 54 0.104
269
TXC005 Toxic Shock Syndrome 62 0.104
270
P LCT001 Lactic Acidosis 51 0.104
271
c GRV008 Graves Disease 1 56 0.103
272
P CTR002 Cataract 60 0.102
273
GLB015 Glioblastoma Multiforme 75 0.101
274
P RTN024 Retinoblastoma 73 0.101
275
c FML008 Familial Retinoblastoma 53 0.101
276
HYP110 Hyperproinsulinemia 37 0.101
277
ANX010 Anxiety 73 0.100
278
P MSC005 Muscular Dystrophy 66 0.100
279
P ALC033 Alcohol Use Disorder 58 0.099
280
P DRR001 Diarrhea 55 0.098
281
CLR108 Colorectal Adenoma 64 0.098
282
P LPS004 Lupus Erythematosus 61 0.098
283
P MYP004 Myopathy 70 0.096
285
c PRM005 Primary Hyperparathyroidism 58 0.095
286
FTL021 Fetal Macrosomia 42 0.095
287
P PSR002 Psoriasis 62 0.094
288
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.094
289
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.094
290
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.094
291
P PTT006 Pituitary Adenoma 55 0.094
292
PST011 Pustulosis of Palm and Sole 52 0.094
293
c PCH010 Pachyonychia Congenita 3 44 0.094
294
GLC008 Glucose Metabolism Disease 40 0.094
295
PLC008 Placenta Disease 50 0.093
296
P MJR001 Major Depressive Disorder 68 0.092
297
P CLC063 Celiac Disease 1 66 0.092
298
P THY023 Thymoma 65 0.092
299
c THY107 Thymoma, Familial 52 0.092
300
BRR012 Berardinelli-Seip Congenital Lipodystrophy 49 0.092
301
c DBT103 Diabetes Mellitus, Permanent Neonatal 4 46 0.092
302
MYL069 Myeloma, Multiple 85 0.091
303
P CRD119 Cardiac Arrest 67 0.091
304
HYP020 Hyperprolactinemia 64 0.091
305
P GST053 Gastric Cancer 83 0.089
306
c SML038 Small Cell Cancer of the Lung 65 0.089
307
DBT002 Diabetic Autonomic Neuropathy 41 0.089
308
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.089
309
P BPL003 Bipolar Disorder 56 0.089
310
INT007 Intermediate Coronary Syndrome 55 0.089
311
GTR002 Goiter 53 0.089
312
TRM010 Traumatic Brain Injury 51 0.089
313
P LKM002 Leukemia 68 0.088
314
P FBR017 Fibrosarcoma 56 0.088
315
c VRL010 Viral Hepatitis 52 0.088
316
c MJR024 Major Affective Disorder 9 41 0.088
317
c MJR022 Major Affective Disorder 8 38 0.088
318
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.087
319
DFC004 Deficiency Anemia 70 0.087
320
SPN186 Spinal Cord Injury 60 0.087
321
P ALP008 Alopecia 54 0.087
322
BRN071 Brain Injury 49 0.087
323
P LNG064 Lung Cancer Susceptibility 3 78 0.086
324
SQM006 Squamous Cell Carcinoma 60 0.086
325
PPT005 Peptic Ulcer Disease 59 0.085
326
HMC014 Homocysteinemia 53 0.085
327
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.085
328
P ATX030 Ataxia-Telangiectasia 82 0.084
329
P NPH012 Nephrotic Syndrome 60 0.084
330
P URT039 Urticaria 58 0.084
331
WRN001 Werner Syndrome 69 0.083
332
P ART022 Arthritis 69 0.083
333
AST005 Asthma 76 0.082
334
P LKM062 Leukemia, Acute Lymphoblastic 69 0.082
335
PLC005 Placental Insufficiency 57 0.082
336
RST023 Resting Heart Rate, Variation in 41 0.082
337
OVR094 Ovarian Epithelial Cancer 38 0.082
338
APN008 Apnea, Obstructive Sleep 64 0.082
339
P HYP730 Hypogonadotropic Hypogonadism 52 0.082
340
P BLD134 Bladder Cancer 79 0.081
341
c HMC039 Hemochromatosis, Type 1 74 0.081
342
ALC007 Alcohol Dependence 66 0.081
343
SRC014 Sarcoma 65 0.081
344
P DBT100 Diabetes Mellitus, Permanent Neonatal 1 59 0.081
345
P GND004 Gonadal Dysgenesis 48 0.081
346
MDD011 Mood Disorder 62 0.080
347
P PRD006 Prader-Willi Syndrome 59 0.080
348
P GLM007 Glomerulonephritis 57 0.080
349
BLR008 Bilirubin Metabolic Disorder 57 0.080
350
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 55 0.080
351
PRT038 Protein-Energy Malnutrition 54 0.080
352
CRD137 Cardiogenic Shock 47 0.080
353
EWN003 Ewing Sarcoma 69 0.079
354
c BRN108 Branchiootic Syndrome 1 62 0.079
355
HSH003 Hashimoto Thyroiditis 62 0.079
356
P END084 Endocrine System Disease 45 0.079
357
CRV035 Cervical Cancer 76 0.078
358
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.078
359
TTN003 Tetanus 65 0.078
360
GT001 Gout 64 0.078
361
c LPD015 Lipodystrophy, Familial Partial, Type 2 64 0.078
362
P END044 Endometriosis 63 0.078
363
c CNG012 Congenital Generalized Lipodystrophy 52 0.078
364
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.078
365
HMN044 Human Immunodeficiency Virus Type 1 71 0.077
366
P THL005 Thalassemia 60 0.077
367
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.077
368
P SZR006 Seizure Disorder 56 0.077
369
GST037 Gastroparesis 54 0.077
370
P INF037 Inflammatory Bowel Disease 54 0.077
371
LMY002 Leiomyoma 52 0.077
372
c SCN007 Secondary Hyperparathyroidism 51 0.077
373
ISL003 Isolated Growth Hormone Deficiency 49 0.077
374
ATS010 Autosomal Recessive Disease 48 0.077
375
DBT008 Diabetic Angiopathy 44 0.077
376
ANX004 Anoxia 40 0.077
377
P HNT016 Huntington Disease 72 0.076
378
P TBR001 Tuberous Sclerosis 70 0.076
379
c FNC043 Fanconi Anemia, Complementation Group E 62 0.076
380
DRM006 Dermatitis 61 0.076
381
c HPT016 Hepatitis B 59 0.076
382
IRN002 Iron Metabolism Disease 57 0.076
383
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 50 0.076
384
CRB004 Cerebral Artery Occlusion 45 0.076
385
ASP026 Asplenia, Isolated Congenital 44 0.076
386
PRT013 Portal Hypertension 59 0.075
387
P BRS044 Breast Adenocarcinoma 59 0.075
388
P BCL017 B-Cell Lymphoma 58 0.075
389
VSC002 Vascular Dementia 57 0.075
390
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 55 0.075
391
49X006 49, Xxxxy Syndrome 41 0.075
392
GNT167 Genetic Obesity 33 0.075
393
PLY150 Polykaryocytosis Inducer 31 0.075
394
c DLT002 Dilated Cardiomyopathy 79 0.074
395
IMM167 Immune Deficiency Disease 78 0.074
396
c EXD008 Exudative Vitreoretinopathy 1 71 0.074
397
PNC129 Pancreatic Adenocarcinoma 68 0.074
398
P PLM036 Pulmonary Fibrosis 65 0.074
399
P BND020 Bone Disease 59 0.074
400
P MLN008 Melanoma 69 0.073
401
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.073
402
PRT036 Peritonitis 64 0.073
403
P MMP001 Mumps 58 0.073
404
P CHN012 Chondrosarcoma 56 0.073
405
HPT022 Hepatoblastoma 56 0.073
406
c MGR028 Migraine with or Without Aura 1 67 0.072
407
THY030 Thyroid Gland Disease 52 0.072
408
MNG006 Monogenic Diabetes 46 0.072
409
CNN003 Conn's Syndrome 79 0.071
410
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.071
411
TRN015 Transient Cerebral Ischemia 63 0.071
412
BRS051 Breast Disease 58 0.071
413
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.071
414
P FML012 Familial Partial Lipodystrophy 54 0.071
415
TLN003 Telangiectasis 52 0.071
416
P ATR011 Atrial Fibrillation 66 0.070
417
c ACT068 Acute Cystitis 63 0.070
418
P GLY013 Glycogen Storage Disease 60 0.070
419
MCL006 Macular Retinal Edema 55 0.070
420
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.070
421
PTT009 Pituitary Gland Disease 54 0.070
422
PRP080 Peripheral Artery Disease 53 0.070
423
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.070
424
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.070
425
P MDL005 Medulloblastoma 77 0.068
426
CRH001 Crohn's Disease 74 0.068
427
KHL003 Kohlschutter-Tonz Syndrome 65 0.068
428
P MYL006 Myeloid Leukemia 60 0.068
429
ACQ007 Acquired Immunodeficiency Syndrome 60 0.068
430
PRT058 Pure Autonomic Failure 59 0.068
431
VSL002 Visual Epilepsy 59 0.068
432
BLM002 Bulimia Nervosa 57 0.068
433
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.068
434
P RSP003 Respiratory Failure 74 0.067
435
P HYP061 Hypertrophic Cardiomyopathy 70 0.067
436
DPH001 Diphtheria 60 0.067
437
EYD002 Eye Disease 58 0.067
438
P TRM003 Tremor 54 0.067
439
c GLL024 Gallbladder Disease 1 53 0.067
440
P RCT021 Rectum Cancer 52 0.067
441
HYP017 Hypophosphatemia 50 0.067
442
CHR074 Choriocarcinoma 47 0.067
443
P PRC019 Precocious Puberty 46 0.067
444
ARG004 Argyria 27 0.067
445
c SPN225 Spondyloarthropathy 1 73 0.066
446
PLM001 Pulmonary Tuberculosis 69 0.066
447
P LYM118 Lymphoma 68 0.066
448
c HPT003 Hepatitis a 62 0.066
449
P TRC086 Trichohepatoenteric Syndrome 1 62 0.066
450
c WLF013 Wolfram Syndrome 1 60 0.066
451
FBR047 Fibromyalgia 58 0.066
452
RTN020 Retinal Vascular Disease 46 0.066
453
P BNG032 Benign Mesothelioma 46 0.066
454
HPT004 Hepatic Coma 45 0.066
455
c SCL052 Scleroderma, Familial Progressive 61 0.065
456
HLC007 Helicobacter Pylori Infection 59 0.065
457
END040 Endogenous Depression 55 0.065
458
HYP835 Hypothalamic Obesity 38 0.065
459
ATM052 Autoimmune Disease 1 37 0.065
460
DBT081 Diabetic Encephalopathy 37 0.065
461
GST019 Gastrointestinal Stromal Tumor 78 0.064
462
c TBR025 Tuberous Sclerosis 1 77 0.064
463
P ATS364 Autism 70 0.064
464
CLN015 Colon Adenocarcinoma 65 0.064
465
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.064
466
P MLN007 Male Infertility 55 0.064
467
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 0.064
468
P DBT005 Diabetes Insipidus 55 0.064
469
SPN035 Spindle Cell Sarcoma 53 0.064
470
AND014 Androgenic Alopecia 46 0.064
471
MMM006 Mammographic Density 41 0.064
472
P CNR004 Cone-Rod Dystrophy 2 73 0.063
473
PSY004 Psychotic Disorder 67 0.063
474
SKN016 Skin Disease 63 0.063
475
P BCK002 Beckwith-Wiedemann Syndrome 62 0.063
476
P SLP005 Sleep Disorder 59 0.063
477
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.063
478
c LPD032 Lipodystrophy, Congenital Generalized, Type 1 57 0.063
479
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.063
480
LMY014 Leiomyoma, Uterine 56 0.063
481
THR013 Thoracic Outlet Syndrome 54 0.063
482
P RTN018 Retinal Disease 53 0.063
483
P AST007 Astrocytoma 51 0.063
484
c SVR005 Severe Pre-Eclampsia 50 0.063
485
GLC036 Glucagonoma 45 0.063
486
c LKM061 Leukemia, Acute Myeloid 84 0.061
487
P SYS005 Systemic Scleroderma 68 0.061
488
P SHR029 Short Syndrome 63 0.061
489
P SNS001 Sensorineural Hearing Loss 60 0.061
490
VRC005 Varicose Veins 60 0.061
491
c HYP272 Hypercholesterolemia, Familial, 3 44 0.061
492
IDP033 Idiopathic Edema 44 0.061
493
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.061
494
P PRK057 Parkinson Disease, Late-Onset 78 0.060
495
P KDN017 Kidney Cancer 60 0.060
496
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.060
497
P MLT074 Multiple Endocrine Neoplasia 56 0.060
498
P GST044 Gastritis 56 0.060
499
PLM010 Pulmonary Edema 54 0.060
500
SNS003 Sensory Peripheral Neuropathy 54 0.060
501
P TRT010 Teratoma 52 0.060
502
DBT004 Diabetic Polyneuropathy 49 0.060
503
BCK003 Background Diabetic Retinopathy 46 0.060
504
SBC016 Subacute Delirium 44 0.060
505
ESP021 Esophageal Cancer 90 0.059
506
c FML021 Familial Hypercholesterolemia 66 0.059
507
P ANR048 Aniridia 1 63 0.059
508
EMB004 Embryonal Carcinoma 56 0.059
509
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.059
510
HYP781 Hypoascorbemia 51 0.059
511
ADR016 Adrenal Cortical Carcinoma 48 0.059
512
ADR004 Adrenal Cortical Adenocarcinoma 39 0.059
513
P GLM040 Glioma Susceptibility 1 81 0.058
514
END041 Endometrial Adenocarcinoma 63 0.058
515
P LMY004 Leiomyosarcoma 63 0.058
516
CHL068 Cholestasis 61 0.058
517
HPT019 Hepatic Encephalopathy 60 0.058
518
ANR040 Aneurysm 59 0.058
519
P PLY018 Polycythemia 56 0.058
520
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.058
521
ERY051 Erythroleukemia, Familial 56 0.058
522
PPL022 Papilloma 54 0.058
523
PNG002 Pain Agnosia 51 0.058
524
CRN030 Coronary Stenosis 50 0.058
525
CHL004 Cholelithiasis 49 0.058
526
P ALP061 Alopecia, Androgenetic, 1 49 0.058
527
RDN001 Reading Disorder 40 0.058
528
P FML187 Familial Hypertension 37 0.058
529
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.058
530
CHL131 Chlorpropamide-Alcohol Flushing 22 0.058
531
P MLT020 Multiple Sclerosis 72 0.056
532
BRK010 Burkitt Lymphoma 67 0.056
533
P HYP098 Hypereosinophilic Syndrome 67 0.056
534
c ATS007 Autism Spectrum Disorder 67 0.056
535
CRN036 Craniopharyngioma 65 0.056
536
P MTR014 Motor Neuron Disease 65 0.056
537
INT002 Intermittent Claudication 61 0.056
538
GNG013 Gingivitis 59 0.056
539
GLS018 Glass Syndrome 57 0.056
540
NPH009 Nephrolithiasis 55 0.056
541
DNT012 Dental Caries 53 0.056
542
ANT039 Antisynthetase Syndrome 46 0.056
543
HDN002 Head Injury 46 0.056
544
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.056
545
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.055
546
P PLM037 Pulmonary Hypertension 67 0.055
547
P NTR004 Neutropenia 63 0.055
548
P PLY014 Polycystic Kidney Disease 62 0.055
549
VRL011 Viral Infectious Disease 61 0.055
550
P RBL001 Rubella 59 0.055
551
P MCR010 Microcephaly 59 0.055
552
P EXN002 Exanthem 57 0.055
553
THR024 Thrombosis 57 0.055
554
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.055
555
NRT001 Neurotic Disorder 53 0.055
556
c PNC106 Pancreatic Agenesis 1 51 0.055
557
ORL015 Oral Squamous Cell Carcinoma 43 0.055
558
GST020 Gastric Antral Vascular Ectasia 41 0.055
559
ART016 Aortic Aneurysm 69 0.054
560
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.054
561
P WLF004 Wolfram Syndrome 60 0.054
562
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.054
563
DSS008 Disease of Mental Health 58 0.054
564
CNS004 Constipation 58 0.054
565
NRN004 Neuroendocrine Tumor 55 0.054
566
LMB062 Limb Ischemia 55 0.054
567
PRP030 Purpura 54 0.054
568
PST021 Postpartum Depression 50 0.054
569
P OBS001 Obstructive Jaundice 50 0.054
570
DBT006 Diabetic Macular Edema 48 0.054
571
P PRD021 Periodic Paralysis 45 0.054
572
P RTT002 Rett Syndrome 80 0.052
573
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.052
574
MSC157 Muscular Dystrophy, Duchenne Type 72 0.052
575
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.052
576
P SRC025 Sarcoidosis 1 70 0.052
577
c HYP768 Hyperlipoproteinemia, Type I 67 0.052
578
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.052
579
P SKN015 Skin Carcinoma 66 0.052
580
c WLM013 Wilms Tumor 1 65 0.052
581
NRM005 Neuromuscular Disease 64 0.052
582
OVR029 Ovarian Hyperstimulation Syndrome 64 0.052
583
P THR117 Three M Syndrome 1 63 0.052
584
c ACT073 Acute Leukemia 58 0.052
585
P HDC001 Headache 57 0.052
586
P FTL001 Fetal Alcohol Syndrome 57 0.052
587
P INS002 in Situ Carcinoma 53 0.052
588
HRT012 Heart Valve Disease 53 0.052
589
GST023 Gastric Ulcer 53 0.052
590
NRT004 Neuritis 52 0.052
591
SXL003 Sexual Disorder 47 0.052
592
KWS001 Kwashiorkor 44 0.052
593
c TRN032 Transient Neonatal Diabetes Mellitus 41 0.052
594
GLM044 Glomerular Disease 37 0.052
595
P VSC018 Visceral Steatosis 33 0.052
596
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.051
597
ART001 Arterial Tortuosity Syndrome 66 0.051
598
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.051
599
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.051
600
CHC001 Chickenpox 60 0.051
601
ORL011 Oral Cancer 60 0.051
602
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.051
603
c ACT134 Acute Liver Failure 56 0.051
604
BCT022 Bacterial Infectious Disease 56 0.051
605
CHR100 Chronic Ulcer of Skin 55 0.051
606
P ALP106 Alport Syndrome 1, X-Linked 55 0.051
607
c PRD040 Periodontitis, Chronic 53 0.051
608
SPN051 Spondylitis 51 0.051
609
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.051
610
SCH012 Schizoaffective Disorder 50 0.051
611
CRT013 Carotid Stenosis 50 0.051
612
LPT006 Leptin Receptor Deficiency 48 0.051
613
DMP001 Dumping Syndrome 44 0.051
614
ALL014 Allergic Encephalomyelitis 38 0.051
615
P GRF003 Graft-Versus-Host Disease 72 0.049
616
MYL009 Myelodysplastic Syndrome 70 0.049
617
c MYT021 Myotonic Dystrophy 1 69 0.049
618
P PNM007 Pneumonia 68 0.049
619
BRR014 Barrett Esophagus 65 0.049
620
STF001 Stiff-Person Syndrome 60 0.049
621
P MLN069 Melanoma, Uveal 59 0.049
622
LYM027 Lymphopenia 58 0.049
623
SFT003 Soft Tissue Sarcoma 56 0.049
624
MST005 Mastitis 53 0.049
625
P SHR001 Short Bowel Syndrome 53 0.049
626
PLT004 Platelet Glycoprotein Iv Deficiency 53 0.049
627
DMY004 Demyelinating Disease 52 0.049
628
ENT011 Enterocolitis 51 0.049
629
P HYP077 Hypertrichosis 50 0.049
630
IGG001 Iga Glomerulonephritis 48 0.049
631
P OVR046 Ovarian Cyst 47 0.049
632
RTN023 Retinitis 46 0.049
633
NRR001 Neuroretinitis 42 0.049
634
HYP784 Hypogonadism, Male 40 0.049
635
PRM329 Premature Aging 35 0.049
636
ATX010 Ataxia Neuropathy Spectrum 34 0.049
637
ACT064 Acute Necrotizing Encephalitis 33 0.049
638
INF009 Inflammatory Spondylopathy 31 0.049
639
PST092 Posttransplant Acute Limbic Encephalitis 29 0.049
640
BLD137 Blood Group--Ahonen 16 0.049
641
NRL016 Neural Tube Defects 82 0.048
642
ULC004 Ulcerative Colitis 73 0.048
643
P BRD002 Bardet-Biedl Syndrome 66 0.048
644
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.048
645
CLT003 Colitis 62 0.048
646
P ART023 Arthropathy 62 0.048
647
MNN042 Meningioma, Radiation-Induced 62 0.048
648
P PRM006 Primary Biliary Cirrhosis 62 0.048
649
P SBS003 Substance Abuse 55 0.048
650
P SPP010 Suppressor of Tumorigenicity 3 51 0.048
651
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.048
652
PNC034 Pancreas Disease 48 0.048
653
P RNL015 Renal Hypertension 47 0.048
654
P ACQ022 Acquired Generalized Lipodystrophy 47 0.048
655
c CNT075 Central Precocious Puberty 46 0.048
656
NSP002 Nasopharyngitis 43 0.048
657
P MJR007 Major Affective Disorder 1 43 0.048
658
c CHR682 Chronic Bilirubin Encephalopathy 39 0.048
659
P ADP010 Adiponectin, Serum Level of, Quantitative Trait Locus 1 24 0.048
660
JVN026 Jeavons Syndrome 24 0.048
662
BRN028 Brain Cancer 74 0.046
663
P EPL164 Epilepsy 71 0.046
664
MLT157 Multiple System Atrophy 1 70 0.046
665
LYM133 Lymphoma, Hodgkin, Classic 69 0.046
666
CRP001 Carpal Tunnel Syndrome 67 0.046
667
AND002 Androgen Insensitivity Syndrome 66 0.046
668
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.046
669
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.046
670
c JVN010 Juvenile Rheumatoid Arthritis 64 0.046
671
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.046
672
P VSC011 Vasculitis 62 0.046
673
MSL001 Measles 62 0.046
674
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 61 0.046
675
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.046
676
CRD223 Cardiac Arrhythmia 60 0.046
677
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.046
678
RNL024 Renal Glucosuria 58 0.046
679
CRD132 Cardiac Conduction Defect 58 0.046
680
NWB001 Newborn Respiratory Distress Syndrome 58 0.046
681
c MST023 Mesothelioma, Malignant 57 0.046
682
P HYP024 Hypoparathyroidism 56 0.046
683
P MYP006 Myopia 55 0.046
684
AMN003 Amnestic Disorder 54 0.046
685
NNT012 Neonatal Jaundice 53 0.046
686
KRT009 Keratosis 51 0.046
687
VCC001 Vaccinia 49 0.046
688
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 48 0.046
689
HYP068 Hyperostosis 48 0.046
690
END062 Endometrial Hyperplasia 48 0.046
691
NDL007 Nodular Goiter 47 0.046
692
SQM002 Squamous Cell Papilloma 46 0.046
693
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.046
694
HPT082 Hepatic Adenomas, Familial 44 0.046
695
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.046
696
c SCN052 Secondary Adrenal Insufficiency 36 0.046
698
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.046
699
c MJR008 Major Affective Disorder 2 35 0.046
700
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.046
701
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.044
702
CNN005 Connective Tissue Disease 68 0.044
703
P THR014 Thrombocytopenia 67 0.044
704
c FML001 Familial Atrial Fibrillation 65 0.044
705
P HRP006 Herpes Simplex 65 0.044
706
P ADL010 Adult Respiratory Distress Syndrome 65 0.044
707
c CNG006 Congenital Hypothyroidism 64 0.044
708
c LPM012 Lipomatosis, Multiple 60 0.044
709
P AXN002 Axenfeld-Rieger Syndrome 59 0.044
710
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.044
711
IGR001 Ige Responsiveness, Atopic 59 0.044
712
CHL123 Chlamydia 59 0.044
713
IRN001 Iron Deficiency Anemia 59 0.044
714
CNT047 Contact Dermatitis 58 0.044
715
SCH003 Schizophreniform Disorder 56 0.044
716
ZLL002 Zollinger-Ellison Syndrome 55 0.044
717
c OST164 Osteoporosis, Juvenile 53 0.044
718
ALC009 Alcoholic Liver Cirrhosis 53 0.044
719
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.044
720
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 0.044
721
ESP002 Esophageal Varix 51 0.044
722
STM007 Stomatitis 50 0.044
723
P SCK005 Sickle Cell Disease 50 0.044
724
KRT008 Keratopathy 47 0.044
725
RNL077 Renal Fibrosis 47 0.044
726
TRP008 Tropical Calcific Pancreatitis 46 0.044
727
c MLG068 Malignant Glioma 46 0.044
728
P HYP265 Hypotonia 43 0.044
729
EXC002 Exocrine Pancreatic Insufficiency 42 0.044
730
GGN002 Gigantism 33 0.044
731
c PRG106 Progressive Muscular Dystrophy 33 0.044
732
c MJR023 Major Affective Disorder 7 33 0.044
733
ALR002 Al-Raqad Syndrome 33 0.044
734
c MJR003 Major Affective Disorder 6 33 0.044
735
c MJR006 Major Affective Disorder 5 33 0.044
736
CRT009 Critical Illness Polyneuropathy 32 0.044
737
c MJR004 Major Affective Disorder 4 28 0.044
738
P LKM071 Leukemia, Chronic Lymphocytic 79 0.043
739
KPS004 Kaposi Sarcoma 75 0.043
740
c BTT014 Beta-Thalassemia 74 0.043
741
GST040 Gastric Adenocarcinoma 70 0.043
742
P OCL013 Oculodentodigital Dysplasia 69 0.043
743
P ANG001 Angelman Syndrome 69 0.043
744
P DRM053 Dermatitis, Atopic 66 0.043
745
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.043
746
ALS001 Alstrom Syndrome 64 0.043
747
PLM031 Poliomyelitis 64 0.043
748
OST017 Osteomyelitis 64 0.043
749
PHL006 Phelan-Mcdermid Syndrome 62 0.043
750
ALC006 Alcoholic Hepatitis 61 0.043
751
P ALP009 Alopecia Areata 60 0.043
752
PRN019 Perinatal Necrotizing Enterocolitis 59 0.043
753
DCT002 Ductal Carcinoma in Situ 59 0.043
754
BRN056 Bronchopulmonary Dysplasia 57 0.043
755
HMR039 Hemorrhage, Intracerebral 57 0.043
756
TND005 Tendinitis 54 0.043
757
P RTN016 Retinal Degeneration 53 0.043
758
PRN011 Pernicious Anemia 53 0.043
759
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 52 0.043
760
BLL003 Bell's Palsy 51 0.043
761
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.043
762
NRN001 Neuroendocrine Carcinoma 47 0.043
763
LYM019 Lymphosarcoma 46 0.043
764
c DRR009 Diarrhea 6 46 0.043
765
DBT090 Diabetes and Deafness, Maternally Inherited 44 0.043
766
P CHR345 Chronic Pain 44 0.043
767
TRP009 Triple X Syndrome 42 0.043
768
MRS001 Marasmus 42 0.043
769
P CRB088 Cerebral Atrophy 37 0.043
770
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.043
771
CHR178 Chromosomal Triplication 35 0.043
772
MTY003 Mutyh Polyposis 30 0.043
773
OBS067 Obesity Due to Melanocortin 4 Receptor Deficiency 22 0.043
774
AND005 Androgen Insensitivity Syndrome, Mild 19 0.043
775
P MYS003 Myasthenia Gravis 68 0.041
776
BRN024 Bronchitis 68 0.041
777
GST092 Gastroesophageal Reflux 67 0.041
778
P NSP012 Nasopharyngeal Carcinoma 66 0.041
779
c DPH024 Diaphragmatic Hernia, Congenital 63 0.041
780
c BRD010 Bardet-Biedl Syndrome 1 62 0.041
781
CHR066 Chronic Fatigue Syndrome 61 0.041
782
SPP011 Suppression of Tumorigenicity 12 59 0.041
783
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.041
784
c DWL002 Dowling-Degos Disease 1 58 0.041
785
CHL067 Cholecystitis 57 0.041
786
PRL032 Perlman Syndrome 57 0.041
787
EPP024 Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus 56 0.041
788
ARM001 Aromatase Deficiency 54 0.041
789
CLL003 Cellulitis 54 0.041
790
OST016 Osteochondrosis 53 0.041
791
P SLV027 Silver-Russell Syndrome 1 53 0.041
792
PRP016 Paraplegia 52 0.041
793
P MND003 Mandibuloacral Dysplasia with Type a Lipodystrophy 51 0.041
794
P SMP003 Simpson-Golabi-Behmel Syndrome 50 0.041
795
HST010 Histiocytosis 48 0.041
796
CHL147 Chlamydia Pneumonia 48 0.041
797
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.041
798
GST071 Gastrointestinal Carcinoma 47 0.041
799
P ATM019 Autoimmune Polyendocrine Syndrome 46 0.041
800
EXS001 Exostosis 46 0.041
801
SYN036 Syncope 45 0.041
802
ACT003 Acute Kidney Tubular Necrosis 45 0.041
803
IMM064 Immunodeficiency, Common Variable, 10 44 0.041
804
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.041
805
ALD013 Aldosterone-Producing Adenoma 39 0.041
806
NCR002 Necrobiosis Lipoidica 38 0.041
807
CRY036 Cryptogenic Cirrhosis 36 0.041
808
c FNC027 Fanconi Anemia, Complementation Group a 81 0.039
809
c THR092 Thrombophilia Due to Thrombin Defect 73 0.039
810
c LKM063 Leukemia, Chronic Myeloid 72 0.039
811
OBS002 Obsessive-Compulsive Disorder 68 0.039
812
THY111 Thyroid Carcinoma, Familial Medullary 67 0.039
813
CHG001 Chagas Disease 66 0.039
814
P NRV007 Nervous System Disease 66 0.039
815
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.039
816
LSH001 Leishmaniasis 63 0.039
817
P ACR001 Aicardi-Goutieres Syndrome 62 0.039
818
P ENC004 Encephalitis 61 0.039
819
DCB001 Decubitus Ulcer 61 0.039
820
P HMN036 Hemangiopericytoma, Malignant 59 0.039
821
SRC027 Sarcoma, Synovial 58 0.039
822
FML063 Familial Glucocorticoid Deficiency 58 0.039
823
P GLL020 Gallbladder Disease 57 0.039
824
APH002 Aphasia 57 0.039
825
CYT008 Cytomegalovirus Infection 57 0.039
826
SCH014 Schistosomiasis 57 0.039
827
ALL010 Allergic Contact Dermatitis 56 0.039
828
c LPD033 Lipodystrophy, Congenital Generalized, Type 2 54 0.039
829
CLR030 Clear Cell Renal Cell Carcinoma 53 0.039
830
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.039
831
NPH003 Nephrocalcinosis 51 0.039
832
CLR109 Colorectal Adenocarcinoma 51 0.039
833
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.039
834
THY125 Thyroid Gland Medullary Carcinoma 50 0.039
835
P TMP001 Temporal Lobe Epilepsy 50 0.039
836
SYS003 Systolic Heart Failure 49 0.039
837
P OPN001 Open-Angle Glaucoma 49 0.039
838
LRN003 Learning Disability 49 0.039
839
P RNV001 Renovascular Hypertension 48 0.039
840
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.039
841
c BRD013 Bardet-Biedl Syndrome 12 45 0.039
842
PPL001 Papillary Adenoma 44 0.039
843
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.039
844
ADR041 Adrenal Cortical Adenoma 43 0.039
845
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.039
846
P KLZ004 Kala-Azar 1 41 0.039
847
CRV045 Cervical Intraepithelial Neoplasia 39 0.039
848
ADP007 Adie Pupil 39 0.039
849
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.039
850
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.039
851
MYT011 Myotonia 34 0.039
852
c LKM005 Leukemia, T-Cell, Chronic 34 0.039
853
P PLY188 Polyendocrinopathy 32 0.039
854
PRX085 Preaxial Hallucal Polydactyly 28 0.039
855
HNM002 Hinman Syndrome 27 0.039
856
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.037
857
P RTN008 Retinitis Pigmentosa 79 0.037
858
P NNN008 Noonan Syndrome 1 76 0.037
859
P FRG001 Fragile X Syndrome 70 0.037
860
CRB037 Cerebral Palsy 69 0.037
861
P HYD006 Hydrocephalus 66 0.037
862
P LPS002 Liposarcoma 65 0.037
863
c OPT053 Optic Atrophy 1 63 0.037
864
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.037
865
c SVR001 Severe Acute Respiratory Syndrome 62 0.037
866
PSR001 Psoriatic Arthritis 61 0.037
867
YLL002 Yellow Fever 61 0.037
868
ALV005 Alveolar Soft Part Sarcoma 61 0.037
869
RTN017 Retinal Detachment 61 0.037
870
NRL005 Neurilemmoma 60 0.037
871
c JVN061 Juvenile Arthritis 60 0.037
872
P SCL018 Scoliosis 60 0.037
873
INT066 Interstitial Lung Disease 60 0.037
874
P MYC008 Myocarditis 59 0.037
875
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.037
876
P UVT001 Uveitis 57 0.037
877
P RHN004 Rhinitis 57 0.037
878
P FCL005 Focal Segmental Glomerulosclerosis 57 0.037
879
ALL006 Allergic Asthma 56 0.037
880
MCS002 Mucositis 56 0.037
881
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.037
882
ADR008 Adrenal Adenoma 55 0.037
883
P ANT006 Antiphospholipid Syndrome 55 0.037
884
HDR002 Hidradenitis Suppurativa 55 0.037
885
CRC006 Carcinoid Syndrome 55 0.037
886
c BRD011 Bardet-Biedl Syndrome 10 53 0.037
887
c BRD014 Bardet-Biedl Syndrome 2 52 0.037
888
c BRD012 Bardet-Biedl Syndrome 11 51 0.037
889
RTN003 Retinal Ischemia 50 0.037
890
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.037
891
GYN001 Gynecomastia 49 0.037
892
HDR003 Hidradenitis 49 0.037
893
GST049 Gastrointestinal System Cancer 49 0.037
894
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.037
895
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.037
896
LYM009 Lymphocytic Choriomeningitis 47 0.037
897
TST014 Testicular Cancer 46 0.037
898
GST010 Gestational Trophoblastic Neoplasm 46 0.037
899
URT010 Ureteral Obstruction 45 0.037
900
TRT001 Teratocarcinoma 45 0.037
901
GRN007 Granuloma Annulare 44 0.037
902
MYX004 Myxedema 43 0.037
903
LWC001 Low Compliance Bladder 43 0.037
904
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.037
905
PRM020 Premenstrual Tension 40 0.037
906
KLD004 Keloid Disorder 40 0.037
907
c MTR044 Maturity-Onset Diabetes of the Young, Type 10 39 0.037
908
WLL004 Wallerian Degeneration 39 0.037
909
DBT007 Diabetic Cataract 38 0.037
910
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.037
911
MLD002 Mild Pre-Eclampsia 36 0.037
912
c BLD140 Blood Group, I System 32 0.037
913
FNT004 Fainting 30 0.037
914
MYC088 Mycobacterium Avium Complex Infections 29 0.037
915
INS034 Insulinomatosis and Diabetes Mellitus 27 0.037
916
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 16 0.037
917
RCR030 Recurrent Idiopathic Neuroretinitis 11 0.037
918
MLR004 Malaria 81 0.035
919
SCH036 Scheie Syndrome 72 0.035
920
c PNC108 Pancreatitis, Hereditary 70 0.035
921
PLY001 Polycythemia Vera 69 0.035
922
P MYC084 Mycobacterium Tuberculosis 1 68 0.035
923
CMM004 Common Variable Immunodeficiency 68 0.035
924
P FRN006 Frontotemporal Dementia 68 0.035
925
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.035
926
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.035
927
SPT006 Septooptic Dysplasia 64 0.035
928
HYP780 Hypoadrenocorticism, Familial 63 0.035
929
c ATM011 Autoimmune Hepatitis 63 0.035
930
ING001 Inguinal Hernia 60 0.035
931
PLM033 Pulmonary Embolism 59 0.035
932
PST028 Post-Traumatic Stress Disorder 58 0.035
933
THY122 Thyroid Gland Cancer 57 0.035
934
P PRN023 Prion Disease 57 0.035
935
P ANG015 Angioedema 57 0.035
936
P MTC069 Mitochondrial Disorders 56 0.035
937
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.035
938
MCR141 Mucormycosis 56 0.035
939
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.035
940
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.035
941
HMP005 Hemiplegia 55 0.035
942
P LCH002 Lichen Planus 53 0.035
943
P EMB005 Embryonal Rhabdomyosarcoma 53 0.035
944
INT075 Intracranial Hypertension 53 0.035
945
CHR073 Choreatic Disease 52 0.035
946
LNG031 Lung Benign Neoplasm 51 0.035
947
PNN001 Panniculitis 51 0.035
948
P CHL066 Cholangitis 51 0.035
949
ENT004 Enthesopathy 49 0.035
950
P END046 Endometritis 49 0.035
951
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.035
952
ART004 Aortic Atherosclerosis 47 0.035
953
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.035
954
P THY054 Thyrotoxic Periodic Paralysis 46 0.035
955
P LPM005 Lipomatosis 46 0.035
956
MDS022 Mediastinitis 46 0.035
957
PLY012 Polyhydramnios 46 0.035
958
GST030 Gastrinoma 45 0.035
959
TND004 Tendinopathy 43 0.035
960
c RHB023 Rhabdomyosarcoma, Embryonal, 1 43 0.035
961
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.035
962
P MLG074 Malignant Mesenchymoma 40 0.035
963
NRV004 Nerve Compression Syndrome 40 0.035
964
PNC008 Pancreatic Endocrine Carcinoma 39 0.035
965
PTT003 Pituitary-Dependent Cushing's Disease 39 0.035
966
P PNC045 Pancreatic Agenesis 37 0.035
967
DNC004 Diencephalic Syndrome 36 0.035
968
c RNL113 Renal Failure, Progressive, with Hypertension 34 0.035
969
c LPD036 Lipodystrophy, Familial Partial, Type 6 34 0.035
970
c PRS136 Prostate Cancer, Hereditary, 6 33 0.035
971
c PRS130 Prostate Cancer, Hereditary, 8 32 0.035
972
KDN013 Kidney Hypertrophy 32 0.035
973
INF021 Infant Gynecomastia 31 0.035
974
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.035
975
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 26 0.035
976
P CRT085 Carotid Intimal Medial Thickness 2 24 0.035
977
c PSD047 Pseudo-Turner Syndrome 21 0.035
978
ADN072 Adenoma of Pancreas 20 0.035
979
PNC049 Pancreatic Adenoma 17 0.035
980
PHN003 Phenylketonuria 75 0.033
981
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.033
982
P FML011 Familial Adenomatous Polyposis 72 0.033
983
P LPR021 Leprosy 3 69 0.033
984
CHL065 Cholangiocarcinoma 68 0.033
985
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 68 0.033
986
P DYS154 Dystonia 65 0.033
987
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.033
988
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.033
989
P PRS038 Personality Disorder 65 0.033
990
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.033
991
PLG002 Plague 63 0.033
992
RHB001 Rhabdoid Cancer 63 0.033
993
P DRM010 Dermatomyositis 61 0.033
994
c PNS012 Paine Syndrome 61 0.033
995
P HMN010 Hemangioma 61 0.033
996
P OPT006 Optic Nerve Disease 60 0.033
997
c PTT056 Pituitary Adenoma 1, Multiple Types 58 0.033
998
P MYS005 Myositis 56 0.033
999
PLS011 Plasmacytoma 56 0.033
1000
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.033
1001
P PSD015 Pseudohypoparathyroidism 56 0.033
1002
P NRF002 Neurofibromatosis 56 0.033
1003
BRN004 Brain Edema 56 0.033
1004
P SCL048 Sclerosteosis 55 0.033
1005
LYM040 Lymphoblastic Lymphoma 54 0.033
1006
NVS001 Neovascular Glaucoma 53 0.033
1007
DSM007 Desmoplastic Small Round Cell Tumor 52 0.033
1008
INT079 Intrahepatic Cholangiocarcinoma 51 0.033
1009
PRT029 Parathyroid Adenoma 50 0.033
1010
P FNC004 Fanconi Syndrome 50 0.033
1011
AZS001 Azoospermia 50 0.033
1012
c LRG001 Large Cell Carcinoma 50 0.033
1013
HRT011 Heart Septal Defect 50 0.033
1014
RNL011 Renal Osteodystrophy 50 0.033
1015
MTC005 Mitochondrial Metabolism Disease 49 0.033
1016
P SCL009 Sclerosing Cholangitis 48 0.033
1017
SPL018 Splenomegaly 48 0.033
1018
c PRM093 Premature Ovarian Failure 7 47 0.033
1019
FCL012 Facial Paralysis 46 0.033
1020
CHD004 Chudley-Mccullough Syndrome 46 0.033
1021
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.033
1022
MCR037 Macroglossia 45 0.033
1023
CRT015 Carotid Artery Occlusion 45 0.033
1024
CVD001 Covid-19 44 0.033
1025
FBR054 Fibroma 44 0.033
1026
CLN044 Colon Adenoma 44 0.033
1027
FNC007 Functioning Pituitary Adenoma 43 0.033
1028
PRS042 Prostate Disease 43 0.033
1029
ALC010 Alcoholic Cardiomyopathy 42 0.033
1030
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.033
1031
MCH006 Mechanical Strabismus 42 0.033
1032
CRB025 Carbohydrate Metabolic Disorder 41 0.033
1033
MSN004 Mesenchymal Cell Neoplasm 41 0.033
1034
P CRB045 Cerebellar Hypoplasia 41 0.033
1035
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.033
1036
PLM005 Pleomorphic Lipoma 40 0.033
1037
EST004 Estrogen Excess 40 0.033
1038
ART008 Arteriosclerosis Obliterans 40 0.033
1039
HYP344 Hyperthyroidism, Familial Gestational 39 0.033
1040
P PRC031 Preeclampsia/eclampsia 1 38 0.033
1041
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.033
1042
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 32 0.033
1043
c RNG008 Ring Chromosome 13 31 0.033
1044
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.033
1045
DBT018 Diabetic Mastopathy 18 0.033
1046
P APL001 Aplastic Anemia 74 0.030
1047
c MNN043 Meningioma, Familial 74 0.030
1048
P WSK001 Wiskott-Aldrich Syndrome 72 0.030
1049
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.030
1050
SKN019 Skin Melanoma 68 0.030
1051
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.030
1052
c PRM196 Premature Ovarian Failure 1 67 0.030
1053
P LNG028 Long Qt Syndrome 66 0.030
1054
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.030
1055
GTL001 Gitelman Syndrome 65 0.030
1056
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.030
1057
ACR006 Aceruloplasminemia 65 0.030
1058
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.030
1059
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.030
1060
MSM014 Mismatch Repair Cancer Syndrome 65 0.030
1061
CLF027 Cleft Palate, Isolated 64 0.030
1062
TBC004 Tobacco Addiction 64 0.030
1063
P GLC113 Galactosemia I 64 0.030
1064
P GCH001 Gaucher's Disease 63 0.030
1065
P HML002 Hemolytic Anemia 63 0.030
1066
PRM126 Primary Peritoneal Carcinoma 62 0.030
1067
BRS099 Breast Ductal Carcinoma 62 0.030
1068
CRC021 Carcinosarcoma 62 0.030
1069
P BNG030 Benign Ependymoma 60 0.030
1070