Search results for (R)-p-Mentha-1,8-dien-7-ol

2060 hits were found for (R)-p-Mentha-1,8-dien-7-ol

# Family MCID Name MIFTS Score
1
c FNC058 Fanconi Anemia, Complementation Group R 35 5.135
2
TRN067 Transcobalamin I Deficiency 19 2.776
3
c RNG020 Ring Chromosome 4 34 2.746
4
c RNG024 Ring Chromosome 8 23 1.982
5
INT318 Intrinsic Factor and R Binder, Combined Congenital Deficiency of 7 1.982
6
ATR048 Atrial Tachyarrhythmia with Short Pr Interval 37 1.967
7
c RNG018 Ring Chromosome 22 29 1.967
8
c RNG016 Ring Chromosome 20 28 1.958
9
c RNG004 Ring Chromosome 1 34 1.948
10
c PRX050 Peroxisome Biogenesis Disorder 9b 29 1.948
11
c RNG006 Ring Chromosome 11 19 1.948
12
LRN002 Laron Syndrome 62 1.935
13
JBR007 Joubert Syndrome with Renal Anomalies 29 1.935
14
c RNG031 Ring Chromosome Y Syndrome 13 1.935
15
ANM076 Anomalous Aortic Origin of the Right Coronary Artery 11 1.935
16
c SCN042 Secondary Hypereosinophilic Syndrome 11 1.935
17
P BCL017 B-Cell Lymphoma 61 0.444
18
DFF005 Diffuse Large B-Cell Lymphoma 56 0.416
19
P LYM118 Lymphoma 70 0.380
20
LYM019 Lymphosarcoma 48 0.351
21
RTC005 Reticulosarcoma 48 0.260
22
HMN044 Human Immunodeficiency Virus Type 1 73 0.236
23
LYM133 Lymphoma, Hodgkin, Classic 70 0.236
24
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.221
25
48X005 48,xyyy 37 0.218
26
DWN001 Down Syndrome 70 0.214
27
P PRS038 Personality Disorder 66 0.213
28
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.205
29
P NTR004 Neutropenia 64 0.189
30
P FLL037 Follicular Lymphoma 67 0.188
31
MNT001 Mantle Cell Lymphoma 69 0.188
32
AVD001 Avoidant Personality Disorder 45 0.181
33
ACQ007 Acquired Immunodeficiency Syndrome 61 0.174
34
c RHB024 Rhabdomyosarcoma 2 64 0.169
35
P LKM002 Leukemia 69 0.157
36
IMM167 Immune Deficiency Disease 79 0.155
37
c PRM038 Primary Agammaglobulinemia 45 0.154
38
P INF032 Infertility 60 0.151
39
ANX010 Anxiety 75 0.146
40
P ATS364 Autism 68 0.146
41
P LYM031 Lymphocytic Leukemia 56 0.146
42
47X002 47,xyy 49 0.146
43
P RNG032 Ring Chromosome 43 0.145
44
IMM064 Immunodeficiency, Common Variable, 10 51 0.142
45
HLX001 Helix Syndrome 46 0.142
46
c FLL041 Follicular Lymphoma 1 50 0.141
47
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.141
48
MYL069 Myeloma, Multiple 85 0.135
49
SVR004 Severe Combined Immunodeficiency 74 0.134
50
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.134
51
P HPT021 Hepatitis 69 0.132
52
ADL002 Adult Syndrome 62 0.132
53
c HPT001 Hepatitis C 62 0.132
54
P NRP001 Neuropathy 57 0.132
55
DFC004 Deficiency Anemia 77 0.131
56
P NRB010 Neuroblastoma 1 66 0.129
57
MYL009 Myelodysplastic Syndrome 72 0.127
58
P BRS047 Breast Cancer 99 0.126
59
DPR016 Depression 64 0.126
60
ALC007 Alcohol Dependence 68 0.125
61
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.117
62
P THR014 Thrombocytopenia 67 0.117
63
P LTR001 Lateral Sclerosis 56 0.116
64
c LKM071 Leukemia, Chronic Lymphocytic 81 0.115
65
c HPT073 Hepatitis C Virus 74 0.115
66
P KDN018 Kidney Disease 73 0.115
67
BRK010 Burkitt Lymphoma 68 0.114
68
P TRN020 Turner Syndrome 66 0.114
69
P DRR001 Diarrhea 55 0.114
70
CYS001 Cystic Fibrosis 84 0.112
71
MNT002 Mental Depression 60 0.112
72
ISC004 Ischemia 62 0.110
73
P ATR011 Atrial Fibrillation 67 0.109
74
c LKM061 Leukemia, Acute Myeloid 84 0.108
75
P BLD134 Bladder Cancer 79 0.108
76
P CRN018 Coronary Artery Anomaly 67 0.108
77
c HYP595 Hypertension, Essential 87 0.107
78
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.107
79
ATM095 Autoimmune Disease 62 0.107
80
c LKM004 Leukemia, B-Cell, Chronic 35 0.107
81
c ATS007 Autism Spectrum Disorder 69 0.105
82
P LNG032 Lung Cancer 99 0.104
83
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.104
84
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.104
85
P CLR023 Colorectal Cancer 100 0.103
86
DRM006 Dermatitis 63 0.103
87
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.103
88
GLB002 Glioblastoma 74 0.102
89
P ADN016 Adenocarcinoma 65 0.102
90
ALL026 Allergic Hypersensitivity Disease 65 0.102
91
c HPT003 Hepatitis a 60 0.102
92
CNG034 Congestive Heart Failure 69 0.100
93
P ALZ034 Alzheimer Disease 90 0.099
94
GLB015 Glioblastoma Multiforme 60 0.099
95
ART140 Arteries, Anomalies of 60 0.099
96
P OVR042 Ovarian Cancer 89 0.098
97
c PRG042 Progressive Familial Heart Block, Type Ia 62 0.098
98
P DBT009 Diabetes Mellitus 66 0.096
99
P GLM045 Glioma 64 0.096
100
VRL011 Viral Infectious Disease 62 0.096
101
c PRC016 Pre-Eclampsia 63 0.095
102
P MYL006 Myeloid Leukemia 61 0.095
103
P SBS003 Substance Abuse 56 0.095
104
P PNC025 Panic Disorder 53 0.095
105
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.095
106
P HRT032 Heart Disease 78 0.093
107
c HYP836 Hypercholesterolemia, Familial, 1 74 0.093
108
P LKM062 Leukemia, Acute Lymphoblastic 68 0.093
109
ETN001 Eating Disorder 61 0.093
110
GLL048 Glial Tumor 48 0.093
111
CYT002 Cytokine Deficiency 46 0.093
112
P MJR001 Major Depressive Disorder 69 0.092
113
LVR012 Liver Cirrhosis 67 0.092
114
ANG054 Angina Pectoris 66 0.092
115
P ALC033 Alcohol Use Disorder 58 0.092
116
P BCL004 B-Cell Non-Hodgkin Lymphoma 38 0.092
117
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.091
118
P PRP019 Peripheral Nervous System Disease 64 0.091
119
P CRN300 Coronary Heart Disease 1 59 0.091
120
P PRS040 Prostate Cancer 97 0.089
121
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.089
122
P MYC007 Myocardial Infarction 74 0.089
123
MDD011 Mood Disorder 62 0.089
124
GNR004 Generalized Anxiety Disorder 55 0.089
125
ATN005 Autonomic Dysfunction 48 0.089
126
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.088
127
P ENC004 Encephalitis 64 0.088
128
P SZR006 Seizure Disorder 59 0.088
129
ATN004 Autonomic Neuropathy 43 0.088
130
P PRM293 Primary Mediastinal B-Cell Lymphoma 41 0.088
131
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.086
132
PRT037 Pertussis 66 0.086
133
c ACT075 Acute Myocardial Infarction 59 0.086
134
CRV035 Cervical Cancer 77 0.085
135
MRG003 Marginal Zone B-Cell Lymphoma 55 0.085
136
P CHR345 Chronic Pain 52 0.085
137
LRN003 Learning Disability 51 0.085
138
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.085
139
SCL003 Social Phobia 49 0.085
140
CHR178 Chromosomal Triplication 36 0.085
141
HRW001 Hair Whorl 36 0.085
142
OST012 Osteoarthritis 80 0.083
143
P PRK057 Parkinson Disease, Late-Onset 77 0.083
144
P HRP006 Herpes Simplex 66 0.083
145
HYP066 Hyperglycemia 63 0.083
146
IRN002 Iron Metabolism Disease 58 0.083
147
PRS045 Prostatic Hypertrophy 55 0.083
148
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.083
149
AST005 Asthma 80 0.081
150
P LVR013 Liver Disease 71 0.081
151
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.081
152
TRM010 Traumatic Brain Injury 54 0.081
153
P CNT005 Central Nervous System Lymphoma 52 0.081
154
HMP009 Haemophilus Influenzae 46 0.081
155
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 27 0.081
156
P GST053 Gastric Cancer 85 0.080
157
OCL069 Ocular Motor Apraxia 53 0.080
158
PNG002 Pain Agnosia 52 0.080
159
VCC001 Vaccinia 50 0.080
160
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.080
161
CRB039 Cerebrovascular Disease 71 0.078
162
PSY004 Psychotic Disorder 68 0.078
163
TYP007 Typhoid Fever 61 0.078
164
MSL001 Measles 61 0.078
165
ADN018 Adenoma 60 0.078
166
CHC001 Chickenpox 53 0.078
167
c PRM226 Primary Central Nervous System Lymphoma 50 0.078
168
DYS009 Dysthymic Disorder 48 0.078
169
DYS015 Dysentery 45 0.078
170
P HPT023 Hepatocellular Carcinoma 99 0.076
171
c SYS001 Systemic Lupus Erythematosus 88 0.076
172
STR067 Stroke, Ischemic 82 0.076
173
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.076
174
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.076
175
P LYM033 Lymphoproliferative Syndrome 62 0.076
176
c ACT073 Acute Leukemia 59 0.076
177
VSL002 Visual Epilepsy 58 0.076
178
PRS021 Prostatic Adenoma 52 0.076
179
c LKM056 Leukemia, Chronic Lymphocytic 2 49 0.076
180
PRS129 Prostatic Hyperplasia, Benign 49 0.076
181
HPR003 Heparin-Induced Thrombocytopenia 49 0.076
182
P RHM011 Rheumatoid Arthritis 82 0.075
183
P SLP006 Sleep Apnea 71 0.075
184
HYP056 Hypoglycemia 68 0.075
185
P MNN013 Meningitis 67 0.075
186
P VSC007 Vascular Disease 65 0.075
187
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.075
188
P ALP008 Alopecia 58 0.075
189
c FML035 Familial Hyperlipidemia 56 0.075
190
P TRM003 Tremor 55 0.075
191
SPT005 Spotted Fever 48 0.075
192
P PNC035 Pancreatic Cancer 86 0.073
193
c ATR087 Atrial Standstill 1 76 0.073
194
P EPL164 Epilepsy 73 0.073
195
c SML038 Small Cell Cancer of the Lung 67 0.073
196
OVR029 Ovarian Hyperstimulation Syndrome 63 0.073
197
THY029 Thyroid Carcinoma 62 0.073
198
P CTR002 Cataract 62 0.073
199
P BPL003 Bipolar Disorder 59 0.073
200
CHL014 Cholera 58 0.073
201
ATR057 Atrioventricular Block 56 0.073
202
LYM040 Lymphoblastic Lymphoma 54 0.073
203
BRN071 Brain Injury 51 0.073
204
BCK006 Back Pain 44 0.073
205
P ART022 Arthritis 71 0.071
206
OBS002 Obsessive-Compulsive Disorder 69 0.071
207
MLN008 Melanoma 68 0.071
208
LNG099 Lung Disease 62 0.071
209
TTN003 Tetanus 62 0.071
210
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.071
211
SQM006 Squamous Cell Carcinoma 60 0.071
212
END030 End Stage Renal Failure 60 0.071
213
HMT018 Hematopoietic Stem Cell Transplantation 54 0.071
214
BRD004 Borderline Personality Disorder 51 0.071
215
P GND004 Gonadal Dysgenesis 47 0.071
216
EPD015 Epidemic Typhus 47 0.071
217
c MJR024 Major Affective Disorder 9 42 0.071
218
c MJR022 Major Affective Disorder 8 39 0.071
219
CRB004 Cerebral Artery Occlusion 38 0.071
220
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.071
221
P SRC025 Sarcoidosis 1 72 0.069
222
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.069
223
c ACT068 Acute Cystitis 63 0.069
224
P CRD132 Cardiac Conduction Defect 61 0.069
225
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.069
226
BLM002 Bulimia Nervosa 56 0.069
227
LWC001 Low Compliance Bladder 45 0.069
229
P DMN002 Dementia 68 0.067
230
SKN019 Skin Melanoma 68 0.067
231
P KDN017 Kidney Cancer 60 0.067
232
CNS004 Constipation 59 0.067
233
P GLM007 Glomerulonephritis 58 0.067
234
P SLP005 Sleep Disorder 58 0.067
235
P MMP001 Mumps 57 0.067
236
CMR002 Coumarin Resistance 56 0.067
237
CND002 Conduct Disorder 52 0.067
238
STM007 Stomatitis 51 0.067
239
MCR004 Macroglobulinemia 50 0.067
240
GRW007 Growth Hormone Deficiency 48 0.067
241
c PRG043 Progressive Familial Heart Block, Type Ib 48 0.067
242
ATX019 Ataxia with Vitamin E Deficiency 46 0.067
243
P HYP086 Hypothyroidism 70 0.065
244
SKN016 Skin Disease 64 0.065
245
P ENC018 Encephalopathy 64 0.065
246
SPN186 Spinal Cord Injury 63 0.065
247
P HDC001 Headache 59 0.065
248
P EXN002 Exanthem 58 0.065
249
AGN016 Aging 58 0.065
250
P ECL001 Eclampsia 53 0.065
251
RGH001 Right Bundle Branch Block 48 0.065
252
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 44 0.065
253
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.065
254
INS024 Insulin-Like Growth Factor I 79 0.063
255
P SCH015 Schizophrenia 76 0.063
256
P RSP003 Respiratory Failure 75 0.063
257
P MLT020 Multiple Sclerosis 73 0.063
258
WLF001 Wolff-Parkinson-White Syndrome 65 0.063
259
ANR007 Anorexia Nervosa 64 0.063
260
P HML002 Hemolytic Anemia 64 0.063
261
P PSR002 Psoriasis 63 0.063
262
ART002 Arts Syndrome 63 0.063
263
P END044 Endometriosis 63 0.063
264
P SYP003 Syphilis 59 0.063
265
P FBR017 Fibrosarcoma 57 0.063
266
VSC002 Vascular Dementia 57 0.063
267
APH002 Aphasia 56 0.063
268
P RBL001 Rubella 56 0.063
269
IMP005 Impotence 53 0.063
270
P ART018 Aortic Valve Insufficiency 47 0.063
271
HDN002 Head Injury 47 0.063
272
AGR002 Agoraphobia 44 0.063
273
P DYS021 Dysautonomia 41 0.063
274
HDG004 Hodgkin's Granuloma 27 0.063
275
HDG006 Hodgkin's Paragranuloma 23 0.063
276
MLR004 Malaria 82 0.061
277
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.061
278
P OST002 Osteoporosis 79 0.061
279
PLM001 Pulmonary Tuberculosis 72 0.061
280
c MGR028 Migraine with or Without Aura 1 70 0.061
281
FRN006 Frontotemporal Dementia 70 0.061
282
c CHR684 Chronic Kidney Disease 68 0.061
283
P DRM053 Dermatitis, Atopic 68 0.061
284
P SKN015 Skin Carcinoma 67 0.061
285
HMT002 Hematologic Cancer 64 0.061
286
LYM012 Lymphoplasmacytic Lymphoma 62 0.061
287
HYP266 Hypoxia 58 0.061
288
P GRV001 Graves' Disease 57 0.061
289
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.061
290
P PLY019 Polyneuropathy 55 0.061
291
P RCT021 Rectum Cancer 54 0.061
292
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.061
293
PST011 Pustulosis of Palm and Sole 51 0.061
294
OPP004 Oppositional Defiant Disorder 50 0.061
295
ANT011 Antisocial Personality Disorder 47 0.061
296
SYN036 Syncope 46 0.061
297
DWR001 Dwarfism 45 0.061
298
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.061
299
ALL014 Allergic Encephalomyelitis 40 0.061
300
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.059
301
P APL001 Aplastic Anemia 76 0.059
302
c LKM063 Leukemia, Chronic Myeloid 74 0.059
303
GST092 Gastroesophageal Reflux 68 0.059
304
ATH013 Atherosclerosis Susceptibility 68 0.059
305
SRC014 Sarcoma 67 0.059
306
P PRD008 Periodontitis 66 0.059
307
LPD008 Lipid Metabolism Disorder 64 0.059
308
ING001 Inguinal Hernia 61 0.059
309
P SCL018 Scoliosis 61 0.059
310
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.059
311
GST045 Gastroenteritis 60 0.059
312
PST028 Post-Traumatic Stress Disorder 60 0.059
313
P RHN004 Rhinitis 59 0.059
314
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.059
315
P HMP007 Hemophilia 58 0.059
316
ISL014 Isolated Growth Hormone Deficiency, Type Ia 58 0.059
317
SCH014 Schistosomiasis 57 0.059
318
BCT022 Bacterial Infectious Disease 57 0.059
319
SPN035 Spindle Cell Sarcoma 57 0.059
320
P MCR010 Microcephaly 56 0.059
321
P INS002 in Situ Carcinoma 55 0.059
322
P SLM003 Salmonellosis 54 0.059
323
PRP036 Peripheral T-Cell Lymphoma 53 0.059
324
SPL018 Splenomegaly 48 0.059
325
LFT001 Left Bundle Branch Hemiblock 47 0.059
326
c PCH010 Pachyonychia Congenita 3 43 0.059
327
ACT084 Acute Stress Disorder 42 0.059
328
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.059
329
c DLT002 Dilated Cardiomyopathy 81 0.056
330
c THR092 Thrombophilia Due to Thrombin Defect 74 0.056
331
END057 Endometrial Cancer 74 0.056
332
P GRF003 Graft-Versus-Host Disease 71 0.056
333
P CRD119 Cardiac Arrest 71 0.056
334
BRN024 Bronchitis 70 0.056
335
CRB037 Cerebral Palsy 69 0.056
336
P INF038 Influenza 69 0.056
337
CHG001 Chagas Disease 66 0.056
338
FCT007 Factor Vii Deficiency 65 0.056
339
c FNC043 Fanconi Anemia, Complementation Group E 64 0.056
340
PLM033 Pulmonary Embolism 60 0.056
341
P THR117 Three M Syndrome 1 58 0.056
342
PLM031 Poliomyelitis 58 0.056
343
RHM027 Rheumatic Disease 56 0.056
344
P SCK002 Sick Sinus Syndrome 56 0.056
345
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 0.056
346
HMS001 Hemosiderosis 54 0.056
347
LNG031 Lung Benign Neoplasm 52 0.056
348
P AST007 Astrocytoma 52 0.056
349
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.056
351
HYP080 Hypogonadism 51 0.056
352
SCH012 Schizoaffective Disorder 50 0.056
353
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.056
354
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.056
355
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.056
356
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.056
357
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.056
358
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.056
359
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.056
360
GRN017 Granulocytopenia 46 0.056
361
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.056
362
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.056
363
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.056
364
P RRH023 Rare Hereditary Hemochromatosis 41 0.056
365
HYP064 Hypogonadotropism 40 0.056
366
PPL052 Papillomatosis, Confluent and Reticulated 34 0.056
367
RRS014 Rare Surgical Neurologic Disease 33 0.056
368
CHL079 Children's Interstitial Lung Disease 27 0.056
369
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 27 0.056
370
KPS004 Kaposi Sarcoma 75 0.054
371
CRH001 Crohn's Disease 75 0.054
372
P PHC003 Pheochromocytoma 71 0.054
373
P MYC084 Mycobacterium Tuberculosis 1 69 0.054
374
ALL003 Allergic Rhinitis 69 0.054
375
P FRG001 Fragile X Syndrome 69 0.054
376
P GLM040 Glioma Susceptibility 1 68 0.054
377
P LPR021 Leprosy 3 67 0.054
378
DSS008 Disease of Mental Health 66 0.054
379
P MTR014 Motor Neuron Disease 66 0.054
380
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.054
381
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 62 0.054
382
PPT005 Peptic Ulcer Disease 60 0.054
383
c ACT210 Acute Respiratory Distress Syndrome 59 0.054
384
P PRV006 Pervasive Developmental Disorder 58 0.054
385
SFT003 Soft Tissue Sarcoma 57 0.054
386
MCS002 Mucositis 56 0.054
387
GLS001 Gliosarcoma 56 0.054
388
PPL022 Papilloma 56 0.054
389
AMN003 Amnestic Disorder 55 0.054
390
PNC001 Pancytopenia 54 0.054
391
P TMP001 Temporal Lobe Epilepsy 53 0.054
392
ADR040 Adrenal Gland Pheochromocytoma 51 0.054
393
CRN030 Coronary Stenosis 49 0.054
394
P BNG032 Benign Mesothelioma 47 0.054
395
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.054
396
HNS001 Hansen's Disease 35 0.054
397
PST092 Posttransplant Acute Limbic Encephalitis 29 0.054
398
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 23 0.054
399
ULC004 Ulcerative Colitis 75 0.051
400
c ART101 Aortic Valve Disease 2 67 0.051
401
TBC004 Tobacco Addiction 65 0.051
402
c HPT016 Hepatitis B 63 0.051
403
P LPS004 Lupus Erythematosus 62 0.051
404
c PNS012 Paine Syndrome 61 0.051
405
STT001 Status Epilepticus 61 0.051
406
DPH001 Diphtheria 61 0.051
407
c ACT071 Acute Kidney Failure 60 0.051
408
INS001 Insulinoma 60 0.051
409
THY122 Thyroid Gland Cancer 59 0.051
410
P BRS044 Breast Adenocarcinoma 59 0.051
411
CYT008 Cytomegalovirus Infection 58 0.051
412
HRP004 Herpes Zoster 58 0.051
413
INT007 Intermediate Coronary Syndrome 58 0.051
414
PST046 Post-Transplant Lymphoproliferative Disease 55 0.051
415
PLM017 Pulmonary Alveolar Microlithiasis 54 0.051
416
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.051
417
P MSC003 Muscular Atrophy 52 0.051
418
ISL003 Isolated Growth Hormone Deficiency 50 0.051
419
SCH003 Schizophreniform Disorder 49 0.051
420
SQM002 Squamous Cell Papilloma 49 0.051
421
P TCL004 T-Cell Leukemia 48 0.051
422
PLS025 Plasmablastic Lymphoma 48 0.051
423
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.051
424
CHR074 Choriocarcinoma 47 0.051
425
c HYP272 Hypercholesterolemia, Familial, 3 44 0.051
426
c CHR064 Chronic Monocytic Leukemia 43 0.051
427
49X002 49,xxxxy Syndrome 39 0.051
428
WHP002 Whiplash 37 0.051
429
c LKM005 Leukemia, T-Cell, Chronic 35 0.051
431
LYM048 Lymphoma, Large-Cell, Immunoblastic 30 0.051
432
P HNT016 Huntington Disease 72 0.049
433
LPT014 Leptin Deficiency or Dysfunction 72 0.049
434
EWN003 Ewing Sarcoma 69 0.049
435
ADR054 Adrenocortical Carcinoma, Hereditary 68 0.049
436
P MSC005 Muscular Dystrophy 68 0.049
437
P MCR115 Microvascular Complications of Diabetes 5 67 0.049
438
c FML021 Familial Hypercholesterolemia 67 0.049
439
PRT036 Peritonitis 66 0.049
440
P PLM036 Pulmonary Fibrosis 66 0.049
441
IDP011 Idiopathic Interstitial Pneumonia 65 0.049
442
NTR005 Nutritional Deficiency Disease 61 0.049
443
IGR001 Ige Responsiveness, Atopic 61 0.049
444
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.049
445
INT002 Intermittent Claudication 60 0.049
446
P PLY011 Polycystic Ovary Syndrome 58 0.049
447
LYM027 Lymphopenia 58 0.049
448
P INF037 Inflammatory Bowel Disease 57 0.049
449
P HYP076 Hyperthyroidism 55 0.049
450
PLG002 Plague 54 0.049
451
HRT011 Heart Septal Defect 52 0.049
452
PST021 Postpartum Depression 51 0.049
453
BNR002 Bone Resorption Disease 51 0.049
454
P DDN001 Duodenal Ulcer 50 0.049
455
ANV001 Anovulation 47 0.049
456
ENT004 Enthesopathy 46 0.049
457
SMT001 Somatization Disorder 45 0.049
458
SCH011 Schizotypal Personality Disorder 36 0.049
459
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.049
460
c RNG008 Ring Chromosome 13 29 0.049
461
ESP021 Esophageal Cancer 90 0.046
462
c FNC027 Fanconi Anemia, Complementation Group a 81 0.046
463
P NRF023 Neurofibromatosis, Type Ii 77 0.046
464
MLT157 Multiple System Atrophy 1 71 0.046
465
ACR007 Acromegaly 70 0.046
466
P HYP061 Hypertrophic Cardiomyopathy 68 0.046
467
P CLC063 Celiac Disease 1 66 0.046
468
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.046
469
P DYS154 Dystonia 65 0.046
470
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.046
471
P MVM001 Movement Disease 63 0.046
472
TXC005 Toxic Shock Syndrome 63 0.046
473
P THL005 Thalassemia 62 0.046
474
P ART023 Arthropathy 61 0.046
475
P CHR285 Chronic Myelomonocytic Leukemia 60 0.046
476
P PTN014 Patent Ductus Arteriosus 1 60 0.046
477
P CYS018 Cystitis 59 0.046
478
EYD002 Eye Disease 59 0.046
479
DSS009 Disseminated Intravascular Coagulation 58 0.046
480
P MLN007 Male Infertility 57 0.046
481
HRY003 Hairy Cell Leukemia 57 0.046
482
ALL006 Allergic Asthma 56 0.046
483
c SVR001 Severe Acute Respiratory Syndrome 56 0.046
484
MTH009 Mouth Disease 56 0.046
485
c MCR113 Microvascular Complications of Diabetes 3 55 0.046
486
HYP005 Hypokalemia 55 0.046
487
P HYP730 Hypogonadotropic Hypogonadism 54 0.046
488
PRC013 Pericarditis 54 0.046
489
P MTR003 Mitral Valve Stenosis 54 0.046
490
SPN051 Spondylitis 53 0.046
491
P TRT010 Teratoma 52 0.046
492
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.046
493
OPT003 Opiate Dependence 50 0.046
494
c MTR002 Mitral Valve Insufficiency 49 0.046
495
c MCR120 Microvascular Complications of Diabetes 7 48 0.046
496
SBS004 Substance Dependence 48 0.046
497
DRG003 Drug Dependence 48 0.046
498
c MLG068 Malignant Glioma 46 0.046
499
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 43 0.046
500
SBC016 Subacute Delirium 43 0.046
501
c MCR130 Microvascular Complications of Diabetes 6 42 0.046
502
c MCR133 Microvascular Complications of Diabetes 4 42 0.046
503
IDP070 Idiopathic Scoliosis 39 0.046
504
INF013 Inferior Myocardial Infarction 35 0.046
505
c RNG029 Ring Chromosome 14 Syndrome 31 0.046
506
INF009 Inflammatory Spondylopathy 29 0.046
507
c PST001 Posterior Myocardial Infarction 25 0.046
508
P ATX030 Ataxia-Telangiectasia 83 0.043
509
NRL016 Neural Tube Defects 83 0.043
510
P LNG064 Lung Cancer Susceptibility 3 79 0.043
511
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.043
512
P CNR004 Cone-Rod Dystrophy 2 72 0.043
513
c HMP029 Hemophilia a 69 0.043
514
PNC129 Pancreatic Adenocarcinoma 69 0.043
515
c FML001 Familial Atrial Fibrillation 67 0.043
516
P HYP098 Hypereosinophilic Syndrome 67 0.043
517
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.043
518
P SPN046 Spinal Muscular Atrophy 65 0.043
519
IRR002 Irritable Bowel Syndrome 65 0.043
520
LSH001 Leishmaniasis 64 0.043
521
CLT003 Colitis 63 0.043
522
P RHB003 Rhabdomyosarcoma 62 0.043
523
P HYP750 Hypertriglyceridemia, Familial 62 0.043
524
CRD223 Cardiac Arrhythmia 61 0.043
525
P PLY014 Polycystic Kidney Disease 61 0.043
526
c ACT027 Acute Pancreatitis 60 0.043
527
P END033 Endocarditis 58 0.043
528
P MYP006 Myopia 58 0.043
529
HYD002 Hydronephrosis 58 0.043
530
CNT047 Contact Dermatitis 58 0.043
531
PYR041 Pyruvate Kinase Deficiency of Red Cells 58 0.043
532
THR024 Thrombosis 58 0.043
533
ERY051 Erythroleukemia, Familial 58 0.043
534
P STR020 Strabismus 57 0.043
535
PRP030 Purpura 56 0.043
536
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.043
537
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.043
538
END040 Endogenous Depression 55 0.043
539
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.043
540
PRM042 Primary Effusion Lymphoma 55 0.043
541
P FBR031 Febrile Seizures 54 0.043
542
FCT001 Factor Viii Deficiency 54 0.043
543
P HYP040 Hypospadias 54 0.043
544
TLN003 Telangiectasis 53 0.043
545
P SCK005 Sickle Cell Disease 53 0.043
546
NRT001 Neurotic Disorder 53 0.043
547
GST023 Gastric Ulcer 53 0.043
548
NNL006 Non-Alcoholic Steatohepatitis 53 0.043
549
c ACT135 Acute Graft Versus Host Disease 52 0.043
550
IMM136 Immune System Disease 52 0.043
551
P MYT002 Myotonic Dystrophy 52 0.043
552
CRD137 Cardiogenic Shock 50 0.043
553
c MLG074 Malignant Mesenchymoma 50 0.043
554
SXL003 Sexual Disorder 49 0.043
555
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.043
556
DGN001 Degenerative Disc Disease 49 0.043
557
DBT004 Diabetic Polyneuropathy 48 0.043
558
RCH001 Richter's Syndrome 47 0.043
559
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 46 0.043
560
P SMK004 Smoking As a Quantitative Trait Locus 3 46 0.043
561
DBT002 Diabetic Autonomic Neuropathy 45 0.043
562
ANX004 Anoxia 44 0.043
563
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.043
564
P KLZ004 Kala-Azar 1 43 0.043
565
c PRM163 Primary Mediastinal Large B-Cell Lymphoma 41 0.043
566
SPS057 Spasticity 38 0.043
567
ADJ001 Adjustment Disorder 38 0.043
568
MCH006 Mechanical Strabismus 31 0.043
569
BNG077 Benign Idiopathic Neonatal Seizures 27 0.043
570
MYT026 Myotonia Atrophica 25 0.043
571
IND005 Indolent B Cell Lymphoma 21 0.043
572
SCK003 Sickle Cell Anemia 74 0.040
573
c SPN225 Spondyloarthropathy 1 74 0.040
574
c ATM006 Autoimmune Lymphoproliferative Syndrome 73 0.040
575
OTT002 Otitis Media 71 0.040
576
P BRG001 Brugada Syndrome 70 0.040
577
P PLM037 Pulmonary Hypertension 69 0.040
578
P HYD006 Hydrocephalus 68 0.040
579
P NSP012 Nasopharyngeal Carcinoma 67 0.040
580
OST017 Osteomyelitis 65 0.040
581
LYM017 Lyme Disease 64 0.040
582
P VNW001 Von Willebrand's Disease 64 0.040
583
P LMY004 Leiomyosarcoma 63 0.040
584
FTT001 Fatty Liver Disease 63 0.040
585
c SCL052 Scleroderma, Familial Progressive 62 0.040
586
SDD001 Sudden Infant Death Syndrome 61 0.040
587
CHR066 Chronic Fatigue Syndrome 61 0.040
588
P ATR010 Atrial Heart Septal Defect 61 0.040
589
BND020 Bone Disease 60 0.040
590
BRN002 Bronchiolitis 60 0.040
591
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.040
592
c MST023 Mesothelioma, Malignant 59 0.040
593
P UVT001 Uveitis 58 0.040
594
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.040
595
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 57 0.040
596
ANT024 Anthrax Disease 56 0.040
597
JPN002 Japanese Encephalitis 56 0.040
598
P NRC002 Narcolepsy 56 0.040
599
AVN001 Avian Influenza 56 0.040
600
c CNG216 Congenital Hydrocephalus 55 0.040
601
GLC003 Glucose Intolerance 55 0.040
602
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.040
603
DCB001 Decubitus Ulcer 54 0.040
604
P MMB011 Membranous Nephropathy 54 0.040
605
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.040
606
TXC002 Toxic Encephalopathy 54 0.040
607
c PRM092 Primary Lateral Sclerosis, Adult, 1 54 0.040
608
SPP010 Suppressor of Tumorigenicity 3 54 0.040
609
SPN019 Spondylolisthesis 54 0.040
610
P PTT006 Pituitary Adenoma 53 0.040
611
FDL002 Food Allergy 52 0.040
612
P THY032 Thyroiditis 52 0.040
613
PRN011 Pernicious Anemia 51 0.040
614
URM002 Uremia 50 0.040
615
APR001 Apraxia 50 0.040
616
IGG001 Iga Glomerulonephritis 50 0.040
617
OPD006 Opioid Addiction 49 0.040
618
SPC005 Speech Disorder 44 0.040
619
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.040
620
BNS003 Binswanger's Disease 43 0.040
621
GST020 Gastric Antral Vascular Ectasia 42 0.040
622
SCR015 Scarlet Fever 41 0.040
623
PLY100 Polyploidy 41 0.040
624
KLB003 Klebsiella Pneumonia 36 0.040
625
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 36 0.040
626
DSS010 Dissociative Disorder 35 0.040
627
CYT004 Cytomegalic Inclusion Disease 32 0.040
629
HST001 Histrionic Personality Disorder 28 0.040
630
c RNG010 Ring Chromosome 15 27 0.040
631
c RNG025 Ring Chromosome 9 20 0.040
632
RSP008 Respiratory Rhythmicity in Sleep 17 0.040
633
PFF001 Pfeiffer Syndrome 79 0.036
634
GST019 Gastrointestinal Stromal Tumor 76 0.036
635
c ART115 Aortic Valve Disease 1 76 0.036
636
P RTN024 Retinoblastoma 74 0.036
637
P TBR001 Tuberous Sclerosis 72 0.036
638
P WSK001 Wiskott-Aldrich Syndrome 71 0.036
639
P AMY004 Amyloidosis 71 0.036
640
CHL065 Cholangiocarcinoma 68 0.036
641
FBR012 Fabry Disease 68 0.036
642
c BSL007 Basal Cell Carcinoma 68 0.036
643
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.036
644
c HMP004 Hemophilia B 66 0.036
645
CLN015 Colon Adenocarcinoma 65 0.036
646
INT146 Intervertebral Disc Disease 64 0.036
647
P VSC011 Vasculitis 64 0.036
648
P THY023 Thymoma 64 0.036
649
APN008 Apnea, Obstructive Sleep 64 0.036
650
KHL003 Kohlschutter-Tonz Syndrome 63 0.036
651
OST003 Osteonecrosis 62 0.036
652
c VSC019 Vesicoureteral Reflux 1 62 0.036
653
P INT143 Interstitial Cystitis 62 0.036
654
ORL011 Oral Cancer 62 0.036
655
P ANP001 Anaplastic Large Cell Lymphoma 62 0.036
656
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.036
657
CTN007 Cutaneous Leishmaniasis 61 0.036
658
ANR040 Aneurysm 60 0.036
659
c DWL002 Dowling-Degos Disease 1 59 0.036
660
BRS051 Breast Disease 59 0.036
661
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.036
662
QFV001 Q Fever 58 0.036
663
P PYL005 Pyelonephritis 58 0.036
664
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 58 0.036
665
P SJG008 Sjogren Syndrome 57 0.036
666
CMP010 Complex Regional Pain Syndrome 57 0.036
667
BRN004 Brain Edema 57 0.036
668
PRS047 Prostatitis 57 0.036
669
ENH001 Enhanced S-Cone Syndrome 56 0.036
670
PLM010 Pulmonary Edema 56 0.036
671
SYN007 Synovitis 55 0.036
672
HYP060 Hyperinsulinism 55 0.036
673
c THY107 Thymoma, Familial 55 0.036
674
NRG002 Neurogenic Bladder 55 0.036
675
THY124 Thyroid Gland Papillary Carcinoma 54 0.036
676
INT079 Intrahepatic Cholangiocarcinoma 54 0.036
677
PRP016 Paraplegia 54 0.036
678
AMN001 Amenorrhea 54 0.036
679
TCK001 Tick-Borne Encephalitis 53 0.036
680
KRT006 Keratoconjunctivitis 53 0.036
681
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 53 0.036
682
MMM001 Mammary Paget's Disease 53 0.036
683
DNT012 Dental Caries 52 0.036
684
GNT002 Giant Cell Glioblastoma 52 0.036
685
DXT001 Dextrocardia 52 0.036
686
RDC002 Radiculopathy 51 0.036
687
AZS001 Azoospermia 51 0.036
688
PLC008 Placenta Disease 51 0.036
689
HYP081 Hypolipoproteinemia 51 0.036
690
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 51 0.036
691
ONC002 Onchocerciasis 50 0.036
692
RTN020 Retinal Vascular Disease 49 0.036
693
c LTN004 Late-Onset Retinal Degeneration 49 0.036
694
P HMN032 Human Herpesvirus 8 49 0.036
695
LYM024 Lymphatic System Disease 48 0.036
696
MTB004 Metabolic Acidosis 48 0.036
697
PTH002 Pathological Gambling 48 0.036
698
CCN001 Cocaine Dependence 48 0.036
699
PPL002 Papillary Carcinoma 47 0.036
700
BRN014 Bronchopneumonia 47 0.036
701
P PRR002 Pure Red-Cell Aplasia 47 0.036
702
PLL012 Pollen Allergy 46 0.036
703
c FML008 Familial Retinoblastoma 46 0.036
704
TRC003 Trichomoniasis 46 0.036
705
PRS063 Paresthesia 46 0.036
706
RTC009 Reticulum Cell Sarcoma 45 0.036
707
RDC006 Red Cell Aplasia 45 0.036
708
HYP016 Hypochondriasis 42 0.036
709
P HYP073 Hypersensitivity Reaction Type Iv Disease 42 0.036
710
OBS003 Obsessive-Compulsive Personality Disorder 42 0.036
711
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.036
712
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 41 0.036
713
P SCL057 Scoliosis, Isolated 1 41 0.036
714
MLN003 Melancholia 38 0.036
715
c CHR682 Chronic Bilirubin Encephalopathy 36 0.036
716
MXD026 Mixed Glioma 36 0.036
717
c PRS136 Prostate Cancer, Hereditary, 6 34 0.036
718
c PRS130 Prostate Cancer, Hereditary, 8 33 0.036
719
ARG004 Argyria 28 0.036
720
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.036
721
PRP027 Peripheral Vascular Disease 72 0.033
722
PLY001 Polycythemia Vera 70 0.033
723
CMM004 Common Variable Immunodeficiency 69 0.033
724
P LNG028 Long Qt Syndrome 68 0.033
725
P ORT004 Orthostatic Intolerance 68 0.033
726
P CNJ013 Conjunctivitis 67 0.033
727
P ASP006 Aspergillosis 67 0.033
728
CLF027 Cleft Palate, Isolated 67 0.033
729
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.033
730
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.033
731
P NPH012 Nephrotic Syndrome 65 0.033
732
P HYP069 Hyperparathyroidism 64 0.033
733
MNN042 Meningioma, Radiation-Induced 64 0.033
734
P MYP004 Myopathy 63 0.033
735
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.033
736
P ESP024 Esophagitis 62 0.033
737
P PLV020 Pelvic Organ Prolapse 61 0.033
738
APP008 Appendicitis 61 0.033
739
P TXP001 Toxoplasmosis 61 0.033
740
P CND004 Candidiasis 61 0.033
741
SPP011 Suppression of Tumorigenicity 12 61 0.033
742
P MYC008 Myocarditis 60 0.033
743
FBR047 Fibromyalgia 60 0.033
744
P PRD006 Prader-Willi Syndrome 60 0.033
745
P OPT006 Optic Nerve Disease 59 0.033
746
NRN004 Neuroendocrine Tumor 59 0.033
747
NWB001 Newborn Respiratory Distress Syndrome 58 0.033
748
BLR008 Bilirubin Metabolic Disorder 58 0.033
749
ALL010 Allergic Contact Dermatitis 56 0.033
750
P PLY018 Polycythemia 56 0.033
751
c CHR417 Chronic Graft Versus Host Disease 56 0.033
752
P RTN016 Retinal Degeneration 56 0.033
753
FCL014 Focal Epilepsy 56 0.033
754
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.033
755
DBT010 Diabetic Neuropathy 56 0.033
756
RHM001 Rheumatic Fever 56 0.033
757
SNS003 Sensory Peripheral Neuropathy 56 0.033
758
CHK001 Chikungunya 55 0.033
759
VSC003 Visceral Leishmaniasis 55 0.033
760
HMP005 Hemiplegia 55 0.033
761
CYS005 Cysticercosis 55 0.033
762
P LYM025 Lymphedema 54 0.033
763
CCC001 Coccidioidomycosis 54 0.033
764
DMY004 Demyelinating Disease 54 0.033
765
PLS007 Plasmodium Falciparum Malaria 53 0.033
766
PTH003 Pathologic Nystagmus 53 0.033
767
CHR100 Chronic Ulcer of Skin 53 0.033
768
KRT001 Keratoconjunctivitis Sicca 53 0.033
769
DYS073 Dysphagia 52 0.033
770
CHL122 Cholesteatoma of Middle Ear 52 0.033
771
NRT004 Neuritis 52 0.033
772
KRT009 Keratosis 52 0.033
773
P THR015 Thrombophilia 51 0.033
774
DYS014 Dyspepsia 51 0.033
775
OVR082 Overgrowth Syndrome 51 0.033
776
PRP080 Peripheral Artery Disease 51 0.033
777
CLR109 Colorectal Adenocarcinoma 51 0.033
778
P KRT007 Keratoconus 51 0.033
779
ADR016 Adrenal Cortical Carcinoma 51 0.033
780
P END047 Endophthalmitis 50 0.033
781
DRY001 Dry Eye Syndrome 50 0.033
782
HYD061 Hydrocephalus, Normal-Pressure 49 0.033
783
ANG046 Angioimmunoblastic T-Cell Lymphoma 49 0.033
784
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 0.033
785
ATS010 Autosomal Recessive Disease 49 0.033
786
MTN003 Motion Sickness 48 0.033
787
PRM020 Premenstrual Tension 48 0.033
788
c BPL002 Bipolar I Disorder 48 0.033
789
PTT037 Pituitary Tumors 47 0.033
790
P MYC033 Myoclonus 47 0.033
791
LPT006 Leptin Receptor Deficiency 47 0.033
792
ANH002 Anhidrosis 47 0.033
793
URT010 Ureteral Obstruction 46 0.033
794
RTN023 Retinitis 46 0.033
795
NRR001 Neuroretinitis 46 0.033
796
ERY004 Erysipelas 46 0.033
797
P CRN025 Corneal Dystrophy 45 0.033
798
NWC001 Newcastle Disease 45 0.033
799
c DRM054 Dermatitis, Atopic, 2 45 0.033
800
P OCY003 Oocyte Maturation Defect 1 44 0.033
801
ADR004 Adrenal Cortical Adenocarcinoma 44 0.033
802
P RRT020 Rare Tumor 43 0.033
803
RST023 Resting Heart Rate, Variation in 43 0.033
804
ACT003 Acute Kidney Tubular Necrosis 42 0.033
805
P DYS005 Dyslexia 42 0.033
806
P SBR004 Seborrheic Dermatitis 41 0.033
807
DPR002 Depersonalization Disorder 41 0.033
808
ALX002 Alexithymia 40 0.033
809
c NLD014 Nail Disorder, Nonsyndromic Congenital, 4 38 0.033
810
c PLY105 Polycystic Ovary Syndrome 1 38 0.033
811
SYS071 Systemic Autoimmune Disease 38 0.033
812
INT221 Intravascular Large B-Cell Lymphoma 36 0.033
813
HND015 Hand Skill, Relative 33 0.033
814
FNT004 Fainting 31 0.033
815
RRD056 Rare Disease in Surgical Orthopedic 29 0.033
816
c RNG005 Ring Chromosome 10 28 0.033
817
TCK004 Tick Infestation 25 0.033
818
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.033
819
c RNG013 Ring Chromosome 18 25 0.033
820
LTR004 Lateral Myocardial Infarction 23 0.033
821
ART109 Arterial Thoracic Outlet Syndrome 23 0.033
822
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 21 0.033
823
c MNN043 Meningioma, Familial 74 0.028
824
ART016 Aortic Aneurysm 71 0.028
825
P PNM007 Pneumonia 71 0.028
826
c PRM196 Premature Ovarian Failure 1 70 0.028
827
MSC157 Muscular Dystrophy, Duchenne Type 70 0.028
828
P MYS003 Myasthenia Gravis 68 0.028
829
THY111 Thyroid Carcinoma, Familial Medullary 68 0.028
830
GST040 Gastric Adenocarcinoma 67 0.028
831
c ATS013 Autosomal Recessive Congenital Ichthyosis 65 0.028
832
P CHR071 Charcot-Marie-Tooth Disease 65 0.028
833
MGK001 Megakaryocytic Leukemia 65 0.028
834
P ANR048 Aniridia 1 64 0.028
835
P ART005 Arteriovenous Malformation 63 0.028
836
GT001 Gout 63 0.028
837
c WLM018 Wilms Tumor 5 63 0.028
838
P MST009 Mastocytosis 62 0.028
839
NRM005 Neuromuscular Disease 62 0.028
840
BRC012 Brucellosis 62 0.028
841
TRN015 Transient Cerebral Ischemia 62 0.028
842
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.028
843
THY121 Thyroid Gland Anaplastic Carcinoma 62 0.028
844
P ALP009 Alopecia Areata 61 0.028
845
PRT013 Portal Hypertension 61 0.028
846
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.028
847
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.028
848
P VNT002 Ventricular Septal Defect 61 0.028
849
c ANM038 Anemia, Autoimmune Hemolytic 61 0.028
850
PRT058 Pure Autonomic Failure 60 0.028
851
HYP458 Hyper Ige Syndrome 60 0.028
852
P INT070 Intestinal Obstruction 60 0.028
853
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.028
854
P HRD011 Hereditary Spherocytosis 59 0.028
855
ANG020 Angiosarcoma 59 0.028
856
P MLN069 Melanoma, Uveal 59 0.028
857
c SVR003 Severe Congenital Neutropenia 59 0.028
858
P MTR012 Mitral Valve Disease 59 0.028
859
P LRY044 Larynx Cancer 59 0.028
860
URN010 Urinary Tract Obstruction 59 0.028
861
P PLY006 Polydactyly 58 0.028
862
SPN027 Spinal Stenosis 58 0.028
863
YLL002 Yellow Fever 58 0.028
864
PRM236 Primary Biliary Cholangitis 57 0.028
865
SPN041 Spinal Cord Disease 57 0.028
866
P GLL022 Guillain-Barre Syndrome 56 0.028
867
PNM008 Pneumothorax 56 0.028
868
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 56 0.028
869
P ART021 Arteriosclerosis 56 0.028
870
P INT068 Intestinal Disease 56 0.028
871
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.028
872
ORP003 Oropharynx Cancer 55 0.028
873
SLC006 Silicosis 55 0.028
874
ANN002 Anencephaly 55 0.028
875
MST005 Mastitis 55 0.028
876
c PSR017 Psoriasis 2 55 0.028
877
P NRV006 Nervous System Cancer 55 0.028
878
P SML001 Small Cell Carcinoma 55 0.028
879
c GRV008 Graves Disease 1 55 0.028
880
HYP691 Hypomelanosis of Ito 55 0.028
881
SML019 Smallpox 55 0.028
882
P PRM006 Primary Biliary Cirrhosis 54 0.028
883
PTT009 Pituitary Gland Disease 54 0.028
884
SHG001 Shigellosis 54 0.028
885
GTR002 Goiter 54 0.028
886
P HYP838 Hyperlipidemia, Familial Combined, 3 54 0.028
887
INF034 Infective Endocarditis 53 0.028
888
P PTS002 Ptosis 53 0.028
889
c LRG017 Large Intestine Cancer 53 0.028
890
THY030 Thyroid Gland Disease 53 0.028
891
AST006 Astigmatism 53 0.028
892
LMY002 Leiomyoma 52 0.028
893
OCL006 Ocular Hypertension 52 0.028
894
THY125 Thyroid Gland Medullary Carcinoma 52 0.028
895
FML037 Female Breast Cancer 52 0.028
896
c CNT033 Central Nervous System Cancer 51 0.028
897
CRY005 Cryptococcosis 51 0.028
898
ILS001 Ileus 51 0.028
899
VRC001 Varicocele 51 0.028
900
GLS018 Glass Syndrome 51 0.028
901
VTR016 Vater/vacterl Association 51 0.028
902
HYP748 Hypertelorism 50 0.028
903
c PSR023 Psoriasis 1 50 0.028
904
ECT026 Ectopic Pregnancy 50 0.028
905
CRT013 Carotid Stenosis 50 0.028
906
c PTT057 Pituitary Adenoma 4, Acth-Secreting 50 0.028
907
PLR008 Pleurisy 50 0.028
908
c INF145 Infantile Liver Failure Syndrome 1 50 0.028
909
DRM011 Dermatophytosis 49 0.028
910
CRN027 Corneal Neovascularization 48 0.028
911
SPL004 Splenic Marginal Zone Lymphoma 48 0.028
912
c HNT004 Huntington Disease-Like 2 48 0.028
913
CCN002 Cocaine Abuse 48 0.028
914
BNM001 Bone Marrow Cancer 48 0.028
915
VTM002 Vitamin B12 Deficiency 48 0.028
916
MCR141 Mucormycosis 48 0.028
917
KRT002 Keratomalacia 47 0.028
918
TTH006 Tooth Disease 47 0.028
919
LYM051 Lymphomatoid Granulomatosis 47 0.028
920
SNT005 Sinoatrial Node Disease 46 0.028
921
RFT001 Rift Valley Fever 46 0.028
922
HRN026 Hernia, Hiatus 46 0.028
923
NPH010 Nephrosclerosis 46 0.028
924
SPS007 Spastic Cerebral Palsy 45 0.028
925
c LRG001 Large Cell Carcinoma 45 0.028
926
CWP001 Cowpox 45 0.028
927
ORL015 Oral Squamous Cell Carcinoma 44 0.028
928
AMB001 Amebiasis 44 0.028
929
P MJR007 Major Affective Disorder 1 44 0.028
930
PLY068 Polysubstance Abuse 44 0.028
931
DLS001 Delusional Disorder 44 0.028
932
FNC007 Functioning Pituitary Adenoma 44 0.028
933
P HYP265 Hypotonia 43 0.028
934
FLL031 Follicular Adenoma 43 0.028
935
SMN007 Seminoma 43 0.028
936
BTN002 Boutonneuse Fever 43 0.028
937
P CPL003 Capillary Leak Syndrome 42 0.028
938
MRG013 Mirage Syndrome 42 0.028
939
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.028
940
PTT003 Pituitary-Dependent Cushing's Disease 42 0.028
941
PHB001 Phobic Disorder 42 0.028
942
TRP009 Triple X Syndrome 42 0.028
943
PPL001 Papillary Adenoma 42 0.028
944
RLP003 Relapsing Fever 41 0.028
945
CRB086 Cerebral Aneurysms 41 0.028
946
c SYS007 Systemic Capillary Leak Syndrome 41 0.028
947
P OTT001 Otitis Externa 41 0.028
948
SPN021 Spinal Meningioma 40 0.028
949
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.028
950
c PSR028 Psoriasis 7 40 0.028
951
c PSR018 Psoriasis 13 40 0.028
952
c PSR032 Psoriasis 11 40 0.028
953
c ATM075 Autoimmune Encephalitis 39 0.028
954
GNT029 Genetic Hypertension 39 0.028
955
c MYC083 Myoclonic Epilepsy, Familial Infantile 39 0.028
956
PHB003 Phobia, Specific 39 0.028
957
P DNT007 Dentin Sensitivity 39 0.028
958
SCR001 Secretory Meningioma 38 0.028
959
c HNT011 Huntington Disease-Like 3 37 0.028
960
SCR011 Scrapie 37 0.028
961
NMN001 Nominal Aphasia 37 0.028
962
c PRG020 Paragangliomas 3 36 0.028
963
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.028
964
SPR012 Separation Anxiety Disorder 36 0.028
965
c SBR001 Seborrheic Infantile Dermatitis 36 0.028
966
VGN019 Vaginal Discharge 35 0.028
967
P FML187 Familial Hypertension 35 0.028
968
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.028
969
VRS002 Virus-Associated Trichodysplasia Spinulosa 33 0.028
970
PCD001 Pica Disease 33 0.028
971
NRC003 Narcissistic Personality Disorder 33 0.028
972
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 32 0.028
973
PRT112 Portal Hypertension, Noncirrhotic 31 0.028
974
VNT037 Ventral Hernia 31 0.028
975
PTT001 Pituitary Hypoplasia 30 0.028
976
TMR016 Tumor Suppressor Gene on Chromosome 11 29 0.028
977
c RNG022 Ring Chromosome 6 28 0.028
978
CYT018 Cytochrome P450 2d6 Variant 28 0.028
979
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 28 0.028
980
ANT005 Anteroseptal Myocardial Infarction 26 0.028
981
JVN026 Jeavons Syndrome 24 0.028
982
c RNG019 Ring Chromosome 3 22 0.028
983
ATR089 Atrioventricular Dissociation 20 0.028
984
RFS002 Refsum Disease with Increased Pipecolic Acidemia 7 0.028
985
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.023
986
P MDL005 Medulloblastoma 78 0.023
987
BRN028 Brain Cancer 75 0.023
988
RNL065 Renal Cell Carcinoma, Papillary, 1 75 0.023
989
c TBR025 Tuberous Sclerosis 1 74 0.023
990
P FML011 Familial Adenomatous Polyposis 73 0.023
991
BRT054 Brittle Bone Disorder 71 0.023
992
P NJM001 Nijmegen Breakage Syndrome 70 0.023
993
RCK004 Rickets 70 0.023
994
P CHR012 Chronic Granulomatous Disease 69 0.023
995
MYL005 Myelofibrosis 69 0.023
996
c JVN004 Juvenile Myelomonocytic Leukemia 68 0.023
997
P SYS005 Systemic Scleroderma 68 0.023
998
P MPL001 Maple Syrup Urine Disease 68 0.023
999
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.023
1000
c GLY008 Glycogen Storage Disease Ii 68 0.023
1001
P HLP001 Holoprosencephaly 67 0.023
1002
P OLG002 Oligodendroglioma 67 0.023
1003
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.023
1004
c MCR129 Microvascular Complications of Diabetes 1 67 0.023
1005
MYC006 Mycosis Fungoides 67 0.023
1006
P CCK001 Cockayne Syndrome 66 0.023
1007
P OCL013 Oculodentodigital Dysplasia 65 0.023
1008
P ANG001 Angelman Syndrome 65 0.023
1009
P FRD012 Friedreich Ataxia 1 65 0.023
1010
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.023
1011
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 64 0.023
1012
CLR108 Colorectal Adenoma 64 0.023
1013
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 64 0.023
1014
KRN002 Kearns-Sayre Syndrome 64 0.023
1015
END041 Endometrial Adenocarcinoma 64 0.023
1016
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.023
1017
P TST021 Testicular Germ Cell Tumor 63 0.023
1018
HSH003 Hashimoto Thyroiditis 63 0.023
1019
ACT119 Acute Promyelocytic Leukemia 63 0.023
1020
PSR001 Psoriatic Arthritis 63 0.023
1021
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.023
1022
PPL049 Papillon-Lefevre Syndrome 63 0.023
1023
BRS099 Breast Ductal Carcinoma 63 0.023
1024
MCR013 Microphthalmia 62 0.023
1025
HYP020 Hyperprolactinemia 62 0.023
1026
INC021 Incontinentia Pigmenti 62 0.023
1027
c BRN108 Branchiootic Syndrome 1 62 0.023
1028
P HMN010 Hemangioma 62 0.023
1029
MRK001 Merkel Cell Carcinoma 62 0.023
1030
P SNS001 Sensorineural Hearing Loss 62 0.023
1031
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.023
1032
CRC021 Carcinosarcoma 62 0.023
1033
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.023
1034
CHL068 Cholestasis 61 0.023
1035
DGR001 Digeorge Syndrome 61 0.023
1036
INT066 Interstitial Lung Disease 61 0.023
1037
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.023
1038
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.023
1039
VRC005 Varicose Veins 61 0.023
1040
P PNC044 Pancreatitis 61 0.023
1041
HLC007 Helicobacter Pylori Infection 61 0.023
1042
P ADL010 Adult Respiratory Distress Syndrome 61 0.023
1043
GNG013 Gingivitis 60 0.023
1044
PNM010 Pneumothorax, Primary Spontaneous 60 0.023
1045
c LPM012 Lipomatosis, Multiple 60 0.023
1046
P BRN022 Bronchiectasis 60 0.023
1047
c MCL013 Mucolipidosis Iv 60 0.023
1048
c PRM005 Primary Hyperparathyroidism 60 0.023
1049
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 60 0.023
1050
c ADL017 Adult T-Cell Leukemia 59 0.023
1051
GRD007 Grade Iii Astrocytoma 59 0.023
1052
P PGT001 Paget's Disease of Bone 59 0.023
1053
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 59 0.023
1054
ADR005 Adrenal Carcinoma 58 0.023
1055
GST033 Gestational Diabetes 58 0.023
1056
HYP042 Hypochondroplasia 58 0.023
1057
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.023
1058
BRG013 Buerger Disease 58 0.023
1059
P GST044 Gastritis 58 0.023
1060