Search results for Estradiol

1197 hits were found for Estradiol

# Family MCID Name MIFTS Score
1
P BRS047 Breast Cancer 97 0.311
2
P PLY011 Polycystic Ovary Syndrome 56 0.249
3
AMN001 Amenorrhea 54 0.238
4
INS024 Insulin-Like Growth Factor I 80 0.222
5
P INF032 Infertility 58 0.222
6
P OST002 Osteoporosis 74 0.215
7
P END044 Endometriosis 61 0.213
8
END057 Endometrial Cancer 75 0.204
9
48X005 48,xyyy 39 0.200
10
DWN001 Down Syndrome 71 0.194
11
BNR002 Bone Resorption Disease 49 0.193
12
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.184
13
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.184
14
P NRF023 Neurofibromatosis, Type Ii 77 0.183
15
END062 Endometrial Hyperplasia 48 0.182
16
HYP064 Hypogonadotropism 41 0.167
17
P TRN020 Turner Syndrome 65 0.166
18
HYP080 Hypogonadism 50 0.166
19
c PRM196 Premature Ovarian Failure 1 69 0.158
20
P ADN016 Adenocarcinoma 64 0.152
21
CHL068 Cholestasis 61 0.152
22
VGN023 Vaginitis 55 0.145
23
HYP043 Hyperandrogenism 48 0.142
24
LMY002 Leiomyoma 51 0.139
25
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.139
26
PST029 Postmenopausal Atrophic Vaginitis 38 0.139
27
P PRS040 Prostate Cancer 98 0.138
28
ANX010 Anxiety 73 0.138
29
P BLD124 Bleeding Disorder, Platelet-Type, 11 62 0.138
30
ANV001 Anovulation 48 0.138
31
PTT037 Pituitary Tumors 45 0.138
32
HYP020 Hyperprolactinemia 64 0.136
33
OVR029 Ovarian Hyperstimulation Syndrome 63 0.136
34
P GND004 Gonadal Dysgenesis 49 0.132
35
P CRD246 Cardiovascular System Disease 56 0.130
36
ATH013 Atherosclerosis Susceptibility 66 0.129
37
PRS045 Prostatic Hypertrophy 52 0.129
38
P OVR042 Ovarian Cancer 90 0.127
39
DPR016 Depression 64 0.125
40
c PLY105 Polycystic Ovary Syndrome 1 38 0.125
41
c RHB024 Rhabdomyosarcoma 2 66 0.124
42
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.124
43
END041 Endometrial Adenocarcinoma 64 0.122
44
ISC004 Ischemia 61 0.122
45
MNT002 Mental Depression 57 0.122
46
ADL002 Adult Syndrome 70 0.121
47
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 67 0.121
48
P BDY004 Body Mass Index Quantitative Trait Locus 11 77 0.119
49
c THR092 Thrombophilia Due to Thrombin Defect 73 0.119
50
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 37 0.119
51
PRM020 Premenstrual Tension 39 0.117
52
P INT143 Interstitial Cystitis 62 0.115
53
LMY014 Leiomyoma, Uterine 56 0.114
54
CRB004 Cerebral Artery Occlusion 45 0.114
55
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.112
56
PRS021 Prostatic Adenoma 51 0.110
57
PRS129 Prostatic Hyperplasia, Benign 49 0.110
58
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.108
59
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.108
60
P NRB001 Neuroblastoma 72 0.108
61
c BDY021 Body Mass Index Quantitative Trait Locus 20 53 0.108
62
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.108
63
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.108
64
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.108
65
c BDY010 Body Mass Index Quantitative Trait Locus 4 47 0.108
66
c BDY015 Body Mass Index Quantitative Trait Locus 12 47 0.108
67
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.108
68
c BDY011 Body Mass Index Quantitative Trait Locus 10 46 0.108
69
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.108
70
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.108
71
c PRC016 Pre-Eclampsia 64 0.106
72
P CRN018 Coronary Artery Anomaly 64 0.106
73
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.106
74
P OVR049 Ovarian Disease 53 0.106
75
MYF001 Myofibroma 42 0.106
76
c MGR028 Migraine with or Without Aura 1 70 0.104
77
P CRN300 Coronary Heart Disease 1 64 0.104
78
AGN016 Aging 56 0.104
79
P EST001 Estrogen-Receptor Positive Breast Cancer 50 0.104
80
P OVR046 Ovarian Cyst 45 0.104
81
PST021 Postpartum Depression 51 0.102
82
P PRC019 Precocious Puberty 47 0.102
83
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.100
84
ANR007 Anorexia Nervosa 63 0.100
85
MDD011 Mood Disorder 62 0.100
86
ATM095 Autoimmune Disease 61 0.100
87
HYP060 Hyperinsulinism 55 0.100
88
c HNT004 Huntington Disease-Like 2 49 0.100
89
ALL026 Allergic Hypersensitivity Disease 64 0.098
90
LVR012 Liver Cirrhosis 64 0.098
91
GYN001 Gynecomastia 49 0.098
92
CYT002 Cytokine Deficiency 44 0.098
93
INF021 Infant Gynecomastia 31 0.098
94
P ALZ034 Alzheimer Disease 89 0.096
95
P SZR006 Seizure Disorder 59 0.096
96
THR024 Thrombosis 57 0.096
97
PRM013 Premature Menopause 42 0.096
98
P SCH015 Schizophrenia 75 0.094
99
HYP056 Hypoglycemia 66 0.094
100
HYP066 Hyperglycemia 61 0.094
101
ART140 Arteries, Anomalies of 53 0.094
102
ATX019 Ataxia with Vitamin E Deficiency 48 0.094
103
c SYS001 Systemic Lupus Erythematosus 87 0.092
104
CRB039 Cerebrovascular Disease 69 0.092
105
PSY004 Psychotic Disorder 67 0.092
106
RPD005 Rapidly Involuting Congenital Hemangioma 39 0.092
107
HMN044 Human Immunodeficiency Virus Type 1 71 0.090
108
P ALP008 Alopecia 56 0.090
109
IMM167 Immune Deficiency Disease 78 0.088
110
P HRT032 Heart Disease 76 0.088
111
c PNS012 Paine Syndrome 61 0.088
112
P LPS004 Lupus Erythematosus 61 0.088
113
ADN018 Adenoma 59 0.088
114
BRN071 Brain Injury 50 0.088
115
c EPS039 Episodic Pain Syndrome, Familial, 1 41 0.088
116
c HNT011 Huntington Disease-Like 3 38 0.088
117
OVR094 Ovarian Epithelial Cancer 38 0.088
118
c HYP836 Hypercholesterolemia, Familial, 1 73 0.085
119
P VSC007 Vascular Disease 64 0.085
120
ETN001 Eating Disorder 60 0.085
121
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.085
122
END040 Endogenous Depression 55 0.085
123
NRT001 Neurotic Disorder 53 0.085
124
SXL003 Sexual Disorder 48 0.085
125
P CLR023 Colorectal Cancer 99 0.083
126
STR067 Stroke, Ischemic 80 0.083
127
OST159 Osteogenic Sarcoma 67 0.083
128
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.083
129
ACQ007 Acquired Immunodeficiency Syndrome 60 0.083
130
CHL123 Chlamydia 59 0.083
131
P BRS044 Breast Adenocarcinoma 59 0.083
132
VSL002 Visual Epilepsy 57 0.083
133
P HYP730 Hypogonadotropic Hypogonadism 53 0.083
134
47X002 47,xyy 49 0.083
135
ECT026 Ectopic Pregnancy 49 0.083
136
EST004 Estrogen Excess 41 0.083
137
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.083
138
CHL079 Children's Interstitial Lung Disease 27 0.083
139
CRV035 Cervical Cancer 76 0.080
140
P ART022 Arthritis 71 0.080
141
P MJR001 Major Depressive Disorder 68 0.080
142
P DBT009 Diabetes Mellitus 65 0.080
143
LPD008 Lipid Metabolism Disorder 63 0.080
144
BRS051 Breast Disease 58 0.080
145
HYP266 Hypoxia 57 0.080
146
GLC003 Glucose Intolerance 54 0.080
147
IMP005 Impotence 52 0.080
148
P HYP086 Hypothyroidism 69 0.078
149
P HPT021 Hepatitis 68 0.078
150
LNG099 Lung Disease 61 0.078
151
PLM033 Pulmonary Embolism 59 0.078
152
P HDC001 Headache 58 0.078
153
SCH003 Schizophreniform Disorder 57 0.078
154
HYP081 Hypolipoproteinemia 51 0.078
155
P CHR345 Chronic Pain 50 0.078
156
c HYP595 Hypertension, Essential 85 0.075
157
LPT014 Leptin Deficiency or Dysfunction 74 0.075
158
P PLM037 Pulmonary Hypertension 69 0.075
159
c HPT001 Hepatitis C 63 0.075
160
c ACT068 Acute Cystitis 63 0.075
161
DRM006 Dermatitis 62 0.075
162
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.075
163
ARM001 Aromatase Deficiency 54 0.075
164
P GST053 Gastric Cancer 84 0.072
165
P RHM011 Rheumatoid Arthritis 81 0.072
166
P MYC007 Myocardial Infarction 71 0.072
167
P KDN018 Kidney Disease 71 0.072
168
P LVR013 Liver Disease 68 0.072
169
P HYP750 Hypertriglyceridemia, Familial 62 0.072
170
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.072
171
P MLN007 Male Infertility 56 0.072
172
AZS001 Azoospermia 51 0.072
173
49X002 49,xxxxy Syndrome 42 0.072
174
MMM006 Mammographic Density 42 0.072
175
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.072
176
P HPT023 Hepatocellular Carcinoma 100 0.070
177
P LNG032 Lung Cancer 98 0.070
178
OST012 Osteoarthritis 78 0.070
179
PRT037 Pertussis 66 0.070
180
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.070
181
P BCL017 B-Cell Lymphoma 58 0.070
182
CNT047 Contact Dermatitis 58 0.070
183
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 56 0.070
184
LYM019 Lymphosarcoma 47 0.070
185
P OVR075 Ovarian Dysgenesis 1 36 0.070
186
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.067
187
DFC004 Deficiency Anemia 75 0.067
188
P EPL164 Epilepsy 72 0.067
189
c CHR684 Chronic Kidney Disease 67 0.067
190
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.067
191
P CYS018 Cystitis 60 0.067
192
P BND020 Bone Disease 60 0.067
193
DSS008 Disease of Mental Health 57 0.067
194
ADN027 Adenomyosis 57 0.067
195
c ACT075 Acute Myocardial Infarction 57 0.067
196
P ART021 Arteriosclerosis 55 0.067
197
P ECL001 Eclampsia 51 0.067
198
P HYP040 Hypospadias 51 0.067
199
P OCY003 Oocyte Maturation Defect 1 46 0.067
200
PPL052 Papillomatosis, Confluent and Reticulated 34 0.067
201
c PRS136 Prostate Cancer, Hereditary, 6 33 0.067
202
c PRS130 Prostate Cancer, Hereditary, 8 33 0.067
203
P MLT020 Multiple Sclerosis 72 0.064
204
c HPT073 Hepatitis C Virus 71 0.064
205
P SYS005 Systemic Scleroderma 70 0.064
206
P SLP006 Sleep Apnea 69 0.064
207
P LYM118 Lymphoma 69 0.064
208
RCK004 Rickets 69 0.064
209
P DMN002 Dementia 68 0.064
210
ANG054 Angina Pectoris 66 0.064
211
IRR002 Irritable Bowel Syndrome 64 0.064
212
FTT001 Fatty Liver Disease 62 0.064
213
P ALP009 Alopecia Areata 60 0.064
214
PST028 Post-Traumatic Stress Disorder 59 0.064
215
GST033 Gestational Diabetes 58 0.064
216
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.064
217
SCH012 Schizoaffective Disorder 51 0.064
218
CHR074 Choriocarcinoma 47 0.064
219
VGN019 Vaginal Discharge 44 0.064
220
c SYS043 Systemic Lupus Erythematosus 1 43 0.064
221
LWC001 Low Compliance Bladder 43 0.064
222
GST020 Gastric Antral Vascular Ectasia 42 0.064
223
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.064
224
CYT018 Cytochrome P450 2d6 Variant 27 0.064
225
P PNC035 Pancreatic Cancer 85 0.060
226
P RSP003 Respiratory Failure 75 0.060
227
ALC007 Alcohol Dependence 67 0.060
228
P LNG028 Long Qt Syndrome 66 0.060
229
c SML038 Small Cell Cancer of the Lung 66 0.060
230
PRT036 Peritonitis 65 0.060
231
P PRD008 Periodontitis 63 0.060
232
P NTR004 Neutropenia 63 0.060
233
P ART023 Arthropathy 63 0.060
234
P CTR002 Cataract 61 0.060
235
VRC005 Varicose Veins 61 0.060
236
HLC007 Helicobacter Pylori Infection 59 0.060
237
P PLV020 Pelvic Organ Prolapse 59 0.060
238
P ALC033 Alcohol Use Disorder 59 0.060
239
c DWL002 Dowling-Degos Disease 1 58 0.060
240
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.060
241
PRS047 Prostatitis 57 0.060
242
P DRR001 Diarrhea 56 0.060
243
P HYP076 Hyperthyroidism 56 0.060
244
CHL014 Cholera 56 0.060
245
PTT009 Pituitary Gland Disease 54 0.060
246
MYM001 Myoma 54 0.060
247
ALN001 Aland Island Eye Disease 49 0.060
248
ACT084 Acute Stress Disorder 48 0.060
249
ALL014 Allergic Encephalomyelitis 40 0.060
250
ESP021 Esophageal Cancer 91 0.057
251
c AMY091 Amyotrophic Lateral Sclerosis 1 90 0.057
252
CYS001 Cystic Fibrosis 80 0.057
253
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.057
254
PRP027 Peripheral Vascular Disease 72 0.057
255
LYM133 Lymphoma, Hodgkin, Classic 70 0.057
256
P LKM002 Leukemia 67 0.057
257
P CNJ013 Conjunctivitis 66 0.057
258
c SCL052 Scleroderma, Familial Progressive 63 0.057
259
c FNC043 Fanconi Anemia, Complementation Group E 63 0.057
260
HMT002 Hematologic Cancer 62 0.057
261
TXC005 Toxic Shock Syndrome 62 0.057
262
P PNC044 Pancreatitis 61 0.057
263
THY029 Thyroid Carcinoma 60 0.057
264
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.057
265
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 59 0.057
266
IRN002 Iron Metabolism Disease 58 0.057
267
BCT022 Bacterial Infectious Disease 56 0.057
268
P INF037 Inflammatory Bowel Disease 56 0.057
269
P GST044 Gastritis 56 0.057
270
ALL010 Allergic Contact Dermatitis 56 0.057
271
INT007 Intermediate Coronary Syndrome 55 0.057
272
P RST001 Restless Legs Syndrome 55 0.057
273
P LTR001 Lateral Sclerosis 54 0.057
274
P PNC025 Panic Disorder 53 0.057
275
BCT002 Bacterial Vaginosis 53 0.057
276
INT078 Intracranial Thrombosis 49 0.057
277
GST010 Gestational Trophoblastic Neoplasm 46 0.057
278
P SBR004 Seborrheic Dermatitis 45 0.057
279
HYP784 Hypogonadism, Male 39 0.057
280
ADH001 Adhesions of Uterus 33 0.057
281
ASH001 Asherman's Syndrome 32 0.057
282
INT076 Intracranial Sinus Thrombosis 29 0.057
283
MLG164 Malignant Epithelial Tumor of Ovary 26 0.057
285
c LKM071 Leukemia, Chronic Lymphocytic 80 0.053
286
P PRK057 Parkinson Disease, Late-Onset 77 0.053
287
c ATR087 Atrial Standstill 1 74 0.053
288
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.053
289
SVR004 Severe Combined Immunodeficiency 74 0.053
290
c SPN225 Spondyloarthropathy 1 74 0.053
291
P RTN024 Retinoblastoma 73 0.053
292
P PHC003 Pheochromocytoma 72 0.053
293
P MYC084 Mycobacterium Tuberculosis 1 69 0.053
294
P INF038 Influenza 68 0.053
295
P PNM007 Pneumonia 68 0.053
296
CNN005 Connective Tissue Disease 67 0.053
297
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.053
298
KHL003 Kohlschutter-Tonz Syndrome 64 0.053
299
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.053
300
P PSR002 Psoriasis 63 0.053
301
MNN042 Meningioma, Radiation-Induced 62 0.053
302
PSR001 Psoriatic Arthritis 62 0.053
303
INT002 Intermittent Claudication 62 0.053
304
NTR005 Nutritional Deficiency Disease 62 0.053
305
SPN186 Spinal Cord Injury 61 0.053
306
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.053
307
INT066 Interstitial Lung Disease 60 0.053
308
c HPT016 Hepatitis B 60 0.053
309
FBR047 Fibromyalgia 59 0.053
310
ANR040 Aneurysm 59 0.053
311
P URT039 Urticaria 58 0.053
312
P RHN004 Rhinitis 58 0.053
313
P EXN002 Exanthem 58 0.053
314
GNR004 Generalized Anxiety Disorder 56 0.053
315
HYP005 Hypokalemia 56 0.053
316
FCT001 Factor Viii Deficiency 55 0.053
317
P PTT006 Pituitary Adenoma 55 0.053
318
c PRD040 Periodontitis, Chronic 54 0.053
319
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 54 0.053
320
P TRM003 Tremor 54 0.053
321
c FML008 Familial Retinoblastoma 53 0.053
322
PST011 Pustulosis of Palm and Sole 53 0.053
323
c GLL024 Gallbladder Disease 1 52 0.053
324
SPP010 Suppressor of Tumorigenicity 3 51 0.053
325
P OVR082 Overgrowth Syndrome 50 0.053
326
c PSR017 Psoriasis 2 50 0.053
327
c PSR023 Psoriasis 1 49 0.053
328
P END046 Endometritis 48 0.053
329
P TCL004 T-Cell Leukemia 47 0.053
330
KRT013 Keratolytic Winter Erythema 46 0.053
331
ADR040 Adrenal Gland Pheochromocytoma 46 0.053
332
OLG001 Oligospermia 45 0.053
333
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.053
334
TRP009 Triple X Syndrome 43 0.053
335
PRG014 Progesterone Resistance 42 0.053
336
RST023 Resting Heart Rate, Variation in 42 0.053
337
PRM329 Premature Aging 39 0.053
338
c PSR028 Psoriasis 7 39 0.053
339
c PSR032 Psoriasis 11 39 0.053
340
c PSR018 Psoriasis 13 39 0.053
341
HRW001 Hair Whorl 36 0.053
342
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 34 0.053
343
PST103 Postpartum Psychosis 33 0.053
344
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.053
345
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 31 0.053
346
PST092 Posttransplant Acute Limbic Encephalitis 29 0.053
347
TMP019 Temporomandibular Joint Anomaly 29 0.053
348
URN022 Urinary Tract Infections, Recurrent 25 0.053
349
P APL001 Aplastic Anemia 75 0.049
350
ADR007 Adrenoleukodystrophy 75 0.049
351
P GRF003 Graft-Versus-Host Disease 72 0.049
352
P CNR004 Cone-Rod Dystrophy 2 72 0.049
353
P AMY004 Amyloidosis 71 0.049
354
LYM007 Lymphangioleiomyomatosis 69 0.049
355
P THR014 Thrombocytopenia 68 0.049
356
KRT019 Keratitis, Hereditary 68 0.049
357
ALL003 Allergic Rhinitis 68 0.049
358
FCT007 Factor Vii Deficiency 67 0.049
359
P HYP098 Hypereosinophilic Syndrome 66 0.049
360
MYC006 Mycosis Fungoides 66 0.049
361
MSM014 Mismatch Repair Cancer Syndrome 65 0.049
362
GST092 Gastroesophageal Reflux 65 0.049
363
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.049
364
GT001 Gout 64 0.049
365
SKN016 Skin Disease 63 0.049
366
P GLM045 Glioma 63 0.049
367
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 63 0.049
368
CHL067 Cholecystitis 62 0.049
369
P PRM006 Primary Biliary Cirrhosis 62 0.049
370
CHR066 Chronic Fatigue Syndrome 62 0.049
371
P BRN022 Bronchiectasis 60 0.049
372
CRD132 Cardiac Conduction Defect 59 0.049
373
EYD002 Eye Disease 59 0.049
374
c ACT073 Acute Leukemia 58 0.049
375
CNS004 Constipation 58 0.049
376
c ADL017 Adult T-Cell Leukemia 57 0.049
377
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.049
378
CMR002 Coumarin Resistance 56 0.049
379
c FML035 Familial Hyperlipidemia 56 0.049
380
P PLY018 Polycythemia 56 0.049
381
PLV003 Pelvic Inflammatory Disease 56 0.049
382
P LYM031 Lymphocytic Leukemia 55 0.049
383
HDR002 Hidradenitis Suppurativa 54 0.049
384
MST005 Mastitis 53 0.049
385
FML037 Female Breast Cancer 52 0.049
386
P INS002 in Situ Carcinoma 52 0.049
388
TLN003 Telangiectasis 52 0.049
389
PNG002 Pain Agnosia 51 0.049
390
P THR015 Thrombophilia 51 0.049
391
VRC001 Varicocele 50 0.049
392
VGN020 Vaginal Disease 50 0.049
393
PLC008 Placenta Disease 50 0.049
394
HDR003 Hidradenitis 49 0.049
395
c CNT075 Central Precocious Puberty 49 0.049
396
GLL048 Glial Tumor 46 0.049
397
SYN036 Syncope 46 0.049
398
AND014 Androgenic Alopecia 45 0.049
399
SBC016 Subacute Delirium 44 0.049
400
MYF002 Myofascial Pain Syndrome 43 0.049
401
GLC096 Galactorrhea 43 0.049
402
BCK006 Back Pain 42 0.049
403
DFF003 Diffuse Scleroderma 42 0.049
404
CRB086 Cerebral Aneurysms 40 0.049
405
ANG049 Angioedema Induced by Ace Inhibitors 39 0.049
406
HYP030 Hypoactive Sexual Desire Disorder 39 0.049
407
c CHR682 Chronic Bilirubin Encephalopathy 39 0.049
408
TRP005 Trophoblastic Neoplasm 38 0.049
409
P PRG002 Progesterone-Receptor Positive Breast Cancer 35 0.049
410
c SCH085 Schizophrenia 2 33 0.049
411
ACN029 Acne, Adult 10 0.049
412
MYL069 Myeloma, Multiple 85 0.045
413
P ATX030 Ataxia-Telangiectasia 84 0.045
414
c LKM061 Leukemia, Acute Myeloid 83 0.045
415
NRL016 Neural Tube Defects 83 0.045
416
MLR004 Malaria 81 0.045
417
P LYN001 Lynch Syndrome 78 0.045
418
PHN003 Phenylketonuria 76 0.045
419
c MNN043 Meningioma, Familial 75 0.045
420
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.045
421
LPD012 Lipoid Congenital Adrenal Hyperplasia 72 0.045
422
c LKM063 Leukemia, Chronic Myeloid 72 0.045
423
OTT002 Otitis Media 71 0.045
424
P SRC025 Sarcoidosis 1 71 0.045
425
MYL009 Myelodysplastic Syndrome 71 0.045
426
PLM001 Pulmonary Tuberculosis 70 0.045
427
CNG034 Congestive Heart Failure 70 0.045
428
P ESS003 Essential Thrombocythemia 70 0.045
429
PLY001 Polycythemia Vera 70 0.045
430
P OCL013 Oculodentodigital Dysplasia 69 0.045
431
P LKM062 Leukemia, Acute Lymphoblastic 69 0.045
432
BRN024 Bronchitis 69 0.045
433
P CRD119 Cardiac Arrest 68 0.045
434
MYL005 Myelofibrosis 68 0.045
435
BRK010 Burkitt Lymphoma 68 0.045
436
P LPR021 Leprosy 3 67 0.045
437
MNT001 Mantle Cell Lymphoma 67 0.045
438
c FML001 Familial Atrial Fibrillation 67 0.045
439
P FLL037 Follicular Lymphoma 67 0.045
440
P ATR011 Atrial Fibrillation 66 0.045
441
P MNN013 Meningitis 66 0.045
442
MYL031 Myeloproliferative Neoplasm 65 0.045
443
P PRS038 Personality Disorder 65 0.045
444
APN008 Apnea, Obstructive Sleep 65 0.045
445
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 65 0.045
446
c MCL013 Mucolipidosis Iv 65 0.045
447
P MTR014 Motor Neuron Disease 65 0.045
448
OST017 Osteomyelitis 64 0.045
449
TBC004 Tobacco Addiction 64 0.045
450
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 0.045
451
P ORT004 Orthostatic Intolerance 63 0.045
452
ART002 Arts Syndrome 63 0.045
453
BRS099 Breast Ductal Carcinoma 63 0.045
454
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.045
455
P HML002 Hemolytic Anemia 63 0.045
456
CLT003 Colitis 63 0.045
457
HYP780 Hypoadrenocorticism, Familial 62 0.045
458
TMT001 Timothy Syndrome 62 0.045
459
BRC012 Brucellosis 62 0.045
460
P ANP001 Anaplastic Large Cell Lymphoma 61 0.045
461
P TST021 Testicular Germ Cell Tumor 61 0.045
462
VRL011 Viral Infectious Disease 61 0.045
463
LYM012 Lymphoplasmacytic Lymphoma 61 0.045
464
SZR001 Sezary's Disease 61 0.045
465
P MYL006 Myeloid Leukemia 60 0.045
466
APP008 Appendicitis 60 0.045
467
GNG013 Gingivitis 60 0.045
468
BRN002 Bronchiolitis 59 0.045
469
P CHR285 Chronic Myelomonocytic Leukemia 59 0.045
470
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.045
471
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.045
472
TNS005 Tonsillitis 57 0.045
473
P HYP726 Hypercalcemia, Infantile, 1 57 0.045
474
HPT046 Hepatic Veno-Occlusive Disease 57 0.045
475
P NRP001 Neuropathy 57 0.045
476
PGM001 Pigmented Villonodular Synovitis 57 0.045
477
PLS011 Plasmacytoma 57 0.045
478
CMM005 Common Cold 56 0.045
479
MCL006 Macular Retinal Edema 56 0.045
480
HRY003 Hairy Cell Leukemia 55 0.045
481
P SBS003 Substance Abuse 55 0.045
482
LYM040 Lymphoblastic Lymphoma 54 0.045
483
c ACT020 Acute T Cell Leukemia 54 0.045
484
MRG003 Marginal Zone B-Cell Lymphoma 54 0.045
485
BRN038 Bronchial Disease 54 0.045
486
c FML191 Familial Long Qt Syndrome 53 0.045
487
c HYP768 Hyperlipoproteinemia, Type I 53 0.045
488
PLS007 Plasmodium Falciparum Malaria 53 0.045
489
c MCR113 Microvascular Complications of Diabetes 3 53 0.045
490
ACR041 Acromelic Frontonasal Dysostosis 53 0.045
491
ANG046 Angioimmunoblastic T-Cell Lymphoma 53 0.045
492
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.045
493
P END047 Endophthalmitis 53 0.045
494
c PRM012 Primary Polycythemia 52 0.045
495
OVR059 Ovary Adenocarcinoma 52 0.045
496
SPL004 Splenic Marginal Zone Lymphoma 51 0.045
497
c ALM001 Al Amyloidosis 51 0.045
498
P ATR005 Atrophic Gastritis 51 0.045
499
LGN006 Legionnaire Disease 51 0.045
500
STM007 Stomatitis 51 0.045
501
P CHL066 Cholangitis 51 0.045
502
PLS006 Plasmodium Vivax Malaria 51 0.045
503
P AGG001 Aggressive Periodontitis 51 0.045
504
DYS073 Dysphagia 51 0.045
505
MCR004 Macroglobulinemia 50 0.045
506
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.045
507
MYC087 Mycoplasma Pneumoniae Pneumonia 50 0.045
508
RSP006 Respiratory System Disease 50 0.045
509
AMB002 Amblyopia 50 0.045
510
APL002 Aplasia of Lacrimal and Salivary Glands 50 0.045
511
LNG095 Lung Abscess 50 0.045
512
P KRT007 Keratoconus 50 0.045
513
P INT099 Intrahepatic Cholestasis of Pregnancy 50 0.045
514
P ALP061 Alopecia, Androgenetic, 1 50 0.045
515
MYL075 Myelodysplastic/myeloproliferative Neoplasm 50 0.045
516
BLP005 Blepharitis 50 0.045
517
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.045
518
c FLL041 Follicular Lymphoma 1 49 0.045
519
c DYS119 Dystonia 9 49 0.045
520
ATY042 Atypical Chronic Myeloid Leukemia 49 0.045
521
PPL021 Papilledema 49 0.045
522
KRT002 Keratomalacia 49 0.045
523
c THR090 Thrombocythemia 1 49 0.045
524
c LKM056 Leukemia, Chronic Lymphocytic 2 49 0.045
525
CHR563 Chronic Eosinophilic Leukemia 48 0.045
526
TBR011 Tuberculous Meningitis 48 0.045
527
ASP007 Aspiration Pneumonia 48 0.045
528
INT054 Intraocular Lymphoma 48 0.045
529
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.045
530
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.045
531
P CRN028 Corneal Ulcer 48 0.045
532
GRM005 Germ Cell Cancer 48 0.045
533
PRL017 Prolymphocytic Leukemia 48 0.045
534
c MCR120 Microvascular Complications of Diabetes 7 47 0.045
535
SPN021 Spinal Meningioma 47 0.045
536
c BCT013 Bacterial Pneumonia 47 0.045
537
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.045
538
MLT006 Multidrug-Resistant Tuberculosis 47 0.045
539
GLS007 Glossitis 47 0.045
540
PLS025 Plasmablastic Lymphoma 47 0.045
541
P BLD051 Blood Coagulation Disease 47 0.045
542
INT067 Interstitial Nephritis 47 0.045
543
ACT113 Acute Myeloblastic Leukemia with Maturation 47 0.045
544
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 0.045
545
END080 Endometrial Disease 46 0.045
546
EXT010 Extramedullary Plasmacytoma 46 0.045
547
GRN017 Granulocytopenia 45 0.045
548
LRY022 Laryngoonychocutaneous Syndrome 45 0.045
549
P TST026 Testicular Germ Cell Cancer 44 0.045
550
P BCT020 Bacteremia 2 44 0.045
551
RFR003 Refractive Error 44 0.045
552
FNT005 Fontaine Progeroid Syndrome 44 0.045
553
c PCH010 Pachyonychia Congenita 3 44 0.045
554
P LYD001 Leydig Cell Tumor 44 0.045
555
P PRC031 Preeclampsia/eclampsia 1 44 0.045
556
ADR052 Adrenal Hyperplasia, Congenital, Due to 17-Alpha-Hydroxylase Deficiency 44 0.045
557
BNM001 Bone Marrow Cancer 43 0.045
558
P CRN024 Corneal Disease 43 0.045
559
OVR112 Ovarian Germ Cell Cancer 43 0.045
560
PRS063 Paresthesia 43 0.045
561
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 43 0.045
562
HMP009 Haemophilus Influenzae 43 0.045
563
ASP008 Aspiration Pneumonitis 43 0.045
564
c SPR086 Spermatogenic Failure 3 42 0.045
565
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 42 0.045
566
LCN001 Lice Infestation 42 0.045
567
P AVS003 Avascular Necrosis 42 0.045
568
CHR286 Chronic Neutrophilic Leukemia 42 0.045
569
c MCR130 Microvascular Complications of Diabetes 6 41 0.045
570
c MCR133 Microvascular Complications of Diabetes 4 41 0.045
571
LRG008 Large Granular Lymphocyte Leukemia 41 0.045
572
RDN001 Reading Disorder 41 0.045
573
UTR043 Uterine Sarcoma 40 0.045
574
P CRN026 Corneal Edema 40 0.045
575
SPS057 Spasticity 40 0.045
576
ACT011 Acute Contagious Conjunctivitis 40 0.045
577
EST007 Estrogen Resistance 40 0.045
578
OPT010 Optic Papillitis 39 0.045
579
P OTT001 Otitis Externa 39 0.045
580
SPP007 Suppression Amblyopia 39 0.045
581
IMM166 Immunodeficiency 27a 39 0.045
582
HYP084 Hypopyon 39 0.045
583
CVT001 Cavitary Optic Disc Anomalies 39 0.045
584
c OVR114 Ovarian Cancer 1 39 0.045
585
DPR002 Depersonalization Disorder 38 0.045
586
HYP141 Hyperphenylalaninemia 38 0.045
587
PRR004 Preretinal Fibrosis 38 0.045
588
SCR001 Secretory Meningioma 38 0.045
589
c LPR022 Leprosy 2 37 0.045
590
MYC017 Mycobacterium Kansasii 37 0.045
591
P MXL015 Maxillary Sinusitis 37 0.045
592
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.045
593
ACL001 Acalculous Cholecystitis 36 0.045
594
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 35 0.045
595
HNS001 Hansen's Disease 35 0.045
596
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.045
597
GRM010 Germ Cells Tumors 34 0.045
598
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.045
599
c RST012 Restless Legs Syndrome 1 34 0.045
600
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.045
601
c BCT006 Bacterial Conjunctivitis 33 0.045
602
CNR033 Cone-Rod Synaptic Disorder, Congenital Nonprogressive 33 0.045
603
ACT216 Acute Leukemia of Ambiguous Lineage 33 0.045
604
RFR002 Refractory Hairy Cell Leukemia 32 0.045
605
PLR005 Pleuropneumonia 32 0.045
606
CLC017 Calcification of Joints and Arteries 32 0.045
607
c ACT047 Acute Endophthalmitis 30 0.045
608
c TST046 Testicular Germ Cell Tumor 1 29 0.045
609
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.045
610
ARG004 Argyria 28 0.045
611
KLB004 Klebsiella Infection 28 0.045
612
CLS052 Classic Hairy Cell Leukemia 27 0.045
613
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.045
614
ACT162 Acute Sensory Ataxic Neuropathy 27 0.045
615
HDG004 Hodgkin's Granuloma 26 0.045
616
c LNG052 Long Qt Syndrome 8 26 0.045
617
MYC021 Mycobacterium Xenopi 26 0.045
618
P CRT085 Carotid Intimal Medial Thickness 2 25 0.045
619
HDG006 Hodgkin's Paragranuloma 25 0.045
620
JVN026 Jeavons Syndrome 24 0.045
621
PLL009 Pellucid Marginal Degeneration 22 0.045
622
HML018 Homologous Wasting Disease 22 0.045
623
c QTN001 Qt Interval, Variation in 14 0.045
624
P LNG064 Lung Cancer Susceptibility 3 78 0.040
625
ACR006 Aceruloplasminemia 74 0.040
626
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.040
627
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.040
628
ADR054 Adrenocortical Carcinoma, Hereditary 67 0.040
629
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.040
630
c PRD013 Periodic Fever, Familial, Autosomal Dominant 66 0.040
631
DSM004 Desmoid Tumor 65 0.040
632
P KLL001 Kallmann Syndrome 64 0.040
633
SPT006 Septooptic Dysplasia 64 0.040
634
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.040
635
P PRP029 Porphyria 62 0.040
636
P THL005 Thalassemia 60 0.040
637
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 59 0.040
638
DCT002 Ductal Carcinoma in Situ 59 0.040
639
END030 End Stage Renal Failure 58 0.040
640
BRN056 Bronchopulmonary Dysplasia 58 0.040
641
P GLM007 Glomerulonephritis 57 0.040
642
P SJG008 Sjogren Syndrome 57 0.040
643
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 56 0.040
644
INT030 Intracranial Aneurysm 56 0.040
645
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.040
646
PSD021 Pseudovaginal Perineoscrotal Hypospadias 56 0.040
647
P DBT005 Diabetes Insipidus 55 0.040
648
CLL003 Cellulitis 55 0.040
649
GNT003 Genital Herpes 55 0.040
650
CRT017 Cartilage Disease 55 0.040
651
HMS001 Hemosiderosis 54 0.040
652
P LRY044 Larynx Cancer 54 0.040
653
CYS005 Cysticercosis 54 0.040
654
GLS018 Glass Syndrome 53 0.040
655
HMT008 Hematuria, Benign Familial 53 0.040
656
TRM010 Traumatic Brain Injury 53 0.040
657
P CTN003 Cutaneous Lupus Erythematosus 53 0.040
658
CRT016 Carotid Artery Disease 52 0.040
659
OCL069 Ocular Motor Apraxia 52 0.040
660
THR016 Thrombophlebitis 52 0.040
661
c BRS049 Breast Carcinoma in Situ 51 0.040
662
NNL006 Non-Alcoholic Steatohepatitis 51 0.040
663
SMT006 Somatoform Disorder 51 0.040
664
THY030 Thyroid Gland Disease 51 0.040
665
P MRR011 Mirror Movements 1 51 0.040
666
LNG031 Lung Benign Neoplasm 51 0.040
667
NTR046 Neutrophil Migration 50 0.040
668
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 50 0.040
669
P BRS053 Breast Fibroadenoma 48 0.040
670
P UTR058 Uterine Anomalies 48 0.040
671
SMT001 Somatization Disorder 48 0.040
672
DRY001 Dry Eye Syndrome 48 0.040
673
LPT006 Leptin Receptor Deficiency 47 0.040
674
ATN005 Autonomic Dysfunction 47 0.040
675
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.040
676
c CNT015 Central Sleep Apnea 47 0.040
677
TST014 Testicular Cancer 47 0.040
678
VLV036 Vulvar Disease 47 0.040
679
P HYP733 Hypercalciuria, Absorptive, 2 46 0.040
680
PNT038 Peanut Allergy 46 0.040
681
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 45 0.040
682
c HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 45 0.040
683
c CRV002 Cervix Uteri Carcinoma in Situ 44 0.040
684
FBR019 Fibromatosis 44 0.040
685
c HYP272 Hypercholesterolemia, Familial, 3 44 0.040
686
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 44 0.040
687
c PRM038 Primary Agammaglobulinemia 44 0.040
688
IDP033 Idiopathic Edema 43 0.040
689
GRW007 Growth Hormone Deficiency 43 0.040
690
c 46X002 46 Xx Gonadal Dysgenesis 43 0.040
691
IDP073 Idiopathic Hypercalciuria 43 0.040
692
ACR002 Acrocapitofemoral Dysplasia 42 0.040
693
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.040
694
P RRH023 Rare Hereditary Hemochromatosis 41 0.040
695
TRN007 Transsexualism 41 0.040
696
CRN020 Coronary Restenosis 40 0.040
697
P PRG092 Pregnancy Loss, Recurrent 1 40 0.040
698
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 40 0.040
699
CRV045 Cervical Intraepithelial Neoplasia 39 0.040
700
BRS050 Breast Cyst 39 0.040
701
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.040
702
VLV042 Vulvar Vestibulitis Syndrome 38 0.040
703
c BNG079 Benign Adult Familial Myoclonic Epilepsy 36 0.040
704
PSD088 Pseudobulbar Affect 36 0.040
705
TNF001 Tinea Favosa 34 0.040
706
P VSC018 Visceral Steatosis 33 0.040
707
RRS014 Rare Surgical Neurologic Disease 32 0.040
708
c SPN295 Spinocerebellar Ataxia, Autosomal Recessive 3 30 0.040
709
c RNG005 Ring Chromosome 10 29 0.040
710
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 26 0.040
711
c DRR021 Diarrhea 11, Malabsorptive, Congenital 24 0.040
712
GYN002 Gynatresia 20 0.040
713
GLB015 Glioblastoma Multiforme 75 0.035
714
c BTT014 Beta-Thalassemia 73 0.035
715
P FML011 Familial Adenomatous Polyposis 72 0.035
716
MSC157 Muscular Dystrophy, Duchenne Type 72 0.035
717
ACR007 Acromegaly 71 0.035
718
P TBR001 Tuberous Sclerosis 71 0.035
719
P BRG001 Brugada Syndrome 71 0.035
720
c FML346 Familial Adenomatous Polyposis 1 70 0.035
721
ART016 Aortic Aneurysm 69 0.035
722
P FRG001 Fragile X Syndrome 69 0.035
723
P ANG001 Angelman Syndrome 67 0.035
724
P MSC005 Muscular Dystrophy 66 0.035
725
SRC014 Sarcoma 66 0.035
726
P HRP006 Herpes Simplex 65 0.035
727
NRM005 Neuromuscular Disease 64 0.035
728
c EPS035 Episodic Ataxia, Type 2 63 0.035
729
c ALP101 Alpha-Thalassemia 62 0.035
730
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.035
731
CRC021 Carcinosarcoma 62 0.035
732
P SNS001 Sensorineural Hearing Loss 61 0.035
733
INS001 Insulinoma 60 0.035
734
CHC001 Chickenpox 60 0.035
735
P SCL018 Scoliosis 60 0.035
736
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.035
737
P SLP005 Sleep Disorder 60 0.035
738
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.035
739
P SYP003 Syphilis 60 0.035
740
NWB001 Newborn Respiratory Distress Syndrome 58 0.035
741
c CHL119 Cholangitis, Primary Sclerosing 58 0.035
742
P CND004 Candidiasis 58 0.035
743
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.035
744
SCH014 Schistosomiasis 57 0.035
745
P BPL003 Bipolar Disorder 57 0.035
746
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.035
747
TRD006 Tardive Dyskinesia 56 0.035
748
P FTL001 Fetal Alcohol Syndrome 55 0.035
749
PPL022 Papilloma 55 0.035
750
KRT006 Keratoconjunctivitis 54 0.035
751
HMC014 Homocysteinemia 53 0.035
752
P HYP083 Hypopituitarism 53 0.035
753
FRS002 Frasier Syndrome 53 0.035
754
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 53 0.035
755
GTR002 Goiter 53 0.035
756
DMY004 Demyelinating Disease 52 0.035
757
KRT009 Keratosis 52 0.035
758
P TRT010 Teratoma 52 0.035
759
HYP014 Hyperuricemia 52 0.035
760
c VRL010 Viral Hepatitis 52 0.035
761
SPN035 Spindle Cell Sarcoma 51 0.035
762
HYP781 Hypoascorbemia 51 0.035
763
P AST007 Astrocytoma 50 0.035
764
DSM003 Desmoid Disease, Hereditary 50 0.035
765
KRT001 Keratoconjunctivitis Sicca 50 0.035
766
c SVR005 Severe Pre-Eclampsia 49 0.035
767
URM002 Uremia 49 0.035
768
NRL018 Neural Tube Defects, Folate-Sensitive 49 0.035
769
P RNL015 Renal Hypertension 48 0.035
770
ART004 Aortic Atherosclerosis 48 0.035
771
ADR016 Adrenal Cortical Carcinoma 48 0.035
772
P CRV031 Cervical Adenocarcinoma 47 0.035
773
P SCL009 Sclerosing Cholangitis 47 0.035
774
NDL013 Nodular Regenerative Hyperplasia 47 0.035
775
ARM004 Aromatase Excess Syndrome 47 0.035
776
PSD009 Pseudohermaphroditism 46 0.035
777
TTR005 Tetrahydrobiopterin Deficiency 46 0.035
778
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 46 0.035
779
P BNG032 Benign Mesothelioma 45 0.035
780
HYP034 Hypertensive Encephalopathy 45 0.035
781
FBR054 Fibroma 44 0.035
782
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.035
783
CRD221 Cardiospondylocarpofacial Syndrome 43 0.035
784
SQM002 Squamous Cell Papilloma 43 0.035
785
c CHR579 Chiari Malformation Type Ii 41 0.035
786
PHB001 Phobic Disorder 41 0.035
787
c MJR024 Major Affective Disorder 9 41 0.035
788
GND002 Gender Identity Disorder 41 0.035
789
PHB003 Phobia, Specific 41 0.035
790
P CHR342 Chiari Malformation 41 0.035
791
END011 Endometriosis of Ovary 40 0.035
792
PLY100 Polyploidy 40 0.035
793
WDH003 Woodhouse-Sakati Syndrome 40 0.035
795
P INT260 Intracranial Berry Aneurysm 39 0.035
796
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.035
797
c MJR022 Major Affective Disorder 8 38 0.035
798
IDP070 Idiopathic Scoliosis 38 0.035
799
INC003 Inclusion Conjunctivitis 37 0.035
800
c HYP647 Hypogonadotropic Hypogonadism 24 Without Anosmia 36 0.035
801
ADN075 Adenomyoma 36 0.035
803
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.035
804
HND015 Hand Skill, Relative 33 0.035
805
ADR057 Adrenogenital Syndrome 32 0.035
806
MDR006 Moderate and Severe Traumatic Brain Injury 27 0.035
807
HRP008 Herpes Simiae 25 0.035
808
URT049 Urate Oxidase, Pseudogene 25 0.035
809
ENC002 Eunuchism 24 0.035
810
HPT066 Hepatoportal Sclerosis 24 0.035
811
EXT062 Extracranial Carotid Artery Aneurysm 21 0.035
812
AST005 Asthma 77 0.028
813
c TBR025 Tuberous Sclerosis 1 77 0.028
814
c ATS007 Autism Spectrum Disorder 68 0.028
815
THY111 Thyroid Carcinoma, Familial Medullary 68 0.028
816
P HYP061 Hypertrophic Cardiomyopathy 67 0.028
817
P NRV007 Nervous System Disease 66 0.028
818
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.028
819
NRF007 Neurofibroma 65 0.028
820
NRF026 Neurofibromatosis, Type Iv, of Riccardi 64 0.028
821
P NPH012 Nephrotic Syndrome 63 0.028
822
P HYP069 Hyperparathyroidism 63 0.028
823
P LMY004 Leiomyosarcoma 63 0.028
824
TRN015 Transient Cerebral Ischemia 62 0.028
825
P ENC018 Encephalopathy 61 0.028
826
P KDN017 Kidney Cancer 61 0.028
827
ACN002 Acanthosis Nigricans 61 0.028
828
P TXP001 Toxoplasmosis 61 0.028
829
CRD223 Cardiac Arrhythmia 61 0.028
830
WST001 West Syndrome 61 0.028
831
SQM006 Squamous Cell Carcinoma 60 0.028
832
HRP004 Herpes Zoster 60 0.028
833
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.028
834
P MYC008 Myocarditis 60 0.028
835
STT001 Status Epilepticus 60 0.028
836
c ACT027 Acute Pancreatitis 60 0.028
837
c ACT071 Acute Kidney Failure 60 0.028
838
CRV038 Cervical Squamous Cell Carcinoma 59 0.028
839
P GLL020 Gallbladder Disease 58 0.028
840
c PRM005 Primary Hyperparathyroidism 58 0.028
841
BLM002 Bulimia Nervosa 58 0.028
842
BLR008 Bilirubin Metabolic Disorder 58 0.028
843
VSC002 Vascular Dementia 57 0.028
844
P PYL005 Pyelonephritis 57 0.028
845
HPT022 Hepatoblastoma 56 0.028
846
BRN004 Brain Edema 56 0.028
847
P GRV001 Graves' Disease 56 0.028
848
P MYP006 Myopia 55 0.028
849
P ANG015 Angioedema 54 0.028
850
PRC002 Paracoccidioidomycosis 54 0.028
851
CLF001 Cleft Lip 53 0.028
852
c HNT010 Huntington Disease-Like 1 53 0.028
853
DNT012 Dental Caries 51 0.028
854
THY125 Thyroid Gland Medullary Carcinoma 51 0.028
855
P TMP001 Temporal Lobe Epilepsy 51 0.028
856
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 51 0.028
857
P DDN001 Duodenal Ulcer 50 0.028
858
CRT013 Carotid Stenosis 50 0.028
859
P 46X052 46,xx Sex Reversal 1 50 0.028
860
BCT004 Bacteriuria 49 0.028
861
FLT006 Floating-Harbor Syndrome 48 0.028
862
DYS009 Dysthymic Disorder 48 0.028
863
DGN001 Degenerative Disc Disease 48 0.028
864
THY128 Thyroid Tumor 48 0.028
865
HLX001 Helix Syndrome 48 0.028
866
c PRM093 Premature Ovarian Failure 7 47 0.028
867
WDM005 Wiedemann-Rautenstrauch Syndrome 47 0.028
868
P MYC033 Myoclonus 46 0.028
869
SHH001 Sheehan Syndrome 46 0.028
870
PRS042 Prostate Disease 44 0.028
871
LMY003 Leiomyomatosis 44 0.028
872
P MJR007 Major Affective Disorder 1 44 0.028
873
ADR041 Adrenal Cortical Adenoma 44 0.028
874
P SCL057 Scoliosis, Isolated 1 41 0.028
875
c PRG020 Paragangliomas 3 38 0.028
876
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.028
877
GND003 Gonadal Disease 38 0.028
878
46X012 46,xy Partial Gonadal Dysgenesis 38 0.028
879
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 37 0.028
880
CNG041 Congenital Cataracts, Facial Dysmorphism, and Neuropathy 36 0.028
881
INT020 Intravenous Leiomyomatosis 36 0.028
882
TTH004 Tethered Spinal Cord Syndrome 36 0.028
883
ADN064 Adenohypophysitis 35 0.028
884
CHR178 Chromosomal Triplication 35 0.028
885
c MJR008 Major Affective Disorder 2 35 0.028
886
c MJR003 Major Affective Disorder 6 33 0.028
887
c MJR006 Major Affective Disorder 5 33 0.028
888
PRG023 Progeroid Short Stature with Pigmented Nevi 33 0.028
889
c MJR023 Major Affective Disorder 7 33 0.028
890
RHS001 Rh Isoimmunization 32 0.028
892
CMP063 Complement Factor B Deficiency 31 0.028
893
46X053 46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy 30 0.028
894
c HYP547 Hypogonadotropic Hypogonadism 12 with or Without Anosmia 29 0.028
895
c MJR004 Major Affective Disorder 4 29 0.028
896
c OVR076 Ovarian Dysgenesis 2 28 0.028
897
PTC005 Pituicytoma 28 0.028
898
c RNG015 Ring Chromosome 2 27 0.028
899
c PRM089 Premature Ovarian Failure 3 25 0.028
900
c PRM091 Premature Ovarian Failure 2b 24 0.028
901
c PRM192 Premature Ovarian Failure 8 23 0.028
902
c PRM094 Premature Ovarian Failure 5 22 0.028
903
c PRM090 Premature Ovarian Failure 6 22 0.028
904
c PRM295 Premature Ovarian Failure 15 21 0.028
905
PNH004 Panhypophysitis 20 0.028
906
HYP685 Hypergonadotropic Hypogonadism and Partial Alopecia 20 0.028
907
c PRM191 Premature Ovarian Failure 9 19 0.028
908
c PRM292 Premature Ovarian Failure 14 19 0.028
909
c PRM255 Premature Ovarian Failure 12 18 0.028
910
c FNC027 Fanconi Anemia, Complementation Group a 82 0.020
911
P BLD134 Bladder Cancer 79 0.020
912
P RTN008 Retinitis Pigmentosa 78 0.020
913
P MDL005 Medulloblastoma 78 0.020
914
CRH001 Crohn's Disease 75 0.020
915
P HNT016 Huntington Disease 72 0.020
916
c TBR026 Tuberous Sclerosis 2 72 0.020
917
P WSK001 Wiskott-Aldrich Syndrome 72 0.020
918
ADN011 Adenoid Cystic Carcinoma 71 0.020
919
MCC012 Mccune-Albright Syndrome 71 0.020
920
c EXD008 Exudative Vitreoretinopathy 1 70 0.020
921
MLN008 Melanoma 69 0.020
922
c FML021 Familial Hypercholesterolemia 69 0.020
923
c NMN015 Niemann-Pick Disease, Type C1 68 0.020
924
P MYS003 Myasthenia Gravis 68 0.020
925
CRB037 Cerebral Palsy 68 0.020
926
SKN019 Skin Melanoma 68 0.020
927
CRP001 Carpal Tunnel Syndrome 67 0.020
928
P SKN015 Skin Carcinoma 67 0.020
929
FLL027 Fallopian Tube Carcinoma 67 0.020
930
P MCR115 Microvascular Complications of Diabetes 5 67 0.020
931
LNG039 Lung Squamous Cell Carcinoma 66 0.020
932
c CNG006 Congenital Hypothyroidism 66 0.020
933
P ATS364 Autism 65 0.020
934
AFB002 Afibrinogenemia, Congenital 65 0.020
935
c WLM013 Wilms Tumor 1 65 0.020
936
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.020
937
P ART005 Arteriovenous Malformation 65 0.020
938
P MYP004 Myopathy 65 0.020
939
TTN003 Tetanus 64 0.020
940
PRP083 Porphyria, Acute Intermittent 64 0.020
941
IDP011 Idiopathic Interstitial Pneumonia 64 0.020
942
MSC007 Muscle Hypertrophy 64 0.020
943
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.020
944
TYP007 Typhoid Fever 63 0.020
945
P RHB003 Rhabdomyosarcoma 63 0.020
946
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.020
947
c WLM018 Wilms Tumor 5 62 0.020
948
c ATM011 Autoimmune Hepatitis 62 0.020
949
P PLM036 Pulmonary Fibrosis 62 0.020
950
P THR005 Thrombotic Thrombocytopenic Purpura 62 0.020
951
SDD001 Sudden Infant Death Syndrome 61 0.020
952
MSL001 Measles 61 0.020
953
NRL005 Neurilemmoma 61 0.020
954
PRT013 Portal Hypertension 61 0.020
955
HPT019 Hepatic Encephalopathy 61 0.020
956
RTN017 Retinal Detachment 60 0.020
957
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.020
958
P NMN002 Niemann-Pick Disease 60 0.020
959
HYD002 Hydronephrosis 60 0.020
960
GST045 Gastroenteritis 60 0.020
961
DST005 Diastrophic Dysplasia 59 0.020
962
P PRD006 Prader-Willi Syndrome 59 0.020
963
c LNG047 Long Qt Syndrome 2 59 0.020
964
PPT005 Peptic Ulcer Disease 59 0.020
965
ADR005 Adrenal Carcinoma 58 0.020
966
c THY102 Thyroid Cancer, Nonmedullary, 2 58 0.020
967
URN010 Urinary Tract Obstruction 58 0.020
968
P ACT010 Acth-Secreting Pituitary Adenoma 58 0.020
969
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 58 0.020
970
LYM027 Lymphopenia 58 0.020
971
EMB004 Embryonal Carcinoma 58 0.020
972
PLM031 Poliomyelitis 57 0.020
973
P STR020 Strabismus 57 0.020
974
P CHN012 Chondrosarcoma 57 0.020
975
P FBR017 Fibrosarcoma 57 0.020
976
ANN002 Anencephaly 56 0.020
977
ORL005 Oral Candidiasis 56 0.020
978
GLL018 Gallbladder Cancer 56 0.020
979
P PLY019 Polyneuropathy 56 0.020
980
GST050 Gastrointestinal System Disease 56 0.020
981
ALL006 Allergic Asthma 56 0.020
982
DFF005 Diffuse Large B-Cell Lymphoma 56 0.020
983
P HYP024 Hypoparathyroidism 56 0.020
984
PRP030 Purpura 56 0.020
985
c SVR001 Severe Acute Respiratory Syndrome 56 0.020
986
LMB062 Limb Ischemia 56 0.020
987
FLR002 Filariasis 55 0.020
988
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.020
989
P VNS003 Venous Insufficiency 55 0.020
990
TNG003 Tongue Cancer 55 0.020
991
PLM010 Pulmonary Edema 55 0.020
992
PYD001 Pyoderma Gangrenosum 55 0.020
993
P ANT006 Antiphospholipid Syndrome 55 0.020
994
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.020
995
PRN019 Perinatal Necrotizing Enterocolitis 55 0.020
996
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.020
997
AMN003 Amnestic Disorder 55 0.020
998
HMP005 Hemiplegia 55 0.020
999
P LCH002 Lichen Planus 55 0.020
1000
FCL014 Focal Epilepsy 54 0.020
1001
GNG004 Ganglioglioma 54 0.020
1002
BRN015 Bronchiolo-Alveolar Adenocarcinoma 54 0.020
1003
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 54 0.020
1004
c CNT035 Central Nervous System Disease 54 0.020
1005
c CNG021 Congenital Toxoplasmosis 54 0.020
1006
HLL004 Hellp Syndrome 54 0.020
1007
GST037 Gastroparesis 54 0.020
1008
CHR100 Chronic Ulcer of Skin 54 0.020
1009
HYP706 Hypermobile Ehlers-Danlos Syndrome 54 0.020
1010
P RCT021 Rectum Cancer 53 0.020
1011
BRD004 Borderline Personality Disorder 53 0.020
1012
GST023 Gastric Ulcer 53 0.020
1013
P THY032 Thyroiditis 53 0.020
1014
P RTN018 Retinal Disease 53 0.020
1015
P SHR001 Short Bowel Syndrome 53 0.020
1016
EXP004 Exophthalmos 53 0.020
1017
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.020
1018
P SML001 Small Cell Carcinoma 53 0.020
1019
STT041 Stuttering 52 0.020
1020
P ACT105 Acute Mountain Sickness 52 0.020
1021
THY124 Thyroid Gland Papillary Carcinoma 52 0.020
1022
ISL003 Isolated Growth Hormone Deficiency 52 0.020
1023
TRC003 Trichomoniasis 52 0.020
1024
P OVR106 Ovarian Clear Cell Carcinoma 52 0.020
1025
PRV004 Periventricular Leukomalacia 52 0.020
1026
PYD002 Pyoderma 52 0.020
1027
P MSC003 Muscular Atrophy 52 0.020
1028
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.020
1029
c VRL007 Viral Encephalitis 51 0.020
1030
c PYR010 Peyronie's Disease 51 0.020
1031
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.020
1032
CLR003 Clear Cell Adenocarcinoma 51 0.020
1033
RTN003 Retinal Ischemia 51 0.020
1034
ENT011 Enterocolitis 51 0.020
1035
P HYP077 Hypertrichosis 51 0.020
1036
CCC002 Coccidiosis 50 0.020
1037
CRN030 Coronary Stenosis 50 0.020
1038
TRC010 Trichotillomania 50 0.020
1039
P OTS001 Otosclerosis 50 0.020
1040
c INF023 Inflammatory Breast Carcinoma 50 0.020
1041
CHL004 Cholelithiasis 50 0.020
1042
LRN003 Learning Disability 49 0.020
1043
MCP006 Mucoepidermoid Carcinoma 49 0.020
1044
PNN001 Panniculitis 49 0.020
1045
VCC001 Vaccinia 49 0.020
1046
AMB001 Amebiasis 49 0.020
1047
PRN009 Paranoid Schizophrenia 49 0.020
1048
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.020
1049
RTC005 Reticulosarcoma 49 0.020
1050
HPT009 Hepatopulmonary Syndrome 49 0.020
1051
URT001 Urethritis 49 0.020
1052
VTM002 Vitamin B12 Deficiency 49 0.020
1053
CCN001 Cocaine Dependence 49 0.020
1054
SCL003 Social Phobia 49 0.020
1055
DBT006 Diabetic Macular Edema 49 0.020
1056
ATS010 Autosomal Recessive Disease 49 0.020
1057
THY123 Thyroid Gland Follicular Carcinoma 49 0.020
1058
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.020
1059
HYP068 Hyperostosis 48 0.020
1060
CRD137 Cardiogenic Shock 48 0.020
1061
IGG001 Iga Glomerulonephritis 48 0.020
1062
KHN001 Kuhnt-Junius Degeneration 48 0.020
1063
PLC007 Placental Abruption 48 0.020
1064
SPL018 Splenomegaly 48 0.020
1065
GLC106 Glucocorticoid Resistance, Generalized 48 0.020
1066
c HMN021 Human T-Cell Leukemia Virus Type 1 48 0.020
1067
PRP007 Priapism 48 0.020
1068
CMP034 Complete Androgen Insensitivity Syndrome 47 0.020
1069
P CRC039 Coarctation of Aorta 47 0.020
1070
c LRG017 Large Intestine Cancer 47 0.020
1071
CRN017 Coronary Thrombosis 47 0.020
1072
PPL018 Papillary Adenocarcinoma 47 0.020
1073
RYN005 Raynaud Phenomenon 47 0.020
1074
RTN023 Retinitis 47 0.020
1075
ALB002 Albinism 47 0.020
1076
MYC005 Myocardial Stunning 46 0.020
1077
END031 Endometrial Stromal Sarcoma 46 0.020
1078
CTS011 Cutis Marmorata Telangiectatica Congenita 46 0.020
1079
KDN015 Kidney Angiomyolipoma 46 0.020