Search results for Neurotransmitter Agents

2267 hits were found for Neurotransmitter Agents

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 88 0.174
2
P ENC018 Encephalopathy 61 0.164
3
P NRB001 Neuroblastoma 72 0.160
4
HYP056 Hypoglycemia 66 0.157
5
P LNG032 Lung Cancer 98 0.153
6
P DRR001 Diarrhea 55 0.147
7
P CLR023 Colorectal Cancer 99 0.140
8
P OVR042 Ovarian Cancer 88 0.140
9
P NTR004 Neutropenia 63 0.140
10
CNG034 Congestive Heart Failure 69 0.139
11
DPR016 Depression 63 0.138
12
P LKM002 Leukemia 68 0.138
13
MYL069 Myeloma, Multiple 85 0.138
14
GLL048 Glial Tumor 45 0.137
15
P GLM045 Glioma 63 0.136
16
P BRS047 Breast Cancer 97 0.136
17
ALL026 Allergic Hypersensitivity Disease 62 0.136
18
P KDN018 Kidney Disease 72 0.131
19
HYP266 Hypoxia 57 0.131
20
GLB015 Glioblastoma Multiforme 75 0.129
21
P PNC035 Pancreatic Cancer 84 0.129
22
P MYL006 Myeloid Leukemia 60 0.129
23
c LKM061 Leukemia, Acute Myeloid 84 0.129
24
ISC004 Ischemia 58 0.128
25
P PSR002 Psoriasis 62 0.126
26
PST011 Pustulosis of Palm and Sole 52 0.125
27
SCR011 Scrapie 39 0.125
28
c SML038 Small Cell Cancer of the Lung 65 0.124
29
MYL009 Myelodysplastic Syndrome 70 0.123
30
P PRS040 Prostate Cancer 97 0.123
31
P TRM003 Tremor 54 0.121
32
P SZR006 Seizure Disorder 56 0.119
33
ALC007 Alcohol Dependence 66 0.119
34
BCT022 Bacterial Infectious Disease 56 0.119
35
P HRP006 Herpes Simplex 65 0.119
36
c HYP595 Hypertension, Essential 84 0.118
37
ATM095 Autoimmune Disease 62 0.118
38
VSL002 Visual Epilepsy 59 0.117
39
48X005 48,xyyy 39 0.116
40
MNT002 Mental Depression 58 0.116
41
P PHC003 Pheochromocytoma 71 0.114
42
ADR040 Adrenal Gland Pheochromocytoma 46 0.114
43
c HPT073 Hepatitis C Virus 72 0.114
44
P SCH015 Schizophrenia 74 0.114
45
ANX010 Anxiety 73 0.113
46
P INF037 Inflammatory Bowel Disease 54 0.112
47
P RHM011 Rheumatoid Arthritis 80 0.111
48
c HPT001 Hepatitis C 62 0.111
49
PRT037 Pertussis 65 0.110
50
HRW001 Hair Whorl 36 0.110
51
c MGR028 Migraine with or Without Aura 1 67 0.109
52
HMP009 Haemophilus Influenzae 43 0.108
53
LVR012 Liver Cirrhosis 62 0.108
54
DWN001 Down Syndrome 70 0.108
55
P HNT016 Huntington Disease 72 0.108
56
c SVR001 Severe Acute Respiratory Syndrome 62 0.108
57
P NRP001 Neuropathy 56 0.108
58
TTN003 Tetanus 65 0.107
59
PNG002 Pain Agnosia 51 0.107
60
P HRT032 Heart Disease 75 0.107
61
CYT002 Cytokine Deficiency 42 0.106
62
P ADN016 Adenocarcinoma 64 0.106
63
P MJR001 Major Depressive Disorder 68 0.105
64
HYP066 Hyperglycemia 61 0.104
65
CRH001 Crohn's Disease 74 0.104
66
c PCH010 Pachyonychia Congenita 3 44 0.103
67
DRM006 Dermatitis 61 0.102
68
CNS004 Constipation 58 0.102
69
CHL014 Cholera 59 0.102
70
LSH001 Leishmaniasis 63 0.101
71
P KLZ004 Kala-Azar 1 41 0.101
72
HMN044 Human Immunodeficiency Virus Type 1 71 0.101
73
P LTR001 Lateral Sclerosis 54 0.101
74
P DMN002 Dementia 66 0.101
75
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.100
76
OCL069 Ocular Motor Apraxia 51 0.099
77
P BLD134 Bladder Cancer 79 0.099
78
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.099
79
AGN016 Aging 56 0.099
80
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.099
81
SPN186 Spinal Cord Injury 60 0.098
82
P OST002 Osteoporosis 74 0.098
83
BRN071 Brain Injury 49 0.098
84
P PRK057 Parkinson Disease, Late-Onset 78 0.098
85
P LVR013 Liver Disease 68 0.098
86
TRM010 Traumatic Brain Injury 51 0.097
87
P DBT009 Diabetes Mellitus 64 0.097
88
P PNM007 Pneumonia 68 0.097
89
P ART022 Arthritis 69 0.096
90
P EXN002 Exanthem 57 0.096
91
P LKM071 Leukemia, Chronic Lymphocytic 79 0.096
92
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.096
93
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.096
94
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.096
95
LPD008 Lipid Metabolism Disorder 62 0.096
96
P ENC004 Encephalitis 61 0.096
97
LYM017 Lyme Disease 64 0.095
98
ANG054 Angina Pectoris 66 0.095
99
P VSC007 Vascular Disease 63 0.094
100
P PRP019 Peripheral Nervous System Disease 58 0.094
101
P CHR345 Chronic Pain 44 0.093
102
P HPT021 Hepatitis 67 0.093
103
GST045 Gastroenteritis 59 0.093
104
MDD011 Mood Disorder 62 0.093
105
P DYS154 Dystonia 65 0.093
106
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.092
107
SKN016 Skin Disease 63 0.092
108
P BPL003 Bipolar Disorder 56 0.092
109
P MVM001 Movement Disease 63 0.092
110
PLG002 Plague 63 0.092
111
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.092
112
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.092
113
CHG001 Chagas Disease 66 0.091
114
PPT005 Peptic Ulcer Disease 59 0.091
115
P THR014 Thrombocytopenia 67 0.091
116
P HDC001 Headache 57 0.090
117
P LKM062 Leukemia, Acute Lymphoblastic 69 0.090
118
P MLT020 Multiple Sclerosis 72 0.090
119
OST159 Osteogenic Sarcoma 66 0.090
120
HPT004 Hepatic Coma 45 0.090
121
c MJR024 Major Affective Disorder 9 41 0.090
122
c MJR022 Major Affective Disorder 8 38 0.090
123
BNR002 Bone Resorption Disease 48 0.089
124
SRC014 Sarcoma 65 0.089
125
HPT019 Hepatic Encephalopathy 60 0.089
126
SPN035 Spindle Cell Sarcoma 53 0.089
127
ACQ007 Acquired Immunodeficiency Syndrome 60 0.088
128
c THR092 Thrombophilia Due to Thrombin Defect 73 0.088
129
P BCL017 B-Cell Lymphoma 58 0.088
130
SQM006 Squamous Cell Carcinoma 60 0.088
131
SVR004 Severe Combined Immunodeficiency 73 0.087
132
IMP005 Impotence 52 0.087
133
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.087
134
ULC004 Ulcerative Colitis 73 0.087
135
AMN003 Amnestic Disorder 54 0.087
136
P EPL164 Epilepsy 71 0.086
137
LYM133 Lymphoma, Hodgkin, Classic 69 0.086
138
CRB039 Cerebrovascular Disease 67 0.086
139
ATH013 Atherosclerosis Susceptibility 65 0.086
140
P MNN013 Meningitis 66 0.086
141
c NRF023 Neurofibromatosis, Type Ii 80 0.086
142
c HPT016 Hepatitis B 59 0.085
143
ANX004 Anoxia 40 0.085
144
P MLN008 Melanoma 69 0.085
145
CRB004 Cerebral Artery Occlusion 45 0.084
146
OST012 Osteoarthritis 78 0.084
147
P ALP008 Alopecia 54 0.084
148
STT001 Status Epilepticus 60 0.084
149
PSR001 Psoriatic Arthritis 61 0.084
150
P GST053 Gastric Cancer 83 0.084
151
P ATR011 Atrial Fibrillation 66 0.084
152
P KDN017 Kidney Cancer 60 0.083
153
c HYP836 Hypercholesterolemia, Familial, 1 73 0.083
154
STR067 Stroke, Ischemic 81 0.083
155
STM007 Stomatitis 50 0.083
156
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.083
157
IRN002 Iron Metabolism Disease 57 0.082
158
c SPN225 Spondyloarthropathy 1 73 0.082
159
ADN018 Adenoma 59 0.082
160
LWC001 Low Compliance Bladder 43 0.082
161
P SKN015 Skin Carcinoma 66 0.082
162
DNT012 Dental Caries 53 0.082
163
47X002 47,xyy 49 0.082
164
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.082
165
PLY150 Polykaryocytosis Inducer 31 0.081
166
P ASP006 Aspergillosis 69 0.081
167
OBS002 Obsessive-Compulsive Disorder 68 0.081
168
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.081
169
P HYP086 Hypothyroidism 69 0.081
170
DRM011 Dermatophytosis 52 0.081
172
P PRD008 Periodontitis 64 0.080
173
PLM001 Pulmonary Tuberculosis 69 0.080
174
P CTR002 Cataract 60 0.080
175
AST005 Asthma 76 0.080
176
CYS001 Cystic Fibrosis 81 0.080
177
GST023 Gastric Ulcer 53 0.079
178
BRN028 Brain Cancer 74 0.079
179
PLM033 Pulmonary Embolism 59 0.079
180
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.079
181
TRD006 Tardive Dyskinesia 54 0.079
182
P INF038 Influenza 68 0.079
183
P SLP005 Sleep Disorder 59 0.079
184
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.078
185
CHC001 Chickenpox 60 0.078
186
P DRM053 Dermatitis, Atopic 66 0.078
187
PRT036 Peritonitis 64 0.078
188
IRR002 Irritable Bowel Syndrome 65 0.077
189
P AST007 Astrocytoma 51 0.077
190
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.077
191
P FBR017 Fibrosarcoma 56 0.076
192
P ATS364 Autism 70 0.076
193
SPS057 Spasticity 45 0.076
194
P HYP076 Hyperthyroidism 55 0.075
195
WTH001 Withdrawal Disorder 48 0.075
196
BRN004 Brain Edema 56 0.075
197
P UVT001 Uveitis 57 0.075
198
CVD001 Covid-19 44 0.075
199
P CRD119 Cardiac Arrest 67 0.075
200
P END033 Endocarditis 57 0.075
201
P AMY004 Amyloidosis 70 0.074
202
P CYS018 Cystitis 59 0.074
203
P VSC011 Vasculitis 62 0.074
204
MLR004 Malaria 81 0.074
205
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.074
206
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.074
207
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.074
208
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.074
209
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.074
210
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.074
211
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.074
212
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.074
213
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.074
214
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.074
215
END040 Endogenous Depression 55 0.074
216
P URT039 Urticaria 58 0.074
217
END057 Endometrial Cancer 74 0.073
218
P GLM007 Glomerulonephritis 57 0.073
219
SFT003 Soft Tissue Sarcoma 56 0.073
220
P PLY011 Polycystic Ovary Syndrome 56 0.073
221
c LKM063 Leukemia, Chronic Myeloid 72 0.072
222
ORL011 Oral Cancer 60 0.072
223
P ALC033 Alcohol Use Disorder 58 0.072
224
P MCR115 Microvascular Complications of Diabetes 5 66 0.072
225
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.072
226
OVR094 Ovarian Epithelial Cancer 38 0.072
227
P MYS003 Myasthenia Gravis 68 0.072
228
PRT058 Pure Autonomic Failure 59 0.072
229
P TRN020 Turner Syndrome 67 0.072
230
P HYD006 Hydrocephalus 66 0.072
231
VSC002 Vascular Dementia 57 0.071
232
P INF032 Infertility 57 0.071
233
VCC001 Vaccinia 49 0.071
234
c MLG068 Malignant Glioma 46 0.071
235
HYP060 Hyperinsulinism 54 0.071
236
HLX001 Helix Syndrome 47 0.071
237
P MYP004 Myopathy 70 0.071
238
c VRL010 Viral Hepatitis 52 0.070
239
PLM010 Pulmonary Edema 54 0.070
240
GT001 Gout 64 0.070
241
ANT024 Anthrax Disease 58 0.070
242
FTT001 Fatty Liver Disease 61 0.070
243
c HPT003 Hepatitis a 62 0.070
244
DYS015 Dysentery 52 0.070
245
P BNG032 Benign Mesothelioma 46 0.070
246
c ATS007 Autism Spectrum Disorder 67 0.070
247
PRT013 Portal Hypertension 59 0.070
248
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.070
249
CNT047 Contact Dermatitis 58 0.070
250
P GRF003 Graft-Versus-Host Disease 72 0.069
251
P BND020 Bone Disease 59 0.069
252
HDN002 Head Injury 46 0.069
253
PRS045 Prostatic Hypertrophy 53 0.069
254
SBC016 Subacute Delirium 44 0.069
255
P SBS003 Substance Abuse 55 0.069
256
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.069
257
MSL001 Measles 62 0.069
258
THY029 Thyroid Carcinoma 59 0.069
259
SCH014 Schistosomiasis 57 0.069
260
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.069
261
ESP021 Esophageal Cancer 90 0.069
262
P TXP001 Toxoplasmosis 60 0.069
263
HYP005 Hypokalemia 55 0.068
264
P HYP098 Hypereosinophilic Syndrome 67 0.068
265
MCL006 Macular Retinal Edema 55 0.068
266
P DDN001 Duodenal Ulcer 52 0.068
267
P HYP069 Hyperparathyroidism 63 0.068
268
PHN003 Phenylketonuria 75 0.068
269
P RTN024 Retinoblastoma 73 0.068
270
c FML008 Familial Retinoblastoma 53 0.068
272
ACT119 Acute Promyelocytic Leukemia 63 0.068
273
P END044 Endometriosis 63 0.068
274
CHL068 Cholestasis 61 0.067
275
c DWL002 Dowling-Degos Disease 1 58 0.067
276
P PLM036 Pulmonary Fibrosis 65 0.067
277
OST017 Osteomyelitis 64 0.067
278
P RCT021 Rectum Cancer 52 0.067
279
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.067
280
PRS021 Prostatic Adenoma 51 0.067
281
TRN015 Transient Cerebral Ischemia 63 0.067
282
NRT001 Neurotic Disorder 53 0.067
283
c CHR064 Chronic Monocytic Leukemia 33 0.067
284
P SRC025 Sarcoidosis 1 70 0.066
285
P GST044 Gastritis 56 0.066
286
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.066
287
P GLM040 Glioma Susceptibility 1 81 0.066
288
SKN019 Skin Melanoma 68 0.066
289
OST003 Osteonecrosis 61 0.066
290
c MCR113 Microvascular Complications of Diabetes 3 52 0.066
291
c MCR120 Microvascular Complications of Diabetes 7 47 0.066
292
c PRS136 Prostate Cancer, Hereditary, 6 33 0.066
293
c PRS130 Prostate Cancer, Hereditary, 8 32 0.066
294
P RSP003 Respiratory Failure 74 0.066
295
c MCR130 Microvascular Complications of Diabetes 6 41 0.066
296
c MCR133 Microvascular Complications of Diabetes 4 41 0.066
297
RCK004 Rickets 68 0.065
298
PRS129 Prostatic Hyperplasia, Benign 49 0.065
299
HRP004 Herpes Zoster 60 0.065
300
MNT001 Mantle Cell Lymphoma 69 0.065
301
P HMN010 Hemangioma 61 0.065
302
PST028 Post-Traumatic Stress Disorder 58 0.065
303
VRC005 Varicose Veins 60 0.065
304
c ACT027 Acute Pancreatitis 60 0.065
305
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.065
306
SXL003 Sexual Disorder 47 0.065
307
P PRS038 Personality Disorder 65 0.065
308
CTN007 Cutaneous Leishmaniasis 62 0.064
309
P SPP010 Suppressor of Tumorigenicity 3 51 0.064
310
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.064
311
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.064
312
P OVR082 Overgrowth Syndrome 50 0.064
313
P NSP012 Nasopharyngeal Carcinoma 66 0.064
314
P NPH012 Nephrotic Syndrome 60 0.064
315
P TCD001 Tic Disorder 53 0.064
316
P HMP007 Hemophilia 51 0.064
317
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.064
318
CRD223 Cardiac Arrhythmia 60 0.064
319
TRN018 Transitional Cell Carcinoma 56 0.064
320
PRP030 Purpura 54 0.064
321
P ART023 Arthropathy 62 0.063
322
CHL065 Cholangiocarcinoma 68 0.063
323
PNC129 Pancreatic Adenocarcinoma 68 0.063
324
P PNC044 Pancreatitis 61 0.063
325
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.063
326
c BCT007 Bacterial Meningitis 55 0.063
327
P MSC005 Muscular Dystrophy 66 0.063
328
c PRC016 Pre-Eclampsia 63 0.063
329
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.063
330
c ACT134 Acute Liver Failure 56 0.063
331
P MTR014 Motor Neuron Disease 65 0.063
332
CHR073 Choreatic Disease 52 0.063
333
P RHB003 Rhabdomyosarcoma 63 0.063
334
GNG013 Gingivitis 59 0.063
335
HMS001 Hemosiderosis 54 0.063
336
PPL022 Papilloma 54 0.063
337
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.063
338
P ART005 Arteriovenous Malformation 65 0.063
339
ACT084 Acute Stress Disorder 47 0.063
340
P PRN023 Prion Disease 57 0.063
341
ENT004 Enthesopathy 49 0.063
342
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.063
343
ALL014 Allergic Encephalomyelitis 38 0.062
344
INT079 Intrahepatic Cholangiocarcinoma 51 0.062
345
KPS004 Kaposi Sarcoma 75 0.062
346
DPH001 Diphtheria 60 0.062
347
SLP001 Sleeping Sickness 54 0.062
348
P MYC033 Myoclonus 46 0.062
349
P NRC002 Narcolepsy 52 0.062
350
P MYC008 Myocarditis 59 0.062
351
DFF005 Diffuse Large B-Cell Lymphoma 55 0.062
352
HNS001 Hansen's Disease 34 0.062
353
P MSC003 Muscular Atrophy 52 0.062
354
P SLP006 Sleep Apnea 69 0.062
355
VRL011 Viral Infectious Disease 61 0.062
356
P HYP265 Hypotonia 43 0.062
357
P LPR021 Leprosy 3 69 0.061
358
P RRH023 Rare Hereditary Hemochromatosis 41 0.061
359
INS024 Insulin-Like Growth Factor I 79 0.061
360
OTT002 Otitis Media 72 0.061
361
c OVR114 Ovarian Cancer 1 38 0.061
362
P ART021 Arteriosclerosis 54 0.061
363
CRD132 Cardiac Conduction Defect 58 0.061
364
PLS009 Plasma Cell Neoplasm 51 0.061
365
GRN017 Granulocytopenia 44 0.061
366
ILS001 Ileus 51 0.061
367
c JVN010 Juvenile Rheumatoid Arthritis 64 0.061
368
GLC003 Glucose Intolerance 54 0.061
369
P PRP029 Porphyria 62 0.060
370
CRB037 Cerebral Palsy 69 0.060
371
P PNC025 Panic Disorder 53 0.060
372
P MDL005 Medulloblastoma 77 0.060
373
BRK010 Burkitt Lymphoma 67 0.060
374
ATX019 Ataxia with Vitamin E Deficiency 42 0.060
375
P MLG074 Malignant Mesenchymoma 40 0.060
376
KRT006 Keratoconjunctivitis 53 0.060
377
P CTN015 Cutaneous T Cell Lymphoma 49 0.060
378
SQM002 Squamous Cell Papilloma 46 0.060
379
P THL005 Thalassemia 60 0.060
380
P ATX030 Ataxia-Telangiectasia 82 0.059
381
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.059
382
SYN007 Synovitis 54 0.059
383
PLC002 Plica Syndrome 36 0.059
384
URM002 Uremia 49 0.059
385
DSS008 Disease of Mental Health 58 0.059
386
VSC003 Visceral Leishmaniasis 55 0.059
387
P ANP001 Anaplastic Large Cell Lymphoma 58 0.059
388
GST033 Gestational Diabetes 61 0.059
389
EMB004 Embryonal Carcinoma 56 0.059
390
c DLT002 Dilated Cardiomyopathy 79 0.059
391
P SYS005 Systemic Scleroderma 68 0.059
392
P MYC084 Mycobacterium Tuberculosis 1 68 0.059
393
c JVN061 Juvenile Arthritis 60 0.059
394
ERY051 Erythroleukemia, Familial 56 0.059
395
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.058
396
HYP014 Hyperuricemia 52 0.058
397
INT075 Intracranial Hypertension 53 0.058
398
KRT009 Keratosis 51 0.058
399
P ECL001 Eclampsia 50 0.058
400
c INV001 Invasive Aspergillosis 49 0.058
401
P NRV007 Nervous System Disease 66 0.058
402
CRC021 Carcinosarcoma 62 0.058
403
NNL006 Non-Alcoholic Steatohepatitis 54 0.057
404
c CHR682 Chronic Bilirubin Encephalopathy 39 0.057
405
PST092 Posttransplant Acute Limbic Encephalitis 29 0.057
406
DBT010 Diabetic Neuropathy 54 0.057
407
c HMP029 Hemophilia a 67 0.057
408
P CHR285 Chronic Myelomonocytic Leukemia 60 0.057
409
MYL005 Myelofibrosis 70 0.056
410
KHN001 Kuhnt-Junius Degeneration 47 0.056
411
ADG002 Audiogenic Seizures 25 0.056
412
c FML001 Familial Atrial Fibrillation 65 0.056
413
P HYP750 Hypertriglyceridemia, Familial 62 0.056
414
INT066 Interstitial Lung Disease 60 0.056
415
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.056
416
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.056
417
GST050 Gastrointestinal System Disease 56 0.056
418
INF034 Infective Endocarditis 53 0.056
419
HYP020 Hyperprolactinemia 64 0.056
420
c INF145 Infantile Liver Failure Syndrome 1 50 0.056
421
P HML002 Hemolytic Anemia 63 0.056
422
c MST023 Mesothelioma, Malignant 57 0.056
423
P PYL005 Pyelonephritis 56 0.056
424
P INT068 Intestinal Disease 53 0.056
425
P PTS002 Ptosis 53 0.056
426
c SCL052 Scleroderma, Familial Progressive 61 0.056
427
DYS073 Dysphagia 50 0.056
428
RTN017 Retinal Detachment 61 0.055
429
P DNG005 Dengue Virus 59 0.055
430
LYM027 Lymphopenia 58 0.055
431
CRN030 Coronary Stenosis 50 0.055
432
P MYP006 Myopia 55 0.055
433
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.055
434
FBR047 Fibromyalgia 58 0.055
435
CRY005 Cryptococcosis 58 0.055
436
c GLL024 Gallbladder Disease 1 53 0.055
437
SPL018 Splenomegaly 48 0.055
438
MXD026 Mixed Glioma 45 0.055
439
P HYP061 Hypertrophic Cardiomyopathy 70 0.055
440
ATN005 Autonomic Dysfunction 46 0.055
441
LMY002 Leiomyoma 52 0.055
442
c MCR129 Microvascular Complications of Diabetes 1 66 0.055
443
CYT008 Cytomegalovirus Infection 57 0.055
444
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.054
445
P ADL010 Adult Respiratory Distress Syndrome 65 0.054
446
HMT002 Hematologic Cancer 62 0.054
447
DRM009 Dermatomycosis 36 0.054
448
PHR003 Pharyngitis 57 0.054
449
P INS002 in Situ Carcinoma 53 0.054
450
CRH005 Crohn's Colitis 53 0.054
451
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.054
452
ALL006 Allergic Asthma 56 0.054
453
c BRN108 Branchiootic Syndrome 1 62 0.054
454
PST021 Postpartum Depression 50 0.054
455
GLL008 Gilles De La Tourette Syndrome 66 0.054
456
CNN005 Connective Tissue Disease 68 0.054
457
c DBT099 Diabetes Mellitus, Type I 65 0.054
458
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.054
459
GLS001 Gliosarcoma 54 0.054
460
P MJR007 Major Affective Disorder 1 43 0.054
461
P NRF002 Neurofibromatosis 56 0.053
462
ART016 Aortic Aneurysm 69 0.053
463
P ESP024 Esophagitis 62 0.053
464
CHR100 Chronic Ulcer of Skin 55 0.053
465
ORL015 Oral Squamous Cell Carcinoma 43 0.053
466
NRR001 Neuroretinitis 42 0.053
467
DRG003 Drug Dependence 47 0.053
468
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.053
469
EWN003 Ewing Sarcoma 69 0.053
470
PSY004 Psychotic Disorder 67 0.053
471
P PLY018 Polycythemia 56 0.053
472
CRD137 Cardiogenic Shock 47 0.053
473
TRP009 Triple X Syndrome 42 0.053
474
CHR066 Chronic Fatigue Syndrome 61 0.053
475
ETN001 Eating Disorder 60 0.053
476
c CNT035 Central Nervous System Disease 52 0.053
477
c INH020 Inherited Metabolic Disorder 47 0.053
478
CHR178 Chromosomal Triplication 35 0.053
479
FDB001 Foodborne Botulism 55 0.053
480
GST019 Gastrointestinal Stromal Tumor 78 0.053
481
NTR005 Nutritional Deficiency Disease 62 0.053
482
c PSR028 Psoriasis 7 42 0.053
483
RYN005 Raynaud Phenomenon 47 0.053
484
RTN023 Retinitis 46 0.053
485
ANR007 Anorexia Nervosa 63 0.052
486
c PSR017 Psoriasis 2 53 0.052
487
c PSR023 Psoriasis 1 52 0.052
488
c PSR032 Psoriasis 11 47 0.052
489
CHR074 Choriocarcinoma 47 0.052
490
c PSR018 Psoriasis 13 41 0.052
491
c MCR112 Microvascular Complications of Diabetes 2 41 0.052
492
P TMP001 Temporal Lobe Epilepsy 50 0.052
493
P RTN016 Retinal Degeneration 53 0.052
494
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.052
495
PLS011 Plasmacytoma 56 0.052
496
CCN001 Cocaine Dependence 48 0.052
497
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.052
498
FLL027 Fallopian Tube Carcinoma 67 0.052
499
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.052
500
P CHL066 Cholangitis 51 0.052
501
MCR004 Macroglobulinemia 49 0.052
502
NRM005 Neuromuscular Disease 64 0.052
503
c WLM018 Wilms Tumor 5 61 0.052
504
TND005 Tendinitis 54 0.052
505
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.052
506
c BSL007 Basal Cell Carcinoma 68 0.052
507
BRN002 Bronchiolitis 59 0.052
508
TXC002 Toxic Encephalopathy 53 0.052
509
c BCT013 Bacterial Pneumonia 48 0.052
510
SYN036 Syncope 45 0.052
511
TBC004 Tobacco Addiction 64 0.052
512
P PRM006 Primary Biliary Cirrhosis 62 0.051
513
P BRN022 Bronchiectasis 59 0.051
514
IGR001 Ige Responsiveness, Atopic 59 0.051
515
EXT034 Extrinsic Allergic Alveolitis 58 0.051
516
c FLL041 Follicular Lymphoma 1 49 0.051
517
TST014 Testicular Cancer 46 0.051
518
BCK006 Back Pain 42 0.051
519
PPL052 Papillomatosis, Confluent and Reticulated 33 0.051
520
RBS001 Rabies 58 0.051
521
BLR008 Bilirubin Metabolic Disorder 57 0.051
522
MTN003 Motion Sickness 53 0.051
523
ATS010 Autosomal Recessive Disease 48 0.051
524
MYL031 Myeloproliferative Neoplasm 66 0.051
525
MTH009 Mouth Disease 56 0.051
526
c FML035 Familial Hyperlipidemia 55 0.051
527
P PMP001 Pemphigus 54 0.051
529
HYP025 Hyperphosphatemia 48 0.051
530
TNP001 Tinea Pedis 46 0.051
531
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.051
532
CRC006 Carcinoid Syndrome 55 0.051
533
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.051
534
HLC007 Helicobacter Pylori Infection 59 0.051
535
CLL003 Cellulitis 54 0.051
536
c PRD040 Periodontitis, Chronic 53 0.051
537
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.051
538
ANV001 Anovulation 47 0.051
539
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.051
540
GST037 Gastroparesis 54 0.050
541
HYP081 Hypolipoproteinemia 51 0.050
542
49X006 49, Xxxxy Syndrome 41 0.050
543
ANG049 Angioedema Induced by Ace Inhibitors 40 0.050
544
PRM020 Premenstrual Tension 40 0.050
545
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.050
546
PTH003 Pathologic Nystagmus 52 0.050
547
c MNN043 Meningioma, Familial 74 0.050
548
P LMY004 Leiomyosarcoma 63 0.050
549
MNN042 Meningioma, Radiation-Induced 62 0.050
550
SPP011 Suppression of Tumorigenicity 12 59 0.050
551
P PLY019 Polyneuropathy 56 0.050
552
P RTN022 Retinal Vein Occlusion 53 0.050
553
SPN021 Spinal Meningioma 50 0.050
554
NWC001 Newcastle Disease 45 0.050
555
SCR001 Secretory Meningioma 41 0.050
556
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.050
557
FDL002 Food Allergy 51 0.050
558
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.050
559
c GLC092 Glaucoma, Primary Open Angle 62 0.050
560
c PNS012 Paine Syndrome 61 0.050
561
P BNG030 Benign Ependymoma 60 0.050
562
P ALP009 Alopecia Areata 60 0.050
563
CLL010 Cellular Ependymoma 54 0.050
564
AMN001 Amenorrhea 54 0.050
565
MDD018 Middle East Respiratory Syndrome 43 0.050
566
P SNS001 Sensorineural Hearing Loss 60 0.050
567
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.049
568
c ATM011 Autoimmune Hepatitis 63 0.049
569
P INT143 Interstitial Cystitis 61 0.049
570
ATR057 Atrioventricular Block 55 0.049
571
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.049
572
RTC005 Reticulosarcoma 47 0.049
573
CNT033 Central Nervous System Cancer 47 0.049
574
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.049
575
c INF071 Inflammatory Bowel Disease 1 67 0.049
576
P BNC003 Bone Cancer 58 0.049
577
DSS009 Disseminated Intravascular Coagulation 57 0.049
578
HRT012 Heart Valve Disease 53 0.049
579
P PRR002 Pure Red-Cell Aplasia 47 0.049
580
MSC157 Muscular Dystrophy, Duchenne Type 72 0.049
581
P OLG002 Oligodendroglioma 67 0.049
582
CRT015 Carotid Artery Occlusion 45 0.049
583
P DRM010 Dermatomyositis 61 0.049
584
PRS047 Prostatitis 56 0.049
585
P MNC007 Monocytic Leukemia 53 0.049
586
P HMR005 Hemorrhoid 46 0.049
587
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.049
588
RDC006 Red Cell Aplasia 43 0.049
589
DRG024 Drug Allergy 42 0.049
590
GST020 Gastric Antral Vascular Ectasia 41 0.049
591
P SJG008 Sjogren Syndrome 61 0.048
592
HYP043 Hyperandrogenism 48 0.048
593
CRN017 Coronary Thrombosis 47 0.048
594
c HYP272 Hypercholesterolemia, Familial, 3 44 0.048
595
ATM052 Autoimmune Disease 1 37 0.048
596
BLM002 Bulimia Nervosa 57 0.048
597
P PLY014 Polycystic Kidney Disease 62 0.048
598
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.048
599
RDC002 Radiculopathy 50 0.048
600
TND004 Tendinopathy 43 0.048
601
P ESS003 Essential Thrombocythemia 68 0.048
602
P LNG028 Long Qt Syndrome 66 0.048
603
APN008 Apnea, Obstructive Sleep 64 0.048
604
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.048
605
NWB001 Newborn Respiratory Distress Syndrome 58 0.048
606
P MMP001 Mumps 58 0.048
607
c VSC019 Vesicoureteral Reflux 1 57 0.048
608
TNS005 Tonsillitis 57 0.048
609
HMR039 Hemorrhage, Intracerebral 57 0.048
610
AYM001 Ayme-Gripp Syndrome 57 0.048
611
ACR041 Acromelic Frontonasal Dysostosis 52 0.048
612
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.048
613
CRN322 Coronavirus Infectious Disease 40 0.048
614
c ESS001 Essential Tremor 56 0.048
615
MLT157 Multiple System Atrophy 1 70 0.047
616
PRC013 Pericarditis 54 0.047
617
GST040 Gastric Adenocarcinoma 70 0.047
618
PLY001 Polycythemia Vera 69 0.047
619
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.047
620
c MCL013 Mucolipidosis Iv 66 0.047
621
THY122 Thyroid Gland Cancer 57 0.047
622
MRG003 Marginal Zone B-Cell Lymphoma 52 0.047
623
THR004 Thrombocytosis 51 0.047
624
PPL001 Papillary Adenoma 44 0.047
625
c MJR008 Major Affective Disorder 2 35 0.047
626
c MJR023 Major Affective Disorder 7 33 0.047
627
c MJR003 Major Affective Disorder 6 33 0.047
628
c MJR006 Major Affective Disorder 5 33 0.047
629
c MJR004 Major Affective Disorder 4 28 0.047
630
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.047
631
ANG020 Angiosarcoma 64 0.047
632
P LYM033 Lymphoproliferative Syndrome 59 0.047
633
LMB062 Limb Ischemia 55 0.047
634
SNS003 Sensory Peripheral Neuropathy 54 0.047
635
PRP036 Peripheral T-Cell Lymphoma 53 0.047
636
CRY014 Cryptococcal Meningitis 48 0.047
637
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.047
638
PLY068 Polysubstance Abuse 43 0.047
639
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.047
640
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.047
641
c DNG003 Dengue Disease 59 0.047
642
P RNL015 Renal Hypertension 47 0.047
643
RFR003 Refractive Error 43 0.047
644
P MYS005 Myositis 56 0.047
645
c GRV008 Graves Disease 1 56 0.047
646
NRN004 Neuroendocrine Tumor 55 0.047
647
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.047
648
P HMR003 Hemorrhagic Disease 53 0.047
649
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.047
650
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.047
651
CCN002 Cocaine Abuse 49 0.047
652
P EPN001 Ependymoblastoma 44 0.047
653
SMN007 Seminoma 43 0.047
654
OPD006 Opioid Addiction 48 0.046
655
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.046
656
CLF027 Cleft Palate, Isolated 64 0.046
657
c BTT014 Beta-Thalassemia 74 0.046
658
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.046
659
HRY003 Hairy Cell Leukemia 55 0.046
660
P ACT008 Actinic Keratosis 53 0.046
661
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.046
662
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.046
663
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.046
664
P PRV006 Pervasive Developmental Disorder 57 0.046
665
PRV004 Periventricular Leukomalacia 52 0.046
666
NRF007 Neurofibroma 64 0.046
667
GRD007 Grade Iii Astrocytoma 59 0.046
668
ERY003 Erythema Multiforme 58 0.046
669
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.046
670
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.046
671
GSG001 Gas Gangrene 53 0.046
672
PLC008 Placenta Disease 50 0.046
673
c PRM226 Primary Central Nervous System Lymphoma 48 0.046
674
MYF001 Myofibroma 45 0.046
675
APP009 Appendix Adenocarcinoma 44 0.046
676
CRB086 Cerebral Aneurysms 40 0.046
677
HDG004 Hodgkin's Granuloma 23 0.046
678
HDG006 Hodgkin's Paragranuloma 22 0.046
679
INS001 Insulinoma 60 0.046
680
LMY014 Leiomyoma, Uterine 56 0.046
681
P RST001 Restless Legs Syndrome 54 0.046
682
HYP080 Hypogonadism 50 0.046
683
ADR007 Adrenoleukodystrophy 75 0.045
684
BRR014 Barrett Esophagus 65 0.045
685
P THY023 Thymoma 65 0.045
686
BRS099 Breast Ductal Carcinoma 62 0.045
687
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.045
688
P MLN007 Male Infertility 55 0.045
689
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.045
690
c THY107 Thymoma, Familial 52 0.045
691
c ALM001 Al Amyloidosis 50 0.045
692
AZS001 Azoospermia 50 0.045
693
OPT003 Opiate Dependence 50 0.045
694
c CHR418 Chronic Leukemia 49 0.045
695
GST049 Gastrointestinal System Cancer 49 0.045
696
BCT004 Bacteriuria 49 0.045
697
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.045
698
GST071 Gastrointestinal Carcinoma 47 0.045
699
MNN020 Meningococcal Infection 46 0.045
700
CLN045 Colonic Benign Neoplasm 46 0.045
701
URL001 Urolithiasis 45 0.045
702
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.045
703
CRV045 Cervical Intraepithelial Neoplasia 39 0.045
704
GRM010 Germ Cells Tumors 34 0.045
705
P SPN046 Spinal Muscular Atrophy 62 0.045
706
AVD001 Avoidant Personality Disorder 51 0.045
707
SBS004 Substance Dependence 48 0.045
708
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.045
709
P CLS010 Cluster Headache 42 0.045
710
HND015 Hand Skill, Relative 33 0.045
711
HYP141 Hyperphenylalaninemia 39 0.045
712
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.045
713
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.045
714
BRN056 Bronchopulmonary Dysplasia 57 0.045
715
TCK001 Tick-Borne Encephalitis 56 0.045
716
PLS016 Plasma Cell Leukemia 53 0.045
717
P SML001 Small Cell Carcinoma 52 0.045
718
FCT001 Factor Viii Deficiency 51 0.045
719
THR016 Thrombophlebitis 51 0.045
720
CYS014 Cystadenocarcinoma 51 0.045
721
ESP002 Esophageal Varix 51 0.045
722
SKN013 Skin Benign Neoplasm 51 0.045
723
HYP781 Hypoascorbemia 51 0.045
724
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.045
725
RST023 Resting Heart Rate, Variation in 41 0.045
726
PRS063 Paresthesia 41 0.045
727
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.045
728
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.045
729
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.045
730
P FRN006 Frontotemporal Dementia 68 0.045
731
c EXD008 Exudative Vitreoretinopathy 1 71 0.045
732
P LPS002 Liposarcoma 65 0.045
733
c WLM013 Wilms Tumor 1 65 0.045
734
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.045
735
P TST021 Testicular Germ Cell Tumor 60 0.045
736
PMP006 Pemphigus Vulgaris, Familial 57 0.045
737
c LKM070 Leukemia, Acute Monocytic 57 0.045
738
PNM008 Pneumothorax 56 0.045
739
P LRY044 Larynx Cancer 55 0.045
740
PRP016 Paraplegia 52 0.045
741
P MMB011 Membranous Nephropathy 50 0.045
742
RSP006 Respiratory System Disease 50 0.045
743
KRT001 Keratoconjunctivitis Sicca 49 0.045
744
CHL004 Cholelithiasis 49 0.045
745
NSS002 Neisseria Meningitidis Infection 47 0.045
746
IMM136 Immune System Disease 45 0.045
747
PTT009 Pituitary Gland Disease 54 0.044
748
P MLG056 Malignant Hyperthermia 67 0.044
749
WLD007 Waldenstroem's Macroglobulinemia 61 0.044
750
P SCL018 Scoliosis 60 0.044
751
INT030 Intracranial Aneurysm 56 0.044
752
DMY004 Demyelinating Disease 52 0.044
753
c VRL005 Viral Pneumonia 52 0.044
754
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.044
755
ADR016 Adrenal Cortical Carcinoma 48 0.044
756
GRM005 Germ Cell Cancer 47 0.044
757
PRD004 Prediabetes Syndrome 47 0.044
758
P MTH007 Methemoglobinemia 46 0.044
759
ORB013 Orbital Disease 42 0.044
760
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.044
761
c PLY105 Polycystic Ovary Syndrome 1 38 0.044
762
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.044
763
MLG164 Malignant Epithelial Tumor of Ovary 26 0.044
764
HRP008 Herpes Simiae 25 0.044
765
P FRG001 Fragile X Syndrome 70 0.044
766
P MTC069 Mitochondrial Disorders 56 0.044
767
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.044
768
P VNS003 Venous Insufficiency 55 0.044
769
CLR030 Clear Cell Renal Cell Carcinoma 53 0.044
770
P CRN028 Corneal Ulcer 47 0.044
771
GST010 Gestational Trophoblastic Neoplasm 46 0.044
772
P SBR004 Seborrheic Dermatitis 45 0.044
773
ADR004 Adrenal Cortical Adenocarcinoma 39 0.044
774
TRP005 Trophoblastic Neoplasm 38 0.044
775
c WLM011 Wilms Tumor 6 37 0.044
776
RSP007 Respiratory Distress Syndrome, Infant 30 0.044
777
HML018 Homologous Wasting Disease 22 0.044
778
CMP010 Complex Regional Pain Syndrome 58 0.044
779
NRL004 Neuroleptic Malignant Syndrome 56 0.044
780
FCL014 Focal Epilepsy 54 0.044
781
DCB001 Decubitus Ulcer 61 0.043
782
IDP011 Idiopathic Interstitial Pneumonia 59 0.043
783
PGM001 Pigmented Villonodular Synovitis 56 0.043
784
P STR020 Strabismus 55 0.043
785
P CNT005 Central Nervous System Lymphoma 53 0.043
786
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.043
787
SRS001 Serous Cystadenocarcinoma 52 0.043
788
FSC004 Fasciitis 50 0.043
789
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.043
790
DRY001 Dry Eye Syndrome 47 0.043
791
LYM012 Lymphoplasmacytic Lymphoma 47 0.043
792
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.043
793
BNM001 Bone Marrow Cancer 43 0.043
794
MCH006 Mechanical Strabismus 42 0.043
795
PTT037 Pituitary Tumors 44 0.043
796
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.043
797
PSD088 Pseudobulbar Affect 36 0.043
798
P DBT005 Diabetes Insipidus 55 0.043
799
BRD004 Borderline Personality Disorder 53 0.043
800
RTN003 Retinal Ischemia 50 0.043
801
CRB090 Cerebral Hypoxia 44 0.043
802
c HMC039 Hemochromatosis, Type 1 74 0.043
803
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.043
804
MGK001 Megakaryocytic Leukemia 64 0.043
805
BRS051 Breast Disease 58 0.043
806
P GLL018 Gallbladder Cancer 57 0.043
807
BRN012 Bronchiolitis Obliterans 55 0.043
808
ORP003 Oropharynx Cancer 55 0.043
809
NTR018 Neutrophilia, Hereditary 52 0.043
810
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.043
811
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.043
812
LPT006 Leptin Receptor Deficiency 48 0.043
813
SRT004 Serotonin Syndrome 47 0.043
814
PLS025 Plasmablastic Lymphoma 47 0.043
815
P TST026 Testicular Germ Cell Cancer 43 0.043
816
DFF003 Diffuse Scleroderma 41 0.043
817
P DNT007 Dentin Sensitivity 36 0.043
818
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.043
819
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.043
820
TRG002 Trigeminal Neuralgia 60 0.043
821
MYM001 Myoma 54 0.043
822
P OVR049 Ovarian Disease 52 0.043
823
ATN004 Autonomic Neuropathy 45 0.043
824
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.043
825
c ALP101 Alpha-Thalassemia 62 0.042
826
CHL067 Cholecystitis 57 0.042
827
c BSL024 Basal Cell Carcinoma 1 56 0.042
828
HMG005 Hemoglobinopathy 56 0.042
829
HPT022 Hepatoblastoma 56 0.042
830
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.042
831
GNT002 Giant Cell Glioblastoma 50 0.042
832
INT067 Interstitial Nephritis 48 0.042
833
SMT001 Somatization Disorder 46 0.042
834
OPD001 Opioid Abuse 46 0.042
835
IMM064 Immunodeficiency, Common Variable, 10 44 0.042
836
HYP344 Hyperthyroidism, Familial Gestational 39 0.042
837
ACH005 Achalasia 51 0.042
838
ONC002 Onchocerciasis 52 0.042
839
ASP004 Asphyxia Neonatorum 46 0.042
840
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.042
841
ALC006 Alcoholic Hepatitis 61 0.042
842
APH001 Aphthous Stomatitis 57 0.042
843
P FCL005 Focal Segmental Glomerulosclerosis 57 0.042
844
P BRN035 Brain Stem Glioma 52 0.042
845
P HYP040 Hypospadias 51 0.042
846
HPT014 Hepatorenal Syndrome 50 0.042
847
ACT029 Acute Interstitial Pneumonia 49 0.042
848
c HPT015 Hepatitis D 49 0.042
849
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.042
850
P HMN032 Human Herpesvirus 8 47 0.042
851
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.042
852
c CNG216 Congenital Hydrocephalus 47 0.042
853
CYN002 Cyanosis, Transient Neonatal 45 0.042
854
P OCY003 Oocyte Maturation Defect 1 45 0.042
855
ANP009 Anaplastic Oligodendroglioma 43 0.042
856
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.042
857
P RTN008 Retinitis Pigmentosa 79 0.042
858
LRN003 Learning Disability 49 0.042
859
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.042
860
P FTL001 Fetal Alcohol Syndrome 57 0.042
861
ADN011 Adenoid Cystic Carcinoma 70 0.041
862
SVR097 Severe Cutaneous Adverse Reaction 69 0.041
863
c ART101 Aortic Valve Disease 2 65 0.041
864
P TRC086 Trichohepatoenteric Syndrome 1 62 0.041
865
ING001 Inguinal Hernia 60 0.041
866
IRN001 Iron Deficiency Anemia 59 0.041
867
ADR005 Adrenal Carcinoma 58 0.041
868
P GLL020 Gallbladder Disease 57 0.041
869
BRD001 Brody Myopathy 57 0.041
870
PLM012 Pulmonary Sarcoidosis 53 0.041
871
c HRD202 Hereditary Lymphedema I 50 0.041
872
NTR046 Neutrophil Migration 50 0.041
873
PRL017 Prolymphocytic Leukemia 47 0.041
874
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.041
875
c DRM054 Dermatitis, Atopic, 2 44 0.041
876
P BCT020 Bacteremia 2 44 0.041
877
c SRC023 Sarcoidosis 2 43 0.041
878
ENT001 Enterocele 39 0.041
879
ERY066 Erythema Multiforme Major 30 0.041
880
c TST046 Testicular Germ Cell Tumor 1 29 0.041
881
P RTT002 Rett Syndrome 80 0.041
882
P BRB001 Beriberi 46 0.041
883
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.041
884
P MST009 Mastocytosis 64 0.041
885
APP008 Appendicitis 61 0.041
886
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.041
887
SRC027 Sarcoma, Synovial 58 0.041
888
P PLY041 Polymyositis 57 0.041
889
P CHN012 Chondrosarcoma 56 0.041
890
CRT017 Cartilage Disease 54 0.041
891
MCN017 Meconium Ileus 52 0.041
892
c PRM012 Primary Polycythemia 50 0.041
893
c THR090 Thrombocythemia 1 49 0.041
894
RYN001 Raynaud Disease 48 0.041
895
CLS016 Clostridium Difficile Colitis 48 0.041
896
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.041
897
BRN032 Brain Glioma 45 0.041
898
PRT035 Peritoneum Cancer 44 0.041
899
P AVS003 Avascular Necrosis 42 0.041
900
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.041
901
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.041
902
CLS052 Classic Hairy Cell Leukemia 27 0.041
903
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.041
904
P CNG001 Congenital Myasthenic Syndrome 66 0.041
905
P BLD062 Bile Duct Cancer 67 0.041
906
ACR006 Aceruloplasminemia 65 0.041
907
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.041
908
c LPM012 Lipomatosis, Multiple 60 0.041
909
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.041
910
NRT004 Neuritis 52 0.041
911
CRT016 Carotid Artery Disease 52 0.041
912
HPR003 Heparin-Induced Thrombocytopenia 48 0.041
913
P BLD051 Blood Coagulation Disease 46 0.041
914
CLL014 Cll/sll 45 0.041
915
CYS009 Cystadenoma 44 0.041
916
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.041
917
RFR002 Refractory Hairy Cell Leukemia 33 0.041
918
P VSC018 Visceral Steatosis 33 0.041
919
VLV047 Volvulus of Midgut 49 0.040
920
STF001 Stiff-Person Syndrome 60 0.040
921
MLN003 Melancholia 38 0.040
922
P CLC063 Celiac Disease 1 66 0.040
923
c CHR417 Chronic Graft Versus Host Disease 57 0.040
924
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.040
925
URN010 Urinary Tract Obstruction 55 0.040
926
BRN014 Bronchopneumonia 54 0.040
927
ACT200 Acute Monoblastic Leukemia 52 0.040
928
SPL004 Splenic Marginal Zone Lymphoma 51 0.040
929
TNG007 Tongue Carcinoma 51 0.040
930
PNM005 Pneumonic Plague 51 0.040
931
LNG020 Lung Oat Cell Carcinoma 47 0.040
932
OBS003 Obsessive-Compulsive Personality Disorder 46 0.040
933
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.040
934
HMR023 Hemorrhagic Cystitis 45 0.040
935
OVR112 Ovarian Germ Cell Cancer 45 0.040
936
P ATX024 Ataxia-Oculomotor Apraxia 3 44 0.040
937
P CRN024 Corneal Disease 44 0.040
938
SKN005 Skin Atrophy 43 0.040
939
BLR013 Biliary Tract Cancer 42 0.040
940
UTR043 Uterine Sarcoma 39 0.040
941
P INT260 Intracranial Berry Aneurysm 39 0.040
942
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.040
943
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.040
944
MNR012 Meniere Disease 57 0.040
945
HPT046 Hepatic Veno-Occlusive Disease 56 0.040
946
SPN041 Spinal Cord Disease 56 0.040
947
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.040
948
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.040
949
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.040
950
ACT017 Acute Chest Syndrome 51 0.040
951
CRT013 Carotid Stenosis 50 0.040
952
STT002 Status Asthmaticus 50 0.040
953
INT054 Intraocular Lymphoma 48 0.040
954
ACT098 Acute Erythroid Leukemia 48 0.040
955
PLL012 Pollen Allergy 46 0.040
956
EXT010 Extramedullary Plasmacytoma 45 0.040
957
CNT017 Central Nervous System Origin Vertigo 45 0.040
958
GNG003 Gingival Recession 44 0.040
959
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.040
960
IDP033 Idiopathic Edema 44 0.040
961
P CRN026 Corneal Edema 43 0.040
962
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 40 0.040
963
JVN026 Jeavons Syndrome 24 0.040
964
ADS004 Aids Dementia Complex 40 0.039
965
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.039
966
P NJM001 Nijmegen Breakage Syndrome 74 0.039
967
THY111 Thyroid Carcinoma, Familial Medullary 67 0.039
968
PRT010 Parathyroid Carcinoma 67 0.039
969
MYX005 Myxoid Liposarcoma 66 0.039
970
CRN036 Craniopharyngioma 65 0.039
971
PRM126 Primary Peritoneal Carcinoma 62 0.039
972
P ORT004 Orthostatic Intolerance 62 0.039
973
MSS001 Masa Syndrome 62 0.039
974
c HRD002 Hereditary Angioedema 60 0.039
975
P SLV026 Salivary Gland Carcinoma 57 0.039
976
NRG002 Neurogenic Bladder 55 0.039
977
P ANT006 Antiphospholipid Syndrome 55 0.039
978
P PTT006 Pituitary Adenoma 55 0.039
979
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.039
980
P ORL007 Oral Cavity Cancer 53 0.039
981
P PRC012 Pericardial Effusion 51 0.039
982
P THR015 Thrombophilia 51 0.039
983
CHL018 Childhood Medulloblastoma 49 0.039
984
STP011 Stapes Ankylosis with Broad Thumbs and Toes 49 0.039
985
CHL061 Childhood Leukemia 48 0.039
986
P SCL015 Scleritis 48 0.039
987
HMP001 Hemopericardium 48 0.039
988
KRT008 Keratopathy 47 0.039
989
c ORT011 Orthostatic Hypotension 1 44 0.039
990
MCR011 Microinvasive Gastric Cancer 43 0.039
991
MCN008 Mucinous Cystadenocarcinoma 40 0.039
992
FML039 Female Reproductive System Disease 39 0.039
993
c ADL008 Adult Oligodendroglioma 34 0.039
994
LRY047 Laryngeal Abductor Paralysis 28 0.039
995
LSC001 Lesch-Nyhan Syndrome 62 0.039
996
HYP264 Hypertonia 38 0.039
997
P OLV001 Olivopontocerebellar Atrophy 51 0.039
998
CRP001 Carpal Tunnel Syndrome 67 0.039
999
HYD002 Hydronephrosis 60 0.039
1000
SPN027 Spinal Stenosis 59 0.039
1001
HMT008 Hematuria, Benign Familial 56 0.039
1002
P DYS193 Dystonia 11, Myoclonic 55 0.039
1003
P SPN052 Spondyloarthropathy 54 0.039
1004
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.039
1005
P KRT007 Keratoconus 50 0.039
1006
HRT011 Heart Septal Defect 50 0.039
1007
c INF023 Inflammatory Breast Carcinoma 50 0.039
1008
VRR004 Verrucous Carcinoma 49 0.039
1009
HDR003 Hidradenitis 49 0.039
1010
QDR001 Quadriplegia 48 0.039
1011
CRC014 Carcinoid Tumors, Intestinal 47 0.039
1012
MYC005 Myocardial Stunning 46 0.039
1013
ANP006 Anaplastic Ependymoma 46 0.039
1014
INT253 Intestinal Benign Neoplasm 45 0.039
1015
ORL013 Oral Lichen Planus 45 0.039
1016
CHL149 Childhood Acute Myeloid Leukemia 44 0.039
1017
SPR008 Supratentorial Primitive Neuroectodermal Tumor 43 0.039
1018
DBT002 Diabetic Autonomic Neuropathy 41 0.039
1019
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.039
1020
SWL001 Swallowing Disorders 38 0.039
1021
TST043 Testicular Seminoma 35 0.039
1022
PDT014 Pediatric Ependymoma 32 0.039
1023
TMP019 Temporomandibular Joint Anomaly 28 0.039
1024
P CNT036 Central Nervous System Germ Cell Tumor 28 0.039
1025
HMP005 Hemiplegia 55 0.038
1026
c DMN023 Diamond-Blackfan Anemia 1 53 0.038
1027
c CRS016 Crisponi/cold-Induced Sweating Syndrome 1 52 0.038
1028
ADT003 Auditory System Disease 48 0.038
1029
c ATM075 Autoimmune Encephalitis 38 0.038
1030
c NRF024 Neurofibromatosis, Type I 77 0.038
1031
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.038
1032
INC002 Inclusion Body Myositis 58 0.038
1033
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.038
1034
ANG005 Anogenital Venereal Wart 55 0.038
1035
FLR002 Filariasis 55 0.038
1036
RHM028 Rheumatic Heart Disease 53 0.038
1037
LYS002 Lysosomal Storage Disease 52 0.038
1038
PPT001 Peptic Esophagitis 52 0.038
1039
c PRM108 Primary Progressive Multiple Sclerosis 51 0.038
1040
THY125 Thyroid Gland Medullary Carcinoma 50 0.038
1041
HMG002 Hemoglobinuria 50 0.038
1042
GYN001 Gynecomastia 49 0.038
1043
c BPL002 Bipolar I Disorder 49 0.038
1044
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.038
1045
CRP002 Croup 44 0.038
1046
DMP001 Dumping Syndrome 44 0.038
1047
c MLG064 Malignant Ependymoma 41 0.038
1048
KLD004 Keloid Disorder 40 0.038
1049
PLC009 Placenta Praevia 39 0.038
1050
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.038
1051
INF021 Infant Gynecomastia 31 0.038
1052
STT009 Sutton Disease 2 30 0.038
1053
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.038
1054
FNT004 Fainting 30 0.038
1055
BRN049 Brain Tumor, Childhood 29 0.038
1056
FTL073 Fetal Anticonvulsant Syndrome 26 0.038
1057
CYS005 Cysticercosis 53 0.038
1058
MTC005 Mitochondrial Metabolism Disease 49 0.038
1059
HPT085 Hepatitis, Fulminant Viral 32 0.038
1060
NRL016 Neural Tube Defects 82 0.038
1061
MRF001 Marfan Syndrome 77 0.038
1062
c TBR025 Tuberous Sclerosis 1 77 0.038
1063
P ANR048 Aniridia 1 63 0.038
1064
CHN016 Cohen Syndrome 63 0.038
1065
PRG017 Paraganglioma and Gastric Stromal Sarcoma 61 0.038
1066
PNM010 Pneumothorax, Primary Spontaneous 60 0.038
1067
RHM001 Rheumatic Fever 60 0.038