Search results for Coagulation factor VII human

972 hits were found for Coagulation factor VII human

# Family MCID Name MIFTS Score
1
DSS009 Disseminated Intravascular Coagulation 58 0.654
2
P HMP007 Hemophilia 58 0.593
3
IMM167 Immune Deficiency Disease 79 0.533
4
P CLR023 Colorectal Cancer 100 0.481
5
P BRS047 Breast Cancer 99 0.476
6
HMN044 Human Immunodeficiency Virus Type 1 73 0.457
7
c HMP029 Hemophilia a 69 0.448
8
FCT007 Factor Vii Deficiency 65 0.448
9
FCT001 Factor Viii Deficiency 54 0.446
10
P HPT023 Hepatocellular Carcinoma 99 0.426
11
P LKM002 Leukemia 69 0.425
12
P ADN016 Adenocarcinoma 65 0.421
13
P LNG032 Lung Cancer 99 0.415
14
P LVR013 Liver Disease 71 0.403
15
P CRN300 Coronary Heart Disease 1 59 0.395
16
P OVR042 Ovarian Cancer 89 0.394
17
c THR092 Thrombophilia Due to Thrombin Defect 74 0.391
18
P THR014 Thrombocytopenia 67 0.389
19
LVR012 Liver Cirrhosis 67 0.389
20
P VSC007 Vascular Disease 65 0.387
21
ATH013 Atherosclerosis Susceptibility 68 0.381
22
THR024 Thrombosis 58 0.374
23
GLB002 Glioblastoma 74 0.369
24
ATM095 Autoimmune Disease 62 0.366
25
GLB015 Glioblastoma Multiforme 60 0.365
26
SQM006 Squamous Cell Carcinoma 60 0.363
27
P KDN018 Kidney Disease 73 0.361
28
CYT002 Cytokine Deficiency 46 0.361
29
P GLM045 Glioma 64 0.359
30
c PRC016 Pre-Eclampsia 63 0.354
31
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.350
32
CRV035 Cervical Cancer 77 0.349
33
GLL048 Glial Tumor 48 0.345
34
HYP266 Hypoxia 58 0.342
35
P PNC035 Pancreatic Cancer 86 0.341
36
P NRB010 Neuroblastoma 1 66 0.340
37
P LYM031 Lymphocytic Leukemia 56 0.337
38
P PRS040 Prostate Cancer 97 0.335
39
P BLD134 Bladder Cancer 79 0.331
40
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.331
41
HLX001 Helix Syndrome 46 0.331
42
P HRT032 Heart Disease 78 0.326
43
SVR004 Severe Combined Immunodeficiency 74 0.325
44
P NTR004 Neutropenia 64 0.322
45
ADN018 Adenoma 60 0.321
46
MLN008 Melanoma 68 0.321
47
TXC005 Toxic Shock Syndrome 63 0.315
48
c HMP004 Hemophilia B 66 0.313
49
P DRR001 Diarrhea 55 0.307
50
CRB039 Cerebrovascular Disease 71 0.306
51
P CRN018 Coronary Artery Anomaly 67 0.303
52
48X005 48,xyyy 37 0.299
53
c SYS001 Systemic Lupus Erythematosus 88 0.296
54
P MYL006 Myeloid Leukemia 61 0.295
55
P INF032 Infertility 60 0.295
56
P BLD051 Blood Coagulation Disease 48 0.294
57
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.290
58
P VNW001 Von Willebrand's Disease 64 0.290
59
ISC004 Ischemia 62 0.290
60
ACQ007 Acquired Immunodeficiency Syndrome 61 0.290
61
c SML038 Small Cell Cancer of the Lung 67 0.289
62
P MCR115 Microvascular Complications of Diabetes 5 67 0.287
63
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.287
64
c LKM061 Leukemia, Acute Myeloid 84 0.286
65
P LYM118 Lymphoma 70 0.285
66
LPD008 Lipid Metabolism Disorder 64 0.283
67
LNG099 Lung Disease 62 0.281
68
P INF037 Inflammatory Bowel Disease 57 0.280
69
P HRP006 Herpes Simplex 66 0.279
70
ART140 Arteries, Anomalies of 60 0.278
71
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.276
72
P GLM007 Glomerulonephritis 58 0.275
73
PRT037 Pertussis 66 0.275
74
STR067 Stroke, Ischemic 82 0.274
75
P LPS004 Lupus Erythematosus 62 0.273
76
c HYP836 Hypercholesterolemia, Familial, 1 74 0.273
77
PPL022 Papilloma 56 0.273
78
P MYC007 Myocardial Infarction 74 0.271
79
P DBT009 Diabetes Mellitus 66 0.268
80
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.268
81
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.268
82
MYL069 Myeloma, Multiple 85 0.265
83
c ACT210 Acute Respiratory Distress Syndrome 59 0.264
84
ALL026 Allergic Hypersensitivity Disease 65 0.264
85
THY029 Thyroid Carcinoma 62 0.261
86
PRP030 Purpura 56 0.260
87
SKN016 Skin Disease 64 0.260
88
PLM033 Pulmonary Embolism 60 0.260
89
SQM002 Squamous Cell Papilloma 49 0.259
90
CNG034 Congestive Heart Failure 69 0.257
91
DFC004 Deficiency Anemia 77 0.255
92
c CHR684 Chronic Kidney Disease 68 0.254
93
END057 Endometrial Cancer 74 0.254
94
P LKM062 Leukemia, Acute Lymphoblastic 68 0.253
95
HYP066 Hyperglycemia 63 0.253
96
P THR015 Thrombophilia 51 0.253
97
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.253
98
P PRD008 Periodontitis 66 0.253
100
P LNG064 Lung Cancer Susceptibility 3 79 0.246
101
END030 End Stage Renal Failure 60 0.246
102
ANR040 Aneurysm 60 0.246
103
P ALZ034 Alzheimer Disease 90 0.246
104
c HYP595 Hypertension, Essential 87 0.245
105
CRH001 Crohn's Disease 75 0.243
106
MLR004 Malaria 82 0.243
107
TRM010 Traumatic Brain Injury 54 0.243
108
P RHM011 Rheumatoid Arthritis 82 0.241
109
HYP056 Hypoglycemia 68 0.241
110
PRS045 Prostatic Hypertrophy 55 0.239
111
P ECL001 Eclampsia 53 0.239
112
P END044 Endometriosis 63 0.239
113
BRN071 Brain Injury 51 0.238
114
OST012 Osteoarthritis 80 0.237
115
47X002 47,xyy 49 0.237
116
c ACT075 Acute Myocardial Infarction 59 0.237
117
ESP021 Esophageal Cancer 90 0.237
118
P RTN024 Retinoblastoma 74 0.236
119
c FML008 Familial Retinoblastoma 46 0.236
120
BNR002 Bone Resorption Disease 51 0.235
121
P CTR002 Cataract 62 0.235
122
ULC004 Ulcerative Colitis 75 0.235
123
P BCL017 B-Cell Lymphoma 61 0.235
124
P EPD016 Epidermolysis Bullosa 54 0.234
125
P ART021 Arteriosclerosis 56 0.232
126
P ATR011 Atrial Fibrillation 67 0.232
127
FTT001 Fatty Liver Disease 63 0.231
128
PRS021 Prostatic Adenoma 52 0.231
129
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.230
130
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.230
131
CRV045 Cervical Intraepithelial Neoplasia 41 0.230
132
c CRV002 Cervix Uteri Carcinoma in Situ 47 0.230
133
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.230
134
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.230
135
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.230
136
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.230
137
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.230
138
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.230
139
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.230
140
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.230
141
P GRF003 Graft-Versus-Host Disease 71 0.230
142
OCL069 Ocular Motor Apraxia 53 0.229
143
c ACT071 Acute Kidney Failure 60 0.228
144
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.228
145
CHL014 Cholera 58 0.228
146
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.228
147
AGN016 Aging 58 0.228
148
SPP010 Suppressor of Tumorigenicity 3 54 0.227
149
P PSR002 Psoriasis 63 0.227
150
c ACT073 Acute Leukemia 59 0.226
151
c HPT001 Hepatitis C 62 0.226
152
PRS129 Prostatic Hyperplasia, Benign 49 0.226
153
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.224
154
P HYP086 Hypothyroidism 70 0.224
155
P VSC011 Vasculitis 64 0.223
156
ART016 Aortic Aneurysm 71 0.222
157
PST011 Pustulosis of Palm and Sole 51 0.222
158
PRP027 Peripheral Vascular Disease 72 0.221
159
P PNM007 Pneumonia 71 0.220
160
DRM006 Dermatitis 63 0.219
161
P ENC018 Encephalopathy 64 0.217
162
P CRD119 Cardiac Arrest 71 0.217
163
c HPT016 Hepatitis B 63 0.216
164
ALC007 Alcohol Dependence 68 0.216
165
P AST007 Astrocytoma 52 0.215
166
HMT018 Hematopoietic Stem Cell Transplantation 54 0.215
167
PRT036 Peritonitis 66 0.214
168
P EXN002 Exanthem 58 0.214
169
SRC014 Sarcoma 67 0.214
170
P INF038 Influenza 69 0.213
171
DPR016 Depression 64 0.212
172
P RSP003 Respiratory Failure 75 0.211
173
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.210
174
P NRP001 Neuropathy 57 0.210
175
KPS004 Kaposi Sarcoma 75 0.210
176
P RHN004 Rhinitis 59 0.209
177
P ENC004 Encephalitis 64 0.208
178
BCT022 Bacterial Infectious Disease 57 0.208
179
LSH001 Leishmaniasis 64 0.207
180
P KLZ004 Kala-Azar 1 43 0.207
181
P SYP003 Syphilis 59 0.206
182
TTN003 Tetanus 62 0.206
183
P HYP750 Hypertriglyceridemia, Familial 62 0.204
184
SPN035 Spindle Cell Sarcoma 57 0.204
185
PLM001 Pulmonary Tuberculosis 72 0.204
186
GST045 Gastroenteritis 60 0.202
187
HDN002 Head Injury 47 0.202
188
ANX010 Anxiety 75 0.201
189
CLT003 Colitis 63 0.201
190
SCH014 Schistosomiasis 57 0.201
191
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.199
192
c ACT027 Acute Pancreatitis 60 0.199
193
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.199
194
ANG054 Angina Pectoris 66 0.199
195
P PLM037 Pulmonary Hypertension 69 0.199
196
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.199
197
P PNC044 Pancreatitis 61 0.198
198
P OST002 Osteoporosis 79 0.197
199
P END033 Endocarditis 58 0.197
200
IDP011 Idiopathic Interstitial Pneumonia 65 0.196
201
P PLM036 Pulmonary Fibrosis 66 0.196
202
VCC001 Vaccinia 50 0.195
203
PPT005 Peptic Ulcer Disease 60 0.195
204
RRS014 Rare Surgical Neurologic Disease 33 0.194
205
MYL009 Myelodysplastic Syndrome 72 0.194
206
CYS001 Cystic Fibrosis 84 0.194
207
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.194
208
P NPH012 Nephrotic Syndrome 65 0.193
209
ORL015 Oral Squamous Cell Carcinoma 44 0.193
210
AST005 Asthma 80 0.193
211
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.190
212
DWN001 Down Syndrome 70 0.189
213
P DRM053 Dermatitis, Atopic 68 0.189
214
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.189
215
P AMY004 Amyloidosis 71 0.188
216
INT007 Intermediate Coronary Syndrome 58 0.187
217
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.187
218
P ART022 Arthritis 71 0.187
219
P FBR017 Fibrosarcoma 57 0.186
220
c VRL010 Viral Hepatitis 56 0.186
221
c ACT134 Acute Liver Failure 53 0.186
222
P HYP098 Hypereosinophilic Syndrome 67 0.185
223
RTN017 Retinal Detachment 62 0.185
224
CYT008 Cytomegalovirus Infection 58 0.184
225
c ACT068 Acute Cystitis 63 0.184
226
P ART023 Arthropathy 61 0.184
227
IRN002 Iron Metabolism Disease 58 0.183
228
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.182
229
P GST044 Gastritis 58 0.182
230
P HPT021 Hepatitis 69 0.181
231
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.181
232
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.181
233
c CNG216 Congenital Hydrocephalus 55 0.180
234
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.180
235
P NSP012 Nasopharyngeal Carcinoma 67 0.180
236
P ALC033 Alcohol Use Disorder 58 0.180
237
P HYD006 Hydrocephalus 68 0.180
238
P MLT020 Multiple Sclerosis 73 0.180
239
c SCL052 Scleroderma, Familial Progressive 62 0.179
240
P INS002 in Situ Carcinoma 55 0.179
241
BCK006 Back Pain 44 0.179
242
MSL001 Measles 61 0.178
243
HRW001 Hair Whorl 36 0.177
244
P CHR345 Chronic Pain 52 0.177
245
MNT002 Mental Depression 60 0.176
246
c ACQ014 Acquired Hemophilia 47 0.176
247
P SCK005 Sickle Cell Disease 53 0.176
248
LYM133 Lymphoma, Hodgkin, Classic 70 0.175
249
DNT012 Dental Caries 52 0.174
250
P RCT021 Rectum Cancer 54 0.174
251
VRC005 Varicose Veins 61 0.174
252
c ATR087 Atrial Standstill 1 76 0.173
253
P HML002 Hemolytic Anemia 64 0.173
254
P MSC005 Muscular Dystrophy 68 0.173
255
P MNN013 Meningitis 67 0.172
256
c LKM071 Leukemia, Chronic Lymphocytic 81 0.172
257
TLN003 Telangiectasis 53 0.171
258
ALL003 Allergic Rhinitis 69 0.171
259
P SLP006 Sleep Apnea 71 0.171
260
ENT011 Enterocolitis 51 0.170
261
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.170
262
GTR002 Goiter 54 0.169
263
BND020 Bone Disease 60 0.169
264
RHM027 Rheumatic Disease 56 0.169
265
CHC001 Chickenpox 53 0.169
266
P SZR006 Seizure Disorder 59 0.169
267
c PRM038 Primary Agammaglobulinemia 45 0.168
268
P KDN017 Kidney Cancer 60 0.168
269
DPH001 Diphtheria 61 0.168
270
IMP005 Impotence 53 0.168
271
NRR001 Neuroretinitis 46 0.168
272
P THL005 Thalassemia 62 0.168
273
RTN023 Retinitis 46 0.168
274
MNN042 Meningioma, Radiation-Induced 64 0.167
275
P ANT006 Antiphospholipid Syndrome 56 0.167
276
c MLG068 Malignant Glioma 46 0.167
277
HNS001 Hansen's Disease 35 0.167
278
PRT013 Portal Hypertension 61 0.167
279
STM007 Stomatitis 51 0.167
280
P LPR021 Leprosy 3 67 0.166
281
ERY051 Erythroleukemia, Familial 58 0.166
282
P HYP076 Hyperthyroidism 55 0.166
283
P DMN002 Dementia 68 0.166
284
BRC012 Brucellosis 62 0.166
285
FCT002 Factor Xi Deficiency 59 0.166
286
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.165
287
FCT003 Factor X Deficiency 57 0.165
288
CHL068 Cholestasis 61 0.165
289
BRK010 Burkitt Lymphoma 68 0.164
290
P HMR003 Hemorrhagic Disease 54 0.163
291
c HPT003 Hepatitis a 60 0.163
292
PLM010 Pulmonary Edema 56 0.163
293
CHR178 Chromosomal Triplication 36 0.162
294
SPN021 Spinal Meningioma 40 0.162
295
c MNN043 Meningioma, Familial 74 0.162
296
P MYP004 Myopathy 63 0.162
297
P TXP001 Toxoplasmosis 61 0.162
298
BRN024 Bronchitis 70 0.162
299
FCT005 Factor Xiii Deficiency 50 0.161
300
SCR001 Secretory Meningioma 38 0.161
301
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.161
302
P EPL164 Epilepsy 73 0.161
303
P SCH015 Schizophrenia 76 0.161
304
AVN001 Avian Influenza 56 0.160
305
c MGR028 Migraine with or Without Aura 1 70 0.160
306
BLL006 Bullous Pemphigoid 63 0.159
307
P RHB003 Rhabdomyosarcoma 62 0.158
308
GST040 Gastric Adenocarcinoma 67 0.158
309
c DLT002 Dilated Cardiomyopathy 81 0.157
310
VTM033 Vitamin K Deficiency Bleeding 47 0.157
311
c SPN225 Spondyloarthropathy 1 74 0.157
312
OVR082 Overgrowth Syndrome 51 0.156
313
ATS010 Autosomal Recessive Disease 49 0.156
314
LPT001 Leptospirosis 60 0.156
315
VSL002 Visual Epilepsy 58 0.156
316
PNC129 Pancreatic Adenocarcinoma 69 0.156
317
HLC007 Helicobacter Pylori Infection 61 0.156
318
P APL001 Aplastic Anemia 76 0.156
319
P MLN007 Male Infertility 57 0.156
320
c BRN108 Branchiootic Syndrome 1 62 0.155
321
P CND004 Candidiasis 61 0.155
322
DYS073 Dysphagia 52 0.155
323
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.155
325
THR035 Thrombasthenia 42 0.154
326
URM002 Uremia 50 0.153
327
P SCL018 Scoliosis 61 0.153
328
P PYL005 Pyelonephritis 58 0.153
329
OTT002 Otitis Media 71 0.153
330
P SYS005 Systemic Scleroderma 68 0.152
331
P MJR001 Major Depressive Disorder 69 0.152
332
EYD002 Eye Disease 59 0.152
333
c MCR129 Microvascular Complications of Diabetes 1 67 0.151
334
c ACT135 Acute Graft Versus Host Disease 52 0.150
335
P ATS364 Autism 68 0.150
336
PLM031 Poliomyelitis 58 0.150
337
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.149
338
VRL011 Viral Infectious Disease 62 0.149
339
FCT006 Factor V Deficiency 53 0.149
340
ADL002 Adult Syndrome 62 0.149
341
P GRV001 Graves' Disease 57 0.149
342
PLC007 Placental Abruption 47 0.148
343
TRY001 Trypanosomiasis 50 0.148
344
PRN019 Perinatal Necrotizing Enterocolitis 55 0.148
345
P MYP006 Myopia 58 0.148
346
P TRN020 Turner Syndrome 66 0.148
347
P THY032 Thyroiditis 52 0.148
348
THR004 Thrombocytosis 52 0.147
349
ANT024 Anthrax Disease 56 0.147
350
CRT013 Carotid Stenosis 50 0.146
351
P UVT001 Uveitis 58 0.146
352
GLC003 Glucose Intolerance 55 0.146
353
LMY002 Leiomyoma 52 0.146
354
P MYC084 Mycobacterium Tuberculosis 1 69 0.145
355
P DDN001 Duodenal Ulcer 50 0.145
356
SPL018 Splenomegaly 48 0.145
357
P CYS018 Cystitis 59 0.145
358
c MCR112 Microvascular Complications of Diabetes 2 42 0.145
359
P HYP069 Hyperparathyroidism 64 0.144
360
SKN019 Skin Melanoma 68 0.144
361
PLY150 Polykaryocytosis Inducer 31 0.144
362
ALL014 Allergic Encephalomyelitis 40 0.143
363
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.143
364
PNG002 Pain Agnosia 52 0.143
365
BRR014 Barrett Esophagus 67 0.143
366
MST005 Mastitis 55 0.142
367
CHG001 Chagas Disease 66 0.142
368
HMP009 Haemophilus Influenzae 46 0.141
369
P PRS038 Personality Disorder 66 0.141
370
ANR007 Anorexia Nervosa 64 0.141
371
APP008 Appendicitis 61 0.140
372
VSC003 Visceral Leishmaniasis 55 0.140
373
P HMN010 Hemangioma 62 0.140
374
RRD056 Rare Disease in Surgical Orthopedic 29 0.139
375
P PRK057 Parkinson Disease, Late-Onset 77 0.139
376
ECH003 Echinococcosis 54 0.139
377
CRB037 Cerebral Palsy 69 0.139
378
SPN051 Spondylitis 53 0.138
379
TYP007 Typhoid Fever 61 0.138
380
INF009 Inflammatory Spondylopathy 29 0.138
381
MDD011 Mood Disorder 62 0.137
382
P PLY018 Polycythemia 56 0.136
383
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.136
384
FCT004 Factor Xii Deficiency 54 0.136
385
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.136
386
P ATX030 Ataxia-Telangiectasia 83 0.136
387
P PTT006 Pituitary Adenoma 53 0.136
388
HYP014 Hyperuricemia 52 0.135
389
P CHL066 Cholangitis 53 0.135
390
IGG001 Iga Glomerulonephritis 50 0.135
391
NRL016 Neural Tube Defects 83 0.134
392
GST023 Gastric Ulcer 53 0.134
393
PLG002 Plague 54 0.134
394
CHL067 Cholecystitis 60 0.134
395
THR016 Thrombophlebitis 50 0.133
396
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.133
397
PLM017 Pulmonary Alveolar Microlithiasis 54 0.133
398
P HDC001 Headache 59 0.133
399
ACR007 Acromegaly 70 0.132
400
ENT004 Enthesopathy 46 0.132
401
P SRC025 Sarcoidosis 1 72 0.131
402
P MSC003 Muscular Atrophy 52 0.131
403
LMB062 Limb Ischemia 50 0.131
404
P RTN018 Retinal Disease 53 0.131
405
P ADL010 Adult Respiratory Distress Syndrome 61 0.131
406
CNS004 Constipation 59 0.131
407
KRT019 Keratitis, Hereditary 69 0.130
408
HPT022 Hepatoblastoma 58 0.130
409
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.129
410
MCS002 Mucositis 56 0.129
411
TRN015 Transient Cerebral Ischemia 62 0.129
412
ANG005 Anogenital Venereal Wart 51 0.129
413
P CNJ013 Conjunctivitis 67 0.129
414
c WLM018 Wilms Tumor 5 63 0.129
415
ETN001 Eating Disorder 61 0.129
416
GRW007 Growth Hormone Deficiency 48 0.129
417
ANX004 Anoxia 44 0.128
418
c SVR001 Severe Acute Respiratory Syndrome 56 0.128
419
c EXD008 Exudative Vitreoretinopathy 1 69 0.128
420
PNM008 Pneumothorax 56 0.127
421
SYN007 Synovitis 55 0.127
422
P PLY019 Polyneuropathy 55 0.127
423
c JVN010 Juvenile Rheumatoid Arthritis 67 0.127
424
THR123 Thrombotic Microangiopathy 41 0.127
425
P SLM003 Salmonellosis 54 0.126
426
CLF027 Cleft Palate, Isolated 67 0.126
427
CRN017 Coronary Thrombosis 45 0.126
428
ATX019 Ataxia with Vitamin E Deficiency 46 0.126
429
SLP001 Sleeping Sickness 47 0.126
430
P HYP061 Hypertrophic Cardiomyopathy 68 0.126
431
P CRD132 Cardiac Conduction Defect 61 0.126
432
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.125
433
BLR008 Bilirubin Metabolic Disorder 58 0.125
434
BRN028 Brain Cancer 75 0.125
435
CHR100 Chronic Ulcer of Skin 53 0.125
436
c GLL024 Gallbladder Disease 1 53 0.125
437
c PRD040 Periodontitis, Chronic 56 0.124
438
INF034 Infective Endocarditis 53 0.124
439
P GLY013 Glycogen Storage Disease 59 0.124
440
GRN017 Granulocytopenia 46 0.124
441
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.124
442
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.123
443
NTR005 Nutritional Deficiency Disease 61 0.123
444
PRT011 Protein C Deficiency 45 0.123
445
DNG002 Dengue Hemorrhagic Fever 59 0.122
446
P TRM003 Tremor 55 0.122
447
PRM236 Primary Biliary Cholangitis 57 0.122
448
CNN005 Connective Tissue Disease 68 0.122
449
OST017 Osteomyelitis 65 0.122
450
KRT009 Keratosis 52 0.121
451
HRT011 Heart Septal Defect 52 0.121
452
HYP064 Hypogonadotropism 40 0.121
453
SCK003 Sickle Cell Anemia 74 0.121
454
HYP080 Hypogonadism 51 0.121
455
GNG013 Gingivitis 60 0.120
456
P PRM006 Primary Biliary Cirrhosis 54 0.120
457
INT066 Interstitial Lung Disease 61 0.120
458
P MTR003 Mitral Valve Stenosis 54 0.119
459
GT001 Gout 63 0.119
460
ARG004 Argyria 28 0.119
461
c RHB024 Rhabdomyosarcoma 2 64 0.119
462
HPR003 Heparin-Induced Thrombocytopenia 49 0.119
463
CLR108 Colorectal Adenoma 64 0.119
464
P ANG015 Angioedema 54 0.119
465
HPT004 Hepatic Coma 42 0.118
466
P ART005 Arteriovenous Malformation 63 0.118
467
P SLP005 Sleep Disorder 58 0.118
468
ALL006 Allergic Asthma 56 0.117
469
P RTN016 Retinal Degeneration 56 0.117
470
P RTN022 Retinal Vein Occlusion 50 0.117
471
P PMP001 Pemphigus 56 0.117
472
P PLY014 Polycystic Kidney Disease 61 0.117
473
CHR005 Chorioamnionitis 51 0.117
474
P CLC063 Celiac Disease 1 66 0.117
475
DYS015 Dysentery 45 0.117
476
PPL052 Papillomatosis, Confluent and Reticulated 34 0.117
477
LYM019 Lymphosarcoma 48 0.116
478
PRT014 Protein S Deficiency 50 0.116
479
PST092 Posttransplant Acute Limbic Encephalitis 29 0.116
480
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.115
481
c DNG003 Dengue Disease 61 0.115
482
HRP004 Herpes Zoster 58 0.115
483
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.114
484
DYS014 Dyspepsia 51 0.114
485
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.114
486
RCK004 Rickets 70 0.113
487
P SNS001 Sensorineural Hearing Loss 62 0.113
488
NRL005 Neurilemmoma 62 0.113
489
BRS051 Breast Disease 59 0.113
490
MSC157 Muscular Dystrophy, Duchenne Type 70 0.112
491
AMN001 Amenorrhea 54 0.112
492
P LMY004 Leiomyosarcoma 63 0.112
493
RTN020 Retinal Vascular Disease 49 0.112
494
PRT018 Portal Vein Thrombosis 50 0.111
495
c MTR002 Mitral Valve Insufficiency 49 0.111
496
PLY001 Polycythemia Vera 70 0.110
497
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.110
498
c BTT014 Beta-Thalassemia 73 0.109
499
CHL004 Cholelithiasis 50 0.109
500
CRN030 Coronary Stenosis 49 0.109
501
P OPT006 Optic Nerve Disease 59 0.109
502
SHW001 Shwartzman Phenomenon 35 0.109
503
ESP002 Esophageal Varix 49 0.109
504
P ESP024 Esophagitis 62 0.108
505
DBT010 Diabetic Neuropathy 56 0.108
506
HYD012 Hydrops Fetalis 49 0.108
507
PLS007 Plasmodium Falciparum Malaria 53 0.108
508
LPT014 Leptin Deficiency or Dysfunction 72 0.107
509
MYL005 Myelofibrosis 69 0.107
510
INT052 Intestinal Volvulus 44 0.106
511
THY030 Thyroid Gland Disease 53 0.106
512
P FML011 Familial Adenomatous Polyposis 73 0.105
513
HPT019 Hepatic Encephalopathy 60 0.105
514
HRT012 Heart Valve Disease 56 0.105
515
MNN009 Meningoencephalitis 50 0.105
516
FTL016 Fetal Edema 24 0.104
517
P MCR010 Microcephaly 56 0.104
518
RHM001 Rheumatic Fever 56 0.104
519
PRP016 Paraplegia 54 0.104
520
GLN010 Glanzmann Thrombasthenia 66 0.104
521
STT001 Status Epilepticus 61 0.103
522
P CNR004 Cone-Rod Dystrophy 2 72 0.103
523
c HRD002 Hereditary Angioedema 59 0.103
524
GST050 Gastrointestinal System Disease 57 0.103
525
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 0.102
526
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.102
527
P HMC002 Homocystinuria 52 0.102
528
P LCH002 Lichen Planus 55 0.102
530
P EHL001 Ehlers-Danlos Syndrome 60 0.102
531
P OBS001 Obstructive Jaundice 49 0.101
532
P MST009 Mastocytosis 62 0.101
533
ILS001 Ileus 51 0.101
534
ACT058 Active Peptic Ulcer Disease 55 0.101
535
PLS011 Plasmacytoma 57 0.100
536
TNS005 Tonsillitis 58 0.100
537
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.099
538
SPT005 Spotted Fever 48 0.099
539
c FML021 Familial Hypercholesterolemia 67 0.099
540
HYD002 Hydronephrosis 58 0.099
541
KWS002 Kawasaki Disease 65 0.098
542
LKP003 Leukoplakia 40 0.098
543
ANG020 Angiosarcoma 59 0.098
544
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.098
545
MCR011 Microinvasive Gastric Cancer 43 0.098
546
P SCL009 Sclerosing Cholangitis 47 0.098
547
P DYS154 Dystonia 65 0.098
548
PLC009 Placenta Praevia 35 0.097
549
P GCH001 Gaucher's Disease 63 0.097
550
P VNT002 Ventricular Septal Defect 61 0.097
551
GST019 Gastrointestinal Stromal Tumor 76 0.097
552
P LYM025 Lymphedema 54 0.097
553
PPL002 Papillary Carcinoma 47 0.097
554
HMR002 Hemarthrosis 46 0.097
555
P MMB011 Membranous Nephropathy 54 0.097
556
INT075 Intracranial Hypertension 54 0.096
557
NRM005 Neuromuscular Disease 62 0.096
558
ING001 Inguinal Hernia 61 0.096
559
PRS047 Prostatitis 57 0.096
560
P PRP029 Porphyria 58 0.096
561
PFF001 Pfeiffer Syndrome 79 0.096
562
P DRM010 Dermatomyositis 62 0.096
563
HMR039 Hemorrhage, Intracerebral 59 0.095
564
P LCT001 Lactic Acidosis 52 0.095
565
LMY014 Leiomyoma, Uterine 57 0.095
566
EPD015 Epidemic Typhus 47 0.095
567
P CRN037 Craniosynostosis 69 0.095
568
HLL004 Hellp Syndrome 53 0.095
569
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 33 0.094
570
NRT004 Neuritis 52 0.094
571
PRT082 Preterm Premature Rupture of the Membranes 53 0.094
572
P PLY041 Polymyositis 57 0.094
573
PTH003 Pathologic Nystagmus 53 0.094
574
P NRV007 Nervous System Disease 68 0.094
575
P CMP008 Compartment Syndrome 45 0.093
576
PMP006 Pemphigus Vulgaris, Familial 56 0.093
577
ACN002 Acanthosis Nigricans 62 0.093
578
c DWL002 Dowling-Degos Disease 1 59 0.093
579
MYL031 Myeloproliferative Neoplasm 66 0.092
580
P AGM001 Agammaglobulinemia 66 0.092
581
c PNS012 Paine Syndrome 61 0.092
582
QFV001 Q Fever 58 0.092
583
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.092
584
HPT046 Hepatic Veno-Occlusive Disease 56 0.091
585
BDD001 Budd-Chiari Syndrome 62 0.091
586
CRD137 Cardiogenic Shock 50 0.091
587
CRB086 Cerebral Aneurysms 41 0.091
588
P AFB001 Afibrinogenemia 49 0.091
589
c FML035 Familial Hyperlipidemia 56 0.091
590
ACS001 Acoustic Neuroma 57 0.091
591
CMM005 Common Cold 57 0.091
592
SLC006 Silicosis 55 0.091
593
P MYS005 Myositis 54 0.091
594
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.091
595
FDL002 Food Allergy 52 0.090
596
PRN011 Pernicious Anemia 51 0.090
597
c ATM011 Autoimmune Hepatitis 63 0.090
598
HYP005 Hypokalemia 55 0.090
599
c GRV008 Graves Disease 1 55 0.089
600
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.089
601
c CNT016 Central Retinal Vein Occlusion 48 0.089
602
P INT143 Interstitial Cystitis 62 0.089
603
c ACQ042 Acquired Hemophilia a 38 0.089
604
TNG003 Tongue Cancer 57 0.089
605
P FCL005 Focal Segmental Glomerulosclerosis 63 0.089
606
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.088
607
P ANR048 Aniridia 1 64 0.088
608
ADN011 Adenoid Cystic Carcinoma 71 0.088
609
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.088
610
P PLV020 Pelvic Organ Prolapse 61 0.088
611
PRS034 Parasitic Helminthiasis Infectious Disease 48 0.088
612
HMP001 Hemopericardium 44 0.087
613
P HYP024 Hypoparathyroidism 56 0.087
614
YLL002 Yellow Fever 58 0.087
615
RYN005 Raynaud Phenomenon 50 0.087
616
P ATR010 Atrial Heart Septal Defect 61 0.086
617
c ACQ017 Acquired Von Willebrand Syndrome 42 0.086
618
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.086
619
HYP020 Hyperprolactinemia 62 0.086
620
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.085
621
MRF001 Marfan Syndrome 75 0.085
622
BRT054 Brittle Bone Disorder 71 0.084
623
P FRG001 Fragile X Syndrome 69 0.084
624
P INT070 Intestinal Obstruction 60 0.084
625
PRC013 Pericarditis 54 0.084
626
P CLL015 Collagen Disease 46 0.084
627
P HMP002 Hemophagocytic Lymphohistiocytosis 68 0.084
628
P PRP034 Purpura Fulminans 42 0.084
629
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.083
630
INT030 Intracranial Aneurysm 57 0.083
631
P PLM034 Pulmonary Emphysema 55 0.083
632
NRN004 Neuroendocrine Tumor 59 0.083
633
P BRN019 Bernard-Soulier Syndrome 60 0.083
634
THR013 Thoracic Outlet Syndrome 49 0.083
635
c PRM005 Primary Hyperparathyroidism 60 0.083
636
HYP457 Hypertrophic Scars 44 0.083
637
TRG002 Trigeminal Neuralgia 58 0.083
638
P ART018 Aortic Valve Insufficiency 47 0.082
639
KRT008 Keratopathy 46 0.082
640
HRY003 Hairy Cell Leukemia 57 0.082
641
c CNT035 Central Nervous System Disease 56 0.082
642
P GNT008 Giant Cell Tumor 45 0.082
643
P FBR031 Febrile Seizures 54 0.082
644
c WLM013 Wilms Tumor 1 69 0.082
645
MST004 Mast Cell Neoplasm 40 0.082
646
CRD001 Cardiac Tamponade 45 0.082
647
EXT007 Extracutaneous Mastocytoma 39 0.081
648
P DBT005 Diabetes Insipidus 54 0.081
649
KRT006 Keratoconjunctivitis 53 0.081
650
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.080
651
c FNC043 Fanconi Anemia, Complementation Group E 64 0.080
652
P PRC012 Pericardial Effusion 51 0.080
653
MLD001 Melioidosis 66 0.080
654
CRP001 Carpal Tunnel Syndrome 68 0.080
655
TRC008 Trachoma 49 0.080
656
SPT004 Septic Arthritis 55 0.080
657
PHR003 Pharyngitis 56 0.079
658
c ACT004 Acute Diarrhea 38 0.079
659
P HYP265 Hypotonia 43 0.079
660
CRC021 Carcinosarcoma 62 0.079
661
P TRC086 Trichohepatoenteric Syndrome 1 57 0.079
662
c AFB002 Afibrinogenemia, Congenital 62 0.079
663
P HST010 Histiocytosis 54 0.079
664
THY122 Thyroid Gland Cancer 59 0.078
665
END040 Endogenous Depression 55 0.078
666
BLD053 Blood Platelet Disease 51 0.078
667
AND002 Androgen Insensitivity Syndrome 66 0.078
668
URT001 Urethritis 44 0.078
669
ANT009 Antithrombin Iii Deficiency 57 0.078
670
APH002 Aphasia 56 0.078
671
P DYS026 Dysfibrinogenemia 42 0.078
672
c GCH015 Gaucher Disease, Type I 65 0.077
673
MMM001 Mammary Paget's Disease 53 0.077
674
P ANG001 Angelman Syndrome 65 0.077
675
DNG001 Dengue Shock Syndrome 43 0.076
676
HMP005 Hemiplegia 55 0.076
677
RRC033 Rare Coagulation Disorder 16 0.076
678
NRT001 Neurotic Disorder 53 0.076
679
c DPH024 Diaphragmatic Hernia, Congenital 66 0.076
680
END062 Endometrial Hyperplasia 49 0.075
681
c ALM001 Al Amyloidosis 50 0.075
682
FCT034 Factor V and Factor Viii, Combined Deficiency of, 2 37 0.075
683
VRS002 Virus-Associated Trichodysplasia Spinulosa 33 0.075
684
MNN020 Meningococcal Infection 46 0.075
685
ATN004 Autonomic Neuropathy 43 0.075
686
P ORT004 Orthostatic Intolerance 68 0.075
687
c FML001 Familial Atrial Fibrillation 67 0.075
688
GNG003 Gingival Recession 43 0.075
689
P ACT232 Acute Necrotizing Encephalopathy 28 0.075
690
NRM004 Neuroma 50 0.075
691
ATR057 Atrioventricular Block 56 0.074
692
c INF145 Infantile Liver Failure Syndrome 1 50 0.073
693
PNM001 Pneumocystosis 53 0.073
694
c ANM038 Anemia, Autoimmune Hemolytic 61 0.073
695
SCT005 Scott Syndrome 48 0.073
696
HMR023 Hemorrhagic Cystitis 40 0.073
697
P OVR049 Ovarian Disease 55 0.073
698
PLL012 Pollen Allergy 46 0.073
699
LYM021 Lymphadenitis 58 0.073
700
VTM009 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1 25 0.072
701
ANG011 Angiodysplasia 45 0.072
702
P SPN046 Spinal Muscular Atrophy 65 0.072
703
ATX010 Ataxia Neuropathy Spectrum 39 0.072
704
ORN001 Ornithosis 40 0.072
705
VGN023 Vaginitis 54 0.072
706
BLD137 Blood Group--Ahonen 17 0.072
707
INT078 Intracranial Thrombosis 48 0.072
708
PRT012 Prothrombin Deficiency 37 0.071
709
LPD004 Lipoid Nephrosis 48 0.071
710
ORL013 Oral Lichen Planus 47 0.071
711
P ACT008 Actinic Keratosis 50 0.071
712
SNL007 Senile Cataract 41 0.070
713
c PRS130 Prostate Cancer, Hereditary, 8 33 0.070
714
CRY004 Cryoglobulinemia 47 0.070
715
P PTS002 Ptosis 53 0.070
716
c PRS136 Prostate Cancer, Hereditary, 6 34 0.070
717
c TRC022 Tricuspid Valve Insufficiency 41 0.070
718
ERY004 Erysipelas 46 0.070
719
LRN003 Learning Disability 51 0.070
720
MYL020 Myelomeningocele 51 0.069
721
INT051 Intussusception 48 0.069
722
P END046 Endometritis 49 0.069
723
P CRN024 Corneal Disease 42 0.069
724
MCP006 Mucoepidermoid Carcinoma 53 0.069
725
c RRH015 Rare Hemorrhagic Disorder 21 0.069
726
MSN004 Mesenchymal Cell Neoplasm 45 0.069
727
HRD083 Hereditary Antithrombin Deficiency 30 0.069
728
DVR002 Diverticulitis 44 0.069
729
P MTR012 Mitral Valve Disease 59 0.069
730
CCN002 Cocaine Abuse 48 0.068
731
TBR011 Tuberculous Meningitis 50 0.068
732
TLR001 Tularemia 44 0.068
733
RCK002 Rocky Mountain Spotted Fever 40 0.068
734
CLC006 Calcinosis 48 0.067
735
URN010 Urinary Tract Obstruction 59 0.067
736
HRN026 Hernia, Hiatus 46 0.067
737
PLC001 Placenta Accreta 44 0.067
738
P RNL015 Renal Hypertension 47 0.066
739
HPT082 Hepatic Adenomas, Familial 40 0.066
740
AMB001 Amebiasis 44 0.066
741
P RNV001 Renovascular Hypertension 49 0.066
742
PLP001 Pulpitis 48 0.066
743
BLL003 Bell's Palsy 50 0.066
744
P AXN002 Axenfeld-Rieger Syndrome 58 0.066
745
EXP004 Exophthalmos 53 0.066
746
P MLG056 Malignant Hyperthermia 60 0.066
747
CMR002 Coumarin Resistance 56 0.066
748
SPN027 Spinal Stenosis 58 0.066
749
PRT129 Prothrombin Deficiency, Congenital 52 0.065
750
CRT004 Carotid Artery Thrombosis 37 0.065
751
ORL012 Oral Leukoplakia 42 0.064
752
EBL001 Ebola Hemorrhagic Fever 48 0.064
753
CHL061 Childhood Leukemia 49 0.064
754
RDC006 Red Cell Aplasia 45 0.064
755
INT067 Interstitial Nephritis 46 0.064
756
P OPT009 Optic Neuritis 55 0.064
757
P FML018 Familial Mediterranean Fever 70 0.064
758
THY128 Thyroid Tumor 49 0.064
759
P PST095 Post-Thrombotic Syndrome 50 0.064
760
CRT017 Cartilage Disease 54 0.063
761
CRT016 Carotid Artery Disease 53 0.063
762
ART031 Aortic Coarctation 45 0.063
763
PNM013 Pneumococcal Meningitis 45 0.062
764
P BCK002 Beckwith-Wiedemann Syndrome 62 0.062
765
c VNW005 Von Willebrand Disease, Type 1 49 0.062
766
MGK001 Megakaryocytic Leukemia 65 0.062
767
PYD002 Pyoderma 51 0.062
768
DFF031 Diffuse Alveolar Hemorrhage 28 0.062
769
c CHR682 Chronic Bilirubin Encephalopathy 36 0.062
770
c VNW010 Von Willebrand Disease, Type 2 58 0.061
771
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.061
772
WLS001 Wilson Disease 69 0.061
773
P PLY017 Polyarteritis Nodosa 52 0.061
774
END011 Endometriosis of Ovary 35 0.061
775
P HYP055 Hypoplastic Left Heart Syndrome 63 0.061
776
P PRR002 Pure Red-Cell Aplasia 47 0.061
777
HYP781 Hypoascorbemia 48 0.061
778
NRG002 Neurogenic Bladder 55 0.061
779
MST024 Mastocytosis, Cutaneous 65 0.061
780
P GLM040 Glioma Susceptibility 1 68 0.060
781
ANC002 Anca-Associated Vasculitis 43 0.060
782
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.060
783
c OVR114 Ovarian Cancer 1 39 0.060
784
P OTS001 Otosclerosis 51 0.060
785
MCR141 Mucormycosis 48 0.060
786
P HRD011 Hereditary Spherocytosis 59 0.060
787
ART017 Aortic Disease 49 0.059
788
C1N001 C1 Inhibitor Deficiency 39 0.059
789
MDS022 Mediastinitis 42 0.059
790
DBN001 Dubin-Johnson Syndrome 58 0.059
791
BRN032 Brain Glioma 44 0.059
792
CHR073 Choreatic Disease 52 0.059
793
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.059
794
LNG108 Langerhans Cell Histiocytosis 60 0.059
795
CMP040 Complement Component 4, Partial Deficiency of 34 0.058
796
CVR006 Cavernous Hemangioma 49 0.058
797
GLS018 Glass Syndrome 51 0.058
798
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.058
799
CYS009 Cystadenoma 43 0.058
800
P MGL001 Megaloblastic Anemia 54 0.058
801
ALR002 Al-Raqad Syndrome 32 0.058
802
P HMF004 Hemifacial Spasm 40 0.058
803
c HMF011 Hemifacial Spasm, Familial 34 0.058
804
P CRN028 Corneal Ulcer 49 0.058
805
LCH001 Leech Infestation 40 0.057
806
KRT001 Keratoconjunctivitis Sicca 53 0.057
807
APH001 Aphthous Stomatitis 56 0.057
808
P RTN014 Retinal Artery Occlusion 46 0.057
809
GLL008 Gilles De La Tourette Syndrome 66 0.057
810
BLL004 Bullous Keratopathy 47 0.057
811
HMP018 Hemophilic Arthropathy 35 0.057
812
MYC088 Mycobacterium Avium Complex Infections 30 0.057
813
MCR088 Microscopic Polyangiitis 51 0.057
814
ANC001 Ancylostomiasis 39 0.056
815
GLC006 Galactosemia 63 0.055
816
PPL049 Papillon-Lefevre Syndrome 63 0.055
817
LWC002 Lowe Oculocerebrorenal Syndrome 63 0.055
818
ART001 Arterial Tortuosity Syndrome 60 0.055
819
GST037 Gastroparesis 52 0.055
820
c PST005 Posterior Uveitis 52 0.055
821
P ALP106 Alport Syndrome 1, X-Linked 55 0.054
822
TKY002 Takayasu Arteritis 61 0.054
823
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.054
824
PYD001 Pyoderma Gangrenosum 53 0.054
825
VLV044 Vulvar Intraepithelial Neoplasia 44 0.054
826
HYP458 Hyper Ige Syndrome 60 0.054
827
P MYG005 Myoglobinuria 43 0.054
828
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 56 0.054
829
HNT002 Hantavirus Pulmonary Syndrome 48 0.054
830
ANG046 Angioimmunoblastic T-Cell Lymphoma 49 0.054
831
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.053
832
FRN014 Fournier Gangrene 38 0.053
833
P NMN002 Niemann-Pick Disease 60 0.053
834
HMN035 Hemangioma-Thrombocytopenia Syndrome 40 0.053
835
AML001 Amelanotic Melanoma 38 0.053
836
c INH004 Inherited Blood Coagulation Disease 31 0.053
837
c BLD140 Blood Group, I System 29 0.052
838
DDN006 Duodenitis 44 0.052
839
ELP001 Elephantiasis 37 0.052
840
c GLY008 Glycogen Storage Disease Ii 68 0.051
841
ADP007 Adie Pupil 40 0.051
842
HNM002 Hinman Syndrome 26 0.051
843
ORC001 Orchitis 41 0.051
844
CHL013 Cholecystolithiasis 37 0.051
845
c LSS005 Lissencephaly 1 54 0.051
846
UMB002 Umbilical Hernia 45 0.051
847
P PRM011 Primary Ciliary Dyskinesia 67 0.051
848
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 65 0.050
849
AND005 Androgen Insensitivity Syndrome, Mild 20 0.050
850
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.050
851
P ACR001 Aicardi-Goutieres Syndrome 63 0.050
852
APR006 Apert Syndrome 70 0.050
853
HYD038 Hydrops Fetalis, Nonimmune 55 0.050
854
49X002 49,xxxxy Syndrome 39 0.050
855
CHD001 Chediak-Higashi Syndrome 68 0.050
856
P SYR001 Syringomyelia 51 0.050
857
SYR010 Syringomyelia, Noncommunicating Isolated 37 0.050
858
ACR008 Acrocallosal Syndrome 66 0.049
859
OBS524 Obsolete: Benign Exophthalmos Syndrome 13 0.049
861
P ALP004 Alport Syndrome 66 0.048
862
HMN016 Hemangioendothelioma 41 0.048
863
P HRM001 Hermansky-Pudlak Syndrome 64 0.048
864
c ACR116 Aicardi-Goutieres Syndrome 1 53 0.048
865
ICH001 Ichthyosis Vulgaris 54 0.048
866
ANL022 Anal Fistula 47 0.048
867
END081 Endosteal Hyperostosis, Autosomal Dominant 59 0.047
868
VRL017 Viral Hemorrhagic Fever 36 0.047
869
CHR008 Choroiditis 41 0.047
870
PRC051 Paracetamol Poisoning 31 0.047
871
SCR015 Scarlet Fever 41 0.047
872
P HMN036 Hemangiopericytoma, Malignant 57 0.047
873
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 46 0.047
874
ACT049 Acute Disseminated Encephalomyelitis 50 0.046
875
DFF015 Diffuse Glomerulonephritis 33 0.046
876
ENT001 Enterocele 44 0.046
877
SPL006 Splenic Infarction 35 0.046
878
P ECT005 Ectropion 44 0.046
879
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 48 0.046
880
PPL058 Papilloma of Choroid Plexus 57 0.046
881
HYD005 Hydrocele 47 0.045
882
CRD016 Cardiac Rupture 33 0.045
883
CLD007 Cold Agglutinin Disease 47 0.045
884
P OMP004 Omphalocele 51 0.045
885
ACT055 Actinomycosis 43 0.044
886
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.044
887
LYM022 Lymphangioma 52 0.044
888
CRB079 Cerebrospinal Fluid Leak 36 0.044
889
WTR001 Waterhouse-Friderichsen Syndrome 39 0.044
890
IMM001 Immune-Complex Glomerulonephritis 40 0.044
891
c LTN004 Late-Onset Retinal Degeneration 49 0.044
892
CRB009 Cerebritis 31 0.044
893
HRD160 Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors 15 0.044
894
HMT008 Hematuria, Benign Familial 53 0.043
895
SWL001 Swallowing Disorders 39 0.043
896
BLD163 Blood Group, Dombrock System 24 0.043
897
CRB132 Cerebral Sinovenous Thrombosis 33 0.043
898
P SHR029 Short Syndrome 56 0.043
899
IRT001 Iritis 37 0.043
900
LYM014 Lymphangitis 32 0.043
901
KLP010 Klippel-Trenaunay-Weber Syndrome 55 0.042
902
VTM010 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 2 18 0.042
903
DFF003 Diffuse Scleroderma 43 0.042
904
HYP706 Hypermobile Ehlers-Danlos Syndrome 44 0.042
905
CMP064 Complement Component 3 Deficiency 30 0.042
906
c RRL003 Rare Lymphatic Malformation 32 0.042
907
LYM116 Lymph Node Disease 43 0.042
908
P HRN001 Horner's Syndrome 46 0.042
909
P JNC001 Junctional Epidermolysis Bullosa 54 0.042
910
SPC030 Specific Language Disorder 27 0.042
911
CNS002 Constrictive Pericarditis 37 0.041
912
P ANT088 Anterior Segment Dysgenesis 41 0.041
913
P BLP003 Blepharospasm 43 0.040
914
MLL004 Mallory-Weiss Syndrome 28 0.040
915
GST007 Gastric Dilatation 30 0.040
917
MRS001 Marasmus 39 0.040
918
PCT003 Pectus Excavatum 48 0.040
919
NRN002 Neuronitis 37 0.040
920
RNL012 Renal Tuberculosis 36 0.040
921
c PSD048 Pseudo-Von Willebrand Disease 44 0.039
922
RTR011 Retroperitoneal Fibrosis 41 0.039
923
CHR177 Chromophobe Renal Cell Carcinoma 58 0.039
924
END072 Endotheliitis 36 0.039
925
CHR103 Charge Syndrome 62 0.039
926
PYR041 Pyruvate Kinase Deficiency of Red Cells 58 0.038
927
RYN001 Raynaud Disease 48 0.038
928
c CNG124 Congenital Rubella 44 0.038
929
ANK010 Ankylostomiasis 30 0.037
930
HPT081 Hepatic Infarction 32 0.037
931
HMN004 Hemangioma of Liver 35 0.037
932
TRG019 Trigonocephaly with Short Stature and Developmental Delay 31 0.037
933
BLD165 Blood Group, Colton System 21 0.036
934
BRR002 Barrett's Adenocarcinoma 36 0.036
935
P MLT007 Multiple Epiphyseal Dysplasia 56 0.036
936
P LRS001 Larsen Syndrome 55 0.036
937
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 27 0.036
938
WHM001 Whim Syndrome 55 0.036
939
ALT002 Aleutian Mink Disease 35 0.035
940
c RNG019 Ring Chromosome 3 22 0.035
941
P CRB045 Cerebellar Hypoplasia 53 0.035
942
P RST002 Restrictive Cardiomyopathy 55 0.035
943
c CLR131 Ciliary Dyskinesia, Primary, 1 59 0.035
944
FMR003 Femoral Neuropathy 36 0.034
945
RGH009 Right Atrial Isomerism 52 0.034
946
ARC007 Arachnoid Cysts 40 0.034
947
SLV025 Salivary Gland Adenoma, Pleomorphic 37 0.034
948
MLK003 Melkersson-Rosenthal Syndrome 50 0.033
949
CHL109 Childhood Apraxia of Speech 43 0.033
950
FBR089 Fibrosclerosis, Multifocal 37 0.033
951
PLM180 Pulmonary Artery Disease 33 0.033
952
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 58 0.033
953
EPT010 Epithelial-Myoepithelial Carcinoma 53 0.032
954
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.032
955
P BRN120 Bronchus Cancer 45 0.032
956
P PLM149 Palmoplantar Keratoderma and Congenital Alopecia 2 35 0.032
957
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 52 0.032
958
c PTT056 Pituitary Adenoma 1, Multiple Types 59 0.032
959
SPN331 Spondyloocular Syndrome 35 0.031
960
P CWD010 Cowden Syndrome 66 0.031
961
WRF003 Warfarin Syndrome 29 0.031
962
c WLM011 Wilms Tumor 6 38 0.031
963
c CWD006 Cowden Syndrome 1 76 0.030
964
KLT001 Klatskin's Tumor 50 0.030
965
P EPT020 Epithelioid Hemangioendothelioma 45 0.030
966
KND001 Kindler Syndrome 58 0.029
967
FLT006 Floating-Harbor Syndrome 46 0.028
968
P APL006 Aplasia Cutis Congenita 49 0.027
969
RTN179 Retinal Arteries, Tortuosity of 42 0.027
970
FNT005 Fontaine Progeroid Syndrome 43 0.027
971
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 41 0.026
972
c LYM150 Lymphatic Malformation 7 40 0.025
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