Search results for deoxyadenosine

403 hits were found for deoxyadenosine

# Family MCID Name MIFTS Score
1
ADN001 Adenosine Deaminase Deficiency 59 6.252
2
P LKM071 Leukemia, Chronic Lymphocytic 74 4.542
3
HRY003 Hairy Cell Leukemia 61 4.194
4
SVR004 Severe Combined Immunodeficiency 71 3.279
5
CMB007 Combined Immunodeficiency 56 3.143
6
P LKM002 Leukemia 66 3.064
7
HLX001 Helix Syndrome 47 2.664
8
LYM027 Lymphopenia 56 2.644
9
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 2.428
10
IMM167 Immune Deficiency Disease 77 2.423
11
P LKM062 Leukemia, Acute Lymphoblastic 69 2.399
12
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 2.326
13
HMN044 Human Immunodeficiency Virus Type 1 76 2.158
14
XRD010 Xeroderma Pigmentosum, Variant Type 72 2.151
15
P GLM040 Glioma Susceptibility 1 70 2.097
16
MLG169 Malignant Astrocytoma 57 2.097
17
c LKM061 Leukemia, Acute Myeloid 83 2.085
18
P MYL006 Myeloid Leukemia 60 2.064
19
c LKM005 Leukemia, T-Cell, Chronic 33 2.059
20
MYL009 Myelodysplastic Syndrome 67 2.041
21
MDD018 Middle East Respiratory Syndrome 44 1.977
22
VCC001 Vaccinia 49 1.945
23
MCR004 Macroglobulinemia 48 1.795
24
P GRF003 Graft-Versus-Host Disease 71 1.639
25
P NRB001 Neuroblastoma 66 1.590
26
c ACT073 Acute Leukemia 59 1.505
27
SLP001 Sleeping Sickness 56 1.439
28
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 1.426
29
P LYM118 Lymphoma 69 1.362
30
LNG108 Langerhans Cell Histiocytosis 57 1.329
31
ACQ007 Acquired Immunodeficiency Syndrome 58 1.329
32
P HPT021 Hepatitis 68 1.329
33
HST010 Histiocytosis 49 1.329
34
P BCL017 B-Cell Lymphoma 57 1.290
35
P CTN015 Cutaneous T Cell Lymphoma 48 1.275
36
MCR013 Microphthalmia 60 1.252
37
MNT001 Mantle Cell Lymphoma 65 1.239
38
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 72 1.239
39
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.215
40
P HML002 Hemolytic Anemia 62 1.174
41
CHC001 Chickenpox 56 1.174
42
P CNT005 Central Nervous System Lymphoma 51 1.124
43
PRM226 Primary Central Nervous System Lymphoma 47 1.124
44
P MNC007 Monocytic Leukemia 48 1.095
45
PLR008 Pleurisy 49 1.077
46
c ANM038 Anemia, Autoimmune Hemolytic 63 1.062
47
SKN016 Skin Disease 62 1.023
48
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.008
49
P MYC084 Mycobacterium Tuberculosis 1 68 0.989
50
P HRP006 Herpes Simplex 65 0.989
51
c HPT073 Hepatitis C Virus 71 0.972
52
c HPT001 Hepatitis C 61 0.972
53
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.969
54
URT010 Ureteral Obstruction 45 0.969
55
PLR007 Pleural Empyema 51 0.969
56
TRY001 Trypanosomiasis 50 0.926
57
STM007 Stomatitis 52 0.926
58
P CCK001 Cockayne Syndrome 68 0.901
59
P FBR017 Fibrosarcoma 55 0.901
60
P THR014 Thrombocytopenia 66 0.875
61
P MLT020 Multiple Sclerosis 79 0.864
62
PRL017 Prolymphocytic Leukemia 47 0.846
63
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.846
64
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.813
65
c LKM070 Leukemia, Acute Monocytic 56 0.813
66
PLM031 Poliomyelitis 62 0.813
67
ACT200 Acute Monoblastic Leukemia 40 0.813
68
c RNG015 Ring Chromosome 2 22 0.813
69
c LKM063 Leukemia, Chronic Myeloid 71 0.791
70
48X005 48,xyyy 39 0.791
71
P RTN024 Retinoblastoma 72 0.774
72
ATH013 Atherosclerosis Susceptibility 63 0.774
73
P EXN002 Exanthem 58 0.774
74
c SYS001 Systemic Lupus Erythematosus 86 0.774
75
NWC001 Newcastle Disease 48 0.774
76
OST159 Osteogenic Sarcoma 66 0.774
77
DFF016 Diffuse Astrocytoma 48 0.774
78
P LPS004 Lupus Erythematosus 61 0.774
79
P ENC004 Encephalitis 61 0.774
80
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.774
81
c ACT134 Acute Liver Failure 57 0.774
82
HMT002 Hematologic Cancer 61 0.762
83
P HYP098 Hypereosinophilic Syndrome 66 0.762
84
P ANR048 Aniridia 1 66 0.729
85
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.723
87
INF158 Infections, Recurrent, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations 30 0.723
88
ACT119 Acute Promyelocytic Leukemia 62 0.723
89
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.723
90
DFF005 Diffuse Large B-Cell Lymphoma 55 0.723
91
CST005 Castleman Disease 56 0.723
92
P END033 Endocarditis 58 0.723
93
P OST002 Osteoporosis 77 0.723
94
c ATR087 Atrial Standstill 1 74 0.723
95
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.723
96
LYM012 Lymphoplasmacytic Lymphoma 50 0.723
97
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.723
98
NRL016 Neural Tube Defects 81 0.723
99
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.723
100
P WSK001 Wiskott-Aldrich Syndrome 72 0.723
101
HND015 Hand Skill, Relative 29 0.723
102
WLD007 Waldenstroem's Macroglobulinemia 65 0.723
103
P CND004 Candidiasis 57 0.723
104
CRY004 Cryoglobulinemia 47 0.723
105
CLR007 Colorado Tick Fever 31 0.723
106
P MLN008 Melanoma 75 0.723
107
TBR009 Tuberculous Empyema 23 0.723
108
c DLT002 Dilated Cardiomyopathy 79 0.723
109
LYM009 Lymphocytic Choriomeningitis 46 0.723
110
PNM001 Pneumocystosis 60 0.723
111
P GLM007 Glomerulonephritis 59 0.723
112
P OLG002 Oligodendroglioma 66 0.723
113
HYP066 Hyperglycemia 60 0.723
114
PTR032 Peters-Plus Syndrome 63 0.723
115
P SYS005 Systemic Scleroderma 73 0.723
116
CHR178 Chromosomal Triplication 34 0.723
117
P INF038 Influenza 68 0.723
118
VNZ002 Venezuelan Equine Encephalitis 46 0.723
119
c CHR417 Chronic Graft Versus Host Disease 55 0.723
120
HMP009 Haemophilus Influenzae 41 0.723
121
PLS002 Peliosis Hepatis 32 0.723
122
TCL024 T-Cell Non-Hodgkin Lymphoma 39 0.723
123
PRM329 Premature Aging 36 0.723
124
P OVR082 Overgrowth Syndrome 42 0.723
125
c LKM056 Leukemia, Chronic Lymphocytic 2 47 0.690
126
SRC014 Sarcoma 64 0.690
127
SPN035 Spindle Cell Sarcoma 51 0.690
128
LYM133 Lymphoma, Hodgkin, Classic 74 0.639
129
LYM143 Lymphoma, Non-Hodgkin, Familial 79 0.639
130
DFC004 Deficiency Anemia 74 0.639
131
HML018 Homologous Wasting Disease 21 0.639
132
LYM019 Lymphosarcoma 46 0.639
133
P BCL004 B-Cell Non-Hodgkin Lymphoma 42 0.639
134
NRR001 Neuroretinitis 42 0.600
135
P END044 Endometriosis 62 0.600
136
SVR001 Severe Acute Respiratory Syndrome 68 0.600
137
P SKN015 Skin Carcinoma 71 0.600
138
RTN023 Retinitis 45 0.600
139
ADL002 Adult Syndrome 69 0.516
140
DWN001 Down Syndrome 70 0.516
141
CHP002 Chops Syndrome 47 0.516
142
ANT039 Antisynthetase Syndrome 55 0.516
143
LTT002 Letterer-Siwe Disease 33 0.516
144
c PNT037 Pontocerebellar Hypoplasia, Type 3 42 0.516
145
SLT014 Salt and Pepper Developmental Regression Syndrome 43 0.516
146
HYP810 Hypereosinophilic Syndrome, Idiopathic 61 0.516
147
JVN004 Juvenile Myelomonocytic Leukemia 67 0.516
148
MST024 Mastocytosis, Cutaneous 66 0.516
149
c CHL119 Cholangitis, Primary Sclerosing 57 0.516
150
ALN001 Aland Island Eye Disease 55 0.516
151
P CHR285 Chronic Myelomonocytic Leukemia 59 0.516
152
c HPT003 Hepatitis a 63 0.516
153
IND002 Indolent Systemic Mastocytosis 41 0.516
154
MYL031 Myeloproliferative Neoplasm 66 0.516
155
P SCL009 Sclerosing Cholangitis 46 0.516
156
P MST009 Mastocytosis 64 0.516
157
SYS004 Systemic Mastocytosis 62 0.516
158
P TRN020 Turner Syndrome 67 0.516
159
ART002 Arts Syndrome 66 0.516
160
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.516
161
SFT003 Soft Tissue Sarcoma 57 0.516
162
P MXD050 Mixed Phenotype Acute Leukemia 45 0.516
163
ACT250 Acute Megakaryocytic Leukemia 63 0.516
164
BNM001 Bone Marrow Cancer 45 0.516
165
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.516
166
P MLG074 Malignant Mesenchymoma 40 0.516
167
AND005 Androgen Insensitivity Syndrome, Mild 21 0.516
168
ATM021 Autoimmune Inner Ear Disease 36 0.516
169
c CHR064 Chronic Monocytic Leukemia 36 0.516
170
GST050 Gastrointestinal System Disease 55 0.516
171
MYL003 Myeloid Sarcoma 48 0.516
172
P CHL066 Cholangitis 51 0.516
173
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.516
174
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.516
175
ACT118 Acute Non Lymphoblastic Leukemia 26 0.516
176
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.516
177
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.516
178
RFR007 Refractory Anemia with Excess Blasts in Transformation 26 0.516
179
SML040 Smoldering Systemic Mastocytosis 14 0.516
180
CLS052 Classic Hairy Cell Leukemia 25 0.516
181
RFR010 Refractory Anemia 49 0.516
182
PRT037 Pertussis 49 0.507
183
PLR001 Pleural Tuberculosis 49 0.477
184
RNL077 Renal Fibrosis 46 0.426
185
CHL014 Cholera 62 0.389
186
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.369
187
47X002 47,xyy 48 0.369
188
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.348
189
CHG001 Chagas Disease 65 0.326
190
P PYL005 Pyelonephritis 56 0.326
191
CYT002 Cytokine Deficiency 43 0.301
192
LNG099 Lung Disease 62 0.301
193
SVR096 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative 54 0.275
194
P GST053 Gastric Cancer 82 0.275
195
P BLD134 Bladder Cancer 79 0.246
196
P BRS047 Breast Cancer 97 0.246
197
c HPT016 Hepatitis B 62 0.246
198
PLM010 Pulmonary Edema 54 0.246
199
FTT001 Fatty Liver Disease 61 0.246
200
MYL069 Myeloma, Multiple 77 0.213
201
WRN001 Werner Syndrome 69 0.213
202
MYC006 Mycosis Fungoides 65 0.213
203
P TMR010 Tumor Predisposition Syndrome 69 0.213
204
P ADL017 Adult T-Cell Leukemia 54 0.213
205
P FML011 Familial Adenomatous Polyposis 71 0.213
206
P LNG064 Lung Cancer Susceptibility 3 70 0.213
207
CHL065 Cholangiocarcinoma 58 0.213
208
LYM040 Lymphoblastic Lymphoma 53 0.213
209
PNC001 Pancytopenia 52 0.213
210
INT079 Intrahepatic Cholangiocarcinoma 51 0.213
211
PPL022 Papilloma 53 0.213
212
HYP014 Hyperuricemia 51 0.213
213
SQM002 Squamous Cell Papilloma 45 0.213
214
P NTR004 Neutropenia 62 0.213
215
c CHR418 Chronic Leukemia 48 0.213
216
HRP004 Herpes Zoster 60 0.213
217
P TRM003 Tremor 50 0.213
218
SPL018 Splenomegaly 47 0.213
219
DSR074 Disorder of Purine Metabolism 23 0.213
220
c CCK007 Cockayne Syndrome B 56 0.174
221
c MTC063 Mitochondrial Dna Depletion Syndrome 3 51 0.174
222
SVR098 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Positive 47 0.174
223
MND025 Mandibulofacial Dysostosis with Alopecia 39 0.174
224
P SNS001 Sensorineural Hearing Loss 59 0.174
225
P CHL156 Childhood T-Cell Acute Lymphoblastic Leukemia 38 0.174
226
P OVR042 Ovarian Cancer 88 0.174
227
P RHM011 Rheumatoid Arthritis 81 0.174
228
END057 Endometrial Cancer 71 0.174
229
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.174
230
P CLR023 Colorectal Cancer 100 0.174
231
ADN084 Adenosine Deaminase, Elevated, Hemolytic Anemia Due to 11 0.174
232
PPL052 Papillomatosis, Confluent and Reticulated 34 0.174
233
c CND033 Candidiasis, Familial, 1 27 0.174
234
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.174
235
BLM001 Bloom Syndrome 65 0.174
236
STT001 Status Epilepticus 58 0.174
237
P ALC033 Alcohol Use Disorder 67 0.174
238
P MTC010 Mitochondrial Dna Depletion Syndrome 46 0.174
239
GT001 Gout 63 0.174
240
GLB002 Glioblastoma 67 0.174
241
P ANT006 Antiphospholipid Syndrome 55 0.174
242
ADN018 Adenoma 58 0.174
243
P INF032 Infertility 60 0.174
244
P ESN008 Eosinophilic Pneumonia 50 0.174
245
BRN024 Bronchitis 67 0.174
246
P CNJ013 Conjunctivitis 66 0.174
247
OLG001 Oligospermia 45 0.174
248
PLS007 Plasmodium Falciparum Malaria 52 0.174
249
CHL123 Chlamydia 58 0.174
250
ALL029 Allergic Disease 61 0.174
251
LYM017 Lyme Disease 63 0.174
252
TST014 Testicular Cancer 51 0.174
253
c ACT071 Acute Kidney Failure 60 0.174
254
CLN015 Colon Adenocarcinoma 64 0.174
255
c SPR086 Spermatogenic Failure 3 47 0.174
256
HYP266 Hypoxia 56 0.174
257
INT078 Intracranial Thrombosis 50 0.174
258
ANT024 Anthrax Disease 58 0.174
259
PLM033 Pulmonary Embolism 58 0.174
260
PLM035 Pulmonary Eosinophilia 49 0.174
261
ORL011 Oral Cancer 60 0.174
262
c ACT135 Acute Graft Versus Host Disease 51 0.174
263
PST092 Posttransplant Acute Limbic Encephalitis 29 0.174
264
INH023 Inherited Cancer-Predisposing Syndrome 53 0.174
265
LRG008 Large Granular Lymphocyte Leukemia 34 0.174
266
CYS001 Cystic Fibrosis 77 0.123
267
c HMC039 Hemochromatosis, Type 1 73 0.123
268
HLC007 Helicobacter Pylori Infection 67 0.123
269
P SPP010 Suppressor of Tumorigenicity 3 51 0.123
270
VSC063 Vasculopathy, Retinal, with Cerebral Leukoencephalopathy and Systemic Manifestations 57 0.123
271
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.123
272
LSC001 Lesch-Nyhan Syndrome 62 0.123
273
CRV035 Cervical Cancer 72 0.123
274
c MTC055 Mitochondrial Dna Depletion Syndrome 4b 53 0.123
275
c MYC083 Myoclonic Epilepsy, Familial Infantile 41 0.123
276
c MTC062 Mitochondrial Dna Depletion Syndrome 2 43 0.123
277
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.123
278
PRT112 Portal Hypertension, Noncirrhotic 29 0.123
279
c PRG128 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 4 28 0.123
280
P ACR001 Aicardi-Goutieres Syndrome 63 0.123
281
ATS010 Autosomal Recessive Disease 42 0.123
282
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.123
283
P INF037 Inflammatory Bowel Disease 53 0.123
284
MRG003 Marginal Zone B-Cell Lymphoma 52 0.123
285
BCT022 Bacterial Infectious Disease 56 0.123
286
CRB004 Cerebral Artery Occlusion 46 0.123
287
ADN011 Adenoid Cystic Carcinoma 68 0.123
288
MCS002 Mucositis 55 0.123
289
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.123
290
NDL024 Nodal Marginal Zone Lymphoma 37 0.123
291
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.123
292
NNL006 Non-Alcoholic Steatohepatitis 54 0.123
293
PLY150 Polykaryocytosis Inducer 29 0.123
294
BCL014 B-Cell Growth Factor 32 0.123
295
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.123
296
P LNG032 Lung Cancer 98 0.123
297
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 0.123
298
c ACR116 Aicardi-Goutieres Syndrome 1 46 0.123
299
c ATS007 Autism Spectrum Disorder 72 0.123
300
ORL015 Oral Squamous Cell Carcinoma 43 0.123
301
VTM002 Vitamin B12 Deficiency 48 0.123
302
P LYM033 Lymphoproliferative Syndrome 59 0.123
303
CLR108 Colorectal Adenoma 63 0.123
304
CLR109 Colorectal Adenocarcinoma 50 0.123
305
P FLL037 Follicular Lymphoma 73 0.123
306
c CHL140 Chilblain Lupus 1 59 0.123
307
MTG002 Mutagen Sensitivity 35 0.123
308
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 40 0.123
309
MLR004 Malaria 78 0.123
310
P KLZ004 Kala-Azar 1 41 0.123
311
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.123
312
ATM095 Autoimmune Disease 61 0.123
313
PHS025 Phosphatase, Acid, of Tissues 28 0.123
314
PHS027 Phosphoglycoprotein 1 14 0.123
315
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.123
316
c SML038 Small Cell Cancer of the Lung 69 0.123
317
LKD025 Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 48 0.123
318
CLF027 Cleft Palate, Isolated 64 0.123
319
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.123
320
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 0.123
321
P HMN032 Human Herpesvirus 8 47 0.123
322
c MJR024 Major Affective Disorder 9 40 0.123
323
P MMB011 Membranous Nephropathy 50 0.123
324
c MJR022 Major Affective Disorder 8 37 0.123
325
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.123
326
P CRN026 Corneal Edema 42 0.123
327
HRW001 Hair Whorl 35 0.123
328
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 16 0.123
329
P HPT023 Hepatocellular Carcinoma 95 0.123
330
c THR092 Thrombophilia Due to Thrombin Defect 74 0.123
331
URT049 Urate Oxidase, Pseudogene 24 0.123
332
WLL001 Williams-Beuren Syndrome 60 0.123
333
P ATS364 Autism 72 0.123
334
c VRL010 Viral Hepatitis 52 0.123
335
NRT004 Neuritis 53 0.123
336
P BND020 Bone Disease 60 0.123
337
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.123
338
ACT098 Acute Erythroid Leukemia 55 0.123
339
CHR100 Chronic Ulcer of Skin 57 0.123
340
OPS001 Opisthorchiasis 41 0.123
341
PNP001 Panophthalmitis 28 0.123
342
c ACT068 Acute Cystitis 61 0.123
343
ISC004 Ischemia 61 0.123
344
IGG001 Iga Glomerulonephritis 50 0.123
345
LVR012 Liver Cirrhosis 62 0.123
346
c CNG027 Congenital Hemolytic Anemia 49 0.123
347
P BNG030 Benign Ependymoma 51 0.123
348
AMN003 Amnestic Disorder 54 0.123
349
TRC003 Trichomoniasis 53 0.123
350
IRN002 Iron Metabolism Disease 56 0.123
351
QDR001 Quadriplegia 49 0.123
352
P CRD246 Cardiovascular System Disease 55 0.123
353
PLR005 Pleuropneumonia 33 0.123
354
P OPT009 Optic Neuritis 57 0.123
355
P MLN007 Male Infertility 56 0.123
356
GST023 Gastric Ulcer 52 0.123
357
WST002 Western Equine Encephalitis 40 0.123
358
DPH001 Diphtheria 59 0.123
359
PNC129 Pancreatic Adenocarcinoma 65 0.123
360
P LVR013 Liver Disease 68 0.123
361
P PLM036 Pulmonary Fibrosis 65 0.123
362
MSN004 Mesenchymal Cell Neoplasm 42 0.123
363
ADR005 Adrenal Carcinoma 61 0.123
364
P BPL003 Bipolar Disorder 56 0.123
365
BCL002 B Cell Deficiency 40 0.123
366
P BNG032 Benign Mesothelioma 53 0.123
367
DMY004 Demyelinating Disease 50 0.123
368
ANP005 Anaplastic Astrocytoma 59 0.123
369
ORT008 Orotic Aciduria 56 0.123
370
P PNC035 Pancreatic Cancer 86 0.123
371
AML001 Amelanotic Melanoma 37 0.123
372
ERD001 Erdheim-Chester Disease 53 0.123
373
GST045 Gastroenteritis 58 0.123
374
PLR022 Pleural Disease 45 0.123
375
GLM045 Glioma 62 0.123
376
PST046 Post-Transplant Lymphoproliferative Disease 53 0.123
377
ANX004 Anoxia 40 0.123
378
P VSC011 Vasculitis 61 0.123
379
P INS002 in Situ Carcinoma 53 0.123
380
GLL048 Glial Tumor 52 0.123
381
CLL010 Cellular Ependymoma 58 0.123
382
PDT014 Pediatric Ependymoma 28 0.123
383
P MYP004 Myopathy 67 0.123
384
P EYD002 Eye Disease 57 0.123
385
P CRB059 Cerebellar Degeneration 36 0.123
386
DSM007 Desmoplastic Small Round Cell Tumor 54 0.123
387
LSH001 Leishmaniasis 63 0.123
388
OST012 Osteoarthritis 77 0.123
389
P ART022 Arthritis 70 0.123
390
SKN019 Skin Melanoma 70 0.123
391
P AMY004 Amyloidosis 69 0.123
392
ACT055 Actinomycosis 55 0.123
393
c SPR009 Sporadic Breast Cancer 42 0.123
394
CRT015 Carotid Artery Occlusion 45 0.123
395
MSL001 Measles 61 0.123
396
PRN035 Perniosis 27 0.123
397
HRP011 Herpes Zoster Ophthalmicus 24 0.123
398
P ACT105 Acute Mountain Sickness 52 0.123
400
P VTR007 Vitreoretinopathy 45 0.123
401
MTH086 Methotrexate Toxicity 32 0.123
402
P RRT020 Rare Tumor 39 0.123
403
PLY100 Polyploidy 36 0.123
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