Search results for Niacin

749 hits were found for Niacin

# Family MCID Name MIFTS Score
1
P PLL002 Pellagra 47 4.460
2
LPD008 Lipid Metabolism Disorder 64 0.399
3
c HYP836 Hypercholesterolemia, Familial, 1 74 0.276
4
ATH013 Atherosclerosis Susceptibility 68 0.230
5
HYP081 Hypolipoproteinemia 51 0.230
6
P CRN018 Coronary Artery Anomaly 67 0.211
7
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.207
8
P CRN300 Coronary Heart Disease 1 59 0.207
9
c HYP272 Hypercholesterolemia, Familial, 3 44 0.193
10
ART140 Arteries, Anomalies of 60 0.186
11
ISC004 Ischemia 62 0.179
12
c FML035 Familial Hyperlipidemia 56 0.175
13
P HRT032 Heart Disease 78 0.161
14
P HYP750 Hypertriglyceridemia, Familial 62 0.157
15
CRB039 Cerebrovascular Disease 71 0.148
16
STR067 Stroke, Ischemic 82 0.137
17
P SCH015 Schizophrenia 76 0.132
18
P VSC007 Vascular Disease 65 0.132
19
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.129
20
PRP027 Peripheral Vascular Disease 72 0.129
21
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.127
22
P MYC007 Myocardial Infarction 74 0.127
23
P MYP004 Myopathy 63 0.127
24
c HYP740 Hyperlipoproteinemia, Type V 53 0.127
25
c HRM017 Hermansky-Pudlak Syndrome 2 54 0.124
26
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.113
27
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.113
28
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.113
29
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.113
30
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.113
31
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.113
32
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.113
33
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.113
34
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.113
35
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.113
36
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.113
37
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.110
38
48X005 48,xyyy 37 0.110
39
P KDN018 Kidney Disease 73 0.107
40
HYP066 Hyperglycemia 63 0.107
41
P DBT009 Diabetes Mellitus 66 0.103
42
P HYP838 Hyperlipidemia, Familial Combined, 3 54 0.103
43
c HYP839 Hyperlipidemia, Familial Combined, 1 28 0.103
44
OBS529 Obsolete: Combined Hyperlipidemia 22 0.103
45
c CHR684 Chronic Kidney Disease 68 0.097
46
PRP080 Peripheral Artery Disease 51 0.093
47
c HNT004 Huntington Disease-Like 2 48 0.093
48
HYP025 Hyperphosphatemia 47 0.093
49
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.093
50
P PLM036 Pulmonary Fibrosis 66 0.090
51
FTT001 Fatty Liver Disease 63 0.090
52
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.090
53
c HYP595 Hypertension, Essential 87 0.086
54
IDP011 Idiopathic Interstitial Pneumonia 65 0.086
55
P DRR001 Diarrhea 55 0.086
56
c RHB024 Rhabdomyosarcoma 2 64 0.082
57
P EXN002 Exanthem 58 0.082
58
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.082
59
CRT016 Carotid Artery Disease 53 0.082
60
MCL006 Macular Retinal Edema 52 0.082
61
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.082
62
DFC004 Deficiency Anemia 77 0.078
63
P LKM002 Leukemia 69 0.078
64
P ENC018 Encephalopathy 64 0.078
65
INT002 Intermittent Claudication 60 0.078
66
END030 End Stage Renal Failure 60 0.078
67
HMN044 Human Immunodeficiency Virus Type 1 73 0.073
68
PLM001 Pulmonary Tuberculosis 72 0.073
69
c FML021 Familial Hypercholesterolemia 67 0.073
70
P SKN015 Skin Carcinoma 67 0.073
71
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.073
72
P ART021 Arteriosclerosis 56 0.073
73
P HYP733 Hypercalciuria, Absorptive, 2 45 0.073
74
PSY004 Psychotic Disorder 68 0.068
75
P THR014 Thrombocytopenia 67 0.068
76
ADL002 Adult Syndrome 62 0.068
77
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.068
78
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.068
79
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.068
80
c HNT011 Huntington Disease-Like 3 37 0.068
81
P LVR013 Liver Disease 71 0.063
82
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.063
83
P HDC001 Headache 59 0.063
84
P RTN022 Retinal Vein Occlusion 50 0.063
85
CRN030 Coronary Stenosis 49 0.063
86
CHL079 Children's Interstitial Lung Disease 27 0.063
87
P ALZ034 Alzheimer Disease 90 0.058
88
SCK003 Sickle Cell Anemia 74 0.058
89
P HPT021 Hepatitis 69 0.058
90
ALC007 Alcohol Dependence 68 0.058
91
PRT037 Pertussis 66 0.058
92
DSS008 Disease of Mental Health 66 0.058
93
ANG054 Angina Pectoris 66 0.058
94
P TRN020 Turner Syndrome 66 0.058
95
P NTR004 Neutropenia 64 0.058
96
TRN015 Transient Cerebral Ischemia 62 0.058
97
ACQ007 Acquired Immunodeficiency Syndrome 61 0.058
98
P BPL003 Bipolar Disorder 59 0.058
99
P THR117 Three M Syndrome 1 58 0.058
100
ISL014 Isolated Growth Hormone Deficiency, Type Ia 58 0.058
101
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.058
102
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.058
103
P MYS005 Myositis 54 0.058
104
c HYP841 Hypoalphalipoproteinemia, Primary, 1 53 0.058
105
DYS014 Dyspepsia 51 0.058
106
ISL003 Isolated Growth Hormone Deficiency 50 0.058
107
P HYP121 Hypoalphalipoproteinemia 49 0.058
108
LPD009 Lipid Storage Disease 49 0.058
109
GRW007 Growth Hormone Deficiency 48 0.058
110
ATX019 Ataxia with Vitamin E Deficiency 46 0.058
111
DWR001 Dwarfism 45 0.058
112
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.058
113
c MJR024 Major Affective Disorder 9 42 0.058
114
c MJR022 Major Affective Disorder 8 39 0.058
115
FML235 Familial Combined Hyperlipoproteinemia 29 0.058
116
P CLR023 Colorectal Cancer 100 0.052
117
P PRK057 Parkinson Disease, Late-Onset 77 0.052
118
c MGR028 Migraine with or Without Aura 1 70 0.052
119
P MYC084 Mycobacterium Tuberculosis 1 69 0.052
120
DPR016 Depression 64 0.052
121
GT001 Gout 63 0.052
122
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 62 0.052
123
MNT002 Mental Depression 60 0.052
124
c ACT210 Acute Respiratory Distress Syndrome 59 0.052
125
THR024 Thrombosis 58 0.052
126
HPT022 Hepatoblastoma 58 0.052
127
INT007 Intermediate Coronary Syndrome 58 0.052
128
BCT022 Bacterial Infectious Disease 57 0.052
129
c ACT134 Acute Liver Failure 53 0.052
130
P SCK005 Sickle Cell Disease 53 0.052
131
GLS018 Glass Syndrome 51 0.052
132
MTB004 Metabolic Acidosis 48 0.052
133
c CNT016 Central Retinal Vein Occlusion 48 0.052
134
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.052
135
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.052
136
HYD030 Hydroxykynureninuria 26 0.052
138
ANX010 Anxiety 75 0.045
139
DWN001 Down Syndrome 70 0.045
140
P PLM037 Pulmonary Hypertension 69 0.045
141
CNG034 Congestive Heart Failure 69 0.045
142
HYP056 Hypoglycemia 68 0.045
143
P MCR115 Microvascular Complications of Diabetes 5 67 0.045
144
LVR012 Liver Cirrhosis 67 0.045
145
ALL026 Allergic Hypersensitivity Disease 65 0.045
146
P HYP069 Hyperparathyroidism 64 0.045
147
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.045
148
PPT005 Peptic Ulcer Disease 60 0.045
149
c HPT003 Hepatitis a 60 0.045
150
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.045
151
P PLY011 Polycystic Ovary Syndrome 58 0.045
152
P HYP726 Hypercalcemia, Infantile, 1 58 0.045
153
IRN002 Iron Metabolism Disease 58 0.045
154
GST050 Gastrointestinal System Disease 57 0.045
155
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.045
156
GRN034 Grange Syndrome 55 0.045
157
END040 Endogenous Depression 55 0.045
158
NRT001 Neurotic Disorder 53 0.045
159
NNL006 Non-Alcoholic Steatohepatitis 53 0.045
160
HYP014 Hyperuricemia 52 0.045
161
c SCN007 Secondary Hyperparathyroidism 52 0.045
162
P LCT001 Lactic Acidosis 52 0.045
163
BRN071 Brain Injury 51 0.045
164
P OPN001 Open-Angle Glaucoma 50 0.045
165
SCH003 Schizophreniform Disorder 49 0.045
166
ATS010 Autosomal Recessive Disease 49 0.045
167
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.045
168
HRT031 Hartnup Disorder 47 0.045
169
P MYC033 Myoclonus 47 0.045
170
MCL027 Macular Dystrophy, Dominant Cystoid 47 0.045
171
CYT002 Cytokine Deficiency 46 0.045
172
RBF001 Riboflavin Deficiency 46 0.045
173
P MJR007 Major Affective Disorder 1 44 0.045
174
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 44 0.045
175
OPD001 Opioid Abuse 42 0.045
176
c HMG029 Hemoglobin Se Disease 40 0.045
177
SPR126 Superior Semicircular Canal Dehiscence 39 0.045
178
MYC017 Mycobacterium Kansasii 39 0.045
179
DBT081 Diabetic Encephalopathy 30 0.045
180
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.045
181
P HPT023 Hepatocellular Carcinoma 99 0.037
182
P BRS047 Breast Cancer 99 0.037
183
NRL016 Neural Tube Defects 83 0.037
184
MLR004 Malaria 82 0.037
185
IMM167 Immune Deficiency Disease 79 0.037
186
P NRF023 Neurofibromatosis, Type Ii 77 0.037
187
c ART115 Aortic Valve Disease 1 76 0.037
188
ULC004 Ulcerative Colitis 75 0.037
189
BRN028 Brain Cancer 75 0.037
190
c LKM063 Leukemia, Chronic Myeloid 74 0.037
191
LPT014 Leptin Deficiency or Dysfunction 72 0.037
192
P CRD119 Cardiac Arrest 71 0.037
193
LYM133 Lymphoma, Hodgkin, Classic 70 0.037
194
P LYM118 Lymphoma 70 0.037
195
P MJR001 Major Depressive Disorder 69 0.037
196
OBS002 Obsessive-Compulsive Disorder 69 0.037
197
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.037
198
P DMN002 Dementia 68 0.037
199
P NRV007 Nervous System Disease 68 0.037
200
c BSL007 Basal Cell Carcinoma 68 0.037
201
P DRM053 Dermatitis, Atopic 68 0.037
202
c MCR129 Microvascular Complications of Diabetes 1 67 0.037
203
c SML038 Small Cell Cancer of the Lung 67 0.037
204
c ART101 Aortic Valve Disease 2 67 0.037
205
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.037
206
P PRS038 Personality Disorder 66 0.037
207
INC002 Inclusion Body Myositis 66 0.037
208
TNG002 Tangier Disease 64 0.037
209
KRN002 Kearns-Sayre Syndrome 64 0.037
210
SKN016 Skin Disease 64 0.037
211
c FNC043 Fanconi Anemia, Complementation Group E 64 0.037
212
DRM006 Dermatitis 63 0.037
213
KHL003 Kohlschutter-Tonz Syndrome 63 0.037
214
P PSR002 Psoriasis 63 0.037
215
CLT003 Colitis 63 0.037
216
TXC005 Toxic Shock Syndrome 63 0.037
217
SPN186 Spinal Cord Injury 63 0.037
218
MDD011 Mood Disorder 62 0.037
219
P LPS004 Lupus Erythematosus 62 0.037
220
BRC012 Brucellosis 62 0.037
221
ACN002 Acanthosis Nigricans 62 0.037
222
NTR005 Nutritional Deficiency Disease 61 0.037
223
c ACT027 Acute Pancreatitis 60 0.037
224
c ACT071 Acute Kidney Failure 60 0.037
225
INS001 Insulinoma 60 0.037
226
ADN018 Adenoma 60 0.037
227
PST028 Post-Traumatic Stress Disorder 60 0.037
228
NRN004 Neuroendocrine Tumor 59 0.037
229
CNS004 Constipation 59 0.037
230
P ALC033 Alcohol Use Disorder 58 0.037
231
AGN016 Aging 58 0.037
232
P INF037 Inflammatory Bowel Disease 57 0.037
233
P MTC069 Mitochondrial Disorders 57 0.037
234
PRT038 Protein-Energy Malnutrition 56 0.037
235
HRT012 Heart Valve Disease 56 0.037
236
P SBS003 Substance Abuse 56 0.037
237
c MCR113 Microvascular Complications of Diabetes 3 55 0.037
238
HYP005 Hypokalemia 55 0.037
239
P HYP076 Hyperthyroidism 55 0.037
240
CRC006 Carcinoid Syndrome 55 0.037
241
RSC001 Rosacea 55 0.037
242
HMC014 Homocysteinemia 54 0.037
243
MSC190 Muscular Disease 54 0.037
244
EXP004 Exophthalmos 53 0.037
245
IMP005 Impotence 53 0.037
246
P MTC133 Mitochondrial Myopathy 53 0.037
247
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.037
248
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 52 0.037
249
KRT009 Keratosis 52 0.037
250
PRN011 Pernicious Anemia 51 0.037
251
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.037
252
PST011 Pustulosis of Palm and Sole 51 0.037
253
OPT003 Opiate Dependence 50 0.037
254
LMB062 Limb Ischemia 50 0.037
255
SCH012 Schizoaffective Disorder 50 0.037
256
CRT013 Carotid Stenosis 50 0.037
257
P IDP024 Idiopathic Inflammatory Myopathy 49 0.037
258
NTR046 Neutrophil Migration 49 0.037
259
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.037
260
c MCR120 Microvascular Complications of Diabetes 7 48 0.037
261
HYP781 Hypoascorbemia 48 0.037
262
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.037
263
KRT002 Keratomalacia 47 0.037
264
CRB008 Cerebral Atherosclerosis 47 0.037
265
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.037
266
CTS005 Catastrophic Antiphospholipid Syndrome 44 0.037
267
ACT084 Acute Stress Disorder 42 0.037
268
c MCR130 Microvascular Complications of Diabetes 6 42 0.037
269
c MCR133 Microvascular Complications of Diabetes 4 42 0.037
270
OBS003 Obsessive-Compulsive Personality Disorder 42 0.037
271
c MCR112 Microvascular Complications of Diabetes 2 42 0.037
272
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.037
273
DRG002 Drug-Induced Hepatitis 41 0.037
274
c PLY105 Polycystic Ovary Syndrome 1 38 0.037
275
c MJR008 Major Affective Disorder 2 35 0.037
276
c MJR003 Major Affective Disorder 6 34 0.037
277
c MJR006 Major Affective Disorder 5 34 0.037
278
PPL052 Papillomatosis, Confluent and Reticulated 34 0.037
279
c MJR023 Major Affective Disorder 7 34 0.037
280
CND006 Candida Glabrata 33 0.037
281
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 32 0.037
282
PYR009 Pyridoxine Deficiency Anemia 32 0.037
283
c MJR004 Major Affective Disorder 4 29 0.037
284
c HYP843 Hypoalphalipoproteinemia, Primary, 2 29 0.037
285
P OVR096 Overlap Myositis 28 0.037
286
CRD220 Cardiac Valvular Defect, Developmental 27 0.037
287
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.037
288
INT074 Intracranial Arteriosclerosis 17 0.037
289
P PRS040 Prostate Cancer 97 0.026
290
ESP021 Esophageal Cancer 90 0.026
291
P OVR042 Ovarian Cancer 89 0.026
292
c SYS001 Systemic Lupus Erythematosus 88 0.026
293
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.026
294
P PNC035 Pancreatic Cancer 86 0.026
295
c LKM061 Leukemia, Acute Myeloid 84 0.026
296
P ATX030 Ataxia-Telangiectasia 83 0.026
297
P RHM011 Rheumatoid Arthritis 82 0.026
298
c DLT002 Dilated Cardiomyopathy 81 0.026
299
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.026
300
AST005 Asthma 80 0.026
301
OST012 Osteoarthritis 80 0.026
302
INS024 Insulin-Like Growth Factor I 79 0.026
303
P BLD134 Bladder Cancer 79 0.026
304
CNN003 Conn's Syndrome 78 0.026
305
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.026
306
GST019 Gastrointestinal Stromal Tumor 76 0.026
307
c ATR087 Atrial Standstill 1 76 0.026
308
P RSP003 Respiratory Failure 75 0.026
309
GLB002 Glioblastoma 74 0.026
310
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.026
311
END057 Endometrial Cancer 74 0.026
312
SVR004 Severe Combined Immunodeficiency 74 0.026
313
ACR006 Aceruloplasminemia 74 0.026
314
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.026
315
c SPN225 Spondyloarthropathy 1 74 0.026
316
P EPL164 Epilepsy 73 0.026
317
P MLT020 Multiple Sclerosis 73 0.026
318
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.026
319
P CNR004 Cone-Rod Dystrophy 2 72 0.026
320
P HNT016 Huntington Disease 72 0.026
321
P SRC025 Sarcoidosis 1 72 0.026
322
MYL009 Myelodysplastic Syndrome 72 0.026
323
P LFR001 Li-Fraumeni Syndrome 71 0.026
324
P ART022 Arthritis 71 0.026
325
P PNM007 Pneumonia 71 0.026
326
P BRG001 Brugada Syndrome 70 0.026
327
c PRM196 Premature Ovarian Failure 1 70 0.026
328
BSL036 Basal Cell Nevus Syndrome 70 0.026
329
PLY001 Polycythemia Vera 70 0.026
330
BRN024 Bronchitis 70 0.026
331
P HYP086 Hypothyroidism 70 0.026
332
RCK004 Rickets 70 0.026
333
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.026
334
P MLN066 Melanoma, Cutaneous Malignant 1 69 0.026
335
MNT001 Mantle Cell Lymphoma 69 0.026
336
CRB037 Cerebral Palsy 69 0.026
337
P ESS003 Essential Thrombocythemia 69 0.026
338
P CHR012 Chronic Granulomatous Disease 69 0.026
339
KRT019 Keratitis, Hereditary 69 0.026
340
MYL005 Myelofibrosis 69 0.026
341
ALL003 Allergic Rhinitis 69 0.026
342
PNC129 Pancreatic Adenocarcinoma 69 0.026
343
P SYS005 Systemic Scleroderma 68 0.026
344
BRK010 Burkitt Lymphoma 68 0.026
345
P LKM062 Leukemia, Acute Lymphoblastic 68 0.026
346
P GLM040 Glioma Susceptibility 1 68 0.026
347
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.026
348
SKN019 Skin Melanoma 68 0.026
349
MLN008 Melanoma 68 0.026
350
c JVN010 Juvenile Rheumatoid Arthritis 67 0.026
351
P LPR021 Leprosy 3 67 0.026
352
SRC014 Sarcoma 67 0.026
353
P OLG002 Oligodendroglioma 67 0.026
354
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.026
355
P FLL037 Follicular Lymphoma 67 0.026
356
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.026
357
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.026
358
MYC006 Mycosis Fungoides 67 0.026
359
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.026
360
PRT036 Peritonitis 66 0.026
361
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.026
362
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.026
363
MYL031 Myeloproliferative Neoplasm 66 0.026
364
P PRD008 Periodontitis 66 0.026
365
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.026
366
P MTR014 Motor Neuron Disease 66 0.026
367
P CCK001 Cockayne Syndrome 66 0.026
368
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 65 0.026
369
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 65 0.026
370
P ADN016 Adenocarcinoma 65 0.026
371
MSC007 Muscle Hypertrophy 65 0.026
372
P FRD012 Friedreich Ataxia 1 65 0.026
373
FCT007 Factor Vii Deficiency 65 0.026
374
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.026
375
P PRP019 Peripheral Nervous System Disease 64 0.026
376
P HML002 Hemolytic Anemia 64 0.026
377
HMT002 Hematologic Cancer 64 0.026
378
P GLM045 Glioma 64 0.026
379
P ANR048 Aniridia 1 64 0.026
380
P TST021 Testicular Germ Cell Tumor 63 0.026
381
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.026
382
c ACT068 Acute Cystitis 63 0.026
383
c HPT016 Hepatitis B 63 0.026
384
c PRC016 Pre-Eclampsia 63 0.026
385
PSR001 Psoriatic Arthritis 63 0.026
386
BLL006 Bullous Pemphigoid 63 0.026
387
c ALP101 Alpha-Thalassemia 63 0.026
388
P MVM001 Movement Disease 63 0.026
389
c GLC092 Glaucoma, Primary Open Angle 63 0.026
390
PPL049 Papillon-Lefevre Syndrome 63 0.026
391
BLD131 Bladder Urothelial Carcinoma 62 0.026
392
LNG099 Lung Disease 62 0.026
393
LYM012 Lymphoplasmacytic Lymphoma 62 0.026
394
P THL005 Thalassemia 62 0.026
395
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 62 0.026
396
P LYM033 Lymphoproliferative Syndrome 62 0.026
397
c HPT001 Hepatitis C 62 0.026
398
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 62 0.026
399
P DRM010 Dermatomyositis 62 0.026
400
ATM095 Autoimmune Disease 62 0.026
401
P ANP001 Anaplastic Large Cell Lymphoma 62 0.026
402
P CTR002 Cataract 62 0.026
403
TYP007 Typhoid Fever 61 0.026
404
CHL068 Cholestasis 61 0.026
405
c PNS012 Paine Syndrome 61 0.026
406
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.026
407
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.026
408
P BCL017 B-Cell Lymphoma 61 0.026
409
P MYL006 Myeloid Leukemia 61 0.026
410
P EPN002 Ependymoma 61 0.026
411
P PLY014 Polycystic Kidney Disease 61 0.026
412
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.026
413
GLB015 Glioblastoma Multiforme 60 0.026
414
SQM006 Squamous Cell Carcinoma 60 0.026
415
GNG013 Gingivitis 60 0.026
416
P MYC008 Myocarditis 60 0.026
417
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.026
418
c MCL013 Mucolipidosis Iv 60 0.026
419
HPT019 Hepatic Encephalopathy 60 0.026
420
P INF032 Infertility 60 0.026
421
c DWL002 Dowling-Degos Disease 1 59 0.026
422
P RHN004 Rhinitis 59 0.026
423
c ACT073 Acute Leukemia 59 0.026
424
EYD002 Eye Disease 59 0.026
425
GRD007 Grade Iii Astrocytoma 59 0.026
426
P SZR006 Seizure Disorder 59 0.026
427
SZR001 Sezary's Disease 59 0.026
428
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.026
429
P THR005 Thrombotic Thrombocytopenic Purpura 59 0.026
430
c ACT075 Acute Myocardial Infarction 59 0.026
431
IRN001 Iron Deficiency Anemia 59 0.026
432
P LRY044 Larynx Cancer 59 0.026
433
VSL002 Visual Epilepsy 58 0.026
434
P PRP029 Porphyria 58 0.026
435
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 58 0.026
436
P ALP008 Alopecia 58 0.026
437
MLN065 Melanocytic Nevus Syndrome, Congenital 58 0.026
438
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 58 0.026
439
LYM027 Lymphopenia 58 0.026
440
DSS009 Disseminated Intravascular Coagulation 58 0.026
441
BLR008 Bilirubin Metabolic Disorder 58 0.026
442
ERY029 Erythermalgia, Primary 58 0.026
443
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 57 0.026
444
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.026
445
BRN045 Brunner Syndrome 57 0.026
446
P NRP001 Neuropathy 57 0.026
447
SCH014 Schistosomiasis 57 0.026
448
LMY014 Leiomyoma, Uterine 57 0.026
449
TRN018 Transitional Cell Carcinoma 57 0.026
450
HMG005 Hemoglobinopathy 57 0.026
451
P MLN007 Male Infertility 57 0.026
452
SFT003 Soft Tissue Sarcoma 57 0.026
453
P PLC011 Pilocytic Astrocytoma 57 0.026
454
SPN035 Spindle Cell Sarcoma 57 0.026
455
PRP030 Purpura 56 0.026
456
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.026
457
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 56 0.026
458
P LYM031 Lymphocytic Leukemia 56 0.026
459
CMR002 Coumarin Resistance 56 0.026
460
c VRL010 Viral Hepatitis 56 0.026
461
P PLY018 Polycythemia 56 0.026
462
LBL001 Lobular Neoplasia 56 0.026
463
DBT010 Diabetic Neuropathy 56 0.026
464
GLS001 Gliosarcoma 56 0.026
465
MNR012 Meniere Disease 56 0.026
466
P LTR001 Lateral Sclerosis 56 0.026
467
SNS003 Sensory Peripheral Neuropathy 56 0.026
468
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.026
469
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.026
470
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 0.026
471
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.026
472
SLC006 Silicosis 55 0.026
473
ACD008 Acid-Labile Subunit Deficiency 55 0.026
474
HYP060 Hyperinsulinism 55 0.026
475
P ICH004 Ichthyosis 55 0.026
476
c PSR017 Psoriasis 2 55 0.026
477
GLC003 Glucose Intolerance 55 0.026
478
P PLY019 Polyneuropathy 55 0.026
479
P NRV006 Nervous System Cancer 55 0.026
480
PST046 Post-Transplant Lymphoproliferative Disease 55 0.026
481
P INS002 in Situ Carcinoma 55 0.026
482
GNR004 Generalized Anxiety Disorder 55 0.026
483
P CYS039 Cystic Kidney Disease 55 0.026
484
DRR016 Diarrhea 2, with Microvillus Atrophy 54 0.026
485
INT075 Intracranial Hypertension 54 0.026
486
P RCT021 Rectum Cancer 54 0.026
487
ZLL002 Zollinger-Ellison Syndrome 54 0.026
488
GTR002 Goiter 54 0.026
489
P RST001 Restless Legs Syndrome 54 0.026
490
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.026
491
LYM040 Lymphoblastic Lymphoma 54 0.026
492
TXC002 Toxic Encephalopathy 54 0.026
493
AMN001 Amenorrhea 54 0.026
494
c PRM092 Primary Lateral Sclerosis, Adult, 1 54 0.026
495
NTR018 Neutrophilia, Hereditary 53 0.026
496
PRP036 Peripheral T-Cell Lymphoma 53 0.026
497
TLN003 Telangiectasis 53 0.026
498
c LRG017 Large Intestine Cancer 53 0.026
499
P ECL001 Eclampsia 53 0.026
500
P PTT006 Pituitary Adenoma 53 0.026
501
THY030 Thyroid Gland Disease 53 0.026
502
ALC009 Alcoholic Liver Cirrhosis 53 0.026
503
c GLL024 Gallbladder Disease 1 53 0.026
504
c HPT007 Hepatitis E 53 0.026
505
SPS003 Spastic Diplegia 53 0.026
506
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 52 0.026
507
FDL002 Food Allergy 52 0.026
508
LMY002 Leiomyoma 52 0.026
509
c CHL140 Chilblain Lupus 1 52 0.026
510
LNG031 Lung Benign Neoplasm 52 0.026
511
INT303 Intracranial Hypertension, Idiopathic 52 0.026
512
P NLD001 Nail Disease 52 0.026
513
GNT002 Giant Cell Glioblastoma 52 0.026
514
THR004 Thrombocytosis 52 0.026
515
PRG017 Paraganglioma and Gastric Stromal Sarcoma 52 0.026
516
P CTN015 Cutaneous T Cell Lymphoma 52 0.026
517
P TRT010 Teratoma 52 0.026
518
c PRM012 Primary Polycythemia 52 0.026
519
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.026
520
P AST007 Astrocytoma 52 0.026
521
P PNB001 Pineoblastoma 52 0.026
522
c CNT033 Central Nervous System Cancer 51 0.026
523
PLC008 Placenta Disease 51 0.026
524
STM007 Stomatitis 51 0.026
525
c MLG054 Malignant Histiocytosis 51 0.026
526
FBR008 Fibrillary Astrocytoma 51 0.026
527
P BRN035 Brain Stem Glioma 51 0.026
528
c INH020 Inherited Metabolic Disorder 51 0.026
529
QDR001 Quadriplegia 51 0.026
530
FML063 Familial Glucocorticoid Deficiency 51 0.026
532
ENT011 Enterocolitis 51 0.026
533
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 51 0.026
534
IMM064 Immunodeficiency, Common Variable, 10 51 0.026
535
VTR016 Vater/vacterl Association 51 0.026
536
CHL004 Cholelithiasis 50 0.026
537
P ACT008 Actinic Keratosis 50 0.026
538
GLM004 Gliomatosis Cerebri 50 0.026
539
ACR041 Acromelic Frontonasal Dysostosis 50 0.026
540
c FLL041 Follicular Lymphoma 1 50 0.026
541
INT253 Intestinal Benign Neoplasm 50 0.026
542
c PSR023 Psoriasis 1 50 0.026
543
MTC005 Mitochondrial Metabolism Disease 50 0.026
544
P OVR046 Ovarian Cyst 50 0.026
545
MCR004 Macroglobulinemia 50 0.026
546
NRL018 Neural Tube Defects, Folate-Sensitive 50 0.026
547
P CTN003 Cutaneous Lupus Erythematosus 50 0.026
548
c MLG074 Malignant Mesenchymoma 50 0.026
549
SXL003 Sexual Disorder 49 0.026
550
GST049 Gastrointestinal System Cancer 49 0.026
551
c PRM108 Primary Progressive Multiple Sclerosis 49 0.026
552
SMT003 Somatostatinoma 49 0.026
553
RTN020 Retinal Vascular Disease 49 0.026
554
ANG046 Angioimmunoblastic T-Cell Lymphoma 49 0.026
555
SCL003 Social Phobia 49 0.026
556
RNL011 Renal Osteodystrophy 49 0.026
557
CRC014 Carcinoid Tumors, Intestinal 49 0.026
558
P OBS001 Obstructive Jaundice 49 0.026
559
BWN001 Bowen-Conradi Syndrome 49 0.026
560
PRD004 Prediabetes Syndrome 49 0.026
561
SKN013 Skin Benign Neoplasm 49 0.026
562
P END046 Endometritis 49 0.026
563
SPL018 Splenomegaly 48 0.026
564
c BNG030 Benign Ependymoma 48 0.026
565
PRS034 Parasitic Helminthiasis Infectious Disease 48 0.026
566
SBP001 Subependymal Giant Cell Astrocytoma 48 0.026
567
PLS025 Plasmablastic Lymphoma 48 0.026
568
RTC005 Reticulosarcoma 48 0.026
569
LYM019 Lymphosarcoma 48 0.026
570
HYP043 Hyperandrogenism 48 0.026
571
SBS004 Substance Dependence 48 0.026
572
LGN006 Legionnaire Disease 48 0.026
573
NRN001 Neuroendocrine Carcinoma 48 0.026
574
DBT004 Diabetic Polyneuropathy 48 0.026
575
GLL048 Glial Tumor 48 0.026
576
HMZ003 Homozygous Familial Hypercholesterolemia 48 0.026
577
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 48 0.026
578
HYP017 Hypophosphatemia 48 0.026
579
SRT004 Serotonin Syndrome 48 0.026
580
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.026
581
c THR090 Thrombocythemia 1 47 0.026
582
c HRD026 Hereditary Ataxia 47 0.026
583
CHR074 Choriocarcinoma 47 0.026
584
VTM033 Vitamin K Deficiency Bleeding 47 0.026
585
VPM001 Vipoma 47 0.026
586
LYM051 Lymphomatoid Granulomatosis 47 0.026
587
ISL001 Islet Cell Tumor 47 0.026
588
LNT004 Lentigines 47 0.026
589
PRN014 Paronychia 47 0.026
590
LRY017 Laryngeal Disease 47 0.026
591
c BSL024 Basal Cell Carcinoma 1 47 0.026
592
ART004 Aortic Atherosclerosis 47 0.026
593
GLC008 Glucose Metabolism Disease 47 0.026
594
DBT006 Diabetic Macular Edema 46 0.026
595
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.026
596
c MLG068 Malignant Glioma 46 0.026
597
KWS001 Kwashiorkor 46 0.026
598
PPL021 Papilledema 46 0.026
599
ACT029 Acute Interstitial Pneumonia 46 0.026
600
KRT013 Keratolytic Winter Erythema 45 0.026
601
GLC036 Glucagonoma 45 0.026
602
MLN073 Melanosis, Neurocutaneous 45 0.026
603
INT054 Intraocular Lymphoma 45 0.026
604
c PRM038 Primary Agammaglobulinemia 45 0.026
605
c DRM054 Dermatitis, Atopic, 2 45 0.026
606
DBT002 Diabetic Autonomic Neuropathy 45 0.026
607
CRN017 Coronary Thrombosis 45 0.026
608
GRM004 Germinoma 45 0.026
609
KHN001 Kuhnt-Junius Degeneration 45 0.026
610
c SCH085 Schizophrenia 2 45 0.026
611
c SCH079 Schizophrenia 1 44 0.026
612
GLC042 Glucocorticoid Deficiency 1 44 0.026
613
PLM020 Pleomorphic Xanthoastrocytoma 44 0.026
614
BCK006 Back Pain 44 0.026
615
GLS007 Glossitis 44 0.026
616
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 44 0.026
617
ANP009 Anaplastic Oligodendroglioma 44 0.026
618
MTC004 Mitochondrial Encephalomyopathy 44 0.026
619
FNC007 Functioning Pituitary Adenoma 44 0.026
620
P END039 Endodermal Sinus Tumor 44 0.026
621
HYP082 Hypopharynx Cancer 44 0.026
622
c CHR064 Chronic Monocytic Leukemia 43 0.026
623
DFF037 Diffuse Intrinsic Pontine Glioma 43 0.026
624
ATN004 Autonomic Neuropathy 43 0.026
625
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.026
626
P CNT037 Central Nervous System Germinoma 43 0.026
627
PLM021 Pilomyxoid Astrocytoma 43 0.026
628
VCT001 Vacterl Association 43 0.026
630
SYS003 Systolic Heart Failure 43 0.026
631
DST006 Diastolic Heart Failure 43 0.026
632
SBC016 Subacute Delirium 43 0.026
633
MMM006 Mammographic Density 43 0.026
634
GST030 Gastrinoma 43 0.026
635
ACT088 Acute Insulin Response 42 0.026
636
P PRC031 Preeclampsia/eclampsia 1 42 0.026
637
PHY002 Physical Disorder 42 0.026
638
GST071 Gastrointestinal Carcinoma 42 0.026
639
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 42 0.026
640
ASP030 Aspirin Resistance 42 0.026
641
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 42 0.026
642
HPT004 Hepatic Coma 42 0.026
643
PTT003 Pituitary-Dependent Cushing's Disease 42 0.026
644
c NLD016 Nail Disorder, Nonsyndromic Congenital, 10 42 0.026
645
PPL001 Papillary Adenoma 42 0.026
646
P DYS005 Dyslexia 42 0.026
647
CNN001 Cannabis Dependence 41 0.026
648
c LFR007 Li-Fraumeni Syndrome 2 41 0.026
649
P SBR004 Seborrheic Dermatitis 41 0.026
650
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 41 0.026
651
P HRD086 Hereditary Hypophosphatemic Rickets 41 0.026
652
P BRB001 Beriberi 41 0.026
653
c TRC022 Tricuspid Valve Insufficiency 41 0.026
654
MYF001 Myofibroma 40 0.026
656
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.026
657
P PRG092 Pregnancy Loss, Recurrent 1 40 0.026
658
CNN002 Cannabis Abuse 40 0.026
659
c PSR028 Psoriasis 7 40 0.026
660
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.026
661
c CHR521 Charcot-Marie-Tooth Disease, Type 4b1 40 0.026
662
WLL004 Wallerian Degeneration 40 0.026
663
c PSR018 Psoriasis 13 40 0.026
664
c PSR032 Psoriasis 11 40 0.026
665
TST018 Testicular Yolk Sac Tumor 39 0.026
666
TNN002 Tinea Unguium 39 0.026
667
c OVR114 Ovarian Cancer 1 39 0.026
668
PSD001 Pseudobulbar Palsy 39 0.026
669
PRT005 Protoplasmic Astrocytoma 39 0.026
670
OVR094 Ovarian Epithelial Cancer 39 0.026
671
HPT070 Hepatosplenic T-Cell Lymphoma 39 0.026
672
c SYS043 Systemic Lupus Erythematosus 1 39 0.026
673
c HRD088 Hereditary Neuropathies 39 0.026
674
CRB004 Cerebral Artery Occlusion 38 0.026
675
SPS057 Spasticity 38 0.026
676
P BCL004 B-Cell Non-Hodgkin Lymphoma 38 0.026
677
CNT017 Central Nervous System Origin Vertigo 38 0.026
678
c CTR132 Cataract 3, Multiple Types 38 0.026
679
TBS001 Tabes Dorsalis 38 0.026
680
SML008 Small Intestine Lymphoma 37 0.026
681
c TCL024 T-Cell Non-Hodgkin Lymphoma 37 0.026
682
c LPR022 Leprosy 2 37 0.026
683
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 37 0.026
684
TNS014 Tenosynovitis 37 0.026
685
OPT010 Optic Papillitis 37 0.026
686
PNC008 Pancreatic Endocrine Carcinoma 36 0.026
687
HRD016 Hereditary Retinal Dystrophy 36 0.026
688
c SCH051 Schizophrenia 4 36 0.026
689
OLG006 Oligoastrocytoma 36 0.026
690
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 36 0.026
691
c CHR682 Chronic Bilirubin Encephalopathy 36 0.026
692
MXD026 Mixed Glioma 36 0.026
693
SCH011 Schizotypal Personality Disorder 36 0.026
694
HNS001 Hansen's Disease 35 0.026
695
GRM010 Germ Cells Tumors 35 0.026
696
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.026
697
GMS001 Gemistocytic Astrocytoma 35 0.026
698
LNT002 Lentigo Maligna Melanoma 34 0.026
699
MYC078 Myoclonus and Ataxia 34 0.026
700
XRD026 Xeroderma Pigmentosum-Cockayne Syndrome Complex 34 0.026
701
c PRS136 Prostate Cancer, Hereditary, 6 34 0.026
702
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 34 0.026
703
OPT032 Optic Pathway Glioma 34 0.026
704
c PRS130 Prostate Cancer, Hereditary, 8 33 0.026
705
c NLD006 Nail Disorder, Nonsyndromic Congenital, 9 33 0.026
706
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 32 0.026
707
ATR073 Atrophic Glossitis 32 0.026
708
MXD032 Mixed Germ Cell Tumor 32 0.026
709
WDH001 Wdha Syndrome 32 0.026
710
VCT005 Vacterl Association, X-Linked, with or Without Hydrocephalus 31 0.026
711
PYR016 Pyridoxine Deficiency 31 0.026
712
CRB026 Cerebellar Astrocytoma 31 0.026
713
CHL006 Childhood Oligodendroglioma 31 0.026
714
FNT004 Fainting 31 0.026
715
ANP008 Anaplastic Oligoastrocytoma 31 0.026
716
PNC012 Punctate Epithelial Keratoconjunctivitis 30 0.026
717
LYM048 Lymphoma, Large-Cell, Immunoblastic 30 0.026
718
c MYC058 Myocardial Infarction 2 30 0.026
719
CLS047 Classic Progressive Supranuclear Palsy Syndrome 30 0.026
720
TMR016 Tumor Suppressor Gene on Chromosome 11 29 0.026
721
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.026
722
CHL062 Childhood Pilocytic Astrocytoma 29 0.026
723
BRN048 Brain Stem Cancer 28 0.026
724
SPR038 Supranuclear Ocular Palsy 28 0.026
725
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.026
726
PPM002 Ppoma 28 0.026
727
P CNT036 Central Nervous System Germ Cell Tumor 28 0.026
728
c ICH023 Ichthyosis, Acquired 28 0.026
729
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 28 0.026
730
c SCH087 Schizophrenia 18 28 0.026
731
DFC001 Defective Apolipoprotein B-100 27 0.026
732
BNG077 Benign Idiopathic Neonatal Seizures 27 0.026
733
ACT162 Acute Sensory Ataxic Neuropathy 27 0.026
734
c TYP028 Type 1 Diabetes Mellitus 2 27 0.026
735
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 27 0.026
736
HDG004 Hodgkin's Granuloma 27 0.026
737
MLR020 Malaria, Mild 27 0.026
738
MXD025 Mixed Germ Cell Cancer 26 0.026
739
P CRT085 Carotid Intimal Medial Thickness 2 25 0.026
740
CRB087 Cerebral Arteriosclerosis 23 0.026
741
HDG006 Hodgkin's Paragranuloma 23 0.026
742
SYP005 Syphilitic Myelopathy 22 0.026
743
P RRN010 Rare Neurodegenerative Disease 21 0.026
744
P VRT014 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 1 21 0.026
745
CHL057 Childhood Brain Stem Glioma 19 0.026
746
c VRT015 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 2 18 0.026
747
CHL009 Childhood Cerebral Astrocytoma 15 0.026
748
CHL046 Childhood Central Nervous System Mixed Germ Cell Tumor 11 0.026
749
CHL027 Childhood Central Nervous System Germinoma 11 0.026
Content
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