Search results for Mitogens

1740 hits were found for Mitogens

# Family MCID Name MIFTS Score
1
RSP023 Rasopathy 51 2.903
2
PRT037 Pertussis 65 0.285
3
INS024 Insulin-Like Growth Factor I 79 0.219
4
P BRS047 Breast Cancer 97 0.191
5
CYT002 Cytokine Deficiency 42 0.173
6
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.162
7
P RTN024 Retinoblastoma 73 0.137
8
c FML008 Familial Retinoblastoma 53 0.137
9
P NRB001 Neuroblastoma 72 0.135
10
P CLR023 Colorectal Cancer 99 0.134
11
P PHC003 Pheochromocytoma 71 0.129
12
CHL014 Cholera 59 0.129
13
P PRS040 Prostate Cancer 97 0.128
14
ADR040 Adrenal Gland Pheochromocytoma 46 0.128
15
P LKM002 Leukemia 68 0.125
16
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.124
17
P GLM045 Glioma 63 0.120
18
OST159 Osteogenic Sarcoma 66 0.118
19
P MLN008 Melanoma 69 0.117
20
GLL048 Glial Tumor 45 0.117
21
TTN003 Tetanus 65 0.114
22
P OVR042 Ovarian Cancer 88 0.112
23
P PNC035 Pancreatic Cancer 84 0.111
24
THY029 Thyroid Carcinoma 59 0.110
25
P LKM071 Leukemia, Chronic Lymphocytic 79 0.108
26
P VSC007 Vascular Disease 63 0.107
27
ALL026 Allergic Hypersensitivity Disease 62 0.106
28
ATM095 Autoimmune Disease 62 0.105
29
P BCL017 B-Cell Lymphoma 58 0.105
30
HYP266 Hypoxia 57 0.105
31
P AST007 Astrocytoma 51 0.102
32
48X005 48,xyyy 39 0.102
33
P HPT023 Hepatocellular Carcinoma 100 0.101
34
GLB015 Glioblastoma Multiforme 75 0.101
35
HMN044 Human Immunodeficiency Virus Type 1 71 0.095
36
TXC005 Toxic Shock Syndrome 62 0.095
37
HLX001 Helix Syndrome 47 0.095
38
P LYM118 Lymphoma 68 0.093
39
MCK005 Mckusick-Kaufman Syndrome 61 0.093
40
LNG099 Lung Disease 60 0.093
41
BNR002 Bone Resorption Disease 48 0.093
42
P LNG032 Lung Cancer 98 0.092
43
ATH013 Atherosclerosis Susceptibility 65 0.092
44
c SYS001 Systemic Lupus Erythematosus 86 0.091
45
END057 Endometrial Cancer 74 0.091
46
P RHM011 Rheumatoid Arthritis 80 0.089
47
P ADN016 Adenocarcinoma 64 0.089
48
P PSR002 Psoriasis 62 0.087
49
ISC004 Ischemia 58 0.087
50
OST012 Osteoarthritis 78 0.086
51
c ACT027 Acute Pancreatitis 60 0.086
52
P GLM007 Glomerulonephritis 57 0.086
53
c MCR113 Microvascular Complications of Diabetes 3 52 0.086
54
c MCR120 Microvascular Complications of Diabetes 7 47 0.086
55
c MCR130 Microvascular Complications of Diabetes 6 41 0.086
56
c MCR133 Microvascular Complications of Diabetes 4 41 0.086
57
IMM167 Immune Deficiency Disease 78 0.084
58
c PCH010 Pachyonychia Congenita 3 44 0.084
59
HYP066 Hyperglycemia 61 0.083
60
SQM006 Squamous Cell Carcinoma 60 0.083
61
P FBR017 Fibrosarcoma 56 0.083
62
P MYL006 Myeloid Leukemia 60 0.081
63
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.081
64
SVR004 Severe Combined Immunodeficiency 73 0.079
65
MSC007 Muscle Hypertrophy 64 0.079
66
HYP060 Hyperinsulinism 54 0.079
67
MYL069 Myeloma, Multiple 85 0.078
68
P GST053 Gastric Cancer 83 0.078
69
ACQ007 Acquired Immunodeficiency Syndrome 60 0.078
70
PST011 Pustulosis of Palm and Sole 52 0.078
71
P PRD008 Periodontitis 64 0.076
72
P INF037 Inflammatory Bowel Disease 54 0.076
73
P PLM037 Pulmonary Hypertension 67 0.074
74
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.074
75
KPS004 Kaposi Sarcoma 75 0.072
76
P SKN015 Skin Carcinoma 66 0.072
77
CRH001 Crohn's Disease 74 0.070
78
P LKM062 Leukemia, Acute Lymphoblastic 69 0.070
79
P PLM036 Pulmonary Fibrosis 65 0.070
80
ERY051 Erythroleukemia, Familial 56 0.070
81
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.070
82
CRB004 Cerebral Artery Occlusion 45 0.070
83
c LKM061 Leukemia, Acute Myeloid 84 0.068
84
P BLD134 Bladder Cancer 79 0.068
85
P LVR013 Liver Disease 68 0.068
86
P DRM053 Dermatitis, Atopic 66 0.068
87
SKN016 Skin Disease 63 0.068
88
SPN186 Spinal Cord Injury 60 0.068
89
CHR074 Choriocarcinoma 47 0.068
90
P ALZ034 Alzheimer Disease 88 0.066
91
P LNG064 Lung Cancer Susceptibility 3 78 0.066
92
BRK010 Burkitt Lymphoma 67 0.066
93
c SML038 Small Cell Cancer of the Lung 65 0.066
94
P THY023 Thymoma 65 0.066
95
ADN018 Adenoma 59 0.066
96
c THY107 Thymoma, Familial 52 0.066
97
VCC001 Vaccinia 49 0.066
98
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.066
99
PPL052 Papillomatosis, Confluent and Reticulated 33 0.066
100
AST005 Asthma 76 0.064
101
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.064
102
P HRP006 Herpes Simplex 65 0.064
103
LYM027 Lymphopenia 58 0.064
104
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.064
105
RNL077 Renal Fibrosis 47 0.064
106
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.064
107
BCL014 B-Cell Growth Factor 35 0.064
108
c ANT081 Antigen Defined by Monoclonal Antibody T87 13 0.064
109
DRM006 Dermatitis 61 0.062
110
BCT022 Bacterial Infectious Disease 56 0.062
111
NTR046 Neutrophil Migration 50 0.062
112
HMP009 Haemophilus Influenzae 43 0.062
113
c LKM005 Leukemia, T-Cell, Chronic 34 0.062
114
P GLM040 Glioma Susceptibility 1 81 0.060
115
c DLT002 Dilated Cardiomyopathy 79 0.060
116
P ART022 Arthritis 69 0.060
117
P HYP098 Hypereosinophilic Syndrome 67 0.060
118
P NSP012 Nasopharyngeal Carcinoma 66 0.060
119
P MCR115 Microvascular Complications of Diabetes 5 66 0.060
120
P END044 Endometriosis 63 0.060
121
ANT024 Anthrax Disease 58 0.060
122
P CRD246 Cardiovascular System Disease 57 0.060
123
SPL018 Splenomegaly 48 0.060
124
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.057
125
c HYP836 Hypercholesterolemia, Familial, 1 73 0.057
126
c HPT073 Hepatitis C Virus 72 0.057
127
P GRF003 Graft-Versus-Host Disease 72 0.057
128
P SYS005 Systemic Scleroderma 68 0.057
129
CHL065 Cholangiocarcinoma 68 0.057
130
P INF038 Influenza 68 0.057
131
LYM017 Lyme Disease 64 0.057
132
ORL011 Oral Cancer 60 0.057
133
P NRF002 Neurofibromatosis 56 0.057
134
INT079 Intrahepatic Cholangiocarcinoma 51 0.057
135
P BNG032 Benign Mesothelioma 46 0.057
136
ALL014 Allergic Encephalomyelitis 38 0.057
137
CYS001 Cystic Fibrosis 81 0.055
138
c MNN043 Meningioma, Familial 74 0.055
139
P KDN018 Kidney Disease 72 0.055
140
DWN001 Down Syndrome 70 0.055
141
P LPR021 Leprosy 3 69 0.055
142
LSH001 Leishmaniasis 63 0.055
143
c PRC016 Pre-Eclampsia 63 0.055
144
MNN042 Meningioma, Radiation-Induced 62 0.055
145
FTT001 Fatty Liver Disease 61 0.055
146
c SCL052 Scleroderma, Familial Progressive 61 0.055
147
MCR013 Microphthalmia 57 0.055
148
SCH014 Schistosomiasis 57 0.055
149
ALL006 Allergic Asthma 56 0.055
150
BRN004 Brain Edema 56 0.055
151
LMY002 Leiomyoma 52 0.055
152
TRM010 Traumatic Brain Injury 51 0.055
153
SPN021 Spinal Meningioma 50 0.055
154
PTT037 Pituitary Tumors 44 0.055
155
P KLZ004 Kala-Azar 1 41 0.055
156
SCR001 Secretory Meningioma 41 0.055
157
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.055
158
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.055
159
HNS001 Hansen's Disease 34 0.055
160
P ATX030 Ataxia-Telangiectasia 82 0.052
161
P MDL005 Medulloblastoma 77 0.052
162
ULC004 Ulcerative Colitis 73 0.052
163
c LKM063 Leukemia, Chronic Myeloid 72 0.052
164
MYL009 Myelodysplastic Syndrome 70 0.052
165
P MSC005 Muscular Dystrophy 66 0.052
166
CHG001 Chagas Disease 66 0.052
167
P NTR004 Neutropenia 63 0.052
168
MSL001 Measles 62 0.052
169
P LPS004 Lupus Erythematosus 61 0.052
170
EMB004 Embryonal Carcinoma 56 0.052
171
PRS045 Prostatic Hypertrophy 53 0.052
172
P MNC007 Monocytic Leukemia 53 0.052
173
TLN003 Telangiectasis 52 0.052
174
STM007 Stomatitis 50 0.052
175
BRN071 Brain Injury 49 0.052
176
P PRL003 Proliferative Glomerulonephritis 44 0.052
177
ANX004 Anoxia 40 0.052
178
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.050
179
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.050
180
P MYS003 Myasthenia Gravis 68 0.050
181
c JVN010 Juvenile Rheumatoid Arthritis 64 0.050
182
P RHB003 Rhabdomyosarcoma 63 0.050
183
ACT119 Acute Promyelocytic Leukemia 63 0.050
184
END041 Endometrial Adenocarcinoma 63 0.050
185
P CND004 Candidiasis 58 0.050
186
P EXN002 Exanthem 57 0.050
187
PPL022 Papilloma 54 0.050
188
PRS021 Prostatic Adenoma 51 0.050
189
TRY001 Trypanosomiasis 50 0.050
190
PRS129 Prostatic Hyperplasia, Benign 49 0.050
191
SQM002 Squamous Cell Papilloma 46 0.050
192
c MLG068 Malignant Glioma 46 0.050
193
ORL015 Oral Squamous Cell Carcinoma 43 0.050
194
CHR178 Chromosomal Triplication 35 0.050
195
ESP021 Esophageal Cancer 90 0.047
196
MLR004 Malaria 81 0.047
197
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.047
198
CRV035 Cervical Cancer 76 0.047
199
c ATR087 Atrial Standstill 1 75 0.047
200
P MLT020 Multiple Sclerosis 72 0.047
201
GST040 Gastric Adenocarcinoma 70 0.047
202
LYM133 Lymphoma, Hodgkin, Classic 69 0.047
203
SKN019 Skin Melanoma 68 0.047
204
BRN024 Bronchitis 68 0.047
205
HYP056 Hypoglycemia 66 0.047
206
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.047
207
DPR016 Depression 63 0.047
208
CLT003 Colitis 62 0.047
209
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.047
210
P PNC044 Pancreatitis 61 0.047
211
DPH001 Diphtheria 60 0.047
212
c ACT071 Acute Kidney Failure 60 0.047
213
c HPT016 Hepatitis B 59 0.047
214
CHL123 Chlamydia 59 0.047
215
P ANP001 Anaplastic Large Cell Lymphoma 58 0.047
216
BRN056 Bronchopulmonary Dysplasia 57 0.047
217
THY122 Thyroid Gland Cancer 57 0.047
218
P MLT074 Multiple Endocrine Neoplasia 56 0.047
219
SYN007 Synovitis 54 0.047
220
PLM010 Pulmonary Edema 54 0.047
221
P ART021 Arteriosclerosis 54 0.047
222
DBT010 Diabetic Neuropathy 54 0.047
223
P SPP010 Suppressor of Tumorigenicity 3 51 0.047
224
RTN003 Retinal Ischemia 50 0.047
225
LYM019 Lymphosarcoma 46 0.047
226
P VTR007 Vitreoretinopathy 46 0.047
227
TCL003 T Cell Deficiency 46 0.047
228
TRT001 Teratocarcinoma 45 0.047
229
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.047
230
OVR094 Ovarian Epithelial Cancer 38 0.047
231
GLM044 Glomerular Disease 37 0.047
232
PLC002 Plica Syndrome 36 0.047
233
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.044
234
BRN028 Brain Cancer 74 0.044
235
P OST002 Osteoporosis 74 0.044
236
c SPN225 Spondyloarthropathy 1 73 0.044
237
MSC157 Muscular Dystrophy, Duchenne Type 72 0.044
238
P HYP086 Hypothyroidism 69 0.044
239
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.044
240
P ADL010 Adult Respiratory Distress Syndrome 65 0.044
241
NRF007 Neurofibroma 64 0.044
242
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.044
243
c HPT001 Hepatitis C 62 0.044
244
LVR012 Liver Cirrhosis 62 0.044
245
NRL005 Neurilemmoma 60 0.044
246
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.044
247
P BRS044 Breast Adenocarcinoma 59 0.044
248
c ACT073 Acute Leukemia 58 0.044
249
IRN002 Iron Metabolism Disease 57 0.044
250
c ACT075 Acute Myocardial Infarction 57 0.044
251
P CHN012 Chondrosarcoma 56 0.044
252
P GST044 Gastritis 56 0.044
253
GLC003 Glucose Intolerance 54 0.044
254
P LTR001 Lateral Sclerosis 54 0.044
255
SLP001 Sleeping Sickness 54 0.044
256
c PRD040 Periodontitis, Chronic 53 0.044
257
SPN051 Spondylitis 51 0.044
258
47X002 47,xyy 49 0.044
259
P CHR345 Chronic Pain 44 0.044
260
PLY100 Polyploidy 40 0.044
261
INF009 Inflammatory Spondylopathy 31 0.044
262
P NNN008 Noonan Syndrome 1 76 0.040
263
P HRT032 Heart Disease 75 0.040
264
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.040
265
P HNT016 Huntington Disease 72 0.040
266
OTT002 Otitis Media 72 0.040
267
P AMY004 Amyloidosis 70 0.040
268
c CHR684 Chronic Kidney Disease 70 0.040
269
P MYP004 Myopathy 70 0.040
270
WRN001 Werner Syndrome 69 0.040
271
SRC014 Sarcoma 65 0.040
272
P ART023 Arthropathy 62 0.040
273
P KDN017 Kidney Cancer 60 0.040
274
P TXP001 Toxoplasmosis 60 0.040
275
INS001 Insulinoma 60 0.040
276
HLC007 Helicobacter Pylori Infection 59 0.040
277
P MMP001 Mumps 58 0.040
278
MNT002 Mental Depression 58 0.040
279
P BNC003 Bone Cancer 58 0.040
280
P RHN004 Rhinitis 57 0.040
281
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.040
282
c MST023 Mesothelioma, Malignant 57 0.040
283
P NRP001 Neuropathy 56 0.040
284
P GRV001 Graves' Disease 55 0.040
285
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.040
286
P HYP076 Hyperthyroidism 55 0.040
287
FLR002 Filariasis 55 0.040
288
HRY003 Hairy Cell Leukemia 55 0.040
289
NNL006 Non-Alcoholic Steatohepatitis 54 0.040
290
MST005 Mastitis 53 0.040
291
SPN035 Spindle Cell Sarcoma 53 0.040
292
P RTN018 Retinal Disease 53 0.040
293
c VRL010 Viral Hepatitis 52 0.040
294
c ACT135 Acute Graft Versus Host Disease 52 0.040
295
END086 End Stage Renal Disease 51 0.040
296
P OVR082 Overgrowth Syndrome 50 0.040
297
IGG001 Iga Glomerulonephritis 48 0.040
298
RTN020 Retinal Vascular Disease 46 0.040
299
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.040
300
MST004 Mast Cell Neoplasm 42 0.040
301
EXT007 Extracutaneous Mastocytoma 38 0.040
302
c PSD047 Pseudo-Turner Syndrome 21 0.040
303
c NRF023 Neurofibromatosis, Type Ii 80 0.037
304
P APL001 Aplastic Anemia 74 0.037
305
P RSP003 Respiratory Failure 74 0.037
306
P SCH015 Schizophrenia 74 0.037
307
MYL005 Myelofibrosis 70 0.037
308
P TBR001 Tuberous Sclerosis 70 0.037
309
P MYC084 Mycobacterium Tuberculosis 1 68 0.037
310
P MJR001 Major Depressive Disorder 68 0.037
311
PNC129 Pancreatic Adenocarcinoma 68 0.037
312
P CRD119 Cardiac Arrest 67 0.037
313
P HPT021 Hepatitis 67 0.037
314
ALL003 Allergic Rhinitis 67 0.037
315
P AGM001 Agammaglobulinemia 65 0.037
316
KRT019 Keratitis, Hereditary 65 0.037
317
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.037
318
BRC012 Brucellosis 64 0.037
319
P LMY004 Leiomyosarcoma 63 0.037
320
c SVR001 Severe Acute Respiratory Syndrome 62 0.037
321
P PRP029 Porphyria 62 0.037
322
P ENC018 Encephalopathy 61 0.037
323
P ENC004 Encephalitis 61 0.037
324
VRL011 Viral Infectious Disease 61 0.037
325
RHM001 Rheumatic Fever 60 0.037
326
P RBL001 Rubella 59 0.037
327
P BND020 Bone Disease 59 0.037
328
P MLN069 Melanoma, Uveal 59 0.037
329
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.037
330
P PLY011 Polycystic Ovary Syndrome 56 0.037
331
LMY014 Leiomyoma, Uterine 56 0.037
332
CHR100 Chronic Ulcer of Skin 55 0.037
333
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.037
334
P PMP001 Pemphigus 54 0.037
335
ECH003 Echinococcosis 53 0.037
336
P HML001 Hemolytic-Uremic Syndrome 53 0.037
337
GTR002 Goiter 53 0.037
338
P INT068 Intestinal Disease 53 0.037
339
OVR059 Ovary Adenocarcinoma 53 0.037
340
SVR096 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative 53 0.037
341
DMY004 Demyelinating Disease 52 0.037
342
P THY032 Thyroiditis 52 0.037
344
P SCK005 Sickle Cell Disease 50 0.037
345
LPR001 Lepromatous Leprosy 50 0.037
346
URT010 Ureteral Obstruction 45 0.037
347
CRB090 Cerebral Hypoxia 44 0.037
348
SCR011 Scrapie 39 0.037
349
PLY150 Polykaryocytosis Inducer 31 0.037
350
NRL016 Neural Tube Defects 82 0.033
351
P PRK057 Parkinson Disease, Late-Onset 78 0.033
352
c TBR025 Tuberous Sclerosis 1 77 0.033
353
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.033
354
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.033
355
P SRC025 Sarcoidosis 1 70 0.033
356
CNG034 Congestive Heart Failure 69 0.033
357
P ASP006 Aspergillosis 69 0.033
358
CMM004 Common Variable Immunodeficiency 68 0.033
359
MLD001 Melioidosis 68 0.033
360
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 68 0.033
361
THY111 Thyroid Carcinoma, Familial Medullary 67 0.033
362
MYC006 Mycosis Fungoides 66 0.033
363
MYL031 Myeloproliferative Neoplasm 66 0.033
364
SVR066 Severe Combined Immunodeficiency, X-Linked 66 0.033
365
P DBT009 Diabetes Mellitus 64 0.033
366
PRP083 Porphyria, Acute Intermittent 64 0.033
367
P HML002 Hemolytic Anemia 63 0.033
368
c GLC092 Glaucoma, Primary Open Angle 62 0.033
369
LPD008 Lipid Metabolism Disorder 62 0.033
370
CHL068 Cholestasis 61 0.033
371
PSR001 Psoriatic Arthritis 61 0.033
372
P INT143 Interstitial Cystitis 61 0.033
373
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.033
374
P HMN010 Hemangioma 61 0.033
375
P NPH012 Nephrotic Syndrome 60 0.033
376
INT066 Interstitial Lung Disease 60 0.033
377
HPT019 Hepatic Encephalopathy 60 0.033
378
P THL005 Thalassemia 60 0.033
379
IGR001 Ige Responsiveness, Atopic 59 0.033
380
P CYS018 Cystitis 59 0.033
381
GNG013 Gingivitis 59 0.033
382
GST045 Gastroenteritis 59 0.033
383
RBS001 Rabies 58 0.033
384
ADR005 Adrenal Carcinoma 58 0.033
385
c DWL002 Dowling-Degos Disease 1 58 0.033
386
P PRP019 Peripheral Nervous System Disease 58 0.033
387
c CHR417 Chronic Graft Versus Host Disease 57 0.033
388
P PRN023 Prion Disease 57 0.033
389
P BPL003 Bipolar Disorder 56 0.033
390
P MYS005 Myositis 56 0.033
391
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.033
392
TRN018 Transitional Cell Carcinoma 56 0.033
393
SLC006 Silicosis 56 0.033
394
VSC003 Visceral Leishmaniasis 55 0.033
395
P ANT006 Antiphospholipid Syndrome 55 0.033
396
HMS001 Hemosiderosis 54 0.033
397
P RTN016 Retinal Degeneration 53 0.033
398
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.033
399
IMP005 Impotence 52 0.033
400
P MSC003 Muscular Atrophy 52 0.033
401
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.033
402
PNG002 Pain Agnosia 51 0.033
403
THR004 Thrombocytosis 51 0.033
404
LNG031 Lung Benign Neoplasm 51 0.033
405
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.033
406
THY125 Thyroid Gland Medullary Carcinoma 50 0.033
407
P OPN001 Open-Angle Glaucoma 49 0.033
408
c INV001 Invasive Aspergillosis 49 0.033
409
HYP043 Hyperandrogenism 48 0.033
410
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.033
411
DGN001 Degenerative Disc Disease 48 0.033
412
CHL147 Chlamydia Pneumonia 48 0.033
413
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.033
414
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.033
415
TST044 Testicular Torsion 47 0.033
416
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.033
417
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.033
418
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.033
419
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.033
420
HPT004 Hepatic Coma 45 0.033
421
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.033
422
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.033
423
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.033
424
FBR019 Fibromatosis 41 0.033
425
c MJR024 Major Affective Disorder 9 41 0.033
426
P RRH023 Rare Hereditary Hemochromatosis 41 0.033
427
WLL004 Wallerian Degeneration 39 0.033
428
RTC012 Reticuloendotheliosis, X-Linked 39 0.033
429
c MJR022 Major Affective Disorder 8 38 0.033
430
STR077 Streptococcal Toxic-Shock Syndrome 37 0.033
431
PRM329 Premature Aging 35 0.033
432
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.033
433
ARG004 Argyria 27 0.033
435
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.029
436
c HMC039 Hemochromatosis, Type 1 74 0.029
437
P FML011 Familial Adenomatous Polyposis 72 0.029
438
ACR007 Acromegaly 71 0.029
439
P ATS364 Autism 70 0.029
440
ADN011 Adenoid Cystic Carcinoma 70 0.029
441
P HYP061 Hypertrophic Cardiomyopathy 70 0.029
442
PLM001 Pulmonary Tuberculosis 69 0.029
443
P SLP006 Sleep Apnea 69 0.029
444
P PNM007 Pneumonia 68 0.029
445
GST092 Gastroesophageal Reflux 67 0.029
446
c MGR028 Migraine with or Without Aura 1 67 0.029
447
c FML021 Familial Hypercholesterolemia 66 0.029
448
c MCR129 Microvascular Complications of Diabetes 1 66 0.029
449
P BRL012 Bare Lymphocyte Syndrome, Type Ii 66 0.029
450
BRR014 Barrett Esophagus 65 0.029
451
IRR002 Irritable Bowel Syndrome 65 0.029
452
c DBT099 Diabetes Mellitus, Type I 65 0.029
453
ANG020 Angiosarcoma 64 0.029
454
P MST009 Mastocytosis 64 0.029
455
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.029
456
HYP020 Hyperprolactinemia 64 0.029
457
P HYP069 Hyperparathyroidism 63 0.029
458
P CRN300 Coronary Heart Disease 1 63 0.029
459
c ACT068 Acute Cystitis 63 0.029
460
c ATM011 Autoimmune Hepatitis 63 0.029
461
P VSC011 Vasculitis 62 0.029
462
CRC021 Carcinosarcoma 62 0.029
463
RTN017 Retinal Detachment 61 0.029
464
P BNG030 Benign Ependymoma 60 0.029
465
P ALP009 Alopecia Areata 60 0.029
466
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.029
467
STT001 Status Epilepticus 60 0.029
468
P CHR285 Chronic Myelomonocytic Leukemia 60 0.029
469
SPP011 Suppression of Tumorigenicity 12 59 0.029
470
VSL002 Visual Epilepsy 59 0.029
471
P DNG005 Dengue Virus 59 0.029
472
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.029
473
PPT005 Peptic Ulcer Disease 59 0.029
474
SRC027 Sarcoma, Synovial 58 0.029
475
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.029
476
EXT034 Extrinsic Allergic Alveolitis 58 0.029
477
P INF032 Infertility 57 0.029
478
P UVT001 Uveitis 57 0.029
479
THR024 Thrombosis 57 0.029
480
P END033 Endocarditis 57 0.029
481
P FTL001 Fetal Alcohol Syndrome 57 0.029
482
CYT008 Cytomegalovirus Infection 57 0.029
483
P PYL005 Pyelonephritis 56 0.029
484
c ACT134 Acute Liver Failure 56 0.029
485
P SZR006 Seizure Disorder 56 0.029
486
HPT022 Hepatoblastoma 56 0.029
487
P DRR001 Diarrhea 55 0.029
488
c BCT007 Bacterial Meningitis 55 0.029
489
DFF005 Diffuse Large B-Cell Lymphoma 55 0.029
490
P ALP008 Alopecia 54 0.029
491
CLL010 Cellular Ependymoma 54 0.029
492
HLL004 Hellp Syndrome 54 0.029
493
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.029
494
P LCH002 Lichen Planus 53 0.029
495
RHM028 Rheumatic Heart Disease 53 0.029
496
P INS002 in Situ Carcinoma 53 0.029
497
OCL006 Ocular Hypertension 53 0.029
498
INF034 Infective Endocarditis 53 0.029
499
FNG017 Fungal Infectious Disease 53 0.029
500
GST023 Gastric Ulcer 53 0.029
501
OST011 Osteomalacia 52 0.029
502
THY030 Thyroid Gland Disease 52 0.029
503
DFF036 Differentiated Thyroid Carcinoma 52 0.029
504
ENT011 Enterocolitis 51 0.029
505
P HYP040 Hypospadias 51 0.029
506
c SVR005 Severe Pre-Eclampsia 50 0.029
507
PLC008 Placenta Disease 50 0.029
508
ENT004 Enthesopathy 49 0.029
509
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.029
510
ALV002 Alveolar Echinococcosis 49 0.029
511
PRN014 Paronychia 49 0.029
512
MNN009 Meningoencephalitis 49 0.029
513
URM002 Uremia 49 0.029
514
GLC106 Glucocorticoid Resistance, Generalized 48 0.029
515
OPD006 Opioid Addiction 48 0.029
516
ASB001 Asbestosis 47 0.029
517
P CLL015 Collagen Disease 47 0.029
518
KRT002 Keratomalacia 47 0.029
519
RTC005 Reticulosarcoma 47 0.029
520
ANV001 Anovulation 47 0.029
521
TXC011 Toxocariasis 46 0.029
522
GRW007 Growth Hormone Deficiency 46 0.029
523
HDN002 Head Injury 46 0.029
524
EPD015 Epidemic Typhus 45 0.029
525
DWR001 Dwarfism 44 0.029
526
BLR013 Biliary Tract Cancer 42 0.029
527
c MCR112 Microvascular Complications of Diabetes 2 41 0.029
528
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.029
529
KLD004 Keloid Disorder 40 0.029
530
c ACT079 Acute Proliferative Glomerulonephritis 39 0.029
531
CMB081 Combined Immunodeficiency, X-Linked 36 0.029
532
HMN002 Human Granulocytic Anaplasmosis 32 0.029
533
ASB003 Asbestos Intoxication 26 0.029
534
c HYP595 Hypertension, Essential 84 0.023
535
STR067 Stroke, Ischemic 81 0.023
536
PFF001 Pfeiffer Syndrome 79 0.023
537
c NRF024 Neurofibromatosis, Type I 77 0.023
538
SCK003 Sickle Cell Anemia 74 0.023
539
c BTT014 Beta-Thalassemia 74 0.023
540
P NJM001 Nijmegen Breakage Syndrome 74 0.023
541
c THR092 Thrombophilia Due to Thrombin Defect 73 0.023
542
ANX010 Anxiety 73 0.023
543
PRP027 Peripheral Vascular Disease 71 0.023
544
P FRG001 Fragile X Syndrome 70 0.023
545
PLY001 Polycythemia Vera 69 0.023
546
EWN003 Ewing Sarcoma 69 0.023
547
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.023
548
c BSL007 Basal Cell Carcinoma 68 0.023
549
CST001 Costello Syndrome 68 0.023
550
CNN005 Connective Tissue Disease 68 0.023
551
P THR014 Thrombocytopenia 67 0.023
552
HYL004 Hyaline Fibromatosis Syndrome 67 0.023
553
P CRB048 Cerebral Cavernous Malformations 67 0.023
554
P BLD062 Bile Duct Cancer 67 0.023
555
c ATS007 Autism Spectrum Disorder 67 0.023
556
ALC007 Alcohol Dependence 66 0.023
557
ANG054 Angina Pectoris 66 0.023
558
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.023
559
P MNN013 Meningitis 66 0.023
560
LNG039 Lung Squamous Cell Carcinoma 66 0.023
561
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 65 0.023
562
P LPS002 Liposarcoma 65 0.023
563
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.023
564
P MTR014 Motor Neuron Disease 65 0.023
565
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.023
566
KWS002 Kawasaki Disease 65 0.023
567
CLN015 Colon Adenocarcinoma 65 0.023
568
PRT036 Peritonitis 64 0.023
569
APN008 Apnea, Obstructive Sleep 64 0.023
570
PLG002 Plague 63 0.023
571
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.023
572
TRN015 Transient Cerebral Ischemia 63 0.023
573
ANR007 Anorexia Nervosa 63 0.023
574
RHB001 Rhabdoid Cancer 63 0.023
575
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.023
576
P PLY014 Polycystic Kidney Disease 62 0.023
577
c HPT003 Hepatitis a 62 0.023
578
LPP008 Lipoprotein Quantitative Trait Locus 62 0.023
579
c ANM038 Anemia, Autoimmune Hemolytic 62 0.023
580
HSH003 Hashimoto Thyroiditis 62 0.023
581
BLD131 Bladder Urothelial Carcinoma 62 0.023
582
P DRM010 Dermatomyositis 61 0.023
583
P SJG008 Sjogren Syndrome 61 0.023
584
GST033 Gestational Diabetes 61 0.023
585
CRD223 Cardiac Arrhythmia 60 0.023
586
DNG002 Dengue Hemorrhagic Fever 60 0.023
587
CHC001 Chickenpox 60 0.023
588
P CTR002 Cataract 60 0.023
589
QFV001 Q Fever 60 0.023
590
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.023
591
P MYC008 Myocarditis 59 0.023
592
P MCR010 Microcephaly 59 0.023
593
P BRN022 Bronchiectasis 59 0.023
594
c DNG003 Dengue Disease 59 0.023
595
PRN019 Perinatal Necrotizing Enterocolitis 59 0.023
596
AVN001 Avian Influenza 59 0.023
597
IRN001 Iron Deficiency Anemia 59 0.023
598
ANR040 Aneurysm 59 0.023
599
INC002 Inclusion Body Myositis 58 0.023
600
P SYP003 Syphilis 58 0.023
601
SCR008 Scrub Typhus 58 0.023
602
c PRM005 Primary Hyperparathyroidism 58 0.023
603
CNT047 Contact Dermatitis 58 0.023
604
BRS051 Breast Disease 58 0.023
605
NWB001 Newborn Respiratory Distress Syndrome 58 0.023
606
EYD002 Eye Disease 58 0.023
607
CNS004 Constipation 58 0.023
608
PMP006 Pemphigus Vulgaris, Familial 57 0.023
609
P PLV020 Pelvic Organ Prolapse 57 0.023
610
P MYM013 Moyamoya Disease 1 57 0.023
611
P PLY041 Polymyositis 57 0.023
612
CHK001 Chikungunya 57 0.023
613
CPR004 Coproporphyria, Hereditary 57 0.023
614
P FCL005 Focal Segmental Glomerulosclerosis 57 0.023
615
CMM005 Common Cold 57 0.023
616
VSC002 Vascular Dementia 57 0.023
617
JPN002 Japanese Encephalitis 57 0.023
618
P PLY018 Polycythemia 56 0.023
619
PLS011 Plasmacytoma 56 0.023
620
SFT003 Soft Tissue Sarcoma 56 0.023
621
ALL010 Allergic Contact Dermatitis 56 0.023
622
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.023
623
CYS008 Cystic Echinococcosis 56 0.023
624
HMG005 Hemoglobinopathy 56 0.023
625
GST050 Gastrointestinal System Disease 56 0.023
626
MCS002 Mucositis 56 0.023
627
AGN016 Aging 56 0.023
628
FLR001 Filarial Elephantiasis 55 0.023
629
LMB062 Limb Ischemia 55 0.023
630
FND002 Fundus Dystrophy 55 0.023
631
P MLN007 Male Infertility 55 0.023
632
P PLM034 Pulmonary Emphysema 55 0.023
633
P PTT006 Pituitary Adenoma 55 0.023
634
JVN009 Juvenile Pilocytic Astrocytoma 55 0.023
635
INT007 Intermediate Coronary Syndrome 55 0.023
636
P LRY044 Larynx Cancer 55 0.023
637
PRP030 Purpura 54 0.023
638
BRN015 Bronchiolo-Alveolar Adenocarcinoma 54 0.023
639
PRT082 Preterm Premature Rupture of the Membranes 54 0.023
640
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.023
641
P TRM003 Tremor 54 0.023
642
PNC001 Pancytopenia 54 0.023
643
CLR030 Clear Cell Renal Cell Carcinoma 53 0.023
644
PLS016 Plasma Cell Leukemia 53 0.023
645
CRH005 Crohn's Colitis 53 0.023
646
NVS001 Neovascular Glaucoma 53 0.023
647
HMC014 Homocysteinemia 53 0.023
648
ERD001 Erdheim-Chester Disease 53 0.023
649
DNT012 Dental Caries 53 0.023
650
P RTN022 Retinal Vein Occlusion 53 0.023
651
TRC003 Trichomoniasis 53 0.023
652
P SML001 Small Cell Carcinoma 52 0.023
653
P DDN001 Duodenal Ulcer 52 0.023
654
c INH030 Inherited Retinal Disorder 51 0.023
655
P HMP007 Hemophilia 51 0.023
656
OCL069 Ocular Motor Apraxia 51 0.023
657
ILS001 Ileus 51 0.023
658
CLR109 Colorectal Adenocarcinoma 51 0.023
659
NRM004 Neuroma 51 0.023
660
ASP003 Aseptic Meningitis 51 0.023
661
SKN013 Skin Benign Neoplasm 51 0.023
662
P MMB011 Membranous Nephropathy 50 0.023
663
PLR008 Pleurisy 50 0.023
664
P ECL001 Eclampsia 50 0.023
665
P ESN008 Eosinophilic Pneumonia 50 0.023
666
CHL122 Cholesteatoma of Middle Ear 50 0.023
667
FSC004 Fasciitis 50 0.023
668
c HRD202 Hereditary Lymphedema I 50 0.023
669
P TMP001 Temporal Lobe Epilepsy 50 0.023
670
ECT026 Ectopic Pregnancy 50 0.023
671
CLR003 Clear Cell Adenocarcinoma 50 0.023
672
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.023
673
OCL022 Ocular Melanoma 50 0.023
674
c INF023 Inflammatory Breast Carcinoma 50 0.023
675
ISL003 Isolated Growth Hormone Deficiency 49 0.023
676
P MYT002 Myotonic Dystrophy 49 0.023
677
P IGN003 Iga Nephropathy 1 49 0.023
678
PLP001 Pulpitis 49 0.023
679
P CRV031 Cervical Adenocarcinoma 49 0.023
680
P CTN015 Cutaneous T Cell Lymphoma 49 0.023
681
c 46X049 46,xy Sex Reversal 2 48 0.023
682
HST010 Histiocytosis 48 0.023
683
INT017 Intestinal Schistosomiasis 48 0.023
684
NCR007 Necrotizing Fasciitis 48 0.023
685
ATS010 Autosomal Recessive Disease 48 0.023
686
CLC006 Calcinosis 48 0.023
687
RFR010 Refractory Anemia 48 0.023
688
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.023
689
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.023
690
P RNV001 Renovascular Hypertension 48 0.023
691
PLM035 Pulmonary Eosinophilia 48 0.023
692
BBS001 Babesiosis 48 0.023
693
END062 Endometrial Hyperplasia 48 0.023
694
PNC013 Pancreatic Ductal Carcinoma 48 0.023
695
SVR098 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Positive 48 0.023
696
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.023
697
PRL017 Prolymphocytic Leukemia 47 0.023
698
CRC014 Carcinoid Tumors, Intestinal 47 0.023
699
PPL002 Papillary Carcinoma 47 0.023
700
ADN001 Adenosine Deaminase Deficiency 47 0.023
701
THY128 Thyroid Tumor 47 0.023
702
P HMN032 Human Herpesvirus 8 47 0.023
703
AML029 Ameloblastoma 46 0.023
704
PLL012 Pollen Allergy 46 0.023
705
FLL008 Folliculitis 46 0.023
706
CWP001 Cowpox 46 0.023
707
c ACT042 Acute Pyelonephritis 46 0.023
708
STP004 Staphylococcal Toxic Shock Syndrome 45 0.023
709
ORL013 Oral Lichen Planus 45 0.023
710
PLR022 Pleural Disease 45 0.023
711
IMM003 Immunoglobulin Alpha Deficiency 45 0.023
712
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.023
713
ACT003 Acute Kidney Tubular Necrosis 45 0.023
714
P DSR089 Disorders of Sexual Development 45 0.023
715
c CLR017 Clear Cell Sarcoma 45 0.023
716
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.023
717
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.023
718
PLX002 Plexiform Neurofibroma 44 0.023
719
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.023
720
c PRM038 Primary Agammaglobulinemia 44 0.023
721
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.023
722
CHN010 Chondroma 43 0.023
723
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.023
724
NRF003 Neurofibrosarcoma 43 0.023
725
CRS001 Crescentic Glomerulonephritis 43 0.023
726
P HYP265 Hypotonia 43 0.023
727
ONC003 Oncogenic Osteomalacia 42 0.023
728
c MLG079 Malignant Pleural Mesothelioma 42 0.023
729
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.023
730
MSN004 Mesenchymal Cell Neoplasm 41 0.023
731
MMM006 Mammographic Density 41 0.023
732
DBT002 Diabetic Autonomic Neuropathy 41 0.023
733
PRS063 Paresthesia 41 0.023
734
P MLG074 Malignant Mesenchymoma 40 0.023
735
FNG016 Fungal Keratitis 40 0.023
736
P BRY005 Beryllium Disease 40 0.023
737
LNG030 Lung Adenoma 39 0.023
739
P PRP021 Peripheral Nervous System Neoplasm 39 0.023
740
PRS123 Persistent Generalized Lymphadenopathy 37 0.023
741
KRT003 Keratinizing Squamous Cell Carcinoma 37 0.023
742
SYS071 Systemic Autoimmune Disease 37 0.023
743
TRC020 Tracheitis 36 0.023
744
BRN018 Borna Disease 36 0.023
746
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.023
747
P PRG002 Progesterone-Receptor Positive Breast Cancer 35 0.023
749
IMM143 Immunodeficiency 48 33 0.023
750
CND006 Candida Glabrata 32 0.023
751
P PLY188 Polyendocrinopathy 32 0.023
752
BLD047 Bladder Squamous Cell Carcinoma 31 0.023
753
PLR005 Pleuropneumonia 31 0.023
754
NLL001 Null-Cell Leukemia 30 0.023
755
ENC014 Enchondroma 29 0.023
756
IMM071 Immunodeficiency 12 29 0.023
757
CD4001 Cd45 Deficiency 28 0.023
758
BLD028 Bladder Lymphoma 27 0.023
759
NRL008 Neural Crest Tumor 27 0.023
760
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.023
761
THY006 Thymus Lymphoma 26 0.023
762
PRQ002 Paraquat Poisoning 26 0.023
763
TBS005 T-B+ Severe Combined Immunodeficiency Due to Cd3delta/cd3epsilon/cd3zeta 24 0.023
764
MD2001 Med23 22 0.023
765
HML018 Homologous Wasting Disease 22 0.023
766
STP007 Staphylococcal Scarlet Fever 21 0.023
767
CD4008 Cd4/cd8 T-Cell Ratio 20 0.023
768
SKL031 Skeletal Dysplasia-T-Cell Immunodeficiency-Developmental Delay Syndrome 18 0.023
769
c FNC027 Fanconi Anemia, Complementation Group a 81 0.017
770
P RTT002 Rett Syndrome 80 0.017
771
P RTN008 Retinitis Pigmentosa 79 0.017
772
CNN003 Conn's Syndrome 79 0.017
773
GST019 Gastrointestinal Stromal Tumor 78 0.017
774
P LYN001 Lynch Syndrome 77 0.017
775
PHN003 Phenylketonuria 75 0.017
776
ADR007 Adrenoleukodystrophy 75 0.017
777
LPT014 Leptin Deficiency or Dysfunction 74 0.017
778
VNH007 Von Hippel-Lindau Syndrome 73 0.017
779
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.017
780
P CNR004 Cone-Rod Dystrophy 2 73 0.017
781
P FML018 Familial Mediterranean Fever 73 0.017
782
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.017
783
P WSK001 Wiskott-Aldrich Syndrome 72 0.017
784
c EXD008 Exudative Vitreoretinopathy 1 71 0.017
785
BHC003 Behcet Syndrome 71 0.017
786
P EPL164 Epilepsy 71 0.017
787
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.017
788
P MYC007 Myocardial Infarction 70 0.017
789
DFC004 Deficiency Anemia 70 0.017
790
MLT157 Multiple System Atrophy 1 70 0.017
791
P CRD224 Cardiofaciocutaneous Syndrome 1 70 0.017
792
P TTR001 Tetralogy of Fallot 70 0.017
793
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.017
794
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.017
795
ADL002 Adult Syndrome 70 0.017
796
c PNC108 Pancreatitis, Hereditary 70 0.017
797
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.017
798
SVR097 Severe Cutaneous Adverse Reaction 69 0.017
799
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.017
800
CRB037 Cerebral Palsy 69 0.017
801
ART016 Aortic Aneurysm 69 0.017
802
LYM007 Lymphangioleiomyomatosis 69 0.017
803
MST024 Mastocytosis, Cutaneous 69 0.017
804
c MYT021 Myotonic Dystrophy 1 69 0.017
805
NVS017 Nevus, Epidermal 68 0.017
806
ODN023 Odontochondrodysplasia 68 0.017
807
OBS002 Obsessive-Compulsive Disorder 68 0.017
808
PCK003 Pick Disease of Brain 68 0.017
809
c NMN015 Niemann-Pick Disease, Type C1 68 0.017
810
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.017
811
P ESS003 Essential Thrombocythemia 68 0.017
812
P ALP004 Alport Syndrome 68 0.017
813
RCK004 Rickets 68 0.017
814
P FRN006 Frontotemporal Dementia 68 0.017
815
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.017
816
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.017
817
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.017
818
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.017
819
c INF071 Inflammatory Bowel Disease 1 67 0.017
820
FCT007 Factor Vii Deficiency 67 0.017
821
P OLG002 Oligodendroglioma 67 0.017
822
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.017
823
CRB039 Cerebrovascular Disease 67 0.017
824
P FLL037 Follicular Lymphoma 67 0.017
825
P TRN020 Turner Syndrome 67 0.017
826
FLL027 Fallopian Tube Carcinoma 67 0.017
827
CRP001 Carpal Tunnel Syndrome 67 0.017
828
c RHB024 Rhabdomyosarcoma 2 67 0.017
829
c PRM196 Premature Ovarian Failure 1 67 0.017
830
c TYR012 Tyrosinemia, Type I 66 0.017
831
P DMN002 Dementia 66 0.017
832
MYX005 Myxoid Liposarcoma 66 0.017
833
c PSD108 Pseudohypoparathyroidism, Type Ia 66 0.017
834
c FML346 Familial Adenomatous Polyposis 1 66 0.017
835
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.017
836
ACH004 Achondroplasia 66 0.017
837
P ATR011 Atrial Fibrillation 66 0.017
838
P HYD006 Hydrocephalus 66 0.017
839
P NRV007 Nervous System Disease 66 0.017
840
c MCL013 Mucolipidosis Iv 66 0.017
841
KHL003 Kohlschutter-Tonz Syndrome 65 0.017
842
CRN036 Craniopharyngioma 65 0.017
843
CNC002 Cinca Syndrome 65 0.017
844
c FML001 Familial Atrial Fibrillation 65 0.017
845
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.017
846
P HRS035 Hirschsprung Disease 1 65 0.017
847
P ART005 Arteriovenous Malformation 65 0.017
848
P DYS154 Dystonia 65 0.017
849
ACR006 Aceruloplasminemia 65 0.017
850
PPL049 Papillon-Lefevre Syndrome 65 0.017
851
P PSD087 Pseudoxanthoma Elasticum 65 0.017
852
PRP001 Propionic Acidemia 65 0.017
853
MSM014 Mismatch Repair Cancer Syndrome 65 0.017
854
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.017
855
DRM014 Dermatofibrosarcoma Protuberans 65 0.017
856
MRK001 Merkel Cell Carcinoma 65 0.017
857
c WLM013 Wilms Tumor 1 65 0.017
858
P PLR004 Pleuropulmonary Blastoma 65 0.017
859
P PRS038 Personality Disorder 65 0.017
860
MCK007 Muckle-Wells Syndrome 65 0.017
861
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.017
862
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.017
863
c MCP001 Mucopolysaccharidosis Iii 65 0.017
864
NRM005 Neuromuscular Disease 64 0.017
865
OVR029 Ovarian Hyperstimulation Syndrome 64 0.017
866
TBC004 Tobacco Addiction 64 0.017
867
GT001 Gout 64 0.017
868
ALS001 Alstrom Syndrome 64 0.017
869
CLR108 Colorectal Adenoma 64 0.017
870
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.017
871
ART002 Arts Syndrome 64 0.017
872
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.017
873
PLM031 Poliomyelitis 64 0.017
874
RBR001 Roberts Syndrome 64 0.017
875
OST017 Osteomyelitis 64 0.017
876
c EPS035 Episodic Ataxia, Type 2 63 0.017
877
c DPH024 Diaphragmatic Hernia, Congenital 63 0.017
878
P GCH001 Gaucher's Disease 63 0.017
879
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.017
880
TYP007 Typhoid Fever 63 0.017
881
CNT061 Conotruncal Heart Malformations 63 0.017
882
c MLG084 Malignant Fibrous Histiocytoma 63 0.017
883
INT146 Intervertebral Disc Disease 63 0.017
884
HYP780 Hypoadrenocorticism, Familial 63 0.017
885
c ALP101 Alpha-Thalassemia 62 0.017
886
P ECT006 Ectodermal Dysplasia 62 0.017
887
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.017
888
LRN002 Laron Syndrome 62 0.017
889
c FNC043 Fanconi Anemia, Complementation Group E 62 0.017
890
NNN026 Noonan Syndrome with Multiple Lentigines 62 0.017
891
RTN209 Retinoschisis 1, X-Linked, Juvenile 62 0.017
892
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.017
893
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.017
894
PRM126 Primary Peritoneal Carcinoma 62 0.017
895
P LRS001 Larsen Syndrome 62 0.017
896
P ESP024 Esophagitis 62 0.017
897
P TRC086 Trichohepatoenteric Syndrome 1 62 0.017
898
BLL006 Bullous Pemphigoid 62 0.017
899
LSC001 Lesch-Nyhan Syndrome 62 0.017
900
PHL006 Phelan-Mcdermid Syndrome 62 0.017
901
BRS099 Breast Ductal Carcinoma 62 0.017
902
NRM019 Neuraminidase Deficiency 62 0.017
903
CTN007 Cutaneous Leishmaniasis 62 0.017
904
MDD011 Mood Disorder 62 0.017
905
P OST009 Osteochondritis Dissecans 62 0.017
906
P PRM006 Primary Biliary Cirrhosis 62 0.017
907
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 62 0.017
908
P CRN038 Carney Complex Variant 61 0.017
909
ATY005 Atypical Teratoid Rhabdoid Tumor 61 0.017
910
c MCP043 Mucopolysaccharidosis, Type Iiia 61 0.017
911
P HYP097 Hyperekplexia 61 0.017
912
OST003 Osteonecrosis 61 0.017
913
INT002 Intermittent Claudication 61 0.017
914
CHR001 Churg-Strauss Syndrome 61 0.017
915
c PNS012 Paine Syndrome 61 0.017
916
YLL002 Yellow Fever 61 0.017
917
ALC006 Alcoholic Hepatitis 61 0.017
918
CHR066 Chronic Fatigue Syndrome 61 0.017
919
ALV005 Alveolar Soft Part Sarcoma 61 0.017
920
c WLM018 Wilms Tumor 5 61 0.017
921
RCT015 Reactive Arthritis 61 0.017
922
SDD001 Sudden Infant Death Syndrome 61 0.017
923
FBR086 Fibrolamellar Carcinoma 61 0.017
924
PRG017 Paraganglioma and Gastric Stromal Sarcoma 61 0.017
925
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.017
926
SZR001 Sezary's Disease 60 0.017
927
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.017
928
c LPM012 Lipomatosis, Multiple 60 0.017
929
c JVN061 Juvenile Arthritis 60 0.017
930
P SCL018 Scoliosis 60 0.017
931
P VNT002 Ventricular Septal Defect 60 0.017
932
c LYN004 Lynch Syndrome I 60 0.017
933
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.017
934
P HRD011 Hereditary Spherocytosis 60 0.017
935
P OPT006 Optic Nerve Disease 60 0.017
936
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.017
937
PRT013 Portal Hypertension 59 0.017
938
IDP011 Idiopathic Interstitial Pneumonia 59 0.017
939
PNM001 Pneumocystosis 59 0.017
940
LGS001 Legius Syndrome 59 0.017
941
P SLP005 Sleep Disorder 59 0.017
942
PLM033 Pulmonary Embolism 59 0.017
943
P PRD006 Prader-Willi Syndrome 59 0.017
944
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 59 0.017
945
P LYM033 Lymphoproliferative Syndrome 59 0.017
946
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.017
947
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.017
948
c LTN004 Late-Onset Retinal Degeneration 59 0.017
949
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.017
950
c HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 59 0.017
951
c MCP045 Mucopolysaccharidosis, Type Iiic 59 0.017
952
GRD007 Grade Iii Astrocytoma 59 0.017
953
KLP010 Klippel-Trenaunay-Weber Syndrome 59 0.017
954
P HMN036 Hemangiopericytoma, Malignant 59 0.017
955
P NMN002 Niemann-Pick Disease 59 0.017
956
P GLL022 Guillain-Barre Syndrome 59 0.017
957
ACH043 Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans 59 0.017
958
c MCP044 Mucopolysaccharidosis, Type Iiib 59 0.017
959
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.017
960
RNL024 Renal Glucosuria 58 0.017
961
P FML052 Familial Cold Autoinflammatory Syndrome 58 0.017
962
KRT071 Keratosis, Seborrheic 58 0.017
963
P PLY017 Polyarteritis Nodosa 58 0.017
964
P TYR004 Tyrosinemia 58 0.017
965
P INT070 Intestinal Obstruction 58 0.017
966
P HYP726 Hypercalcemia, Infantile, 1 58 0.017
967
FBR047 Fibromyalgia 58 0.017
968
c SHR072 Short-Rib Thoracic Dysplasia 3 with or Without Polydactyly 58 0.017
969
CHR072 Chordoma 58 0.017
970
c PRG018 Paragangliomas 1 58 0.017
971
P ALC033 Alcohol Use Disorder 58 0.017
972
HYP458 Hyper Ige Syndrome 58 0.017
973
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.017
974
ERY003 Erythema Multiforme 58 0.017
975
P URT039 Urticaria 58 0.017
976
DSS008 Disease of Mental Health 58 0.017
977
LNG108 Langerhans Cell Histiocytosis 58 0.017
978
c THY102 Thyroid Cancer, Nonmedullary, 2 58 0.017
979
P GLL018 Gallbladder Cancer 57 0.017
980
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.017
981
CST005 Castleman Disease 57 0.017
982
BLM002 Bulimia Nervosa 57 0.017
983
P SLV026 Salivary Gland Carcinoma 57 0.017
984
P HDC001 Headache 57 0.017
985
DSS009 Disseminated Intravascular Coagulation 57 0.017
986
PRL032 Perlman Syndrome 57 0.017
987
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 57 0.017
988
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.017
989
THY022 Thymic Carcinoma 57 0.017
990
P PRV006 Pervasive Developmental Disorder 57 0.017
991
TNS005 Tonsillitis 57 0.017
992
c LKM070 Leukemia, Acute Monocytic 57 0.017
993
HMR039 Hemorrhage, Intracerebral 57 0.017
994
CRT033 Corticobasal Degeneration 57 0.017
995
c SML009 Small Intestine Adenocarcinoma 57 0.017
996
PHR003 Pharyngitis 57 0.017
997
AYM001 Ayme-Gripp Syndrome 57 0.017
998
P ADL017 Adult T-Cell Leukemia 56 0.017
999
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.017
1000
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 56 0.017
1001
CMR002 Coumarin Resistance 56 0.017
1002
DNN002 Donnai-Barrow Syndrome 56 0.017
1003
HMT008 Hematuria, Benign Familial 56 0.017
1004
EXF001 Exfoliation Syndrome 56 0.017
1005
SPN041 Spinal Cord Disease 56 0.017
1006
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.017
1007
FNC009 Fanconi-Bickel Syndrome 56 0.017
1008
ISL001 Islet Cell Tumor 56 0.017
1009
ACS001 Acoustic Neuroma 56 0.017
1010
ANN002 Anencephaly 56 0.017
1011
P PSD015 Pseudohypoparathyroidism 56 0.017
1012
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.017
1013
SBC001 Subacute Sclerosing Panencephalitis 56 0.017
1014
MTH009 Mouth Disease 56 0.017
1015
c MCR256 Microphthalmia, Syndromic 9 56 0.017
1016
P LBR014 Leber Congenital Amaurosis 4 56 0.017
1017
ORL005 Oral Candidiasis 56 0.017
1018
P INF049 Infantile Myofibromatosis 56 0.017
1019
P HYP024 Hypoparathyroidism 56 0.017
1020
P PNM006 Pneumoconiosis 56 0.017
1021
c GRV008 Graves Disease 1 56 0.017
1022
P PLY019 Polyneuropathy 56 0.017
1023
PSD014 Pseudopseudohypoparathyroidism 55 0.017
1024
c FML035 Familial Hyperlipidemia 55 0.017
1025
HYP005 Hypokalemia 55 0.017
1026
ORP003 Oropharynx Cancer 55 0.017
1027
MCL006 Macular Retinal Edema 55 0.017
1028
NRG002 Neurogenic Bladder 55 0.017
1029
ZLL002 Zollinger-Ellison Syndrome 55 0.017
1030
SCH016 Schimke Immunoosseous Dysplasia 55 0.017
1031
AMB001 Amebiasis 55 0.017
1032
PLV003 Pelvic Inflammatory Disease 55 0.017
1033
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.017
1034
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.017
1035
P MYP006 Myopia 55 0.017
1036
P STR020 Strabismus 55 0.017
1037
CPL003 Capillary Leak Syndrome 55 0.017
1038
P SBS003 Substance Abuse 55 0.017
1039
HDR002 Hidradenitis Suppurativa 55 0.017
1040
CRC006 Carcinoid Syndrome 55 0.017
1041
c INT064 Intermediate Uveitis 55 0.017
1042
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.017
1043
PRN001 Purine Nucleoside Phosphorylase Deficiency 55 0.017
1044
P VNS003 Venous Insufficiency 55 0.017
1045
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.017
1046
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.017
1047
P SCL048 Sclerosteosis 55 0.017
1048
END040 Endogenous Depression 55 0.017
1049
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.017
1050
P NRM002 Normal Pressure Hydrocephalus 54 0.017
1051
P SPN052 Spondyloarthropathy 54 0.017
1052
RSC001 Rosacea 54 0.017
1053
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.017
1054
GLS001 Gliosarcoma 54 0.017
1055
ACD008 Acid-Labile Subunit Deficiency 54 0.017
1056
HMN009 Hemangioblastoma 54 0.017
1057
AMN003 Amnestic Disorder 54 0.017
1058
CRT017 Cartilage Disease 54 0.017
1059
VGN023 Vaginitis 54 0.017
1060
P FML068 Familial Hypocalciuric Hypercalcemia 54 0.017
1061
GNG004 Ganglioglioma 54 0.017
1062
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.017
1063
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.017
1064
PRT038 Protein-Energy Malnutrition 54 0.017
1065
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.017
1066
TND005 Tendinitis 54 0.017
1067
PRC013 Pericarditis 54 0.017
1068
PSD007 Pseudomyxoma Peritonei 54 0.017
1069
ANL018 Analbuminemia 54 0.017
1070
AMN001 Amenorrhea 54 0.017
1071
c FML116 Familial Cold Autoinflammatory Syndrome 1 54 0.017
1072
c PST005 Posterior Uveitis 54 0.017
1073
P LNG035 Lung Large Cell Carcinoma 54 0.017
1074
SVR010 Severe Combined Immunodeficiency with Sensitivity to Ionizing Radiation 54 0.017
1075
c CNG021 Congenital Toxoplasmosis 54 0.017
1076
WST005 West Nile Virus 54 0.017
1077
SNS003 Sensory Peripheral Neuropathy 54 0.017