Search results for myeloid malignancy

1335 hits were found for myeloid malignancy

# Family MCID Name MIFTS Score
1
PLT019 Platelet Disorder, Familial, with Associated Myeloid Malignancy 30 4.035
2
ERY024 Erythropoietic Uroporphyria Associated with Myeloid Malignancy 8 2.165
3
FML146 Familial Platelet Disorder with Propensity to Acute Myelogenous Leukemia 9 1.524
4
P LKM002 Leukemia 71 1.255
5
P MYL006 Myeloid Leukemia 66 1.192
6
c LKM061 Leukemia, Acute Myeloid 73 0.588
7
c CHR064 Chronic Monocytic Leukemia 42 0.514
8
c ACT073 Acute Leukemia 60 0.511
9
ACT118 Acute Non Lymphoblastic Leukemia 30 0.481
10
BNM001 Bone Marrow Cancer 51 0.419
11
MYL009 Myelodysplastic Syndrome 73 0.406
12
MRG013 Mirage Syndrome 29 0.396
13
SRC014 Sarcoma 66 0.370
14
PRM243 Primary Bone Cancer 29 0.370
15
P LYM118 Lymphoma 69 0.353
16
MLN008 Melanoma 62 0.352
17
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.346
18
BNC003 Bone Cancer 58 0.337
19
HMT002 Hematologic Cancer 64 0.336
20
c CHR418 Chronic Leukemia 47 0.328
21
MYL031 Myeloproliferative Neoplasm 58 0.314
22
P CHR562 Chronic Myelocytic Leukemia 41 0.302
23
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.298
24
c PRM023 Pre-Malignant Neoplasm 41 0.285
25
MYL003 Myeloid Sarcoma 48 0.281
26
c ACT020 Acute T Cell Leukemia 35 0.279
27
P LYM026 Lymphoblastic Leukemia 62 0.272
28
P GLM045 Glioma 60 0.271
29
HMT018 Hematopoietic Stem Cell Transplantation 41 0.264
30
RFR004 Refractory Hematologic Cancer 28 0.250
31
P NRV006 Nervous System Cancer 60 0.242
32
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 49 0.239
33
c MLG068 Malignant Glioma 51 0.236
34
LYM067 Lymphoid Leukemia 44 0.234
35
INC022 Inclusion-Cell Disease 46 0.232
36
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 15 0.218
37
MYL004 Myelodysplastic Myeloproliferative Cancer 45 0.214
38
LYM023 Lymphatic System Cancer 33 0.213
39
P LYM033 Lymphoproliferative Syndrome 56 0.211
40
LYM024 Lymphatic System Disease 52 0.208
41
P ACT074 Acute Lymphocytic Leukemia 56 0.207
42
ACT113 Acute Myeloblastic Leukemia with Maturation 37 0.205
43
ACT114 Acute Myeloblastic Leukemia Without Maturation 29 0.205
44
BNS002 Bone Structure Disease 37 0.205
45
PRP021 Peripheral Nervous System Neoplasm 46 0.204
46
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.204
47
OCL009 Ocular Cancer 59 0.203
48
c LKM062 Leukemia, Acute Lymphoblastic 64 0.201
49
c CHR090 Chronic Lymphocytic Leukemia 76 0.200
50
ACD009 Acid-Labile Subunit, Deficiency of 45 0.193
51
c ADL052 Adult Acute Lymphocytic Leukemia 44 0.193
52
LYM019 Lymphosarcoma 53 0.191
53
LYM040 Lymphoblastic Lymphoma 53 0.189
54
CHR285 Chronic Myelomonocytic Leukemia 56 0.188
55
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.186
56
c ADL001 Adult Lymphoma 39 0.185
57
P MNC007 Monocytic Leukemia 55 0.184
58
CHL061 Childhood Leukemia 49 0.184
59
ADL002 Adult Syndrome 52 0.182
60
MGK001 Megakaryocytic Leukemia 55 0.182
61
P ACT135 Acute Graft Versus Host Disease 53 0.179
62
ACT098 Acute Erythroid Leukemia 47 0.178
63
LKC003 Leukocyte Disease 43 0.178
64
c ACT009 Acute Monocytic Leukemia 52 0.177
65
P MYL005 Myelofibrosis 67 0.177
66
END072 Endotheliitis 42 0.175
67
ACT200 Acute Monoblastic Leukemia 42 0.175
68
c CLL013 Cell Type Cancer 46 0.175
69
BRT030 Birth Defects 43 0.174
70
PLS009 Plasma Cell Neoplasm 48 0.172
71
SNS023 Sensory System Cancer 43 0.172
72
BNL002 Bone Lymphoma 32 0.172
73
P BRS047 Breast Cancer 100 0.171
74
WLL006 Wells Syndrome 59 0.171
75
GDS001 Good Syndrome 44 0.170
76
P TCL004 T-Cell Leukemia 47 0.169
77
P HST010 Histiocytosis 58 0.169
78
c LKM055 Leukemia, Acute Lymphoblastic 2 19 0.169
79
c ADL093 Adult Acute Monocytic Leukemia 19 0.168
80
BLD053 Blood Platelet Disease 46 0.168
81
DFC004 Deficiency Anemia 64 0.167
82
c ADL017 Adult T-Cell Leukemia 60 0.167
83
KDS001 Kid Syndrome 53 0.165
84
NRL004 Neuroleptic Malignant Syndrome 41 0.165
85
P MLT019 Multiple Myeloma 83 0.164
86
CHL071 Child Syndrome 58 0.164
87
BND014 Bone Development Disease 40 0.164
88
ACR002 Acrocapitofemoral Dysplasia 33 0.164
89
P ORL007 Oral Cavity Cancer 59 0.163
90
PRS047 Prostatitis 56 0.162
91
CSY001 C Syndrome 50 0.161
92
ORL011 Oral Cancer 56 0.161
93
P NTR004 Neutropenia 59 0.161
94
P MDL005 Medulloblastoma 77 0.158
95
c CHR417 Chronic Graft Versus Host Disease 51 0.157
96
EWN003 Ewing Sarcoma 66 0.156
97
P BCL006 B-Cell Lymphomas 65 0.155
98
GRF001 Graft-Versus-Host Disease, Protection Against 52 0.155
99
CNT018 Central Nervous System Leukemia 37 0.153
100
PRM151 Primary Bone Lymphoma 26 0.153
101
HML018 Homologous Wasting Disease 13 0.152
102
c LKM060 Leukemia, Acute Lymphoblastic 3 50 0.150
103
TST021 Testicular Germ Cell Tumor 69 0.149
104
VSC006 Vascular Cancer 51 0.149
105
P ADN016 Adenocarcinoma 69 0.149
106
PLS016 Plasma Cell Leukemia 42 0.148
107
BLD054 Blood Protein Disease 37 0.145
108
P HPT021 Hepatitis 69 0.144
109
P THY032 Thyroiditis 54 0.144
110
c MLG054 Malignant Histiocytosis 49 0.144
111
GRM001 Germ Cell and Embryonal Cancer 36 0.143
112
PRT036 Peritonitis 63 0.142
113
c LYM107 Lymphoproliferative Syndrome 2 50 0.141
114
RFR010 Refractory Anemia 45 0.141
115
c LYM106 Lymphoproliferative Syndrome 1 32 0.141
116
FRB001 Farber Lipogranulomatosis 53 0.140
117
c LKM056 Leukemia, Chronic Lymphocytic 2 21 0.139
118
P LNG032 Lung Cancer 95 0.138
119
HRT007 Heart Cancer 46 0.137
120
c LKM050 Leukemia, Chronic Lymphocytic 1 19 0.137
121
P TRT010 Teratoma 52 0.137
122
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 34 0.136
123
P PNC044 Pancreatitis 61 0.136
124
ACR041 Acromelic Frontonasal Dysostosis 45 0.135
125
ATY042 Atypical Chronic Myeloid Leukemia 48 0.134
126
P HRT017 Heart Tumor 32 0.134
127
LYM115 Lymphoma, Non-Hodgkin 63 0.133
128
c ADL079 Adult Heart Tumor 16 0.133
129
c LKM004 Leukemia, B-Cell, Chronic 24 0.132
130
P HPT023 Hepatocellular Carcinoma 92 0.131
131
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.131
132
ADN018 Adenoma 58 0.130
133
P CHR084 Chromosomal Disease 32 0.130
134
SQM006 Squamous Cell Carcinoma 70 0.129
135
CRB138 Core Binding Factor Acute Myeloid Leukemia 42 0.129
136
P AST007 Astrocytoma 65 0.127
137
CNT010 Central Nervous System Hematologic Cancer 18 0.125
138
P GLB002 Glioblastoma 68 0.124
139
MXD023 Mixed Cell Type Cancer 44 0.124
140
P BLD051 Blood Coagulation Disease 42 0.124
141
P RFR008 Refractory Anemia with Excess Blasts 31 0.124
142
P HMR003 Hemorrhagic Disease 57 0.123
143
ACT228 Acute Radiation Syndrome 20 0.122
144
CRD118 Cardiovascular Cancer 44 0.122
145
VSC008 Vascular Hemostatic Disease 30 0.122
146
c LKM005 Leukemia, T-Cell, Chronic 20 0.120
147
P CLR023 Colorectal Cancer 97 0.118
148
c LKM051 Leukemia, Chronic Lymphocytic 3 19 0.117
149
ARG006 Aregenerative Anemia 22 0.117
150
PCK002 Pick Disease 68 0.116
151
BRN028 Brain Cancer 70 0.116
152
P PRT096 Peritoneal Mesothelioma 52 0.115
153
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 39 0.115
154
NTR003 Natural Killer Cell Leukemia 47 0.115
155
P GST049 Gastrointestinal System Cancer 60 0.113
156
HDG012 Hodgkin Lymphoma 77 0.113
157
c MLG002 Malignant Peritoneal Mesothelioma 46 0.112
158
c PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 22 0.112
159
c RTN162 Retinitis Pigmentosa 2 48 0.111
160
P PNC035 Pancreatic Cancer 87 0.111
161
P MST009 Mastocytosis 56 0.111
162
P PLR004 Pleuropulmonary Blastoma 65 0.110
163
GST019 Gastrointestinal Stromal Tumor 73 0.110
164
P RNL014 Renal Cell Carcinoma 82 0.110
165
P NRF002 Neurofibromatosis 71 0.109
166
P APL001 Aplastic Anemia 75 0.109
167
CHR563 Chronic Eosinophilic Leukemia 46 0.109
168
P THR014 Thrombocytopenia 64 0.108
169
GLM004 Gliomatosis Cerebri 49 0.108
170
MDS022 Mediastinitis 41 0.108
171
P PLY018 Polycythemia 58 0.107
172
c RFR014 Refractory Anemia with Excess Blasts Type 2 16 0.107
173
CRC006 Carcinoid Syndrome 52 0.107
174
c BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.107
175
P OVR042 Ovarian Cancer 76 0.107
176
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.107
177
HYP266 Hypoxia 56 0.106
178
P KDN017 Kidney Cancer 65 0.106
179
ENG004 Engraftment Syndrome 32 0.106
180
P ESS003 Essential Thrombocythemia 70 0.106
181
ACT184 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Alkylating Agent 13 0.106
182
MST016 Mesothelioma, Somatic 51 0.105
183
P CRV039 Cervicitis 45 0.105
184
c RFR015 Refractory Anemia with Excess Blasts Type 1 15 0.105
185
ALR002 Al-Raqad Syndrome 36 0.104
186
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.104
187
LKM067 Leukemia, Acute Promyelocytic, Somatic 52 0.104
188
GST053 Gastric Cancer 78 0.104
189
RFR007 Refractory Anemia with Excess Blasts in Transformation 20 0.104
190
PLS003 Plasmacytic Leukemia 21 0.104
191
VND001 Vein Disease 47 0.103
192
VSC001 Vascular Myelopathy 23 0.103
193
P PRS040 Prostate Cancer 90 0.102
194
RFR001 Refractory Plasma Cell Neoplasm 16 0.102
195
c SYS004 Systemic Mastocytosis 60 0.101
196
THR024 Thrombosis 57 0.101
197
P ART022 Arthritis 75 0.100
198
PRD011 Proud Syndrome 42 0.100
199
THR004 Thrombocytosis 55 0.100
200
ALN001 Aland Island Eye Disease 45 0.100
201
WLM007 Wilms Tumor Susceptibility-5 63 0.100
202
PLR006 Pleural Cancer 44 0.099
203
P ASP006 Aspergillosis 61 0.099
204
PLR022 Pleural Disease 51 0.099
205
NRN004 Neuroendocrine Tumor 56 0.098
206
DFF005 Diffuse Large B-Cell Lymphoma 59 0.098
207
c MLG081 Malignant Teratoma 46 0.097
208
CRB009 Cerebritis 39 0.097
209
c SML023 Small Cell Lung Cancer, Adult 15 0.097
210
P SPS003 Spastic Diplegia 52 0.096
211
ACT177 Acute Basophilic Leukemia 34 0.096
212
GLB015 Glioblastoma Multiforme 63 0.096
213
ACT158 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Radiation 12 0.096
214
RDT005 Radiation Induced Cancer 28 0.094
215
P BNG032 Benign Mesothelioma 40 0.094
216
ACT103 Acute Lymphoblastic Leukemia, Childhood 41 0.093
217
SFT003 Soft Tissue Sarcoma 57 0.092
218
MNT001 Mantle Cell Lymphoma 72 0.092
219
P PNM007 Pneumonia 68 0.092
220
LYM127 Lymphatic Malformations 39 0.092
221
GRN017 Granulocytopenia 44 0.091
222
DWN001 Down Syndrome 66 0.091
223
BNM011 Bone Marrow Failure Syndrome 2 25 0.090
224
PRL032 Perlman Syndrome 50 0.090
225
MLG012 Malignant Epithelial Mesothelioma 33 0.090
226
HRT029 Heart Tumor of the Child 15 0.090
227
c CNN010 Connective Tissue Benign Neoplasm 32 0.089
228
IMM136 Immune System Disease 51 0.089
229
ISC004 Ischemia 61 0.089
230
WTH001 Withdrawal Disorder 37 0.088
231
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 56 0.088
232
PRP036 Peripheral T-Cell Lymphoma 45 0.088
233
c INV001 Invasive Aspergillosis 47 0.088
234
DND018 Dendritic Cell Tumor 41 0.087
235
P RHM011 Rheumatoid Arthritis 89 0.087
236
CLV009 Clove Syndrome, Somatic 41 0.087
237
P ESP024 Esophagitis 61 0.087
238
C3D001 C3 Deficiency 53 0.086
239
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 24 0.086
240
NSY001 N Syndrome 36 0.086
241
OBS001 Obstructive Jaundice 48 0.086
242
P SKN013 Skin Benign Neoplasm 43 0.086
243
c SVR003 Severe Congenital Neutropenia 56 0.086
244
P FLL037 Follicular Lymphoma 70 0.085
245
P CNN004 Connective Tissue Cancer 40 0.085
246
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 41 0.084
247
LPD004 Lipoid Nephrosis 48 0.083
248
P MNN013 Meningitis 67 0.083
249
MCR004 Macroglobulinemia 50 0.082
250
DDN006 Duodenitis 42 0.082
251
P HYP098 Hypereosinophilic Syndrome 63 0.081
252
BNM010 Bone Marrow Failure Syndrome 1 29 0.081
253
c NRF018 Neurofibromatosis, Type 1 67 0.081
254
PRP027 Peripheral Vascular Disease 68 0.080
255
CLL014 Cll/sll 42 0.080
256
c WLM005 Wilms Tumor 2 20 0.080
257
P OVR049 Ovarian Disease 56 0.080
258
c CRN214 Coronary Heart Disease 5 22 0.080
259
ATN003 Autonomic Nervous System Neoplasm 40 0.080
260
RTC005 Reticulosarcoma 48 0.080
261
WST001 West Syndrome 57 0.080
262
SML033 Small Cell Cancer of the Lung, Somatic 54 0.080
263
P OST001 Osteopetrosis 63 0.079
264
END035 Endocrine Gland Cancer 49 0.079
265
c FLL041 Follicular Lymphoma 1 45 0.079
266
WHT007 White Platelet Syndrome 15 0.079
267
SKN023 Skin Tag 44 0.079
268
AML051 Aml with Myelodysplasia-Related Features 18 0.079
269
RTC009 Reticulum Cell Sarcoma 47 0.079
270
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.079
271
CNT098 Central Core Disease 65 0.078
272
PLY125 Polycythemia Vera, Somatic 63 0.078
273
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 13 0.077
274
MTH009 Mouth Disease 61 0.077
275
P SML001 Small Cell Carcinoma 56 0.077
276
P HRT032 Heart Disease 75 0.077
277
PRC012 Pericardial Effusion 51 0.077
278
HRY003 Hairy Cell Leukemia 57 0.077
279
P OLG002 Oligodendroglioma 56 0.077
280
P NRB001 Neuroblastoma 70 0.076
281
SPL018 Splenomegaly 44 0.076
282
NWC001 Newcastle Disease 54 0.076
283
INT253 Intestinal Benign Neoplasm 47 0.076
284
SPL011 Spleen Cancer 36 0.076
285
LYM126 Lymphoma Aids Related 15 0.076
286
c CRN173 Coronary Heart Disease 8 18 0.076
287
MRG003 Marginal Zone B-Cell Lymphoma 52 0.075
288
P RTN024 Retinoblastoma 74 0.075
289
ACT095 Acute Biphenotypic Leukemia 32 0.075
290
LYM104 Lymphoma, Malt, Somatic 54 0.074
291
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.074
292
MCS002 Mucositis 55 0.074
293
BRK010 Burkitt Lymphoma 69 0.074
294
LYM012 Lymphoplasmacytic Lymphoma 44 0.074
295
BND002 B- and T-Cell Mixed Leukemia 17 0.073
296
HV1006 Hiv-1 80 0.073
297
P ANP001 Anaplastic Large Cell Lymphoma 57 0.073
298
WSC001 Wisconsin Syndrome 14 0.073
299
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.073
300
P PNC001 Pancytopenia 52 0.072
301
P ACT080 Acute Pulmonary Heart Disease 31 0.072
302
c PRM012 Primary Polycythemia 52 0.072
303
MYL015 Myeloproliferative Disorder with Eosinophilia 34 0.072
304
P NSP012 Nasopharyngeal Carcinoma 66 0.072
305
ESP021 Esophageal Cancer 76 0.072
306
LNG030 Lung Adenoma 40 0.072
307
SPR035 Superior Vena Cava Syndrome 31 0.072
308
THR106 Therapy Related Acute Myeloid Leukemia and Myelodysplastic Syndrome 14 0.072
309
SPL012 Splenic Disease 46 0.072
310
TBR010 Tuberculosis 70 0.072
311
RHB003 Rhabdomyosarcoma 57 0.071
312
CNN005 Connective Tissue Disease 62 0.071
313
LRN003 Learning Disability 49 0.071
314
PLS011 Plasmacytoma 56 0.071
315
VRL011 Viral Infectious Disease 55 0.071
316
ADJ001 Adjustment Disorder 38 0.071
317
BCL012 B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue 37 0.071
318
PRP007 Priapism 46 0.071
319
P BRN120 Bronchus Cancer 44 0.071
320
c PRM149 Primary Hypereosinophilic Syndrome 38 0.071
321
UTR033 Uterine Corpus Cancer 49 0.071
322
DSS003 Disseminated Eosinophilic Collagen Disease 15 0.070
323
PST046 Post-Transplant Lymphoproliferative Disease 54 0.070
324
c CNT035 Central Nervous System Disease 60 0.070
325
FML038 Female Reproductive Organ Cancer 50 0.070
326
c HPT016 Hepatitis B 64 0.070
327
c CHR096 Chronic Pulmonary Heart Disease 40 0.069
328
P LMY004 Leiomyosarcoma 55 0.069
329
P NRV007 Nervous System Disease 71 0.069
330
ACT217 Acute Myeloid Leukemia with Recurrent Genetic Anomaly 10 0.069
331
BLS007 Blastic Plasmacytoid Dendritic Cell 41 0.069
332
SPL004 Splenic Marginal Zone Lymphoma 44 0.068
333
THY028 Thyroid Cancer 69 0.068
334
RNL101 Renal Cell Carcinoma, Papillary 63 0.068
335
c CRN177 Coronary Heart Disease 7 20 0.068
336
P CTN015 Cutaneous T Cell Lymphoma 50 0.068
337
LKP003 Leukoplakia 38 0.068
338
BRN106 Burns 52 0.068
339
MYC006 Mycosis Fungoides 66 0.067
340
P LRY019 Laryngitis 54 0.067
341
MLG041 Malignant Triton Tumor 36 0.067
342
BNM013 Bone Marrow Failure Syndrome 3 17 0.067
343
FML039 Female Reproductive System Disease 48 0.067
344
P ENC004 Encephalitis 63 0.066
345
P FBR017 Fibrosarcoma 56 0.066
346
BNM005 Bone Marrow Necrosis 32 0.066
347
c THR037 Thrombocytopenia 2 35 0.066
348
c TRC078 Trichohepatoenteric Syndrome 2 29 0.066
349
LYM041 Lymphocytes Absent 13 0.066
350
P INF038 Influenza 72 0.065
351
P SNS014 Sinusitis 60 0.065
352
ACT216 Acute Leukemia of Ambiguous Lineage 34 0.065
353
URT010 Ureteral Obstruction 45 0.065
354
RTN023 Retinitis 50 0.065
355
RBR001 Roberts Syndrome 60 0.065
356
c PRM225 Primary Thrombocytopenia 39 0.065
357
P WLD002 Waldenstrom Macroglobulinemia 58 0.065
358
P INT070 Intestinal Obstruction 57 0.065
359
NDL020 Nodal Marginal Zone B-Cell Lymphoma 35 0.065
360
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.064
361
MST002 Mast-Cell Leukemia 48 0.064
362
P GLM007 Glomerulonephritis 59 0.064
363
MN1001 Mn1 30 0.064
364
ACT234 Acute Myeloid Leukemia with Minimal Differentiation 22 0.064
365
P HML002 Hemolytic Anemia 62 0.064
366
P DBT005 Diabetes Insipidus 53 0.064
367
P LPS004 Lupus Erythematosus 64 0.063
368
LNG013 Lung Lymphoma 38 0.063
369
OLV001 Olivopontocerebellar Atrophy 53 0.063
370
TST014 Testicular Cancer 53 0.063
371
P LPS002 Liposarcoma 55 0.062
372
FXF002 Fox-Fordyce Disease 36 0.062
373
LYM048 Lymphoma, Large-Cell, Immunoblastic 25 0.062
374
PNC034 Pancreas Disease 58 0.062
375
ALL026 Allergic Hypersensitivity Disease 52 0.062
376
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 60 0.062
377
CLT003 Colitis 60 0.061
378
c PNC106 Pancreatic Agenesis 1 37 0.061
379
P CNT005 Central Nervous System Lymphoma 53 0.061
380
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.061
381
MYL052 Myeloproliferative Neoplasms, Familial 15 0.061
382
NTR005 Nutritional Deficiency Disease 36 0.061
383
P INF037 Inflammatory Bowel Disease 63 0.061
384
GLC077 Glucocorticoid Therapy, Response to 16 0.061
385
c MCR161 Macroglobulinemia, Waldenstrom 1 27 0.061
386
TTR011 Tetraploidy 41 0.061
387
BRN038 Bronchial Disease 51 0.061
388
MLN013 Melanoma Metastasis 40 0.061
389
c MCR162 Macroglobulinemia, Waldenstrom 2 17 0.060
390
P MYC007 Myocardial Infarction 79 0.060
391
c ACT195 Acute Myeloid Leukemia with T(9;11)(p22;q23) 22 0.060
392
PRP019 Peripheral Nervous System Disease 55 0.060
393
CLN015 Colon Adenocarcinoma 50 0.060
394
LYM051 Lymphomatoid Granulomatosis 47 0.060
395
SKN016 Skin Disease 66 0.059
396
c SCN042 Secondary Hypereosinophilic Syndrome 14 0.059
397
SHW002 Shwachman-Diamond Syndrome 61 0.059
398
c SYS001 Systemic Lupus Erythematosus 86 0.059
399
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 29 0.059
400
SPC003 Specific Developmental Disorder 38 0.059
401
PLS025 Plasmablastic Lymphoma 46 0.059
402
PRN039 Paraneoplastic Syndromes 32 0.059
403
HRT003 Heart Lymphoma 30 0.059
404
c CLR075 Colorectal Cancer 3 28 0.059
405
BCK006 Back Pain 43 0.058
406
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.058
407
ANR040 Aneurysm 57 0.058
408
c CRN176 Coronary Heart Disease 9 18 0.058
409
CHR286 Chronic Neutrophilic Leukemia 43 0.058
410
c PRM226 Primary Central Nervous System Lymphoma 49 0.058
411
AND005 Androgen Insensitivity Syndrome, Mild 16 0.058
412
GST050 Gastrointestinal System Disease 56 0.058
413
P MYP004 Myopathy 67 0.058
414
CHR062 Chronic Erythremia 13 0.058
415
PYD002 Pyoderma 48 0.057
416
c THR090 Thrombocythemia 1 30 0.057
417
ERY051 Erythroleukemia, Familial 23 0.057
418
OVR094 Ovarian Epithelial Cancer 43 0.057
419
ZYG002 Zygomycosis 33 0.057
420
PHY001 Physiological Polycythemia 28 0.057
421
LMY002 Leiomyoma 54 0.057
422
ACN002 Acanthosis Nigricans 57 0.056
423
c PNC094 Pancreatic Cancer 1 27 0.056
424
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 39 0.056
425
P EXP004 Exophthalmos 53 0.056
426
P CHR345 Chronic Pain 50 0.056
427
GND003 Gonadal Disease 39 0.056
428
c HPT001 Hepatitis C 68 0.056
429
P TRC086 Trichohepatoenteric Syndrome 1 48 0.056
430
PRM025 Primary Bacterial Infectious Disease 41 0.056
431
c WLM011 Wilms Tumor 6 19 0.056
432
PRT035 Peritoneum Cancer 35 0.056
433
OVR069 Ovarian Germ Cell Tumor 24 0.056
434
DPH001 Diphtheria 59 0.056
435
MSC072 Muscle Cancer 49 0.056
436
RCT018 Rectal Neoplasm 54 0.055
437
P MYS005 Myositis 57 0.055
438
PYD001 Pyoderma Gangrenosum 51 0.055
439
P OBS005 Obesity 92 0.055
440
P PLM006 Pulmonary Alveolar Proteinosis 48 0.055
441
ORL015 Oral Squamous Cell Carcinoma 57 0.055
442
HPT070 Hepatosplenic T-Cell Lymphoma 39 0.055
443
VSC011 Vasculitis 62 0.054
444
STT009 Sutton Disease 2 18 0.054
445
P END044 Endometriosis 66 0.054
446
ANP010 Anaplastic Plasmacytoma 19 0.054
447
FML037 Female Breast Cancer 50 0.054
448
P BCL005 B Cell Prolymphocytic Leukemia 43 0.054
449
OLG006 Oligoastrocytoma 35 0.054
450
ANP008 Anaplastic Oligoastrocytoma 25 0.054
451
P RSP003 Respiratory Failure 71 0.054
452
DRM006 Dermatitis 66 0.054
453
c FML108 Familial Breast Cancer 57 0.054
454
NRN002 Neuronitis 41 0.054
455
c ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 34 0.054
456
MST017 Mast Cell Disease 50 0.054
457
HMG002 Hemoglobinuria 48 0.054
458
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.053
459
PRR002 Pure Red-Cell Aplasia 47 0.053
460
RPR002 Reproductive System Disease 41 0.053
461
CNT067 Central Cord Syndrome 23 0.053
462
LKS001 Leukostasis 35 0.053
463
c CLR085 Colorectal Cancer 1 45 0.053
464
INS024 Insulin-Like Growth Factor I 75 0.053
465
GNG004 Ganglioglioma 50 0.053
466
P UTR038 Uterine Disease 37 0.053
467
CRD001 Cardiac Tamponade 44 0.053
468
FSR001 Fusariosis 31 0.053
469
P LPC002 Lip Cancer 53 0.053
470
ACQ007 Acquired Immunodeficiency Syndrome 60 0.053
471
PRT018 Portal Vein Thrombosis 49 0.053
472
VGN023 Vaginitis 42 0.053
473
MYC002 Mycobacterium Avium Complex Disease 52 0.052
474
YNG002 Young Syndrome 26 0.052
475
PDT001 Pediatric Lymphoma 38 0.052
476
ADM013 Adamantinoma of Long Bones 57 0.052
477
DFF027 Diffuse Lymphatic Malformation 22 0.052
478
PRL017 Prolymphocytic Leukemia 47 0.052
479
PRM133 Primary Pulmonary Lymphoma 23 0.052
480
c ANP011 Anaplastic Small Cell Lymphoma 14 0.052
481
PRS042 Prostate Disease 52 0.052
482
STM006 Stomach Disease 50 0.052
483
CHR008 Choroiditis 44 0.052
484
BRN048 Brain Stem Cancer 36 0.052
485
P CRD011 Cardiomyopathy 68 0.052
486
ATN002 Autonomic Nervous System Disease 48 0.052
487
LRG008 Large Granular Lymphocyte Leukemia 39 0.052
488
MYL059 Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 29 0.051
489
P INF032 Infertility 59 0.051
490
P CRN178 Coronary Heart Disease 6 21 0.051
491
PLR008 Pleurisy 50 0.051
492
P DRM010 Dermatomyositis 62 0.051
493
EMB004 Embryonal Carcinoma 57 0.051
494
P AST005 Asthma 82 0.051
495
WRT001 Worth's Syndrome 34 0.051
496
P LCH002 Lichen Planus 53 0.051
497
P SML016 Small Intestine Cancer 52 0.051
498
MLR004 Malaria 83 0.051
499
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.051
500
END030 End Stage Renal Failure 55 0.051
501
c THR048 Thrombocytopenia 4 26 0.050
502
c CLR079 Colorectal Cancer 2 29 0.050
503
HYP084 Hypopyon 31 0.050
504
BCT015 Bacteremia 48 0.050
505
ACC008 Accelerated Tumor Formation 17 0.050
506
P CND004 Candidiasis 57 0.050
507
c FML303 Familial/multiple Cancer 14 0.050
508
PNN001 Panniculitis 51 0.050
509
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 27 0.050
510
TCL018 T-Cell Childhood Acute Lymphocytic Leukemia 18 0.050
511
TCL019 T-Cell Childhood Lymphoblastic Lymphoma 14 0.050
512
SCT005 Scott Syndrome 53 0.050
513
P 8P1002 8p11 Myeloproliferative Syndrome 36 0.050
514
P UVT001 Uveitis 58 0.049
515
P PLY041 Polymyositis 52 0.049
516
DSS009 Disseminated Intravascular Coagulation 51 0.049
517
GNG013 Gingivitis 61 0.049
518
ATR060 Atrial Standstill, Digenic 51 0.049
519
RDC002 Radiculopathy 50 0.049
520
c PND001 Pain Disorder 54 0.049
521
VSC047 Vascular Malformation 45 0.048
522
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.048
523
THR016 Thrombophlebitis 53 0.048
524
ACT017 Acute Chest Syndrome 48 0.048
525
EPD001 Epidermodysplasia Verruciformis 50 0.048
526
P LFR001 Li-Fraumeni Syndrome 75 0.047
527
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.047
528
c INH015 Inherited Acute Myeloid Leukemia 25 0.047
529
APP008 Appendicitis 60 0.047
530
HPT074 Hepatic Adenoma, Somatic 50 0.047
531
FBR009 Fibrous Dysplasia 45 0.047
532
MLR006 Male Reproductive Organ Cancer 43 0.047
533
GST014 Gastrointestinal Lymphoma 31 0.047
534
c ADL096 Adult Hepatocellular Carcinoma 24 0.047
535
P CHL066 Cholangitis 42 0.047
536
MYX005 Myxoid Liposarcoma 57 0.047
537
CNG034 Congestive Heart Failure 72 0.047
538
P INT068 Intestinal Disease 60 0.046
539
SZR001 Sezary's Disease 52 0.046
540
c PRS116 Prostate Cancer 1 37 0.046
541
c LRG001 Large Cell Carcinoma 51 0.046
542
BRS001 Breast Lymphoma 32 0.046
543
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.046
544
CNT045 Central Nervous System Sarcoma 16 0.046
545
P KDN018 Kidney Disease 66 0.046
546
LYM021 Lymphadenitis 58 0.046
547
c THR102 Thrombocytopenia 5 27 0.046
548
SVR004 Severe Combined Immunodeficiency 69 0.046
549
MCR013 Microphthalmia 60 0.046
550
ULC004 Ulcerative Colitis 76 0.046
551
RSP006 Respiratory System Disease 58 0.046
552
PRC013 Pericarditis 51 0.046
553
P SLV002 Salivary Gland Cancer 61 0.046
554
GNG002 Ganglioneuroma 47 0.046
555
c ACT194 Acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation 28 0.046
556
ATH003 Atherosclerosis 65 0.045
557
MSL001 Measles 61 0.045
558
ALL006 Allergic Asthma 58 0.045
559
PTR006 Peters Anomaly 65 0.045
560
MND006 Mondor Disease 21 0.045
561
MYL055 Myeloid/lymphoid or Mixed Lineage Leukemia 29 0.045
562
WLL001 Williams-Beuren Syndrome 60 0.045
563
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.045
564
INT051 Intussusception 50 0.045
565
P ATX004 Ataxia 53 0.045
566
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 40 0.045
567
P THL005 Thalassemia 64 0.045
568
CYT008 Cytomegalovirus Infection 52 0.045
569
GLL018 Gallbladder Cancer 63 0.044
570
EPS006 Epstein Syndrome 38 0.044
571
OST017 Osteomyelitis 61 0.044
572
BRN004 Brain Edema 52 0.044
573
P KRT005 Keratoacanthoma 46 0.044
574
SPN051 Spondylitis 51 0.044
575
BRC012 Brucellosis 66 0.044
576
P ALX003 Alexander Disease 63 0.044
577
PLM012 Pulmonary Sarcoidosis 54 0.044
578
KRT009 Keratosis 52 0.044
579
P HRP006 Herpes Simplex 65 0.044
580
P HMN010 Hemangioma 59 0.044
581
PRP030 Purpura 58 0.043
582
CNG028 Congenital Hypoplastic Anemia 48 0.043
583
NNH003 Non-Hodgkin Lymphoma, Childhood 12 0.043
584
P ACT105 Acute Mountain Sickness 52 0.043
585
NTR040 Neutropenia, Cyclic 51 0.043
586
RCM004 Recombinant 8 Syndrome 22 0.043
587
NVD002 Nevada Syndrome 14 0.043
588
c ACT198 Acute Myeloid Leukemia with T(6;9)(p23;q34) 17 0.043
589
ACT196 Acute Myeloid Leukemia with Inv3(p21;q26.2) or T(3;3)(p21;q26.2) 8 0.043
590
P PRT013 Portal Hypertension 60 0.043
591
LYM027 Lymphopenia 56 0.043
592
c THR086 Thrombocythemia 3 25 0.043
593
P SZR006 Seizure Disorder 56 0.043
594
P HYP014 Hyperuricemia 50 0.043
595
ADR005 Adrenal Carcinoma 57 0.043
596
OVR104 Ovarian Melanoma 36 0.043
597
c DLT001 Delta Chain Disease 13 0.042
598
P CNJ013 Conjunctivitis 64 0.042
599
PMP001 Pemphigus 50 0.042
600
KDN020 Kidney Cancer, Childhood 11 0.042
601
c THR092 Thrombophilia Due to Thrombin Defect 54 0.042
602
NSP002 Nasopharyngitis 40 0.042
603
LNG099 Lung Disease 64 0.042
604
ANG046 Angioimmunoblastic T-Cell Lymphoma 43 0.042
605
PNL014 Pineal Gland Cancer 32 0.042
606
P ATX030 Ataxia-Telangiectasia 77 0.042
607
c HPT073 Hepatitis C Virus 73 0.042
608
c FNC027 Fanconi Anemia, Complementation Group a 71 0.042
609
LSH001 Leishmaniasis 66 0.042
610
P PRP029 Porphyria 59 0.042
611
P PLY019 Polyneuropathy 56 0.042
612
P MSC005 Muscular Dystrophy 65 0.041
613
HPT022 Hepatoblastoma 55 0.041
614
c INH020 Inherited Metabolic Disorder 49 0.041
615
P SCH015 Schizophrenia 77 0.041
616
SXL003 Sexual Disorder 42 0.041
617
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.041
618
TCL002 T-Cell Large Granular Lymphocyte Leukemia 42 0.041
619
P SML002 Small Cell Sarcoma 25 0.041
620
c JVN003 Juvenile Xanthogranuloma 44 0.041
621
PYM001 Pyomyositis 40 0.041
622
CYC007 Cyclic Thrombocytopenia 37 0.041
623
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.041
624
OST085 Osteosarcoma, Somatic 63 0.041
625
PLM039 Pulmonary Neuroendocrine Tumor 42 0.041
626
SPN040 Spinal Cancer 39 0.041
627
c ACT075 Acute Myocardial Infarction 60 0.041
628
HRP004 Herpes Zoster 56 0.041
629
HYP063 Hypersplenism 48 0.041
630
IDP064 Idiopathic Neutropenia 45 0.041
631
c ACT219 Acute Myeloid Leukemia, Flt3-Related 29 0.041
632
P ACT190 Acute Myeloid Leukemia with T(8;16)(p11;p13) Translocation 16 0.041
633
P DRR001 Diarrhea 60 0.041
634
PHR003 Pharyngitis 56 0.041
635
c THR110 Thrombocytopenia 6 20 0.041
636
MNT045 Montefiore Syndrome 10 0.041
637
HYP066 Hyperglycemia 61 0.040
638
P EXN002 Exanthem 57 0.040
639
PRM097 Primary Immunodeficiency Disease 60 0.040
640
SCK003 Sickle Cell Anemia 71 0.040
641
P RTN022 Retinal Vein Occlusion 38 0.040
642
c CNT016 Central Retinal Vein Occlusion 36 0.040
643
PLX004 Plexopathy 34 0.040
644
CRB040 Cerebrum Cancer 32 0.039
645
P GST044 Gastritis 56 0.039
646
NRT004 Neuritis 52 0.039
647
P INT063 Intellectual Disability 49 0.039
648
P CMP008 Compartment Syndrome 48 0.039
649
GYN001 Gynecomastia 48 0.039
650
MMB001 Membranoproliferative Glomerulonephritis 46 0.039
651
c ACT027 Acute Pancreatitis 57 0.039
652
P FNC004 Fanconi Syndrome 49 0.039
653
FSC004 Fasciitis 48 0.039
654
c ATM024 Autoimmune Pancreatitis 47 0.039
655
SVR077 Severe Combined Immune Deficiency 36 0.039
656
P GRV001 Graves' Disease 59 0.039
657
FLL013 Follicular Dendritic Cell Sarcoma 41 0.039
658
PRM165 Primary Plasmacytoma of the Bone 12 0.039
659
MCP006 Mucoepidermoid Carcinoma 48 0.039
660
P VGN017 Vaginal Cancer 47 0.039
661
c RNL034 Renal Cell Carcinoma 4 18 0.039
662
c CHR089 Chronic Kidney Failure 66 0.038
663
TTH006 Tooth Disease 52 0.038
664
HST011 Histoplasmosis 52 0.038
665
HYP005 Hypokalemia 51 0.038
666
c RNL016 Renal Infectious Disease 20 0.038
667
c CRN175 Coronary Heart Disease 4 19 0.038
668
P DMN001 Diamond-Blackfan Anemia 69 0.038
669
VSC007 Vascular Disease 67 0.038
670
BLM001 Bloom Syndrome 63 0.038
671
FCL012 Facial Paralysis 50 0.038
672
DRM014 Dermatofibrosarcoma Protuberans 61 0.038
673
P TST026 Testicular Germ Cell Cancer 39 0.038
674
c MLG036 Malignant Spiradenoma 32 0.038
675
MLL012 Miller Syndrome 49 0.038
676
TTR021 Tetrasomy 21 20 0.038
677
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 17 0.038
678
P HNT016 Huntington Disease 80 0.038
679
WLS001 Wilson Disease 72 0.038
680
CHR012 Chronic Granulomatous Disease 65 0.038
681
EXF001 Exfoliation Syndrome 57 0.038
682
P END033 Endocarditis 54 0.038
683
OPT009 Optic Neuritis 50 0.038
684
P PLN008 Peeling Skin Syndrome 45 0.038
685
HYP017 Hypophosphatemia 43 0.038
686
c PLN021 Peeling Skin Syndrome 3 29 0.038
687
c BCT007 Bacterial Meningitis 54 0.038
688
PRT011 Protein C Deficiency 52 0.038
689
P SDR003 Sideroblastic Anemia 40 0.038
690
c PRM126 Primary Peritoneal Carcinoma 54 0.037
691
GST045 Gastroenteritis 59 0.037
692
SCK005 Sickle Cell Disease 51 0.037
693
PHY002 Physical Disorder 43 0.037
694
AGG002 Aggressive Systemic Mastocytosis 42 0.037
695
PRM026 Primary Systemic Mycosis 36 0.037
696
SLT001 Solitary Osseous Plasmacytoma 36 0.037
697
SKN021 Skin Sarcoma 25 0.037
698
P TXP001 Toxoplasmosis 61 0.037
699
P WGN003 Wagner Syndrome 36 0.037
700
INH011 Inherited Bone Marrow Failure Syndromes 27 0.037
701
GRW021 Growing Teratoma Syndrome 18 0.037
702
MXD005 Mixed Connective Tissue Disease 62 0.037
703
PRS039 Prostate Adenocarcinoma 46 0.037
704
c OVR058 Ovarian Small Cell Carcinoma 36 0.037
705
P LPR003 Leprosy 69 0.036
706
P CLD001 Cleidocranial Dysplasia 62 0.036
707
WGR001 Wagr Syndrome 53 0.036
708
c SCN036 Secondary Progressive Multiple Sclerosis 49 0.036
709
c PLN018 Peeling Skin Syndrome 2 40 0.036
710
SPL006 Splenic Infarction 35 0.036
711
CND006 Candida Glabrata 34 0.036
712
SYN036 Syncope 47 0.036
713
CLN044 Colon Adenoma 44 0.036
714
PRN049 Paraneoplastic Pemphigus 40 0.036
715
CRD119 Cardiac Arrest 61 0.036
716
CTS003 Coats Disease 57 0.036
717
KDN019 Kidney Sarcoma 31 0.036
718
c NRB015 Neuroblastoma 2 28 0.036
719
SML025 Small Non-Cleaved Cell Lymphoma 22 0.036
720
P PLM037 Pulmonary Hypertension 79 0.036
721
CHG001 Chagas Disease 67 0.036
722
OTT002 Otitis Media 66 0.036
723
ATP002 Atopy 66 0.036
724
TXC005 Toxic Shock Syndrome 60 0.036
725
TNS005 Tonsillitis 57 0.036
726
VSC003 Visceral Leishmaniasis 56 0.036
727
PRC002 Paracoccidioidomycosis 55 0.036
728
PLN006 Poland Syndrome 54 0.036
729
P MTC069 Mitochondrial Disorders 53 0.036
730
P LMB006 Limb-Girdle Muscular Dystrophy 51 0.036
731
HDR003 Hidradenitis 45 0.036
732
IMM078 Immunodeficiency 21 35 0.036
733
c PRM200 Primary Fanconi Syndrome 24 0.036
734
CRS005 Crest Syndrome 51 0.035
735
ALK003 Aleukemic Leukemia Cutis 31 0.035
736
MGK005 Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) 13 0.035
737
ACT185 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Topoisomerase Type 2 Inhibitor 10 0.035
738
ACT166 Acute Myeloid Leukemia with Cebpa Somatic Mutations 10 0.035
739
ACT199 Acute Myeloid Leukemia with Npm1 Somatic Mutations 10 0.035
740
P AMY004 Amyloidosis 65 0.035
741
P LYM025 Lymphedema 61 0.035
742
ABL002 Ablepharon-Macrostomia Syndrome 57 0.035
743
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.035
744
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 41 0.035
745
LMB024 Limbic Encephalitis 38 0.035
746
SML022 Small Cell Lung Cancer, Childhood 12 0.035
747
UPP004 Upper Respiratory Tract Disease 46 0.035
748
MST004 Mast Cell Neoplasm 40 0.035
749
SPN369 Spinal Disease 39 0.035
750
APP010 Appendix Cancer 39 0.035
751
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.035
752
ACR007 Acromegaly 66 0.035
753
P GLY013 Glycogen Storage Disease 60 0.035
754
LPR001 Lepromatous Leprosy 50 0.035
755
HYP068 Hyperostosis 40 0.035
756
TLR001 Tularemia 39 0.035
757
SGT001 Sagittal Sinus Thrombosis 35 0.035
758
LYM045 Lymphocytic Vasculitis 33 0.035
759
TRC006 Trichosporonosis 29 0.035
760
ACT176 Acute Panmyelosis with Myelofibrosis 19 0.035
761
P CRN211 Coronary Artery Disease 74 0.035
762
P AGM001 Agammaglobulinemia 64 0.035
763
P BRG001 Brugada Syndrome 59 0.035
764
c ACT210 Acute Respiratory Distress Syndrome 57 0.035
765
HDC001 Headache 54 0.035
766
CCC002 Coccidiosis 51 0.035
767
P HRD001 Hereditary Multiple Exostoses 46 0.035
768
IDP024 Idiopathic Inflammatory Myopathy 46 0.035
769
NTR018 Neutrophilia, Hereditary 42 0.035
770
ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 37 0.035
771
c HRD009 Hereditary Wilms' Tumor 36 0.035
772
c HMG004 Hemoglobin D Disease 31 0.035
773
c WGN005 Wagner Syndrome 1 28 0.035
774
c BNG076 Benign Exophthalmos Syndrome 15 0.035
775
PGM001 Pigmented Villonodular Synovitis 49 0.034
776
EWN002 Ewing's Family of Tumors 43 0.034
777
c SML034 Small Cell Neuroendocrine Carcinoma 42 0.034
778
HST016 Histiocytic Sarcoma 40 0.034
779
VSC009 Vascular Skin Disease 19 0.034
780
ANX002 Anxiety Disorder 67 0.034
781
BRN002 Bronchiolitis 56 0.034
782
FDL002 Food Allergy 53 0.034
783
CLL003 Cellulitis 51 0.034
784
STM007 Stomatitis 50 0.034
785
c ACT071 Acute Kidney Failure 49 0.034
786
BLR008 Bilirubin Metabolic Disorder 42 0.034
787
ADN014 Adenomatoid Tumor 34 0.034
788
ALV010 Alveolar Soft-Part Sarcoma 54 0.034
789
ADR014 Adrenal Medulla Cancer 36 0.034
790
MLR007 Male Reproductive System Disease 34 0.034
791
c NRB011 Neuroblastoma 4 17 0.034
792
PDT026 Pediatric T-Cell Leukemia 11 0.034
793
CRH001 Crohn's Disease 75 0.033
794
ART016 Aortic Aneurysm 69 0.033
795
ISC006 Ischemic Heart Disease 68 0.033
796
P NJM001 Nijmegen Breakage Syndrome 67 0.033
797
P TMP003 Temporal Arteritis 60 0.033
798
ART111 Artery Disease 55 0.033
799
ECH003 Echinococcosis 54 0.033
800
TMR010 Tumor Predisposition Syndrome 47 0.033
801
VCC001 Vaccinia 46 0.033
802
P PRD008 Periodontitis 63 0.033
803
HSH003 Hashimoto Thyroiditis 62 0.033
804
PRD007 Periodontal Disease 60 0.033
805
PMS001 Poems Syndrome 52 0.033
806
MGL001 Megaloblastic Anemia 50 0.033
807
ACT049 Acute Disseminated Encephalomyelitis 49 0.033
808
c ACQ014 Acquired Hemophilia 42 0.033
809
HPT020 Hepatic Vascular Disease 42 0.033
810
c CHR091 Chronic Meningitis 39 0.033
811
c PLN017 Peeling Skin Syndrome 1 34 0.033
812
ANG049 Angioedema Induced by Ace Inhibitors 34 0.033
813
ABD004 Abdominal Tuberculosis 32 0.033
814
PLY010 Polyclonal Hypergammaglobulinemia 32 0.033
815
ANP007 Anaplastic Ganglioglioma 27 0.033
816
CNT017 Central Nervous System Origin Vertigo 24 0.033
817
TCR004 Tacrolimus Dose Selection 20 0.033
818
STT044 Statin Toxicity 14 0.033
819
SYS059 Systemic Mastocytosis with an Associated Clonal Hematologic Non-Mast Cell Lineage Disease 13 0.033
820
ERY003 Erythema Multiforme 55 0.033
821
BRN071 Brain Injury 52 0.033
822
PRN021 Paranasal Sinus Disease 49 0.033
823
HPT067 Hepatocellular Adenoma 42 0.033
824
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.033
825
SFT004 Soft Tissue Sarcoma Childhood 12 0.033
826
SPT004 Septic Arthritis 60 0.032
827
P AVS004 Avascular Necrosis of the Femoral Head 56 0.032
828
THR013 Thoracic Outlet Syndrome 50 0.032
829
CRN017 Coronary Thrombosis 48 0.032
830
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.032
831
P PLG001 Pelger-Huet Anomaly 45 0.032
832
ESP018 Esophageal Candidiasis 41 0.032
833
c CNG031 Congenital Nervous System Abnormality 37 0.032
834
GST020 Gastric Antral Vascular Ectasia 33 0.032
835
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.032
836
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 14 0.032
837
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 14 0.032
838
CHL067 Cholecystitis 57 0.032
839
GNR004 Generalized Anxiety Disorder 51 0.032
840
KLN001 Klinefelter's Syndrome 50 0.032
841
BCL002 B Cell Deficiency 49 0.032
842
MST001 Mast-Cell Sarcoma 40 0.032
843
P LNG035 Lung Large Cell Carcinoma 38 0.032
844
VRS001 Virus Associated Hemophagocytic Syndrome 35 0.032
845
PLS010 Plasma Protein Metabolism Disease 34 0.032
846
SWL001 Swallowing Disorders 33 0.032
847
LPN002 Lip and Oral Cavity Cancer 15 0.032
848
P PSR002 Psoriasis 61 0.032
849
RTN017 Retinal Detachment 56 0.032
850
CHR177 Chromophobe Renal Cell Carcinoma 56 0.032
851
HDR002 Hidradenitis Suppurativa 51 0.032
852
RLP001 Relapsing Polychondritis 50 0.032
853
PRP016 Paraplegia 49 0.032
854
P SCL015 Scleritis 49 0.032
855
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.032
856
DYS164 Dyskeratosis Congenita, X-Linked 44 0.032
857
CHR276 Chronic Active Epstein-Barr Virus Infection 44 0.032
858
GNG008 Ganglioneuroblastoma 40 0.032
859
P TRC005 Tracheal Stenosis 39 0.032
860
c ACT036 Acute Cholangitis 34 0.032
861
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.032
862
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 12 0.032
863
KWS002 Kawasaki Disease 70 0.031
864
PLM001 Pulmonary Tuberculosis 67 0.031
865
MLD001 Melioidosis 67 0.031
866
c ATM010 Autoimmune Hemolytic Anemia 60 0.031
867
c ATM011 Autoimmune Hepatitis 60 0.031
868
P MMP001 Mumps 58 0.031
869
ASP003 Aseptic Meningitis 51 0.031
870
TRY001 Trypanosomiasis 51 0.031
871
CDQ001 Cauda Equina Syndrome 41 0.031
872
c RNG023 Ring Chromosome 7 37 0.031
873
ECT004 Ecthyma 35 0.031
874
HNS001 Hansen's Disease 30 0.031
875
GRN011 Granulomatous Gastritis 28 0.031
876
EXF003 Exfoliative Dermatitis 25 0.031
877
ATM052 Autoimmune Disease 1 25 0.031
878
c SCN051 Secondary Pulmonary Alveolar Proteinosis 18 0.031
879
ATM053 Autoimmune Disease 2 16 0.031
880
P MYS003 Myasthenia Gravis 67 0.031
881
BLL006 Bullous Pemphigoid 59 0.031
882
RHM027 Rheumatic Disease 58 0.031
883
P SYP003 Syphilis 53 0.031
884
P URF003 Urofacial Syndrome 1 50 0.031
885
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 47 0.031
886
ADR038 Adermatoglyphia 46 0.031
887
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 42 0.031
888
LYM052 Lymphomatoid Papulosis 41 0.031
889
GST078 Gastrointestinal Allergy 40 0.031
890
HRT010 Heart Sarcoma 37 0.031
891
OVR050 Ovarian Embryonal Carcinoma 36 0.031
892
MTG002 Mutagen Sensitivity 36 0.031
893
MLG005 Malignant Spindle Cell Melanoma 32 0.031
894
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 31 0.031
895
BNM004 Bone Marrow Failure, Familial 14 0.031
896
c ATM006 Autoimmune Lymphoproliferative Syndrome 71 0.030
897
KRT004 Keratitis 71 0.030
898
P FML161 Familial Mediterranean Fever, Ar 63 0.030
899
P ATP001 Atopic Dermatitis 62 0.030
900
FCT003 Factor X Deficiency 61 0.030
901
P FCL005 Focal Segmental Glomerulosclerosis 60 0.030
902
P HMP007 Hemophilia 57 0.030
903
c EHL032 Ehlers-Danlos Syndrome, Type Viib 49 0.030
904
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.030
905
RLP003 Relapsing Fever 45 0.030
906
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 45 0.030
907
P DMY001 Demyelinating Polyneuropathy 43 0.030
908
NCR004 Nocardiosis 43 0.030
909
RDN001 Reading Disorder 34 0.030
910
RNL021 Renal Tubular Transport Disease 32 0.030
911
DMN002 Dementia 65 0.030
912
TTN003 Tetanus 61 0.030
913
LPM004 Lipoma 60 0.030
914
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.030
915
SPT005 Spotted Fever 53 0.030
916
URN009 Urinary System Disease 50 0.030
917
c MTR002 Mitral Valve Insufficiency 44 0.030
918
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.030
919
PRS002 Prostate Lymphoma 29 0.030
920
PRS008 Prostate Small Cell Carcinoma 29 0.030
921
c NRB014 Neuroblastoma 3 28 0.030
922
EXT007 Extracutaneous Mastocytoma 28 0.030
923
BRN104 Bronchial Endocrine Tumor 21 0.030
924
PLY039 Polymorphic Reticulosis 19 0.030
925
PLM024 Pulmonary Type Ovarian Small Cell Carcinoma 13 0.030
926
WGN006 Wegener Granulomatosis 63 0.029
927
APH001 Aphthous Stomatitis 62 0.029
928
P ALP009 Alopecia Areata 62 0.029
929
P THR015 Thrombophilia 59 0.029
930
ALP001 Alopecia Universalis 58 0.029
931
SNS001 Sensorineural Hearing Loss 57 0.029
932
P BCK002 Beckwith-Wiedemann Syndrome 56 0.029
933
P MYC008 Myocarditis 54 0.029
934
END040 Endogenous Depression 53 0.029
935
MNT002 Mental Depression 53 0.029
936
LMB062 Limb Ischemia 48 0.029
937
MCR191 Microscopic Colitis 47 0.029
938
HMS001 Hemosiderosis 46 0.029
939
RNL025 Renal Hypoplasia 42 0.029
940
CYS036 Cystinosis, Nephropathic 41 0.029
941
SPP004 Suppurative Cholangitis 33 0.029
942
HRF001 Hair Follicle Neoplasm 32 0.029
943
PYR004 Pyuria 32 0.029
944
GRN016 Grant Syndrome 29 0.029
945
ALL003 Allergic Rhinitis 63 0.029
946
P ADL010 Adult Respiratory Distress Syndrome 61 0.029
947
EPD016 Epidermolysis Bullosa 57 0.029
948
TRM010 Traumatic Brain Injury 52 0.029
949
INT007 Intermediate Coronary Syndrome 50 0.029
950
TCL003 T Cell Deficiency 45 0.029
951
ACR014 Acral Lentiginous Melanoma 45 0.029
952
MST006 Mast Syndrome 43 0.029
953
VGN020 Vaginal Disease 41 0.029
954
c DMN023 Diamond-Blackfan Anemia 1 38 0.029
955
c INF086 Inflammatory Bowel Disease 3 38 0.029
956
ENT008 Enteropathy-Associated T-Cell Lymphoma 35 0.029
957
HNM002 Hinman Syndrome 25 0.029
958
c NRB013 Neuroblastoma 6 16 0.029
959
P PRP003 Porphyria Cutanea Tarda 64 0.029
960
GLN010 Glanzmann Thrombasthenia 63 0.029
961
P WVR001 Weaver Syndrome 56 0.029
962
MCN017 Meconium Ileus 54 0.029
963
HMR002 Hemarthrosis 48 0.029
964
RNL077 Renal Fibrosis 47 0.029
965
KRT008 Keratopathy 44 0.029
966
PRT026 Parotitis 42 0.029
967
c NTR038 Neutropenia, Severe Congenital 3, Autosomal Recessive 41 0.029
968
CNV002 Conversion Disorder 41 0.029
969
THR035 Thrombasthenia 39 0.029
970
ORL019 Oral Hairy Leukoplakia 34 0.029
971
CRY008 Cryopyrin-Associated Periodic Syndrome 34 0.029
972
FTD001 Foot Drop 33 0.029
973
SPL007 Splenic Abscess 30 0.029
974
P PLM064 Pulmonary Sequestration 27 0.029
975
BLD052 Blood Group Incompatibility 27 0.029
976
PLM139 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 1 27 0.029
977
MYL048 Myelodysplasia and Leukemia Syndrome with Monosomy 7 25 0.029
978
DFF031 Diffuse Alveolar Hemorrhage 24 0.029
979
EPS031 Epstein-Barr Virus-Positive Diffuse Large B-Cell Lymphoma of the Elderly 19 0.029
980
CHR230 Chromosome 20q Deletion 10 0.029
981
ALK014 Aleukemic Mast Cell Leukemia 10 0.029
982
WRN001 Werner Syndrome 67 0.028
983
c SRC025 Sarcoidosis 1 61 0.028
984
BRN012 Bronchiolitis Obliterans 58 0.028
985
P ANT006 Antiphospholipid Syndrome 56 0.028
986
KRT006 Keratoconjunctivitis 52 0.028
987
P GND004 Gonadal Dysgenesis 51 0.028
988
GNG011 Gingival Disease 46 0.028
989
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.028
990
FBR002 Fibrosarcoma of Bone 40 0.028
991
ORC001 Orchitis 31 0.028
992
BRN069 Brain and Spinal Tumors 12 0.028
993
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.027
994
RCT015 Reactive Arthritis 63 0.027
995
LPT001 Leptospirosis 62 0.027
996
BHC003 Behcet Syndrome 60 0.027
997
P SPN052 Spondyloarthropathy 60 0.027
998
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.027
999
BLS001 Blau Syndrome 57 0.027
1000
P HMR012 Hemorrhagic Fever 56 0.027
1001
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.027
1002
P TMT001 Timothy Syndrome 55 0.027
1003
EXT034 Extrinsic Allergic Alveolitis 54 0.027
1004
P SCK004 Seckel Syndrome 54 0.027
1005
c INT064 Intermediate Uveitis 52 0.027
1006
MYL001 Myelitis 51 0.027
1007
ORL005 Oral Candidiasis 48 0.027
1008
CRD003 Cardiac Sarcoidosis 42 0.027
1009
c CHR576 Chronic Beryllium Disease 41 0.027
1010
c CHR546 Chronic Mountain Sickness 40 0.027
1011
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 39 0.027
1012
TXC020 Toxic Oil Syndrome 39 0.027
1013
ORF044 Orofacial Granulomatosis 37 0.027
1014
EPG003 Epiglottitis 33 0.027
1015
THY043 Thymic Hyperplasia 32 0.027
1016
c AST037 Asthma 1 28 0.027
1017
ACQ016 Acquired Pure Red Cell Aplasia 25 0.027
1018
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 18 0.027
1019
EXT039 Extrapontine Myelinolysis 15 0.027
1020
c HYP595 Hypertension, Essential 69 0.026
1021
GLC037 Glucocorticoid Resistance 62 0.026
1022
ACN011 Acne 62 0.026
1023
CNT047 Contact Dermatitis 61 0.026
1024
P RHN004 Rhinitis 60 0.026
1025
P GT001 Gout 58 0.026
1026
SCH014 Schistosomiasis 58 0.026
1027
DSM004 Desmoid Tumor 56 0.026
1028
P RTH001 Rothmund-Thomson Syndrome 55 0.026
1029
DMY004 Demyelinating Disease 53 0.026
1030
SLP005 Sleep Disorder 53 0.026
1031
ERD001 Erdheim-Chester Disease 52 0.026
1032
c INF067 Inflammatory Bowel Disease 10 49 0.026
1033
FLL008 Folliculitis 46 0.026
1034
OST003 Osteonecrosis 45 0.026
1035
CRS001 Crescentic Glomerulonephritis 42 0.026
1036
VRN001 Vernal Conjunctivitis 42 0.026
1037
AYM001 Ayme-Gripp Syndrome 41 0.026
1038
P ACQ009 Acquired Metabolic Disease 38 0.026
1039
BRS015 Breast Medullary Carcinoma 37 0.026
1040
LCH004 Lichen Disease 36 0.026
1041
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.026
1042
PLC008 Placenta Disease 33 0.026
1043
P ATX010 Ataxia Neuropathy Spectrum 30 0.026
1044
c DMN006 Diamond-Blackfan Anemia 3 29 0.026
1045
c DMN019 Diamond-Blackfan Anemia 4 27 0.026
1046
c DMN005 Diamond-Blackfan Anemia 2 22 0.026
1047
UTR037 Uterine Corpus Sarcoma 20 0.026
1048
P PLM036 Pulmonary Fibrosis 71 0.025
1049
OMN001 Omenn Syndrome 67 0.025
1050
P ATR011 Atrial Fibrillation 66 0.025
1051
BRN024 Bronchitis 64 0.025
1052
CHR063 Chronic Mucocutaneous Candidiasis 63 0.025
1053
ADL030 Adult-Onset Still's Disease 59 0.025
1054
PGT001 Paget's Disease of Bone 59 0.025
1055
LPD008 Lipid Metabolism Disorder 58 0.025
1056
c SVR001 Severe Acute Respiratory Syndrome 57 0.025
1057
ALL010 Allergic Contact Dermatitis 57 0.025
1058
SVR066 Severe Combined Immunodeficiency, X-Linked 57 0.025
1059
P HYP076 Hyperthyroidism 55 0.025
1060
CRH005 Crohn's Colitis 52 0.025
1061
P HRD018 Hair Disease 51 0.025
1062
P PLY017 Polyarteritis Nodosa 51 0.025
1063
NNL002 Nonalcoholic Steatohepatitis 50 0.025
1064
P PNV001 Panuveitis 50 0.025
1065
CMR002 Coumarin Resistance 48 0.025
1066
ELS001 Eales Disease 47 0.025
1067
P RPD001 Rapidly Progressive Glomerulonephritis 45 0.025
1068
BNN003 Bone Inflammation Disease 44 0.025
1069
ERY004 Erysipelas 41 0.025
1070
MYC017 Mycobacterium Kansasii 40 0.025
1071
c DMN021 Diamond-Blackfan Anemia 6 35 0.025
1072
ADP007 Adie Pupil 34 0.025
1073
LWR001 Lower Lip Cancer 33 0.025
1074
TXC007 Toxic Pneumonitis 33 0.025
1075
ESP026 Esophagus Sarcoma 33 0.025
1076
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.025
1077
SML015 Small Intestinal Sarcoma 32 0.025
1078
CYT004 Cytomegalic Inclusion Disease 31 0.025
1079
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 30 0.025
1080
P DRM012 Dermis Tumor 26 0.025
1081
EYC003 Eye Accommodation Disease 24 0.025
1082
c PRX067 Paroxysmal Nocturnal Hemoglobinuria 2 21 0.025
1083
c NRB012 Neuroblastoma 5 18 0.025
1084
c INF136 Influenza, Severe 15 0.025
1085
P FML321 Familial Stomach Cancer 13 0.025
1086
CHR066 Chronic Fatigue Syndrome 64 0.024
1087
DNG002 Dengue Hemorrhagic Fever 63 0.024
1088
P VLC001 Velocardiofacial Syndrome 62 0.024
1089
P KLL001 Kallmann Syndrome 61 0.024
1090
CHL123 Chlamydia 60 0.024
1091
P BRC006 Brachydactyly 54 0.024
1092
SML019 Smallpox 54 0.024
1093
DSS008 Disease of Mental Health 52 0.024
1094
QDR001 Quadriplegia 52 0.024
1095
PHL006 Phelan-Mcdermid Syndrome 51 0.024
1096
SCH002 Schnitzler Syndrome 51 0.024
1097
AMN001 Amenorrhea 50 0.024
1098
BRN022 Bronchiectasis 50 0.024
1099
IMG001 Image Syndrome 50 0.024
1100
HYP037 Hyperhomocysteinemia 50 0.024
1101
QBC001 Quebec Platelet Disorder 48 0.024
1102
HYD002 Hydronephrosis 47 0.024
1103
c PST005 Posterior Uveitis 46 0.024
1104
MGC001 Megacolon 45 0.024
1105
RCT011 Rectal Prolapse 43 0.024
1106
FCT005 Factor Xiii Deficiency 43 0.024
1107
c ATM022 Autoimmune Myocarditis 42 0.024
1108
STP004 Staphylococcal Toxic Shock Syndrome 41 0.024
1109
VRL003 Variola Major 41 0.024
1110
SXD001 Sex Differentiation Disease 38 0.024
1111
c ATM075 Autoimmune Encephalitis 38 0.024