Search results for Selenium

1009 hits were found for Selenium

# Family MCID Name MIFTS Score
1
KSH001 Keshan Disease 34 3.138
2
SLN002 Selenium Poisoning 11 3.086
3
P HYP086 Hypothyroidism 69 0.240
4
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.228
5
P PRS040 Prostate Cancer 97 0.216
6
P THY032 Thyroiditis 52 0.215
7
P MYP004 Myopathy 70 0.195
8
P MSC005 Muscular Dystrophy 66 0.187
9
HSH003 Hashimoto Thyroiditis 62 0.184
10
c ATR087 Atrial Standstill 1 75 0.183
11
P CLR023 Colorectal Cancer 99 0.180
12
KSH004 Kashin-Beck Disease 38 0.179
13
MST005 Mastitis 53 0.170
14
P MRC003 Mercury Poisoning 48 0.168
15
GTR002 Goiter 53 0.162
16
ADN018 Adenoma 59 0.150
17
THY030 Thyroid Gland Disease 52 0.150
18
P HYP076 Hyperthyroidism 55 0.146
19
P LVR013 Liver Disease 68 0.141
20
P CTR002 Cataract 60 0.141
21
P GRV001 Graves' Disease 55 0.141
22
P HPT023 Hepatocellular Carcinoma 100 0.139
23
P SKN015 Skin Carcinoma 66 0.136
24
LVR012 Liver Cirrhosis 62 0.134
25
PHN003 Phenylketonuria 75 0.132
26
P INF032 Infertility 57 0.130
27
P KDN018 Kidney Disease 72 0.128
28
c PRC016 Pre-Eclampsia 63 0.126
29
P CRN300 Coronary Heart Disease 1 63 0.126
30
c DLT002 Dilated Cardiomyopathy 79 0.122
31
P MLN007 Male Infertility 55 0.122
32
48X005 48,xyyy 39 0.120
33
P HRT032 Heart Disease 75 0.118
34
P ALZ034 Alzheimer Disease 88 0.116
35
THY029 Thyroid Carcinoma 59 0.116
36
P ALP008 Alopecia 54 0.116
37
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.114
38
CNG034 Congestive Heart Failure 69 0.114
39
P ADN016 Adenocarcinoma 64 0.114
40
ISC004 Ischemia 58 0.114
41
P LTR001 Lateral Sclerosis 54 0.114
42
P LNG032 Lung Cancer 98 0.112
43
P BRS047 Breast Cancer 97 0.112
44
CRH001 Crohn's Disease 74 0.112
45
CYS001 Cystic Fibrosis 81 0.109
46
P RHM011 Rheumatoid Arthritis 80 0.109
47
P BLD134 Bladder Cancer 79 0.109
48
LPD008 Lipid Metabolism Disorder 62 0.109
49
DNT012 Dental Caries 53 0.109
50
ESP021 Esophageal Cancer 90 0.107
51
DFC004 Deficiency Anemia 70 0.107
52
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.107
53
HYP066 Hyperglycemia 61 0.107
54
GST033 Gestational Diabetes 61 0.107
55
P MYC008 Myocarditis 59 0.107
56
P DRR001 Diarrhea 55 0.107
57
P GST053 Gastric Cancer 83 0.105
58
CLR108 Colorectal Adenoma 64 0.105
59
TXC005 Toxic Shock Syndrome 62 0.105
60
DRM006 Dermatitis 61 0.105
61
PTY002 Pityriasis Versicolor 38 0.105
62
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.105
63
PPL052 Papillomatosis, Confluent and Reticulated 33 0.105
64
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.102
65
P MYC007 Myocardial Infarction 70 0.102
66
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.102
67
c PCH010 Pachyonychia Congenita 3 44 0.102
68
c PRS136 Prostate Cancer, Hereditary, 6 33 0.102
69
c PRS130 Prostate Cancer, Hereditary, 8 32 0.102
70
P OVR042 Ovarian Cancer 88 0.100
71
c CHR684 Chronic Kidney Disease 70 0.100
72
P PSR002 Psoriasis 62 0.100
73
NTR005 Nutritional Deficiency Disease 62 0.100
74
ACQ007 Acquired Immunodeficiency Syndrome 60 0.100
75
PRS045 Prostatic Hypertrophy 53 0.100
76
PST011 Pustulosis of Palm and Sole 52 0.100
77
c HYP836 Hypercholesterolemia, Familial, 1 73 0.097
78
P ART022 Arthritis 69 0.097
79
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.097
80
P VSC007 Vascular Disease 63 0.097
81
ATM095 Autoimmune Disease 62 0.097
82
LNG099 Lung Disease 60 0.097
83
P BCL017 B-Cell Lymphoma 58 0.097
84
FTT001 Fatty Liver Disease 61 0.095
85
IRN002 Iron Metabolism Disease 57 0.095
86
PRS021 Prostatic Adenoma 51 0.095
87
PRS129 Prostatic Hyperplasia, Benign 49 0.095
88
OST159 Osteogenic Sarcoma 66 0.092
89
DRM011 Dermatophytosis 52 0.092
90
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.092
91
DWN001 Down Syndrome 70 0.089
92
P DBT009 Diabetes Mellitus 64 0.089
93
P PLY011 Polycystic Ovary Syndrome 56 0.089
94
BCT022 Bacterial Infectious Disease 56 0.089
95
AGN016 Aging 56 0.089
96
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.089
97
CYT002 Cytokine Deficiency 42 0.089
98
IMM167 Immune Deficiency Disease 78 0.086
99
P MPL001 Maple Syrup Urine Disease 69 0.086
100
ALC007 Alcohol Dependence 66 0.086
101
P GLM045 Glioma 63 0.086
102
GLL048 Glial Tumor 45 0.086
103
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.086
104
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.084
105
ATH013 Atherosclerosis Susceptibility 65 0.084
106
LPP008 Lipoprotein Quantitative Trait Locus 62 0.084
107
P BRS044 Breast Adenocarcinoma 59 0.084
108
P SHR001 Short Bowel Syndrome 53 0.084
109
PST092 Posttransplant Acute Limbic Encephalitis 29 0.084
110
GLB015 Glioblastoma Multiforme 75 0.080
111
HMN044 Human Immunodeficiency Virus Type 1 71 0.080
112
P LKM002 Leukemia 68 0.080
113
c RHB024 Rhabdomyosarcoma 2 67 0.080
114
CHG001 Chagas Disease 66 0.080
115
CLT003 Colitis 62 0.080
116
P ALC033 Alcohol Use Disorder 58 0.080
117
P INF037 Inflammatory Bowel Disease 54 0.080
118
47X002 47,xyy 49 0.080
119
P SBR004 Seborrheic Dermatitis 45 0.080
120
END028 Endemic Goiter 37 0.080
121
HRW001 Hair Whorl 36 0.080
122
AST005 Asthma 76 0.077
123
P NRB001 Neuroblastoma 72 0.077
124
P PNC044 Pancreatitis 61 0.077
125
c ACT027 Acute Pancreatitis 60 0.077
126
c ACT071 Acute Kidney Failure 60 0.077
127
BRN056 Bronchopulmonary Dysplasia 57 0.077
128
c ACT075 Acute Myocardial Infarction 57 0.077
129
GLC003 Glucose Intolerance 54 0.077
130
CRV035 Cervical Cancer 76 0.074
131
P OST002 Osteoporosis 74 0.074
132
P LYM118 Lymphoma 68 0.074
133
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.074
134
SQM006 Squamous Cell Carcinoma 60 0.074
135
HYP060 Hyperinsulinism 54 0.074
136
P ECL001 Eclampsia 50 0.074
137
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.074
138
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.074
139
HVY002 Heavy Metal Poisoning 22 0.074
140
P LNG064 Lung Cancer Susceptibility 3 78 0.071
141
ULC004 Ulcerative Colitis 73 0.071
142
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.071
143
P PNM007 Pneumonia 68 0.071
144
P CRD119 Cardiac Arrest 67 0.071
145
P DMN002 Dementia 66 0.071
146
P ENC018 Encephalopathy 61 0.071
147
MCS002 Mucositis 56 0.071
148
P RCT021 Rectum Cancer 52 0.071
149
TLN003 Telangiectasis 52 0.071
150
PLC008 Placenta Disease 50 0.071
151
BRN071 Brain Injury 49 0.071
152
c MCR120 Microvascular Complications of Diabetes 7 47 0.071
153
P PNC035 Pancreatic Cancer 84 0.067
154
P ATX030 Ataxia-Telangiectasia 82 0.067
155
OST012 Osteoarthritis 78 0.067
156
P LKM062 Leukemia, Acute Lymphoblastic 69 0.067
157
P NTR004 Neutropenia 63 0.067
158
SKN016 Skin Disease 63 0.067
159
CHL068 Cholestasis 61 0.067
160
SDD001 Sudden Infant Death Syndrome 61 0.067
161
ORL011 Oral Cancer 60 0.067
162
IRN001 Iron Deficiency Anemia 59 0.067
163
BRS051 Breast Disease 58 0.067
164
c DWL002 Dowling-Degos Disease 1 58 0.067
165
LYM027 Lymphopenia 58 0.067
166
HYP266 Hypoxia 57 0.067
167
HMS001 Hemosiderosis 54 0.067
168
ART140 Arteries, Anomalies of 52 0.067
169
END086 End Stage Renal Disease 51 0.067
170
c HRD202 Hereditary Lymphedema I 50 0.067
171
KWS001 Kwashiorkor 44 0.067
172
STN013 Stenotrophomonas Maltophilia Infection 25 0.067
173
NRL016 Neural Tube Defects 82 0.063
174
c EXD008 Exudative Vitreoretinopathy 1 71 0.063
175
P EPL164 Epilepsy 71 0.063
176
P MLN008 Melanoma 69 0.063
177
P CLC063 Celiac Disease 1 66 0.063
178
P NSP012 Nasopharyngeal Carcinoma 66 0.063
179
P DRM053 Dermatitis, Atopic 66 0.063
180
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.063
181
P HML002 Hemolytic Anemia 63 0.063
182
ALL026 Allergic Hypersensitivity Disease 62 0.063
183
SPN186 Spinal Cord Injury 60 0.063
184
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.063
185
P CRD246 Cardiovascular System Disease 57 0.063
186
P GST044 Gastritis 56 0.063
187
PRT038 Protein-Energy Malnutrition 54 0.063
188
P SPP010 Suppressor of Tumorigenicity 3 51 0.063
189
KRT009 Keratosis 51 0.063
190
TRM010 Traumatic Brain Injury 51 0.063
191
DYS073 Dysphagia 50 0.063
192
KRT002 Keratomalacia 47 0.063
193
NWC001 Newcastle Disease 45 0.063
194
CHR178 Chromosomal Triplication 35 0.063
195
LYM053 Lymphomatous Thyroiditis 22 0.063
197
INS024 Insulin-Like Growth Factor I 79 0.059
198
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.059
199
END057 Endometrial Cancer 74 0.059
200
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.059
201
PLM001 Pulmonary Tuberculosis 69 0.059
202
P TRN020 Turner Syndrome 67 0.059
203
c SML038 Small Cell Cancer of the Lung 65 0.059
204
TTN003 Tetanus 65 0.059
205
P MTR014 Motor Neuron Disease 65 0.059
206
LSH001 Leishmaniasis 63 0.059
207
P BND020 Bone Disease 59 0.059
208
VSL002 Visual Epilepsy 59 0.059
209
c ACT073 Acute Leukemia 58 0.059
210
P ANP001 Anaplastic Large Cell Lymphoma 58 0.059
211
P BNC003 Bone Cancer 58 0.059
212
P HDC001 Headache 57 0.059
213
P SZR006 Seizure Disorder 56 0.059
214
PRS047 Prostatitis 56 0.059
215
PRP009 Peripartum Cardiomyopathy 55 0.059
216
PLM010 Pulmonary Edema 54 0.059
217
c MCR113 Microvascular Complications of Diabetes 3 52 0.059
218
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.059
219
c VRL010 Viral Hepatitis 52 0.059
220
DYS015 Dysentery 52 0.059
221
P END046 Endometritis 49 0.059
222
PPL001 Papillary Adenoma 44 0.059
223
ORL015 Oral Squamous Cell Carcinoma 43 0.059
224
P KLZ004 Kala-Azar 1 41 0.059
225
c MCR130 Microvascular Complications of Diabetes 6 41 0.059
226
c MCR133 Microvascular Complications of Diabetes 4 41 0.059
227
P RRH023 Rare Hereditary Hemochromatosis 41 0.059
228
TNC002 Tinea Capitis 38 0.059
229
ARG004 Argyria 27 0.059
230
c NRF023 Neurofibromatosis, Type Ii 80 0.055
231
P MLT020 Multiple Sclerosis 72 0.055
232
P INF038 Influenza 68 0.055
233
CRB039 Cerebrovascular Disease 67 0.055
234
ANG054 Angina Pectoris 66 0.055
235
P MCR115 Microvascular Complications of Diabetes 5 66 0.055
236
DPR016 Depression 63 0.055
237
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.055
238
MDD011 Mood Disorder 62 0.055
239
P PRM006 Primary Biliary Cirrhosis 62 0.055
240
BLD131 Bladder Urothelial Carcinoma 62 0.055
241
P MYL006 Myeloid Leukemia 60 0.055
242
P SCL018 Scoliosis 60 0.055
243
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.055
244
EYD002 Eye Disease 58 0.055
245
P RHN004 Rhinitis 57 0.055
246
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.055
247
P FBR017 Fibrosarcoma 56 0.055
248
TRN018 Transitional Cell Carcinoma 56 0.055
249
ALL006 Allergic Asthma 56 0.055
250
CLR030 Clear Cell Renal Cell Carcinoma 53 0.055
251
SPL018 Splenomegaly 48 0.055
252
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.055
253
CHL079 Children's Interstitial Lung Disease 26 0.055
254
c LKM061 Leukemia, Acute Myeloid 84 0.050
255
P RSP003 Respiratory Failure 74 0.050
256
c HPT073 Hepatitis C Virus 72 0.050
257
P HNT016 Huntington Disease 72 0.050
258
SKN019 Skin Melanoma 68 0.050
259
RCK004 Rickets 68 0.050
260
KHL003 Kohlschutter-Tonz Syndrome 65 0.050
261
BRR014 Barrett Esophagus 65 0.050
262
CTN007 Cutaneous Leishmaniasis 62 0.050
263
INT066 Interstitial Lung Disease 60 0.050
264
P THL005 Thalassemia 60 0.050
265
IGR001 Ige Responsiveness, Atopic 59 0.050
266
P CND004 Candidiasis 58 0.050
267
P UVT001 Uveitis 57 0.050
268
P GLM007 Glomerulonephritis 57 0.050
269
c GRV008 Graves Disease 1 56 0.050
270
PPL022 Papilloma 54 0.050
271
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.050
272
FDL002 Food Allergy 51 0.050
273
HYP781 Hypoascorbemia 51 0.050
274
STM007 Stomatitis 50 0.050
275
P MYT002 Myotonic Dystrophy 49 0.050
276
VRC001 Varicocele 49 0.050
277
BNR002 Bone Resorption Disease 48 0.050
278
NDL007 Nodular Goiter 47 0.050
279
DNB001 Danubian Endemic Familial Nephropathy 44 0.050
280
c PRM038 Primary Agammaglobulinemia 44 0.050
281
HYP344 Hyperthyroidism, Familial Gestational 39 0.050
282
GLT039 Glutathione Peroxidase Deficiency 34 0.050
283
c HYP595 Hypertension, Essential 84 0.045
284
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.045
285
P SCH015 Schizophrenia 74 0.045
286
MSC157 Muscular Dystrophy, Duchenne Type 72 0.045
287
P PHC003 Pheochromocytoma 71 0.045
288
P MJR001 Major Depressive Disorder 68 0.045
289
P HPT021 Hepatitis 67 0.045
290
P NRV007 Nervous System Disease 66 0.045
291
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.045
292
c CNG006 Congenital Hypothyroidism 64 0.045
293
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.045
294
P END044 Endometriosis 63 0.045
295
c HPT001 Hepatitis C 62 0.045
296
P HYP750 Hypertriglyceridemia, Familial 62 0.045
297
RTN017 Retinal Detachment 61 0.045
298
P LPS004 Lupus Erythematosus 61 0.045
299
P KDN017 Kidney Cancer 60 0.045
300
P TXP001 Toxoplasmosis 60 0.045
301
INS001 Insulinoma 60 0.045
302
SPP011 Suppression of Tumorigenicity 12 59 0.045
303
c HPT016 Hepatitis B 59 0.045
304
HLC007 Helicobacter Pylori Infection 59 0.045
305
RBS001 Rabies 58 0.045
306
FBR047 Fibromyalgia 58 0.045
307
MNT002 Mental Depression 58 0.045
308
BLR008 Bilirubin Metabolic Disorder 57 0.045
309
AYM001 Ayme-Gripp Syndrome 57 0.045
310
ORL005 Oral Candidiasis 56 0.045
311
BRN004 Brain Edema 56 0.045
312
c FML035 Familial Hyperlipidemia 55 0.045
313
HYP005 Hypokalemia 55 0.045
314
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.045
315
P ART021 Arteriosclerosis 54 0.045
316
NNL006 Non-Alcoholic Steatohepatitis 54 0.045
317
P INS002 in Situ Carcinoma 53 0.045
318
GST023 Gastric Ulcer 53 0.045
319
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.045
320
FML037 Female Breast Cancer 52 0.045
321
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.045
322
LMY002 Leiomyoma 52 0.045
323
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.045
324
P OVR082 Overgrowth Syndrome 50 0.045
325
P SCK005 Sickle Cell Disease 50 0.045
326
MYC087 Mycoplasma Pneumoniae Pneumonia 50 0.045
327
TRY001 Trypanosomiasis 50 0.045
328
URM002 Uremia 49 0.045
329
HYP043 Hyperandrogenism 48 0.045
330
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.045
331
HLX001 Helix Syndrome 47 0.045
332
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.045
333
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.045
334
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.045
335
P BNG032 Benign Mesothelioma 46 0.045
336
ADR040 Adrenal Gland Pheochromocytoma 46 0.045
337
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.045
338
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.045
339
CVD001 Covid-19 44 0.045
340
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.045
341
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.045
342
TST015 Testicular Disease 43 0.045
343
ILC002 Ileocolitis 43 0.045
344
IDP070 Idiopathic Scoliosis 42 0.045
345
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.045
346
ANX004 Anoxia 40 0.045
347
CRD005 Cardia Cancer 40 0.045
348
ALL014 Allergic Encephalomyelitis 38 0.045
349
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.045
350
c SYS001 Systemic Lupus Erythematosus 86 0.039
351
STR067 Stroke, Ischemic 81 0.039
352
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.039
353
c BTT014 Beta-Thalassemia 74 0.039
354
SVR004 Severe Combined Immunodeficiency 73 0.039
355
P ATS364 Autism 70 0.039
356
LYM133 Lymphoma, Hodgkin, Classic 69 0.039
357
P SYS005 Systemic Scleroderma 68 0.039
358
P MYC084 Mycobacterium Tuberculosis 1 68 0.039
359
CHL065 Cholangiocarcinoma 68 0.039
360
BRN024 Bronchitis 68 0.039
361
P THR014 Thrombocytopenia 67 0.039
362
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.039
363
P FLL037 Follicular Lymphoma 67 0.039
364
ALL003 Allergic Rhinitis 67 0.039
365
P HYP098 Hypereosinophilic Syndrome 67 0.039
366
c ATS007 Autism Spectrum Disorder 67 0.039
367
c MCR129 Microvascular Complications of Diabetes 1 66 0.039
368
HYP056 Hypoglycemia 66 0.039
369
IRR002 Irritable Bowel Syndrome 65 0.039
370
c DBT099 Diabetes Mellitus, Type I 65 0.039
371
P ADL010 Adult Respiratory Distress Syndrome 65 0.039
372
PRT036 Peritonitis 64 0.039
373
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.039
374
MSC007 Muscle Hypertrophy 64 0.039
375
PLM031 Poliomyelitis 64 0.039
376
P VSC011 Vasculitis 62 0.039
377
MSL001 Measles 62 0.039
378
P NPH012 Nephrotic Syndrome 60 0.039
379
HPT019 Hepatic Encephalopathy 60 0.039
380
AVN001 Avian Influenza 59 0.039
381
CNS004 Constipation 58 0.039
382
P PRP019 Peripheral Nervous System Disease 58 0.039
383
P BPL003 Bipolar Disorder 56 0.039
384
P NRP001 Neuropathy 56 0.039
385
MTH009 Mouth Disease 56 0.039
386
GST050 Gastrointestinal System Disease 56 0.039
387
P PNM006 Pneumoconiosis 56 0.039
388
SLC006 Silicosis 56 0.039
389
HPT022 Hepatoblastoma 56 0.039
390
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.039
391
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.039
392
OCL009 Ocular Cancer 55 0.039
393
HMP005 Hemiplegia 55 0.039
394
MYM001 Myoma 54 0.039
395
LYM022 Lymphangioma 54 0.039
396
CRH005 Crohn's Colitis 53 0.039
397
GSG001 Gas Gangrene 53 0.039
398
P FBR031 Febrile Seizures 53 0.039
399
NRT001 Neurotic Disorder 53 0.039
400
ALC009 Alcoholic Liver Cirrhosis 53 0.039
401
P INT068 Intestinal Disease 53 0.039
402
ACR041 Acromelic Frontonasal Dysostosis 52 0.039
403
PNG002 Pain Agnosia 51 0.039
404
OCL069 Ocular Motor Apraxia 51 0.039
405
P HRD144 Hereditary Mixed Polyposis Syndrome 51 0.039
406
INT079 Intrahepatic Cholangiocarcinoma 51 0.039
407
LNG031 Lung Benign Neoplasm 51 0.039
408
BLP005 Blepharitis 50 0.039
409
NTR046 Neutrophil Migration 50 0.039
410
P ATR005 Atrophic Gastritis 50 0.039
411
MYS061 Myasthenic Syndrome, Congenital, 4c, Associated with Acetylcholine Receptor Deficiency 49 0.039
412
VTM002 Vitamin B12 Deficiency 48 0.039
413
ANT018 Anthracosis 48 0.039
414
P OVR046 Ovarian Cyst 47 0.039
415
LYM019 Lymphosarcoma 46 0.039
416
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.039
417
SQM002 Squamous Cell Papilloma 46 0.039
418
c DRR009 Diarrhea 6 46 0.039
419
SYN036 Syncope 45 0.039
420
HPT004 Hepatic Coma 45 0.039
421
CRT015 Carotid Artery Occlusion 45 0.039
422
CNT017 Central Nervous System Origin Vertigo 45 0.039
423
P CHR345 Chronic Pain 44 0.039
424
P PRL003 Proliferative Glomerulonephritis 44 0.039
425
ENC005 Encephalomalacia 43 0.039
426
PRS042 Prostate Disease 43 0.039
427
MRS001 Marasmus 42 0.039
428
ATX019 Ataxia with Vitamin E Deficiency 42 0.039
429
c MJR024 Major Affective Disorder 9 41 0.039
430
c MCR112 Microvascular Complications of Diabetes 2 41 0.039
431
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.039
432
HYP141 Hyperphenylalaninemia 39 0.039
433
c MJR022 Major Affective Disorder 8 38 0.039
434
ATM052 Autoimmune Disease 1 37 0.039
435
OLG022 Oligoasthenoteratozoospermia 36 0.039
436
AMR003 Amaurosis Fugax 34 0.039
437
P RRL003 Rare Lymphatic Malformation 31 0.039
438
c SBR001 Seborrheic Infantile Dermatitis 30 0.039
439
CYT018 Cytochrome P450 2d6 Variant 27 0.039
440
c RNG015 Ring Chromosome 2 26 0.039
441
ADG002 Audiogenic Seizures 25 0.039
442
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.032
443
P GLM040 Glioma Susceptibility 1 81 0.032
444
P RTN008 Retinitis Pigmentosa 79 0.032
445
P PRK057 Parkinson Disease, Late-Onset 78 0.032
446
BRN028 Brain Cancer 74 0.032
447
SCK003 Sickle Cell Anemia 74 0.032
448
c SPN225 Spondyloarthropathy 1 73 0.032
449
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.032
450
OTT002 Otitis Media 72 0.032
451
PRP027 Peripheral Vascular Disease 71 0.032
452
BHC003 Behcet Syndrome 71 0.032
453
P AMY004 Amyloidosis 70 0.032
454
GST040 Gastric Adenocarcinoma 70 0.032
455
ADL002 Adult Syndrome 70 0.032
456
P SLP006 Sleep Apnea 69 0.032
457
BRK010 Burkitt Lymphoma 67 0.032
458
FLL027 Fallopian Tube Carcinoma 67 0.032
460
P HYD006 Hydrocephalus 66 0.032
461
LNG039 Lung Squamous Cell Carcinoma 66 0.032
462
P PLM036 Pulmonary Fibrosis 65 0.032
463
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.032
464
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.032
465
PRT037 Pertussis 65 0.032
466
P PRS038 Personality Disorder 65 0.032
467
CLN015 Colon Adenocarcinoma 65 0.032
468
c JVN010 Juvenile Rheumatoid Arthritis 64 0.032
469
P PRD008 Periodontitis 64 0.032
470
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.032
471
ANR007 Anorexia Nervosa 63 0.032
472
c OPT053 Optic Atrophy 1 63 0.032
473
c GLC092 Glaucoma, Primary Open Angle 62 0.032
474
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.032
475
c FNC043 Fanconi Anemia, Complementation Group E 62 0.032
476
c SVR001 Severe Acute Respiratory Syndrome 62 0.032
477
PSR001 Psoriatic Arthritis 61 0.032
478
c SCL052 Scleroderma, Familial Progressive 61 0.032
479
P ENC004 Encephalitis 61 0.032
480
ALC006 Alcoholic Hepatitis 61 0.032
481
CHR066 Chronic Fatigue Syndrome 61 0.032
482
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.032
483
CRD223 Cardiac Arrhythmia 60 0.032
484
P ALP009 Alopecia Areata 60 0.032
485
P SNS001 Sensorineural Hearing Loss 60 0.032
486
c DNG003 Dengue Disease 59 0.032
487
P SLP005 Sleep Disorder 59 0.032
488
c LTN004 Late-Onset Retinal Degeneration 59 0.032
489
BRN002 Bronchiolitis 59 0.032
490
CYS010 Cystinosis 59 0.032
491
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.032
492
GST045 Gastroenteritis 59 0.032
493
ANR040 Aneurysm 59 0.032
494
CRD132 Cardiac Conduction Defect 58 0.032
495
CNT047 Contact Dermatitis 58 0.032
496
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.032
497
DSS008 Disease of Mental Health 58 0.032
498
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 57 0.032
499
GLS018 Glass Syndrome 57 0.032
500
MCR013 Microphthalmia 57 0.032
501
DSS009 Disseminated Intravascular Coagulation 57 0.032
502
c MST023 Mesothelioma, Malignant 57 0.032
503
TNS005 Tonsillitis 57 0.032
504
P MYS005 Myositis 56 0.032
505
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.032
506
LST001 Listeriosis 56 0.032
507
HMG005 Hemoglobinopathy 56 0.032
508
ORL004 Oral Submucous Fibrosis 55 0.032
509
DFF005 Diffuse Large B-Cell Lymphoma 55 0.032
510
NPH009 Nephrolithiasis 55 0.032
511
P MYP006 Myopia 55 0.032
512
P DRM007 Dermatitis Herpetiformis 55 0.032
513
END040 Endogenous Depression 55 0.032
514
P LRY044 Larynx Cancer 55 0.032
515
WST005 West Nile Virus 54 0.032
516
P TRM003 Tremor 54 0.032
517
P LCH002 Lichen Planus 53 0.032
518
TRC023 Trichinosis 53 0.032
519
P HMC002 Homocystinuria 53 0.032
520
P MNC007 Monocytic Leukemia 53 0.032
521
ECH003 Echinococcosis 53 0.032
522
P ACT008 Actinic Keratosis 53 0.032
523
PRP080 Peripheral Artery Disease 53 0.032
524
c GLL024 Gallbladder Disease 1 53 0.032
525
OST011 Osteomalacia 52 0.032
526
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.032
527
IMP005 Impotence 52 0.032
528
P MSC003 Muscular Atrophy 52 0.032
529
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 52 0.032
530
HYP014 Hyperuricemia 52 0.032
531
P OVR049 Ovarian Disease 52 0.032
532
P TRT010 Teratoma 52 0.032
533
SPN051 Spondylitis 51 0.032
534
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.032
535
ENT011 Enterocolitis 51 0.032
536
CCC002 Coccidiosis 51 0.032
537
P AST007 Astrocytoma 51 0.032
538
SKN013 Skin Benign Neoplasm 51 0.032
539
PST021 Postpartum Depression 50 0.032
540
c SVR005 Severe Pre-Eclampsia 50 0.032
541
MLL001 Molluscum Contagiosum 50 0.032
542
P KRT007 Keratoconus 50 0.032
543
ENT004 Enthesopathy 49 0.032
544
CCN002 Cocaine Abuse 49 0.032
545
P OPN001 Open-Angle Glaucoma 49 0.032
546
c FLL041 Follicular Lymphoma 1 49 0.032
547
P BRS053 Breast Fibroadenoma 49 0.032
548
P CTN015 Cutaneous T Cell Lymphoma 49 0.032
549
PRC003 Proctitis 47 0.032
550
c INH020 Inherited Metabolic Disorder 47 0.032
551
TTR011 Tetraploidy 47 0.032
552
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.032
553
HYP082 Hypopharynx Cancer 47 0.032
554
NDL013 Nodular Regenerative Hyperplasia 47 0.032
555
RTN023 Retinitis 46 0.032
556
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.032
557
c SPL067 Split-Hand/foot Malformation 1 46 0.032
558
KRT013 Keratolytic Winter Erythema 46 0.032
559
P BRB001 Beriberi 46 0.032
560
P MTH007 Methemoglobinemia 46 0.032
561
GRW007 Growth Hormone Deficiency 46 0.032
562
HDN002 Head Injury 46 0.032
563
c MLG068 Malignant Glioma 46 0.032
564
MXD026 Mixed Glioma 45 0.032
565
CYN002 Cyanosis, Transient Neonatal 45 0.032
566
ORL013 Oral Lichen Planus 45 0.032
567
CRB004 Cerebral Artery Occlusion 45 0.032
568
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.032
569
ISL121 Isolated Split Hand-Split Foot Malformation 45 0.032
570
SPS057 Spasticity 45 0.032
571
DNT001 Dental Fluorosis 43 0.032
572
P MJR007 Major Affective Disorder 1 43 0.032
573
TRP009 Triple X Syndrome 42 0.032
574
ALC010 Alcoholic Cardiomyopathy 42 0.032
575
SNL007 Senile Cataract 42 0.032
576
EXC002 Exocrine Pancreatic Insufficiency 42 0.032
577
NRR001 Neuroretinitis 42 0.032
578
GST020 Gastric Antral Vascular Ectasia 41 0.032
579
49X006 49, Xxxxy Syndrome 41 0.032
580
PRS063 Paresthesia 41 0.032
581
P SCL057 Scoliosis, Isolated 1 41 0.032
582
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.032
583
P PRG092 Pregnancy Loss, Recurrent 1 40 0.032
584
CHL045 Choline Deficiency Disease 39 0.032
585
LKP003 Leukoplakia 39 0.032
586
CRV045 Cervical Intraepithelial Neoplasia 39 0.032
587
P PRC031 Preeclampsia/eclampsia 1 38 0.032
588
c PLY105 Polycystic Ovary Syndrome 1 38 0.032
589
c OVR114 Ovarian Cancer 1 38 0.032
590
ACR005 Acrodermatitis 38 0.032
591
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.032
592
PSD088 Pseudobulbar Affect 36 0.032
593
c DRM040 Dermatitis Herpetiformis, Familial 35 0.032
594
c MJR008 Major Affective Disorder 2 35 0.032
595
INT040 Intrinsic Asthma 34 0.032
596
c PRG106 Progressive Muscular Dystrophy 33 0.032
597
c MJR023 Major Affective Disorder 7 33 0.032
598
P VSC018 Visceral Steatosis 33 0.032
599
c MJR003 Major Affective Disorder 6 33 0.032
600
c MJR006 Major Affective Disorder 5 33 0.032
601
INF009 Inflammatory Spondylopathy 31 0.032
602
OCC001 Occupational Dermatitis 29 0.032
603
c MJR004 Major Affective Disorder 4 28 0.032
604
VSD001 Vas Deferens, Congenital Bilateral Aplasia of, X-Linked 28 0.032
605
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.032
606
PHS025 Phosphatase, Acid, of Tissues 28 0.032
607
ENT007 Enteropathica 26 0.032
608
c PRS080 Prostate Cancer, Hereditary, 7 22 0.032
609
MLR004 Malaria 81 0.022
610
P LKM071 Leukemia, Chronic Lymphocytic 79 0.022
611
P LYN001 Lynch Syndrome 77 0.022
612
c TBR025 Tuberous Sclerosis 1 77 0.022
613
KPS004 Kaposi Sarcoma 75 0.022
614
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.022
615
P APL001 Aplastic Anemia 74 0.022
616
LPT014 Leptin Deficiency or Dysfunction 74 0.022
617
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.022
618
P CNR004 Cone-Rod Dystrophy 2 73 0.022
619
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.022
620
ANX010 Anxiety 73 0.022
621
ACR007 Acromegaly 71 0.022
622
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.022
623
MYL009 Myelodysplastic Syndrome 70 0.022
624
P HYP061 Hypertrophic Cardiomyopathy 70 0.022
625
c PNC108 Pancreatitis, Hereditary 70 0.022
626
P TBR001 Tuberous Sclerosis 70 0.022
627
P ASP006 Aspergillosis 69 0.022
628
WRN001 Werner Syndrome 69 0.022
629
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.022
630
CRB037 Cerebral Palsy 69 0.022
631
P LPR021 Leprosy 3 69 0.022
632
ART016 Aortic Aneurysm 69 0.022
633
c MYT021 Myotonic Dystrophy 1 69 0.022
634
c BSL007 Basal Cell Carcinoma 68 0.022
635
OBS002 Obsessive-Compulsive Disorder 68 0.022
636
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.022
637
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 68 0.022
638
P FRN006 Frontotemporal Dementia 68 0.022
639
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.022
640
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.022
641
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.022
642
c INF071 Inflammatory Bowel Disease 1 67 0.022
643
P BLD062 Bile Duct Cancer 67 0.022
644
c MGR028 Migraine with or Without Aura 1 67 0.022
645
MYC006 Mycosis Fungoides 66 0.022
646
LPT001 Leptospirosis 66 0.022
647
ART001 Arterial Tortuosity Syndrome 66 0.022
648
P LYS001 Loeys-Dietz Syndrome 65 0.022
649
P HRS035 Hirschsprung Disease 1 65 0.022
650
DMN031 Dementia, Lewy Body 65 0.022
651
KRT019 Keratitis, Hereditary 65 0.022
652
PPL049 Papillon-Lefevre Syndrome 65 0.022
653
TNG002 Tangier Disease 65 0.022
654
CHY002 Chylomicron Retention Disease 65 0.022
655
c WLM013 Wilms Tumor 1 65 0.022
656
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.022
657
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.022
658
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.022
659
MYC079 Myoclonic Epilepsy of Lafora 64 0.022
660
CLF027 Cleft Palate, Isolated 64 0.022
661
TBC004 Tobacco Addiction 64 0.022
662
GT001 Gout 64 0.022
663
BRC012 Brucellosis 64 0.022
664
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.022
665
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.022
666
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.022
667
OST017 Osteomyelitis 64 0.022
668
CYS013 Cystinuria 63 0.022
669
P ANR048 Aniridia 1 63 0.022
670
P HYP069 Hyperparathyroidism 63 0.022
671
PLG002 Plague 63 0.022
672
END041 Endometrial Adenocarcinoma 63 0.022
673
P MVM001 Movement Disease 63 0.022
674
c ACT068 Acute Cystitis 63 0.022
675
c ATM011 Autoimmune Hepatitis 63 0.022
676
c ALP101 Alpha-Thalassemia 62 0.022
677
HMT002 Hematologic Cancer 62 0.022
678
P PLY014 Polycystic Kidney Disease 62 0.022
679
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.022
680
P SPN046 Spinal Muscular Atrophy 62 0.022
681
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 62 0.022
682
P ESP024 Esophagitis 62 0.022
683
P TRC086 Trichohepatoenteric Syndrome 1 62 0.022
684
BLL006 Bullous Pemphigoid 62 0.022
685
P ART023 Arthropathy 62 0.022
686
CRC021 Carcinosarcoma 62 0.022
687
OST003 Osteonecrosis 61 0.022
688
c PNS012 Paine Syndrome 61 0.022
689
ALV005 Alveolar Soft Part Sarcoma 61 0.022
690
VRL011 Viral Infectious Disease 61 0.022
691
HRP004 Herpes Zoster 60 0.022
692
DRR016 Diarrhea 2, with Microvillus Atrophy 60 0.022
693
P TST021 Testicular Germ Cell Tumor 60 0.022
694
DPH001 Diphtheria 60 0.022
695
P VNT002 Ventricular Septal Defect 60 0.022
696
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.022
697
ACN002 Acanthosis Nigricans 60 0.022
698
P ATR010 Atrial Heart Septal Defect 60 0.022
699
DNG002 Dengue Hemorrhagic Fever 60 0.022
700
RHM001 Rheumatic Fever 60 0.022
701
VRC005 Varicose Veins 60 0.022
702
HYD002 Hydronephrosis 60 0.022
703
P GLY013 Glycogen Storage Disease 60 0.022
704
PRT013 Portal Hypertension 59 0.022
705
CHL014 Cholera 59 0.022
706
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.022
707
CHL123 Chlamydia 59 0.022
708
PRN019 Perinatal Necrotizing Enterocolitis 59 0.022
709
GRD007 Grade Iii Astrocytoma 59 0.022
710
P CYS018 Cystitis 59 0.022
711
GNG013 Gingivitis 59 0.022
712
P DNG005 Dengue Virus 59 0.022
713
ALP097 Alopecia Universalis Congenita 59 0.022
714
PPT005 Peptic Ulcer Disease 59 0.022
715
P SYP003 Syphilis 58 0.022
716
P MMP001 Mumps 58 0.022
717
LNG108 Langerhans Cell Histiocytosis 58 0.022
718
PMP006 Pemphigus Vulgaris, Familial 57 0.022
719
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.022
720
P PLV020 Pelvic Organ Prolapse 57 0.022
721
c CHL119 Cholangitis, Primary Sclerosing 57 0.022
722
MNR012 Meniere Disease 57 0.022
723
P PLY041 Polymyositis 57 0.022
724
P EXN002 Exanthem 57 0.022
725
CHK001 Chikungunya 57 0.022
726
APH001 Aphthous Stomatitis 57 0.022
727
P PRV006 Pervasive Developmental Disorder 57 0.022
728
P FTL001 Fetal Alcohol Syndrome 57 0.022
729
VSC002 Vascular Dementia 57 0.022
730
c LKM070 Leukemia, Acute Monocytic 57 0.022
731
CYT008 Cytomegalovirus Infection 57 0.022
732
PLC005 Placental Insufficiency 57 0.022
733
JPN002 Japanese Encephalitis 57 0.022
734
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.022
735
P ADL017 Adult T-Cell Leukemia 56 0.022
736
CMR002 Coumarin Resistance 56 0.022
737
PLS011 Plasmacytoma 56 0.022
738
EXF001 Exfoliation Syndrome 56 0.022
739
c ACT134 Acute Liver Failure 56 0.022
740
c INT072 Intestinal Pseudo-Obstruction 56 0.022
741
LMY014 Leiomyoma, Uterine 56 0.022
742
ERY051 Erythroleukemia, Familial 56 0.022
743
P MTC069 Mitochondrial Disorders 56 0.022
744
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.022
745
ANN002 Anencephaly 56 0.022
746
CYS008 Cystic Echinococcosis 56 0.022
747
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.022
748
FLR001 Filarial Elephantiasis 55 0.022
749
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.022
750
ADR008 Adrenal Adenoma 55 0.022
751
FDB001 Foodborne Botulism 55 0.022
752
VSC003 Visceral Leishmaniasis 55 0.022
753
P ANT006 Antiphospholipid Syndrome 55 0.022
754
GNG005 Gangliocytoma 55 0.022
755
P SBS003 Substance Abuse 55 0.022
756
FLR002 Filariasis 55 0.022
757
P ALP106 Alport Syndrome 1, X-Linked 55 0.022
758
BRN045 Brunner Syndrome 55 0.022
759
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.022
760
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.022
761
PRP030 Purpura 54 0.022
762
TRD006 Tardive Dyskinesia 54 0.022
763
P PMP001 Pemphigus 54 0.022
764
ACD008 Acid-Labile Subunit Deficiency 54 0.022
765
PRT082 Preterm Premature Rupture of the Membranes 54 0.022
766
P EPS030 Episodic Kinesigenic Dyskinesia 1 54 0.022
767
P RST001 Restless Legs Syndrome 54 0.022
768
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.022
769
CRY003 Cryptosporidiosis 54 0.022
770
BRN014 Bronchopneumonia 54 0.022
771
TND005 Tendinitis 54 0.022
772
THR013 Thoracic Outlet Syndrome 54 0.022
773
PRC013 Pericarditis 54 0.022
774
AMN001 Amenorrhea 54 0.022
775
DBT010 Diabetic Neuropathy 54 0.022
776
P LNG035 Lung Large Cell Carcinoma 54 0.022
777
SLP001 Sleeping Sickness 54 0.022
778
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.022
779
GST009 Gastroschisis 53 0.022
780
c HNT010 Huntington Disease-Like 1 53 0.022
781
MMM001 Mammary Paget's Disease 53 0.022
782
PST046 Post-Transplant Lymphoproliferative Disease 53 0.022
783
OCL006 Ocular Hypertension 53 0.022
784
c PRD040 Periodontitis, Chronic 53 0.022
785
P ORL007 Oral Cavity Cancer 53 0.022
786
P HMR003 Hemorrhagic Disease 53 0.022
787
P PTS002 Ptosis 53 0.022
788
HMC014 Homocysteinemia 53 0.022
789
OVR059 Ovary Adenocarcinoma 53 0.022
790
c CNT035 Central Nervous System Disease 52 0.022
791
FRY006 Fryns Microphthalmia Syndrome 52 0.022
792
EXP004 Exophthalmos 52 0.022
793
GNG002 Ganglioneuroma 52 0.022
794
CLB010 Coloboma of Macula 52 0.022
795
DMY004 Demyelinating Disease 52 0.022
796
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.022
797
MGC002 Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 52 0.022
798
PLM014 Pleomorphic Adenoma 52 0.022
799
P SML001 Small Cell Carcinoma 52 0.022
800
NRT004 Neuritis 52 0.022
801
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.022
802
BWN001 Bowen-Conradi Syndrome 52 0.022
803
LGN006 Legionnaire Disease 52 0.022
804
ACT200 Acute Monoblastic Leukemia 52 0.022
805
DFF036 Differentiated Thyroid Carcinoma 52 0.022
806
PRV004 Periventricular Leukomalacia 52 0.022
807
SPS003 Spastic Diplegia 51 0.022
808
NPH003 Nephrocalcinosis 51 0.022
810
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.022
811
CLR109 Colorectal Adenocarcinoma 51 0.022
812
c PNC106 Pancreatic Agenesis 1 51 0.022
813
ESP002 Esophageal Varix 51 0.022
814
HND002 Hand, Foot and Mouth Disease 51 0.022
815
TNG007 Tongue Carcinoma 51 0.022
816
P CHL066 Cholangitis 51 0.022
817
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.022
818
HYP081 Hypolipoproteinemia 51 0.022
819
P MMB011 Membranous Nephropathy 50 0.022
820
SCB001 Scabies 50 0.022
821
LNT004 Lentigines 50 0.022
822
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.022
823
RTN003 Retinal Ischemia 50 0.022
824
CRN030 Coronary Stenosis 50 0.022
825
AZS001 Azoospermia 50 0.022
826
MTB004 Metabolic Acidosis 50 0.022
827
BLR001 Biliary Atresia 50 0.022
828
c LRG001 Large Cell Carcinoma 50 0.022
829
OCL022 Ocular Melanoma 50 0.022
830
HRT011 Heart Septal Defect 50 0.022
831
HYP080 Hypogonadism 50 0.022
832
RBF001 Riboflavin Deficiency 49 0.022
833
ERY004 Erysipelas 49 0.022
834
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.022
835
ART017 Aortic Disease 49 0.022
836
GST049 Gastrointestinal System Cancer 49 0.022
837
CHL004 Cholelithiasis 49 0.022
838
MTC005 Mitochondrial Metabolism Disease 49 0.022
839
SLF014 Sulfite Oxidase Deficiency, Isolated 49 0.022
840
HST010 Histiocytosis 48 0.022
841
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.022
842
P HYP058 Hypervitaminosis a 48 0.022
843
CCN001 Cocaine Dependence 48 0.022
844
CLC006 Calcinosis 48 0.022
845
P NGH001 Night Blindness 48 0.022
846
P SCL009 Sclerosing Cholangitis 48 0.022
847
BLT006 Bilateral Breast Cancer 48 0.022
848
VTM033 Vitamin K Deficiency Bleeding 48 0.022
849
INT067 Interstitial Nephritis 48 0.022
850
PNC034 Pancreas Disease 48 0.022
851
IGG001 Iga Glomerulonephritis 48 0.022
852
c MTR002 Mitral Valve Insufficiency 48 0.022
853
P GND004 Gonadal Dysgenesis 48 0.022
854
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.022
855
RCT020 Rectum Adenocarcinoma 48 0.022
856
ART004 Aortic Atherosclerosis 47 0.022
857
SXL003 Sexual Disorder 47 0.022
858
NNT017 Neonatal Adrenoleukodystrophy 47 0.022
859
ASB001 Asbestosis 47 0.022
860
MCC002 Mucocutaneous Leishmaniasis 47 0.022
861
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.022
862
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.022
863
GST071 Gastrointestinal Carcinoma 47 0.022
864
ANV001 Anovulation 47 0.022
865
TST044 Testicular Torsion 47 0.022
866
CRD137 Cardiogenic Shock 47 0.022
867
ATN005 Autonomic Dysfunction 46 0.022
868
PLL012 Pollen Allergy 46 0.022
869
TRP008 Tropical Calcific Pancreatitis 46 0.022
870
FLL008 Folliculitis 46 0.022
871
CHR008 Choroiditis 46 0.022
872
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.022
873
OLG001 Oligospermia 45 0.022
874
URT010 Ureteral Obstruction 45 0.022
875
TRT001 Teratocarcinoma 45 0.022
876
PLR022 Pleural Disease 45 0.022
877
P OCY003 Oocyte Maturation Defect 1 45 0.022
878
KR002 Kuru 45 0.022
879
URL001 Urolithiasis 45 0.022
880
PRT019 Protein-Losing Enteropathy 45 0.022
881
ACT003 Acute Kidney Tubular Necrosis 45 0.022
882
BRN032 Brain Glioma 45 0.022
883
P END084 Endocrine System Disease 45 0.022
884
MLN073 Melanosis, Neurocutaneous 45 0.022
885
MYF001 Myofibroma 45 0.022
886
DBT090 Diabetes and Deafness, Maternally Inherited 44 0.022
887
CHP002 Chops Syndrome 44 0.022
888
TNS004 Tonsil Cancer 44 0.022
889
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 44 0.022
890
LRY022 Laryngoonychocutaneous Syndrome 44 0.022
891
SBC016 Subacute Delirium 44 0.022
892
GRN017 Granulocytopenia 44 0.022
893
PTT037 Pituitary Tumors 44 0.022
894
P END039 Endodermal Sinus Tumor 44 0.022
895
HPT067 Hepatocellular Adenoma 44 0.022
896
DMP001 Dumping Syndrome 44 0.022
897
P MYG005 Myoglobinuria 44 0.022
898
CRB090 Cerebral Hypoxia 44 0.022
899
TND004 Tendinopathy 43 0.022
900
MCR011 Microinvasive Gastric Cancer 43 0.022
901
SDD008 Sudden Sensorineural Hearing Loss 43 0.022
902
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.022
903
P DMY001 Demyelinating Polyneuropathy 43 0.022
904
MDD018 Middle East Respiratory Syndrome 43 0.022
905
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.022
906
MXD050 Mixed Phenotype Acute Leukemia 43 0.022
907
P MLT008 Multinodular Goiter 42 0.022
908
c RTN047 Retinitis Pigmentosa 18 42 0.022
909
PRS115 Prosthetic Joint Infection 42 0.022
910
LRY017 Laryngeal Disease 42 0.022
911
MYF002 Myofascial Pain Syndrome 42 0.022
912
LCH016 Lichen Sclerosus Et Atrophicus 41 0.022
913
PCD001 Pica Disease 41 0.022
914
FNC002 Functional Diarrhea 41 0.022
915
P PRN020 Paranasal Sinus Cancer 41 0.022
916
VLL006 Villous Adenoma 40 0.022
917
OST115 Osteonecrosis of the Jaw 40 0.022
918
ALC005 Alcoholic Pancreatitis 40 0.022
919
GLC008 Glucose Metabolism Disease 40 0.022
920
PYL004 Pyelitis 40 0.022
921
KLD004 Keloid Disorder 40 0.022
922
ORL012 Oral Leukoplakia 39 0.022
923
TST018 Testicular Yolk Sac Tumor 39 0.022
924
AKL001 Au-Kline Syndrome 39 0.022
925
ETH004 Euthyroid Sick Syndrome 38 0.022
926
HYP264 Hypertonia 38 0.022
927
P FML355 Familial Intrahepatic Cholestasis 38 0.022
928
OVR094 Ovarian Epithelial Cancer 38 0.022
929
c SYS043 Systemic Lupus Erythematosus 1 38 0.022
930
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.022
931
CNT060 Central Serous Chorioretinopathy 38 0.022
932
KLD003 Keloid Formation 38 0.022
933
SCL001 Scalp Dermatosis 38 0.022
934
PRS123 Persistent Generalized Lymphadenopathy 37 0.022
935
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.022
936
CRT012 Cortical Blindness 37 0.022
937
P CRB088 Cerebral Atrophy 37 0.022
938
GLM044 Glomerular Disease 37 0.022
939
RHM014 Rheumatoid Vasculitis 37 0.022
940
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.022
941
ABD010 Abdominal Wall Defect 36 0.022
943
c MCR312 Microphthalmia, Syndromic 10 35 0.022
944
PLM011 Plummer's Disease 35 0.022
945
PLN026 Pilonidal Sinus 35 0.022
946
KRN001 Korean Hemorrhagic Fever 35 0.022
947
PRM329 Premature Aging 35 0.022
948
NRX001 Neuroaxonal Dystrophy 35 0.022
949
c PST106 Post-Cardiac Arrest Syndrome 35 0.022
950
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.022
951
ATX010 Ataxia Neuropathy Spectrum 34 0.022
952
HNS001 Hansen's Disease 34 0.022
953
c LKM005 Leukemia, T-Cell, Chronic 34 0.022
954
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.022
955
PST010 Pasteurellosis 34 0.022
957
MCR334 Microcolon 34 0.022
958
LNT002 Lentigo Maligna Melanoma 33 0.022
959
ACT064 Acute Necrotizing Encephalitis 33 0.022
960
LYM095 Lymphangiomatosis 33 0.022
961
LPD026 Lipedema 33 0.022
962
HND015 Hand Skill, Relative 33 0.022
963
c BLD140 Blood Group, I System 32 0.022
964
PRT112 Portal Hypertension, Noncirrhotic 31 0.022
965
ANM001 Anemia of Prematurity 31 0.022
966
TRC025 Tracheal Cancer 31 0.022
967
GST029 Gastric Cardia Adenocarcinoma 31 0.022
968
PLY150 Polykaryocytosis Inducer 31 0.022
969
STT009 Sutton Disease 2 30 0.022
970
ISL119 Isolated Optic Neuritis 30 0.022
971
FNT004 Fainting 30 0.022
972
AML065 Amelia 30 0.022
973
TLG001 Telogen Effluvium 30 0.022
974
GRV012 Grover's Disease 30 0.022
976
c SCK014 Sick Sinus Syndrome 2 30 0.022
977
BRT055 Breath-Holding Spells 30 0.022
978
THY064 Thyroid Hormone Metabolism, Abnormal 29 0.022
979
MXL017 Maxillary Cancer 29 0.022
980
c RNG022 Ring Chromosome 6 28 0.022
981
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.022
982
c PSR031 Psoriasis 10 28 0.022
983
MTR001 Mature Cataract 28 0.022
984
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 28 0.022
985
DSR031 Disorder of Copper Metabolism 27 0.022
986
MLR020 Malaria, Mild 27 0.022
987
DFF010 Diffuse Alopecia Areata 26 0.022
988
FTL064 Fetal Methylmercury Syndrome 26 0.022
989
ASB003 Asbestos Intoxication 26 0.022
990
c DMN005 Diamond-Blackfan Anemia 2 25 0.022
991
c VSC053 Visceral Steatosis, Congenital 25 0.022
992
c PRM243 Primary Bone Cancer 24 0.022
993
ARY002 Aryl Hydrocarbon Hydroxylase Inducibility 24 0.022
994
SST003 Sister Chromatid Exchange, Frequency of 24 0.022
995
NCL001 Nuclear Senile Cataract 23 0.022
996
c RNG021 Ring Chromosome 5 23 0.022
997
ACQ008 Acquired Hyperkeratosis 22 0.022
998
TRC013 Trichostrongylosis 22 0.022
999
c CHR093 Chronic Orbital Inflammation 22 0.022
1000
PSD006 Pseudopterygium 21 0.022
1001
c PST001 Posterior Myocardial Infarction 21 0.022
1002
SPR019 Superficial Keratitis 21 0.022
1003
RCK009 Rickettsial Disease 20 0.022
1004
SPR033 Superficial Spreading Melanoma 18 0.022
1005
CNG101 Congenital Human Immunodeficiency Virus 18 0.022
1006
BLD137 Blood Group--Ahonen 16 0.022
1007
PHS027 Phosphoglycoprotein 1 14 0.022
1008
GNT148 Genetic Hemoglobinopathy 12 0.022
1009
c GLL025 Gallbladder Disease 2 12 0.022
Content
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