Search results for Antilymphocyte Serum

549 hits were found for Antilymphocyte Serum

# Family MCID Name MIFTS Score
1
P HPT021 Hepatitis 76 0.256
2
PRS047 Prostatitis 60 0.225
3
P ART022 Arthritis 76 0.211
4
P RHM011 Rheumatoid Arthritis 80 0.193
5
P DBT009 Diabetes Mellitus 64 0.178
6
P BRS047 Breast Cancer 100 0.175
7
P LPS004 Lupus Erythematosus 68 0.168
8
c SYS001 Systemic Lupus Erythematosus 86 0.165
9
c HPT001 Hepatitis C 71 0.160
10
P LVR013 Liver Disease 75 0.152
11
AST005 Asthma 82 0.148
12
P LYM118 Lymphoma 70 0.147
13
P LKM002 Leukemia 72 0.142
14
c HPT016 Hepatitis B 67 0.141
15
ART140 Arteries, Anomalies of 65 0.141
16
P MYC007 Myocardial Infarction 79 0.135
17
P MLT020 Multiple Sclerosis 78 0.134
18
P OVR042 Ovarian Cancer 81 0.133
19
c CHR089 Chronic Kidney Failure 72 0.128
20
P KDN018 Kidney Disease 68 0.126
21
MYL069 Myeloma, Multiple 83 0.123
22
P HRT032 Heart Disease 74 0.121
23
APL001 Aplastic Anemia 73 0.120
24
P ADN016 Adenocarcinoma 70 0.120
25
MLN008 Melanoma 62 0.119
26
TYP041 Type I 56 0.118
27
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 38 0.114
28
ISC004 Ischemia 65 0.111
29
c SCL052 Scleroderma, Familial Progressive 64 0.105
30
P PNM007 Pneumonia 69 0.105
31
c HPT073 Hepatitis C Virus 72 0.103
32
P HYP086 Hypothyroidism 64 0.101
33
LNG099 Lung Disease 67 0.090
34
RNL114 Renal Cell Carcinoma, Nonpapillary 59 0.089
35
P AMY004 Amyloidosis 68 0.087
36
P GRF003 Graft-Versus-Host Disease 71 0.087
37
P INF032 Infertility 59 0.086
38
BRN071 Brain Injury 53 0.086
39
P MCR115 Microvascular Complications of Diabetes 5 71 0.085
40
c LKM071 Leukemia, Chronic Lymphocytic 75 0.083
41
c LKM004 Leukemia, B-Cell, Chronic 36 0.083
42
P ASP006 Aspergillosis 65 0.082
43
CHL068 Cholestasis 60 0.082
44
GST033 Gestational Diabetes 60 0.081
45
CYS001 Cystic Fibrosis 84 0.080
46
P ENC018 Encephalopathy 62 0.079
47
LYM133 Lymphoma, Hodgkin, Classic 71 0.079
48
P THL005 Thalassemia 64 0.078
49
P BCL006 B-Cell Lymphomas 65 0.078
50
P MYL006 Myeloid Leukemia 68 0.077
51
P PLM036 Pulmonary Fibrosis 69 0.076
52
HMT018 Hematopoietic Stem Cell Transplantation 57 0.076
53
ATM095 Autoimmune Disease 64 0.076
54
URN009 Urinary System Disease 55 0.076
55
LYM027 Lymphopenia 55 0.076
56
MYL009 Myelodysplastic Syndrome 70 0.075
57
c LKM056 Leukemia, Chronic Lymphocytic 2 41 0.074
58
DMN002 Dementia 68 0.074
59
c OVR114 Ovarian Cancer 1 62 0.074
60
BND020 Bone Disease 62 0.073
61
P NRP001 Neuropathy 63 0.073
62
LPD008 Lipid Metabolism Disorder 58 0.072
63
PRP030 Purpura 61 0.072
64
BRN106 Burns 56 0.072
65
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.072
66
CNN005 Connective Tissue Disease 64 0.072
67
VSC011 Vasculitis 65 0.071
68
P INF038 Influenza 76 0.070
69
SRC014 Sarcoma 68 0.069
70
ANG054 Angina Pectoris 66 0.069
71
HYP266 Hypoxia 61 0.069
72
GT001 Gout 57 0.069
73
c LKM061 Leukemia, Acute Myeloid 80 0.069
74
CNG034 Congestive Heart Failure 72 0.068
75
P ENC004 Encephalitis 65 0.068
76
DFF005 Diffuse Large B-Cell Lymphoma 56 0.067
77
VSC007 Vascular Disease 68 0.067
78
P HMR012 Hemorrhagic Fever 57 0.067
79
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.067
80
LYM019 Lymphosarcoma 55 0.067
81
NRL016 Neural Tube Defects 78 0.067
82
GST050 Gastrointestinal System Disease 64 0.067
83
P DRM010 Dermatomyositis 64 0.066
84
P GRM010 Germ Cells Tumors 36 0.066
85
SKN016 Skin Disease 66 0.065
86
P PLY019 Polyneuropathy 57 0.065
87
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.065
88
c ACT073 Acute Leukemia 60 0.065
89
RHM027 Rheumatic Disease 62 0.064
90
ENT004 Enthesopathy 46 0.064
91
P NTR004 Neutropenia 60 0.063
92
MCS002 Mucositis 60 0.063
93
P OVR049 Ovarian Disease 59 0.063
94
P PLY041 Polymyositis 56 0.063
95
SCK005 Sickle Cell Disease 54 0.063
96
HMS001 Hemosiderosis 51 0.063
97
P ATR011 Atrial Fibrillation 68 0.063
98
ACQ007 Acquired Immunodeficiency Syndrome 63 0.063
99
P NRB001 Neuroblastoma 72 0.062
100
P THR014 Thrombocytopenia 64 0.062
101
END030 End Stage Renal Failure 56 0.062
102
P FLL037 Follicular Lymphoma 69 0.062
103
P ART023 Arthropathy 67 0.061
104
P LYM026 Lymphoblastic Leukemia 64 0.061
105
ANX010 Anxiety 72 0.061
106
c ACT135 Acute Graft Versus Host Disease 56 0.061
107
SKN027 Skin Conditions 48 0.061
108
c BTT014 Beta-Thalassemia 69 0.060
109
CRB039 Cerebrovascular Disease 67 0.060
110
c HPT003 Hepatitis a 61 0.060
111
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.060
112
c LKM062 Leukemia, Acute Lymphoblastic 69 0.060
113
HRY003 Hairy Cell Leukemia 59 0.060
114
P MYP004 Myopathy 68 0.059
115
P CTN015 Cutaneous T Cell Lymphoma 55 0.059
116
c CHR417 Chronic Graft Versus Host Disease 64 0.059
117
P DRR001 Diarrhea 56 0.059
118
GLC008 Glucose Metabolism Disease 52 0.059
119
P INT068 Intestinal Disease 64 0.058
120
BRN002 Bronchiolitis 59 0.058
121
HYP066 Hyperglycemia 63 0.057
122
THR024 Thrombosis 61 0.057
123
MYC006 Mycosis Fungoides 72 0.057
124
P NRV007 Nervous System Disease 73 0.057
125
BRS051 Breast Disease 66 0.057
126
HYP056 Hypoglycemia 62 0.056
127
P HST010 Histiocytosis 59 0.056
128
PRP080 Peripheral Artery Disease 53 0.055
129
P CLL015 Collagen Disease 52 0.055
130
P TCL004 T-Cell Leukemia 50 0.055
131
c CNT035 Central Nervous System Disease 63 0.055
132
NRN004 Neuroendocrine Tumor 58 0.055
133
c ALM001 Al Amyloidosis 57 0.055
134
TST014 Testicular Cancer 53 0.055
135
P PLM037 Pulmonary Hypertension 75 0.054
136
VRL011 Viral Infectious Disease 63 0.054
137
P MYL005 Myelofibrosis 70 0.054
138
HMN044 Human Immunodeficiency Virus Type 1 70 0.053
139
RSP006 Respiratory System Disease 63 0.053
140
P PLY018 Polycythemia 58 0.053
141
BNF002 Bone Fracture 55 0.053
142
URM002 Uremia 52 0.053
143
P CND004 Candidiasis 60 0.052
144
JNT002 Joint Disorders 59 0.052
145
P ACT074 Acute Lymphocytic Leukemia 59 0.051
146
c ADL017 Adult T-Cell Leukemia 62 0.051
147
GLC003 Glucose Intolerance 56 0.051
148
IMM136 Immune System Disease 56 0.051
149
THY030 Thyroid Gland Disease 51 0.051
150
GND003 Gonadal Disease 46 0.051
151
c LKM063 Leukemia, Chronic Myeloid 70 0.050
152
SCK003 Sickle Cell Anemia 72 0.050
153
c JVN010 Juvenile Rheumatoid Arthritis 69 0.050
154
TTN003 Tetanus 64 0.050
155
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 59 0.050
156
P KDN017 Kidney Cancer 58 0.050
157
MCR004 Macroglobulinemia 53 0.050
158
EXC002 Exocrine Pancreatic Insufficiency 43 0.050
159
P HMR003 Hemorrhagic Disease 60 0.049
160
SKN019 Skin Melanoma 69 0.049
161
PRP019 Peripheral Nervous System Disease 60 0.049
162
THR004 Thrombocytosis 54 0.049
163
SPS003 Spastic Diplegia 54 0.049
164
CLR030 Clear Cell Renal Cell Carcinoma 49 0.049
165
PLY001 Polycythemia Vera 74 0.048
166
P TYS001 Tay-Sachs Disease 71 0.048
167
c PLM164 Pulmonary Hypertension, Primary, 1 66 0.048
168
P TMP003 Temporal Arteritis 66 0.048
169
c LCL006 Localized Scleroderma 64 0.048
170
P HYP024 Hypoparathyroidism 54 0.048
171
c ACT071 Acute Kidney Failure 54 0.048
172
CHL061 Childhood Leukemia 55 0.048
173
P BLD051 Blood Coagulation Disease 50 0.048
174
CMM004 Common Variable Immunodeficiency 70 0.047
175
P EXN002 Exanthem 61 0.047
176
LYM024 Lymphatic System Disease 54 0.046
177
PLS009 Plasma Cell Neoplasm 51 0.046
178
THR100 Thrombocytopenic Purpura, Autoimmune 62 0.046
179
DMY004 Demyelinating Disease 57 0.046
180
ANC002 Anca-Associated Vasculitis 45 0.046
181
P RSP003 Respiratory Failure 70 0.045
182
P TRN020 Turner Syndrome 68 0.045
183
P HYP098 Hypereosinophilic Syndrome 65 0.045
184
P TST021 Testicular Germ Cell Tumor 61 0.045
185
BRN012 Bronchiolitis Obliterans 60 0.045
186
HDC001 Headache 59 0.045
187
SFT003 Soft Tissue Sarcoma 58 0.045
188
NRT004 Neuritis 57 0.045
189
PNC034 Pancreas Disease 57 0.045
190
CHR001 Churg-Strauss Syndrome 51 0.045
191
MNC006 Monoclonal Gammopathy of Uncertain Significance 51 0.045
192
OVR094 Ovarian Epithelial Cancer 38 0.045
193
ALL012 Allergic Angiitis 25 0.045
194
PNC001 Pancytopenia 51 0.045
195
VSC008 Vascular Hemostatic Disease 36 0.045
196
MXD005 Mixed Connective Tissue Disease 65 0.044
197
P HML002 Hemolytic Anemia 62 0.044
198
EPD016 Epidermolysis Bullosa 56 0.044
199
IMM003 Immunoglobulin Alpha Deficiency 41 0.044
200
SCR015 Scarlet Fever 40 0.044
201
c TRC078 Trichohepatoenteric Syndrome 2 34 0.044
202
BRK010 Burkitt Lymphoma 68 0.043
203
P THY023 Thymoma 65 0.043
204
P CHR285 Chronic Myelomonocytic Leukemia 62 0.043
205
PLS011 Plasmacytoma 60 0.043
206
PDT001 Pediatric Lymphoma 45 0.043
207
c ADL001 Adult Lymphoma 39 0.043
208
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.043
209
INS001 Insulinoma 65 0.043
210
P MYS005 Myositis 63 0.043
211
P PLY014 Polycystic Kidney Disease 60 0.043
212
NRM005 Neuromuscular Disease 60 0.043
213
RTN018 Retinal Disease 56 0.043
214
SPP010 Suppressor of Tumorigenicity 3 54 0.043
215
CHR074 Choriocarcinoma 47 0.043
216
GRN017 Granulocytopenia 43 0.043
217
P ESS003 Essential Thrombocythemia 70 0.042
218
P SYS005 Systemic Scleroderma 66 0.042
219
IDP011 Idiopathic Interstitial Pneumonia 60 0.042
220
P CYS018 Cystitis 56 0.042
221
P PLY017 Polyarteritis Nodosa 51 0.042
222
c ADL052 Adult Acute Lymphocytic Leukemia 46 0.041
223
LYM067 Lymphoid Leukemia 44 0.041
224
NDL024 Nodal Marginal Zone Lymphoma 41 0.041
225
P AGM001 Agammaglobulinemia 69 0.041
226
DNG002 Dengue Hemorrhagic Fever 66 0.041
227
c MCL062 Mucolipidosis Ii Alpha/beta 63 0.041
228
LNG108 Langerhans Cell Histiocytosis 63 0.041
229
PLM033 Pulmonary Embolism 62 0.041
230
c WLM018 Wilms Tumor 5 60 0.041
231
SLP005 Sleep Disorder 59 0.041
232
BRN038 Bronchial Disease 56 0.041
233
P RHB003 Rhabdomyosarcoma 56 0.041
234
EWN002 Ewing's Family of Tumors 56 0.041
235
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 55 0.041
236
DYS014 Dyspepsia 54 0.041
237
GNR004 Generalized Anxiety Disorder 53 0.041
238
PRT030 Parathyroid Gland Disease 49 0.041
239
P ART084 Arteriovenous Fistula 45 0.041
240
WGN006 Wegener Granulomatosis 70 0.039
241
TKY002 Takayasu Arteritis 66 0.039
242
IMM174 Immunodeficiency with Hyper-Igm, Type 1 63 0.039
243
P OST001 Osteopetrosis 61 0.039
244
P MNC007 Monocytic Leukemia 57 0.039
245
PRP036 Peripheral T-Cell Lymphoma 56 0.039
246
CYT008 Cytomegalovirus Infection 56 0.039
247
P MYP006 Myopia 56 0.039
248
BRN022 Bronchiectasis 55 0.039
249
P MSC033 Muscle Disorders 52 0.039
250
ANX004 Anoxia 49 0.039
251
RNL077 Renal Fibrosis 48 0.039
252
MSC004 Muscle Tissue Disease 39 0.039
253
MNT001 Mantle Cell Lymphoma 73 0.039
254
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 69 0.039
255
SZR001 Sezary's Disease 63 0.039
256
LYM040 Lymphoblastic Lymphoma 57 0.039
257
MRG003 Marginal Zone B-Cell Lymphoma 56 0.039
258
CHR563 Chronic Eosinophilic Leukemia 50 0.039
259
CHR286 Chronic Neutrophilic Leukemia 48 0.039
260
INT038 Interdigitating Dendritic Cell Sarcoma 44 0.039
261
HDG004 Hodgkin's Granuloma 28 0.039
262
HDG006 Hodgkin's Paragranuloma 21 0.039
263
GST092 Gastroesophageal Reflux 64 0.038
264
P GCH001 Gaucher's Disease 62 0.038
265
CNS004 Constipation 56 0.038
266
P INT070 Intestinal Obstruction 56 0.038
267
PNM001 Pneumocystosis 55 0.038
268
P PRC012 Pericardial Effusion 53 0.038
269
c MTR002 Mitral Valve Insufficiency 46 0.038
270
P AST055 Asthma-Related Traits 1 30 0.038
271
SVR004 Severe Combined Immunodeficiency 69 0.036
272
P MCL013 Mucolipidosis Iv 67 0.036
273
CMB081 Combined Immunodeficiency, X-Linked 64 0.036
274
P FCS002 Fucosidosis 60 0.036
275
P ANP001 Anaplastic Large Cell Lymphoma 59 0.036
276
c ANM038 Anemia, Autoimmune Hemolytic 59 0.036
277
TRN015 Transient Cerebral Ischemia 56 0.036
278
ART017 Aortic Disease 56 0.036
279
P TRC086 Trichohepatoenteric Syndrome 1 54 0.036
280
DFF035 Diffuse Cutaneous Systemic Sclerosis 52 0.036
281
ANR004 Anuria 50 0.036
282
IDP024 Idiopathic Inflammatory Myopathy 49 0.036
283
ANG046 Angioimmunoblastic T-Cell Lymphoma 47 0.036
284
ALP012 Alpha-Methylacyl-Coa Racemase Deficiency 46 0.036
285
LKC003 Leukocyte Disease 46 0.036
286
DFF003 Diffuse Scleroderma 44 0.036
287
HMP001 Hemopericardium 41 0.036
288
P TST026 Testicular Germ Cell Cancer 41 0.036
289
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.036
290
P DYS007 Dyskeratosis Congenita 67 0.036
291
MYL031 Myeloproliferative Neoplasm 63 0.036
292
MYL004 Myelodysplastic Myeloproliferative Cancer 53 0.036
293
PLS025 Plasmablastic Lymphoma 53 0.036
294
RTC009 Reticulum Cell Sarcoma 52 0.036
295
SPL004 Splenic Marginal Zone Lymphoma 51 0.036
296
ATY042 Atypical Chronic Myeloid Leukemia 50 0.036
297
RTC005 Reticulosarcoma 49 0.036
298
ACT103 Acute Lymphoblastic Leukemia, Childhood 48 0.036
299
NDL020 Nodal Marginal Zone B-Cell Lymphoma 38 0.036
300
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 36 0.036
301
RFR002 Refractory Hairy Cell Leukemia 35 0.036
302
ACT118 Acute Non Lymphoblastic Leukemia 32 0.036
303
LYM048 Lymphoma, Large-Cell, Immunoblastic 31 0.036
304
CLS052 Classic Hairy Cell Leukemia 25 0.036
305
RFR001 Refractory Plasma Cell Neoplasm 19 0.036
306
P WSK001 Wiskott-Aldrich Syndrome 77 0.035
307
ADR007 Adrenoleukodystrophy 71 0.035
308
P AGM019 Agammaglobulinemia, X-Linked 68 0.035
309
P NMN002 Niemann-Pick Disease 60 0.035
310
P ZLL001 Zellweger Syndrome 56 0.035
311
P TRM003 Tremor 54 0.035
312
HMG005 Hemoglobinopathy 53 0.035
313
EXT010 Extramedullary Plasmacytoma 49 0.035
314
RFR010 Refractory Anemia 49 0.035
315
PRD004 Prediabetes Syndrome 45 0.035
316
P ATS366 Autism X-Linked 2 43 0.035
317
P CHR084 Chromosomal Disease 40 0.035
318
VRS001 Virus Associated Hemophagocytic Syndrome 36 0.035
319
AST054 Australia Antigen 27 0.035
320
VSC009 Vascular Skin Disease 20 0.035
321
HML018 Homologous Wasting Disease 18 0.035
322
P MTC003 Metachromatic Leukodystrophy 71 0.033
323
P CHR012 Chronic Granulomatous Disease 69 0.033
324
P TBR001 Tuberous Sclerosis 68 0.033
325
c NMN015 Niemann-Pick Disease, Type C1 68 0.033
326
P FRN006 Frontotemporal Dementia 67 0.033
327
P DBT085 Diabetes Mellitus, Insulin-Dependent 65 0.033
328
SND001 Sandhoff Disease 64 0.033
329
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 63 0.033
330
P SHW006 Shwachman-Diamond Syndrome 1 62 0.033
331
P WLD002 Waldenstrom Macroglobulinemia 61 0.033
332
THY025 Thymus Cancer 60 0.033
333
LYS012 Lysosomal Acid Lipase Deficiency 60 0.033
334
P MTR004 Maturity-Onset Diabetes of the Young 60 0.033
335
P BRS044 Breast Adenocarcinoma 58 0.033
336
HYP810 Hypereosinophilic Syndrome, Idiopathic 58 0.033
337
LKC009 Leukocyte Adhesion Deficiency, Type I 57 0.033
338
P LKD001 Leukodystrophy 57 0.033
339
DBF001 D-Bifunctional Protein Deficiency 57 0.033
340
ASP002 Aspartylglucosaminuria 56 0.033
341
LYS002 Lysosomal Storage Disease 56 0.033
342
OST015 Osteochondrodysplasia 53 0.033
343
P FNC004 Fanconi Syndrome 52 0.033
344
c VRL007 Viral Encephalitis 52 0.033
345
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 52 0.033
346
HMG002 Hemoglobinuria 52 0.033
347
PRX028 Peroxisomal Acyl-Coa Oxidase Deficiency 52 0.033
348
ADR012 Adrenal Gland Disease 51 0.033
349
PRL017 Prolymphocytic Leukemia 50 0.033
350
LYM051 Lymphomatoid Granulomatosis 50 0.033
351
LYM012 Lymphoplasmacytic Lymphoma 50 0.033
352
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 50 0.033
353
CRB025 Carbohydrate Metabolic Disorder 50 0.033
354
HNC001 Henoch-Schoenlein Purpura 47 0.033
355
LRG008 Large Granular Lymphocyte Leukemia 47 0.033
356
TCL002 T-Cell Large Granular Lymphocyte Leukemia 47 0.033
357
EPD070 Epidermoid Cysts 47 0.033
358
P CNN004 Connective Tissue Cancer 45 0.033
359
OVR112 Ovarian Germ Cell Cancer 44 0.033
360
MTC061 Mitochondrial Dna Depletion Syndrome 1 44 0.033
361
CHL010 Childhood Kidney Cell Carcinoma 43 0.033
362
PLS016 Plasma Cell Leukemia 42 0.033
363
c INH004 Inherited Blood Coagulation Disease 41 0.033
364
VSC012 Vesiculobullous Skin Disease 41 0.033
365
CYT004 Cytomegalic Inclusion Disease 34 0.033
366
FRN030 Frontotemporal Dementia with Parkinsonism-17 31 0.033
367
EXF003 Exfoliative Dermatitis 29 0.033
368
P DMN001 Diamond-Blackfan Anemia 69 0.031
369
P KRB001 Krabbe Disease 69 0.031
370
EWN003 Ewing Sarcoma 68 0.031
371
CHD001 Chediak-Higashi Syndrome 65 0.031
372
P CHR071 Charcot-Marie-Tooth Disease 65 0.031
373
c MCP050 Mucopolysaccharidosis, Type Ii 63 0.031
374
VLC001 Velocardiofacial Syndrome 63 0.031
375
HMT002 Hematologic Cancer 63 0.031
376
MST017 Mast Cell Disease 63 0.031
377
c TBR025 Tuberous Sclerosis 1 62 0.031
378
P NRN021 Neuronal Ceroid Lipofuscinosis 61 0.031
379
c MCP004 Mucopolysaccharidosis Iv 59 0.031
380
c SVR003 Severe Congenital Neutropenia 58 0.031
381
c INT072 Intestinal Pseudo-Obstruction 57 0.031
382
c GCH015 Gaucher Disease, Type I 57 0.031
383
c GNG001 Gangliosidosis Gm1 57 0.031
384
HPT046 Hepatic Veno-Occlusive Disease 57 0.031
385
c MNN047 Mannosidosis, Alpha B, Lysosomal 56 0.031
386
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 56 0.031
387
DGR001 Digeorge Syndrome 55 0.031
388
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 55 0.031
389
PST046 Post-Transplant Lymphoproliferative Disease 55 0.031
390
c LKM070 Leukemia, Acute Monocytic 55 0.031
391
CRD223 Cardiac Arrhythmia 54 0.031
392
P MTC133 Mitochondrial Myopathy 54 0.031
393
c ACT020 Acute T Cell Leukemia 52 0.031
394
ACT098 Acute Erythroid Leukemia 52 0.031
395
c TCL005 T-Cell Prolymphocytic Leukemia 52 0.031
396
SPC010 Speech and Communication Disorders 52 0.031
397
HYP074 Hypersensitivity Vasculitis 51 0.031
398
LPD009 Lipid Storage Disease 51 0.031
399
PRR002 Pure Red-Cell Aplasia 51 0.031
400
P GND004 Gonadal Dysgenesis 50 0.031
401
P MTC069 Mitochondrial Disorders 49 0.031
402
SKL017 Skeletal Dysplasias 48 0.031
403
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.031
404
ESN020 Eosinophilic Granulomatosis with Polyangiitis 47 0.031
405
c CHR418 Chronic Leukemia 47 0.031
406
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 46 0.031
407
LYM127 Lymphatic Malformations 45 0.031
408
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 44 0.031
409
P MTC004 Mitochondrial Encephalomyopathy 43 0.031
410
ACT088 Acute Insulin Response 43 0.031
411
HYP189 Hypoadrenalism 43 0.031
412
BCL014 B-Cell Growth Factor 41 0.031
413
CMP009 Complement Deficiency 41 0.031
414
FXF002 Fox-Fordyce Disease 40 0.031
415
ADR010 Adrenal Cortical Hypofunction 40 0.031
416
P ENC011 Encephalomyopathy 40 0.031
417
PDT021 Pediatric Osteosarcoma 40 0.031
418
DYS016 Dysgammaglobulinemia 38 0.031
419
ACT003 Acute Kidney Tubular Necrosis 38 0.031
420
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 36 0.031
421
MCP033 Mucopolysaccharidoses 36 0.031
422
CYL001 Cayler Cardiofacial Syndrome 36 0.031
423
MCN011 Mucinoses 36 0.031
424
ACQ031 Acquired Idiopathic Sideroblastic Anemia 36 0.031
425
NRV004 Nerve Compression Syndrome 35 0.031
426
P MRQ003 Morquio Syndrome 31 0.031
427
c PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 30 0.031
428
URN022 Urinary Tract Infections, Recurrent 29 0.031
429
MST020 Mast Cell Activation Syndrome 27 0.031
430
c BKV001 Bk-Virus Nephropathy 26 0.031
431
MNS002 Mini Stroke 23 0.031
432
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 23 0.031
433
ATY022 Atypical Coarctation of Aorta 22 0.031
434
DSS003 Disseminated Eosinophilic Collagen Disease 18 0.031
435
ALL002 Allergic Cutaneous Vasculitis 18 0.031
436
P FNC027 Fanconi Anemia, Complementation Group a 78 0.028
437
PCK003 Pick Disease of Brain 65 0.028
438
GLN010 Glanzmann Thrombasthenia 65 0.028
439
c WLM013 Wilms Tumor 1 64 0.028
440
FCT002 Factor Xi Deficiency 64 0.028
441
MGK001 Megakaryocytic Leukemia 63 0.028
442
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.028
443
RFS006 Refsum Disease, Classic 62 0.028
444
c MCP024 Mucopolysaccharidosis Type Vi 62 0.028
445
BNC003 Bone Cancer 59 0.028
446
IMM167 Immune Deficiency Disease 59 0.028
447
OST159 Osteogenic Sarcoma 59 0.028
448
ACT119 Acute Promyelocytic Leukemia 59 0.028
449
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 59 0.028
450
c NMN013 Niemann-Pick Disease, Type a 59 0.028
451
APH002 Aphasia 58 0.028
452
c PRX045 Peroxisome Biogenesis Disorder 1b 56 0.028
453
P GRS003 Griscelli Syndrome 56 0.028
454
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 56 0.028
455
HRL003 Hurler Syndrome 56 0.028
456
TXC002 Toxic Encephalopathy 55 0.028
457
BLD053 Blood Platelet Disease 55 0.028
458
P LYM033 Lymphoproliferative Syndrome 55 0.028
459
c MLG074 Malignant Mesenchymoma 54 0.028
460
SMN008 Semantic Dementia 54 0.028
461
c PRM012 Primary Polycythemia 52 0.028
462
FRN051 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related 52 0.028
463
NNT017 Neonatal Adrenoleukodystrophy 52 0.028
464
MYL003 Myeloid Sarcoma 51 0.028
465
MST002 Mast-Cell Leukemia 51 0.028
466
P SML016 Small Intestine Cancer 50 0.028
467
P LPM005 Lipomatosis 50 0.028
468
INT054 Intraocular Lymphoma 50 0.028
469
CNG028 Congenital Hypoplastic Anemia 48 0.028
470
c INH020 Inherited Metabolic Disorder 48 0.028
471
SPH010 Sphingolipidosis 47 0.028
472
SPC005 Speech Disorder 47 0.028
473
ACT200 Acute Monoblastic Leukemia 46 0.028
474
c ADL066 Adult Neuronal Ceroid Lipofuscinosis 46 0.028
475
THR035 Thrombasthenia 45 0.028
476
CLL014 Cll/sll 45 0.028
477
NRN005 Neuronal Ceroid-Lipofuscinoses 44 0.028
478
SML008 Small Intestine Lymphoma 44 0.028
479
CD4003 Cd40 Ligand Deficiency 44 0.028
480
PRX001 Peroxisomal Disease 44 0.028
481
c HYP072 Hypersensitivity Reaction Type Iii Disease 44 0.028
482
P MNN018 Mannosidosis 43 0.028
483
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 43 0.028
484
c GM1004 Gm1-Gangliosidosis, Type I 42 0.028
485
NNL001 Non-Langerhans-Cell Histiocytosis 41 0.028
486
LTH001 Lethal Midline Granuloma 41 0.028
487
GNT050 Genitourinary Tract Anomalies 40 0.028
488
P SCL057 Scoliosis, Isolated 1 40 0.028
489
c ADL027 Adult Dermatomyositis 40 0.028
490
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.028
491
PRX077 Peroxisomal Biogenesis Disorders 40 0.028
492
MTR007 Motor Peripheral Neuropathy 40 0.028
493
LTT002 Letterer-Siwe Disease 39 0.028
494
ADR022 Adrenomyeloneuropathy 39 0.028
495
RNL021 Renal Tubular Transport Disease 38 0.028
496
BNS001 Bone Osteosarcoma 38 0.028
497
SLT001 Solitary Osseous Plasmacytoma 38 0.028
498
TTH004 Tethered Spinal Cord Syndrome 38 0.028
499
CPL005 Capillary Disease 38 0.028
500
c CNG413 Congenital Short Bowel Syndrome 38 0.028
501
c MYL058 Myeloproliferative Syndrome, Transient 37 0.028
502
CHL050 Cholesterol Ester Storage Disease 37 0.028
503
LYM005 Lymphocele 37 0.028
504
c GRN014 Grn-Related Frontotemporal Dementia 37 0.028
505
IMM078 Immunodeficiency 21 37 0.028
506
END014 Endemic Typhus 37 0.028
507
CRD043 Ceroid Storage Disease 36 0.028
508
HMR023 Hemorrhagic Cystitis 36 0.028
509
c CRD226 Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive 36 0.028
510
ACT177 Acute Basophilic Leukemia 36 0.028
511
c NTR049 Neutropenia, Severe Congenital, 3, Autosomal Recessive 36 0.028
512
ENG004 Engraftment Syndrome 35 0.028
513
PHG002 Phagocyte Bactericidal Dysfunction 35 0.028
514
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 34 0.028
515
c TYP010 Type C Thymoma 34 0.028
516
P RFR008 Refractory Anemia with Excess Blasts 33 0.028
517
INC022 Inclusion-Cell Disease 32 0.028
518
ACT216 Acute Leukemia of Ambiguous Lineage 32 0.028
519
ACT114 Acute Myeloblastic Leukemia Without Maturation 31 0.028
520
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 31 0.028
521
MTC016 Mitochondrial Neurogastrointestinal Encephalopathy Disease 30 0.028
522
RFR004 Refractory Hematologic Cancer 29 0.028
523
ACT095 Acute Biphenotypic Leukemia 29 0.028
524
P PRX010 Paroxysmal Ventricular Fibrillation 28 0.028
525
c WSK002 Wiskott-Aldrich Syndrome 2 27 0.028
526
SDN002 Sudanophilic Cerebral Sclerosis 27 0.028
527
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 27 0.028
528
PRX034 Peroxisome Disorders 27 0.028
529
MCL022 Mucolipidoses 26 0.028
530
c PRM200 Primary Fanconi Syndrome 26 0.028
531
c LKM005 Leukemia, T-Cell, Chronic 26 0.028
532
PDT020 Pediatric Germ Cell Cancer 25 0.028
533
ARG006 Aregenerative Anemia 25 0.028
534
c ALP039 Alopecia Areata 1 25 0.028
535
ACT234 Acute Myeloid Leukemia with Minimal Differentiation 25 0.028
536
RFR007 Refractory Anemia with Excess Blasts in Transformation 24 0.028
537
SML025 Small Non-Cleaved Cell Lymphoma 24 0.028
538
RFS003 Refsum Disease, Infantile Form 23 0.028
539
CLN039 Cln4 Disease 22 0.028
540
c ADL093 Adult Acute Monocytic Leukemia 22 0.028
541
PRM153 Primary Progressive Apraxia of Speech 21 0.028
542
PLS003 Plasmacytic Leukemia 21 0.028
543
HDG009 Hodgkin Lymphoma, Childhood 21 0.028
544
AML051 Aml with Myelodysplasia-Related Features 18 0.028
545
BND002 B- and T-Cell Mixed Leukemia 18 0.028
546
TCL018 T-Cell Childhood Acute Lymphocytic Leukemia 17 0.028
547
c LKM051 Leukemia, Chronic Lymphocytic 3 17 0.028
548
c 46X002 46 Xx Gonadal Dysgenesis 16 0.028
549
NNN002 Noninvasive Malignant Thymoma 12 0.028
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