Search results for Lenalidomide

869 hits were found for Lenalidomide

# Family MCID Name MIFTS Score
1
MYL069 Myeloma, Multiple 76 36.761
2
P LYM118 Lymphoma 66 19.653
3
MYL009 Myelodysplastic Syndrome 67 18.530
4
PLS009 Plasma Cell Neoplasm 64 17.408
5
P LKM002 Leukemia 65 15.067
6
P BCL017 B-Cell Lymphoma 57 14.378
7
P LKM071 Leukemia, Chronic Lymphocytic 74 13.958
8
DWN001 Down Syndrome 70 13.767
9
P NTR004 Neutropenia 62 13.104
10
LYM019 Lymphosarcoma 46 12.756
11
DFF005 Diffuse Large B-Cell Lymphoma 55 12.051
12
c LKM061 Leukemia, Acute Myeloid 83 11.555
13
LYM133 Lymphoma, Hodgkin, Classic 69 11.501
14
MNT001 Mantle Cell Lymphoma 65 11.020
15
LYM143 Lymphoma, Non-Hodgkin, Familial 74 10.636
16
P FLL037 Follicular Lymphoma 66 10.343
17
P MYL006 Myeloid Leukemia 60 10.192
18
P ANR048 Aniridia 1 66 10.094
19
P THR014 Thrombocytopenia 66 9.710
20
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 8.209
21
P AMY004 Amyloidosis 69 7.755
22
P NRP001 Neuropathy 59 7.038
23
PMS001 Poems Syndrome 59 6.982
24
CHR635 Chromosome 5q Deletion Syndrome 50 6.977
25
RHB024 Rhabdomyosarcoma 2 65 6.949
26
c ALM001 Al Amyloidosis 54 6.777
27
RTC005 Reticulosarcoma 47 6.375
28
P PRP019 Peripheral Nervous System Disease 57 6.097
29
ANT039 Antisynthetase Syndrome 55 5.999
30
c LKM056 Leukemia, Chronic Lymphocytic 2 47 5.963
31
P EXN002 Exanthem 58 5.888
32
c THR092 Thrombophilia Due to Thrombin Defect 74 5.806
33
P BCL004 B-Cell Non-Hodgkin Lymphoma 41 5.562
34
FLL041 Follicular Lymphoma 1 44 5.424
35
PLS011 Plasmacytoma 56 5.392
36
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 69 5.337
37
DFC004 Deficiency Anemia 74 5.267
38
PRP036 Peripheral T-Cell Lymphoma 52 5.177
39
MYL005 Myelofibrosis 70 5.158
40
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 5.066
41
AGN016 Aging 53 4.939
42
MCR004 Macroglobulinemia 48 4.917
43
P TRN020 Turner Syndrome 67 4.911
44
c CHR064 Chronic Monocytic Leukemia 35 4.791
45
MRG003 Marginal Zone B-Cell Lymphoma 52 4.726
46
ADL002 Adult Syndrome 69 4.667
47
P PRS040 Prostate Cancer 95 4.593
48
P SRC025 Sarcoidosis 1 70 4.517
49
P CNT005 Central Nervous System Lymphoma 51 4.503
50
PRM226 Primary Central Nervous System Lymphoma 47 4.503
51
ANG046 Angioimmunoblastic T-Cell Lymphoma 50 4.486
52
P LKM062 Leukemia, Acute Lymphoblastic 69 4.468
53
IND017 Indolent Plasma Cell Myeloma 41 4.439
54
PLS016 Plasma Cell Leukemia 53 4.421
55
AND005 Androgen Insensitivity Syndrome, Mild 21 4.333
56
P GRF003 Graft-Versus-Host Disease 71 4.332
57
ACT113 Acute Myeloblastic Leukemia with Maturation 46 4.304
58
CRT084 Creatinine Clearance Quantitative Trait Locus 25 4.256
59
CLL014 Cll/sll 45 4.234
60
P ADL017 Adult T-Cell Leukemia 53 4.164
61
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 4.164
62
c LKM005 Leukemia, T-Cell, Chronic 33 4.164
63
LYM012 Lymphoplasmacytic Lymphoma 50 4.043
64
P CHR285 Chronic Myelomonocytic Leukemia 59 3.915
65
MYC006 Mycosis Fungoides 64 3.829
66
RFR010 Refractory Anemia 49 3.778
67
P CTN015 Cutaneous T Cell Lymphoma 48 3.762
68
LYM027 Lymphopenia 56 3.750
69
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 3.689
70
P DRR001 Diarrhea 55 3.688
71
c PRM038 Primary Agammaglobulinemia 47 3.680
72
HMT002 Hematologic Cancer 61 3.529
73
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 36 3.494
74
CHP002 Chops Syndrome 47 3.494
75
P KDN018 Kidney Disease 71 3.479
76
BRK010 Burkitt Lymphoma 65 3.445
77
CYT002 Cytokine Deficiency 43 3.444
78
P PLY019 Polyneuropathy 52 3.435
79
P CTN003 Cutaneous Lupus Erythematosus 52 3.405
80
P HYP086 Hypothyroidism 68 3.403
81
c ACT073 Acute Leukemia 59 3.376
82
SPL018 Splenomegaly 47 3.370
83
FCT007 Factor Vii Deficiency 64 3.362
84
CRH001 Crohn's Disease 80 3.355
85
THR004 Thrombocytosis 52 3.346
86
WLD007 Waldenstroem's Macroglobulinemia 59 3.328
87
PLS025 Plasmablastic Lymphoma 47 3.323
88
HDG004 Hodgkin's Granuloma 22 3.266
89
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 3.266
90
HDG006 Hodgkin's Paragranuloma 22 3.266
91
KPS004 Kaposi Sarcoma 76 3.229
92
SML011 Smoldering Myeloma 32 3.208
93
GLM045 Glioma 62 3.204
94
GLL048 Glial Tumor 51 3.204
95
RNL114 Renal Cell Carcinoma, Nonpapillary 79 3.202
96
HGH043 High Grade Glioma 46 3.191
97
CNS004 Constipation 56 3.164
98
THR024 Thrombosis 56 3.150
99
P LYM033 Lymphoproliferative Syndrome 59 3.132
100
GLB002 Glioblastoma 67 3.128
101
P HYP098 Hypereosinophilic Syndrome 66 3.089
102
P HPT023 Hepatocellular Carcinoma 95 3.083
103
ALL029 Allergic Disease 61 3.072
104
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 3.041
105
PLM033 Pulmonary Embolism 58 3.026
106
MYL031 Myeloproliferative Neoplasm 66 2.991
107
P PNC035 Pancreatic Cancer 87 2.947
108
P GLM040 Glioma Susceptibility 1 70 2.887
109
TCL024 T-Cell Non-Hodgkin Lymphoma 39 2.850
110
HST010 Histiocytosis 49 2.843
111
P KDN017 Kidney Cancer 60 2.839
112
LNG108 Langerhans Cell Histiocytosis 57 2.812
113
c SCN036 Secondary Progressive Multiple Sclerosis 55 2.803
114
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.742
115
P NRB001 Neuroblastoma 66 2.714
116
CMP010 Complex Regional Pain Syndrome 59 2.712
117
END086 End Stage Renal Disease 54 2.711
118
SPN035 Spindle Cell Sarcoma 51 2.695
119
SRC014 Sarcoma 64 2.695
120
HRP004 Herpes Zoster 60 2.689
121
HMN044 Human Immunodeficiency Virus Type 1 76 2.682
122
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 2.673
123
LGH004 Light Chain Deposition Disease 40 2.665
124
48X005 48,xyyy 39 2.655
125
P CLR023 Colorectal Cancer 100 2.655
126
INT054 Intraocular Lymphoma 48 2.611
127
c LKM060 Leukemia, Acute Lymphoblastic 3 49 2.605
128
P MLN008 Melanoma 75 2.524
129
c PRS130 Prostate Cancer, Hereditary, 8 32 2.514
130
c PRS136 Prostate Cancer, Hereditary, 6 33 2.514
131
PRS047 Prostatitis 57 2.514
132
ADN011 Adenoid Cystic Carcinoma 68 2.467
134
FNG017 Fungal Infectious Disease 54 2.451
135
SZR001 Sezary's Disease 60 2.451
136
CTS005 Catastrophic Antiphospholipid Syndrome 43 2.451
137
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 2.451
138
CRY008 Cryopyrin-Associated Periodic Syndrome 48 2.451
139
ERD001 Erdheim-Chester Disease 53 2.440
140
MLG169 Malignant Astrocytoma 57 2.440
141
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.438
142
c SML038 Small Cell Cancer of the Lung 68 2.411
143
MTR088 Mature T-Cell and Nk-Cell Lymphoma 42 2.400
144
IMM167 Immune Deficiency Disease 76 2.363
145
P ADN016 Adenocarcinoma 63 2.363
146
P PLY018 Polycythemia 56 2.354
147
P ANP001 Anaplastic Large Cell Lymphoma 59 2.352
148
PLY001 Polycythemia Vera 69 2.340
149
RSP007 Respiratory Distress Syndrome, Infant 41 2.316
150
P ESS003 Essential Thrombocythemia 68 2.311
151
c SYS001 Systemic Lupus Erythematosus 85 2.289
152
P OVR042 Ovarian Cancer 88 2.289
153
P LPS004 Lupus Erythematosus 61 2.289
154
NSL029 Nasal Type Extranodal Nk/t-Cell Lymphoma 41 2.246
155
HNT002 Hantavirus Pulmonary Syndrome 55 2.241
156
c OVR114 Ovarian Cancer 1 60 2.219
157
SCT005 Scott Syndrome 51 2.204
158
P BRS047 Breast Cancer 97 2.204
159
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 42 2.190
160
PRM126 Primary Peritoneal Carcinoma 61 2.185
161
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 2.171
162
P BLD134 Bladder Cancer 79 2.167
163
P THY032 Thyroiditis 56 2.167
164
SVR004 Severe Combined Immunodeficiency 70 2.154
165
P BND020 Bone Disease 60 2.147
166
LYM040 Lymphoblastic Lymphoma 53 2.147
167
SNS003 Sensory Peripheral Neuropathy 51 2.140
168
ALK016 Alk-Negative Anaplastic Large Cell Lymphoma 44 2.122
169
THY029 Thyroid Carcinoma 55 2.122
170
P CNJ013 Conjunctivitis 66 2.122
171
MLD018 Mild Cognitive Impairment 48 2.113
172
AGG012 Aggressive Nk-Cell Leukemia 47 2.097
173
JVN004 Juvenile Myelomonocytic Leukemia 66 2.096
174
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 2.089
175
MXD026 Mixed Glioma 45 2.089
176
OCL022 Ocular Melanoma 54 2.076
177
SFT003 Soft Tissue Sarcoma 43 2.068
178
IND016 Indolent B-Cell Non-Hodgkin Lymphoma 20 2.064
179
CVD001 Covid-19 59 2.036
180
ACT011 Acute Contagious Conjunctivitis 41 2.014
181
PRL017 Prolymphocytic Leukemia 47 2.014
182
FBR002 Fibrosarcoma of Bone 47 2.014
183
P VSC011 Vasculitis 61 2.008
184
ERY003 Erythema Multiforme 56 1.973
185
SKN019 Skin Melanoma 70 1.944
186
NDL024 Nodal Marginal Zone Lymphoma 36 1.942
187
c HPT016 Hepatitis B 62 1.917
188
P TRC086 Trichohepatoenteric Syndrome 1 59 1.917
189
NCR009 Necrobiotic Xanthogranuloma 26 1.896
190
PNC001 Pancytopenia 52 1.892
191
NRN004 Neuroendocrine Tumor 55 1.879
192
c HMP029 Hemophilia a 69 1.861
193
P HPT021 Hepatitis 68 1.861
194
SYN036 Syncope 44 1.861
195
HYP066 Hyperglycemia 60 1.853
196
CNT033 Central Nervous System Cancer 47 1.844
197
P NRV006 Nervous System Cancer 47 1.844
198
BNR002 Bone Resorption Disease 47 1.843
199
P DMN001 Diamond-Blackfan Anemia 73 1.840
200
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 47 1.840
201
AMD002 Amed Syndrome, Digenic 36 1.840
202
P OCL013 Oculodentodigital Dysplasia 66 1.840
203
P RSP003 Respiratory Failure 73 1.825
204
SVR097 Severe Cutaneous Adverse Reaction 68 1.823
205
ERY066 Erythema Multiforme Major 29 1.823
206
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 1.823
207
MYL064 Myeloproliferative/lymphoproliferative Neoplasms, Familial 24 1.821
208
CYS036 Cystinosis, Nephropathic 51 1.821
209
P ATS364 Autism 72 1.817
210
LYM048 Lymphoma, Large-Cell, Immunoblastic 27 1.806
211
LYM051 Lymphomatoid Granulomatosis 44 1.806
212
HRY003 Hairy Cell Leukemia 53 1.802
213
P PLC011 Pilocytic Astrocytoma 55 1.791
214
JVN009 Juvenile Pilocytic Astrocytoma 34 1.791
215
OPT032 Optic Pathway Glioma 34 1.791
216
HML018 Homologous Wasting Disease 21 1.791
217
47X002 47,xyy 47 1.781
218
EXT010 Extramedullary Plasmacytoma 45 1.778
219
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.762
220
ADR054 Adrenocortical Carcinoma, Hereditary 47 1.762
221
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 1.745
222
CST005 Castleman Disease 56 1.715
223
SPL004 Splenic Marginal Zone Lymphoma 50 1.708
224
HYP005 Hypokalemia 55 1.688
225
c HPT003 Hepatitis a 63 1.683
226
ACT119 Acute Promyelocytic Leukemia 62 1.650
227
ART002 Arts Syndrome 66 1.642
228
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 35 1.642
229
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 43 1.642
230
P PNC044 Pancreatitis 61 1.642
231
c ACT027 Acute Pancreatitis 60 1.642
232
ACQ007 Acquired Immunodeficiency Syndrome 58 1.642
233
P LNG032 Lung Cancer 98 1.632
234
c ACT135 Acute Graft Versus Host Disease 51 1.630
235
P CHL066 Cholangitis 51 1.630
236
RNL065 Renal Cell Carcinoma, Papillary, 1 79 1.615
237
P CNR004 Cone-Rod Dystrophy 2 74 1.615
238
CHR178 Chromosomal Triplication 33 1.609
239
P AGM001 Agammaglobulinemia 67 1.595
240
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.564
241
P NPH012 Nephrotic Syndrome 61 1.564
242
P PLM037 Pulmonary Hypertension 69 1.563
243
IND005 Indolent B Cell Lymphoma 20 1.561
244
DND018 Dendritic Cell Tumor 40 1.548
245
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.530
246
KWS002 Kawasaki Disease 65 1.530
247
NTR005 Nutritional Deficiency Disease 60 1.530
248
AGM019 Agammaglobulinemia, X-Linked 71 1.516
249
SQM006 Squamous Cell Carcinoma 59 1.516
250
BNM001 Bone Marrow Cancer 45 1.516
251
P HML002 Hemolytic Anemia 62 1.516
252
EXT034 Extrinsic Allergic Alveolitis 56 1.516
253
PRT251 Proteinuria, Chronic Benign 58 1.486
254
PRP030 Purpura 54 1.486
255
PRR013 Prurigo Nodularis 38 1.462
256
PNN001 Panniculitis 52 1.441
257
P MXD050 Mixed Phenotype Acute Leukemia 46 1.434
258
RTR011 Retroperitoneal Fibrosis 47 1.434
259
BLS007 Blastic Plasmacytoid Dendritic Cell 37 1.432
260
TCL002 T-Cell Large Granular Lymphocyte Leukemia 48 1.408
261
P FNG006 Feingold Syndrome 1 61 1.408
262
ERY051 Erythroleukemia, Familial 37 1.408
263
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 56 1.408
264
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 1.408
265
c LKM070 Leukemia, Acute Monocytic 56 1.408
266
RCH001 Richter's Syndrome 44 1.408
267
P RCT021 Rectum Cancer 54 1.408
268
CLN045 Colonic Benign Neoplasm 48 1.408
269
ATY005 Atypical Teratoid Rhabdoid Tumor 69 1.408
270
THY122 Thyroid Gland Cancer 59 1.408
271
P MLG074 Malignant Mesenchymoma 40 1.408
272
THY030 Thyroid Gland Disease 50 1.408
273
THY123 Thyroid Gland Follicular Carcinoma 53 1.408
274
P NRV007 Nervous System Disease 65 1.408
275
ACT250 Acute Megakaryocytic Leukemia 63 1.408
276
ATX019 Ataxia with Vitamin E Deficiency 44 1.408
277
LRG008 Large Granular Lymphocyte Leukemia 34 1.408
278
P ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 39 1.408
279
P PNM007 Pneumonia 64 1.392
280
c ANM038 Anemia, Autoimmune Hemolytic 63 1.392
281
P MYC008 Myocarditis 59 1.391
282
ANG037 Angiomatosis 31 1.391
283
LNG031 Lung Benign Neoplasm 51 1.383
284
PRT036 Peritonitis 65 1.383
285
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 1.350
287
c HMN021 Human T-Cell Leukemia Virus Type 1 46 1.319
288
c THR111 Thrombocytopenia 3 35 1.288
289
P URT039 Urticaria 57 1.288
290
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.278
291
ATM095 Autoimmune Disease 61 1.278
292
c ACT071 Acute Kidney Failure 60 1.278
293
P LTR001 Lateral Sclerosis 57 1.278
294
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 1.277
295
KPR003 Keipert Syndrome 43 1.277
296
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 1.261
297
c SYS043 Systemic Lupus Erythematosus 1 38 1.261
298
c CHL140 Chilblain Lupus 1 59 1.261
299
GST020 Gastric Antral Vascular Ectasia 40 1.261
300
TXC002 Toxic Encephalopathy 51 1.261
301
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.255
302
MDD018 Middle East Respiratory Syndrome 44 1.255
303
STM007 Stomatitis 52 1.252
304
c PNS012 Paine Syndrome 60 1.249
305
ACR041 Acromelic Frontonasal Dysostosis 53 1.249
306
RFL001 Reflex Sympathetic Dystrophy 51 1.249
307
SMT001 Somatization Disorder 49 1.249
308
ALG001 Algoneurodystrophy 37 1.249
309
c ATS007 Autism Spectrum Disorder 71 1.211
310
P HMN032 Human Herpesvirus 8 47 1.211
311
TRN018 Transitional Cell Carcinoma 56 1.211
312
P INT068 Intestinal Disease 53 1.211
313
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 34 1.211
314
c CHR417 Chronic Graft Versus Host Disease 55 1.211
315
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 37 1.210
316
P THR005 Thrombotic Thrombocytopenic Purpura 64 1.194
317
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 45 1.194
318
HYP017 Hypophosphatemia 49 1.178
319
c THR110 Thrombocytopenia 6 26 1.178
320
c THR037 Thrombocytopenia 2 36 1.178
321
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 1.178
323
P CRD119 Cardiac Arrest 68 1.176
324
MLT113 Multicentric Castleman Disease 46 1.176
325
P ADL010 Adult Respiratory Distress Syndrome 70 1.161
326
CYT005 Cytomegalovirus Retinitis 50 1.143
327
BLR008 Bilirubin Metabolic Disorder 57 1.143
328
NRR001 Neuroretinitis 42 1.143
329
CRY004 Cryoglobulinemia 47 1.143
330
P FNC004 Fanconi Syndrome 60 1.143
331
RTN023 Retinitis 45 1.143
332
P HRP006 Herpes Simplex 65 1.143
333
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 1.133
334
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 1.133
335
CNG034 Congestive Heart Failure 69 1.115
336
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 1.102
337
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.102
338
MNN042 Meningioma, Radiation-Induced 51 1.102
339
P ALZ034 Alzheimer Disease 87 1.102
340
NRF026 Neurofibromatosis, Type Iv, of Riccardi 24 1.102
341
c NRF024 Neurofibromatosis, Type I 76 1.102
342
P MDL005 Medulloblastoma 75 1.102
343
EPT021 Epithelial Recurrent Erosion Dystrophy 45 1.102
344
c CRN139 Cornelia De Lange Syndrome 1 61 1.102
345
LRY022 Laryngoonychocutaneous Syndrome 43 1.102
346
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 56 1.102
347
c THR090 Thrombocythemia 1 50 1.102
348
c THY102 Thyroid Cancer, Nonmedullary, 2 54 1.102
349
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 1.102
350
XRD010 Xeroderma Pigmentosum, Variant Type 72 1.102
351
P HMP002 Hemophagocytic Lymphohistiocytosis 60 1.102
352
MRG013 Mirage Syndrome 44 1.102
353
LTT002 Letterer-Siwe Disease 33 1.102
354
MNN043 Meningioma, Familial 79 1.102
355
FCL084 Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature 39 1.102
357
c DMN023 Diamond-Blackfan Anemia 1 68 1.102
358
P MLN069 Melanoma, Uveal 59 1.102
359
HYL004 Hyaline Fibromatosis Syndrome 67 1.102
360
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 53 1.102
361
P SLV026 Salivary Gland Carcinoma 59 1.102
362
P PNB001 Pineoblastoma 49 1.102
363
PTH001 Pthirus Pubis Infestation 33 1.102
364
PPL002 Papillary Carcinoma 46 1.102
365
P OLG002 Oligodendroglioma 66 1.102
366
CYS009 Cystadenoma 42 1.102
367
FLL027 Fallopian Tube Carcinoma 66 1.102
368
URT001 Urethritis 52 1.102
369
P BNG030 Benign Ependymoma 51 1.102
370
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.102
371
PNL014 Pineal Gland Cancer 40 1.102
372
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.102
373
CLL010 Cellular Ependymoma 58 1.102
374
CNJ009 Conjunctival Cancer 34 1.102
375
SPN041 Spinal Cord Disease 54 1.102
376
GRY001 Gray Zone Lymphoma 35 1.102
377
c PST022 Posterior Uveal Melanoma 41 1.102
378
ACT177 Acute Basophilic Leukemia 35 1.102
379
SCR001 Secretory Meningioma 40 1.102
380
P EPN001 Ependymoblastoma 44 1.102
381
CRN036 Craniopharyngioma 63 1.102
382
THY124 Thyroid Gland Papillary Carcinoma 38 1.102
383
GLS001 Gliosarcoma 63 1.102
384
RDC002 Radiculopathy 51 1.102
385
P CRN015 Cornelia De Lange Syndrome 67 1.102
386
c PRM012 Primary Polycythemia 58 1.102
387
INT395 Intracranial Meningioma 47 1.102
388
P PRS038 Personality Disorder 65 1.102
389
P DNR001 Duane Retraction Syndrome 53 1.102
390
SPN021 Spinal Meningioma 43 1.102
391
MLG142 Malignant Conjunctival Melanoma 37 1.102
392
VRR004 Verrucous Carcinoma 48 1.102
393
P CHR573 Choroid Plexus Cancer 48 1.102
394
RHB001 Rhabdoid Cancer 68 1.102
395
URT035 Urethral Benign Neoplasm 38 1.102
396
P NRF002 Neurofibromatosis 60 1.102
397
VRL011 Viral Infectious Disease 60 1.102
398
P ENC004 Encephalitis 61 1.102
399
CNG092 Congenital Extrahepatic Portosystemic Shunt 24 1.102
400
NRF007 Neurofibroma 63 1.102
401
P BCL005 B Cell Prolymphocytic Leukemia 39 1.102
402
LPG001 Lipogranulomatosis 29 1.102
403
LYM052 Lymphomatoid Papulosis 37 1.102
404
DFF036 Differentiated Thyroid Carcinoma 51 1.102
405
PNC056 Pineocytoma 44 1.102
406
ENT008 Enteropathy-Associated T-Cell Lymphoma 36 1.102
407
CHR682 Chronic Bilirubin Encephalopathy 37 1.102
408
HST016 Histiocytic Sarcoma 38 1.102
409
FLL042 Folliculotropic Mycosis Fungoides 28 1.102
410
P RFR014 Refractory Anemia with Excess Blasts Type 2 18 1.102
411
ALL014 Allergic Encephalomyelitis 34 1.101
412
c LKM063 Leukemia, Chronic Myeloid 70 1.094
413
c ACQ017 Acquired Von Willebrand Syndrome 48 1.088
414
P ERY036 Erythema Nodosum 49 1.088
415
TLN003 Telangiectasis 51 1.088
416
SCL025 Scleromyxedema 37 1.084
417
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 22 1.080
418
BRN024 Bronchitis 67 1.073
419
DSC009 Discoid Lupus Erythematosus 42 1.073
420
DPH001 Diphtheria 59 1.054
421
P VNW001 Von Willebrand's Disease 64 1.043
422
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 64 1.043
423
PYD002 Pyoderma 49 1.035
424
P ANG015 Angioedema 56 1.035
425
PYD001 Pyoderma Gangrenosum 53 1.035
426
P INF037 Inflammatory Bowel Disease 53 1.027
427
P ZNC008 Zinc Finger Protein 1 22 1.027
428
P SCL015 Scleritis 47 1.027
429
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.011
430
STR067 Stroke, Ischemic 79 1.011
431
c THR125 Thrombocytopenia 7 22 1.011
432
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.011
433
OST003 Osteonecrosis 60 1.011
434
P URN019 Urinary Tract Infection 48 1.011
435
GRN017 Granulocytopenia 42 1.011
436
OST115 Osteonecrosis of the Jaw 40 1.011
437
PRG009 Progressive Multifocal Leukoencephalopathy 58 1.006
438
CRD223 Cardiac Arrhythmia 63 0.993
440
c MCR115 Microvascular Complications of Diabetes 5 65 0.993
441
HMN016 Hemangioendothelioma 35 0.993
442
EXP004 Exophthalmos 50 0.993
443
P EPT020 Epithelioid Hemangioendothelioma 43 0.993
444
GLB001 Gilbert Syndrome 53 0.975
445
CLL003 Cellulitis 53 0.975
446
GST027 Gastric Lymphoma 43 0.975
447
P CHR345 Chronic Pain 50 0.975
448
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.961
449
P LPR021 Leprosy 3 71 0.957
450
HNS001 Hansen's Disease 32 0.957
451
CLT003 Colitis 63 0.955
452
ISC015 Ischemic Colitis 43 0.955
453
c ACQ014 Acquired Hemophilia 45 0.955
454
P HMP007 Hemophilia 52 0.955
455
HYP266 Hypoxia 56 0.946
456
P MYP004 Myopathy 67 0.934
457
P ART022 Arthritis 70 0.934
458
P PRR002 Pure Red-Cell Aplasia 46 0.927
459
OST008 Osteosclerotic Myeloma 23 0.919
460
P RHM011 Rheumatoid Arthritis 81 0.910
461
c DWL002 Dowling-Degos Disease 1 58 0.910
462
NRT004 Neuritis 53 0.910
463
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.907
464
SLT001 Solitary Osseous Plasmacytoma 32 0.907
465
TRN015 Transient Cerebral Ischemia 62 0.885
466
PPL021 Papilledema 49 0.878
467
INT066 Interstitial Lung Disease 60 0.878
468
LNG099 Lung Disease 62 0.878
469
ATN004 Autonomic Neuropathy 42 0.863
470
SYS004 Systemic Mastocytosis 62 0.856
471
PTS001 Patau Syndrome 55 0.856
472
P MST009 Mastocytosis 64 0.856
473
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.832
474
P TMR010 Tumor Predisposition Syndrome 69 0.832
475
P RST002 Restrictive Cardiomyopathy 54 0.832
476
HYP056 Hypoglycemia 65 0.832
477
INH023 Inherited Cancer-Predisposing Syndrome 53 0.832
478
INT067 Interstitial Nephritis 46 0.821
479
OCL069 Ocular Motor Apraxia 57 0.815
480
ANG011 Angiodysplasia 42 0.815
481
APH002 Aphasia 55 0.797
482
P NSP012 Nasopharyngeal Carcinoma 60 0.797
483
ESP021 Esophageal Cancer 84 0.797
484
c CLR075 Colorectal Cancer 3 31 0.797
485
MCS002 Mucositis 55 0.797
486
DSS009 Disseminated Intravascular Coagulation 56 0.797
487
P THR015 Thrombophilia 51 0.797
488
c VRL010 Viral Hepatitis 52 0.797
489
c BSL007 Basal Cell Carcinoma 67 0.779
490
c HPT001 Hepatitis C 61 0.779
491
GLC003 Glucose Intolerance 53 0.779
492
LYM116 Lymph Node Disease 42 0.779
493
ISL001 Islet Cell Tumor 55 0.777
494
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 41 0.777
495
FCT001 Factor Viii Deficiency 61 0.759
496
OST159 Osteogenic Sarcoma 66 0.759
497
TLG001 Telogen Effluvium 31 0.759
498
HMG005 Hemoglobinopathy 55 0.759
499
P AXN001 Axonal Neuropathy 33 0.759
500
P SCK005 Sickle Cell Disease 56 0.759
501
c ACQ042 Acquired Hemophilia a 37 0.759
502
P THL005 Thalassemia 56 0.759
503
P ALP008 Alopecia 53 0.759
504
PDT035 Pediatric Systemic Lupus Erythematosus 47 0.759
505
RYN005 Raynaud Phenomenon 45 0.759
506
LGH007 Leigh Syndrome 70 0.748
507
c DRR009 Diarrhea 6 46 0.748
508
CMR002 Coumarin Resistance 59 0.748
509
MTC112 Mitochondrial Dna-Associated Leigh Syndrome 39 0.748
510
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.748
511
P APL001 Aplastic Anemia 72 0.738
512
TRD006 Tardive Dyskinesia 53 0.738
514
P KLZ004 Kala-Azar 1 41 0.738
515
TXC005 Toxic Shock Syndrome 61 0.738
516
P ESN008 Eosinophilic Pneumonia 50 0.738
517
GLM004 Gliomatosis Cerebri 51 0.738
518
LSH001 Leishmaniasis 63 0.738
519
CHC001 Chickenpox 56 0.738
520
PRT178 Partial Deletion of the Long Arm of Chromosome 5 10 0.738
521
P TRM003 Tremor 50 0.738
522
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 31 0.737
523
BLD054 Blood Protein Disease 33 0.737
524
P NJM001 Nijmegen Breakage Syndrome 75 0.719
525
c CHL119 Cholangitis, Primary Sclerosing 57 0.719
526
RBN014 Robin Sequence with Cleft Mandible and Limb Anomalies 36 0.719
527
HYP781 Hypoascorbemia 52 0.719
528
FBR089 Fibrosclerosis, Multifocal 35 0.719
529
INT253 Intestinal Benign Neoplasm 46 0.719
530
ADL054 Adult Brain Stem Glioma 30 0.719
531
SML008 Small Intestine Lymphoma 33 0.719
532
P SCL009 Sclerosing Cholangitis 46 0.719
533
P CRV039 Cervicitis 52 0.719
534
KRT002 Keratomalacia 54 0.719
536
MLG023 Malignant Adult Ependymoma 15 0.719
537
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.719
538
49X006 49, Xxxxy Syndrome 40 0.719
539
ADL045 Adult Ependymoblastoma 14 0.719
540
P PTS002 Ptosis 52 0.715
541
DBT090 Diabetes and Deafness, Maternally Inherited 44 0.715
542
c GRV008 Graves Disease 1 54 0.715
543
c BTT014 Beta-Thalassemia 72 0.715
544
c THR071 Thrombocytopenia 1 48 0.715
545
HPT019 Hepatic Encephalopathy 59 0.715
546
HYP068 Hyperostosis 47 0.715
547
NNS002 Nonspecific Interstitial Pneumonia 42 0.715
548
MCR017 Macrocytic Anemia 44 0.715
549
BNS007 Bone Sarcoma 50 0.715
550
HPT004 Hepatic Coma 43 0.715
551
CLD007 Cold Agglutinin Disease 43 0.715
552
P DBT005 Diabetes Insipidus 54 0.715
553
ENG004 Engraftment Syndrome 26 0.715
554
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.689
555
c EXD008 Exudative Vitreoretinopathy 1 71 0.689
556
c RTN047 Retinitis Pigmentosa 18 45 0.689
557
PRT010 Parathyroid Carcinoma 68 0.689
558
HYP080 Hypogonadism 49 0.689
559
CHL068 Cholestasis 61 0.689
560
PRM236 Primary Biliary Cholangitis 62 0.689
561
NRN001 Neuroendocrine Carcinoma 47 0.689
562
OVR059 Ovary Adenocarcinoma 49 0.689
563
MSL001 Measles 61 0.689
564
P HYP076 Hyperthyroidism 53 0.689
565
BCK006 Back Pain 43 0.689
566
ATN005 Autonomic Dysfunction 45 0.689
567
c BCT013 Bacterial Pneumonia 47 0.689
568
ATM069 Autoimmune Hemolytic Anemia, Warm Type 26 0.689
569
P RRT020 Rare Tumor 39 0.689
570
FLL008 Folliculitis 45 0.668
571
P PMP001 Pemphigus 54 0.668
572
DFF031 Diffuse Alveolar Hemorrhage 31 0.668
573
P HVY001 Heavy Chain Disease 32 0.660
574
SXL003 Sexual Disorder 49 0.660
575
c GMM003 Gamma Heavy Chain Disease 37 0.660
576
ADR016 Adrenal Cortical Carcinoma 61 0.660
577
P HYP750 Hypertriglyceridemia, Familial 61 0.660
578
INT051 Intussusception 53 0.660
579
DRG002 Drug-Induced Hepatitis 42 0.660
580
P HMN010 Hemangioma 61 0.660
581
P LMY004 Leiomyosarcoma 62 0.660
582
PLM012 Pulmonary Sarcoidosis 52 0.660
583
P GLM007 Glomerulonephritis 59 0.660
584
CLR017 Clear Cell Sarcoma 44 0.660
585
ADR004 Adrenal Cortical Adenocarcinoma 38 0.660
586
NRD001 Neurodermatitis 39 0.660
587
P PRL003 Proliferative Glomerulonephritis 43 0.660
588
CRB001 Cerebral Lymphoma 37 0.660
589
c HPT007 Hepatitis E 50 0.660
590
P HYP083 Hypopituitarism 51 0.660
591
GRM010 Germ Cells Tumors 33 0.660
592
HMP009 Haemophilus Influenzae 41 0.660
593
TTR011 Tetraploidy 43 0.660
594
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 30 0.660
595
ALK017 Alk-Positive Large B-Cell Lymphoma 19 0.660
596
PRS063 Paresthesia 39 0.660
597
c MCR133 Microvascular Complications of Diabetes 4 41 0.626
598
c MCR113 Microvascular Complications of Diabetes 3 52 0.626
599
c MCR130 Microvascular Complications of Diabetes 6 41 0.626
600
c MCR120 Microvascular Complications of Diabetes 7 47 0.626
601
P MYS005 Myositis 55 0.626
602
P MMP001 Mumps 56 0.626
603
TTH006 Tooth Disease 51 0.626
604
MYL075 Myelodysplastic/myeloproliferative Neoplasm 51 0.626
605
LVR012 Liver Cirrhosis 62 0.626
606
P EYD002 Eye Disease 57 0.626
607
P NML001 Nemaline Myopathy 49 0.626
608
RLP001 Relapsing Polychondritis 55 0.626
609
P GRV001 Graves' Disease 54 0.626
610
P CHR071 Charcot-Marie-Tooth Disease 64 0.626
611
CRY005 Cryptococcosis 61 0.626
612
P OPT009 Optic Neuritis 57 0.626
613
P RBL001 Rubella 58 0.626
614
ACT176 Acute Panmyelosis with Myelofibrosis 25 0.626
615
NNS003 Non-Secretory Myeloma 24 0.626
616
APH001 Aphthous Stomatitis 57 0.626
617
MCR141 Mucormycosis 59 0.626
618
MYC019 Mycobacterium Marinum 29 0.626
619
MGC006 Magic Syndrome 14 0.626
620
RSD004 Rosai-Dorfman Disease 49 0.626
621
UNC014 Unicentric Castleman Disease 22 0.626
622
RRS004 Rare Systemic Disease 12 0.626
623
ETH013 Euthyroid Graves Orbitopathy 13 0.626
624
RFR009 Refractory Cytopenia with Multilineage Dysplasia 30 0.626
625
PLS037 Plasma Cell Tumor 20 0.626
626
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.626
627
ACT164 Actinic Prurigo 44 0.581
628
P GST053 Gastric Cancer 82 0.581
629
c PCH010 Pachyonychia Congenita 3 43 0.581
630
P PLY041 Polymyositis 58 0.581
631
INP001 Inappropriate Adh Syndrome 48 0.581
632
NCR004 Nocardiosis 52 0.581
633
PLM031 Poliomyelitis 62 0.581
634
PNC129 Pancreatic Adenocarcinoma 64 0.581
635
TTN003 Tetanus 64 0.581
636
CRT013 Carotid Stenosis 51 0.581
637
PRT037 Pertussis 49 0.581
638
CRB039 Cerebrovascular Disease 65 0.581
639
P DBT009 Diabetes Mellitus 67 0.581
640
FSC004 Fasciitis 49 0.581
641
NCR007 Necrotizing Fasciitis 48 0.581
642
RRS010 Rare Soft Tissue Tumor 18 0.581
643
RCT024 Reactive Angioendotheliomatosis 14 0.581
644
c RNG023 Ring Chromosome 7 43 0.581
645
DPR016 Depression 64 0.581
646
P RNG032 Ring Chromosome 39 0.581
647
P BRG001 Brugada Syndrome 69 0.473
648
P MYC007 Myocardial Infarction 69 0.473
649
NTR042 Neutrophilic Dermatosis, Acute Febrile 56 0.473
650
P MYC084 Mycobacterium Tuberculosis 1 68 0.473
651
CRT072 Creutzfeldt-Jakob Disease 67 0.473
652
P PRK039 Parkinsonism 55 0.473
653
P SPN052 Spondyloarthropathy 54 0.473
654
IGP001 Iga Pemphigus 28 0.473
655
P DYS154 Dystonia 64 0.473
656
SKN006 Skin Sarcoidosis 42 0.473
657
PRN014 Paronychia 50 0.473
658
P DMN002 Dementia 65 0.473
659
CHL056 Cheilitis 46 0.473
660
VSC003 Visceral Leishmaniasis 54 0.473
661
P LCH002 Lichen Planus 54 0.473
662
TMP008 Tempi Syndrome 23 0.473
663
TCL012 T-Cell/histiocyte Rich Large B Cell Lymphoma 31 0.473
664
JSS002 Jessner Lymphocytic Infiltration of the Skin 15 0.473
665
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.473
666
STV009 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis Overlap Syndrome 14 0.473
667
c ACT134 Acute Liver Failure 57 0.473
668
HMS001 Hemosiderosis 48 0.472
669
P RRH023 Rare Hereditary Hemochromatosis 52 0.472
670
CRH005 Crohn's Colitis 53 0.365
671
c INF071 Inflammatory Bowel Disease 1 65 0.365
672
P LYM024 Lymphatic System Disease 46 0.365
673
c THR082 Thrombophilia Due to Activated Protein C Resistance 58 0.325
674
P PLY020 Polyradiculoneuropathy 47 0.325
675
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 56 0.325
676
DSS032 Disease by Infectious Agent 55 0.286
677
BHC003 Behcet Syndrome 70 0.265
678
P ART005 Arteriovenous Malformation 64 0.265
679
HGH041 High-Grade Astrocytoma 36 0.242
680
P NNN008 Noonan Syndrome 1 76 0.216
681
NKC002 Nk Cell Deficiency 31 0.216
682
HYP014 Hyperuricemia 51 0.216
683
BCT022 Bacterial Infectious Disease 55 0.216
684
P DMY001 Demyelinating Polyneuropathy 41 0.216
685
SVR001 Severe Acute Respiratory Syndrome 68 0.216
686
P PLM036 Pulmonary Fibrosis 65 0.216
687
PLM010 Pulmonary Edema 54 0.216
688
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.216
689
NDL020 Nodal Marginal Zone B-Cell Lymphoma 29 0.216
690
c PSD047 Pseudo-Turner Syndrome 52 0.216
691
RFR015 Refractory Anemia with Excess Blasts Type 1 14 0.216
692
VRC005 Varicose Veins 59 0.187
693
P RTN024 Retinoblastoma 72 0.187
694
HSH003 Hashimoto Thyroiditis 60 0.187
695
DRM006 Dermatitis 61 0.187
696
P GST044 Gastritis 55 0.187
697
CNN003 Conn's Syndrome 77 0.187
698
PRT013 Portal Hypertension 59 0.187
699
ORL011 Oral Cancer 60 0.187
700
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.187
701
PSR001 Psoriatic Arthritis 61 0.153
702
ASP007 Aspiration Pneumonia 49 0.153
703
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.153
704
ERY029 Erythermalgia, Primary 57 0.153
705
P CRY007 Cryoglobulinemia, Familial Mixed 48 0.153
706
P DRM053 Dermatitis, Atopic 65 0.153
707
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.153
708
P ATX030 Ataxia-Telangiectasia 80 0.153
709
P CRP001 Carpal Tunnel Syndrome 65 0.153
710
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.153
711
HYP020 Hyperprolactinemia 63 0.153
712
c ACR084 Aicardi-Goutieres Syndrome 7 30 0.153
713
MLT157 Multiple System Atrophy 1 69 0.153
714
c ACR090 Aicardi-Goutieres Syndrome 2 32 0.153
715
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.153
716
CMB007 Combined Immunodeficiency 56 0.153
717
HMR023 Hemorrhagic Cystitis 43 0.153
718
P CYS018 Cystitis 58 0.153
719
IMP005 Impotence 52 0.153
720
MCL006 Macular Retinal Edema 56 0.153
721
ADN018 Adenoma 58 0.153
722
IRN002 Iron Metabolism Disease 56 0.153
723
P PRM293 Primary Mediastinal B-Cell Lymphoma 42 0.153
724
GRN003 Granulomatous Dermatitis 32 0.153
725
CRB009 Cerebritis 43 0.153
726
P LKD001 Leukodystrophy 58 0.153
727
AMN003 Amnestic Disorder 53 0.153
728
CMM004 Common Variable Immunodeficiency 71 0.153
729
EMP001 Empty Sella Syndrome 41 0.153
730
SKN016 Skin Disease 63 0.153
731
ACT118 Acute Non Lymphoblastic Leukemia 26 0.153
732
MTR008 Mature B-Cell Neoplasm 36 0.153
733
OST012 Osteoarthritis 77 0.153
734
SHH001 Sheehan Syndrome 45 0.153
735
c CHR684 Chronic Kidney Disease 73 0.153
736
ANX004 Anoxia 40 0.153
737
P PPL026 Papular Mucinosis 24 0.153
738
P AVS003 Avascular Necrosis 41 0.153
739
TFR002 Tafro Syndrome 34 0.153
740
THR123 Thrombotic Microangiopathy 40 0.153
741
PRR019 Perioral Myoclonia with Absences 26 0.153
742
PST046 Post-Transplant Lymphoproliferative Disease 53 0.153
743
DYS073 Dysphagia 53 0.153
744
MLR004 Malaria 77 0.108
745
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 63 0.108
746
P ATR011 Atrial Fibrillation 66 0.108
747
ATR057 Atrioventricular Block 54 0.108
748
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.108
749
ART140 Arteries, Anomalies of 52 0.108
750
c SCL052 Scleroderma, Familial Progressive 60 0.108
751
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.108
752
P HML033 Hemolytic Uremic Syndrome, Atypical 1 67 0.108
753
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 0.108
754
c FNC027 Fanconi Anemia, Complementation Group a 80 0.108
755
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 0.108
756
INS024 Insulin-Like Growth Factor I 77 0.108
757
SCK003 Sickle Cell Anemia 74 0.108
758
IMM202 Immunodeficiency 64 25 0.108
759
ANG054 Angina Pectoris 65 0.108
760
HYP025 Hyperphosphatemia 47 0.108
761
VRL003 Variola Major 43 0.108
762
CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 29 0.108
763
P MYS003 Myasthenia Gravis 67 0.108
764
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.108
765
P AST005 Asthma 75 0.108
766
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.108
767
c THR048 Thrombocytopenia 4 28 0.108
768
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.108
769
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.108
770
P LFR001 Li-Fraumeni Syndrome 73 0.108
771
END057 Endometrial Cancer 76 0.108
772
P LNG064 Lung Cancer Susceptibility 3 69 0.108
773
P MLT008 Multinodular Goiter 41 0.108
774
MLG145 Malignant Epithelioid Hemangioendothelioma 26 0.108
775
c ALP087 Alpha-Heavy Chain Disease 28 0.108
776
ESP002 Esophageal Varix 51 0.108
777
CHR008 Choroiditis 48 0.108
778
CRD001 Cardiac Tamponade 44 0.108
779
PRP080 Peripheral Artery Disease 54 0.108
780
LMB062 Limb Ischemia 55 0.108
781
TLR001 Tularemia 56 0.108
782
P TMP001 Temporal Lobe Epilepsy 49 0.108
783
VCC001 Vaccinia 49 0.108
784
P STR021 Struma Ovarii 39 0.108
785
MTR007 Motor Peripheral Neuropathy 41 0.108
786
BCL002 B Cell Deficiency 40 0.108
787
P VSC007 Vascular Disease 62 0.108
788
CHL067 Cholecystitis 59 0.108
789
HMP001 Hemopericardium 47 0.108
790
CLR030 Clear Cell Renal Cell Carcinoma 53 0.108
791
JVN003 Juvenile Xanthogranuloma 43 0.108
792
NNL001 Non-Langerhans-Cell Histiocytosis 35 0.108
793
ISC004 Ischemia 61 0.108
794
CNN005 Connective Tissue Disease 66 0.108
795
PTT009 Pituitary Gland Disease 52 0.108
796
P HRT032 Heart Disease 84 0.108
797
INF021 Infant Gynecomastia 30 0.108
798
IRN001 Iron Deficiency Anemia 58 0.108
799
STT001 Status Epilepticus 58 0.108
800
P EPL164 Epilepsy 70 0.108
801
P ESP024 Esophagitis 60 0.108
802
P OBS001 Obstructive Jaundice 49 0.108
803
MGL001 Megaloblastic Anemia 59 0.108
804
P HYP077 Hypertrichosis 48 0.108
805
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.108
806
MRK001 Merkel Cell Carcinoma 64 0.108
807
P PTT006 Pituitary Adenoma 55 0.108
808
GRN007 Granuloma Annulare 43 0.108
809
P CRN035 Cranial Nerve Palsy 42 0.108
810
DMY004 Demyelinating Disease 50 0.108
811
TST014 Testicular Cancer 51 0.108
812
P HYP061 Hypertrophic Cardiomyopathy 68 0.108
813
GTR002 Goiter 52 0.108
814
NPH010 Nephrosclerosis 50 0.108
815
P PRC012 Pericardial Effusion 50 0.108
816
LPR001 Lepromatous Leprosy 49 0.108
817
RTN003 Retinal Ischemia 48 0.108
818
RCK004 Rickets 64 0.108
819
P MTH007 Methemoglobinemia 46 0.108
820
JPN002 Japanese Encephalitis 61 0.108
821
GYN001 Gynecomastia 48 0.108
822
P HRD011 Hereditary Spherocytosis 63 0.108
823
ABD002 Abducens Nerve Disease 38 0.108
824
CRY003 Cryptosporidiosis 55 0.108
825
CPL003 Capillary Leak Syndrome 54 0.108
826
TRC012 Trichuriasis 44 0.108
827
P HML001 Hemolytic-Uremic Syndrome 52 0.108
828
GT001 Gout 63 0.108
829
HMG002 Hemoglobinuria 50 0.108
830
NCR002 Necrobiosis Lipoidica 38 0.108
831
MDS019 Mediastinal Malignant Lymphoma 30 0.108
832
ILS001 Ileus 49 0.108
833
PRL008 Paralytic Ileus 44 0.108
834
FSC002 Fascioliasis 43 0.108
835
RTN011 Retina Lymphoma 25 0.108
836
EVN001 Evans' Syndrome 46 0.108
837
P BNL002 Bone Lymphoma 34 0.108
838
FCT013 Factor V Leiden Thrombophilia 20 0.108
839
BNT001 Banti's Syndrome 21 0.108
840
P SDR003 Sideroblastic Anemia 49 0.108
841
GST014 Gastrointestinal Lymphoma 31 0.108
842
ACT058 Active Peptic Ulcer Disease 55 0.108
843
DDN006 Duodenitis 49 0.108
844
P C1Q005 C1q Nephropathy 21 0.108
845
RFR004 Refractory Hematologic Cancer 31 0.108
846
HPR003 Heparin-Induced Thrombocytopenia 47 0.108
847
TCL008 T-Cell Lymphoma 1a 18 0.108
848
PST053 Postherpetic Neuralgia 39 0.108
849
P TRS029 Trisomy 1q 27 0.108
850
SML019 Smallpox 55 0.108
851
P PLY017 Polyarteritis Nodosa 59 0.108
852
CHR208 Chromosome 17p Deletion 21 0.108
853
c HRD039 Hereditary Amyloidosis 45 0.108
854
c AMY009 Amyloidosis Aa 47 0.108
855
WLD005 Wild Type Attr Amyloidosis 29 0.108
856
PNM013 Pneumococcal Meningitis 43 0.108
857
PLY100 Polyploidy 36 0.108
858
HVY003 Heavy Chain Deposition Disease 18 0.108
859
ARG006 Aregenerative Anemia 28 0.108
860
c AHM002 Ah Amyloidosis 14 0.108
861
NNS045 Non-Specific Syndromic Intellectual Disability 41 0.108
862
PRM151 Primary Bone Lymphoma 19 0.108
863
FTL029 Fetal Thalidomide Syndrome 27 0.108
864
MRK002 Marek Disease 22 0.108
865
P DYS021 Dysautonomia 38 0.108
866
P ENC018 Encephalopathy 62 0.108
867
PRN039 Paraneoplastic Syndromes 37 0.108
868
PST092 Posttransplant Acute Limbic Encephalitis 29 0.108
869
HPT066 Hepatoportal Sclerosis 21 0.108
Content
Loading form....