Search results for (S)-famoxadone

3484 hits were found for (S)-famoxadone

# Family MCID Name MIFTS Score
1
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 29 6.914
2
ENH001 Enhanced S-Cone Syndrome 57 6.597
3
HRL004 Hurler-Scheie Syndrome 55 6.481
4
PRT014 Protein S Deficiency 44 6.301
5
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 28 4.994
6
P THP004 Thiopurines, Poor Metabolism of, 1 47 4.934
7
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 25 4.610
8
c FNC062 Fanconi Anemia, Complementation Group S 34 3.879
9
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 56 3.876
10
SCK003 Sickle Cell Anemia 74 3.687
11
P THL005 Thalassemia 60 2.729
12
P SCK005 Sickle Cell Disease 50 2.704
13
THP001 Thiopurine S Methyltranferase Deficiency 20 2.546
14
SCH036 Scheie Syndrome 72 2.518
15
STN013 Stenotrophomonas Maltophilia Infection 25 2.494
16
SVR099 Severe Hereditary Thrombophilia Due to Congenital Protein S Deficiency 16 2.494
17
BLC001 Blue Cone Monochromacy 45 2.474
18
LTT002 Letterer-Siwe Disease 33 2.438
19
IMM165 Immunoglobulin Switch Sequences 15 1.849
20
c HMG029 Hemoglobin Se Disease 39 1.790
21
HYP003 Hypermethioninemia 40 1.777
22
PRT104 Protein S Acquired Deficiency 9 1.747
23
SYM028 Symphalangism, C. S. Lewis Type 7 1.747
24
P SCK034 Sickle Beta Thalassemia 28 1.733
25
TNG001 Tungiasis 25 1.724
26
STR108 Streptococcus Pneumoniae-Associated Hemolytic Uremic Syndrome 13 1.724
27
SCH014 Schistosomiasis 57 0.190
28
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.188
29
c THR092 Thrombophilia Due to Thrombin Defect 73 0.184
30
LYM133 Lymphoma, Hodgkin, Classic 69 0.178
31
HLX001 Helix Syndrome 47 0.178
32
c HPT016 Hepatitis B 59 0.174
33
P BRS047 Breast Cancer 97 0.172
34
P BLD134 Bladder Cancer 79 0.157
35
P CLR023 Colorectal Cancer 99 0.156
36
P NRB001 Neuroblastoma 72 0.154
37
48X005 48,xyyy 39 0.154
38
P LVR013 Liver Disease 68 0.153
39
P ALZ034 Alzheimer Disease 88 0.152
40
BRK010 Burkitt Lymphoma 67 0.149
41
P LNG032 Lung Cancer 98 0.147
42
EWN003 Ewing Sarcoma 69 0.146
43
DPR016 Depression 63 0.145
44
THR024 Thrombosis 57 0.140
45
P HPT023 Hepatocellular Carcinoma 100 0.138
46
P THR015 Thrombophilia 51 0.135
47
P RTN024 Retinoblastoma 73 0.134
48
MNT002 Mental Depression 58 0.133
49
c FML008 Familial Retinoblastoma 53 0.133
50
P DRR001 Diarrhea 55 0.133
51
P UVT001 Uveitis 57 0.132
52
P OVR042 Ovarian Cancer 88 0.131
53
PRT037 Pertussis 65 0.129
54
47X002 47,xyy 49 0.129
55
P HRP006 Herpes Simplex 65 0.128
56
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.127
57
P ADN016 Adenocarcinoma 64 0.126
58
ATM095 Autoimmune Disease 62 0.126
59
P LYM118 Lymphoma 68 0.125
60
LVR012 Liver Cirrhosis 62 0.125
61
c SVR001 Severe Acute Respiratory Syndrome 62 0.124
62
P MYL006 Myeloid Leukemia 60 0.124
63
CRH001 Crohn's Disease 74 0.122
64
TYP007 Typhoid Fever 63 0.120
65
P LKM002 Leukemia 68 0.119
66
P MJR001 Major Depressive Disorder 68 0.117
67
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.116
68
HRW001 Hair Whorl 36 0.116
69
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.115
70
BRR014 Barrett Esophagus 65 0.114
71
CHL014 Cholera 59 0.114
72
P GLM045 Glioma 63 0.113
73
P INF037 Inflammatory Bowel Disease 54 0.113
74
P PRS040 Prostate Cancer 97 0.112
75
MLR004 Malaria 81 0.112
76
HMN044 Human Immunodeficiency Virus Type 1 71 0.112
77
GLL048 Glial Tumor 45 0.112
78
P GST053 Gastric Cancer 83 0.111
79
HMG005 Hemoglobinopathy 56 0.111
80
P PRK057 Parkinson Disease, Late-Onset 78 0.110
81
TLN003 Telangiectasis 52 0.110
82
VCC001 Vaccinia 49 0.110
83
P ATX030 Ataxia-Telangiectasia 82 0.109
84
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.109
85
c BTT014 Beta-Thalassemia 74 0.109
86
P LKM062 Leukemia, Acute Lymphoblastic 69 0.108
87
PNG002 Pain Agnosia 51 0.107
88
LNG099 Lung Disease 60 0.106
89
ISC004 Ischemia 58 0.106
90
SQM006 Squamous Cell Carcinoma 60 0.105
91
P END033 Endocarditis 57 0.105
92
c HYP595 Hypertension, Essential 84 0.104
93
TXC005 Toxic Shock Syndrome 62 0.104
94
P VSC007 Vascular Disease 63 0.103
95
P CHR345 Chronic Pain 44 0.103
96
ALL026 Allergic Hypersensitivity Disease 62 0.102
97
ADN018 Adenoma 59 0.102
98
c LKM061 Leukemia, Acute Myeloid 84 0.102
99
HMC014 Homocysteinemia 53 0.102
100
CHL068 Cholestasis 61 0.100
101
P SLM003 Salmonellosis 55 0.100
102
c SYS001 Systemic Lupus Erythematosus 86 0.099
103
GST045 Gastroenteritis 59 0.098
104
P HRS035 Hirschsprung Disease 1 65 0.098
105
ANX010 Anxiety 73 0.097
106
PRP030 Purpura 54 0.096
107
DFC004 Deficiency Anemia 70 0.096
108
P PNC035 Pancreatic Cancer 84 0.095
109
OST012 Osteoarthritis 78 0.095
110
GLB015 Glioblastoma Multiforme 75 0.095
111
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.095
112
SRC014 Sarcoma 65 0.095
113
PLM033 Pulmonary Embolism 59 0.095
114
DWN001 Down Syndrome 70 0.094
115
MST005 Mastitis 53 0.094
116
SPN035 Spindle Cell Sarcoma 53 0.094
117
CYS001 Cystic Fibrosis 81 0.094
118
P KDN018 Kidney Disease 72 0.094
119
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.094
120
c SML038 Small Cell Cancer of the Lung 65 0.094
121
P NTR004 Neutropenia 63 0.094
122
DNT012 Dental Caries 53 0.094
123
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.093
124
c ATM099 Autoimmune Uveitis 45 0.093
125
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.093
126
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.092
127
OST159 Osteogenic Sarcoma 66 0.092
128
c PRC016 Pre-Eclampsia 63 0.092
129
P CTR002 Cataract 60 0.092
130
P HPT021 Hepatitis 67 0.091
131
PRT011 Protein C Deficiency 44 0.091
132
BRR002 Barrett's Adenocarcinoma 36 0.091
133
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.091
134
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.090
135
DRM006 Dermatitis 61 0.089
136
P BCL017 B-Cell Lymphoma 58 0.089
137
LPP008 Lipoprotein Quantitative Trait Locus 62 0.089
138
c PNS012 Paine Syndrome 61 0.089
139
AST005 Asthma 76 0.088
140
FTT001 Fatty Liver Disease 61 0.088
141
ULC004 Ulcerative Colitis 73 0.087
142
ADL002 Adult Syndrome 70 0.087
143
c ALP101 Alpha-Thalassemia 62 0.087
144
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.087
145
HYP066 Hyperglycemia 61 0.086
146
CHC001 Chickenpox 60 0.086
147
BCT022 Bacterial Infectious Disease 56 0.086
148
END040 Endogenous Depression 55 0.086
149
HMP009 Haemophilus Influenzae 43 0.086
150
MYL069 Myeloma, Multiple 85 0.085
151
P TRN020 Turner Syndrome 67 0.085
152
NRT001 Neurotic Disorder 53 0.085
153
CRB039 Cerebrovascular Disease 67 0.084
154
P TRM003 Tremor 54 0.084
155
CYT002 Cytokine Deficiency 42 0.084
156
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.083
157
ALC007 Alcohol Dependence 66 0.083
158
P DMN002 Dementia 66 0.083
159
PRT036 Peritonitis 64 0.083
160
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.082
161
P CRN300 Coronary Heart Disease 1 63 0.082
162
ESP021 Esophageal Cancer 90 0.082
163
HYP266 Hypoxia 57 0.082
164
CRV035 Cervical Cancer 76 0.081
165
P DBT009 Diabetes Mellitus 64 0.081
166
STM007 Stomatitis 50 0.081
167
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.080
168
STR067 Stroke, Ischemic 81 0.080
169
SVR004 Severe Combined Immunodeficiency 73 0.080
170
P PNM007 Pneumonia 68 0.080
171
ORL011 Oral Cancer 60 0.080
172
P INF032 Infertility 57 0.080
173
P NRP001 Neuropathy 56 0.080
174
IMM167 Immune Deficiency Disease 78 0.079
175
P MLN008 Melanoma 69 0.079
176
ATH013 Atherosclerosis Susceptibility 65 0.079
177
ART140 Arteries, Anomalies of 52 0.079
178
P PRP034 Purpura Fulminans 43 0.079
179
c HPT073 Hepatitis C Virus 72 0.078
180
P PSR002 Psoriasis 62 0.078
181
DSS009 Disseminated Intravascular Coagulation 57 0.078
182
PRS045 Prostatic Hypertrophy 53 0.078
183
CVD001 Covid-19 44 0.078
184
BRN024 Bronchitis 68 0.078
185
P MNN013 Meningitis 66 0.078
186
P VSC011 Vasculitis 62 0.077
187
FBR047 Fibromyalgia 58 0.077
188
PST011 Pustulosis of Palm and Sole 52 0.077
189
LYM019 Lymphosarcoma 46 0.077
190
P LPS004 Lupus Erythematosus 61 0.076
191
THY029 Thyroid Carcinoma 59 0.076
192
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.076
193
VLV047 Volvulus of Midgut 49 0.076
194
P INF038 Influenza 68 0.075
195
DYS015 Dysentery 52 0.075
196
PRS021 Prostatic Adenoma 51 0.075
197
P RHM011 Rheumatoid Arthritis 80 0.074
198
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.074
199
END057 Endometrial Cancer 74 0.074
200
P THR014 Thrombocytopenia 67 0.074
201
HYP056 Hypoglycemia 66 0.074
202
P DRM053 Dermatitis, Atopic 66 0.074
203
SKN016 Skin Disease 63 0.074
204
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.073
205
P PLM037 Pulmonary Hypertension 67 0.073
206
ANG054 Angina Pectoris 66 0.073
207
CLT003 Colitis 62 0.073
208
ERY051 Erythroleukemia, Familial 56 0.073
209
PRS129 Prostatic Hyperplasia, Benign 49 0.073
210
INT017 Intestinal Schistosomiasis 48 0.073
212
PPL052 Papillomatosis, Confluent and Reticulated 33 0.073
213
P LKM071 Leukemia, Chronic Lymphocytic 79 0.072
214
c CHR684 Chronic Kidney Disease 70 0.072
215
c RHB024 Rhabdomyosarcoma 2 67 0.072
216
P END044 Endometriosis 63 0.072
217
P NPH012 Nephrotic Syndrome 60 0.072
218
P SZR006 Seizure Disorder 56 0.072
219
RTN023 Retinitis 46 0.072
220
c PCH010 Pachyonychia Congenita 3 44 0.072
221
ATX019 Ataxia with Vitamin E Deficiency 42 0.072
222
NRR001 Neuroretinitis 42 0.072
223
P HRT032 Heart Disease 75 0.071
224
P SCL018 Scoliosis 60 0.070
225
ACQ007 Acquired Immunodeficiency Syndrome 60 0.070
226
P AST007 Astrocytoma 51 0.070
227
c LKM063 Leukemia, Chronic Myeloid 72 0.070
228
P MYC007 Myocardial Infarction 70 0.070
229
OST017 Osteomyelitis 64 0.070
230
TRN018 Transitional Cell Carcinoma 56 0.070
231
P LTR001 Lateral Sclerosis 54 0.070
232
END086 End Stage Renal Disease 51 0.070
233
P HNT016 Huntington Disease 72 0.069
234
CNG034 Congestive Heart Failure 69 0.069
235
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.069
236
c ACT075 Acute Myocardial Infarction 57 0.069
237
P BPL003 Bipolar Disorder 56 0.069
238
BNR002 Bone Resorption Disease 48 0.069
239
c HYP836 Hypercholesterolemia, Familial, 1 73 0.068
240
c HPT001 Hepatitis C 62 0.068
241
VSL002 Visual Epilepsy 59 0.068
242
P GLM007 Glomerulonephritis 57 0.068
243
P FBR017 Fibrosarcoma 56 0.068
244
TRM010 Traumatic Brain Injury 51 0.068
245
c PRM038 Primary Agammaglobulinemia 44 0.068
246
c MJR024 Major Affective Disorder 9 41 0.068
247
WLL004 Wallerian Degeneration 39 0.068
248
c MJR022 Major Affective Disorder 8 38 0.068
249
TTN003 Tetanus 65 0.067
250
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.067
251
P ALC033 Alcohol Use Disorder 58 0.067
252
P EXN002 Exanthem 57 0.067
253
P RTN016 Retinal Degeneration 53 0.067
254
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.067
255
c MGR028 Migraine with or Without Aura 1 67 0.066
256
P SKN015 Skin Carcinoma 66 0.066
257
P PRD008 Periodontitis 64 0.066
258
P ENC004 Encephalitis 61 0.066
259
P HDC001 Headache 57 0.066
260
BRN071 Brain Injury 49 0.066
261
SPL018 Splenomegaly 48 0.066
262
MDD018 Middle East Respiratory Syndrome 43 0.066
263
HNS001 Hansen's Disease 34 0.066
264
MYL009 Myelodysplastic Syndrome 70 0.065
265
P LPR021 Leprosy 3 69 0.065
266
P HYP098 Hypereosinophilic Syndrome 67 0.065
267
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.065
268
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.065
269
DPH001 Diphtheria 60 0.065
270
P ECL001 Eclampsia 50 0.065
271
OVR094 Ovarian Epithelial Cancer 38 0.065
272
P RTN008 Retinitis Pigmentosa 79 0.064
273
P PHC003 Pheochromocytoma 71 0.064
274
P MYP004 Myopathy 70 0.064
275
GST092 Gastroesophageal Reflux 67 0.064
276
TBC004 Tobacco Addiction 64 0.064
277
c HPT003 Hepatitis a 62 0.064
278
P CRD246 Cardiovascular System Disease 57 0.064
279
INF034 Infective Endocarditis 53 0.064
280
c MCR113 Microvascular Complications of Diabetes 3 52 0.064
281
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.064
282
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.064
283
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.064
284
c MCR120 Microvascular Complications of Diabetes 7 47 0.064
285
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.064
286
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.064
287
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.064
288
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.064
289
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.064
290
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.064
291
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.064
292
c MCR130 Microvascular Complications of Diabetes 6 41 0.064
293
c MCR133 Microvascular Complications of Diabetes 4 41 0.064
294
P LNG064 Lung Cancer Susceptibility 3 78 0.063
295
P ART022 Arthritis 69 0.063
296
P HYP086 Hypothyroidism 69 0.063
297
P NSP012 Nasopharyngeal Carcinoma 66 0.063
298
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.063
299
LPD008 Lipid Metabolism Disorder 62 0.063
300
P KDN017 Kidney Cancer 60 0.063
301
P ANT006 Antiphospholipid Syndrome 55 0.063
302
IMP005 Impotence 52 0.063
303
ADR040 Adrenal Gland Pheochromocytoma 46 0.063
304
CRB004 Cerebral Artery Occlusion 45 0.063
305
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.062
306
ONC002 Onchocerciasis 52 0.062
307
THR016 Thrombophlebitis 51 0.062
308
BCK006 Back Pain 42 0.062
309
PST053 Postherpetic Neuralgia 40 0.062
310
ARG004 Argyria 27 0.062
311
KPS004 Kaposi Sarcoma 75 0.060
312
c ACT073 Acute Leukemia 58 0.060
313
ANT024 Anthrax Disease 58 0.060
314
IRN002 Iron Metabolism Disease 57 0.060
315
CRH005 Crohn's Colitis 53 0.060
316
PRT018 Portal Vein Thrombosis 50 0.060
317
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.059
318
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.059
319
c BSL007 Basal Cell Carcinoma 68 0.059
320
P CRD119 Cardiac Arrest 67 0.059
321
P ENC018 Encephalopathy 61 0.059
322
HRP004 Herpes Zoster 60 0.059
323
RHM001 Rheumatic Fever 60 0.059
324
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.059
325
DSS008 Disease of Mental Health 58 0.059
326
AGN016 Aging 56 0.059
327
AMN003 Amnestic Disorder 54 0.059
328
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.059
329
P HMP007 Hemophilia 51 0.059
330
ALL014 Allergic Encephalomyelitis 38 0.059
331
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.059
332
P RSP003 Respiratory Failure 74 0.058
333
P SCH015 Schizophrenia 74 0.058
334
P PLM036 Pulmonary Fibrosis 65 0.058
335
CLN015 Colon Adenocarcinoma 65 0.058
336
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.058
337
LSH001 Leishmaniasis 63 0.058
338
P HML002 Hemolytic Anemia 63 0.058
339
c ACT068 Acute Cystitis 63 0.058
340
PHR003 Pharyngitis 57 0.058
341
P MLN007 Male Infertility 55 0.058
342
P LRY044 Larynx Cancer 55 0.058
343
PPL022 Papilloma 54 0.058
344
P OVR082 Overgrowth Syndrome 50 0.058
345
P OPN001 Open-Angle Glaucoma 49 0.058
346
MYF002 Myofascial Pain Syndrome 42 0.058
347
P KLZ004 Kala-Azar 1 41 0.058
348
OTT002 Otitis Media 72 0.057
349
P MCR115 Microvascular Complications of Diabetes 5 66 0.057
350
P PRS038 Personality Disorder 65 0.057
351
P ESP024 Esophagitis 62 0.057
352
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.057
353
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.057
354
DFF005 Diffuse Large B-Cell Lymphoma 55 0.057
355
P THY032 Thyroiditis 52 0.057
356
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.057
357
c LKM005 Leukemia, T-Cell, Chronic 34 0.057
358
c ATR087 Atrial Standstill 1 75 0.056
359
P EPL164 Epilepsy 71 0.056
360
PLM001 Pulmonary Tuberculosis 69 0.056
361
CHL065 Cholangiocarcinoma 68 0.056
362
c INF071 Inflammatory Bowel Disease 1 67 0.056
363
CHG001 Chagas Disease 66 0.056
364
NTR005 Nutritional Deficiency Disease 62 0.056
365
c ACT027 Acute Pancreatitis 60 0.056
366
P HMC002 Homocystinuria 53 0.056
367
SQM002 Squamous Cell Papilloma 46 0.056
368
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.056
369
ORL015 Oral Squamous Cell Carcinoma 43 0.056
370
PLY150 Polykaryocytosis Inducer 31 0.056
371
INS024 Insulin-Like Growth Factor I 79 0.055
372
GST040 Gastric Adenocarcinoma 70 0.055
373
KHL003 Kohlschutter-Tonz Syndrome 65 0.055
374
CRD132 Cardiac Conduction Defect 58 0.055
375
NNL006 Non-Alcoholic Steatohepatitis 54 0.055
376
PLS007 Plasmodium Falciparum Malaria 52 0.055
377
INT079 Intrahepatic Cholangiocarcinoma 51 0.055
378
TRY001 Trypanosomiasis 50 0.055
379
P NGH001 Night Blindness 48 0.055
380
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.055
381
c LNG109 Lung Cancer Susceptibility 1 27 0.055
383
c DLT002 Dilated Cardiomyopathy 79 0.054
384
P ATS364 Autism 70 0.054
385
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.054
386
c GLC092 Glaucoma, Primary Open Angle 62 0.054
387
P PRM006 Primary Biliary Cirrhosis 62 0.054
388
MSL001 Measles 62 0.054
389
SPN186 Spinal Cord Injury 60 0.054
390
VRC005 Varicose Veins 60 0.054
391
c ACT071 Acute Kidney Failure 60 0.054
392
INT007 Intermediate Coronary Syndrome 55 0.054
393
c VRL010 Viral Hepatitis 52 0.054
394
ENT011 Enterocolitis 51 0.054
395
P BNG032 Benign Mesothelioma 46 0.054
396
ANX004 Anoxia 40 0.054
397
c SPN225 Spondyloarthropathy 1 73 0.052
398
P SRC025 Sarcoidosis 1 70 0.052
399
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.052
400
P CYS018 Cystitis 59 0.052
401
P SYP003 Syphilis 58 0.052
402
P PRP019 Peripheral Nervous System Disease 58 0.052
403
CYT008 Cytomegalovirus Infection 57 0.052
404
DYS073 Dysphagia 50 0.052
405
PST092 Posttransplant Acute Limbic Encephalitis 29 0.052
406
CHL079 Children's Interstitial Lung Disease 26 0.052
407
MDD011 Mood Disorder 62 0.051
408
P PNC044 Pancreatitis 61 0.051
409
P RBL001 Rubella 59 0.051
410
ANR040 Aneurysm 59 0.051
411
EYD002 Eye Disease 58 0.051
412
P GLL018 Gallbladder Cancer 57 0.051
413
ALL006 Allergic Asthma 56 0.051
414
SFT003 Soft Tissue Sarcoma 56 0.051
415
P GST044 Gastritis 56 0.051
416
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.051
417
P SBS003 Substance Abuse 55 0.051
418
P ART021 Arteriosclerosis 54 0.051
419
GST023 Gastric Ulcer 53 0.051
420
P MSC003 Muscular Atrophy 52 0.051
422
P SPP010 Suppressor of Tumorigenicity 3 51 0.051
423
URM002 Uremia 49 0.051
424
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.051
425
URN003 Urinary Schistosomiasis 46 0.051
426
IDP070 Idiopathic Scoliosis 42 0.051
427
c FNC027 Fanconi Anemia, Complementation Group a 81 0.050
428
P APL001 Aplastic Anemia 74 0.050
429
P CNR004 Cone-Rod Dystrophy 2 73 0.050
430
P HYP061 Hypertrophic Cardiomyopathy 70 0.050
431
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.050
432
P DYS154 Dystonia 65 0.050
433
SHG001 Shigellosis 60 0.050
434
IGR001 Ige Responsiveness, Atopic 59 0.050
435
SPT004 Septic Arthritis 58 0.050
436
APH002 Aphasia 57 0.050
437
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.050
438
PLS011 Plasmacytoma 56 0.050
439
P HYP076 Hyperthyroidism 55 0.050
440
HMS001 Hemosiderosis 54 0.050
441
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.050
442
P CHL066 Cholangitis 51 0.050
443
ATS010 Autosomal Recessive Disease 48 0.050
444
PTT037 Pituitary Tumors 44 0.050
445
P RRH023 Rare Hereditary Hemochromatosis 41 0.050
446
ANS003 Anisakiasis 40 0.050
447
P MLT020 Multiple Sclerosis 72 0.048
448
P SLP006 Sleep Apnea 69 0.048
449
PSY004 Psychotic Disorder 67 0.048
450
c ATS007 Autism Spectrum Disorder 67 0.048
451
P ATR011 Atrial Fibrillation 66 0.048
452
PLM031 Poliomyelitis 64 0.048
453
P HYP069 Hyperparathyroidism 63 0.048
454
c ATM011 Autoimmune Hepatitis 63 0.048
455
c FNC043 Fanconi Anemia, Complementation Group E 62 0.048
456
P HYP750 Hypertriglyceridemia, Familial 62 0.048
457
P MCR010 Microcephaly 59 0.048
458
CHL123 Chlamydia 59 0.048
459
VSC002 Vascular Dementia 57 0.048
460
P PLY019 Polyneuropathy 56 0.048
461
c PST005 Posterior Uveitis 54 0.048
462
SLP001 Sleeping Sickness 54 0.048
463
P PNC025 Panic Disorder 53 0.048
464
P RCT021 Rectum Cancer 52 0.048
465
P HMN032 Human Herpesvirus 8 47 0.048
466
SGT001 Sagittal Sinus Thrombosis 32 0.048
467
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.047
468
P OST002 Osteoporosis 74 0.047
469
c HMP004 Hemophilia B 68 0.047
470
CNN005 Connective Tissue Disease 68 0.047
471
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.047
472
TRN015 Transient Cerebral Ischemia 63 0.047
473
P BRS044 Breast Adenocarcinoma 59 0.047
474
PPT005 Peptic Ulcer Disease 59 0.047
475
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.047
476
P RHN004 Rhinitis 57 0.047
477
P MYS005 Myositis 56 0.047
478
FLR002 Filariasis 55 0.047
479
P INS002 in Situ Carcinoma 53 0.047
480
P SML001 Small Cell Carcinoma 52 0.047
481
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.047
482
ADN022 Adenylosuccinase Deficiency 44 0.047
483
P MDL005 Medulloblastoma 77 0.046
484
LPT014 Leptin Deficiency or Dysfunction 74 0.046
485
LYM017 Lyme Disease 64 0.046
486
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.046
487
P MVM001 Movement Disease 63 0.046
488
c SCL052 Scleroderma, Familial Progressive 61 0.046
489
GST033 Gestational Diabetes 61 0.046
490
PRT013 Portal Hypertension 59 0.046
491
MCS002 Mucositis 56 0.046
492
P RTN022 Retinal Vein Occlusion 53 0.046
493
P RTN018 Retinal Disease 53 0.046
494
SPN051 Spondylitis 51 0.046
495
HRT011 Heart Septal Defect 50 0.046
496
ENT004 Enthesopathy 49 0.046
497
VRC001 Varicocele 49 0.046
498
RYN005 Raynaud Phenomenon 47 0.046
499
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.046
500
LWC001 Low Compliance Bladder 43 0.046
501
P SCL057 Scoliosis, Isolated 1 41 0.046
502
INF009 Inflammatory Spondylopathy 31 0.046
503
c FTL067 Fetal Hemoglobin Quantitative Trait Locus 6 28 0.046
504
P GRF003 Graft-Versus-Host Disease 72 0.044
505
WRN001 Werner Syndrome 69 0.044
506
RCK004 Rickets 68 0.044
507
P PRP029 Porphyria 62 0.044
508
YLL002 Yellow Fever 61 0.044
509
ANT009 Antithrombin Iii Deficiency 59 0.044
510
P CND004 Candidiasis 58 0.044
511
P PRN023 Prion Disease 57 0.044
512
P ADL017 Adult T-Cell Leukemia 56 0.044
513
c FML035 Familial Hyperlipidemia 55 0.044
514
RHM028 Rheumatic Heart Disease 53 0.044
515
OCL069 Ocular Motor Apraxia 51 0.044
516
KRT009 Keratosis 51 0.044
517
CRN030 Coronary Stenosis 50 0.044
518
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.044
519
SBC016 Subacute Delirium 44 0.044
520
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.044
521
BCL014 B-Cell Growth Factor 35 0.044
522
HND015 Hand Skill, Relative 33 0.044
523
P AMY004 Amyloidosis 70 0.043
524
OBS002 Obsessive-Compulsive Disorder 68 0.043
525
P FLL037 Follicular Lymphoma 67 0.043
526
P MSC005 Muscular Dystrophy 66 0.043
527
P NRV007 Nervous System Disease 66 0.043
528
GT001 Gout 64 0.043
529
P FRD001 Friedreich Ataxia 64 0.043
530
PLG002 Plague 63 0.043
531
ACT119 Acute Promyelocytic Leukemia 63 0.043
532
ANR007 Anorexia Nervosa 63 0.043
533
P PLY014 Polycystic Kidney Disease 62 0.043
534
OST003 Osteonecrosis 61 0.043
535
P HMN010 Hemangioma 61 0.043
536
P TXP001 Toxoplasmosis 60 0.043
537
ETN001 Eating Disorder 60 0.043
538
HLC007 Helicobacter Pylori Infection 59 0.043
539
P ANP001 Anaplastic Large Cell Lymphoma 58 0.043
540
CNS004 Constipation 58 0.043
541
P PLY018 Polycythemia 56 0.043
542
GLC003 Glucose Intolerance 54 0.043
543
CLL003 Cellulitis 54 0.043
544
PNC001 Pancytopenia 54 0.043
545
PPT001 Peptic Esophagitis 52 0.043
546
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.043
547
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.043
548
c HPT015 Hepatitis D 49 0.043
549
P MLG074 Malignant Mesenchymoma 40 0.043
550
CHR178 Chromosomal Triplication 35 0.043
551
PRS131 Prostate Cancer/brain Cancer Susceptibility 25 0.043
552
c NRF023 Neurofibromatosis, Type Ii 80 0.041
553
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.041
554
P TBR001 Tuberous Sclerosis 70 0.041
555
ART016 Aortic Aneurysm 69 0.041
556
P MYC084 Mycobacterium Tuberculosis 1 68 0.041
557
c HMP029 Hemophilia a 67 0.041
558
KRT019 Keratitis, Hereditary 65 0.041
559
c DBT099 Diabetes Mellitus, Type I 65 0.041
560
P ADL010 Adult Respiratory Distress Syndrome 65 0.041
561
c BRN108 Branchiootic Syndrome 1 62 0.041
562
P VNT002 Ventricular Septal Defect 60 0.041
563
ING001 Inguinal Hernia 60 0.041
564
PRN019 Perinatal Necrotizing Enterocolitis 59 0.041
565
CCC001 Coccidioidomycosis 58 0.041
566
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.041
567
MTH009 Mouth Disease 56 0.041
568
HPT022 Hepatoblastoma 56 0.041
569
PLM010 Pulmonary Edema 54 0.041
570
P END047 Endophthalmitis 53 0.041
571
P MNC007 Monocytic Leukemia 53 0.041
572
c GLL024 Gallbladder Disease 1 53 0.041
573
PTH003 Pathologic Nystagmus 52 0.041
574
LNG031 Lung Benign Neoplasm 51 0.041
575
BCT004 Bacteriuria 49 0.041
576
c BCT013 Bacterial Pneumonia 48 0.041
577
RTN001 Retinal Vasculitis 47 0.041
578
HDN002 Head Injury 46 0.041
579
BNG077 Benign Idiopathic Neonatal Seizures 26 0.041
580
P FML011 Familial Adenomatous Polyposis 72 0.040
581
PRP027 Peripheral Vascular Disease 71 0.040
582
P ASP006 Aspergillosis 69 0.040
583
CRB037 Cerebral Palsy 69 0.040
584
ART002 Arts Syndrome 64 0.040
585
P RHB003 Rhabdomyosarcoma 63 0.040
586
BDD001 Budd-Chiari Syndrome 63 0.040
587
P ART023 Arthropathy 62 0.040
588
c WLM018 Wilms Tumor 5 61 0.040
589
P SJG008 Sjogren Syndrome 61 0.040
590
P SLP005 Sleep Disorder 59 0.040
591
P URT039 Urticaria 58 0.040
592
BRN056 Bronchopulmonary Dysplasia 57 0.040
593
P PLY011 Polycystic Ovary Syndrome 56 0.040
594
c ACT134 Acute Liver Failure 56 0.040
595
EMB004 Embryonal Carcinoma 56 0.040
596
AMN001 Amenorrhea 54 0.040
597
WST005 West Nile Virus 54 0.040
598
CLR030 Clear Cell Renal Cell Carcinoma 53 0.040
599
P PTS002 Ptosis 53 0.040
600
ALC009 Alcoholic Liver Cirrhosis 53 0.040
601
CLR109 Colorectal Adenocarcinoma 51 0.040
602
PST021 Postpartum Depression 50 0.040
603
FSC004 Fasciitis 50 0.040
604
CHL004 Cholelithiasis 49 0.040
605
LYM009 Lymphocytic Choriomeningitis 47 0.040
606
RFT001 Rift Valley Fever 47 0.040
607
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.040
608
ALB002 Albinism 46 0.040
609
GRN017 Granulocytopenia 44 0.040
610
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.040
611
P AVS003 Avascular Necrosis 42 0.040
612
PLY100 Polyploidy 40 0.040
613
LKP003 Leukoplakia 39 0.040
614
c OVR114 Ovarian Cancer 1 38 0.040
615
PHN003 Phenylketonuria 75 0.038
616
c MNN043 Meningioma, Familial 74 0.038
617
P TTR001 Tetralogy of Fallot 70 0.038
618
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.038
619
P SYS005 Systemic Scleroderma 68 0.038
620
P MYS003 Myasthenia Gravis 68 0.038
621
ALL003 Allergic Rhinitis 67 0.038
622
P CLC063 Celiac Disease 1 66 0.038
623
CLF027 Cleft Palate, Isolated 64 0.038
624
P TRC086 Trichohepatoenteric Syndrome 1 62 0.038
625
APP008 Appendicitis 61 0.038
626
HYD002 Hydronephrosis 60 0.038
627
STT001 Status Epilepticus 60 0.038
628
P BRN022 Bronchiectasis 59 0.038
629
GNG013 Gingivitis 59 0.038
630
RBS001 Rabies 58 0.038
631
CNT047 Contact Dermatitis 58 0.038
632
NWB001 Newborn Respiratory Distress Syndrome 58 0.038
633
HPT046 Hepatic Veno-Occlusive Disease 56 0.038
634
DBL002 Double Outlet Right Ventricle 56 0.038
635
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.038
636
BRN004 Brain Edema 56 0.038
637
MCL006 Macular Retinal Edema 55 0.038
638
P PMP001 Pemphigus 54 0.038
639
c CNT016 Central Retinal Vein Occlusion 53 0.038
640
IRD001 Iridocyclitis 53 0.038
641
PLS009 Plasma Cell Neoplasm 51 0.038
642
SPN019 Spondylolisthesis 51 0.038
643
ACT017 Acute Chest Syndrome 51 0.038
644
SCB001 Scabies 50 0.038
645
CRT013 Carotid Stenosis 50 0.038
646
P TMP001 Temporal Lobe Epilepsy 50 0.038
647
IMP004 Impetigo 49 0.038
648
NCR007 Necrotizing Fasciitis 48 0.038
649
HPR003 Heparin-Induced Thrombocytopenia 48 0.038
650
ACT084 Acute Stress Disorder 47 0.038
651
TST014 Testicular Cancer 46 0.038
652
KRT013 Keratolytic Winter Erythema 46 0.038
653
CWP001 Cowpox 46 0.038
654
NWC001 Newcastle Disease 45 0.038
655
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.038
656
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 44 0.038
657
FSC002 Fascioliasis 42 0.038
658
KRN001 Korean Hemorrhagic Fever 35 0.038
659
INF013 Inferior Myocardial Infarction 33 0.038
660
NRL016 Neural Tube Defects 82 0.036
661
P GLM040 Glioma Susceptibility 1 81 0.036
662
PFF001 Pfeiffer Syndrome 79 0.036
663
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.036
664
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.036
665
BHC003 Behcet Syndrome 71 0.036
666
MCC012 Mccune-Albright Syndrome 70 0.036
667
PLY001 Polycythemia Vera 69 0.036
668
KWS002 Kawasaki Disease 65 0.036
669
CLR108 Colorectal Adenoma 64 0.036
670
BRC012 Brucellosis 64 0.036
671
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.036
672
MNN042 Meningioma, Radiation-Induced 62 0.036
673
RTN017 Retinal Detachment 61 0.036
674
DCB001 Decubitus Ulcer 61 0.036
675
INT066 Interstitial Lung Disease 60 0.036
676
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.036
677
P HRD011 Hereditary Spherocytosis 60 0.036
678
P MYC008 Myocarditis 59 0.036
679
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.036
680
P BND020 Bone Disease 59 0.036
681
AVN001 Avian Influenza 59 0.036
682
INC002 Inclusion Body Myositis 58 0.036
683
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.036
684
PST028 Post-Traumatic Stress Disorder 58 0.036
685
P INT070 Intestinal Obstruction 58 0.036
686
CMP010 Complex Regional Pain Syndrome 58 0.036
687
FLR001 Filarial Elephantiasis 55 0.036
688
HYP005 Hypokalemia 55 0.036
689
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.036
690
P PLM034 Pulmonary Emphysema 55 0.036
691
KRT006 Keratoconjunctivitis 53 0.036
692
INT075 Intracranial Hypertension 53 0.036
693
NRT004 Neuritis 52 0.036
694
P HYP040 Hypospadias 51 0.036
695
P MMB011 Membranous Nephropathy 50 0.036
696
PLR007 Pleural Empyema 50 0.036
697
SPN021 Spinal Meningioma 50 0.036
698
HYP080 Hypogonadism 50 0.036
699
INT078 Intracranial Thrombosis 49 0.036
700
VTM002 Vitamin B12 Deficiency 48 0.036
701
SXL003 Sexual Disorder 47 0.036
702
CRD137 Cardiogenic Shock 47 0.036
703
P BRB001 Beriberi 46 0.036
704
c MLG068 Malignant Glioma 46 0.036
705
SMN007 Seminoma 43 0.036
706
P HYP265 Hypotonia 43 0.036
707
SNL007 Senile Cataract 42 0.036
708
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.036
709
SCR001 Secretory Meningioma 41 0.036
710
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.036
711
P NJM001 Nijmegen Breakage Syndrome 74 0.034
712
c EXD008 Exudative Vitreoretinopathy 1 71 0.034
713
SKN019 Skin Melanoma 68 0.034
714
P ESS003 Essential Thrombocythemia 68 0.034
715
c MCR129 Microvascular Complications of Diabetes 1 66 0.034
716
P CCK001 Cockayne Syndrome 66 0.034
717
c ART101 Aortic Valve Disease 2 65 0.034
718
c WLM013 Wilms Tumor 1 65 0.034
719
P THY023 Thymoma 65 0.034
720
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.034
721
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.034
722
P ANR048 Aniridia 1 63 0.034
723
HSH003 Hashimoto Thyroiditis 62 0.034
724
BRS099 Breast Ductal Carcinoma 62 0.034
725
BLD131 Bladder Urothelial Carcinoma 62 0.034
726
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.034
727
ALC006 Alcoholic Hepatitis 61 0.034
728
PNM001 Pneumocystosis 59 0.034
729
P DNG005 Dengue Virus 59 0.034
730
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.034
731
P EHL001 Ehlers-Danlos Syndrome 58 0.034
732
P MMP001 Mumps 58 0.034
733
CHL067 Cholecystitis 57 0.034
734
THY122 Thyroid Gland Cancer 57 0.034
735
TNS005 Tonsillitis 57 0.034
736
BLR008 Bilirubin Metabolic Disorder 57 0.034
737
P NRF002 Neurofibromatosis 56 0.034
738
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.034
739
LMB062 Limb Ischemia 55 0.034
740
P GRV001 Graves' Disease 55 0.034
741
P MYP006 Myopia 55 0.034
742
HMP005 Hemiplegia 55 0.034
743
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.034
744
DBT010 Diabetic Neuropathy 54 0.034
745
LYM040 Lymphoblastic Lymphoma 54 0.034
746
TRC023 Trichinosis 53 0.034
747
HRT012 Heart Valve Disease 53 0.034
748
P ACT008 Actinic Keratosis 53 0.034
749
DMY004 Demyelinating Disease 52 0.034
750
c THY107 Thymoma, Familial 52 0.034
751
HYP014 Hyperuricemia 52 0.034
752
LMY002 Leiomyoma 52 0.034
753
AVD001 Avoidant Personality Disorder 51 0.034
754
FDL002 Food Allergy 51 0.034
755
c SCN007 Secondary Hyperparathyroidism 51 0.034
756
c SVR005 Severe Pre-Eclampsia 50 0.034
757
CHR078 Chorioretinitis 50 0.034
758
PLC008 Placenta Disease 50 0.034
759
OPT003 Opiate Dependence 50 0.034
760
LPR001 Lepromatous Leprosy 50 0.034
761
ADR016 Adrenal Cortical Carcinoma 48 0.034
762
VTM033 Vitamin K Deficiency Bleeding 48 0.034
763
ADN001 Adenosine Deaminase Deficiency 47 0.034
764
AST006 Astigmatism 47 0.034
765
KRT002 Keratomalacia 47 0.034
766
c INH020 Inherited Metabolic Disorder 47 0.034
767
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.034
768
FCL012 Facial Paralysis 46 0.034
769
SYN036 Syncope 45 0.034
770
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.034
771
CRT015 Carotid Artery Occlusion 45 0.034
772
49X006 49, Xxxxy Syndrome 41 0.034
773
c HMG001 Hemoglobin C Disease 40 0.034
774
SCR015 Scarlet Fever 39 0.034
775
CRV045 Cervical Intraepithelial Neoplasia 39 0.034
776
AML001 Amelanotic Melanoma 39 0.034
777
SPL006 Splenic Infarction 38 0.034
778
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.034
779
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 35 0.034
780
PYR009 Pyridoxine Deficiency Anemia 34 0.034
781
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.034
782
TCK004 Tick Infestation 28 0.034
783
NNS059 Non-Syndromic Limb Reduction Defect 7 0.034
784
c HMC039 Hemochromatosis, Type 1 74 0.032
785
P CRN037 Craniosynostosis 68 0.032
786
P FRN006 Frontotemporal Dementia 68 0.032
787
PNC129 Pancreatic Adenocarcinoma 68 0.032
788
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.032
789
P MTR014 Motor Neuron Disease 65 0.032
790
HRL003 Hurler Syndrome 65 0.032
791
P LMY004 Leiomyosarcoma 63 0.032
792
CTN007 Cutaneous Leishmaniasis 62 0.032
793
PSR001 Psoriatic Arthritis 61 0.032
794
SDD001 Sudden Infant Death Syndrome 61 0.032
795
ACN002 Acanthosis Nigricans 60 0.032
796
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.032
797
P SNS001 Sensorineural Hearing Loss 60 0.032
798
INS001 Insulinoma 60 0.032
799
P OPT006 Optic Nerve Disease 60 0.032
800
SPP011 Suppression of Tumorigenicity 12 59 0.032
801
P MLN069 Melanoma, Uveal 59 0.032
802
GRD007 Grade Iii Astrocytoma 59 0.032
803
P GLL022 Guillain-Barre Syndrome 59 0.032
804
c DWL002 Dowling-Degos Disease 1 58 0.032
805
P OPT009 Optic Neuritis 57 0.032
806
c CHL119 Cholangitis, Primary Sclerosing 57 0.032
807
JPN002 Japanese Encephalitis 57 0.032
808
P PYL005 Pyelonephritis 56 0.032
809
PNM008 Pneumothorax 56 0.032
810
LST001 Listeriosis 56 0.032
811
ALL010 Allergic Contact Dermatitis 56 0.032
812
P PSD015 Pseudohypoparathyroidism 56 0.032
813
PRT002 Paratyphoid Fever 55 0.032
814
HYP060 Hyperinsulinism 54 0.032
815
P ALP008 Alopecia 54 0.032
816
THR013 Thoracic Outlet Syndrome 54 0.032
817
PRC013 Pericarditis 54 0.032
818
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.032
819
HYP706 Hypermobile Ehlers-Danlos Syndrome 53 0.032
820
P EPD016 Epidermolysis Bullosa 53 0.032
821
OCL006 Ocular Hypertension 53 0.032
822
CYS005 Cysticercosis 53 0.032
823
CLF001 Cleft Lip 53 0.032
824
PRP016 Paraplegia 52 0.032
825
CLC001 Calciphylaxis 51 0.032
826
ESP002 Esophageal Varix 51 0.032
827
STR008 Strongyloidiasis 51 0.032
828
P MTR003 Mitral Valve Stenosis 50 0.032
829
P MYT002 Myotonic Dystrophy 49 0.032
830
TRT020 Tritanopia 49 0.032
831
MNN009 Meningoencephalitis 49 0.032
832
P SCL009 Sclerosing Cholangitis 48 0.032
834
P BCT020 Bacteremia 2 44 0.032
835
SPC005 Speech Disorder 43 0.032
836
EPC002 Epicondylitis 41 0.032
837
MLY001 Molybdenum Cofactor Deficiency 40 0.032
838
ADR004 Adrenal Cortical Adenocarcinoma 39 0.032
839
ORL012 Oral Leukoplakia 39 0.032
840
P DVL012 Developmental Dysplasia of the Hip 1 38 0.032
841
PRM329 Premature Aging 35 0.032
842
ATX010 Ataxia Neuropathy Spectrum 34 0.032
843
ACT064 Acute Necrotizing Encephalitis 33 0.032
844
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.032
845
BLD137 Blood Group--Ahonen 16 0.032
846
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.030
847
FCT007 Factor Vii Deficiency 67 0.030
848
P PRP003 Porphyria Cutanea Tarda 67 0.030
849
P HYD006 Hydrocephalus 66 0.030
850
c FML001 Familial Atrial Fibrillation 65 0.030
851
P ART005 Arteriovenous Malformation 65 0.030
852
P CNJ013 Conjunctivitis 65 0.030
853
DMN031 Dementia, Lewy Body 65 0.030
854
IRR002 Irritable Bowel Syndrome 65 0.030
855
KRN002 Kearns-Sayre Syndrome 63 0.030
856
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.030
857
RTN209 Retinoschisis 1, X-Linked, Juvenile 62 0.030
858
P SPN046 Spinal Muscular Atrophy 62 0.030
859
BLL006 Bullous Pemphigoid 62 0.030
860
NRM001 Neuromyelitis Optica 61 0.030
861
VRL011 Viral Infectious Disease 61 0.030
862
P AXN002 Axenfeld-Rieger Syndrome 59 0.030
863
DCT002 Ductal Carcinoma in Situ 59 0.030
864
LYM027 Lymphopenia 58 0.030
865
MXD005 Mixed Connective Tissue Disease 58 0.030
866
GLS018 Glass Syndrome 57 0.030
867
P PLV020 Pelvic Organ Prolapse 57 0.030
868
P MYM013 Moyamoya Disease 1 57 0.030
869
CHK001 Chikungunya 57 0.030
870
c MST023 Mesothelioma, Malignant 57 0.030
871
TCK001 Tick-Borne Encephalitis 56 0.030
872
GNR004 Generalized Anxiety Disorder 56 0.030
873
FND002 Fundus Dystrophy 55 0.030
874
VSC003 Visceral Leishmaniasis 55 0.030
875
c BCT007 Bacterial Meningitis 55 0.030
876
P PTT006 Pituitary Adenoma 55 0.030
877
CHR100 Chronic Ulcer of Skin 55 0.030
878
P STR020 Strabismus 55 0.030
879
SYN007 Synovitis 54 0.030
880
HLL004 Hellp Syndrome 54 0.030
881
P HML001 Hemolytic-Uremic Syndrome 53 0.030
882
PRP080 Peripheral Artery Disease 53 0.030
883
P INT068 Intestinal Disease 53 0.030
884
STT041 Stuttering 52 0.030
885
TRC096 Trichothiodystrophy 52 0.030
886
P DDN001 Duodenal Ulcer 52 0.030
887
SRS001 Serous Cystadenocarcinoma 52 0.030
888
P TRT010 Teratoma 52 0.030
889
c INH030 Inherited Retinal Disorder 51 0.030
890
THR004 Thrombocytosis 51 0.030
891
ILS001 Ileus 51 0.030
892
BLL003 Bell's Palsy 51 0.030
893
AZS001 Azoospermia 50 0.030
894
CCN002 Cocaine Abuse 49 0.030
895
RYN001 Raynaud Disease 48 0.030
896
FBR009 Fibrous Dysplasia 48 0.030
897
PLC007 Placental Abruption 48 0.030
898
ASB001 Asbestosis 47 0.030
899
CHR074 Choriocarcinoma 47 0.030
900
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.030
901
GST010 Gestational Trophoblastic Neoplasm 46 0.030
902
c DRR009 Diarrhea 6 46 0.030
903
EPD015 Epidemic Typhus 45 0.030
904
CYN002 Cyanosis, Transient Neonatal 45 0.030
905
HPT004 Hepatic Coma 45 0.030
906
DWR001 Dwarfism 44 0.030
907
c HYP272 Hypercholesterolemia, Familial, 3 44 0.030
908
RFR003 Refractive Error 43 0.030
909
MST004 Mast Cell Neoplasm 42 0.030
910
MCH006 Mechanical Strabismus 42 0.030
911
CLR033 Color Vision Deficiency 41 0.030
912
P OGC005 Oguchi Disease 39 0.030
913
ADP007 Adie Pupil 39 0.030
914
EXT007 Extracutaneous Mastocytoma 38 0.030
915
PRG008 Paragonimiasis 38 0.030
916
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.030
917
HRN029 Hearing Loss, Noise-Induced 37 0.030
918
PLC002 Plica Syndrome 36 0.030
919
c CHR064 Chronic Monocytic Leukemia 33 0.030
920
CND006 Candida Glabrata 32 0.030
921
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.030
922
ASB003 Asbestos Intoxication 26 0.030
923
HRP008 Herpes Simiae 25 0.030
924
HML018 Homologous Wasting Disease 22 0.030
925
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 20 0.030
926
BRN028 Brain Cancer 74 0.028
927
ACR007 Acromegaly 71 0.028
928
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.028
929
P ANG001 Angelman Syndrome 69 0.028
930
THY111 Thyroid Carcinoma, Familial Medullary 67 0.028
931
FLL027 Fallopian Tube Carcinoma 67 0.028
932
LPT001 Leptospirosis 66 0.028
933
c PSD108 Pseudohypoparathyroidism, Type Ia 66 0.028
934
LNG039 Lung Squamous Cell Carcinoma 66 0.028
935
P VNW001 Von Willebrand's Disease 65 0.028
936
APN008 Apnea, Obstructive Sleep 64 0.028
937
NRF007 Neurofibroma 64 0.028
938
END041 Endometrial Adenocarcinoma 63 0.028
939
CHR063 Chronic Mucocutaneous Candidiasis 63 0.028
940
CRC021 Carcinosarcoma 62 0.028
941
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.028
942
P BNG030 Benign Ependymoma 60 0.028
943
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.028
944
HPT019 Hepatic Encephalopathy 60 0.028
945
QFV001 Q Fever 60 0.028
946
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.028
947
P PLY006 Polydactyly 59 0.028
948
c PRM005 Primary Hyperparathyroidism 58 0.028
949
ADR005 Adrenal Carcinoma 58 0.028
950
HMR039 Hemorrhage, Intracerebral 57 0.028
951
AYM001 Ayme-Gripp Syndrome 57 0.028
952
SCH003 Schizophreniform Disorder 56 0.028
953
PRS047 Prostatitis 56 0.028
954
SBC001 Subacute Sclerosing Panencephalitis 56 0.028
955
SLC006 Silicosis 56 0.028
956
ATR057 Atrioventricular Block 55 0.028
957
ORP003 Oropharynx Cancer 55 0.028
958
NRN004 Neuroendocrine Tumor 55 0.028
959
P ALP106 Alport Syndrome 1, X-Linked 55 0.028
960
P VNS003 Venous Insufficiency 55 0.028
961
P DBT005 Diabetes Insipidus 55 0.028
962
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.028
963
GLS001 Gliosarcoma 54 0.028
964
GST037 Gastroparesis 54 0.028
965
P ICH004 Ichthyosis 54 0.028
966
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.028
967
CLL010 Cellular Ependymoma 54 0.028
968
CRM001 Crimean-Congo Hemorrhagic Fever 53 0.028
969
P TCD001 Tic Disorder 53 0.028
970
P RNL017 Renal Oncocytoma 53 0.028
971
ECH003 Echinococcosis 53 0.028
972
GTR002 Goiter 53 0.028
973
CHR073 Choreatic Disease 52 0.028
974
OST011 Osteomalacia 52 0.028
975
THY030 Thyroid Gland Disease 52 0.028
976
c ACT135 Acute Graft Versus Host Disease 52 0.028
977
MYL001 Myelitis 51 0.028
978
P LCT001 Lactic Acidosis 51 0.028
979
CYS014 Cystadenocarcinoma 51 0.028
980
CRV040 Cervix Carcinoma 51 0.028
981
PYD002 Pyoderma 50 0.028
982
P PNV001 Panuveitis 50 0.028
983
MTB004 Metabolic Acidosis 50 0.028
984
SCR037 Sucrase-Isomaltase Deficiency, Congenital 50 0.028
985
KRT001 Keratoconjunctivitis Sicca 49 0.028
986
MCR004 Macroglobulinemia 49 0.028
987
P CMP008 Compartment Syndrome 49 0.028
988
HYP043 Hyperandrogenism 48 0.028
989
RGH001 Right Bundle Branch Block 48 0.028
990
SCL003 Social Phobia 48 0.028
991
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.028
992
CHL147 Chlamydia Pneumonia 48 0.028
993
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.028
994
MLK006 Milk Allergy 48 0.028
995
SYM002 Sympathetic Ophthalmia 47 0.028
996
PRP007 Priapism 47 0.028
997
DRY001 Dry Eye Syndrome 47 0.028
998
RTC005 Reticulosarcoma 47 0.028
999
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.028
1000
ATN005 Autonomic Dysfunction 46 0.028
1001
RTN020 Retinal Vascular Disease 46 0.028
1002
P MTH007 Methemoglobinemia 46 0.028
1003
OBS003 Obsessive-Compulsive Personality Disorder 46 0.028
1004
TRT001 Teratocarcinoma 45 0.028
1005
HMR023 Hemorrhagic Cystitis 45 0.028
1006
CYS019 Cystathioninuria 45 0.028
1007
c SPR009 Sporadic Breast Cancer 45 0.028
1008
c DRM054 Dermatitis, Atopic, 2 44 0.028
1009
DMP001 Dumping Syndrome 44 0.028
1010
P MJR007 Major Affective Disorder 1 43 0.028
1011
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.028
1012
PRM020 Premenstrual Tension 40 0.028
1013
SCR011 Scrapie 39 0.028
1014
CVT001 Cavitary Optic Disc Anomalies 38 0.028
1015
ATM052 Autoimmune Disease 1 37 0.028
1016
STR077 Streptococcal Toxic-Shock Syndrome 37 0.028
1017
CHL013 Cholecystolithiasis 37 0.028
1018
c HMG004 Hemoglobin D Disease 36 0.028
1019
SPL009 Splenic Sequestration 35 0.028
1020
STC004 Stachybotrys Chartarum 34 0.028
1021
P VSC018 Visceral Steatosis 33 0.028
1022
BWN006 Bowen's Disease 32 0.028
1023
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 32 0.028
1024
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.028
1025
c TBR025 Tuberous Sclerosis 1 77 0.026
1026
P FML018 Familial Mediterranean Fever 73 0.026
1027
MSC157 Muscular Dystrophy, Duchenne Type 72 0.026
1028
MYL005 Myelofibrosis 70 0.026
1029
P FRG001 Fragile X Syndrome 70 0.026
1030
MNT001 Mantle Cell Lymphoma 69 0.026
1031
MLD001 Melioidosis 68 0.026
1032
P CHR012 Chronic Granulomatous Disease 67 0.026
1033
P MLG056 Malignant Hyperthermia 67 0.026
1034
c FML021 Familial Hypercholesterolemia 66 0.026
1035
AND002 Androgen Insensitivity Syndrome 66 0.026
1036
SVR066 Severe Combined Immunodeficiency, X-Linked 66 0.026
1037
MRK001 Merkel Cell Carcinoma 65 0.026
1038
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.026
1039
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.026
1040
c JVN010 Juvenile Rheumatoid Arthritis 64 0.026
1041
HYP020 Hyperprolactinemia 64 0.026
1042
P GCH001 Gaucher's Disease 63 0.026
1043
P SHR029 Short Syndrome 63 0.026
1044
HYP780 Hypoadrenocorticism, Familial 63 0.026
1045
c OPT053 Optic Atrophy 1 63 0.026
1046
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.026
1047
LSC001 Lesch-Nyhan Syndrome 62 0.026
1048
P ORT004 Orthostatic Intolerance 62 0.026
1049
P INT143 Interstitial Cystitis 61 0.026
1050
INT002 Intermittent Claudication 61 0.026
1051
NRL005 Neurilemmoma 60 0.026
1052
PTN001 Patent Foramen Ovale 60 0.026
1053
IDP011 Idiopathic Interstitial Pneumonia 59 0.026
1054
PRT058 Pure Autonomic Failure 59 0.026
1055
P LYM033 Lymphoproliferative Syndrome 59 0.026
1056
c LTN004 Late-Onset Retinal Degeneration 59 0.026
1057
IRN001 Iron Deficiency Anemia 59 0.026
1058
MCR013 Microphthalmia 57 0.026
1059
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.026
1060
P MTC069 Mitochondrial Disorders 56 0.026
1061
SML019 Smallpox 56 0.026
1062
P PNM006 Pneumoconiosis 56 0.026
1063
AND020 Androgen Insensitivity, Partial 56 0.026
1064
AMB001 Amebiasis 55 0.026
1065
PLV003 Pelvic Inflammatory Disease 55 0.026
1066
NPH009 Nephrolithiasis 55 0.026
1067
CRC006 Carcinoid Syndrome 55 0.026
1068
PRN001 Purine Nucleoside Phosphorylase Deficiency 55 0.026
1069
HRY003 Hairy Cell Leukemia 55 0.026
1070
P CNG010 Congenital Stationary Night Blindness 54 0.026
1071
FRZ001 Frozen Shoulder 53 0.026
1072
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.026
1073
FCT005 Factor Xiii Deficiency 52 0.026
1074
LGN006 Legionnaire Disease 52 0.026
1075
ART074 Aortic Dissection 52 0.026
1076
P OVR049 Ovarian Disease 52 0.026
1077
FCT001 Factor Viii Deficiency 51 0.026
1078
c PNC106 Pancreatic Agenesis 1 51 0.026