Search results for Metformin

1080 hits were found for Metformin

# Family MCID Name MIFTS Score
1
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 1.034
2
P DBT009 Diabetes Mellitus 64 0.996
3
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.885
4
P PLY011 Polycystic Ovary Syndrome 56 0.736
5
HYP056 Hypoglycemia 66 0.635
6
P LCT001 Lactic Acidosis 51 0.557
7
HYP066 Hyperglycemia 61 0.436
8
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.402
9
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.399
10
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.399
11
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.399
12
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.399
13
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.399
14
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.399
15
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.399
16
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.399
17
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.399
18
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.399
19
HYP060 Hyperinsulinism 54 0.396
20
GST033 Gestational Diabetes 57 0.390
21
c PLY105 Polycystic Ovary Syndrome 1 38 0.368
22
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.354
23
P TRN020 Turner Syndrome 65 0.343
24
LPD008 Lipid Metabolism Disorder 62 0.316
25
HYP043 Hyperandrogenism 48 0.306
26
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.301
27
FTT001 Fatty Liver Disease 61 0.290
28
P KDN018 Kidney Disease 70 0.280
29
GLC003 Glucose Intolerance 54 0.276
30
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.275
31
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.269
32
P LVR013 Liver Disease 68 0.265
33
P INF032 Infertility 57 0.265
34
c RHB024 Rhabdomyosarcoma 2 65 0.261
35
END057 Endometrial Cancer 74 0.259
36
ANV001 Anovulation 47 0.259
37
P CRD246 Cardiovascular System Disease 56 0.256
38
P BRS047 Breast Cancer 96 0.254
39
P PNC035 Pancreatic Cancer 84 0.249
40
P PRS040 Prostate Cancer 97 0.235
41
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.231
42
c HYP595 Hypertension, Essential 84 0.230
43
P HRT032 Heart Disease 75 0.229
44
P CLR023 Colorectal Cancer 98 0.227
45
CNG034 Congestive Heart Failure 70 0.222
46
c CHR684 Chronic Kidney Disease 66 0.220
47
PRD004 Prediabetes Syndrome 47 0.217
48
ADL002 Adult Syndrome 69 0.216
49
P LNG032 Lung Cancer 97 0.214
50
P ADN016 Adenocarcinoma 64 0.212
51
P DRR001 Diarrhea 57 0.212
52
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.210
53
48X005 48,xyyy 39 0.210
54
NNL006 Non-Alcoholic Steatohepatitis 51 0.206
55
P HPT023 Hepatocellular Carcinoma 100 0.205
56
ATH013 Atherosclerosis Susceptibility 66 0.202
57
P OVR042 Ovarian Cancer 89 0.193
58
P CRN018 Coronary Artery Anomaly 63 0.193
59
c ACT071 Acute Kidney Failure 59 0.191
60
MTB004 Metabolic Acidosis 50 0.191
61
VTM002 Vitamin B12 Deficiency 48 0.188
62
P NRF023 Neurofibromatosis, Type Ii 76 0.187
63
P CRN300 Coronary Heart Disease 1 63 0.185
64
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.183
65
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.181
66
c PRC016 Pre-Eclampsia 63 0.176
67
NTR005 Nutritional Deficiency Disease 61 0.176
68
ART140 Arteries, Anomalies of 53 0.176
69
ISC004 Ischemia 60 0.175
70
DWN001 Down Syndrome 70 0.173
71
P MYC007 Myocardial Infarction 70 0.168
72
c PRS136 Prostate Cancer, Hereditary, 6 33 0.168
73
c PRS130 Prostate Cancer, Hereditary, 8 32 0.168
74
HYP081 Hypolipoproteinemia 50 0.163
75
P NRP001 Neuropathy 56 0.161
76
AGN016 Aging 56 0.161
77
c SML038 Small Cell Cancer of the Lung 65 0.160
78
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.158
79
ATX019 Ataxia with Vitamin E Deficiency 48 0.158
80
SQM006 Squamous Cell Carcinoma 60 0.157
81
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.156
82
LPT014 Leptin Deficiency or Dysfunction 73 0.153
83
P VSC007 Vascular Disease 63 0.153
84
CRB039 Cerebrovascular Disease 69 0.150
85
P SCH015 Schizophrenia 75 0.147
86
P HYP086 Hypothyroidism 68 0.147
87
GLB015 Glioblastoma Multiforme 75 0.144
88
P HPT021 Hepatitis 67 0.144
89
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.142
90
P PRD008 Periodontitis 62 0.139
91
P HYP750 Hypertriglyceridemia, Familial 61 0.137
92
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.137
93
OVR029 Ovarian Hyperstimulation Syndrome 63 0.134
94
THY029 Thyroid Carcinoma 59 0.134
95
c FML035 Familial Hyperlipidemia 55 0.132
96
c MCR113 Microvascular Complications of Diabetes 3 52 0.132
97
PLC008 Placenta Disease 49 0.132
98
c MCR120 Microvascular Complications of Diabetes 7 47 0.132
99
c MCR130 Microvascular Complications of Diabetes 6 41 0.132
100
c MCR133 Microvascular Complications of Diabetes 4 41 0.132
101
STR067 Stroke, Ischemic 80 0.131
102
P BLD134 Bladder Cancer 78 0.131
103
END062 Endometrial Hyperplasia 48 0.131
104
ADN018 Adenoma 58 0.129
105
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.129
106
HYP266 Hypoxia 56 0.129
107
LVR012 Liver Cirrhosis 63 0.127
108
P ECL001 Eclampsia 51 0.125
109
c LPD015 Lipodystrophy, Familial Partial, Type 2 62 0.123
110
P KDN017 Kidney Cancer 61 0.123
111
CHL079 Children's Interstitial Lung Disease 27 0.123
112
LNG031 Lung Benign Neoplasm 50 0.122
113
GLC008 Glucose Metabolism Disease 40 0.122
114
PRP027 Peripheral Vascular Disease 71 0.120
115
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.118
116
DFC004 Deficiency Anemia 75 0.118
117
P PRP019 Peripheral Nervous System Disease 57 0.118
118
c PRD040 Periodontitis, Chronic 54 0.118
119
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.118
120
P LYM031 Lymphocytic Leukemia 55 0.116
121
P LYM118 Lymphoma 68 0.114
122
P GLM045 Glioma 63 0.114
123
ACN002 Acanthosis Nigricans 60 0.114
124
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.114
125
GLL048 Glial Tumor 45 0.114
126
P BCL017 B-Cell Lymphoma 58 0.112
127
AMN001 Amenorrhea 54 0.112
128
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.112
129
c PRM038 Primary Agammaglobulinemia 43 0.110
130
P GST053 Gastric Cancer 83 0.108
131
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.108
132
MLN008 Melanoma 69 0.108
133
ALL026 Allergic Hypersensitivity Disease 64 0.108
134
c ACT068 Acute Cystitis 63 0.108
135
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.108
136
PNC129 Pancreatic Adenocarcinoma 67 0.106
137
P LKM002 Leukemia 66 0.106
138
P MCR115 Microvascular Complications of Diabetes 5 66 0.106
139
c MCR129 Microvascular Complications of Diabetes 1 66 0.106
140
c HPT001 Hepatitis C 63 0.106
141
P OVR049 Ovarian Disease 53 0.106
142
P ALZ034 Alzheimer Disease 88 0.104
143
ANX010 Anxiety 72 0.104
144
P DMN002 Dementia 67 0.104
145
END030 End Stage Renal Failure 58 0.104
146
P LKM062 Leukemia, Acute Lymphoblastic 68 0.102
147
DPR016 Depression 63 0.102
148
MNT002 Mental Depression 57 0.102
149
c ACT075 Acute Myocardial Infarction 56 0.102
150
47X002 47,xyy 49 0.102
151
c LRG017 Large Intestine Cancer 47 0.102
152
P LNG064 Lung Cancer Susceptibility 3 77 0.099
153
PSY004 Psychotic Disorder 67 0.099
154
FCT007 Factor Vii Deficiency 66 0.099
155
HYP020 Hyperprolactinemia 64 0.099
156
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.099
157
SCH012 Schizoaffective Disorder 50 0.099
158
LYM019 Lymphosarcoma 47 0.099
159
P END084 Endocrine System Disease 44 0.099
160
CRV035 Cervical Cancer 76 0.097
161
CLR108 Colorectal Adenoma 64 0.097
162
END041 Endometrial Adenocarcinoma 63 0.097
163
P BPL003 Bipolar Disorder 56 0.097
164
c MJR024 Major Affective Disorder 9 41 0.097
165
c MJR022 Major Affective Disorder 8 38 0.097
166
ESP021 Esophageal Cancer 90 0.095
167
RCK004 Rickets 69 0.095
168
P ALC033 Alcohol Use Disorder 58 0.095
169
OVR094 Ovarian Epithelial Cancer 38 0.095
170
c HYP836 Hypercholesterolemia, Familial, 1 72 0.092
171
CHL065 Cholangiocarcinoma 67 0.092
172
KHL003 Kohlschutter-Tonz Syndrome 64 0.092
173
P ENC018 Encephalopathy 61 0.092
174
INT079 Intrahepatic Cholangiocarcinoma 50 0.092
175
SKN019 Skin Melanoma 67 0.090
176
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.090
177
TRP009 Triple X Syndrome 42 0.090
178
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.090
179
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.090
180
P VSC018 Visceral Steatosis 33 0.090
181
MYL069 Myeloma, Multiple 85 0.087
182
IMM167 Immune Deficiency Disease 78 0.087
183
P ART022 Arthritis 70 0.087
184
P SLP006 Sleep Apnea 69 0.087
185
P PLM037 Pulmonary Hypertension 68 0.087
186
P MSC005 Muscular Dystrophy 66 0.087
187
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.087
188
THR024 Thrombosis 56 0.087
189
c LKM061 Leukemia, Acute Myeloid 83 0.085
190
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.085
191
SVR004 Severe Combined Immunodeficiency 73 0.085
192
P PSR002 Psoriasis 62 0.085
193
P PNC044 Pancreatitis 61 0.085
194
P PLY014 Polycystic Kidney Disease 59 0.085
195
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.085
196
P RCT021 Rectum Cancer 53 0.085
197
PST011 Pustulosis of Palm and Sole 52 0.085
198
IMP005 Impotence 52 0.085
199
TLN003 Telangiectasis 51 0.085
200
CYT002 Cytokine Deficiency 44 0.085
201
P MJR007 Major Affective Disorder 1 43 0.085
202
P ATX030 Ataxia-Telangiectasia 83 0.082
203
BRN028 Brain Cancer 73 0.082
204
MSC157 Muscular Dystrophy, Duchenne Type 71 0.082
205
P FRG001 Fragile X Syndrome 68 0.082
206
P CRD119 Cardiac Arrest 67 0.082
207
MSC007 Muscle Hypertrophy 63 0.082
208
c FNC043 Fanconi Anemia, Complementation Group E 62 0.082
209
ATM095 Autoimmune Disease 61 0.082
210
P MYL006 Myeloid Leukemia 60 0.082
211
OCL069 Ocular Motor Apraxia 51 0.082
212
c MJR008 Major Affective Disorder 2 34 0.082
213
c MJR003 Major Affective Disorder 6 33 0.082
214
c MJR006 Major Affective Disorder 5 33 0.082
215
c MJR023 Major Affective Disorder 7 33 0.082
216
c MJR004 Major Affective Disorder 4 28 0.082
217
P RTN024 Retinoblastoma 72 0.079
218
HMN044 Human Immunodeficiency Virus Type 1 71 0.079
219
ART016 Aortic Aneurysm 68 0.079
220
c ATS007 Autism Spectrum Disorder 67 0.079
221
ORL011 Oral Cancer 60 0.079
222
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.079
223
c HPT016 Hepatitis B 59 0.079
224
DBT010 Diabetic Neuropathy 55 0.079
225
c FML008 Familial Retinoblastoma 53 0.079
226
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.079
227
c OVR114 Ovarian Cancer 1 38 0.079
228
c HPT073 Hepatitis C Virus 70 0.076
229
OST159 Osteogenic Sarcoma 66 0.076
230
P ATS364 Autism 65 0.076
231
MDD011 Mood Disorder 62 0.076
232
LNG099 Lung Disease 61 0.076
233
CHL068 Cholestasis 60 0.076
234
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.076
235
NRN004 Neuroendocrine Tumor 55 0.076
236
PRP080 Peripheral Artery Disease 53 0.076
237
P INS002 in Situ Carcinoma 52 0.076
238
HYP080 Hypogonadism 50 0.076
239
CRB004 Cerebral Artery Occlusion 44 0.076
240
ACT088 Acute Insulin Response 41 0.076
241
HYP064 Hypogonadotropism 40 0.076
242
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.076
243
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.076
244
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.076
245
INS024 Insulin-Like Growth Factor I 79 0.073
246
CNN003 Conn's Syndrome 79 0.073
247
OST012 Osteoarthritis 78 0.073
248
P TBR001 Tuberous Sclerosis 70 0.073
249
IDP011 Idiopathic Interstitial Pneumonia 63 0.073
250
c HPT003 Hepatitis a 63 0.073
251
P PLM036 Pulmonary Fibrosis 61 0.073
252
DSS008 Disease of Mental Health 57 0.073
253
HYP005 Hypokalemia 55 0.073
254
P OCY003 Oocyte Maturation Defect 1 45 0.073
255
c HYP272 Hypercholesterolemia, Familial, 3 43 0.073
257
P GLM040 Glioma Susceptibility 1 81 0.070
258
P RHM011 Rheumatoid Arthritis 80 0.070
259
c TBR025 Tuberous Sclerosis 1 76 0.070
260
P RSP003 Respiratory Failure 74 0.070
261
c ACT027 Acute Pancreatitis 59 0.070
262
ANR040 Aneurysm 58 0.070
263
P EXN002 Exanthem 57 0.070
264
SCH003 Schizophreniform Disorder 56 0.070
265
DFF005 Diffuse Large B-Cell Lymphoma 56 0.070
266
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.070
267
SRS001 Serous Cystadenocarcinoma 52 0.070
268
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 0.070
269
DMP001 Dumping Syndrome 44 0.070
270
c PCH010 Pachyonychia Congenita 3 43 0.070
271
49X006 49, Xxxxy Syndrome 41 0.070
272
c LKM071 Leukemia, Chronic Lymphocytic 79 0.067
273
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.067
274
P NRB001 Neuroblastoma 71 0.067
275
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.067
276
P HML002 Hemolytic Anemia 62 0.067
277
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.067
278
VSC002 Vascular Dementia 57 0.067
279
LYM040 Lymphoblastic Lymphoma 54 0.067
280
CYS014 Cystadenocarcinoma 51 0.067
281
SYS003 Systolic Heart Failure 50 0.067
282
APP009 Appendix Adenocarcinoma 44 0.067
283
ORL015 Oral Squamous Cell Carcinoma 43 0.067
284
c SYS001 Systemic Lupus Erythematosus 86 0.064
285
c ATR087 Atrial Standstill 1 74 0.064
286
P HNT016 Huntington Disease 71 0.064
287
LYM133 Lymphoma, Hodgkin, Classic 69 0.064
288
P ATR011 Atrial Fibrillation 66 0.064
289
ANG054 Angina Pectoris 66 0.064
290
SKN016 Skin Disease 63 0.064
291
P LPS004 Lupus Erythematosus 61 0.064
292
CNS004 Constipation 57 0.064
293
P ACT010 Acth-Secreting Pituitary Adenoma 57 0.064
294
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.064
295
P HYP076 Hyperthyroidism 55 0.064
296
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.064
297
P ART021 Arteriosclerosis 54 0.064
298
P MSC003 Muscular Atrophy 52 0.064
299
THY030 Thyroid Gland Disease 51 0.064
300
BNR002 Bone Resorption Disease 48 0.064
301
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.064
302
PPL001 Papillary Adenoma 45 0.064
303
RST023 Resting Heart Rate, Variation in 41 0.064
304
c THR092 Thrombophilia Due to Thrombin Defect 73 0.060
305
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.060
306
P SKN015 Skin Carcinoma 67 0.060
307
FLL027 Fallopian Tube Carcinoma 67 0.060
308
BRR014 Barrett Esophagus 64 0.060
309
P SLP005 Sleep Disorder 59 0.060
310
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.060
311
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.060
312
INT007 Intermediate Coronary Syndrome 55 0.060
313
P SBS003 Substance Abuse 54 0.060
314
P CHR345 Chronic Pain 50 0.060
315
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.060
316
BRN071 Brain Injury 49 0.060
317
P PRC031 Preeclampsia/eclampsia 1 37 0.060
318
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 35 0.060
319
CYT018 Cytochrome P450 2d6 Variant 27 0.060
321
AST005 Asthma 77 0.056
322
P PRK057 Parkinson Disease, Late-Onset 76 0.056
323
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.056
324
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.056
325
c TBR026 Tuberous Sclerosis 2 71 0.056
326
P MJR001 Major Depressive Disorder 68 0.056
327
ALC007 Alcohol Dependence 66 0.056
328
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.056
329
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.056
330
P THY023 Thymoma 65 0.056
331
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.056
332
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 61 0.056
333
INT002 Intermittent Claudication 61 0.056
334
P THL005 Thalassemia 60 0.056
335
c DWL002 Dowling-Degos Disease 1 58 0.056
336
P HDC001 Headache 57 0.056
337
P FBR017 Fibrosarcoma 56 0.056
338
P ALP008 Alopecia 56 0.056
339
P MLN007 Male Infertility 56 0.056
340
P INF037 Inflammatory Bowel Disease 56 0.056
341
P MGL001 Megaloblastic Anemia 55 0.056
342
P PTT006 Pituitary Adenoma 54 0.056
343
END040 Endogenous Depression 54 0.056
344
c THY107 Thymoma, Familial 54 0.056
345
ACR041 Acromelic Frontonasal Dysostosis 52 0.056
346
c PSR017 Psoriasis 2 52 0.056
347
PLS009 Plasma Cell Neoplasm 51 0.056
348
PRS021 Prostatic Adenoma 51 0.056
349
c PSR023 Psoriasis 1 49 0.056
350
RTC005 Reticulosarcoma 49 0.056
351
P PRC019 Precocious Puberty 47 0.056
352
RNL077 Renal Fibrosis 47 0.056
353
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.056
354
ANR004 Anuria 46 0.056
355
FTL021 Fetal Macrosomia 42 0.056
356
GST020 Gastric Antral Vascular Ectasia 41 0.056
357
c MCR112 Microvascular Complications of Diabetes 2 41 0.056
358
RDN001 Reading Disorder 40 0.056
359
LKP003 Leukoplakia 39 0.056
360
c PSR028 Psoriasis 7 39 0.056
361
c PSR032 Psoriasis 11 38 0.056
362
c PSR018 Psoriasis 13 38 0.056
363
c SYS043 Systemic Lupus Erythematosus 1 38 0.056
364
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.056
365
ERY023 Erythroplakia 24 0.056
366
NRL016 Neural Tube Defects 82 0.052
367
c FNC027 Fanconi Anemia, Complementation Group a 81 0.052
368
P OST002 Osteoporosis 73 0.052
369
P CNR004 Cone-Rod Dystrophy 2 71 0.052
370
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.052
371
P FLL037 Follicular Lymphoma 66 0.052
372
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.052
373
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.052
374
APN008 Apnea, Obstructive Sleep 65 0.052
375
GT001 Gout 63 0.052
376
MSC152 Muscular Dystrophy, Becker Type 63 0.052
377
P NTR004 Neutropenia 63 0.052
378
P END044 Endometriosis 62 0.052
379
BRS099 Breast Ductal Carcinoma 62 0.052
380
c ALP101 Alpha-Thalassemia 62 0.052
381
TRN015 Transient Cerebral Ischemia 62 0.052
382
TXC005 Toxic Shock Syndrome 61 0.052
383
P SNS001 Sensorineural Hearing Loss 61 0.052
384
PRT013 Portal Hypertension 60 0.052
385
SPN186 Spinal Cord Injury 60 0.052
386
HPT019 Hepatic Encephalopathy 60 0.052
387
BLR008 Bilirubin Metabolic Disorder 57 0.052
388
ISL001 Islet Cell Tumor 56 0.052
389
GNR004 Generalized Anxiety Disorder 56 0.052
390
GST050 Gastrointestinal System Disease 56 0.052
391
MCS002 Mucositis 55 0.052
392
LMB062 Limb Ischemia 55 0.052
393
P DBT005 Diabetes Insipidus 55 0.052
394
P TCD001 Tic Disorder 54 0.052
395
P CYS039 Cystic Kidney Disease 54 0.052
396
CLR030 Clear Cell Renal Cell Carcinoma 53 0.052
397
HDR002 Hidradenitis Suppurativa 53 0.052
398
NRT001 Neurotic Disorder 52 0.052
399
GTR002 Goiter 52 0.052
400
PRS045 Prostatic Hypertrophy 52 0.052
401
CRT016 Carotid Artery Disease 52 0.052
402
SPP010 Suppressor of Tumorigenicity 3 51 0.052
403
CLR109 Colorectal Adenocarcinoma 50 0.052
404
DYS073 Dysphagia 50 0.052
405
P SCK005 Sickle Cell Disease 50 0.052
406
P MYT002 Myotonic Dystrophy 49 0.052
407
PRS129 Prostatic Hyperplasia, Benign 49 0.052
408
HDR003 Hidradenitis 49 0.052
409
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.052
410
ADR016 Adrenal Cortical Carcinoma 48 0.052
411
LPT006 Leptin Receptor Deficiency 47 0.052
412
PRT035 Peritoneum Cancer 44 0.052
413
HPT004 Hepatic Coma 43 0.052
414
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.052
415
MMM006 Mammographic Density 41 0.052
416
ADR004 Adrenal Cortical Adenocarcinoma 38 0.052
417
CYS001 Cystic Fibrosis 80 0.047
418
P MLT020 Multiple Sclerosis 72 0.047
419
c LKM063 Leukemia, Chronic Myeloid 71 0.047
420
GST040 Gastric Adenocarcinoma 70 0.047
421
EWN003 Ewing Sarcoma 68 0.047
422
P THR014 Thrombocytopenia 68 0.047
423
P NSP012 Nasopharyngeal Carcinoma 67 0.047
424
c FML001 Familial Atrial Fibrillation 66 0.047
425
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 66 0.047
426
P NRV007 Nervous System Disease 66 0.047
427
CRN036 Craniopharyngioma 65 0.047
428
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.047
429
P VSC011 Vasculitis 62 0.047
430
CRC021 Carcinosarcoma 61 0.047
431
c PNS012 Paine Syndrome 61 0.047
432
INS001 Insulinoma 60 0.047
433
ACQ007 Acquired Immunodeficiency Syndrome 60 0.047
434
P SYP003 Syphilis 59 0.047
435
P BRS044 Breast Adenocarcinoma 59 0.047
436
THY122 Thyroid Gland Cancer 58 0.047
437
ADR005 Adrenal Carcinoma 58 0.047
438
P PRV006 Pervasive Developmental Disorder 57 0.047
439
BCT022 Bacterial Infectious Disease 56 0.047
440
GLL018 Gallbladder Cancer 56 0.047
441
TRD006 Tardive Dyskinesia 55 0.047
442
BRN004 Brain Edema 55 0.047
443
PLM010 Pulmonary Edema 55 0.047
444
PPL022 Papilloma 54 0.047
445
EPT010 Epithelial-Myoepithelial Carcinoma 53 0.047
446
HMC014 Homocysteinemia 53 0.047
447
ECH003 Echinococcosis 53 0.047
448
NNT012 Neonatal Jaundice 53 0.047
449
P SML001 Small Cell Carcinoma 52 0.047
450
FML037 Female Breast Cancer 52 0.047
451
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 52 0.047
452
c GLL024 Gallbladder Disease 1 52 0.047
453
HYP014 Hyperuricemia 51 0.047
454
c VRL010 Viral Hepatitis 51 0.047
455
CLR003 Clear Cell Adenocarcinoma 50 0.047
456
c BRS049 Breast Carcinoma in Situ 50 0.047
457
APL002 Aplasia of Lacrimal and Salivary Glands 50 0.047
458
HYP781 Hypoascorbemia 50 0.047
459
c INF145 Infantile Liver Failure Syndrome 1 50 0.047
460
c FLL041 Follicular Lymphoma 1 49 0.047
461
END021 Endomyocardial Fibrosis 48 0.047
462
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.047
463
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.047
464
URT010 Ureteral Obstruction 46 0.047
465
c MLG068 Malignant Glioma 45 0.047
466
ACN001 Acinar Cell Carcinoma 45 0.047
467
P OVR046 Ovarian Cyst 45 0.047
468
END035 Endocrine Gland Cancer 44 0.047
469
P HYP121 Hypoalphalipoproteinemia 43 0.047
470
P ATS366 Autism X-Linked 2 42 0.047
471
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.047
472
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.047
473
PNC015 Pancreatic Acinar Cell Adenocarcinoma 40 0.047
474
HYP784 Hypogonadism, Male 39 0.047
475
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.047
476
c HYP841 Hypoalphalipoproteinemia, Primary, 1 37 0.047
477
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.047
478
ACN026 Acinar Cell Carcinoma of Pancreas 28 0.047
479
c SPN225 Spondyloarthropathy 1 73 0.042
480
P LFR001 Li-Fraumeni Syndrome 72 0.042
481
P FML011 Familial Adenomatous Polyposis 72 0.042
482
ACR007 Acromegaly 71 0.042
483
c FML346 Familial Adenomatous Polyposis 1 70 0.042
484
c MGR028 Migraine with or Without Aura 1 69 0.042
485
P OCL013 Oculodentodigital Dysplasia 69 0.042
486
MNT001 Mantle Cell Lymphoma 66 0.042
487
P MTR004 Maturity-Onset Diabetes of the Young 66 0.042
488
LNG039 Lung Squamous Cell Carcinoma 65 0.042
489
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.042
490
MGK001 Megakaryocytic Leukemia 64 0.042
491
ACT119 Acute Promyelocytic Leukemia 63 0.042
492
CLT003 Colitis 62 0.042
493
DRM006 Dermatitis 61 0.042
494
VRL011 Viral Infectious Disease 61 0.042
495
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 61 0.042
496
P MYC008 Myocarditis 59 0.042
497
GST045 Gastroenteritis 59 0.042
498
DCT002 Ductal Carcinoma in Situ 59 0.042
499
FBR047 Fibromyalgia 59 0.042
500
HLC007 Helicobacter Pylori Infection 59 0.042
501
CRD132 Cardiac Conduction Defect 59 0.042
502
P SZR006 Seizure Disorder 58 0.042
503
c ACT073 Acute Leukemia 58 0.042
504
VSL002 Visual Epilepsy 58 0.042
505
EMB004 Embryonal Carcinoma 57 0.042
506
IRN002 Iron Metabolism Disease 57 0.042
507
P UVT001 Uveitis 57 0.042
508
P CHN012 Chondrosarcoma 56 0.042
509
LMY014 Leiomyoma, Uterine 56 0.042
510
P MTC069 Mitochondrial Disorders 56 0.042
511
HMG005 Hemoglobinopathy 55 0.042
512
TNG003 Tongue Cancer 55 0.042
513
MRG003 Marginal Zone B-Cell Lymphoma 53 0.042
514
P THY032 Thyroiditis 53 0.042
515
SPL004 Splenic Marginal Zone Lymphoma 51 0.042
516
LMY002 Leiomyoma 50 0.042
517
CYS008 Cystic Echinococcosis 50 0.042
518
P OPN001 Open-Angle Glaucoma 49 0.042
519
URM002 Uremia 49 0.042
520
SPL018 Splenomegaly 48 0.042
521
GRM005 Germ Cell Cancer 47 0.042
522
RCT020 Rectum Adenocarcinoma 46 0.042
523
MNC019 Monocarboxylate Transporter 1 Deficiency 46 0.042
524
MXD026 Mixed Glioma 45 0.042
525
MLN073 Melanosis, Neurocutaneous 45 0.042
526
P BRB001 Beriberi 44 0.042
527
ATN004 Autonomic Neuropathy 44 0.042
528
LMY003 Leiomyomatosis 43 0.042
529
IDP033 Idiopathic Edema 43 0.042
530
CYS009 Cystadenoma 43 0.042
531
c LFR007 Li-Fraumeni Syndrome 2 42 0.042
532
NSP002 Nasopharyngitis 41 0.042
533
GRM004 Germinoma 40 0.042
534
c HNT011 Huntington Disease-Like 3 38 0.042
535
HYP835 Hypothalamic Obesity 38 0.042
536
CRY036 Cryptogenic Cirrhosis 36 0.042
537
INT020 Intravenous Leiomyomatosis 36 0.042
538
P OVR010 Ovarian Brenner Tumor 35 0.042
539
HND015 Hand Skill, Relative 33 0.042
540
PGM030 Pigmentation Anomaly of the Skin 25 0.042
541
CHR176 Chromophil Renal Cell Carcinoma 23 0.042
542
P MDL005 Medulloblastoma 77 0.037
543
ACR006 Aceruloplasminemia 73 0.037
544
ULC004 Ulcerative Colitis 73 0.037
545
c BTT014 Beta-Thalassemia 72 0.037
546
SCK003 Sickle Cell Anemia 72 0.037
547
PLM001 Pulmonary Tuberculosis 70 0.037
548
c BSL007 Basal Cell Carcinoma 68 0.037
549
P INF038 Influenza 68 0.037
550
CRB037 Cerebral Palsy 68 0.037
551
BRK010 Burkitt Lymphoma 67 0.037
552
P DRM053 Dermatitis, Atopic 66 0.037
553
MYC006 Mycosis Fungoides 66 0.037
554
SRC014 Sarcoma 65 0.037
555
c PRD013 Periodic Fever, Familial, Autosomal Dominant 65 0.037
556
MSM014 Mismatch Repair Cancer Syndrome 65 0.037
557
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.037
558
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.037
559
c MCL013 Mucolipidosis Iv 64 0.037
560
TBC004 Tobacco Addiction 64 0.037
561
CLN015 Colon Adenocarcinoma 63 0.037
562
PTT046 Pituitary Hormone Deficiency, Combined, 2 63 0.037
563
NRM005 Neuromuscular Disease 63 0.037
564
P ADL010 Adult Respiratory Distress Syndrome 63 0.037
565
PPL049 Papillon-Lefevre Syndrome 63 0.037
566
PRM126 Primary Peritoneal Carcinoma 62 0.037
567
c GLC092 Glaucoma, Primary Open Angle 62 0.037
568
PSR001 Psoriatic Arthritis 62 0.037
569
P PRM006 Primary Biliary Cirrhosis 61 0.037
570
P MVM001 Movement Disease 61 0.037
571
P ANP001 Anaplastic Large Cell Lymphoma 61 0.037
572
P MCR256 Microphthalmia, Syndromic 9 61 0.037
573
LYM012 Lymphoplasmacytic Lymphoma 61 0.037
574
P CTR002 Cataract 60 0.037
575
SZR001 Sezary's Disease 60 0.037
576
CRD223 Cardiac Arrhythmia 60 0.037
577
P ALP009 Alopecia Areata 60 0.037
578
GNG013 Gingivitis 59 0.037
579
SPP011 Suppression of Tumorigenicity 12 59 0.037
580
P BND020 Bone Disease 59 0.037
581
EYD002 Eye Disease 58 0.037
582
NWB001 Newborn Respiratory Distress Syndrome 58 0.037
583
ERY003 Erythema Multiforme 57 0.037
584
P BNC003 Bone Cancer 57 0.037
585
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 57 0.037
586
c ADL017 Adult T-Cell Leukemia 57 0.037
587
ADN027 Adenomyosis 57 0.037
588
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.037
589
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 56 0.037
590
ERY051 Erythroleukemia, Familial 56 0.037
591
SFT003 Soft Tissue Sarcoma 56 0.037
592
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.037
593
CMR002 Coumarin Resistance 56 0.037
594
P PLY019 Polyneuropathy 56 0.037
595
GRN034 Grange Syndrome 55 0.037
596
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 55 0.037
597
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.037
598
CLL003 Cellulitis 54 0.037
599
GLS001 Gliosarcoma 54 0.037
600
ORP003 Oropharynx Cancer 54 0.037
601
HMS001 Hemosiderosis 54 0.037
602
BRN015 Bronchiolo-Alveolar Adenocarcinoma 54 0.037
603
OCL008 Oculopharyngeal Muscular Dystrophy 54 0.037
604
HLL004 Hellp Syndrome 53 0.037
605
c LKM070 Leukemia, Acute Monocytic 53 0.037
606
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 53 0.037
607
SNS003 Sensory Peripheral Neuropathy 53 0.037
608
TRM010 Traumatic Brain Injury 53 0.037
609
KRT009 Keratosis 53 0.037
610
GLS018 Glass Syndrome 53 0.037
611
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 53 0.037
612
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.037
613
c PNT034 Pontocerebellar Hypoplasia, Type 2e 52 0.037
614
THY124 Thyroid Gland Papillary Carcinoma 52 0.037
615
CYS036 Cystinosis, Nephropathic 51 0.037
616
c ACT134 Acute Liver Failure 51 0.037
617
SPN035 Spindle Cell Sarcoma 51 0.037
618
AZS001 Azoospermia 50 0.037
619
P FNC004 Fanconi Syndrome 50 0.037
620
SPS003 Spastic Diplegia 50 0.037
621
P AST007 Astrocytoma 50 0.037
622
MCR004 Macroglobulinemia 50 0.037
623
c MLG054 Malignant Histiocytosis 50 0.037
624
KRT001 Keratoconjunctivitis Sicca 50 0.037
625
P INT099 Intrahepatic Cholestasis of Pregnancy 49 0.037
626
c HNT004 Huntington Disease-Like 2 49 0.037
627
JCB001 Jacobsen Syndrome 49 0.037
628
OPP004 Oppositional Defiant Disorder 49 0.037
629
ADN009 Adenosquamous Carcinoma 49 0.037
630
c DYS119 Dystonia 9 49 0.037
631
CLN045 Colonic Benign Neoplasm 49 0.037
632
VTM033 Vitamin K Deficiency Bleeding 48 0.037
633
MTC005 Mitochondrial Metabolism Disease 48 0.037
634
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 48 0.037
635
SXL003 Sexual Disorder 48 0.037
636
c PNT049 Pontocerebellar Hypoplasia, Type 2d 48 0.037
637
ADN089 Adenosquamous Lung Carcinoma 48 0.037
638
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.037
639
ART004 Aortic Atherosclerosis 48 0.037
640
DRY001 Dry Eye Syndrome 47 0.037
641
c BSL024 Basal Cell Carcinoma 1 47 0.037
642
TST044 Testicular Torsion 47 0.037
643
NDL007 Nodular Goiter 47 0.037
644
P TCL004 T-Cell Leukemia 47 0.037
645
c CTR098 Cataract 1, Multiple Types 47 0.037
646
PLS025 Plasmablastic Lymphoma 47 0.037
647
PLY012 Polyhydramnios 46 0.037
648
CNG028 Congenital Hypoplastic Anemia 46 0.037
649
P MYC033 Myoclonus 46 0.037
650
PLS016 Plasma Cell Leukemia 46 0.037
651
HDN002 Head Injury 45 0.037
652
P BNG032 Benign Mesothelioma 45 0.037
654
LYM051 Lymphomatoid Granulomatosis 45 0.037
655
OLG001 Oligospermia 45 0.037
656
c EST002 Estrogen-Receptor Negative Breast Cancer 44 0.037
657
THR012 Thoracic Cancer 44 0.037
658
c ATM099 Autoimmune Uveitis 44 0.037
659
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.037
660
IMM064 Immunodeficiency, Common Variable, 10 44 0.037
661
FNC007 Functioning Pituitary Adenoma 44 0.037
662
LTH001 Lethal Midline Granuloma 43 0.037
663
CHL152 Childhood Acute Lymphocytic Leukemia 43 0.037
664
PLY068 Polysubstance Abuse 43 0.037
665
CLN044 Colon Adenoma 42 0.037
666
MYF002 Myofascial Pain Syndrome 42 0.037
667
PHY002 Physical Disorder 42 0.037
668
MXD023 Mixed Cell Type Cancer 42 0.037
669
XRP001 Xerophthalmia 42 0.037
670
BCK006 Back Pain 42 0.037
671
c ADN012 Adenocarcinoma in Situ 42 0.037
672
DBT002 Diabetic Autonomic Neuropathy 41 0.037
673
BNB002 Bainbridge-Ropers Syndrome 41 0.037
674
c PRS097 Prostate Cancer, Hereditary, 1 41 0.037
675
P RRH023 Rare Hereditary Hemochromatosis 41 0.037
676
SPS057 Spasticity 41 0.037
677
CYC005 Cyclothymic Disorder 40 0.037
678
P PRG092 Pregnancy Loss, Recurrent 1 40 0.037
679
SPR126 Superior Semicircular Canal Dehiscence 40 0.037
680
CMB021 Combined Pituitary Hormone Deficiency 40 0.037
681
ALL014 Allergic Encephalomyelitis 39 0.037
682
PTT003 Pituitary-Dependent Cushing's Disease 39 0.037
683
ORL012 Oral Leukoplakia 39 0.037
684
c MLG074 Malignant Mesenchymoma 39 0.037
685
c CHR682 Chronic Bilirubin Encephalopathy 38 0.037
686
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 0.037
687
c HMG029 Hemoglobin Se Disease 38 0.037
688
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.037
689
c BNG079 Benign Adult Familial Myoclonic Epilepsy 36 0.037
690
c GLC078 Glaucoma 1, Open Angle, F 35 0.037
691
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.037
692
TTH004 Tethered Spinal Cord Syndrome 35 0.037
693
P PRG002 Progesterone-Receptor Positive Breast Cancer 34 0.037
694
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.037
695
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 34 0.037
696
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.037
697
c CHR064 Chronic Monocytic Leukemia 34 0.037
698
c PRG003 Progesterone-Receptor Negative Breast Cancer 33 0.037
699
c PRC047 Precocious Puberty, Central, 1 32 0.037
700
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.037
701
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.037
702
PRX085 Preaxial Hallucal Polydactyly 28 0.037
703
HRP008 Herpes Simiae 25 0.037
704
ORL006 Oral Mucosa Leukoplakia 24 0.037
705
CD4008 Cd4/cd8 T-Cell Ratio 20 0.037
706
P RTN008 Retinitis Pigmentosa 77 0.030
707
P PHC003 Pheochromocytoma 71 0.030
708
P EPL164 Epilepsy 71 0.030
709
P SRC025 Sarcoidosis 1 70 0.030
710
P MYC084 Mycobacterium Tuberculosis 1 68 0.030
711
P PNM007 Pneumonia 68 0.030
712
P TMP003 Temporal Arteritis 67 0.030
713
SVR097 Severe Cutaneous Adverse Reaction 67 0.030
714
P BRD002 Bardet-Biedl Syndrome 66 0.030
715
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.030
716
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.030
717
GST092 Gastroesophageal Reflux 65 0.030
718
PRT036 Peritonitis 65 0.030
719
P DYS154 Dystonia 65 0.030
720
P MYP004 Myopathy 64 0.030
721
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.030
722
MYC079 Myoclonic Epilepsy of Lafora 64 0.030
723
IRR002 Irritable Bowel Syndrome 63 0.030
724
THY121 Thyroid Gland Anaplastic Carcinoma 63 0.030
725
P FRD001 Friedreich Ataxia 63 0.030
726
ANR007 Anorexia Nervosa 63 0.030
727
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.030
728
HSH003 Hashimoto Thyroiditis 62 0.030
729
BLL006 Bullous Pemphigoid 62 0.030
730
P ESP024 Esophagitis 62 0.030
731
c BRD010 Bardet-Biedl Syndrome 1 61 0.030
732
INT066 Interstitial Lung Disease 59 0.030
733
P WLF004 Wolfram Syndrome 59 0.030
734
STT001 Status Epilepticus 59 0.030
735
PLM033 Pulmonary Embolism 59 0.030
736
P PRD006 Prader-Willi Syndrome 59 0.030
737
IRN001 Iron Deficiency Anemia 58 0.030
738
PPT005 Peptic Ulcer Disease 58 0.030
739
CHL067 Cholecystitis 58 0.030
740
PRL032 Perlman Syndrome 58 0.030
741
P GLL020 Gallbladder Disease 58 0.030
742
ERY029 Erythermalgia, Primary 58 0.030
743
P URT039 Urticaria 58 0.030
744
c WLF013 Wolfram Syndrome 1 58 0.030
745
LYM027 Lymphopenia 57 0.030
746
c MST023 Mesothelioma, Malignant 57 0.030
747
P PYL005 Pyelonephritis 56 0.030
748
CMM005 Common Cold 56 0.030
749
P GST044 Gastritis 55 0.030
750
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 55 0.030
751
P LCH002 Lichen Planus 54 0.030
752
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 0.030
753
P ANG015 Angioedema 54 0.030
754
c BRD011 Bardet-Biedl Syndrome 10 54 0.030
755
P RTN016 Retinal Degeneration 53 0.030
756
INT075 Intracranial Hypertension 53 0.030
757
P TRM003 Tremor 53 0.030
758
GST023 Gastric Ulcer 53 0.030
759
P RTN018 Retinal Disease 52 0.030
760
P PRG013 Paraganglioma 52 0.030
761
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.030
762
DMY004 Demyelinating Disease 52 0.030
763
P ACT105 Acute Mountain Sickness 52 0.030
764
c BRD014 Bardet-Biedl Syndrome 2 51 0.030
765
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.030
766
LRN001 Laurence-Moon Syndrome 51 0.030
767
P THR015 Thrombophilia 50 0.030
768
PST021 Postpartum Depression 50 0.030
769
DYS015 Dysentery 50 0.030
770
c BRD012 Bardet-Biedl Syndrome 11 50 0.030
771
P OVR082 Overgrowth Syndrome 50 0.030
772
P RNL007 Renal Tubular Acidosis 50 0.030
773
HYP017 Hypophosphatemia 49 0.030
774
c SVR005 Severe Pre-Eclampsia 49 0.030
775
ALN001 Aland Island Eye Disease 49 0.030
776
HPT009 Hepatopulmonary Syndrome 49 0.030
777
RDC002 Radiculopathy 48 0.030
778
BRR012 Berardinelli-Seip Congenital Lipodystrophy 48 0.030
779
CRD137 Cardiogenic Shock 48 0.030
780
RTN020 Retinal Vascular Disease 48 0.030
781
DGN001 Degenerative Disc Disease 48 0.030
782
THY128 Thyroid Tumor 47 0.030
783
HYP082 Hypopharynx Cancer 47 0.030
784
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.030
785
RTN023 Retinitis 46 0.030
786
ADR040 Adrenal Gland Pheochromocytoma 46 0.030
787
CYN002 Cyanosis, Transient Neonatal 45 0.030
788
c BRD013 Bardet-Biedl Syndrome 12 44 0.030
789
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.030
790
DVR002 Diverticulitis 44 0.030
791
SBC016 Subacute Delirium 44 0.030
792
SDD008 Sudden Sensorineural Hearing Loss 43 0.030
793
GRW007 Growth Hormone Deficiency 43 0.030
794
NRR001 Neuroretinitis 43 0.030
795
c SRC023 Sarcoidosis 2 43 0.030
796
BLR013 Biliary Tract Cancer 42 0.030
797
LWC001 Low Compliance Bladder 42 0.030
798
GLC096 Galactorrhea 42 0.030
799
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.030
800
ANX004 Anoxia 42 0.030
801
PPL007 Papillary Serous Adenocarcinoma 41 0.030
802
c WLF009 Wolfram Syndrome 2 40 0.030
803
KLD004 Keloid Disorder 40 0.030
804
PRM329 Premature Aging 39 0.030
805
HYP026 Hypoglycemic Coma 38 0.030
806
GND003 Gonadal Disease 38 0.030
807
HRN029 Hearing Loss, Noise-Induced 37 0.030
808
DBT081 Diabetic Encephalopathy 36 0.030
809
MYT011 Myotonia 35 0.030
810
FXD003 Fixed Drug Eruption 35 0.030
811
FST010 Fasting Hypoglycemia 35 0.030
812
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.030
813
c DRR009 Diarrhea 6 32 0.030
814
RRS014 Rare Surgical Neurologic Disease 32 0.030
815
PNT003 Pinta Disease 31 0.030
816
PRG074 Progressive Myoclonus Epilepsy, Lafora Type 29 0.030
817
ERY066 Erythema Multiforme Major 28 0.030
818
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.030
819
UTR054 Uterine Hypoplasia 25 0.030
820
c CHR465 Chronic Diarrhea Due to Guanylate Cyclase 2c Overactivity 20 0.030
821
NNC012 Non-Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 17 0.030
822
HYP158 Hyperinsulinism, Diffuse 3 0.030
823
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.021
824
MLR004 Malaria 80 0.021
825
c DLT002 Dilated Cardiomyopathy 79 0.021
826
P LYN001 Lynch Syndrome 77 0.021
827
ADR007 Adrenoleukodystrophy 74 0.021
828
c MNN043 Meningioma, Familial 74 0.021
829
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.021
830
P GRF003 Graft-Versus-Host Disease 71 0.021
831
OTT002 Otitis Media 71 0.021
832
P AMY004 Amyloidosis 70 0.021
833
MYL009 Myelodysplastic Syndrome 70 0.021
834
P SYS005 Systemic Scleroderma 70 0.021
835
PLY001 Polycythemia Vera 69 0.021
836
c PNC108 Pancreatitis, Hereditary 69 0.021
837
P MPL001 Maple Syrup Urine Disease 69 0.021
838
P MYS003 Myasthenia Gravis 68 0.021
839
c CNG411 Congenital Disorder of Glycosylation, Type in 68 0.021
840
c FML021 Familial Hypercholesterolemia 68 0.021
841
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.021
842
ALL003 Allergic Rhinitis 67 0.021
843
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.021
844
P HYP098 Hypereosinophilic Syndrome 66 0.021
845
P ART005 Arteriovenous Malformation 65 0.021
847
P MNN013 Meningitis 65 0.021
848
P BLD062 Bile Duct Cancer 65 0.021
849
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.021
850
OST017 Osteomyelitis 64 0.021
851
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.021
852
P HYP069 Hyperparathyroidism 62 0.021
853
P HRD008 Hereditary Hemorrhagic Telangiectasia 62 0.021
854
P RHB003 Rhabdomyosarcoma 62 0.021
855
DNH001 Donohue Syndrome 62 0.021
856
MNN042 Meningioma, Radiation-Induced 62 0.021
857
ALC006 Alcoholic Hepatitis 61 0.021
858
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.021
859
c ANM038 Anemia, Autoimmune Hemolytic 61 0.021
860
P HMN010 Hemangioma 61 0.021
861
RHM001 Rheumatic Fever 61 0.021
862
ERL001 Early Myoclonic Encephalopathy 61 0.021
863
MSL001 Measles 61 0.021
864
c THR082 Thrombophilia Due to Activated Protein C Resistance 60 0.021
865
NRL005 Neurilemmoma 60 0.021
866
VRC005 Varicose Veins 60 0.021
867
P ATR010 Atrial Heart Septal Defect 60 0.021
868
P SLV026 Salivary Gland Carcinoma 60 0.021
869
MCR013 Microphthalmia 60 0.021
870
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.021
871
RTN017 Retinal Detachment 60 0.021
872
P SCL018 Scoliosis 60 0.021
873
DNG002 Dengue Hemorrhagic Fever 60 0.021
874
ETN001 Eating Disorder 59 0.021
875
PRT058 Pure Autonomic Failure 59 0.021
876
UTR024 Uterine Carcinosarcoma 59 0.021
877
GRD007 Grade Iii Astrocytoma 59 0.021
878
CMP010 Complex Regional Pain Syndrome 58 0.021
879
CRV038 Cervical Squamous Cell Carcinoma 58 0.021
880
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 58 0.021
881
PST028 Post-Traumatic Stress Disorder 58 0.021
882
BRS051 Breast Disease 58 0.021
883
P FNC044 Fanconi Anemia, Complementation Group C 58 0.021
884
ADL030 Adult-Onset Still's Disease 58 0.021
885
CNT047 Contact Dermatitis 57 0.021
886
P CND004 Candidiasis 57 0.021
887
URN010 Urinary Tract Obstruction 57 0.021
888
P RHN004 Rhinitis 57 0.021
889
BRN056 Bronchopulmonary Dysplasia 57 0.021
890
P PRN023 Prion Disease 57 0.021
891
P SHR029 Short Syndrome 57 0.021
892
P GLM007 Glomerulonephritis 57 0.021
893
PRS047 Prostatitis 56 0.021
894
P ORL007 Oral Cavity Cancer 56 0.021
895
ORL005 Oral Candidiasis 56 0.021
896
ACS001 Acoustic Neuroma 56 0.021
897
ADR008 Adrenal Adenoma 56 0.021
898
HPT022 Hepatoblastoma 56 0.021
899
PRP030 Purpura 55 0.021
900
MCL006 Macular Retinal Edema 55 0.021
901
P FML012 Familial Partial Lipodystrophy 55 0.021
902
P GRV001 Graves' Disease 55 0.021
903
P PLY018 Polycythemia 55 0.021
904
ATR057 Atrioventricular Block 55 0.021
905
ALL010 Allergic Contact Dermatitis 55 0.021
906
PLV003 Pelvic Inflammatory Disease 55 0.021
907
ACT058 Active Peptic Ulcer Disease 55 0.021
908
c NPH055 Nephrotic Syndrome, Type 1 55 0.021
909
RSC001 Rosacea 55 0.021
910
P FTL001 Fetal Alcohol Syndrome 55 0.021
911
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.021
912
CRT017 Cartilage Disease 54 0.021
913
c OPT053 Optic Atrophy 1 54 0.021
914
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.021
915
P MNC007 Monocytic Leukemia 54 0.021
916
P SCL048 Sclerosteosis 53 0.021
917
GST037 Gastroparesis 53 0.021
918
c ACT020 Acute T Cell Leukemia 53 0.021
919
P LTR001 Lateral Sclerosis 53 0.021
920
MYM001 Myoma 53 0.021
921
ALC009 Alcoholic Liver Cirrhosis 53 0.021
922
ARM001 Aromatase Deficiency 53 0.021
923
P HYP730 Hypogonadotropic Hypogonadism 53 0.021
924
c HYP768 Hyperlipoproteinemia, Type I 52 0.021
925
P INT068 Intestinal Disease 52 0.021
926
SPN051 Spondylitis 52 0.021
927
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.021
928
TND005 Tendinitis 52 0.021
929
NVS001 Neovascular Glaucoma 52 0.021
930
P RTN022 Retinal Vein Occlusion 52 0.021
931
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.021
932
PTH003 Pathologic Nystagmus 51 0.021
933
P TRT010 Teratoma 51 0.021
934
c ACT135 Acute Graft Versus Host Disease 51 0.021
935
OVR059 Ovary Adenocarcinoma 51 0.021
936
MCR141 Mucormycosis 51 0.021
937
c HYP739 Hyperlipoproteinemia, Type Iv 51 0.021
938
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 51 0.021
939
VLV011 Vulvovaginal Candidiasis 51 0.021
940
ACT017 Acute Chest Syndrome 50 0.021
941
HRT011 Heart Septal Defect 50 0.021
942
P HYP077 Hypertrichosis 50 0.021
943
c PNC106 Pancreatic Agenesis 1 50 0.021
944
P TMP001 Temporal Lobe Epilepsy 50 0.021
945
P SMP003 Simpson-Golabi-Behmel Syndrome 50 0.021
946
VLV047 Volvulus of Midgut 50 0.021
947
CRT013 Carotid Stenosis 50 0.021
948
P DDN001 Duodenal Ulcer 50 0.021
949
TRY001 Trypanosomiasis 50 0.021
950
CRN030 Coronary Stenosis 50 0.021
951
P NNT009 Neonatal Diabetes Mellitus 50 0.021
952
HYP006 Hypertensive Heart Disease 49 0.021
953
RNL011 Renal Osteodystrophy 49 0.021
954
IMP004 Impetigo 49 0.021
955
PNN001 Panniculitis 49 0.021
956
BHR001 Behr Syndrome 49 0.021
957
PPL021 Papilledema 48 0.021
958
P CMP008 Compartment Syndrome 48 0.021
959
DBT006 Diabetic Macular Edema 48 0.021
960
ATS010 Autosomal Recessive Disease 48 0.021
961
c FML053 Familial Colorectal Cancer 48 0.021
962
c FNC028 Fanconi Anemia, Complementation Group L 48 0.021
963
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.021
964
ACT084 Acute Stress Disorder 48 0.021
965
HLX001 Helix Syndrome 47 0.021
966
DRG003 Drug Dependence 47 0.021
967
P ACQ022 Acquired Generalized Lipodystrophy 47 0.021
968
HYP025 Hyperphosphatemia 47 0.021
969
SCH038 Schopf-Schulz-Passarge Syndrome 47 0.021
970
CRN027 Corneal Neovascularization 47 0.021
971
ATN005 Autonomic Dysfunction 47 0.021
972
SPN021 Spinal Meningioma 47 0.021
973
c BCT013 Bacterial Pneumonia 47 0.021
974
PRC003 Proctitis 47 0.021
975
INT067 Interstitial Nephritis 46 0.021
976
PNC034 Pancreas Disease 46 0.021
977
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.021
978
c ACT076 Acute Myocarditis 46 0.021
979
P BLR006 Biliary Tract Disease 46 0.021
980
TRT001 Teratocarcinoma 46 0.021
981
END080 Endometrial Disease 45 0.021
982
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.021
983
P LPM005 Lipomatosis 45 0.021
984
PTT037 Pituitary Tumors 44 0.021
985
RMS001 Rem Sleep Behavior Disorder 44 0.021
987
MNG006 Monogenic Diabetes 44 0.021
988
CRT015 Carotid Artery Occlusion 44 0.021
989
GST027 Gastric Lymphoma 44 0.021
990
CHD004 Chudley-Mccullough Syndrome 44 0.021
991
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.021
992
PRS042 Prostate Disease 44 0.021
993
c RTN047 Retinitis Pigmentosa 18 44 0.021
994
PNM013 Pneumococcal Meningitis 43 0.021
995
OVR063 Overnutrition 43 0.021
996
TST015 Testicular Disease 43 0.021
997
HPT067 Hepatocellular Adenoma 43 0.021
998
GLL017 Gallbladder Adenocarcinoma 43 0.021
999
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.021
1000
ADP001 Adiposis Dolorosa 43 0.021
1001
MCR019 Microglandular Adenosis 43 0.021
1002
PRG014 Progesterone Resistance 43 0.021
1003
PRS063 Paresthesia 43 0.021
1004
DNG001 Dengue Shock Syndrome 43 0.021
1005
c FTL006 Fetal Alcohol Spectrum Disorder 42 0.021
1006
SQM002 Squamous Cell Papilloma 42 0.021
1007
UTR011 Uterine Corpus Serous Adenocarcinoma 42 0.021
1008
BNS007 Bone Sarcoma 42 0.021
1009
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.021
1010
c PRG011 Progressive Myoclonus Epilepsy 42 0.021
1011
P AVS003 Avascular Necrosis 42 0.021
1012
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.021
1013
VLV010 Vulvovaginitis 41 0.021
1014
MRP001 Morphine Dependence 41 0.021
1015
P RRT020 Rare Tumor 41 0.021
1016
P GRW001 Growth Hormone Secreting Pituitary Adenoma 41 0.021
1017
EST004 Estrogen Excess 40 0.021
1018
c CTR132 Cataract 3, Multiple Types 40 0.021
1019
P MCR364 Macrodactyly 40 0.021
1020
C1N001 C1 Inhibitor Deficiency 40 0.021
1022
PLM052 Pulmonary Arteriovenous Malformation 39 0.021
1023
LNG030 Lung Adenoma 39 0.021
1024
MNN017 Mononeuropathy 39 0.021
1025
ADR022 Adrenomyeloneuropathy 38 0.021
1026
SVR002 Severe Nonproliferative Diabetic Retinopathy 38 0.021
1027
CRD016 Cardiac Rupture 38 0.021
1028
MCK029 Meckel Diverticulum 37 0.021
1029
SCR001 Secretory Meningioma 37 0.021
1030
IDP070 Idiopathic Scoliosis 37 0.021
1031
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 37 0.021
1032
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 37 0.021
1033
FRN014 Fournier Gangrene 37 0.021
1034
SYS071 Systemic Autoimmune Disease 37 0.021
1035
BLN010 Balanitis 36 0.021
1036
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.021
1037
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.021
1038
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.021
1040
P MYC026 Myoclonus Epilepsy 35 0.021
1041
AMR003 Amaurosis Fugax 34 0.021
1042
NNT024 Neonatal Stroke 34 0.021
1043
PLM151 Pulmonary Arteriovenous Fistulas 34 0.021
1044
HYP114 Hypertensive Nephropathy 34 0.021
1045
c CNT101 Central Congenital Hypothyroidism 34 0.021
1046
c FTL070 Fetal Akinesia Deformation Sequence 2 33 0.021
1047
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.021
1048
c CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.021
1049
INF009 Inflammatory Spondylopathy 32 0.021
1050
PRX097 Paroxysmal Dystonia 31 0.021
1051
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 31 0.021
1052
HMN004 Hemangioma of Liver 31 0.021
1053
PLY150 Polykaryocytosis Inducer 31 0.021
1054
PST014 Postsurgical Hypothyroidism 30 0.021
1055
c PNC095 Pancreatic Cancer 3 28 0.021
1056
IMP001 Impetigo Herpetiformis 28 0.021
1057
c CLB022 Coloboma, Ocular, Autosomal Recessive 28 0.021
1058
ARG004 Argyria 28 0.021
1059
EPS001 Epstein-Barr Virus Hepatitis 28 0.021
1060
ACT162 Acute Sensory Ataxic Neuropathy 26 0.021
1061
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 26 0.021
1063
XLN228 X-Linked Recessive Disease 26 0.021
1064
GRW027 Growth Restriction, Severe, with Distinctive Facies 25 0.021
1065
NRM022 Neurometabolic Disease 25 0.021
1066
PRQ002 Paraquat Poisoning 25 0.021
1067
BRT037 Brittle Diabetes 25 0.021
1068
c PRS134 Prostate Cancer, Hereditary, 3 25 0.021
1069
TRP003 Triple-Receptor Negative Breast Cancer 24 0.021
1070
c INT262 Intermediate Maple Syrup Urine Disease 24 0.021
1071
SPT003 Septic Myocarditis 23 0.021
1072
HML018 Homologous Wasting Disease 22 0.021
1074
GLC025 Galactorrhoea-Hyperprolactinaemia 21 0.021
1075
c CHR688 Chronic Acquired Demyelinating Polyneuropathy