Search results for Asparagine

1486 hits were found for Asparagine

# Family MCID Name MIFTS Score
1
ASP024 Asparagine Synthetase Deficiency 37 46.359
2
P LKM062 Leukemia, Acute Lymphoblastic 69 12.698
3
P LKM002 Leukemia 67 6.677
4
CHL152 Childhood Acute Lymphocytic Leukemia 50 6.499
5
RPD005 Rapidly Involuting Congenital Hemangioma 46 6.389
6
HLX001 Helix Syndrome 48 6.234
7
P MCR010 Microcephaly 60 6.116
8
P ENC018 Encephalopathy 62 4.206
9
P CRB088 Cerebral Atrophy 33 4.129
10
HMN044 Human Immunodeficiency Virus Type 1 78 4.116
11
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 3.862
12
LYM019 Lymphosarcoma 46 3.853
13
P SZR006 Seizure Disorder 70 3.795
14
HYP266 Hypoxia 57 3.767
15
47X002 47,xyy 48 3.476
16
VCC001 Vaccinia 47 3.454
17
P HRP006 Herpes Simplex 65 3.364
18
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.304
19
48X005 48,xyyy 39 3.170
20
P LYM118 Lymphoma 67 3.156
21
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 3.136
22
AGN016 Aging 54 3.041
23
P NRB001 Neuroblastoma 66 3.029
24
QDR001 Quadriplegia 50 3.017
25
ATS010 Autosomal Recessive Disease 42 2.999
26
P OVR042 Ovarian Cancer 88 2.990
27
CHR074 Choriocarcinoma 46 2.950
28
P INF038 Influenza 68 2.905
29
CHL014 Cholera 62 2.874
30
c CNG411 Congenital Disorder of Glycosylation, Type in 67 2.778
31
P HYP097 Hyperekplexia 62 2.759
32
c AMY091 Amyotrophic Lateral Sclerosis 1 88 2.743
33
P LTR001 Lateral Sclerosis 58 2.743
34
IMM167 Immune Deficiency Disease 78 2.707
35
SPN035 Spindle Cell Sarcoma 54 2.693
36
SRC014 Sarcoma 65 2.693
37
SPS004 Spastic Quadriplegia 40 2.652
38
P AMY004 Amyloidosis 70 2.601
39
ASP002 Aspartylglucosaminuria 58 2.588
40
STM007 Stomatitis 54 2.583
41
P BCL017 B-Cell Lymphoma 59 2.575
42
P ALZ034 Alzheimer Disease 87 2.564
43
SCR011 Scrapie 39 2.526
44
c LKM061 Leukemia, Acute Myeloid 83 2.511
45
P HNT016 Huntington Disease 73 2.507
46
SPS057 Spasticity 42 2.494
47
P HYP265 Hypotonia 42 2.485
48
GLB002 Glioblastoma 67 2.447
49
c INH020 Inherited Metabolic Disorder 48 2.440
50
PPL052 Papillomatosis, Confluent and Reticulated 34 2.416
51
LYM040 Lymphoblastic Lymphoma 53 2.379
52
P PRN023 Prion Disease 60 2.324
53
P MLN008 Melanoma 76 2.320
54
MLR004 Malaria 80 2.320
55
P ADN016 Adenocarcinoma 63 2.293
56
PRT037 Pertussis 65 2.254
57
AVN001 Avian Influenza 61 2.217
58
P EPL164 Epilepsy 68 2.203
59
P CLR023 Colorectal Cancer 100 2.191
60
P PNC035 Pancreatic Cancer 86 2.191
61
HMP009 Haemophilus Influenzae 41 2.180
62
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 2.109
63
c ACT073 Acute Leukemia 58 2.109
64
P CTR002 Cataract 60 2.103
65
P PRS040 Prostate Cancer 95 2.080
66
OST159 Osteogenic Sarcoma 66 2.079
67
SVR001 Severe Acute Respiratory Syndrome 67 2.079
68
TTN003 Tetanus 65 2.063
69
GLM045 Glioma 63 2.063
70
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 2.062
71
c LKM005 Leukemia, T-Cell, Chronic 34 2.062
72
CRT012 Cortical Blindness 42 2.059
73
ALL029 Allergic Disease 59 2.028
74
GLL048 Glial Tumor 52 2.022
75
P PLY019 Polyneuropathy 52 2.014
76
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.980
77
LYS002 Lysosomal Storage Disease 51 1.980
78
MLY001 Molybdenum Cofactor Deficiency 40 1.975
79
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.964
80
PLG002 Plague 58 1.964
81
THY029 Thyroid Carcinoma 51 1.955
82
HYP066 Hyperglycemia 61 1.936
83
P FBR017 Fibrosarcoma 56 1.936
84
RBS001 Rabies 58 1.936
85
WST001 West Syndrome 59 1.912
86
c CNG191 Congenital Disorder of Glycosylation, Type Iia 50 1.866
87
FCS002 Fucosidosis 62 1.858
88
INV018 Invasive Mole 23 1.858
89
P GST053 Gastric Cancer 83 1.858
90
c HYD046 Hydatidiform Mole, Recurrent, 1 59 1.858
91
ARG004 Argyria 26 1.858
92
GST010 Gestational Trophoblastic Neoplasm 52 1.858
93
P DNG005 Dengue Virus 56 1.858
94
ATM095 Autoimmune Disease 61 1.845
95
LPP008 Lipoprotein Quantitative Trait Locus 65 1.845
96
ACT098 Acute Erythroid Leukemia 55 1.845
97
P PRK039 Parkinsonism 55 1.845
98
MTR088 Mature T-Cell and Nk-Cell Lymphoma 42 1.842
99
P LNG032 Lung Cancer 98 1.810
100
P MYL006 Myeloid Leukemia 61 1.810
101
PNC129 Pancreatic Adenocarcinoma 65 1.810
102
c TYP009 Type 2 Diabetes Mellitus 92 1.801
103
EPL131 Epilepsy, Pyridoxine-Dependent 45 1.769
104
P MYC084 Mycobacterium Tuberculosis 1 68 1.747
105
PRT251 Proteinuria, Chronic Benign 57 1.747
106
P MLT020 Multiple Sclerosis 79 1.740
107
DBT010 Diabetic Neuropathy 54 1.740
108
P LKM071 Leukemia, Chronic Lymphocytic 75 1.727
109
c ACT027 Acute Pancreatitis 60 1.719
110
ART140 Arteries, Anomalies of 53 1.695
111
KPS004 Kaposi Sarcoma 77 1.695
112
P TRM003 Tremor 48 1.695
113
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.695
114
c HPT016 Hepatitis B 62 1.695
115
P RTN016 Retinal Degeneration 52 1.676
116
KRT009 Keratosis 53 1.676
117
STT001 Status Epilepticus 59 1.676
118
SQM006 Squamous Cell Carcinoma 60 1.676
119
P HPT023 Hepatocellular Carcinoma 96 1.641
120
PLS011 Plasmacytoma 56 1.641
121
P LNG064 Lung Cancer Susceptibility 3 70 1.641
122
c ADL052 Adult Acute Lymphocytic Leukemia 46 1.641
123
c HRD039 Hereditary Amyloidosis 45 1.641
124
THY111 Thyroid Carcinoma, Familial Medullary 67 1.632
125
DRM006 Dermatitis 62 1.632
126
DPH006 Diaphragmatic Eventration 34 1.622
127
RNL114 Renal Cell Carcinoma, Nonpapillary 80 1.606
128
P PLY014 Polycystic Kidney Disease 69 1.583
129
WST005 West Nile Virus 57 1.583
130
P GCH001 Gaucher's Disease 70 1.583
131
P HPT021 Hepatitis 69 1.583
132
JPN002 Japanese Encephalitis 61 1.583
133
P ICH004 Ichthyosis 56 1.583
134
P HYP086 Hypothyroidism 69 1.555
135
DPH001 Diphtheria 59 1.539
136
P SPR120 Supranuclear Palsy, Progressive, 1 69 1.531
137
MYL069 Myeloma, Multiple 77 1.523
138
P AMY084 Amyloidosis, Finnish Type 51 1.523
139
ANT024 Anthrax Disease 58 1.523
140
CHL061 Childhood Leukemia 47 1.523
141
P ENC004 Encephalitis 61 1.523
142
P MYC033 Myoclonus 47 1.523
143
FML249 Familial Amyloidosis, Finnish Type 35 1.523
144
MSL001 Measles 61 1.498
145
P PNC044 Pancreatitis 61 1.495
146
P CRN300 Coronary Heart Disease 1 73 1.458
147
MNN047 Mannosidosis, Alpha B, Lysosomal 67 1.458
148
P MDL005 Medulloblastoma 75 1.458
149
CNS004 Constipation 56 1.458
150
P HYP035 Hypophosphatasia 62 1.458
151
P TBR001 Tuberous Sclerosis 69 1.458
152
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.455
153
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.455
154
ISC004 Ischemia 61 1.448
155
P BLD134 Bladder Cancer 79 1.430
156
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 62 1.422
157
c BRN108 Branchiootic Syndrome 1 62 1.412
158
c HPT073 Hepatitis C Virus 71 1.412
159
NWC001 Newcastle Disease 47 1.412
160
MCR004 Macroglobulinemia 49 1.408
161
P SLM003 Salmonellosis 54 1.389
162
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.389
163
P MYC007 Myocardial Infarction 70 1.389
164
URM002 Uremia 47 1.389
165
PPT005 Peptic Ulcer Disease 58 1.389
166
ALL014 Allergic Encephalomyelitis 34 1.389
167
LYM133 Lymphoma, Hodgkin, Classic 74 1.367
168
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.367
169
LYM143 Lymphoma, Non-Hodgkin, Familial 75 1.367
170
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.361
171
PHN003 Phenylketonuria 76 1.353
172
PRS045 Prostatic Hypertrophy 53 1.353
173
P RHN004 Rhinitis 57 1.353
174
CRT033 Corticobasal Degeneration 47 1.353
175
c CNG415 Congenital Disorder of Glycosylation, Type Ia 59 1.341
176
FTT001 Fatty Liver Disease 62 1.321
177
c HPT001 Hepatitis C 62 1.321
178
BLR008 Bilirubin Metabolic Disorder 57 1.321
179
EPD002 Epidermolytic Hyperkeratosis 56 1.314
180
BRK010 Burkitt Lymphoma 66 1.314
181
c HYP864 Hypoparathyroidism, Familial Isolated, 1 30 1.314
182
ACQ007 Acquired Immunodeficiency Syndrome 59 1.314
183
P NRN021 Neuronal Ceroid Lipofuscinosis 65 1.314
184
P CNG003 Congenital Dyserythropoietic Anemia 48 1.314
185
P KDN017 Kidney Cancer 61 1.273
186
CHL079 Children's Interstitial Lung Disease 26 1.243
187
PRS129 Prostatic Hyperplasia, Benign 49 1.241
188
HRT040 Hirata Disease 38 1.241
190
CHR048 Chronic Rhinitis 46 1.241
191
PRS021 Prostatic Adenoma 43 1.241
192
HRT015 Heritable Pulmonary Arterial Hypertension 46 1.241
193
P WSK001 Wiskott-Aldrich Syndrome 72 1.230
194
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 1.230
195
STL007 Steel Syndrome 42 1.230
196
ACT119 Acute Promyelocytic Leukemia 62 1.230
197
c SML038 Small Cell Cancer of the Lung 69 1.230
198
P SCL018 Scoliosis 57 1.230
199
MDD018 Middle East Respiratory Syndrome 44 1.230
200
BRN004 Brain Edema 54 1.230
201
P ATS411 Autosomal Dominant Epidermolytic Ichthyosis 36 1.230
202
CMM004 Common Variable Immunodeficiency 72 1.230
203
P GLY013 Glycogen Storage Disease 60 1.230
204
CHL123 Chlamydia 58 1.230
205
P HYP750 Hypertriglyceridemia, Familial 62 1.223
206
DWN001 Down Syndrome 70 1.202
207
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 1.202
208
c CNG195 Congenital Disorder of Glycosylation, Type Id 37 1.195
209
c CNG189 Congenital Disorder of Glycosylation, Type Ib 39 1.195
210
P RTN008 Retinitis Pigmentosa 80 1.171
211
P PHC003 Pheochromocytoma 69 1.171
212
P FTL002 Fatal Familial Insomnia 50 1.171
213
ADR040 Adrenal Gland Pheochromocytoma 46 1.171
214
NRR001 Neuroretinitis 42 1.171
215
RTN023 Retinitis 46 1.171
216
P NRP001 Neuropathy 60 1.171
217
NPH009 Nephrolithiasis 54 1.171
218
HYP056 Hypoglycemia 65 1.171
219
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.136
220
c DWL002 Dowling-Degos Disease 1 58 1.136
221
ANX010 Anxiety 70 1.136
222
GST092 Gastroesophageal Reflux 61 1.136
223
MTB004 Metabolic Acidosis 48 1.136
224
P MJR001 Major Depressive Disorder 68 1.136
225
P CMP072 Camptodactyly Syndrome, Guadalajara, Type I 31 1.136
226
PNG002 Pain Agnosia 51 1.136
227
MNT002 Mental Depression 57 1.136
228
THY125 Thyroid Gland Medullary Carcinoma 48 1.136
229
CRB004 Cerebral Artery Occlusion 45 1.136
230
P AGM001 Agammaglobulinemia 68 1.136
231
LST001 Listeriosis 59 1.136
232
GST052 Gestational Choriocarcinoma 35 1.136
233
P RCT021 Rectum Cancer 54 1.136
234
DPR016 Depression 65 1.136
235
ANX004 Anoxia 40 1.116
236
P MPL001 Maple Syrup Urine Disease 70 1.116
237
HRW001 Hair Whorl 35 1.116
238
P MYP004 Myopathy 67 1.116
239
CLN015 Colon Adenocarcinoma 65 1.116
240
HMG005 Hemoglobinopathy 56 1.116
241
IRN002 Iron Metabolism Disease 57 1.116
242
MYL009 Myelodysplastic Syndrome 67 1.108
244
c HYP699 Hyperekplexia 1 44 1.098
245
CRT072 Creutzfeldt-Jakob Disease 68 1.059
246
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.059
247
P MSC005 Muscular Dystrophy 67 1.059
248
P THR015 Thrombophilia 51 1.059
249
PLS007 Plasmodium Falciparum Malaria 52 1.059
250
HYP060 Hyperinsulinism 54 1.059
251
NRM022 Neurometabolic Disease 24 1.024
252
c MCR247 Microcephaly 1, Primary, Autosomal Recessive 42 1.024
253
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 53 1.024
254
UMB002 Umbilical Hernia 47 1.024
255
LKC009 Leukocyte Adhesion Deficiency, Type I 70 1.024
256
ICH002 Ichthyosis Bullosa of Siemens 41 1.024
257
c HNT011 Huntington Disease-Like 3 34 1.024
258
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 1.024
259
c HNT004 Huntington Disease-Like 2 52 1.024
260
c RTN150 Retinitis Pigmentosa 10 44 1.024
261
VRL011 Viral Infectious Disease 61 1.024
262
IGG001 Iga Glomerulonephritis 50 1.024
263
FDL002 Food Allergy 47 1.024
264
P SKN015 Skin Carcinoma 71 1.024
265
INS001 Insulinoma 59 1.024
266
BLD164 Blood Group, Gerbich System 19 1.024
267
CHL147 Chlamydia Pneumonia 47 1.024
268
LRY018 Laryngeal Squamous Cell Carcinoma 44 1.024
269
c HPT007 Hepatitis E 51 1.024
270
c GM1007 Gm1 Gangliosidosis 65 1.024
271
MDD011 Mood Disorder 62 1.024
272
GLY031 Glycoproteinosis 49 1.024
273
P BNG032 Benign Mesothelioma 53 1.024
274
PLS006 Plasmodium Vivax Malaria 51 1.024
275
HST011 Histoplasmosis 55 1.024
276
SPL018 Splenomegaly 49 1.024
277
P GNG009 Gangliosidosis 44 1.024
278
INS024 Insulin-Like Growth Factor I 78 0.998
279
PLY150 Polykaryocytosis Inducer 29 0.998
280
CYS001 Cystic Fibrosis 78 0.998
281
P DYS154 Dystonia 64 0.998
282
P PSR002 Psoriasis 63 0.998
283
PST011 Pustulosis of Palm and Sole 52 0.998
284
P HYP061 Hypertrophic Cardiomyopathy 69 0.998
285
LYM009 Lymphocytic Choriomeningitis 46 0.998
286
P MLN007 Male Infertility 56 0.998
287
PPL022 Papilloma 53 0.998
288
GST045 Gastroenteritis 58 0.998
289
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.995
290
P BRS047 Breast Cancer 98 0.995
291
ALC007 Alcohol Dependence 66 0.995
292
P FLL037 Follicular Lymphoma 74 0.995
293
FRN006 Frontotemporal Dementia 68 0.934
294
END057 Endometrial Cancer 72 0.934
295
c ATR087 Atrial Standstill 1 74 0.934
296
P PRK057 Parkinson Disease, Late-Onset 80 0.934
297
P GLC113 Galactosemia I 66 0.934
298
URT049 Urate Oxidase, Pseudogene 24 0.934
299
BCT022 Bacterial Infectious Disease 56 0.934
300
P MSC003 Muscular Atrophy 52 0.934
301
P DBT009 Diabetes Mellitus 67 0.934
302
CHC001 Chickenpox 57 0.934
303
P LVR013 Liver Disease 69 0.934
304
P ANT006 Antiphospholipid Syndrome 55 0.934
305
TRT001 Teratocarcinoma 42 0.934
306
MTH009 Mouth Disease 57 0.934
307
GST040 Gastric Adenocarcinoma 67 0.934
308
P ART022 Arthritis 71 0.934
309
SQM002 Squamous Cell Papilloma 46 0.934
310
LVR012 Liver Cirrhosis 63 0.934
311
P INF032 Infertility 57 0.934
312
P HYP076 Hyperthyroidism 53 0.934
313
EMB004 Embryonal Carcinoma 56 0.934
314
P GLM007 Glomerulonephritis 60 0.934
315
HYP014 Hyperuricemia 51 0.934
316
P HMP007 Hemophilia 52 0.934
317
ACT248 Acute Monoblastic/monocytic Leukemia 26 0.877
318
P NSP012 Nasopharyngeal Carcinoma 61 0.877
319
OBN001 Ouabain Resistance 16 0.877
320
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 63 0.877
321
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.877
322
PLL017 Pallister-Hall-Like Syndrome 37 0.877
323
ANG054 Angina Pectoris 66 0.877
324
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.877
325
c GM1004 Gm1-Gangliosidosis, Type I 58 0.877
326
P CRP001 Carpal Tunnel Syndrome 66 0.877
327
ENC038 Encephalopathy, Progressive, with or Without Lipodystrophy 40 0.877
328
DBT020 Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 40 0.877
329
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 55 0.877
330
OVR105 Ovarian Serous Carcinoma 37 0.877
331
PRC002 Paracoccidioidomycosis 54 0.877
332
P RBL001 Rubella 58 0.877
333
MLG079 Malignant Pleural Mesothelioma 42 0.877
334
P FCL005 Focal Segmental Glomerulosclerosis 57 0.877
335
HYP043 Hyperandrogenism 48 0.877
336
LMY003 Leiomyomatosis 44 0.877
337
INT020 Intravenous Leiomyomatosis 36 0.877
338
AMN001 Amenorrhea 54 0.877
339
ENM001 Enamel Caries 27 0.877
340
VSC006 Vascular Cancer 46 0.877
341
HML018 Homologous Wasting Disease 21 0.877
342
P THL005 Thalassemia 56 0.865
343
ATH013 Atherosclerosis Susceptibility 63 0.865
344
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.865
345
P LPR021 Leprosy 3 71 0.865
346
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.865
347
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.865
348
P KLZ004 Kala-Azar 1 41 0.865
349
c PCH015 Pachyonychia Congenita 1 60 0.865
350
FCT001 Factor Viii Deficiency 60 0.865
351
JMP002 Jumping Frenchmen of Maine 21 0.865
352
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.865
353
NNL006 Non-Alcoholic Steatohepatitis 54 0.865
354
c CNG006 Congenital Hypothyroidism 63 0.865
355
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.865
356
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 0.865
357
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.865
358
PRP001 Propionic Acidemia 65 0.865
359
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.865
360
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.865
361
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.865
362
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.865
363
c HMP029 Hemophilia a 68 0.865
364
P RTN024 Retinoblastoma 73 0.865
365
TBC004 Tobacco Addiction 63 0.865
366
c TBR025 Tuberous Sclerosis 1 84 0.865
367
P EPD003 Epidermolysis Bullosa Simplex 57 0.865
368
P KDN018 Kidney Disease 72 0.865
369
URC002 Urea Cycle Disorder 51 0.865
370
LSH001 Leishmaniasis 64 0.865
371
P CNG001 Congenital Myasthenic Syndrome 68 0.865
372
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.865
373
TXC005 Toxic Shock Syndrome 62 0.865
374
CCC001 Coccidioidomycosis 58 0.865
375
P HRT032 Heart Disease 81 0.865
376
SVR004 Severe Combined Immunodeficiency 72 0.865
377
P EYD002 Eye Disease 57 0.865
378
LPD008 Lipid Metabolism Disorder 62 0.865
379
P EPD016 Epidermolysis Bullosa 53 0.865
380
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.865
381
HNS001 Hansen's Disease 32 0.865
382
P DRM053 Dermatitis, Atopic 65 0.849
383
MNT001 Mantle Cell Lymphoma 67 0.849
384
ADL002 Adult Syndrome 70 0.849
385
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.849
386
PRS047 Prostatitis 58 0.849
387
P ALC033 Alcohol Use Disorder 61 0.849
388
LNG031 Lung Benign Neoplasm 51 0.849
389
P THY032 Thyroiditis 57 0.849
390
NRN004 Neuroendocrine Tumor 59 0.849
391
SFT003 Soft Tissue Sarcoma 57 0.849
392
MYL003 Myeloid Sarcoma 48 0.849
393
16P004 16p13.11 Microduplication Syndrome 17 0.842
394
ADR022 Adrenomyeloneuropathy 39 0.789
395
STN013 Stenotrophomonas Maltophilia Infection 26 0.789
396
c LTT008 Lattice Corneal Dystrophy Type Ii 26 0.789
397
ADR007 Adrenoleukodystrophy 73 0.789
398
AND002 Androgen Insensitivity Syndrome 63 0.789
399
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.789
400
PSR001 Psoriatic Arthritis 62 0.789
401
HMC014 Homocysteinemia 52 0.789
402
CRV035 Cervical Cancer 73 0.789
403
OVR029 Ovarian Hyperstimulation Syndrome 63 0.789
404
P RHM011 Rheumatoid Arthritis 82 0.789
405
P SCH015 Schizophrenia 74 0.789
406
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.789
407
c SPN225 Spondyloarthropathy 1 70 0.789
408
THR024 Thrombosis 56 0.789
409
c ANM042 Anemia, Congenital Dyserythropoietic, Type Ii 50 0.789
410
c ERY064 Erythrocytosis, Familial, 6 30 0.789
412
DSS032 Disease by Infectious Agent 55 0.789
413
ERL027 Early-Onset Non-Syndromic Cataract 31 0.789
414
c HPT003 Hepatitis a 63 0.789
415
HPT004 Hepatic Coma 43 0.789
416
P OPN001 Open-Angle Glaucoma 55 0.789
417
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.789
418
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 0.789
419
P RHB003 Rhabdomyosarcoma 66 0.789
420
P HMC002 Homocystinuria 53 0.789
421
SPN051 Spondylitis 51 0.789
422
P PLY018 Polycythemia 56 0.789
423
P GRV001 Graves' Disease 55 0.789
424
INF009 Inflammatory Spondylopathy 30 0.789
425
GTR002 Goiter 53 0.789
426
HPT019 Hepatic Encephalopathy 59 0.789
427
P VSC007 Vascular Disease 63 0.789
428
P LNG028 Long Qt Syndrome 64 0.789
429
MST005 Mastitis 53 0.789
430
P INT068 Intestinal Disease 53 0.789
431
GST050 Gastrointestinal System Disease 55 0.789
432
P CRN025 Corneal Dystrophy 49 0.789
433
P DRR001 Diarrhea 55 0.789
434
P MNN013 Meningitis 65 0.789
435
P NRF002 Neurofibromatosis 57 0.789
436
P MYC008 Myocarditis 59 0.789
437
HYP264 Hypertonia 36 0.789
438
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.745
439
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 0.745
440
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.745
441
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.745
442
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.745
443
VSL002 Visual Epilepsy 39 0.745
444
P ATS364 Autism 69 0.706
445
CNG429 Congenital Myasthenic Syndromes with Glycosylation Defect 33 0.706
446
CNG506 Congenital Amyoplasia 27 0.706
447
c PNC108 Pancreatitis, Hereditary 69 0.706
448
P PLM037 Pulmonary Hypertension 72 0.706
449
P ALT001 Alternating Hemiplegia of Childhood 57 0.706
450
P EXN002 Exanthem 58 0.706
451
KRT019 Keratitis, Hereditary 66 0.706
452
c MYS077 Myasthenic Syndrome, Congenital, 15 28 0.706
453
c MYS078 Myasthenic Syndrome, Congenital, 14 40 0.706
454
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.706
455
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.706
456
PYR037 Pyruvate Carboxylase Deficiency 45 0.706
457
c NRF024 Neurofibromatosis, Type I 72 0.706
458
GST019 Gastrointestinal Stromal Tumor 78 0.706
459
GLC003 Glucose Intolerance 54 0.706
460
P ISL078 Isolated Ectopia Lentis 58 0.706
461
CTN007 Cutaneous Leishmaniasis 62 0.706
462
P HML002 Hemolytic Anemia 62 0.706
463
HPT022 Hepatoblastoma 54 0.706
464
PST092 Posttransplant Acute Limbic Encephalitis 28 0.706
465
P THR014 Thrombocytopenia 66 0.706
466
SKN016 Skin Disease 63 0.706
467
CHL067 Cholecystitis 60 0.706
468
SGT001 Sagittal Sinus Thrombosis 35 0.706
469
HYP005 Hypokalemia 55 0.706
470
PRP016 Paraplegia 52 0.706
471
TCK001 Tick-Borne Encephalitis 59 0.706
472
c DLT002 Dilated Cardiomyopathy 78 0.706
473
GT001 Gout 64 0.706
474
CHG001 Chagas Disease 66 0.706
475
P NTR004 Neutropenia 63 0.706
476
SHG001 Shigellosis 63 0.706
477
PSY004 Psychotic Disorder 66 0.706
478
THR004 Thrombocytosis 53 0.706
479
HMP005 Hemiplegia 54 0.706
480
MCR013 Microphthalmia 60 0.706
481
CNG034 Congestive Heart Failure 69 0.706
482
P PRP019 Peripheral Nervous System Disease 58 0.706
483
RFR004 Refractory Hematologic Cancer 32 0.706
484
PLM029 Palmoplantar Keratosis 48 0.706
485
MSN004 Mesenchymal Cell Neoplasm 42 0.706
486
CHR028 Chronic Wasting Disease 33 0.706
487
P PRP029 Porphyria 60 0.706
488
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.706
489
SNL007 Senile Cataract 40 0.706
490
CND006 Candida Glabrata 30 0.706
491
DWR001 Dwarfism 44 0.706
492
c GCH015 Gaucher Disease, Type I 68 0.611
493
DSR074 Disorder of Purine Metabolism 23 0.611
494
SPR166 Sporadic Fatal Insomnia 14 0.611
495
TBR011 Tuberculous Meningitis 48 0.611
496
c ART068 Aortic Aneurysm, Familial Thoracic 2 33 0.611
497
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 58 0.611
498
CRD132 Cardiac Conduction Defect 60 0.611
499
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.611
500
c SYS001 Systemic Lupus Erythematosus 87 0.611
501
c PRG042 Progressive Familial Heart Block, Type Ia 66 0.611
502
ABT001 Abetalipoproteinemia 68 0.611
503
ARG002 Argininosuccinic Aciduria 61 0.611
504
P CLC063 Celiac Disease 1 66 0.611
505
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.611
506
P BRG001 Brugada Syndrome 69 0.611
507
c MJR022 Major Affective Disorder 8 38 0.611
508
MSC007 Muscle Hypertrophy 64 0.611
509
DFC004 Deficiency Anemia 74 0.611
510
c ATM045 Autoimmune Glomerulonephritis 35 0.611
511
P URN019 Urinary Tract Infection 49 0.611
512
P HVY001 Heavy Chain Disease 33 0.611
513
CLT003 Colitis 63 0.611
514
CMP034 Complete Androgen Insensitivity Syndrome 55 0.611
515
WTH001 Withdrawal Disorder 48 0.611
516
P CRB045 Cerebellar Hypoplasia 40 0.611
517
BNR002 Bone Resorption Disease 47 0.611
518
P HYP760 Hypothyroidism, Congenital, Nongoitrous, 2 55 0.611
519
P BRN019 Bernard-Soulier Syndrome 61 0.611
520
c CTR098 Cataract 1, Multiple Types 39 0.611
521
P KRT028 Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant 54 0.611
522
FCT034 Factor V and Factor Viii, Combined Deficiency of, 2 42 0.611
523
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.611
524
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.611
525
c MJR024 Major Affective Disorder 9 41 0.611
526
P MTC003 Metachromatic Leukodystrophy 71 0.611
527
CTR172 Citrullinemia, Classic 65 0.611
528
c GLY008 Glycogen Storage Disease Ii 72 0.611
529
SBC001 Subacute Sclerosing Panencephalitis 53 0.611
530
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.611
531
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 0.611
532
c HYP595 Hypertension, Essential 85 0.611
533
FCS014 Fucosidase Regulator 15 0.611
534
PLM102 Palmoplantar Keratoderma, Epidermolytic 55 0.611
535
HYP042 Hypochondroplasia 59 0.611
536
P NNN008 Noonan Syndrome 1 77 0.611
537
c GLC041 Glaucoma 1, Open Angle, a 34 0.611
538
c GLC092 Glaucoma, Primary Open Angle 62 0.611
539
P GLM040 Glioma Susceptibility 1 71 0.611
540
ACH004 Achondroplasia 66 0.611
541
ORL015 Oral Squamous Cell Carcinoma 43 0.611
542
P LKD001 Leukodystrophy 59 0.611
543
P MYP006 Myopia 56 0.611
544
P LTT001 Lattice Corneal Dystrophy 31 0.611
545
CLF001 Cleft Lip 53 0.611
546
PLM001 Pulmonary Tuberculosis 69 0.611
547
c VRL010 Viral Hepatitis 53 0.611
548
P BPL003 Bipolar Disorder 56 0.611
549
P BRS044 Breast Adenocarcinoma 58 0.611
550
P GST044 Gastritis 55 0.611
551
ADN018 Adenoma 59 0.611
552
PRT036 Peritonitis 65 0.611
553
OST012 Osteoarthritis 77 0.611
554
P SNS001 Sensorineural Hearing Loss 59 0.611
555
P GRF003 Graft-Versus-Host Disease 71 0.611
556
CYS005 Cysticercosis 60 0.611
557
P DMN002 Dementia 66 0.611
558
P SPN046 Spinal Muscular Atrophy 63 0.611
559
c ACT068 Acute Cystitis 61 0.611
560
MLG169 Malignant Astrocytoma 57 0.611
561
PPL002 Papillary Carcinoma 46 0.611
562
P END044 Endometriosis 62 0.611
563
ATN004 Autonomic Neuropathy 42 0.611
564
GST033 Gestational Diabetes 61 0.611
565
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.611
566
BRC012 Brucellosis 66 0.611
567
BRN024 Bronchitis 67 0.611
568
P CNJ013 Conjunctivitis 66 0.611
569
PRP030 Purpura 54 0.611
570
P MLT074 Multiple Endocrine Neoplasia 59 0.611
571
P MTR014 Motor Neuron Disease 65 0.611
572
DMY004 Demyelinating Disease 50 0.611
573
RFT001 Rift Valley Fever 48 0.611
574
CHL068 Cholestasis 61 0.611
575
MGC001 Megacolon 48 0.611
576
CHR073 Choreatic Disease 54 0.611
577
AZS001 Azoospermia 45 0.611
578
TLR001 Tularemia 56 0.611
579
HYP141 Hyperphenylalaninemia 42 0.611
580
ALB002 Albinism 47 0.611
582
NNT017 Neonatal Adrenoleukodystrophy 54 0.611
583
ORL011 Oral Cancer 60 0.611
584
INH007 Inherited Thyroxine-Binding Globulin Deficiency 13 0.611
585
OPD006 Opioid Addiction 48 0.611
586
P DYS021 Dysautonomia 38 0.611
587
CYT002 Cytokine Deficiency 43 0.611
588
c CRD185 Ceroid Lipofuscinosis, Neuronal, 6 53 0.525
589
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.525
590
ACN002 Acanthosis Nigricans 56 0.525
591
c RTN036 Retinal Cone Dystrophy 4 35 0.525
592
c CRD183 Ceroid Lipofuscinosis, Neuronal, 2 56 0.525
593
ADN022 Adenylosuccinase Deficiency 44 0.525
594
FRT005 Fruit Allergy 33 0.525
595
c CHR684 Chronic Kidney Disease 69 0.525
596
CRC021 Carcinosarcoma 64 0.525
597
P MNC007 Monocytic Leukemia 47 0.525
598
FLR001 Filarial Elephantiasis 59 0.525
599
FLR002 Filariasis 55 0.525
600
DFC001 Defective Apolipoprotein B-100 24 0.525
601
c BRD010 Bardet-Biedl Syndrome 1 64 0.499
602
P PLY180 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 1 56 0.499
603
c HMC039 Hemochromatosis, Type 1 73 0.499
604
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 0.499
605
P KRB001 Krabbe Disease 69 0.499
606
SPN050 Spinocerebellar Degeneration 39 0.499
607
FML304 Familial Isolated Dilated Cardiomyopathy 49 0.499
608
CLF004 Cleft Lip/palate 57 0.499
609
P DBT005 Diabetes Insipidus 54 0.499
610
SKL017 Skeletal Dysplasias 41 0.499
611
c FML294 Familial Short Qt Syndrome 43 0.499
612
ERY014 Erythrokeratoderma 26 0.499
613
P HRD217 Hereditary Optic Neuropathy 36 0.499
614
SPN186 Spinal Cord Injury 61 0.499
615
c INH030 Inherited Retinal Disorder 28 0.499
616
SPS019 Spastic Paraparesis 38 0.499
617
CNG491 Congenital Portosystemic Shunt 17 0.499
618
c ACT134 Acute Liver Failure 59 0.499
619
c SCL052 Scleroderma, Familial Progressive 61 0.499
620
P FML018 Familial Mediterranean Fever 73 0.499
621
c ANM036 Anemia, Sideroblastic, 1 56 0.499
622
P FRG001 Fragile X Syndrome 70 0.499
623
CRD223 Cardiac Arrhythmia 63 0.499
624
c ANM038 Anemia, Autoimmune Hemolytic 64 0.499
625
ART002 Arts Syndrome 66 0.499
626
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.499
627
MSC157 Muscular Dystrophy, Duchenne Type 79 0.499
628
c THR087 Thrombocythemia 2 22 0.499
629
P TRM004 Trimethylaminuria 45 0.499
630
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 45 0.499
631
P MTR004 Maturity-Onset Diabetes of the Young 68 0.499
632
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.499
633
c PCH012 Pachyonychia Congenita 2 40 0.499
634
c EXD008 Exudative Vitreoretinopathy 1 71 0.499
635
VLV047 Volvulus of Midgut 52 0.499
636
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.499
637
c MGR028 Migraine with or Without Aura 1 64 0.499
638
c PGT008 Paget Disease of Bone 5, Juvenile-Onset 46 0.499
639
GRN037 Granulomatosis with Polyangiitis 64 0.499
640
P OCL002 Oculocutaneous Albinism 59 0.499
641
PLY023 Polycystic Liver Disease 60 0.499
642
c LTH047 Lethal Congenital Contracture Syndrome 3 26 0.499
643
c CTR166 Cataract 33, Multiple Types 26 0.499
644
c MCR115 Microvascular Complications of Diabetes 5 65 0.499
645
c MCR130 Microvascular Complications of Diabetes 6 41 0.499
646
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 27 0.499
647
c SHR030 Short Qt Syndrome 44 0.499
648
ATR057 Atrioventricular Block 54 0.499
649
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.499
650
CHK001 Chikungunya 60 0.499
651
NPH113 Nephroma 37 0.499
652
c GMM003 Gamma Heavy Chain Disease 37 0.499
653
c ERL056 Early-Onset Parkinson's Disease 40 0.499
654
P CHN012 Chondrosarcoma 57 0.499
655
SCR037 Sucrase-Isomaltase Deficiency, Congenital 49 0.499
656
c BRT050 Bartter Syndrome, Type 2, Antenatal 46 0.499
657
c GRV008 Graves Disease 1 54 0.499
658
PTZ001 Peutz-Jeghers Syndrome 70 0.499
659
P PRP003 Porphyria Cutanea Tarda 66 0.499
660
IGR001 Ige Responsiveness, Atopic 59 0.499
661
c SPL067 Split-Hand/foot Malformation 1 46 0.499
663
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.499
664
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 0.499
665
ALV005 Alveolar Soft Part Sarcoma 61 0.499
666
c MTC055 Mitochondrial Dna Depletion Syndrome 4b 54 0.499
667
c LNG047 Long Qt Syndrome 2 59 0.499
668
c ART101 Aortic Valve Disease 2 66 0.499
669
P CNG436 Congenital Disorder of Deglycosylation 51 0.499
670
c PCH010 Pachyonychia Congenita 3 43 0.499
671
GLC106 Glucocorticoid Resistance, Generalized 48 0.499
672
NLX003 Neu-Laxova Syndrome 2 46 0.499
673
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.499
674
c MTC062 Mitochondrial Dna Depletion Syndrome 2 43 0.499
675
FCT002 Factor Xi Deficiency 62 0.499
676
c MCR120 Microvascular Complications of Diabetes 7 47 0.499
677
P MNN019 Mannosidosis, Beta a, Lysosomal 49 0.499
678
MTC019 Metachromatic Leukodystrophy Due to Saposin B Deficiency 32 0.499
679
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 0.499
680
LGN006 Legionnaire Disease 52 0.499
681
CHN016 Cohen Syndrome 60 0.499
682
c GCH017 Gaucher Disease, Type Iii 52 0.499
683
MYX004 Myxedema 43 0.499
684
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 53 0.499
685
RTC009 Reticulum Cell Sarcoma 44 0.499
686
c SZR022 Seizures, Benign Familial Neonatal, 1 43 0.499
687
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.499
688
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 53 0.499
689
c HYP836 Hypercholesterolemia, Familial, 1 73 0.499
690
IMM165 Immunoglobulin Switch Sequences 14 0.499
691
DMN031 Dementia, Lewy Body 65 0.499
692
CLS005 Clouston Syndrome 58 0.499
693
ESP021 Esophageal Cancer 83 0.499
694
PNM010 Pneumothorax, Primary Spontaneous 58 0.499
695
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 0.499
696
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.499
697
SPN428 Spinal Muscular Atrophy, Lower Extremity-Predominant, 2b, Prenatal Onset, Autosomal Dominant 23 0.499
698
MNN043 Meningioma, Familial 79 0.499
699
P SPS008 Spastic Ataxia 41 0.499
700
PRM329 Premature Aging 36 0.499
701
P ANT061 Antenatal Bartter Syndrome 36 0.499
702
c CTR128 Cataract 33 19 0.499
703
LBR036 Leber Plus Disease 66 0.499
704
c HMP004 Hemophilia B 68 0.499
705
ICH054 Ichthyosis, X-Linked 52 0.499
706
NPH003 Nephrocalcinosis 49 0.499
707
P FML068 Familial Hypocalciuric Hypercalcemia 55 0.499
708
P LPS004 Lupus Erythematosus 61 0.499
709
P SDR003 Sideroblastic Anemia 51 0.499
710
P BLD062 Bile Duct Cancer 67 0.499
711
P NRC002 Narcolepsy 56 0.499
712
CRV002 Cervix Uteri Carcinoma in Situ 47 0.499
713
ULC004 Ulcerative Colitis 74 0.499
714
P MTC133 Mitochondrial Myopathy 50 0.499
715
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 43 0.499
716
FND002 Fundus Dystrophy 55 0.499
717
ADN001 Adenosine Deaminase Deficiency 59 0.499
718
YLL002 Yellow Fever 61 0.499
719
P ALP008 Alopecia 54 0.499
720
ISL121 Isolated Split Hand-Split Foot Malformation 41 0.499
721
P VNT002 Ventricular Septal Defect 58 0.499
722
HRT011 Heart Septal Defect 49 0.499
723
INT002 Intermittent Claudication 61 0.499
724
P OPT006 Optic Nerve Disease 58 0.499
725
PNM008 Pneumothorax 54 0.499
726
ART016 Aortic Aneurysm 68 0.499
727
P SYS005 Systemic Scleroderma 74 0.499
728
P ART023 Arthropathy 61 0.499
729
SCR001 Secretory Meningioma 40 0.499
730
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.499
731
END086 End Stage Renal Disease 52 0.499
732
P JVN008 Juvenile Glaucoma 50 0.499
733
GNG002 Ganglioneuroma 52 0.499
734
P INT070 Intestinal Obstruction 57 0.499
735
MLT177 Multisystem Proteinopathy 31 0.499
736
P MMP001 Mumps 57 0.499
737
c MCR113 Microvascular Complications of Diabetes 3 52 0.499
738
c MCR133 Microvascular Complications of Diabetes 4 41 0.499
739
KRN001 Korean Hemorrhagic Fever 35 0.499
740
c VRL012 Viral Meningitis 46 0.499
741
P CHR071 Charcot-Marie-Tooth Disease 64 0.499
742
DNG003 Dengue Disease 65 0.499
743
NRG002 Neurogenic Bladder 55 0.499
744
BRN014 Bronchopneumonia 53 0.499
745
DNT012 Dental Caries 53 0.499
746
LYD001 Leydig Cell Tumor 45 0.499
747
HRY003 Hairy Cell Leukemia 61 0.499
748
c HPT015 Hepatitis D 49 0.499
749
c HRD010 Hereditary Spastic Paraplegia 66 0.499
750
P ECT006 Ectodermal Dysplasia 63 0.499
751
P HMR003 Hemorrhagic Disease 59 0.499
752
FCL014 Focal Epilepsy 53 0.499
753
CYS014 Cystadenocarcinoma 51 0.499
754
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 0.499
755
P CRD119 Cardiac Arrest 67 0.499
756
LPR001 Lepromatous Leprosy 49 0.499
757
TTH006 Tooth Disease 51 0.499
758
ONC002 Onchocerciasis 51 0.499
759
PRG008 Paragonimiasis 37 0.499
760
PRM013 Premature Menopause 58 0.499
761
DSS009 Disseminated Intravascular Coagulation 57 0.499
762
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 44 0.499
763
PLS009 Plasma Cell Neoplasm 64 0.499
764
P BRT004 Bartter Disease 58 0.499
765
TST018 Testicular Yolk Sac Tumor 39 0.499
766
P OVR046 Ovarian Cyst 46 0.499
767
c ACT071 Acute Kidney Failure 60 0.499
768
ERL001 Early Myoclonic Encephalopathy 62 0.499
769
PPL003 Papillary Cystadenocarcinoma 29 0.499
770
P CTS001 Cutis Laxa 65 0.499
771
GNG005 Gangliocytoma 55 0.499
772
MMM001 Mammary Paget's Disease 53 0.499
773
P OBS001 Obstructive Jaundice 48 0.499
774
P EHL001 Ehlers-Danlos Syndrome 58 0.499
775
CLN003 Clonorchiasis 43 0.499
776
SPN021 Spinal Meningioma 50 0.499
777
P URT039 Urticaria 58 0.499
778
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.499
779
HND002 Hand, Foot and Mouth Disease 50 0.499
780
AMN003 Amnestic Disorder 54 0.499
781
FML026 Familial Lipoprotein Lipase Deficiency 52 0.499
782
P END039 Endodermal Sinus Tumor 41 0.499
783
HYP080 Hypogonadism 50 0.499
784
NNS008 Nonsyndromic Hearing Loss and Deafness, Dfna3 16 0.499
785
CLS031 Classic Galactosemia and Clinical Variant Galactosemia 18 0.499
786
PRM209 Primary Trimethylaminuria 19 0.499
787
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.499
788
GNT003 Genital Herpes 54 0.499
789
RTC005 Reticulosarcoma 48 0.499
790
GLC036 Glucagonoma 46 0.499
791
DST006 Diastolic Heart Failure 45 0.499
792
P EPS003 Episodic Ataxia 59 0.499
793
DRG003 Drug Dependence 46 0.499
794
P PRC019 Precocious Puberty 47 0.499
795
c PSD047 Pseudo-Turner Syndrome 52 0.499
796
NGL005 Ngly1-Congenital Disorder of Deglycosylation 13 0.499
797
HDN002 Head Injury 44 0.499
798
P MTC069 Mitochondrial Disorders 57 0.499
799
P CHR345 Chronic Pain 50 0.499
800
PTT037 Pituitary Tumors 44 0.499
801
P FBR031 Febrile Seizures 52 0.499
802
BDR001 Bidirectional Tachycardia 14 0.499
803
CLS040 Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 37 0.499
804
CNG065 Congenital Contractures 25 0.499
805
CTR014 Cataract Microcornea Syndrome 35 0.499
806
CRV045 Cervical Intraepithelial Neoplasia 39 0.499
807
c RNG015 Ring Chromosome 2 22 0.499
808
c ATS418 Autosomal Dominant Spinal Muscular Atrophy, Lower Extremity-Predominant 2 12 0.499
809
CHR178 Chromosomal Triplication 34 0.499
810
FML330 Familial Lcat Deficiency 33 0.499
811
OVR094 Ovarian Epithelial Cancer 39 0.499
812
c CHR417 Chronic Graft Versus Host Disease 55 0.499
813
PHS011 Phosphomannoisomerase Deficiency 3 0.499
814
CHR682 Chronic Bilirubin Encephalopathy 37 0.496
815
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.496
816
MLN065 Melanocytic Nevus Syndrome, Congenital 62 0.496
817
BSL036 Basal Cell Nevus Syndrome 73 0.496
818
PRP036 Peripheral T-Cell Lymphoma 53 0.496
819
BRR014 Barrett Esophagus 66 0.496
820
HYP458 Hyper Ige Syndrome 60 0.496
821
VTM028 Vitamin E, Familial Isolated Deficiency of 53 0.496
822
c BSL024 Basal Cell Carcinoma 1 55 0.496
823
c DRM054 Dermatitis, Atopic, 2 46 0.496
824
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 63 0.496
825
FLL041 Follicular Lymphoma 1 45 0.496
826
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.496
827
c PRS136 Prostate Cancer, Hereditary, 6 33 0.496
828
RHB024 Rhabdomyosarcoma 2 67 0.496
829
MYL005 Myelofibrosis 71 0.496
830
EPT021 Epithelial Recurrent Erosion Dystrophy 46 0.496
831
P ANR048 Aniridia 1 64 0.496
832
c PRS130 Prostate Cancer, Hereditary, 8 32 0.496
833
ANT039 Antisynthetase Syndrome 55 0.496
834
BNM001 Bone Marrow Cancer 46 0.496
835
P MLG074 Malignant Mesenchymoma 40 0.496
836
NDL009 Nodular Basal Cell Carcinoma 40 0.496
837
NRN001 Neuroendocrine Carcinoma 47 0.496
838
P ESP024 Esophagitis 60 0.496
839
THY122 Thyroid Gland Cancer 59 0.496
840
c BSL007 Basal Cell Carcinoma 68 0.496
841
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.496
842
MYL031 Myeloproliferative Neoplasm 66 0.496
843
SKN013 Skin Benign Neoplasm 50 0.496
844
THY030 Thyroid Gland Disease 50 0.496
845
P PNM007 Pneumonia 67 0.496
846
CLN045 Colonic Benign Neoplasm 48 0.496
847
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.496
848
ATX019 Ataxia with Vitamin E Deficiency 44 0.496
849
AND005 Androgen Insensitivity Syndrome, Mild 21 0.496
850
CNG092 Congenital Extrahepatic Portosystemic Shunt 24 0.496
851
c PRM038 Primary Agammaglobulinemia 47 0.496
852
P NRV007 Nervous System Disease 67 0.496
853
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.496
854
c CHR064 Chronic Monocytic Leukemia 36 0.496
855
c WLF013 Wolfram Syndrome 1 60 0.353
856
P URF003 Urofacial Syndrome 1 56 0.353
857
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 47 0.353
858
c INF122 Infantile Krabbe Disease 32 0.353
859
P PRM011 Primary Ciliary Dyskinesia 69 0.353
860
P SLW003 Slow-Channel Congenital Myasthenic Syndrome 35 0.353
862
MTC005 Mitochondrial Metabolism Disease 45 0.353
863
VNZ002 Venezuelan Equine Encephalitis 46 0.353
864
ACT120 Acute Zonal Occult Outer Retinopathy 24 0.353
865
LCH014 Lichen Amyloidosis 28 0.353
866
FNG016 Fungal Keratitis 39 0.353
867
PLY100 Polyploidy 36 0.353
868
OLG024 Oligosaccharidosis 10 0.353
869
STR108 Streptococcus Pneumoniae-Associated Hemolytic Uremic Syndrome 13 0.353
870
ATH010 Athyreosis 34 0.353
871
ERL042 Early-Onset Partial Cataract 20 0.353
872
c ERL044 Early-Onset Posterior Polar Cataract 22 0.353
873
SMT007 Smith-Fineman-Myers Syndrome 32 0.353
874
PRC051 Paracetamol Poisoning 29 0.353
875
MCN019 Mucinous Adenocarcinoma of Ovary 16 0.353
876
c SPS021 Spastic Paraplegia 10 27 0.353
877
P FML313 Familial Progressive Hyperpigmentation 28 0.353
879
NRM021 Neurometabolic Disorder Due to Serine Deficiency 15 0.353
880
P OVR082 Overgrowth Syndrome 49 0.353
881
c NRF023 Neurofibromatosis, Type Ii 71 0.353
882
PFF001 Pfeiffer Syndrome 77 0.353
883
P MCH002 Machado-Joseph Disease 62 0.353
884
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 56 0.353
885
RTC012 Reticuloendotheliosis, X-Linked 35 0.353
886
P SPS133 Spastic Paraplegia 2, X-Linked 50 0.353
887
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 0.353
888
P EPL140 Epilepsy, Idiopathic Generalized 62 0.353
889
c CHR646 Charcot-Marie-Tooth Disease, Axonal, Type 2b 50 0.353
890
c GLL024 Gallbladder Disease 1 52 0.353
891
c DFN098 Deafness, Autosomal Dominant 3a 39 0.353
892
P RNL115 Renal Tubular Acidosis, Proximal 32 0.353
893
KR002 Kuru 45 0.353
894
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.353
895
c MSC171 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5 42 0.353
896
c MSC172 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 8 44 0.353
897
c MYS033 Miyoshi Muscular Dystrophy 1 52 0.353
898
P MYS003 Myasthenia Gravis 68 0.353
899
TWN007 Twinning, Dizygotic 22 0.353
900
c XRD022 Xeroderma Pigmentosum, Complementation Group D 56 0.353
901
ALL001 Allan-Herndon-Dudley Syndrome 54 0.353
902
IMM099 Immunodeficiency 33 37 0.353
903
PHS014 Phosphoglycerate Kinase 1 Deficiency 45 0.353
904
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 49 0.353
905
c DVL030 Developmental and Epileptic Encephalopathy 36 40 0.353
906
CHN055 Chanarin-Dorfman Syndrome 60 0.353
907
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.353
908
ADR049 Adrenal Hypoplasia, Congenital 53 0.353
909
LSC001 Lesch-Nyhan Syndrome 62 0.353
910
IMM026 Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia 47 0.353
911
SJG002 Sjogren-Larsson Syndrome 54 0.353
912
ALP099 Alopecia, Congenital 23 0.353
913
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 61 0.353
914
c MCP043 Mucopolysaccharidosis, Type Iiia 61 0.353
915
ALK013 Alkaptonuria 59 0.353
916
FBR012 Fabry Disease 70 0.353
917
ARS001 Aarskog-Scott Syndrome 54 0.353
918
SND001 Sandhoff Disease 66 0.353
919
GLY015 Glycine N-Methyltransferase Deficiency 40 0.353
920
c SPR086 Spermatogenic Failure 3 46 0.353
921
MYP035 Myopathy, Distal, with Anterior Tibial Onset 33 0.353
922
CRG004 Crigler-Najjar Syndrome, Type Ii 46 0.353
923
ANR007 Anorexia Nervosa 60 0.353
924
c CNG194 Congenital Disorder of Glycosylation, Type Ig 47 0.353
925
ALL003 Allergic Rhinitis 67 0.353
926
c LTH008 Lethal Congenital Contracture Syndrome 2 34 0.353
927
c PRM196 Premature Ovarian Failure 1 59 0.353
928
P PLZ001 Pelizaeus-Merzbacher Disease 65 0.353
929
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 64 0.353
930
c EPD080 Epidermolysis Bullosa Simplex, Autosomal Recessive 1 35 0.353
931
P AST005 Asthma 76 0.353
932
c AGM013 Agammaglobulinemia 1, Autosomal Recessive 37 0.353
933
FCL078 Facial Dysmorphism, Lens Dislocation, Anterior Segment Abnormalities, and Spontaneous Filtering Blebs 27 0.353
934
HYP332 Hypotrichosis, Congenital, with Juvenile Macular Dystrophy 41 0.353
935
FRY006 Fryns Microphthalmia Syndrome 52 0.353
936
c CRD099 Cardiomyopathy, Dilated, 1e 53 0.353
937
P CRD234 Cardiomyopathy, Dilated, 1c, with or Without Left Ventricular Noncompaction 41 0.353
938
c DFN136 Deafness, Autosomal Dominant 9 44 0.353
939
BLR030 Bilirubin, Serum Level of, Quantitative Trait Locus 1 33 0.353
940