Search results for Estradiol

1223 hits were found for Estradiol

# Family MCID Name MIFTS Score
1
P BRS047 Breast Cancer 97 0.301
2
P PLY011 Polycystic Ovary Syndrome 56 0.246
3
AMN001 Amenorrhea 54 0.233
4
INS024 Insulin-Like Growth Factor I 79 0.216
5
P INF032 Infertility 57 0.212
6
P OST002 Osteoporosis 74 0.207
7
P END044 Endometriosis 63 0.207
8
END057 Endometrial Cancer 74 0.199
9
48X005 48,xyyy 39 0.198
10
BNR002 Bone Resorption Disease 48 0.189
11
DWN001 Down Syndrome 70 0.188
12
c NRF023 Neurofibromatosis, Type Ii 80 0.180
13
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.177
14
END062 Endometrial Hyperplasia 48 0.177
15
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.177
16
P TRN020 Turner Syndrome 67 0.165
17
HYP080 Hypogonadism 50 0.162
18
P ADN016 Adenocarcinoma 64 0.145
19
CHL068 Cholestasis 61 0.143
20
HYP043 Hyperandrogenism 48 0.139
21
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.137
22
VGN023 Vaginitis 54 0.136
23
LMY002 Leiomyoma 52 0.136
24
PST029 Postmenopausal Atrophic Vaginitis 38 0.136
25
P PRS040 Prostate Cancer 97 0.134
26
ANX010 Anxiety 73 0.134
27
HYP020 Hyperprolactinemia 64 0.134
28
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.134
29
ANV001 Anovulation 47 0.134
30
PTT037 Pituitary Tumors 44 0.134
31
OVR029 Ovarian Hyperstimulation Syndrome 64 0.133
32
P CRD246 Cardiovascular System Disease 57 0.131
33
c PRM196 Premature Ovarian Failure 1 67 0.130
34
ATH013 Atherosclerosis Susceptibility 65 0.127
35
PRS045 Prostatic Hypertrophy 53 0.127
36
DPR016 Depression 63 0.124
37
P GND004 Gonadal Dysgenesis 48 0.124
38
c PLY105 Polycystic Ovary Syndrome 1 38 0.124
39
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.122
40
ADL002 Adult Syndrome 70 0.121
41
MNT002 Mental Depression 58 0.121
42
P OVR042 Ovarian Cancer 88 0.119
43
END041 Endometrial Adenocarcinoma 63 0.119
44
c THR092 Thrombophilia Due to Thrombin Defect 73 0.118
45
ISC004 Ischemia 58 0.118
46
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.118
47
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.116
48
PRM020 Premenstrual Tension 40 0.116
49
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.113
50
P INT143 Interstitial Cystitis 61 0.113
51
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.113
52
c RHB024 Rhabdomyosarcoma 2 67 0.111
53
LMY014 Leiomyoma, Uterine 56 0.111
54
CRB004 Cerebral Artery Occlusion 45 0.111
55
PRS021 Prostatic Adenoma 51 0.109
56
PRS129 Prostatic Hyperplasia, Benign 49 0.109
57
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.107
58
c PRC016 Pre-Eclampsia 63 0.106
59
AGN016 Aging 56 0.106
60
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.106
61
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.104
62
P NRB001 Neuroblastoma 72 0.104
63
c MGR028 Migraine with or Without Aura 1 67 0.104
64
LPP008 Lipoprotein Quantitative Trait Locus 62 0.104
65
P OVR049 Ovarian Disease 52 0.104
66
PST021 Postpartum Depression 50 0.104
67
MYF001 Myofibroma 45 0.104
68
P CRN300 Coronary Heart Disease 1 63 0.102
69
ATM095 Autoimmune Disease 62 0.102
70
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.102
71
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.102
72
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.102
73
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.102
74
P OVR046 Ovarian Cyst 47 0.102
75
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.102
76
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.102
77
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.102
78
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.102
79
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.102
80
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.102
81
MDD011 Mood Disorder 62 0.100
82
P PRC019 Precocious Puberty 46 0.100
83
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.098
84
ANR007 Anorexia Nervosa 63 0.098
85
HYP060 Hyperinsulinism 54 0.098
86
c HNT004 Huntington Disease-Like 2 50 0.098
87
GYN001 Gynecomastia 49 0.098
88
INF021 Infant Gynecomastia 31 0.098
89
LVR012 Liver Cirrhosis 62 0.096
90
THR024 Thrombosis 57 0.096
91
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.096
92
P ALZ034 Alzheimer Disease 88 0.094
93
P SZR006 Seizure Disorder 56 0.094
94
SXL003 Sexual Disorder 47 0.094
95
PRM013 Premature Menopause 41 0.094
96
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.094
97
ALL026 Allergic Hypersensitivity Disease 62 0.092
98
ART140 Arteries, Anomalies of 52 0.092
99
CYT002 Cytokine Deficiency 42 0.092
100
ATX019 Ataxia with Vitamin E Deficiency 42 0.092
101
c SYS001 Systemic Lupus Erythematosus 86 0.090
102
HMN044 Human Immunodeficiency Virus Type 1 71 0.090
103
ETN001 Eating Disorder 60 0.090
104
P ALP008 Alopecia 54 0.090
105
IMM167 Immune Deficiency Disease 78 0.088
106
P SCH015 Schizophrenia 74 0.088
107
PSY004 Psychotic Disorder 67 0.088
108
IMP005 Impotence 52 0.088
109
BRN071 Brain Injury 49 0.088
110
P HRT032 Heart Disease 75 0.085
111
P VSC007 Vascular Disease 63 0.085
112
P LPS004 Lupus Erythematosus 61 0.085
113
ADN018 Adenoma 59 0.085
114
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.085
115
OVR094 Ovarian Epithelial Cancer 38 0.085
116
c HNT011 Huntington Disease-Like 3 38 0.085
117
c HYP836 Hypercholesterolemia, Familial, 1 73 0.083
118
P MJR001 Major Depressive Disorder 68 0.083
119
CRB039 Cerebrovascular Disease 67 0.083
120
HYP056 Hypoglycemia 66 0.083
121
c PNS012 Paine Syndrome 61 0.083
122
ACQ007 Acquired Immunodeficiency Syndrome 60 0.083
123
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.083
124
HYP266 Hypoxia 57 0.083
125
END040 Endogenous Depression 55 0.083
126
NRT001 Neurotic Disorder 53 0.083
127
ECT026 Ectopic Pregnancy 50 0.083
128
EST004 Estrogen Excess 40 0.083
129
CHL079 Children's Interstitial Lung Disease 26 0.083
130
P CLR023 Colorectal Cancer 99 0.081
131
STR067 Stroke, Ischemic 81 0.081
132
P HPT021 Hepatitis 67 0.081
133
P PLM037 Pulmonary Hypertension 67 0.081
134
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.081
135
OST159 Osteogenic Sarcoma 66 0.081
136
P DBT009 Diabetes Mellitus 64 0.081
137
c HPT001 Hepatitis C 62 0.081
138
HYP066 Hyperglycemia 61 0.081
139
CHL123 Chlamydia 59 0.081
140
VSL002 Visual Epilepsy 59 0.081
141
P BRS044 Breast Adenocarcinoma 59 0.081
142
P HYP730 Hypogonadotropic Hypogonadism 52 0.081
143
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.081
144
CRV035 Cervical Cancer 76 0.078
145
P ART022 Arthritis 69 0.078
146
LPD008 Lipid Metabolism Disorder 62 0.078
147
LNG099 Lung Disease 60 0.078
148
BRS051 Breast Disease 58 0.078
149
47X002 47,xyy 49 0.078
150
c HYP595 Hypertension, Essential 84 0.076
151
LPT014 Leptin Deficiency or Dysfunction 74 0.076
152
P HYP086 Hypothyroidism 69 0.076
153
P HDC001 Headache 57 0.076
154
GLC003 Glucose Intolerance 54 0.076
155
HYP081 Hypolipoproteinemia 51 0.076
156
P MYC007 Myocardial Infarction 70 0.073
157
RCK004 Rickets 68 0.073
158
c ACT068 Acute Cystitis 63 0.073
159
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.073
160
DRM006 Dermatitis 61 0.073
161
PLM033 Pulmonary Embolism 59 0.073
162
SCH003 Schizophreniform Disorder 56 0.073
163
ARM001 Aromatase Deficiency 54 0.073
164
P CHR345 Chronic Pain 44 0.073
165
P RHM011 Rheumatoid Arthritis 80 0.071
166
P KDN018 Kidney Disease 72 0.071
167
P EPL164 Epilepsy 71 0.071
168
P LVR013 Liver Disease 68 0.071
169
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.071
170
P HYP750 Hypertriglyceridemia, Familial 62 0.071
171
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.071
172
P MLN007 Male Infertility 55 0.071
173
AZS001 Azoospermia 50 0.071
174
49X006 49, Xxxxy Syndrome 41 0.071
175
MMM006 Mammographic Density 41 0.071
176
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.071
177
P LNG032 Lung Cancer 98 0.068
178
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.068
179
PRT037 Pertussis 65 0.068
180
P CYS018 Cystitis 59 0.068
181
P BCL017 B-Cell Lymphoma 58 0.068
182
CNT047 Contact Dermatitis 58 0.068
183
HYP005 Hypokalemia 55 0.068
184
LYM019 Lymphosarcoma 46 0.068
185
P OVR075 Ovarian Dysgenesis 1 37 0.068
186
OST012 Osteoarthritis 78 0.065
187
DFC004 Deficiency Anemia 70 0.065
188
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.065
189
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.065
190
FTT001 Fatty Liver Disease 61 0.065
191
P BND020 Bone Disease 59 0.065
192
DSS008 Disease of Mental Health 58 0.065
193
c ACT075 Acute Myocardial Infarction 57 0.065
194
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.065
195
ADN027 Adenomyosis 56 0.065
196
P ART021 Arteriosclerosis 54 0.065
197
P HYP040 Hypospadias 51 0.065
198
P ECL001 Eclampsia 50 0.065
199
P OCY003 Oocyte Maturation Defect 1 45 0.065
200
PPL052 Papillomatosis, Confluent and Reticulated 33 0.065
201
c PRS136 Prostate Cancer, Hereditary, 6 33 0.065
202
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.065
203
c PRS130 Prostate Cancer, Hereditary, 8 32 0.065
204
CYT018 Cytochrome P450 2d6 Variant 27 0.065
205
P MLT020 Multiple Sclerosis 72 0.062
206
c HPT073 Hepatitis C Virus 72 0.062
207
P SLP006 Sleep Apnea 69 0.062
208
P LYM118 Lymphoma 68 0.062
209
P SYS005 Systemic Scleroderma 68 0.062
210
ANG054 Angina Pectoris 66 0.062
211
IRR002 Irritable Bowel Syndrome 65 0.062
212
GST033 Gestational Diabetes 61 0.062
213
P ALP009 Alopecia Areata 60 0.062
214
PST028 Post-Traumatic Stress Disorder 58 0.062
215
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.062
216
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.062
217
PRS047 Prostatitis 56 0.062
218
CHR074 Choriocarcinoma 47 0.062
219
VGN019 Vaginal Discharge 46 0.062
220
LWC001 Low Compliance Bladder 43 0.062
221
GST020 Gastric Antral Vascular Ectasia 41 0.062
222
c SYS043 Systemic Lupus Erythematosus 1 38 0.062
223
P PNC035 Pancreatic Cancer 84 0.059
224
CYS001 Cystic Fibrosis 81 0.059
225
P RSP003 Respiratory Failure 74 0.059
226
c CHR684 Chronic Kidney Disease 70 0.059
227
CNG034 Congestive Heart Failure 69 0.059
228
P LKM002 Leukemia 68 0.059
229
P LNG028 Long Qt Syndrome 66 0.059
230
ALC007 Alcohol Dependence 66 0.059
231
P DMN002 Dementia 66 0.059
232
c SML038 Small Cell Cancer of the Lung 65 0.059
233
P PRD008 Periodontitis 64 0.059
234
P NTR004 Neutropenia 63 0.059
235
c FNC043 Fanconi Anemia, Complementation Group E 62 0.059
236
P ART023 Arthropathy 62 0.059
237
VRC005 Varicose Veins 60 0.059
238
P CTR002 Cataract 60 0.059
239
CHL014 Cholera 59 0.059
240
HLC007 Helicobacter Pylori Infection 59 0.059
241
P ALC033 Alcohol Use Disorder 58 0.059
242
c DWL002 Dowling-Degos Disease 1 58 0.059
243
P PLV020 Pelvic Organ Prolapse 57 0.059
244
BLM002 Bulimia Nervosa 57 0.059
245
P HYP076 Hyperthyroidism 55 0.059
246
MYM001 Myoma 54 0.059
247
PTT009 Pituitary Gland Disease 54 0.059
248
SCH012 Schizoaffective Disorder 50 0.059
249
ALN001 Aland Island Eye Disease 50 0.059
250
ACT084 Acute Stress Disorder 47 0.059
251
ALL014 Allergic Encephalomyelitis 38 0.059
252
ESP021 Esophageal Cancer 90 0.055
253
P GST053 Gastric Cancer 83 0.055
254
P LKM071 Leukemia, Chronic Lymphocytic 79 0.055
255
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.055
256
PRP027 Peripheral Vascular Disease 71 0.055
257
LYM133 Lymphoma, Hodgkin, Classic 69 0.055
258
P CNJ013 Conjunctivitis 65 0.055
259
PRT036 Peritonitis 64 0.055
260
HMT002 Hematologic Cancer 62 0.055
261
c SVR001 Severe Acute Respiratory Syndrome 62 0.055
262
TXC005 Toxic Shock Syndrome 62 0.055
263
c SCL052 Scleroderma, Familial Progressive 61 0.055
264
THY029 Thyroid Carcinoma 59 0.055
265
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.055
266
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.055
267
IRN002 Iron Metabolism Disease 57 0.055
268
ALL010 Allergic Contact Dermatitis 56 0.055
269
P DRR001 Diarrhea 55 0.055
270
INT007 Intermediate Coronary Syndrome 55 0.055
271
P RST001 Restless Legs Syndrome 54 0.055
272
P INF037 Inflammatory Bowel Disease 54 0.055
273
BCT002 Bacterial Vaginosis 53 0.055
274
P PNC025 Panic Disorder 53 0.055
275
INT078 Intracranial Thrombosis 49 0.055
276
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.055
277
GST010 Gestational Trophoblastic Neoplasm 46 0.055
278
P SBR004 Seborrheic Dermatitis 45 0.055
279
HYP784 Hypogonadism, Male 40 0.055
280
HYP030 Hypoactive Sexual Desire Disorder 40 0.055
281
ADH001 Adhesions of Uterus 36 0.055
282
ASH001 Asherman's Syndrome 31 0.055
283
INT076 Intracranial Sinus Thrombosis 29 0.055
284
URN022 Urinary Tract Infections, Recurrent 27 0.055
285
MLG164 Malignant Epithelial Tumor of Ovary 26 0.055
286
P HPT023 Hepatocellular Carcinoma 100 0.052
288
SVR004 Severe Combined Immunodeficiency 73 0.052
289
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.052
290
c SPN225 Spondyloarthropathy 1 73 0.052
291
P RTN024 Retinoblastoma 73 0.052
292
P PHC003 Pheochromocytoma 71 0.052
293
P PNM007 Pneumonia 68 0.052
294
P MYC084 Mycobacterium Tuberculosis 1 68 0.052
295
CNN005 Connective Tissue Disease 68 0.052
296
KHL003 Kohlschutter-Tonz Syndrome 65 0.052
297
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.052
298
P PSR002 Psoriasis 62 0.052
299
MNN042 Meningioma, Radiation-Induced 62 0.052
300
NTR005 Nutritional Deficiency Disease 62 0.052
301
PSR001 Psoriatic Arthritis 61 0.052
302
P PNC044 Pancreatitis 61 0.052
303
VRL011 Viral Infectious Disease 61 0.052
304
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.052
305
SPN186 Spinal Cord Injury 60 0.052
306
INT066 Interstitial Lung Disease 60 0.052
307
c HPT016 Hepatitis B 59 0.052
308
ANR040 Aneurysm 59 0.052
309
GNR004 Generalized Anxiety Disorder 56 0.052
310
P PTT006 Pituitary Adenoma 55 0.052
311
c PRD040 Periodontitis, Chronic 53 0.052
312
c FML008 Familial Retinoblastoma 53 0.052
313
c PSR017 Psoriasis 2 53 0.052
314
PST011 Pustulosis of Palm and Sole 52 0.052
315
c PSR023 Psoriasis 1 52 0.052
316
P SPP010 Suppressor of Tumorigenicity 3 51 0.052
317
FCT001 Factor Viii Deficiency 51 0.052
318
P END046 Endometritis 49 0.052
319
c PSR032 Psoriasis 11 47 0.052
320
KRT013 Keratolytic Winter Erythema 46 0.052
321
AND014 Androgenic Alopecia 46 0.052
322
ADR040 Adrenal Gland Pheochromocytoma 46 0.052
323
c DRR009 Diarrhea 6 46 0.052
324
OLG001 Oligospermia 45 0.052
325
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.052
326
TRP009 Triple X Syndrome 42 0.052
327
c PSR028 Psoriasis 7 42 0.052
328
c PSR018 Psoriasis 13 41 0.052
329
HRW001 Hair Whorl 36 0.052
330
PRM329 Premature Aging 35 0.052
331
c LKM005 Leukemia, T-Cell, Chronic 34 0.052
332
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 34 0.052
333
PST103 Postpartum Psychosis 32 0.052
334
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.052
335
PST092 Posttransplant Acute Limbic Encephalitis 29 0.052
336
TMP019 Temporomandibular Joint Anomaly 28 0.052
337
ADR007 Adrenoleukodystrophy 75 0.048
338
P CNR004 Cone-Rod Dystrophy 2 73 0.048
339
P GRF003 Graft-Versus-Host Disease 72 0.048
340
P AMY004 Amyloidosis 70 0.048
341
LYM007 Lymphangioleiomyomatosis 69 0.048
342
FCT007 Factor Vii Deficiency 67 0.048
343
MYC006 Mycosis Fungoides 66 0.048
344
KRT019 Keratitis, Hereditary 65 0.048
345
MSM014 Mismatch Repair Cancer Syndrome 65 0.048
346
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.048
347
P GLM045 Glioma 63 0.048
348
SKN016 Skin Disease 63 0.048
349
P PRM006 Primary Biliary Cirrhosis 62 0.048
350
CHR066 Chronic Fatigue Syndrome 61 0.048
351
c ACT027 Acute Pancreatitis 60 0.048
352
c ACT073 Acute Leukemia 58 0.048
353
FBR047 Fibromyalgia 58 0.048
354
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.048
355
EYD002 Eye Disease 58 0.048
356
P PLY018 Polycythemia 56 0.048
357
P ADL017 Adult T-Cell Leukemia 56 0.048
358
CMR002 Coumarin Resistance 56 0.048
359
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.048
360
PLV003 Pelvic Inflammatory Disease 55 0.048
361
HDR002 Hidradenitis Suppurativa 55 0.048
362
P INS002 in Situ Carcinoma 53 0.048
363
MST005 Mastitis 53 0.048
364
FML037 Female Breast Cancer 52 0.048
365
TLN003 Telangiectasis 52 0.048
366
PNG002 Pain Agnosia 51 0.048
367
TRM010 Traumatic Brain Injury 51 0.048
368
P THR015 Thrombophilia 51 0.048
369
P OVR082 Overgrowth Syndrome 50 0.048
370
PLC008 Placenta Disease 50 0.048
371
VGN020 Vaginal Disease 49 0.048
372
VRC001 Varicocele 49 0.048
373
HDR003 Hidradenitis 49 0.048
374
c CNT075 Central Precocious Puberty 46 0.048
375
GLL048 Glial Tumor 45 0.048
376
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.048
377
SBC016 Subacute Delirium 44 0.048
378
PRG014 Progesterone Resistance 42 0.048
379
GLC096 Galactorrhea 42 0.048
380
BCK006 Back Pain 42 0.048
381
DFF003 Diffuse Scleroderma 41 0.048
382
ANG049 Angioedema Induced by Ace Inhibitors 40 0.048
383
CRB086 Cerebral Aneurysms 40 0.048
384
c CHR682 Chronic Bilirubin Encephalopathy 39 0.048
385
TRP005 Trophoblastic Neoplasm 38 0.048
386
P PRG002 Progesterone-Receptor Positive Breast Cancer 35 0.048
387
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.048
388
c SCH085 Schizophrenia 2 33 0.048
389
ACN029 Acne, Adult 10 0.048
390
MYL069 Myeloma, Multiple 85 0.044
391
c LKM061 Leukemia, Acute Myeloid 84 0.044
392
NRL016 Neural Tube Defects 82 0.044
393
P ATX030 Ataxia-Telangiectasia 82 0.044
394
MLR004 Malaria 81 0.044
395
P LYN001 Lynch Syndrome 77 0.044
396
c MNN043 Meningioma, Familial 74 0.044
397
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.044
398
c LKM063 Leukemia, Chronic Myeloid 72 0.044
399
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.044
400
MYL009 Myelodysplastic Syndrome 70 0.044
401
MYL005 Myelofibrosis 70 0.044
402
PLY001 Polycythemia Vera 69 0.044
403
P OCL013 Oculodentodigital Dysplasia 69 0.044
404
P LKM062 Leukemia, Acute Lymphoblastic 69 0.044
405
MNT001 Mantle Cell Lymphoma 69 0.044
406
P INF038 Influenza 68 0.044
407
P ESS003 Essential Thrombocythemia 68 0.044
408
BRN024 Bronchitis 68 0.044
409
c HYP768 Hyperlipoproteinemia, Type I 67 0.044
410
P CRD119 Cardiac Arrest 67 0.044
411
BRK010 Burkitt Lymphoma 67 0.044
412
P FLL037 Follicular Lymphoma 67 0.044
413
MYL031 Myeloproliferative Neoplasm 66 0.044
414
P PRS038 Personality Disorder 65 0.044
415
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.044
416
APN008 Apnea, Obstructive Sleep 64 0.044
417
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.044
418
TBC004 Tobacco Addiction 64 0.044
419
ART002 Arts Syndrome 64 0.044
420
OST017 Osteomyelitis 64 0.044
421
HYP780 Hypoadrenocorticism, Familial 63 0.044
422
CLT003 Colitis 62 0.044
423
P ORT004 Orthostatic Intolerance 62 0.044
424
BRS099 Breast Ductal Carcinoma 62 0.044
425
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.044
426
WLD007 Waldenstroem's Macroglobulinemia 61 0.044
427
P MYL006 Myeloid Leukemia 60 0.044
428
SZR001 Sezary's Disease 60 0.044
429
P TST021 Testicular Germ Cell Tumor 60 0.044
430
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.044
431
P CHR285 Chronic Myelomonocytic Leukemia 60 0.044
432
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.044
433
GNG013 Gingivitis 59 0.044
434
P ANP001 Anaplastic Large Cell Lymphoma 58 0.044
435
CRD132 Cardiac Conduction Defect 58 0.044
436
CNS004 Constipation 58 0.044
437
TNS005 Tonsillitis 57 0.044
438
CMM005 Common Cold 57 0.044
439
AYM001 Ayme-Gripp Syndrome 57 0.044
440
PGM001 Pigmented Villonodular Synovitis 56 0.044
441
HPT046 Hepatic Veno-Occlusive Disease 56 0.044
442
PLS011 Plasmacytoma 56 0.044
443
c FML035 Familial Hyperlipidemia 55 0.044
444
P SBS003 Substance Abuse 55 0.044
445
HRY003 Hairy Cell Leukemia 55 0.044
446
LYM040 Lymphoblastic Lymphoma 54 0.044
447
P END047 Endophthalmitis 53 0.044
448
BRN038 Bronchial Disease 53 0.044
449
FNG017 Fungal Infectious Disease 53 0.044
450
OVR059 Ovary Adenocarcinoma 53 0.044
451
c MCR113 Microvascular Complications of Diabetes 3 52 0.044
452
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.044
453
ACR041 Acromelic Frontonasal Dysostosis 52 0.044
454
PLS007 Plasmodium Falciparum Malaria 52 0.044
455
MRG003 Marginal Zone B-Cell Lymphoma 52 0.044
456
PLS009 Plasma Cell Neoplasm 51 0.044
457
LNG095 Lung Abscess 51 0.044
458
SPL004 Splenic Marginal Zone Lymphoma 51 0.044
459
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.044
460
c ALM001 Al Amyloidosis 50 0.044
461
c PRM012 Primary Polycythemia 50 0.044
462
SPN021 Spinal Meningioma 50 0.044
463
RSP006 Respiratory System Disease 50 0.044
464
BLP005 Blepharitis 50 0.044
465
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.044
466
ATY042 Atypical Chronic Myeloid Leukemia 49 0.044
467
c THR090 Thrombocythemia 1 49 0.044
468
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.044
469
MCR004 Macroglobulinemia 49 0.044
470
c FLL041 Follicular Lymphoma 1 49 0.044
471
P ALP061 Alopecia, Androgenetic, 1 49 0.044
472
INT054 Intraocular Lymphoma 48 0.044
473
ASP007 Aspiration Pneumonia 48 0.044
474
CHR563 Chronic Eosinophilic Leukemia 48 0.044
475
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.044
476
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.044
477
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.044
478
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.044
479
GRM005 Germ Cell Cancer 47 0.044
480
PRL017 Prolymphocytic Leukemia 47 0.044
481
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.044
482
P CRN028 Corneal Ulcer 47 0.044
483
c MCR120 Microvascular Complications of Diabetes 7 47 0.044
484
LYM012 Lymphoplasmacytic Lymphoma 47 0.044
485
PLS025 Plasmablastic Lymphoma 47 0.044
486
P BLD051 Blood Coagulation Disease 46 0.044
487
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.044
488
END080 Endometrial Disease 46 0.044
489
EXT010 Extramedullary Plasmacytoma 45 0.044
490
LYD001 Leydig Cell Tumor 45 0.044
491
OVR112 Ovarian Germ Cell Cancer 45 0.044
492
ASP008 Aspiration Pneumonitis 45 0.044
493
LRY022 Laryngoonychocutaneous Syndrome 44 0.044
494
c PCH010 Pachyonychia Congenita 3 44 0.044
495
P BCT020 Bacteremia 2 44 0.044
496
FNT005 Fontaine Progeroid Syndrome 44 0.044
497
c SPR086 Spermatogenic Failure 3 44 0.044
498
ADR052 Adrenal Hyperplasia, Congenital, Due to 17-Alpha-Hydroxylase Deficiency 44 0.044
499
P TST026 Testicular Germ Cell Cancer 43 0.044
500
RFR003 Refractive Error 43 0.044
501
BNM001 Bone Marrow Cancer 43 0.044
502
HYP084 Hypopyon 43 0.044
503
P CRN026 Corneal Edema 43 0.044
504
P AVS003 Avascular Necrosis 42 0.044
505
CHR286 Chronic Neutrophilic Leukemia 42 0.044
506
MYF002 Myofascial Pain Syndrome 42 0.044
507
LCN001 Lice Infestation 42 0.044
508
c MCR130 Microvascular Complications of Diabetes 6 41 0.044
509
c MCR133 Microvascular Complications of Diabetes 4 41 0.044
510
EST007 Estrogen Resistance 41 0.044
511
LRG008 Large Granular Lymphocyte Leukemia 41 0.044
512
SCR001 Secretory Meningioma 41 0.044
513
RDN001 Reading Disorder 40 0.044
514
ACT011 Acute Contagious Conjunctivitis 40 0.044
515
UTR043 Uterine Sarcoma 39 0.044
516
P PRC031 Preeclampsia/eclampsia 1 38 0.044
517
c OVR114 Ovarian Cancer 1 38 0.044
518
c BCT006 Bacterial Conjunctivitis 37 0.044
519
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.044
520
P MXL015 Maxillary Sinusitis 36 0.044
521
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.044
522
CNR033 Cone-Rod Synaptic Disorder, Congenital Nonprogressive 35 0.044
523
GRM010 Germ Cells Tumors 34 0.044
524
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.044
525
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.044
526
c RST012 Restless Legs Syndrome 1 34 0.044
527
RFR002 Refractory Hairy Cell Leukemia 33 0.044
528
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.044
529
c ACT047 Acute Endophthalmitis 29 0.044
530
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.044
531
c TST046 Testicular Germ Cell Tumor 1 29 0.044
532
KLB004 Klebsiella Infection 27 0.044
533
CLS052 Classic Hairy Cell Leukemia 27 0.044
534
ARG004 Argyria 27 0.044
535
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.044
536
P CRT085 Carotid Intimal Medial Thickness 2 24 0.044
537
JVN026 Jeavons Syndrome 24 0.044
538
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.039
539
P LNG064 Lung Cancer Susceptibility 3 78 0.039
540
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.039
541
P SRC025 Sarcoidosis 1 70 0.039
542
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.039
543
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.039
544
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.039
545
P ATR011 Atrial Fibrillation 66 0.039
546
c FML001 Familial Atrial Fibrillation 65 0.039
547
ACR006 Aceruloplasminemia 65 0.039
548
c DBT099 Diabetes Mellitus, Type I 65 0.039
549
SPT006 Septooptic Dysplasia 64 0.039
550
DSM004 Desmoid Tumor 64 0.039
551
P PRP029 Porphyria 62 0.039
552
P KLL001 Kallmann Syndrome 61 0.039
553
P SJG008 Sjogren Syndrome 61 0.039
554
P THL005 Thalassemia 60 0.039
555
DCT002 Ductal Carcinoma in Situ 59 0.039
556
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.039
557
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 58 0.039
558
P GLM007 Glomerulonephritis 57 0.039
559
GLS018 Glass Syndrome 57 0.039
560
BRN056 Bronchopulmonary Dysplasia 57 0.039
561
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 57 0.039
562
HMT008 Hematuria, Benign Familial 56 0.039
563
BCT022 Bacterial Infectious Disease 56 0.039
564
INT030 Intracranial Aneurysm 56 0.039
565
P GST044 Gastritis 56 0.039
566
PSD021 Pseudovaginal Perineoscrotal Hypospadias 55 0.039
567
P DBT005 Diabetes Insipidus 55 0.039
568
P LRY044 Larynx Cancer 55 0.039
569
GNT003 Genital Herpes 54 0.039
570
CRT017 Cartilage Disease 54 0.039
571
P LTR001 Lateral Sclerosis 54 0.039
572
HMS001 Hemosiderosis 54 0.039
573
NNL006 Non-Alcoholic Steatohepatitis 54 0.039
574
CYS005 Cysticercosis 53 0.039
575
P CTN003 Cutaneous Lupus Erythematosus 53 0.039
576
CRT016 Carotid Artery Disease 52 0.039
577
THY030 Thyroid Gland Disease 52 0.039
578
OCL069 Ocular Motor Apraxia 51 0.039
579
P MRR011 Mirror Movements 1 51 0.039
580
THR016 Thrombophlebitis 51 0.039
581
LNG031 Lung Benign Neoplasm 51 0.039
582
c BRS049 Breast Carcinoma in Situ 51 0.039
583
END086 End Stage Renal Disease 51 0.039
584
P CHL066 Cholangitis 51 0.039
585
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.039
586
SMT006 Somatoform Disorder 50 0.039
587
NTR046 Neutrophil Migration 50 0.039
588
P BRS053 Breast Fibroadenoma 49 0.039
589
ACR002 Acrocapitofemoral Dysplasia 48 0.039
590
LPT006 Leptin Receptor Deficiency 48 0.039
591
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.039
592
DRY001 Dry Eye Syndrome 47 0.039
593
P UTR058 Uterine Anomalies 47 0.039
594
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.039
595
ATN005 Autonomic Dysfunction 46 0.039
596
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.039
597
TST014 Testicular Cancer 46 0.039
598
SMT001 Somatization Disorder 46 0.039
599
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.039
600
VLV036 Vulvar Disease 46 0.039
601
GRW007 Growth Hormone Deficiency 46 0.039
602
P HYP733 Hypercalciuria, Absorptive, 2 45 0.039
603
c CNT015 Central Sleep Apnea 45 0.039
604
c HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 45 0.039
605
P END084 Endocrine System Disease 45 0.039
606
PNT038 Peanut Allergy 45 0.039
607
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 44 0.039
608
CNN002 Cannabis Abuse 44 0.039
609
P ATX024 Ataxia-Oculomotor Apraxia 3 44 0.039
610
c HYP272 Hypercholesterolemia, Familial, 3 44 0.039
611
c PRM038 Primary Agammaglobulinemia 44 0.039
612
IDP033 Idiopathic Edema 44 0.039
613
IDP073 Idiopathic Hypercalciuria 43 0.039
614
c SPN295 Spinocerebellar Ataxia, Autosomal Recessive 3 42 0.039
615
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.039
616
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.039
617
FBR019 Fibromatosis 41 0.039
618
P RRH023 Rare Hereditary Hemochromatosis 41 0.039
619
c FML363 Familial Adult Myoclonic Epilepsy 41 0.039
620
c 46X002 46 Xx Gonadal Dysgenesis 41 0.039
621
HPR006 Heparin Cofactor Ii Deficiency 40 0.039
622
BRS050 Breast Cyst 40 0.039
623
P PRG092 Pregnancy Loss, Recurrent 1 40 0.039
624
CNN001 Cannabis Dependence 40 0.039
625
CRN020 Coronary Restenosis 39 0.039
626
CRV045 Cervical Intraepithelial Neoplasia 39 0.039
627
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.039
628
TRN007 Transsexualism 39 0.039
629
VLV042 Vulvar Vestibulitis Syndrome 38 0.039
630
PSD088 Pseudobulbar Affect 36 0.039
631
CRB031 Cerebral Arterial Disease 33 0.039
632
P VSC018 Visceral Steatosis 33 0.039
633
TNF001 Tinea Favosa 33 0.039
634
c RNG005 Ring Chromosome 10 29 0.039
635
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 26 0.039
636
c DRR021 Diarrhea 11, Malabsorptive, Congenital 25 0.039
637
HDG004 Hodgkin's Granuloma 23 0.039
638
HDG006 Hodgkin's Paragranuloma 22 0.039
639
GYN002 Gynatresia 21 0.039
640
c PRM344 Premature Ovarian Failure 16 20 0.039
641
P PRK057 Parkinson Disease, Late-Onset 78 0.034
642
GLB015 Glioblastoma Multiforme 75 0.034
643
c ATR087 Atrial Standstill 1 75 0.034
644
c BTT014 Beta-Thalassemia 74 0.034
645
MSC157 Muscular Dystrophy, Duchenne Type 72 0.034
646
P FML011 Familial Adenomatous Polyposis 72 0.034
647
ACR007 Acromegaly 71 0.034
648
P BRG001 Brugada Syndrome 71 0.034
649
P FRG001 Fragile X Syndrome 70 0.034
650
P TBR001 Tuberous Sclerosis 70 0.034
651
ART016 Aortic Aneurysm 69 0.034
652
P ANG001 Angelman Syndrome 69 0.034
653
P MSC005 Muscular Dystrophy 66 0.034
654
c FML346 Familial Adenomatous Polyposis 1 66 0.034
655
SRC014 Sarcoma 65 0.034
656
P HRP006 Herpes Simplex 65 0.034
657
NRM005 Neuromuscular Disease 64 0.034
658
c EPS035 Episodic Ataxia, Type 2 63 0.034
659
c ALP101 Alpha-Thalassemia 62 0.034
660
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.034
661
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.034
662
CRC021 Carcinosarcoma 62 0.034
663
INT002 Intermittent Claudication 61 0.034
664
P SCL018 Scoliosis 60 0.034
665
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.034
666
P SNS001 Sensorineural Hearing Loss 60 0.034
667
CHC001 Chickenpox 60 0.034
668
INS001 Insulinoma 60 0.034
669
P SLP005 Sleep Disorder 59 0.034
670
P SYP003 Syphilis 58 0.034
671
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.034
672
P URT039 Urticaria 58 0.034
673
NWB001 Newborn Respiratory Distress Syndrome 58 0.034
674
P CND004 Candidiasis 58 0.034
675
c CHL119 Cholangitis, Primary Sclerosing 57 0.034
676
P EXN002 Exanthem 57 0.034
677
P RHN004 Rhinitis 57 0.034
678
P FTL001 Fetal Alcohol Syndrome 57 0.034
679
SCH014 Schistosomiasis 57 0.034
680
P BPL003 Bipolar Disorder 56 0.034
681
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.034
682
FRS002 Frasier Syndrome 55 0.034
683
TRD006 Tardive Dyskinesia 54 0.034
684
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.034
685
PPL022 Papilloma 54 0.034
686
P TRM003 Tremor 54 0.034
687
KRT006 Keratoconjunctivitis 53 0.034
688
P HYP083 Hypopituitarism 53 0.034
689
GTR002 Goiter 53 0.034
690
HMC014 Homocysteinemia 53 0.034
691
SPN035 Spindle Cell Sarcoma 53 0.034
692
c GLL024 Gallbladder Disease 1 53 0.034
693
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.034
694
DMY004 Demyelinating Disease 52 0.034
695
c VRL010 Viral Hepatitis 52 0.034
696
HYP014 Hyperuricemia 52 0.034
697
P TRT010 Teratoma 52 0.034
698
SPN051 Spondylitis 51 0.034
699
KRT009 Keratosis 51 0.034
700
P AST007 Astrocytoma 51 0.034
701
HYP781 Hypoascorbemia 51 0.034
702
c SVR005 Severe Pre-Eclampsia 50 0.034
703
KRT001 Keratoconjunctivitis Sicca 49 0.034
704
P CRV031 Cervical Adenocarcinoma 49 0.034
705
URM002 Uremia 49 0.034
706
ADR016 Adrenal Cortical Carcinoma 48 0.034
707
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.034
708
P SCL009 Sclerosing Cholangitis 48 0.034
709
DSM003 Desmoid Disease, Hereditary 48 0.034
710
ARM004 Aromatase Excess Syndrome 48 0.034
711
ART004 Aortic Atherosclerosis 47 0.034
712
P RNL015 Renal Hypertension 47 0.034
713
NDL013 Nodular Regenerative Hyperplasia 47 0.034
714
HYP034 Hypertensive Encephalopathy 46 0.034
715
PSD009 Pseudohermaphroditism 46 0.034
716
P BNG032 Benign Mesothelioma 46 0.034
717
SQM002 Squamous Cell Papilloma 46 0.034
718
TTR005 Tetrahydrobiopterin Deficiency 45 0.034
719
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.034
720
c CHR579 Chiari Malformation Type Ii 44 0.034
721
CRD221 Cardiospondylocarpofacial Syndrome 44 0.034
722
FBR054 Fibroma 44 0.034
723
MDD018 Middle East Respiratory Syndrome 43 0.034
725
IDP070 Idiopathic Scoliosis 42 0.034
726
PHB001 Phobic Disorder 41 0.034
727
P CHR342 Chiari Malformation 41 0.034
728
RST023 Resting Heart Rate, Variation in 41 0.034
729
c MJR024 Major Affective Disorder 9 41 0.034
730
PHB003 Phobia, Specific 41 0.034
731
GND002 Gender Identity Disorder 40 0.034
732
WDH003 Woodhouse-Sakati Syndrome 40 0.034
733
PLY100 Polyploidy 40 0.034
734
P INT260 Intracranial Berry Aneurysm 39 0.034
735
END011 Endometriosis of Ovary 39 0.034
736
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.034
737
c MJR022 Major Affective Disorder 8 38 0.034
738
ADN075 Adenomyoma 38 0.034
739
INC003 Inclusion Conjunctivitis 37 0.034
740
c HYP647 Hypogonadotropic Hypogonadism 24 Without Anosmia 36 0.034
742
HND015 Hand Skill, Relative 33 0.034
743
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.034
744
ADR057 Adrenogenital Syndrome 32 0.034
745
INF009 Inflammatory Spondylopathy 31 0.034
746
MDR006 Moderate and Severe Traumatic Brain Injury 27 0.034
747
URT049 Urate Oxidase, Pseudogene 25 0.034
748
ENC002 Eunuchism 25 0.034
749
HRP008 Herpes Simiae 25 0.034
750
HPT066 Hepatoportal Sclerosis 23 0.034
751
EXT062 Extracranial Carotid Artery Aneurysm 21 0.034
752
c TBR025 Tuberous Sclerosis 1 77 0.028
753
AST005 Asthma 76 0.028
754
P APL001 Aplastic Anemia 74 0.028
755
P HYP061 Hypertrophic Cardiomyopathy 70 0.028
756
P THR014 Thrombocytopenia 67 0.028
757
GST092 Gastroesophageal Reflux 67 0.028
758
ALL003 Allergic Rhinitis 67 0.028
759
THY111 Thyroid Carcinoma, Familial Medullary 67 0.028
760
P HYP098 Hypereosinophilic Syndrome 67 0.028
761
c ATS007 Autism Spectrum Disorder 67 0.028
762
P NRV007 Nervous System Disease 66 0.028
763
NRF007 Neurofibroma 64 0.028
764
GT001 Gout 64 0.028
765
P HYP069 Hyperparathyroidism 63 0.028
766
P LMY004 Leiomyosarcoma 63 0.028
767
TRN015 Transient Cerebral Ischemia 63 0.028
768
WST001 West Syndrome 61 0.028
769
P ENC018 Encephalopathy 61 0.028
770
P KDN017 Kidney Cancer 60 0.028
771
HRP004 Herpes Zoster 60 0.028
772
P NPH012 Nephrotic Syndrome 60 0.028
773
P TXP001 Toxoplasmosis 60 0.028
774
CRD223 Cardiac Arrhythmia 60 0.028
775
ACN002 Acanthosis Nigricans 60 0.028
776
SQM006 Squamous Cell Carcinoma 60 0.028
777
STT001 Status Epilepticus 60 0.028
778
c ACT071 Acute Kidney Failure 60 0.028
779
P MYC008 Myocarditis 59 0.028
780
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.028
781
P BRN022 Bronchiectasis 59 0.028
782
c PRM005 Primary Hyperparathyroidism 58 0.028
783
CRV038 Cervical Squamous Cell Carcinoma 58 0.028
784
P GLL020 Gallbladder Disease 57 0.028
785
CHL067 Cholecystitis 57 0.028
786
BLR008 Bilirubin Metabolic Disorder 57 0.028
787
VSC002 Vascular Dementia 57 0.028
788
P ANG015 Angioedema 57 0.028
789
P PYL005 Pyelonephritis 56 0.028
790
P NRF002 Neurofibromatosis 56 0.028
791
BRN004 Brain Edema 56 0.028
792
HPT022 Hepatoblastoma 56 0.028
793
P GRV001 Graves' Disease 55 0.028
794
P MYP006 Myopia 55 0.028
795
FLT006 Floating-Harbor Syndrome 55 0.028
796
PRC002 Paracoccidioidomycosis 54 0.028
797
c HNT010 Huntington Disease-Like 1 53 0.028
798
CLF001 Cleft Lip 53 0.028
799
DNT012 Dental Caries 53 0.028
800
P DDN001 Duodenal Ulcer 52 0.028
802
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.028
803
P 46X052 46,xx Sex Reversal 1 50 0.028
804
CRT013 Carotid Stenosis 50 0.028
805
THY125 Thyroid Gland Medullary Carcinoma 50 0.028
806
P TMP001 Temporal Lobe Epilepsy 50 0.028
807
WDM005 Wiedemann-Rautenstrauch Syndrome 49 0.028
808
DYS009 Dysthymic Disorder 49 0.028
809
BCT004 Bacteriuria 49 0.028
810
DGN001 Degenerative Disc Disease 48 0.028
811
HLX001 Helix Syndrome 47 0.028
812
THY128 Thyroid Tumor 47 0.028
813
c PRM093 Premature Ovarian Failure 7 47 0.028
814
SHH001 Sheehan Syndrome 46 0.028
815
P MYC033 Myoclonus 46 0.028
816
SYN036 Syncope 45 0.028
817
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.028
818
CVD001 Covid-19 44 0.028
819
ADR041 Adrenal Cortical Adenoma 43 0.028
820
LMY003 Leiomyomatosis 43 0.028
821
PRS042 Prostate Disease 43 0.028
822
P MJR007 Major Affective Disorder 1 43 0.028
823
P SCL057 Scoliosis, Isolated 1 41 0.028
824
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 40 0.028
825
c PRG020 Paragangliomas 3 39 0.028
826
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.028
827
46X012 46,xy Partial Gonadal Dysgenesis 37 0.028
828
CNG041 Congenital Cataracts, Facial Dysmorphism, and Neuropathy 36 0.028
829
INT020 Intravenous Leiomyomatosis 36 0.028
830
CHR178 Chromosomal Triplication 35 0.028
831
TTH004 Tethered Spinal Cord Syndrome 35 0.028
832
ADN064 Adenohypophysitis 35 0.028
833
c MJR008 Major Affective Disorder 2 35 0.028
834
c HYP547 Hypogonadotropic Hypogonadism 12 with or Without Anosmia 34 0.028
835
c MJR023 Major Affective Disorder 7 33 0.028
836
c MJR003 Major Affective Disorder 6 33 0.028
837
c MJR006 Major Affective Disorder 5 33 0.028
838
PRG023 Progeroid Short Stature with Pigmented Nevi 33 0.028
839
CMP063 Complement Factor B Deficiency 32 0.028
840
RHS001 Rh Isoimmunization 32 0.028
841
46X053 46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy 30 0.028
843
c OVR076 Ovarian Dysgenesis 2 29 0.028
844
c MJR004 Major Affective Disorder 4 28 0.028
845
PTC005 Pituicytoma 28 0.028
846
c RNG015 Ring Chromosome 2 26 0.028
847
c PRM094 Premature Ovarian Failure 5 24 0.028
848
c PRM091 Premature Ovarian Failure 2b 24 0.028
849
c PRM090 Premature Ovarian Failure 6 24 0.028
850
c PRM089 Premature Ovarian Failure 3 23 0.028
851
c PRM192 Premature Ovarian Failure 8 22 0.028
852
c PRM295 Premature Ovarian Failure 15 20 0.028
853
PNH004 Panhypophysitis 20 0.028
854
HYP685 Hypergonadotropic Hypogonadism and Partial Alopecia 20 0.028
855
c PRM191 Premature Ovarian Failure 9 19 0.028
856
c PRM292 Premature Ovarian Failure 14 19 0.028
857
HYP865 Hypogonadotropic Hypogonadism 25 with Anosmia 18 0.028
858
c PRM255 Premature Ovarian Failure 12 18 0.028
859
c FNC027 Fanconi Anemia, Complementation Group a 81 0.020
860
P BLD134 Bladder Cancer 79 0.020
861
P RTN008 Retinitis Pigmentosa 79 0.020
862
P MDL005 Medulloblastoma 77 0.020
863
PHN003 Phenylketonuria 75 0.020
864
CRH001 Crohn's Disease 74 0.020
865
c TBR026 Tuberous Sclerosis 2 72 0.020
866
P HNT016 Huntington Disease 72 0.020
867
OTT002 Otitis Media 72 0.020
868
P WSK001 Wiskott-Aldrich Syndrome 72 0.020
869
c EXD008 Exudative Vitreoretinopathy 1 71 0.020
870
P ATS364 Autism 70 0.020
871
MCC012 Mccune-Albright Syndrome 70 0.020
872
ADN011 Adenoid Cystic Carcinoma 70 0.020
873
P MYP004 Myopathy 70 0.020
874
PLM001 Pulmonary Tuberculosis 69 0.020
875
P MLN008 Melanoma 69 0.020
876
CRB037 Cerebral Palsy 69 0.020
877
P LPR021 Leprosy 3 69 0.020
878
SKN019 Skin Melanoma 68 0.020
879
c NMN015 Niemann-Pick Disease, Type C1 68 0.020
880
P MYS003 Myasthenia Gravis 68 0.020
881
FLL027 Fallopian Tube Carcinoma 67 0.020
882
CRP001 Carpal Tunnel Syndrome 67 0.020
883
c FML021 Familial Hypercholesterolemia 66 0.020
884
P SKN015 Skin Carcinoma 66 0.020
885
P MCR115 Microvascular Complications of Diabetes 5 66 0.020
886
P MNN013 Meningitis 66 0.020
887
LNG039 Lung Squamous Cell Carcinoma 66 0.020
888
c MCL013 Mucolipidosis Iv 66 0.020
889
P PLM036 Pulmonary Fibrosis 65 0.020
890
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.020
891
TTN003 Tetanus 65 0.020
892
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.020
893
P ART005 Arteriovenous Malformation 65 0.020
894
AFB002 Afibrinogenemia, Congenital 65 0.020
895
P MTR014 Motor Neuron Disease 65 0.020
896
c WLM013 Wilms Tumor 1 65 0.020
897
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.020
898
BRC012 Brucellosis 64 0.020
899
PRP083 Porphyria, Acute Intermittent 64 0.020
900
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 0.020
901
c CNG006 Congenital Hypothyroidism 64 0.020
902
MSC007 Muscle Hypertrophy 64 0.020
903
PLM031 Poliomyelitis 64 0.020
904
P RHB003 Rhabdomyosarcoma 63 0.020
905
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.020
906
P HML002 Hemolytic Anemia 63 0.020
907
TYP007 Typhoid Fever 63 0.020
908
c ATM011 Autoimmune Hepatitis 63 0.020
909
MSL001 Measles 62 0.020
910
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.020
911
TMT001 Timothy Syndrome 61 0.020
912
c WLM018 Wilms Tumor 5 61 0.020
913
RTN017 Retinal Detachment 61 0.020
914
SDD001 Sudden Infant Death Syndrome 61 0.020
915
APP008 Appendicitis 61 0.020
916
NRL005 Neurilemmoma 60 0.020
917
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.020
918
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.020
919
HPT019 Hepatic Encephalopathy 60 0.020
920
HYD002 Hydronephrosis 60 0.020
921
PRT013 Portal Hypertension 59 0.020
922
PRN019 Perinatal Necrotizing Enterocolitis 59 0.020
923
P PRD006 Prader-Willi Syndrome 59 0.020
924
BRN002 Bronchiolitis 59 0.020
925
P NMN002 Niemann-Pick Disease 59 0.020
926
GST045 Gastroenteritis 59 0.020
927
PPT005 Peptic Ulcer Disease 59 0.020
928
CRY005 Cryptococcosis 58 0.020
929
c LNG047 Long Qt Syndrome 2 58 0.020
930
P HYP726 Hypercalcemia, Infantile, 1 58 0.020
931
DST005 Diastrophic Dysplasia 58 0.020
932
ADR005 Adrenal Carcinoma 58 0.020
933
LYM027 Lymphopenia 58 0.020
934
c THY102 Thyroid Cancer, Nonmedullary, 2 58 0.020
935
P GLL018 Gallbladder Cancer 57 0.020
936
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.020
937
P CHN012 Chondrosarcoma 56 0.020
938
P FBR017 Fibrosarcoma 56 0.020
939
ALL006 Allergic Asthma 56 0.020
940
P NRP001 Neuropathy 56 0.020
941
ANN002 Anencephaly 56 0.020
942
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.020
943
EMB004 Embryonal Carcinoma 56 0.020
944
GST050 Gastrointestinal System Disease 56 0.020
945
ORL005 Oral Candidiasis 56 0.020
946
P HYP024 Hypoparathyroidism 56 0.020
947
P PLY019 Polyneuropathy 56 0.020
948
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.020
949
MCL006 Macular Retinal Edema 55 0.020
950
LMB062 Limb Ischemia 55 0.020
951
AMB001 Amebiasis 55 0.020
952
DFF005 Diffuse Large B-Cell Lymphoma 55 0.020
953
NPH009 Nephrolithiasis 55 0.020
954
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.020
955
P ANT006 Antiphospholipid Syndrome 55 0.020
956
CHR100 Chronic Ulcer of Skin 55 0.020
957
P STR020 Strabismus 55 0.020
958
FLR002 Filariasis 55 0.020
959
P VNS003 Venous Insufficiency 55 0.020
960
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.020
961
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.020
962
URN010 Urinary Tract Obstruction 55 0.020
963
HMP005 Hemiplegia 55 0.020
964
PRP030 Purpura 54 0.020
965
BRN015 Bronchiolo-Alveolar Adenocarcinoma 54 0.020
966
PYD001 Pyoderma Gangrenosum 54 0.020
967
AMN003 Amnestic Disorder 54 0.020
968
GNG004 Ganglioglioma 54 0.020
969
FCL014 Focal Epilepsy 54 0.020
970
GST037 Gastroparesis 54 0.020
971
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.020
972
PLM010 Pulmonary Edema 54 0.020
973
HLL004 Hellp Syndrome 54 0.020
974
c CNG021 Congenital Toxoplasmosis 54 0.020
975
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 53 0.020
976
P LCH002 Lichen Planus 53 0.020
977
HYP706 Hypermobile Ehlers-Danlos Syndrome 53 0.020
978
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.020
979
BRD004 Borderline Personality Disorder 53 0.020
980
P SHR001 Short Bowel Syndrome 53 0.020
981
GST023 Gastric Ulcer 53 0.020
982
TRC003 Trichomoniasis 53 0.020
983
P RTN018 Retinal Disease 53 0.020
984
c FML191 Familial Long Qt Syndrome 53 0.020
985
c CNT035 Central Nervous System Disease 52 0.020
986
EXP004 Exophthalmos 52 0.020
987
STT041 Stuttering 52 0.020
988
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.020
989
P SML001 Small Cell Carcinoma 52 0.020
990
P RCT021 Rectum Cancer 52 0.020
991
P MSC003 Muscular Atrophy 52 0.020
992
P THY032 Thyroiditis 52 0.020
993
P ACT105 Acute Mountain Sickness 52 0.020
994
LGN006 Legionnaire Disease 52 0.020
995
ART074 Aortic Dissection 52 0.020
996
PRV004 Periventricular Leukomalacia 52 0.020
997
ENT011 Enterocolitis 51 0.020
998
CCC002 Coccidiosis 51 0.020
999
PLS006 Plasmodium Vivax Malaria 51 0.020
1000
TNG007 Tongue Carcinoma 51 0.020
1001
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.020
1002
c VRL007 Viral Encephalitis 51 0.020
1003
PNN001 Panniculitis 51 0.020
1004
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.020
1005
P HYP077 Hypertrichosis 50 0.020
1006
c PYR010 Peyronie's Disease 50 0.020
1007
RTN003 Retinal Ischemia 50 0.020
1008
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.020
1009
CRN030 Coronary Stenosis 50 0.020
1010
STM007 Stomatitis 50 0.020
1011
MYC087 Mycoplasma Pneumoniae Pneumonia 50 0.020
1012
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.020
1013
MCP006 Mucoepidermoid Carcinoma 50 0.020
1014
PYD002 Pyoderma 50 0.020
1015
P AGG001 Aggressive Periodontitis 50 0.020
1016
P KRT007 Keratoconus 50 0.020
1017
PRN009 Paranoid Schizophrenia 50 0.020
1018
CLR003 Clear Cell Adenocarcinoma 50 0.020
1019
DYS073 Dysphagia 50 0.020
1020
c INF023 Inflammatory Breast Carcinoma 50 0.020
1021
P ATR005 Atrophic Gastritis 50 0.020
1022
c DYS119 Dystonia 9 50 0.020
1023
ISL003 Isolated Growth Hormone Deficiency 49 0.020
1024
P OTS001 Otosclerosis 49 0.020
1025
URT001 Urethritis 49 0.020
1026
PPL021 Papilledema 49 0.020
1027
AMB002 Amblyopia 49 0.020
1028
ART017 Aortic Disease 49 0.020
1029
CHL004 Cholelithiasis 49 0.020
1030
VCC001 Vaccinia 49 0.020
1031
LRN003 Learning Disability 49 0.020
1032
c BCT013 Bacterial Pneumonia 48 0.020
1033
ATS010 Autosomal Recessive Disease 48 0.020
1034
CCN001 Cocaine Dependence 48 0.020
1035
HPT009 Hepatopulmonary Syndrome 48 0.020
1036
BLT006 Bilateral Breast Cancer 48 0.020
1037
SCL003 Social Phobia 48 0.020
1038
INT067 Interstitial Nephritis 48 0.020
1039
DBT006 Diabetic Macular Edema 48 0.020
1040
SPL018 Splenomegaly 48 0.020
1041
HYP068 Hyperostosis 48 0.020
1042
GLC106 Glucocorticoid Resistance, Generalized 48 0.020
1043
IGG001 Iga Glomerulonephritis 48 0.020
1044
TBR011 Tuberculous Meningitis 48 0.020
1045
OPD006 Opioid Addiction 48 0.020
1046
PLC007 Placental Abruption 48 0.020
1047
VTM002 Vitamin B12 Deficiency 48 0.020
1048
MLT006 Multidrug-Resistant Tuberculosis 48 0.020
1049
PRP007 Priapism 47 0.020
1050
c NLX003 Neu-Laxova Syndrome 2 47 0.020
1051
CRN017 Coronary Thrombosis 47 0.020
1052
KRT002 Keratomalacia 47 0.020
1053
GLS007 Glossitis 47 0.020
1054
RTC005 Reticulosarcoma 47 0.020
1055
KHN001 Kuhnt-Junius Degeneration 47 0.020
1056
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.020
1057
P CRC039 Coarctation of Aorta 47 0.020
1058
CRD137 Cardiogenic Shock 47 0.020
1059
NSS002 Neisseria Meningitidis Infection 47 0.020
1060
RYN005 Raynaud Phenomenon 47 0.020
1061
RTN023 Retinitis 46 0.020
1062
ALB002 Albinism 46 0.020
1063
c CHR048 Chronic Rhinitis 46 0.020
1064
MYC005 Myocardial Stunning 46 0.020
1065
MNN020 Meningococcal Infection 46 0.020
1066
CMP034 Complete Androgen Insensitivity Syndrome 46 0.020
1067
EXS001 Exostosis 46 0.020
1068
END031 Endometrial Stromal Sarcoma 46 0.020
1069
c SCH079 Schizophrenia 1 46 0.020
1070
ANG018 Angiomyolipoma 46 0.020
1071
PLC001 Placenta Accreta 46 0.020
1072
c EST002 Estrogen-Receptor Negative Breast Cancer 45 0.020
1073
JVN033 Juvenile Nasopharyngeal Angiofibroma 45 0.020
1074
PPL018 Papillary Adenocarcinoma 45 0.020
1075
CYN002 Cyanosis, Transient Neonatal 45 0.020
1076
ORL013 Oral Lichen Planus 45 0.020
1077
HPT004 Hepatic Coma 45 0.020
1078
KDN015 Kidney Angiomyolipoma 45 0.020
1079
c SPR009 Sporadic Breast Cancer 45 0.020