Search results for Protein C

5786 hits were found for Protein C

# Family MCID Name MIFTS Score
1
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 31 7.180
2
c THR082 Thrombophilia Due to Activated Protein C Resistance 60 6.808
3
PRT011 Protein C Deficiency 45 6.698
4
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 27 4.337
5
c SRF003 Surfactant Metabolism Dysfunction, Pulmonary, 2 36 4.072
6
FCT013 Factor V Leiden Thrombophilia 24 3.887
7
FCT030 Factor V and Factor Viii, Combined Deficiency of, with Normal Protein C and Protein C Inhibitor 7 2.463
8
CRC043 C-Reactive Protein, Serum Level of, Quantitative Trait Locus 1 6 1.742
9
c HPT073 Hepatitis C Virus 70 0.933
10
c HPT001 Hepatitis C 63 0.925
11
P HPT021 Hepatitis 67 0.490
12
HLX001 Helix Syndrome 47 0.480
13
P BRS047 Breast Cancer 96 0.421
14
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.419
15
PRT037 Pertussis 65 0.412
16
INH023 Inherited Cancer-Predisposing Syndrome 46 0.392
17
P LVR013 Liver Disease 68 0.376
18
LVR012 Liver Cirrhosis 63 0.371
19
P HPT023 Hepatocellular Carcinoma 100 0.355
20
P CLR023 Colorectal Cancer 98 0.336
21
P NRB001 Neuroblastoma 71 0.334
22
c HPT016 Hepatitis B 59 0.330
23
HMN044 Human Immunodeficiency Virus Type 1 71 0.328
24
P ALZ034 Alzheimer Disease 88 0.307
25
P ADN016 Adenocarcinoma 64 0.299
26
P RTN024 Retinoblastoma 72 0.295
27
P KDN018 Kidney Disease 70 0.293
28
ATM095 Autoimmune Disease 61 0.289
29
P LKM002 Leukemia 66 0.286
30
INS024 Insulin-Like Growth Factor I 79 0.285
31
P HRP006 Herpes Simplex 65 0.285
32
c FML008 Familial Retinoblastoma 53 0.283
33
P LNG032 Lung Cancer 97 0.278
34
VCC001 Vaccinia 49 0.274
35
CHL014 Cholera 55 0.272
36
48X005 48,xyyy 39 0.269
37
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.267
38
P OVR042 Ovarian Cancer 89 0.265
39
IMM167 Immune Deficiency Disease 78 0.261
40
P GLM045 Glioma 63 0.256
41
P LYM118 Lymphoma 68 0.256
42
ISC004 Ischemia 60 0.251
43
c VRL010 Viral Hepatitis 51 0.249
44
SQM006 Squamous Cell Carcinoma 60 0.247
45
P PRS040 Prostate Cancer 97 0.247
46
GLL048 Glial Tumor 45 0.247
47
P GST053 Gastric Cancer 83 0.246
48
c LKM061 Leukemia, Acute Myeloid 83 0.245
49
GLB015 Glioblastoma Multiforme 75 0.244
50
c HYP836 Hypercholesterolemia, Familial, 1 72 0.244
51
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.243
52
c HPT003 Hepatitis a 63 0.241
53
P PRN023 Prion Disease 57 0.240
54
c THR092 Thrombophilia Due to Thrombin Defect 73 0.238
55
P BCL017 B-Cell Lymphoma 58 0.237
56
c CHR684 Chronic Kidney Disease 66 0.237
57
P BLD134 Bladder Cancer 78 0.237
58
P MYL006 Myeloid Leukemia 60 0.237
59
P PNC035 Pancreatic Cancer 84 0.236
60
ATH013 Atherosclerosis Susceptibility 66 0.234
61
CYT002 Cytokine Deficiency 44 0.234
62
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.232
63
P ENC018 Encephalopathy 61 0.231
64
P LYM031 Lymphocytic Leukemia 55 0.230
65
P HYP061 Hypertrophic Cardiomyopathy 66 0.227
66
P ATX030 Ataxia-Telangiectasia 83 0.224
67
P PHC003 Pheochromocytoma 71 0.223
68
P CRN300 Coronary Heart Disease 1 63 0.223
69
ADN018 Adenoma 58 0.221
70
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.221
71
OST159 Osteogenic Sarcoma 66 0.219
72
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.216
73
STM007 Stomatitis 49 0.216
74
47X002 47,xyy 49 0.214
75
P LYN001 Lynch Syndrome 77 0.214
76
P LTR001 Lateral Sclerosis 53 0.214
77
FTT001 Fatty Liver Disease 61 0.214
78
CHL123 Chlamydia 59 0.212
79
P DRR001 Diarrhea 57 0.212
80
MLN008 Melanoma 69 0.210
81
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.210
82
c ATR087 Atrial Standstill 1 74 0.209
83
c SYS001 Systemic Lupus Erythematosus 86 0.209
84
P VSC007 Vascular Disease 63 0.208
85
P GLM007 Glomerulonephritis 57 0.207
86
HYP066 Hyperglycemia 61 0.207
87
ALL026 Allergic Hypersensitivity Disease 64 0.205
88
TTN003 Tetanus 64 0.204
89
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.203
90
END030 End Stage Renal Failure 58 0.202
91
TXC005 Toxic Shock Syndrome 61 0.202
92
CYS001 Cystic Fibrosis 80 0.200
93
BCT022 Bacterial Infectious Disease 56 0.198
94
P CRN018 Coronary Artery Anomaly 63 0.197
95
HMP009 Haemophilus Influenzae 42 0.197
96
P MSC005 Muscular Dystrophy 66 0.196
97
c SML038 Small Cell Cancer of the Lung 65 0.196
98
P AMY004 Amyloidosis 70 0.196
99
c FNC027 Fanconi Anemia, Complementation Group a 81 0.196
100
c PRC016 Pre-Eclampsia 63 0.195
101
MYL069 Myeloma, Multiple 85 0.194
102
SCR011 Scrapie 38 0.191
103
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.191
104
c MCR120 Microvascular Complications of Diabetes 7 47 0.190
105
c MCR113 Microvascular Complications of Diabetes 3 52 0.190
106
c MCR130 Microvascular Complications of Diabetes 6 41 0.190
107
c MCR133 Microvascular Complications of Diabetes 4 41 0.190
108
PRT014 Protein S Deficiency 50 0.190
109
BNR002 Bone Resorption Disease 48 0.189
110
LPD008 Lipid Metabolism Disorder 62 0.187
111
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.187
112
LNG099 Lung Disease 61 0.187
113
P PRD008 Periodontitis 62 0.187
114
HYP266 Hypoxia 56 0.185
115
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.184
116
PRP030 Purpura 55 0.184
117
P DNG005 Dengue Virus 57 0.184
118
P MYP004 Myopathy 64 0.184
119
SVR004 Severe Combined Immunodeficiency 73 0.184
120
P INF038 Influenza 68 0.183
121
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.182
122
P TCL004 T-Cell Leukemia 47 0.182
123
ART140 Arteries, Anomalies of 53 0.182
124
ALL014 Allergic Encephalomyelitis 39 0.181
125
THY029 Thyroid Carcinoma 59 0.179
126
P ENC004 Encephalitis 61 0.179
127
LSH001 Leishmaniasis 63 0.179
128
P KLZ004 Kala-Azar 1 41 0.179
129
THR024 Thrombosis 56 0.179
130
P INF037 Inflammatory Bowel Disease 56 0.179
131
c DLT002 Dilated Cardiomyopathy 79 0.177
132
P HRT032 Heart Disease 75 0.177
133
c SVR001 Severe Acute Respiratory Syndrome 55 0.177
134
P LNG064 Lung Cancer Susceptibility 3 77 0.176
135
P RHM011 Rheumatoid Arthritis 80 0.176
136
MSL001 Measles 61 0.175
137
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.175
138
P THR014 Thrombocytopenia 68 0.174
139
DPH001 Diphtheria 60 0.174
140
P NRP001 Neuropathy 56 0.174
141
P NTR004 Neutropenia 63 0.173
142
P CTR002 Cataract 60 0.173
143
CRV035 Cervical Cancer 76 0.173
144
DFC004 Deficiency Anemia 75 0.171
145
ARG004 Argyria 28 0.170
146
PLY150 Polykaryocytosis Inducer 31 0.169
147
P VSC011 Vasculitis 62 0.169
148
P THR015 Thrombophilia 50 0.169
149
ADR040 Adrenal Gland Pheochromocytoma 46 0.169
150
P NSP012 Nasopharyngeal Carcinoma 67 0.169
151
BRK010 Burkitt Lymphoma 67 0.169
152
P MYC007 Myocardial Infarction 70 0.167
153
P LKM062 Leukemia, Acute Lymphoblastic 68 0.167
154
VRL011 Viral Infectious Disease 61 0.167
155
P MSC003 Muscular Atrophy 52 0.167
156
P PSR002 Psoriasis 62 0.166
158
P NPH012 Nephrotic Syndrome 63 0.165
159
P DBT009 Diabetes Mellitus 64 0.164
160
P HNT016 Huntington Disease 71 0.164
161
DWN001 Down Syndrome 70 0.164
162
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.164
163
ERY051 Erythroleukemia, Familial 56 0.164
164
PPL052 Papillomatosis, Confluent and Reticulated 34 0.163
165
P LPS004 Lupus Erythematosus 61 0.161
166
PST011 Pustulosis of Palm and Sole 52 0.161
167
MTH009 Mouth Disease 56 0.159
168
P HYP086 Hypothyroidism 68 0.159
169
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.158
170
c ACT075 Acute Myocardial Infarction 56 0.157
171
END057 Endometrial Cancer 74 0.157
172
CRY004 Cryoglobulinemia 49 0.156
173
P CRD246 Cardiovascular System Disease 56 0.156
174
P AST007 Astrocytoma 50 0.155
175
ESP021 Esophageal Cancer 90 0.154
176
KPS004 Kaposi Sarcoma 75 0.154
177
OST012 Osteoarthritis 78 0.154
178
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.153
179
CRT072 Creutzfeldt-Jakob Disease 69 0.152
180
P MNN013 Meningitis 65 0.152
181
CNG034 Congestive Heart Failure 70 0.152
182
P LNG028 Long Qt Syndrome 65 0.152
183
P THL005 Thalassemia 60 0.152
184
P TBR001 Tuberous Sclerosis 70 0.152
185
PRT038 Protein-Energy Malnutrition 54 0.152
186
DRM006 Dermatitis 61 0.151
187
CRH001 Crohn's Disease 74 0.151
188
c ACT027 Acute Pancreatitis 59 0.151
189
ULC004 Ulcerative Colitis 73 0.150
190
LGH007 Leigh Syndrome 70 0.150
191
AGN016 Aging 56 0.150
192
BRN071 Brain Injury 49 0.150
193
SRC014 Sarcoma 65 0.150
194
ACQ007 Acquired Immunodeficiency Syndrome 60 0.150
195
GST045 Gastroenteritis 59 0.149
196
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 65 0.149
197
STR067 Stroke, Ischemic 80 0.149
198
c TBR025 Tuberous Sclerosis 1 76 0.148
199
HYP056 Hypoglycemia 66 0.147
200
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 61 0.147
201
P FBR017 Fibrosarcoma 56 0.147
202
IDP011 Idiopathic Interstitial Pneumonia 63 0.147
203
c ACT073 Acute Leukemia 58 0.146
204
HYP060 Hyperinsulinism 54 0.146
205
SPP010 Suppressor of Tumorigenicity 3 51 0.146
206
c CNG411 Congenital Disorder of Glycosylation, Type in 68 0.146
207
P GST044 Gastritis 55 0.146
208
MLR004 Malaria 80 0.146
209
P PLM036 Pulmonary Fibrosis 61 0.145
210
TLN003 Telangiectasis 51 0.145
211
P HMP007 Hemophilia 51 0.145
212
c LKM071 Leukemia, Chronic Lymphocytic 79 0.145
213
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.144
214
ORL015 Oral Squamous Cell Carcinoma 43 0.144
215
P FRN006 Frontotemporal Dementia 70 0.144
216
VSL002 Visual Epilepsy 58 0.144
217
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.143
218
c LKM063 Leukemia, Chronic Myeloid 71 0.142
219
c PCH010 Pachyonychia Congenita 3 43 0.142
220
PRT019 Protein-Losing Enteropathy 46 0.142
221
INT007 Intermediate Coronary Syndrome 55 0.141
222
PRT036 Peritonitis 65 0.140
223
P CHR071 Charcot-Marie-Tooth Disease 64 0.140
224
SPN035 Spindle Cell Sarcoma 51 0.139
225
NWC001 Newcastle Disease 44 0.139
226
CLT003 Colitis 62 0.139
227
GST019 Gastrointestinal Stromal Tumor 76 0.139
228
SKN016 Skin Disease 63 0.139
229
DFF005 Diffuse Large B-Cell Lymphoma 56 0.139
230
P MCR115 Microvascular Complications of Diabetes 5 66 0.138
231
P PRM011 Primary Ciliary Dyskinesia 69 0.138
232
c HYP595 Hypertension, Essential 84 0.138
233
LYM133 Lymphoma, Hodgkin, Classic 69 0.137
234
LYM017 Lyme Disease 63 0.137
235
TRM010 Traumatic Brain Injury 53 0.137
236
PPL022 Papilloma 54 0.137
237
DPR016 Depression 63 0.136
238
CRB039 Cerebrovascular Disease 69 0.135
239
CRB004 Cerebral Artery Occlusion 44 0.135
240
P LBR001 Leber Congenital Amaurosis 67 0.135
241
P JBR020 Joubert Syndrome 1 72 0.135
242
P INS002 in Situ Carcinoma 52 0.135
243
P PNM007 Pneumonia 68 0.135
244
P HYP750 Hypertriglyceridemia, Familial 61 0.135
245
IRN002 Iron Metabolism Disease 57 0.135
246
MSC157 Muscular Dystrophy, Duchenne Type 71 0.134
247
c NMN015 Niemann-Pick Disease, Type C1 68 0.134
248
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.134
249
SPN186 Spinal Cord Injury 60 0.134
250
RCK004 Rickets 69 0.134
251
ATS010 Autosomal Recessive Disease 48 0.134
252
P ART022 Arthritis 70 0.133
253
P DRM053 Dermatitis, Atopic 66 0.133
254
P INF032 Infertility 57 0.133
255
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.133
256
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.133
257
P SYP003 Syphilis 59 0.133
258
P RTN016 Retinal Degeneration 53 0.132
259
SQM002 Squamous Cell Papilloma 42 0.132
260
GLC003 Glucose Intolerance 54 0.132
261
HMS001 Hemosiderosis 54 0.132
262
NSS002 Neisseria Meningitidis Infection 46 0.132
263
P NMN002 Niemann-Pick Disease 60 0.132
264
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.131
265
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.131
266
SCH014 Schistosomiasis 56 0.131
267
P ZLL001 Zellweger Syndrome 64 0.131
268
P BRG001 Brugada Syndrome 70 0.129
269
P PRK057 Parkinson Disease, Late-Onset 76 0.129
270
P BRD002 Bardet-Biedl Syndrome 66 0.128
271
DSS009 Disseminated Intravascular Coagulation 57 0.128
272
P RTN008 Retinitis Pigmentosa 77 0.128
273
P HML002 Hemolytic Anemia 62 0.128
274
PLM001 Pulmonary Tuberculosis 70 0.128
275
P PRP019 Peripheral Nervous System Disease 57 0.128
276
c FML346 Familial Adenomatous Polyposis 1 70 0.128
277
CHL068 Cholestasis 60 0.128
278
AST005 Asthma 77 0.128
279
GST040 Gastric Adenocarcinoma 70 0.127
280
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 54 0.127
281
P RRH023 Rare Hereditary Hemochromatosis 41 0.127
282
P HYP098 Hypereosinophilic Syndrome 66 0.127
283
P MLT020 Multiple Sclerosis 72 0.127
284
P PRP034 Purpura Fulminans 42 0.127
285
NTR005 Nutritional Deficiency Disease 61 0.126
286
BRN024 Bronchitis 68 0.126
287
MNT002 Mental Depression 57 0.126
288
URM002 Uremia 49 0.126
289
MYL009 Myelodysplastic Syndrome 70 0.126
290
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.126
291
P SKN015 Skin Carcinoma 67 0.125
292
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.125
293
P BPL003 Bipolar Disorder 56 0.125
294
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.124
295
WRN001 Werner Syndrome 69 0.124
296
ANX004 Anoxia 42 0.124
297
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.123
298
c MJR024 Major Affective Disorder 9 41 0.123
299
c MJR022 Major Affective Disorder 8 38 0.123
300
FML089 Familial Thoracic Aortic Aneurysm and Dissection 66 0.123
301
INS001 Insulinoma 60 0.123
302
P OST002 Osteoporosis 73 0.122
303
P CRD119 Cardiac Arrest 67 0.122
304
c CRD080 Cardiomyopathy, Dilated, 1g 37 0.122
305
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.122
306
P GLM040 Glioma Susceptibility 1 81 0.122
307
OVR094 Ovarian Epithelial Cancer 38 0.122
308
CHC001 Chickenpox 60 0.122
309
P ALC033 Alcohol Use Disorder 58 0.121
310
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.121
311
FDL002 Food Allergy 49 0.121
312
P PLY014 Polycystic Kidney Disease 59 0.121
313
ENT011 Enterocolitis 50 0.120
314
P PNC044 Pancreatitis 61 0.120
315
CHL065 Cholangiocarcinoma 67 0.120
316
MSC007 Muscle Hypertrophy 63 0.120
317
P PLM037 Pulmonary Hypertension 68 0.120
318
P END044 Endometriosis 62 0.120
319
c NRF024 Neurofibromatosis, Type I 71 0.119
320
c MSC179 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 10 35 0.119
321
NRR001 Neuroretinitis 43 0.119
322
RTN023 Retinitis 46 0.119
323
ACT119 Acute Promyelocytic Leukemia 63 0.119
324
INT079 Intrahepatic Cholangiocarcinoma 50 0.119
325
HRW001 Hair Whorl 36 0.119
326
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 63 0.118
327
MRF001 Marfan Syndrome 75 0.118
328
ANG054 Angina Pectoris 66 0.118
329
P ECL001 Eclampsia 51 0.117
330
c PRM038 Primary Agammaglobulinemia 43 0.117
331
EMB004 Embryonal Carcinoma 57 0.117
332
P HYP076 Hyperthyroidism 55 0.117
333
c ATS007 Autism Spectrum Disorder 67 0.117
334
HYP781 Hypoascorbemia 50 0.117
335
P RSP003 Respiratory Failure 74 0.117
336
P SZR006 Seizure Disorder 58 0.117
337
c WLM018 Wilms Tumor 5 62 0.117
338
P LCH002 Lichen Planus 54 0.116
339
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.116
340
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.116
341
TRN018 Transitional Cell Carcinoma 56 0.116
342
ORL011 Oral Cancer 60 0.116
343
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.116
344
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.116
345
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.116
346
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.116
347
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.116
348
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.116
349
NNL006 Non-Alcoholic Steatohepatitis 51 0.116
350
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.116
351
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.116
352
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.116
353
P DYS154 Dystonia 65 0.116
354
P PLY011 Polycystic Ovary Syndrome 56 0.116
355
P RHN004 Rhinitis 57 0.116
356
c ACT071 Acute Kidney Failure 59 0.115
357
P THY032 Thyroiditis 53 0.115
358
PNC129 Pancreatic Adenocarcinoma 67 0.115
359
ALC007 Alcohol Dependence 66 0.115
360
PLM033 Pulmonary Embolism 59 0.115
361
P FML011 Familial Adenomatous Polyposis 72 0.115
362
NRL016 Neural Tube Defects 82 0.115
363
PLS011 Plasmacytoma 56 0.115
364
RHM027 Rheumatic Disease 56 0.115
365
P NNN008 Noonan Syndrome 1 76 0.115
366
HNS001 Hansen's Disease 34 0.115
367
P MYC008 Myocarditis 59 0.115
368
P LPR021 Leprosy 3 67 0.114
369
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.114
370
VSC003 Visceral Leishmaniasis 55 0.114
371
JPN002 Japanese Encephalitis 54 0.114
372
P MDL005 Medulloblastoma 77 0.114
373
PRT013 Portal Hypertension 60 0.114
374
P WSK001 Wiskott-Aldrich Syndrome 71 0.114
375
WST005 West Nile Virus 55 0.113
376
c PRD040 Periodontitis, Chronic 54 0.113
377
c ATM011 Autoimmune Hepatitis 62 0.113
378
AVN001 Avian Influenza 56 0.113
379
P SRC025 Sarcoidosis 1 70 0.113
380
P EXN002 Exanthem 57 0.113
381
P KDN017 Kidney Cancer 61 0.113
382
P SPN046 Spinal Muscular Atrophy 64 0.112
383
P MLN007 Male Infertility 56 0.112
384
MTC097 Mitochondrial Complex Iv Deficiency 56 0.112
385
SPL018 Splenomegaly 48 0.112
386
P SCH015 Schizophrenia 75 0.112
387
CHG001 Chagas Disease 66 0.112
388
P TXP001 Toxoplasmosis 60 0.111
389
OTT002 Otitis Media 71 0.111
390
P MTR004 Maturity-Onset Diabetes of the Young 66 0.111
391
PRP027 Peripheral Vascular Disease 71 0.111
392
c HPT007 Hepatitis E 52 0.111
393
P FRG001 Fragile X Syndrome 68 0.110
394
P DMN002 Dementia 67 0.110
395
c BRS110 Breast-Ovarian Cancer, Familial 1 51 0.110
396
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.110
397
P PLY019 Polyneuropathy 56 0.109
398
OCL069 Ocular Motor Apraxia 51 0.109
399
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.109
400
DMY004 Demyelinating Disease 52 0.109
401
P MJR001 Major Depressive Disorder 68 0.108
402
P END033 Endocarditis 57 0.108
403
P EMR001 Emery-Dreifuss Muscular Dystrophy 61 0.108
404
PRS045 Prostatic Hypertrophy 52 0.108
405
RTN187 Retinitis Pigmentosa-Deafness Syndrome 47 0.108
406
c FML021 Familial Hypercholesterolemia 68 0.107
407
P BND020 Bone Disease 59 0.107
408
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.107
409
HLC007 Helicobacter Pylori Infection 59 0.106
410
P BNG032 Benign Mesothelioma 45 0.106
411
c GLC092 Glaucoma, Primary Open Angle 62 0.106
412
P ATS364 Autism 65 0.106
413
c SCL052 Scleroderma, Familial Progressive 62 0.106
414
c BRN108 Branchiootic Syndrome 1 61 0.106
415
CHR074 Choriocarcinoma 46 0.105
416
CHL147 Chlamydia Pneumonia 45 0.105
417
c SPN225 Spondyloarthropathy 1 73 0.105
418
CNN005 Connective Tissue Disease 66 0.105
419
c HMC039 Hemochromatosis, Type 1 74 0.105
420
INT066 Interstitial Lung Disease 59 0.105
421
CTN007 Cutaneous Leishmaniasis 61 0.104
422
c HMP029 Hemophilia a 65 0.104
423
PHN003 Phenylketonuria 75 0.104
424
CLN015 Colon Adenocarcinoma 63 0.104
425
P SLP006 Sleep Apnea 69 0.104
426
CHR178 Chromosomal Triplication 35 0.104
427
c BTT014 Beta-Thalassemia 72 0.104
428
GNT033 Genetic Prion Diseases 35 0.104
429
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.104
430
P HYP069 Hyperparathyroidism 62 0.104
431
c HMN021 Human T-Cell Leukemia Virus Type 1 48 0.104
432
PLG002 Plague 57 0.104
433
P FCL005 Focal Segmental Glomerulosclerosis 58 0.103
434
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.103
435
BRC012 Brucellosis 61 0.103
436
c ADL017 Adult T-Cell Leukemia 57 0.103
437
P PRM006 Primary Biliary Cirrhosis 61 0.103
438
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.103
439
P HRM001 Hermansky-Pudlak Syndrome 65 0.103
440
P TRN020 Turner Syndrome 65 0.103
441
HPT004 Hepatic Coma 43 0.102
442
P UVT001 Uveitis 57 0.102
443
c BCT007 Bacterial Meningitis 55 0.102
444
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.102
445
ACR006 Aceruloplasminemia 73 0.102
446
P CND004 Candidiasis 57 0.102
447
P OVR082 Overgrowth Syndrome 50 0.102
448
P ART021 Arteriosclerosis 54 0.102
449
TRT001 Teratocarcinoma 46 0.101
450
P NPH005 Nephronophthisis 58 0.101
451
c PRX059 Peroxisome Biogenesis Disorder 1a 57 0.101
452
c MLG068 Malignant Glioma 45 0.101
453
YLL002 Yellow Fever 60 0.101
454
PRS021 Prostatic Adenoma 51 0.101
455
P ATR011 Atrial Fibrillation 66 0.100
456
PRS129 Prostatic Hyperplasia, Benign 49 0.100
457
P GRF003 Graft-Versus-Host Disease 71 0.100
458
P SYS005 Systemic Scleroderma 70 0.100
459
HPT019 Hepatic Encephalopathy 60 0.100
460
P CHR345 Chronic Pain 50 0.100
461
c RHB024 Rhabdomyosarcoma 2 65 0.099
462
SPN051 Spondylitis 52 0.099
463
GST033 Gestational Diabetes 57 0.099
464
c LNG044 Long Qt Syndrome 1 66 0.099
465
P MYC084 Mycobacterium Tuberculosis 1 68 0.099
466
c ACT134 Acute Liver Failure 51 0.099
467
P MLT074 Multiple Endocrine Neoplasia 55 0.099
468
ALL006 Allergic Asthma 56 0.099
469
LYM019 Lymphosarcoma 47 0.099
470
P NRF023 Neurofibromatosis, Type Ii 76 0.099
471
P RHB003 Rhabdomyosarcoma 62 0.099
472
P SCK005 Sickle Cell Disease 50 0.099
473
RBS001 Rabies 58 0.098
474
c CNG006 Congenital Hypothyroidism 65 0.098
475
INF009 Inflammatory Spondylopathy 32 0.098
476
P LYM033 Lymphoproliferative Syndrome 60 0.098
477
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 61 0.098
478
MST005 Mastitis 53 0.098
479
P OPN001 Open-Angle Glaucoma 49 0.098
480
FCT001 Factor Viii Deficiency 55 0.098
481
c HPT015 Hepatitis D 49 0.098
482
P BRS044 Breast Adenocarcinoma 59 0.097
483
ALL003 Allergic Rhinitis 67 0.097
484
APP008 Appendicitis 60 0.097
485
P CCK001 Cockayne Syndrome 66 0.097
486
P RBL001 Rubella 58 0.097
487
MDD011 Mood Disorder 62 0.097
488
P GRV001 Graves' Disease 55 0.097
489
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.096
490
KRT019 Keratitis, Hereditary 67 0.096
491
P HLP001 Holoprosencephaly 68 0.096
492
c ACT068 Acute Cystitis 63 0.096
493
PPT005 Peptic Ulcer Disease 58 0.096
494
BRS099 Breast Ductal Carcinoma 62 0.095
495
SKN019 Skin Melanoma 67 0.095
496
ANT024 Anthrax Disease 58 0.095
498
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.095
499
HMC014 Homocysteinemia 53 0.095
500
c FML053 Familial Colorectal Cancer 48 0.094
501
P MYS005 Myositis 56 0.094
502
PTT037 Pituitary Tumors 44 0.094
503
P MTH008 Methylmalonic Acidemia 51 0.094
504
BLD131 Bladder Urothelial Carcinoma 61 0.094
505
BRN028 Brain Cancer 73 0.094
506
P RCT021 Rectum Cancer 53 0.094
507
LYS003 Lysinuric Protein Intolerance 56 0.094
508
PLM010 Pulmonary Edema 55 0.094
509
BLM001 Bloom Syndrome 66 0.093
510
ATX019 Ataxia with Vitamin E Deficiency 48 0.093
511
GTR002 Goiter 52 0.093
512
P PRP029 Porphyria 62 0.093
513
CLR108 Colorectal Adenoma 64 0.093
514
PFF001 Pfeiffer Syndrome 79 0.093
515
P ANT006 Antiphospholipid Syndrome 54 0.092
516
P URT039 Urticaria 58 0.092
517
P JVN014 Juvenile Polyposis Syndrome 68 0.092
518
P MCR010 Microcephaly 58 0.092
519
CLR030 Clear Cell Renal Cell Carcinoma 53 0.092
520
PRM329 Premature Aging 39 0.092
521
P OST001 Osteopetrosis 71 0.092
522
CNS004 Constipation 57 0.091
523
TRN015 Transient Cerebral Ischemia 62 0.091
524
P THY023 Thymoma 65 0.090
525
P RTT002 Rett Syndrome 80 0.090
526
VRC005 Varicose Veins 60 0.090
527
P EPL164 Epilepsy 71 0.090
528
c CRV002 Cervix Uteri Carcinoma in Situ 44 0.090
529
CRV045 Cervical Intraepithelial Neoplasia 39 0.090
530
c THY107 Thymoma, Familial 54 0.090
531
P HML001 Hemolytic-Uremic Syndrome 52 0.090
532
P MMP001 Mumps 57 0.090
533
WLS001 Wilson Disease 70 0.090
534
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 59 0.090
535
ADL002 Adult Syndrome 69 0.090
536
CRD132 Cardiac Conduction Defect 59 0.089
537
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 67 0.089
538
ANX010 Anxiety 72 0.089
539
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.089
540
P MYT002 Myotonic Dystrophy 49 0.089
541
P MCK013 Meckel Syndrome, Type 1 65 0.089
542
MTB004 Metabolic Acidosis 50 0.089
543
P LYS001 Loeys-Dietz Syndrome 66 0.089
544
c MNN043 Meningioma, Familial 74 0.089
545
VNH007 Von Hippel-Lindau Syndrome 73 0.089
546
P ALP008 Alopecia 56 0.089
547
P FLL037 Follicular Lymphoma 66 0.088
548
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.088
549
CLR109 Colorectal Adenocarcinoma 50 0.088
550
TYP007 Typhoid Fever 63 0.088
551
MNN042 Meningioma, Radiation-Induced 62 0.088
552
ART016 Aortic Aneurysm 68 0.088
553
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.088
554
P HYD006 Hydrocephalus 65 0.088
555
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.088
557
P MPL001 Maple Syrup Urine Disease 69 0.088
558
P NJM001 Nijmegen Breakage Syndrome 72 0.088
559
P CLC063 Celiac Disease 1 68 0.088
560
P DMN001 Diamond-Blackfan Anemia 69 0.087
561
MMB001 Membranoproliferative Glomerulonephritis 53 0.087
562
IGG001 Iga Glomerulonephritis 48 0.087
563
DNT012 Dental Caries 51 0.087
564
HDN002 Head Injury 45 0.087
565
KWS001 Kwashiorkor 45 0.087
566
P ART023 Arthropathy 62 0.087
567
ENT004 Enthesopathy 48 0.087
568
P MMB011 Membranous Nephropathy 50 0.087
569
BRN002 Bronchiolitis 59 0.087
570
P MTR014 Motor Neuron Disease 64 0.087
571
c CWD006 Cowden Syndrome 1 77 0.087
572
THY111 Thyroid Carcinoma, Familial Medullary 67 0.086
573
RNL077 Renal Fibrosis 47 0.086
574
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.086
575
P CYS018 Cystitis 59 0.086
576
CNT047 Contact Dermatitis 57 0.086
577
P TRM003 Tremor 53 0.086
578
TTH006 Tooth Disease 46 0.086
579
P SBS003 Substance Abuse 54 0.085
580
c MGR028 Migraine with or Without Aura 1 69 0.085
581
P TRC031 Trichorhinophalangeal Syndrome 40 0.085
582
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 0.085
583
DWR001 Dwarfism 44 0.085
584
TCK001 Tick-Borne Encephalitis 52 0.085
585
DSR002 Disorders of Intracellular Cobalamin Metabolism 30 0.085
586
P CHN012 Chondrosarcoma 56 0.085
587
IRR002 Irritable Bowel Syndrome 63 0.085
588
RHM001 Rheumatic Fever 61 0.085
589
STT001 Status Epilepticus 59 0.085
590
LYM027 Lymphopenia 57 0.085
591
c HNT011 Huntington Disease-Like 3 38 0.085
592
c FNC025 Fanconi Anemia, Complementation Group J 51 0.084
593
DBT010 Diabetic Neuropathy 55 0.084
594
PST092 Posttransplant Acute Limbic Encephalitis 29 0.084
595
c DNG003 Dengue Disease 59 0.084
596
c XRD030 Xeroderma Pigmentosum, Complementation Group C 54 0.083
597
LPT001 Leptospirosis 66 0.083
598
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.083
599
IGR001 Ige Responsiveness, Atopic 59 0.083
600
EYD002 Eye Disease 58 0.083
601
LYS002 Lysosomal Storage Disease 52 0.083
602
c FRS014 Fraser Syndrome 1 58 0.083
603
P MTC069 Mitochondrial Disorders 56 0.083
604
ACR007 Acromegaly 71 0.082
605
SPN021 Spinal Meningioma 47 0.082
606
ANR040 Aneurysm 58 0.082
607
CYT008 Cytomegalovirus Infection 56 0.082
608
c WLM013 Wilms Tumor 1 65 0.082
609
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 54 0.082
610
SCR001 Secretory Meningioma 37 0.082
611
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.082
612
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.082
613
GT001 Gout 63 0.082
614
FND002 Fundus Dystrophy 51 0.081
615
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 57 0.081
616
BLR008 Bilirubin Metabolic Disorder 57 0.081
617
P ANR048 Aniridia 1 63 0.081
618
c INH030 Inherited Retinal Disorder 47 0.081
619
THY125 Thyroid Gland Medullary Carcinoma 51 0.081
620
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.081
621
BRN004 Brain Edema 55 0.081
622
P GLL022 Guillain-Barre Syndrome 59 0.081
623
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.081
624
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 66 0.081
625
KRT002 Keratomalacia 48 0.081
626
P EPS003 Episodic Ataxia 60 0.081
627
MCR013 Microphthalmia 60 0.081
628
P LRY044 Larynx Cancer 54 0.080
629
c ATS307 Autosomal Recessive Cerebellar Ataxia 41 0.080
630
THY124 Thyroid Gland Papillary Carcinoma 52 0.080
631
DCT002 Ductal Carcinoma in Situ 59 0.080
632
P HML033 Hemolytic Uremic Syndrome, Atypical 1 69 0.080
633
BDD001 Budd-Chiari Syndrome 62 0.080
634
P HYP265 Hypotonia 42 0.080
635
P MNC007 Monocytic Leukemia 54 0.080
636
SYN007 Synovitis 55 0.080
637
AZS001 Azoospermia 50 0.080
638
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.080
639
ADR007 Adrenoleukodystrophy 74 0.080
640
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.080
641
FDB001 Foodborne Botulism 56 0.080
642
RTN017 Retinal Detachment 60 0.079
643
PLM031 Poliomyelitis 57 0.079
644
LPT014 Leptin Deficiency or Dysfunction 73 0.079
645
EWN003 Ewing Sarcoma 68 0.079
646
c TBR026 Tuberous Sclerosis 2 71 0.079
647
HPT022 Hepatoblastoma 56 0.079
648
P VTR007 Vitreoretinopathy 46 0.079
649
P MST009 Mastocytosis 63 0.078
650
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.078
651
P FML018 Familial Mediterranean Fever 72 0.078
652
SCK003 Sickle Cell Anemia 72 0.078
653
GLM044 Glomerular Disease 39 0.078
654
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.078
655
c BSL007 Basal Cell Carcinoma 68 0.078
656
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.078
657
P CRN037 Craniosynostosis 68 0.078
658
P MTC010 Mitochondrial Dna Depletion Syndrome 45 0.077
659
PSR001 Psoriatic Arthritis 62 0.077
660
SML019 Smallpox 56 0.077
661
c MYT021 Myotonic Dystrophy 1 66 0.077
662
P APL001 Aplastic Anemia 74 0.077
663
PRP016 Paraplegia 53 0.077
664
NNS032 Non-Syndromic X-Linked Intellectual Disability 44 0.077
665
NRT004 Neuritis 53 0.077
666
PLS007 Plasmodium Falciparum Malaria 52 0.077
667
OST017 Osteomyelitis 64 0.077
668
P VNW001 Von Willebrand's Disease 64 0.076
669
KRT009 Keratosis 53 0.076
670
ADN011 Adenoid Cystic Carcinoma 70 0.076
671
c FML001 Familial Atrial Fibrillation 66 0.076
672
PHR003 Pharyngitis 56 0.076
673
BLL006 Bullous Pemphigoid 62 0.076
674
P RTN018 Retinal Disease 52 0.076
675
P PRP003 Porphyria Cutanea Tarda 67 0.076
676
P FNC044 Fanconi Anemia, Complementation Group C 58 0.076
677
CHK001 Chikungunya 53 0.076
678
P PTT006 Pituitary Adenoma 54 0.076
679
P MYS003 Myasthenia Gravis 68 0.076
680
c PRS097 Prostate Cancer, Hereditary, 1 41 0.075
681
ORL013 Oral Lichen Planus 45 0.075
682
P PLY006 Polydactyly 58 0.075
683
P LCT001 Lactic Acidosis 51 0.075
684
NRM005 Neuromuscular Disease 63 0.075
685
VSC002 Vascular Dementia 57 0.075
686
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.075
687
P TMP001 Temporal Lobe Epilepsy 50 0.075
688
BSL036 Basal Cell Nevus Syndrome 72 0.075
689
P PYL005 Pyelonephritis 56 0.075
690
MNT001 Mantle Cell Lymphoma 66 0.075
691
c MST023 Mesothelioma, Malignant 57 0.075
692
LNG039 Lung Squamous Cell Carcinoma 65 0.075
693
MNN020 Meningococcal Infection 45 0.075
694
c GLL024 Gallbladder Disease 1 52 0.074
695
P CHL066 Cholangitis 50 0.074
696
P GCH001 Gaucher's Disease 64 0.074
697
c PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 63 0.074
698
MNN009 Meningoencephalitis 49 0.074
699
P BRC006 Brachydactyly 53 0.074
700
DYS073 Dysphagia 50 0.074
701
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.074
702
c FML191 Familial Long Qt Syndrome 53 0.074
703
c JVN010 Juvenile Rheumatoid Arthritis 67 0.074
704
PNG002 Pain Agnosia 51 0.074
705
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 0.074
706
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.074
707
P MYP006 Myopia 55 0.074
708
c HMP004 Hemophilia B 67 0.074
709
P ALP004 Alport Syndrome 68 0.074
710
MCS002 Mucositis 55 0.073
711
MLD001 Melioidosis 67 0.073
712
P CRB048 Cerebral Cavernous Malformations 67 0.073
713
LMY002 Leiomyoma 50 0.073
714
CMM005 Common Cold 56 0.073
715
P LMY004 Leiomyosarcoma 62 0.073
716
CHD001 Chediak-Higashi Syndrome 66 0.073
717
P HMN032 Human Herpesvirus 8 46 0.073
718
P PLY041 Polymyositis 57 0.073
719
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.073
720
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.073
721
CHR005 Chorioamnionitis 51 0.073
722
DYS015 Dysentery 50 0.073
723
ALC006 Alcoholic Hepatitis 61 0.073
724
AMN003 Amnestic Disorder 54 0.073
725
P MTC003 Metachromatic Leukodystrophy 70 0.073
726
P PMP001 Pemphigus 55 0.073
727
P ASP006 Aspergillosis 66 0.073
728
SLP001 Sleeping Sickness 48 0.072
729
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.072
730
P ANG001 Angelman Syndrome 67 0.072
731
MTC027 Mitochondrial Trifunctional Protein Deficiency 56 0.072
732
P MYC033 Myoclonus 46 0.072
733
LNG031 Lung Benign Neoplasm 50 0.072
734
END041 Endometrial Adenocarcinoma 63 0.072
735
NTR046 Neutrophil Migration 50 0.072
736
INC002 Inclusion Body Myositis 64 0.072
737
PRN019 Perinatal Necrotizing Enterocolitis 54 0.072
738
MCC012 Mccune-Albright Syndrome 70 0.072
739
GST023 Gastric Ulcer 53 0.072
740
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 69 0.072
741
SPP011 Suppression of Tumorigenicity 12 59 0.072
742
P DRM010 Dermatomyositis 61 0.072
743
P LFR001 Li-Fraumeni Syndrome 72 0.072
744
PTZ001 Peutz-Jeghers Syndrome 69 0.072
745
BRR014 Barrett Esophagus 64 0.072
746
PRT018 Portal Vein Thrombosis 50 0.072
747
P TRT010 Teratoma 51 0.071
748
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 0.071
749
PRP080 Peripheral Artery Disease 53 0.071
750
c MCR129 Microvascular Complications of Diabetes 1 66 0.071
751
P PLR004 Pleuropulmonary Blastoma 65 0.071
752
c GCH015 Gaucher Disease, Type I 70 0.071
753
PND002 Pendred Syndrome 60 0.071
754
ANR007 Anorexia Nervosa 63 0.070
755
BRS051 Breast Disease 58 0.070
756
c BCT013 Bacterial Pneumonia 47 0.070
757
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.070
758
P ADL010 Adult Respiratory Distress Syndrome 63 0.070
759
c SVR005 Severe Pre-Eclampsia 49 0.070
760
PPL002 Papillary Carcinoma 47 0.070
762
ALX003 Alexander Disease 61 0.070
763
MLK006 Milk Allergy 48 0.070
764
GLL018 Gallbladder Cancer 56 0.070
765
HSH003 Hashimoto Thyroiditis 62 0.070
766
PLY100 Polyploidy 40 0.070
767
CHL079 Children's Interstitial Lung Disease 27 0.070
768
ABT001 Abetalipoproteinemia 67 0.070
769
GST050 Gastrointestinal System Disease 56 0.070
770
c HNT004 Huntington Disease-Like 2 49 0.070
771
TBL022 Tibial Muscular Dystrophy, Tardive 36 0.070
772
ALP103 Alpha-1-Antitrypsin Deficiency 63 0.070
773
MTC005 Mitochondrial Metabolism Disease 48 0.070
774
MCR004 Macroglobulinemia 50 0.070
775
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.070
776
c PTT042 Pitt-Hopkins-Like Syndrome 36 0.070
777
P AGM001 Agammaglobulinemia 65 0.070
778
P LPS002 Liposarcoma 65 0.070
779
P OPT006 Optic Nerve Disease 57 0.069
780
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.069
781
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.069
782
HYP014 Hyperuricemia 51 0.069
783
P SML001 Small Cell Carcinoma 52 0.069
784
URT010 Ureteral Obstruction 46 0.069
785
CHR003 Cherubism 57 0.069
786
c GST103 Gastric Cancer, Hereditary Diffuse 64 0.069
787
P MLN069 Melanoma, Uveal 58 0.069
788
MST004 Mast Cell Neoplasm 38 0.069
789
INF034 Infective Endocarditis 52 0.069
790
HYP081 Hypolipoproteinemia 50 0.069
791
MYP153 Myopathy, Myofibrillar, 9, with Early Respiratory Failure 40 0.069
792
HYP080 Hypogonadism 50 0.069
793
P CNJ013 Conjunctivitis 65 0.069
794
P CHN059 Chondrocalcinosis 51 0.069
795
c FML035 Familial Hyperlipidemia 55 0.069
796
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.069
797
PRC013 Pericarditis 54 0.069
798
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.069
799
HYP064 Hypogonadotropism 40 0.069
800
P VSC013 Visceral Heterotaxy 52 0.069
801
SFT003 Soft Tissue Sarcoma 56 0.068
802
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.068
803
IMP005 Impotence 52 0.068
804
P SNS001 Sensorineural Hearing Loss 61 0.068
805
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.068
806
MLT157 Multiple System Atrophy 1 70 0.068
808
P ERY058 Erythrocytosis, Familial, 1 61 0.068
809
CYS010 Cystinosis 60 0.068
810
P HMC002 Homocystinuria 54 0.068
811
P ATR005 Atrophic Gastritis 50 0.068
812
c WRB002 Warburg Micro Syndrome 1 50 0.068
813
EXT007 Extracutaneous Mastocytoma 38 0.068
814
P RST002 Restrictive Cardiomyopathy 56 0.068
815
HMG002 Hemoglobinuria 49 0.068
816
CCC001 Coccidioidomycosis 53 0.068
817
P PLY018 Polycythemia 55 0.068
818
MMM001 Mammary Paget's Disease 53 0.067
819
TNG002 Tangier Disease 65 0.067
820
LYM009 Lymphocytic Choriomeningitis 46 0.067
821
PCK003 Pick Disease of Brain 68 0.067
822
GNG013 Gingivitis 59 0.067
823
CMB008 Combined Oxidative Phosphorylation Deficiency 38 0.067
824
TRY001 Trypanosomiasis 50 0.067
825
THR004 Thrombocytosis 51 0.067
826
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.067
827
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.067
828
SCH038 Schopf-Schulz-Passarge Syndrome 47 0.067
829
VRL003 Variola Major 43 0.067
830
P ANP001 Anaplastic Large Cell Lymphoma 61 0.067
831
P WRB001 Warburg Micro Syndrome 40 0.067
832
P PGT001 Paget's Disease of Bone 60 0.067
833
c GRV008 Graves Disease 1 55 0.067
834
P HRD011 Hereditary Spherocytosis 60 0.066
835
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 64 0.066
836
CRD043 Ceroid Storage Disease 43 0.066
837
P KLL001 Kallmann Syndrome 64 0.066
838
SPN008 Spondyloepiphyseal Dysplasia Congenita 52 0.066
839
c MCR112 Microvascular Complications of Diabetes 2 41 0.066
840
THY030 Thyroid Gland Disease 51 0.066
841
CRN030 Coronary Stenosis 50 0.066
842
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.066
843
P SCL018 Scoliosis 60 0.066
844
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.066
845
HMG005 Hemoglobinopathy 55 0.065
846
THR016 Thrombophlebitis 51 0.065
847
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 0.065
848
c ACT135 Acute Graft Versus Host Disease 51 0.065
849
KWS002 Kawasaki Disease 64 0.065
850
PTR032 Peters-Plus Syndrome 62 0.065
851
P WRD001 Waardenburg's Syndrome 59 0.065
852
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.065
853
HYP346 Hypotrichosis and Recurrent Skin Vesicles 29 0.065
854
P CRN038 Carney Complex Variant 63 0.065
855
P RTN022 Retinal Vein Occlusion 52 0.065
856
c CHR020 Chronic Interstitial Cystitis 37 0.065
857
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.065
858
P SLM003 Salmonellosis 54 0.065
859
P SJG008 Sjogren Syndrome 56 0.065
860
PLC008 Placenta Disease 49 0.065
861
GLY010 Glycine Encephalopathy 60 0.065
862
c DWL002 Dowling-Degos Disease 1 58 0.064
863
c MSC173 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 6 49 0.064
864
HND015 Hand Skill, Relative 33 0.064
865
IRN001 Iron Deficiency Anemia 58 0.064
866
CRT015 Carotid Artery Occlusion 44 0.064
867
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.064
868
MRS001 Marasmus 43 0.064
869
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.064
870
PRN029 Parainfluenza Virus Type 3 36 0.064
871
DNG002 Dengue Hemorrhagic Fever 60 0.064
872
CHL067 Cholecystitis 58 0.064
873
P RHZ001 Rhizomelic Chondrodysplasia Punctata 54 0.064
874
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.064
875
P WLL002 Weill-Marchesani Syndrome 55 0.064
876
P PNT019 Pontocerebellar Hypoplasia 46 0.064
877
NRL005 Neurilemmoma 60 0.064
878
RTN020 Retinal Vascular Disease 48 0.064
879
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.064
881
P ERL057 Early Infantile Epileptic Encephalopathy 62 0.064
882
P CNR004 Cone-Rod Dystrophy 2 71 0.064
883
FCT007 Factor Vii Deficiency 66 0.063
884
P MLG056 Malignant Hyperthermia 67 0.063
885
P PLZ001 Pelizaeus-Merzbacher Disease 62 0.063
886
c PNC108 Pancreatitis, Hereditary 69 0.063
887
SPT004 Septic Arthritis 57 0.063
888
P HMR003 Hemorrhagic Disease 52 0.063
889
P JNC001 Junctional Epidermolysis Bullosa 54 0.063
890
CRY003 Cryptosporidiosis 54 0.063
891
THY122 Thyroid Gland Cancer 58 0.063
892
MNN032 Meningococcal Meningitis 46 0.063
893
HYP732 Hyperalphalipoproteinemia 1 56 0.063
894
SPS019 Spastic Paraparesis 40 0.063
895
c CHR064 Chronic Monocytic Leukemia 34 0.063
896
CND006 Candida Glabrata 32 0.063
897
P KRB001 Krabbe Disease 69 0.063
898
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.063
899
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 62 0.063
900
c HRD010 Hereditary Spastic Paraplegia 66 0.063
901
ORT008 Orotic Aciduria 54 0.063
902
c THY112 Thyroid Hormone Resistance, Generalized, Autosomal Dominant 51 0.063
903
c MYS033 Miyoshi Muscular Dystrophy 1 56 0.062
904
CLP005 Ciliopathy 40 0.062
905
GRG001 Greig Cephalopolysyndactyly Syndrome 67 0.062
906
FLR002 Filariasis 55 0.062
907
c PRM005 Primary Hyperparathyroidism 58 0.062
908
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 62 0.062
909
SMN007 Seminoma 44 0.062
910
ALS001 Alstrom Syndrome 62 0.062
911
DGN001 Degenerative Disc Disease 48 0.062
912
MCK005 Mckusick-Kaufman Syndrome 58 0.062
913
QFV001 Q Fever 58 0.062
914
P MYS079 Miyoshi Muscular Dystrophy 53 0.062
915
CLF027 Cleft Palate, Isolated 64 0.062
916
VLV047 Volvulus of Midgut 50 0.062
917
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 63 0.062
918
c MCP001 Mucopolysaccharidosis Iii 65 0.062
919
P SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 60 0.062
920
WLL004 Wallerian Degeneration 39 0.062
921
FML307 Familial Calcium Pyrophosphate Deposition 38 0.062
922
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.062
923
NWB001 Newborn Respiratory Distress Syndrome 58 0.062
924
PNC001 Pancytopenia 54 0.062
925
P INT068 Intestinal Disease 52 0.062
926
c OPT053 Optic Atrophy 1 54 0.062
927
P DDN001 Duodenal Ulcer 50 0.062
928
P CHR012 Chronic Granulomatous Disease 67 0.062
929
SBC016 Subacute Delirium 44 0.062
930
P HNN005 Hennekam Lymphangiectasia-Lymphedema Syndrome 1 40 0.062
931
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.062
932
LKP003 Leukoplakia 39 0.062
933
CWP001 Cowpox 45 0.062
934
P PTT014 Pitt-Hopkins Syndrome 60 0.061
935
CRT013 Carotid Stenosis 50 0.061
936
LMB062 Limb Ischemia 55 0.061
937
P LKD001 Leukodystrophy 59 0.061
938
P NML001 Nemaline Myopathy 51 0.061
939
FML063 Familial Glucocorticoid Deficiency 51 0.061
940
SLC006 Silicosis 56 0.061
941
c SHR030 Short Qt Syndrome 48 0.061
942
CRC021 Carcinosarcoma 61 0.061
943
MSN004 Mesenchymal Cell Neoplasm 41 0.061
944
P MTC133 Mitochondrial Myopathy 49 0.061
945
c GLY008 Glycogen Storage Disease Ii 70 0.061
946
HMM004 Hamamy Syndrome 37 0.061
947
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.061
948
c MLG079 Malignant Pleural Mesothelioma 42 0.061
949
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.061
950
P ALP106 Alport Syndrome 1, X-Linked 55 0.061
951
ESP002 Esophageal Varix 51 0.061
952
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.061
953
c FML023 Familial Hemiplegic Migraine 54 0.061
954
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.061
955
LYM035 Lymphangiectasis 30 0.061
956
P SCK004 Seckel Syndrome 57 0.061
957
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 27 0.061
958
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 59 0.060
959
MYL031 Myeloproliferative Neoplasm 65 0.060
960
P GNT009 Giant Axonal Neuropathy 51 0.060
961
P MCP040 Mucopolysaccharidosis-Plus Syndrome 64 0.060
962
P LRS001 Larsen Syndrome 62 0.060
963
PRT010 Parathyroid Carcinoma 66 0.060
964
ACR013 Acrodysostosis 53 0.060
965
SRC027 Sarcoma, Synovial 56 0.060
966
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.060
967
c LRG017 Large Intestine Cancer 47 0.060
968
c NRB010 Neuroblastoma 1 49 0.060
969
APN008 Apnea, Obstructive Sleep 65 0.060
970
FCL081 Focal Cortical Dysplasia, Type Ii 60 0.060
971
c HMG001 Hemoglobin C Disease 40 0.060
972
SNS003 Sensory Peripheral Neuropathy 53 0.060
973
WLK001 Walker-Warburg Syndrome 63 0.060
974
CYS036 Cystinosis, Nephropathic 51 0.060
975
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 45 0.060
976
c ACT020 Acute T Cell Leukemia 53 0.060
977
P GLP001 Geleophysic Dysplasia 42 0.060
978
CRY005 Cryptococcosis 58 0.060
979
MNK001 Menkes Disease 64 0.060
980
PRT082 Preterm Premature Rupture of the Membranes 54 0.060
981
VNZ002 Venezuelan Equine Encephalitis 46 0.059
982
RFT001 Rift Valley Fever 47 0.059
983
P ACH011 Achondrogenesis 53 0.059
984
LST001 Listeriosis 54 0.059
985
P ATR010 Atrial Heart Septal Defect 60 0.059
986
WLF002 Wolf-Hirschhorn Syndrome 56 0.059
987
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.059
988
SBC001 Subacute Sclerosing Panencephalitis 52 0.059
989
BRN056 Bronchopulmonary Dysplasia 57 0.059
990
P TRC086 Trichohepatoenteric Syndrome 1 59 0.059
991
P CRN015 Cornelia De Lange Syndrome 63 0.059
992
P LYM025 Lymphedema 53 0.059
993
SHR044 Short Rib-Polydactyly Syndrome 49 0.059
994
ANT009 Antithrombin Iii Deficiency 59 0.059
995
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.059
996
P NRV007 Nervous System Disease 66 0.059
997
CRH005 Crohn's Colitis 52 0.059
998
P MCH002 Machado-Joseph Disease 63 0.059
999
P PRL003 Proliferative Glomerulonephritis 44 0.059
1000
ADR022 Adrenomyeloneuropathy 38 0.059
1001
c PRG020 Paragangliomas 3 38 0.059
1002
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.059
1003
KRN002 Kearns-Sayre Syndrome 63 0.058
1004
P EXD001 Exudative Vitreoretinopathy 56 0.058
1005
P ESP024 Esophagitis 62 0.058
1006
ALP077 Alpha-Methylacetoacetic Aciduria 56 0.058
1007
GLC106 Glucocorticoid Resistance, Generalized 48 0.058
1008
PRS047 Prostatitis 56 0.058
1009
DBF001 D-Bifunctional Protein Deficiency 56 0.058
1010
c MGL009 Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 48 0.058
1011
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 0.058
1012
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.058
1013
HYP005 Hypokalemia 55 0.058
1014
P ESS003 Essential Thrombocythemia 67 0.058
1015
BRT054 Brittle Bone Disorder 70 0.058
1016
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.058
1017
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.058
1018
ECH003 Echinococcosis 53 0.058
1019
P FML012 Familial Partial Lipodystrophy 55 0.058
1020
MRG003 Marginal Zone B-Cell Lymphoma 53 0.058
1021
TMT001 Timothy Syndrome 62 0.058
1022
CHR103 Charge Syndrome 66 0.058
1023
BLL001 Baller-Gerold Syndrome 59 0.058
1024
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.058
1025
P CTN015 Cutaneous T Cell Lymphoma 49 0.058
1026
RTC012 Reticuloendotheliosis, X-Linked 40 0.058
1027
PRX015 Paroxysmal Extreme Pain Disorder 53 0.058
1028
KLD004 Keloid Disorder 40 0.058
1029
OPT003 Opiate Dependence 50 0.057
1030
FBR012 Fabry Disease 71 0.057
1031
P CRD224 Cardiofaciocutaneous Syndrome 1 70 0.057
1032
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.057
1033
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.057
1034
PLM014 Pleomorphic Adenoma 52 0.057
1035
c LRG001 Large Cell Carcinoma 49 0.057
1036
P HDC001 Headache 57 0.057
1037
RHM028 Rheumatic Heart Disease 53 0.057
1038
P CRN108 Cranioectodermal Dysplasia 1 62 0.057
1039
c MYC083 Myoclonic Epilepsy, Familial Infantile 39 0.057
1040
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.057
1041
P HYP818 Hypobetalipoproteinemia, Familial, 1 58 0.057
1042
RSP023 Rasopathy 47 0.057
1043
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.057
1044
OMN001 Omenn Syndrome 66 0.057
1045
P PLM006 Pulmonary Alveolar Proteinosis 52 0.057
1046
P DST002 Distal Arthrogryposis 58 0.057
1047
c FML347 Familial Adenomatous Polyposis 2 50 0.057
1048
PSD012 Pseudoachondroplasia 58 0.057
1049
PSY004 Psychotic Disorder 67 0.057
1050
P HYP726 Hypercalcemia, Infantile, 1 57 0.057
1051
OST003 Osteonecrosis 61 0.057
1052
P SCL009 Sclerosing Cholangitis 47 0.057
1053
c SCN007 Secondary Hyperparathyroidism 50 0.057
1054
GRD007 Grade Iii Astrocytoma 59 0.057
1055
EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.057
1056
P TYS001 Tay-Sachs Disease 68 0.057
1057
P ISL078 Isolated Ectopia Lentis 56 0.057
1058
FCT006 Factor V Deficiency 56 0.057
1059
c PTT029 Pitt-Hopkins-Like Syndrome 1 48 0.057
1060
EPD015 Epidemic Typhus 46 0.057
1061
PPL049 Papillon-Lefevre Syndrome 63 0.057
1062
c PRM196 Premature Ovarian Failure 1 68 0.056
1063
FBR047 Fibromyalgia 59 0.056
1064
PLY001 Polycythemia Vera 69 0.056
1065