Search results for rel

3402 hits were found for rel

# Family MCID Name MIFTS Score
1
P NBS002 Nabais Sa-De Vries Syndrome, Type 2 16 4.653
2
P LYM118 Lymphoma 68 4.552
3
P BCL017 B-Cell Lymphoma 58 4.059
4
HND015 Hand Skill, Relative 33 3.906
5
P RHM011 Rheumatoid Arthritis 80 3.541
6
ULC004 Ulcerative Colitis 73 3.522
7
DFF005 Diffuse Large B-Cell Lymphoma 55 3.503
8
P ART022 Arthritis 69 3.498
9
CLT003 Colitis 62 3.482
10
IMM167 Immune Deficiency Disease 78 2.932
11
P LKM071 Leukemia, Chronic Lymphocytic 79 2.890
12
LYM133 Lymphoma, Hodgkin, Classic 69 2.890
13
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 2.866
14
RBS001 Rabies 58 2.823
15
P PRM293 Primary Mediastinal B-Cell Lymphoma 43 2.783
16
HYP063 Hypersplenism 53 2.777
17
FNG015 Fingers, Relative Length of 13 2.718
18
TSR001 Toes, Relative Length of First and Second 5 2.713
19
RTC012 Reticuloendotheliosis, X-Linked 39 2.112
20
MYL069 Myeloma, Multiple 85 2.082
21
P RTN008 Retinitis Pigmentosa 79 2.038
22
c PRX055 Peroxisome Biogenesis Disorder 11a 36 1.953
23
INH002 Inhibited Male Orgasm 28 1.953
24
ADL002 Adult Syndrome 70 0.188
25
P BPL003 Bipolar Disorder 56 0.182
26
c MJR024 Major Affective Disorder 9 41 0.178
27
c MJR022 Major Affective Disorder 8 38 0.178
28
P SCH015 Schizophrenia 74 0.163
29
P TRN020 Turner Syndrome 67 0.150
30
P CLR023 Colorectal Cancer 99 0.146
31
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.142
32
DPR016 Depression 63 0.142
33
ATM095 Autoimmune Disease 62 0.137
34
ANX010 Anxiety 73 0.135
35
MNT002 Mental Depression 58 0.132
36
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.126
37
P CRN300 Coronary Heart Disease 1 63 0.125
38
P PRS038 Personality Disorder 65 0.125
39
P DBT009 Diabetes Mellitus 64 0.124
40
P BRS047 Breast Cancer 97 0.118
41
PNG002 Pain Agnosia 51 0.118
42
HMN044 Human Immunodeficiency Virus Type 1 71 0.118
43
CRH001 Crohn's Disease 74 0.117
44
P DMN002 Dementia 66 0.117
45
ALC007 Alcohol Dependence 66 0.116
46
P ALZ034 Alzheimer Disease 88 0.116
47
P KDN018 Kidney Disease 72 0.114
48
P CLC063 Celiac Disease 1 66 0.114
49
c DBT099 Diabetes Mellitus, Type I 65 0.113
50
P ATS364 Autism 70 0.113
51
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.113
52
ADN018 Adenoma 59 0.112
53
c SYS001 Systemic Lupus Erythematosus 86 0.110
54
P GST053 Gastric Cancer 83 0.109
55
P MJR001 Major Depressive Disorder 68 0.108
56
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.108
57
MDD011 Mood Disorder 62 0.106
58
PSY004 Psychotic Disorder 67 0.102
59
c HYP836 Hypercholesterolemia, Familial, 1 73 0.101
60
OBS002 Obsessive-Compulsive Disorder 68 0.101
61
LPP008 Lipoprotein Quantitative Trait Locus 62 0.101
62
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.101
63
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.100
64
END086 End Stage Renal Disease 51 0.100
65
P LVR013 Liver Disease 68 0.099
66
HLX001 Helix Syndrome 47 0.099
67
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.098
68
LVR012 Liver Cirrhosis 62 0.098
69
P INF037 Inflammatory Bowel Disease 54 0.098
70
48X005 48,xyyy 39 0.098
71
DWN001 Down Syndrome 70 0.097
72
P OVR042 Ovarian Cancer 88 0.096
73
c HYP595 Hypertension, Essential 84 0.096
74
P HYP086 Hypothyroidism 69 0.095
75
c ATS007 Autism Spectrum Disorder 67 0.095
76
HYP056 Hypoglycemia 66 0.095
77
BRN071 Brain Injury 49 0.095
78
ETN001 Eating Disorder 60 0.095
79
SCH011 Schizotypal Personality Disorder 40 0.094
80
GLC003 Glucose Intolerance 54 0.093
81
TRM010 Traumatic Brain Injury 51 0.093
82
P DRR001 Diarrhea 55 0.092
83
ART140 Arteries, Anomalies of 52 0.092
84
P HRT032 Heart Disease 75 0.091
85
c CHR684 Chronic Kidney Disease 70 0.091
86
HRW001 Hair Whorl 36 0.091
87
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.090
88
P LKM002 Leukemia 68 0.090
89
P MSC005 Muscular Dystrophy 66 0.090
90
THY029 Thyroid Carcinoma 59 0.090
91
CNG034 Congestive Heart Failure 69 0.089
92
PST028 Post-Traumatic Stress Disorder 58 0.089
93
ISC004 Ischemia 58 0.089
94
P SBS003 Substance Abuse 55 0.089
95
HYP060 Hyperinsulinism 54 0.089
96
CYS001 Cystic Fibrosis 81 0.088
97
OST012 Osteoarthritis 78 0.088
98
P LPS004 Lupus Erythematosus 61 0.088
99
P GST044 Gastritis 56 0.088
100
c ATR087 Atrial Standstill 1 75 0.086
101
P PSR002 Psoriasis 62 0.086
102
c ACT075 Acute Myocardial Infarction 57 0.086
103
PST011 Pustulosis of Palm and Sole 52 0.086
104
P LNG032 Lung Cancer 98 0.085
105
c SPN225 Spondyloarthropathy 1 73 0.085
106
DFC004 Deficiency Anemia 70 0.085
107
HYP066 Hyperglycemia 61 0.085
108
SCH012 Schizoaffective Disorder 50 0.085
109
P PNC035 Pancreatic Cancer 84 0.085
110
DSS008 Disease of Mental Health 58 0.084
111
ACT084 Acute Stress Disorder 47 0.084
112
P PRS040 Prostate Cancer 97 0.083
113
P HYP061 Hypertrophic Cardiomyopathy 70 0.083
114
P MLN008 Melanoma 69 0.083
115
P SCL018 Scoliosis 60 0.083
116
P CTR002 Cataract 60 0.083
117
IRN002 Iron Metabolism Disease 57 0.083
118
P OST002 Osteoporosis 74 0.082
119
P PNC025 Panic Disorder 53 0.082
120
AVD001 Avoidant Personality Disorder 51 0.082
121
P CRD119 Cardiac Arrest 67 0.081
122
SPN051 Spondylitis 51 0.081
123
BCK006 Back Pain 42 0.081
124
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.081
125
INF009 Inflammatory Spondylopathy 31 0.081
126
LPD008 Lipid Metabolism Disorder 62 0.080
127
FTT001 Fatty Liver Disease 61 0.080
128
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.080
129
P HPT023 Hepatocellular Carcinoma 100 0.079
130
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.079
131
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.079
132
P GLM045 Glioma 63 0.079
133
LNG099 Lung Disease 60 0.079
134
ANR040 Aneurysm 59 0.079
135
P SZR006 Seizure Disorder 56 0.079
136
P NTR004 Neutropenia 63 0.078
137
47X002 47,xyy 49 0.078
138
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.078
139
GLL048 Glial Tumor 45 0.078
140
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.078
141
P MLT020 Multiple Sclerosis 72 0.077
142
P ADN016 Adenocarcinoma 64 0.077
143
ANR007 Anorexia Nervosa 63 0.077
144
TXC005 Toxic Shock Syndrome 62 0.077
145
ACQ007 Acquired Immunodeficiency Syndrome 60 0.077
146
P ALC033 Alcohol Use Disorder 58 0.077
147
ATX019 Ataxia with Vitamin E Deficiency 42 0.077
148
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.076
149
P NRP001 Neuropathy 56 0.076
150
OCL069 Ocular Motor Apraxia 51 0.076
151
CRV035 Cervical Cancer 76 0.075
152
P MYC007 Myocardial Infarction 70 0.075
153
P SKN015 Skin Carcinoma 66 0.075
154
P HRP006 Herpes Simplex 65 0.075
155
P PRD008 Periodontitis 64 0.075
156
c HPT001 Hepatitis C 62 0.075
157
END040 Endogenous Depression 55 0.075
158
P THY032 Thyroiditis 52 0.075
159
CYT002 Cytokine Deficiency 42 0.075
160
P BLD134 Bladder Cancer 79 0.074
161
c DLT002 Dilated Cardiomyopathy 79 0.074
162
P PRK057 Parkinson Disease, Late-Onset 78 0.074
163
GLB015 Glioblastoma Multiforme 75 0.074
164
P THL005 Thalassemia 60 0.074
165
P TRM003 Tremor 54 0.074
166
STR067 Stroke, Ischemic 81 0.073
167
CHL123 Chlamydia 59 0.073
168
P RCT021 Rectum Cancer 52 0.073
169
HDN002 Head Injury 46 0.073
170
c HPT073 Hepatitis C Virus 72 0.072
171
P VSC007 Vascular Disease 63 0.072
172
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.072
173
MLR004 Malaria 81 0.071
174
c PRC016 Pre-Eclampsia 63 0.071
175
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.071
176
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.071
177
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.071
178
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.070
179
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.070
180
c MGR028 Migraine with or Without Aura 1 67 0.070
181
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.070
182
P OPT006 Optic Nerve Disease 60 0.070
183
CRD132 Cardiac Conduction Defect 58 0.070
184
HYP266 Hypoxia 57 0.070
185
P PLY011 Polycystic Ovary Syndrome 56 0.070
186
P MYP006 Myopia 55 0.070
187
c BPL002 Bipolar I Disorder 49 0.070
188
P RTN024 Retinoblastoma 73 0.069
189
CRB039 Cerebrovascular Disease 67 0.069
190
GST033 Gestational Diabetes 61 0.069
191
P LTR001 Lateral Sclerosis 54 0.069
192
CLF001 Cleft Lip 53 0.069
193
c FML008 Familial Retinoblastoma 53 0.069
194
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.069
195
c THR092 Thrombophilia Due to Thrombin Defect 73 0.068
196
P AMY004 Amyloidosis 70 0.068
197
P HYP750 Hypertriglyceridemia, Familial 62 0.068
198
P MYL006 Myeloid Leukemia 60 0.068
199
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.068
200
IMP005 Impotence 52 0.068
201
P HNT016 Huntington Disease 72 0.067
202
ART016 Aortic Aneurysm 69 0.067
203
P INF038 Influenza 68 0.067
204
ATH013 Atherosclerosis Susceptibility 65 0.067
205
VSL002 Visual Epilepsy 59 0.067
206
HLC007 Helicobacter Pylori Infection 59 0.067
207
P RHN004 Rhinitis 57 0.067
208
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.067
209
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.067
210
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.067
211
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.067
212
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.067
213
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.067
214
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.067
215
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.067
216
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.067
217
IDP070 Idiopathic Scoliosis 42 0.067
218
c LKM005 Leukemia, T-Cell, Chronic 34 0.067
219
AST005 Asthma 76 0.066
220
P EPL164 Epilepsy 71 0.066
221
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.066
222
P OPN001 Open-Angle Glaucoma 49 0.066
223
SVR004 Severe Combined Immunodeficiency 73 0.065
224
RCK004 Rickets 68 0.065
225
P HPT021 Hepatitis 67 0.065
226
DRM006 Dermatitis 61 0.065
227
CHL014 Cholera 59 0.065
228
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.065
229
P GRV001 Graves' Disease 55 0.065
230
BNR002 Bone Resorption Disease 48 0.065
231
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.065
232
P CHR345 Chronic Pain 44 0.065
233
CLF027 Cleft Palate, Isolated 64 0.063
234
P HYP069 Hyperparathyroidism 63 0.063
235
P SYP003 Syphilis 58 0.063
236
BCT022 Bacterial Infectious Disease 56 0.063
237
BRD004 Borderline Personality Disorder 53 0.063
238
c MCR113 Microvascular Complications of Diabetes 3 52 0.063
239
c MCR120 Microvascular Complications of Diabetes 7 47 0.063
240
c MCR130 Microvascular Complications of Diabetes 6 41 0.063
241
c MCR133 Microvascular Complications of Diabetes 4 41 0.063
242
CHR178 Chromosomal Triplication 35 0.063
244
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.062
245
c HPT003 Hepatitis a 62 0.062
246
SPN186 Spinal Cord Injury 60 0.062
247
c HPT016 Hepatitis B 59 0.062
248
P HDC001 Headache 57 0.062
249
APH002 Aphasia 57 0.062
250
P PLY018 Polycythemia 56 0.062
251
GTR002 Goiter 53 0.062
252
DNT012 Dental Caries 53 0.062
253
P LYN001 Lynch Syndrome 77 0.061
254
P LKM062 Leukemia, Acute Lymphoblastic 69 0.061
255
c FNC043 Fanconi Anemia, Complementation Group E 62 0.061
256
PLM033 Pulmonary Embolism 59 0.061
257
P INF032 Infertility 57 0.061
258
P HYP076 Hyperthyroidism 55 0.061
259
RFR003 Refractive Error 43 0.061
260
P SCL057 Scoliosis, Isolated 1 41 0.061
261
NRL016 Neural Tube Defects 82 0.060
262
END057 Endometrial Cancer 74 0.060
263
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.060
264
MYL009 Myelodysplastic Syndrome 70 0.060
265
P PNM007 Pneumonia 68 0.060
266
P THR014 Thrombocytopenia 67 0.060
267
SQM006 Squamous Cell Carcinoma 60 0.060
268
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.060
269
CNS004 Constipation 58 0.060
270
P HYP024 Hypoparathyroidism 56 0.060
271
OPT003 Opiate Dependence 50 0.060
272
P NRB001 Neuroblastoma 72 0.059
273
P SLP006 Sleep Apnea 69 0.059
274
ALL003 Allergic Rhinitis 67 0.059
275
P DYS154 Dystonia 65 0.059
276
TYP007 Typhoid Fever 63 0.059
277
NTR005 Nutritional Deficiency Disease 62 0.059
278
P ENC018 Encephalopathy 61 0.059
279
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.059
280
GST045 Gastroenteritis 59 0.059
281
LYM027 Lymphopenia 58 0.059
282
P CRD246 Cardiovascular System Disease 57 0.059
283
PLY100 Polyploidy 40 0.059
284
DYS182 Dysphasia, Familial Developmental 35 0.059
285
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.057
286
P GLM007 Glomerulonephritis 57 0.057
287
BLM002 Bulimia Nervosa 57 0.057
288
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.057
289
PRS045 Prostatic Hypertrophy 53 0.057
290
P SPC019 Specific Language Impairment 33 0.057
291
ESP021 Esophageal Cancer 90 0.056
292
P LPR021 Leprosy 3 69 0.056
293
ANG054 Angina Pectoris 66 0.056
294
c BRN108 Branchiootic Syndrome 1 62 0.056
295
P PRM006 Primary Biliary Cirrhosis 62 0.056
296
RTN017 Retinal Detachment 61 0.056
297
c ACT027 Acute Pancreatitis 60 0.056
298
c ACT071 Acute Kidney Failure 60 0.056
299
c ACT073 Acute Leukemia 58 0.056
300
AMN003 Amnestic Disorder 54 0.056
301
HMS001 Hemosiderosis 54 0.056
302
P DDN001 Duodenal Ulcer 52 0.056
303
P SCK005 Sickle Cell Disease 50 0.056
304
KRT002 Keratomalacia 47 0.056
305
P RRH023 Rare Hereditary Hemochromatosis 41 0.056
306
HNS001 Hansen's Disease 34 0.056
307
INS024 Insulin-Like Growth Factor I 79 0.055
308
c HMC039 Hemochromatosis, Type 1 74 0.055
309
P GRF003 Graft-Versus-Host Disease 72 0.055
310
BRN024 Bronchitis 68 0.055
311
OST159 Osteogenic Sarcoma 66 0.055
312
PRT037 Pertussis 65 0.055
313
TBC004 Tobacco Addiction 64 0.055
314
c ACT068 Acute Cystitis 63 0.055
315
P ENC004 Encephalitis 61 0.055
316
SCH014 Schistosomiasis 57 0.055
317
P MSC003 Muscular Atrophy 52 0.055
318
TLN003 Telangiectasis 52 0.055
319
CND002 Conduct Disorder 51 0.055
320
P MJR007 Major Affective Disorder 1 43 0.055
321
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.055
322
CHL079 Children's Interstitial Lung Disease 26 0.055
323
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.055
324
c LKM061 Leukemia, Acute Myeloid 84 0.053
325
P FLL037 Follicular Lymphoma 67 0.053
326
P PLM037 Pulmonary Hypertension 67 0.053
327
c FML021 Familial Hypercholesterolemia 66 0.053
328
P MNN013 Meningitis 66 0.053
329
TTN003 Tetanus 65 0.053
330
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.053
331
c SVR001 Severe Acute Respiratory Syndrome 62 0.053
332
MSL001 Measles 62 0.053
333
SCH003 Schizophreniform Disorder 56 0.053
334
AGN016 Aging 56 0.053
335
NRT001 Neurotic Disorder 53 0.053
336
P OVR082 Overgrowth Syndrome 50 0.053
337
P TMP001 Temporal Lobe Epilepsy 50 0.053
338
HRT011 Heart Septal Defect 50 0.053
339
RTN023 Retinitis 46 0.053
340
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.053
341
NRR001 Neuroretinitis 42 0.053
342
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.053
343
P ATX030 Ataxia-Telangiectasia 82 0.052
344
MSC157 Muscular Dystrophy, Duchenne Type 72 0.052
345
P MYP004 Myopathy 70 0.052
346
P HYP098 Hypereosinophilic Syndrome 67 0.052
347
CRP001 Carpal Tunnel Syndrome 67 0.052
348
P ATR011 Atrial Fibrillation 66 0.052
349
IRR002 Irritable Bowel Syndrome 65 0.052
350
c GLC092 Glaucoma, Primary Open Angle 62 0.052
351
ALL026 Allergic Hypersensitivity Disease 62 0.052
352
c SCL052 Scleroderma, Familial Progressive 61 0.052
353
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.052
354
P BND020 Bone Disease 59 0.052
355
FML037 Female Breast Cancer 52 0.052
356
PRS021 Prostatic Adenoma 51 0.052
357
CRN030 Coronary Stenosis 50 0.052
358
TST014 Testicular Cancer 46 0.052
359
AGR002 Agoraphobia 45 0.052
360
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.052
361
c BTT014 Beta-Thalassemia 74 0.050
362
PLM001 Pulmonary Tuberculosis 69 0.050
363
SKN019 Skin Melanoma 68 0.050
364
P DRM053 Dermatitis, Atopic 66 0.050
365
c SML038 Small Cell Cancer of the Lung 65 0.050
366
P CNJ013 Conjunctivitis 65 0.050
367
LSH001 Leishmaniasis 63 0.050
368
INS001 Insulinoma 60 0.050
369
P SLP005 Sleep Disorder 59 0.050
370
THR024 Thrombosis 57 0.050
371
P MLT074 Multiple Endocrine Neoplasia 56 0.050
372
INT007 Intermediate Coronary Syndrome 55 0.050
373
P ALP008 Alopecia 54 0.050
374
AMN001 Amenorrhea 54 0.050
375
P AST007 Astrocytoma 51 0.050
376
P CHL066 Cholangitis 51 0.050
377
P MYT002 Myotonic Dystrophy 49 0.050
378
PRS129 Prostatic Hyperplasia, Benign 49 0.050
379
VCC001 Vaccinia 49 0.050
380
ATS010 Autosomal Recessive Disease 48 0.050
381
SPL018 Splenomegaly 48 0.050
382
P KLZ004 Kala-Azar 1 41 0.050
383
SCK003 Sickle Cell Anemia 74 0.049
384
c LKM063 Leukemia, Chronic Myeloid 72 0.049
385
PRP027 Peripheral Vascular Disease 71 0.049
386
BRK010 Burkitt Lymphoma 67 0.049
387
P MCR115 Microvascular Complications of Diabetes 5 66 0.049
388
BRC012 Brucellosis 64 0.049
389
PLM031 Poliomyelitis 64 0.049
390
LYM017 Lyme Disease 64 0.049
391
SKN016 Skin Disease 63 0.049
392
P END044 Endometriosis 63 0.049
393
P SNS001 Sensorineural Hearing Loss 60 0.049
394
ORL011 Oral Cancer 60 0.049
395
PRP030 Purpura 54 0.049
396
P INS002 in Situ Carcinoma 53 0.049
397
P ECL001 Eclampsia 50 0.049
398
HYP080 Hypogonadism 50 0.049
399
ENT004 Enthesopathy 49 0.049
400
P ART018 Aortic Valve Insufficiency 49 0.049
401
AMB002 Amblyopia 49 0.049
402
IMM003 Immunoglobulin Alpha Deficiency 45 0.049
403
CVD001 Covid-19 44 0.049
404
SPP007 Suppression Amblyopia 39 0.049
405
OVR094 Ovarian Epithelial Cancer 38 0.049
406
CRB037 Cerebral Palsy 69 0.047
407
P MYS003 Myasthenia Gravis 68 0.047
408
P HYD006 Hydrocephalus 66 0.047
409
GT001 Gout 64 0.047
410
P MVM001 Movement Disease 63 0.047
411
PSR001 Psoriatic Arthritis 61 0.047
412
P PNC044 Pancreatitis 61 0.047
413
PRT013 Portal Hypertension 59 0.047
414
P UVT001 Uveitis 57 0.047
415
c ESS001 Essential Tremor 56 0.047
416
c VRL010 Viral Hepatitis 52 0.047
417
P HMP007 Hemophilia 51 0.047
418
P THR015 Thrombophilia 51 0.047
419
c SCN007 Secondary Hyperparathyroidism 51 0.047
420
DYS073 Dysphagia 50 0.047
421
P ATR005 Atrophic Gastritis 50 0.047
422
URM002 Uremia 49 0.047
423
SYN036 Syncope 45 0.047
424
MDD018 Middle East Respiratory Syndrome 43 0.047
425
PPL052 Papillomatosis, Confluent and Reticulated 33 0.047
426
c NRF023 Neurofibromatosis, Type Ii 80 0.046
427
P LFR001 Li-Fraumeni Syndrome 72 0.046
428
P FML011 Familial Adenomatous Polyposis 72 0.046
429
c RHB024 Rhabdomyosarcoma 2 67 0.046
430
PRT036 Peritonitis 64 0.046
431
P PRP029 Porphyria 62 0.046
432
HPT019 Hepatic Encephalopathy 60 0.046
433
IGR001 Ige Responsiveness, Atopic 59 0.046
434
PPT005 Peptic Ulcer Disease 59 0.046
435
FBR047 Fibromyalgia 58 0.046
436
P PRP019 Peripheral Nervous System Disease 58 0.046
437
P NRF002 Neurofibromatosis 56 0.046
438
FLR002 Filariasis 55 0.046
439
OPD001 Opioid Abuse 46 0.046
440
HPT004 Hepatic Coma 45 0.046
441
ORL015 Oral Squamous Cell Carcinoma 43 0.046
442
PST092 Posttransplant Acute Limbic Encephalitis 29 0.046
443
KPS004 Kaposi Sarcoma 75 0.044
444
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.044
445
c ART115 Aortic Valve Disease 1 75 0.044
446
P SRC025 Sarcoidosis 1 70 0.044
447
P LNG028 Long Qt Syndrome 66 0.044
448
GLL008 Gilles De La Tourette Syndrome 66 0.044
449
P RHB003 Rhabdomyosarcoma 63 0.044
450
P KDN017 Kidney Cancer 60 0.044
451
DPH001 Diphtheria 60 0.044
452
P TXP001 Toxoplasmosis 60 0.044
453
VRC005 Varicose Veins 60 0.044
454
P OPT009 Optic Neuritis 57 0.044
455
GNR004 Generalized Anxiety Disorder 56 0.044
456
MTH009 Mouth Disease 56 0.044
457
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.044
458
NPH009 Nephrolithiasis 55 0.044
459
CLF004 Cleft Lip/palate 54 0.044
460
P PMP001 Pemphigus 54 0.044
461
FCL014 Focal Epilepsy 54 0.044
462
PRN011 Pernicious Anemia 53 0.044
463
NRT004 Neuritis 52 0.044
464
THY030 Thyroid Gland Disease 52 0.044
465
PTH003 Pathologic Nystagmus 52 0.044
466
P SPP010 Suppressor of Tumorigenicity 3 51 0.044
467
LRN003 Learning Disability 49 0.044
468
HYP043 Hyperandrogenism 48 0.044
469
ATN005 Autonomic Dysfunction 46 0.044
470
ASP026 Asplenia, Isolated Congenital 44 0.044
471
c DRM040 Dermatitis Herpetiformis, Familial 35 0.044
473
GST019 Gastrointestinal Stromal Tumor 78 0.042
474
P MDL005 Medulloblastoma 77 0.042
475
P FRG001 Fragile X Syndrome 70 0.042
476
P FRN006 Frontotemporal Dementia 68 0.042
477
GST092 Gastroesophageal Reflux 67 0.042
478
P NSP012 Nasopharyngeal Carcinoma 66 0.042
479
CLR108 Colorectal Adenoma 64 0.042
480
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 0.042
481
P PLY014 Polycystic Kidney Disease 62 0.042
482
P ART023 Arthropathy 62 0.042
483
HSH003 Hashimoto Thyroiditis 62 0.042
484
YLL002 Yellow Fever 61 0.042
485
P RBL001 Rubella 59 0.042
486
c DNG003 Dengue Disease 59 0.042
487
GNG013 Gingivitis 59 0.042
488
c CHL119 Cholangitis, Primary Sclerosing 57 0.042
489
P END033 Endocarditis 57 0.042
490
P ADL017 Adult T-Cell Leukemia 56 0.042
491
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.042
492
P DRM007 Dermatitis Herpetiformis 55 0.042
493
PLM010 Pulmonary Edema 54 0.042
494
OCL006 Ocular Hypertension 53 0.042
495
DYS015 Dysentery 52 0.042
496
STM007 Stomatitis 50 0.042
497
P SCL009 Sclerosing Cholangitis 48 0.042
498
CRD137 Cardiogenic Shock 47 0.042
499
c PRM038 Primary Agammaglobulinemia 44 0.042
500
HMP009 Haemophilus Influenzae 43 0.042
501
ACT088 Acute Insulin Response 41 0.042
502
ANP008 Anaplastic Oligoastrocytoma 30 0.042
503
BNG077 Benign Idiopathic Neonatal Seizures 26 0.042
504
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.041
505
P RSP003 Respiratory Failure 74 0.041
506
OTT002 Otitis Media 72 0.041
507
P SYS005 Systemic Scleroderma 68 0.041
508
c BSL007 Basal Cell Carcinoma 68 0.041
509
P PLM036 Pulmonary Fibrosis 65 0.041
510
KRT019 Keratitis, Hereditary 65 0.041
511
CHL068 Cholestasis 61 0.041
512
P VNT002 Ventricular Septal Defect 60 0.041
513
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.041
514
CHC001 Chickenpox 60 0.041
515
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.041
516
CNT047 Contact Dermatitis 58 0.041
517
P EXN002 Exanthem 57 0.041
518
VSC002 Vascular Dementia 57 0.041
519
SFT003 Soft Tissue Sarcoma 56 0.041
520
PPL022 Papilloma 54 0.041
521
PNC001 Pancytopenia 54 0.041
522
c ACT135 Acute Graft Versus Host Disease 52 0.041
523
P KRT007 Keratoconus 50 0.041
524
PRN009 Paranoid Schizophrenia 50 0.041
525
P GND004 Gonadal Dysgenesis 48 0.041
526
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.041
527
P BNG032 Benign Mesothelioma 46 0.041
528
SQM002 Squamous Cell Papilloma 46 0.041
529
SBC016 Subacute Delirium 44 0.041
530
RST023 Resting Heart Rate, Variation in 41 0.041
531
CRV045 Cervical Intraepithelial Neoplasia 39 0.041
532
SCR011 Scrapie 39 0.041
533
ALX002 Alexithymia 38 0.041
534
ALL014 Allergic Encephalomyelitis 38 0.041
535
MSC148 Musical Perfect Pitch 22 0.041
536
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.039
537
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.039
538
P PHC003 Pheochromocytoma 71 0.039
539
P BRG001 Brugada Syndrome 71 0.039
540
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.039
541
P MYC084 Mycobacterium Tuberculosis 1 68 0.039
542
MYC006 Mycosis Fungoides 66 0.039
543
P ART005 Arteriovenous Malformation 65 0.039
544
c ATM011 Autoimmune Hepatitis 63 0.039
545
OST003 Osteonecrosis 61 0.039
546
HYD002 Hydronephrosis 60 0.039
547
P CYS018 Cystitis 59 0.039
548
BRS051 Breast Disease 58 0.039
549
P CND004 Candidiasis 58 0.039
550
CYT008 Cytomegalovirus Infection 57 0.039
551
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.039
552
HYP005 Hypokalemia 55 0.039
553
P ART021 Arteriosclerosis 54 0.039
554
NNL006 Non-Alcoholic Steatohepatitis 54 0.039
555
MMM001 Mammary Paget's Disease 53 0.039
556
P RTN016 Retinal Degeneration 53 0.039
557
MST005 Mastitis 53 0.039
558
GST023 Gastric Ulcer 53 0.039
559
PRP016 Paraplegia 52 0.039
560
c PSR023 Psoriasis 1 52 0.039
561
FDL002 Food Allergy 51 0.039
562
ENT011 Enterocolitis 51 0.039
563
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.039
564
c HNT004 Huntington Disease-Like 2 50 0.039
565
PLC008 Placenta Disease 50 0.039
566
MTB004 Metabolic Acidosis 50 0.039
567
DYS009 Dysthymic Disorder 49 0.039
568
IGG001 Iga Glomerulonephritis 48 0.039
569
AST006 Astigmatism 47 0.039
570
LYM019 Lymphosarcoma 46 0.039
571
SCT002 Scotoma 44 0.039
572
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.039
573
PLY150 Polykaryocytosis Inducer 31 0.039
574
SDD004 Sudden Arrhythmia Death Syndrome 22 0.039
575
ADR007 Adrenoleukodystrophy 75 0.037
576
BRN028 Brain Cancer 74 0.037
577
CRT072 Creutzfeldt-Jakob Disease 70 0.037
578
P ASP006 Aspergillosis 69 0.037
579
PNC129 Pancreatic Adenocarcinoma 68 0.037
580
THY111 Thyroid Carcinoma, Familial Medullary 67 0.037
581
SRC014 Sarcoma 65 0.037
582
P VNW001 Von Willebrand's Disease 65 0.037
583
P MTR014 Motor Neuron Disease 65 0.037
584
BRR014 Barrett Esophagus 65 0.037
585
c JVN010 Juvenile Rheumatoid Arthritis 64 0.037
586
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.037
587
PLG002 Plague 63 0.037
588
P ESP024 Esophagitis 62 0.037
589
P DRM010 Dermatomyositis 61 0.037
590
INT002 Intermittent Claudication 61 0.037
591
P NPH012 Nephrotic Syndrome 60 0.037
592
P TST021 Testicular Germ Cell Tumor 60 0.037
593
P MCR010 Microcephaly 59 0.037
594
SPN027 Spinal Stenosis 59 0.037
595
P MLN069 Melanoma, Uveal 59 0.037
596
IRN001 Iron Deficiency Anemia 59 0.037
597
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.037
598
P PRV006 Pervasive Developmental Disorder 57 0.037
599
P PYL005 Pyelonephritis 56 0.037
600
PNM008 Pneumothorax 56 0.037
601
SML019 Smallpox 56 0.037
602
INT030 Intracranial Aneurysm 56 0.037
603
P STR020 Strabismus 55 0.037
604
WST005 West Nile Virus 54 0.037
605
P TCD001 Tic Disorder 53 0.037
606
c PRD040 Periodontitis, Chronic 53 0.037
607
P PTS002 Ptosis 53 0.037
608
SPN035 Spindle Cell Sarcoma 53 0.037
609
STT041 Stuttering 52 0.037
610
CHR073 Choreatic Disease 52 0.037
611
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 52 0.037
612
CRT013 Carotid Stenosis 50 0.037
613
THY125 Thyroid Gland Medullary Carcinoma 50 0.037
614
ECT026 Ectopic Pregnancy 50 0.037
615
BLR001 Biliary Atresia 50 0.037
616
SBS004 Substance Dependence 48 0.037
617
SCL003 Social Phobia 48 0.037
618
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.037
619
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.037
620
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.037
621
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.037
622
ADR040 Adrenal Gland Pheochromocytoma 46 0.037
623
c TRC022 Tricuspid Valve Insufficiency 45 0.037
624
URL001 Urolithiasis 45 0.037
625
MCH006 Mechanical Strabismus 42 0.037
626
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.037
627
ANX004 Anoxia 40 0.037
628
P DYS005 Dyslexia 40 0.037
629
c HMG029 Hemoglobin Se Disease 39 0.037
630
ADR022 Adrenomyeloneuropathy 38 0.037
631
TTH032 Tooth Size 36 0.037
632
GRM010 Germ Cells Tumors 34 0.037
633
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.037
634
c FNC027 Fanconi Anemia, Complementation Group a 81 0.035
635
P APL001 Aplastic Anemia 74 0.035
636
c MNN043 Meningioma, Familial 74 0.035
637
P FML018 Familial Mediterranean Fever 73 0.035
638
MYL005 Myelofibrosis 70 0.035
639
CNN005 Connective Tissue Disease 68 0.035
640
c INF071 Inflammatory Bowel Disease 1 67 0.035
641
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.035
642
ART002 Arts Syndrome 64 0.035
643
c CNG006 Congenital Hypothyroidism 64 0.035
644
MSC007 Muscle Hypertrophy 64 0.035
645
P GCH001 Gaucher's Disease 63 0.035
646
P HML002 Hemolytic Anemia 63 0.035
647
TRN015 Transient Cerebral Ischemia 63 0.035
648
c ALP101 Alpha-Thalassemia 62 0.035
649
MNN042 Meningioma, Radiation-Induced 62 0.035
650
CHR066 Chronic Fatigue Syndrome 61 0.035
651
APP008 Appendicitis 61 0.035
652
P BNG030 Benign Ependymoma 60 0.035
653
INT066 Interstitial Lung Disease 60 0.035
654
P ALP009 Alopecia Areata 60 0.035
655
STT001 Status Epilepticus 60 0.035
656
EYD002 Eye Disease 58 0.035
657
P GLL018 Gallbladder Cancer 57 0.035
658
MCR013 Microphthalmia 57 0.035
659
P FBR017 Fibrosarcoma 56 0.035
660
c GRV008 Graves Disease 1 56 0.035
661
P PLY019 Polyneuropathy 56 0.035
662
HRY003 Hairy Cell Leukemia 55 0.035
663
PRT038 Protein-Energy Malnutrition 54 0.035
664
CLL010 Cellular Ependymoma 54 0.035
665
P FBR031 Febrile Seizures 53 0.035
666
c PSR017 Psoriasis 2 53 0.035
667
PLS007 Plasmodium Falciparum Malaria 52 0.035
668
P NRC002 Narcolepsy 52 0.035
670
ACH005 Achalasia 51 0.035
671
SPN021 Spinal Meningioma 50 0.035
672
P MTR003 Mitral Valve Stenosis 50 0.035
673
OPP004 Oppositional Defiant Disorder 49 0.035
674
VLV047 Volvulus of Midgut 49 0.035
675
CHL004 Cholelithiasis 49 0.035
676
P ASP001 Asperger Syndrome 48 0.035
677
c MTR002 Mitral Valve Insufficiency 48 0.035
678
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.035
679
CLF056 Cleft Lip with or Without Cleft Palate 47 0.035
680
c PSR032 Psoriasis 11 47 0.035
681
CHR074 Choriocarcinoma 47 0.035
682
c PRM093 Premature Ovarian Failure 7 47 0.035
683
P LPM005 Lipomatosis 46 0.035
684
GRW007 Growth Hormone Deficiency 46 0.035
685
EPD015 Epidemic Typhus 45 0.035
686
c LFR007 Li-Fraumeni Syndrome 2 45 0.035
687
P TST026 Testicular Germ Cell Cancer 43 0.035
688
P HYP265 Hypotonia 43 0.035
689
VRL003 Variola Major 42 0.035
690
CRV043 Cervical Dystonia 42 0.035
691
c PSR028 Psoriasis 7 42 0.035
692
c PSR018 Psoriasis 13 41 0.035
693
SPS019 Spastic Paraparesis 38 0.035
694
c HNT011 Huntington Disease-Like 3 38 0.035
695
PRN010 Paranoid Personality Disorder 29 0.035
696
CYT018 Cytochrome P450 2d6 Variant 27 0.035
697
P LNG064 Lung Cancer Susceptibility 3 78 0.032
698
LPT014 Leptin Deficiency or Dysfunction 74 0.032
699
FBR012 Fabry Disease 72 0.032
700
ACR007 Acromegaly 71 0.032
701
c HMP029 Hemophilia a 67 0.032
702
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.032
703
OST017 Osteomyelitis 64 0.032
704
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 0.032
705
P SPN046 Spinal Muscular Atrophy 62 0.032
706
P VSC011 Vasculitis 62 0.032
707
c WLM018 Wilms Tumor 5 61 0.032
708
SDD001 Sudden Infant Death Syndrome 61 0.032
709
P HMN010 Hemangioma 61 0.032
710
NRL005 Neurilemmoma 60 0.032
711
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.032
712
HRP004 Herpes Zoster 60 0.032
713
CRD223 Cardiac Arrhythmia 60 0.032
714
LGG001 Legg-Calve-Perthes Disease 60 0.032
715
PRN019 Perinatal Necrotizing Enterocolitis 59 0.032
716
P GLL022 Guillain-Barre Syndrome 59 0.032
717
CRY005 Cryptococcosis 58 0.032
718
P URT039 Urticaria 58 0.032
719
GLS018 Glass Syndrome 57 0.032
720
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.032
721
VSC003 Visceral Leishmaniasis 55 0.032
722
P ANT006 Antiphospholipid Syndrome 55 0.032
723
CRH005 Crohn's Colitis 53 0.032
724
P HML001 Hemolytic-Uremic Syndrome 53 0.032
725
INF034 Infective Endocarditis 53 0.032
726
P ACT008 Actinic Keratosis 53 0.032
727
c GLL024 Gallbladder Disease 1 53 0.032
728
OST011 Osteomalacia 52 0.032
729
P SML001 Small Cell Carcinoma 52 0.032
730
HYP014 Hyperuricemia 52 0.032
731
APR001 Apraxia 52 0.032
732
ONC002 Onchocerciasis 52 0.032
733
KRT009 Keratosis 51 0.032
734
c SVR005 Severe Pre-Eclampsia 50 0.032
735
TRY001 Trypanosomiasis 50 0.032
736
QDR001 Quadriplegia 48 0.032
737
OPD006 Opioid Addiction 48 0.032
738
DRG003 Drug Dependence 47 0.032
739
NSS002 Neisseria Meningitidis Infection 47 0.032
740
AML029 Ameloblastoma 46 0.032
741
c ERL020 Early-Onset Schizophrenia 44 0.032
742
LWC001 Low Compliance Bladder 43 0.032
743
PHY002 Physical Disorder 42 0.032
744
OCL052 Ocular Dominance 42 0.032
745
HYP466 Hyperplastic Polyposis Syndrome 41 0.032
746
SCR001 Secretory Meningioma 41 0.032
747
RDN001 Reading Disorder 40 0.032
748
SPR126 Superior Semicircular Canal Dehiscence 40 0.032
749
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.032
750
c FML053 Familial Colorectal Cancer 35 0.032
751
c MJR008 Major Affective Disorder 2 35 0.032
752
c MJR003 Major Affective Disorder 6 33 0.032
753
c MJR006 Major Affective Disorder 5 33 0.032
754
CND006 Candida Glabrata 32 0.032
755
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.032
756
RDT005 Radiation Induced Cancer 25 0.032
757
P CNR004 Cone-Rod Dystrophy 2 73 0.030
758
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.030
759
PLY001 Polycythemia Vera 69 0.030
760
MNT001 Mantle Cell Lymphoma 69 0.030
761
c MYT021 Myotonic Dystrophy 1 69 0.030
762
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.030
763
P TMP003 Temporal Arteritis 68 0.030
764
CMM004 Common Variable Immunodeficiency 68 0.030
765
P OLG002 Oligodendroglioma 67 0.030
766
P MLG056 Malignant Hyperthermia 67 0.030
767
c PRM196 Premature Ovarian Failure 1 67 0.030
768
CHG001 Chagas Disease 66 0.030
769
KHL003 Kohlschutter-Tonz Syndrome 65 0.030
770
CRN036 Craniopharyngioma 65 0.030
771
P THY023 Thymoma 65 0.030
772
P CHR071 Charcot-Marie-Tooth Disease 65 0.030
773
c DPH024 Diaphragmatic Hernia, Congenital 63 0.030
774
MSC152 Muscular Dystrophy, Becker Type 63 0.030
775
P LMY004 Leiomyosarcoma 63 0.030
776
HMT002 Hematologic Cancer 62 0.030
777
P ORT004 Orthostatic Intolerance 62 0.030
778
P INT143 Interstitial Cystitis 61 0.030
779
ALC006 Alcoholic Hepatitis 61 0.030
780
VRL011 Viral Infectious Disease 61 0.030
781
SHG001 Shigellosis 60 0.030
782
WLL001 Williams-Beuren Syndrome 60 0.030
783
c JVN061 Juvenile Arthritis 60 0.030
784
P ATR010 Atrial Heart Septal Defect 60 0.030
785
DCT002 Ductal Carcinoma in Situ 59 0.030
786
BRN002 Bronchiolitis 59 0.030
787
P DNG005 Dengue Virus 59 0.030
788
P ANP001 Anaplastic Large Cell Lymphoma 58 0.030
789
c PRM005 Primary Hyperparathyroidism 58 0.030
790
PMP006 Pemphigus Vulgaris, Familial 57 0.030
791
c VSC019 Vesicoureteral Reflux 1 57 0.030
792
P PRN023 Prion Disease 57 0.030
793
CMM005 Common Cold 57 0.030
794
TRN018 Transitional Cell Carcinoma 56 0.030
795
PLS011 Plasmacytoma 56 0.030
796
ALL010 Allergic Contact Dermatitis 56 0.030
797
FND002 Fundus Dystrophy 55 0.030
798
AMB001 Amebiasis 55 0.030
799
P MLN007 Male Infertility 55 0.030
800
P PLM034 Pulmonary Emphysema 55 0.030
801
P PTT006 Pituitary Adenoma 55 0.030
802
CHR100 Chronic Ulcer of Skin 55 0.030
803
P LRY044 Larynx Cancer 55 0.030
804
GLS001 Gliosarcoma 54 0.030
805
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.030
806
c CNT016 Central Retinal Vein Occlusion 53 0.030
807
ECH003 Echinococcosis 53 0.030
808
P HYP083 Hypopituitarism 53 0.030
809
P RTN022 Retinal Vein Occlusion 53 0.030
810
PRP080 Peripheral Artery Disease 53 0.030
811
P RTN018 Retinal Disease 53 0.030
812
P HYP730 Hypogonadotropic Hypogonadism 52 0.030
813
c THY107 Thymoma, Familial 52 0.030
814
ART074 Aortic Dissection 52 0.030
815
LMY002 Leiomyoma 52 0.030
816
PLS009 Plasma Cell Neoplasm 51 0.030
817
ESP002 Esophageal Varix 51 0.030
818
ALL009 Allergic Conjunctivitis 50 0.030
819
AZS001 Azoospermia 50 0.030
820
P AGG001 Aggressive Periodontitis 50 0.030
821
URT001 Urethritis 49 0.030
822
KRT001 Keratoconjunctivitis Sicca 49 0.030
823
LFT001 Left Bundle Branch Hemiblock 49 0.030
824
P MGR001 Migraine Without Aura 49 0.030
825
c BCT013 Bacterial Pneumonia 48 0.030
826
P NGH001 Night Blindness 48 0.030
827
BNN003 Bone Inflammation Disease 48 0.030
828
HYP025 Hyperphosphatemia 48 0.030
829
SXL003 Sexual Disorder 47 0.030
830
HYP016 Hypochondriasis 47 0.030
831
LYM009 Lymphocytic Choriomeningitis 47 0.030
832
ANT011 Antisocial Personality Disorder 47 0.030
833
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.030
834
RMS001 Rem Sleep Behavior Disorder 46 0.030
835
c MLG068 Malignant Glioma 46 0.030
836
URT010 Ureteral Obstruction 45 0.030
837
CRB004 Cerebral Artery Occlusion 45 0.030
838
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.030
839
SPS057 Spasticity 45 0.030
840
DWR001 Dwarfism 44 0.030
841
PPL001 Papillary Adenoma 44 0.030
842
DMP001 Dumping Syndrome 44 0.030
843
PRT014 Protein S Deficiency 44 0.030
844
SMN007 Seminoma 43 0.030
845
MYX004 Myxedema 43 0.030
846
MMM006 Mammographic Density 41 0.030
847
MYL057 Myelopathy, Htlv-1-Associated 39 0.030
848
OPS002 Opsismodysplasia 37 0.030
849
DVL001 Developmental Coordination Disorder 34 0.030
850
BNN005 Bunion 33 0.030
851
ANS006 Anosognosia 30 0.030
852
SPN136 Spondyloepimetaphyseal Dysplasia, Aggrecan Type 25 0.030
853
P GLM040 Glioma Susceptibility 1 81 0.027
854
PHN003 Phenylketonuria 75 0.027
855
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.027
856
BRT054 Brittle Bone Disorder 72 0.027
857
WLS001 Wilson Disease 71 0.027
858
GST040 Gastric Adenocarcinoma 70 0.027
859
MLT157 Multiple System Atrophy 1 70 0.027
860
c GCH015 Gaucher Disease, Type I 70 0.027
861
P OST001 Osteopetrosis 70 0.027
862
P TTR001 Tetralogy of Fallot 70 0.027
863
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.027
864
P TBR001 Tuberous Sclerosis 70 0.027
865
P ESS003 Essential Thrombocythemia 68 0.027
866
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.027
867
P CHR012 Chronic Granulomatous Disease 67 0.027
868
P PRP003 Porphyria Cutanea Tarda 67 0.027
869
LBR036 Leber Plus Disease 66 0.027
870
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.027
871
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.027
872
APN008 Apnea, Obstructive Sleep 64 0.027
873
NRM005 Neuromuscular Disease 64 0.027
874
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.027
875
PRP083 Porphyria, Acute Intermittent 64 0.027
876
HYP020 Hyperprolactinemia 64 0.027
877
ACT119 Acute Promyelocytic Leukemia 63 0.027
878
LRN002 Laron Syndrome 62 0.027
879
BLL006 Bullous Pemphigoid 62 0.027
880
RCT015 Reactive Arthritis 61 0.027
881
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.027
882
TRG002 Trigeminal Neuralgia 60 0.027
883
DNG002 Dengue Hemorrhagic Fever 60 0.027
884
RHM001 Rheumatic Fever 60 0.027
885
P PTN014 Patent Ductus Arteriosus 1 60 0.027
886
QFV001 Q Fever 60 0.027
887
P MYC008 Myocarditis 59 0.027
888
P LYM033 Lymphoproliferative Syndrome 59 0.027
889
P BRS044 Breast Adenocarcinoma 59 0.027
890
GRD007 Grade Iii Astrocytoma 59 0.027
891
ANT024 Anthrax Disease 58 0.027
892
P MLT007 Multiple Epiphyseal Dysplasia 58 0.027
893
CHR072 Chordoma 58 0.027
894
SCR008 Scrub Typhus 58 0.027
895
CCC001 Coccidioidomycosis 58 0.027
896
P MMP001 Mumps 58 0.027
897
P MYM013 Moyamoya Disease 1 57 0.027
898
DSS009 Disseminated Intravascular Coagulation 57 0.027
899
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.027
900
P MYS005 Myositis 56 0.027
901
LST001 Listeriosis 56 0.027
902
ALL006 Allergic Asthma 56 0.027
903
ANN002 Anencephaly 56 0.027
904
EMB004 Embryonal Carcinoma 56 0.027
905
GST050 Gastrointestinal System Disease 56 0.027
906
P PNM006 Pneumoconiosis 56 0.027
907
MCS002 Mucositis 56 0.027
908
SLC006 Silicosis 56 0.027
909
BRN004 Brain Edema 56 0.027
910
HPT022 Hepatoblastoma 56 0.027
911
FLR001 Filarial Elephantiasis 55 0.027
912
ATR057 Atrioventricular Block 55 0.027
913
c FML035 Familial Hyperlipidemia 55 0.027
914
ORP003 Oropharynx Cancer 55 0.027
915
P ATR001 Atrioventricular Septal Defect 55 0.027
916
LMB062 Limb Ischemia 55 0.027
917
HMP005 Hemiplegia 55 0.027
918
P SLM003 Salmonellosis 55 0.027
919
RSC001 Rosacea 54 0.027
920
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.027
921
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.027
922
OPT054 Opitz-Kaveggia Syndrome 54 0.027
923
PRC002 Paracoccidioidomycosis 54 0.027
924
MTN003 Motion Sickness 53 0.027
925
IRD001 Iridocyclitis 53 0.027
926
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.027
927
TRC008 Trachoma 53 0.027
928
DRM011 Dermatophytosis 52 0.027
929
P ACT105 Acute Mountain Sickness 52 0.027
930
c INH030 Inherited Retinal Disorder 51 0.027
931
THR004 Thrombocytosis 51 0.027
932
RYS001 Reye Syndrome 51 0.027
933
ILS001 Ileus 51 0.027
934
ANK001 Ankylosis 51 0.027
935
LNG031 Lung Benign Neoplasm 51 0.027
936
SPN019 Spondylolisthesis 51 0.027
937
P PRC012 Pericardial Effusion 51 0.027
938
HND002 Hand, Foot and Mouth Disease 51 0.027
939
TNG007 Tongue Carcinoma 51 0.027
940
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 51 0.027
941
P MMB011 Membranous Nephropathy 50 0.027
942
HPT014 Hepatorenal Syndrome 50 0.027
943
P OBS001 Obstructive Jaundice 50 0.027
944
TRP002 Tropical Spastic Paraparesis 50 0.027
945
HYP017 Hypophosphatemia 50 0.027
946
SYS003 Systolic Heart Failure 49 0.027
947
ART017 Aortic Disease 49 0.027
948
MRS004 Marshall-Smith Syndrome 49 0.027
949
PTH002 Pathological Gambling 49 0.027
950
WTH001 Withdrawal Disorder 48 0.027
951
BLT006 Bilateral Breast Cancer 48 0.027
952
HMP001 Hemopericardium 48 0.027
953
MLK006 Milk Allergy 48 0.027
954
PLC007 Placental Abruption 48 0.027
955
ANT018 Anthracosis 48 0.027
956
ASB001 Asbestosis 47 0.027
957
KHN001 Kuhnt-Junius Degeneration 47 0.027
958
TST044 Testicular Torsion 47 0.027
959
TTH006 Tooth Disease 46 0.027
960
SMT001 Somatization Disorder 46 0.027
961
P MYC033 Myoclonus 46 0.027
962
c DRR009 Diarrhea 6 46 0.027
963
c PCH010 Pachyonychia Congenita 3 44 0.027
964
GNG003 Gingival Recession 44 0.027
965
P BLP003 Blepharospasm 44 0.027
966
c HYP272 Hypercholesterolemia, Familial, 3 44 0.027
967
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.027
968
P SYR001 Syringomyelia 44 0.027
969
DNT001 Dental Fluorosis 43 0.027
971
EST005 Esotropia 42 0.027
972
49X006 49, Xxxxy Syndrome 41 0.027
973
c ACT004 Acute Diarrhea 39 0.027
974
MCK029 Meckel Diverticulum 38 0.027
975
c PLY105 Polycystic Ovary Syndrome 1 38 0.027
976
SYR010 Syringomyelia, Noncommunicating Isolated 37 0.027
977
HRM002 Hermaphroditism 36 0.027
978
P HRD217 Hereditary Optic Neuropathy 36 0.027
979
c SPN325 Spinocerebellar Ataxia, Autosomal Recessive 20 36 0.027
980
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 35 0.027
981
ENP001 Enophthalmos 35 0.027
982
CYC001 Cycloplegia 35 0.027
983
STC004 Stachybotrys Chartarum 34 0.027
984
c MJR023 Major Affective Disorder 7 33 0.027
985
c PRS136 Prostate Cancer, Hereditary, 6 33 0.027
986
c PRS130 Prostate Cancer, Hereditary, 8 32 0.027
987
MNC001 Monocular Esotropia 30 0.027
988
c MJR004 Major Affective Disorder 4 28 0.027
989
ANS021 Anisocoria 27 0.027
990
MTH071 Methane Production 26 0.027
991
ASB003 Asbestos Intoxication 26 0.027
992
DVL005 Developmental Dyspraxia 23 0.027
993
SSS001 Sessile Serrated Polyposis Cancer Syndrome 21 0.027
994
PFF001 Pfeiffer Syndrome 79 0.024
995
MRF001 Marfan Syndrome 77 0.024
996
c NRF024 Neurofibromatosis, Type I 77 0.024
997
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.024
998
c EXD008 Exudative Vitreoretinopathy 1 71 0.024
999
P OCL013 Oculodentodigital Dysplasia 69 0.024
1000
CHL065 Cholangiocarcinoma 68 0.024
1001
c HMP004 Hemophilia B 68 0.024
1002
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 0.024
1003
c MCR129 Microvascular Complications of Diabetes 1 66 0.024
1004
MYL031 Myeloproliferative Neoplasm 66 0.024
1005
P BRD002 Bardet-Biedl Syndrome 66 0.024
1006
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.024
1007
P MST009 Mastocytosis 64 0.024
1008
DGR001 Digeorge Syndrome 64 0.024
1009
P MCH002 Machado-Joseph Disease 62 0.024
1010
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.024
1011
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 62 0.024
1012
CTN007 Cutaneous Leishmaniasis 62 0.024
1013
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.024
1014
c PNS012 Paine Syndrome 61 0.024
1015
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.024
1016
c LYN004 Lynch Syndrome I 60 0.024
1017
P CHR285 Chronic Myelomonocytic Leukemia 60 0.024
1018
c HRD002 Hereditary Angioedema 60 0.024
1019
SPP011 Suppression of Tumorigenicity 12 59 0.024
1020
P HYP760 Hypothyroidism, Congenital, Nongoitrous, 2 59 0.024
1021
P LKD001 Leukodystrophy 59 0.024
1022
AVN001 Avian Influenza 59 0.024
1023
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.024
1024
VLV032 Vulva Cancer 59 0.024
1025
P PLY006 Polydactyly 59 0.024
1026
P PGT001 Paget's Disease of Bone 58 0.024
1027
SPT004 Septic Arthritis 58 0.024
1028
P EHL001 Ehlers-Danlos Syndrome 58 0.024
1029
P BNC003 Bone Cancer 58 0.024
1030
c CHR417 Chronic Graft Versus Host Disease 57 0.024
1031
BRN056 Bronchopulmonary Dysplasia 57 0.024
1032
LYM021 Lymphadenitis 57 0.024
1033
P ANG015 Angioedema 57 0.024
1034
P CHN012 Chondrosarcoma 56 0.024
1035
CMR002 Coumarin Resistance 56 0.024
1036
TCK001 Tick-Borne Encephalitis 56 0.024
1037
c ACT134 Acute Liver Failure 56 0.024
1038
ERY051 Erythroleukemia, Familial 56 0.024
1039
P MTC069 Mitochondrial Disorders 56 0.024
1040
ACS001 Acoustic Neuroma 56 0.024
1041
VGT001 Vogt-Koyanagi-Harada Disease 55 0.024
1042
PTS001 Patau Syndrome 55 0.024
1043
ZLL002 Zollinger-Ellison Syndrome 55 0.024
1044
c BCT007 Bacterial Meningitis 55 0.024
1045
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.024
1046
P DBT005 Diabetes Insipidus 55 0.024
1047
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.024
1048
GNT003 Genital Herpes 54 0.024
1049
SYN007 Synovitis 54 0.024
1050
P SPN052 Spondyloarthropathy 54 0.024
1051
TRD006 Tardive Dyskinesia 54 0.024
1052
GNG004 Ganglioglioma 54 0.024
1053
P RST001 Restless Legs Syndrome 54 0.024
1054
VLC001 Velocardiofacial Syndrome 54 0.024
1055
THR013 Thoracic Outlet Syndrome 54 0.024
1056
PRC013 Pericarditis 54 0.024
1057
LYM040 Lymphoblastic Lymphoma 54 0.024
1058
SNS003 Sensory Peripheral Neuropathy 54 0.024
1059
P BRC006 Brachydactyly 53 0.024
1060
RHM028 Rheumatic Heart Disease 53 0.024
1061
KRT006 Keratoconjunctivitis 53 0.024
1062
PRP036 Peripheral T-Cell Lymphoma 53 0.024
1063
P CNT005 Central Nervous System Lymphoma 53 0.024
1064
HMC014 Homocysteinemia 53 0.024
1065
P INT068 Intestinal Disease 53 0.024
1066
P SLV027 Silver-Russell Syndrome 1 53 0.024
1067
EXP004 Exophthalmos 52 0.024
1068
MRG003 Marginal Zone B-Cell Lymphoma 52 0.024
1069
PRV004 Periventricular Leukomalacia 52 0.024
1070
SPS003 Spastic Diplegia 51 0.024
1071
OLG003 Oligohydramnios 51 0.024
1072
P LCT001 Lactic Acidosis 51 0.024
1073
INT079 Intrahepatic Cholangiocarcinoma 51 0.024
1074
NRM004 Neuroma 51 0.024
1075
P HYP040 Hypospadias 51 0.024
1076
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.024
1077
BRX001 Bruxism 50 0.024
1078
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.024
1079
RSP006 Respiratory System Disease 50 0.024
1080
BLS002 Blastomycosis 50 0.024
1081
P OTS001 Otosclerosis 49 0.024
1082
P CRV039 Cervicitis 49 0.024
1083
VRC001 Varicocele 49 0.024
1084
PLP001 Pulpitis 49 0.024
1085
P END046 Endometritis 49 0.024
1086
SPT005 Spotted Fever 49 0.024
1087
MCR004 Macroglobulinemia 49 0.024
1088
CNG069 Congenital Cytomegalovirus 49 0.024
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