Search results for Ceramide NG

1060 hits were found for Ceramide NG

# Family MCID Name MIFTS Score
1
FBR012 Fabry Disease 71 20.901
2
P PRS040 Prostate Cancer 95 10.186
3
P NRB001 Neuroblastoma 66 9.172
4
P DRM053 Dermatitis, Atopic 65 9.167
5
GLM045 Glioma 62 9.062
6
GLL048 Glial Tumor 52 8.936
7
CHL123 Chlamydia 58 8.926
8
P LKM002 Leukemia 66 8.520
9
c LKM061 Leukemia, Acute Myeloid 83 7.919
10
P MYL006 Myeloid Leukemia 60 7.772
11
DRM006 Dermatitis 62 7.247
12
NNL005 Non-Alcoholic Fatty Liver Disease 63 6.970
13
P LNG032 Lung Cancer 98 6.909
14
FTT001 Fatty Liver Disease 61 6.548
15
PRT037 Pertussis 49 6.546
16
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 6.495
17
P ADN016 Adenocarcinoma 63 6.380
18
AGN016 Aging 54 6.368
19
c TYP009 Type 2 Diabetes Mellitus 92 6.274
20
PRS045 Prostatic Hypertrophy 52 6.149
21
RCK004 Rickets 65 6.085
22
P BRS047 Breast Cancer 97 5.981
23
P HPT023 Hepatocellular Carcinoma 95 5.941
24
P CRN300 Coronary Heart Disease 1 73 5.939
25
RPD005 Rapidly Involuting Congenital Hemangioma 48 5.922
26
P DBT009 Diabetes Mellitus 67 5.918
27
INS024 Insulin-Like Growth Factor I 77 5.892
28
LPP008 Lipoprotein Quantitative Trait Locus 65 5.885
29
c HYP595 Hypertension, Essential 84 5.881
30
P CLR023 Colorectal Cancer 100 5.854
31
PRS021 Prostatic Adenoma 43 5.851
32
ART140 Arteries, Anomalies of 52 5.849
33
PRS129 Prostatic Hyperplasia, Benign 48 5.784
34
LPD008 Lipid Metabolism Disorder 61 5.746
35
CYS001 Cystic Fibrosis 77 5.745
36
P LNG064 Lung Cancer Susceptibility 3 70 5.732
37
TXC005 Toxic Shock Syndrome 62 5.546
38
c SML038 Small Cell Cancer of the Lung 69 5.502
39
48X005 48,xyyy 39 5.302
40
SKN016 Skin Disease 62 5.275
41
CHL014 Cholera 62 5.201
42
CYT002 Cytokine Deficiency 43 5.149
43
P OVR042 Ovarian Cancer 88 5.129
44
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 5.086
45
P LVR013 Liver Disease 68 5.059
46
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 5.057
47
P LKM062 Leukemia, Acute Lymphoblastic 69 5.027
48
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 4.993
49
P KDN018 Kidney Disease 72 4.887
50
47X002 47,xyy 48 4.881
51
P RTN024 Retinoblastoma 72 4.861
52
NRR001 Neuroretinitis 42 4.855
53
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 4.836
54
IRN002 Iron Metabolism Disease 56 4.836
55
THY029 Thyroid Carcinoma 54 4.825
56
P MLN008 Melanoma 75 4.733
57
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 4.726
58
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.725
59
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.725
60
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.725
61
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 4.725
62
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.725
63
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.725
64
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 4.725
65
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 4.725
66
P LYM118 Lymphoma 69 4.720
67
P MYC007 Myocardial Infarction 69 4.703
68
ATH013 Atherosclerosis Susceptibility 63 4.695
69
BCT022 Bacterial Infectious Disease 56 4.661
70
CNG034 Congestive Heart Failure 69 4.656
71
c PRC016 Pre-Eclampsia 64 4.585
72
P HRT032 Heart Disease 84 4.453
73
P PHC003 Pheochromocytoma 70 4.433
74
DFC004 Deficiency Anemia 74 4.425
75
ADR040 Adrenal Gland Pheochromocytoma 45 4.415
76
LNG099 Lung Disease 62 4.413
77
P PSR002 Psoriasis 63 4.400
78
P PNC035 Pancreatic Cancer 86 4.336
79
PST011 Pustulosis of Palm and Sole 52 4.326
80
NNL006 Non-Alcoholic Steatohepatitis 54 4.273
81
HYP066 Hyperglycemia 60 4.272
82
ISC004 Ischemia 61 4.242
83
P RTN008 Retinitis Pigmentosa 79 4.202
84
SQM006 Squamous Cell Carcinoma 59 4.176
85
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 4.175
86
c ATR087 Atrial Standstill 1 74 4.116
87
P PLM037 Pulmonary Hypertension 69 4.109
88
PRT251 Proteinuria, Chronic Benign 58 4.103
89
MYL069 Myeloma, Multiple 77 4.094
90
c LKM063 Leukemia, Chronic Myeloid 71 4.074
91
MNT002 Mental Depression 56 4.049
92
c CHR684 Chronic Kidney Disease 74 4.045
93
HYP060 Hyperinsulinism 53 3.999
94
SPP011 Suppression of Tumorigenicity 12 61 3.992
95
SVR004 Severe Combined Immunodeficiency 71 3.989
96
GLB002 Glioblastoma 67 3.976
97
RTN023 Retinitis 45 3.971
98
HYP266 Hypoxia 56 3.964
99
P ALZ034 Alzheimer Disease 87 3.941
100
CRH001 Crohn's Disease 80 3.927
101
P THL005 Thalassemia 56 3.891
102
P INF032 Infertility 60 3.878
103
P PRD008 Periodontitis 64 3.848
104
END057 Endometrial Cancer 71 3.796
105
PLM010 Pulmonary Edema 54 3.778
106
P GCH001 Gaucher's Disease 69 3.761
107
P BCL017 B-Cell Lymphoma 57 3.749
108
HMN044 Human Immunodeficiency Virus Type 1 76 3.726
109
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 3.722
110
ADN018 Adenoma 58 3.707
111
P FBR017 Fibrosarcoma 55 3.680
112
RNL114 Renal Cell Carcinoma, Nonpapillary 79 3.671
113
DPR016 Depression 65 3.641
114
P LPS004 Lupus Erythematosus 61 3.628
115
ULC004 Ulcerative Colitis 74 3.577
116
GLC003 Glucose Intolerance 53 3.556
117
P GLM007 Glomerulonephritis 59 3.551
118
P CNR004 Cone-Rod Dystrophy 2 75 3.549
119
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.500
120
P ICH004 Ichthyosis 56 3.481
121
P INF037 Inflammatory Bowel Disease 53 3.466
122
c SYS001 Systemic Lupus Erythematosus 86 3.457
123
SPN186 Spinal Cord Injury 61 3.450
124
OST159 Osteogenic Sarcoma 66 3.420
125
c AMY091 Amyotrophic Lateral Sclerosis 1 88 3.409
126
P AST005 Asthma 76 3.406
127
LVR012 Liver Cirrhosis 62 3.389
128
CLT003 Colitis 63 3.384
129
DSS032 Disease by Infectious Agent 55 3.362
131
P MSC003 Muscular Atrophy 52 3.333
132
P MLT020 Multiple Sclerosis 79 3.290
133
c MCR133 Microvascular Complications of Diabetes 4 41 3.289
134
c MCR113 Microvascular Complications of Diabetes 3 52 3.289
135
c MCR130 Microvascular Complications of Diabetes 6 41 3.289
136
c MCR120 Microvascular Complications of Diabetes 7 47 3.289
137
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 3.272
138
c HYP836 Hypercholesterolemia, Familial, 1 73 3.260
139
P HYP069 Hyperparathyroidism 62 3.235
140
BNR002 Bone Resorption Disease 47 3.219
141
c ACT075 Acute Myocardial Infarction 55 3.184
142
MLR004 Malaria 78 3.178
143
PLM129 Pulmonary Disease, Chronic Obstructive 74 3.177
144
DWN001 Down Syndrome 70 3.164
145
P MJR001 Major Depressive Disorder 68 3.149
146
P RSP003 Respiratory Failure 74 3.149
147
ATM095 Autoimmune Disease 61 3.135
148
P SKN015 Skin Carcinoma 71 3.109
149
P GLM040 Glioma Susceptibility 1 70 3.103
150
TTN003 Tetanus 64 3.091
151
P MYP004 Myopathy 67 3.080
152
HYP080 Hypogonadism 49 3.070
153
P PLY011 Polycystic Ovary Syndrome 57 3.068
154
P PNM007 Pneumonia 64 3.053
155
P CRD246 Cardiovascular System Disease 55 3.052
156
P HYP086 Hypothyroidism 69 3.048
157
c PCH010 Pachyonychia Congenita 3 43 3.043
158
c ACT071 Acute Kidney Failure 60 3.029
159
GST033 Gestational Diabetes 61 3.028
160
c BTT014 Beta-Thalassemia 72 3.020
161
P PRP019 Peripheral Nervous System Disease 57 3.020
162
ACT113 Acute Myeloblastic Leukemia with Maturation 46 3.018
163
P NTR004 Neutropenia 62 3.016
164
P LKM071 Leukemia, Chronic Lymphocytic 74 3.008
165
P NMN002 Niemann-Pick Disease 60 3.003
166
P LTR001 Lateral Sclerosis 58 2.992
167
c MCR115 Microvascular Complications of Diabetes 5 65 2.988
168
P RTN016 Retinal Degeneration 52 2.948
169
PPL022 Papilloma 53 2.932
170
SQM002 Squamous Cell Papilloma 45 2.921
171
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.897
172
P GRF003 Graft-Versus-Host Disease 71 2.891
173
INT007 Intermediate Coronary Syndrome 53 2.884
174
P LKD001 Leukodystrophy 58 2.874
175
ANG054 Angina Pectoris 65 2.867
176
P NRP001 Neuropathy 59 2.860
177
P ACN011 Acne 55 2.838
178
P BRS044 Breast Adenocarcinoma 58 2.837
179
HMC014 Homocysteinemia 52 2.829
180
HGH043 High Grade Glioma 46 2.826
181
ALL006 Allergic Asthma 56 2.825
182
P ECL001 Eclampsia 52 2.798
183
SPH010 Sphingolipidosis 47 2.796
184
P TRN020 Turner Syndrome 67 2.790
185
BRK010 Burkitt Lymphoma 66 2.771
186
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 2.771
187
P ALC033 Alcohol Use Disorder 67 2.757
188
ACR007 Acromegaly 70 2.753
189
BRN071 Brain Injury 50 2.737
190
CNT047 Contact Dermatitis 57 2.712
191
SRC014 Sarcoma 64 2.690
192
LYS002 Lysosomal Storage Disease 51 2.669
193
SQM013 Squamous Cell Carcinoma, Head and Neck 75 2.668
194
c ACT027 Acute Pancreatitis 60 2.665
195
P INF038 Influenza 68 2.659
196
SPN035 Spindle Cell Sarcoma 51 2.640
197
P MSC005 Muscular Dystrophy 66 2.640
198
P GST053 Gastric Cancer 82 2.639
199
P PNC044 Pancreatitis 61 2.636
200
P HYP076 Hyperthyroidism 53 2.623
201
IMP005 Impotence 52 2.600
202
c HPT001 Hepatitis C 61 2.599
203
P HML001 Hemolytic-Uremic Syndrome 52 2.595
204
P SYS005 Systemic Scleroderma 73 2.591
205
PRT036 Peritonitis 65 2.576
206
P PLM036 Pulmonary Fibrosis 65 2.567
207
STR067 Stroke, Ischemic 79 2.551
208
c HPT073 Hepatitis C Virus 71 2.541
209
ALL014 Allergic Encephalomyelitis 34 2.525
210
ALL029 Allergic Disease 61 2.493
211
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.490
212
INT066 Interstitial Lung Disease 60 2.489
213
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 2.486
214
c LKM005 Leukemia, T-Cell, Chronic 33 2.470
215
STM007 Stomatitis 52 2.467
216
CRB004 Cerebral Artery Occlusion 46 2.450
217
P KLZ004 Kala-Azar 1 41 2.436
218
LSH001 Leishmaniasis 63 2.436
219
P PLY018 Polycythemia 56 2.431
220
MYL009 Myelodysplastic Syndrome 67 2.418
221
P OPN001 Open-Angle Glaucoma 55 2.414
222
P ENC004 Encephalitis 61 2.407
223
P PRK039 Parkinsonism 55 2.386
224
P PLY014 Polycystic Kidney Disease 71 2.385
225
P BLD134 Bladder Cancer 79 2.382
226
P END044 Endometriosis 62 2.379
227
OVR094 Ovarian Epithelial Cancer 39 2.377
228
P RTN018 Retinal Disease 53 2.367
229
P ENC018 Encephalopathy 62 2.360
230
P ADL010 Adult Respiratory Distress Syndrome 71 2.353
231
c TYP008 Type 1 Diabetes Mellitus 77 2.348
232
P NSP012 Nasopharyngeal Carcinoma 60 2.346
233
P CTR002 Cataract 59 2.343
234
P PRK057 Parkinson Disease, Late-Onset 79 2.337
235
MLG169 Malignant Astrocytoma 57 2.331
236
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 2.331
237
P THR014 Thrombocytopenia 66 2.328
238
P KDN017 Kidney Cancer 60 2.324
239
PLY150 Polykaryocytosis Inducer 29 2.323
240
c GLC092 Glaucoma, Primary Open Angle 61 2.321
241
BRN024 Bronchitis 67 2.314
242
c CHR064 Chronic Monocytic Leukemia 36 2.300
243
INS001 Insulinoma 59 2.289
244
P SCK005 Sickle Cell Disease 56 2.286
245
IMM167 Immune Deficiency Disease 77 2.281
246
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.269
247
SPL018 Splenomegaly 47 2.267
248
P ART022 Arthritis 70 2.265
249
P SZR006 Seizure Disorder 69 2.245
250
P ART021 Arteriosclerosis 53 2.244
251
NRL016 Neural Tube Defects 81 2.242
252
P URN019 Urinary Tract Infection 49 2.240
253
c DLT002 Dilated Cardiomyopathy 79 2.240
254
P OLG002 Oligodendroglioma 66 2.239
255
TLN003 Telangiectasis 51 2.239
256
FND002 Fundus Dystrophy 55 2.234
257
P ATR011 Atrial Fibrillation 66 2.231
258
ALC007 Alcohol Dependence 65 2.229
259
P GNG009 Gangliosidosis 44 2.224
260
c PLM164 Pulmonary Hypertension, Primary, 1 80 2.201
261
P BND020 Bone Disease 60 2.199
262
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.190
263
c ACT073 Acute Leukemia 59 2.181
264
P SLP006 Sleep Apnea 69 2.177
265
P RHM011 Rheumatoid Arthritis 81 2.176
266
P HYP061 Hypertrophic Cardiomyopathy 69 2.167
267
P MYC084 Mycobacterium Tuberculosis 1 68 2.164
268
P PLY019 Polyneuropathy 53 2.162
269
EWN003 Ewing Sarcoma 70 2.159
270
P RHN004 Rhinitis 57 2.152
271
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.150
272
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.150
273
c ACT134 Acute Liver Failure 57 2.149
274
P OST002 Osteoporosis 77 2.145
275
P EPL164 Epilepsy 70 2.134
276
PNG002 Pain Agnosia 51 2.132
277
ACQ007 Acquired Immunodeficiency Syndrome 58 2.124
278
P HPT021 Hepatitis 68 2.122
279
P ATX030 Ataxia-Telangiectasia 80 2.114
280
GST023 Gastric Ulcer 52 2.112
281
AMN001 Amenorrhea 53 2.110
282
DPH001 Diphtheria 59 2.105
283
c PRM005 Primary Hyperparathyroidism 59 2.094
284
c ACT135 Acute Graft Versus Host Disease 51 2.091
285
END086 End Stage Renal Disease 54 2.088
286
P NPH012 Nephrotic Syndrome 62 2.087
287
DFF005 Diffuse Large B-Cell Lymphoma 55 2.079
288
CRN030 Coronary Stenosis 50 2.068
289
ACD003 Acid Sphingomyelinase Deficiency 30 2.065
290
TRM010 Traumatic Brain Injury 50 2.064
291
HYD002 Hydronephrosis 58 2.062
292
P GRV001 Graves' Disease 54 2.060
293
CRV035 Cervical Cancer 72 2.059
294
c BRN108 Branchiootic Syndrome 1 63 2.048
295
ORL015 Oral Squamous Cell Carcinoma 43 2.047
296
CHL065 Cholangiocarcinoma 58 2.046
297
INT079 Intrahepatic Cholangiocarcinoma 51 2.045
298
KRT009 Keratosis 52 2.040
299
P ALP008 Alopecia 53 2.038
300
ALL003 Allergic Rhinitis 66 2.033
301
DMY004 Demyelinating Disease 50 2.030
302
CHR074 Choriocarcinoma 46 2.023
303
HNS001 Hansen's Disease 32 2.023
304
P OVR082 Overgrowth Syndrome 42 2.021
305
P NRN021 Neuronal Ceroid Lipofuscinosis 64 2.012
306
P LPR021 Leprosy 3 71 2.008
307
IRN001 Iron Deficiency Anemia 58 1.997
308
P GST044 Gastritis 55 1.993
309
P MYC033 Myoclonus 46 1.990
310
P CRD119 Cardiac Arrest 68 1.985
311
IGR001 Ige Responsiveness, Atopic 59 1.984
312
MCS002 Mucositis 55 1.977
313
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.976
314
P SPN046 Spinal Muscular Atrophy 62 1.973
315
c NMN013 Niemann-Pick Disease, Type a 63 1.968
316
P EYD002 Eye Disease 57 1.967
317
OVR063 Overnutrition 42 1.963
318
ATS010 Autosomal Recessive Disease 42 1.959
319
SVR001 Severe Acute Respiratory Syndrome 68 1.955
320
P THY032 Thyroiditis 56 1.944
321
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.938
322
c VRL010 Viral Hepatitis 52 1.937
323
LYM143 Lymphoma, Non-Hodgkin, Familial 79 1.936
324
LYM133 Lymphoma, Hodgkin, Classic 74 1.932
325
P SCH015 Schizophrenia 74 1.929
326
P HML002 Hemolytic Anemia 62 1.927
327
ANX004 Anoxia 40 1.926
328
c OPT053 Optic Atrophy 1 62 1.925
329
SYN036 Syncope 44 1.914
330
NPH009 Nephrolithiasis 54 1.910
331
c INH030 Inherited Retinal Disorder 28 1.906
332
MDD018 Middle East Respiratory Syndrome 44 1.903
333
P THY023 Thymoma 64 1.897
334
c THY107 Thymoma, Familial 42 1.897
335
CRD132 Cardiac Conduction Defect 59 1.896
336
P TRM003 Tremor 50 1.883
337
P HYP750 Hypertriglyceridemia, Familial 62 1.877
338
c ATS013 Autosomal Recessive Congenital Ichthyosis 65 1.877
339
PPL052 Papillomatosis, Confluent and Reticulated 34 1.871
340
CVD001 Covid-19 58 1.868
341
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.867
342
c SCL052 Scleroderma, Familial Progressive 60 1.861
343
MLD018 Mild Cognitive Impairment 48 1.858
344
STT001 Status Epilepticus 58 1.858
345
MDD011 Mood Disorder 62 1.857
346
CHR005 Chorioamnionitis 50 1.855
347
URM002 Uremia 47 1.842
348
P APL001 Aplastic Anemia 73 1.837
349
P HYP098 Hypereosinophilic Syndrome 66 1.830
351
ART016 Aortic Aneurysm 69 1.824
352
P HNT016 Huntington Disease 73 1.823
353
c THR092 Thrombophilia Due to Thrombin Defect 74 1.811
354
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.809
355
P DMN002 Dementia 65 1.803
356
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.798
357
CLN015 Colon Adenocarcinoma 64 1.796
358
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.796
359
P DYS154 Dystonia 64 1.789
360
P MTC003 Metachromatic Leukodystrophy 71 1.785
361
P RHB003 Rhabdomyosarcoma 66 1.780
362
P RCT021 Rectum Cancer 54 1.770
363
KPS004 Kaposi Sarcoma 76 1.763
364
P TRT010 Teratoma 50 1.763
365
HRW001 Hair Whorl 35 1.761
366
LYM019 Lymphosarcoma 46 1.759
367
P SPP010 Suppressor of Tumorigenicity 3 51 1.757
368
P BPL003 Bipolar Disorder 56 1.751
369
c MJR024 Major Affective Disorder 9 40 1.748
370
c MJR022 Major Affective Disorder 8 37 1.748
371
BRN004 Brain Edema 54 1.746
372
PRP016 Paraplegia 52 1.742
373
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.732
374
MTC005 Mitochondrial Metabolism Disease 45 1.730
375
P MTR004 Maturity-Onset Diabetes of the Young 66 1.727
376
P ZLL001 Zellweger Syndrome 65 1.721
377
HMP009 Haemophilus Influenzae 41 1.719
378
HLC007 Helicobacter Pylori Infection 67 1.719
379
SCK003 Sickle Cell Anemia 74 1.718
380
P KRB001 Krabbe Disease 69 1.716
381
P MDL005 Medulloblastoma 75 1.714
382
P TBR001 Tuberous Sclerosis 69 1.707
383
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.705
384
NRN005 Neuronal Ceroid-Lipofuscinoses 61 1.694
385
P DRR001 Diarrhea 55 1.683
386
c INH020 Inherited Metabolic Disorder 47 1.670
387
HLX001 Helix Syndrome 47 1.665
388
BRN056 Bronchopulmonary Dysplasia 57 1.660
389
P CHR345 Chronic Pain 50 1.659
390
P MLN007 Male Infertility 56 1.652
391
c JVN010 Juvenile Rheumatoid Arthritis 66 1.645
392
c TBR025 Tuberous Sclerosis 1 84 1.645
393
ANR040 Aneurysm 60 1.642
394
P UVT001 Uveitis 57 1.641
395
P AGG001 Aggressive Periodontitis 55 1.638
396
P HYP730 Hypogonadotropic Hypogonadism 54 1.634
397
ACT119 Acute Promyelocytic Leukemia 62 1.627
398
P LCT001 Lactic Acidosis 50 1.625
399
ILS001 Ileus 49 1.624
400
P SNS001 Sensorineural Hearing Loss 59 1.620
401
P PLM034 Pulmonary Emphysema 58 1.617
402
P DNG005 Dengue Virus 55 1.615
403
ANX010 Anxiety 70 1.609
404
P MYC008 Myocarditis 59 1.604
405
RTN017 Retinal Detachment 60 1.600
406
GRM010 Germ Cells Tumors 33 1.600
407
P HRP006 Herpes Simplex 65 1.599
408
P PRM011 Primary Ciliary Dyskinesia 69 1.599
409
P PRC019 Precocious Puberty 49 1.595
410
c HPT016 Hepatitis B 62 1.592
411
P VSC007 Vascular Disease 62 1.587
412
URT010 Ureteral Obstruction 45 1.583
413
P RRT020 Rare Tumor 39 1.582
414
WST005 West Nile Virus 55 1.581
415
P ADL017 Adult T-Cell Leukemia 54 1.577
416
P MCR010 Microcephaly 59 1.577
417
c MGR028 Migraine with or Without Aura 1 64 1.574
418
CRB039 Cerebrovascular Disease 65 1.572
419
DBT010 Diabetic Neuropathy 54 1.572
420
MSL001 Measles 61 1.568
421
PRM013 Premature Menopause 57 1.555
422
P BNG032 Benign Mesothelioma 53 1.549
423
PLY100 Polyploidy 36 1.545
424
MCR013 Microphthalmia 60 1.538
425
ERL001 Early Myoclonic Encephalopathy 63 1.538
426
P INT070 Intestinal Obstruction 57 1.537
427
SMN007 Seminoma 42 1.535
428
P SRC025 Sarcoidosis 1 70 1.529
429
TRC003 Trichomoniasis 53 1.507
430
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 1.496
431
RNL077 Renal Fibrosis 46 1.495
432
THY121 Thyroid Gland Anaplastic Carcinoma 66 1.495
433
BRN028 Brain Cancer 73 1.495
434
CNS004 Constipation 56 1.494
435
c GM2006 Gm2 Gangliosidosis 46 1.493
436
P HYP024 Hypoparathyroidism 55 1.492
437
c HYP724 Hyperlipoproteinemia, Type Iii 66 1.481
438
P STR022 Stargardt Disease 61 1.473
439
NRX001 Neuroaxonal Dystrophy 38 1.473
440
P PYL005 Pyelonephritis 56 1.472
441
LKP003 Leukoplakia 39 1.472
442
MNT001 Mantle Cell Lymphoma 65 1.471
443
P HMP007 Hemophilia 52 1.467
444
LBR036 Leber Plus Disease 67 1.466
445
P MYC026 Myoclonus Epilepsy 35 1.465
446
GST092 Gastroesophageal Reflux 60 1.463
447
CHG001 Chagas Disease 65 1.463
448
THY030 Thyroid Gland Disease 50 1.462
449
HYP043 Hyperandrogenism 47 1.459
450
LPT014 Leptin Deficiency or Dysfunction 77 1.458
451
P CLC063 Celiac Disease 1 66 1.448
452
c ICH069 Ichthyosis, Congenital, Autosomal Recessive 4b 51 1.447
453
P LRY044 Larynx Cancer 53 1.445
454
c GM1007 Gm1 Gangliosidosis 65 1.439
455
P HRD011 Hereditary Spherocytosis 63 1.431
456
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.429
457
MSC157 Muscular Dystrophy, Duchenne Type 79 1.427
458
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.427
459
P GLL018 Gallbladder Cancer 53 1.418
461
P ATT013 Attention Deficit-Hyperactivity Disorder 66 1.412
462
NRL005 Neurilemmoma 60 1.409
463
OST012 Osteoarthritis 77 1.406
464
PLR008 Pleurisy 49 1.405
465
c ACT068 Acute Cystitis 61 1.404
466
P LTH003 Lethal Congenital Contracture Syndrome 40 1.397
467
P CHL066 Cholangitis 51 1.396
468
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 1.394
469
PNC129 Pancreatic Adenocarcinoma 65 1.392
470
FRN006 Frontotemporal Dementia 68 1.388
471
SYN007 Synovitis 54 1.387
472
PLC002 Plica Syndrome 35 1.387
473
P MNN013 Meningitis 65 1.386
474
P ART023 Arthropathy 60 1.383
475
VCC001 Vaccinia 49 1.379
476
P VTL001 Vitelliform Macular Dystrophy 45 1.375
477
ADR007 Adrenoleukodystrophy 74 1.368
478
ADR022 Adrenomyeloneuropathy 39 1.368
479
GST045 Gastroenteritis 58 1.366
480
c FML021 Familial Hypercholesterolemia 71 1.363
481
HMN047 Human Cytomegalovirus Infection 59 1.361
482
P VSC011 Vasculitis 61 1.358
483
CRB090 Cerebral Hypoxia 42 1.357
484
c PRG042 Progressive Familial Heart Block, Type Ia 65 1.356
485
CMB007 Combined Immunodeficiency 56 1.355
486
P FML011 Familial Adenomatous Polyposis 71 1.355
487
DSS009 Disseminated Intravascular Coagulation 56 1.353
488
c RTN047 Retinitis Pigmentosa 18 45 1.352
489
ORL011 Oral Cancer 60 1.349
490
CRY035 Cryptorchidism, Unilateral or Bilateral 57 1.348
491
IGG001 Iga Glomerulonephritis 50 1.337
492
GRN017 Granulocytopenia 42 1.334
493
WLS001 Wilson Disease 70 1.333
494
DGN001 Degenerative Disc Disease 48 1.332
495
P EXN002 Exanthem 58 1.331
496
c NMN015 Niemann-Pick Disease, Type C1 68 1.325
497
THR024 Thrombosis 56 1.324
498
PRM329 Premature Aging 36 1.320
499
P TYS001 Tay-Sachs Disease 69 1.317
500
P FTL001 Fetal Alcohol Syndrome 55 1.315
501
c HNT011 Huntington Disease-Like 3 33 1.312
502
P USH001 Usher Syndrome 64 1.306
503
VRL011 Viral Infectious Disease 60 1.305
505
SYS003 Systolic Heart Failure 49 1.302
506
NRM005 Neuromuscular Disease 63 1.297
507
PRM236 Primary Biliary Cholangitis 62 1.291
508
GNG013 Gingivitis 59 1.291
509
P ESP024 Esophagitis 60 1.278
510
P ATS364 Autism 72 1.277
511
DWR001 Dwarfism 45 1.277
512
PRP030 Purpura 54 1.270
513
P GLC113 Galactosemia I 65 1.269
514
c PRG020 Paragangliomas 3 39 1.266
515
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.265
516
c NMN016 Niemann-Pick Disease, Type B 56 1.264
517
P INS002 in Situ Carcinoma 53 1.261
518
ADN011 Adenoid Cystic Carcinoma 68 1.260
519
c HRD010 Hereditary Spastic Paraplegia 65 1.252
520
P CYS018 Cystitis 59 1.249
521
SKN019 Skin Melanoma 70 1.249
522
P MTR014 Motor Neuron Disease 65 1.243
523
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.236
524
P PGT001 Paget's Disease of Bone 60 1.229
525
LFT001 Left Bundle Branch Hemiblock 47 1.229
526
GST040 Gastric Adenocarcinoma 66 1.228
528
P END033 Endocarditis 58 1.218
529
GSG001 Gas Gangrene 52 1.205
530
LPD009 Lipid Storage Disease 45 1.204
531
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 62 1.203
532
ESP021 Esophageal Cancer 84 1.194
533
HLL004 Hellp Syndrome 53 1.192
534
MYM001 Myoma 54 1.192
535
NTH001 Netherton Syndrome 60 1.190
536
CHL068 Cholestasis 61 1.189
537
THY123 Thyroid Gland Follicular Carcinoma 53 1.180
538
c STR040 Stargardt Disease 3 34 1.177
539
IRR003 Irritant Dermatitis 47 1.177
540
P ASP006 Aspergillosis 71 1.176
541
KLD004 Keloid Disorder 39 1.173
542
HRT015 Heritable Pulmonary Arterial Hypertension 46 1.167
543
PSR001 Psoriatic Arthritis 61 1.165
544
P LYM033 Lymphoproliferative Syndrome 59 1.158
545
END041 Endometrial Adenocarcinoma 63 1.156
546
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.155
547
VSC003 Visceral Leishmaniasis 54 1.154
548
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.141
549
P MTC069 Mitochondrial Disorders 57 1.141
550
GLS018 Glass Syndrome 60 1.138
551
MYL005 Myelofibrosis 70 1.138
552
QDR001 Quadriplegia 49 1.136
553
RRG078 Rare Genetic Deafness 38 1.132
554
P PRG013 Paraganglioma 57 1.129
555
c BLD140 Blood Group, I System 47 1.126
556
CLR030 Clear Cell Renal Cell Carcinoma 54 1.121
557
ARG004 Argyria 26 1.115
558
P CTN015 Cutaneous T Cell Lymphoma 48 1.112
559
OST017 Osteomyelitis 63 1.112
560
P SCL009 Sclerosing Cholangitis 46 1.110
561
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 1.107
562
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.106
563
NRT004 Neuritis 53 1.106
564
RTN020 Retinal Vascular Disease 45 1.105
565
P SML001 Small Cell Carcinoma 52 1.094
566
CHL045 Choline Deficiency Disease 39 1.088
567
c PRG011 Progressive Myoclonus Epilepsy 40 1.086
568
PRT013 Portal Hypertension 59 1.083
569
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 30 1.082
570
P DDN001 Duodenal Ulcer 53 1.081
571
c CHL119 Cholangitis, Primary Sclerosing 57 1.081
572
ALL010 Allergic Contact Dermatitis 56 1.080
573
LNG039 Lung Squamous Cell Carcinoma 57 1.080
574
P HYD006 Hydrocephalus 63 1.079
575
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 1.078
576
P OVR046 Ovarian Cyst 44 1.070
577
P AMY004 Amyloidosis 69 1.070
578
AZS001 Azoospermia 45 1.067
579
CWP001 Cowpox 44 1.067
580
NSS002 Neisseria Meningitidis Infection 47 1.061
581
P CRB059 Cerebellar Degeneration 36 1.056
582
PST092 Posttransplant Acute Limbic Encephalitis 29 1.056
583
PPT001 Peptic Esophagitis 51 1.047
584
c HNT004 Huntington Disease-Like 2 51 1.041
585
c SVR005 Severe Pre-Eclampsia 50 1.041
586
PLY001 Polycythemia Vera 69 1.032
587
P TST021 Testicular Germ Cell Tumor 61 1.026
588
P PRP029 Porphyria 60 1.020
589
SJG002 Sjogren-Larsson Syndrome 53 1.020
590
HRN029 Hearing Loss, Noise-Induced 37 1.020
591
ING001 Inguinal Hernia 59 1.014
592
OBS082 Obstructive Nephropathy 41 1.012
593
P CHR071 Charcot-Marie-Tooth Disease 64 1.011
594
PLM001 Pulmonary Tuberculosis 69 1.011
595
TTH006 Tooth Disease 51 1.008
596
OBS002 Obsessive-Compulsive Disorder 68 1.004
597
P NRD007 Neurodegeneration with Brain Iron Accumulation 51 1.004
598
P HDC001 Headache 56 1.002
599
FNG017 Fungal Infectious Disease 54 1.001
600
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.001
601
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.993
602
ANR007 Anorexia Nervosa 59 0.990
603
CHR072 Chordoma 57 0.988
604
P HRM001 Hermansky-Pudlak Syndrome 65 0.985
605
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.985
606
BRT005 Barth Syndrome 55 0.978
607
P EHL001 Ehlers-Danlos Syndrome 57 0.978
608
RHB024 Rhabdomyosarcoma 2 65 0.975
609
SCH014 Schistosomiasis 56 0.971
610
OVR059 Ovary Adenocarcinoma 49 0.968
611
CRT015 Carotid Artery Occlusion 45 0.967
612
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.965
613
P CND004 Candidiasis 57 0.963
614
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 0.962
615
c RTN141 Retinitis Pigmentosa 39 44 0.954
616
c USH035 Usher Syndrome Type 2 52 0.954
617
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.953
618
P PMP001 Pemphigus 55 0.951
619
HYP025 Hyperphosphatemia 47 0.950
620
P OVR049 Ovarian Disease 50 0.950
621
c NMN014 Niemann-Pick Disease, Type C2 49 0.948
622
LYM017 Lyme Disease 63 0.945
623
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.940
624
ENT011 Enterocolitis 55 0.940
625
c PLM163 Palmoplantar Keratoderma, Punctate Type Ii 29 0.937
626
PNC060 Punctate Porokeratosis 28 0.937
627
CHD004 Chudley-Mccullough Syndrome 47 0.931
628
c USH037 Usher Syndrome, Type Iia 50 0.929
629
LYM009 Lymphocytic Choriomeningitis 46 0.927
630
P PRP003 Porphyria Cutanea Tarda 66 0.925
631
BRN002 Bronchiolitis 57 0.923
632
SND001 Sandhoff Disease 66 0.921
633
P GLY013 Glycogen Storage Disease 59 0.917
634
EXS001 Exostosis 49 0.917
635
IRR002 Irritable Bowel Syndrome 65 0.916
636
PRV004 Periventricular Leukomalacia 52 0.914
637
P LNG028 Long Qt Syndrome 63 0.911
638
P HMP002 Hemophagocytic Lymphohistiocytosis 60 0.910
639
JPN002 Japanese Encephalitis 61 0.903
640
ATR057 Atrioventricular Block 54 0.899
641
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.897
642
RSC001 Rosacea 55 0.895
643
P CYS039 Cystic Kidney Disease 52 0.886
644
GDP001 Goodpasture Syndrome 55 0.886
645
P CNJ013 Conjunctivitis 66 0.882
646
c ATM075 Autoimmune Encephalitis 39 0.882
647
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 0.881
648
ABT001 Abetalipoproteinemia 68 0.880
649
BLR008 Bilirubin Metabolic Disorder 57 0.876
650
c HRM009 Hermansky-Pudlak Syndrome 6 45 0.875
651
P FCL005 Focal Segmental Glomerulosclerosis 57 0.871
652
KWS002 Kawasaki Disease 65 0.867
653
MYC006 Mycosis Fungoides 65 0.866
654
ART074 Aortic Dissection 53 0.863
655
c ATS007 Autism Spectrum Disorder 72 0.863
656
MCP033 Mucopolysaccharidoses 44 0.862
657
GT001 Gout 63 0.861
658
ANH002 Anhidrosis 45 0.856
659
PRX001 Peroxisomal Disease 46 0.856
660
TRC008 Trachoma 53 0.855
661
HDN002 Head Injury 44 0.853
662
LST001 Listeriosis 59 0.852
663
c HRD202 Hereditary Lymphedema I 55 0.849
664
PMP006 Pemphigus Vulgaris, Familial 58 0.846
665
FDL002 Food Allergy 47 0.844
666
CRV040 Cervix Carcinoma 50 0.844
667
P DMY001 Demyelinating Polyneuropathy 41 0.843
668
BRC012 Brucellosis 66 0.841
669
CNN005 Connective Tissue Disease 66 0.841
670
P MMB011 Membranous Nephropathy 50 0.836
671
CND006 Candida Glabrata 29 0.835
672
HSH003 Hashimoto Thyroiditis 60 0.835
673
P ANT001 Anterolateral Myocardial Infarction 34 0.834
674
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 0.827
675
EHR002 Ehrlichiosis 39 0.827
676
P ECT006 Ectodermal Dysplasia 62 0.827
677
PTH003 Pathologic Nystagmus 52 0.826
678
GLC106 Glucocorticoid Resistance, Generalized 48 0.825
679
CLR108 Colorectal Adenoma 63 0.824
680
PRN019 Perinatal Necrotizing Enterocolitis 60 0.821
681
GST071 Gastrointestinal Carcinoma 46 0.819
682
ICH001 Ichthyosis Vulgaris 53 0.818
683
RTC012 Reticuloendotheliosis, X-Linked 35 0.818
684
P SLV026 Salivary Gland Carcinoma 60 0.818
685
BCT002 Bacterial Vaginosis 53 0.816
686
PMP004 Pemphigus Foliaceus 43 0.814
687
HYD038 Hydrops Fetalis, Nonimmune 57 0.813
688
c LYM150 Lymphatic Malformation 7 43 0.813
689
ACT228 Acute Radiation Syndrome 30 0.813
690
PLS009 Plasma Cell Neoplasm 64 0.813
691
HPT022 Hepatoblastoma 54 0.810
692
MNN009 Meningoencephalitis 48 0.808
693
P SBR004 Seborrheic Dermatitis 44 0.805
694
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.804
695
MST005 Mastitis 52 0.804
696
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.803
697
PLC008 Placenta Disease 49 0.800
698
P SCL018 Scoliosis 57 0.799
699
c GLC114 Glaucoma, Primary Closed-Angle 36 0.797
700
APP008 Appendicitis 62 0.794
701
HPT067 Hepatocellular Adenoma 42 0.793
702
SHG001 Shigellosis 61 0.793
703
P GLL022 Guillain-Barre Syndrome 59 0.792
704
HVY002 Heavy Metal Poisoning 22 0.786
705
P WSK001 Wiskott-Aldrich Syndrome 72 0.785
706
LMY002 Leiomyoma 51 0.784
707
TLR001 Tularemia 56 0.775
708
EST002 Estrogen-Receptor Negative Breast Cancer 45 0.768
709
SMT004 Smith-Lemli-Opitz Syndrome 69 0.768
710
c OPT051 Opitz Gbbb Syndrome, Type I 45 0.768
711
CRN020 Coronary Restenosis 39 0.767
712
MNN043 Meningioma, Familial 79 0.761
713
CLR109 Colorectal Adenocarcinoma 50 0.758
714
HMN002 Human Granulocytic Anaplasmosis 31 0.757
715
INT395 Intracranial Meningioma 48 0.757
716
SCR001 Secretory Meningioma 40 0.757
717
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.757
718
c DWL002 Dowling-Degos Disease 1 58 0.757
719
FBR047 Fibromyalgia 58 0.756
720
c CRD185 Ceroid Lipofuscinosis, Neuronal, 6 54 0.755
721
P AVS003 Avascular Necrosis 41 0.753
722
c EXS019 Exostoses, Multiple, Type I 54 0.743
723
ACT098 Acute Erythroid Leukemia 55 0.743
724
P FML018 Familial Mediterranean Fever 73 0.742
725
NWC001 Newcastle Disease 48 0.741
726
PRP080 Peripheral Artery Disease 54 0.737
727
PNC034 Pancreas Disease 49 0.731
728
LMB062 Limb Ischemia 55 0.730
729
SKN005 Skin Atrophy 41 0.729
730
CHR081 Choroideremia 58 0.727
731
P AXN001 Axonal Neuropathy 33 0.727
732
c PNC106 Pancreatic Agenesis 1 51 0.725
733
P HYP265 Hypotonia 42 0.720
734
MLD001 Melioidosis 67 0.716
735
MSC007 Muscle Hypertrophy 64 0.704
736
CHR031 Chromoblastomycosis 48 0.703
737
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.701
738
PNC001 Pancytopenia 52 0.699
739
MLL001 Molluscum Contagiosum 48 0.696
740
P AML002 Amelogenesis Imperfecta 56 0.691
741
MLG079 Malignant Pleural Mesothelioma 42 0.689
742
HYP014 Hyperuricemia 51 0.686
743
TRN015 Transient Cerebral Ischemia 62 0.684
744
GST050 Gastrointestinal System Disease 55 0.682
745
BLP005 Blepharitis 50 0.682
746
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.680
747
SFT003 Soft Tissue Sarcoma 57 0.680
748
ATN004 Autonomic Neuropathy 42 0.679
749
MMM001 Mammary Paget's Disease 53 0.678
750
P OBS001 Obstructive Jaundice 49 0.676
751
GNG012 Gingival Overgrowth 49 0.673
752
ACN002 Acanthosis Nigricans 56 0.670
753
c CLR080 Colorectal Cancer 5 24 0.670
754
TRY001 Trypanosomiasis 50 0.667
755
EMB004 Embryonal Carcinoma 55 0.666
756
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.664
757
BLR013 Biliary Tract Cancer 43 0.663
758
P PLY041 Polymyositis 59 0.660
759
RTN003 Retinal Ischemia 48 0.660
760
VTM033 Vitamin K Deficiency Bleeding 50 0.657
761
ALX003 Alexander Disease 61 0.657
762
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.652
763
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.652
764
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.645
765
DCB001 Decubitus Ulcer 61 0.644
766
SPS057 Spasticity 43 0.643
767
CHL147 Chlamydia Pneumonia 47 0.641
768
GLM044 Glomerular Disease 34 0.641
769
c HRM005 Hermansky-Pudlak Syndrome 1 55 0.639
770
VSC002 Vascular Dementia 59 0.627
771
NRD001 Neurodermatitis 39 0.625
772
HST011 Histoplasmosis 54 0.620
773
CYS014 Cystadenocarcinoma 51 0.619
774
ENT004 Enthesopathy 51 0.616
775
P HMN010 Hemangioma 61 0.616
776
HYP457 Hypertrophic Scars 42 0.615
777
NRN001 Neuroendocrine Carcinoma 47 0.613
778
RST023 Resting Heart Rate, Variation in 40 0.613
779
BRR014 Barrett Esophagus 66 0.610
780
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.610
781
SDD001 Sudden Infant Death Syndrome 60 0.610
782
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.607
783
P PRM327 Primary Lymphedema 35 0.607
784
DNG003 Dengue Disease 65 0.607
785
HST010 Histiocytosis 49 0.607
786
P PRD006 Prader-Willi Syndrome 60 0.604
787
PST028 Post-Traumatic Stress Disorder 59 0.604
788
VLV047 Volvulus of Midgut 55 0.603
789
P MNC007 Monocytic Leukemia 48 0.599
790
c GLL024 Gallbladder Disease 1 53 0.599
791
CHL004 Cholelithiasis 48 0.599
792
THY128 Thyroid Tumor 33 0.594
793
P MVM001 Movement Disease 61 0.590
794
THR123 Thrombotic Microangiopathy 40 0.586
795
P NRM002 Normal Pressure Hydrocephalus 49 0.585
796
P TXP001 Toxoplasmosis 60 0.583
797
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.579
798
PLG002 Plague 58 0.576
799
ALC009 Alcoholic Liver Cirrhosis 54 0.571
800
HRY003 Hairy Cell Leukemia 61 0.568
801
PST046 Post-Transplant Lymphoproliferative Disease 53 0.568
802
SBC001 Subacute Sclerosing Panencephalitis 53 0.564
803
PHN003 Phenylketonuria 76 0.561
804
CRY005 Cryptococcosis 61 0.560
805
P FLL037 Follicular Lymphoma 73 0.560
806
KRT019 Keratitis, Hereditary 66 0.558
807
MTR002 Mitral Valve Insufficiency 51 0.558
808
HMG002 Hemoglobinuria 50 0.552
809
SNS003 Sensory Peripheral Neuropathy 51 0.551
810
c GCH015 Gaucher Disease, Type I 67 0.550
811
P HRD021 Hereditary Sensory Neuropathy 48 0.548
812
P PLM006 Pulmonary Alveolar Proteinosis 53 0.546
813
SPT004 Septic Arthritis 58 0.545
814
P PRL003 Proliferative Glomerulonephritis 43 0.538
815
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.538
816
MLK006 Milk Allergy 47 0.537
817
PLS011 Plasmacytoma 56 0.533
818
PRS063 Paresthesia 39 0.532
819
EXC002 Exocrine Pancreatic Insufficiency 42 0.528
820
OCL006 Ocular Hypertension 53 0.525
821
END062 Endometrial Hyperplasia 48 0.521
822
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.518
823
LPR001 Lepromatous Leprosy 49 0.513
824
P ORT004 Orthostatic Intolerance 62 0.511
825
ATN005 Autonomic Dysfunction 45 0.511
826
SLP001 Sleeping Sickness 56 0.510
827
YLL002 Yellow Fever 61 0.508
828
CTN007 Cutaneous Leishmaniasis 61 0.506
829
P INT068 Intestinal Disease 53 0.503
830
TRT001 Teratocarcinoma 41 0.503
831
FTL006 Fetal Alcohol Spectrum Disorder 43 0.503
833
MYF001 Myofibroma 42 0.500
834
CYS005 Cysticercosis 60 0.492
835
DNT012 Dental Caries 53 0.492
836
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.491
837
P ALP009 Alopecia Areata 59 0.488
838
CCC002 Coccidiosis 50 0.486
839
URL001 Urolithiasis 45 0.485
840
c CHR417 Chronic Graft Versus Host Disease 55 0.481
841
c BSL007 Basal Cell Carcinoma 68 0.478
842
P KRT007 Keratoconus 50 0.477
843
WST001 West Syndrome 64 0.473
844
KRN002 Kearns-Sayre Syndrome 63 0.473
845
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.471
846
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 19 0.467
847
ART002 Arts Syndrome 66 0.465
848
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.453
849
HYP063 Hypersplenism 52 0.451
850
ADR005 Adrenal Carcinoma 61 0.451
851
APH002 Aphasia 55 0.448
852
P ART005 Arteriovenous Malformation 65 0.448
853
c HPT007 Hepatitis E 50 0.448
854
P LPS002 Liposarcoma 64 0.446
855
CHD001 Chediak-Higashi Syndrome 67 0.443
856
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.440
857
P ACT105 Acute Mountain Sickness 52 0.437
858
ACT084 Acute Stress Disorder 53 0.435
859
HMP005 Hemiplegia 53 0.431
860
ECH003 Echinococcosis 52 0.431
861
P BLD062 Bile Duct Cancer 68 0.431
862
P RBL001 Rubella 58 0.431
863
ICH054 Ichthyosis, X-Linked 51 0.430
864
P CRN025 Corneal Dystrophy 49 0.424
865
P BNG030 Benign Ependymoma 51 0.422
866
THY122 Thyroid Gland Cancer 59 0.422
867
CLL010 Cellular Ependymoma 58 0.422
868
P BNC003 Bone Cancer 58 0.418
869
HMR023 Hemorrhagic Cystitis 43 0.417
870
TNG002 Tangier Disease 64 0.417
871
KSH004 Kashin-Beck Disease 37 0.413
872
c PRM340 Primary Adrenal Insufficiency 37 0.413
873
PRC002 Paracoccidioidomycosis 53 0.410
874
APR001 Apraxia 51 0.408
875
KRT002 Keratomalacia 54 0.408
876
P RNL007 Renal Tubular Acidosis 52 0.408
877
c DPH024 Diaphragmatic Hernia, Congenital 64 0.406
878
CHL056 Cheilitis 46 0.406
879
CHR066 Chronic Fatigue Syndrome 60 0.406
880
P AGM001 Agammaglobulinemia 67 0.403
881
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.398
882
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.398
883
SNL007 Senile Cataract 40 0.398
884
DRM011 Dermatophytosis 52 0.398
885
HDR003 Hidradenitis 50 0.398
886
HDR002 Hidradenitis Suppurativa 54 0.398
887
SPS019 Spastic Paraparesis 38 0.394
888
CHK001 Chikungunya 60 0.393
889
CHR100 Chronic Ulcer of Skin 57 0.389
890
c CNT035 Central Nervous System Disease 53 0.389
891
LNG108 Langerhans Cell Histiocytosis 57 0.388
892
MCN008 Mucinous Cystadenocarcinoma 39 0.383
893
P MCL001 Mucolipidosis 49 0.383
894
DRY001 Dry Eye Syndrome 49 0.378
895
PNT038 Peanut Allergy 46 0.371
896
GNG005 Gangliocytoma 54 0.367
897
P HYP818 Hypobetalipoproteinemia, Familial, 1 60 0.366
898
c PRM108 Primary Progressive Multiple Sclerosis 51 0.364
899
NNT021 Neonatal Meningitis 22 0.364
900
GRD001 Giardiasis 46 0.363
901
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.362
902
c WLM013 Wilms Tumor 1 65 0.362
903
RGH001 Right Bundle Branch Block 47 0.362
904
ADG002 Audiogenic Seizures 25 0.362
905
FBR002 Fibrosarcoma of Bone 47 0.358
906
MRK001 Merkel Cell Carcinoma 65 0.358
907
WLF001 Wolff-Parkinson-White Syndrome 63 0.356
908
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.356
909
P CRN024 Corneal Disease 43 0.356
910
BRN014 Bronchopneumonia 52 0.356
911
MCR141 Mucormycosis 59 0.356
912
SCR011 Scrapie 39 0.356
913
CHR176 Chromophil Renal Cell Carcinoma 23 0.356
914
DNB001 Danubian Endemic Familial Nephropathy 41 0.351
915
P CNG003 Congenital Dyserythropoietic Anemia 48 0.351
916
EXR008 Exercise-Induced Malignant Hyperthermia 20 0.351
917
CHL122 Cholesteatoma of Middle Ear 51 0.350
918
P PRN023 Prion Disease 60 0.350
919
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 56 0.350
920
VRL003 Variola Major 43 0.344
921
SML019 Smallpox 55 0.344
922
MCR004 Macroglobulinemia 48 0.344
923
PPL058 Papilloma of Choroid Plexus 54 0.344
924
P LNG035 Lung Large Cell Carcinoma 53 0.343
925
PLY179 Polyomavirus-Associated Nephropathy 25 0.338
926
SCR003 Secretory Diarrhea 35 0.338
927
GNG002 Ganglioneuroma 52 0.338
928
P SPN052 Spondyloarthropathy 54 0.332
929
INT078 Intracranial Thrombosis 50 0.332
930
GNT167 Genetic Obesity 32 0.331
931
WRN001 Werner Syndrome 69 0.329
932
P ACT008 Actinic Keratosis 54 0.329
933
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.326
934
TCK001 Tick-Borne Encephalitis 59 0.326
935
DMN031 Dementia, Lewy Body 65 0.326
936
P GLL020 Gallbladder Disease 57 0.319
937
P ANG001 Angelman Syndrome 65 0.319
938
P SCK002 Sick Sinus Syndrome 55 0.319
939
P CRV031 Cervical Adenocarcinoma 48 0.319
940
CLL003 Cellulitis 53 0.319
941
P MLG056 Malignant Hyperthermia 65 0.319
942
FRS012 First-Degree Atrioventricular Block 39 0.312
943
DGR001 Digeorge Syndrome 62 0.312
944
MSC190 Muscular Disease 36 0.309
945
P MCH002 Machado-Joseph Disease 63 0.305