Search results for Antilymphocyte Serum

1178 hits were found for Antilymphocyte Serum

# Family MCID Name MIFTS Score
1
P HPT021 Hepatitis 69 0.223
2
P ART022 Arthritis 75 0.174
3
P BRS047 Breast Cancer 100 0.163
4
P RHM011 Rheumatoid Arthritis 89 0.158
5
c HPT001 Hepatitis C 68 0.144
6
P HPT023 Hepatocellular Carcinoma 92 0.143
7
P LVR013 Liver Disease 75 0.136
8
P LPS004 Lupus Erythematosus 64 0.133
9
P AST005 Asthma 82 0.132
10
c SYS001 Systemic Lupus Erythematosus 86 0.129
11
P LKM002 Leukemia 71 0.128
12
P LYM118 Lymphoma 69 0.128
13
ART111 Artery Disease 55 0.123
14
P MYC007 Myocardial Infarction 79 0.121
15
P OVR042 Ovarian Cancer 76 0.113
16
GST053 Gastric Cancer 78 0.109
17
P HRT032 Heart Disease 75 0.109
18
c HPT016 Hepatitis B 64 0.109
19
MLN008 Melanoma 62 0.107
20
P ADN016 Adenocarcinoma 69 0.105
21
P KDN018 Kidney Disease 66 0.104
22
P MLT019 Multiple Myeloma 83 0.102
23
P PNM007 Pneumonia 68 0.092
24
c ACT075 Acute Myocardial Infarction 60 0.091
25
TBR010 Tuberculosis 70 0.090
26
c HPT073 Hepatitis C Virus 73 0.090
27
P PNC035 Pancreatic Cancer 87 0.083
28
P APL001 Aplastic Anemia 75 0.079
29
P INF037 Inflammatory Bowel Disease 63 0.077
30
P RNL014 Renal Cell Carcinoma 82 0.077
31
P AMY004 Amyloidosis 65 0.075
32
c VRL010 Viral Hepatitis 60 0.074
33
ISC004 Ischemia 61 0.073
34
P INF032 Infertility 59 0.073
35
LNG099 Lung Disease 64 0.073
36
BLD054 Blood Protein Disease 37 0.070
37
CRH001 Crohn's Disease 75 0.070
38
c CHR090 Chronic Lymphocytic Leukemia 76 0.068
39
P THL005 Thalassemia 64 0.067
40
P BCL006 B-Cell Lymphomas 65 0.066
41
P PLM036 Pulmonary Fibrosis 71 0.066
42
P ENC018 Encephalopathy 59 0.066
43
PLM001 Pulmonary Tuberculosis 67 0.065
44
ATP002 Atopy 66 0.064
45
HDG012 Hodgkin Lymphoma 77 0.064
46
DMN002 Dementia 65 0.063
47
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.063
48
P NRP001 Neuropathy 59 0.063
49
MYL009 Myelodysplastic Syndrome 73 0.062
50
PRP030 Purpura 58 0.062
51
GRW007 Growth Hormone Deficiency 50 0.062
52
HMT018 Hematopoietic Stem Cell Transplantation 41 0.062
53
P INF038 Influenza 72 0.062
54
VSC011 Vasculitis 62 0.062
55
CYS001 Cystic Fibrosis 83 0.061
56
P OVR049 Ovarian Disease 56 0.061
57
NTR005 Nutritional Deficiency Disease 36 0.061
58
c ACT073 Acute Leukemia 60 0.060
59
INT066 Interstitial Lung Disease 59 0.059
60
HYP266 Hypoxia 56 0.059
61
P URF003 Urofacial Syndrome 1 50 0.059
62
IMP003 Impaired Renal Function Disease 34 0.059
63
P MYL006 Myeloid Leukemia 66 0.059
64
CNN005 Connective Tissue Disease 62 0.059
65
URN009 Urinary System Disease 50 0.059
66
c CHR089 Chronic Kidney Failure 66 0.058
67
SRC014 Sarcoma 66 0.058
68
P ENC004 Encephalitis 63 0.058
69
LYM027 Lymphopenia 56 0.058
70
CNG034 Congestive Heart Failure 72 0.057
71
P HMR012 Hemorrhagic Fever 56 0.057
72
LPD008 Lipid Metabolism Disorder 58 0.057
73
DFF005 Diffuse Large B-Cell Lymphoma 59 0.057
74
P DRM010 Dermatomyositis 62 0.056
75
P PLY019 Polyneuropathy 56 0.056
76
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.056
77
DFC004 Deficiency Anemia 64 0.055
78
END030 End Stage Renal Failure 55 0.055
79
PRP027 Peripheral Vascular Disease 68 0.055
80
P GT001 Gout 58 0.055
81
FML039 Female Reproductive System Disease 48 0.055
82
MCS002 Mucositis 55 0.054
83
P TCL004 T-Cell Leukemia 47 0.054
84
P PLY041 Polymyositis 52 0.053
85
NRL016 Neural Tube Defects 76 0.053
86
P NRB001 Neuroblastoma 70 0.053
87
RHM027 Rheumatic Disease 58 0.053
88
BNS002 Bone Structure Disease 37 0.053
89
P MYP004 Myopathy 67 0.052
90
P NTR004 Neutropenia 59 0.052
91
MTH009 Mouth Disease 61 0.052
92
P RCK004 Rickets 61 0.052
93
ACD009 Acid-Labile Subunit, Deficiency of 45 0.052
94
P FLL037 Follicular Lymphoma 70 0.051
95
SKN016 Skin Disease 66 0.051
96
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.051
97
P ACT135 Acute Graft Versus Host Disease 53 0.050
98
P LYM026 Lymphoblastic Leukemia 62 0.050
99
HRY003 Hairy Cell Leukemia 57 0.050
100
RPR002 Reproductive System Disease 41 0.050
101
CRB039 Cerebrovascular Disease 63 0.049
102
c HPT003 Hepatitis a 59 0.049
103
ORL011 Oral Cancer 56 0.049
104
PRP080 Peripheral Artery Disease 37 0.049
105
c ADL017 Adult T-Cell Leukemia 60 0.049
106
VSC007 Vascular Disease 67 0.048
107
P THR014 Thrombocytopenia 64 0.048
108
HYP056 Hypoglycemia 61 0.048
109
P CTN015 Cutaneous T Cell Lymphoma 50 0.048
110
P ART023 Arthropathy 64 0.048
111
ADL002 Adult Syndrome 52 0.048
112
SCK005 Sickle Cell Disease 51 0.048
113
P FML035 Familial Hyperlipidemia 48 0.048
114
THL018 Thalassemia Major 48 0.048
115
c CLL013 Cell Type Cancer 46 0.047
116
c CHR417 Chronic Graft Versus Host Disease 51 0.047
117
NRN004 Neuroendocrine Tumor 56 0.047
118
HYP066 Hyperglycemia 61 0.046
119
BRS051 Breast Disease 61 0.046
120
P DRR001 Diarrhea 60 0.046
121
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.046
122
GST045 Gastroenteritis 59 0.046
123
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.046
124
ALN001 Aland Island Eye Disease 45 0.046
125
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.046
126
MYC006 Mycosis Fungoides 66 0.046
127
P HST010 Histiocytosis 58 0.046
128
PRM243 Primary Bone Cancer 29 0.046
129
TST014 Testicular Cancer 53 0.046
130
KRT002 Keratomalacia 52 0.046
131
ALL026 Allergic Hypersensitivity Disease 52 0.046
132
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.046
133
P PLY018 Polycythemia 58 0.045
134
THR024 Thrombosis 57 0.045
135
CSY001 C Syndrome 50 0.045
136
URM002 Uremia 48 0.045
137
BNC003 Bone Cancer 58 0.045
138
VSC006 Vascular Cancer 51 0.045
139
PLS009 Plasma Cell Neoplasm 48 0.045
140
CRD118 Cardiovascular Cancer 44 0.045
141
PCK002 Pick Disease 68 0.044
142
ALC007 Alcohol Dependence 63 0.044
143
c ACT134 Acute Liver Failure 50 0.044
144
c ALM001 Al Amyloidosis 49 0.044
145
PRT030 Parathyroid Gland Disease 47 0.044
146
SXL003 Sexual Disorder 42 0.044
147
VTM003 Vitamin Metabolic Disorder 30 0.044
148
P INT068 Intestinal Disease 60 0.043
149
ETN001 Eating Disorder 58 0.043
150
P CND004 Candidiasis 57 0.043
151
P CLL015 Collagen Disease 50 0.043
152
P DMY001 Demyelinating Polyneuropathy 43 0.043
153
c CRN214 Coronary Heart Disease 5 22 0.043
154
c CRN175 Coronary Heart Disease 4 19 0.043
155
LYM115 Lymphoma, Non-Hodgkin 63 0.043
156
WLL006 Wells Syndrome 59 0.043
157
LYM019 Lymphosarcoma 53 0.043
158
GDS001 Good Syndrome 44 0.043
159
VSC008 Vascular Hemostatic Disease 30 0.043
160
P PLM037 Pulmonary Hypertension 79 0.042
161
TST021 Testicular Germ Cell Tumor 69 0.042
162
TTN003 Tetanus 61 0.042
163
P NRV006 Nervous System Cancer 60 0.042
164
GLC003 Glucose Intolerance 55 0.042
165
FDL002 Food Allergy 53 0.042
166
MCR004 Macroglobulinemia 50 0.042
167
EXC002 Exocrine Pancreatic Insufficiency 43 0.042
168
GLC008 Glucose Metabolism Disease 42 0.042
169
GND003 Gonadal Disease 39 0.042
170
P CRN178 Coronary Heart Disease 6 21 0.042
171
P ACT074 Acute Lymphocytic Leukemia 56 0.042
172
P BLD051 Blood Coagulation Disease 42 0.042
173
SCK003 Sickle Cell Anemia 71 0.042
174
P PRM019 Premature Ovarian Failure 64 0.042
175
APH001 Aphthous Stomatitis 62 0.042
176
THR004 Thrombocytosis 55 0.042
177
c ACT071 Acute Kidney Failure 49 0.042
178
SKN023 Skin Tag 44 0.042
179
SKN027 Skin Conditions 43 0.042
180
PRM025 Primary Bacterial Infectious Disease 41 0.042
181
P NRV007 Nervous System Disease 71 0.041
182
P TYS001 Tay-Sachs Disease 71 0.041
183
P KDN017 Kidney Cancer 65 0.041
184
c LCL006 Localized Scleroderma 61 0.041
185
P ORL007 Oral Cavity Cancer 59 0.041
186
FML038 Female Reproductive Organ Cancer 50 0.041
187
VND001 Vein Disease 47 0.041
188
CRB025 Carbohydrate Metabolic Disorder 46 0.041
189
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.041
190
ATM052 Autoimmune Disease 1 25 0.041
191
P RSP003 Respiratory Failure 71 0.040
192
CHL071 Child Syndrome 58 0.040
193
C3D001 C3 Deficiency 53 0.040
194
KDS001 Kid Syndrome 53 0.040
195
CLR030 Clear Cell Renal Cell Carcinoma 53 0.040
196
STM006 Stomach Disease 50 0.040
197
END035 Endocrine Gland Cancer 49 0.040
198
LPD004 Lipoid Nephrosis 48 0.040
199
P MYL005 Myelofibrosis 67 0.039
200
HMT002 Hematologic Cancer 64 0.039
201
P HMR003 Hemorrhagic Disease 57 0.039
202
c INF071 Inflammatory Bowel Disease 1 51 0.039
203
STR067 Stroke, Ischemic 75 0.039
204
WLS001 Wilson Disease 72 0.039
205
CMM004 Common Variable Immunodeficiency 68 0.039
206
c BSL007 Basal Cell Carcinoma 65 0.039
207
P GST049 Gastrointestinal System Cancer 60 0.039
208
PRM097 Primary Immunodeficiency Disease 60 0.039
209
c CNT035 Central Nervous System Disease 60 0.039
210
RSP006 Respiratory System Disease 58 0.039
211
c ACT210 Acute Respiratory Distress Syndrome 57 0.039
212
GST050 Gastrointestinal System Disease 56 0.039
213
VSC002 Vascular Dementia 54 0.039
214
P HYP024 Hypoparathyroidism 53 0.039
215
P SHR001 Short Bowel Syndrome 49 0.039
216
LRN003 Learning Disability 49 0.039
217
GST071 Gastrointestinal Carcinoma 42 0.039
218
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.039
219
BND014 Bone Development Disease 40 0.039
220
ACR002 Acrocapitofemoral Dysplasia 33 0.039
221
P TRN020 Turner Syndrome 65 0.038
222
P HYP098 Hypereosinophilic Syndrome 63 0.038
223
MXD005 Mixed Connective Tissue Disease 62 0.038
224
JNT002 Joint Disorders 55 0.038
225
c HPT015 Hepatitis D 52 0.038
226
MYC002 Mycobacterium Avium Complex Disease 52 0.038
227
IMM136 Immune System Disease 51 0.038
228
CHR001 Churg-Strauss Syndrome 49 0.038
229
NSD001 Nose Disease 48 0.038
230
PRP021 Peripheral Nervous System Neoplasm 46 0.038
231
BLD053 Blood Platelet Disease 46 0.038
232
c AST037 Asthma 1 28 0.038
233
c CRN173 Coronary Heart Disease 8 18 0.038
234
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.037
235
P HML002 Hemolytic Anemia 62 0.037
236
SPT004 Septic Arthritis 60 0.037
237
PNC034 Pancreas Disease 58 0.037
238
SFT003 Soft Tissue Sarcoma 57 0.037
239
EPD016 Epidermolysis Bullosa 57 0.037
240
P SZR006 Seizure Disorder 56 0.037
241
P MLT074 Multiple Endocrine Neoplasia 56 0.037
242
GST023 Gastric Ulcer 56 0.037
243
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.037
244
INT007 Intermediate Coronary Syndrome 50 0.037
245
BRT030 Birth Defects 43 0.037
246
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.037
247
ANC002 Anca-Associated Vasculitis 42 0.037
248
SCR015 Scarlet Fever 38 0.037
249
SPC003 Specific Developmental Disorder 38 0.037
250
MSC004 Muscle Tissue Disease 34 0.037
251
LYM024 Lymphatic System Disease 52 0.037
252
CHL061 Childhood Leukemia 49 0.037
253
INC022 Inclusion-Cell Disease 46 0.037
254
OCL009 Ocular Cancer 59 0.036
255
PRP019 Peripheral Nervous System Disease 55 0.036
256
P MSC033 Muscle Disorders 52 0.036
257
P SPS003 Spastic Diplegia 52 0.036
258
BRN038 Bronchial Disease 51 0.036
259
FML037 Female Breast Cancer 50 0.036
260
P CTN003 Cutaneous Lupus Erythematosus 48 0.036
261
CRB085 Cerebral Hemorrhage 46 0.036
262
CHR074 Choriocarcinoma 46 0.036
263
ACR041 Acromelic Frontonasal Dysostosis 45 0.036
264
THL017 Thalassemia Intermedia 40 0.036
265
c INF067 Inflammatory Bowel Disease 10 49 0.035
266
VSC047 Vascular Malformation 45 0.035
267
c INF087 Inflammatory Bowel Disease 4 40 0.035
268
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.035
269
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.035
270
INS001 Insulinoma 61 0.035
271
ART017 Aortic Disease 57 0.035
272
WST001 West Syndrome 57 0.035
273
NRM005 Neuromuscular Disease 56 0.035
274
P MCR129 Microvascular Complications of Diabetes 1 54 0.035
275
DMY004 Demyelinating Disease 53 0.035
276
RTN018 Retinal Disease 53 0.035
277
CRC006 Carcinoid Syndrome 52 0.035
278
GNR004 Generalized Anxiety Disorder 51 0.035
279
P PLY017 Polyarteritis Nodosa 51 0.035
280
P CHR345 Chronic Pain 50 0.035
281
P INT063 Intellectual Disability 49 0.035
282
HRT007 Heart Cancer 46 0.035
283
PHY002 Physical Disorder 43 0.035
284
LKC003 Leukocyte Disease 43 0.035
285
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.035
286
c PNC106 Pancreatic Agenesis 1 37 0.035
287
ATM012 Autoimmune Disease of Blood 35 0.035
288
P HRT017 Heart Tumor 32 0.035
289
c AST039 Asthma 2 28 0.035
290
c ADL079 Adult Heart Tumor 16 0.035
291
ATM053 Autoimmune Disease 2 16 0.035
292
ATM055 Autoimmune Disease 4 15 0.035
293
BRK010 Burkitt Lymphoma 69 0.034
294
P THY023 Thymoma 57 0.034
295
PLS011 Plasmacytoma 56 0.034
296
CHR285 Chronic Myelomonocytic Leukemia 56 0.034
297
c PRM023 Pre-Malignant Neoplasm 41 0.034
298
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.034
299
c ADL001 Adult Lymphoma 39 0.034
300
ALR002 Al-Raqad Syndrome 36 0.034
301
c INF089 Inflammatory Bowel Disease 6 34 0.034
302
BNL002 Bone Lymphoma 32 0.034
303
c INF078 Inflammatory Bowel Disease 2 31 0.034
304
c INF073 Inflammatory Bowel Disease 12 21 0.034
305
BRN028 Brain Cancer 70 0.033
306
P ESS003 Essential Thrombocythemia 70 0.033
307
EWN003 Ewing Sarcoma 66 0.033
308
ADM013 Adamantinoma of Long Bones 57 0.033
309
c SVR001 Severe Acute Respiratory Syndrome 57 0.033
310
EXF001 Exfoliation Syndrome 57 0.033
311
P MYS005 Myositis 57 0.033
312
P CYS018 Cystitis 52 0.033
313
ATR060 Atrial Standstill, Digenic 51 0.033
314
ISL001 Islet Cell Tumor 50 0.033
315
ATN002 Autonomic Nervous System Disease 48 0.033
316
P RNL015 Renal Hypertension 48 0.033
317
INT253 Intestinal Benign Neoplasm 47 0.033
318
P ART084 Arteriovenous Fistula 44 0.033
319
GRN017 Granulocytopenia 44 0.033
320
SPN369 Spinal Disease 39 0.033
321
THL010 Thalassemia Minor 39 0.033
322
ADJ001 Adjustment Disorder 38 0.033
323
PLS010 Plasma Protein Metabolism Disease 34 0.033
324
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.033
325
c RNL016 Renal Infectious Disease 20 0.033
326
P MDL005 Medulloblastoma 77 0.032
327
P AGM001 Agammaglobulinemia 64 0.032
328
DNG002 Dengue Hemorrhagic Fever 63 0.032
329
P OST001 Osteopetrosis 63 0.032
330
SKN019 Skin Melanoma 62 0.032
331
RHB003 Rhabdomyosarcoma 57 0.032
332
CRT016 Carotid Artery Disease 57 0.032
333
P SML001 Small Cell Carcinoma 56 0.032
334
IDP011 Idiopathic Interstitial Pneumonia 56 0.032
335
VRL011 Viral Infectious Disease 55 0.032
336
P MNC007 Monocytic Leukemia 55 0.032
337
NWC001 Newcastle Disease 54 0.032
338
CYT008 Cytomegalovirus Infection 52 0.032
339
BRN022 Bronchiectasis 50 0.032
340
ACT017 Acute Chest Syndrome 48 0.032
341
RNL077 Renal Fibrosis 47 0.032
342
PRP036 Peripheral T-Cell Lymphoma 45 0.032
343
P SKN013 Skin Benign Neoplasm 43 0.032
344
OVR094 Ovarian Epithelial Cancer 43 0.032
345
RNL097 Renal Artery Disease 43 0.032
346
SNS023 Sensory System Cancer 43 0.032
347
RHM014 Rheumatoid Vasculitis 42 0.032
348
WTH001 Withdrawal Disorder 37 0.032
349
GRM001 Germ Cell and Embryonal Cancer 36 0.032
350
IMM065 Immunodeficiency 10 36 0.032
351
IMM071 Immunodeficiency 12 26 0.032
352
ATM059 Autoimmune Disease 6 22 0.032
353
ATM054 Autoimmune Disease 3 15 0.032
354
P LYM033 Lymphoproliferative Syndrome 56 0.032
355
LYM067 Lymphoid Leukemia 44 0.032
356
c ADL052 Adult Acute Lymphocytic Leukemia 44 0.032
357
PLS016 Plasma Cell Leukemia 42 0.032
358
c INF086 Inflammatory Bowel Disease 3 38 0.032
359
LYM023 Lymphatic System Cancer 33 0.032
360
MRG013 Mirage Syndrome 29 0.032
361
PRM151 Primary Bone Lymphoma 26 0.032
362
c INF093 Inflammatory Bowel Disease 14 23 0.032
363
c INF091 Inflammatory Bowel Disease 8 22 0.032
364
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.031
365
TKY002 Takayasu Arteritis 61 0.031
366
P SYS005 Systemic Scleroderma 61 0.031
367
P MCP010 Mucopolysaccharidosis 60 0.031
368
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.031
369
P SHR029 Short Syndrome 58 0.031
370
P HYP192 Hypocalcemia, Autosomal Dominant 56 0.031
371
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 56 0.031
372
IMM111 Immunodeficiency, X-Linked, with Hyper-Igm 54 0.031
373
BLD044 Bladder Disease 51 0.031
374
c MLG054 Malignant Histiocytosis 49 0.031
375
c INH020 Inherited Metabolic Disorder 49 0.031
376
ADR012 Adrenal Gland Disease 48 0.031
377
GLT021 Glutaricaciduria, Type I 46 0.031
378
PLM035 Pulmonary Eosinophilia 46 0.031
379
c VRL005 Viral Pneumonia 42 0.031
380
PRD011 Proud Syndrome 42 0.031
381
CLV009 Clove Syndrome, Somatic 41 0.031
382
GST078 Gastrointestinal Allergy 40 0.031
383
c ACT004 Acute Diarrhea 39 0.031
384
NSY001 N Syndrome 36 0.031
385
c HMG004 Hemoglobin D Disease 31 0.031
386
c MYC058 Myocardial Infarction 2 28 0.031
387
c CRN177 Coronary Heart Disease 7 20 0.031
388
ATM013 Autoimmune Disease of Cardiovascular System 13 0.031
389
MNT001 Mantle Cell Lymphoma 72 0.030
390
LYM040 Lymphoblastic Lymphoma 53 0.030
391
SZR001 Sezary's Disease 52 0.030
392
BNM001 Bone Marrow Cancer 51 0.030
393
c LYM107 Lymphoproliferative Syndrome 2 50 0.030
394
c CHR418 Chronic Leukemia 47 0.030
395
CHR563 Chronic Eosinophilic Leukemia 46 0.030
396
MXD023 Mixed Cell Type Cancer 44 0.030
397
CHR286 Chronic Neutrophilic Leukemia 43 0.030
398
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.030
399
LYM127 Lymphatic Malformations 39 0.030
400
c ACT020 Acute T Cell Leukemia 35 0.030
401
c LYM106 Lymphoproliferative Syndrome 1 32 0.030
402
HDG004 Hodgkin's Granuloma 24 0.030
403
c INF074 Inflammatory Bowel Disease 15 19 0.030
404
HDG006 Hodgkin's Paragranuloma 17 0.030
405
RFR001 Refractory Plasma Cell Neoplasm 16 0.030
406
c FML303 Familial/multiple Cancer 14 0.030
407
URN008 Urinary Bladder Cancer 66 0.029
408
RNL101 Renal Cell Carcinoma, Papillary 63 0.029
409
c ATM010 Autoimmune Hemolytic Anemia 60 0.029
410
P BRS044 Breast Adenocarcinoma 58 0.029
411
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.029
412
CTS003 Coats Disease 57 0.029
413
P FCS002 Fucosidosis 57 0.029
414
SNS001 Sensorineural Hearing Loss 57 0.029
415
P INT070 Intestinal Obstruction 57 0.029
416
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.029
417
P PLY014 Polycystic Kidney Disease 53 0.029
418
P CNT005 Central Nervous System Lymphoma 53 0.029
419
DSS008 Disease of Mental Health 52 0.029
420
PRC012 Pericardial Effusion 51 0.029
421
PNM001 Pneumocystosis 50 0.029
422
DRG003 Drug Dependence 50 0.029
423
c HMG001 Hemoglobin C Disease 47 0.029
424
CMP004 Complement Factor I Deficiency 47 0.029
425
IDP024 Idiopathic Inflammatory Myopathy 46 0.029
426
c MCR113 Microvascular Complications of Diabetes 3 45 0.029
427
P PLN008 Peeling Skin Syndrome 45 0.029
428
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.029
429
IRN002 Iron Metabolism Disease 41 0.029
430
CNV002 Conversion Disorder 41 0.029
431
END038 Endocrine Pancreas Disease 41 0.029
432
P TST026 Testicular Germ Cell Cancer 39 0.029
433
HYP540 Hypertension, Diastolic 39 0.029
434
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.029
435
c CNN010 Connective Tissue Benign Neoplasm 32 0.029
436
P CHR084 Chromosomal Disease 32 0.029
437
IMM068 Immunodeficiency 8 30 0.029
438
CTN019 Cutaneous Polyarteritis Nodosa 28 0.029
439
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.029
440
c ADL096 Adult Hepatocellular Carcinoma 24 0.029
441
c MLT093 Multiple Sclerosis 2 18 0.029
442
c MLT136 Multiple Endocrine Neoplasia 1 69 0.028
443
P GCH001 Gaucher's Disease 62 0.028
444
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.028
445
ADR005 Adrenal Carcinoma 57 0.028
446
P ANP001 Anaplastic Large Cell Lymphoma 57 0.028
447
ZLL001 Zellweger Syndrome 56 0.028
448
PHR003 Pharyngitis 56 0.028
449
CND002 Conduct Disorder 54 0.028
450
GRF001 Graft-Versus-Host Disease, Protection Against 52 0.028
451
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.028
452
SPN041 Spinal Cord Disease 51 0.028
453
c PRM226 Primary Central Nervous System Lymphoma 49 0.028
454
EXT010 Extramedullary Plasmacytoma 49 0.028
455
MSS002 Mass Syndrome 48 0.028
456
CRN017 Coronary Thrombosis 48 0.028
457
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.028
458
RFR010 Refractory Anemia 45 0.028
459
c PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 44 0.028
460
c MTR002 Mitral Valve Insufficiency 44 0.028
461
ANG046 Angioimmunoblastic T-Cell Lymphoma 43 0.028
462
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.028
463
SPC010 Speech and Communication Disorders 41 0.028
464
P CNN004 Connective Tissue Cancer 40 0.028
465
c PLN018 Peeling Skin Syndrome 2 40 0.028
466
ACT088 Acute Insulin Response 39 0.028
467
MLG088 Malignant Germ Cell Tumor 38 0.028
468
c CNG031 Congenital Nervous System Abnormality 37 0.028
469
ATM014 Autoimmune Disease of Endocrine System 36 0.028
470
c PLN017 Peeling Skin Syndrome 1 34 0.028
471
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.028
472
c TRC078 Trichohepatoenteric Syndrome 2 29 0.028
473
TYP027 Type 1 Diabetes Mellitus 10 27 0.028
474
c ATM007 Autoimmune Disease of Central Nervous System 25 0.028
475
VSC009 Vascular Skin Disease 19 0.028
476
CGL001 Coagulation Protein Disease 14 0.028
477
HML018 Homologous Wasting Disease 13 0.028
478
c LKM061 Leukemia, Acute Myeloid 73 0.027
479
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.027
480
c LKM062 Leukemia, Acute Lymphoblastic 64 0.027
481
P DYS007 Dyskeratosis Congenita 63 0.027
482
MYL031 Myeloproliferative Neoplasm 58 0.027
483
LYM104 Lymphoma, Malt, Somatic 54 0.027
484
MRG003 Marginal Zone B-Cell Lymphoma 52 0.027
485
c LKM060 Leukemia, Acute Lymphoblastic 3 50 0.027
486
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 49 0.027
487
RTC005 Reticulosarcoma 48 0.027
488
ATY042 Atypical Chronic Myeloid Leukemia 48 0.027
489
RTC009 Reticulum Cell Sarcoma 47 0.027
490
PLS025 Plasmablastic Lymphoma 46 0.027
491
SPL012 Splenic Disease 46 0.027
492
MYL004 Myelodysplastic Myeloproliferative Cancer 45 0.027
493
c FLL041 Follicular Lymphoma 1 45 0.027
494
SPL004 Splenic Marginal Zone Lymphoma 44 0.027
495
c CHR064 Chronic Monocytic Leukemia 42 0.027
496
CLL014 Cll/sll 42 0.027
497
P CHR562 Chronic Myelocytic Leukemia 41 0.027
498
ACT103 Acute Lymphoblastic Leukemia, Childhood 41 0.027
499
BCL012 B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue 37 0.027
500
SPL011 Spleen Cancer 36 0.027
501
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 35 0.027
502
NDL020 Nodal Marginal Zone B-Cell Lymphoma 35 0.027
503
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.027
504
c BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.027
505
ACT118 Acute Non Lymphoblastic Leukemia 30 0.027
506
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 29 0.027
507
RFR002 Refractory Hairy Cell Leukemia 29 0.027
508
RFR004 Refractory Hematologic Cancer 28 0.027
509
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 27 0.027
510
c INF090 Inflammatory Bowel Disease 7 26 0.027
511
PRM128 Primary Cutaneous Follicle Center Lymphoma 26 0.027
512
LYM048 Lymphoma, Large-Cell, Immunoblastic 25 0.027
513
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 24 0.027
514
c LKM004 Leukemia, B-Cell, Chronic 24 0.027
515
VSC001 Vascular Myelopathy 23 0.027
516
DFF027 Diffuse Lymphatic Malformation 22 0.027
517
c LKM056 Leukemia, Chronic Lymphocytic 2 21 0.027
518
PLS003 Plasmacytic Leukemia 21 0.027
519
c LKM005 Leukemia, T-Cell, Chronic 20 0.027
520
c LKM050 Leukemia, Chronic Lymphocytic 1 19 0.027
521
ANP010 Anaplastic Plasmacytoma 19 0.027
522
c LKM055 Leukemia, Acute Lymphoblastic 2 19 0.027
523
c LKM051 Leukemia, Chronic Lymphocytic 3 19 0.027
524
c INF081 Inflammatory Bowel Disease 22 18 0.027
525
TCL018 T-Cell Childhood Acute Lymphocytic Leukemia 18 0.027
526
FML125 Familial Hodgkin Disease 17 0.027
527
BND002 B- and T-Cell Mixed Leukemia 17 0.027
528
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 15 0.027
529
MYL052 Myeloproliferative Neoplasms, Familial 15 0.027
530
LYM126 Lymphoma Aids Related 15 0.027
531
TCL019 T-Cell Childhood Lymphoblastic Lymphoma 14 0.027
532
HDG009 Hodgkin Lymphoma, Childhood 14 0.027
533
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 13 0.027
534
ACT184 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Alkylating Agent 13 0.027
535
PRM165 Primary Plasmacytoma of the Bone 12 0.027
536
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 12 0.027
537
NNH003 Non-Hodgkin Lymphoma, Childhood 12 0.027
538
c FML078 Familial Myelofibrosis 11 0.027
539
P WSK001 Wiskott-Aldrich Syndrome 73 0.026
540
ADR007 Adrenoleukodystrophy 72 0.026
541
P MTC003 Metachromatic Leukodystrophy 70 0.026
542
P NMN002 Niemann-Pick Disease 65 0.026
543
P ALX003 Alexander Disease 63 0.026
544
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.026
545
P LNG064 Lung Cancer Susceptibility 3 62 0.026
546
FCT003 Factor X Deficiency 61 0.026
547
P TMP003 Temporal Arteritis 60 0.026
548
WLL001 Williams-Beuren Syndrome 60 0.026
549
P LKD001 Leukodystrophy 59 0.026
550
P WLD002 Waldenstrom Macroglobulinemia 58 0.026
551
CLR003 Clear Cell Adenocarcinoma 56 0.026
552
LKC001 Leukocyte Adhesion Deficiency 55 0.026
553
ASP002 Aspartylglucosaminuria 55 0.026
554
PST046 Post-Transplant Lymphoproliferative Disease 54 0.026
555
SML033 Small Cell Cancer of the Lung, Somatic 54 0.026
556
P MTC069 Mitochondrial Disorders 53 0.026
557
LYS002 Lysosomal Storage Disease 52 0.026
558
OST015 Osteochondrodysplasia 52 0.026
559
P PNC001 Pancytopenia 52 0.026
560
HMG005 Hemoglobinopathy 52 0.026
561
c LRG001 Large Cell Carcinoma 51 0.026
562
c ACT068 Acute Cystitis 50 0.026
563
LPD009 Lipid Storage Disease 49 0.026
564
MSC072 Muscle Cancer 49 0.026
565
P FNC004 Fanconi Syndrome 49 0.026
566
ATN005 Autonomic Dysfunction 49 0.026
567
HMG002 Hemoglobinuria 48 0.026
568
c CNG027 Congenital Hemolytic Anemia 48 0.026
569
LYM051 Lymphomatoid Granulomatosis 47 0.026
570
PRL017 Prolymphocytic Leukemia 47 0.026
571
TCL003 T Cell Deficiency 45 0.026
572
HNC001 Henoch-Schoenlein Purpura 45 0.026
573
LYM012 Lymphoplasmacytic Lymphoma 44 0.026
574
ACT058 Active Peptic Ulcer Disease 43 0.026
575
CHL028 Childhood Type Dermatomyositis 42 0.026
576
TCL002 T-Cell Large Granular Lymphocyte Leukemia 42 0.026
577
P CHR102 Charcot-Marie-Tooth Neuropathy 41 0.026
578
ACT029 Acute Interstitial Pneumonia 41 0.026
579
DFF003 Diffuse Scleroderma 41 0.026
580
GRN006 Granulomatous Angiitis 40 0.026
581
c CHR096 Chronic Pulmonary Heart Disease 40 0.026
582
ATN003 Autonomic Nervous System Neoplasm 40 0.026
583
LRG008 Large Granular Lymphocyte Leukemia 39 0.026
584
SPN040 Spinal Cancer 39 0.026
585
SXD001 Sex Differentiation Disease 38 0.026
586
LNG013 Lung Lymphoma 38 0.026
587
P CRN276 Corneal Endothelial Dystrophy 37 0.026
588
FNC002 Functional Diarrhea 37 0.026
589
VSC012 Vesiculobullous Skin Disease 36 0.026
590
c INH004 Inherited Blood Coagulation Disease 36 0.026
591
MTC005 Mitochondrial Metabolism Disease 36 0.026
592
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.026
593
VRS001 Virus Associated Hemophagocytic Syndrome 35 0.026
594
PNC053 Pancreatic Islet Cell Tumors 35 0.026
595
MXD032 Mixed Germ Cell Tumor 34 0.026
596
P XLN007 X-Linked Disease 34 0.026
597
P ATS049 Autism Susceptibility, X-Linked 2 33 0.026
598
c PST001 Posterior Myocardial Infarction 31 0.026
599
CYT004 Cytomegalic Inclusion Disease 31 0.026
600
IMM102 Immunodeficiency 14 31 0.026
601
c ATM068 Autoimmune Hypoparathyroidism 30 0.026
602
c PLN021 Peeling Skin Syndrome 3 29 0.026
603
c PNC103 Pancreatic Cancer 4 29 0.026
604
c PNC094 Pancreatic Cancer 1 27 0.026
605
IMM075 Immunodeficiency 22 26 0.026
606
OVR069 Ovarian Germ Cell Tumor 24 0.026
607
IMM025 Immunoglobulin a Deficiency 2 24 0.026
608
c AGM011 Agammaglobulinemia 1 24 0.026
609
CNT067 Central Cord Syndrome 23 0.026
610
IMM142 Immunodeficiency 50 20 0.026
611
SPC022 Specific Antibody Deficiency 18 0.026
612
CML001 Cumulative Trauma Disorders 18 0.026
613
CD4004 Cd4 Deficiency 14 0.026
614
PLY028 Polycystic Bone Disease 13 0.026
615
TCL006 T Cell Immunodeficiency Primary 12 0.026
616
ORL014 Oral Pharyngeal Disorders 11 0.026
617
P DMN001 Diamond-Blackfan Anemia 69 0.024
618
SVR004 Severe Combined Immunodeficiency 69 0.024
619
P CHR071 Charcot-Marie-Tooth Disease 67 0.024
620
CHR012 Chronic Granulomatous Disease 65 0.024
621
CHD001 Chediak-Higashi Syndrome 64 0.024
622
c NMN015 Niemann-Pick Disease, Type C1 63 0.024
623
WGN006 Wegener Granulomatosis 63 0.024
624
P MCL013 Mucolipidosis Iv 62 0.024
625
P VLC001 Velocardiofacial Syndrome 62 0.024
626
c MCP009 Mucopolysaccharidosis Ii 62 0.024
627
FCT007 Factor Vii Deficiency 61 0.024
628
SHW002 Shwachman-Diamond Syndrome 61 0.024
629
c MCP004 Mucopolysaccharidosis Iv 60 0.024
630
P NRN021 Neuronal Ceroid Lipofuscinosis 59 0.024
631
ARM001 Aromatase Deficiency 58 0.024
632
P MTR004 Maturity-Onset Diabetes of the Young 58 0.024
633
P AGM005 Agammaglobulinemia, X-Linked 1 57 0.024
634
c SVR003 Severe Congenital Neutropenia 56 0.024
635
c THR092 Thrombophilia Due to Thrombin Defect 54 0.024
636
c VRL007 Viral Encephalitis 54 0.024
637
c RNL003 Renal Clear Cell Carcinoma 54 0.024
638
MCN017 Meconium Ileus 54 0.024
639
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.024
640
P VNS003 Venous Insufficiency 54 0.024
641
OLV001 Olivopontocerebellar Atrophy 53 0.024
642
P DGR001 Digeorge Syndrome 53 0.024
643
c TCL005 T-Cell Prolymphocytic Leukemia 52 0.024
644
NRP015 Neuropathy, Congenital Hypomyelinating 52 0.024
645
c ACT009 Acute Monocytic Leukemia 52 0.024
646
PHL006 Phelan-Mcdermid Syndrome 51 0.024
647
P GND004 Gonadal Dysgenesis 51 0.024
648
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 50 0.024
649
MST017 Mast Cell Disease 50 0.024
650
DBF001 D-Bifunctional Protein Deficiency 50 0.024
651
P PRM001 Primary Cutaneous Amyloidosis 50 0.024
652
RSS002 Roussy-Levy Syndrome 50 0.024
653
HYP074 Hypersensitivity Vasculitis 48 0.024
654
P TRC086 Trichohepatoenteric Syndrome 1 48 0.024
655
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.024
656
ACT098 Acute Erythroid Leukemia 47 0.024
657
P GRN010 Granular Cell Tumor 47 0.024
658
PRR002 Pure Red-Cell Aplasia 47 0.024
659
c INT072 Intestinal Pseudo-Obstruction 46 0.024
660
ADR038 Adermatoglyphia 46 0.024
661
SKL014 Skeletal Dysplasia 46 0.024
662
P ACT150 Acute Adrenal Insufficiency 45 0.024
663
RLP003 Relapsing Fever 45 0.024
664
SNS003 Sensory Peripheral Neuropathy 45 0.024
665
ALP012 Alpha-Methylacyl-Coa Racemase Deficiency 45 0.024
666
SKL017 Skeletal Dysplasias 45 0.024
667
MNC006 Monoclonal Gammopathy of Uncertain Significance 44 0.024
668
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 43 0.024
669
c LYM114 Lymphoproliferative Syndrome, X-Linked, 2 43 0.024
670
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.024
671
ADT003 Auditory System Disease 40 0.024
672
RNL012 Renal Tuberculosis 40 0.024
673
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 39 0.024
674
LYM020 Lymph Node Cancer 39 0.024
675
CMP009 Complement Deficiency 39 0.024
676
FST010 Fasting Hypoglycemia 39 0.024
677
ESN020 Eosinophilic Granulomatosis with Polyangiitis 39 0.024
678
MCP033 Mucopolysaccharidoses 39 0.024
679
PRX034 Peroxisome Disorders 39 0.024
680
TMP012 Temple Syndrome 38 0.024
681
MTR007 Motor Peripheral Neuropathy 37 0.024
682
DYS016 Dysgammaglobulinemia 37 0.024
683
PRM026 Primary Systemic Mycosis 36 0.024
684
IDP074 Idiopathic Bronchiectasis 36 0.024
685
P WGN003 Wagner Syndrome 36 0.024
686
FXF002 Fox-Fordyce Disease 36 0.024
687
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.024
688
NNF001 Non-Functioning Pancreatic Endocrine Tumor 35 0.024
689
WRT001 Worth's Syndrome 34 0.024
690
c ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 34 0.024
691
FLC001 Folic Acid Deficiency Anemia 34 0.024
692
c DBT038 Diabetes Mellitus, Insulin-Dependent, 5 34 0.024
693
IMM044 Immunoglobulin G Deficiency 33 0.024
694
c SYS043 Systemic Lupus Erythematosus 1 33 0.024
695
PDT021 Pediatric Osteosarcoma 33 0.024
696
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 33 0.024
697
FNC006 Functional Gastric Disease 32 0.024
698
MCR021 Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies 32 0.024
699
OVR021 Ovarian Lymphoma 32 0.024
700
BLD028 Bladder Lymphoma 32 0.024
701
BRS001 Breast Lymphoma 32 0.024
702
c INF088 Inflammatory Bowel Disease 5 31 0.024
703
P ACT080 Acute Pulmonary Heart Disease 31 0.024
704
P ATM076 Autoimmune Retinopathy 31 0.024
705
FNC012 Functioning Pancreatic Endocrine Tumor 31 0.024
706
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 31 0.024
707
IMM082 Immunodeficiency 18 31 0.024
708
NRV004 Nerve Compression Syndrome 31 0.024
709
c PNC095 Pancreatic Cancer 3 30 0.024
710
IMM066 Immunodeficiency 9 30 0.024
711
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 30 0.024
712
CYL001 Cayler Cardiofacial Syndrome 29 0.024
713
MCN011 Mucinoses 29 0.024
714
GRN016 Grant Syndrome 29 0.024
715
c DBT052 Diabetes Mellitus, Insulin-Dependent, 18 29 0.024
716
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.024
717
IMM095 Immunodeficiency 35 28 0.024
718
c WGN005 Wagner Syndrome 1 28 0.024
719
GLC073 Glucocorticoid Deficiency 4 28 0.024
720
THY026 Thymus Gland Disease 27 0.024
721
c CHR565 Chromosomal Deletion Syndrome 27 0.024
722
INH011 Inherited Bone Marrow Failure Syndromes 27 0.024
723
c INF002 Inflammatory Diarrhea 27 0.024
724
IMM096 Immunodeficiency 30 27 0.024
725
c SYS038 Systemic Lupus Erythematosus 2 27 0.024
726
LVR006 Liver Lymphoma 27 0.024
727
IMM063 Immunodeficiency 15 26 0.024
728
IMM062 Immunodeficiency 11 26 0.024
729
c ATM089 Autoimmune Neuropathy 26 0.024
730
c DBT055 Diabetes Mellitus, Insulin-Dependent, 3 26 0.024
731
c WSK002 Wiskott-Aldrich Syndrome 2 25 0.024
732
c BKV001 Bk-Virus Nephropathy 25 0.024
733
IMM120 Immunodeficiency 40 24 0.024
734
IST006 Isotretinoin Syndrome 24 0.024
735
c MLT094 Multiple Sclerosis 3 24 0.024
736
c MLT124 Multiple Sclerosis 5 23 0.024
737
PRM133 Primary Pulmonary Lymphoma 23 0.024
738
CMP063 Complement Factor B Deficiency 23 0.024
739
c SYS040 Systemic Lupus Erythematosus 10 22 0.024
740
c RNL034 Renal Cell Carcinoma 4 18 0.024
741
c ALP039 Alopecia Areata 1 18 0.024
742
ALL002 Allergic Cutaneous Vasculitis 17 0.024
743
c MLT095 Multiple Sclerosis 4 16 0.024
744
GLC077 Glucocorticoid Therapy, Response to 16 0.024
745
CHR235 Chromosome 22q Deletion 15 0.024
746
c INF136 Influenza, Severe 15 0.024
747
c SML023 Small Cell Lung Cancer, Adult 15 0.024
748
HRT029 Heart Tumor of the Child 15 0.024
749
NVD002 Nevada Syndrome 14 0.024
750
c DGR004 Digeorge Syndrome 2 14 0.024
751
P MYC054 Mycobacterium Tuberculosis 2 14 0.024
752
MXD024 Mixed Epithelial Tumor of Ovary 13 0.024
753
PNC040 Pancreatic Delta Cell Neoplasm 13 0.024
754
c DLT001 Delta Chain Disease 13 0.024
755
c VLC003 Velocardiofacial Syndrome 2 12 0.024
756
MLG035 Malignant Ovarian Mixed Epithelial Neoplasm 12 0.024
757
PRM053 Primary Release Disorder of Platelets 11 0.024
758
c ATM006 Autoimmune Lymphoproliferative Syndrome 71 0.021
759
c FNC027 Fanconi Anemia, Complementation Group a 71 0.021
760
P KRB001 Krabbe Disease 69 0.021
761
c MCP037 Mucopolysaccharidosis is 64 0.021
762
WLM007 Wilms Tumor Susceptibility-5 63 0.021
763
PLY125 Polycythemia Vera, Somatic 63 0.021
764
GLN010 Glanzmann Thrombasthenia 63 0.021
765
OST085 Osteosarcoma, Somatic 63 0.021
766
P RFS001 Refsum Disease 63 0.021
767
P DMN033 Dementia, Frontotemporal 62 0.021
768
c MCP003 Mucopolysaccharidosis Vii 62 0.021
769
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.021
770
LPM004 Lipoma 60 0.021
771
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 60 0.021
772
c MCP024 Mucopolysaccharidosis Type Vi 60 0.021
773
RBR001 Roberts Syndrome 60 0.021
774
c MNN043 Meningioma, Familial 59 0.021
775
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 59 0.021
776
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 59 0.021
777
c GCH015 Gaucher Disease, Type I 59 0.021
778
c MCP001 Mucopolysaccharidosis Iii 58 0.021
779
P THY102 Thyroid Cancer, Nonmedullary, 2 58 0.021
780
FCT006 Factor V Deficiency 57 0.021
781
WLM001 Wolman Disease 57 0.021
782
SND007 Sandhoff Disease, Infantile, Juvenile, and Adult Forms 57 0.021
783
SVR066 Severe Combined Immunodeficiency, X-Linked 57 0.021
784
c NMN013 Niemann-Pick Disease, Type a 56 0.021
785
LTT002 Letterer-Siwe Disease 56 0.021
786
c MNN025 Mannosidosis, Alpha-, Types I and Ii 55 0.021
787
P TMT001 Timothy Syndrome 55 0.021
788
MGK001 Megakaryocytic Leukemia 55 0.021
789
P EMB005 Embryonal Rhabdomyosarcoma 54 0.021
790
APH002 Aphasia 54 0.021
791
P RNL100 Renal Hypodysplasia/aplasia 1 53 0.021
792
FRB001 Farber Lipogranulomatosis 53 0.021
793
THL016 Thalassemias, Alpha- 53 0.021
794
SCT005 Scott Syndrome 53 0.021
795
P SML016 Small Intestine Cancer 52 0.021
796
LKM067 Leukemia, Acute Promyelocytic, Somatic 52 0.021
797
P APL006 Aplasia Cutis Congenita 52 0.021
798
c PRX045 Peroxisome Biogenesis Disorder 1b 52 0.021
799
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 52 0.021
800
c PRM012 Primary Polycythemia 52 0.021
801
TXC002 Toxic Encephalopathy 51 0.021
802
P GRS003 Griscelli Syndrome 51 0.021
803
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 51 0.021
804
c GNG001 Gangliosidosis Gm1 51 0.021
805
c PLY060 Polycystic Kidney Disease 2 51 0.021
806
P RNL028 Renal Tubular Dysgenesis 51 0.021
807
THY025 Thymus Cancer 50 0.021
808
HND003 Hand-Foot-Uterus Syndrome 50 0.021
809
PRX028 Peroxisomal Acyl-Coa Oxidase Deficiency 50 0.021
810
PRL032 Perlman Syndrome 50 0.021
811
GLM004 Gliomatosis Cerebri 49 0.021
812
c CRD183 Ceroid Lipofuscinosis, Neuronal, 2 49 0.021
813
BCL002 B Cell Deficiency 49 0.021
814
MLL012 Miller Syndrome 49 0.021
815
c CNG464 Congenital Myopathy 49 0.021
816
MST002 Mast-Cell Leukemia 48 0.021
817
QBC001 Quebec Platelet Disorder 48 0.021
818
MYL003 Myeloid Sarcoma 48 0.021
819
CNG028 Congenital Hypoplastic Anemia 48 0.021
820
LYM116 Lymph Node Disease 47 0.021
821
NNT017 Neonatal Adrenoleukodystrophy 47 0.021
822
NTR003 Natural Killer Cell Leukemia 47 0.021
823
TMR010 Tumor Predisposition Syndrome 47 0.021
824
LPM005 Lipomatosis 47 0.021
825
NLS001 Nelson Syndrome 47 0.021
826
P MNN018 Mannosidosis 47 0.021
827
CNT046 Central Nervous System Vasculitis 46 0.021
828
EMB007 Embryonal Sarcoma 46 0.021
829
c GCH017 Gaucher Disease, Type Iii 46 0.021
830
P HRD021 Hereditary Sensory Neuropathy 46 0.021
831
CD4003 Cd40 Ligand Deficiency 46 0.021
832
INT054 Intraocular Lymphoma 45 0.021
833
c ADL066 Adult Neuronal Ceroid Lipofuscinosis 45 0.021
834
RNL078 Renal Dysplasia 45 0.021
835
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 45 0.021
836
IPX001 Ipex Syndrome 45 0.021
837
FBR086 Fibrolamellar Carcinoma 45 0.021
838
SPH010 Sphingolipidosis 45 0.021
839
ACH037 Achalasia-Addisonianism-Alacrimia Syndrome 45 0.021
840
P RPR003 Reproductive Organ Cancer 44 0.021
841
DYS164 Dyskeratosis Congenita, X-Linked 44 0.021
842
CRB033 Cerebral Degeneration 44 0.021
843
SMN008 Semantic Dementia 44 0.021
844
CHR276 Chronic Active Epstein-Barr Virus Infection 44 0.021
845
TST015 Testicular Disease 44 0.021
846
c CHR431 Chronic Venous Insufficiency 44 0.021
847
c HMN022 Human T-Cell Leukemia Virus Type 2 44 0.021
848
c HMG003 Hemoglobin E Disease 44 0.021
849
BNW001 Bone Ewing's Sarcoma 43 0.021
850
c GCH016 Gaucher Disease, Type Ii 43 0.021
851
P BCL005 B Cell Prolymphocytic Leukemia 43 0.021
852
MST006 Mast Syndrome 43 0.021
853
EWN002 Ewing's Family of Tumors 43 0.021
854
c ART120 Arthrogryposis, Distal, Type 3 42 0.021
855
NRN005 Neuronal Ceroid-Lipofuscinoses 42 0.021
856
CMB003 Combined T Cell and B Cell Immunodeficiency 42 0.021
857
P PNC045 Pancreatic Agenesis 42 0.021
858
HPT020 Hepatic Vascular Disease 42 0.021
859
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 42 0.021
860
PLM039 Pulmonary Neuroendocrine Tumor 42 0.021
861
RNL025 Renal Hypoplasia 42 0.021
862
P MTC004 Mitochondrial Encephalomyopathy 42 0.021
863
ACT200 Acute Monoblastic Leukemia 42 0.021
864
c MCP012 Mucopolysaccharidosis Ih 41 0.021
865
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 41 0.021
866
OPP002 Opportunistic Mycosis 41 0.021
867
CYS036 Cystinosis, Nephropathic 41 0.021
868
GNT001 Giant Cell Reparative Granuloma 41 0.021
869
DND018 Dendritic Cell Tumor 41 0.021
870
SPC005 Speech Disorder 41 0.021
871
CMB023 Combined Immunodeficiency, X-Linked, Moderate 40 0.021
872
SML008 Small Intestine Lymphoma 40 0.021
873
ENT001 Enterocele 40 0.021
874
P XLN110 X-Linked Charcot-Marie-Tooth Disease 40 0.021
875
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 40 0.021
876
ATX003 Ataxia with Isolated Vitamin E Deficiency 40 0.021
877
c HRD088 Hereditary Neuropathies 40 0.021
878
MNC019 Monocarboxylate Transporter 1 Deficiency 40 0.021
879
c GRN014 Grn-Related Frontotemporal Dementia 40 0.021
880
c GM1004 Gm1-Gangliosidosis, Type I 40 0.021
881
MST004 Mast Cell Neoplasm 40 0.021
882
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.021
883
c PRM225 Primary Thrombocytopenia 39 0.021
884
GST093 Gastrointestinal Defects and Immunodeficiency Syndrome 39 0.021
885
PRX077 Peroxisomal Biogenesis Disorders 39 0.021
886
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 39 0.021
887
c CRD185 Ceroid Lipofuscinosis, Neuronal, 6 39 0.021
888
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 39 0.021
889
THR035 Thrombasthenia 39 0.021
890
P ATM020 Autoimmune Enteropathy 39 0.021
891
EPS006 Epstein Syndrome 38 0.021
892
c DMN023 Diamond-Blackfan Anemia 1 38 0.021
893
c PRM149 Primary Hypereosinophilic Syndrome 38 0.021
894
RHM009 Rheumatoid Lung Disease 38 0.021
895
PDT001 Pediatric Lymphoma 38 0.021
896
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.021
897
CHL050 Cholesterol Ester Storage Disease 38 0.021
898
P HRT035 Heart Block, Congenital 38 0.021
899
NNT004 Neonatal Respiratory Failure 37 0.021
900
ACT113 Acute Myeloblastic Leukemia with Maturation 37 0.021
901
c PLY139 Polycystic Kidney Disease 3 37 0.021
902
ADR022 Adrenomyeloneuropathy 37 0.021
903
CMP001 Composite Lymphoma 37 0.021
904
HYP189 Hypoadrenalism 37 0.021
905
TST004 Testicular Lymphoma 37 0.021
906
AMY002 Amyloid Tumor 37 0.021
907
P CNT036 Central Nervous System Germ Cell Tumor 37 0.021
908
LNG004 Langerhans Cell Sarcoma 37 0.021
909
LTH001 Lethal Midline Granuloma 37 0.021
910
CNT018 Central Nervous System Leukemia 37 0.021
911
c DBT057 Diabetes Mellitus, Insulin-Dependent, 6 37 0.021
912
P ENC011 Encephalomyopathy 37 0.021
913
PRX001 Peroxisomal Disease 37 0.021
914
CPL005 Capillary Disease 36 0.021
915
ISC005 Ischemic Bone Disease 36 0.021
916
c CNG413 Congenital Short Bowel Syndrome 36 0.021
917
BRN048 Brain Stem Cancer 36 0.021
918
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 36 0.021
919
SVR077 Severe Combined Immune Deficiency 36 0.021
920
NNL001 Non-Langerhans-Cell Histiocytosis 36 0.021
921
ADR010 Adrenal Cortical Hypofunction 36 0.021
922
OVR104 Ovarian Melanoma 36 0.021
923
RDT001 Radiation Cystitis 36 0.021
924
FML063 Familial Glucocorticoid Deficiency 36 0.021
925
SLT001 Solitary Osseous Plasmacytoma 36 0.021
926
c DMN021 Diamond-Blackfan Anemia 6 35 0.021
927
c CHR087 Chronic Cystitis 35 0.021
928
c MTR071 Maturity-Onset Diabetes of the Young 6 35 0.021
929
DFF012 Differentiating Neuroblastoma 35 0.021
930
c THR037 Thrombocytopenia 2 35 0.021
931
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 35 0.021
932
BNS001 Bone Osteosarcoma 35 0.021
933
LYM005 Lymphocele 35 0.021
934
IMM078 Immunodeficiency 21 35 0.021
935
CHR340 Chronic Granulomatous Disease, X-Linked 35 0.021
936
LNG037 Lung Sarcoma 35 0.021
937
ACT216 Acute Leukemia of Ambiguous Lineage 34 0.021
938
GLS018 Glass Syndrome 34 0.021
939
PRP024 Peripheral Osteosarcoma 34 0.021
940
c BRN108 Branchiootic Syndrome 1 34 0.021
941
MYL015 Myeloproliferative Disorder with Eosinophilia 34 0.021
942
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 34 0.021
943
PLM013 Pulmonary Immaturity 34 0.021
944
MTC061 Mitochondrial Dna Depletion Syndrome 1 34 0.021
945
ACT177 Acute Basophilic Leukemia 34 0.021
946
c CNG007 Congenital Adrenal Insufficiency 34 0.021
947
MNC004 Monoclonal Paraproteinemia 34 0.021
948
MSN004 Mesenchymal Cell Neoplasm 34 0.021
949
ATM015 Autoimmune Disease of Gastrointestinal Tract 34 0.021
950
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.021
951
c DFN036 Deafness, X-Linked 2 33 0.021
952
BWN006 Bowen's Disease 33 0.021
953
HYP114 Hypertensive Nephropathy 33 0.021
954
CHL010 Childhood Kidney Cell Carcinoma 33 0.021
955
TXC007 Toxic Pneumonitis 33 0.021
956
c MYL058 Myeloproliferative Syndrome, Transient 33 0.021
957
c DBT050 Diabetes Mellitus, Insulin-Dependent, 15 33 0.021
958
HMR023 Hemorrhagic Cystitis 33 0.021
959
c GM1005 Gm1-Gangliosidosis, Type Ii 33 0.021
960
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.021
961
ENG004 Engraftment Syndrome 32 0.021
962
RNL021 Renal Tubular Transport Disease 32 0.021
963
CRB040 Cerebrum Cancer 32 0.021
964
ACT095 Acute Biphenotypic Leukemia 32 0.021
965
P GNG010 Gangliosidosis Gm2 32 0.021
966
LNG054 Lung Agenesis 32 0.021
967
c GM1006 Gm1-Gangliosidosis, Type Iii 32 0.021
968
BNM005 Bone Marrow Necrosis 32 0.021
969
HDG003 Hodgkin's Lymphoma, Lymphocytic Depletion 32 0.021
970
END014 Endemic Typhus 31 0.021
971
P RFR008 Refractory Anemia with Excess Blasts 31 0.021
972
IMM027 Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome 31 0.021
973
KDN019 Kidney Sarcoma 31 0.021
974
c LNG072 Lung Cancer Susceptibility 2 31 0.021
975
TST003 Testicular Leukemia 31 0.021
976
GST014 Gastrointestinal Lymphoma 31 0.021
977
TTH004 Tethered Spinal Cord Syndrome 31 0.021
978
c ADL027 Adult Dermatomyositis 31 0.021
979
MXD025 Mixed Germ Cell Cancer 31 0.021
980
c THR090 Thrombocythemia 1 30 0.021
981
c CHR373 Charcot-Marie-Tooth Neuropathy, X-Linked Recessive, 2 30 0.021
982
MXD027 Mixed Type Thymoma 30 0.021
983
P SCK034 Sickle Beta Thalassemia 30 0.021
984
c DBT034 Diabetes Mellitus, Insulin-Dependent, 20 30 0.021
985
c TYP010 Type C Thymoma 30 0.021
986
P CNT044 Central Nervous System Primitive Neuroectodermal Neoplasm 30 0.021
987
PLT019 Platelet Disorder, Familial, with Associated Myeloid Malignancy 30 0.021
988
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 30 0.021
989
c PRM038 Primary Agammaglobulinemia 30 0.021
990
PRG090 Progressive Relapsing Multiple Sclerosis 30 0.021
991
HRT003 Heart Lymphoma 30 0.021
992
c DMN017 Diamond-Blackfan Anemia 10 29 0.021
993
IMM073 Immunoglobulin a Vasculitis 29 0.021
994
c DMN006 Diamond-Blackfan Anemia 3 29 0.021
995
BRW006 Brown Syndrome 29 0.021
996
P ENC021 Encephalopathy, Neonatal Severe 29 0.021
997
ATM016 Autoimmune Disease of Skin and Connective Tissue 29 0.021
998
c DRR009 Diarrhea 6 29 0.021
999
HYP377 Hypomyelination, Global Cerebral 29 0.021
1000
BNM010 Bone Marrow Failure Syndrome 1 29 0.021
1001
c MNT149 Mental Retardation, X-Linked 3 29 0.021
1002
ACT114 Acute Myeloblastic Leukemia Without Maturation 29 0.021
1003
FRN030 Frontotemporal Dementia with Parkinsonism-17 29 0.021
1004
c DMN018 Diamond-Blackfan Anemia 5 29 0.021
1005
CRB005 Cerebral Arteritis 29 0.021
1006
PHY001 Physiological Polycythemia 28 0.021
1007
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.021
1008
c NRB015 Neuroblastoma 2 28 0.021
1009
TMR001 Tumor of Exocrine Pancreas 28 0.021
1010
RDT005 Radiation Induced Cancer 28 0.021
1011
c NRB014 Neuroblastoma 3 28 0.021
1012
c PNC111 Pancreatic Cancer 2 28 0.021
1013
BRS061 Breast Sarcoma 28 0.021
1014
THY042 Thymic Epithelial Tumor 28 0.021
1015
ACT003 Acute Kidney Tubular Necrosis 28 0.021
1016
GLC043 Glucocorticoid Deficiency 2 28 0.021
1017
PHG002 Phagocyte Bactericidal Dysfunction 28 0.021
1018
THY024 Thymus Adenocarcinoma 28 0.021
1019
c MCR161 Macroglobulinemia, Waldenstrom 1 27 0.021
1020
IMM038 Immunodeficiency, Common Variable, 1 27 0.021
1021
c CHR316 Charcot-Marie-Tooth Neuropathy X 27 0.021
1022
c DMN019 Diamond-Blackfan Anemia 4 27 0.021
1023
IMM070 Immunodeficiency 13 27 0.021
1024
CRB018 Cerebral Lipidosis 27 0.021
1025
BRS031 Breast Rhabdomyosarcoma 27 0.021
1026
c INF122 Infantile Krabbe Disease 27 0.021
1027
c DMN029 Diamond-Blackfan Anemia 11 27 0.021
1028
MTC016 Mitochondrial Neurogastrointestinal Encephalopathy Disease 27 0.021
1029
EPT007 Epithelial Malignant Thymoma 27 0.021
1030
c THR102 Thrombocytopenia 5 27 0.021
1031
c DMN028 Diamond-Blackfan Anemia 12 27 0.021
1032
c THR048 Thrombocytopenia 4 26 0.021
1033
DFN003 Deafness and Hereditary Hearing Loss 26 0.021
1034
c DMN022 Diamond-Blackfan Anemia 9 26 0.021
1035
c DMN020 Diamond-Blackfan Anemia 8 26 0.021
1036
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 26 0.021
1037
HRN022 Hearing Loss/deafness 26 0.021
1038
NMN003 Niemann–pick Disease 26 0.021
1039
YNG002 Young Syndrome 26 0.021
1040
c THR086 Thrombocythemia 3 25 0.021
1041
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 25 0.021
1042
P MCL022 Mucolipidoses 25 0.021
1043
P SML002 Small Cell Sarcoma 25 0.021
1044
c INF145 Infantile Liver Failure Syndrome 1 25 0.021
1045
BNM011 Bone Marrow Failure Syndrome 2 25 0.021
1046
MYL048 Myelodysplasia and Leukemia Syndrome with Monosomy 7 25 0.021
1047
c JVN019 Juvenile Temporal Arteritis 24 0.021
1048
c PRM200 Primary Fanconi Syndrome 24 0.021
1049
c TST017 Testicular Malignant Germ Cell Cancer 24 0.021
1050
c DBT059 Diabetes Mellitus, Insulin-Dependent, 8 24 0.021
1051
c DFN194 Deafness, X-Linked 1 24 0.021
1052
c INF138 Infantile Liver Failure Syndrome 2 24 0.021
1053
c MTC074 Metachromatic Leukodystrophy, Adult Form 23 0.021
1054
ERY051 Erythroleukemia, Familial 23 0.021
1055
PLM015 Pulmonary Systemic Sclerosis 23 0.021
1056
IND005 Indolent B Cell Lymphoma 23 0.021
1057
c PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 22 0.021
1058
GRM003 German Syndrome 22 0.021
1059
GRW032 Growth Factors, Combined Defect of 22 0.021
1060
ARG006 Aregenerative Anemia 22 0.021
1061
c DMN005 Diamond-Blackfan Anemia 2 22 0.021
1062
c PRC018 Precursor T-Lymphoblastic Lymphoma/leukemia 22 0.021
1063
c SYS066 Systemic Polyarteritis Nodosa 22 0.021
1064
ACT234 Acute Myeloid Leukemia with Minimal Differentiation 22 0.021
1065
RCM004 Recombinant 8 Syndrome 22 0.021
1066
SML025 Small Non-Cleaved Cell Lymphoma 22 0.021
1067
c RHB021 Rhabdomyosarcoma, Embryonal, 2 21 0.021
1068
OPP001 Opportunistic Bacterial Infectious Disease 21 0.021
1069
OVR015 Ovarian Mixed Germ Cell Neoplasm 21 0.021
1070
MND006 Mondor Disease 21 0.021
1071
c PNC105 Pancreatic Agenesis 2 21 0.021
1072
ADL082 Adult Pulmonary Langerhans Cell Histiocytosis 21 0.021
1073
c PRX067 Paroxysmal Nocturnal Hemoglobinuria 2 21 0.021
1074
ESN014 Eosinophilic Enteropathy 21 0.021
1075
c DBT077 Diabetes Mellitus, Insulin-Dependent, 19 20 0.021
1076
c WLM005 Wilms Tumor 2 20 0.021
1077
RFR007 Refractory Anemia with Excess Blasts in Transformation 20 0.021
1078
TCR004 Tacrolimus Dose Selection 20 0.021
1079
DFF029 Diffuse Large B-Cell Lymphoma of the Central Nervous System 20 0.021
1080
c DMN030 Diamond-Blackfan Anemia 13 20 0.021
1081
c JVN046 Juvenile Polymyositis 20 0.021
1082
c THR110 Thrombocytopenia 6 20 0.021
1083
ACT228 Acute Radiation Syndrome 20 0.021
1084
c MNT223 Mental Retardation, X-Linked 100 19 0.021
1085
c ADL093 Adult Acute Monocytic Leukemia 19 0.021
1086
c WLM011 Wilms Tumor 6 19 0.021
1087
c RFS003 Refsum Disease, Infantile Form 18 0.021
1088
CNT010 Central Nervous System Hematologic Cancer 18 0.021
1089
c THY085 Thymoma Type a 18 0.021
1090
c