Search results for ar

6801 hits were found for ar

# Family MCID Name MIFTS Score
1
AND002 Androgen Insensitivity Syndrome 57 13.044
2
P PRS040 Prostate Cancer 88 6.076
3
P BRS047 Breast Cancer 100 5.386
4
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 59 4.892
5
AND020 Androgen Insensitivity, Partial 49 4.659
6
c HYP373 Hyper-Ige Recurrent Infection Syndrome, Autosomal Recessive 30 4.014
7
RNL118 Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness 22 3.992
8
P MSC003 Muscular Atrophy 55 3.613
9
P HYP040 Hypospadias 60 3.595
10
END057 Endometrial Cancer 76 3.325
11
AZS001 Azoospermia 47 3.300
12
PRS042 Prostate Disease 56 2.979
13
P ALP008 Alopecia 56 2.969
14
P SPN046 Spinal Muscular Atrophy 63 2.965
15
MLN007 Male Infertility 53 2.965
16
CMP034 Complete Androgen Insensitivity Syndrome 47 2.942
17
MTR014 Motor Neuron Disease 62 2.940
18
PLM014 Pleomorphic Adenoma 55 2.934
19
BRS099 Breast Ductal Carcinoma 55 2.934
20
PSD009 Pseudohermaphroditism 42 2.915
21
OLG001 Oligospermia 39 2.912
22
P FML018 Familial Mediterranean Fever 73 2.854
23
c MYP131 Myopathy, Centronuclear, 2 35 2.838
24
RNL054 Renal Tubular Acidosis, Distal, with Hemolytic Anemia 24 2.825
25
c HYP788 Hypophosphatemic Rickets, Autosomal Recessive, 1 22 2.825
26
ALR002 Al-Raqad Syndrome 30 2.821
27
P OST002 Osteoporosis 75 2.612
28
DCT002 Ductal Carcinoma in Situ 56 2.568
29
TST014 Testicular Cancer 54 2.556
30
CRY035 Cryptorchidism, Unilateral or Bilateral 58 2.554
31
c SPN294 Spinocerebellar Ataxia 1 58 2.548
32
AND014 Androgenic Alopecia 39 2.542
33
P HYP284 Hypospadias 1, X-Linked 11 2.542
34
P TST026 Testicular Germ Cell Cancer 44 2.540
35
ING001 Inguinal Hernia 59 2.537
36
c EST002 Estrogen-Receptor Negative Breast Cancer 44 2.532
37
TRN007 Transsexualism 44 2.532
38
FML037 Female Breast Cancer 52 2.529
39
PRS045 Prostatic Hypertrophy 51 2.529
40
GYN001 Gynecomastia 47 2.525
41
PGT003 Paget Disease, Extramammary 44 2.525
42
WTH001 Withdrawal Disorder 40 2.525
43
END035 Endocrine Gland Cancer 48 2.521
44
GND002 Gender Identity Disorder 46 2.521
45
SWT002 Sweat Gland Cancer 35 2.521
46
VGN023 Vaginitis 59 2.124
47
GND003 Gonadal Disease 32 2.109
48
PRS129 Prostatic Hyperplasia, Benign 47 2.101
49
c WLM013 Wilms Tumor 1 69 2.097
50
SPP011 Suppression of Tumorigenicity 12 41 2.096
51
P TST021 Testicular Germ Cell Tumor 70 2.092
52
c ALP061 Alopecia, Androgenetic, 1 44 2.079
53
SXD001 Sex Differentiation Disease 37 2.076
54
47X003 47, Xxy 33 2.076
55
c SPR089 Spermatogenic Failure 4 27 2.071
56
HRM002 Hermaphroditism 42 2.067
57
APC004 Apocrine Adenocarcinoma 38 2.067
58
PRS021 Prostatic Adenoma 39 2.063
59
DBT007 Diabetic Cataract 38 2.063
60
PST029 Postmenopausal Atrophic Vaginitis 36 2.063
61
MBM001 Meibomian Cyst 30 2.063
62
END025 Endometrial Squamous Cell Carcinoma 39 2.059
63
c MLG088 Malignant Germ Cell Tumor 39 2.059
64
P RPR003 Reproductive Organ Cancer 38 2.059
65
BRS023 Breast Adenoid Cystic Carcinoma 36 2.059
66
MLR006 Male Reproductive Organ Cancer 34 2.059
67
BRT014 Bartholin's Duct Cyst 33 2.059
68
CYS003 Cystitis Cystica 32 2.059
69
PPL017 Papillary Hidradenoma 30 2.059
70
PNS014 Penis Agenesis 29 2.059
71
ONC001 Oncocytic Breast Carcinoma 29 2.059
72
MRP002 Morpheaform Basal Cell Carcinoma 27 2.059
73
INF027 Infiltrative Basal Cell Carcinoma 26 2.059
74
VLV038 Vulvar Sarcoma 25 2.059
75
CRN004 Corneal Abscess 24 2.059
76
PRS006 Prostatic Acinar Adenocarcinoma 24 2.059
77
LWR004 Lower Urinary Tract Calculus 22 2.059
78
PRS007 Prostate Calculus 22 2.059
79
NDL006 Nodular Prostate 22 2.059
80
VLV026 Vulvar Leiomyosarcoma 17 2.059
81
ISL069 Isolated Micropenis 12 2.059
82
IMM166 Immunodeficiency 27a 22 2.027
83
P AXN002 Axenfeld-Rieger Syndrome 53 2.012
84
EPD055 Epidermolysis Bullosa, Nonspecific, Autosomal Recessive 18 2.009
85
c OCL047 Oculodentodigital Dysplasia, Autosomal Recessive 24 2.005
86
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 47 2.000
87
c PLY141 Polycystic Kidney Disease 5 42 2.000
88
c EPD080 Epidermolysis Bullosa Simplex, Autosomal Recessive 1 31 2.000
89
ECT009 Ectopia Pupillae 12 2.000
90
SVR096 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative 44 1.994
91
HYP206 Hypohidrotic Ectodermal Dysplasia Autosomal Recessive 34 1.994
92
MYL059 Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 31 1.994
93
c EMR020 Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive 25 1.994
94
ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 23 1.994
95
RNL120 Renal Tubular Acidosis, Proximal, with Ocular Abnormalities and Mental Retardation 23 1.994
96
MTC138 Mitochondrial Dna Depletion Syndrome 12b , Autosomal Recessive 19 1.994
97
c EPD068 Epidermolysis Bullosa Simplex, Autosomal Recessive 2 19 1.994
98
MLR007 Male Reproductive System Disease 24 1.462
99
RPR002 Reproductive System Disease 33 1.456
100
P LKM002 Leukemia 75 0.185
101
END072 Endotheliitis 46 0.171
102
PRS047 Prostatitis 59 0.163
103
P HPT021 Hepatitis 75 0.162
104
P LYM118 Lymphoma 71 0.160
105
AGN016 Aging 65 0.156
106
c BLD140 Blood Group, I System 37 0.152
107
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.152
108
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.152
109
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.152
110
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.152
111
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.152
112
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.152
113
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.152
114
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.152
115
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.152
116
NRN002 Neuronitis 43 0.145
117
P ART022 Arthritis 77 0.142
118
P LNG032 Lung Cancer 99 0.134
119
P PNC044 Pancreatitis 64 0.127
120
P RHM011 Rheumatoid Arthritis 91 0.126
121
P ALZ034 Alzheimer Disease 95 0.126
122
P CLR023 Colorectal Cancer 98 0.122
123
P THY032 Thyroiditis 56 0.122
124
P ADN016 Adenocarcinoma 71 0.121
125
P DBT009 Diabetes Mellitus 72 0.117
126
AST005 Asthma 83 0.116
127
SQM006 Squamous Cell Carcinoma 74 0.112
128
MLN008 Melanoma 72 0.112
129
P MYL006 Myeloid Leukemia 69 0.107
130
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.105
131
ART140 Arteries, Anomalies of 51 0.103
132
P CRN018 Coronary Artery Anomaly 69 0.101
133
CRB009 Cerebritis 41 0.100
134
P MLT020 Multiple Sclerosis 85 0.099
135
P SCH015 Schizophrenia 71 0.099
136
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.097
137
c HPT001 Hepatitis C 73 0.096
138
c SML038 Small Cell Cancer of the Lung 67 0.096
139
BRR014 Barrett Esophagus 64 0.096
140
P LPS004 Lupus Erythematosus 69 0.095
141
P OVR042 Ovarian Cancer 82 0.094
142
c LKM061 Leukemia, Acute Myeloid 81 0.092
143
GST053 Gastric Cancer 84 0.091
144
P BCL006 B-Cell Lymphomas 70 0.091
145
P CRV039 Cervicitis 49 0.090
146
c SYS001 Systemic Lupus Erythematosus 86 0.089
147
DRM006 Dermatitis 67 0.089
148
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.088
149
P MYC007 Myocardial Infarction 81 0.088
150
P ESP024 Esophagitis 64 0.087
151
P HPT023 Hepatocellular Carcinoma 94 0.085
152
P HRT032 Heart Disease 80 0.085
153
RTN023 Retinitis 52 0.083
154
MYL069 Myeloma, Multiple 86 0.082
155
P KDN018 Kidney Disease 69 0.082
156
P LVR013 Liver Disease 76 0.082
157
P GLM045 Glioma 61 0.082
158
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.081
159
P LYM026 Lymphoblastic Leukemia 66 0.081
160
P MYC084 Mycobacterium Tuberculosis 1 69 0.081
161
P PSR002 Psoriasis 65 0.079
162
c LKM071 Leukemia, Chronic Lymphocytic 75 0.079
163
P EPL164 Epilepsy 70 0.077
164
HMN044 Human Immunodeficiency Virus Type 1 71 0.076
165
c LKM004 Leukemia, B-Cell, Chronic 37 0.076
166
P PLY011 Polycystic Ovary Syndrome 65 0.076
167
c HPT073 Hepatitis C Virus 73 0.075
168
SRC014 Sarcoma 68 0.075
169
DMN002 Dementia 68 0.075
170
ADN018 Adenoma 63 0.074
171
c HPT016 Hepatitis B 68 0.074
172
HYP266 Hypoxia 61 0.073
173
MLR004 Malaria 86 0.073
174
MYL009 Myelodysplastic Syndrome 75 0.073
175
P NRB001 Neuroblastoma 73 0.073
176
CLT003 Colitis 63 0.072
177
P INF032 Infertility 59 0.072
178
DFF005 Diffuse Large B-Cell Lymphoma 64 0.072
179
CRH001 Crohn's Disease 80 0.071
180
LYM133 Lymphoma, Hodgkin, Classic 78 0.071
181
P PNC035 Pancreatic Cancer 89 0.070
182
P DRM053 Dermatitis, Atopic 68 0.070
183
P NRP001 Neuropathy 63 0.070
184
GLB002 Glioblastoma 74 0.069
185
ANX010 Anxiety 72 0.069
186
OST012 Osteoarthritis 88 0.068
187
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.068
188
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.068
189
P PNM007 Pneumonia 70 0.068
190
PST011 Pustulosis of Palm and Sole 47 0.068
191
BRS051 Breast Disease 67 0.067
192
ANR040 Aneurysm 61 0.067
193
ISC004 Ischemia 66 0.067
194
c LKM063 Leukemia, Chronic Myeloid 80 0.067
195
c CHR089 Chronic Kidney Failure 72 0.065
196
P END044 Endometriosis 71 0.065
197
ACQ007 Acquired Immunodeficiency Syndrome 65 0.065
198
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.065
199
THR024 Thrombosis 61 0.065
200
P INF037 Inflammatory Bowel Disease 52 0.065
201
SKN016 Skin Disease 68 0.065
202
LNG099 Lung Disease 67 0.065
203
VRL011 Viral Infectious Disease 64 0.065
204
P INF038 Influenza 77 0.064
205
P CRN300 Coronary Heart Disease 1 57 0.064
206
ULC004 Ulcerative Colitis 80 0.063
207
P ATS364 Autism 70 0.063
208
P LTR001 Lateral Sclerosis 58 0.063
209
LYM019 Lymphosarcoma 58 0.063
210
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.063
211
CYS001 Cystic Fibrosis 85 0.063
212
P BLD134 Bladder Cancer 78 0.063
213
ATM095 Autoimmune Disease 66 0.063
214
ALL026 Allergic Hypersensitivity Disease 59 0.063
215
SKN027 Skin Conditions 48 0.063
216
P PRD008 Periodontitis 67 0.062
217
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.062
218
P ENC018 Encephalopathy 58 0.061
219
LYM024 Lymphatic System Disease 45 0.061
220
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.061
221
PRT036 Peritonitis 67 0.060
222
P GRF003 Graft-Versus-Host Disease 72 0.060
223
c OVR114 Ovarian Cancer 1 54 0.060
224
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.059
225
CNN005 Connective Tissue Disease 65 0.058
226
FTT001 Fatty Liver Disease 62 0.057
227
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.057
228
GST033 Gestational Diabetes 62 0.057
229
IMM136 Immune System Disease 57 0.057
230
P FLL037 Follicular Lymphoma 76 0.056
231
P CRV035 Cervical Cancer 72 0.056
232
P RHN004 Rhinitis 62 0.056
233
INS024 Insulin-Like Growth Factor I 83 0.055
234
c MCL042 Macular Degeneration, Age-Related, 1 79 0.054
235
P HYP086 Hypothyroidism 62 0.054
236
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.054
237
c SPN225 Spondyloarthropathy 1 71 0.054
238
P MSC005 Muscular Dystrophy 66 0.054
239
VSC007 Vascular Disease 71 0.053
240
P HRP006 Herpes Simplex 70 0.053
241
MYL031 Myeloproliferative Neoplasm 64 0.053
242
MNT001 Mantle Cell Lymphoma 76 0.053
243
ALL003 Allergic Rhinitis 68 0.053
244
P ATR011 Atrial Fibrillation 68 0.053
245
SPS057 Spasticity 41 0.053
246
P ENC004 Encephalitis 66 0.052
247
VSC011 Vasculitis 66 0.052
248
RHM027 Rheumatic Disease 62 0.052
249
SPN051 Spondylitis 55 0.052
250
INF009 Inflammatory Spondylopathy 32 0.052
251
P PRK057 Parkinson Disease, Late-Onset 78 0.051
252
c LKM062 Leukemia, Acute Lymphoblastic 64 0.051
253
MGR028 Migraine with or Without Aura 1 55 0.051
254
LYM067 Lymphoid Leukemia 43 0.051
255
ART016 Aortic Aneurysm 70 0.051
256
P HMR003 Hemorrhagic Disease 61 0.051
257
P BPL003 Bipolar Disorder 61 0.051
258
c SCL052 Scleroderma, Familial Progressive 60 0.051
259
P ECL001 Eclampsia 57 0.051
260
NRL016 Neural Tube Defects 79 0.050
261
MCS002 Mucositis 61 0.050
262
THY028 Thyroid Cancer 72 0.050
263
P AST007 Astrocytoma 66 0.050
264
NSP002 Nasopharyngitis 46 0.050
265
P ACT074 Acute Lymphocytic Leukemia 61 0.049
266
SPS003 Spastic Diplegia 55 0.049
267
c HYP595 Hypertension, Essential 78 0.049
268
P ART023 Arthropathy 68 0.049
269
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.049
270
P INT068 Intestinal Disease 65 0.049
271
P THR014 Thrombocytopenia 65 0.049
272
URN009 Urinary System Disease 58 0.049
273
GLC008 Glucose Metabolism Disease 38 0.049
274
P BLD051 Blood Coagulation Disease 38 0.049
275
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 67 0.048
276
P MCR115 Microvascular Complications of Diabetes 5 66 0.048
277
P SLP006 Sleep Apnea 65 0.048
278
c PRC016 Pre-Eclampsia 65 0.048
279
P CTR002 Cataract 60 0.048
280
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.048
281
c ACT075 Acute Myocardial Infarction 64 0.048
282
HMT018 Hematopoietic Stem Cell Transplantation 58 0.048
283
P PMP001 Pemphigus 55 0.048
284
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.048
285
P MJR001 Major Depressive Disorder 70 0.047
286
ACT118 Acute Non Lymphoblastic Leukemia 32 0.047
287
P RNG031 Ring Chromosome Y Syndrome 29 0.047
288
P DLT002 Dilated Cardiomyopathy 76 0.047
289
P NSP012 Nasopharyngeal Carcinoma 71 0.047
290
P CLC063 Celiac Disease 1 65 0.047
291
NRN004 Neuroendocrine Tumor 58 0.047
292
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.047
293
VSC008 Vascular Hemostatic Disease 36 0.047
294
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.047
295
P PLM037 Pulmonary Hypertension 79 0.046
296
DWN001 Down Syndrome 70 0.046
297
P MYP004 Myopathy 69 0.046
298
GT001 Gout 60 0.046
299
BRN002 Bronchiolitis 59 0.046
300
IGR001 Ige Responsiveness, Atopic 56 0.046
301
P TRM003 Tremor 54 0.046
302
BRK010 Burkitt Lymphoma 71 0.046
303
IRR002 Irritable Bowel Syndrome 63 0.046
304
P DYS154 Dystonia 61 0.046
305
P DRR001 Diarrhea 60 0.046
306
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.046
307
PLS009 Plasma Cell Neoplasm 51 0.046
308
P TCL004 T-Cell Leukemia 50 0.046
309
ESP021 Esophageal Cancer 79 0.045
310
P RTN024 Retinoblastoma 76 0.045
311
LVR012 Liver Cirrhosis 73 0.045
312
c HPT003 Hepatitis a 63 0.045
313
JNT002 Joint Disorders 60 0.045
314
ORL015 Oral Squamous Cell Carcinoma 59 0.045
315
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.045
316
P MYL005 Myelofibrosis 75 0.045
317
P KDN017 Kidney Cancer 66 0.045
318
c ACT135 Acute Graft Versus Host Disease 57 0.045
319
HDC001 Headache 55 0.045
320
P CLL015 Collagen Disease 53 0.045
321
ENT004 Enthesopathy 38 0.045
322
SCK003 Sickle Cell Anemia 73 0.044
323
BRN071 Brain Injury 54 0.044
324
P PLM036 Pulmonary Fibrosis 68 0.043
325
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.043
326
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.043
327
GST019 Gastrointestinal Stromal Tumor 74 0.043
328
ISC006 Ischemic Heart Disease 73 0.043
329
PLM001 Pulmonary Tuberculosis 72 0.043
330
CHL065 Cholangiocarcinoma 70 0.043
331
CRB037 Cerebral Palsy 70 0.043
332
MNT002 Mental Depression 60 0.043
333
P CTN015 Cutaneous T Cell Lymphoma 56 0.043
334
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.043
335
c ATS007 Autism Spectrum Disorder 68 0.042
336
P PRS038 Personality Disorder 65 0.042
337
P THY109 Thyroid Cancer, Nonmedullary, 1 64 0.042
338
P GRV001 Graves' Disease 62 0.042
339
LMY014 Leiomyoma, Uterine 61 0.042
340
P ANT006 Antiphospholipid Syndrome 59 0.042
341
LMY002 Leiomyoma 58 0.042
342
P PRM006 Primary Biliary Cirrhosis 55 0.042
343
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.042
344
ATM052 Autoimmune Disease 1 30 0.042
345
PSY004 Psychotic Disorder 72 0.042
346
ALC007 Alcohol Dependence 65 0.042
347
MSL001 Measles 64 0.042
348
P SNS014 Sinusitis 62 0.042
349
HRY003 Hairy Cell Leukemia 60 0.042
350
c MCR113 Microvascular Complications of Diabetes 3 55 0.042
351
TRM010 Traumatic Brain Injury 54 0.042
352
RTC005 Reticulosarcoma 49 0.042
353
c MCR130 Microvascular Complications of Diabetes 6 42 0.042
354
c MCR120 Microvascular Complications of Diabetes 7 34 0.042
355
c MCR133 Microvascular Complications of Diabetes 4 32 0.042
356
PLY001 Polycythemia Vera 75 0.041
357
P AMY004 Amyloidosis 69 0.041
358
P THL005 Thalassemia 65 0.041
359
SLP005 Sleep Disorder 59 0.041
360
BRN106 Burns 57 0.041
361
P NRF023 Neurofibromatosis, Type Ii 69 0.040
362
GLB015 Glioblastoma Multiforme 68 0.040
363
P CHR285 Chronic Myelomonocytic Leukemia 63 0.040
364
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 62 0.040
365
LYM040 Lymphoblastic Lymphoma 58 0.040
366
P MDL005 Medulloblastoma 76 0.040
367
LSH001 Leishmaniasis 71 0.040
368
c MNN043 Meningioma, Familial 69 0.040
369
APN008 Apnea, Obstructive Sleep 67 0.040
370
c ACT027 Acute Pancreatitis 61 0.040
371
P PLY018 Polycythemia 60 0.040
372
SFT003 Soft Tissue Sarcoma 58 0.040
373
c BLM008 Bulimia Nervosa 2 53 0.040
374
RTC009 Reticulum Cell Sarcoma 51 0.040
375
INT038 Interdigitating Dendritic Cell Sarcoma 46 0.040
376
P DYS005 Dyslexia 39 0.040
377
P MNN013 Meningitis 71 0.039
378
OBS002 Obsessive-Compulsive Disorder 68 0.039
379
c BSL007 Basal Cell Carcinoma 66 0.039
380
MLT157 Multiple System Atrophy 1 65 0.039
381
HMT002 Hematologic Cancer 64 0.039
382
P MYS005 Myositis 63 0.039
383
P GST044 Gastritis 61 0.039
384
P LPR021 Leprosy 3 59 0.039
385
c ESS001 Essential Tremor 58 0.039
386
MRG003 Marginal Zone B-Cell Lymphoma 56 0.039
387
CLR030 Clear Cell Renal Cell Carcinoma 55 0.039
388
WHP002 Whiplash 39 0.039
389
P NRM001 Neuromyelitis Optica 67 0.038
390
HSH003 Hashimoto Thyroiditis 67 0.038
391
P GLM007 Glomerulonephritis 61 0.038
392
RST001 Restless Legs Syndrome 54 0.038
393
SPL004 Splenic Marginal Zone Lymphoma 52 0.038
394
PLS025 Plasmablastic Lymphoma 51 0.038
395
c BRN108 Branchiootic Syndrome 1 47 0.038
396
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.038
397
NRL018 Neural Tube Defects, Folate-Sensitive 44 0.038
398
EWN003 Ewing Sarcoma 72 0.038
399
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.038
400
BRN024 Bronchitis 67 0.038
401
P HYP061 Hypertrophic Cardiomyopathy 65 0.038
402
HLC007 Helicobacter Pylori Infection 64 0.038
403
P MYP006 Myopia 56 0.038
404
P OPN001 Open-Angle Glaucoma 51 0.038
405
EWN002 Ewing's Family of Tumors 49 0.038
406
LYM048 Lymphoma, Large-Cell, Immunoblastic 31 0.038
407
HDG004 Hodgkin's Granuloma 28 0.038
408
HDG006 Hodgkin's Paragranuloma 21 0.038
409
P RTT002 Rett Syndrome 82 0.037
410
P HYP607 Hypercholesterolemia, Familial 81 0.037
411
P ESS003 Essential Thrombocythemia 71 0.037
412
PRT037 Pertussis 70 0.037
413
CRB039 Cerebrovascular Disease 68 0.037
414
PNC041 Pancreatic Ductal Adenocarcinoma 67 0.037
415
PSR001 Psoriatic Arthritis 66 0.037
416
P ASP006 Aspergillosis 65 0.037
417
CHL123 Chlamydia 64 0.037
418
BLL006 Bullous Pemphigoid 64 0.037
419
P NTR004 Neutropenia 60 0.037
420
P LRY019 Laryngitis 57 0.037
421
PRP080 Peripheral Artery Disease 54 0.037
422
SCR011 Scrapie 40 0.037
423
SQM013 Squamous Cell Carcinoma, Head and Neck 79 0.036
424
P NNN008 Noonan Syndrome 1 77 0.036
425
P NRV007 Nervous System Disease 75 0.036
426
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.036
427
P PHC003 Pheochromocytoma 72 0.036
428
P TRN020 Turner Syndrome 69 0.036
429
P HYD006 Hydrocephalus 68 0.036
430
TTN003 Tetanus 65 0.036
431
HYP056 Hypoglycemia 62 0.036
432
P HMP007 Hemophilia 61 0.036
433
TNS005 Tonsillitis 61 0.036
434
ORL011 Oral Cancer 60 0.036
435
EPD016 Epidermolysis Bullosa 57 0.036
436
CLN019 Colonic Disease 55 0.036
437
VCC001 Vaccinia 50 0.036
438
c LBR014 Leber Congenital Amaurosis 4 48 0.036
439
BCK006 Back Pain 46 0.036
440
P BRN120 Bronchus Cancer 39 0.036
441
RCT017 Rectal Disease 38 0.036
442
KPS004 Kaposi Sarcoma 73 0.036
443
P MYS003 Myasthenia Gravis 73 0.036
444
c JVN004 Juvenile Myelomonocytic Leukemia 70 0.036
445
GST050 Gastrointestinal System Disease 66 0.036
446
P DRM010 Dermatomyositis 65 0.036
447
PLM033 Pulmonary Embolism 62 0.036
448
P PLY019 Polyneuropathy 58 0.036
449
P OVR049 Ovarian Disease 58 0.036
450
P CRB048 Cerebral Cavernous Malformations 57 0.036
451
P PTT006 Pituitary Adenoma 57 0.036
452
CYT008 Cytomegalovirus Infection 57 0.036
453
ANG054 Angina Pectoris 53 0.036
454
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 36 0.036
455
CNG034 Congestive Heart Failure 74 0.035
456
BRC012 Brucellosis 71 0.035
457
FRN006 Frontotemporal Dementia 70 0.035
458
INS001 Insulinoma 66 0.035
459
MDD011 Mood Disorder 64 0.035
460
VRC005 Varicose Veins 64 0.035
461
PRD007 Periodontal Disease 64 0.035
462
HYP066 Hyperglycemia 64 0.035
463
INT066 Interstitial Lung Disease 63 0.035
464
c ACT073 Acute Leukemia 61 0.035
465
P ANP001 Anaplastic Large Cell Lymphoma 60 0.035
466
BRN012 Bronchiolitis Obliterans 60 0.035
467
GLC003 Glucose Intolerance 58 0.035
468
CNS004 Constipation 57 0.035
469
P PNC025 Panic Disorder 57 0.035
470
FDL002 Food Allergy 55 0.035
471
CLF001 Cleft Lip 54 0.035
472
P GLM040 Glioma Susceptibility 1 51 0.035
473
P MYT002 Myotonic Dystrophy 50 0.035
474
c WLM018 Wilms Tumor 5 49 0.035
475
c GLL024 Gallbladder Disease 1 39 0.035
476
P RTN008 Retinitis Pigmentosa 81 0.034
477
CHG001 Chagas Disease 72 0.034
478
CMM004 Common Variable Immunodeficiency 71 0.034
479
GST045 Gastroenteritis 65 0.034
480
CRT072 Creutzfeldt-Jakob Disease 65 0.034
481
ALC006 Alcoholic Hepatitis 62 0.034
482
ALL006 Allergic Asthma 60 0.034
483
P HMR012 Hemorrhagic Fever 60 0.034
484
c GLC092 Glaucoma, Primary Open Angle 58 0.034
485
DYS014 Dyspepsia 54 0.034
486
PRP016 Paraplegia 53 0.034
487
ACT103 Acute Lymphoblastic Leukemia, Childhood 53 0.034
488
GRW007 Growth Hormone Deficiency 52 0.034
489
ARC007 Arachnoid Cysts 39 0.034
490
NDL020 Nodal Marginal Zone B-Cell Lymphoma 38 0.034
491
P FNC027 Fanconi Anemia, Complementation Group a 78 0.033
492
APL001 Aplastic Anemia 74 0.033
493
KWS002 Kawasaki Disease 72 0.033
494
c PRM196 Premature Ovarian Failure 1 68 0.033
495
GNG013 Gingivitis 64 0.033
496
RSP006 Respiratory System Disease 63 0.033
497
SCH014 Schistosomiasis 62 0.033
498
ETN001 Eating Disorder 61 0.033
499
P SJG008 Sjogren Syndrome 58 0.033
500
BCT002 Bacterial Vaginosis 56 0.033
501
c PNS012 Paine Syndrome 52 0.033
502
HYP043 Hyperandrogenism 50 0.033
503
P HRD009 Hereditary Wilms' Tumor 46 0.033
504
HML018 Homologous Wasting Disease 18 0.033
505
STR067 Stroke, Ischemic 84 0.033
506
P LYN001 Lynch Syndrome 71 0.033
507
P SPR120 Supranuclear Palsy, Progressive, 1 70 0.033
508
P TBR001 Tuberous Sclerosis 69 0.033
509
LYM017 Lyme Disease 68 0.033
510
CHR066 Chronic Fatigue Syndrome 67 0.033
511
c MLG068 Malignant Glioma 66 0.033
512
ACT119 Acute Promyelocytic Leukemia 64 0.033
513
WLL001 Williams-Beuren Syndrome 63 0.033
514
PNC033 Pancreas Adenocarcinoma 63 0.033
515
OST003 Osteonecrosis 63 0.033
516
P ALC004 Alcohol Abuse 63 0.033
517
PRP030 Purpura 61 0.033
518
P CND004 Candidiasis 61 0.033
519
BRN056 Bronchopulmonary Dysplasia 61 0.033
520
c THR092 Thrombophilia Due to Thrombin Defect 61 0.033
521
P RHB003 Rhabdomyosarcoma 61 0.033
522
URT039 Urticaria 59 0.033
523
GNT003 Genital Herpes 58 0.033
524
P SCL018 Scoliosis 56 0.033
525
BLR001 Biliary Atresia 56 0.033
526
TBC004 Tobacco Addiction 55 0.033
527
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.033
528
GNR004 Generalized Anxiety Disorder 53 0.033
529
OVR094 Ovarian Epithelial Cancer 46 0.033
530
DDN006 Duodenitis 46 0.033
531
IRN002 Iron Metabolism Disease 45 0.033
532
c BSL024 Basal Cell Carcinoma 1 42 0.033
533
P GRM010 Germ Cells Tumors 37 0.033
534
c PMP006 Pemphigus Vulgaris, Familial 26 0.033
535
BRN028 Brain Cancer 72 0.032
536
c CNT035 Central Nervous System Disease 65 0.032
537
P RBL001 Rubella 61 0.032
538
P THR015 Thrombophilia 58 0.032
539
TRN018 Transitional Cell Carcinoma 58 0.032
540
P LPD010 Lipodystrophy 57 0.032
541
P DNG005 Dengue Virus 56 0.032
542
SCK005 Sickle Cell Disease 54 0.032
543
MCR004 Macroglobulinemia 54 0.032
544
STM007 Stomatitis 52 0.032
545
P FBR031 Febrile Seizures 52 0.032
546
PRN023 Prion Disease 51 0.032
547
HDN002 Head Injury 48 0.032
548
MYL004 Myelodysplastic Myeloproliferative Cancer 45 0.032
549
P KLZ004 Kala-Azar 1 31 0.032
550
RFR001 Refractory Plasma Cell Neoplasm 19 0.032
551
P WSK001 Wiskott-Aldrich Syndrome 76 0.031
552
MYC006 Mycosis Fungoides 73 0.031
553
INC002 Inclusion Body Myositis 64 0.031
554
CRP001 Carpal Tunnel Syndrome 64 0.031
555
GST092 Gastroesophageal Reflux 64 0.031
556
MRB003 Morbid Obesity 61 0.031
557
P MMP001 Mumps 61 0.031
558
CHL068 Cholestasis 60 0.031
559
PLS011 Plasmacytoma 60 0.031
560
DBT010 Diabetic Neuropathy 60 0.031
561
P OLG002 Oligodendroglioma 59 0.031
562
CHL014 Cholera 56 0.031
563
P PMP005 Pemphigus Vulgaris 56 0.031
564
P RTN016 Retinal Degeneration 56 0.031
565
THR004 Thrombocytosis 55 0.031
566
TTH006 Tooth Disease 54 0.031
567
P EPN002 Ependymoma 53 0.031
568
P CHL066 Cholangitis 52 0.031
569
ECT026 Ectopic Pregnancy 52 0.031
570
PTT037 Pituitary Tumors 49 0.031
571
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.031
572
CHR008 Choroiditis 47 0.031
573
c WLM011 Wilms Tumor 6 44 0.031
574
ALX002 Alexithymia 40 0.031
575
FXF002 Fox-Fordyce Disease 40 0.031
576
DVL001 Developmental Coordination Disorder 37 0.031
577
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 21 0.031
578
P ATX030 Ataxia-Telangiectasia 80 0.030
579
ACR007 Acromegaly 70 0.030
580
P ORT004 Orthostatic Intolerance 68 0.030
581
c HRD010 Hereditary Spastic Paraplegia 68 0.030
582
SPN186 Spinal Cord Injury 67 0.030
583
c EXD008 Exudative Vitreoretinopathy 1 65 0.030
584
c CHR417 Chronic Graft Versus Host Disease 65 0.030
585
ART005 Arteriovenous Malformation 64 0.030
586
P LNG028 Long Qt Syndrome 63 0.030
587
DPH001 Diphtheria 63 0.030
588
c ATM011 Autoimmune Hepatitis 63 0.030
589
c ADL017 Adult T-Cell Leukemia 63 0.030
590
P PRP029 Porphyria 62 0.030
591
SDD001 Sudden Infant Death Syndrome 61 0.030
592
SYN007 Synovitis 61 0.030
593
P UVT001 Uveitis 61 0.030
594
VNW001 Von Willebrand's Disease 61 0.030
595
HRP004 Herpes Zoster 61 0.030
596
GST040 Gastric Adenocarcinoma 60 0.030
597
P HYP069 Hyperparathyroidism 58 0.030
598
P CYS018 Cystitis 57 0.030
599
NNL002 Nonalcoholic Steatohepatitis 56 0.030
600
P CHN012 Chondrosarcoma 56 0.030
601
P HYP750 Hypertriglyceridemia, Familial 55 0.030
602
P SYP003 Syphilis 55 0.030
603
TMP001 Temporal Lobe Epilepsy 54 0.030
604
HYP080 Hypogonadism 54 0.030
605
CRV045 Cervical Intraepithelial Neoplasia 43 0.030
606
CRV002 Cervix Uteri Carcinoma in Situ 40 0.030
607
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.030
608
c INF145 Infantile Liver Failure Syndrome 1 33 0.030
609
MNT310 Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type 32 0.030
610
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 67 0.029
611
BRT054 Brittle Bone Disorder 67 0.029
612
MTH009 Mouth Disease 64 0.029
613
RBS001 Rabies 63 0.029
614
RCK004 Rickets 63 0.029
615
P NRN021 Neuronal Ceroid Lipofuscinosis 62 0.029
616
CLF027 Cleft Palate, Isolated 61 0.029
617
P GLY013 Glycogen Storage Disease 61 0.029
618
ALL010 Allergic Contact Dermatitis 60 0.029
619
CCC001 Coccidioidomycosis 60 0.029
620
SPN027 Spinal Stenosis 60 0.029
621
EMB004 Embryonal Carcinoma 59 0.029
622
P SML001 Small Cell Carcinoma 58 0.029
623
VSC002 Vascular Dementia 58 0.029
624
LKD001 Leukodystrophy 57 0.029
625
P PRM011 Primary Ciliary Dyskinesia 57 0.029
626
P STS008 Sotos Syndrome 1 56 0.029
627
SPP010 Suppressor of Tumorigenicity 3 55 0.029
628
P CHR345 Chronic Pain 52 0.029
629
SMN007 Seminoma 49 0.029
630
P RNL045 Renal Tubular Acidosis, Distal 42 0.029
631
P SMK004 Smoking As a Quantitative Trait Locus 3 34 0.029
632
c MYS011 Myasthenia Gravis Congenital 28 0.029
633
c PSD047 Pseudo-Turner Syndrome 15 0.029
634
CNN003 Conn's Syndrome 70 0.029
635
P DMN001 Diamond-Blackfan Anemia 70 0.029
636
P NJM001 Nijmegen Breakage Syndrome 69 0.029
637
P CNJ013 Conjunctivitis 67 0.029
638
P PRD006 Prader-Willi Syndrome 66 0.029
639
c DNG003 Dengue Disease 66 0.029
640
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.029
641
P ALP009 Alopecia Areata 64 0.029
642
P MLG056 Malignant Hyperthermia 60 0.029
643
ERY003 Erythema Multiforme 60 0.029
644
PHR003 Pharyngitis 59 0.029
645
LPD008 Lipid Metabolism Disorder 59 0.029
646
P USH001 Usher Syndrome 59 0.029
647
CRB172 Cerebral Amyloid Angiopathy, Cst3-Related 58 0.029
648
P END033 Endocarditis 58 0.029
649
SML019 Smallpox 57 0.029
650
P SBS003 Substance Abuse 57 0.029
651
P PYL005 Pyelonephritis 56 0.029
652
BNF002 Bone Fracture 56 0.029
653
GST009 Gastroschisis 55 0.029
654
P MLT074 Multiple Endocrine Neoplasia 55 0.029
655
IRN001 Iron Deficiency Anemia 55 0.029
656
HPT022 Hepatoblastoma 55 0.029
657
P CNG001 Congenital Myasthenic Syndrome 55 0.029
658
PLG002 Plague 55 0.029
659
LMB062 Limb Ischemia 52 0.029
660
P PRC019 Precocious Puberty 52 0.029
661
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.029
662
P INF049 Infantile Myofibromatosis 49 0.029
663
TND004 Tendinopathy 45 0.029
664
MDS022 Mediastinitis 44 0.029
665
P HNT016 Huntington Disease 78 0.028
666
WRN001 Werner Syndrome 70 0.028
667
c BTT014 Beta-Thalassemia 70 0.028
668
P CHR071 Charcot-Marie-Tooth Disease 67 0.028
669
OTT002 Otitis Media 67 0.028
670
P PRP003 Porphyria Cutanea Tarda 67 0.028
671
P TXP001 Toxoplasmosis 65 0.028
672
SYS004 Systemic Mastocytosis 65 0.028
673
CNT047 Contact Dermatitis 64 0.028
674
c CNG006 Congenital Hypothyroidism 62 0.028
675
P LPS002 Liposarcoma 61 0.028
676
P EHL001 Ehlers-Danlos Syndrome 61 0.028
677
CHK001 Chikungunya 61 0.028
678
AVN001 Avian Influenza 60 0.028
679
HPT019 Hepatic Encephalopathy 59 0.028
680
END030 End Stage Renal Failure 59 0.028
681
P HYP083 Hypopituitarism 59 0.028
682
PPL022 Papilloma 58 0.028
683
WST005 West Nile Virus 58 0.028
684
P PLY041 Polymyositis 57 0.028
685
P PRG013 Paraganglioma 57 0.028
686
P SLV001 Silver-Russell Syndrome 57 0.028
687
HYP060 Hyperinsulinism 56 0.028
688
c INS002 in Situ Carcinoma 56 0.028
689
CRT049 Critical Limb Ischemia 56 0.028
690
P LMB006 Limb-Girdle Muscular Dystrophy 55 0.028
691
NRT004 Neuritis 55 0.028
692
P SZR006 Seizure Disorder 55 0.028
693
P ICH004 Ichthyosis 54 0.028
694
CND002 Conduct Disorder 54 0.028
695
GTR002 Goiter 53 0.028
696
PRP019 Peripheral Nervous System Disease 53 0.028
697
P DDN001 Duodenal Ulcer 53 0.028
698
PRV004 Periventricular Leukomalacia 53 0.028
699
HMG002 Hemoglobinuria 52 0.028
700
ATY042 Atypical Chronic Myeloid Leukemia 51 0.028
701
SCB001 Scabies 50 0.028
702
ANX004 Anoxia 49 0.028
703
P PTN014 Patent Ductus Arteriosus 1 45 0.028
704
OST097 Osteoporotic Fracture 41 0.028
705
c PSR017 Psoriasis 2 40 0.028
706
c PSR018 Psoriasis 13 39 0.028
707
FCL044 Fecal Incontinence 38 0.028
708
c PSR028 Psoriasis 7 37 0.028
709
c PSR032 Psoriasis 11 35 0.028
710
c DNT051 Dentin Dysplasia, Type I 34 0.028
711
SPS019 Spastic Paraparesis 33 0.028
712
MSC157 Muscular Dystrophy, Duchenne Type 74 0.027
713
MLD001 Melioidosis 73 0.027
714
SVR004 Severe Combined Immunodeficiency 71 0.027
715
P TMP003 Temporal Arteritis 67 0.027
716
GLL008 Gilles De La Tourette Syndrome 64 0.027
717
SKN019 Skin Melanoma 63 0.027
718
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.027
719
P PLC011 Pilocytic Astrocytoma 63 0.027
720
CMM005 Common Cold 62 0.027
721
P MTR004 Maturity-Onset Diabetes of the Young 62 0.027
722
MCR013 Microphthalmia 61 0.027
723
CHR072 Chordoma 61 0.027
724
P HMN010 Hemangioma 61 0.027
725
P MCP040 Mucopolysaccharidosis-Plus Syndrome 61 0.027
726
LNG039 Lung Squamous Cell Carcinoma 60 0.027
727
PNC034 Pancreas Disease 59 0.027
728
P BCK002 Beckwith-Wiedemann Syndrome 58 0.027
729
IMM158 Immune Suppression 57 0.027
730
GST023 Gastric Ulcer 57 0.027
731
P CNT005 Central Nervous System Lymphoma 57 0.027
732
HYP730 Hypogonadotropic Hypogonadism 56 0.027
733
P DRM007 Dermatitis Herpetiformis 56 0.027
734
P UTR058 Uterine Anomalies 55 0.027
735
CLR109 Colorectal Adenocarcinoma 54 0.027
736
CLN015 Colon Adenocarcinoma 53 0.027
737
EPD001 Epidermodysplasia Verruciformis 52 0.027
738
c ACT134 Acute Liver Failure 52 0.027
739
OCL006 Ocular Hypertension 51 0.027
740
MCL006 Macular Retinal Edema 51 0.027
741
KLD001 Keloids 50 0.027
742
ANG018 Angiomyolipoma 50 0.027
743
SLP001 Sleeping Sickness 48 0.027
744
SYN036 Syncope 46 0.027
745
SYS003 Systolic Heart Failure 44 0.027
746
P PST059 Pustular Psoriasis 40 0.027
747
CND006 Candida Glabrata 38 0.027
748
PRS025 Presbyopia 37 0.027
749
c CTR119 Cataract 32, Multiple Types 32 0.027
750
P SCL057 Scoliosis, Isolated 1 28 0.027
751
ADR007 Adrenoleukodystrophy 72 0.026
752
P FRG001 Fragile X Syndrome 69 0.026
753
c HMP029 Hemophilia a 69 0.026
754
P DYS007 Dyskeratosis Congenita 68 0.026
755
P ADL010 Adult Respiratory Distress Syndrome 67 0.026
756
LPD012 Lipoid Congenital Adrenal Hyperplasia 66 0.026
757
OVR029 Ovarian Hyperstimulation Syndrome 64 0.026
758
LNG108 Langerhans Cell Histiocytosis 63 0.026
759
c ACT210 Acute Respiratory Distress Syndrome 63 0.026
760
c TBR025 Tuberous Sclerosis 1 63 0.026
761
THY111 Thyroid Carcinoma, Familial Medullary 63 0.026
762
P ART021 Arteriosclerosis 62 0.026
763
FLL027 Fallopian Tube Carcinoma 62 0.026
764
c MCR129 Microvascular Complications of Diabetes 1 62 0.026
765
P BRG001 Brugada Syndrome 61 0.026
766
TXC005 Toxic Shock Syndrome 61 0.026
767
QFV001 Q Fever 61 0.026
768
NRM005 Neuromuscular Disease 60 0.026
769
INT079 Intrahepatic Cholangiocarcinoma 60 0.026
770
P PRT013 Portal Hypertension 59 0.026
771
PST028 Post-Traumatic Stress Disorder 59 0.026
772
c PRM005 Primary Hyperparathyroidism 59 0.026
773
MRK001 Merkel Cell Carcinoma 59 0.026
774
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.026
775
PLS007 Plasmodium Falciparum Malaria 59 0.026
776
SZR001 Sezary's Disease 58 0.026
777
P INT030 Intracranial Aneurysm 58 0.026
778
c CNG021 Congenital Toxoplasmosis 57 0.026
779
ADN027 Adenomyosis 57 0.026
780
RTN018 Retinal Disease 56 0.026
781
LYM027 Lymphopenia 56 0.026
782
P HYP076 Hyperthyroidism 56 0.026
783
P BLM007 Bulimia Nervosa 1 53 0.026
784
CHR005 Chorioamnionitis 52 0.026
785
P EST001 Estrogen-Receptor Positive Breast Cancer 52 0.026
786
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 52 0.026
787
c PRM226 Primary Central Nervous System Lymphoma 51 0.026
788
DRG003 Drug Dependence 51 0.026
789
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.026
790
LRN003 Learning Disability 49 0.026
791
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.026
792
P CLS010 Cluster Headache 47 0.026
793
LYM009 Lymphocytic Choriomeningitis 46 0.026
794
PMP004 Pemphigus Foliaceus 46 0.026
795
IMP004 Impetigo 45 0.026
796
DCB001 Decubitus Ulcer 44 0.026
797
URT001 Urethritis 44 0.026
798
P SPS133 Spastic Paraplegia 2, X-Linked 41 0.026
799
P CRB088 Cerebral Atrophy 38 0.026
800
TST043 Testicular Seminoma 36 0.026
801
ALP072 Alpha-Fetoprotein Deficiency 32 0.026
802
PRK066 Parkinsonism with Spasticity, X-Linked 31 0.026
803
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 29 0.026
804
CLS047 Classic Progressive Supranuclear Palsy Syndrome 25 0.026
805
SML025 Small Non-Cleaved Cell Lymphoma 25 0.026
806
MLR020 Malaria, Mild 23 0.026
807
BLD138 Blood Group--Diego System 18 0.026
808
HPD002 Hepadnavirus Infection 14 0.026
809
P FML011 Familial Adenomatous Polyposis 71 0.025
810
c MYT021 Myotonic Dystrophy 1 68 0.025
811
LYM007 Lymphangioleiomyomatosis 68 0.025
812
P NMN002 Niemann-Pick Disease 68 0.025
813
P HLP001 Holoprosencephaly 67 0.025
814
GLL018 Gallbladder Cancer 67 0.025
815
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.025
816
MXD005 Mixed Connective Tissue Disease 66 0.025
817
SVR097 Severe Cutaneous Adverse Reaction 64 0.025
818
c DPH024 Diaphragmatic Hernia, Congenital 63 0.025
819
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 63 0.025
820
P LYM025 Lymphedema 63 0.025
821
P HML002 Hemolytic Anemia 62 0.025
822
DFC004 Deficiency Anemia 62 0.025
823
P FCL005 Focal Segmental Glomerulosclerosis 60 0.025
824
c HRD002 Hereditary Angioedema 59 0.025
825
JPN002 Japanese Encephalitis 59 0.025
826
ICH054 Ichthyosis, X-Linked 59 0.025
827
VSC003 Visceral Leishmaniasis 59 0.025
828
TRN015 Transient Cerebral Ischemia 58 0.025
829
CMP010 Complex Regional Pain Syndrome 58 0.025
830
P LCH002 Lichen Planus 58 0.025
831
TRP002 Tropical Spastic Paraparesis 58 0.025
832
ALX003 Alexander Disease 58 0.025
833
c PRX045 Peroxisome Biogenesis Disorder 1b 57 0.025
834
P ANG015 Angioedema 57 0.025
835
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 57 0.025
836
PNM008 Pneumothorax 57 0.025
837
P ZLL001 Zellweger Syndrome 56 0.025
838
INF034 Infective Endocarditis 56 0.025
839
PLV003 Pelvic Inflammatory Disease 56 0.025
840
PRG009 Progressive Multifocal Leukoencephalopathy 55 0.025
841
P CNG411 Congenital Disorder of Glycosylation, Type in 55 0.025
842
P HYP014 Hyperuricemia 54 0.025
843
c MLG079 Malignant Pleural Mesothelioma 54 0.025
844
P RTN022 Retinal Vein Occlusion 53 0.025
845
INT075 Intracranial Hypertension 53 0.025
846
HLL004 Hellp Syndrome 53 0.025
847
P OVR046 Ovarian Cyst 52 0.025
848
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.025
849
P ATR005 Atrophic Gastritis 51 0.025
850
NSD001 Nose Disease 51 0.025
851
c SPN393 Spinal Muscular Atrophy, Type I 50 0.025
852
c BPL002 Bipolar I Disorder 50 0.025
853
P MYM013 Moyamoya Disease 1 50 0.025
854
DBT006 Diabetic Macular Edema 49 0.025
855
PNC119 Pancreatic Neuroendocrine Tumor 49 0.025
856
CHC001 Chickenpox 48 0.025
857
ANV001 Anovulation 48 0.025
858
ATN004 Autonomic Neuropathy 46 0.025
859
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 43 0.025
860
IDP070 Idiopathic Scoliosis 42 0.025
861
LKP003 Leukoplakia 42 0.025
862
PCH007 Pouchitis 42 0.025
863
PNM010 Pneumothorax, Primary Spontaneous 41 0.025
864
CRP002 Croup 41 0.025
865
PRP056 Porphyria, Acute Hepatic 41 0.025
866
TRT001 Teratocarcinoma 41 0.025
867
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.025
868
c DRM040 Dermatitis Herpetiformis, Familial 32 0.025
869
OTD001 Otodental Dysplasia 31 0.025
870
P STR035 Streptococcal Group a Invasive Disease 28 0.025
871
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.025
872
HDG009 Hodgkin Lymphoma, Childhood 20 0.025
873
c MLT156 Multiple Endocrine Neoplasia, Type I 70 0.024
874
ACR006 Aceruloplasminemia 65 0.024
875
P WLD002 Waldenstrom Macroglobulinemia 65 0.024
876
P LBR001 Leber Congenital Amaurosis 65 0.024
877
RCT015 Reactive Arthritis 65 0.024
878
LPT001 Leptospirosis 64 0.024
879
CRD119 Cardiac Arrest 63 0.024
880
KRT019 Keratitis, Hereditary 62 0.024
881
P XRD010 Xeroderma Pigmentosum, Variant Type 62 0.024
882
P EXN002 Exanthem 62 0.024
883
GLS001 Gliosarcoma 61 0.024
884
STT001 Status Epilepticus 60 0.024
885
CLR108 Colorectal Adenoma 60 0.024
886
PRP083 Porphyria, Acute Intermittent 60 0.024
887
P HST010 Histiocytosis 60 0.024
888
c CHL119 Cholangitis, Primary Sclerosing 60 0.024
889
UND005 Undifferentiated Pleomorphic Sarcoma 59 0.024
890
ADR005 Adrenal Carcinoma 59 0.024
891
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.024
892
APH002 Aphasia 58 0.024
893
CRT016 Carotid Artery Disease 58 0.024
894
P EPL140 Epilepsy, Idiopathic Generalized 58 0.024
895
P HYP614 Hyperlipidemia, Familial Combined 57 0.024
896
P MCR010 Microcephaly 57 0.024
897
ECT006 Ectodermal Dysplasia 57 0.024
898
P BRC006 Brachydactyly 57 0.024
899
P ACR001 Aicardi-Goutieres Syndrome 57 0.024
900
LYS002 Lysosomal Storage Disease 56 0.024
901
P MGR003 Migraine with Aura 56 0.024
902
P ESP035 Esophagitis, Eosinophilic, 1 55 0.024
903
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 55 0.024
904
P MMB011 Membranous Nephropathy 55 0.024
905
RCT018 Rectal Neoplasm 53 0.024
906
P SCL009 Sclerosing Cholangitis 53 0.024
907
P CRD132 Cardiac Conduction Defect 53 0.024
908
CCN001 Cocaine Dependence 52 0.024
909
ACH005 Achalasia 52 0.024
910
CRV040 Cervix Carcinoma 52 0.024
911
ORL013 Oral Lichen Planus 51 0.024
912
ATN005 Autonomic Dysfunction 51 0.024
913
AML029 Ameloblastoma 51 0.024
914
CHR563 Chronic Eosinophilic Leukemia 51 0.024
915
BRD004 Borderline Personality Disorder 50 0.024
916
HMS001 Hemosiderosis 50 0.024
917
THR013 Thoracic Outlet Syndrome 50 0.024
918
CRY004 Cryoglobulinemia 49 0.024
919
c ATM024 Autoimmune Pancreatitis 49 0.024
920
MTC069 Mitochondrial Disorders 49 0.024
921
LRG008 Large Granular Lymphocyte Leukemia 49 0.024
922
ONC007 Oncocytoma 48 0.024
923
c ACT042 Acute Pyelonephritis 48 0.024
924
P ENC008 Encephalocele 48 0.024
925
DWR001 Dwarfism 48 0.024
926
PRM003 Premature Ejaculation 47 0.024
927
HYD061 Hydrocephalus, Normal-Pressure 47 0.024
928
P GRN010 Granular Cell Tumor 47 0.024
929
P BLP003 Blepharospasm 46 0.024
930
CLB002 Clubfoot 46 0.024
931
SPN035 Spindle Cell Sarcoma 46 0.024
932
LKM006 Leukomalacia 46 0.024
933
P CHR342 Chiari Malformation 45 0.024
934
c PSR021 Psoriasis 14, Pustular 44 0.024
935
P CRB059 Cerebellar Degeneration 40 0.024
936
MYL057 Myelopathy, Htlv-1-Associated 38 0.024
937
c ACT059 Acute Maxillary Sinusitis 38 0.024
938
c CTR122 Cataract 5, Multiple Types 38 0.024
939
ALL014 Allergic Encephalomyelitis 37 0.024
940
BNG006 Benign Familial Neonatal Epilepsy 36 0.024
941
FLL029 Fallopian Tube Disease 35 0.024
942
MNG003 Mungan Syndrome 34 0.024
943
CHR391 Chromosome 15q24 Deletion Syndrome 32 0.024
944
RFR002 Refractory Hairy Cell Leukemia 32 0.024
945
c MCR112 Microvascular Complications of Diabetes 2 30 0.024
946
RTN187 Retinitis Pigmentosa-Deafness Syndrome 30 0.024
947
END016 Endocervicitis 28 0.024
948
MSM016 Mesomelic Dysplasia, Kantaputra Type 28 0.024
949
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 24 0.024
950
CLS052 Classic Hairy Cell Leukemia 16 0.024
951
PHN003 Phenylketonuria 73 0.023
952
VNH007 Von Hippel-Lindau Syndrome 72 0.023
953
P RSP003 Respiratory Failure 71 0.023
954
c JVN010 Juvenile Rheumatoid Arthritis 71 0.023
955
P TTR001 Tetralogy of Fallot 70 0.023
956
CNR004 Cone-Rod Dystrophy 2 69 0.023
957
P CRN037 Craniosynostosis 68 0.023
958
P PLZ001 Pelizaeus-Merzbacher Disease 68 0.023
959
CST001 Costello Syndrome 67 0.023
960
DMN031 Dementia, Lewy Body 66 0.023
961
PCK003 Pick Disease of Brain 66 0.023
962
P THY023 Thymoma 65 0.023
963
c GLY008 Glycogen Storage Disease Ii 64 0.023
964
PLM031 Poliomyelitis 64 0.023
965
P NRC002 Narcolepsy 64 0.023
966
CMB081 Combined Immunodeficiency, X-Linked 64 0.023
967
ADR054 Adrenocortical Carcinoma, Hereditary 63 0.023
968
P INT143 Interstitial Cystitis 63 0.023
969
CRN036 Craniopharyngioma 63 0.023
970
P HRM001 Hermansky-Pudlak Syndrome 62 0.023
971
P INT001 Intrahepatic Cholestasis 62 0.023
972
P ANG001 Angelman Syndrome 61 0.023
973
INT002 Intermittent Claudication 61 0.023
974
P FBR017 Fibrosarcoma 61 0.023
975
CRV038 Cervical Squamous Cell Carcinoma 61 0.023
976
c MST023 Mesothelioma, Malignant 61 0.023
977
P PLY014 Polycystic Kidney Disease 60 0.023
978
c ALP101 Alpha-Thalassemia 60 0.023
979
MYC079 Myoclonic Epilepsy of Lafora 60 0.023
980
MLG077 Malignant Peripheral Nerve Sheath Tumor 59 0.023
981
DBT062 Diabetic Foot Ulcers 59 0.023
982
MSC165 Muscular Dystrophy, Congenital, Lmna-Related 59 0.023
983
PTN001 Patent Foramen Ovale 58 0.023
984
c SVR001 Severe Acute Respiratory Syndrome 58 0.023
985
RSC001 Rosacea 58 0.023
986
P PNL012 Penile Cancer 58 0.023
987
P ACT105 Acute Mountain Sickness 58 0.023
988
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.023
989
FCL009 Focal Dermal Hypoplasia 57 0.023
990
MSC007 Muscle Hypertrophy 57 0.023
991
c HPT007 Hepatitis E 57 0.023
992
LBR002 Leber Hereditary Optic Neuropathy 57 0.023
993
GNT002 Giant Cell Glioblastoma 56 0.023
994
LST001 Listeriosis 55 0.023
995
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.023
996
HYP068 Hyperostosis 52 0.023
997
URM002 Uremia 52 0.023
998
STM006 Stomach Disease 52 0.023
999
P ASP001 Asperger Syndrome 51 0.023
1000
CLC006 Calcinosis 51 0.023
1001
CRY003 Cryptosporidiosis 51 0.023
1002
BRX001 Bruxism 51 0.023
1003
c MLG074 Malignant Mesenchymoma 51 0.023
1004
SBS004 Substance Dependence 51 0.023
1005
PRL017 Prolymphocytic Leukemia 51 0.023
1006
LYM012 Lymphoplasmacytic Lymphoma 50 0.023
1007
ADN024 Adenine Phosphoribosyltransferase Deficiency 49 0.023
1008
CHR286 Chronic Neutrophilic Leukemia 49 0.023
1009
GRN017 Granulocytopenia 49 0.023
1010
HPR003 Heparin-Induced Thrombocytopenia 48 0.023
1011
HYP457 Hypertrophic Scars 48 0.023
1012
RFR010 Refractory Anemia 48 0.023
1013
P LRS001 Larsen Syndrome 47 0.023
1014
FCL022 Focal Dystonia 47 0.023
1015
MGR001 Migraine Without Aura 47 0.023
1016
P ICH001 Ichthyosis Vulgaris 47 0.023
1017
MLK006 Milk Allergy 46 0.023
1018
CHR100 Chronic Ulcer of Skin 46 0.023
1019
c ART144 Arthrogryposis, Distal, Type 1a 46 0.023
1020
LCH009 Lichen Sclerosus 45 0.023
1021
BSL008 Basal Ganglia Disease 44 0.023
1022
P ACH011 Achondrogenesis 44 0.023
1023
DVR002 Diverticulitis 44 0.023
1024
CRT009 Critical Illness Polyneuropathy 44 0.023
1025
CVR010 Cavernous Malformation 40 0.023
1026
GRN007 Granuloma Annulare 40 0.023
1027
CRV069 Cervix Disease 39 0.023
1028
AMY098 Amyotrophy, Monomelic 35 0.023
1029
P BCT020 Bacteremia 2 34 0.023
1030
GST059 Gestational Trophoblastic Tumor 30 0.023
1031
P FTT008 Fatty Liver Disease, Nonalcoholic 1 25 0.023
1032
PLY150 Polykaryocytosis Inducer 20 0.023
1033
PLM051 Pulmonary Arterio-Veinous Fistula 17 0.023
1034
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.021
1035
P AGM019 Agammaglobulinemia, X-Linked 69 0.021
1036
LGH007 Leigh Syndrome 68 0.021
1037
P ALG028 Alagille Syndrome 1 68 0.021
1038
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.021
1039
ADL030 Adult-Onset Still's Disease 65 0.021
1040
P HRS035 Hirschsprung Disease 1 64 0.021
1041
FBR011 Fibrodysplasia Ossificans Progressiva 64 0.021
1042
OST017 Osteomyelitis 64 0.021
1043
APH001 Aphthous Stomatitis 64 0.021
1044
MST017 Mast Cell Disease 63 0.021
1045
DSM004 Desmoid Tumor 63 0.021
1046
PTT048 Pituitary Adenoma, Prolactin-Secreting 63 0.021
1047
BLM001 Bloom Syndrome 62 0.021
1048
NRV006 Nervous System Cancer 61 0.021
1049
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 61 0.021
1050
P SPN052 Spondyloarthropathy 61 0.021
1051
PPT005 Peptic Ulcer Disease 60 0.021
1052
BLD034 Bile Duct Carcinoma 60 0.021
1053
JVN014 Juvenile Polyposis Syndrome 60 0.021
1054
ATH013 Atherosclerosis Susceptibility 59 0.021
1055
c VRL010 Viral Hepatitis 59 0.021
1056
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 59 0.021
1057
P HYP035 Hypophosphatasia 58 0.021
1058
PLM012 Pulmonary Sarcoidosis 58 0.021
1059
BRN038 Bronchial Disease 58 0.021
1060
SHG001 Shigellosis 57 0.021
1061
PLM010 Pulmonary Edema 57 0.021
1062
CYS005 Cysticercosis 57 0.021
1063
c ALM001 Al Amyloidosis 56 0.021
1064
PLS006 Plasmodium Vivax Malaria 56 0.021
1065
PRP082 Porphyria, Congenital Erythropoietic 56 0.021
1066
KRT006 Keratoconjunctivitis 56 0.021
1067
GST037 Gastroparesis 56 0.021
1068
P HRD011 Hereditary Spherocytosis 55 0.021
1069
c ANM036 Anemia, Sideroblastic, 1 55 0.021
1070
c EPL209 Epilepsy, Idiopathic Generalized 10 55 0.021
1071
HDR002 Hidradenitis Suppurativa 54 0.021
1072
c INF071 Inflammatory Bowel Disease 1 54 0.021
1073
ESP020 Esophageal Atresia 54 0.021
1074
OPT003 Opiate Dependence 54 0.021
1075
c VSC019 Vesicoureteral Reflux 1 54 0.021
1076
MBS002 Moebius Syndrome 53 0.021
1077
HMG005 Hemoglobinopathy 53 0.021
1078
c CNT075 Central Precocious Puberty 52 0.021
1079
ARM001 Aromatase Deficiency 52 0.021
1080
APR001 Apraxia 52 0.021
1081
ILT001 Ileitis 52 0.021
1082
TRC008 Trachoma 52 0.021
1083
PRN021 Paranasal Sinus Disease 51 0.021
1084
c HYP760 Hypothyroidism, Congenital, Nongoitrous, 2 51 0.021
1085
BBS001 Babesiosis 51 0.021
1086
P ERY053 Erythrokeratodermia Variabilis Et Progressiva 1 51 0.021
1087
HYP006 Hypertensive Heart Disease 51 0.021
1088
DNT012 Dental Caries 50 0.021
1089
TMR011 Tumoral Calcinosis, Hyperphosphatemic, Familial 50 0.021
1090
EPD006 Epidermolysis Bullosa Acquisita 50 0.021
1091
FLL008 Folliculitis 50 0.021
1092
P HMC002 Homocystinuria 50 0.021
1093
SBP001 Subependymal Giant Cell Astrocytoma 50 0.021
1094
ACR012 Aicardi Syndrome 49 0.021
1095
HMP009 Haemophilus Influenzae 49 0.021
1096
MTB004 Metabolic Acidosis 49 0.021
1097
CYS039 Cystic Kidney Disease 49 0.021
1098
BCT004 Bacteriuria 49 0.021
1099
CHR074 Choriocarcinoma 49 0.021
1100
BLL003 Bell's Palsy 49 0.021
1101
P MYP087 Myopathy, Tubular Aggregate, 1 48 0.021
1102
c FTL006 Fetal Alcohol Spectrum Disorder 48 0.021
1103
MLT006 Multidrug-Resistant Tuberculosis 48 0.021
1104
PRP036 Peripheral T-Cell Lymphoma 48 0.021
1105
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.021
1106
EXT033 Extrapulmonary Tuberculosis 48 0.021
1107
P NML001 Nemaline Myopathy 47 0.021
1108
P DNT011 Dentinogenesis Imperfecta 47 0.021
1109
HTR003 Heterotaxy 46 0.021
1110
c ACH033 Achondrogenesis, Type Ia 46 0.021
1111
ANG046 Angioimmunoblastic T-Cell Lymphoma 46 0.021
1112
LYM127 Lymphatic Malformations 45 0.021
1113
AMB002 Amblyopia 45 0.021
1114
CRD137 Cardiogenic Shock 45 0.021
1115
ARC002 Arachnoiditis 45 0.021
1116
P HYP263 Hypersomnia 45 0.021
1117
MYC013 Mycobacterium Abscessus 45 0.021
1118
CRV043 Cervical Dystonia 45 0.021
1119
RFR003 Refractive Error 45 0.021
1120
PST053 Postherpetic Neuralgia 44 0.021
1121
PNN005 Panencephalitis, Subacute Sclerosing 44 0.021
1122
c ICH069 Ichthyosis, Congenital, Autosomal Recessive 4b 44 0.021