Search results for "myeloid malignancy"

The MalaCard for "myeloid malignancy" has been retired.
Searching MalaCards for entries containing "myeloid malignancy"

1396 hits were found for 'myeloid malignancy'

# Family MCID Name MIFTS Score
1
PLT019 Platelet Disorder, Familial, with Associated Myeloid Malignancy 31 4.030
2
ERY024 Erythropoietic Uroporphyria Associated with Myeloid Malignancy 8 2.164
3
FML146 Familial Platelet Disorder with Propensity to Acute Myelogenous Leukemia 9 1.523
4
P LKM002 Leukemia 70 1.216
5
P MYL006 Myeloid Leukemia 67 1.151
6
c LKM061 Leukemia, Acute Myeloid 71 0.567
7
c CHR064 Chronic Monocytic Leukemia 43 0.495
8
c ACT073 Acute Leukemia 62 0.493
9
ACT118 Acute Non Lymphoblastic Leukemia 29 0.463
10
BNM001 Bone Marrow Cancer 52 0.406
11
MYL009 Myelodysplastic Syndrome 74 0.394
12
MRG013 Mirage Syndrome 26 0.386
13
SRC014 Sarcoma 66 0.365
14
P LYM118 Lymphoma 70 0.351
15
HMT002 Hematologic Cancer 64 0.341
16
BNC003 Bone Cancer 45 0.338
17
P LKM068 Leukemia, Chronic Myeloid, Somatic 66 0.336
18
c CHR418 Chronic Leukemia 48 0.318
19
CMP005 Campomelic Dysplasia 72 0.298
20
P CHR562 Chronic Myelocytic Leukemia 41 0.293
21
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.292
22
c PRM023 Pre-Malignant Neoplasm 43 0.277
23
MYL003 Myeloid Sarcoma 48 0.276
24
P GLM045 Glioma 58 0.274
25
c ACT020 Acute T Cell Leukemia 39 0.272
26
P LYM026 Lymphoblastic Leukemia 60 0.262
27
HMT018 Hematopoietic Stem Cell Transplantation 41 0.256
28
IMM127 Immune System Cancer 42 0.250
29
P NRV006 Nervous System Cancer 62 0.246
30
RFR004 Refractory Hematologic Cancer 29 0.241
31
c MLG068 Malignant Glioma 50 0.240
32
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 48 0.235
33
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.229
34
LYM067 Lymphoid Leukemia 43 0.226
35
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 17 0.215
36
LYM023 Lymphatic System Cancer 35 0.210
37
MYL004 Myelodysplastic Myeloproliferative Cancer 47 0.208
38
LYM024 Lymphatic System Disease 50 0.204
39
P LYM033 Lymphoproliferative Syndrome 53 0.204
40
P ACT074 Acute Lymphocytic Leukemia 55 0.203
41
BNS002 Bone Structure Disease 36 0.200
42
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.200
43
OCL009 Ocular Cancer 62 0.200
44
PRP021 Peripheral Nervous System Neoplasm 50 0.199
45
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.199
46
ACT114 Acute Myeloblastic Leukemia Without Maturation 30 0.199
47
c CHR090 Chronic Lymphocytic Leukemia 74 0.197
48
c LKM062 Leukemia, Acute Lymphoblastic 64 0.195
49
ACD009 Acid-Labile Subunit, Deficiency of 48 0.195
50
c ADL001 Adult Lymphoma 41 0.193
51
LYM019 Lymphosarcoma 53 0.189
52
c ADL052 Adult Acute Lymphocytic Leukemia 42 0.187
53
LYM040 Lymphoblastic Lymphoma 54 0.185
54
CHR285 Chronic Myelomonocytic Leukemia 55 0.184
55
P MNC007 Monocytic Leukemia 55 0.184
56
BRT030 Birth Defects 43 0.182
57
ACR041 Acromelic Frontonasal Dysostosis 46 0.181
58
CHL061 Childhood Leukemia 48 0.180
59
ADL002 Adult Syndrome 53 0.179
60
MGK001 Megakaryocytic Leukemia 53 0.178
61
c CLL013 Cell Type Cancer 48 0.176
62
c ACT009 Acute Monocytic Leukemia 52 0.175
63
ACT098 Acute Erythroid Leukemia 48 0.175
64
P MYL005 Myelofibrosis 67 0.175
65
LKC003 Leukocyte Disease 47 0.174
66
END072 Endotheliitis 42 0.174
67
P ACT135 Acute Graft Versus Host Disease 53 0.174
68
NRL004 Neuroleptic Malignant Syndrome 45 0.173
69
PLS009 Plasma Cell Neoplasm 48 0.172
70
ACT200 Acute Monoblastic Leukemia 44 0.171
71
P BRS047 Breast Cancer 100 0.170
72
P HST010 Histiocytosis 55 0.170
73
BNL002 Bone Lymphoma 33 0.170
74
P ORL007 Oral Cavity Cancer 58 0.169
75
DFC004 Deficiency Anemia 65 0.167
76
BLD053 Blood Platelet Disease 46 0.167
77
c ADL093 Adult Acute Monocytic Leukemia 20 0.166
78
SNS023 Sensory System Cancer 46 0.166
79
WLL006 Wells Syndrome 56 0.165
80
GDS001 Good Syndrome 45 0.165
81
HST009 Histiocytoma 47 0.165
82
c LKM055 Leukemia, Acute Lymphoblastic 2 22 0.165
83
P MLT019 Multiple Myeloma 80 0.164
84
ORL011 Oral Cancer 55 0.164
85
P TCL004 T-Cell Leukemia 46 0.163
86
PRS047 Prostatitis 56 0.163
87
c ADL017 Adult T-Cell Leukemia 58 0.162
88
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.162
89
BND014 Bone Development Disease 42 0.161
90
ACR002 Acrocapitofemoral Dysplasia 36 0.161
91
KDS001 Kid Syndrome 53 0.160
92
CHL071 Child Syndrome 58 0.160
93
EWN003 Ewing Sarcoma 64 0.160
94
P MDL005 Medulloblastoma 77 0.159
95
P NTR004 Neutropenia 59 0.158
96
CSY001 C Syndrome 49 0.157
97
P BCL006 B-Cell Lymphomas 64 0.155
98
TST021 Testicular Germ Cell Tumor 70 0.155
99
MNM003 Minimally Differentiated Acute Myeloblastic Leukemia 17 0.153
100
c CHR417 Chronic Graft Versus Host Disease 50 0.153
101
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.152
102
PRM151 Primary Bone Lymphoma 27 0.150
103
CNT018 Central Nervous System Leukemia 39 0.149
104
HML018 Homologous Wasting Disease 17 0.149
105
P ADN016 Adenocarcinoma 69 0.148
106
PLS016 Plasma Cell Leukemia 42 0.147
107
VSC006 Vascular Cancer 54 0.146
108
c MLG054 Malignant Histiocytosis 55 0.146
109
GRM001 Germ Cell and Embryonal Cancer 39 0.145
110
P LNG032 Lung Cancer 94 0.143
111
BLD054 Blood Protein Disease 40 0.143
112
P THY032 Thyroiditis 54 0.143
113
P HPT021 Hepatitis 70 0.143
114
RFR010 Refractory Anemia 45 0.142
115
c LKM060 Leukemia, Acute Lymphoblastic 3 52 0.141
116
P TRT010 Teratoma 52 0.139
117
c LYM106 Lymphoproliferative Syndrome 1 34 0.138
118
c LYM107 Lymphoproliferative Syndrome 2 34 0.137
119
PLV005 Pelviureteric Junction Obstruction 45 0.137
120
c LKM056 Leukemia, Chronic Lymphocytic 2 24 0.136
121
PRT036 Peritonitis 62 0.136
122
c LKM050 Leukemia, Chronic Lymphocytic 1 22 0.136
123
HRT007 Heart Cancer 50 0.134
124
P PNC044 Pancreatitis 60 0.134
125
FRB001 Farber Lipogranulomatosis 51 0.134
126
P AST007 Astrocytoma 65 0.132
127
LYM115 Lymphoma, Non-Hodgkin 65 0.131
128
ADN018 Adenoma 59 0.131
129
P HRT017 Heart Tumor 35 0.130
130
P ESN007 Eosinophilia 61 0.130
131
HPT023 Hepatocellular Carcinoma 91 0.130
132
ATY042 Atypical Chronic Myeloid Leukemia 45 0.130
133
c ADL079 Adult Heart Tumor 19 0.129
134
c LKM004 Leukemia, B-Cell, Chronic 25 0.129
135
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 36 0.127
136
MXD023 Mixed Cell Type Cancer 47 0.127
137
P BLD051 Blood Coagulation Disease 45 0.126
138
P HMR003 Hemorrhagic Disease 57 0.125
139
P CHR084 Chromosomal Disease 37 0.125
140
P GLB002 Glioblastoma 66 0.124
141
MLG108 Malignant Melanoma, Somatic 67 0.124
142
P RFR008 Refractory Anemia with Excess Blasts 30 0.122
143
P PRT096 Peritoneal Mesothelioma 51 0.122
144
CNT010 Central Nervous System Hematologic Cancer 21 0.122
145
ACT228 Acute Radiation Syndrome 21 0.121
146
VSC008 Vascular Hemostatic Disease 33 0.120
147
CRD118 Cardiovascular Cancer 47 0.120
148
c MLG002 Malignant Peritoneal Mesothelioma 45 0.119
149
c LKM005 Leukemia, T-Cell, Chronic 22 0.118
150
c LKM051 Leukemia, Chronic Lymphocytic 3 22 0.118
151
P PLR004 Pleuropulmonary Blastoma 64 0.117
152
ARG006 Aregenerative Anemia 23 0.117
153
BRN028 Brain Cancer 70 0.116
154
P CLR023 Colorectal Cancer 97 0.115
155
PCK002 Pick Disease 67 0.115
156
GLM004 Gliomatosis Cerebri 53 0.114
157
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 39 0.114
158
HDG012 Hodgkin Lymphoma 73 0.113
159
P PNC035 Pancreatic Cancer 85 0.112
160
VND001 Vein Disease 52 0.112
161
NTR003 Natural Killer Cell Leukemia 47 0.111
162
MST016 Mesothelioma, Somatic 53 0.111
163
c PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 25 0.111
164
P GST049 Gastrointestinal System Cancer 60 0.110
165
P APL001 Aplastic Anemia 73 0.110
166
P RNL014 Renal Cell Carcinoma 81 0.109
167
P PLY018 Polycythemia 57 0.109
168
P MST009 Mastocytosis 54 0.109
169
CRC006 Carcinoid Syndrome 51 0.108
170
MDS022 Mediastinitis 41 0.108
171
P THR014 Thrombocytopenia 64 0.107
172
CHR563 Chronic Eosinophilic Leukemia 47 0.107
173
c RFR014 Refractory Anemia with Excess Blasts Type 2 18 0.107
174
GST019 Gastrointestinal Stromal Tumor 72 0.107
175
c BCL013 B-Cell Adult Acute Lymphocytic Leukemia 22 0.107
176
c RTN162 Retinitis Pigmentosa 2 51 0.107
177
P OVR042 Ovarian Cancer 75 0.106
178
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.106
179
P CRV039 Cervicitis 44 0.105
180
P KDN017 Kidney Cancer 67 0.105
181
c RFR015 Refractory Anemia with Excess Blasts Type 1 15 0.105
182
PLS003 Plasmacytic Leukemia 23 0.105
183
ACT184 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Alkylating Agent 15 0.104
184
ENG004 Engraftment Syndrome 35 0.104
185
P ESS003 Essential Thrombocythemia 68 0.104
186
PLR006 Pleural Cancer 46 0.104
187
HYP266 Hypoxia 55 0.104
188
ALN001 Aland Island Eye Disease 45 0.103
189
RFR007 Refractory Anemia with Excess Blasts in Transformation 22 0.103
190
PLR022 Pleural Disease 52 0.103
191
P PRS040 Prostate Cancer 89 0.102
192
RFR001 Refractory Plasma Cell Neoplasm 18 0.102
193
VSC001 Vascular Myelopathy 25 0.102
194
GST053 Gastric Cancer 77 0.102
195
MLG012 Malignant Epithelial Mesothelioma 35 0.101
196
LKM067 Leukemia, Acute Promyelocytic, Somatic 53 0.101
197
c SYS004 Systemic Mastocytosis 59 0.101
198
THR004 Thrombocytosis 55 0.099
199
P BNG032 Benign Mesothelioma 41 0.099
200
NRN004 Neuroendocrine Tumor 54 0.099
201
ALR002 Al-Raqad Syndrome 36 0.099
202
c MLG081 Malignant Teratoma 46 0.099
203
c SML023 Small Cell Lung Cancer, Adult 17 0.098
204
DFF005 Diffuse Large B-Cell Lymphoma 56 0.098
205
CRB009 Cerebritis 38 0.098
206
P ART022 Arthritis 75 0.098
207
CRB002 Cerebral Primitive Neuroectodermal Tumor 45 0.097
208
PRD011 Proud Syndrome 42 0.097
209
WLM007 Wilms Tumor Susceptibility-5 64 0.097
210
GLB015 Glioblastoma Multiforme 62 0.096
211
P SPS003 Spastic Diplegia 53 0.096
212
P ASP006 Aspergillosis 60 0.095
213
SFT003 Soft Tissue Sarcoma 56 0.095
214
ACT177 Acute Basophilic Leukemia 34 0.095
215
RDT005 Radiation Induced Cancer 28 0.094
216
ACT158 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Radiation 14 0.093
217
MNT001 Mantle Cell Lymphoma 70 0.093
218
LYM127 Lymphatic Malformations 37 0.093
219
ACT103 Acute Lymphoblastic Leukemia, Childhood 42 0.093
220
GRN017 Granulocytopenia 42 0.092
221
c CRN214 Coronary Heart Disease 5 23 0.090
222
c CNN010 Connective Tissue Benign Neoplasm 35 0.089
223
HRT029 Heart Tumor of the Child 17 0.089
224
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 28 0.089
225
BNM011 Bone Marrow Failure Syndrome 2 26 0.089
226
PRL032 Perlman Syndrome 55 0.089
227
P PNM007 Pneumonia 66 0.089
228
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 58 0.088
229
PRP036 Peripheral T-Cell Lymphoma 45 0.088
230
CLV009 Clove Syndrome, Somatic 42 0.087
231
P CNN004 Connective Tissue Cancer 45 0.087
232
DND018 Dendritic Cell Tumor 40 0.087
233
P ESP024 Esophagitis 62 0.087
234
DWN001 Down Syndrome 65 0.087
235
IMM136 Immune System Disease 50 0.087
236
P FLL037 Follicular Lymphoma 66 0.087
237
MLG097 Malignant Mesenchymal Tumor 37 0.086
238
OBS001 Obstructive Jaundice 48 0.086
239
C3D001 C3 Deficiency 53 0.085
240
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 41 0.085
241
P RHM011 Rheumatoid Arthritis 88 0.085
242
MCR004 Macroglobulinemia 50 0.085
243
c SVR003 Severe Congenital Neutropenia 56 0.084
244
CLL014 Cll/sll 43 0.084
245
c INV001 Invasive Aspergillosis 47 0.084
246
WTH001 Withdrawal Disorder 41 0.084
247
P SKN013 Skin Benign Neoplasm 46 0.082
248
GRD007 Grade Iii Astrocytoma 51 0.082
249
LPD004 Lipoid Nephrosis 48 0.082
250
RTC009 Reticulum Cell Sarcoma 48 0.082
251
RTC005 Reticulosarcoma 48 0.082
252
BNM010 Bone Marrow Failure Syndrome 1 30 0.082
253
DDN006 Duodenitis 44 0.081
254
SKN019 Skin Melanoma 62 0.081
255
ATN003 Autonomic Nervous System Neoplasm 43 0.081
256
LNG030 Lung Adenoma 41 0.081
257
c NRF018 Neurofibromatosis, Type 1 68 0.081
258
P OST001 Osteopetrosis 62 0.080
259
LRN003 Learning Disability 51 0.080
260
P SML001 Small Cell Carcinoma 57 0.080
261
SML033 Small Cell Cancer of the Lung, Somatic 53 0.080
262
PRP027 Peripheral Vascular Disease 69 0.080
263
NSY001 N Syndrome 39 0.080
264
WST001 West Syndrome 61 0.080
265
WHT007 White Platelet Syndrome 18 0.080
266
P OVR049 Ovarian Disease 55 0.080
267
END035 Endocrine Gland Cancer 52 0.079
268
c WLM005 Wilms Tumor 2 24 0.079
269
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.078
270
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 17 0.078
271
c FLL041 Follicular Lymphoma 1 46 0.078
272
P HYP098 Hypereosinophilic Syndrome 51 0.078
273
MTH009 Mouth Disease 63 0.078
274
MRG003 Marginal Zone B-Cell Lymphoma 50 0.078
275
SPL011 Spleen Cancer 37 0.078
276
HRY003 Hairy Cell Leukemia 60 0.078
277
PRC012 Pericardial Effusion 50 0.078
278
PLY125 Polycythemia Vera, Somatic 63 0.078
279
AML051 Aml with Myelodysplasia-Related Features 19 0.077
280
P MNN013 Meningitis 65 0.077
281
P OLG002 Oligodendroglioma 55 0.077
282
P NRB001 Neuroblastoma 69 0.077
283
NWC001 Newcastle Disease 54 0.076
284
HV1006 Hiv-1 82 0.076
285
P ANP001 Anaplastic Large Cell Lymphoma 58 0.075
286
P HRT032 Heart Disease 76 0.075
287
BND002 B- and T-Cell Mixed Leukemia 20 0.075
288
PLS011 Plasmacytoma 56 0.075
289
SPL018 Splenomegaly 44 0.075
290
P NSP012 Nasopharyngeal Carcinoma 67 0.075
291
ACT095 Acute Biphenotypic Leukemia 33 0.074
292
P RTN024 Retinoblastoma 75 0.074
293
SPR035 Superior Vena Cava Syndrome 32 0.074
294
LYM104 Lymphoma, Malt, Somatic 54 0.074
295
LYM126 Lymphoma Aids Related 18 0.074
296
CNN005 Connective Tissue Disease 61 0.074
297
WSC001 Wisconsin Syndrome 17 0.073
298
BRK010 Burkitt Lymphoma 66 0.073
299
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.073
300
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.073
301
P ACT080 Acute Pulmonary Heart Disease 32 0.073
302
MYL015 Myeloproliferative Disorder with Eosinophilia 35 0.072
303
CNT098 Central Core Disease 66 0.072
304
RHB003 Rhabdomyosarcoma 58 0.072
305
PST046 Post-Transplant Lymphoproliferative Disease 53 0.072
306
P PNC001 Pancytopenia 52 0.072
307
c CRN173 Coronary Heart Disease 8 20 0.072
308
SPL012 Splenic Disease 47 0.071
309
c ADL008 Adult Oligodendroglioma 37 0.071
310
ESP021 Esophageal Cancer 75 0.071
311
P BRN120 Bronchus Cancer 46 0.071
312
INT253 Intestinal Benign Neoplasm 50 0.071
313
BCL012 B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue 37 0.071
314
PPL022 Papilloma 55 0.070
315
c PRM012 Primary Polycythemia 51 0.070
316
P NRV007 Nervous System Disease 71 0.070
317
PRP007 Priapism 47 0.070
318
ADJ001 Adjustment Disorder 38 0.070
319
THR106 Therapy Related Acute Myeloid Leukemia and Myelodysplastic Syndrome 15 0.070
320
c CHR096 Chronic Pulmonary Heart Disease 40 0.070
321
VRL011 Viral Infectious Disease 59 0.070
322
P LMY004 Leiomyosarcoma 53 0.069
323
TBR010 Tuberculosis 69 0.069
324
UTR033 Uterine Corpus Cancer 50 0.069
325
MYC006 Mycosis Fungoides 66 0.069
326
BRN038 Bronchial Disease 54 0.069
327
DSS003 Disseminated Eosinophilic Collagen Disease 18 0.069
328
c PRM225 Primary Thrombocytopenia 42 0.069
329
RNL101 Renal Cell Carcinoma, Papillary 67 0.069
330
c HPT016 Hepatitis B 64 0.069
331
ANP009 Anaplastic Oligodendroglioma 41 0.068
332
MLG041 Malignant Triton Tumor 36 0.068
333
BNM013 Bone Marrow Failure Syndrome 3 19 0.068
334
FML038 Female Reproductive Organ Cancer 51 0.068
335
SKN023 Skin Tag 46 0.068
336
c THR037 Thrombocytopenia 2 37 0.068
337
P THY023 Thymoma 53 0.068
338
THY028 Thyroid Cancer 68 0.068
339
SPL004 Splenic Marginal Zone Lymphoma 43 0.068
340
c PRM149 Primary Hypereosinophilic Syndrome 39 0.068
341
ACT217 Acute Myeloid Leukemia with Recurrent Genetic Anomaly 12 0.068
342
BLS007 Blastic Plasmacytoid Dendritic Cell 40 0.067
343
NDL020 Nodal Marginal Zone B-Cell Lymphoma 35 0.067
344
FML039 Female Reproductive System Disease 48 0.067
345
c CRN177 Coronary Heart Disease 7 22 0.067
346
LNG013 Lung Lymphoma 40 0.067
347
P LRY019 Laryngitis 55 0.066
348
ACT216 Acute Leukemia of Ambiguous Lineage 36 0.066
349
P ENC004 Encephalitis 61 0.066
350
GNT002 Giant Cell Glioblastoma 51 0.066
351
P WLD002 Waldenstrom Macroglobulinemia 62 0.066
352
c ACT195 Acute Myeloid Leukemia with T(9;11)(p22;q23) 23 0.066
353
P FBR017 Fibrosarcoma 56 0.066
354
c CNT035 Central Nervous System Disease 59 0.066
355
URT010 Ureteral Obstruction 45 0.065
356
P INF038 Influenza 74 0.065
357
BNM005 Bone Marrow Necrosis 31 0.065
358
BRN106 Burns 52 0.064
359
P LPS002 Liposarcoma 50 0.064
360
c TRC078 Trichohepatoenteric Syndrome 2 31 0.064
361
P SNS014 Sinusitis 60 0.064
362
P HML002 Hemolytic Anemia 60 0.064
363
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 62 0.064
364
LYM041 Lymphocytes Absent 16 0.064
365
TNG003 Tongue Cancer 60 0.064
366
MXD026 Mixed Glioma 32 0.064
367
RTN023 Retinitis 49 0.064
368
LKP003 Leukoplakia 41 0.064
369
MST002 Mast-Cell Leukemia 48 0.064
370
c PRM226 Primary Central Nervous System Lymphoma 49 0.064
371
P CTN015 Cutaneous T Cell Lymphoma 50 0.063
372
P LPS004 Lupus Erythematosus 63 0.063
373
P CNT005 Central Nervous System Lymphoma 53 0.063
374
PLS025 Plasmablastic Lymphoma 45 0.063
375
P GLM007 Glomerulonephritis 56 0.063
376
MN1001 Mn1 31 0.063
377
GLC077 Glucocorticoid Therapy, Response to 19 0.063
378
NRF007 Neurofibroma 52 0.063
379
TST014 Testicular Cancer 52 0.062
380
RBR001 Roberts Syndrome 59 0.062
381
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.062
382
LYM048 Lymphoma, Large-Cell, Immunoblastic 27 0.062
383
MRC001 Marchiafava Bignami Disease 50 0.062
384
CLT003 Colitis 59 0.062
385
PNC034 Pancreas Disease 57 0.062
386
P CRN178 Coronary Heart Disease 6 24 0.061
387
HRT003 Heart Lymphoma 31 0.061
388
P DBT005 Diabetes Insipidus 53 0.061
389
c PNC106 Pancreatic Agenesis 1 40 0.061
390
ORL015 Oral Squamous Cell Carcinoma 56 0.061
391
P INT070 Intestinal Obstruction 56 0.061
392
c MCR161 Macroglobulinemia, Waldenstrom 1 27 0.061
393
c THR090 Thrombocythemia 1 34 0.060
394
GND003 Gonadal Disease 43 0.060
395
PHY001 Physiological Polycythemia 31 0.060
396
TTR011 Tetraploidy 41 0.060
397
c MCR162 Macroglobulinemia, Waldenstrom 2 20 0.060
398
PDT001 Pediatric Lymphoma 40 0.060
399
MSC072 Muscle Cancer 51 0.059
400
P MYC007 Myocardial Infarction 79 0.059
401
PRR002 Pure Red-Cell Aplasia 46 0.059
402
MLG065 Malignant Fibroxanthoma 38 0.059
403
CHR062 Chronic Erythremia 16 0.059
404
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 31 0.059
405
FXF002 Fox-Fordyce Disease 39 0.059
406
LYM051 Lymphomatoid Granulomatosis 46 0.059
407
ANR040 Aneurysm 57 0.059
408
SHW002 Shwachman-Diamond Syndrome 60 0.058
409
NTR005 Nutritional Deficiency Disease 39 0.058
410
MYL052 Myeloproliferative Neoplasms, Familial 17 0.058
411
c SCN042 Secondary Hypereosinophilic Syndrome 16 0.058
412
P PRP019 Peripheral Nervous System Disease 54 0.058
413
PRM025 Primary Bacterial Infectious Disease 43 0.058
414
SPC003 Specific Developmental Disorder 40 0.058
415
c CRN176 Coronary Heart Disease 9 20 0.057
416
ALL026 Allergic Hypersensitivity Disease 53 0.057
417
c PNC094 Pancreatic Cancer 1 29 0.057
418
ERY051 Erythroleukemia, Familial 23 0.057
419
P MYP004 Myopathy 67 0.057
420
CHR286 Chronic Neutrophilic Leukemia 44 0.057
421
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.057
422
P SPN301 Spinocerebellar Ataxia 2 63 0.057
423
GST050 Gastrointestinal System Disease 54 0.057
424
P EXP004 Exophthalmos 54 0.057
425
P BCL005 B Cell Prolymphocytic Leukemia 43 0.057
426
CLN015 Colon Adenocarcinoma 49 0.057
427
DPH001 Diphtheria 58 0.057
428
OVR094 Ovarian Epithelial Cancer 45 0.057
429
ACN002 Acanthosis Nigricans 57 0.056
430
PRT035 Peritoneum Cancer 39 0.056
431
OVR069 Ovarian Germ Cell Tumor 23 0.056
432
ANP010 Anaplastic Plasmacytoma 21 0.056
433
CNT067 Central Cord Syndrome 24 0.056
434
c SYS001 Systemic Lupus Erythematosus 87 0.056
435
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 28 0.056
436
ZYG002 Zygomycosis 33 0.056
437
PRN039 Paraneoplastic Syndromes 33 0.056
438
DFF027 Diffuse Lymphatic Malformation 30 0.056
439
PRL017 Prolymphocytic Leukemia 47 0.056
440
LMY002 Leiomyoma 42 0.056
441
P CHR345 Chronic Pain 49 0.056
442
BCK006 Back Pain 42 0.055
443
P MYS005 Myositis 56 0.055
444
MYC002 Mycobacterium Avium Complex Disease 51 0.055
445
HMG002 Hemoglobinuria 49 0.055
446
HDN004 Head and Neck Carcinoma 55 0.055
447
c ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 35 0.055
448
c WLM011 Wilms Tumor 6 21 0.055
449
NRN002 Neuronitis 42 0.055
450
LRG008 Large Granular Lymphocyte Leukemia 38 0.055
451
P TRC086 Trichohepatoenteric Syndrome 1 46 0.055
452
MST017 Mast Cell Disease 52 0.055
453
RPR002 Reproductive System Disease 46 0.054
454
RCT018 Rectal Neoplasm 55 0.054
455
P END044 Endometriosis 53 0.054
456
c THR048 Thrombocytopenia 4 29 0.054
457
P OBS005 Obesity 93 0.054
458
YNG002 Young Syndrome 26 0.054
459
STT009 Sutton Disease 2 20 0.054
460
AND005 Androgen Insensitivity Syndrome, Mild 16 0.054
461
c CLR075 Colorectal Cancer 3 30 0.054
462
SKN016 Skin Disease 68 0.053
463
PYD002 Pyoderma 49 0.053
464
P PLM006 Pulmonary Alveolar Proteinosis 48 0.053
465
P RSP003 Respiratory Failure 70 0.053
466
TCL018 T-Cell Childhood Acute Lymphocytic Leukemia 17 0.053
467
TCL019 T-Cell Childhood Lymphoblastic Lymphoma 17 0.053
468
GNG004 Ganglioglioma 49 0.053
469
P INF032 Infertility 61 0.053
470
INS024 Insulin-Like Growth Factor I 74 0.053
471
ISC004 Ischemia 59 0.053
472
EMB004 Embryonal Carcinoma 56 0.053
473
P LPC002 Lip Cancer 53 0.053
474
CLN019 Colonic Disease 50 0.053
475
c CLR085 Colorectal Cancer 1 42 0.053
476
c FML108 Familial Breast Cancer 57 0.053
477
P UTR038 Uterine Disease 40 0.053
478
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 41 0.052
479
OVR104 Ovarian Melanoma 36 0.052
480
ANP008 Anaplastic Oligoastrocytoma 24 0.052
481
LKS001 Leukostasis 39 0.052
482
PRS042 Prostate Disease 52 0.052
483
c HPT001 Hepatitis C 68 0.052
484
VGN023 Vaginitis 42 0.052
485
P CHL066 Cholangitis 49 0.052
486
c ANP011 Anaplastic Small Cell Lymphoma 17 0.052
487
ACC008 Accelerated Tumor Formation 20 0.052
488
DRM006 Dermatitis 61 0.052
489
PRT018 Portal Vein Thrombosis 49 0.052
490
EPT020 Epithelioid Hemangioendothelioma 45 0.052
491
P CRD011 Cardiomyopathy 67 0.052
492
ADM013 Adamantinoma of Long Bones 59 0.052
493
OLG006 Oligoastrocytoma 34 0.052
494
PRM133 Primary Pulmonary Lymphoma 24 0.052
495
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.051
496
END030 End Stage Renal Failure 52 0.051
497
VSC011 Vasculitis 62 0.051
498
ATN002 Autonomic Nervous System Disease 47 0.051
499
FSR001 Fusariosis 33 0.051
500
c INH015 Inherited Acute Myeloid Leukemia 27 0.051
501
c THR102 Thrombocytopenia 5 30 0.051
502
P SML016 Small Intestine Cancer 54 0.051
503
BRN048 Brain Stem Cancer 38 0.051
504
MLR004 Malaria 79 0.050
505
APP008 Appendicitis 60 0.050
506
P LFR001 Li-Fraumeni Syndrome 75 0.050
507
P DRM010 Dermatomyositis 58 0.050
508
BLR007 Biliary Tract Neoplasm 52 0.050
509
CRD001 Cardiac Tamponade 44 0.050
510
STM006 Stomach Disease 50 0.050
511
HPT070 Hepatosplenic T-Cell Lymphoma 41 0.050
512
CNT045 Central Nervous System Sarcoma 19 0.050
513
GNG013 Gingivitis 60 0.050
514
ACT017 Acute Chest Syndrome 48 0.050
515
c CLR079 Colorectal Cancer 2 31 0.049
516
HYP084 Hypopyon 30 0.049
517
c ACT198 Acute Myeloid Leukemia with T(6;9)(p23;q34) 17 0.049
518
DSS009 Disseminated Intravascular Coagulation 51 0.049
519
c FML303 Familial/multiple Cancer 16 0.049
520
CRV047 Cervical Cancer, Somatic 65 0.049
521
P INT068 Intestinal Disease 61 0.049
522
P AST005 Asthma 82 0.049
523
MYL055 Myeloid/lymphoid or Mixed Lineage Leukemia 30 0.049
524
VSC047 Vascular Malformation 45 0.049
525
PTR006 Peters Anomaly 64 0.048
526
P 8P1002 8p11 Myeloproliferative Syndrome 35 0.048
527
MYL059 Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 11 0.048
528
CNG034 Congestive Heart Failure 71 0.048
529
P PLY041 Polymyositis 51 0.048
530
EPD001 Epidermodysplasia Verruciformis 50 0.048
531
BLD087 Bladder Cancer, Somatic 67 0.048
532
ATR060 Atrial Standstill, Digenic 53 0.048
533
FML037 Female Breast Cancer 51 0.048
534
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.048
535
P CND004 Candidiasis 57 0.048
536
c PND001 Pain Disorder 55 0.048
537
FBR009 Fibrous Dysplasia 44 0.048
538
THR016 Thrombophlebitis 52 0.048
539
c HYP072 Hypersensitivity Reaction Type Iii Disease 41 0.048
540
ADR005 Adrenal Carcinoma 56 0.047
541
P SML002 Small Cell Sarcoma 41 0.047
542
PYD001 Pyoderma Gangrenosum 49 0.047
543
SZR001 Sezary's Disease 53 0.047
544
CNG028 Congenital Hypoplastic Anemia 49 0.047
545
SCT005 Scott Syndrome 50 0.047
546
c HMN021 Human T-Cell Leukemia Virus Type 1 51 0.047
547
GNG002 Ganglioneuroma 48 0.047
548
MLR006 Male Reproductive Organ Cancer 47 0.047
549
c PRS116 Prostate Cancer 1 41 0.047
550
BCT015 Bacteremia 48 0.047
551
P ACT105 Acute Mountain Sickness 53 0.047
552
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.047
553
MND006 Mondor Disease 21 0.046
554
MYX005 Myxoid Liposarcoma 57 0.046
555
INT051 Intussusception 50 0.046
556
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 31 0.046
557
TXC002 Toxic Encephalopathy 51 0.046
558
THY025 Thymus Cancer 51 0.046
559
RSP006 Respiratory System Disease 62 0.046
560
HPT074 Hepatic Adenoma, Somatic 51 0.046
561
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.046
562
OCL022 Ocular Melanoma 51 0.046
563
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 40 0.046
564
OST085 Osteosarcoma, Somatic 63 0.046
565
c THR086 Thrombocythemia 3 28 0.046
566
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.045
567
KDN020 Kidney Cancer, Childhood 13 0.045
568
PLR008 Pleurisy 50 0.045
569
RDC002 Radiculopathy 53 0.045
570
c THR110 Thrombocytopenia 6 22 0.045
571
NVD002 Nevada Syndrome 16 0.045
572
MST004 Mast Cell Neoplasm 42 0.045
573
SVR004 Severe Combined Immunodeficiency 68 0.045
574
MCR013 Microphthalmia 59 0.045
575
P ATX004 Ataxia 53 0.045
576
SLT001 Solitary Osseous Plasmacytoma 38 0.045
577
EPS006 Epstein Syndrome 40 0.045
578
ACT196 Acute Myeloid Leukemia with Inv3(p21;q26.2) or T(3;3)(p21;q26.2) 8 0.044
579
IDP064 Idiopathic Neutropenia 45 0.044
580
c DLT001 Delta Chain Disease 16 0.044
581
P HMN010 Hemangioma 60 0.044
582
PNN001 Panniculitis 50 0.044
583
GLL018 Gallbladder Cancer 63 0.044
584
P PNL012 Penile Cancer 60 0.044
585
P CRV031 Cervical Adenocarcinoma 52 0.044
586
CRN036 Craniopharyngioma 52 0.044
587
THY030 Thyroid Gland Disease 51 0.044
588
KRT009 Keratosis 50 0.044
589
HPT022 Hepatoblastoma 53 0.044
590
CYT008 Cytomegalovirus Infection 51 0.044
591
HYP063 Hypersplenism 48 0.044
592
P HRP006 Herpes Simplex 65 0.044
593
P SZR006 Seizure Disorder 57 0.044
594
PNL014 Pineal Gland Cancer 33 0.043
595
P ALX003 Alexander Disease 64 0.043
596
ATH003 Atherosclerosis 62 0.043
597
c FNC027 Fanconi Anemia, Complementation Group a 73 0.043
598
MSL001 Measles 61 0.043
599
PRP030 Purpura 59 0.043
600
PMP001 Pemphigus 49 0.043
601
MST001 Mast-Cell Sarcoma 46 0.043
602
PRM165 Primary Plasmacytoma of the Bone 15 0.043
603
P THL005 Thalassemia 61 0.043
604
c THR092 Thrombophilia Due to Thrombin Defect 56 0.043
605
P HYP014 Hyperuricemia 50 0.043
606
INF058 Inflammatory Myofibroblastic Tumor 46 0.043
607
RCM004 Recombinant 8 Syndrome 18 0.042
608
MNT045 Montefiore Syndrome 13 0.042
609
NTR040 Neutropenia, Cyclic 50 0.042
610
c ACT194 Acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation 29 0.042
611
P ACT190 Acute Myeloid Leukemia with T(8;16)(p11;p13) Translocation 16 0.042
612
P PLC011 Pilocytic Astrocytoma 58 0.042
613
ANG046 Angioimmunoblastic T-Cell Lymphoma 45 0.042
614
SPN040 Spinal Cancer 43 0.042
615
UND005 Undifferentiated Pleomorphic Sarcoma 43 0.042
616
PRC013 Pericarditis 52 0.042
617
c INH020 Inherited Metabolic Disorder 49 0.042
618
NSP002 Nasopharyngitis 41 0.042
619
BRC012 Brucellosis 65 0.042
620
WLL001 Williams-Beuren Syndrome 61 0.042
621
GYN001 Gynecomastia 49 0.042
622
c JVN003 Juvenile Xanthogranuloma 40 0.042
623
LNG099 Lung Disease 62 0.042
624
PNC033 Pancreas Adenocarcinoma 55 0.042
625
TCL002 T-Cell Large Granular Lymphocyte Leukemia 41 0.042
626
P ATX030 Ataxia-Telangiectasia 76 0.041
627
c ACT075 Acute Myocardial Infarction 60 0.041
628
P PRT013 Portal Hypertension 59 0.041
629
P PRP029 Porphyria 58 0.041
630
P PLY019 Polyneuropathy 54 0.041
631
PLM012 Pulmonary Sarcoidosis 54 0.041
632
BRN004 Brain Edema 51 0.041
633
c SML034 Small Cell Neuroendocrine Carcinoma 40 0.041
634
SXL003 Sexual Disorder 47 0.041
635
AGG002 Aggressive Systemic Mastocytosis 42 0.041
636
SKN021 Skin Sarcoma 30 0.041
637
OST017 Osteomyelitis 59 0.041
638
MCP006 Mucoepidermoid Carcinoma 47 0.041
639
PLM039 Pulmonary Neuroendocrine Tumor 42 0.041
640
CRB040 Cerebrum Cancer 36 0.041
641
CHR012 Chronic Granulomatous Disease 65 0.041
642
P UVT001 Uveitis 59 0.041
643
P INT063 Intellectual Disability 53 0.041
644
SPN051 Spondylitis 50 0.041
645
PYM001 Pyomyositis 39 0.041
646
SCK003 Sickle Cell Anemia 68 0.041
647
P MSC005 Muscular Dystrophy 64 0.041
648
HRP004 Herpes Zoster 56 0.040
649
P WGN003 Wagner Syndrome 37 0.040
650
P SLV002 Salivary Gland Cancer 61 0.040
651
c TCL005 T-Cell Prolymphocytic Leukemia 53 0.040
652
c LRG001 Large Cell Carcinoma 51 0.040
653
CLL001 Cellular Schwannoma 44 0.040
654
SML008 Small Intestine Lymphoma 41 0.040
655
AML001 Amelanotic Melanoma 39 0.040
656
P SCH015 Schizophrenia 76 0.040
657
HYP066 Hyperglycemia 60 0.040
658
LYM021 Lymphadenitis 58 0.040
659
P EXN002 Exanthem 57 0.040
660
MLL012 Miller Syndrome 49 0.040
661
CYC007 Cyclic Thrombocytopenia 37 0.040
662
ULC004 Ulcerative Colitis 75 0.040
663
PHR003 Pharyngitis 58 0.040
664
P DRR001 Diarrhea 51 0.040
665
HST016 Histiocytic Sarcoma 40 0.040
666
BRS001 Breast Lymphoma 32 0.040
667
LSH001 Leishmaniasis 62 0.039
668
c ACT027 Acute Pancreatitis 56 0.039
669
SVR077 Severe Combined Immune Deficiency 36 0.039
670
SML022 Small Cell Lung Cancer, Childhood 15 0.039
671
P GST044 Gastritis 58 0.039
672
P FNC026 Fanconi Renotubular Syndrome 1 51 0.039
673
P CMP008 Compartment Syndrome 48 0.039
674
MMB001 Membranoproliferative Glomerulonephritis 45 0.039
675
NTR018 Neutrophilia, Hereditary 45 0.039
676
IMM078 Immunodeficiency 21 35 0.039
677
PRM200 Primary Fanconi Syndrome 24 0.039
678
P RTN022 Retinal Vein Occlusion 37 0.039
679
c CNT016 Central Retinal Vein Occlusion 35 0.039
680
PLX004 Plexopathy 33 0.039
681
P BRS044 Breast Adenocarcinoma 60 0.039
682
P VGN017 Vaginal Cancer 45 0.039
683
SPT007 Spitz Nevus 34 0.039
684
c RNL034 Renal Cell Carcinoma 4 21 0.039
685
P DMN001 Diamond-Blackfan Anemia 68 0.039
686
P KRT005 Keratoacanthoma 45 0.039
687
FLL013 Follicular Dendritic Cell Sarcoma 41 0.039
688
c NRB011 Neuroblastoma 4 20 0.039
689
c HMN022 Human T-Cell Leukemia Virus Type 2 44 0.038
690
RFR002 Refractory Hairy Cell Leukemia 31 0.038
691
c HPT073 Hepatitis C Virus 72 0.038
692
P LPR003 Leprosy 68 0.038
693
c CHR089 Chronic Kidney Failure 66 0.038
694
TXC005 Toxic Shock Syndrome 61 0.038
695
STM007 Stomatitis 50 0.038
696
BLR008 Bilirubin Metabolic Disorder 47 0.038
697
c RNL016 Renal Infectious Disease 24 0.038
698
c CRN175 Coronary Heart Disease 4 21 0.038
699
BLM001 Bloom Syndrome 62 0.038
700
SCK005 Sickle Cell Disease 49 0.038
701
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.038
702
PRN049 Paraneoplastic Pemphigus 39 0.038
703
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 31 0.038
704
P HNT016 Huntington Disease 80 0.038
705
ACR007 Acromegaly 65 0.038
706
LPR001 Lepromatous Leprosy 49 0.038
707
OPT009 Optic Neuritis 48 0.038
708
PLN006 Poland Syndrome 48 0.038
709
HYP017 Hypophosphatemia 42 0.038
710
c HRD009 Hereditary Wilms' Tumor 41 0.038
711
PLY010 Polyclonal Hypergammaglobulinemia 32 0.038
712
c WGN005 Wagner Syndrome 1 29 0.038
713
P TST026 Testicular Germ Cell Cancer 41 0.038
714
CRS005 Crest Syndrome 47 0.037
715
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 17 0.037
716
P CLD001 Cleidocranial Dysplasia 62 0.037
717
P SDR003 Sideroblastic Anemia 39 0.037
718
ALK003 Aleukemic Leukemia Cutis 31 0.037
719
FCL012 Facial Paralysis 50 0.037
720
SYN036 Syncope 47 0.037
721
FSC004 Fasciitis 46 0.037
722
PHY002 Physical Disorder 44 0.037
723
P LNG035 Lung Large Cell Carcinoma 40 0.037
724
ADN014 Adenomatoid Tumor 31 0.037
725
TNS005 Tonsillitis 58 0.037
726
NRT004 Neuritis 52 0.037
727
HYP005 Hypokalemia 51 0.037
728
INH011 Inherited Bone Marrow Failure Syndromes 25 0.037
729
GRW021 Growing Teratoma Syndrome 18 0.037
730
CRD119 Cardiac Arrest 63 0.037
731
UTR043 Uterine Sarcoma 44 0.037
732
ANS011 Anus Cancer 44 0.037
733
RCH001 Richter's Syndrome 44 0.037
734
SPN369 Spinal Disease 41 0.037
735
MDS018 Mediastinal Cancer 36 0.037
736
VSC007 Vascular Disease 67 0.036
737
P CNJ013 Conjunctivitis 65 0.036
738
P LYM025 Lymphedema 61 0.036
739
c ATM024 Autoimmune Pancreatitis 46 0.036
740
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 41 0.036
741
HRT010 Heart Sarcoma 39 0.036
742
c MLG053 Malignant Ovarian Brenner Tumor 40 0.036
743
c OVR058 Ovarian Small Cell Carcinoma 37 0.036
744
c MLG036 Malignant Spiradenoma 33 0.036
745
c NRB015 Neuroblastoma 2 31 0.036
746
KDN019 Kidney Sarcoma 30 0.036
747
PNS010 Penis Squamous Cell Carcinoma 25 0.036
748
SML025 Small Non-Cleaved Cell Lymphoma 23 0.036
749
SPL006 Splenic Infarction 35 0.036
750
CNT017 Central Nervous System Origin Vertigo 28 0.036
751
STT044 Statin Toxicity 17 0.036
752
P PLM037 Pulmonary Hypertension 79 0.036
753
HSH003 Hashimoto Thyroiditis 61 0.036
754
P BRG001 Brugada Syndrome 59 0.036
755
P MTC069 Mitochondrial Disorders 52 0.036
756
P LMB006 Limb-Girdle Muscular Dystrophy 50 0.036
757
c HMG004 Hemoglobin D Disease 33 0.036
758
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 15 0.036
759
PNC041 Pancreatic Ductal Adenocarcinoma 63 0.035
760
CTS003 Coats Disease 57 0.035
761
RTN015 Retinal Cancer 51 0.035
762
PRS039 Prostate Adenocarcinoma 46 0.035
763
BLD032 Bile Duct Adenocarcinoma 40 0.035
764
APP010 Appendix Cancer 40 0.035
765
SCR035 Sacral Agenesis with Vertebral Anomalies 33 0.035
766
STR067 Stroke, Ischemic 77 0.035
767
P AMY004 Amyloidosis 64 0.035
768
P TMP003 Temporal Arteritis 60 0.035
769
ABL002 Ablepharon-Macrostomia Syndrome 57 0.035
770
LYM027 Lymphopenia 54 0.035
771
c DMN023 Diamond-Blackfan Anemia 1 38 0.035
772
LMB024 Limbic Encephalitis 36 0.035
773
BNM004 Bone Marrow Failure, Familial 15 0.035
774
INC002 Inclusion Body Myositis 63 0.035
775
ACT167 Acute Generalized Exanthematous Pustulosis 40 0.035
776
c CNG031 Congenital Nervous System Abnormality 39 0.035
777
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 15 0.035
778
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 14 0.035
779
MGK005 Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) 13 0.035
780
ACT185 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Topoisomerase Type 2 Inhibitor 10 0.035
781
ACT166 Acute Myeloid Leukemia with Cebpa Somatic Mutations 10 0.035
782
ACT199 Acute Myeloid Leukemia with Npm1 Somatic Mutations 10 0.035
783
c PRM126 Primary Peritoneal Carcinoma 54 0.034
784
PGM001 Pigmented Villonodular Synovitis 48 0.034
785
THY009 Thyroid Lymphoma 47 0.034
786
PTT037 Pituitary Tumors 45 0.034
787
EWN002 Ewing's Family of Tumors 45 0.034
788
TNS004 Tonsil Cancer 44 0.034
789
c LNG031 Lung Benign Neoplasm 44 0.034
790
CHL006 Childhood Oligodendroglioma 37 0.034
791
OVR021 Ovarian Lymphoma 33 0.034
792
VSC009 Vascular Skin Disease 22 0.034
793
WLS001 Wilson Disease 72 0.034
794
P AGM001 Agammaglobulinemia 64 0.034
795
EXF001 Exfoliation Syndrome 57 0.034
796
PMS001 Poems Syndrome 55 0.034
797
PRC002 Paracoccidioidomycosis 55 0.034
798
TTH006 Tooth Disease 52 0.034
799
CCC002 Coccidiosis 49 0.034
800
ACT049 Acute Disseminated Encephalomyelitis 49 0.034
801
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 46 0.034
802
RNL021 Renal Tubular Transport Disease 35 0.034
803
HRF001 Hair Follicle Neoplasm 35 0.034
804
P GLY013 Glycogen Storage Disease 59 0.034
805
ALL006 Allergic Asthma 58 0.034
806
c BCT007 Bacterial Meningitis 54 0.034
807
WGR001 Wagr Syndrome 52 0.034
808
TLR001 Tularemia 42 0.034
809
HYP068 Hyperostosis 40 0.034
810
SGT001 Sagittal Sinus Thrombosis 33 0.034
811
TRC006 Trichosporonosis 28 0.034
812
ACT176 Acute Panmyelosis with Myelofibrosis 19 0.034
813
ANX002 Anxiety Disorder 69 0.034
814
ART016 Aortic Aneurysm 67 0.034
815
HST011 Histoplasmosis 54 0.034
816
CLL003 Cellulitis 49 0.034
817
PRS002 Prostate Lymphoma 31 0.034
818
P GRV001 Graves' Disease 61 0.034
819
PTT006 Pituitary Adenoma 55 0.034
820
ALV010 Alveolar Soft-Part Sarcoma 53 0.034
821
EXT010 Extramedullary Plasmacytoma 49 0.034
822
PRM026 Primary Systemic Mycosis 41 0.034
823
ADR014 Adrenal Medulla Cancer 38 0.034
824
MLR007 Male Reproductive System Disease 37 0.034
825
END036 Endocrine Organ Benign Neoplasm 37 0.034
826
c INV003 Invasive Malignant Thymoma 33 0.034
827
CLL006 Cellular Neurofibroma 33 0.034
828
CRH001 Crohn's Disease 76 0.033
829
P NJM001 Nijmegen Breakage Syndrome 66 0.033
830
RTN017 Retinal Detachment 57 0.033
831
c ACT071 Acute Kidney Failure 50 0.033
832
RLP001 Relapsing Polychondritis 49 0.033
833
VCC001 Vaccinia 46 0.033
834
ACR014 Acral Lentiginous Melanoma 44 0.033
835
GNG008 Ganglioneuroblastoma 42 0.033
836
ATY019 Atypical Mole Syndrome 37 0.033
837
c DMN006 Diamond-Blackfan Anemia 3 30 0.033
838
c DMN005 Diamond-Blackfan Anemia 2 23 0.033
839
P LRY044 Larynx Cancer 59 0.033
840
BRN071 Brain Injury 52 0.033
841
BCL002 B Cell Deficiency 50 0.033
842
NCR003 Necrotizing Sialometaplasia 34 0.033
843
THY042 Thymic Epithelial Tumor 28 0.033
844
SFT004 Soft Tissue Sarcoma Childhood 14 0.033
845
KWS002 Kawasaki Disease 70 0.033
846
P FCL005 Focal Segmental Glomerulosclerosis 59 0.033
847
c ATM011 Autoimmune Hepatitis 58 0.033
848
c ACT210 Acute Respiratory Distress Syndrome 57 0.033
849
P PLN008 Peeling Skin Syndrome 47 0.033
850
HDR003 Hidradenitis 46 0.033
851
VRL003 Variola Major 43 0.033
852
c CHR546 Chronic Mountain Sickness 42 0.033
853
c ACQ014 Acquired Hemophilia 42 0.033
854
CYS036 Cystinosis, Nephropathic 41 0.033
855
RNL025 Renal Hypoplasia 41 0.033
856
c CHR091 Chronic Meningitis 40 0.033
857
ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 36 0.033
858
ANG049 Angioedema Induced by Ace Inhibitors 35 0.033
859
CND006 Candida Glabrata 34 0.033
860
CRY008 Cryopyrin-Associated Periodic Syndrome 34 0.033
861
c PLN021 Peeling Skin Syndrome 3 31 0.033
862
BLL006 Bullous Pemphigoid 58 0.032
863
KLN001 Klinefelter's Syndrome 55 0.032
864
GNR004 Generalized Anxiety Disorder 51 0.032
865
HYP085 Hypothalamic Disease 44 0.032
866
OVR054 Ovarian Mucinous Neoplasm 38 0.032
867
CRB024 Cerebral Neuroblastoma 38 0.032
868
PLS010 Plasma Protein Metabolism Disease 38 0.032
869
P CYS007 Cystic Nephroma 35 0.032
870
SWL001 Swallowing Disorders 34 0.032
871
CLR112 Clear Cell Papillary Renal Cell Carcinoma 31 0.032
872
ENC014 Enchondroma 28 0.032
873
LPN002 Lip and Oral Cavity Cancer 18 0.032
874
P AVS004 Avascular Necrosis of the Femoral Head 56 0.032
875
PRT011 Protein C Deficiency 51 0.032
876
MYD002 Myd88 Deficiency 46 0.032
877
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 29 0.032
878
PLM001 Pulmonary Tuberculosis 68 0.032
879
P PSR002 Psoriasis 63 0.032
880
DNG002 Dengue Hemorrhagic Fever 62 0.032
881
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.032
882
PGT001 Paget's Disease of Bone 59 0.032
883
ART111 Artery Disease 57 0.032
884
P HMP007 Hemophilia 56 0.032
885
MNT002 Mental Depression 54 0.032
886
TRY001 Trypanosomiasis 52 0.032
887
PRP016 Paraplegia 49 0.032
888
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.032
889
P TRC005 Tracheal Stenosis 38 0.032
890
c DMN021 Diamond-Blackfan Anemia 6 36 0.032
891
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.032
892
c ACT036 Acute Cholangitis 32 0.032
893
c DMN019 Diamond-Blackfan Anemia 4 28 0.032
894
EPD016 Epidermolysis Bullosa 57 0.031
895
CHL067 Cholecystitis 56 0.031
896
ECH003 Echinococcosis 53 0.031
897
SRS001 Serous Cystadenocarcinoma 52 0.031
898
BNN003 Bone Inflammation Disease 46 0.031
899
PTT008 Pituitary Carcinoma 44 0.031
900
MNN006 Meninges Hemangiopericytoma 44 0.031
901
LVR002 Liver Angiosarcoma 44 0.031
902
OVR050 Ovarian Embryonal Carcinoma 39 0.031
903
c PNC108 Pancreatitis, Hereditary 67 0.031
904
P PRP003 Porphyria Cutanea Tarda 64 0.031
905
GLN010 Glanzmann Thrombasthenia 63 0.031
906
P TMT001 Timothy Syndrome 56 0.031
907
PRT026 Parotitis 42 0.031
908
CDQ001 Cauda Equina Syndrome 42 0.031
909
ESP018 Esophageal Candidiasis 40 0.031
910
P DCR003 Dacryoadenitis 37 0.031
911
c PLN018 Peeling Skin Syndrome 2 35 0.031
912
ECT004 Ecthyma 35 0.031
913
FLL019 Follicular Mucinosis 34 0.031
914
HRZ001 Huriez Syndrome 33 0.031
915
THY043 Thymic Hyperplasia 32 0.031
916
HNS001 Hansen's Disease 29 0.031
917
ATM052 Autoimmune Disease 1 28 0.031
918
EXF003 Exfoliative Dermatitis 27 0.031
919
TCR004 Tacrolimus Dose Selection 23 0.031
920
ATM053 Autoimmune Disease 2 19 0.031
921
c SCN051 Secondary Pulmonary Alveolar Proteinosis 18 0.031
922
c ALX007 Alexander Disease Type I 17 0.031
923
P THR015 Thrombophilia 59 0.030
924
VSC003 Visceral Leishmaniasis 55 0.030
925
HDC001 Headache 54 0.030
926
P END033 Endocarditis 52 0.030
927
P HYP237 Hypercalcemia, Infantile 51 0.030
928
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.030
929
DYS164 Dyskeratosis Congenita, X-Linked 44 0.030
930
GLM011 Glomerulosclerosis 44 0.030
931
P DMY001 Demyelinating Polyneuropathy 43 0.030
932
CHR276 Chronic Active Epstein-Barr Virus Infection 43 0.030
933
MCS004 Mucosal Melanoma 42 0.030
934
RDN001 Reading Disorder 39 0.030
935
TXC007 Toxic Pneumonitis 36 0.030
936
P DRM012 Dermis Tumor 28 0.030
937
c PRX067 Paroxysmal Nocturnal Hemoglobinuria 2 23 0.030
938
P FML321 Familial Stomach Cancer 16 0.030
939
DMN002 Dementia 64 0.030
940
P TXP001 Toxoplasmosis 60 0.030
941
INT007 Intermediate Coronary Syndrome 52 0.030
942
HMN014 Human Immunodeficiency Virus Infectious Disease 49 0.030
943
CNT046 Central Nervous System Vasculitis 47 0.030
944
VGN020 Vaginal Disease 45 0.030
945
CLN044 Colon Adenoma 45 0.030
946
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.030
947
EXT035 Extrinsic Cardiomyopathy 39 0.030
948
HDG003 Hodgkin's Lymphoma, Lymphocytic Depletion 33 0.030
949
CNV003 Conventional Fibrosarcoma 32 0.030
950
c NRB014 Neuroblastoma 3 30 0.030
951
BRN104 Bronchial Endocrine Tumor 25 0.030
952
PLY039 Polymorphic Reticulosis 19 0.030
953
PLM024 Pulmonary Type Ovarian Small Cell Carcinoma 16 0.030
954
ISC006 Ischemic Heart Disease 68 0.029
955
WRN001 Werner Syndrome 67 0.029
956
P CSH001 Cushing's Syndrome 64 0.029
957
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.029
958
c HPT003 Hepatitis a 59 0.029
959
LPM004 Lipoma 58 0.029
960
BRN002 Bronchiolitis 56 0.029
961
TRM010 Traumatic Brain Injury 52 0.029
962
CTN014 Cutaneous Mastocytosis 48 0.029
963
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 48 0.029
964
BRC085 Brca2 Hereditary Breast and Ovarian Cancer Syndrome 44 0.029
965
MNC006 Monoclonal Gammopathy of Uncertain Significance 44 0.029
966
MST006 Mast Syndrome 43 0.029
967
SPN018 Spinal Cord Astrocytoma 42 0.029
968
c GST048 Gastrointestinal System Benign Neoplasm 41 0.029
969
ENT008 Enteropathy-Associated T-Cell Lymphoma 36 0.029
970
BLD028 Bladder Lymphoma 35 0.029
971
MLN002 Melanomatosis 33 0.029
972
PRS008 Prostate Small Cell Carcinoma 29 0.029
973
HNM002 Hinman Syndrome 25 0.029
974
c NRB013 Neuroblastoma 6 19 0.029
975
P CRN211 Coronary Artery Disease 75 0.028
976
ATP002 Atopy 63 0.028
977
c ATM010 Autoimmune Hemolytic Anemia 60 0.028
978
P MMP001 Mumps 56 0.028
979
P HMR012 Hemorrhagic Fever 55 0.028
980
LMB062 Limb Ischemia 48 0.028
981
MYL001 Myelitis 48 0.028
982
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.028
983
RLP003 Relapsing Fever 46 0.028
984
MTR008 Mature B-Cell Neoplasm 41 0.028
985
ATM012 Autoimmune Disease of Blood 37 0.028
986
DRM009 Dermatomycosis 36 0.028
987
ABD004 Abdominal Tuberculosis 34 0.028
988
GRN016 Grant Syndrome 30 0.028
989
c DMN028 Diamond-Blackfan Anemia 12 27 0.028
990
LYM117 Lymphocytic Hypereosinophilic Syndrome 16 0.028
991
CHS003 Chest Wall Bone Cancer 16 0.028
992
SYS059 Systemic Mastocytosis with an Associated Clonal Hematologic Non-Mast Cell Lineage Disease 13 0.028
993
PHL006 Phelan-Mcdermid Syndrome 51 0.028
994
P WVR001 Weaver Syndrome 51 0.028
995
AMN001 Amenorrhea 51 0.028
996
QBC001 Quebec Platelet Disorder 50 0.028
997
THR013 Thoracic Outlet Syndrome 49 0.028
998
HMR002 Hemarthrosis 48 0.028
999
CRN017 Coronary Thrombosis 48 0.028
1000
KRT008 Keratopathy 46 0.028
1001
NLS001 Nelson Syndrome 43 0.028
1002
THR035 Thrombasthenia 42 0.028
1003
SXD001 Sex Differentiation Disease 40 0.028
1004
c RNG023 Ring Chromosome 7 38 0.028
1005
SPR006 Sparganosis 33 0.028
1006
FTD001 Foot Drop 32 0.028
1007
GNG006 Gingival Hypertrophy 32 0.028
1008
SPL007 Splenic Abscess 31 0.028
1009
WTS001 Watson Syndrome 29 0.028
1010
PLM139 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 1 27 0.028
1011
GRN011 Granulomatous Gastritis 27 0.028
1012
P PLM064 Pulmonary Sequestration 26 0.028
1013
ANP007 Anaplastic Ganglioglioma 26 0.028
1014
MYL048 Myelodysplasia and Leukemia Syndrome with Monosomy 7 24 0.028
1015
EPS031 Epstein-Barr Virus-Positive Diffuse Large B-Cell Lymphoma of the Elderly 18 0.028
1016
CHR230 Chromosome 20q Deletion 10 0.028
1017
ALK014 Aleukemic Mast Cell Leukemia 10 0.028
1018
OTT002 Otitis Media 66 0.027
1019
P ATR011 Atrial Fibrillation 64 0.027
1020
CNT047 Contact Dermatitis 62 0.027
1021
P ADD001 Addison's Disease 62 0.027
1022
CHR063 Chronic Mucocutaneous Candidiasis 61 0.027
1023
P ADL010 Adult Respiratory Distress Syndrome 60 0.027
1024
DMY004 Demyelinating Disease 55 0.027
1025
P MYC008 Myocarditis 54 0.027
1026
SLP005 Sleep Disorder 53 0.027
1027
P GND004 Gonadal Dysgenesis 53 0.027
1028
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.027
1029
DFF001 Diffuse Cutaneous Mastocytosis 41 0.027
1030
FBR002 Fibrosarcoma of Bone 41 0.027
1031
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.027
1032
SML015 Small Intestinal Sarcoma 35 0.027
1033
ORC001 Orchitis 34 0.027
1034
INT038 Interdigitating Dendritic Cell Sarcoma 33 0.027
1035
EXT007 Extracutaneous Mastocytoma 28 0.027
1036
c ATM006 Autoimmune Lymphoproliferative Syndrome 71 0.027
1037
MLD001 Melioidosis 67 0.027
1038
P FML161 Familial Mediterranean Fever, Ar 63 0.027
1039
P EPS003 Episodic Ataxia 56 0.027
1040
STR026 Star Syndrome 56 0.027
1041
P BCK002 Beckwith-Wiedemann Syndrome 56 0.027
1042
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.027
1043
PTT046 Pituitary Hormone Deficiency, Combined, 2 53 0.027
1044
RSC001 Rosacea 53 0.027
1045