Search results for Adenosine

1714 hits were found for Adenosine

# Family MCID Name MIFTS Score
1
ADN001 Adenosine Deaminase Deficiency 47 8.651
2
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 46 8.336
3
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 32 6.409
4
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 47 5.105
5
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 45 4.979
6
ADN039 Adenosine Triphosphate, Elevated, of Erythrocytes 19 4.968
7
ADN079 Adenosine Triphosphatase Deficiency, Anemia Due to 9 3.537
8
ADN084 Adenosine Deaminase, Elevated, Hemolytic Anemia Due to 11 2.943
9
SVR066 Severe Combined Immunodeficiency, X-Linked 65 2.068
10
c HML041 Hemolytic Anemia Due to Erythrocyte Adenosine Deaminase Overproduction 6 2.052
11
OBS267 Obsolete: Anemia Due to Adenosine Triphosphatase Deficiency 2 2.052
12
TNG002 Tangier Disease 65 2.042
13
ERY039 Erythrocyte Amp Deaminase Deficiency 20 2.031
14
PRT037 Pertussis 65 0.377
15
SVR004 Severe Combined Immunodeficiency 73 0.333
16
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.330
17
ISC004 Ischemia 60 0.307
18
CHL014 Cholera 55 0.298
19
HYP266 Hypoxia 56 0.277
20
P CRN018 Coronary Artery Anomaly 63 0.249
21
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.243
22
ART140 Arteries, Anomalies of 53 0.238
23
ATR057 Atrioventricular Block 55 0.237
24
IMM167 Immune Deficiency Disease 78 0.233
25
CRN030 Coronary Stenosis 50 0.214
26
P NRB001 Neuroblastoma 71 0.207
27
ANX004 Anoxia 42 0.175
28
P SZR006 Seizure Disorder 58 0.174
29
VSL002 Visual Epilepsy 58 0.174
30
P ATR011 Atrial Fibrillation 66 0.170
31
PLR008 Pleurisy 51 0.170
32
PLR001 Pleural Tuberculosis 50 0.170
33
P MYC084 Mycobacterium Tuberculosis 1 68 0.167
34
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.161
35
P MNN013 Meningitis 65 0.161
36
P CRD119 Cardiac Arrest 67 0.156
37
c ACT075 Acute Myocardial Infarction 56 0.156
38
ANG054 Angina Pectoris 66 0.155
39
CNG034 Congestive Heart Failure 70 0.154
40
P CRN300 Coronary Heart Disease 1 63 0.152
41
P HRT032 Heart Disease 75 0.151
42
LNG099 Lung Disease 61 0.151
43
48X005 48,xyyy 39 0.151
44
GLL048 Glial Tumor 45 0.149
45
P PHC003 Pheochromocytoma 71 0.148
46
P GLM045 Glioma 63 0.148
47
ADR040 Adrenal Gland Pheochromocytoma 46 0.148
48
TBR011 Tuberculous Meningitis 48 0.144
49
P LYM031 Lymphocytic Leukemia 55 0.142
50
P HNT016 Huntington Disease 71 0.141
51
SYN036 Syncope 45 0.140
52
P PRK057 Parkinson Disease, Late-Onset 76 0.139
53
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.137
54
P LKM002 Leukemia 66 0.136
55
AST005 Asthma 77 0.135
56
P PLM037 Pulmonary Hypertension 68 0.134
57
SPN186 Spinal Cord Injury 60 0.134
58
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.133
59
P MYC007 Myocardial Infarction 70 0.132
60
PRT036 Peritonitis 65 0.130
61
P AST007 Astrocytoma 50 0.129
62
HYP066 Hyperglycemia 61 0.128
63
WLF001 Wolff-Parkinson-White Syndrome 65 0.127
64
HLX001 Helix Syndrome 47 0.127
65
MYC005 Myocardial Stunning 46 0.127
66
LYM027 Lymphopenia 57 0.125
67
P TRM003 Tremor 53 0.125
68
CRB004 Cerebral Artery Occlusion 44 0.125
69
P KDN018 Kidney Disease 70 0.124
70
PLM001 Pulmonary Tuberculosis 70 0.124
71
HYP056 Hypoglycemia 66 0.124
72
BRN071 Brain Injury 49 0.124
73
c ACT071 Acute Kidney Failure 59 0.123
74
CYT002 Cytokine Deficiency 44 0.123
75
ALL026 Allergic Hypersensitivity Disease 64 0.121
76
c PRC016 Pre-Eclampsia 63 0.120
77
BNR002 Bone Resorption Disease 48 0.115
78
P BRS047 Breast Cancer 96 0.113
79
CYS001 Cystic Fibrosis 80 0.113
80
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.113
81
GLB015 Glioblastoma Multiforme 75 0.112
82
P HYP086 Hypothyroidism 68 0.112
83
P LVR013 Liver Disease 68 0.112
84
P HYP076 Hyperthyroidism 55 0.112
85
TRM010 Traumatic Brain Injury 53 0.112
86
P CLR023 Colorectal Cancer 98 0.110
87
P OVR042 Ovarian Cancer 89 0.110
88
P HML002 Hemolytic Anemia 62 0.110
89
ATM095 Autoimmune Disease 61 0.110
90
P RHM011 Rheumatoid Arthritis 80 0.109
91
LVR012 Liver Cirrhosis 63 0.109
92
P HYP069 Hyperparathyroidism 62 0.109
93
c HYP595 Hypertension, Essential 84 0.107
94
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.107
95
P RHN004 Rhinitis 57 0.107
96
c MCR113 Microvascular Complications of Diabetes 3 52 0.106
97
P CHR345 Chronic Pain 50 0.106
98
c MCR120 Microvascular Complications of Diabetes 7 47 0.106
99
c MCR130 Microvascular Complications of Diabetes 6 41 0.106
100
c MCR133 Microvascular Complications of Diabetes 4 41 0.106
101
DPR016 Depression 63 0.104
102
P ADN016 Adenocarcinoma 64 0.103
103
P VSC007 Vascular Disease 63 0.103
104
FTT001 Fatty Liver Disease 61 0.103
105
PLM010 Pulmonary Edema 55 0.103
106
c LKM071 Leukemia, Chronic Lymphocytic 79 0.101
107
P LYM118 Lymphoma 68 0.101
108
ALL003 Allergic Rhinitis 67 0.101
109
P EPL164 Epilepsy 71 0.100
110
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.100
111
P DBT009 Diabetes Mellitus 64 0.100
112
ATH013 Atherosclerosis Susceptibility 66 0.098
113
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.098
114
PNG002 Pain Agnosia 51 0.098
115
c SYS001 Systemic Lupus Erythematosus 86 0.096
116
OST159 Osteogenic Sarcoma 66 0.096
117
ADN018 Adenoma 58 0.096
118
GST033 Gestational Diabetes 57 0.096
119
ALL006 Allergic Asthma 56 0.096
120
TBR008 Tuberculous Peritonitis 36 0.096
121
INS024 Insulin-Like Growth Factor I 79 0.095
122
P VSC011 Vasculitis 62 0.095
123
ANX010 Anxiety 72 0.093
124
HMN044 Human Immunodeficiency Virus Type 1 71 0.093
125
P MCR115 Microvascular Complications of Diabetes 5 66 0.093
126
CLT003 Colitis 62 0.093
127
STT001 Status Epilepticus 59 0.093
128
LFT001 Left Bundle Branch Hemiblock 49 0.093
129
CHR074 Choriocarcinoma 46 0.093
130
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.091
131
DFC004 Deficiency Anemia 75 0.091
132
IDP011 Idiopathic Interstitial Pneumonia 63 0.091
133
P PSR002 Psoriasis 62 0.091
134
P NRP001 Neuropathy 56 0.091
135
PST011 Pustulosis of Palm and Sole 52 0.091
136
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.090
137
c ATR087 Atrial Standstill 1 74 0.090
138
c HYP836 Hypercholesterolemia, Familial, 1 72 0.090
139
TTN003 Tetanus 64 0.090
140
P PLM036 Pulmonary Fibrosis 61 0.090
141
TXC005 Toxic Shock Syndrome 61 0.090
142
P SCK005 Sickle Cell Disease 50 0.090
143
P HRP006 Herpes Simplex 65 0.088
144
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.088
145
c PRM005 Primary Hyperparathyroidism 58 0.088
146
PRC013 Pericarditis 54 0.088
147
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.086
148
P NTR004 Neutropenia 63 0.086
149
INT007 Intermediate Coronary Syndrome 55 0.086
150
HYP060 Hyperinsulinism 54 0.086
151
IMP005 Impotence 52 0.086
152
PLR007 Pleural Empyema 49 0.086
153
P LNG032 Lung Cancer 97 0.084
154
P ALZ034 Alzheimer Disease 88 0.084
155
P MSC005 Muscular Dystrophy 66 0.084
156
ANR040 Aneurysm 58 0.084
157
OCL069 Ocular Motor Apraxia 51 0.084
158
P ART022 Arthritis 70 0.082
159
MLN008 Melanoma 69 0.082
160
P LKM062 Leukemia, Acute Lymphoblastic 68 0.082
161
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.082
162
P GRV001 Graves' Disease 55 0.082
163
P SCK002 Sick Sinus Syndrome 55 0.082
164
DBT010 Diabetic Neuropathy 55 0.082
165
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.082
166
ALC007 Alcohol Dependence 66 0.080
167
P HYP098 Hypereosinophilic Syndrome 66 0.080
168
c ACT073 Acute Leukemia 58 0.080
169
P INF037 Inflammatory Bowel Disease 56 0.080
170
P TMP001 Temporal Lobe Epilepsy 50 0.080
171
VCC001 Vaccinia 49 0.080
172
SLP001 Sleeping Sickness 48 0.080
173
PTT037 Pituitary Tumors 44 0.080
174
VLK001 Volkmann Contracture 32 0.080
175
c MGR028 Migraine with or Without Aura 1 69 0.078
176
P SLP005 Sleep Disorder 59 0.078
177
P DRR001 Diarrhea 57 0.078
178
c BCT007 Bacterial Meningitis 55 0.078
179
P LTR001 Lateral Sclerosis 53 0.078
180
MTB004 Metabolic Acidosis 50 0.078
181
ALL014 Allergic Encephalomyelitis 39 0.078
182
MYL069 Myeloma, Multiple 85 0.076
183
P GST053 Gastric Cancer 83 0.076
184
c DLT002 Dilated Cardiomyopathy 79 0.076
185
c CHR684 Chronic Kidney Disease 66 0.076
186
P LPS004 Lupus Erythematosus 61 0.076
187
THY029 Thyroid Carcinoma 59 0.076
188
IGR001 Ige Responsiveness, Atopic 59 0.076
189
P PLY017 Polyarteritis Nodosa 58 0.076
190
P PNC025 Panic Disorder 53 0.076
191
P PRC012 Pericardial Effusion 51 0.076
192
P TCL004 T-Cell Leukemia 47 0.076
193
MST004 Mast Cell Neoplasm 38 0.076
194
EXT007 Extracutaneous Mastocytoma 38 0.076
195
P HPT023 Hepatocellular Carcinoma 100 0.074
196
STR067 Stroke, Ischemic 80 0.074
197
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.074
198
P SRC025 Sarcoidosis 1 70 0.074
199
LSH001 Leishmaniasis 63 0.074
200
ACQ007 Acquired Immunodeficiency Syndrome 60 0.074
201
END030 End Stage Renal Failure 58 0.074
202
STM007 Stomatitis 49 0.074
203
P KLZ004 Kala-Azar 1 41 0.074
204
PPL052 Papillomatosis, Confluent and Reticulated 34 0.074
205
P BLD134 Bladder Cancer 78 0.072
206
c FML001 Familial Atrial Fibrillation 66 0.072
207
P DRM053 Dermatitis, Atopic 66 0.072
208
TYP007 Typhoid Fever 63 0.072
209
LPD008 Lipid Metabolism Disorder 62 0.072
210
TRN015 Transient Cerebral Ischemia 62 0.072
211
P MVM001 Movement Disease 61 0.072
212
c ACT027 Acute Pancreatitis 59 0.072
213
P BCL017 B-Cell Lymphoma 58 0.072
214
ERY051 Erythroleukemia, Familial 56 0.072
215
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 0.072
216
47X002 47,xyy 49 0.072
217
P BNG032 Benign Mesothelioma 45 0.072
218
APN006 Apnea of Prematurity 23 0.072
219
P PRS040 Prostate Cancer 97 0.069
220
P MLT020 Multiple Sclerosis 72 0.069
221
DRM006 Dermatitis 61 0.069
222
P ENC004 Encephalitis 61 0.069
223
MSL001 Measles 61 0.069
224
SQM006 Squamous Cell Carcinoma 60 0.069
225
IRN002 Iron Metabolism Disease 57 0.069
226
P GST044 Gastritis 55 0.069
227
P DBT005 Diabetes Insipidus 55 0.069
228
GSG001 Gas Gangrene 50 0.069
229
SNT005 Sinoatrial Node Disease 49 0.069
230
RNL077 Renal Fibrosis 47 0.069
231
CTY001 Cat Eye Syndrome 44 0.069
232
CRB086 Cerebral Aneurysms 40 0.069
233
CRB039 Cerebrovascular Disease 69 0.067
234
P ATS364 Autism 65 0.067
235
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.067
236
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 0.067
237
P MYL006 Myeloid Leukemia 60 0.067
238
MNT002 Mental Depression 57 0.067
239
OCL006 Ocular Hypertension 53 0.067
240
HMP001 Hemopericardium 46 0.067
241
CRT015 Carotid Artery Occlusion 44 0.067
242
MLR004 Malaria 80 0.065
243
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.065
244
P ENC018 Encephalopathy 61 0.065
245
P ALC033 Alcohol Use Disorder 58 0.065
246
P UVT001 Uveitis 57 0.065
247
P GLM007 Glomerulonephritis 57 0.065
248
P PSD015 Pseudohypoparathyroidism 56 0.065
249
HYP005 Hypokalemia 55 0.065
250
P RST001 Restless Legs Syndrome 54 0.065
251
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.065
252
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.065
253
WTH001 Withdrawal Disorder 48 0.065
254
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.065
255
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.065
256
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.065
257
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.065
258
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.065
259
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.065
260
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.065
261
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.065
262
LWC001 Low Compliance Bladder 42 0.065
263
PRC005 Pericardial Tuberculosis 33 0.065
264
P PNC035 Pancreatic Cancer 84 0.062
265
OST012 Osteoarthritis 78 0.062
266
P SCH015 Schizophrenia 75 0.062
267
MSC157 Muscular Dystrophy, Duchenne Type 71 0.062
268
P SYS005 Systemic Scleroderma 70 0.062
269
P SLP006 Sleep Apnea 69 0.062
270
P MJR001 Major Depressive Disorder 68 0.062
271
P THR014 Thrombocytopenia 68 0.062
272
P PNM007 Pneumonia 68 0.062
273
c ATS007 Autism Spectrum Disorder 67 0.062
274
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.062
275
DPH001 Diphtheria 60 0.062
276
PPT005 Peptic Ulcer Disease 58 0.062
277
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.062
278
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.062
279
BCT022 Bacterial Infectious Disease 56 0.062
280
AGN016 Aging 56 0.062
281
c SVR001 Severe Acute Respiratory Syndrome 55 0.062
282
AMN003 Amnestic Disorder 54 0.062
283
GTR002 Goiter 52 0.062
284
c VRL010 Viral Hepatitis 51 0.062
285
P ECL001 Eclampsia 51 0.062
286
ASP003 Aseptic Meningitis 51 0.062
287
RTN020 Retinal Vascular Disease 48 0.062
288
DYS022 Dyschromatosis Symmetrica Hereditaria 48 0.062
289
CMB081 Combined Immunodeficiency, X-Linked 48 0.062
290
PRP007 Priapism 48 0.062
291
CRN019 Coronary Artery Vasospasm 46 0.062
292
RST023 Resting Heart Rate, Variation in 41 0.062
293
SCN049 Second-Degree Atrioventricular Block 36 0.062
294
P LNG064 Lung Cancer Susceptibility 3 77 0.059
295
ULC004 Ulcerative Colitis 73 0.059
296
PRP027 Peripheral Vascular Disease 71 0.059
297
BRN024 Bronchitis 68 0.059
298
P LPR021 Leprosy 3 67 0.059
299
P ART005 Arteriovenous Malformation 65 0.059
300
P DYS154 Dystonia 65 0.059
301
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.059
302
LSC001 Lesch-Nyhan Syndrome 62 0.059
303
MDD011 Mood Disorder 62 0.059
304
CHL068 Cholestasis 60 0.059
305
c PRG043 Progressive Familial Heart Block, Type Ib 58 0.059
306
P CRD246 Cardiovascular System Disease 56 0.059
307
INT030 Intracranial Aneurysm 56 0.059
308
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.059
309
HYP014 Hyperuricemia 51 0.059
310
RTN003 Retinal Ischemia 50 0.059
311
NTR046 Neutrophil Migration 50 0.059
312
URT010 Ureteral Obstruction 46 0.059
313
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.059
314
c PCH010 Pachyonychia Congenita 3 43 0.059
315
HNS001 Hansen's Disease 34 0.059
316
ESP021 Esophageal Cancer 90 0.057
317
P GRF003 Graft-Versus-Host Disease 71 0.057
318
c LKM063 Leukemia, Chronic Myeloid 71 0.057
319
RCK004 Rickets 69 0.057
320
P MYS003 Myasthenia Gravis 68 0.057
321
P HYP061 Hypertrophic Cardiomyopathy 66 0.057
322
SRC014 Sarcoma 65 0.057
323
c SML038 Small Cell Cancer of the Lung 65 0.057
324
CLN015 Colon Adenocarcinoma 63 0.057
325
SKN016 Skin Disease 63 0.057
326
P TXP001 Toxoplasmosis 60 0.057
327
INS001 Insulinoma 60 0.057
328
P BND020 Bone Disease 59 0.057
329
P DNG005 Dengue Virus 57 0.057
330
P PRP019 Peripheral Nervous System Disease 57 0.057
331
P BPL003 Bipolar Disorder 56 0.057
332
P HYP024 Hypoparathyroidism 55 0.057
333
P MYP006 Myopia 55 0.057
334
GST023 Gastric Ulcer 53 0.057
335
TRY001 Trypanosomiasis 50 0.057
336
HYP017 Hypophosphatemia 49 0.057
337
c BCT013 Bacterial Pneumonia 47 0.057
338
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.057
339
HMP009 Haemophilus Influenzae 42 0.057
340
RDC006 Red Cell Aplasia 42 0.057
341
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.057
342
c MJR024 Major Affective Disorder 9 41 0.057
343
OVR094 Ovarian Epithelial Cancer 38 0.057
344
c MJR022 Major Affective Disorder 8 38 0.057
345
c LKM061 Leukemia, Acute Myeloid 83 0.054
346
P RSP003 Respiratory Failure 74 0.054
347
c HPT073 Hepatitis C Virus 70 0.054
348
P MLG056 Malignant Hyperthermia 67 0.054
349
P MYP004 Myopathy 64 0.054
350
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.054
351
GT001 Gout 63 0.054
352
c SCL052 Scleroderma, Familial Progressive 62 0.054
353
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.054
354
c BRN108 Branchiootic Syndrome 1 61 0.054
355
P INF032 Infertility 57 0.054
356
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.054
357
P EXN002 Exanthem 57 0.054
358
THR024 Thrombosis 56 0.054
359
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.054
360
BRN004 Brain Edema 55 0.054
361
VSC003 Visceral Leishmaniasis 55 0.054
362
HMC014 Homocysteinemia 53 0.054
363
SPN035 Spindle Cell Sarcoma 51 0.054
364
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.054
365
CRD137 Cardiogenic Shock 48 0.054
366
RGH001 Right Bundle Branch Block 47 0.054
367
c ATM099 Autoimmune Uveitis 44 0.054
368
HPT004 Hepatic Coma 43 0.054
369
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.051
370
CRV035 Cervical Cancer 76 0.051
371
P CNR004 Cone-Rod Dystrophy 2 71 0.051
372
P DMN001 Diamond-Blackfan Anemia 69 0.051
373
P CHR012 Chronic Granulomatous Disease 67 0.051
374
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.051
375
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.051
376
P THY023 Thymoma 65 0.051
377
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.051
378
CHC001 Chickenpox 60 0.051
379
INT066 Interstitial Lung Disease 59 0.051
380
P PLY014 Polycystic Kidney Disease 59 0.051
381
BRN002 Bronchiolitis 59 0.051
382
c ESS001 Essential Tremor 56 0.051
383
P FBR017 Fibrosarcoma 56 0.051
384
P ALP008 Alopecia 56 0.051
385
RHM027 Rheumatic Disease 56 0.051
386
c GRV008 Graves Disease 1 55 0.051
387
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.051
388
HRY003 Hairy Cell Leukemia 55 0.051
389
c THY107 Thymoma, Familial 54 0.051
390
PRP016 Paraplegia 53 0.051
391
P THY032 Thyroiditis 53 0.051
392
PRS045 Prostatic Hypertrophy 52 0.051
393
NNL006 Non-Alcoholic Steatohepatitis 51 0.051
394
ATS010 Autosomal Recessive Disease 48 0.051
395
P PRR002 Pure Red-Cell Aplasia 48 0.051
396
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.051
397
LYM019 Lymphosarcoma 47 0.051
398
AGR002 Agoraphobia 44 0.051
399
ASP030 Aspirin Resistance 40 0.051
400
PLY150 Polykaryocytosis Inducer 31 0.051
402
c SPN225 Spondyloarthropathy 1 73 0.047
403
P RTN024 Retinoblastoma 72 0.047
404
DWN001 Down Syndrome 70 0.047
405
c EXD008 Exudative Vitreoretinopathy 1 69 0.047
406
ART016 Aortic Aneurysm 68 0.047
407
BRK010 Burkitt Lymphoma 67 0.047
408
c MCR129 Microvascular Complications of Diabetes 1 66 0.047
409
P LNG028 Long Qt Syndrome 65 0.047
410
P PRD008 Periodontitis 62 0.047
411
P PRP029 Porphyria 62 0.047
412
CRD223 Cardiac Arrhythmia 60 0.047
413
P MYC008 Myocarditis 59 0.047
414
P CYS018 Cystitis 59 0.047
415
PLM033 Pulmonary Embolism 59 0.047
416
CRD132 Cardiac Conduction Defect 59 0.047
417
P BRS044 Breast Adenocarcinoma 59 0.047
418
CMP010 Complex Regional Pain Syndrome 58 0.047
419
PST028 Post-Traumatic Stress Disorder 58 0.047
420
P OPT006 Optic Nerve Disease 57 0.047
421
c MST023 Mesothelioma, Malignant 57 0.047
422
c ADL017 Adult T-Cell Leukemia 57 0.047
423
P MLN007 Male Infertility 56 0.047
424
P PLY011 Polycystic Ovary Syndrome 56 0.047
425
BRN012 Bronchiolitis Obliterans 56 0.047
426
LMB062 Limb Ischemia 55 0.047
427
P ART021 Arteriosclerosis 54 0.047
428
P MNC007 Monocytic Leukemia 54 0.047
429
c FML008 Familial Retinoblastoma 53 0.047
430
THR013 Thoracic Outlet Syndrome 53 0.047
431
PRS021 Prostatic Adenoma 51 0.047
432
c ACT134 Acute Liver Failure 51 0.047
433
CLR109 Colorectal Adenocarcinoma 50 0.047
434
P RNV001 Renovascular Hypertension 49 0.047
435
ATX019 Ataxia with Vitamin E Deficiency 48 0.047
436
ACT084 Acute Stress Disorder 48 0.047
437
c INH020 Inherited Metabolic Disorder 46 0.047
438
CRB090 Cerebral Hypoxia 43 0.047
439
P HYP265 Hypotonia 42 0.047
440
MRP001 Morphine Dependence 41 0.047
441
OCL010 Ocular Hypotension 38 0.047
442
ARG004 Argyria 28 0.047
443
ADG002 Audiogenic Seizures 26 0.047
444
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.047
445
P OST002 Osteoporosis 73 0.044
446
SCK003 Sickle Cell Anemia 72 0.044
447
PNC129 Pancreatic Adenocarcinoma 67 0.044
448
c JVN010 Juvenile Rheumatoid Arthritis 67 0.044
449
P AGM001 Agammaglobulinemia 65 0.044
450
c RHB024 Rhabdomyosarcoma 2 65 0.044
451
P END044 Endometriosis 62 0.044
452
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.044
453
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.044
454
INT002 Intermittent Claudication 61 0.044
455
P INT143 Interstitial Cystitis 61 0.044
456
c PNS012 Paine Syndrome 61 0.044
457
P KDN017 Kidney Cancer 61 0.044
458
P PNC044 Pancreatitis 61 0.044
459
P HRD011 Hereditary Spherocytosis 60 0.044
460
P TRC086 Trichohepatoenteric Syndrome 1 59 0.044
461
EYD002 Eye Disease 58 0.044
462
TRD006 Tardive Dyskinesia 55 0.044
463
WST005 West Nile Virus 55 0.044
464
GLC003 Glucose Intolerance 54 0.044
465
FCL014 Focal Epilepsy 54 0.044
466
NRT004 Neuritis 53 0.044
467
HRT012 Heart Valve Disease 53 0.044
468
PRN011 Pernicious Anemia 52 0.044
469
P NRC002 Narcolepsy 51 0.044
470
PRT029 Parathyroid Adenoma 50 0.044
471
P DDN001 Duodenal Ulcer 50 0.044
472
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.044
473
OPT003 Opiate Dependence 50 0.044
474
PRS129 Prostatic Hyperplasia, Benign 49 0.044
475
BHR001 Behr Syndrome 49 0.044
476
URM002 Uremia 49 0.044
477
c HPT015 Hepatitis D 49 0.044
478
ENT004 Enthesopathy 48 0.044
479
c VRL012 Viral Meningitis 48 0.044
480
CRY014 Cryptococcal Meningitis 48 0.044
481
ADR016 Adrenal Cortical Carcinoma 48 0.044
482
TRT001 Teratocarcinoma 46 0.044
483
HDN002 Head Injury 45 0.044
484
THR099 Third-Degree Atrioventricular Block 45 0.044
485
ATN004 Autonomic Neuropathy 44 0.044
486
HYP003 Hypermethioninemia 44 0.044
487
P LYD001 Leydig Cell Tumor 43 0.044
488
c MCR112 Microvascular Complications of Diabetes 2 41 0.044
489
c PRG020 Paragangliomas 3 38 0.044
490
ADR004 Adrenal Cortical Adenocarcinoma 38 0.044
491
P GLM040 Glioma Susceptibility 1 81 0.040
492
END057 Endometrial Cancer 74 0.040
493
CRH001 Crohn's Disease 74 0.040
494
CRB037 Cerebral Palsy 68 0.040
495
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 67 0.040
496
CHL065 Cholangiocarcinoma 67 0.040
497
CMM004 Common Variable Immunodeficiency 67 0.040
498
CHG001 Chagas Disease 66 0.040
499
KWS002 Kawasaki Disease 64 0.040
500
NRM005 Neuromuscular Disease 63 0.040
501
P ADL010 Adult Respiratory Distress Syndrome 63 0.040
502
ART002 Arts Syndrome 63 0.040
503
NTR005 Nutritional Deficiency Disease 61 0.040
504
P HYP750 Hypertriglyceridemia, Familial 61 0.040
505
VRL011 Viral Infectious Disease 61 0.040
506
PRT013 Portal Hypertension 60 0.040
507
HPT019 Hepatic Encephalopathy 60 0.040
508
YLL002 Yellow Fever 60 0.040
509
ORL011 Oral Cancer 60 0.040
510
P THL005 Thalassemia 60 0.040
511
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.040
512
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.040
513
c HPT016 Hepatitis B 59 0.040
514
THY122 Thyroid Gland Cancer 58 0.040
515
CNS004 Constipation 57 0.040
516
DSS009 Disseminated Intravascular Coagulation 57 0.040
517
BRN056 Bronchopulmonary Dysplasia 57 0.040
518
PLG002 Plague 57 0.040
519
VSC002 Vascular Dementia 57 0.040
520
P CHN012 Chondrosarcoma 56 0.040
521
DFF005 Diffuse Large B-Cell Lymphoma 56 0.040
522
SYN007 Synovitis 55 0.040
523
P SBS003 Substance Abuse 54 0.040
524
PPL022 Papilloma 54 0.040
525
P HMC002 Homocystinuria 54 0.040
526
PNC001 Pancytopenia 54 0.040
527
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.040
528
NNT012 Neonatal Jaundice 53 0.040
529
P PLM006 Pulmonary Alveolar Proteinosis 52 0.040
530
c DMN023 Diamond-Blackfan Anemia 1 52 0.040
531
TRC003 Trichomoniasis 52 0.040
532
P FBR031 Febrile Seizures 51 0.040
533
INT079 Intrahepatic Cholangiocarcinoma 50 0.040
534
VLV047 Volvulus of Midgut 50 0.040
535
ILT001 Ileitis 50 0.040
536
P OVR082 Overgrowth Syndrome 50 0.040
537
P ALP061 Alopecia, Androgenetic, 1 49 0.040
538
HMG002 Hemoglobinuria 49 0.040
539
BCT004 Bacteriuria 48 0.040
540
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.040
541
EPD015 Epidemic Typhus 46 0.040
542
c MLG068 Malignant Glioma 45 0.040
543
NWC001 Newcastle Disease 44 0.040
544
AND014 Androgenic Alopecia 44 0.040
545
c RTN047 Retinitis Pigmentosa 18 44 0.040
546
SQM002 Squamous Cell Papilloma 42 0.040
547
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.040
548
THR035 Thrombasthenia 41 0.040
549
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.040
550
HRN029 Hearing Loss, Noise-Induced 37 0.040
552
CHL079 Children's Interstitial Lung Disease 27 0.040
553
HSB001 His Bundle Tachycardia 25 0.040
554
URT049 Urate Oxidase, Pseudogene 25 0.040
555
PFF001 Pfeiffer Syndrome 79 0.036
556
c TBR025 Tuberous Sclerosis 1 76 0.036
557
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.036
558
c BTT014 Beta-Thalassemia 72 0.036
559
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.036
560
P OST001 Osteopetrosis 71 0.036
561
WLS001 Wilson Disease 70 0.036
562
P TBR001 Tuberous Sclerosis 70 0.036
563
GST040 Gastric Adenocarcinoma 70 0.036
564
MYL009 Myelodysplastic Syndrome 70 0.036
565
BHC003 Behcet Syndrome 70 0.036
566
LYM133 Lymphoma, Hodgkin, Classic 69 0.036
567
P HPT021 Hepatitis 67 0.036
568
CNN005 Connective Tissue Disease 66 0.036
569
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.036
570
OMN001 Omenn Syndrome 66 0.036
571
MYC006 Mycosis Fungoides 66 0.036
572
P HYD006 Hydrocephalus 65 0.036
573
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.036
574
P TRN020 Turner Syndrome 65 0.036
575
P MTR014 Motor Neuron Disease 64 0.036
576
HYP020 Hyperprolactinemia 64 0.036
577
c HPT001 Hepatitis C 63 0.036
578
P NPH012 Nephrotic Syndrome 63 0.036
579
c HPT003 Hepatitis a 63 0.036
580
P RHB003 Rhabdomyosarcoma 62 0.036
581
P ART023 Arthropathy 62 0.036
582
HSH003 Hashimoto Thyroiditis 62 0.036
583
c WLM018 Wilms Tumor 5 62 0.036
584
c ATM011 Autoimmune Hepatitis 62 0.036
585
CTN007 Cutaneous Leishmaniasis 61 0.036
586
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.036
587
P SNS001 Sensorineural Hearing Loss 61 0.036
588
P CTR002 Cataract 60 0.036
589
RTN017 Retinal Detachment 60 0.036
590
ETN001 Eating Disorder 59 0.036
591
PRT058 Pure Autonomic Failure 59 0.036
592
CHL123 Chlamydia 59 0.036
593
ANT024 Anthrax Disease 58 0.036
594
c PRG126 Progressive Familial Heart Block 58 0.036
595
P CND004 Candidiasis 57 0.036
596
SPT004 Septic Arthritis 57 0.036
597
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.036
598
P MMP001 Mumps 57 0.036
599
BLR008 Bilirubin Metabolic Disorder 57 0.036
600
P HDC001 Headache 57 0.036
601
TRN018 Transitional Cell Carcinoma 56 0.036
602
PLS011 Plasmacytoma 56 0.036
603
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.036
604
GST050 Gastrointestinal System Disease 56 0.036
605
MCL006 Macular Retinal Edema 55 0.036
606
P ALP106 Alport Syndrome 1, X-Linked 55 0.036
607
END040 Endogenous Depression 54 0.036
608
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.036
609
LYM040 Lymphoblastic Lymphoma 54 0.036
610
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.036
611
CHK001 Chikungunya 53 0.036
612
P RTN018 Retinal Disease 52 0.036
613
SPN051 Spondylitis 52 0.036
614
c GLL024 Gallbladder Disease 1 52 0.036
615
BLD053 Blood Platelet Disease 51 0.036
616
THY030 Thyroid Gland Disease 51 0.036
617
c SCN007 Secondary Hyperparathyroidism 50 0.036
618
P ATR005 Atrophic Gastritis 50 0.036
619
HPT014 Hepatorenal Syndrome 50 0.036
620
c CHR418 Chronic Leukemia 50 0.036
621
MCR004 Macroglobulinemia 50 0.036
622
P ESN008 Eosinophilic Pneumonia 50 0.036
623
KRT002 Keratomalacia 48 0.036
624
CCN001 Cocaine Dependence 48 0.036
625
DRG003 Drug Dependence 47 0.036
626
STR089 Storage Pool Platelet Disease 47 0.036
627
CRN017 Coronary Thrombosis 47 0.036
628
PLS025 Plasmablastic Lymphoma 47 0.036
629
TCL003 T Cell Deficiency 45 0.036
630
RBF001 Riboflavin Deficiency 45 0.036
631
MYX004 Myxedema 44 0.036
632
PLR022 Pleural Disease 44 0.036
633
MNG006 Monogenic Diabetes 44 0.036
634
BRN032 Brain Glioma 43 0.036
635
c PRM038 Primary Agammaglobulinemia 43 0.036
636
ORL015 Oral Squamous Cell Carcinoma 43 0.036
637
c ATM101 Autoimmune Gastritis 43 0.036
638
CLP006 Clopidogrel Resistance 40 0.036
639
ABD004 Abdominal Tuberculosis 39 0.036
640
c OVR114 Ovarian Cancer 1 38 0.036
641
HRW001 Hair Whorl 36 0.036
642
BRK012 Broken Heart Syndrome 35 0.036
643
CHR178 Chromosomal Triplication 35 0.036
644
c BLD120 Bleeding Disorder, Platelet-Type, 8 34 0.036
645
INF009 Inflammatory Spondylopathy 32 0.036
646
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.036
647
DSR074 Disorder of Purine Metabolism 29 0.036
648
PST092 Posttransplant Acute Limbic Encephalitis 29 0.036
649
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.036
650
P ATX030 Ataxia-Telangiectasia 83 0.031
651
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.031
652
P NRF023 Neurofibromatosis, Type Ii 76 0.031
653
c THR092 Thrombophilia Due to Thrombin Defect 73 0.031
654
AGM019 Agammaglobulinemia, X-Linked 72 0.031
655
P WSK001 Wiskott-Aldrich Syndrome 71 0.031
656
OTT002 Otitis Media 71 0.031
657
ACR007 Acromegaly 71 0.031
658
THY111 Thyroid Carcinoma, Familial Medullary 67 0.031
659
P PSD087 Pseudoxanthoma Elasticum 67 0.031
660
PSY004 Psychotic Disorder 67 0.031
661
P MTR004 Maturity-Onset Diabetes of the Young 66 0.031
662
ART001 Arterial Tortuosity Syndrome 66 0.031
663
P ACR001 Aicardi-Goutieres Syndrome 65 0.031
664
DRM014 Dermatofibrosarcoma Protuberans 65 0.031
665
GST092 Gastroesophageal Reflux 65 0.031
666
APN008 Apnea, Obstructive Sleep 65 0.031
667
DBT083 Diabetes Mellitus, Permanent Neonatal 64 0.031
668
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 64 0.031
669
CLF027 Cleft Palate, Isolated 64 0.031
670
P VNW001 Von Willebrand's Disease 64 0.031
671
c MCL013 Mucolipidosis Iv 64 0.031
672
NRF007 Neurofibroma 64 0.031
673
IRR002 Irritable Bowel Syndrome 63 0.031
674
END041 Endometrial Adenocarcinoma 63 0.031
675
P ANR048 Aniridia 1 63 0.031
676
P CRN038 Carney Complex Variant 63 0.031
677
c ACT068 Acute Cystitis 63 0.031
678
ACT119 Acute Promyelocytic Leukemia 63 0.031
679
ANR007 Anorexia Nervosa 63 0.031
680
P PRM002 Primary Hyperoxaluria 62 0.031
681
PSR001 Psoriatic Arthritis 62 0.031
682
c ANM038 Anemia, Autoimmune Hemolytic 61 0.031
683
BRC012 Brucellosis 61 0.031
684
RHM001 Rheumatic Fever 61 0.031
685
ACN002 Acanthosis Nigricans 60 0.031
686
RCT015 Reactive Arthritis 60 0.031
687
HRP004 Herpes Zoster 60 0.031
688
P BRN022 Bronchiectasis 59 0.031
689
FBR047 Fibromyalgia 59 0.031
690
HLC007 Helicobacter Pylori Infection 59 0.031
691
P URT039 Urticaria 58 0.031
692
PLY023 Polycystic Liver Disease 57 0.031
693
TNS005 Tonsillitis 57 0.031
694
PLM031 Poliomyelitis 57 0.031
695
PNM008 Pneumothorax 56 0.031
696
P PLY019 Polyneuropathy 56 0.031
697
PRP030 Purpura 55 0.031
698
BRD001 Brody Myopathy 55 0.031
699
PRT038 Protein-Energy Malnutrition 54 0.031
700
P PTT006 Pituitary Adenoma 54 0.031
701
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 54 0.031
702
P SLM003 Salmonellosis 54 0.031
703
P CYS039 Cystic Kidney Disease 54 0.031
704
P FML068 Familial Hypocalciuric Hypercalcemia 54 0.031
705
HMS001 Hemosiderosis 54 0.031
706
c ACT020 Acute T Cell Leukemia 53 0.031
707
RFL001 Reflex Sympathetic Dystrophy 53 0.031
708
P RTN016 Retinal Degeneration 53 0.031
709
P ART018 Aortic Valve Insufficiency 53 0.031
710
PLS007 Plasmodium Falciparum Malaria 52 0.031
711
P INT068 Intestinal Disease 52 0.031
712
ACR041 Acromelic Frontonasal Dysostosis 52 0.031
713
DMY004 Demyelinating Disease 52 0.031
714
P ACT105 Acute Mountain Sickness 52 0.031
715
CHR073 Choreatic Disease 52 0.031
716
PTH003 Pathologic Nystagmus 51 0.031
717
c ACR116 Aicardi-Goutieres Syndrome 1 51 0.031
718
c ACT135 Acute Graft Versus Host Disease 51 0.031
719
ILS001 Ileus 51 0.031
720
THY125 Thyroid Gland Medullary Carcinoma 51 0.031
721
c VRL007 Viral Encephalitis 51 0.031
722
P LCT001 Lactic Acidosis 51 0.031
723
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.031
724
P FNC004 Fanconi Syndrome 50 0.031
725
P CHL066 Cholangitis 50 0.031
726
SVR096 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative 50 0.031
727
CRT013 Carotid Stenosis 50 0.031
728
SYS003 Systolic Heart Failure 50 0.031
729
P NNT009 Neonatal Diabetes Mellitus 50 0.031
730
FDL002 Food Allergy 49 0.031
731
P MYT002 Myotonic Dystrophy 49 0.031
732
P OPN001 Open-Angle Glaucoma 49 0.031
733
RFR010 Refractory Anemia 48 0.031
734
P OBS001 Obstructive Jaundice 48 0.031
735
PLM035 Pulmonary Eosinophilia 48 0.031
736
P RNL015 Renal Hypertension 48 0.031
737
SPL018 Splenomegaly 48 0.031
738
OPD006 Opioid Addiction 48 0.031
739
SBS004 Substance Dependence 48 0.031
740
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.031
741
DRY001 Dry Eye Syndrome 47 0.031
742
HYP025 Hyperphosphatemia 47 0.031
743
PPL002 Papillary Carcinoma 47 0.031
744
c MTR002 Mitral Valve Insufficiency 47 0.031
745
RTN023 Retinitis 46 0.031
746
P PRD021 Periodic Paralysis 46 0.031
747
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.031
748
ACT003 Acute Kidney Tubular Necrosis 45 0.031
749
CLL014 Cll/sll 45 0.031
750
OBS082 Obstructive Nephropathy 43 0.031
751
BSL008 Basal Ganglia Disease 43 0.031
752
NRR001 Neuroretinitis 43 0.031
753
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.031
754
MCL003 Macular Holes 42 0.031
755
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.031
756
SPC005 Speech Disorder 42 0.031
757
c MLG079 Malignant Pleural Mesothelioma 42 0.031
758
P HYP263 Hypersomnia 41 0.031
759
P RRH023 Rare Hereditary Hemochromatosis 41 0.031
760
OCL052 Ocular Dominance 41 0.031
761
FRS012 First-Degree Atrioventricular Block 41 0.031
762
SPR126 Superior Semicircular Canal Dehiscence 40 0.031
763
GLM044 Glomerular Disease 39 0.031
764
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 39 0.031
765
ADP007 Adie Pupil 39 0.031
766
WLL004 Wallerian Degeneration 39 0.031
767
c CHR682 Chronic Bilirubin Encephalopathy 38 0.031
768
CRB001 Cerebral Lymphoma 38 0.031
769
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.031
770
c HMG029 Hemoglobin Se Disease 38 0.031
771
ATX010 Ataxia Neuropathy Spectrum 38 0.031
772
HPT082 Hepatic Adenomas, Familial 37 0.031
773
ATM052 Autoimmune Disease 1 37 0.031
774
MYT011 Myotonia 35 0.031
775
P HRD217 Hereditary Optic Neuropathy 34 0.031
776
TRN030 Transient Erythroblastopenia of Childhood 34 0.031
777
c CHR064 Chronic Monocytic Leukemia 34 0.031
778
HYP114 Hypertensive Nephropathy 34 0.031
779
c PRG106 Progressive Muscular Dystrophy 33 0.031
780
INF013 Inferior Myocardial Infarction 33 0.031
781
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.031
782
ACT064 Acute Necrotizing Encephalitis 32 0.031
783
HNM002 Hinman Syndrome 29 0.031
784
MST020 Mast Cell Activation Syndrome 27 0.031
785
BNG077 Benign Idiopathic Neonatal Seizures 26 0.031
786
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.031
787
CYN003 Cyanide Poisoning 24 0.031
788
PLS037 Plasma Cell Tumor 22 0.031
789
c DMN028 Diamond-Blackfan Anemia 12 21 0.031
790
BLD137 Blood Group--Ahonen 19 0.031
791
PLT016 Platelet Adenylate Cyclase Activity 16 0.031
792
CNN003 Conn's Syndrome 79 0.025
793
P RTN008 Retinitis Pigmentosa 77 0.025
794
PHN003 Phenylketonuria 75 0.025
795
ADR007 Adrenoleukodystrophy 74 0.025
796
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.025
797
P AMY004 Amyloidosis 70 0.025
798
LGH007 Leigh Syndrome 70 0.025
799
ADL002 Adult Syndrome 69 0.025
800
CRT072 Creutzfeldt-Jakob Disease 69 0.025
801
P MPL001 Maple Syrup Urine Disease 69 0.025
802
P FRG001 Fragile X Syndrome 68 0.025
803
OBS002 Obsessive-Compulsive Disorder 68 0.025
804
c INF071 Inflammatory Bowel Disease 1 68 0.025
805
PCK003 Pick Disease of Brain 68 0.025
806
P KBK002 Kabuki Syndrome 1 67 0.025
807
MYL005 Myelofibrosis 67 0.025
808
P OLG002 Oligodendroglioma 67 0.025
809
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 67 0.025
810
P ANG001 Angelman Syndrome 67 0.025
811
FCT007 Factor Vii Deficiency 66 0.025
812
AND002 Androgen Insensitivity Syndrome 66 0.025
813
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.025
814
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.025
815
GLC006 Galactosemia 65 0.025
816
LNG039 Lung Squamous Cell Carcinoma 65 0.025
817
P HRM001 Hermansky-Pudlak Syndrome 65 0.025
818
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.025
819
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.025
820
MYL031 Myeloproliferative Neoplasm 65 0.025
821
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.025
822
P PRS038 Personality Disorder 65 0.025
823
c WLM013 Wilms Tumor 1 65 0.025
824
BRR014 Barrett Esophagus 64 0.025
825
c ART101 Aortic Valve Disease 2 63 0.025
826
MSC007 Muscle Hypertrophy 63 0.025
827
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 63 0.025
828
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.025
829
PTT046 Pituitary Hormone Deficiency, Combined, 2 63 0.025
830
PPL049 Papillon-Lefevre Syndrome 63 0.025
831
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.025
832
c FNC043 Fanconi Anemia, Complementation Group E 62 0.025
833
c ALP101 Alpha-Thalassemia 62 0.025
834
c GLC092 Glaucoma, Primary Open Angle 62 0.025
835
P ESP024 Esophagitis 62 0.025
836
ALC006 Alcoholic Hepatitis 61 0.025
837
P EPL140 Epilepsy, Idiopathic Generalized 61 0.025
838
HYD038 Hydrops Fetalis, Nonimmune 61 0.025
839
BLD131 Bladder Urothelial Carcinoma 61 0.025
840
P PRM006 Primary Biliary Cirrhosis 61 0.025
841
P DRM010 Dermatomyositis 61 0.025
842
P ANP001 Anaplastic Large Cell Lymphoma 61 0.025
843
LYM012 Lymphoplasmacytic Lymphoma 61 0.025
844
LBR030 Leber Optic Atrophy 60 0.025
845
VRC005 Varicose Veins 60 0.025
846
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.025
847
CRT002 Cartilage-Hair Hypoplasia 60 0.025
848
DCB001 Decubitus Ulcer 60 0.025
849
P ALP009 Alopecia Areata 60 0.025
850
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.025
851
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.025
852
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.025
853
P GLL022 Guillain-Barre Syndrome 59 0.025
854
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.025
855
P LKD001 Leukodystrophy 59 0.025
856
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.025
857
GST045 Gastroenteritis 59 0.025
858
P RBL001 Rubella 58 0.025
859
IRN001 Iron Deficiency Anemia 58 0.025
860
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.025
861
CRY005 Cryptococcosis 58 0.025
862
P AXN002 Axenfeld-Rieger Syndrome 58 0.025
863
ERY029 Erythermalgia, Primary 58 0.025
864
CNT047 Contact Dermatitis 57 0.025
865
BLM002 Bulimia Nervosa 57 0.025
866
P BNC003 Bone Cancer 57 0.025
867
DSS008 Disease of Mental Health 57 0.025
868
P PRN023 Prion Disease 57 0.025
869
APH001 Aphthous Stomatitis 57 0.025
870
CYT008 Cytomegalovirus Infection 56 0.025
871
SFT003 Soft Tissue Sarcoma 56 0.025
872
GNR004 Generalized Anxiety Disorder 56 0.025
873
CMR002 Coumarin Resistance 56 0.025
874
P NRM002 Normal Pressure Hydrocephalus 56 0.025
875
SML019 Smallpox 56 0.025
876
MTH009 Mouth Disease 56 0.025
877
HPT022 Hepatoblastoma 56 0.025
878
HMG005 Hemoglobinopathy 55 0.025
879
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 55 0.025
880
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.025
881
GNG005 Gangliocytoma 55 0.025
882
RTC002 Reticular Dysgenesis 55 0.025
883
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.025
884
P FTL001 Fetal Alcohol Syndrome 55 0.025
885
ACT200 Acute Monoblastic Leukemia 55 0.025
886
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.025
887
P PMP001 Pemphigus 55 0.025
888
c OST131 Osteopetrosis, Autosomal Dominant 2 54 0.025
889
P ANT006 Antiphospholipid Syndrome 54 0.025
890
c ART144 Arthrogryposis, Distal, Type 1a 54 0.025
891
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.025
892
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 54 0.025
893
c CNT035 Central Nervous System Disease 54 0.025
894
CLR030 Clear Cell Renal Cell Carcinoma 53 0.025
895
c LKM070 Leukemia, Acute Monocytic 53 0.025
896
CCC001 Coccidioidomycosis 53 0.025
897
MYM001 Myoma 53 0.025
898
INT075 Intracranial Hypertension 53 0.025
899
BRN038 Bronchial Disease 53 0.025
900
P RCT021 Rectum Cancer 53 0.025
901
MST005 Mastitis 53 0.025
902
P HYP083 Hypopituitarism 53 0.025
903
PRP036 Peripheral T-Cell Lymphoma 53 0.025
904
GNG002 Ganglioneuroma 53 0.025
905
PRG009 Progressive Multifocal Leukoencephalopathy 53 0.025
906
PRP080 Peripheral Artery Disease 53 0.025
907
NRT001 Neurotic Disorder 52 0.025
908
SBC001 Subacute Sclerosing Panencephalitis 52 0.025
909
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 52 0.025
910
P HMG032 Hemoglobin H Disease 52 0.025
911
P PTS002 Ptosis 52 0.025
912
OST011 Osteomalacia 52 0.025
913
P SML001 Small Cell Carcinoma 52 0.025
914
STT041 Stuttering 52 0.025
915
TCK001 Tick-Borne Encephalitis 52 0.025
916
THY124 Thyroid Gland Papillary Carcinoma 52 0.025
917
ANK001 Ankylosis 52 0.025
918
PLS009 Plasma Cell Neoplasm 51 0.025
919
MSC190 Muscular Disease 51 0.025
920
TLN003 Telangiectasis 51 0.025
921
THR004 Thrombocytosis 51 0.025
922
SPP010 Suppressor of Tumorigenicity 3 51 0.025
923
GLC004 Galactokinase Deficiency 51 0.025
924
ACT049 Acute Disseminated Encephalomyelitis 51 0.025
925
P CHN059 Chondrocalcinosis 51 0.025
926
P CNT056 Cantu Syndrome 51 0.025
927
HRT011 Heart Septal Defect 50 0.025
928
P THR015 Thrombophilia 50 0.025
929
SPS003 Spastic Diplegia 50 0.025
930
P MTR003 Mitral Valve Stenosis 50 0.025
931
LMY002 Leiomyoma 50 0.025
932
MLT134 Multiple Pterygium Syndrome, Lethal Type 50 0.025
933
P MGR003 Migraine with Aura 50 0.025
934
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.025
935
LPR001 Lepromatous Leprosy 50 0.025
936
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 50 0.025
937
MYC087 Mycoplasma Pneumoniae Pneumonia 50 0.025
938
VRC001 Varicocele 49 0.025
939
STT002 Status Asthmaticus 49 0.025
940
LRN003 Learning Disability 49 0.025
941
c SVR005 Severe Pre-Eclampsia 49 0.025
942
MNN009 Meningoencephalitis 49 0.025
943
ECT026 Ectopic Pregnancy 49 0.025
944
P CMP008 Compartment Syndrome 48 0.025
945
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 48 0.025
946
QDR001 Quadriplegia 48 0.025
947
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.025
948
CCN002 Cocaine Abuse 48 0.025
949
P MGR001 Migraine Without Aura 48 0.025
950
c HMN021 Human T-Cell Leukemia Virus Type 1 48 0.025
951
HPR003 Heparin-Induced Thrombocytopenia 47 0.025
952
SPC010 Speech and Communication Disorders 47 0.025
953
TST044 Testicular Torsion 47 0.025
954
SVR098 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Positive 47 0.025
955
NDL007 Nodular Goiter 47 0.025
957
c HYD064 Hydrocephalus, Congenital, 1 47 0.025
958
c LRG017 Large Intestine Cancer 47 0.025
959
CRD001 Cardiac Tamponade 46 0.025
960
P VTR007 Vitreoretinopathy 46 0.025
961
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.025
962
CNG028 Congenital Hypoplastic Anemia 46 0.025
963
P MYC033 Myoclonus 46 0.025
964
VNZ002 Venezuelan Equine Encephalitis 46 0.025
965
PLL012 Pollen Allergy 45 0.025
966
c CRN278 Craniosynostosis 1 45 0.025
967
P BRB001 Beriberi 44 0.025
968
MCR225 Macrophage Activation Syndrome 44 0.025
969
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 44 0.025
970
BCT021 Bacterial Sepsis 44 0.025
971
DWR001 Dwarfism 44 0.025
972
P MYG005 Myoglobinuria 43 0.025
973
P MJR007 Major Affective Disorder 1 43 0.025
974
ADR041 Adrenal Cortical Adenoma 43 0.025
975
BNM001 Bone Marrow Cancer 43 0.025
976
ALK024 Alkuraya-Kucinskas Syndrome 43 0.025
977
IDP073 Idiopathic Hypercalciuria 43 0.025
978
c HMP023 Hemophagocytic Lymphohistiocytosis, Familial, 5 43 0.025
979
TRP009 Triple X Syndrome 42 0.025
980
QBC001 Quebec Platelet Disorder 42 0.025
981
P CLL015 Collagen Disease 42 0.025
982
BNS003 Binswanger's Disease 42 0.025
983
SNL007 Senile Cataract 42 0.025
984
PST053 Postherpetic Neuralgia 42 0.025
985
c HYP072 Hypersensitivity Reaction Type Iii Disease 42 0.025
986
BP1002 Bap1 Tumor Predisposition Syndrome 41 0.025
987
GST020 Gastric Antral Vascular Ectasia 41 0.025
988
49X006 49, Xxxxy Syndrome 41 0.025
989
RDN001 Reading Disorder 40 0.025
990
SPS005 Spastic Hemiplegia 40 0.025
991
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 40 0.025
992
c CNG027 Congenital Hemolytic Anemia 40 0.025
993
PLY100 Polyploidy 40 0.025
994
CNS002 Constrictive Pericarditis 40 0.025
995
P TRC031 Trichorhinophalangeal Syndrome 40 0.025
996
CHL045 Choline Deficiency Disease 39 0.025
998
LNG030 Lung Adenoma 39 0.025
999
BTN002 Boutonneuse Fever 39 0.025
1000
MNN017 Mononeuropathy 39 0.025
1001
ORN001 Ornithosis 39 0.025
1002
ADR022 Adrenomyeloneuropathy 38 0.025
1003
IDP091 Idiopathic Nephrotic Syndrome 38 0.025
1004
P PRC031 Preeclampsia/eclampsia 1 37 0.025
1005
FCL010 Focal Epithelial Hyperplasia 37 0.025
1006
SCR003 Secretory Diarrhea 36 0.025
1007
HMM005 Hemimelia 36 0.025
1009
CGH001 Cough Variant Asthma 35 0.025
1010
ALR002 Al-Raqad Syndrome 34 0.025
1011
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.025
1012
GNT167 Genetic Obesity 34 0.025
1013
AST002 Astroblastoma 34 0.025
1014
c DMN021 Diamond-Blackfan Anemia 6 34 0.025
1015
c SCN069 Secondary Hemophagocytic Lymphohistiocytosis 33 0.025
1016
MTB016 Metabolic Myopathy 33 0.025
1017
c PRS136 Prostate Cancer, Hereditary, 6 33 0.025
1018
c PRS130 Prostate Cancer, Hereditary, 8 32 0.025
1019
RRS014 Rare Surgical Neurologic Disease 32 0.025
1020
BLD052 Blood Group Incompatibility 32 0.025
1021
PRX097 Paroxysmal Dystonia 31 0.025
1022
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.025
1023
c BLD140 Blood Group, I System 30 0.025
1024
c RTH007 Rothmund-Thomson Syndrome, Type 1 30 0.025
1025
NLL001 Null-Cell Leukemia 29 0.025
1026
MTY003 Mutyh Polyposis 29 0.025
1027
HYP346 Hypotrichosis and Recurrent Skin Vesicles 29 0.025
1028
VSC004 Vasculogenic Impotence 28 0.025
1029
LST003 Listeria Meningitis 28 0.025
1030
ARG006 Aregenerative Anemia 28 0.025
1031
KYS001 Kyasanur Forest Disease 27 0.025
1032
c DMN017 Diamond-Blackfan Anemia 10 27 0.025
1033
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 27 0.025
1034
c DMN024 Diamond-Blackfan Anemia 7 26 0.025
1035
c DMN006 Diamond-Blackfan Anemia 3 26 0.025
1036
c DMN019 Diamond-Blackfan Anemia 4 26 0.025
1037
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.025
1038
c DMN018 Diamond-Blackfan Anemia 5 25 0.025
1039
CNG506 Congenital Amyoplasia 25 0.025
1040
c DMN020 Diamond-Blackfan Anemia 8 24 0.025
1041
c DYS090 Dyschromatosis Universalis Hereditaria 1 24 0.025
1042
TBR009 Tuberculous Empyema 24 0.025
1043
INS015 Inosine Triphosphatase Deficiency 23 0.025
1044
THR113 Thiourea Tasting 21 0.025
1045
MTR016 Maternal Hyperphenylalaninemia 21 0.025
1046
ATR089 Atrioventricular Dissociation 20 0.025
1047
BDR001 Bidirectional Tachycardia 19 0.025
1048
c DMN030 Diamond-Blackfan Anemia 13 18 0.025
1049
OBS524 Obsolete: Benign Exophthalmos Syndrome 15 0.025
1050
PNF002 Painful Legs and Moving Toes Syndrome 14 0.025
1051
ISP002 Isoproterenol-Mediated Vasodilatation 8 0.025
1052
P MDL005 Medulloblastoma 77 0.018
1053
KPS004 Kaposi Sarcoma 75 0.018
1054
c ART115 Aortic Valve Disease 1 75 0.018
1055
P APL001 Aplastic Anemia 74 0.018
1056
BRN028 Brain Cancer 73 0.018
1057
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.018
1058
P FML011 Familial Adenomatous Polyposis 72 0.018
1059
P FML018 Familial Mediterranean Fever 72 0.018
1060
c TBR026 Tuberous Sclerosis 2 71 0.018
1061
c GCH015 Gaucher Disease, Type I 70 0.018
1062
MCC012 Mccune-Albright Syndrome 70 0.018
1063
P TTR001 Tetralogy of Fallot 69 0.018
1064
PLY001 Polycythemia Vera 69 0.018
1065
c PNC108 Pancreatitis, Hereditary 69 0.018
1066
P OCL013 Oculodentodigital Dysplasia 69 0.018
1067
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.018
1068
c BSL007 Basal Cell Carcinoma 68 0.018
1069
EWN003 Ewing Sarcoma 68 0.018
1070
P INF038 Influenza 68 0.018
1071
P CLC063 Celiac Disease 1 68 0.018
1072
ACR008 Acrocallosal Syndrome 68 0.018
1073
c FML021 Familial Hypercholesterolemia 68 0.018
1074
SND001 Sandhoff Disease 68 0.018
1075
SKN019 Skin Melanoma 67 0.018
1076
c HMP004 Hemophilia B 67 0.018
1077
KRT019 Keratitis, Hereditary 67 0.018
1078
P LBR001 Leber Congenital Amaurosis 67