Search results for Tyrosine

4152 hits were found for Tyrosine

# Family MCID Name MIFTS Score
1
P LNG032 Lung Cancer 98 33.025
2
c TYR013 Tyrosinemia, Type Ii 48 31.317
3
SGW002 Segawa Syndrome, Autosomal Recessive 44 29.651
4
IMM095 Immunodeficiency 35 50 23.744
5
DSR026 Disorder of Tyrosine Metabolism 10 21.511
6
c LKM063 Leukemia, Chronic Myeloid 70 21.154
7
AGM019 Agammaglobulinemia, X-Linked 71 19.260
8
P MYL006 Myeloid Leukemia 60 19.117
9
TYR006 Tyrosine-Oxidase Temporary Deficiency 1 18.971
10
c SML038 Small Cell Cancer of the Lung 68 18.448
11
DSR073 Disorder of Phenylalanin or Tyrosine Metabolism 3 18.289
12
P LKM002 Leukemia 65 17.916
13
IMM075 Immunodeficiency 22 26 17.498
14
RNL114 Renal Cell Carcinoma, Nonpapillary 79 12.181
15
c LKM061 Leukemia, Acute Myeloid 83 10.628
16
P ADN016 Adenocarcinoma 63 10.463
17
P LNG064 Lung Cancer Susceptibility 3 69 10.338
18
P LYM118 Lymphoma 66 9.963
19
P LKM062 Leukemia, Acute Lymphoblastic 69 9.851
20
GST019 Gastrointestinal Stromal Tumor 78 9.666
21
P TYR004 Tyrosinemia 49 8.837
22
PHN003 Phenylketonuria 76 8.240
23
P PHC003 Pheochromocytoma 70 8.159
24
GLM045 Glioma 62 8.060
25
P LKM071 Leukemia, Chronic Lymphocytic 74 7.975
26
c PRC016 Pre-Eclampsia 64 7.968
27
GLL048 Glial Tumor 51 7.966
28
P NRB001 Neuroblastoma 66 7.908
29
GLB002 Glioblastoma 67 7.862
30
ADR040 Adrenal Gland Pheochromocytoma 45 7.745
31
RPD005 Rapidly Involuting Congenital Hemangioma 48 7.686
32
THY029 Thyroid Carcinoma 55 7.622
33
P BCL017 B-Cell Lymphoma 57 7.017
34
INS024 Insulin-Like Growth Factor I 77 6.927
35
PRT037 Pertussis 49 6.861
36
LNG031 Lung Benign Neoplasm 51 6.721
37
P EXN002 Exanthem 58 6.609
38
P KDN017 Kidney Cancer 60 6.455
39
P AGM001 Agammaglobulinemia 67 6.438
40
P BRS047 Breast Cancer 97 6.330
41
c TYR012 Tyrosinemia, Type I 61 6.206
42
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 6.170
43
SQM006 Squamous Cell Carcinoma 59 6.124
44
SRC014 Sarcoma 64 6.055
45
SPN035 Spindle Cell Sarcoma 51 5.953
46
ALK013 Alkaptonuria 58 5.725
47
P PNC035 Pancreatic Cancer 87 5.647
48
CYT002 Cytokine Deficiency 43 5.549
49
P PRK039 Parkinsonism 55 5.516
50
P OVR042 Ovarian Cancer 88 5.432
51
HYP266 Hypoxia 56 5.412
52
P PRK057 Parkinson Disease, Late-Onset 79 5.369
53
HGH043 High Grade Glioma 46 5.348
54
P HYP098 Hypereosinophilic Syndrome 66 5.340
55
P HYP086 Hypothyroidism 68 5.228
56
LYM019 Lymphosarcoma 46 5.167
57
MNT001 Mantle Cell Lymphoma 65 5.131
58
P GLM040 Glioma Susceptibility 1 70 5.111
59
P ANP001 Anaplastic Large Cell Lymphoma 59 5.079
60
HLX001 Helix Syndrome 47 5.072
61
HWK001 Hawkinsinuria 42 5.053
62
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 5.048
63
MYL069 Myeloma, Multiple 76 4.996
64
c ACT073 Acute Leukemia 59 4.973
65
DWN001 Down Syndrome 70 4.964
66
P HPT023 Hepatocellular Carcinoma 95 4.961
67
MYL031 Myeloproliferative Neoplasm 66 4.942
68
P CLR023 Colorectal Cancer 100 4.935
69
P PRS040 Prostate Cancer 95 4.918
70
P BLD134 Bladder Cancer 79 4.866
71
c CHR064 Chronic Monocytic Leukemia 35 4.774
72
PRT251 Proteinuria, Chronic Benign 58 4.743
73
P DRR001 Diarrhea 55 4.739
74
P MLN008 Melanoma 75 4.698
75
ATM095 Autoimmune Disease 61 4.637
76
THY111 Thyroid Carcinoma, Familial Medullary 67 4.543
77
SFT003 Soft Tissue Sarcoma 43 4.533
78
P MST009 Mastocytosis 64 4.532
79
48X005 48,xyyy 39 4.484
80
DFF005 Diffuse Large B-Cell Lymphoma 55 4.391
81
P GST053 Gastric Cancer 82 4.383
82
BNR002 Bone Resorption Disease 47 4.352
83
P RHM011 Rheumatoid Arthritis 81 4.336
84
VCC001 Vaccinia 49 4.334
85
MYL005 Myelofibrosis 70 4.293
86
P ECL001 Eclampsia 52 4.234
87
CLR030 Clear Cell Renal Cell Carcinoma 53 4.153
88
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 4.150
89
c TYP009 Type 2 Diabetes Mellitus 91 4.116
90
RNL065 Renal Cell Carcinoma, Papillary, 1 79 4.114
91
OST159 Osteogenic Sarcoma 66 4.074
92
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 4.043
93
RHB024 Rhabdomyosarcoma 2 65 4.022
94
P THR014 Thrombocytopenia 66 4.007
95
LYM143 Lymphoma, Non-Hodgkin, Familial 74 3.995
96
TYR015 Tyrosinosis 20 3.966
97
LYM133 Lymphoma, Hodgkin, Classic 69 3.912
98
P FBR017 Fibrosarcoma 55 3.908
99
MLG169 Malignant Astrocytoma 57 3.898
100
P MLT074 Multiple Endocrine Neoplasia 58 3.889
101
c THY109 Thyroid Cancer, Nonmedullary, 1 55 3.879
102
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 3.869
103
SVR004 Severe Combined Immunodeficiency 70 3.863
104
P THY032 Thyroiditis 56 3.840
105
SYS004 Systemic Mastocytosis 62 3.797
106
c TYP008 Type 1 Diabetes Mellitus 77 3.794
107
ALL029 Allergic Disease 61 3.790
108
c SYS001 Systemic Lupus Erythematosus 85 3.788
109
LNG099 Lung Disease 62 3.787
110
ACT098 Acute Erythroid Leukemia 55 3.768
111
CHL065 Cholangiocarcinoma 57 3.760
112
P DYS154 Dystonia 64 3.744
113
P PLM037 Pulmonary Hypertension 69 3.738
114
P PLM036 Pulmonary Fibrosis 65 3.736
115
THY125 Thyroid Gland Medullary Carcinoma 48 3.720
116
MCR004 Macroglobulinemia 48 3.716
117
P ART022 Arthritis 70 3.701
118
MYL009 Myelodysplastic Syndrome 67 3.699
119
47X002 47,xyy 47 3.628
120
AGN016 Aging 53 3.620
121
HYP066 Hyperglycemia 60 3.615
122
P NTR004 Neutropenia 62 3.614
123
P ESS003 Essential Thrombocythemia 68 3.608
124
P RTN024 Retinoblastoma 72 3.553
125
P BNG032 Benign Mesothelioma 53 3.520
126
LYM040 Lymphoblastic Lymphoma 53 3.506
127
P DBT009 Diabetes Mellitus 67 3.497
128
c TYR011 Tyrosinemia, Type Iii 41 3.480
129
P GRF003 Graft-Versus-Host Disease 71 3.471
130
END057 Endometrial Cancer 76 3.470
131
P MYS003 Myasthenia Gravis 67 3.464
132
P LPS004 Lupus Erythematosus 61 3.439
133
P MST002 Mast-Cell Leukemia 50 3.430
134
HYP141 Hyperphenylalaninemia 42 3.425
135
SQM013 Squamous Cell Carcinoma, Head and Neck 75 3.408
136
P PLY018 Polycythemia 56 3.380
137
HMN044 Human Immunodeficiency Virus Type 1 76 3.369
138
P NSP012 Nasopharyngeal Carcinoma 60 3.349
139
P ALZ034 Alzheimer Disease 87 3.321
140
TXC005 Toxic Shock Syndrome 61 3.309
141
P SKN015 Skin Carcinoma 71 3.307
142
BRN028 Brain Cancer 73 3.256
143
CRV035 Cervical Cancer 72 3.229
144
P MYP004 Myopathy 67 3.211
145
INS001 Insulinoma 59 3.204
146
INT066 Interstitial Lung Disease 60 3.182
147
MNT002 Mental Depression 56 3.155
148
c PCH010 Pachyonychia Congenita 3 43 3.129
149
CHL014 Cholera 62 3.128
150
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 3.126
151
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 3.116
152
P RHB003 Rhabdomyosarcoma 66 3.106
153
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 3.103
154
ESP021 Esophageal Cancer 84 3.100
155
BRK010 Burkitt Lymphoma 65 3.091
156
PLY001 Polycythemia Vera 69 3.090
157
P THY023 Thymoma 64 3.086
158
P CHR285 Chronic Myelomonocytic Leukemia 59 3.075
159
INT079 Intrahepatic Cholangiocarcinoma 51 3.074
160
P HPT021 Hepatitis 68 3.050
161
c THY107 Thymoma, Familial 42 3.048
163
THY030 Thyroid Gland Disease 50 3.013
164
P ENC018 Encephalopathy 62 3.005
165
c PLM164 Pulmonary Hypertension, Primary, 1 75 3.000
166
P HRP006 Herpes Simplex 65 2.990
167
c LKM056 Leukemia, Chronic Lymphocytic 2 47 2.983
168
PLM134 Pulmonary Fibrosis, Idiopathic 76 2.973
169
SPL018 Splenomegaly 47 2.972
170
PNC129 Pancreatic Adenocarcinoma 64 2.970
171
IMM167 Immune Deficiency Disease 76 2.969
172
ACT119 Acute Promyelocytic Leukemia 62 2.965
173
c HPT016 Hepatitis B 62 2.964
174
STM007 Stomatitis 52 2.963
175
HYP060 Hyperinsulinism 53 2.961
176
P RHN004 Rhinitis 56 2.941
177
ALL003 Allergic Rhinitis 66 2.936
178
DPR016 Depression 64 2.923
179
MCS002 Mucositis 55 2.906
180
LWG006 Low Grade Glioma 41 2.891
181
P INF037 Inflammatory Bowel Disease 53 2.890
183
PRT036 Peritonitis 65 2.868
184
P NNN008 Noonan Syndrome 1 76 2.867
185
c PSD047 Pseudo-Turner Syndrome 52 2.854
186
c AMY091 Amyotrophic Lateral Sclerosis 1 87 2.843
187
P WSK001 Wiskott-Aldrich Syndrome 72 2.842
188
c LKM005 Leukemia, T-Cell, Chronic 33 2.841
189
ADN018 Adenoma 58 2.839
190
JVN004 Juvenile Myelomonocytic Leukemia 66 2.823
191
P GLM007 Glomerulonephritis 59 2.817
192
P PSR002 Psoriasis 63 2.787
193
PST011 Pustulosis of Palm and Sole 52 2.784
194
P LVR013 Liver Disease 68 2.772
195
NNN026 Noonan Syndrome with Multiple Lentigines 64 2.764
196
P DRM053 Dermatitis, Atopic 65 2.763
197
P SPP010 Suppressor of Tumorigenicity 3 50 2.748
198
CHR074 Choriocarcinoma 46 2.744
199
P MLT020 Multiple Sclerosis 79 2.740
200
c ACT027 Acute Pancreatitis 60 2.736
201
P MYC007 Myocardial Infarction 69 2.715
202
P LTR001 Lateral Sclerosis 57 2.710
203
CRH001 Crohn's Disease 80 2.704
204
KPS004 Kaposi Sarcoma 76 2.692
205
P BND020 Bone Disease 60 2.691
206
ISC004 Ischemia 61 2.685
207
P NRF002 Neurofibromatosis 60 2.673
208
OVR094 Ovarian Epithelial Cancer 39 2.669
209
P FLL037 Follicular Lymphoma 66 2.667
210
P SML001 Small Cell Carcinoma 52 2.667
211
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.665
212
P ANR048 Aniridia 1 66 2.664
213
P PNC044 Pancreatitis 61 2.664
214
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 2.661
215
MSN004 Mesenchymal Cell Neoplasm 42 2.621
216
LVR012 Liver Cirrhosis 62 2.619
217
ANX010 Anxiety 70 2.616
218
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.616
219
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 2.616
220
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.616
221
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 2.616
222
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.616
223
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 2.616
224
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 2.616
225
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.616
226
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.616
227
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.584
228
HPT004 Hepatic Coma 43 2.580
229
SKN019 Skin Melanoma 70 2.573
230
MDD011 Mood Disorder 61 2.572
231
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 2.571
232
P INF032 Infertility 60 2.559
233
P SZR006 Seizure Disorder 69 2.554
234
P HNT016 Huntington Disease 73 2.554
235
P ADL010 Adult Respiratory Distress Syndrome 70 2.547
236
LYM012 Lymphoplasmacytic Lymphoma 50 2.546
237
c HYP836 Hypercholesterolemia, Familial, 1 73 2.522
238
P KDN018 Kidney Disease 71 2.504
239
ORL015 Oral Squamous Cell Carcinoma 43 2.471
240
TRN018 Transitional Cell Carcinoma 56 2.469
241
c SCL052 Scleroderma, Familial Progressive 60 2.468
242
HPT019 Hepatic Encephalopathy 59 2.464
243
PLY150 Polykaryocytosis Inducer 29 2.461
244
PRG017 Paraganglioma and Gastric Stromal Sarcoma 63 2.459
245
GST040 Gastric Adenocarcinoma 66 2.459
246
P MYC084 Mycobacterium Tuberculosis 1 68 2.452
247
CLT003 Colitis 63 2.449
248
GLC003 Glucose Intolerance 53 2.447
249
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 2.447
250
P BPL003 Bipolar Disorder 56 2.442
251
c HYP595 Hypertension, Essential 84 2.440
252
CLN015 Colon Adenocarcinoma 64 2.437
253
HYP056 Hypoglycemia 65 2.435
254
P PLY011 Polycystic Ovary Syndrome 57 2.432
255
ALL006 Allergic Asthma 55 2.422
256
HMT002 Hematologic Cancer 61 2.420
257
ATS010 Autosomal Recessive Disease 42 2.417
258
P VSC007 Vascular Disease 62 2.413
259
c MST023 Mesothelioma, Malignant 56 2.409
260
DWR001 Dwarfism 44 2.395
261
P GST044 Gastritis 55 2.390
262
P MJR001 Major Depressive Disorder 68 2.388
263
SKN016 Skin Disease 63 2.385
264
ATH013 Atherosclerosis Susceptibility 63 2.383
265
P INF038 Influenza 68 2.381
266
c CHR417 Chronic Graft Versus Host Disease 55 2.371
267
c PRM038 Primary Agammaglobulinemia 47 2.364
268
EWN003 Ewing Sarcoma 69 2.348
269
DYS192 Dystonia, Dopa-Responsive 56 2.340
270
BCT022 Bacterial Infectious Disease 55 2.328
271
DRM014 Dermatofibrosarcoma Protuberans 64 2.327
272
P MLN007 Male Infertility 56 2.325
273
c ATR087 Atrial Standstill 1 74 2.319
274
MLG079 Malignant Pleural Mesothelioma 42 2.312
275
MRG003 Marginal Zone B-Cell Lymphoma 52 2.308
276
THY122 Thyroid Gland Cancer 59 2.304
277
c HPT073 Hepatitis C Virus 70 2.304
278
c CHR684 Chronic Kidney Disease 73 2.302
279
c MCR115 Microvascular Complications of Diabetes 5 65 2.300
280
CLL014 Cll/sll 45 2.299
281
ALL014 Allergic Encephalomyelitis 34 2.278
282
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.272
283
P TRN020 Turner Syndrome 67 2.261
284
P MDL005 Medulloblastoma 75 2.259
285
CHR178 Chromosomal Triplication 33 2.257
286
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 2.257
287
DFF036 Differentiated Thyroid Carcinoma 51 2.255
288
OCH001 Ochronosis 40 2.247
289
P ALP008 Alopecia 53 2.247
290
P PNM007 Pneumonia 64 2.245
291
ACH004 Achondroplasia 65 2.244
292
WLD007 Waldenstroem's Macroglobulinemia 59 2.237
293
P AST005 Asthma 75 2.228
294
P LPS002 Liposarcoma 64 2.225
295
RTC005 Reticulosarcoma 47 2.213
296
DRM006 Dermatitis 61 2.209
297
c MCR120 Microvascular Complications of Diabetes 7 47 2.209
298
BRS099 Breast Ductal Carcinoma 61 2.203
299
c MCR133 Microvascular Complications of Diabetes 4 41 2.202
300
c MCR113 Microvascular Complications of Diabetes 3 52 2.202
301
c MCR130 Microvascular Complications of Diabetes 6 41 2.202
302
HYP781 Hypoascorbemia 52 2.201
303
P HRS035 Hirschsprung Disease 1 66 2.201
304
P HYP076 Hyperthyroidism 53 2.200
305
CHR563 Chronic Eosinophilic Leukemia 48 2.198
306
NRN001 Neuroendocrine Carcinoma 47 2.182
307
WTH001 Withdrawal Disorder 47 2.170
308
c ATS007 Autism Spectrum Disorder 71 2.163
309
NRN004 Neuroendocrine Tumor 55 2.159
310
NRL016 Neural Tube Defects 80 2.156
311
KRT019 Keratitis, Hereditary 66 2.148
312
P NML001 Nemaline Myopathy 49 2.140
313
P TRM003 Tremor 50 2.128
314
PPL022 Papilloma 53 2.127
315
c HPT001 Hepatitis C 61 2.117
316
c ACT071 Acute Kidney Failure 60 2.109
317
EMB004 Embryonal Carcinoma 55 2.108
318
SQM002 Squamous Cell Papilloma 45 2.106
319
BRN071 Brain Injury 50 2.102
320
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 2.102
321
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 2.102
322
P LMY004 Leiomyosarcoma 62 2.100
323
TLN003 Telangiectasis 51 2.079
324
P RSP003 Respiratory Failure 73 2.076
325
CNG034 Congestive Heart Failure 69 2.069
326
RNL077 Renal Fibrosis 46 2.064
327
OST012 Osteoarthritis 77 2.061
328
THR004 Thrombocytosis 52 2.058
329
P SCH015 Schizophrenia 74 2.056
330
ART140 Arteries, Anomalies of 52 2.054
331
ADN009 Adenosquamous Carcinoma 49 2.050
332
LRY018 Laryngeal Squamous Cell Carcinoma 47 2.046
333
ISL003 Isolated Growth Hormone Deficiency 56 2.038
334
P VSC011 Vasculitis 61 2.037
335
P PLY014 Polycystic Kidney Disease 71 2.036
336
CYS001 Cystic Fibrosis 77 2.030
337
CMB007 Combined Immunodeficiency 56 2.028
338
END086 End Stage Renal Disease 54 2.027
339
ISL122 Isolated Growth Hormone Deficiency, Type Iii, with Agammaglobulinemia 36 2.026
340
ISL125 Isolated Growth Hormone Deficiency Type Iii 39 2.026
341
ULC004 Ulcerative Colitis 74 2.011
342
CLR109 Colorectal Adenocarcinoma 50 2.007
343
c MJR022 Major Affective Disorder 8 37 2.006
344
c MJR024 Major Affective Disorder 9 40 2.006
345
P ATS364 Autism 72 2.005
346
c INF023 Inflammatory Breast Carcinoma 48 2.003
347
CRB004 Cerebral Artery Occlusion 45 1.997
348
CHL123 Chlamydia 58 1.995
349
P ATX030 Ataxia-Telangiectasia 80 1.979
350
P BCL004 B-Cell Non-Hodgkin Lymphoma 41 1.971
351
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 26 1.967
352
CHC001 Chickenpox 56 1.964
353
c ACT135 Acute Graft Versus Host Disease 51 1.962
354
MST004 Mast Cell Neoplasm 41 1.959
355
ORL011 Oral Cancer 60 1.959
356
P ART023 Arthropathy 59 1.958
357
FTT001 Fatty Liver Disease 61 1.957
358
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 1.952
359
P OLG002 Oligodendroglioma 66 1.951
360
MLG077 Malignant Peripheral Nerve Sheath Tumor 53 1.942
361
PLS009 Plasma Cell Neoplasm 64 1.941
362
LYM027 Lymphopenia 56 1.937
363
MDD018 Middle East Respiratory Syndrome 44 1.933
364
PLG002 Plague 58 1.932
365
HRW001 Hair Whorl 35 1.920
366
IGR001 Ige Responsiveness, Atopic 58 1.916
367
LPD008 Lipid Metabolism Disorder 61 1.908
368
SPP011 Suppression of Tumorigenicity 12 61 1.907
369
P BRS044 Breast Adenocarcinoma 58 1.907
370
P ATT013 Attention Deficit-Hyperactivity Disorder 65 1.898
371
RSP023 Rasopathy 54 1.892
372
c LRG001 Large Cell Carcinoma 48 1.892
373
P SRC025 Sarcoidosis 1 70 1.891
374
P GRV001 Graves' Disease 54 1.891
375
PLL012 Pollen Allergy 44 1.886
376
IRR002 Irritable Bowel Syndrome 64 1.884
377
KRT009 Keratosis 52 1.884
378
c WLM013 Wilms Tumor 1 65 1.881
379
PTT037 Pituitary Tumors 44 1.879
380
CLR108 Colorectal Adenoma 63 1.866
381
P FML011 Familial Adenomatous Polyposis 70 1.866
382
MXD026 Mixed Glioma 45 1.858
383
P MSC005 Muscular Dystrophy 66 1.856
384
HRY003 Hairy Cell Leukemia 53 1.835
385
PRS047 Prostatitis 57 1.831
386
MLG157 Malignant Pheochromocytoma 37 1.825
387
P NRP001 Neuropathy 59 1.820
388
c MLT159 Multiple Endocrine Neoplasia, Type Iib 60 1.819
389
CNS004 Constipation 56 1.819
390
c SVR005 Severe Pre-Eclampsia 49 1.816
391
SPN186 Spinal Cord Injury 60 1.811
392
P RST001 Restless Legs Syndrome 52 1.811
393
PLM010 Pulmonary Edema 54 1.802
394
ADL002 Adult Syndrome 69 1.800
395
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 69 1.800
396
EXT007 Extracutaneous Mastocytoma 38 1.798
397
P SCK005 Sickle Cell Disease 56 1.798
398
P ESP024 Esophagitis 60 1.794
399
MNN043 Meningioma, Familial 79 1.794
400
P INS002 in Situ Carcinoma 52 1.794
401
END041 Endometrial Adenocarcinoma 63 1.789
402
ACN002 Acanthosis Nigricans 56 1.788
403
PRN014 Paronychia 50 1.788
404
PST092 Posttransplant Acute Limbic Encephalitis 29 1.787
405
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.784
406
SCR001 Secretory Meningioma 40 1.784
407
INT395 Intracranial Meningioma 47 1.784
408
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.780
409
c INH020 Inherited Metabolic Disorder 47 1.780
410
GTP002 Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia 17 1.776
411
LNG039 Lung Squamous Cell Carcinoma 57 1.772
412
P TRT010 Teratoma 50 1.771
413
ACQ007 Acquired Immunodeficiency Syndrome 58 1.766
414
MRK001 Merkel Cell Carcinoma 64 1.756
415
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 56 1.755
416
P HRT032 Heart Disease 84 1.753
417
ACT113 Acute Myeloblastic Leukemia with Maturation 46 1.753
418
ISL085 Isolated Agammaglobulinemia 31 1.751
419
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 1.736
420
P TMR010 Tumor Predisposition Syndrome 69 1.734
421
P MLG074 Malignant Mesenchymoma 40 1.732
422
SVR001 Severe Acute Respiratory Syndrome 68 1.730
423
URM002 Uremia 47 1.729
424
P HYP605 Hyperphenylalaninemia, Bh4-Deficient, B 44 1.729
425
PPL052 Papillomatosis, Confluent and Reticulated 34 1.723
426
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.723
427
CRB039 Cerebrovascular Disease 65 1.717
428
PPL002 Papillary Carcinoma 46 1.717
429
ALC007 Alcohol Dependence 65 1.713
430
TTN003 Tetanus 64 1.706
431
AND005 Androgen Insensitivity Syndrome, Mild 21 1.704
432
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.703
433
SCH014 Schistosomiasis 56 1.703
434
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.701
435
P DMN002 Dementia 65 1.700
436
P CNT005 Central Nervous System Lymphoma 51 1.690
437
PRM226 Primary Central Nervous System Lymphoma 47 1.690
438
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 1.687
439
P OVR082 Overgrowth Syndrome 41 1.684
440
P PMP001 Pemphigus 54 1.682
441
c PNS012 Paine Syndrome 60 1.681
442
P KLZ004 Kala-Azar 1 41 1.678
443
STT001 Status Epilepticus 58 1.678
444
ANH002 Anhidrosis 45 1.678
445
LSH001 Leishmaniasis 63 1.678
446
INF058 Inflammatory Myofibroblastic Tumor 45 1.678
447
P ACN011 Acne 55 1.672
448
MLD018 Mild Cognitive Impairment 48 1.672
449
INH023 Inherited Cancer-Predisposing Syndrome 53 1.671
450
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 1.668
451
HYP679 Hypoglossia-Hypodactylia 33 1.667
452
GLS001 Gliosarcoma 63 1.663
453
RTN020 Retinal Vascular Disease 45 1.661
454
P MVM001 Movement Disease 61 1.658
455
DSS032 Disease by Infectious Agent 55 1.654
456
P INT068 Intestinal Disease 53 1.653
457
TRM010 Traumatic Brain Injury 50 1.653
458
c ALB021 Albinism, Oculocutaneous, Type Ii 58 1.645
459
ARG004 Argyria 26 1.643
460
DMY004 Demyelinating Disease 50 1.640
461
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.640
462
P HYP750 Hypertriglyceridemia, Familial 61 1.632
463
TTR005 Tetrahydrobiopterin Deficiency 49 1.630
464
HYP005 Hypokalemia 55 1.628
465
KHN001 Kuhnt-Junius Degeneration 48 1.625
466
P PRG013 Paraganglioma 57 1.624
467
P MNC007 Monocytic Leukemia 48 1.624
468
P RTN008 Retinitis Pigmentosa 79 1.620
469
NRR001 Neuroretinitis 42 1.617
470
RTN023 Retinitis 45 1.617
471
FBR047 Fibromyalgia 57 1.616
472
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.615
473
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 1.613
474
P OCL002 Oculocutaneous Albinism 59 1.611
475
CRC006 Carcinoid Syndrome 55 1.607
476
DFC004 Deficiency Anemia 74 1.606
477
P ATM019 Autoimmune Polyendocrine Syndrome 46 1.605
478
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 1.604
479
c ACT134 Acute Liver Failure 57 1.603
480
GST033 Gestational Diabetes 60 1.598
481
P HYP265 Hypotonia 42 1.595
482
P MSC003 Muscular Atrophy 52 1.594
483
P FRG001 Fragile X Syndrome 70 1.587
484
P LYM033 Lymphoproliferative Syndrome 59 1.586
485
HSH003 Hashimoto Thyroiditis 60 1.585
486
RCK004 Rickets 64 1.581
487
PNG002 Pain Agnosia 51 1.579
488
SRS001 Serous Cystadenocarcinoma 51 1.578
489
THY123 Thyroid Gland Follicular Carcinoma 53 1.577
490
CHR176 Chromophil Renal Cell Carcinoma 23 1.575
491
TRT001 Teratocarcinoma 41 1.570
492
P BRC006 Brachydactyly 52 1.567
493
P CRD246 Cardiovascular System Disease 55 1.566
494
BNM001 Bone Marrow Cancer 45 1.565
495
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.556
496
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.555
497
HYP020 Hyperprolactinemia 63 1.553
498
c CHR418 Chronic Leukemia 48 1.552
499
CLR017 Clear Cell Sarcoma 44 1.545
500
c BRN108 Branchiootic Syndrome 1 63 1.543
501
P PRD008 Periodontitis 63 1.543
502
P PRN023 Prion Disease 60 1.542
503
HNT002 Hantavirus Pulmonary Syndrome 55 1.541
504
MSL001 Measles 61 1.531
505
P THY061 Thyroid Dyshormonogenesis 2a 30 1.529
506
CHG001 Chagas Disease 65 1.528
507
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.526
508
MLR004 Malaria 77 1.523
509
c HPT003 Hepatitis a 63 1.522
510
LNT004 Lentigines 45 1.517
511
P RTN016 Retinal Degeneration 52 1.516
512
ATY005 Atypical Teratoid Rhabdoid Tumor 69 1.513
513
HMP009 Haemophilus Influenzae 41 1.509
514
P ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 39 1.509
515
SYN007 Synovitis 54 1.507
516
PLC002 Plica Syndrome 35 1.507
517
P MXD050 Mixed Phenotype Acute Leukemia 46 1.506
518
CCN001 Cocaine Dependence 47 1.506
519
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 1.500
520
MYF002 Myofascial Pain Syndrome 46 1.499
521
ATN004 Autonomic Neuropathy 42 1.499
522
P HMN010 Hemangioma 61 1.498
523
P CRV039 Cervicitis 52 1.496
524
END072 Endotheliitis 36 1.489
525
INT029 Interleukin-7 Receptor Alpha Deficiency 27 1.485
526
STR067 Stroke, Ischemic 79 1.484
527
P OST001 Osteopetrosis 70 1.482
528
P PRP019 Peripheral Nervous System Disease 57 1.479
529
APP009 Appendix Adenocarcinoma 47 1.470
530
CHL149 Childhood Acute Myeloid Leukemia 42 1.468
531
HRP004 Herpes Zoster 60 1.466
532
SKN013 Skin Benign Neoplasm 49 1.465
533
P CNJ013 Conjunctivitis 66 1.463
534
NNL006 Non-Alcoholic Steatohepatitis 54 1.461
535
P CHN012 Chondrosarcoma 56 1.449
536
THR024 Thrombosis 56 1.448
537
P CTR002 Cataract 59 1.448
538
BLD131 Bladder Urothelial Carcinoma 59 1.446
539
TRN015 Transient Cerebral Ischemia 62 1.441
540
SCT005 Scott Syndrome 51 1.440
541
ETN001 Eating Disorder 59 1.439
542
GTR002 Goiter 52 1.433
543
CLL010 Cellular Ependymoma 58 1.431
544
TMR016 Tumor Suppressor Gene on Chromosome 11 28 1.428
545
ANT039 Antisynthetase Syndrome 55 1.427
546
CHP002 Chops Syndrome 47 1.426
547
P BNG030 Benign Ependymoma 51 1.424
548
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 1.423
549
P URT039 Urticaria 57 1.421
550
CNT033 Central Nervous System Cancer 47 1.416
551
FLL027 Fallopian Tube Carcinoma 66 1.413
552
c MGR028 Migraine with or Without Aura 1 63 1.413
553
P FNC004 Fanconi Syndrome 60 1.407
554
P PTS002 Ptosis 52 1.404
555
P THN009 Thanatophoric Dysplasia, Type I 62 1.399
556
HST010 Histiocytosis 49 1.397
557
MCR013 Microphthalmia 59 1.396
558
P LRY044 Larynx Cancer 53 1.395
559
RFR010 Refractory Anemia 49 1.395
560
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.392
561
c PRS130 Prostate Cancer, Hereditary, 8 32 1.391
562
c PRS136 Prostate Cancer, Hereditary, 6 33 1.391
563
LMY002 Leiomyoma 51 1.389
564
P SYS005 Systemic Scleroderma 73 1.388
565
CRB090 Cerebral Hypoxia 42 1.388
566
HML018 Homologous Wasting Disease 21 1.387
567
CHN040 Choanal Atresia and Lymphedema 21 1.384
568
c DLT002 Dilated Cardiomyopathy 79 1.376
569
LPP008 Lipoprotein Quantitative Trait Locus 65 1.374
570
ANT024 Anthrax Disease 57 1.374
571
P MJR007 Major Affective Disorder 1 42 1.372
572
P NPH012 Nephrotic Syndrome 61 1.372
573
GT001 Gout 63 1.372
574
P END044 Endometriosis 62 1.370
575
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 1.370
576
P CRN037 Craniosynostosis 67 1.368
577
ADN011 Adenoid Cystic Carcinoma 68 1.367
578
ANP005 Anaplastic Astrocytoma 59 1.366
579
P HML002 Hemolytic Anemia 62 1.366
580
ALB002 Albinism 46 1.362
581
ANG020 Angiosarcoma 63 1.360
582
END040 Endogenous Depression 54 1.359
583
VNS013 Venous Malformations, Multiple Cutaneous and Mucosal 46 1.358
584
HLC007 Helicobacter Pylori Infection 67 1.353
585
P GLL018 Gallbladder Cancer 59 1.350
586
P RCT021 Rectum Cancer 54 1.346
587
THR123 Thrombotic Microangiopathy 40 1.342
588
NRF007 Neurofibroma 63 1.342
589
CLS049 Classic Phenylketonuria 34 1.341
590
CCN002 Cocaine Abuse 49 1.341
591
BBN001 Bubonic Plague 40 1.341
592
MYX005 Myxoid Liposarcoma 65 1.341
593
THY022 Thymic Carcinoma 56 1.340
594
HPT022 Hepatoblastoma 54 1.340
595
AML001 Amelanotic Melanoma 37 1.336
596
PLS011 Plasmacytoma 56 1.332
597
DCT002 Ductal Carcinoma in Situ 58 1.331
598
NTR055 Ntrk1 Congenital Insensitivity to Pain with Anhidrosis 12 1.330
599
SYS071 Systemic Autoimmune Disease 35 1.330
600
P RBN002 Robinow Syndrome 56 1.327
601
P HMN032 Human Herpesvirus 8 47 1.323
602
THY128 Thyroid Tumor 33 1.323
603
CVD001 Covid-19 59 1.319
604
ANR040 Aneurysm 60 1.319
605
RHB001 Rhabdoid Cancer 68 1.318
606
LRG014 Large Cell Neuroendocrine Carcinoma 44 1.317
607
MCN001 Mucinous Adenocarcinoma 49 1.316
608
HMS001 Hemosiderosis 48 1.315
609
P MYC008 Myocarditis 59 1.312
610
SKN022 Skin Squamous Cell Carcinoma 53 1.310
611
HYP810 Hypereosinophilic Syndrome, Idiopathic 61 1.309
612
KRT002 Keratomalacia 54 1.309
613
P RRH023 Rare Hereditary Hemochromatosis 52 1.307
614
NRL005 Neurilemmoma 60 1.306
615
P INF049 Infantile Myofibromatosis 55 1.306
616
PRP036 Peripheral T-Cell Lymphoma 52 1.306
617
PLM014 Pleomorphic Adenoma 51 1.305
618
CRN027 Corneal Neovascularization 47 1.305
619
c HMN021 Human T-Cell Leukemia Virus Type 1 46 1.301
620
P AMY004 Amyloidosis 69 1.300
621
DSM004 Desmoid Tumor 65 1.299
622
P PRC031 Preeclampsia/eclampsia 1 43 1.295
623
P ALC033 Alcohol Use Disorder 67 1.291
624
c ERY058 Erythrocytosis, Familial, 1 55 1.291
625
SNS003 Sensory Peripheral Neuropathy 51 1.291
626
P FBR003 Fibrous Histiocytoma 43 1.288
627
P EPL164 Epilepsy 70 1.286
628
c GRV008 Graves Disease 1 54 1.285
629
P CYS018 Cystitis 58 1.285
630
ADR016 Adrenal Cortical Carcinoma 61 1.282
631
ADR054 Adrenocortical Carcinoma, Hereditary 47 1.282
632
ADR004 Adrenal Cortical Adenocarcinoma 38 1.282
633
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.281
634
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.281
635
P EMB005 Embryonal Rhabdomyosarcoma 53 1.281
636
TNG007 Tongue Carcinoma 55 1.281
637
P HRD021 Hereditary Sensory Neuropathy 48 1.280
638
P NRV006 Nervous System Cancer 47 1.278
639
IGG001 Iga Glomerulonephritis 50 1.274
640
SPL004 Splenic Marginal Zone Lymphoma 50 1.272
641
SCR011 Scrapie 39 1.272
642
FCT007 Factor Vii Deficiency 64 1.266
643
MST024 Mastocytosis, Cutaneous 66 1.263
644
c ACT075 Acute Myocardial Infarction 55 1.262
645
P RRT020 Rare Tumor 39 1.260
646
GST045 Gastroenteritis 58 1.258
647
P SPR120 Supranuclear Palsy, Progressive, 1 68 1.257
648
VRL011 Viral Infectious Disease 60 1.257
649
P HYP069 Hyperparathyroidism 62 1.256
650
CNN005 Connective Tissue Disease 66 1.256
651
BLR008 Bilirubin Metabolic Disorder 57 1.253
652
TTT001 Tatton-Brown-Rahman Syndrome 44 1.252
653
IND002 Indolent Systemic Mastocytosis 42 1.250
654
SRC027 Sarcoma, Synovial 58 1.244
655
DPH001 Diphtheria 59 1.244
656
PLC008 Placenta Disease 48 1.244
657
HYP780 Hypoadrenocorticism, Familial 61 1.244
658
P MCR010 Microcephaly 59 1.240
659
KRT008 Keratopathy 46 1.240
660
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 61 1.239
661
P CHR345 Chronic Pain 50 1.238
662
PRS021 Prostatic Adenoma 43 1.235
663
c CNG023 Congenital Fibrosarcoma 42 1.235
664
CHR072 Chordoma 56 1.231
665
P MLN069 Melanoma, Uveal 59 1.231
666
FBR019 Fibromatosis 44 1.231
667
c BRC051 Brachydactyly, Type B1 50 1.230
668
P THL005 Thalassemia 56 1.225
669
P 8P1002 8p11 Myeloproliferative Syndrome 35 1.225
670
P RTT002 Rett Syndrome 79 1.224
671
c NRF024 Neurofibromatosis, Type I 76 1.224
672
AGG002 Aggressive Systemic Mastocytosis 49 1.223
673
LNG108 Langerhans Cell Histiocytosis 57 1.218
674
c JVN010 Juvenile Rheumatoid Arthritis 52 1.217
675
PLY100 Polyploidy 36 1.216
676
c DRR009 Diarrhea 6 46 1.215
677
P PLY180 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 1 56 1.214
678
PRM013 Premature Menopause 57 1.214
680
ANX004 Anoxia 40 1.212
681
c MLG084 Malignant Fibrous Histiocytoma 62 1.211
682
LPM012 Lipomatosis, Multiple 59 1.209
683
P NRV007 Nervous System Disease 65 1.209
684
OST015 Osteochondrodysplasia 60 1.208
685
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.203
686
INT030 Intracranial Aneurysm 55 1.202
687
TRY001 Trypanosomiasis 50 1.202
688
CRC021 Carcinosarcoma 62 1.202
689
P VNT002 Ventricular Septal Defect 58 1.201
690
BCL002 B Cell Deficiency 40 1.201
691
BLR013 Biliary Tract Cancer 43 1.199
692
LYM009 Lymphocytic Choriomeningitis 46 1.197
693
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 1.197
694
GLC036 Glucagonoma 45 1.196
695
OCL069 Ocular Motor Apraxia 57 1.195
696
ANR007 Anorexia Nervosa 59 1.195
697
GST023 Gastric Ulcer 52 1.195
698
PPT005 Peptic Ulcer Disease 58 1.195
699
BRR014 Barrett Esophagus 66 1.193
700
BRN002 Bronchiolitis 57 1.193
701
P ENC004 Encephalitis 61 1.192
702
GST050 Gastrointestinal System Disease 55 1.186
703
c ART101 Aortic Valve Disease 2 65 1.185
704
INT054 Intraocular Lymphoma 48 1.184
705
P CTN003 Cutaneous Lupus Erythematosus 52 1.183
706
URT010 Ureteral Obstruction 44 1.181
707
P SBS003 Substance Abuse 54 1.180
708
c VRL010 Viral Hepatitis 52 1.178
709
P ADL017 Adult T-Cell Leukemia 53 1.176
710
DYS073 Dysphagia 53 1.174
711
PYR021 Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency 50 1.173
712
END085 Endometrial Serous Adenocarcinoma 43 1.169
713
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 1.169
714
c OVR114 Ovarian Cancer 1 60 1.165
715
P ATR005 Atrophic Gastritis 50 1.164
716
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.160
717
IMP005 Impotence 52 1.160
718
BRN012 Bronchiolitis Obliterans 56 1.159
719
MLT157 Multiple System Atrophy 1 69 1.158
720
PRS045 Prostatic Hypertrophy 53 1.155
721
END031 Endometrial Stromal Sarcoma 45 1.152
722
P EST001 Estrogen-Receptor Positive Breast Cancer 49 1.150
723
BRN024 Bronchitis 67 1.150
724
BRN004 Brain Edema 54 1.150
725
PRP027 Peripheral Vascular Disease 71 1.148
726
FLL008 Folliculitis 45 1.148
727
P MYC033 Myoclonus 46 1.148
728
c DWL002 Dowling-Degos Disease 1 58 1.146
729
ALV005 Alveolar Soft Part Sarcoma 61 1.146
730
CRD132 Cardiac Conduction Defect 59 1.146
731
PRS129 Prostatic Hyperplasia, Benign 48 1.146
732
GLM044 Glomerular Disease 34 1.146
733
FLL041 Follicular Lymphoma 1 44 1.144
734
MTR008 Mature B-Cell Neoplasm 36 1.141
735
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.136
736
P BNC003 Bone Cancer 58 1.129
737
PNC001 Pancytopenia 52 1.126
738
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 44 1.124
739
P HDC001 Headache 56 1.124
740
SMN007 Seminoma 42 1.122
741
P CTN015 Cutaneous T Cell Lymphoma 48 1.121
742
HYP017 Hypophosphatemia 49 1.121
743
MTR016 Maternal Hyperphenylalaninemia 20 1.120
744
NTR005 Nutritional Deficiency Disease 60 1.119
745
SML019 Smallpox 55 1.118
746
c HYP331 Hyperphenylalaninemia, Bh4-Deficient, a 59 1.117
747
P RNL100 Renal Hypodysplasia/aplasia 1 63 1.116
748
c CNT035 Central Nervous System Disease 53 1.112
749
P CRD119 Cardiac Arrest 68 1.110
750
HLL004 Hellp Syndrome 53 1.110
751
P CNG001 Congenital Myasthenic Syndrome 68 1.109
752
HMP001 Hemopericardium 47 1.105
753
MRP001 Morphine Dependence 41 1.105
754
P PRC012 Pericardial Effusion 50 1.105
755
c RHB023 Rhabdomyosarcoma, Embryonal, 1 44 1.104
756
PRT013 Portal Hypertension 59 1.100
757
PRL017 Prolymphocytic Leukemia 47 1.097
758
SDD001 Sudden Infant Death Syndrome 60 1.094
759
P UVT001 Uveitis 57 1.094
760
c CNG006 Congenital Hypothyroidism 63 1.091
761
P CHL066 Cholangitis 51 1.089
762
P MTR014 Motor Neuron Disease 65 1.087
763
HRT011 Heart Septal Defect 49 1.084
764
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.083
765
ATN005 Autonomic Dysfunction 45 1.083
766
P ALP009 Alopecia Areata 59 1.083
767
ATX019 Ataxia with Vitamin E Deficiency 44 1.079
768
P HYD006 Hydrocephalus 62 1.077
769
P HYP061 Hypertrophic Cardiomyopathy 68 1.073
770
PRP030 Purpura 54 1.072
771
LMB062 Limb Ischemia 55 1.071
772
CHR286 Chronic Neutrophilic Leukemia 42 1.071
773
P CHR012 Chronic Granulomatous Disease 69 1.067
774
CRT015 Carotid Artery Occlusion 45 1.067
775
MSC007 Muscle Hypertrophy 64 1.067
776
ACT029 Acute Interstitial Pneumonia 49 1.064
777
P PTT006 Pituitary Adenoma 55 1.063
778
AMN003 Amnestic Disorder 53 1.063
780
NTR018 Neutrophilia, Hereditary 49 1.061
781
P FCL005 Focal Segmental Glomerulosclerosis 57 1.058
782
ENT011 Enterocolitis 55 1.053
783
RYN005 Raynaud Phenomenon 45 1.053
784
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.053
785
HST016 Histiocytic Sarcoma 38 1.052
786
MLD011 Mild Hyperphenylalaninemia 24 1.047
787
THY121 Thyroid Gland Anaplastic Carcinoma 66 1.045
788
CHL068 Cholestasis 61 1.045
789
PLM033 Pulmonary Embolism 58 1.045
790
P MPL001 Maple Syrup Urine Disease 69 1.043
791
P TMP001 Temporal Lobe Epilepsy 49 1.043
792
P PRS038 Personality Disorder 65 1.040
793
IRN002 Iron Metabolism Disease 56 1.037
794
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 1.032
795
DBT020 Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 40 1.027
796
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.027
797
P DNG005 Dengue Virus 55 1.027
798
JPN002 Japanese Encephalitis 61 1.027
799
P CLL015 Collagen Disease 47 1.026
800
THR035 Thrombasthenia 48 1.024
801
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 1.021
802
MGC001 Megacolon 48 1.021
803
P CND004 Candidiasis 57 1.021
804
CHR073 Choreatic Disease 53 1.021
805
VSC003 Visceral Leishmaniasis 54 1.020
806
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 1.016
807
P TCD001 Tic Disorder 50 1.016
809
PLX002 Plexiform Neurofibroma 44 1.015
810
ACT084 Acute Stress Disorder 53 1.015
811
VNH007 Von Hippel-Lindau Syndrome 72 1.010
812
ISL001 Islet Cell Tumor 55 1.009
813
c HRD202 Hereditary Lymphedema I 54 1.006
814
ADG002 Audiogenic Seizures 25 1.006
815
CRC014 Carcinoid Tumors, Intestinal 46 1.006
816
THY124 Thyroid Gland Papillary Carcinoma 38 1.004
817
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.002
818
CRZ001 Crouzon Syndrome 64 0.999
819
c THR092 Thrombophilia Due to Thrombin Defect 74 0.999
820
MTC018 Metachondromatosis 48 0.999
821
CLF027 Cleft Palate, Isolated 64 0.999
822
DSS009 Disseminated Intravascular Coagulation 56 0.999
823
ACT162 Acute Sensory Ataxic Neuropathy 24 0.998
824
P ATR011 Atrial Fibrillation 66 0.997
825
TRD006 Tardive Dyskinesia 53 0.993
826
c NRF023 Neurofibromatosis, Type Ii 70 0.993
827
PRM236 Primary Biliary Cholangitis 62 0.993
828
P NJM001 Nijmegen Breakage Syndrome 75 0.992
829
PRP016 Paraplegia 52 0.991
830
PLM001 Pulmonary Tuberculosis 69 0.991
831
HYP042 Hypochondroplasia 58 0.988
832
CD4001 Cd45 Deficiency 27 0.987
833
RTN017 Retinal Detachment 60 0.987
834
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.983
835
GNG002 Ganglioneuroma 52 0.981
836
BNS007 Bone Sarcoma 50 0.979
837
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.978
838
P CRN300 Coronary Heart Disease 1 73 0.975
839
P APL001 Aplastic Anemia 72 0.975
840
c SPN225 Spondyloarthropathy 1 70 0.975
842
EST007 Estrogen Resistance 41 0.975
843
GNG005 Gangliocytoma 54 0.975
844
SPN051 Spondylitis 51 0.975
845
CKT002 Cakut 48 0.975
846
INF009 Inflammatory Spondylopathy 30 0.975
847
P LCT001 Lactic Acidosis 50 0.975
848
DRG003 Drug Dependence 46 0.969
849
HYP043 Hyperandrogenism 47 0.969
850
CYS014 Cystadenocarcinoma 51 0.964
851
P LPR021 Leprosy 3 71 0.962
852
HNS001 Hansen's Disease 32 0.962
853
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.958
854
LMY014 Leiomyoma, Uterine 55 0.957
855
P SLV026 Salivary Gland Carcinoma 59 0.957
856
TST014 Testicular Cancer 51 0.957
857
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.956
858
MYC005 Myocardial Stunning 45 0.956
859
MSC157 Muscular Dystrophy, Duchenne Type 78 0.949
860
P GLN011 Glanzmann Thrombasthenia 1 66 0.949
861
ANG054 Angina Pectoris 65 0.942
862
MNG007 Manganese Poisoning 28 0.942
863
ENT004 Enthesopathy 51 0.939
864
P DDN001 Duodenal Ulcer 52 0.938
865
CRB138 Core Binding Factor Acute Myeloid Leukemia 45 0.938
866
CMM004 Common Variable Immunodeficiency 71 0.938
867
PMP006 Pemphigus Vulgaris, Familial 57 0.937
868
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.937
869
c CRN278 Craniosynostosis 1 55 0.935
870
CHR375 Chromosome 8p11 Myeloproliferative Syndrome 28 0.933
871
P ART021 Arteriosclerosis 53 0.933
872
HRN029 Hearing Loss, Noise-Induced 37 0.928
873
CHR710 Chronic Spontaneous Urticaria 45 0.928
874
ALC006 Alcoholic Hepatitis 61 0.928
875
P NRC002 Narcolepsy 55 0.928
876
P OST002 Osteoporosis 76 0.927
877
SLP001 Sleeping Sickness 56 0.927
878
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.922
879
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.922
880
VRL003 Variola Major 43 0.920
881
GNG004 Ganglioglioma 53 0.920
882
MNN009 Meningoencephalitis 47 0.920
883
BRS051 Breast Disease 58 0.920
884
PPL050 Papillary Tumor of the Pineal Region 32 0.920
885
ACH043 Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans 58 0.918
886
PNN001 Panniculitis 52 0.913
887
HYP458 Hyper Ige Syndrome 60 0.910
888
P CRV031 Cervical Adenocarcinoma 48 0.910
889
c THY063 Thyroid Dyshormonogenesis 4 26 0.910
890
PYD002 Pyoderma 49 0.909
891
NSP002 Nasopharyngitis 45 0.907
892
P SCL009 Sclerosing Cholangitis 46 0.905
893
P SLP006 Sleep Apnea 69 0.904
894
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.904
895
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.901
896
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.901
897
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.901
898
P TST021 Testicular Germ Cell Tumor 61 0.901
899
OST003 Osteonecrosis 60 0.898
900
P LNG028 Long Qt Syndrome 63 0.898
901
LGN006 Legionnaire Disease 52 0.897
902
P RTN018 Retinal Disease 53 0.897
903
FBR054 Fibroma 44 0.896
904
c CHL119 Cholangitis, Primary Sclerosing 57 0.896
905
PLM005 Pleomorphic Lipoma 39 0.896
906
FML029 Familial Renal Papillary Carcinoma 30 0.896
907
PSY004 Psychotic Disorder 66 0.896
908
P PRL003 Proliferative Glomerulonephritis 43 0.896
909
ACT003 Acute Kidney Tubular Necrosis 46 0.896
910
P CYS039 Cystic Kidney Disease 52 0.892
911
RTN003 Retinal Ischemia 48 0.892
912
P TBR001 Tuberous Sclerosis 69 0.892
913
CNT061 Conotruncal Heart Malformations 66 0.890
914
ADR005 Adrenal Carcinoma 58 0.890
915
c HYP368 Hyperphenylalaninemia, Bh4-Deficient, C 35 0.889
916
DYR003 Dyrk1a Syndrome 31 0.889
917
PLC007 Placental Abruption 47 0.888
918
P ASP006 Aspergillosis 71 0.886
919
MTB004 Metabolic Acidosis 48 0.883
920
ART006 Arthus Reaction 40 0.881
921
LTN029 Latent Autoimmune Diabetes in Adults 38 0.880
922
P LNG035 Lung Large Cell Carcinoma 53 0.879
923
ANV001 Anovulation 46 0.879
924
CRN030 Coronary Stenosis 50 0.879
925
BRN056 Bronchopulmonary Dysplasia 57 0.878
926
PYD001 Pyoderma Gangrenosum 53 0.878
927
VRC005 Varicose Veins 59 0.873
928
HYP748 Hypertelorism 46 0.873
929
DYS015 Dysentery 49 0.873
930
ACT200 Acute Monoblastic Leukemia 40 0.873
931
c RNG008 Ring Chromosome 13 31 0.873
932
c FML021 Familial Hypercholesterolemia 71 0.872
933
CRT017 Cartilage Disease 52 0.870
934
TRN049 Transient Tyrosinemia of the Newborn 8 0.870
935
c ERY064 Erythrocytosis, Familial, 6 30 0.870
936
P RNL017 Renal Oncocytoma 54 0.869
937
PFF001 Pfeiffer Syndrome 77 0.867
938
c LKM070 Leukemia, Acute Monocytic 56 0.867
939
c SVR003 Severe Congenital Neutropenia 59 0.867
940
P CNT004 Centronuclear Myopathy 56 0.867
941
DNH001 Donohue Syndrome 60 0.863
942
P LPR012 Leopard Syndrome 1 48 0.863
943
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.861
944
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.861
945
DNT005 Dentatorubral-Pallidoluysian Atrophy 59 0.860
946
CHD004 Chudley-Mccullough Syndrome 47 0.860
947
SLC006 Silicosis 55 0.860
948
MTH009 Mouth Disease 57 0.860
949
c ACT068 Acute Cystitis 60 0.860
950
PST021 Postpartum Depression 50 0.860
951
PRT058 Pure Autonomic Failure 58 0.858
952
PHS025 Phosphatase, Acid, of Tissues 28 0.853
953