Search results for Antilymphocyte Serum

507 hits were found for Antilymphocyte Serum

# Family MCID Name MIFTS Score
1
P HPT021 Hepatitis 75 0.242
2
PRS047 Prostatitis 59 0.217
3
P ART022 Arthritis 77 0.192
4
P BRS047 Breast Cancer 100 0.181
5
P RHM011 Rheumatoid Arthritis 91 0.172
6
P DBT009 Diabetes Mellitus 72 0.168
7
c HPT001 Hepatitis C 73 0.159
8
P HPT023 Hepatocellular Carcinoma 94 0.156
9
P LPS004 Lupus Erythematosus 69 0.154
10
c SYS001 Systemic Lupus Erythematosus 86 0.151
11
P LVR013 Liver Disease 76 0.151
12
AST005 Asthma 83 0.148
13
P LYM118 Lymphoma 71 0.144
14
P LKM002 Leukemia 75 0.143
15
ART140 Arteries, Anomalies of 51 0.140
16
P MYC007 Myocardial Infarction 81 0.135
17
P MLT020 Multiple Sclerosis 85 0.134
18
c CHR089 Chronic Kidney Failure 72 0.129
19
P KDN018 Kidney Disease 69 0.125
20
P OVR042 Ovarian Cancer 82 0.124
21
P HRT032 Heart Disease 80 0.121
22
P ADN016 Adenocarcinoma 71 0.120
23
MLN008 Melanoma 72 0.119
24
MYL069 Myeloma, Multiple 86 0.116
25
APL001 Aplastic Anemia 74 0.114
26
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.107
27
c SCL052 Scleroderma, Familial Progressive 60 0.104
28
P PNM007 Pneumonia 70 0.103
29
c HPT073 Hepatitis C Virus 73 0.102
30
ISC004 Ischemia 66 0.091
31
LNG099 Lung Disease 67 0.089
32
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.088
33
P GRF003 Graft-Versus-Host Disease 72 0.087
34
P AMY004 Amyloidosis 69 0.087
35
BRN071 Brain Injury 54 0.086
36
P INF032 Infertility 59 0.086
37
c LKM071 Leukemia, Chronic Lymphocytic 75 0.081
38
c LKM004 Leukemia, B-Cell, Chronic 37 0.081
39
P BCL006 B-Cell Lymphomas 70 0.079
40
P ENC018 Encephalopathy 58 0.078
41
LYM027 Lymphopenia 56 0.078
42
P THL005 Thalassemia 65 0.078
43
URN009 Urinary System Disease 58 0.077
44
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.077
45
HMT018 Hematopoietic Stem Cell Transplantation 58 0.077
46
LYM133 Lymphoma, Hodgkin, Classic 78 0.076
47
P PLM036 Pulmonary Fibrosis 68 0.074
48
MYL009 Myelodysplastic Syndrome 75 0.074
49
LPD008 Lipid Metabolism Disorder 59 0.074
50
DMN002 Dementia 68 0.074
51
ATM095 Autoimmune Disease 66 0.074
52
P NRP001 Neuropathy 63 0.073
53
CYS001 Cystic Fibrosis 85 0.072
54
VSC011 Vasculitis 66 0.072
55
PRP030 Purpura 61 0.072
56
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.072
57
CNN005 Connective Tissue Disease 65 0.072
58
P INF038 Influenza 77 0.071
59
P MYL006 Myeloid Leukemia 69 0.070
60
CNG034 Congestive Heart Failure 74 0.069
61
P ENC004 Encephalitis 66 0.069
62
c OVR114 Ovarian Cancer 1 54 0.069
63
HYP266 Hypoxia 61 0.069
64
GT001 Gout 60 0.069
65
DFF005 Diffuse Large B-Cell Lymphoma 64 0.069
66
SRC014 Sarcoma 68 0.068
67
NRL016 Neural Tube Defects 79 0.068
68
GST050 Gastrointestinal System Disease 66 0.068
69
P HMR012 Hemorrhagic Fever 60 0.068
70
VSC007 Vascular Disease 71 0.067
71
P DRM010 Dermatomyositis 65 0.066
72
P PLY019 Polyneuropathy 58 0.066
73
P GRM010 Germ Cells Tumors 37 0.066
74
SKN016 Skin Disease 68 0.065
75
RHM027 Rheumatic Disease 62 0.065
76
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.065
77
c LKM061 Leukemia, Acute Myeloid 81 0.064
78
P OVR049 Ovarian Disease 58 0.064
79
HMS001 Hemosiderosis 50 0.064
80
ACQ007 Acquired Immunodeficiency Syndrome 65 0.064
81
MCS002 Mucositis 61 0.064
82
P PLY041 Polymyositis 57 0.064
83
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.063
84
c ACT073 Acute Leukemia 61 0.063
85
END030 End Stage Renal Failure 59 0.063
86
P FLL037 Follicular Lymphoma 76 0.063
87
P NRB001 Neuroblastoma 73 0.062
88
P NTR004 Neutropenia 60 0.062
89
P LYM026 Lymphoblastic Leukemia 66 0.062
90
HRY003 Hairy Cell Leukemia 60 0.061
91
P ART023 Arthropathy 68 0.061
92
c CHR417 Chronic Graft Versus Host Disease 65 0.060
93
CRB039 Cerebrovascular Disease 68 0.060
94
c HPT003 Hepatitis a 63 0.060
95
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.060
96
c ACT135 Acute Graft Versus Host Disease 57 0.060
97
SKN027 Skin Conditions 48 0.060
98
P CTN015 Cutaneous T Cell Lymphoma 56 0.060
99
c BTT014 Beta-Thalassemia 70 0.060
100
P THR014 Thrombocytopenia 65 0.059
101
BRN002 Bronchiolitis 59 0.059
102
MYC006 Mycosis Fungoides 73 0.059
103
P NRV007 Nervous System Disease 75 0.058
104
P INT068 Intestinal Disease 65 0.058
105
P MYP004 Myopathy 69 0.058
106
P DRR001 Diarrhea 60 0.058
107
GLC008 Glucose Metabolism Disease 38 0.058
108
BRS051 Breast Disease 67 0.057
109
c CNT035 Central Nervous System Disease 65 0.057
110
HYP056 Hypoglycemia 62 0.057
111
SCK005 Sickle Cell Disease 54 0.057
112
P HST010 Histiocytosis 60 0.057
113
P CLL015 Collagen Disease 53 0.056
114
P TCL004 T-Cell Leukemia 50 0.056
115
VRL011 Viral Infectious Disease 64 0.056
116
HYP066 Hyperglycemia 64 0.056
117
NRN004 Neuroendocrine Tumor 58 0.056
118
PRP080 Peripheral Artery Disease 54 0.056
119
TST014 Testicular Cancer 54 0.055
120
THR024 Thrombosis 61 0.054
121
URM002 Uremia 52 0.054
122
LYM019 Lymphosarcoma 58 0.054
123
P CND004 Candidiasis 61 0.053
124
P PLY018 Polycythemia 60 0.053
125
c ALM001 Al Amyloidosis 56 0.053
126
P ACT074 Acute Lymphocytic Leukemia 61 0.053
127
RSP006 Respiratory System Disease 63 0.052
128
P PLM037 Pulmonary Hypertension 79 0.052
129
c ADL017 Adult T-Cell Leukemia 63 0.052
130
JNT002 Joint Disorders 60 0.052
131
GND003 Gonadal Disease 32 0.052
132
P MYL005 Myelofibrosis 75 0.051
133
TTN003 Tetanus 65 0.051
134
IMM136 Immune System Disease 57 0.051
135
MCR004 Macroglobulinemia 54 0.051
136
EXC002 Exocrine Pancreatic Insufficiency 45 0.051
137
ENT004 Enthesopathy 38 0.051
138
c LKM063 Leukemia, Chronic Myeloid 80 0.050
139
P HMR003 Hemorrhagic Disease 61 0.050
140
SCK003 Sickle Cell Anemia 73 0.050
141
THR004 Thrombocytosis 55 0.050
142
P BLD051 Blood Coagulation Disease 38 0.049
143
P TYS001 Tay-Sachs Disease 71 0.049
144
c JVN010 Juvenile Rheumatoid Arthritis 71 0.049
145
c LCL006 Localized Scleroderma 66 0.049
146
P HYP024 Hypoparathyroidism 55 0.049
147
c ACT071 Acute Kidney Failure 54 0.049
148
PLY001 Polycythemia Vera 75 0.048
149
CLR030 Clear Cell Renal Cell Carcinoma 55 0.048
150
PLS009 Plasma Cell Neoplasm 51 0.048
151
LYM024 Lymphatic System Disease 45 0.048
152
CMM004 Common Variable Immunodeficiency 71 0.047
153
P TMP003 Temporal Arteritis 67 0.047
154
DMY004 Demyelinating Disease 58 0.047
155
SPS003 Spastic Diplegia 55 0.047
156
ANC002 Anca-Associated Vasculitis 42 0.047
157
PNC001 Pancytopenia 50 0.046
158
VSC008 Vascular Hemostatic Disease 36 0.046
159
P TRN020 Turner Syndrome 69 0.046
160
BRN012 Bronchiolitis Obliterans 60 0.046
161
PNC034 Pancreas Disease 59 0.046
162
NRT004 Neuritis 55 0.046
163
CHR001 Churg-Strauss Syndrome 51 0.046
164
P TST021 Testicular Germ Cell Tumor 70 0.045
165
MXD005 Mixed Connective Tissue Disease 66 0.045
166
P HYP098 Hypereosinophilic Syndrome 65 0.045
167
SKN019 Skin Melanoma 63 0.045
168
SFT003 Soft Tissue Sarcoma 58 0.045
169
EPD016 Epidermolysis Bullosa 57 0.045
170
SCR015 Scarlet Fever 40 0.045
171
BRK010 Burkitt Lymphoma 71 0.044
172
P THY023 Thymoma 65 0.044
173
P CHR285 Chronic Myelomonocytic Leukemia 63 0.044
174
PLS011 Plasmacytoma 60 0.044
175
INS001 Insulinoma 66 0.044
176
P MYS005 Myositis 63 0.044
177
P HML002 Hemolytic Anemia 62 0.044
178
RTN018 Retinal Disease 56 0.044
179
SPP010 Suppressor of Tumorigenicity 3 55 0.044
180
CHR074 Choriocarcinoma 49 0.044
181
IMM003 Immunoglobulin Alpha Deficiency 37 0.044
182
c TRC078 Trichohepatoenteric Syndrome 2 34 0.044
183
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.043
184
P KDN017 Kidney Cancer 66 0.043
185
NRM005 Neuromuscular Disease 60 0.043
186
P CYS018 Cystitis 57 0.043
187
P PLY017 Polyarteritis Nodosa 51 0.043
188
GRN017 Granulocytopenia 49 0.043
189
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.042
190
LYM067 Lymphoid Leukemia 43 0.042
191
P ESS003 Essential Thrombocythemia 71 0.041
192
P AGM001 Agammaglobulinemia 70 0.041
193
DNG002 Dengue Hemorrhagic Fever 66 0.041
194
LNG108 Langerhans Cell Histiocytosis 63 0.041
195
P RHB003 Rhabdomyosarcoma 61 0.041
196
IDP011 Idiopathic Interstitial Pneumonia 60 0.041
197
c MCL062 Mucolipidosis Ii Alpha/beta 58 0.041
198
PRT030 Parathyroid Gland Disease 50 0.041
199
c WLM018 Wilms Tumor 5 49 0.041
200
P ART084 Arteriovenous Fistula 46 0.041
201
OVR094 Ovarian Epithelial Cancer 46 0.041
202
P OST001 Osteopetrosis 70 0.040
203
P SYS005 Systemic Scleroderma 67 0.040
204
TKY002 Takayasu Arteritis 66 0.040
205
IMM174 Immunodeficiency with Hyper-Igm, Type 1 64 0.040
206
P MNC007 Monocytic Leukemia 59 0.040
207
BRN038 Bronchial Disease 58 0.040
208
CYT008 Cytomegalovirus Infection 57 0.040
209
P MYP006 Myopia 56 0.040
210
BRN022 Bronchiectasis 55 0.040
211
HDC001 Headache 55 0.040
212
EWN002 Ewing's Family of Tumors 49 0.040
213
PRP036 Peripheral T-Cell Lymphoma 48 0.040
214
MNT001 Mantle Cell Lymphoma 76 0.040
215
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 67 0.040
216
SZR001 Sezary's Disease 58 0.040
217
LYM040 Lymphoblastic Lymphoma 58 0.040
218
MRG003 Marginal Zone B-Cell Lymphoma 56 0.040
219
CHR563 Chronic Eosinophilic Leukemia 51 0.040
220
CHR286 Chronic Neutrophilic Leukemia 49 0.040
221
INT038 Interdigitating Dendritic Cell Sarcoma 46 0.040
222
HDG004 Hodgkin's Granuloma 28 0.040
223
HDG006 Hodgkin's Paragranuloma 21 0.040
224
WGN006 Wegener Granulomatosis 71 0.039
225
P PLY014 Polycystic Kidney Disease 60 0.039
226
PNM001 Pneumocystosis 55 0.039
227
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.039
228
GNR004 Generalized Anxiety Disorder 53 0.039
229
MSC033 Muscle Disorders 53 0.039
230
P PRC012 Pericardial Effusion 52 0.039
231
ANX004 Anoxia 49 0.039
232
RNL077 Renal Fibrosis 49 0.039
233
c MTR002 Mitral Valve Insufficiency 46 0.039
234
P AST055 Asthma-Related Traits 1 18 0.039
235
P MCL013 Mucolipidosis Iv 67 0.037
236
P FCS002 Fucosidosis 59 0.037
237
ART017 Aortic Disease 57 0.037
238
c ANM038 Anemia, Autoimmune Hemolytic 56 0.037
239
P INT070 Intestinal Obstruction 55 0.037
240
P TRC086 Trichohepatoenteric Syndrome 1 54 0.037
241
PRP019 Peripheral Nervous System Disease 53 0.037
242
DFF035 Diffuse Cutaneous Systemic Sclerosis 53 0.037
243
IDP024 Idiopathic Inflammatory Myopathy 49 0.037
244
ALP012 Alpha-Methylacyl-Coa Racemase Deficiency 46 0.037
245
ANG046 Angioimmunoblastic T-Cell Lymphoma 46 0.037
246
P TST026 Testicular Germ Cell Cancer 44 0.037
247
MSC004 Muscle Tissue Disease 39 0.037
248
HMP001 Hemopericardium 34 0.037
249
c JVN004 Juvenile Myelomonocytic Leukemia 70 0.037
250
P DYS007 Dyskeratosis Congenita 68 0.037
251
MYL031 Myeloproliferative Neoplasm 64 0.037
252
c LKM062 Leukemia, Acute Lymphoblastic 64 0.037
253
ACT103 Acute Lymphoblastic Leukemia, Childhood 53 0.037
254
SPL004 Splenic Marginal Zone Lymphoma 52 0.037
255
PLS025 Plasmablastic Lymphoma 51 0.037
256
RTC009 Reticulum Cell Sarcoma 51 0.037
257
ATY042 Atypical Chronic Myeloid Leukemia 51 0.037
258
RTC005 Reticulosarcoma 49 0.037
259
MYL004 Myelodysplastic Myeloproliferative Cancer 45 0.037
260
NDL020 Nodal Marginal Zone B-Cell Lymphoma 38 0.037
261
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 36 0.037
262
ACT118 Acute Non Lymphoblastic Leukemia 32 0.037
263
RFR002 Refractory Hairy Cell Leukemia 32 0.037
264
LYM048 Lymphoma, Large-Cell, Immunoblastic 31 0.037
265
RFR001 Refractory Plasma Cell Neoplasm 19 0.037
266
CLS052 Classic Hairy Cell Leukemia 16 0.037
267
P AGM019 Agammaglobulinemia, X-Linked 69 0.036
268
P GCH001 Gaucher's Disease 62 0.036
269
P ANP001 Anaplastic Large Cell Lymphoma 60 0.036
270
P RNL003 Renal Clear Cell Carcinoma 58 0.036
271
P ZLL001 Zellweger Syndrome 56 0.036
272
P TRM003 Tremor 54 0.036
273
EXT010 Extramedullary Plasmacytoma 52 0.036
274
RFR010 Refractory Anemia 48 0.036
275
DFF003 Diffuse Scleroderma 44 0.036
276
P CHR084 Chromosomal Disease 40 0.036
277
VRS001 Virus Associated Hemophagocytic Syndrome 36 0.036
278
LKC003 Leukocyte Disease 34 0.036
279
P ATS366 Autism X-Linked 2 34 0.036
280
BLD138 Blood Group--Diego System 18 0.036
281
HML018 Homologous Wasting Disease 18 0.036
282
VSC009 Vascular Skin Disease 10 0.036
283
P WSK001 Wiskott-Aldrich Syndrome 76 0.034
284
P MTC003 Metachromatic Leukodystrophy 72 0.034
285
ADR007 Adrenoleukodystrophy 72 0.034
286
FRN006 Frontotemporal Dementia 70 0.034
287
P NMN002 Niemann-Pick Disease 68 0.034
288
SND001 Sandhoff Disease 65 0.034
289
P WLD002 Waldenstrom Macroglobulinemia 65 0.034
290
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.034
291
SHW002 Shwachman-Diamond Syndrome 63 0.034
292
P MTR004 Maturity-Onset Diabetes of the Young 62 0.034
293
LYS012 Lysosomal Acid Lipase Deficiency 60 0.034
294
P BRS044 Breast Adenocarcinoma 58 0.034
295
DBF001 D-Bifunctional Protein Deficiency 57 0.034
296
ASP002 Aspartylglucosaminuria 57 0.034
297
LKD001 Leukodystrophy 57 0.034
298
LYS002 Lysosomal Storage Disease 56 0.034
299
LKC009 Leukocyte Adhesion Deficiency, Type I 56 0.034
300
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 54 0.034
301
P FNC004 Fanconi Syndrome 54 0.034
302
OST015 Osteochondrodysplasia 54 0.034
303
c VRL007 Viral Encephalitis 53 0.034
304
HMG005 Hemoglobinopathy 53 0.034
305
PRX028 Peroxisomal Acyl-Coa Oxidase Deficiency 52 0.034
306
HMG002 Hemoglobinuria 52 0.034
307
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 51 0.034
308
LYM051 Lymphomatoid Granulomatosis 51 0.034
309
ADR012 Adrenal Gland Disease 51 0.034
310
PRL017 Prolymphocytic Leukemia 51 0.034
311
LYM012 Lymphoplasmacytic Lymphoma 50 0.034
312
LRG008 Large Granular Lymphocyte Leukemia 49 0.034
313
HNC001 Henoch-Schoenlein Purpura 48 0.034
314
TCL002 T-Cell Large Granular Lymphocyte Leukemia 48 0.034
315
PLS016 Plasma Cell Leukemia 43 0.034
316
OVR112 Ovarian Germ Cell Cancer 42 0.034
317
CRB025 Carbohydrate Metabolic Disorder 38 0.034
318
MTC061 Mitochondrial Dna Depletion Syndrome 1 35 0.034
319
P CNN004 Connective Tissue Cancer 35 0.034
320
CYT004 Cytomegalic Inclusion Disease 35 0.034
321
c THY107 Thymoma, Familial 34 0.034
322
VSC012 Vesiculobullous Skin Disease 32 0.034
323
c INH004 Inherited Blood Coagulation Disease 29 0.034
324
EWN003 Ewing Sarcoma 72 0.031
325
SVR004 Severe Combined Immunodeficiency 71 0.031
326
P KRB001 Krabbe Disease 70 0.031
327
P DMN001 Diamond-Blackfan Anemia 70 0.031
328
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.031
329
P CHR012 Chronic Granulomatous Disease 69 0.031
330
P CHR071 Charcot-Marie-Tooth Disease 67 0.031
331
CHD001 Chediak-Higashi Syndrome 67 0.031
332
c MCP050 Mucopolysaccharidosis, Type Ii 64 0.031
333
VLC001 Velocardiofacial Syndrome 64 0.031
334
HMT002 Hematologic Cancer 64 0.031
335
CMB081 Combined Immunodeficiency, X-Linked 64 0.031
336
MST017 Mast Cell Disease 63 0.031
337
c MNN047 Mannosidosis, Alpha B, Lysosomal 63 0.031
338
P NRN021 Neuronal Ceroid Lipofuscinosis 62 0.031
339
c MCP004 Mucopolysaccharidosis Iv 60 0.031
340
c SVR003 Severe Congenital Neutropenia 58 0.031
341
c INT072 Intestinal Pseudo-Obstruction 57 0.031
342
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 57 0.031
343
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.031
344
HYP810 Hypereosinophilic Syndrome, Idiopathic 57 0.031
345
IMM158 Immune Suppression 57 0.031
346
c GCH015 Gaucher Disease, Type I 57 0.031
347
PST046 Post-Transplant Lymphoproliferative Disease 56 0.031
348
c LKM070 Leukemia, Acute Monocytic 55 0.031
349
DGR001 Digeorge Syndrome 55 0.031
350
P MTC133 Mitochondrial Myopathy 53 0.031
351
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 53 0.031
352
LPD009 Lipid Storage Disease 53 0.031
353
c TCL005 T-Cell Prolymphocytic Leukemia 53 0.031
354
ACT098 Acute Erythroid Leukemia 52 0.031
355
HYP074 Hypersensitivity Vasculitis 52 0.031
356
PRR002 Pure Red-Cell Aplasia 52 0.031
357
P GND004 Gonadal Dysgenesis 50 0.031
358
MNC006 Monoclonal Gammopathy of Uncertain Significance 49 0.031
359
SKL017 Skeletal Dysplasias 48 0.031
360
c ACT020 Acute T Cell Leukemia 48 0.031
361
ESN020 Eosinophilic Granulomatosis with Polyangiitis 47 0.031
362
c CHR418 Chronic Leukemia 46 0.031
363
EPD070 Epidermoid Cysts 46 0.031
364
LYM127 Lymphatic Malformations 45 0.031
365
ACT088 Acute Insulin Response 43 0.031
366
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 43 0.031
367
BCL014 B-Cell Growth Factor 42 0.031
368
CMP009 Complement Deficiency 41 0.031
369
SPC010 Speech and Communication Disorders 40 0.031
370
FXF002 Fox-Fordyce Disease 40 0.031
371
END014 Endemic Typhus 38 0.031
372
DYS016 Dysgammaglobulinemia 38 0.031
373
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 37 0.031
374
MCN011 Mucinoses 37 0.031
375
NRV004 Nerve Compression Syndrome 37 0.031
376
CYL001 Cayler Cardiofacial Syndrome 36 0.031
377
MCP033 Mucopolysaccharidoses 36 0.031
378
ACT003 Acute Kidney Tubular Necrosis 34 0.031
379
MST020 Mast Cell Activation Syndrome 30 0.031
380
URN022 Urinary Tract Infections, Recurrent 29 0.031
381
c PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 25 0.031
382
P MRQ003 Morquio Syndrome 25 0.031
383
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 24 0.031
384
ALL002 Allergic Cutaneous Vasculitis 18 0.031
385
ATY022 Atypical Coarctation of Aorta 15 0.031
386
P FNC027 Fanconi Anemia, Complementation Group a 78 0.028
387
OST159 Osteogenic Sarcoma 70 0.028
388
c WLM013 Wilms Tumor 1 69 0.028
389
PCK003 Pick Disease of Brain 66 0.028
390
GLN010 Glanzmann Thrombasthenia 66 0.028
391
FCT002 Factor Xi Deficiency 64 0.028
392
c MCP049 Mucopolysaccharidosis, Type Vii 64 0.028
393
ACT119 Acute Promyelocytic Leukemia 64 0.028
394
MGK001 Megakaryocytic Leukemia 63 0.028
395
RFS006 Refsum Disease, Classic 63 0.028
396
IMM167 Immune Deficiency Disease 62 0.028
397
c MCP024 Mucopolysaccharidosis Type Vi 61 0.028
398
c NMN013 Niemann-Pick Disease, Type a 59 0.028
399
BNC003 Bone Cancer 59 0.028
400
APH002 Aphasia 58 0.028
401
P GRS003 Griscelli Syndrome 58 0.028
402
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 57 0.028
403
c PRX045 Peroxisome Biogenesis Disorder 1b 57 0.028
404
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 57 0.028
405
P LYM033 Lymphoproliferative Syndrome 55 0.028
406
HRL003 Hurler Syndrome 55 0.028
407
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 53 0.028
408
c PRM012 Primary Polycythemia 53 0.028
409
c GNG001 Gangliosidosis Gm1 52 0.028
410
THY025 Thymus Cancer 52 0.028
411
P SML016 Small Intestine Cancer 52 0.028
412
NNT017 Neonatal Adrenoleukodystrophy 52 0.028
413
MYL003 Myeloid Sarcoma 51 0.028
414
MST002 Mast-Cell Leukemia 51 0.028
415
c MLG074 Malignant Mesenchymoma 51 0.028
416
FBR086 Fibrolamellar Carcinoma 50 0.028
417
INT054 Intraocular Lymphoma 50 0.028
418
P LPM005 Lipomatosis 50 0.028
419
CNG028 Congenital Hypoplastic Anemia 50 0.028
420
MTC069 Mitochondrial Disorders 49 0.028
421
c INH020 Inherited Metabolic Disorder 49 0.028
422
SPH010 Sphingolipidosis 48 0.028
423
ACT200 Acute Monoblastic Leukemia 47 0.028
424
c ADL066 Adult Neuronal Ceroid Lipofuscinosis 47 0.028
425
THR035 Thrombasthenia 46 0.028
426
BLD053 Blood Platelet Disease 45 0.028
427
SML008 Small Intestine Lymphoma 45 0.028
428
NRN005 Neuronal Ceroid-Lipofuscinoses 45 0.028
429
CD4003 Cd40 Ligand Deficiency 44 0.028
430
P MNN018 Mannosidosis 44 0.028
431
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 44 0.028
432
SPC005 Speech Disorder 44 0.028
433
CLL014 Cll/sll 43 0.028
434
HYP189 Hypoadrenalism 43 0.028
435
MTC004 Mitochondrial Encephalomyopathy 42 0.028
436
NNL001 Non-Langerhans-Cell Histiocytosis 42 0.028
437
FRN051 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related 42 0.028
438
SMN008 Semantic Dementia 41 0.028
439
GNT050 Genitourinary Tract Anomalies 41 0.028
440
c ADL027 Adult Dermatomyositis 41 0.028
441
c GM1004 Gm1-Gangliosidosis, Type I 41 0.028
442
ADR010 Adrenal Cortical Hypofunction 41 0.028
443
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.028
444
PRX077 Peroxisomal Biogenesis Disorders 40 0.028
445
P ENC011 Encephalomyopathy 40 0.028
446
LTH001 Lethal Midline Granuloma 40 0.028
447
MTR007 Motor Peripheral Neuropathy 39 0.028
448
c CNG413 Congenital Short Bowel Syndrome 39 0.028
449
LTT002 Letterer-Siwe Disease 39 0.028
450
SLT001 Solitary Osseous Plasmacytoma 39 0.028
451
ADR022 Adrenomyeloneuropathy 39 0.028
452
CPL005 Capillary Disease 38 0.028
453
IMM078 Immunodeficiency 21 38 0.028
454
BNS001 Bone Osteosarcoma 38 0.028
455
CHL050 Cholesterol Ester Storage Disease 38 0.028
456
LYM005 Lymphocele 37 0.028
457
c MYL058 Myeloproliferative Syndrome, Transient 37 0.028
458
ACT177 Acute Basophilic Leukemia 37 0.028
459
SXD001 Sex Differentiation Disease 37 0.028
460
HMR023 Hemorrhagic Cystitis 36 0.028
461
c NTR049 Neutropenia, Severe Congenital, 3, Autosomal Recessive 36 0.028
462
c CRD226 Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive 36 0.028
463
ENG004 Engraftment Syndrome 36 0.028
464
PHG002 Phagocyte Bactericidal Dysfunction 36 0.028
465
c HYP072 Hypersensitivity Reaction Type Iii Disease 35 0.028
466
CRD043 Ceroid Storage Disease 34 0.028
467
PRX001 Peroxisomal Disease 34 0.028
468
GRN014 Grn-Related Frontotemporal Dementia 34 0.028
469
c TYP010 Type C Thymoma 34 0.028
470
P RFR008 Refractory Anemia with Excess Blasts 34 0.028
471
INC022 Inclusion-Cell Disease 33 0.028
472
ACT114 Acute Myeloblastic Leukemia Without Maturation 32 0.028
473
RFR004 Refractory Hematologic Cancer 31 0.028
474
ACT216 Acute Leukemia of Ambiguous Lineage 30 0.028
475
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 30 0.028
476
ACT095 Acute Biphenotypic Leukemia 29 0.028
477
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 29 0.028
478
MTC016 Mitochondrial Neurogastrointestinal Encephalopathy Disease 28 0.028
479
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 28 0.028
480
P SCL057 Scoliosis, Isolated 1 28 0.028
481
c PRM200 Primary Fanconi Syndrome 27 0.028
482
c ALP039 Alopecia Areata 1 27 0.028
483
RNL021 Renal Tubular Transport Disease 27 0.028
484
MCL022 Mucolipidoses 27 0.028
485
ARG006 Aregenerative Anemia 26 0.028
486
c LKM005 Leukemia, T-Cell, Chronic 25 0.028
487
SML025 Small Non-Cleaved Cell Lymphoma 25 0.028
488
RFR007 Refractory Anemia with Excess Blasts in Transformation 25 0.028
489
ACT234 Acute Myeloid Leukemia with Minimal Differentiation 24 0.028
490
ACQ031 Acquired Idiopathic Sideroblastic Anemia 24 0.028
491
RFS003 Refsum Disease, Infantile Form 23 0.028
492
SDN002 Sudanophilic Cerebral Sclerosis 23 0.028
493
FRN030 Frontotemporal Dementia with Parkinsonism-17 22 0.028
494
PLS003 Plasmacytic Leukemia 22 0.028
495
c ADL093 Adult Acute Monocytic Leukemia 22 0.028
496
PRM153 Primary Progressive Apraxia of Speech 21 0.028
497
PRX034 Peroxisome Disorders 20 0.028
498
HDG009 Hodgkin Lymphoma, Childhood 20 0.028
499
TCL018 T-Cell Childhood Acute Lymphocytic Leukemia 20 0.028
500
DSS003 Disseminated Eosinophilic Collagen Disease 20 0.028
501
AML051 Aml with Myelodysplasia-Related Features 19 0.028
502
CLN039 Cln4 Disease 17 0.028
503
ALL012 Allergic Angiitis 13 0.028
504
c 46X002 46 Xx Gonadal Dysgenesis 12 0.028
505
NNN002 Noninvasive Malignant Thymoma 11 0.028
506
c LKM051 Leukemia, Chronic Lymphocytic 3 11 0.028
507
BND002 B- and T-Cell Mixed Leukemia 9 0.028
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