Search results for Tyrosine

2018 hits were found for Tyrosine

# Family MCID Name MIFTS Score
1
SGW002 Segawa Syndrome, Autosomal Recessive 51 6.241
2
c TYR013 Tyrosinemia, Type Ii 47 6.199
3
IMM095 Immunodeficiency 35 29 5.272
4
P LNG032 Lung Cancer 98 4.579
5
AGM019 Agammaglobulinemia, X-Linked 71 3.399
6
IMM075 Immunodeficiency 22 26 3.033
7
DSR026 Disorder of Tyrosine Metabolism 14 2.228
8
TYR006 Tyrosine-Oxidase Temporary Deficiency 1 2.184
9
DSR073 Disorder of Phenylalanin or Tyrosine Metabolism 3 2.177
10
P MYL006 Myeloid Leukemia 60 0.535
11
c LKM063 Leukemia, Chronic Myeloid 72 0.507
12
P LKM002 Leukemia 68 0.354
13
c SML038 Small Cell Cancer of the Lung 65 0.340
14
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.309
15
c LKM061 Leukemia, Acute Myeloid 84 0.281
16
P LNG064 Lung Cancer Susceptibility 3 78 0.268
17
P BRS047 Breast Cancer 97 0.264
18
P NRB001 Neuroblastoma 72 0.264
19
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.246
20
P PHC003 Pheochromocytoma 71 0.245
21
ADR040 Adrenal Gland Pheochromocytoma 46 0.242
22
ATM095 Autoimmune Disease 62 0.239
23
P LKM062 Leukemia, Acute Lymphoblastic 69 0.235
24
GLB015 Glioblastoma Multiforme 75 0.234
25
P LYM118 Lymphoma 68 0.233
26
c PRC016 Pre-Eclampsia 63 0.227
27
P ADN016 Adenocarcinoma 64 0.227
28
P GLM045 Glioma 63 0.222
29
THY029 Thyroid Carcinoma 59 0.215
30
P CLR023 Colorectal Cancer 99 0.214
31
INS024 Insulin-Like Growth Factor I 79 0.214
32
GLL048 Glial Tumor 45 0.212
33
P AGM001 Agammaglobulinemia 65 0.210
34
P LKM071 Leukemia, Chronic Lymphocytic 79 0.203
35
PRT037 Pertussis 65 0.201
36
GST019 Gastrointestinal Stromal Tumor 78 0.200
37
P EXN002 Exanthem 57 0.193
38
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.184
39
PHN003 Phenylketonuria 75 0.183
40
P PRS040 Prostate Cancer 97 0.171
41
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.169
42
SQM006 Squamous Cell Carcinoma 60 0.164
43
LNG031 Lung Benign Neoplasm 51 0.164
44
P PNC035 Pancreatic Cancer 84 0.163
45
P BCL017 B-Cell Lymphoma 58 0.163
46
P OVR042 Ovarian Cancer 88 0.160
47
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.153
48
P TYR004 Tyrosinemia 58 0.153
49
LYM019 Lymphosarcoma 46 0.153
50
P KDN017 Kidney Cancer 60 0.151
51
CYT002 Cytokine Deficiency 42 0.151
52
P PRK057 Parkinson Disease, Late-Onset 78 0.150
53
HLX001 Helix Syndrome 47 0.150
54
P GST053 Gastric Cancer 83 0.141
55
IMM167 Immune Deficiency Disease 78 0.141
56
DWN001 Down Syndrome 70 0.140
57
MNT001 Mantle Cell Lymphoma 69 0.139
58
P HPT023 Hepatocellular Carcinoma 100 0.138
59
SRC014 Sarcoma 65 0.138
60
P MLN008 Melanoma 69 0.137
61
c CHR064 Chronic Monocytic Leukemia 33 0.137
62
P HYP086 Hypothyroidism 69 0.135
63
BNR002 Bone Resorption Disease 48 0.132
64
c SYS001 Systemic Lupus Erythematosus 86 0.130
65
SPN035 Spindle Cell Sarcoma 53 0.130
66
P DRR001 Diarrhea 55 0.128
67
MYL031 Myeloproliferative Neoplasm 66 0.124
68
P BLD134 Bladder Cancer 79 0.123
69
P DYS154 Dystonia 65 0.122
70
VCC001 Vaccinia 49 0.122
71
P RHM011 Rheumatoid Arthritis 80 0.121
72
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.121
73
48X005 48,xyyy 39 0.121
74
MYL069 Myeloma, Multiple 85 0.120
75
SVR004 Severe Combined Immunodeficiency 73 0.120
76
OST159 Osteogenic Sarcoma 66 0.119
77
P NTR004 Neutropenia 63 0.118
78
P MLT074 Multiple Endocrine Neoplasia 56 0.118
79
HYP066 Hyperglycemia 61 0.116
80
ADN018 Adenoma 59 0.116
81
ERY051 Erythroleukemia, Familial 56 0.116
82
P HYP098 Hypereosinophilic Syndrome 67 0.114
83
P MST009 Mastocytosis 64 0.114
84
c ACT073 Acute Leukemia 58 0.114
85
HYP266 Hypoxia 57 0.113
86
P GLM040 Glioma Susceptibility 1 81 0.112
87
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.112
88
P ECL001 Eclampsia 50 0.111
89
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.111
90
MYL005 Myelofibrosis 70 0.109
91
P ALZ034 Alzheimer Disease 88 0.108
92
CLR030 Clear Cell Renal Cell Carcinoma 53 0.108
93
c MLG068 Malignant Glioma 46 0.108
94
THY111 Thyroid Carcinoma, Familial Medullary 67 0.106
95
P PLM036 Pulmonary Fibrosis 65 0.106
96
ALL026 Allergic Hypersensitivity Disease 62 0.106
97
P AST007 Astrocytoma 51 0.105
98
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.105
99
ISC004 Ischemia 58 0.104
100
LNG099 Lung Disease 60 0.103
101
P FBR017 Fibrosarcoma 56 0.103
102
LYM133 Lymphoma, Hodgkin, Classic 69 0.102
103
P ANP001 Anaplastic Large Cell Lymphoma 58 0.102
104
P RTN024 Retinoblastoma 73 0.100
105
MYL009 Myelodysplastic Syndrome 70 0.100
106
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.100
107
c FML008 Familial Retinoblastoma 53 0.100
108
THY125 Thyroid Gland Medullary Carcinoma 50 0.100
109
47X002 47,xyy 49 0.100
110
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.099
111
P PLM037 Pulmonary Hypertension 67 0.099
112
DPR016 Depression 63 0.099
113
INS001 Insulinoma 60 0.099
114
STM007 Stomatitis 50 0.098
115
c PCH010 Pachyonychia Congenita 3 44 0.098
116
P GRF003 Graft-Versus-Host Disease 72 0.097
117
P MYS003 Myasthenia Gravis 68 0.097
118
P PLY018 Polycythemia 56 0.097
119
c LKM005 Leukemia, T-Cell, Chronic 34 0.097
120
P LVR013 Liver Disease 68 0.095
121
c DBT099 Diabetes Mellitus, Type I 65 0.095
122
c SYS004 Systemic Mastocytosis 63 0.095
123
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.094
124
HYP056 Hypoglycemia 66 0.094
125
P HRP006 Herpes Simplex 65 0.094
126
P GLM007 Glomerulonephritis 57 0.094
127
DFF005 Diffuse Large B-Cell Lymphoma 55 0.094
128
P NSP012 Nasopharyngeal Carcinoma 66 0.093
129
P VSC007 Vascular Disease 63 0.093
130
MCR004 Macroglobulinemia 49 0.093
131
HMN044 Human Immunodeficiency Virus Type 1 71 0.091
132
P INF037 Inflammatory Bowel Disease 54 0.091
133
P THR014 Thrombocytopenia 67 0.090
134
P THY023 Thymoma 65 0.090
135
MDD011 Mood Disorder 62 0.090
136
LVR012 Liver Cirrhosis 62 0.090
137
P LPS004 Lupus Erythematosus 61 0.090
138
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.090
139
P NNN008 Noonan Syndrome 1 76 0.088
140
TXC005 Toxic Shock Syndrome 62 0.088
141
c THY107 Thymoma, Familial 52 0.088
142
SPL018 Splenomegaly 48 0.088
143
c PSD047 Pseudo-Turner Syndrome 21 0.088
144
PLY001 Polycythemia Vera 69 0.087
145
c TYR012 Tyrosinemia, Type I 66 0.087
146
INT066 Interstitial Lung Disease 60 0.087
147
CHL014 Cholera 59 0.087
148
SFT003 Soft Tissue Sarcoma 56 0.087
149
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.087
150
P BNG032 Benign Mesothelioma 46 0.087
151
END057 Endometrial Cancer 74 0.085
152
P SCH015 Schizophrenia 74 0.085
153
P WSK001 Wiskott-Aldrich Syndrome 72 0.085
154
P BPL003 Bipolar Disorder 56 0.085
155
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.085
156
P PSR002 Psoriasis 62 0.084
157
P ENC018 Encephalopathy 61 0.084
158
PST011 Pustulosis of Palm and Sole 52 0.084
159
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.082
160
BRK010 Burkitt Lymphoma 67 0.082
161
ESP021 Esophageal Cancer 90 0.081
162
CHL065 Cholangiocarcinoma 68 0.081
163
MNT002 Mental Depression 58 0.081
164
HYP060 Hyperinsulinism 54 0.081
165
GLC003 Glucose Intolerance 54 0.081
166
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.079
167
ALL003 Allergic Rhinitis 67 0.079
168
c RHB024 Rhabdomyosarcoma 2 67 0.079
169
INT079 Intrahepatic Cholangiocarcinoma 51 0.079
170
P ESS003 Essential Thrombocythemia 68 0.078
171
BCT022 Bacterial Infectious Disease 56 0.078
172
P ALP008 Alopecia 54 0.078
173
P THY032 Thyroiditis 52 0.078
174
CLL014 Cll/sll 45 0.078
175
HYP141 Hyperphenylalaninemia 39 0.078
176
P KDN018 Kidney Disease 72 0.076
177
P RHB003 Rhabdomyosarcoma 63 0.076
178
SKN016 Skin Disease 63 0.076
179
c SCL052 Scleroderma, Familial Progressive 61 0.076
180
ALL006 Allergic Asthma 56 0.076
181
LYM040 Lymphoblastic Lymphoma 54 0.076
182
P MST002 Mast-Cell Leukemia 49 0.076
183
ORL015 Oral Squamous Cell Carcinoma 43 0.076
184
PLY150 Polykaryocytosis Inducer 31 0.076
186
CNG034 Congestive Heart Failure 69 0.074
187
P ART022 Arthritis 69 0.074
188
PNC129 Pancreatic Adenocarcinoma 68 0.074
189
FCT007 Factor Vii Deficiency 67 0.074
190
P SKN015 Skin Carcinoma 66 0.074
191
ATH013 Atherosclerosis Susceptibility 65 0.074
192
CLT003 Colitis 62 0.074
193
P CHR285 Chronic Myelomonocytic Leukemia 60 0.074
194
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.074
195
ULC004 Ulcerative Colitis 73 0.073
196
c ATS007 Autism Spectrum Disorder 67 0.073
197
CLN015 Colon Adenocarcinoma 65 0.073
198
ALK013 Alkaptonuria 58 0.073
199
P RHN004 Rhinitis 57 0.073
200
P GST044 Gastritis 56 0.073
201
P HYP076 Hyperthyroidism 55 0.073
202
END086 End Stage Renal Disease 51 0.073
203
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.073
204
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.073
205
ALL014 Allergic Encephalomyelitis 38 0.073
206
CHR178 Chromosomal Triplication 35 0.073
207
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.071
208
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.071
209
c HPT073 Hepatitis C Virus 72 0.071
210
P ATS364 Autism 70 0.071
211
P MYP004 Myopathy 70 0.071
212
P MJR001 Major Depressive Disorder 68 0.071
213
P DRM053 Dermatitis, Atopic 66 0.071
214
ACT119 Acute Promyelocytic Leukemia 63 0.071
215
P LTR001 Lateral Sclerosis 54 0.071
216
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.071
217
c PRM038 Primary Agammaglobulinemia 44 0.071
218
c HYP595 Hypertension, Essential 84 0.069
219
CYS001 Cystic Fibrosis 81 0.069
220
CRV035 Cervical Cancer 76 0.069
221
KPS004 Kaposi Sarcoma 75 0.069
222
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.069
223
P FLL037 Follicular Lymphoma 67 0.069
224
PLG002 Plague 63 0.069
225
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.069
226
P BND020 Bone Disease 59 0.069
227
EMB004 Embryonal Carcinoma 56 0.069
228
MCS002 Mucositis 56 0.069
229
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.069
230
c MJR024 Major Affective Disorder 9 41 0.069
231
c MJR022 Major Affective Disorder 8 38 0.069
232
BRN028 Brain Cancer 74 0.067
233
c SVR001 Severe Acute Respiratory Syndrome 62 0.067
234
PRG017 Paraganglioma and Gastric Stromal Sarcoma 61 0.067
235
ATS010 Autosomal Recessive Disease 48 0.067
236
RNL077 Renal Fibrosis 47 0.067
237
CHR074 Choriocarcinoma 47 0.067
238
HPT004 Hepatic Coma 45 0.067
239
GST040 Gastric Adenocarcinoma 70 0.065
240
P HRS035 Hirschsprung Disease 1 65 0.065
241
LPD008 Lipid Metabolism Disorder 62 0.065
242
MRG003 Marginal Zone B-Cell Lymphoma 52 0.065
243
P SPP010 Suppressor of Tumorigenicity 3 51 0.065
244
LYM012 Lymphoplasmacytic Lymphoma 47 0.065
245
ADL002 Adult Syndrome 70 0.063
246
EWN003 Ewing Sarcoma 69 0.063
247
ALC007 Alcohol Dependence 66 0.063
248
P MCR115 Microvascular Complications of Diabetes 5 66 0.063
249
HMT002 Hematologic Cancer 62 0.063
250
HPT019 Hepatic Encephalopathy 60 0.063
251
CHL123 Chlamydia 59 0.063
252
P SZR006 Seizure Disorder 56 0.063
253
P MLN007 Male Infertility 55 0.063
254
P GRV001 Graves' Disease 55 0.063
255
BRN015 Bronchiolo-Alveolar Adenocarcinoma 54 0.063
256
P TRM003 Tremor 54 0.063
257
WTH001 Withdrawal Disorder 48 0.063
258
P FML011 Familial Adenomatous Polyposis 72 0.061
259
P DBT009 Diabetes Mellitus 64 0.061
260
PRT036 Peritonitis 64 0.061
261
WLD007 Waldenstroem's Macroglobulinemia 61 0.061
262
SPN186 Spinal Cord Injury 60 0.061
263
c ACT027 Acute Pancreatitis 60 0.061
264
P BRS044 Breast Adenocarcinoma 59 0.061
265
c CHR417 Chronic Graft Versus Host Disease 57 0.061
266
TRN018 Transitional Cell Carcinoma 56 0.061
267
c MCR113 Microvascular Complications of Diabetes 3 52 0.061
268
THY030 Thyroid Gland Disease 52 0.061
269
BRN071 Brain Injury 49 0.061
270
c MCR120 Microvascular Complications of Diabetes 7 47 0.061
271
RTC005 Reticulosarcoma 47 0.061
272
PTT037 Pituitary Tumors 44 0.061
273
c MCR130 Microvascular Complications of Diabetes 6 41 0.061
274
c MCR133 Microvascular Complications of Diabetes 4 41 0.061
275
PST092 Posttransplant Acute Limbic Encephalitis 29 0.061
276
AST005 Asthma 76 0.059
277
c MNN043 Meningioma, Familial 74 0.059
278
CRH001 Crohn's Disease 74 0.059
279
c HYP836 Hypercholesterolemia, Familial, 1 73 0.059
280
P VSC011 Vasculitis 62 0.059
281
MNN042 Meningioma, Radiation-Induced 62 0.059
282
ACN002 Acanthosis Nigricans 60 0.059
283
VSL002 Visual Epilepsy 59 0.059
284
LYM027 Lymphopenia 58 0.059
285
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 56 0.059
286
P SML001 Small Cell Carcinoma 52 0.059
287
PNG002 Pain Agnosia 51 0.059
288
SPN021 Spinal Meningioma 50 0.059
289
c SVR005 Severe Pre-Eclampsia 50 0.059
290
P SCK005 Sickle Cell Disease 50 0.059
291
NTR046 Neutrophil Migration 50 0.059
292
PRN014 Paronychia 49 0.059
293
CRB004 Cerebral Artery Occlusion 45 0.059
294
DWR001 Dwarfism 44 0.059
295
MST004 Mast Cell Neoplasm 42 0.059
296
SCR001 Secretory Meningioma 41 0.059
297
EXT007 Extracutaneous Mastocytoma 38 0.059
298
c MLG157 Malignant Pheochromocytoma 38 0.059
299
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.059
300
P MDL005 Medulloblastoma 77 0.057
301
ANX010 Anxiety 73 0.057
302
P HNT016 Huntington Disease 72 0.057
303
P MYC007 Myocardial Infarction 70 0.057
304
P MSC005 Muscular Dystrophy 66 0.057
305
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.057
306
P PLY014 Polycystic Kidney Disease 62 0.057
307
HSH003 Hashimoto Thyroiditis 62 0.057
308
BRS099 Breast Ductal Carcinoma 62 0.057
309
P CTR002 Cataract 60 0.057
310
ORL011 Oral Cancer 60 0.057
311
CNS004 Constipation 58 0.057
312
P INF032 Infertility 57 0.057
313
THY122 Thyroid Gland Cancer 57 0.057
314
P CRD246 Cardiovascular System Disease 57 0.057
315
P PLY011 Polycystic Ovary Syndrome 56 0.057
316
P NRP001 Neuropathy 56 0.057
317
P INS002 in Situ Carcinoma 53 0.057
318
c LRG001 Large Cell Carcinoma 50 0.057
319
PPL002 Papillary Carcinoma 47 0.057
320
PLL012 Pollen Allergy 46 0.057
321
OVR094 Ovarian Epithelial Cancer 38 0.057
322
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.057
323
P HRT032 Heart Disease 75 0.055
324
P MLT020 Multiple Sclerosis 72 0.055
325
c CHR684 Chronic Kidney Disease 70 0.055
326
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.055
327
P LPS002 Liposarcoma 65 0.055
328
NNN026 Noonan Syndrome with Multiple Lentigines 62 0.055
329
FTT001 Fatty Liver Disease 61 0.055
330
c MLT159 Multiple Endocrine Neoplasia, Type Iib 60 0.055
331
STT001 Status Epilepticus 60 0.055
332
c MST023 Mesothelioma, Malignant 57 0.055
333
SCH014 Schistosomiasis 57 0.055
334
PLM010 Pulmonary Edema 54 0.055
335
P BRC006 Brachydactyly 53 0.055
336
DMY004 Demyelinating Disease 52 0.055
337
TLN003 Telangiectasis 52 0.055
338
c ACT135 Acute Graft Versus Host Disease 52 0.055
339
ANH002 Anhidrosis 47 0.055
340
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.055
341
MXD026 Mixed Glioma 45 0.055
342
P MJR007 Major Affective Disorder 1 43 0.055
343
c MLG079 Malignant Pleural Mesothelioma 42 0.055
344
HWK001 Hawkinsinuria 42 0.055
345
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.055
346
HRW001 Hair Whorl 36 0.055
347
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 28 0.055
348
TYR015 Tyrosinosis 20 0.055
349
P ATX030 Ataxia-Telangiectasia 82 0.053
350
c ATR087 Atrial Standstill 1 75 0.053
351
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.053
352
DFC004 Deficiency Anemia 70 0.053
353
P TRN020 Turner Syndrome 67 0.053
354
ACH004 Achondroplasia 66 0.053
355
LSH001 Leishmaniasis 63 0.053
356
P MVM001 Movement Disease 63 0.053
357
DRM006 Dermatitis 61 0.053
358
c WLM018 Wilms Tumor 5 61 0.053
359
c HPT016 Hepatitis B 59 0.053
360
IGR001 Ige Responsiveness, Atopic 59 0.053
361
P LYM033 Lymphoproliferative Syndrome 59 0.053
362
NRN004 Neuroendocrine Tumor 55 0.053
363
THR004 Thrombocytosis 51 0.053
364
c INF023 Inflammatory Breast Carcinoma 50 0.053
365
c FLL041 Follicular Lymphoma 1 49 0.053
366
ADN009 Adenosquamous Carcinoma 47 0.053
367
NRN001 Neuroendocrine Carcinoma 47 0.053
368
TRT001 Teratocarcinoma 45 0.053
369
ATN004 Autonomic Neuropathy 45 0.053
370
P HYP265 Hypotonia 43 0.053
371
P KLZ004 Kala-Azar 1 41 0.053
372
P MLG074 Malignant Mesenchymoma 40 0.053
374
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.053
375
ISL085 Isolated Agammaglobulinemia 19 0.053
376
c NRF023 Neurofibromatosis, Type Ii 80 0.050
377
P RSP003 Respiratory Failure 74 0.050
378
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.050
379
LNG039 Lung Squamous Cell Carcinoma 66 0.050
380
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.050
381
LPP008 Lipoprotein Quantitative Trait Locus 62 0.050
382
P HYP750 Hypertriglyceridemia, Familial 62 0.050
383
ACQ007 Acquired Immunodeficiency Syndrome 60 0.050
384
P URT039 Urticaria 58 0.050
385
CMR002 Coumarin Resistance 56 0.050
386
c ACT134 Acute Liver Failure 56 0.050
387
P NRF002 Neurofibromatosis 56 0.050
388
SYN007 Synovitis 54 0.050
389
P MNC007 Monocytic Leukemia 53 0.050
390
KRT009 Keratosis 51 0.050
391
HYP781 Hypoascorbemia 51 0.050
392
P HRD021 Hereditary Sensory Neuropathy 48 0.050
393
c INH020 Inherited Metabolic Disorder 47 0.050
394
RTN020 Retinal Vascular Disease 46 0.050
395
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.050
396
MSN004 Mesenchymal Cell Neoplasm 41 0.050
397
BBN001 Bubonic Plague 41 0.050
398
c TYR011 Tyrosinemia, Type Iii 40 0.050
399
PLC002 Plica Syndrome 36 0.050
400
NRL016 Neural Tube Defects 82 0.048
401
P RTN008 Retinitis Pigmentosa 79 0.048
402
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.048
403
P OST001 Osteopetrosis 70 0.048
404
P FRG001 Fragile X Syndrome 70 0.048
405
MST024 Mastocytosis, Cutaneous 69 0.048
406
CHG001 Chagas Disease 66 0.048
407
TTN003 Tetanus 65 0.048
408
DRM014 Dermatofibrosarcoma Protuberans 65 0.048
409
CLR108 Colorectal Adenoma 64 0.048
410
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.048
411
HYP020 Hyperprolactinemia 64 0.048
412
HYP780 Hypoadrenocorticism, Familial 63 0.048
413
P LMY004 Leiomyosarcoma 63 0.048
414
MSL001 Measles 62 0.048
415
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.048
416
P HMN010 Hemangioma 61 0.048
417
ANT024 Anthrax Disease 58 0.048
418
P PRN023 Prion Disease 57 0.048
419
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.048
420
PPL022 Papilloma 54 0.048
421
P PTS002 Ptosis 53 0.048
422
PLM014 Pleomorphic Adenoma 52 0.048
423
ART140 Arteries, Anomalies of 52 0.048
424
DFF036 Differentiated Thyroid Carcinoma 52 0.048
425
LMY002 Leiomyoma 52 0.048
426
TRM010 Traumatic Brain Injury 51 0.048
427
URM002 Uremia 49 0.048
428
CHR563 Chronic Eosinophilic Leukemia 48 0.048
429
KHN001 Kuhnt-Junius Degeneration 47 0.048
430
RTN023 Retinitis 46 0.048
431
SQM002 Squamous Cell Papilloma 46 0.048
432
P CHR345 Chronic Pain 44 0.048
433
HMP009 Haemophilus Influenzae 43 0.048
434
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.048
435
NRR001 Neuroretinitis 42 0.048
436
TTT001 Tatton-Brown-Rahman Syndrome 41 0.048
437
SYS071 Systemic Autoimmune Disease 37 0.048
438
HYP679 Hypoglossia-Hypodactylia 34 0.048
439
PPL052 Papillomatosis, Confluent and Reticulated 33 0.048
440
ARG004 Argyria 27 0.048
441
NTR055 Ntrk1 Congenital Insensitivity to Pain with Anhidrosis 12 0.048
442
VNH007 Von Hippel-Lindau Syndrome 73 0.045
443
P PNM007 Pneumonia 68 0.045
444
P MYC084 Mycobacterium Tuberculosis 1 68 0.045
445
SKN019 Skin Melanoma 68 0.045
446
CNN005 Connective Tissue Disease 68 0.045
447
P HPT021 Hepatitis 67 0.045
448
c MGR028 Migraine with or Without Aura 1 67 0.045
449
KRT019 Keratitis, Hereditary 65 0.045
450
P PRD008 Periodontitis 64 0.045
451
TRN015 Transient Cerebral Ischemia 63 0.045
452
c BRN108 Branchiootic Syndrome 1 62 0.045
453
HYP810 Hypereosinophilic Syndrome, Idiopathic 62 0.045
454
P PNC044 Pancreatitis 61 0.045
455
GST033 Gestational Diabetes 61 0.045
456
CHC001 Chickenpox 60 0.045
457
P MYC008 Myocarditis 59 0.045
458
P CYS018 Cystitis 59 0.045
459
c ACT075 Acute Myocardial Infarction 57 0.045
460
THR024 Thrombosis 57 0.045
461
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.045
462
P ADL017 Adult T-Cell Leukemia 56 0.045
463
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.045
464
AGN016 Aging 56 0.045
465
END040 Endogenous Depression 55 0.045
466
NNL006 Non-Alcoholic Steatohepatitis 54 0.045
467
P RTN016 Retinal Degeneration 53 0.045
468
GTR002 Goiter 53 0.045
469
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.045
470
CLR109 Colorectal Adenocarcinoma 51 0.045
471
P OVR082 Overgrowth Syndrome 50 0.045
472
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.045
473
P RBN002 Robinow Syndrome 49 0.045
474
HST010 Histiocytosis 48 0.045
475
P CLL015 Collagen Disease 47 0.045
476
c DRR009 Diarrhea 6 46 0.045
477
LRG014 Large Cell Neuroendocrine Carcinoma 44 0.045
478
CRB090 Cerebral Hypoxia 44 0.045
479
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.045
480
INT029 Interleukin-7 Receptor Alpha Deficiency 22 0.045
481
MLR004 Malaria 81 0.042
482
P RTT002 Rett Syndrome 80 0.042
483
c DLT002 Dilated Cardiomyopathy 79 0.042
484
OST012 Osteoarthritis 78 0.042
485
P SRC025 Sarcoidosis 1 70 0.042
486
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.042
487
P SYS005 Systemic Scleroderma 68 0.042
488
P OLG002 Oligodendroglioma 67 0.042
489
IRR002 Irritable Bowel Syndrome 65 0.042
490
c WLM013 Wilms Tumor 1 65 0.042
491
ANG020 Angiosarcoma 64 0.042
492
GT001 Gout 64 0.042
493
P ART023 Arthropathy 62 0.042
494
P THN009 Thanatophoric Dysplasia, Type I 62 0.042
495
CRC021 Carcinosarcoma 62 0.042
496
VRL011 Viral Infectious Disease 61 0.042
497
P BNG030 Benign Ependymoma 60 0.042
498
P VNT002 Ventricular Septal Defect 60 0.042
499
P ALP009 Alopecia Areata 60 0.042
500
c ACT071 Acute Kidney Failure 60 0.042
501
SPP011 Suppression of Tumorigenicity 12 59 0.042
502
DCT002 Ductal Carcinoma in Situ 59 0.042
503
P ALC033 Alcohol Use Disorder 58 0.042
504
THY022 Thymic Carcinoma 57 0.042
505
PLS011 Plasmacytoma 56 0.042
506
c GRV008 Graves Disease 1 56 0.042
507
HRY003 Hairy Cell Leukemia 55 0.042
508
P PMP001 Pemphigus 54 0.042
509
GLS001 Gliosarcoma 54 0.042
510
P RST001 Restless Legs Syndrome 54 0.042
511
CLL010 Cellular Ependymoma 54 0.042
512
SNS003 Sensory Peripheral Neuropathy 54 0.042
513
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.042
514
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.042
515
c BRC051 Brachydactyly, Type B1 51 0.042
516
P NML001 Nemaline Myopathy 49 0.042
517
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.042
518
CRN027 Corneal Neovascularization 47 0.042
519
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.042
520
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.042
521
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.042
522
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.042
523
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.042
524
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.042
525
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.042
526
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.042
527
BCL002 B Cell Deficiency 43 0.042
528
SKL017 Skeletal Dysplasias 40 0.042
529
AML001 Amelanotic Melanoma 39 0.042
530
SCR011 Scrapie 39 0.042
531
THR123 Thrombotic Microangiopathy 36 0.042
532
c PRS136 Prostate Cancer, Hereditary, 6 33 0.042
533
c PRS130 Prostate Cancer, Hereditary, 8 32 0.042
534
CHR176 Chromophil Renal Cell Carcinoma 23 0.042
535
PRP027 Peripheral Vascular Disease 71 0.039
536
P AMY004 Amyloidosis 70 0.039
537
ADN011 Adenoid Cystic Carcinoma 70 0.039
538
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.039
539
ODN023 Odontochondrodysplasia 68 0.039
540
P CRD119 Cardiac Arrest 67 0.039
541
CRB039 Cerebrovascular Disease 67 0.039
542
MRK001 Merkel Cell Carcinoma 65 0.039
543
END041 Endometrial Adenocarcinoma 63 0.039
544
P END044 Endometriosis 63 0.039
545
P ESP024 Esophagitis 62 0.039
546
P NPH012 Nephrotic Syndrome 60 0.039
547
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.039
548
P MLN069 Melanoma, Uveal 59 0.039
549
P ERY058 Erythrocytosis, Familial, 1 59 0.039
550
GRD007 Grade Iii Astrocytoma 59 0.039
551
GST045 Gastroenteritis 59 0.039
552
CHR072 Chordoma 58 0.039
553
P PRP019 Peripheral Nervous System Disease 58 0.039
554
c THY102 Thyroid Cancer, Nonmedullary, 2 58 0.039
555
P FCL005 Focal Segmental Glomerulosclerosis 57 0.039
556
SKN022 Skin Squamous Cell Carcinoma 57 0.039
557
P CHN012 Chondrosarcoma 56 0.039
558
SML019 Smallpox 56 0.039
559
P SBS003 Substance Abuse 55 0.039
560
PRP030 Purpura 54 0.039
561
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.039
562
HMS001 Hemosiderosis 54 0.039
563
P CNT005 Central Nervous System Lymphoma 53 0.039
564
P INT068 Intestinal Disease 53 0.039
565
SRS001 Serous Cystadenocarcinoma 52 0.039
566
P TRT010 Teratoma 52 0.039
567
OCL069 Ocular Motor Apraxia 51 0.039
568
PRS021 Prostatic Adenoma 51 0.039
569
PLS009 Plasma Cell Neoplasm 51 0.039
570
PLC008 Placenta Disease 50 0.039
571
TRY001 Trypanosomiasis 50 0.039
572
HRT011 Heart Septal Defect 50 0.039
573
HYP017 Hypophosphatemia 50 0.039
574
c CHR418 Chronic Leukemia 49 0.039
575
IGG001 Iga Glomerulonephritis 48 0.039
576
THY128 Thyroid Tumor 47 0.039
577
KRT008 Keratopathy 47 0.039
578
LYM009 Lymphocytic Choriomeningitis 47 0.039
579
P ATM019 Autoimmune Polyendocrine Syndrome 46 0.039
580
P MYC033 Myoclonus 46 0.039
581
URT010 Ureteral Obstruction 45 0.039
582
CHL149 Childhood Acute Myeloid Leukemia 44 0.039
583
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.039
584
CVD001 Covid-19 44 0.039
585
c CNG023 Congenital Fibrosarcoma 42 0.039
586
ATX019 Ataxia with Vitamin E Deficiency 42 0.039
587
P RRH023 Rare Hereditary Hemochromatosis 41 0.039
588
PLY100 Polyploidy 40 0.039
589
c OVR114 Ovarian Cancer 1 38 0.039
590
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.039
591
PLM196 Pulmonary Adenocarcinoma in Situ 34 0.039
592
GTP002 Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia 21 0.039
594
c THR092 Thrombophilia Due to Thrombin Defect 73 0.035
595
BRN024 Bronchitis 68 0.035
596
GST092 Gastroesophageal Reflux 67 0.035
597
PSY004 Psychotic Disorder 67 0.035
598
FLL027 Fallopian Tube Carcinoma 67 0.035
599
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.035
600
P HYD006 Hydrocephalus 66 0.035
601
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.035
602
KWS002 Kawasaki Disease 65 0.035
603
P ADL010 Adult Respiratory Distress Syndrome 65 0.035
604
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.035
605
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.035
606
ANR007 Anorexia Nervosa 63 0.035
607
RHB001 Rhabdoid Cancer 63 0.035
608
c HPT001 Hepatitis C 62 0.035
609
BLD131 Bladder Urothelial Carcinoma 62 0.035
610
NTR005 Nutritional Deficiency Disease 62 0.035
611
OST003 Osteonecrosis 61 0.035
612
c PNS012 Paine Syndrome 61 0.035
613
SDD001 Sudden Infant Death Syndrome 61 0.035
614
ETN001 Eating Disorder 60 0.035
615
P THL005 Thalassemia 60 0.035
616
P MCR010 Microcephaly 59 0.035
617
PPT005 Peptic Ulcer Disease 59 0.035
618
SRC027 Sarcoma, Synovial 58 0.035
619
CRD132 Cardiac Conduction Defect 58 0.035
620
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.035
621
LNG108 Langerhans Cell Histiocytosis 58 0.035
622
P GLL018 Gallbladder Cancer 57 0.035
623
P UVT001 Uveitis 57 0.035
624
GLS018 Glass Syndrome 57 0.035
625
MCR013 Microphthalmia 57 0.035
626
BLR008 Bilirubin Metabolic Disorder 57 0.035
627
LMY014 Leiomyoma, Uterine 56 0.035
628
HPT022 Hepatoblastoma 56 0.035
629
HYP005 Hypokalemia 55 0.035
630
VSC003 Visceral Leishmaniasis 55 0.035
631
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.035
632
PNC001 Pancytopenia 54 0.035
633
PRS045 Prostatic Hypertrophy 53 0.035
634
GST023 Gastric Ulcer 53 0.035
635
P PRG013 Paraganglioma 52 0.035
636
PRP016 Paraplegia 52 0.035
637
c VRL010 Viral Hepatitis 52 0.035
638
IMP005 Impotence 52 0.035
640
P PRC012 Pericardial Effusion 51 0.035
641
SKN013 Skin Benign Neoplasm 51 0.035
642
P CHL066 Cholangitis 51 0.035
643
LNT004 Lentigines 50 0.035
644
P PRT096 Peritoneal Mesothelioma 50 0.035
645
ECT026 Ectopic Pregnancy 50 0.035
646
DYS073 Dysphagia 50 0.035
647
P ATR005 Atrophic Gastritis 50 0.035
648
ENT004 Enthesopathy 49 0.035
649
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.035
650
PRS129 Prostatic Hyperplasia, Benign 49 0.035
651
MYL003 Myeloid Sarcoma 49 0.035
652
P CTN015 Cutaneous T Cell Lymphoma 49 0.035
653
HMP001 Hemopericardium 48 0.035
654
c PRM226 Primary Central Nervous System Lymphoma 48 0.035
655
P HMN032 Human Herpesvirus 8 47 0.035
656
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.035
657
CNT033 Central Nervous System Cancer 47 0.035
658
RYN005 Raynaud Phenomenon 47 0.035
659
ATN005 Autonomic Dysfunction 46 0.035
660
ALB002 Albinism 46 0.035
661
c CLR017 Clear Cell Sarcoma 45 0.035
662
P FBR003 Fibrous Histiocytoma 44 0.035
663
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.035
664
MDD018 Middle East Respiratory Syndrome 43 0.035
665
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.035
666
TRP009 Triple X Syndrome 42 0.035
667
CHR286 Chronic Neutrophilic Leukemia 42 0.035
668
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.035
669
FBR019 Fibromatosis 41 0.035
670
MRP001 Morphine Dependence 41 0.035
671
ANX004 Anoxia 40 0.035
672
P ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 40 0.035
673
P 8P1002 8p11 Myeloproliferative Syndrome 39 0.035
674
DBT020 Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 39 0.035
675
OCH001 Ochronosis 38 0.035
676
P PRC031 Preeclampsia/eclampsia 1 38 0.035
677
GLM044 Glomerular Disease 37 0.035
678
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.035
679
ACT162 Acute Sensory Ataxic Neuropathy 26 0.035
680
ADG002 Audiogenic Seizures 25 0.035
681
STR067 Stroke, Ischemic 81 0.032
682
P APL001 Aplastic Anemia 74 0.032
683
P OST002 Osteoporosis 74 0.032
684
c SPN225 Spondyloarthropathy 1 73 0.032
685
P CNR004 Cone-Rod Dystrophy 2 73 0.032
686
MLT157 Multiple System Atrophy 1 70 0.032
687
PLM001 Pulmonary Tuberculosis 69 0.032
688
P LPR021 Leprosy 3 69 0.032
689
P MPL001 Maple Syrup Urine Disease 69 0.032
690
CRZ001 Crouzon Syndrome 68 0.032
691
PCK003 Pick Disease of Brain 68 0.032
692
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.032
693
P CHR012 Chronic Granulomatous Disease 67 0.032
694
MYC006 Mycosis Fungoides 66 0.032
695
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.032
696
ANG054 Angina Pectoris 66 0.032
697
P DMN002 Dementia 66 0.032
698
P CNG001 Congenital Myasthenic Syndrome 66 0.032
699
P NRV007 Nervous System Disease 66 0.032
700
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.032
701
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.032
702
BRR014 Barrett Esophagus 65 0.032
703
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.032
704
NRF007 Neurofibroma 64 0.032
705
CLF027 Cleft Palate, Isolated 64 0.032
706
c JVN010 Juvenile Rheumatoid Arthritis 64 0.032
707
c CNG006 Congenital Hypothyroidism 64 0.032
708
MGK001 Megakaryocytic Leukemia 64 0.032
709
P HML002 Hemolytic Anemia 63 0.032
710
P HYP069 Hyperparathyroidism 63 0.032
711
c MLG084 Malignant Fibrous Histiocytoma 63 0.032
712
c HPT003 Hepatitis a 62 0.032
713
P PRM006 Primary Biliary Cirrhosis 62 0.032
714
P ENC004 Encephalitis 61 0.032
715
RTN017 Retinal Detachment 61 0.032
716
NRL005 Neurilemmoma 60 0.032
717
HRP004 Herpes Zoster 60 0.032
718
SZR001 Sezary's Disease 60 0.032
719
DPH001 Diphtheria 60 0.032
720
c LPM012 Lipomatosis, Multiple 60 0.032
721
P OCL002 Oculocutaneous Albinism 60 0.032
722
PRT058 Pure Autonomic Failure 59 0.032
723
c HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 59 0.032
724
BRN002 Bronchiolitis 59 0.032
725
P DNG005 Dengue Virus 59 0.032
726
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.032
727
FBR047 Fibromyalgia 58 0.032
728
BRS051 Breast Disease 58 0.032
729
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.032
730
P BNC003 Bone Cancer 58 0.032
731
P CND004 Candidiasis 58 0.032
732
c CHL119 Cholangitis, Primary Sclerosing 57 0.032
733
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.032
734
JPN002 Japanese Encephalitis 57 0.032
735
GST050 Gastrointestinal System Disease 56 0.032
736
P PLY180 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 1 56 0.032
737
BRN012 Bronchiolitis Obliterans 55 0.032
738
LMB062 Limb Ischemia 55 0.032
739
P PTT006 Pituitary Adenoma 55 0.032
740
GNG005 Gangliocytoma 55 0.032
741
TRD006 Tardive Dyskinesia 54 0.032
742
AMN003 Amnestic Disorder 54 0.032
743
GNG004 Ganglioglioma 54 0.032
744
P LNG035 Lung Large Cell Carcinoma 54 0.032
745
P TCD001 Tic Disorder 53 0.032
746
PRP036 Peripheral T-Cell Lymphoma 53 0.032
747
P CTN003 Cutaneous Lupus Erythematosus 53 0.032
748
GNG002 Ganglioneuroma 52 0.032
749
CHR073 Choreatic Disease 52 0.032
750
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.032
751
P RCT021 Rectum Cancer 52 0.032
752
P MSC003 Muscular Atrophy 52 0.032
753
P NRC002 Narcolepsy 52 0.032
754
NTR018 Neutrophilia, Hereditary 52 0.032
755
SPN051 Spondylitis 51 0.032
756
ENT011 Enterocolitis 51 0.032
757
SPL004 Splenic Marginal Zone Lymphoma 51 0.032
758
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.032
759
CRN030 Coronary Stenosis 50 0.032
760
P TMP001 Temporal Lobe Epilepsy 50 0.032
761
AGG002 Aggressive Systemic Mastocytosis 49 0.032
762
MNN009 Meningoencephalitis 49 0.032
763
ACT029 Acute Interstitial Pneumonia 49 0.032
764
ADR016 Adrenal Cortical Carcinoma 48 0.032
765
CKT002 Cakut 48 0.032
766
HYP043 Hyperandrogenism 48 0.032
767
CCN001 Cocaine Dependence 48 0.032
768
RFR010 Refractory Anemia 48 0.032
769
P SCL009 Sclerosing Cholangitis 48 0.032
770
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.032
771
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.032
772
PRL017 Prolymphocytic Leukemia 47 0.032
773
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.032
774
MYC005 Myocardial Stunning 46 0.032
775
MGC001 Megacolon 46 0.032
776
FLL008 Folliculitis 46 0.032
777
GLC036 Glucagonoma 45 0.032
778
CRT015 Carotid Artery Occlusion 45 0.032
780
APP009 Appendix Adenocarcinoma 44 0.032
781
P PRL003 Proliferative Glomerulonephritis 44 0.032
782
ART006 Arthus Reaction 44 0.032
783
FBR054 Fibroma 44 0.032
784
ANP009 Anaplastic Oligodendroglioma 43 0.032
785
SMN007 Seminoma 43 0.032
786
MYX004 Myxedema 43 0.032
787
BNM001 Bone Marrow Cancer 43 0.032
788
MXD050 Mixed Phenotype Acute Leukemia 43 0.032
789
VRL003 Variola Major 42 0.032
790
BLR013 Biliary Tract Cancer 42 0.032
791
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.032
792
MYF002 Myofascial Pain Syndrome 42 0.032
793
EST007 Estrogen Resistance 41 0.032
794
P RRT020 Rare Tumor 41 0.032
795
HST016 Histiocytic Sarcoma 39 0.032
796
ADR004 Adrenal Cortical Adenocarcinoma 39 0.032
797
HRN029 Hearing Loss, Noise-Induced 37 0.032
798
HNS001 Hansen's Disease 34 0.032
799
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.032
800
PPL050 Papillary Tumor of the Pineal Region 33 0.032
801
INF009 Inflammatory Spondylopathy 31 0.032
802
FML029 Familial Renal Papillary Carcinoma 31 0.032
803
MNG007 Manganese Poisoning 29 0.032
804
CD4001 Cd45 Deficiency 28 0.032
805
c ERY064 Erythrocytosis, Familial, 6 23 0.032
806
HML018 Homologous Wasting Disease 22 0.032
807
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.032
808
PFF001 Pfeiffer Syndrome 79 0.027
809
c NRF024 Neurofibromatosis, Type I 77 0.027
810
MSC157 Muscular Dystrophy, Duchenne Type 72 0.027
811
OTT002 Otitis Media 72 0.027
812
P EPL164 Epilepsy 71 0.027
813
P HYP061 Hypertrophic Cardiomyopathy 70 0.027
814
P SLP006 Sleep Apnea 69 0.027
815
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.027
816
P CRN037 Craniosynostosis 68 0.027
817
CMM004 Common Variable Immunodeficiency 68 0.027
818
OBS002 Obsessive-Compulsive Disorder 68 0.027
819
P INF038 Influenza 68 0.027
820
RCK004 Rickets 68 0.027
821
P FRN006 Frontotemporal Dementia 68 0.027
822
HYL004 Hyaline Fibromatosis Syndrome 67 0.027
823
c INF071 Inflammatory Bowel Disease 1 67 0.027
824
P BLD062 Bile Duct Cancer 67 0.027
825
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.027
826
P LNG028 Long Qt Syndrome 66 0.027
827
GLL008 Gilles De La Tourette Syndrome 66 0.027
828
GLN010 Glanzmann Thrombasthenia 66 0.027
829
MYX005 Myxoid Liposarcoma 66 0.027
830
P ART005 Arteriovenous Malformation 65 0.027
831
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 65 0.027
832
P MTR014 Motor Neuron Disease 65 0.027
833
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.027
834
P PRS038 Personality Disorder 65 0.027
835
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.027
836
MYC079 Myoclonic Epilepsy of Lafora 64 0.027
837
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 64 0.027
838
TBC004 Tobacco Addiction 64 0.027
839
CNT061 Conotruncal Heart Malformations 63 0.027
840
P CRN300 Coronary Heart Disease 1 63 0.027
841
c ATM011 Autoimmune Hepatitis 63 0.027
842
CHL068 Cholestasis 61 0.027
843
P INT143 Interstitial Cystitis 61 0.027
844
ALC006 Alcoholic Hepatitis 61 0.027
845
ALV005 Alveolar Soft Part Sarcoma 61 0.027
846
SHG001 Shigellosis 60 0.027
847
c JVN061 Juvenile Arthritis 60 0.027
848
HYP042 Hypochondroplasia 60 0.027
849
P ATR010 Atrial Heart Septal Defect 60 0.027
850
DNG002 Dengue Hemorrhagic Fever 60 0.027
851
VRC005 Varicose Veins 60 0.027
852
STF001 Stiff-Person Syndrome 60 0.027
853
c ALB021 Albinism, Oculocutaneous, Type Ii 59 0.027
854
PRT013 Portal Hypertension 59 0.027
855
PLM033 Pulmonary Embolism 59 0.027
856
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.027
857
P CNT004 Centronuclear Myopathy 59 0.027
858
HLC007 Helicobacter Pylori Infection 59 0.027
859
c SVR003 Severe Congenital Neutropenia 59 0.027
860
HYP458 Hyper Ige Syndrome 58 0.027
861
ADR005 Adrenal Carcinoma 58 0.027
862
IRN002 Iron Metabolism Disease 57 0.027
863
c LKM070 Leukemia, Acute Monocytic 57 0.027
864
P ANG015 Angioedema 57 0.027
865
P MYS005 Myositis 56 0.027
866
MTH009 Mouth Disease 56 0.027
867
SLC006 Silicosis 56 0.027
868
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 56 0.027
869
FLR001 Filarial Elephantiasis 55 0.027
870
c BCT007 Bacterial Meningitis 55 0.027
871
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 0.027
872
CHR100 Chronic Ulcer of Skin 55 0.027
873
FLR002 Filariasis 55 0.027
874
JVN009 Juvenile Pilocytic Astrocytoma 55 0.027
875
P LRY044 Larynx Cancer 55 0.027
876
P CYS039 Cystic Kidney Disease 54 0.027
877
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.027
878
P ART021 Arteriosclerosis 54 0.027
879
HLL004 Hellp Syndrome 54 0.027
880
SLP001 Sleeping Sickness 54 0.027
881
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.027
882
HRT012 Heart Valve Disease 53 0.027
883
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.027
884
P RNL017 Renal Oncocytoma 53 0.027
885
P EMB005 Embryonal Rhabdomyosarcoma 53 0.027
886
FNG017 Fungal Infectious Disease 53 0.027
887
NRT001 Neurotic Disorder 53 0.027
888
PRP080 Peripheral Artery Disease 53 0.027
889
OVR059 Ovary Adenocarcinoma 53 0.027
890
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.027
891
P DDN001 Duodenal Ulcer 52 0.027
892
DYS015 Dysentery 52 0.027
893
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.027
894
ACT200 Acute Monoblastic Leukemia 52 0.027
895
CYS014 Cystadenocarcinoma 51 0.027
896
P THR015 Thrombophilia 51 0.027
897
TNG007 Tongue Carcinoma 51 0.027
898
GNT002 Giant Cell Glioblastoma 50 0.027
899
P MMB011 Membranous Nephropathy 50 0.027
900
RTN003 Retinal Ischemia 50 0.027
901
PST021 Postpartum Depression 50 0.027
902
c HRD202 Hereditary Lymphedema I 50 0.027
903
c THR071 Thrombocytopenia 1 50 0.027
904
PRN009 Paranoid Schizophrenia 50 0.027
905
HYP748 Hypertelorism 50 0.027
906
OCL022 Ocular Melanoma 50 0.027
907
OPT003 Opiate Dependence 50 0.027
908
ONC007 Oncocytoma 49 0.027
909
VRR004 Verrucous Carcinoma 49 0.027
910
MCN001 Mucinous Adenocarcinoma 49 0.027
911
CCN002 Cocaine Abuse 49 0.027
912
DYS009 Dysthymic Disorder 49 0.027
913
P MGR001 Migraine Without Aura 49 0.027
914
DDF001 Dedifferentiated Liposarcoma 48 0.027
915
INT054 Intraocular Lymphoma 48 0.027
916
P LYM024 Lymphatic System Disease 48 0.027
917
HYP025 Hyperphosphatemia 48 0.027
918
HPR003 Heparin-Induced Thrombocytopenia 48 0.027
919
CRC014 Carcinoid Tumors, Intestinal 47 0.027
920
PLS025 Plasmablastic Lymphoma 47 0.027
921
ANV001 Anovulation 47 0.027
922
CHD004 Chudley-Mccullough Syndrome 46 0.027
923
END031 Endometrial Stromal Sarcoma 46 0.027
924
GST010 Gestational Trophoblastic Neoplasm 46 0.027
925
c EST002 Estrogen-Receptor Negative Breast Cancer 45 0.027
926
VNS013 Venous Malformations, Multiple Cutaneous and Mucosal 45 0.027
927
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.027
928
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.027
929
ACT003 Acute Kidney Tubular Necrosis 45 0.027
930
URT051 Ureter, Cancer of 45 0.027
931
BRN032 Brain Glioma 45 0.027
932
c CTR096 Cataract 6, Multiple Types 44 0.027
933
ASP026 Asplenia, Isolated Congenital 44 0.027
934
SBC016 Subacute Delirium 44 0.027
935
CYS009 Cystadenoma 44 0.027
936
PLX002 Plexiform Neurofibroma 44 0.027
937
PRT035 Peritoneum Cancer 44 0.027
938
MTR010 Mature Teratoma 44 0.027
939
END085 Endometrial Serous Adenocarcinoma 44 0.027
940
CLP005 Ciliopathy 43 0.027
941
c RHB023 Rhabdomyosarcoma, Embryonal, 1 43 0.027
942
P PRM293 Primary Mediastinal B-Cell Lymphoma 43 0.027
943
CRS001 Crescentic Glomerulonephritis 43 0.027
944
P HYP605 Hyperphenylalaninemia, Bh4-Deficient, B 43 0.027
945
LWC001 Low Compliance Bladder 43 0.027
946
CRB138 Core Binding Factor Acute Myeloid Leukemia 43 0.027
947
PNM013 Pneumococcal Meningitis 42 0.027
948
P CLS010 Cluster Headache 42 0.027
949
c PRG011 Progressive Myoclonus Epilepsy 42 0.027
950
OPS001 Opisthorchiasis 41 0.027
951
c PRM163 Primary Mediastinal Large B-Cell Lymphoma 41 0.027
952
THR035 Thrombasthenia 40 0.027
953
OST115 Osteonecrosis of the Jaw 40 0.027
954
PLM005 Pleomorphic Lipoma 40 0.027
955
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 40 0.027
956
KLD004 Keloid Disorder 40 0.027
957
P DYS021 Dysautonomia 39 0.027
958
P BCL005 B Cell Prolymphocytic Leukemia 39 0.027
959
URT035 Urethral Benign Neoplasm 39 0.027
960
IND002 Indolent Systemic Mastocytosis 39 0.027
961
P PRP021 Peripheral Nervous System Neoplasm 39 0.027
962
THY124 Thyroid Gland Papillary Carcinoma 38 0.027
963
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.027
964
NPH113 Nephroma 37 0.027
965
OVR105 Ovarian Serous Carcinoma 37 0.027
966
c CHR020 Chronic Interstitial Cystitis 37 0.027
967
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.027
968
P MYC026 Myoclonus Epilepsy 35 0.027
969
c MJR008 Major Affective Disorder 2 35 0.027
970
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.027
971
c MJR003 Major Affective Disorder 6 33 0.027
972
c MJR006 Major Affective Disorder 5 33 0.027
973
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 31 0.027
974
EXN003 Exencephaly 31 0.027
975
c RNG008 Ring Chromosome 13 31 0.027
976
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.027
977
CHR375 Chromosome 8p11 Myeloproliferative Syndrome 29 0.027
978
PRG074 Progressive Myoclonus Epilepsy, Lafora Type 29 0.027
979
PHS025 Phosphatase, Acid, of Tissues 28 0.027
980
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.027
981
TST003 Testicular Leukemia 27 0.027
982
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.027
983
MLG164 Malignant Epithelial Tumor of Ovary 26 0.027
984
HRP008 Herpes Simiae 25 0.027
985
c PRM243 Primary Bone Cancer 24 0.027
986
URT040 Urethral Cancer 23 0.027
987
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 23 0.027
988
CHN040 Choanal Atresia and Lymphedema 22 0.027
989
TRN058 Transitional Cell Cancer of the Renal Pelvis and Ureter 12 0.027
990
MTS005 Metastatic Squamous Neck Cancer with Occult Primary 11 0.027
991
ERL027 Early-Onset Non-Syndromic Cataract 10 0.027
992
SCK003 Sickle Cell Anemia 74 0.022
993
LPT014 Leptin Deficiency or Dysfunction 74 0.022
994
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.022
995
c EXD008 Exudative Vitreoretinopathy 1 71 0.022
996
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.022
997
BHC003 Behcet Syndrome 71 0.022
998
PTZ001 Peutz-Jeghers Syndrome 70 0.022
999
P TTR001 Tetralogy of Fallot 70 0.022
1000
P TBR001 Tuberous Sclerosis 70 0.022
1001
P ASP006 Aspergillosis 69 0.022
1002
WRN001 Werner Syndrome 69 0.022
1003
LYM007 Lymphangioleiomyomatosis 69 0.022
1004
P TMP003 Temporal Arteritis 68 0.022
1005
MLD001 Melioidosis 68 0.022
1006
STH001 Saethre-Chotzen Syndrome 67 0.022
1007
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 67 0.022
1008
c FML021 Familial Hypercholesterolemia 66 0.022
1009
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.022
1010
P ATR011 Atrial Fibrillation 66 0.022
1011
P MNN013 Meningitis 66 0.022
1012
KHL003 Kohlschutter-Tonz Syndrome 65 0.022
1013
P CNJ013 Conjunctivitis 65 0.022
1014
DMN031 Dementia, Lewy Body 65 0.022
1015
c ART101 Aortic Valve Disease 2 65 0.022
1016
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.022
1017
P PLR004 Pleuropulmonary Blastoma 65 0.022
1018
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.022
1019
NRM005 Neuromuscular Disease 64 0.022
1020
ART002 Arts Syndrome 64 0.022
1021
MSC007 Muscle Hypertrophy 64 0.022
1022
PLM031 Poliomyelitis 64 0.022
1023
DSM004 Desmoid Tumor 64 0.022
1024
LYM017 Lyme Disease 64 0.022
1025
OST017 Osteomyelitis 64 0.022
1026
c DPH024 Diaphragmatic Hernia, Congenital 63 0.022
1027
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.022
1028
P THR117 Three M Syndrome 1 63 0.022
1029
CHR063 Chronic Mucocutaneous Candidiasis 63 0.022
1030
BDD001 Budd-Chiari Syndrome 63 0.022
1031
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 0.022
1032
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.022
1033
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.022
1034
c FNC043 Fanconi Anemia, Complementation Group E 62 0.022
1035
DNH001 Donohue Syndrome 62 0.022
1036
P SPN046 Spinal Muscular Atrophy 62 0.022
1037
P TRC086 Trichohepatoenteric Syndrome 1 62 0.022
1038
BLL006 Bullous Pemphigoid 62 0.022
1039
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 62 0.022
1040
CTN007 Cutaneous Leishmaniasis 62 0.022
1041
P PRP029 Porphyria 62 0.022
1042
ATY005 Atypical Teratoid Rhabdoid Tumor 61 0.022
1043
PSR001 Psoriatic Arthritis 61 0.022
1044
INT002 Intermittent Claudication 61 0.022
1045
CHR001 Churg-Strauss Syndrome 61 0.022
1046
P TST021 Testicular Germ Cell Tumor 60 0.022
1047
P TXP001 Toxoplasmosis 60 0.022
1048
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.022
1049
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.022
1050
P SNS001 Sensorineural Hearing Loss 60 0.022
1051
HYD002 Hydronephrosis 60 0.022
1052
P OPT006 Optic Nerve Disease 60 0.022
1053
PBL005 Piebald Trait 59 0.022
1054
MYP136 Myopathy, Centronuclear, X-Linked 59 0.022
1055
ACH043 Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans 59 0.022
1056
ANR040 Aneurysm 59 0.022
1057
P INT070 Intestinal Obstruction 58 0.022
1058
P HYP726 Hypercalcemia, Infantile, 1 58 0.022
1059
RBS001 Rabies 58 0.022
1060
THY025 Thymus Cancer 58 0.022
1061
NWB001 Newborn Respiratory Distress Syndrome 58 0.022
1062
DSS008 Disease of Mental Health 58 0.022
1063
c DWL002 Dowling-Degos Disease 1 58 0.022
1064
PMP006 Pemphigus Vulgaris, Familial 57 0.022
1065
P ESP035 Esophagitis, Eosinophilic, 1 57 0.022
1066
CST005 Castleman Disease 57 0.022
1067
BRN056 Bronchopulmonary Dysplasia 57 0.022
1068
P SLV026 Salivary Gland Carcinoma 57 0.022
1069
P HDC001 Headache 57 0.022
1070
DSS009 Disseminated Intravascular Coagulation 57 0.022
1071
LYM021 Lymphadenitis 57 0.022
1072
APH001 Aphthous Stomatitis 57 0.022
1073
TNS005 Tonsillitis 57 0.022
1074
P FTL001 Fetal Alcohol Syndrome 57 0.022
1075
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 57 0.022
1076
VSC002 Vascular Dementia 57 0.022
1077
CRT033 Corticobasal Degeneration 57 0.022
1078
FRC011 Fructose Intolerance, Hereditary 57 0.022
1079
P PYL005 Pyelonephritis 56 0.022