Search results for Melatonin

1108 hits were found for Melatonin

# Family MCID Name MIFTS Score
1
P SLP005 Sleep Disorder 59 0.446
2
ISC004 Ischemia 60 0.267
3
PRT037 Pertussis 65 0.237
4
DPR016 Depression 63 0.231
5
SBC016 Subacute Delirium 44 0.219
6
P MJR001 Major Depressive Disorder 68 0.215
7
BRN071 Brain Injury 49 0.202
8
MNT002 Mental Depression 57 0.197
9
P BRS047 Breast Cancer 96 0.189
10
DLY008 Delayed Sleep Phase Disorder 47 0.189
11
P ALZ034 Alzheimer Disease 88 0.181
12
P NRB001 Neuroblastoma 71 0.179
13
AGN016 Aging 56 0.177
14
HYP066 Hyperglycemia 61 0.176
15
ANX010 Anxiety 72 0.175
16
P ATS364 Autism 65 0.175
17
SPN186 Spinal Cord Injury 60 0.174
18
P HDC001 Headache 57 0.174
19
HYP266 Hypoxia 56 0.169
20
P BPL003 Bipolar Disorder 56 0.167
21
P SZR006 Seizure Disorder 58 0.165
22
c MJR024 Major Affective Disorder 9 41 0.163
23
c MJR022 Major Affective Disorder 8 38 0.163
24
P SCL018 Scoliosis 60 0.162
25
c ATS007 Autism Spectrum Disorder 67 0.161
26
c MGR028 Migraine with or Without Aura 1 69 0.156
27
VSL002 Visual Epilepsy 58 0.154
28
TRM010 Traumatic Brain Injury 53 0.151
29
IDP070 Idiopathic Scoliosis 37 0.148
30
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.146
31
MDD011 Mood Disorder 62 0.146
32
c PRC016 Pre-Eclampsia 63 0.143
33
c ACT027 Acute Pancreatitis 59 0.143
34
P MLT020 Multiple Sclerosis 72 0.140
35
CLT003 Colitis 62 0.136
36
CRB004 Cerebral Artery Occlusion 44 0.136
37
P SCL057 Scoliosis, Isolated 1 41 0.134
38
P PRK057 Parkinson Disease, Late-Onset 76 0.129
39
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.127
40
P MYC007 Myocardial Infarction 70 0.127
41
c HYP595 Hypertension, Essential 84 0.125
42
P KDN018 Kidney Disease 70 0.125
43
P SLP006 Sleep Apnea 69 0.125
44
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.125
45
ATM095 Autoimmune Disease 61 0.125
46
PNG002 Pain Agnosia 51 0.124
47
BNR002 Bone Resorption Disease 48 0.124
48
P PLY011 Polycystic Ovary Syndrome 56 0.122
49
BRN004 Brain Edema 55 0.122
50
PPL052 Papillomatosis, Confluent and Reticulated 34 0.120
51
P HNT016 Huntington Disease 71 0.118
52
CRB039 Cerebrovascular Disease 69 0.118
53
TXC005 Toxic Shock Syndrome 61 0.118
54
FTT001 Fatty Liver Disease 61 0.118
55
c ACT075 Acute Myocardial Infarction 56 0.118
56
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.118
57
CYT002 Cytokine Deficiency 44 0.118
58
P GLM045 Glioma 63 0.116
59
P PRD008 Periodontitis 62 0.116
60
END040 Endogenous Depression 54 0.116
61
GLL048 Glial Tumor 45 0.116
62
48X005 48,xyyy 39 0.116
64
P LVR013 Liver Disease 68 0.115
65
FBR047 Fibromyalgia 59 0.115
66
P CLR023 Colorectal Cancer 98 0.113
67
STR067 Stroke, Ischemic 80 0.113
68
P OST002 Osteoporosis 73 0.113
69
P EPL164 Epilepsy 71 0.113
70
DWN001 Down Syndrome 70 0.113
71
c CHR684 Chronic Kidney Disease 66 0.113
72
P ENC018 Encephalopathy 61 0.113
73
ATX019 Ataxia with Vitamin E Deficiency 48 0.113
74
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.111
75
IRR002 Irritable Bowel Syndrome 63 0.111
76
P CRN300 Coronary Heart Disease 1 63 0.111
77
CHL068 Cholestasis 60 0.111
78
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.111
79
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.111
80
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.111
81
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.111
82
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.111
83
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.111
84
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.111
85
P HYP086 Hypothyroidism 68 0.109
86
LPD008 Lipid Metabolism Disorder 62 0.109
87
P LTR001 Lateral Sclerosis 53 0.109
88
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.109
89
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.109
90
P ADN016 Adenocarcinoma 64 0.107
91
DRM006 Dermatitis 61 0.107
92
P PNC044 Pancreatitis 61 0.107
93
P INF032 Infertility 57 0.107
94
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.107
95
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.107
96
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.107
97
P DBT009 Diabetes Mellitus 64 0.105
98
HYP080 Hypogonadism 50 0.105
99
HYP064 Hypogonadotropism 40 0.105
100
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.102
101
PSY004 Psychotic Disorder 67 0.102
102
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.102
103
P CTR002 Cataract 60 0.102
104
SMT008 Smith-Magenis Syndrome 55 0.102
105
P PRS040 Prostate Cancer 97 0.100
106
P OVR042 Ovarian Cancer 89 0.100
107
P SCH015 Schizophrenia 75 0.100
108
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.100
109
HYP056 Hypoglycemia 66 0.100
110
P END044 Endometriosis 62 0.100
111
P HRT032 Heart Disease 75 0.098
112
P VSC007 Vascular Disease 63 0.098
113
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.098
114
INS001 Insulinoma 60 0.098
115
P INF037 Inflammatory Bowel Disease 56 0.098
116
TRD006 Tardive Dyskinesia 55 0.098
117
CHL079 Children's Interstitial Lung Disease 27 0.098
118
P HPT023 Hepatocellular Carcinoma 100 0.096
119
ULC004 Ulcerative Colitis 73 0.096
120
MLN008 Melanoma 69 0.096
121
ORL011 Oral Cancer 60 0.096
122
RMS001 Rem Sleep Behavior Disorder 44 0.096
123
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 43 0.096
124
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.096
125
CNG034 Congestive Heart Failure 70 0.094
126
LVR012 Liver Cirrhosis 63 0.094
127
P CRN018 Coronary Artery Anomaly 63 0.094
128
c PNS012 Paine Syndrome 61 0.094
129
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.094
130
END057 Endometrial Cancer 74 0.091
131
P MCR115 Microvascular Complications of Diabetes 5 66 0.091
132
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.091
133
GLC003 Glucose Intolerance 54 0.091
134
P CHR345 Chronic Pain 50 0.091
135
P CLS010 Cluster Headache 43 0.091
136
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.091
137
GLB015 Glioblastoma Multiforme 75 0.089
138
P DMN002 Dementia 67 0.089
139
OST159 Osteogenic Sarcoma 66 0.089
140
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.089
141
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.089
142
P HYP076 Hyperthyroidism 55 0.089
143
P RTN016 Retinal Degeneration 53 0.089
144
HMC014 Homocysteinemia 53 0.089
145
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.086
146
c ACT071 Acute Kidney Failure 59 0.086
147
P BCL017 B-Cell Lymphoma 58 0.086
148
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.086
149
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.086
150
P NRP001 Neuropathy 56 0.086
151
P HYP730 Hypogonadotropic Hypogonadism 53 0.086
152
GST023 Gastric Ulcer 53 0.086
153
47X002 47,xyy 49 0.086
154
QDR001 Quadriplegia 48 0.086
155
P PNC035 Pancreatic Cancer 84 0.084
156
P DRM053 Dermatitis, Atopic 66 0.084
157
c RHB024 Rhabdomyosarcoma 2 65 0.084
158
IDP011 Idiopathic Interstitial Pneumonia 63 0.084
159
ANR007 Anorexia Nervosa 63 0.084
160
P PLM036 Pulmonary Fibrosis 61 0.084
161
P BND020 Bone Disease 59 0.084
162
MCS002 Mucositis 55 0.084
163
DMY004 Demyelinating Disease 52 0.084
164
c MCR120 Microvascular Complications of Diabetes 7 47 0.084
165
INS024 Insulin-Like Growth Factor I 79 0.081
166
P ART022 Arthritis 70 0.081
167
ALC007 Alcohol Dependence 66 0.081
168
GST092 Gastroesophageal Reflux 65 0.081
169
P PRP029 Porphyria 62 0.081
170
CHR066 Chronic Fatigue Syndrome 61 0.081
171
CHL014 Cholera 55 0.081
172
P PRC019 Precocious Puberty 47 0.081
173
P MJR007 Major Affective Disorder 1 43 0.081
174
NN2002 Non 24 Hour Sleep Wake Disorder 24 0.081
175
P LNG032 Lung Cancer 97 0.078
176
P GST053 Gastric Cancer 83 0.078
177
P RHM011 Rheumatoid Arthritis 80 0.078
178
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.078
179
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.078
180
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.078
181
END030 End Stage Renal Failure 58 0.078
182
GST033 Gestational Diabetes 57 0.078
183
P UVT001 Uveitis 57 0.078
184
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.078
185
AMN003 Amnestic Disorder 54 0.078
186
AMN001 Amenorrhea 54 0.078
187
P ECL001 Eclampsia 51 0.078
188
P DDN001 Duodenal Ulcer 50 0.078
189
TST044 Testicular Torsion 47 0.078
190
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.078
191
ALL014 Allergic Encephalomyelitis 39 0.078
192
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.075
193
c ATR087 Atrial Standstill 1 74 0.075
194
P PHC003 Pheochromocytoma 71 0.075
195
P MSC005 Muscular Dystrophy 66 0.075
196
ATH013 Atherosclerosis Susceptibility 66 0.075
197
P HYD006 Hydrocephalus 65 0.075
198
APN008 Apnea, Obstructive Sleep 65 0.075
199
PRP083 Porphyria, Acute Intermittent 63 0.075
200
P DRR001 Diarrhea 57 0.075
201
P MLN007 Male Infertility 56 0.075
202
NRT001 Neurotic Disorder 52 0.075
203
c MCR113 Microvascular Complications of Diabetes 3 52 0.075
204
NNL006 Non-Alcoholic Steatohepatitis 51 0.075
205
ADR040 Adrenal Gland Pheochromocytoma 46 0.075
206
c MCR130 Microvascular Complications of Diabetes 6 41 0.075
207
c MCR133 Microvascular Complications of Diabetes 4 41 0.075
208
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.075
209
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.075
210
c SYS001 Systemic Lupus Erythematosus 86 0.072
211
P THR014 Thrombocytopenia 68 0.072
212
CRB037 Cerebral Palsy 68 0.072
213
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.072
214
CHG001 Chagas Disease 66 0.072
215
ALL026 Allergic Hypersensitivity Disease 64 0.072
216
P ESP024 Esophagitis 62 0.072
217
CNS004 Constipation 57 0.072
218
DSS008 Disease of Mental Health 57 0.072
219
P CRD246 Cardiovascular System Disease 56 0.072
220
c PRD040 Periodontitis, Chronic 54 0.072
221
LPT014 Leptin Deficiency or Dysfunction 73 0.069
222
P CNR004 Cone-Rod Dystrophy 2 71 0.069
223
c FNC043 Fanconi Anemia, Complementation Group E 62 0.069
224
P MVM001 Movement Disease 61 0.069
225
LNG099 Lung Disease 61 0.069
226
HPT019 Hepatic Encephalopathy 60 0.069
227
SQM006 Squamous Cell Carcinoma 60 0.069
228
P PRV006 Pervasive Developmental Disorder 57 0.069
229
HYP060 Hyperinsulinism 54 0.069
230
OCL069 Ocular Motor Apraxia 51 0.069
231
P NRC002 Narcolepsy 51 0.069
232
P FBR031 Febrile Seizures 51 0.069
233
c ACT134 Acute Liver Failure 51 0.069
234
P TMP001 Temporal Lobe Epilepsy 50 0.069
235
P AST007 Astrocytoma 50 0.069
236
HDN002 Head Injury 45 0.069
237
HPT004 Hepatic Coma 43 0.069
238
HYP020 Hyperprolactinemia 64 0.066
239
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.066
240
P HYP069 Hyperparathyroidism 62 0.066
241
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.066
242
P LPS004 Lupus Erythematosus 61 0.066
243
SDD001 Sudden Infant Death Syndrome 61 0.066
244
P KDN017 Kidney Cancer 61 0.066
245
ETN001 Eating Disorder 59 0.066
246
P BRS044 Breast Adenocarcinoma 59 0.066
247
SCH003 Schizophreniform Disorder 56 0.066
248
P PNC025 Panic Disorder 53 0.066
249
STM007 Stomatitis 49 0.066
250
PRM329 Premature Aging 39 0.066
251
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 37 0.066
252
PHN003 Phenylketonuria 75 0.063
253
DFC004 Deficiency Anemia 75 0.063
254
c HYP836 Hypercholesterolemia, Familial, 1 72 0.063
255
c EXD008 Exudative Vitreoretinopathy 1 69 0.063
256
P PLM037 Pulmonary Hypertension 68 0.063
257
P CRD119 Cardiac Arrest 67 0.063
258
c SML038 Small Cell Cancer of the Lung 65 0.063
259
STT001 Status Epilepticus 59 0.063
260
P CYS018 Cystitis 59 0.063
261
P ALC033 Alcohol Use Disorder 58 0.063
262
P ALP008 Alopecia 56 0.063
263
P TRM003 Tremor 53 0.063
264
HYP081 Hypolipoproteinemia 50 0.063
265
c PCH010 Pachyonychia Congenita 3 43 0.063
266
ORL015 Oral Squamous Cell Carcinoma 43 0.063
267
TRP009 Triple X Syndrome 42 0.063
268
AST005 Asthma 77 0.059
269
HMN044 Human Immunodeficiency Virus Type 1 71 0.059
270
P TBR001 Tuberous Sclerosis 70 0.059
271
c PRM196 Premature Ovarian Failure 1 68 0.059
272
P LYM118 Lymphoma 68 0.059
273
OBS002 Obsessive-Compulsive Disorder 68 0.059
274
P NRV007 Nervous System Disease 66 0.059
275
P TRN020 Turner Syndrome 65 0.059
276
P OPT006 Optic Nerve Disease 57 0.059
277
SFT003 Soft Tissue Sarcoma 56 0.059
278
DBT010 Diabetic Neuropathy 55 0.059
279
P ART021 Arteriosclerosis 54 0.059
280
ART140 Arteries, Anomalies of 53 0.059
281
IMP005 Impotence 52 0.059
282
PLC008 Placenta Disease 49 0.059
283
c MLG068 Malignant Glioma 45 0.059
284
BCK006 Back Pain 42 0.059
285
P HYP263 Hypersomnia 41 0.059
286
c MJR008 Major Affective Disorder 2 34 0.059
287
c MJR003 Major Affective Disorder 6 33 0.059
288
c MJR006 Major Affective Disorder 5 33 0.059
289
c MJR023 Major Affective Disorder 7 33 0.059
290
c MJR004 Major Affective Disorder 4 28 0.059
291
P RTT002 Rett Syndrome 80 0.055
292
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.055
293
P RTN008 Retinitis Pigmentosa 77 0.055
294
c TBR025 Tuberous Sclerosis 1 76 0.055
295
P RTN024 Retinoblastoma 72 0.055
296
ART016 Aortic Aneurysm 68 0.055
297
CHL065 Cholangiocarcinoma 67 0.055
298
P SKN015 Skin Carcinoma 67 0.055
299
CRN036 Craniopharyngioma 65 0.055
300
NTR005 Nutritional Deficiency Disease 61 0.055
301
P INT143 Interstitial Cystitis 61 0.055
302
PRT013 Portal Hypertension 60 0.055
303
ACQ007 Acquired Immunodeficiency Syndrome 60 0.055
304
LYM027 Lymphopenia 57 0.055
305
IRN002 Iron Metabolism Disease 57 0.055
306
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.055
307
P GST044 Gastritis 55 0.055
308
c SVR001 Severe Acute Respiratory Syndrome 55 0.055
309
c FML035 Familial Hyperlipidemia 55 0.055
310
OCL006 Ocular Hypertension 53 0.055
311
MST005 Mastitis 53 0.055
312
c FML008 Familial Retinoblastoma 53 0.055
313
P RTN018 Retinal Disease 52 0.055
314
SCH012 Schizoaffective Disorder 50 0.055
315
AZS001 Azoospermia 50 0.055
316
HYP781 Hypoascorbemia 50 0.055
317
INT079 Intrahepatic Cholangiocarcinoma 50 0.055
318
CRT013 Carotid Stenosis 50 0.055
319
TRY001 Trypanosomiasis 50 0.055
320
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.055
321
P OBS001 Obstructive Jaundice 48 0.055
322
CRD137 Cardiogenic Shock 48 0.055
323
PRD004 Prediabetes Syndrome 47 0.055
324
ANV001 Anovulation 47 0.055
325
RTN023 Retinitis 46 0.055
326
ASP004 Asphyxia Neonatorum 45 0.055
327
NRR001 Neuroretinitis 43 0.055
328
HRW001 Hair Whorl 36 0.055
329
NRL016 Neural Tube Defects 82 0.051
330
OST012 Osteoarthritis 78 0.051
331
P LNG064 Lung Cancer Susceptibility 3 77 0.051
332
CRV035 Cervical Cancer 76 0.051
333
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.051
334
SVR004 Severe Combined Immunodeficiency 73 0.051
335
GST040 Gastric Adenocarcinoma 70 0.051
336
RCK004 Rickets 69 0.051
337
PNC129 Pancreatic Adenocarcinoma 67 0.051
338
P ANG001 Angelman Syndrome 67 0.051
339
c FML001 Familial Atrial Fibrillation 66 0.051
340
P ATR011 Atrial Fibrillation 66 0.051
341
SRC014 Sarcoma 65 0.051
342
P NTR004 Neutropenia 63 0.051
343
INT002 Intermittent Claudication 61 0.051
344
CRC021 Carcinosarcoma 61 0.051
345
P ENC004 Encephalitis 61 0.051
346
P MYC008 Myocarditis 59 0.051
347
HLC007 Helicobacter Pylori Infection 59 0.051
348
ANR040 Aneurysm 58 0.051
349
PPT005 Peptic Ulcer Disease 58 0.051
350
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 58 0.051
351
EYD002 Eye Disease 58 0.051
352
P MLN069 Melanoma, Uveal 58 0.051
353
BLM002 Bulimia Nervosa 57 0.051
354
GNR004 Generalized Anxiety Disorder 56 0.051
355
P MYP006 Myopia 55 0.051
356
GLS018 Glass Syndrome 53 0.051
357
P HMR003 Hemorrhagic Disease 52 0.051
358
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.051
359
PRS045 Prostatic Hypertrophy 52 0.051
360
PRS021 Prostatic Adenoma 51 0.051
361
PPT001 Peptic Esophagitis 51 0.051
362
PLR008 Pleurisy 51 0.051
363
SPN035 Spindle Cell Sarcoma 51 0.051
364
PRS129 Prostatic Hyperplasia, Benign 49 0.051
365
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.051
366
P MGR001 Migraine Without Aura 48 0.051
367
DGN001 Degenerative Disc Disease 48 0.051
368
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.051
369
URT010 Ureteral Obstruction 46 0.051
370
GST020 Gastric Antral Vascular Ectasia 41 0.051
371
GLC008 Glucose Metabolism Disease 40 0.051
372
PRM020 Premenstrual Tension 39 0.051
373
c PLY105 Polycystic Ovary Syndrome 1 38 0.051
374
ATM052 Autoimmune Disease 1 37 0.051
375
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.051
376
CNR033 Cone-Rod Synaptic Disorder, Congenital Nonprogressive 33 0.051
377
HMC012 Hemicrania Continua 28 0.051
378
CNN003 Conn's Syndrome 79 0.047
379
P BLD134 Bladder Cancer 78 0.047
380
BRN028 Brain Cancer 73 0.047
381
ACR007 Acromegaly 71 0.047
382
ADL002 Adult Syndrome 69 0.047
383
P FRG001 Fragile X Syndrome 68 0.047
384
SKN019 Skin Melanoma 67 0.047
385
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.047
386
c MCR129 Microvascular Complications of Diabetes 1 66 0.047
387
P MNN013 Meningitis 65 0.047
388
PRT036 Peritonitis 65 0.047
389
BRR014 Barrett Esophagus 64 0.047
390
SKN016 Skin Disease 63 0.047
391
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.047
392
P HYP750 Hypertriglyceridemia, Familial 61 0.047
393
ADN018 Adenoma 58 0.047
394
BRS051 Breast Disease 58 0.047
395
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.047
396
P EXN002 Exanthem 57 0.047
397
P PRP019 Peripheral Nervous System Disease 57 0.047
398
VSC002 Vascular Dementia 57 0.047
399
PLC005 Placental Insufficiency 57 0.047
400
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 56 0.047
401
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.047
402
P MTC069 Mitochondrial Disorders 56 0.047
403
LMB062 Limb Ischemia 55 0.047
404
c GRV008 Graves Disease 1 55 0.047
405
c OPT053 Optic Atrophy 1 54 0.047
406
HMS001 Hemosiderosis 54 0.047
407
P MSC003 Muscular Atrophy 52 0.047
408
P TRT010 Teratoma 51 0.047
409
CHR005 Chorioamnionitis 51 0.047
410
ENT011 Enterocolitis 50 0.047
411
CLR109 Colorectal Adenocarcinoma 50 0.047
412
P PNB001 Pineoblastoma 50 0.047
413
BRN009 Burning Mouth Syndrome 49 0.047
414
c SVR005 Severe Pre-Eclampsia 49 0.047
415
P OPN001 Open-Angle Glaucoma 49 0.047
416
c BPL002 Bipolar I Disorder 49 0.047
417
SLP001 Sleeping Sickness 48 0.047
418
RTN020 Retinal Vascular Disease 48 0.047
419
CHR074 Choriocarcinoma 46 0.047
420
LCK001 Locked-in Syndrome 46 0.047
421
P CRN025 Corneal Dystrophy 45 0.047
422
PNC056 Pineocytoma 45 0.047
423
CRT015 Carotid Artery Occlusion 44 0.047
424
P STR092 Striatal Degeneration, Autosomal Dominant 2 43 0.047
425
49X006 49, Xxxxy Syndrome 41 0.047
426
P RRH023 Rare Hereditary Hemochromatosis 41 0.047
427
c MCR112 Microvascular Complications of Diabetes 2 41 0.047
428
PNL014 Pineal Gland Cancer 40 0.047
429
MLN003 Melancholia 39 0.047
430
P DYS021 Dysautonomia 39 0.047
431
HMR023 Hemorrhagic Cystitis 38 0.047
432
GRN055 Granular Corneal Dystrophy 35 0.047
433
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 26 0.047
434
ESP021 Esophageal Cancer 90 0.042
435
MLR004 Malaria 80 0.042
436
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.042
437
MSC157 Muscular Dystrophy, Duchenne Type 71 0.042
438
MLT157 Multiple System Atrophy 1 70 0.042
439
LYM133 Lymphoma, Hodgkin, Classic 69 0.042
440
c INF071 Inflammatory Bowel Disease 1 68 0.042
441
P HYP098 Hypereosinophilic Syndrome 66 0.042
442
P DYS154 Dystonia 65 0.042
443
P PRS038 Personality Disorder 65 0.042
444
TBC004 Tobacco Addiction 64 0.042
445
KHL003 Kohlschutter-Tonz Syndrome 64 0.042
446
LSH001 Leishmaniasis 63 0.042
447
P LMY004 Leiomyosarcoma 62 0.042
448
WLL001 Williams-Beuren Syndrome 62 0.042
449
TRN015 Transient Cerebral Ischemia 62 0.042
450
c GLC092 Glaucoma, Primary Open Angle 62 0.042
451
ERL001 Early Myoclonic Encephalopathy 61 0.042
452
RTN017 Retinal Detachment 60 0.042
453
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.042
454
THY029 Thyroid Carcinoma 59 0.042
455
c PRM005 Primary Hyperparathyroidism 58 0.042
456
P RHN004 Rhinitis 57 0.042
457
BLR008 Bilirubin Metabolic Disorder 57 0.042
458
BRN056 Bronchopulmonary Dysplasia 57 0.042
459
LNN001 Lennox-Gastaut Syndrome 57 0.042
460
BCT022 Bacterial Infectious Disease 56 0.042
461
GST050 Gastrointestinal System Disease 56 0.042
462
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.042
463
INT007 Intermediate Coronary Syndrome 55 0.042
464
PLM010 Pulmonary Edema 55 0.042
465
PRN019 Perinatal Necrotizing Enterocolitis 54 0.042
466
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.042
467
P INT068 Intestinal Disease 52 0.042
468
ACR041 Acromelic Frontonasal Dysostosis 52 0.042
469
GTR002 Goiter 52 0.042
470
NRM004 Neuroma 51 0.042
471
RTN003 Retinal Ischemia 50 0.042
472
CHL061 Childhood Leukemia 50 0.042
473
P CHL066 Cholangitis 50 0.042
474
VRC001 Varicocele 49 0.042
475
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.042
476
CHL004 Cholelithiasis 49 0.042
477
GYN001 Gynecomastia 49 0.042
478
GST049 Gastrointestinal System Cancer 49 0.042
479
P CMP008 Compartment Syndrome 48 0.042
480
WTH001 Withdrawal Disorder 48 0.042
481
HYP043 Hyperandrogenism 48 0.042
482
CLC006 Calcinosis 48 0.042
483
PLC007 Placental Abruption 48 0.042
484
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.042
485
ATN005 Autonomic Dysfunction 47 0.042
486
P SCL009 Sclerosing Cholangitis 47 0.042
487
RNL077 Renal Fibrosis 47 0.042
488
VNZ002 Venezuelan Equine Encephalitis 46 0.042
489
GST071 Gastrointestinal Carcinoma 45 0.042
490
P OCY003 Oocyte Maturation Defect 1 45 0.042
491
ACT003 Acute Kidney Tubular Necrosis 45 0.042
492
P OVR046 Ovarian Cyst 45 0.042
493
c DRM054 Dermatitis, Atopic, 2 45 0.042
494
PTT037 Pituitary Tumors 44 0.042
495
AND014 Androgenic Alopecia 44 0.042
496
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.042
497
PRM003 Premature Ejaculation 44 0.042
498
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.042
499
TST015 Testicular Disease 43 0.042
500
P KLZ004 Kala-Azar 1 41 0.042
501
MRP001 Morphine Dependence 41 0.042
502
P ADV001 Advanced Sleep Phase Syndrome 40 0.042
503
c MLG074 Malignant Mesenchymoma 39 0.042
504
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.042
505
PLC009 Placenta Praevia 37 0.042
506
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.042
507
RRS014 Rare Surgical Neurologic Disease 32 0.042
508
INF021 Infant Gynecomastia 31 0.042
509
c ALC016 Alcohol Sensitivity, Acute 29 0.042
510
HYP188 Hypnic Headache 20 0.042
511
c DLT002 Dilated Cardiomyopathy 79 0.036
512
P RSP003 Respiratory Failure 74 0.036
513
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.036
514
P SRC025 Sarcoidosis 1 70 0.036
515
P AMY004 Amyloidosis 70 0.036
516
CNT097 Central Hypoventilation Syndrome, Congenital 70 0.036
517
MYL009 Myelodysplastic Syndrome 70 0.036
518
P OCL013 Oculodentodigital Dysplasia 69 0.036
519
EWN003 Ewing Sarcoma 68 0.036
520
KRT019 Keratitis, Hereditary 67 0.036
521
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.036
522
c JVN010 Juvenile Rheumatoid Arthritis 67 0.036
523
STH001 Saethre-Chotzen Syndrome 67 0.036
524
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.036
525
FCT007 Factor Vii Deficiency 66 0.036
526
ANG054 Angina Pectoris 66 0.036
527
MSM014 Mismatch Repair Cancer Syndrome 65 0.036
528
INC002 Inclusion Body Myositis 64 0.036
529
LYS012 Lysosomal Acid Lipase Deficiency 64 0.036
530
TTN003 Tetanus 64 0.036
531
END041 Endometrial Adenocarcinoma 63 0.036
532
SPT006 Septooptic Dysplasia 63 0.036
533
OVR029 Ovarian Hyperstimulation Syndrome 63 0.036
534
PPL049 Papillon-Lefevre Syndrome 63 0.036
535
c SCL052 Scleroderma, Familial Progressive 62 0.036
536
P PSR002 Psoriasis 62 0.036
537
c ATM011 Autoimmune Hepatitis 62 0.036
538
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.036
539
P PRM006 Primary Biliary Cirrhosis 61 0.036
540
c BRN108 Branchiootic Syndrome 1 61 0.036
541
PHL006 Phelan-Mcdermid Syndrome 61 0.036
542
ACN002 Acanthosis Nigricans 60 0.036
543
P MYL006 Myeloid Leukemia 60 0.036
544
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.036
545
GNG013 Gingivitis 59 0.036
546
PRT058 Pure Autonomic Failure 59 0.036
547
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.036
548
IGR001 Ige Responsiveness, Atopic 59 0.036
549
CRD132 Cardiac Conduction Defect 59 0.036
550
CHL067 Cholecystitis 58 0.036
551
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.036
552
PST028 Post-Traumatic Stress Disorder 58 0.036
553
P GLL020 Gallbladder Disease 58 0.036
554
P TYR004 Tyrosinemia 58 0.036
555
c PRG126 Progressive Familial Heart Block 58 0.036
556
P ACT010 Acth-Secreting Pituitary Adenoma 57 0.036
557
THR024 Thrombosis 56 0.036
558
P FBR017 Fibrosarcoma 56 0.036
559
P OPT009 Optic Neuritis 56 0.036
560
P MYS005 Myositis 56 0.036
561
ALL006 Allergic Asthma 56 0.036
562
SYN007 Synovitis 55 0.036
563
PRP030 Purpura 55 0.036
564
c BCT007 Bacterial Meningitis 55 0.036
565
JVN009 Juvenile Pilocytic Astrocytoma 55 0.036
566
OCL009 Ocular Cancer 55 0.036
567
P LYM031 Lymphocytic Leukemia 55 0.036
568
HMP005 Hemiplegia 54 0.036
569
P LCH002 Lichen Planus 54 0.036
570
FCL014 Focal Epilepsy 54 0.036
571
AVD001 Avoidant Personality Disorder 54 0.036
572
PRP016 Paraplegia 53 0.036
573
NRT004 Neuritis 53 0.036
574
P HYP083 Hypopituitarism 53 0.036
575
P LCT002 Lactose Intolerance 53 0.036
576
P THY032 Thyroiditis 53 0.036
577
P ATN002 Autonomic Nervous System Disease 52 0.036
578
PST011 Pustulosis of Palm and Sole 52 0.036
579
c ACR116 Aicardi-Goutieres Syndrome 1 51 0.036
580
OVR059 Ovary Adenocarcinoma 51 0.036
581
CND002 Conduct Disorder 51 0.036
582
BWN001 Bowen-Conradi Syndrome 51 0.036
583
THY030 Thyroid Gland Disease 51 0.036
584
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.036
585
APL002 Aplasia of Lacrimal and Salivary Glands 50 0.036
586
SPS003 Spastic Diplegia 50 0.036
587
PRT029 Parathyroid Adenoma 50 0.036
588
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.036
589
NTR046 Neutrophil Migration 50 0.036
590
MTB004 Metabolic Acidosis 50 0.036
591
LRN003 Learning Disability 49 0.036
592
LFT001 Left Bundle Branch Hemiblock 49 0.036
593
P RNV001 Renovascular Hypertension 49 0.036
594
END062 Endometrial Hyperplasia 48 0.036
595
SPL018 Splenomegaly 48 0.036
596
ACT084 Acute Stress Disorder 48 0.036
597
SMT001 Somatization Disorder 48 0.036
598
HLX001 Helix Syndrome 47 0.036
599
c CNT075 Central Precocious Puberty 47 0.036
600
TTR011 Tetraploidy 47 0.036
601
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.036
602
c CNT015 Central Sleep Apnea 46 0.036
603
ALB002 Albinism 46 0.036
604
KRT013 Keratolytic Winter Erythema 46 0.036
605
SYN036 Syncope 45 0.036
606
CYN002 Cyanosis, Transient Neonatal 45 0.036
607
P BNG032 Benign Mesothelioma 45 0.036
608
ORL013 Oral Lichen Planus 45 0.036
609
RFR003 Refractive Error 44 0.036
610
VGN019 Vaginal Discharge 44 0.036
611
P CMM008 Communicating Hydrocephalus 43 0.036
612
c ORT011 Orthostatic Hypotension 1 43 0.036
613
MND023 Mend Syndrome 43 0.036
614
PRS063 Paresthesia 43 0.036
615
LWC001 Low Compliance Bladder 42 0.036
616
MYF002 Myofascial Pain Syndrome 42 0.036
617
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.036
618
ANX004 Anoxia 42 0.036
619
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.036
620
RST023 Resting Heart Rate, Variation in 41 0.036
621
RDN001 Reading Disorder 40 0.036
622
GRM004 Germinoma 40 0.036
623
ESN002 Eosinophilia-Myalgia Syndrome 39 0.036
624
c CHR682 Chronic Bilirubin Encephalopathy 38 0.036
625
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.036
626
P PRC031 Preeclampsia/eclampsia 1 37 0.036
627
AMR003 Amaurosis Fugax 34 0.036
628
GRM010 Germ Cells Tumors 34 0.036
629
c FBR072 Febrile Seizures, Familial, 11 32 0.036
630
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 31 0.036
631
EXN003 Exencephaly 31 0.036
632
RRD056 Rare Disease in Surgical Orthopedic 28 0.036
633
P OVR096 Overlap Myositis 27 0.036
634
CYT018 Cytochrome P450 2d6 Variant 27 0.036
635
c ATS371 Autism 6 26 0.036
636
P PRM227 Primary Orthostatic Hypotension 25 0.036
637
PRQ002 Paraquat Poisoning 25 0.036
638
APN007 Apnea, Central Sleep 18 0.036
639
MYL069 Myeloma, Multiple 85 0.030
640
c LKM061 Leukemia, Acute Myeloid 83 0.030
641
P ATX030 Ataxia-Telangiectasia 83 0.030
642
P GLM040 Glioma Susceptibility 1 81 0.030
643
CYS001 Cystic Fibrosis 80 0.030
644
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.030
645
P NRF023 Neurofibromatosis, Type Ii 76 0.030
646
CRH001 Crohn's Disease 74 0.030
647
c SPN225 Spondyloarthropathy 1 73 0.030
648
c THR092 Thrombophilia Due to Thrombin Defect 73 0.030
649
SCK003 Sickle Cell Anemia 72 0.030
650
OTT002 Otitis Media 71 0.030
651
c TBR026 Tuberous Sclerosis 2 71 0.030
652
MCC012 Mccune-Albright Syndrome 70 0.030
653
P LKM062 Leukemia, Acute Lymphoblastic 68 0.030
654
P OLG002 Oligodendroglioma 67 0.030
655
BRK010 Burkitt Lymphoma 67 0.030
656
ALL003 Allergic Rhinitis 67 0.030
657
P LKM002 Leukemia 66 0.030
658
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.030
659
GLL008 Gilles De La Tourette Syndrome 66 0.030
660
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.030
661
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.030
662
P MYP004 Myopathy 64 0.030
663
CLN015 Colon Adenocarcinoma 63 0.030
664
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.030
665
NRM005 Neuromuscular Disease 63 0.030
666
P ORT004 Orthostatic Intolerance 63 0.030
667
ACT119 Acute Promyelocytic Leukemia 63 0.030
668
P NPH012 Nephrotic Syndrome 63 0.030
669
P RHB003 Rhabdomyosarcoma 62 0.030
670
P ART023 Arthropathy 62 0.030
671
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.030
672
HSH003 Hashimoto Thyroiditis 62 0.030
673
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.030
674
P EPL140 Epilepsy, Idiopathic Generalized 61 0.030
675
OST003 Osteonecrosis 61 0.030
676
VRL011 Viral Infectious Disease 61 0.030
677
P SNS001 Sensorineural Hearing Loss 61 0.030
678
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.030
679
P TXP001 Toxoplasmosis 60 0.030
680
P BNG030 Benign Ependymoma 60 0.030
681
INT066 Interstitial Lung Disease 59 0.030
682
GRD007 Grade Iii Astrocytoma 59 0.030
683
P PRD006 Prader-Willi Syndrome 59 0.030
684
LNG108 Langerhans Cell Histiocytosis 58 0.030
685
NWB001 Newborn Respiratory Distress Syndrome 58 0.030
686
c DWL002 Dowling-Degos Disease 1 58 0.030
687
c CHL119 Cholangitis, Primary Sclerosing 57 0.030
688
DSS009 Disseminated Intravascular Coagulation 57 0.030
689
P BNC003 Bone Cancer 57 0.030
690
P PRN023 Prion Disease 57 0.030
691
TNS005 Tonsillitis 57 0.030
692
STR081 Stormorken Syndrome 57 0.030
693
P GLM007 Glomerulonephritis 57 0.030
694
c ESS001 Essential Tremor 56 0.030
695
P PYL005 Pyelonephritis 56 0.030
696
SCH014 Schistosomiasis 56 0.030
697
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 56 0.030
698
LMY014 Leiomyoma, Uterine 56 0.030
699
P NRM002 Normal Pressure Hydrocephalus 56 0.030
700
P PLY019 Polyneuropathy 56 0.030
701
ANN002 Anencephaly 55 0.030
702
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.030
703
VSC003 Visceral Leishmaniasis 55 0.030
704
P DBT005 Diabetes Insipidus 55 0.030
705
WST005 West Nile Virus 55 0.030
706
GNT003 Genital Herpes 54 0.030
707
CRT017 Cartilage Disease 54 0.030
708
P RST001 Restless Legs Syndrome 54 0.030
709
P HMC002 Homocystinuria 54 0.030
710
P RCT021 Rectum Cancer 53 0.030
711
KRT009 Keratosis 53 0.030
712
P HST010 Histiocytosis 53 0.030
713
CLL010 Cellular Ependymoma 53 0.030
714
P SHR001 Short Bowel Syndrome 52 0.030
715
SPN051 Spondylitis 52 0.030
716
P PTS002 Ptosis 52 0.030
717
OST011 Osteomalacia 52 0.030
718
P ACT105 Acute Mountain Sickness 52 0.030
719
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 52 0.030
720
c GLL024 Gallbladder Disease 1 52 0.030
721
CHR073 Choreatic Disease 52 0.030
722
PRV004 Periventricular Leukomalacia 51 0.030
723
HYP014 Hyperuricemia 51 0.030
724
TLN003 Telangiectasis 51 0.030
725
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.030
726
c VRL007 Viral Encephalitis 51 0.030
727
SPP010 Suppressor of Tumorigenicity 3 51 0.030
728
c PRM108 Primary Progressive Multiple Sclerosis 51 0.030
729
SMT006 Somatoform Disorder 51 0.030
730
PST021 Postpartum Depression 50 0.030
731
P MMB011 Membranous Nephropathy 50 0.030
732
LNG031 Lung Benign Neoplasm 50 0.030
733
LMY002 Leiomyoma 50 0.030
734
P AGG001 Aggressive Periodontitis 50 0.030
735
P OVR082 Overgrowth Syndrome 50 0.030
736
MCP006 Mucoepidermoid Carcinoma 50 0.030
737
P OTS001 Otosclerosis 50 0.030
738
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 50 0.030
739
c ACT078 Acute Porphyria 49 0.030
740
HYP006 Hypertensive Heart Disease 49 0.030
741
P ALP061 Alopecia, Androgenetic, 1 49 0.030
742
CLN045 Colonic Benign Neoplasm 49 0.030
743
MTC005 Mitochondrial Metabolism Disease 48 0.030
744
P CLR019 Color Blindness 48 0.030
745
SXL003 Sexual Disorder 48 0.030
746
KHN001 Kuhnt-Junius Degeneration 48 0.030
747
ADR016 Adrenal Cortical Carcinoma 48 0.030
748
NDL007 Nodular Goiter 47 0.030
749
PRC003 Proctitis 47 0.030
750
P VTR007 Vitreoretinopathy 46 0.030
751
TST014 Testicular Cancer 46 0.030
752
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 0.030
753
P MYC033 Myoclonus 46 0.030
754
ANP006 Anaplastic Ependymoma 46 0.030
755
TRT001 Teratocarcinoma 46 0.030
756
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.030
757
MXD026 Mixed Glioma 45 0.030
758
OBS004 Obstructive Hydrocephalus 45 0.030
759
P SBR004 Seborrheic Dermatitis 45 0.030
760
P HRN001 Horner's Syndrome 44 0.030
761
c ACT042 Acute Pyelonephritis 44 0.030
762
ATN004 Autonomic Neuropathy 44 0.030
763
c ATM099 Autoimmune Uveitis 44 0.030
764
c RTN047 Retinitis Pigmentosa 18 44 0.030
765
CRB090 Cerebral Hypoxia 43 0.030
766
CRD043 Ceroid Storage Disease 43 0.030
767
OBS082 Obstructive Nephropathy 43 0.030
768
c PRM038 Primary Agammaglobulinemia 43 0.030
769
PLY068 Polysubstance Abuse 43 0.030
770
CYS009 Cystadenoma 43 0.030
771
ANP009 Anaplastic Oligodendroglioma 43 0.030
772
P PHT010 Photoparoxysmal Response 1 42 0.030
773
P AVS003 Avascular Necrosis 42 0.030
774
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.030
775
P CRN035 Cranial Nerve Palsy 41 0.030
776
c MLG064 Malignant Ependymoma 41 0.030
777
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.030
778
CRN031 Cranial Nerve Disease 40 0.030
779
PRD002 Periodic Limb Movement Disorder 40 0.030
780
BKR002 Baker-Gordon Syndrome 40 0.030
781
PHT008 Photosensitive Epilepsy 39 0.030
782
HYP784 Hypogonadism, Male 39 0.030
783
OST115 Osteonecrosis of the Jaw 39 0.030
784
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.030
785
HYP141 Hyperphenylalaninemia 38 0.030
786
ADR004 Adrenal Cortical Adenocarcinoma 38 0.030
787
HRN029 Hearing Loss, Noise-Induced 37 0.030
788
MDD003 Middle Cerebral Artery Infarction 36 0.030
789
PLC006 Placental Choriocarcinoma 36 0.030
790
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 36 0.030
792
PPL050 Papillary Tumor of the Pineal Region 33 0.030
793
CRT009 Critical Illness Polyneuropathy 32 0.030
794
c RCR002 Recurrent Hypersomnia 32 0.030
795
INF009 Inflammatory Spondylopathy 32 0.030
796
ALT002 Aleutian Mink Disease 28 0.030
797
CTR027 Cataract-Glaucoma 27 0.030
798
ADG002 Audiogenic Seizures 26 0.030
799
MLG061 Malignant Choroid Melanoma 25 0.030
800
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.030
801
c PNC094 Pancreatic Cancer 1 24 0.030
802
LCH010 Lichtenstein Syndrome 21 0.030
803
MTR016 Maternal Hyperphenylalaninemia 21 0.030
804
c ADV007 Advanced Sleep Phase Syndrome, Familial, 2 20 0.030
805
c LKM071 Leukemia, Chronic Lymphocytic 79 0.021
806
IMM167 Immune Deficiency Disease 78 0.021
807
P MDL005 Medulloblastoma 77 0.021
808
c MNN043 Meningioma, Familial 74 0.021
809
c HMC039 Hemochromatosis, Type 1 74 0.021
810
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.021
811
P FML018 Familial Mediterranean Fever 72 0.021
812
c LKM063 Leukemia, Chronic Myeloid 71 0.021
813
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.021
814
WLS001 Wilson Disease 70 0.021
815
PLM001 Pulmonary Tuberculosis 70 0.021
816
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 69 0.021
817
c BSL007 Basal Cell Carcinoma 68 0.021
818
BRN024 Bronchitis 68 0.021
819
PCK003 Pick Disease of Brain 68 0.021
820
P TMP003 Temporal Arteritis 67 0.021
821
P HPT021 Hepatitis 67 0.021
822
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 67 0.021
823
P PRP003 Porphyria Cutanea Tarda 67 0.021
824
P NSP012 Nasopharyngeal Carcinoma 67 0.021
825
P CCK001 Cockayne Syndrome 66 0.021
826
P CNJ013 Conjunctivitis 65 0.021
827
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.021
828
c MCP001 Mucopolysaccharidosis Iii 65 0.021
829
P HRP006 Herpes Simplex 65 0.021
830
KWS002 Kawasaki Disease 64 0.021
831
CLF027 Cleft Palate, Isolated 64 0.021
832
c MCL013 Mucolipidosis Iv 64 0.021
833
P MTR014 Motor Neuron Disease 64 0.021
834
MSC007 Muscle Hypertrophy 63 0.021
835
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.021
836
PTT046 Pituitary Hormone Deficiency, Combined, 2 63 0.021
837
P MCH002 Machado-Joseph Disease 63 0.021
838
BRS099 Breast Ductal Carcinoma 62 0.021
839
P HML002 Hemolytic Anemia 62 0.021
840
MNN042 Meningioma, Radiation-Induced 62 0.021
841
P VSC011 Vasculitis 62 0.021
842
HMT002 Hematologic Cancer 62 0.021
843
P CRG003 Crigler-Najjar Syndrome, Type I 61 0.021
844
P HMN010 Hemangioma 61 0.021
845
P TST021 Testicular Germ Cell Tumor 61 0.021
846
MSL001 Measles 61 0.021
847
MCR013 Microphthalmia 60 0.021
848
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.021
849
DCB001 Decubitus Ulcer 60 0.021
850
HRP004 Herpes Zoster 60 0.021
851
CHR072 Chordoma 59 0.021
852
P PLY014 Polycystic Kidney Disease 59 0.021
853
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.021
854
CHL123 Chlamydia 59 0.021
855
P CHR285 Chronic Myelomonocytic Leukemia 59 0.021
856
MCK005 Mckusick-Kaufman Syndrome 58 0.021
857
P RBL001 Rubella 58 0.021
858
ANT024 Anthrax Disease 58 0.021
859
P INT070 Intestinal Obstruction 58 0.021
860
ADR005 Adrenal Carcinoma 58 0.021
861
LYM021 Lymphadenitis 58 0.021
862
CNT047 Contact Dermatitis 57 0.021
863
P CND004 Candidiasis 57 0.021
864
MNR012 Meniere Disease 57 0.021
865
P END033 Endocarditis 57 0.021
866
EMB004 Embryonal Carcinoma 57 0.021
867
P DNG005 Dengue Virus 57 0.021
868
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 57 0.021
869
ADN027 Adenomyosis 57 0.021
870
PRS047 Prostatitis 56 0.021
871
WLF002 Wolf-Hirschhorn Syndrome 56 0.021
872
P CHN012 Chondrosarcoma 56 0.021
873
ISL001 Islet Cell Tumor 56 0.021
874
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 56 0.021
875
GLL018 Gallbladder Cancer 56 0.021
876
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.021
877
HPT022 Hepatoblastoma 56 0.021
878
INT030 Intracranial Aneurysm 56 0.021
879
DFF005 Diffuse Large B-Cell Lymphoma 56 0.021
880
HMG005 Hemoglobinopathy 55 0.021
881
HYP005 Hypokalemia 55 0.021
882
P GRV001 Graves' Disease 55 0.021
883
ZLL002 Zollinger-Ellison Syndrome 55 0.021
884
CPL003 Capillary Leak Syndrome 55 0.021
885
FLR002 Filariasis 55 0.021
886
P FTL001 Fetal Alcohol Syndrome 55 0.021
887
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.021
888
TNG003 Tongue Cancer 55 0.021
889
P SBS003 Substance Abuse 54 0.021
890
P PTT006 Pituitary Adenoma 54 0.021
891
GLS001 Gliosarcoma 54 0.021
892
PPL022 Papilloma 54 0.021
893
P LRY044 Larynx Cancer 54 0.021
894
PTT009 Pituitary Gland Disease 54 0.021
895
c CNT035 Central Nervous System Disease 54 0.021
896
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.021
897
FRZ001 Frozen Shoulder 53 0.021
898
c ACT020 Acute T Cell Leukemia 53 0.021
899
SNS003 Sensory Peripheral Neuropathy 53 0.021
900
INT075 Intracranial Hypertension 53 0.021
901
HRT012 Heart Valve Disease 53 0.021
902
BRD004 Borderline Personality Disorder 53 0.021
903
P OVR049 Ovarian Disease 53 0.021
904
HYP063 Hypersplenism 53 0.021
905
P CTN003 Cutaneous Lupus Erythematosus 52 0.021
906
GNT002 Giant Cell Glioblastoma 52 0.021
907
THY124 Thyroid Gland Papillary Carcinoma 52 0.021
908
INF034 Infective Endocarditis 52 0.021
909
FND002 Fundus Dystrophy 51 0.021
910
MSC190 Muscular Disease 51 0.021
911
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 51 0.021
912
GSG001 Gas Gangrene 50 0.021
913
FTL002 Fatal Familial Insomnia 50 0.021
914
P ATR005 Atrophic Gastritis 50 0.021
915
HPT014 Hepatorenal Syndrome 50 0.021
916
TRT020 Tritanopia 50 0.021
917
BRX001 Bruxism 50 0.021
918
P FNC004 Fanconi Syndrome 50 0.021
919
CHR078 Chorioretinitis 50 0.021
920
DYS073 Dysphagia 50 0.021
921
P MGR003 Migraine with Aura 50 0.021
922
c CNG216 Congenital Hydrocephalus 50 0.021
923
P PRT096 Peritoneal Mesothelioma 50 0.021
924
CRV040 Cervix Carcinoma 50 0.021
925
CRN030 Coronary Stenosis 50 0.021
926
c ACH020 Achromatopsia 2 50 0.021
927
HYP017 Hypophosphatemia 49 0.021
928
NPH010 Nephrosclerosis 49 0.021
929
WRN002 Wernicke-Korsakoff Syndrome 49 0.021
930
HRT031 Hartnup Disorder 49 0.021
931
c LRG001 Large Cell Carcinoma 49 0.021
932
OPP004 Oppositional Defiant Disorder 49 0.021
933
ALN001 Aland Island Eye Disease 49 0.021
934
HPT009 Hepatopulmonary Syndrome 49 0.021
935
KRT002 Keratomalacia 48 0.021
936
ENT004 Enthesopathy 48 0.021
937
PLP001 Pulpitis 48 0.021
938
FBR009 Fibrous Dysplasia 48 0.021
939
ATS010 Autosomal Recessive Disease 48 0.021
940
P ASP001 Asperger Syndrome 48 0.021
941
MLK006 Milk Allergy 48 0.021
942
CCN002 Cocaine Abuse 48 0.021
943
P BRS053 Breast Fibroadenoma 48 0.021
944
c VRL012 Viral Meningitis 48 0.021
945
P NRV006 Nervous System Cancer 48 0.021
946
DYS009 Dysthymic Disorder 48 0.021
947
OPD006 Opioid Addiction 48 0.021
948
OPT070 Optic Nerve Hypoplasia, Bilateral 48 0.021
949
SBS004 Substance Dependence 48 0.021
950
PRP007 Priapism 48 0.021
951
P NGH001 Night Blindness 47 0.021
952
PTC002 Potocki-Lupski Syndrome 47 0.021
953
P ENC008 Encephalocele 47 0.021
954
P END046 Endometritis 47 0.021
955
LPT006 Leptin Receptor Deficiency 47 0.021
956
SPN021 Spinal Meningioma 47 0.021
957
c BCT013 Bacterial Pneumonia 47 0.021
958
P TCL004 T-Cell Leukemia 47 0.021
959
c HYD064 Hydrocephalus, Congenital, 1 47 0.021
960
c INH030 Inherited Retinal Disorder 47 0.021
961
c LRG017 Large Intestine Cancer 47 0.021
962
MCR018 Microcytic Anemia 47 0.021
963
SRT004 Serotonin Syndrome 46 0.021
964
EXS001 Exostosis 46 0.021
965
c CNT033 Central Nervous System Cancer 46 0.021
966
CRN019 Coronary Artery Vasospasm 46 0.021
967
MYC005 Myocardial Stunning 46 0.021
968
P BLR006 Biliary Tract Disease 46 0.021
969
GLC084 Glaucoma, Normal Tension 46 0.021
970
LNT004 Lentigines 46 0.021
971
P MTH007 Methemoglobinemia 46 0.021
972
EBL001 Ebola Hemorrhagic Fever 46 0.021
973
P CHR573 Choroid Plexus Cancer 45 0.021
974
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.021
975
GST030 Gastrinoma 45 0.021
976
c CNG124 Congenital Rubella 45 0.021
977
ATY001 Atypical Depressive Disorder 45 0.021
978
RSP021 Respiratory Allergy 45 0.021
979
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 45 0.021
980
GRD001 Giardiasis 45 0.021
981
KWS001 Kwashiorkor 45 0.021
982
c ADL023 Adult Medulloblastoma 44 0.021
983
HYP003 Hypermethioninemia 44 0.021
984
P TST026 Testicular Germ Cell Cancer 44 0.021
985
P SPR086 Spermatogenic Failure 3 44 0.021
986
TNG009 Tongue Squamous Cell Carcinoma 44 0.021
987
DWR001 Dwarfism 44 0.021
988
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 43 0.021
989
DNT001 Dental Fluorosis 43 0.021
990
HPT067 Hepatocellular Adenoma 43 0.021
991
SCT002 Scotoma 43 0.021
992
GRW007 Growth Hormone Deficiency 43 0.021
993
c FTL006 Fetal Alcohol Spectrum Disorder 42 0.021
994
SQM002 Squamous Cell Papilloma 42 0.021
995
FCL022 Focal Dystonia 42 0.021
996
DRG002 Drug-Induced Hepatitis 42 0.021
997
PRS036 Parasitic Protozoa Infectious Disease 42 0.021
998
P CLL015 Collagen Disease 42 0.021
999
P END039 Endodermal Sinus Tumor 42 0.021
1000
SPS004 Spastic Quadriplegia 42 0.021
1001
P MLT008 Multinodular Goiter 42 0.021
1002
P HYP265 Hypotonia 42 0.021
1003
CLR033 Color Vision Deficiency 41 0.021
1004
DBT002 Diabetic Autonomic Neuropathy 41 0.021
1005
c CNG023 Congenital Fibrosarcoma 41 0.021
1006
MCR017 Macrocytic Anemia 41 0.021
1007
SPN050 Spinocerebellar Degeneration 41 0.021
1008
LYM042 Lymphocytic Colitis 41 0.021
1009
SPS057 Spasticity 41 0.021
1010
CYC005 Cyclothymic Disorder 40 0.021
1011
P DYS005 Dyslexia 40 0.021
1012
TRN007 Transsexualism 40 0.021
1013
EXT006 Extrahepatic Cholestasis 40 0.021
1014
KLN009 Kleine-Levin Hibernation Syndrome 40 0.021
1015
P SPR119 Spermatogenic Failure, X-Linked, 1 40 0.021
1016
ELP001 Elephantiasis 40 0.021
1017
RTR011 Retroperitoneal Fibrosis 40 0.021
1018
CRB086 Cerebral Aneurysms 40 0.021
1019
DBT007 Diabetic Cataract 39 0.021
1020
TST018 Testicular Yolk Sac Tumor 39 0.021
1021
SCH011 Schizotypal Personality Disorder 39 0.021
1022
TYM001 Tympanosclerosis 39 0.021
1023
MNN017 Mononeuropathy 39 0.021
1024
CHL039 Choledocholithiasis 39 0.021
1025
BRS050 Breast Cyst 38 0.021
1026
SPN221 Spina Bifida Occulta 38 0.021
1027
SCR011 Scrapie 38 0.021
1028
MST004 Mast Cell Neoplasm 38 0.021
1029
PRM024 Primary Angle-Closure Glaucoma 38 0.021
1030
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.021
1031
HYP264 Hypertonia 38 0.021
1032
EXT007 Extracutaneous Mastocytoma 38 0.021
1033
P CRB088 Cerebral Atrophy 38 0.021
1034
c ATM075 Autoimmune Encephalitis 38 0.021
1035
RHB002 Rhabdoid Meningioma 38 0.021
1036
CNT060 Central Serous Chorioretinopathy 38 0.021
1037
CLR133 Colorblindness, Partial, Protan Series 37 0.021
1038
SCR001 Secretory Meningioma 37 0.021
1039
P FML187 Familial Hypertension 37 0.021
1040
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.021
1041
OLG022 Oligoasthenoteratozoospermia 36 0.021
1042
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.021
1043
CRB159 Cerebral Visual Impairment 35 0.021
1044
FXD003 Fixed Drug Eruption 35 0.021
1045
c ADL008 Adult Oligodendroglioma 35 0.021
1046
END038 Endocrine Pancreas Disease 35 0.021
1047
CHR178 Chromosomal Triplication 35 0.021
1048
c MCR124 Microphthalmia, Isolated 1 35 0.021
1049
PYR009 Pyridoxine Deficiency Anemia 34 0.021
1050
KDN013 Kidney Hypertrophy 34 0.021
1051
KRN001 Korean Hemorrhagic Fever 34 0.021
1052
NNT024 Neonatal Stroke 34 0.021
1053
CMP006 Complex Partial Epilepsy 34 0.021
1054
PLM011 Plummer's Disease 34 0.021
1055
ALZ029 Alzheimer Disease Mitochondrial 34 0.021
1056
PRX009 Paroxysmal Hemicrania 33 0.021
1057
c SBC035 Subacute Cutaneous Lupus Erythematosus 33 0.021
1058
PRS064 Persistent Vegetative State 33 0.021
1059
c FTL070 Fetal Akinesia Deformation Sequence 2 33 0.021
1060
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.021
1061
HND015 Hand Skill, Relative 33 0.021
1062
c PRC047 Precocious Puberty, Central, 1 32 0.021
1063
IDP031 Idiopathic Hypersomnia 32 0.021
1064
ADR057 Adrenogenital Syndrome 32 0.021
1065
c SPR089 Spermatogenic Failure 4 31 0.021
1066
c HRD198 Hereditary Dystonia 31 0.021
1067
MCL057 Macular Dystrophy with Central Cone Involvement 31 0.021
1068
PLY150 Polykaryocytosis Inducer 31 0.021
1069
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.021
1070
BRT055 Breath-Holding Spells 30 0.021
1072
ACT228 Acute Radiation Syndrome 29 0.021
1073
MNG007 Manganese Poisoning 29 0.021
1074
TBL025 Tubulointerstitial Nephritis with Uveitis 29 0.021
1075
TMP019 Temporomandibular Joint Anomaly 28 0.021
1077
SNL009 Senile Plaque Formation 28 0.021
1078
ARG004 Argyria 28 0.021
1079
P LRG016 Large Intestine Adenocarcinoma 27 0.021
1080
HYP187 Hypertryptophanemia 27 0.021
1081
CRL001 Cerulean Cataract