Search results for Vitamin A

3812 hits were found for Vitamin A

# Family MCID Name MIFTS Score
1
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 6.121
2
MTH077 Methylmalonic Aciduria, Cbla Type 42 5.057
3
KRT002 Keratomalacia 47 4.213
4
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 50 4.151
5
HYP796 Hypercarotenemia and Vitamin a Deficiency, Autosomal Recessive 8 1.643
6
HRD143 Hereditary Hypercarotenemia and Vitamin a Deficiency 6 1.637
7
RCK004 Rickets 68 1.037
8
P KDN018 Kidney Disease 72 0.456
9
P HYP069 Hyperparathyroidism 63 0.431
10
P OST002 Osteoporosis 74 0.416
11
VTM002 Vitamin B12 Deficiency 48 0.400
12
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.399
13
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.399
14
c CHR684 Chronic Kidney Disease 70 0.385
15
ATM095 Autoimmune Disease 62 0.380
16
P LVR013 Liver Disease 68 0.365
17
P CLR023 Colorectal Cancer 99 0.362
18
DFC004 Deficiency Anemia 70 0.359
19
P DRR001 Diarrhea 55 0.353
20
P BRS047 Breast Cancer 97 0.338
21
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.331
22
BNR002 Bone Resorption Disease 48 0.318
23
P NRP001 Neuropathy 56 0.317
24
P DBT009 Diabetes Mellitus 64 0.315
25
c SCN007 Secondary Hyperparathyroidism 51 0.315
26
c PRC016 Pre-Eclampsia 63 0.312
27
ADN018 Adenoma 59 0.303
28
LVR012 Liver Cirrhosis 62 0.303
29
P PSR002 Psoriasis 62 0.303
30
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.303
31
DRM006 Dermatitis 61 0.302
32
VTM033 Vitamin K Deficiency Bleeding 48 0.301
33
DPR016 Depression 63 0.301
34
P HRT032 Heart Disease 75 0.300
35
END086 End Stage Renal Disease 51 0.299
36
P INF037 Inflammatory Bowel Disease 54 0.299
37
PST011 Pustulosis of Palm and Sole 52 0.299
38
P PRS040 Prostate Cancer 97 0.297
39
P VSC007 Vascular Disease 63 0.296
40
CNG034 Congestive Heart Failure 69 0.291
41
48X005 48,xyyy 39 0.290
42
P MLT020 Multiple Sclerosis 72 0.288
43
P BND020 Bone Disease 59 0.288
44
IRN002 Iron Metabolism Disease 57 0.287
45
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.287
46
OST011 Osteomalacia 52 0.286
47
P CRN300 Coronary Heart Disease 1 63 0.285
48
OST012 Osteoarthritis 78 0.283
49
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.283
50
CRH001 Crohn's Disease 74 0.283
51
P LNG032 Lung Cancer 98 0.282
52
P ALZ034 Alzheimer Disease 88 0.280
53
P ADN016 Adenocarcinoma 64 0.279
54
FTT001 Fatty Liver Disease 61 0.279
55
P ATR011 Atrial Fibrillation 66 0.278
56
CYS001 Cystic Fibrosis 81 0.276
57
ISC004 Ischemia 58 0.274
58
c SYS001 Systemic Lupus Erythematosus 86 0.273
59
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.272
60
LPP008 Lipoprotein Quantitative Trait Locus 62 0.271
61
P LPS004 Lupus Erythematosus 61 0.268
62
MNT002 Mental Depression 58 0.268
63
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.268
64
P LYM118 Lymphoma 68 0.266
65
LNG099 Lung Disease 60 0.265
66
ATH013 Atherosclerosis Susceptibility 65 0.264
67
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.263
68
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.263
69
P HPT023 Hepatocellular Carcinoma 100 0.263
70
P SKN015 Skin Carcinoma 66 0.260
71
P NTR004 Neutropenia 63 0.260
72
STR067 Stroke, Ischemic 81 0.260
73
LPD008 Lipid Metabolism Disorder 62 0.259
74
P LKM002 Leukemia 68 0.259
75
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.259
76
P MYL006 Myeloid Leukemia 60 0.258
77
CRB039 Cerebrovascular Disease 67 0.256
78
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.256
79
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.256
80
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.255
81
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.255
82
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.255
83
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.255
84
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.255
85
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.255
86
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.255
87
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.255
88
ART140 Arteries, Anomalies of 52 0.255
89
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.254
90
P ATS364 Autism 70 0.252
91
P OVR042 Ovarian Cancer 88 0.251
92
P PNC035 Pancreatic Cancer 84 0.251
93
P CTR002 Cataract 60 0.250
94
HMN044 Human Immunodeficiency Virus Type 1 71 0.249
95
c HYP595 Hypertension, Essential 84 0.249
96
DWN001 Down Syndrome 70 0.249
97
P MYP004 Myopathy 70 0.248
98
ANX010 Anxiety 73 0.248
99
P HYP086 Hypothyroidism 69 0.246
100
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.246
101
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.246
102
P PRD008 Periodontitis 64 0.243
103
ULC004 Ulcerative Colitis 73 0.243
104
P ALP008 Alopecia 54 0.243
105
SKN016 Skin Disease 63 0.242
106
GST033 Gestational Diabetes 61 0.241
107
P CHR345 Chronic Pain 44 0.241
108
HYP781 Hypoascorbemia 51 0.241
109
ALC007 Alcohol Dependence 66 0.240
110
BCK006 Back Pain 42 0.239
111
MSL001 Measles 62 0.239
112
c HYP836 Hypercholesterolemia, Familial, 1 73 0.239
113
P MYC007 Myocardial Infarction 70 0.238
114
CYT002 Cytokine Deficiency 42 0.238
115
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.237
116
c THR092 Thrombophilia Due to Thrombin Defect 73 0.237
117
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.236
118
P SZR006 Seizure Disorder 56 0.236
119
HMC014 Homocysteinemia 53 0.236
120
P MLN008 Melanoma 69 0.236
121
P PRP019 Peripheral Nervous System Disease 58 0.236
122
TXC005 Toxic Shock Syndrome 62 0.234
123
47X002 47,xyy 49 0.234
124
P RHM011 Rheumatoid Arthritis 80 0.234
125
PLM001 Pulmonary Tuberculosis 69 0.234
126
ALL026 Allergic Hypersensitivity Disease 62 0.232
127
THY029 Thyroid Carcinoma 59 0.232
128
AST005 Asthma 76 0.231
129
PLM033 Pulmonary Embolism 59 0.231
130
P INF032 Infertility 57 0.231
131
P EXN002 Exanthem 57 0.231
132
P DRM053 Dermatitis, Atopic 66 0.231
133
NTR005 Nutritional Deficiency Disease 62 0.231
134
P HDC001 Headache 57 0.231
135
P DMN002 Dementia 66 0.230
136
P GST053 Gastric Cancer 83 0.230
137
P ENC018 Encephalopathy 61 0.229
138
P PNM007 Pneumonia 68 0.229
139
P BLD134 Bladder Cancer 79 0.229
140
P THR014 Thrombocytopenia 67 0.229
141
P RSP003 Respiratory Failure 74 0.228
142
c HPT003 Hepatitis a 62 0.228
143
ANR040 Aneurysm 59 0.228
144
c NRF023 Neurofibromatosis, Type Ii 80 0.227
145
P PLY011 Polycystic Ovary Syndrome 56 0.227
146
c LKM061 Leukemia, Acute Myeloid 84 0.227
147
OST159 Osteogenic Sarcoma 66 0.227
148
P CRD246 Cardiovascular System Disease 57 0.226
149
VSL002 Visual Epilepsy 59 0.226
150
HYP066 Hyperglycemia 61 0.225
151
c MGR028 Migraine with or Without Aura 1 67 0.225
152
HYP056 Hypoglycemia 66 0.224
153
CLT003 Colitis 62 0.223
154
THR024 Thrombosis 57 0.223
155
NRL016 Neural Tube Defects 82 0.220
156
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.219
157
IMM167 Immune Deficiency Disease 78 0.219
158
c ATS007 Autism Spectrum Disorder 67 0.219
159
P INF038 Influenza 68 0.218
160
SPN186 Spinal Cord Injury 60 0.217
161
ATX019 Ataxia with Vitamin E Deficiency 42 0.217
162
P RHN004 Rhinitis 57 0.215
163
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.215
164
PRN011 Pernicious Anemia 53 0.214
165
P ECL001 Eclampsia 50 0.214
166
AGN016 Aging 56 0.214
167
c HPT001 Hepatitis C 62 0.214
168
P MJR001 Major Depressive Disorder 68 0.214
169
c ATR087 Atrial Standstill 1 75 0.214
170
HLX001 Helix Syndrome 47 0.213
171
P GST044 Gastritis 56 0.213
173
P HPT021 Hepatitis 67 0.211
174
P BCL017 B-Cell Lymphoma 58 0.210
175
P TRN020 Turner Syndrome 67 0.210
176
SQM006 Squamous Cell Carcinoma 60 0.210
177
ACQ007 Acquired Immunodeficiency Syndrome 60 0.210
178
c PRM005 Primary Hyperparathyroidism 58 0.210
179
P ART022 Arthritis 69 0.209
180
P SRC025 Sarcoidosis 1 70 0.209
181
P CRD119 Cardiac Arrest 67 0.209
182
P LKM062 Leukemia, Acute Lymphoblastic 69 0.208
183
CVD001 Covid-19 44 0.208
184
MYL069 Myeloma, Multiple 85 0.208
185
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.206
186
c RHB024 Rhabdomyosarcoma 2 67 0.206
187
PNG002 Pain Agnosia 51 0.204
188
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.204
189
c SML038 Small Cell Cancer of the Lung 65 0.203
190
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.203
191
P MSC005 Muscular Dystrophy 66 0.203
192
P NRB001 Neuroblastoma 72 0.202
193
c HPT073 Hepatitis C Virus 72 0.202
194
CHL068 Cholestasis 61 0.202
195
P RCT021 Rectum Cancer 52 0.201
196
CNS004 Constipation 58 0.201
197
CHL079 Children's Interstitial Lung Disease 26 0.201
198
DSS008 Disease of Mental Health 58 0.200
199
c ACT075 Acute Myocardial Infarction 57 0.200
200
c MCR120 Microvascular Complications of Diabetes 7 47 0.199
201
ESP021 Esophageal Cancer 90 0.199
202
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.199
203
TTN003 Tetanus 65 0.199
204
PRT037 Pertussis 65 0.198
205
GLL048 Glial Tumor 45 0.198
206
P THL005 Thalassemia 60 0.197
207
BRN071 Brain Injury 49 0.197
208
P GLM045 Glioma 63 0.197
209
c MCR113 Microvascular Complications of Diabetes 3 52 0.197
210
HRW001 Hair Whorl 36 0.196
211
c ACT071 Acute Kidney Failure 60 0.196
212
P SCH015 Schizophrenia 74 0.196
213
OCL069 Ocular Motor Apraxia 51 0.196
214
c MCR130 Microvascular Complications of Diabetes 6 41 0.195
215
c MCR133 Microvascular Complications of Diabetes 4 41 0.195
216
P VSC011 Vasculitis 62 0.195
217
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.195
218
P SLP006 Sleep Apnea 69 0.195
219
TRM010 Traumatic Brain Injury 51 0.194
220
P END044 Endometriosis 63 0.194
221
PRT036 Peritonitis 64 0.193
222
PRP030 Purpura 54 0.193
223
P BPL003 Bipolar Disorder 56 0.191
224
P HYD006 Hydrocephalus 66 0.191
225
PRP027 Peripheral Vascular Disease 71 0.191
226
c HPT016 Hepatitis B 59 0.191
227
P MCR115 Microvascular Complications of Diabetes 5 66 0.191
228
MYL009 Myelodysplastic Syndrome 70 0.190
229
DYS073 Dysphagia 50 0.190
230
c MJR024 Major Affective Disorder 9 41 0.189
231
c MJR022 Major Affective Disorder 8 38 0.189
232
P HYP076 Hyperthyroidism 55 0.189
233
GLB015 Glioblastoma Multiforme 75 0.189
234
c PRM038 Primary Agammaglobulinemia 44 0.188
235
P TRM003 Tremor 54 0.188
236
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.188
237
ADL002 Adult Syndrome 70 0.187
238
LYM133 Lymphoma, Hodgkin, Classic 69 0.187
239
ALL003 Allergic Rhinitis 67 0.187
240
MLR004 Malaria 81 0.186
241
SRC014 Sarcoma 65 0.186
242
P EPL164 Epilepsy 71 0.186
243
SPN035 Spindle Cell Sarcoma 53 0.185
244
c ACT068 Acute Cystitis 63 0.185
245
P LTR001 Lateral Sclerosis 54 0.185
246
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.184
247
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.184
248
CRB037 Cerebral Palsy 69 0.184
249
P GRF003 Graft-Versus-Host Disease 72 0.184
250
P NPH012 Nephrotic Syndrome 60 0.184
251
CRV035 Cervical Cancer 76 0.183
252
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.183
253
P MNN013 Meningitis 66 0.182
254
DNT012 Dental Caries 53 0.181
255
P ALC033 Alcohol Use Disorder 58 0.181
256
NPH009 Nephrolithiasis 55 0.181
257
NNL006 Non-Alcoholic Steatohepatitis 54 0.180
258
P CLC063 Celiac Disease 1 66 0.180
259
P GLM007 Glomerulonephritis 57 0.180
260
P END033 Endocarditis 57 0.180
261
ATS010 Autosomal Recessive Disease 48 0.179
262
ANG054 Angina Pectoris 66 0.177
263
P NGH001 Night Blindness 48 0.177
264
P HML002 Hemolytic Anemia 63 0.177
265
c BRN108 Branchiootic Syndrome 1 62 0.177
266
P PLY019 Polyneuropathy 56 0.177
267
P MYC084 Mycobacterium Tuberculosis 1 68 0.176
268
P PNC044 Pancreatitis 61 0.176
269
P PRK057 Parkinson Disease, Late-Onset 78 0.176
270
PYR009 Pyridoxine Deficiency Anemia 34 0.175
271
c PNS012 Paine Syndrome 61 0.175
272
BCT022 Bacterial Infectious Disease 56 0.175
273
P SCK005 Sickle Cell Disease 50 0.174
274
P HYP024 Hypoparathyroidism 56 0.174
275
P HYP098 Hypereosinophilic Syndrome 67 0.173
276
HYP017 Hypophosphatemia 50 0.173
277
P PLM037 Pulmonary Hypertension 67 0.172
278
P THY032 Thyroiditis 52 0.172
279
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.172
280
KRT009 Keratosis 51 0.172
281
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.171
282
MDD011 Mood Disorder 62 0.171
283
P RTN008 Retinitis Pigmentosa 79 0.171
284
P SCL018 Scoliosis 60 0.170
285
PPT005 Peptic Ulcer Disease 59 0.170
286
GLC003 Glucose Intolerance 54 0.170
287
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.170
288
STM007 Stomatitis 50 0.169
289
c ACT027 Acute Pancreatitis 60 0.169
290
P ENC004 Encephalitis 61 0.168
291
KRT001 Keratoconjunctivitis Sicca 49 0.168
292
PLM031 Poliomyelitis 64 0.168
293
SBC016 Subacute Delirium 44 0.168
294
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.168
295
NRR001 Neuroretinitis 42 0.168
296
ART016 Aortic Aneurysm 69 0.167
297
P SBS003 Substance Abuse 55 0.167
298
IRN001 Iron Deficiency Anemia 59 0.166
299
LYM019 Lymphosarcoma 46 0.166
300
c VRL010 Viral Hepatitis 52 0.166
301
c SPN225 Spondyloarthropathy 1 73 0.166
302
RTN023 Retinitis 46 0.166
303
P HMP007 Hemophilia 51 0.165
304
LMY002 Leiomyoma 52 0.165
305
ETN001 Eating Disorder 60 0.165
306
GTR002 Goiter 53 0.165
307
HYP266 Hypoxia 57 0.164
308
IMP005 Impotence 52 0.164
309
LPT014 Leptin Deficiency or Dysfunction 74 0.164
310
P AMY004 Amyloidosis 70 0.163
311
c DBT099 Diabetes Mellitus, Type I 65 0.163
312
DPH001 Diphtheria 60 0.163
313
BRN024 Bronchitis 68 0.163
314
HNS001 Hansen's Disease 34 0.163
315
SPN051 Spondylitis 51 0.163
316
INF009 Inflammatory Spondylopathy 31 0.163
317
GST045 Gastroenteritis 59 0.162
318
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.162
319
P HRP006 Herpes Simplex 65 0.162
320
END057 Endometrial Cancer 74 0.162
321
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.162
322
OST017 Osteomyelitis 64 0.161
323
P LPR021 Leprosy 3 69 0.161
324
EYD002 Eye Disease 58 0.161
325
c SVR001 Severe Acute Respiratory Syndrome 62 0.161
326
FBR047 Fibromyalgia 58 0.161
327
SVR004 Severe Combined Immunodeficiency 73 0.161
328
P ART021 Arteriosclerosis 54 0.161
329
MGL001 Megaloblastic Anemia 51 0.159
330
PSY004 Psychotic Disorder 67 0.159
331
PRS045 Prostatic Hypertrophy 53 0.158
332
P OVR082 Overgrowth Syndrome 50 0.158
333
c SCL052 Scleroderma, Familial Progressive 61 0.158
334
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.157
335
CHR178 Chromosomal Triplication 35 0.157
336
P PRS038 Personality Disorder 65 0.156
337
MCS002 Mucositis 56 0.155
338
SKN019 Skin Melanoma 68 0.155
339
OTT002 Otitis Media 72 0.155
340
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.154
341
P URT039 Urticaria 58 0.154
342
LSH001 Leishmaniasis 63 0.154
343
P KLZ004 Kala-Azar 1 41 0.154
344
HLC007 Helicobacter Pylori Infection 59 0.154
345
P SYP003 Syphilis 58 0.154
346
HMS001 Hemosiderosis 54 0.154
347
c BSL007 Basal Cell Carcinoma 68 0.153
348
XRP001 Xerophthalmia 41 0.153
349
P SLP005 Sleep Disorder 59 0.153
350
ANR007 Anorexia Nervosa 63 0.153
351
PPL022 Papilloma 54 0.153
352
HDN002 Head Injury 46 0.153
353
P GRV001 Graves' Disease 55 0.153
354
PRT013 Portal Hypertension 59 0.152
355
CLF027 Cleft Palate, Isolated 64 0.152
356
P LKM071 Leukemia, Chronic Lymphocytic 79 0.152
357
ENT011 Enterocolitis 51 0.152
358
CHL123 Chlamydia 59 0.151
359
CMM005 Common Cold 57 0.151
360
c DLT002 Dilated Cardiomyopathy 79 0.151
361
HYP025 Hyperphosphatemia 48 0.151
362
c ACT073 Acute Leukemia 58 0.150
363
P SYS005 Systemic Scleroderma 68 0.150
364
IRR002 Irritable Bowel Syndrome 65 0.150
365
SPL018 Splenomegaly 48 0.149
366
DFF005 Diffuse Large B-Cell Lymphoma 55 0.149
367
PRS021 Prostatic Adenoma 51 0.149
368
IGR001 Ige Responsiveness, Atopic 59 0.149
369
CNT047 Contact Dermatitis 58 0.149
370
PNC001 Pancytopenia 54 0.148
371
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.148
372
P NRF002 Neurofibromatosis 56 0.148
373
PRS129 Prostatic Hyperplasia, Benign 49 0.148
374
c DWL002 Dowling-Degos Disease 1 58 0.147
375
BRN056 Bronchopulmonary Dysplasia 57 0.147
376
P INS002 in Situ Carcinoma 53 0.147
377
URM002 Uremia 49 0.147
378
P CNR004 Cone-Rod Dystrophy 2 73 0.147
379
P HYP265 Hypotonia 43 0.147
380
P HYP750 Hypertriglyceridemia, Familial 62 0.146
381
P MSC003 Muscular Atrophy 52 0.146
382
CHL014 Cholera 59 0.146
383
P PLM036 Pulmonary Fibrosis 65 0.145
384
TRN015 Transient Cerebral Ischemia 63 0.144
385
P UVT001 Uveitis 57 0.144
386
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.144
387
P RTN024 Retinoblastoma 73 0.144
388
P RRH023 Rare Hereditary Hemochromatosis 41 0.143
389
P PRM006 Primary Biliary Cirrhosis 62 0.143
390
P DYS154 Dystonia 65 0.143
391
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.142
392
P LNG064 Lung Cancer Susceptibility 3 78 0.142
393
PNM008 Pneumothorax 56 0.142
394
URL001 Urolithiasis 45 0.142
395
HYP005 Hypokalemia 55 0.142
396
c FML008 Familial Retinoblastoma 53 0.142
397
VRC005 Varicose Veins 60 0.141
398
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.141
399
PST092 Posttransplant Acute Limbic Encephalitis 29 0.141
400
CLF001 Cleft Lip 53 0.141
401
HYP080 Hypogonadism 50 0.141
402
SQM002 Squamous Cell Papilloma 46 0.141
403
FDL002 Food Allergy 51 0.140
404
ALL014 Allergic Encephalomyelitis 38 0.140
405
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.140
406
P MYP006 Myopia 55 0.140
407
MTB004 Metabolic Acidosis 50 0.140
408
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.140
409
c PRS136 Prostate Cancer, Hereditary, 6 33 0.140
410
GST092 Gastroesophageal Reflux 67 0.140
411
MST005 Mastitis 53 0.140
412
HMP009 Haemophilus Influenzae 43 0.140
413
c PRS130 Prostate Cancer, Hereditary, 8 32 0.140
414
PLC008 Placenta Disease 50 0.140
415
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.140
416
HYP060 Hyperinsulinism 54 0.140
417
P DDN001 Duodenal Ulcer 52 0.139
418
c HMP029 Hemophilia a 67 0.139
419
P TRT010 Teratoma 52 0.139
420
INT007 Intermediate Coronary Syndrome 55 0.139
421
c FNC043 Fanconi Anemia, Complementation Group E 62 0.139
422
P HYP058 Hypervitaminosis a 48 0.139
423
P BNG032 Benign Mesothelioma 46 0.139
424
P CHL066 Cholangitis 51 0.139
425
P MYC008 Myocarditis 59 0.138
426
P OPN001 Open-Angle Glaucoma 49 0.137
427
P ART023 Arthropathy 62 0.137
428
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.137
429
ORL011 Oral Cancer 60 0.137
430
c PRD040 Periodontitis, Chronic 53 0.137
431
BRN002 Bronchiolitis 59 0.136
432
CRP001 Carpal Tunnel Syndrome 67 0.136
433
CLR108 Colorectal Adenoma 64 0.136
434
P HMN010 Hemangioma 61 0.136
435
c LKM063 Leukemia, Chronic Myeloid 72 0.136
436
SYN036 Syncope 45 0.135
437
AMN001 Amenorrhea 54 0.135
438
OST003 Osteonecrosis 61 0.135
439
SPS057 Spasticity 45 0.135
440
CRD132 Cardiac Conduction Defect 58 0.135
441
KRT019 Keratitis, Hereditary 65 0.135
442
GT001 Gout 64 0.134
443
END040 Endogenous Depression 55 0.134
444
P ESP024 Esophagitis 62 0.134
445
NRT001 Neurotic Disorder 53 0.133
446
CHC001 Chickenpox 60 0.133
447
P MVM001 Movement Disease 63 0.133
448
P RRT020 Rare Tumor 41 0.133
449
OBS002 Obsessive-Compulsive Disorder 68 0.133
450
P HYP061 Hypertrophic Cardiomyopathy 70 0.133
451
GNG013 Gingivitis 59 0.133
452
P KDN017 Kidney Cancer 60 0.133
453
APP008 Appendicitis 61 0.133
454
CRH005 Crohn's Colitis 53 0.132
455
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.132
456
DBT010 Diabetic Neuropathy 54 0.132
457
SCH014 Schistosomiasis 57 0.131
458
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.131
459
TQP001 Taqi Polymorphism 32 0.131
460
CNN005 Connective Tissue Disease 68 0.130
461
P PHC003 Pheochromocytoma 71 0.130
462
P MLN007 Male Infertility 55 0.130
463
HRP004 Herpes Zoster 60 0.130
464
INF034 Infective Endocarditis 53 0.130
465
NRT004 Neuritis 52 0.130
466
P NSP012 Nasopharyngeal Carcinoma 66 0.130
467
BRC012 Brucellosis 64 0.130
468
CHL067 Cholecystitis 57 0.129
469
c BTT014 Beta-Thalassemia 74 0.129
470
P ANT006 Antiphospholipid Syndrome 55 0.129
471
P ASP006 Aspergillosis 69 0.129
472
PST028 Post-Traumatic Stress Disorder 58 0.129
473
INS024 Insulin-Like Growth Factor I 79 0.128
474
c FML001 Familial Atrial Fibrillation 65 0.128
475
P SNS001 Sensorineural Hearing Loss 60 0.128
476
DSS009 Disseminated Intravascular Coagulation 57 0.128
477
c EXD008 Exudative Vitreoretinopathy 1 71 0.128
478
BLR008 Bilirubin Metabolic Disorder 57 0.127
479
ALL006 Allergic Asthma 56 0.127
480
ACT084 Acute Stress Disorder 47 0.127
481
PRP016 Paraplegia 52 0.127
482
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.127
483
P CND004 Candidiasis 58 0.127
484
CLC006 Calcinosis 48 0.126
485
c MNN043 Meningioma, Familial 74 0.126
486
RNL011 Renal Osteodystrophy 50 0.126
487
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.126
488
P LCH002 Lichen Planus 53 0.126
489
ART074 Aortic Dissection 52 0.126
490
PST021 Postpartum Depression 50 0.126
491
CHL065 Cholangiocarcinoma 68 0.126
492
LNG031 Lung Benign Neoplasm 51 0.126
493
OVR094 Ovarian Epithelial Cancer 38 0.125
494
INT079 Intrahepatic Cholangiocarcinoma 51 0.125
495
STT001 Status Epilepticus 60 0.125
496
P MCR010 Microcephaly 59 0.125
497
ADR040 Adrenal Gland Pheochromocytoma 46 0.125
498
P ATR005 Atrophic Gastritis 50 0.125
499
PNC129 Pancreatic Adenocarcinoma 68 0.125
500
SCK003 Sickle Cell Anemia 74 0.125
502
P INT070 Intestinal Obstruction 58 0.125
503
PLM010 Pulmonary Edema 54 0.124
504
P OPT006 Optic Nerve Disease 60 0.124
505
P CNJ013 Conjunctivitis 65 0.124
506
GST050 Gastrointestinal System Disease 56 0.124
507
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.124
508
TLN003 Telangiectasis 52 0.123
509
ILS001 Ileus 51 0.123
510
PRN019 Perinatal Necrotizing Enterocolitis 59 0.123
511
TRN018 Transitional Cell Carcinoma 56 0.123
512
ENT004 Enthesopathy 49 0.123
513
VCC001 Vaccinia 49 0.123
514
P HNT016 Huntington Disease 72 0.123
515
PRP080 Peripheral Artery Disease 53 0.122
516
c INF071 Inflammatory Bowel Disease 1 67 0.122
517
AVN001 Avian Influenza 59 0.122
518
P FBR017 Fibrosarcoma 56 0.122
519
ING001 Inguinal Hernia 60 0.122
520
GST019 Gastrointestinal Stromal Tumor 78 0.122
521
P HMC002 Homocystinuria 53 0.122
522
GST023 Gastric Ulcer 53 0.122
523
SFT003 Soft Tissue Sarcoma 56 0.122
524
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.121
525
MNN042 Meningioma, Radiation-Induced 62 0.121
526
SPN021 Spinal Meningioma 50 0.121
527
SCR001 Secretory Meningioma 41 0.121
528
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.121
529
HYD002 Hydronephrosis 60 0.121
530
NPH003 Nephrocalcinosis 51 0.121
531
MYL005 Myelofibrosis 70 0.121
532
c PCH010 Pachyonychia Congenita 3 44 0.121
533
P BRB001 Beriberi 46 0.120
534
P MYS005 Myositis 56 0.120
535
PSR001 Psoriatic Arthritis 61 0.120
536
P AST007 Astrocytoma 51 0.120
537
P CYS018 Cystitis 59 0.120
538
c GLL024 Gallbladder Disease 1 53 0.119
539
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.119
540
LYM027 Lymphopenia 58 0.119
541
KPS004 Kaposi Sarcoma 75 0.119
542
INT075 Intracranial Hypertension 53 0.119
543
APH002 Aphasia 57 0.119
544
P PYL005 Pyelonephritis 56 0.119
545
c ACT135 Acute Graft Versus Host Disease 52 0.119
546
P HMR003 Hemorrhagic Disease 53 0.118
547
ACT119 Acute Promyelocytic Leukemia 63 0.118
548
P MYS003 Myasthenia Gravis 68 0.118
549
SXL003 Sexual Disorder 47 0.118
550
MMM001 Mammary Paget's Disease 53 0.118
551
c JVN010 Juvenile Rheumatoid Arthritis 64 0.117
552
CRN030 Coronary Stenosis 50 0.117
553
VSC002 Vascular Dementia 57 0.117
554
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.117
555
DMY004 Demyelinating Disease 52 0.116
556
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.116
557
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.116
558
P ALP009 Alopecia Areata 60 0.116
559
P RTN016 Retinal Degeneration 53 0.115
560
P ART005 Arteriovenous Malformation 65 0.115
561
PPL052 Papillomatosis, Confluent and Reticulated 33 0.115
562
CHR066 Chronic Fatigue Syndrome 61 0.115
563
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.115
564
c DRR009 Diarrhea 6 46 0.115
565
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.115
566
PRS063 Paresthesia 41 0.115
567
c GLC092 Glaucoma, Primary Open Angle 62 0.115
568
P RBL001 Rubella 59 0.114
569
HYP014 Hyperuricemia 52 0.114
570
P LMY004 Leiomyosarcoma 63 0.114
571
P RHB003 Rhabdomyosarcoma 63 0.114
572
P SHR001 Short Bowel Syndrome 53 0.114
573
P LCT001 Lactic Acidosis 51 0.114
574
CHG001 Chagas Disease 66 0.113
575
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.113
576
P ADL010 Adult Respiratory Distress Syndrome 65 0.113
577
PTH003 Pathologic Nystagmus 52 0.113
578
c GRV008 Graves Disease 1 56 0.113
579
P PLY018 Polycythemia 56 0.112
580
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.112
581
CRV045 Cervical Intraepithelial Neoplasia 39 0.112
582
VRL011 Viral Infectious Disease 61 0.112
583
PLC002 Plica Syndrome 36 0.112
584
c MCR129 Microvascular Complications of Diabetes 1 66 0.112
585
P HYP726 Hypercalcemia, Infantile, 1 58 0.112
586
P FLL037 Follicular Lymphoma 67 0.112
587
MSC157 Muscular Dystrophy, Duchenne Type 72 0.112
588
PHN003 Phenylketonuria 75 0.112
589
P THR015 Thrombophilia 51 0.112
590
SYN007 Synovitis 54 0.112
591
HMP001 Hemopericardium 48 0.111
592
P OBS001 Obstructive Jaundice 50 0.111
593
PRT029 Parathyroid Adenoma 50 0.111
594
TRD006 Tardive Dyskinesia 54 0.111
595
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.111
596
RTN017 Retinal Detachment 61 0.111
597
THY030 Thyroid Gland Disease 52 0.111
598
ORL015 Oral Squamous Cell Carcinoma 43 0.110
599
P BRN022 Bronchiectasis 59 0.110
600
TYP007 Typhoid Fever 63 0.110
601
CLL003 Cellulitis 54 0.110
602
PRM020 Premenstrual Tension 40 0.109
603
KHL003 Kohlschutter-Tonz Syndrome 65 0.109
604
HMP005 Hemiplegia 55 0.109
605
ACR007 Acromegaly 71 0.109
607
P ATX030 Ataxia-Telangiectasia 82 0.109
608
IDP070 Idiopathic Scoliosis 42 0.109
609
INT002 Intermittent Claudication 61 0.109
610
P VNT002 Ventricular Septal Defect 60 0.108
611
HPT004 Hepatic Coma 45 0.108
612
P DRM010 Dermatomyositis 61 0.108
613
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.108
614
LKP003 Leukoplakia 39 0.108
615
c ACT134 Acute Liver Failure 56 0.108
616
DYS015 Dysentery 52 0.108
617
CRT013 Carotid Stenosis 50 0.108
618
P PTN014 Patent Ductus Arteriosus 1 60 0.107
619
LWC001 Low Compliance Bladder 43 0.107
620
VSC003 Visceral Leishmaniasis 55 0.107
621
P APL001 Aplastic Anemia 74 0.107
622
c JVN061 Juvenile Arthritis 60 0.107
623
P PMP001 Pemphigus 54 0.107
624
NRN004 Neuroendocrine Tumor 55 0.107
625
BRR014 Barrett Esophagus 65 0.107
626
APN008 Apnea, Obstructive Sleep 64 0.107
627
CHL004 Cholelithiasis 49 0.107
628
BNN003 Bone Inflammation Disease 48 0.107
629
P SPP010 Suppressor of Tumorigenicity 3 51 0.107
630
P DNG005 Dengue Virus 59 0.106
631
CRB004 Cerebral Artery Occlusion 45 0.106
632
P PRC012 Pericardial Effusion 51 0.106
633
CLF004 Cleft Lip/palate 54 0.106
634
P INT068 Intestinal Disease 53 0.106
635
MCL006 Macular Retinal Edema 55 0.106
636
P ICH004 Ichthyosis 54 0.106
637
c HMC039 Hemochromatosis, Type 1 74 0.106
638
GST040 Gastric Adenocarcinoma 70 0.106
639
c ATM011 Autoimmune Hepatitis 63 0.106
640
INT066 Interstitial Lung Disease 60 0.106
641
VLV047 Volvulus of Midgut 49 0.106
642
P PRP029 Porphyria 62 0.106
643
NWC001 Newcastle Disease 45 0.106
644
BRT054 Brittle Bone Disorder 72 0.105
645
HPT019 Hepatic Encephalopathy 60 0.105
646
BRN028 Brain Cancer 74 0.105
647
P TXP001 Toxoplasmosis 60 0.105
648
c FML021 Familial Hypercholesterolemia 66 0.105
649
BLR001 Biliary Atresia 50 0.105
650
CRD137 Cardiogenic Shock 47 0.105
651
MYF001 Myofibroma 45 0.105
652
RBS001 Rabies 58 0.104
653
SNS003 Sensory Peripheral Neuropathy 54 0.104
654
HSH003 Hashimoto Thyroiditis 62 0.104
655
c MTR002 Mitral Valve Insufficiency 48 0.104
656
P PTS002 Ptosis 53 0.104
657
MTH009 Mouth Disease 56 0.104
658
HYP081 Hypolipoproteinemia 51 0.104
659
P STR020 Strabismus 55 0.104
660
BCT002 Bacterial Vaginosis 53 0.104
661
MCH006 Mechanical Strabismus 42 0.104
662
FSC004 Fasciitis 50 0.104
663
ATR057 Atrioventricular Block 55 0.103
664
ECT026 Ectopic Pregnancy 50 0.103
665
P THY023 Thymoma 65 0.103
666
P RTN018 Retinal Disease 53 0.103
667
ALL010 Allergic Contact Dermatitis 56 0.103
668
c THY107 Thymoma, Familial 52 0.103
669
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.103
670
P MTH008 Methylmalonic Acidemia 50 0.103
671
P MMP001 Mumps 58 0.103
672
P SML001 Small Cell Carcinoma 52 0.102
673
AMN003 Amnestic Disorder 54 0.102
674
ATN005 Autonomic Dysfunction 46 0.102
675
BLL006 Bullous Pemphigoid 62 0.102
676
c PSR023 Psoriasis 1 52 0.102
677
SCH012 Schizoaffective Disorder 50 0.102
678
P TBR001 Tuberous Sclerosis 70 0.102
679
CHR074 Choriocarcinoma 47 0.102
680
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.102
681
c PSR017 Psoriasis 2 53 0.102
682
P CMP008 Compartment Syndrome 49 0.102
683
CLN015 Colon Adenocarcinoma 65 0.102
684
MSC007 Muscle Hypertrophy 64 0.102
685
HYP043 Hyperandrogenism 48 0.102
686
PRT038 Protein-Energy Malnutrition 54 0.102
687
P EPD016 Epidermolysis Bullosa 53 0.101
688
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.101
689
LRN003 Learning Disability 49 0.101
690
PLS009 Plasma Cell Neoplasm 51 0.101
691
P MYC033 Myoclonus 46 0.101
692
CMP010 Complex Regional Pain Syndrome 58 0.101
693
P DBT005 Diabetes Insipidus 55 0.100
694
P PLV020 Pelvic Organ Prolapse 57 0.100
695
P NRV007 Nervous System Disease 66 0.100
696
BRK010 Burkitt Lymphoma 67 0.100
697
MYC006 Mycosis Fungoides 66 0.100
698
CRD223 Cardiac Arrhythmia 60 0.100
699
TBC004 Tobacco Addiction 64 0.099
700
P LYM033 Lymphoproliferative Syndrome 59 0.099
701
P MTR003 Mitral Valve Stenosis 50 0.099
702
P MTR014 Motor Neuron Disease 65 0.099
703
c SVR005 Severe Pre-Eclampsia 50 0.099
704
LMB062 Limb Ischemia 55 0.099
705
PRC013 Pericarditis 54 0.099
706
c PSR028 Psoriasis 7 42 0.099
707
c PSR032 Psoriasis 11 47 0.099
708
c PSR018 Psoriasis 13 41 0.099
709
P PNC025 Panic Disorder 53 0.099
710
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.099
711
HRT012 Heart Valve Disease 53 0.099
712
PHR003 Pharyngitis 57 0.099
713
P PLY014 Polycystic Kidney Disease 62 0.099
714
IGG001 Iga Glomerulonephritis 48 0.098
715
49X006 49, Xxxxy Syndrome 41 0.098
716
NRF007 Neurofibroma 64 0.098
717
PRT058 Pure Autonomic Failure 59 0.098
718
FCL012 Facial Paralysis 46 0.098
719
P LYN001 Lynch Syndrome 77 0.098
720
c HYP057 Hypervitaminosis D 42 0.098
721
KRN002 Kearns-Sayre Syndrome 63 0.098
722
P RST001 Restless Legs Syndrome 54 0.098
723
EXP004 Exophthalmos 52 0.098
724
HST010 Histiocytosis 48 0.098
725
DGN001 Degenerative Disc Disease 48 0.098
726
CYN002 Cyanosis, Transient Neonatal 45 0.097
727
GNR004 Generalized Anxiety Disorder 56 0.097
728
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.097
729
CRD001 Cardiac Tamponade 47 0.097
730
MCR017 Macrocytic Anemia 44 0.097
731
c MCR112 Microvascular Complications of Diabetes 2 41 0.097
732
PLG002 Plague 63 0.097
733
LYM040 Lymphoblastic Lymphoma 54 0.096
734
c MLG068 Malignant Glioma 46 0.096
735
NRM005 Neuromuscular Disease 64 0.096
736
P SJG008 Sjogren Syndrome 61 0.096
737
c HRD202 Hereditary Lymphedema I 50 0.096
738
AST006 Astigmatism 47 0.096
739
P OPT009 Optic Neuritis 57 0.096
740
THR004 Thrombocytosis 51 0.096
741
LMY014 Leiomyoma, Uterine 56 0.096
742
DCB001 Decubitus Ulcer 61 0.095
743
RFR003 Refractive Error 43 0.095
744
P ANG015 Angioedema 57 0.095
745
P CHN012 Chondrosarcoma 56 0.095
746
GRN017 Granulocytopenia 44 0.095
747
P CHR071 Charcot-Marie-Tooth Disease 65 0.095
748
c WLM018 Wilms Tumor 5 61 0.095
749
RHM001 Rheumatic Fever 60 0.095
750
P ART018 Aortic Valve Insufficiency 49 0.095
751
BRS051 Breast Disease 58 0.095
752
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.095
753
BRN004 Brain Edema 56 0.095
754
CYT008 Cytomegalovirus Infection 57 0.095
755
c LKM005 Leukemia, T-Cell, Chronic 34 0.094
756
KRT006 Keratoconjunctivitis 53 0.094
757
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.094
758
c CHL119 Cholangitis, Primary Sclerosing 57 0.094
759
AZS001 Azoospermia 50 0.094
760
P FML011 Familial Adenomatous Polyposis 72 0.094
761
P GLL022 Guillain-Barre Syndrome 59 0.094
762
DWR001 Dwarfism 44 0.094
763
P SCL057 Scoliosis, Isolated 1 41 0.094
764
ABT001 Abetalipoproteinemia 69 0.094
765
c DPH024 Diaphragmatic Hernia, Congenital 63 0.094
766
P SCL009 Sclerosing Cholangitis 48 0.094
767
CMR002 Coumarin Resistance 56 0.094
768
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.093
769
c INH020 Inherited Metabolic Disorder 47 0.093
770
CHR073 Choreatic Disease 52 0.093
771
FCT007 Factor Vii Deficiency 67 0.093
772
APH001 Aphthous Stomatitis 57 0.093
773
P PTT006 Pituitary Adenoma 55 0.093
774
SPN027 Spinal Stenosis 59 0.093
775
ATM052 Autoimmune Disease 1 37 0.093
776
NWB001 Newborn Respiratory Distress Syndrome 58 0.093
777
PLY001 Polycythemia Vera 69 0.093
778
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.092
779
AVD001 Avoidant Personality Disorder 51 0.092
780
P GND004 Gonadal Dysgenesis 48 0.092
781
SPT004 Septic Arthritis 58 0.092
782
QDR001 Quadriplegia 48 0.092
783
PRS047 Prostatitis 56 0.092
784
P LPS002 Liposarcoma 65 0.092
785
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.092
786
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.092
787
c ART101 Aortic Valve Disease 2 65 0.092
788
PLY150 Polykaryocytosis Inducer 31 0.092
789
P KRT007 Keratoconus 50 0.092
790
c DNG003 Dengue Disease 59 0.092
791
P BRS044 Breast Adenocarcinoma 59 0.092
792
KWS002 Kawasaki Disease 65 0.092
793
FBR054 Fibroma 44 0.092
794
P TCD001 Tic Disorder 53 0.091
795
MYL031 Myeloproliferative Neoplasm 66 0.091
796
P PLL002 Pellagra 46 0.091
797
PLR007 Pleural Empyema 50 0.091
798
GRW007 Growth Hormone Deficiency 46 0.091
799
RDC002 Radiculopathy 50 0.091
800
P MJR007 Major Affective Disorder 1 43 0.091
801
P TMP001 Temporal Lobe Epilepsy 50 0.091
802
RDN001 Reading Disorder 40 0.090
803
P FRN006 Frontotemporal Dementia 68 0.090
804
P GLM040 Glioma Susceptibility 1 81 0.090
805
P HML001 Hemolytic-Uremic Syndrome 53 0.090
806
MNT001 Mantle Cell Lymphoma 69 0.090
807
RSC001 Rosacea 54 0.090
808
RYN005 Raynaud Phenomenon 47 0.090
809
ERY003 Erythema Multiforme 58 0.090
810
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.090
811
HYP068 Hyperostosis 48 0.090
812
PTN001 Patent Foramen Ovale 60 0.089
813
P PLY041 Polymyositis 57 0.089
814
c MST023 Mesothelioma, Malignant 57 0.089
815
c FML035 Familial Hyperlipidemia 55 0.089
816
PPL002 Papillary Carcinoma 47 0.089
817
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.089
818
FND002 Fundus Dystrophy 55 0.089
819
INS001 Insulinoma 60 0.089
820
CHR100 Chronic Ulcer of Skin 55 0.089
821
DCT002 Ductal Carcinoma in Situ 59 0.089
822
AMB002 Amblyopia 49 0.088
823
SPP007 Suppression Amblyopia 39 0.088
824
P MDL005 Medulloblastoma 77 0.088
825
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.088
826
CRB086 Cerebral Aneurysms 40 0.088
827
P FML018 Familial Mediterranean Fever 73 0.088
828
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.087
829
c OVR114 Ovarian Cancer 1 38 0.087
830
P RNL007 Renal Tubular Acidosis 51 0.087
831
THR016 Thrombophlebitis 51 0.087
832
TRG002 Trigeminal Neuralgia 60 0.087
833
P HYP040 Hypospadias 51 0.087
834
TND005 Tendinitis 54 0.087
835
P AVS003 Avascular Necrosis 42 0.087
836
ANG020 Angiosarcoma 64 0.087
837
NRN001 Neuroendocrine Carcinoma 47 0.087
838
HPR003 Heparin-Induced Thrombocytopenia 48 0.087
839
PRM329 Premature Aging 35 0.086
840
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.086
841
ANX004 Anoxia 40 0.086
842
APR001 Apraxia 52 0.086
843
P GCH001 Gaucher's Disease 63 0.086
844
P MLT074 Multiple Endocrine Neoplasia 56 0.086
845
ESP002 Esophageal Varix 51 0.086
846
MYM001 Myoma 54 0.086
847
c BCT007 Bacterial Meningitis 55 0.086
848
c CHR417 Chronic Graft Versus Host Disease 57 0.086
849
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.086
850
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.086
851
DRY001 Dry Eye Syndrome 47 0.085
852
ART002 Arts Syndrome 64 0.085
853
P OVR046 Ovarian Cyst 47 0.085
854
P END047 Endophthalmitis 53 0.085
855
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.085
856
SMN007 Seminoma 43 0.085
857
ORL013 Oral Lichen Planus 45 0.085
858
NSS002 Neisseria Meningitidis Infection 47 0.085
859
PRP036 Peripheral T-Cell Lymphoma 53 0.085
860
P FCL005 Focal Segmental Glomerulosclerosis 57 0.085
861
GLS018 Glass Syndrome 57 0.085
862
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.085
863
MRF001 Marfan Syndrome 77 0.085
864
c ART115 Aortic Valve Disease 1 75 0.085
865
LYM017 Lyme Disease 64 0.085
866
ATN004 Autonomic Neuropathy 45 0.084
867
ERY051 Erythroleukemia, Familial 56 0.084
868
ACT058 Active Peptic Ulcer Disease 55 0.084
869
RTN020 Retinal Vascular Disease 46 0.084
870
HMG005 Hemoglobinopathy 56 0.084
871
P GLL018 Gallbladder Cancer 57 0.084
872
c MLG084 Malignant Fibrous Histiocytoma 63 0.084
873
P ANP001 Anaplastic Large Cell Lymphoma 58 0.084
874
P PSD015 Pseudohypoparathyroidism 56 0.084
875
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.084
876
MCR013 Microphthalmia 57 0.084
877
c ALP101 Alpha-Thalassemia 62 0.084
878
TNS005 Tonsillitis 57 0.084
879
P RTN022 Retinal Vein Occlusion 53 0.084
880
P CTN015 Cutaneous T Cell Lymphoma 49 0.084
881
TRP009 Triple X Syndrome 42 0.083
882
c PLY105 Polycystic Ovary Syndrome 1 38 0.083
883
LYM021 Lymphadenitis 57 0.083
884
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.083
885
CLR109 Colorectal Adenocarcinoma 51 0.083
886
c FNC027 Fanconi Anemia, Complementation Group a 81 0.082
887
P ACT008 Actinic Keratosis 53 0.082
888
PLS007 Plasmodium Falciparum Malaria 52 0.082
889
THR123 Thrombotic Microangiopathy 36 0.082
890
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.082
891
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.082
892
c INH030 Inherited Retinal Disorder 51 0.082
893
c NRF024 Neurofibromatosis, Type I 77 0.081
894
MYL001 Myelitis 51 0.081
895
PRD004 Prediabetes Syndrome 47 0.081
896
GRM010 Germ Cells Tumors 34 0.081
897
SDD001 Sudden Infant Death Syndrome 61 0.081
898
HMT002 Hematologic Cancer 62 0.081
899
WST001 West Syndrome 61 0.081
900
TST014 Testicular Cancer 46 0.081
901
MNN009 Meningoencephalitis 49 0.081
902
OST016 Osteochondrosis 53 0.081
903
P TMP003 Temporal Arteritis 68 0.081
904
P FRG001 Fragile X Syndrome 70 0.081
905
TTH006 Tooth Disease 46 0.081
906
P OST001 Osteopetrosis 70 0.081
907
CTN007 Cutaneous Leishmaniasis 62 0.081
908
EWN003 Ewing Sarcoma 69 0.081
909
c CHR064 Chronic Monocytic Leukemia 33 0.081
910
CRY005 Cryptococcosis 58 0.080
911
c ACT004 Acute Diarrhea 39 0.080
912
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.080
913
P AGM001 Agammaglobulinemia 65 0.080
914
RFR010 Refractory Anemia 48 0.080
915
EMB004 Embryonal Carcinoma 56 0.080
916
CRC021 Carcinosarcoma 62 0.080
917
P VNW001 Von Willebrand's Disease 65 0.080
918
LNG108 Langerhans Cell Histiocytosis 58 0.080
919
P NRC002 Narcolepsy 52 0.080
920
GRD001 Giardiasis 45 0.080
921
FNG017 Fungal Infectious Disease 53 0.080
922
PTT037 Pituitary Tumors 44 0.080
923
P TTR001 Tetralogy of Fallot 70 0.080
924
PMP006 Pemphigus Vulgaris, Familial 57 0.080
925
PYD002 Pyoderma 50 0.080
926
OVR029 Ovarian Hyperstimulation Syndrome 64 0.080
927
P EHL001 Ehlers-Danlos Syndrome 58 0.080
928
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.080
929
HYP020 Hyperprolactinemia 64 0.080
930
PLC007 Placental Abruption 48 0.080
931
PLL012 Pollen Allergy 46 0.079
932
PPL049 Papillon-Lefevre Syndrome 65 0.079
933
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.079
934
ADN011 Adenoid Cystic Carcinoma 70 0.079
935
c TBR025 Tuberous Sclerosis 1 77 0.079
936
P OCL013 Oculodentodigital Dysplasia 69 0.079
937
P MTC069 Mitochondrial Disorders 56 0.079
938
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.079
939
P ORT004 Orthostatic Intolerance 62 0.079
940
DVR002 Diverticulitis 43 0.079
941
PNN001 Panniculitis 51 0.079
942
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.079
943
P PRC031 Preeclampsia/eclampsia 1 38 0.079
944
ANV001 Anovulation 47 0.079
945
SPS019 Spastic Paraparesis 38 0.079
946
P CHR012 Chronic Granulomatous Disease 67 0.079
947
NRM001 Neuromyelitis Optica 61 0.079
948
c HPT007 Hepatitis E 53 0.079
949
RHM028 Rheumatic Heart Disease 53 0.079
950
RST023 Resting Heart Rate, Variation in 41 0.079
951
P VSC018 Visceral Steatosis 33 0.079
952
YLL002 Yellow Fever 61 0.079
953
SCN001 Secondary Hyperparathyroidism of Renal Origin 27 0.078
954
MCR004 Macroglobulinemia 49 0.078
955
BLM002 Bulimia Nervosa 57 0.078
956
P INT143 Interstitial Cystitis 61 0.078
957
P CRN037 Craniosynostosis 68 0.078
958
GLS007 Glossitis 47 0.078
959
CLR030 Clear Cell Renal Cell Carcinoma 53 0.078
960
P HYP730 Hypogonadotropic Hypogonadism 52 0.078
961
VRC001 Varicocele 49 0.078
962
RTR008 Root Resorption 45 0.078
963
ACN002 Acanthosis Nigricans 60 0.078
964
THY111 Thyroid Carcinoma, Familial Medullary 67 0.078
965
P MYT002 Myotonic Dystrophy 49 0.078
966
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.077
967
P PRC019 Precocious Puberty 46 0.077
968
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.077
969
P HYP083 Hypopituitarism 53 0.077
970
KRT008 Keratopathy 47 0.077
971
P MMB011 Membranous Nephropathy 50 0.077
972
LPT001 Leptospirosis 66 0.077
973
FLR002 Filariasis 55 0.077
974
URT010 Ureteral Obstruction 45 0.077
975
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.077
976
OCL006 Ocular Hypertension 53 0.077
977
P FBR003 Fibrous Histiocytoma 44 0.077
978
VGN019 Vaginal Discharge 46 0.077
979
P VNS003 Venous Insufficiency 55 0.077
980
DRM011 Dermatophytosis 52 0.077
981
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.077
982
BLD131 Bladder Urothelial Carcinoma 62 0.077
983
SCH003 Schizophreniform Disorder 56 0.076
984
BRD004 Borderline Personality Disorder 53 0.076
985
HST011 Histoplasmosis 55 0.076
986
RTC005 Reticulosarcoma 47 0.076
987
ADR007 Adrenoleukodystrophy 75 0.076
988
IRD001 Iridocyclitis 53 0.076
989
CMM004 Common Variable Immunodeficiency 68 0.076
990
c CHR682 Chronic Bilirubin Encephalopathy 39 0.076
991
MYL020 Myelomeningocele 51 0.076
992
PRT018 Portal Vein Thrombosis 50 0.076
993
THY125 Thyroid Gland Medullary Carcinoma 50 0.076
994
WLL001 Williams-Beuren Syndrome 60 0.076
995
SPS003 Spastic Diplegia 51 0.076
996
P MLG074 Malignant Mesenchymoma 40 0.076
997
ANN002 Anencephaly 56 0.076
998
c DRM054 Dermatitis, Atopic, 2 44 0.076
999
c MLG079 Malignant Pleural Mesothelioma 42 0.076
1000
P LKD001 Leukodystrophy 59 0.076
1001
MLT006 Multidrug-Resistant Tuberculosis 48 0.076
1002
GST020 Gastric Antral Vascular Ectasia 41 0.076
1003
CHR005 Chorioamnionitis 51 0.076
1004
P VTM026 Vitamin D Hydroxylation-Deficient Rickets, Type 1a 38 0.075
1005
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.075
1006
c HYP272 Hypercholesterolemia, Familial, 3 44 0.075
1007
CYT018 Cytochrome P450 2d6 Variant 27 0.075
1008
EXS001 Exostosis 46 0.075
1009
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.075
1010
PNM010 Pneumothorax, Primary Spontaneous 60 0.075
1011
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.075
1012
INT303 Intracranial Hypertension, Idiopathic 57 0.075
1013
ASP007 Aspiration Pneumonia 48 0.075
1014
EXC002 Exocrine Pancreatic Insufficiency 42 0.075
1015
c WLM013 Wilms Tumor 1 65 0.075
1016
P FTL001 Fetal Alcohol Syndrome 57 0.075
1017
WRN003 Wernicke Encephalopathy 47 0.075
1018
GST010 Gestational Trophoblastic Neoplasm 46 0.075
1019
PFF001 Pfeiffer Syndrome 79 0.075
1020
c MJR003 Major Affective Disorder 6 33 0.074
1021
c MJR006 Major Affective Disorder 5 33 0.074
1022
EPD015 Epidemic Typhus 45 0.074
1023
P SLM003 Salmonellosis 55 0.074
1024
NCR007 Necrotizing Fasciitis 48 0.074
1025
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.074
1026
MCR011 Microinvasive Gastric Cancer 43 0.074
1027
MDS022 Mediastinitis 46 0.074
1028
KLD004 Keloid Disorder 40 0.074
1029
P PSD087 Pseudoxanthoma Elasticum 65 0.074
1030
FBR012 Fabry Disease 72 0.074
1031
MLT157 Multiple System Atrophy 1 70 0.074
1032
ISL099 Isolated Methylmalonic Acidemia 29 0.074
1033
P ANG001 Angelman Syndrome 69 0.074
1034
BCT004 Bacteriuria 49 0.074
1035
HLL004 Hellp Syndrome 54 0.074
1036
CLC001 Calciphylaxis 51 0.074
1037
P BNG030 Benign Ependymoma 60 0.074
1038
P IMR002 Imerslund-Grasbeck Syndrome 1 43 0.074
1039
CRT017 Cartilage Disease 54 0.074
1040
CLL010 Cellular Ependymoma 54 0.074
1041
CYS005 Cysticercosis 53 0.074
1042
WTH001 Withdrawal Disorder 48 0.074
1043
SVR097 Severe Cutaneous Adverse Reaction 69 0.074
1044
HPT022 Hepatoblastoma 56 0.074
1045
ACH005 Achalasia 51 0.074
1046
BSL036 Basal Cell Nevus Syndrome 73 0.074
1047
ORL012 Oral Leukoplakia 39 0.073
1048
INT030 Intracranial Aneurysm 56 0.073
1049
ERY066 Erythema Multiforme Major 30 0.073
1050
FBR019 Fibromatosis 41 0.073
1051
ORL005 Oral Candidiasis 56 0.073
1052
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.073
1053
SPN019 Spondylolisthesis 51 0.073
1054
c PYR010 Peyronie's Disease 50 0.073
1055
MDD018 Middle East Respiratory Syndrome 43 0.073
1056
TBR011 Tuberculous Meningitis 48 0.073
1057
FCL014 Focal Epilepsy 54 0.073
1058
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.073
1059
P ANR048 Aniridia 1 63 0.073
1060
MYF002 Myofascial Pain Syndrome 42 0.073
1061
HND015 Hand Skill, Relative 33 0.073
1062
P HMR005 Hemorrhoid 46 0.073
1063
ARG004 Argyria 27 0.073
1064
P ADL017 Adult T-Cell Leukemia 56 0.073
1065
DBT006 Diabetic Macular Edema 48 0.073
1066
RNL077 Renal Fibrosis 47 0.073
1067
FBR009 Fibrous Dysplasia 48 0.073
1068
STT009 Sutton Disease 2 30 0.072
1069
OST115 Osteonecrosis of the Jaw 40 0.072
1070
P PTY003 Pityriasis Rubra Pilaris 58 0.072
1071
TND004 Tendinopathy 43 0.072
1072
PPL001 Papillary Adenoma 44 0.072
1073
KHN001 Kuhnt-Junius Degeneration 47 0.072
1074
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.072
1075
CHR072 Chordoma 58 0.072
1076
c SYS043 Systemic Lupus Erythematosus 1 38 0.072
1077
HMG002 Hemoglobinuria 50 0.072
1078
P ESS003 Essential Thrombocythemia 68 0.072
1079
ANK001 Ankylosis 51 0.072
1080
SPN020 Spondylosis 46 0.072
1081
P LRY044 Larynx Cancer 55 0.072
1082
CYS009 Cystadenoma 44 0.072
1083
c GCH015 Gaucher Disease, Type I 70 0.072