Search results for Folic acid

1842 hits were found for Folic acid

# Family MCID Name MIFTS Score
1
FLC001 Folic Acid Deficiency Anemia 34 3.912
2
FLT009 Folate Malabsorption, Hereditary 38 3.858
3
P FRG001 Fragile X Syndrome 69 2.821
4
NRL016 Neural Tube Defects 83 0.583
5
DFC004 Deficiency Anemia 77 0.326
6
P LVR013 Liver Disease 71 0.314
7
HMC014 Homocysteinemia 54 0.310
8
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.307
9
P CLR023 Colorectal Cancer 100 0.295
10
P KDN018 Kidney Disease 73 0.282
11
LVR012 Liver Cirrhosis 67 0.261
12
FTT001 Fatty Liver Disease 63 0.254
13
P VSC007 Vascular Disease 65 0.253
14
IRN002 Iron Metabolism Disease 58 0.249
15
P SZR006 Seizure Disorder 59 0.239
16
c PRC016 Pre-Eclampsia 63 0.235
17
VTM002 Vitamin B12 Deficiency 48 0.235
18
CHL068 Cholestasis 61 0.231
19
P NRB010 Neuroblastoma 1 66 0.231
20
P DRR001 Diarrhea 55 0.230
21
P CRN300 Coronary Heart Disease 1 59 0.229
22
48X005 48,xyyy 37 0.228
23
ATH013 Atherosclerosis Susceptibility 68 0.226
24
HYP014 Hyperuricemia 52 0.225
25
VSL002 Visual Epilepsy 58 0.222
26
P CRN018 Coronary Artery Anomaly 67 0.222
27
ISC004 Ischemia 62 0.218
28
P LKM002 Leukemia 69 0.217
29
ACT119 Acute Promyelocytic Leukemia 63 0.215
30
P PSR002 Psoriasis 63 0.214
31
LPD008 Lipid Metabolism Disorder 64 0.213
32
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.213
33
PST011 Pustulosis of Palm and Sole 51 0.212
34
P BRS047 Breast Cancer 99 0.209
35
ART140 Arteries, Anomalies of 60 0.209
36
HLX001 Helix Syndrome 46 0.207
37
CLT003 Colitis 63 0.202
38
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.202
39
c CHR684 Chronic Kidney Disease 68 0.199
40
P GLM045 Glioma 64 0.198
41
ADN018 Adenoma 60 0.197
42
GLL048 Glial Tumor 48 0.196
43
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.195
44
MTB004 Metabolic Acidosis 48 0.195
45
PRN011 Pernicious Anemia 51 0.192
46
P MGL001 Megaloblastic Anemia 54 0.191
47
P NRF023 Neurofibromatosis, Type Ii 77 0.190
48
ANN002 Anencephaly 55 0.188
49
c HYP595 Hypertension, Essential 87 0.187
50
HYP066 Hyperglycemia 63 0.186
51
GST092 Gastroesophageal Reflux 68 0.185
52
P RHM011 Rheumatoid Arthritis 82 0.184
53
P INF037 Inflammatory Bowel Disease 57 0.183
54
BNR002 Bone Resorption Disease 51 0.183
55
ULC004 Ulcerative Colitis 75 0.183
56
OST012 Osteoarthritis 80 0.182
57
ALL026 Allergic Hypersensitivity Disease 65 0.182
58
GT001 Gout 63 0.182
59
P HPT023 Hepatocellular Carcinoma 99 0.181
60
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.181
61
P HRT032 Heart Disease 78 0.181
62
DRM006 Dermatitis 63 0.180
63
P ATS364 Autism 68 0.179
64
CRB039 Cerebrovascular Disease 71 0.177
65
DWN001 Down Syndrome 70 0.177
66
P OVR042 Ovarian Cancer 89 0.175
67
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.175
68
P NRP001 Neuropathy 57 0.174
69
END030 End Stage Renal Failure 60 0.174
70
c HYP836 Hypercholesterolemia, Familial, 1 74 0.173
71
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.173
72
P ENC018 Encephalopathy 64 0.172
73
DPR016 Depression 64 0.172
74
P PRS040 Prostate Cancer 97 0.171
75
P GST044 Gastritis 58 0.170
76
HYP056 Hypoglycemia 68 0.169
77
GLB002 Glioblastoma 74 0.169
78
GLB015 Glioblastoma Multiforme 60 0.169
79
P ADN016 Adenocarcinoma 65 0.168
80
P MYC007 Myocardial Infarction 74 0.168
81
P ART022 Arthritis 71 0.167
82
ATM095 Autoimmune Disease 62 0.165
83
P LNG032 Lung Cancer 99 0.162
84
P OST002 Osteoporosis 79 0.162
85
NTR005 Nutritional Deficiency Disease 61 0.161
86
PRM236 Primary Biliary Cholangitis 57 0.161
87
P DBT009 Diabetes Mellitus 66 0.161
88
STR067 Stroke, Ischemic 82 0.161
89
PPT005 Peptic Ulcer Disease 60 0.160
90
PRT037 Pertussis 66 0.160
91
CLF027 Cleft Palate, Isolated 67 0.159
92
P HYP750 Hypertriglyceridemia, Familial 62 0.159
93
P LYM031 Lymphocytic Leukemia 56 0.158
94
HRW001 Hair Whorl 36 0.156
95
P EPL164 Epilepsy 73 0.155
96
ALC007 Alcohol Dependence 68 0.155
97
c GLL024 Gallbladder Disease 1 53 0.155
98
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.155
99
P NTR004 Neutropenia 64 0.155
100
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.155
101
HYP781 Hypoascorbemia 48 0.155
102
c RHB024 Rhabdomyosarcoma 2 64 0.154
103
PLM001 Pulmonary Tuberculosis 72 0.154
104
P ALZ034 Alzheimer Disease 90 0.153
105
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.151
106
P PRM006 Primary Biliary Cirrhosis 54 0.151
107
MNT002 Mental Depression 60 0.150
108
HMN044 Human Immunodeficiency Virus Type 1 73 0.149
109
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.149
110
c ATS007 Autism Spectrum Disorder 69 0.148
111
CYS001 Cystic Fibrosis 84 0.148
112
HYP060 Hyperinsulinism 55 0.147
113
P PNC035 Pancreatic Cancer 86 0.147
114
c ACT073 Acute Leukemia 59 0.147
115
c ACT071 Acute Kidney Failure 60 0.146
116
P BPL003 Bipolar Disorder 59 0.146
117
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.146
118
c MJR024 Major Affective Disorder 9 42 0.145
119
c MJR022 Major Affective Disorder 8 39 0.145
120
CRV035 Cervical Cancer 77 0.144
121
P HNT016 Huntington Disease 72 0.144
122
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.144
123
HYP266 Hypoxia 58 0.144
124
47X002 47,xyy 49 0.144
125
c ACT210 Acute Respiratory Distress Syndrome 59 0.143
126
c ACT075 Acute Myocardial Infarction 59 0.143
127
CRH001 Crohn's Disease 75 0.142
128
P ESP024 Esophagitis 62 0.140
129
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.139
130
P ECL001 Eclampsia 53 0.139
131
PHN003 Phenylketonuria 73 0.139
132
CYT002 Cytokine Deficiency 46 0.138
133
IRN001 Iron Deficiency Anemia 59 0.138
134
OCL069 Ocular Motor Apraxia 53 0.138
135
NNL006 Non-Alcoholic Steatohepatitis 53 0.138
136
OST159 Osteogenic Sarcoma 67 0.138
137
P BLD134 Bladder Cancer 79 0.138
138
P GST053 Gastric Cancer 85 0.138
139
STM007 Stomatitis 51 0.137
140
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.136
141
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.136
142
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.136
143
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.136
144
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.136
145
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.136
146
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.136
147
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.136
148
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.136
149
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.136
150
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.136
151
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.136
152
c THR092 Thrombophilia Due to Thrombin Defect 74 0.135
153
CLR108 Colorectal Adenoma 64 0.134
154
STT001 Status Epilepticus 61 0.134
155
CNG034 Congestive Heart Failure 69 0.134
156
P HYP086 Hypothyroidism 70 0.134
157
c MCR120 Microvascular Complications of Diabetes 7 48 0.133
158
P INF032 Infertility 60 0.133
159
URM002 Uremia 50 0.132
160
c HPT073 Hepatitis C Virus 74 0.131
161
SKN016 Skin Disease 64 0.131
162
HPT004 Hepatic Coma 42 0.131
163
RCK004 Rickets 70 0.131
164
P ART021 Arteriosclerosis 56 0.131
165
P TRN020 Turner Syndrome 66 0.130
166
c PCH010 Pachyonychia Congenita 3 43 0.130
167
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.130
168
GST023 Gastric Ulcer 53 0.129
169
P DRM053 Dermatitis, Atopic 68 0.129
170
c MCR113 Microvascular Complications of Diabetes 3 55 0.129
171
CHL079 Children's Interstitial Lung Disease 27 0.129
172
c MCR130 Microvascular Complications of Diabetes 6 42 0.128
173
c MCR133 Microvascular Complications of Diabetes 4 42 0.128
174
MCR017 Macrocytic Anemia 41 0.128
175
MYL069 Myeloma, Multiple 85 0.127
176
BND020 Bone Disease 60 0.127
177
P HMC002 Homocystinuria 52 0.126
178
THR024 Thrombosis 58 0.125
179
OVR082 Overgrowth Syndrome 51 0.125
180
CLF001 Cleft Lip 53 0.125
181
SQM006 Squamous Cell Carcinoma 60 0.125
182
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.123
183
P THR014 Thrombocytopenia 67 0.123
184
P SCH015 Schizophrenia 76 0.123
185
c LKM061 Leukemia, Acute Myeloid 84 0.123
186
MDD011 Mood Disorder 62 0.122
187
P PRP019 Peripheral Nervous System Disease 64 0.122
188
c SML038 Small Cell Cancer of the Lung 67 0.122
189
HPT019 Hepatic Encephalopathy 60 0.122
190
c MGR028 Migraine with or Without Aura 1 70 0.121
191
c SYS001 Systemic Lupus Erythematosus 88 0.121
192
BRN071 Brain Injury 51 0.121
193
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.121
194
LNG099 Lung Disease 62 0.121
195
MLR004 Malaria 82 0.121
196
DYS014 Dyspepsia 51 0.120
197
P LYM118 Lymphoma 70 0.120
198
GLC003 Glucose Intolerance 55 0.120
199
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.119
200
P CTR002 Cataract 62 0.119
201
BCT022 Bacterial Infectious Disease 57 0.119
202
INS024 Insulin-Like Growth Factor I 79 0.119
203
P LTR001 Lateral Sclerosis 56 0.119
204
P LKM062 Leukemia, Acute Lymphoblastic 68 0.119
205
CRB004 Cerebral Artery Occlusion 38 0.118
206
P PRD008 Periodontitis 66 0.118
207
P MYP004 Myopathy 63 0.118
208
AGN016 Aging 58 0.118
209
c LRG017 Large Intestine Cancer 53 0.118
210
P HRP006 Herpes Simplex 66 0.118
211
PPL052 Papillomatosis, Confluent and Reticulated 34 0.118
212
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.117
213
P SKN015 Skin Carcinoma 67 0.117
214
P MJR001 Major Depressive Disorder 69 0.117
215
P PLY011 Polycystic Ovary Syndrome 58 0.116
216
P PLY019 Polyneuropathy 55 0.116
217
PRP027 Peripheral Vascular Disease 72 0.115
219
SPP010 Suppressor of Tumorigenicity 3 54 0.115
220
BRR014 Barrett Esophagus 67 0.115
221
MCS002 Mucositis 56 0.115
222
ADR007 Adrenoleukodystrophy 72 0.114
223
SPN186 Spinal Cord Injury 63 0.114
224
c CRV002 Cervix Uteri Carcinoma in Situ 47 0.114
225
CRV045 Cervical Intraepithelial Neoplasia 41 0.114
226
TRM010 Traumatic Brain Injury 54 0.114
227
P HPT021 Hepatitis 69 0.114
228
P MCR115 Microvascular Complications of Diabetes 5 67 0.113
229
KRT002 Keratomalacia 47 0.112
230
RHM027 Rheumatic Disease 56 0.112
231
GST033 Gestational Diabetes 58 0.112
232
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.111
233
MLN008 Melanoma 68 0.111
234
CHL123 Chlamydia 60 0.111
235
SRC014 Sarcoma 67 0.111
236
SPN035 Spindle Cell Sarcoma 57 0.111
237
KRT009 Keratosis 52 0.111
238
P RTN024 Retinoblastoma 74 0.111
239
c VRL010 Viral Hepatitis 56 0.111
240
P LPS004 Lupus Erythematosus 62 0.111
241
c FML008 Familial Retinoblastoma 46 0.111
242
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.110
243
P BCL017 B-Cell Lymphoma 61 0.110
244
HMP009 Haemophilus Influenzae 46 0.110
245
P DMN002 Dementia 68 0.110
246
c INH020 Inherited Metabolic Disorder 51 0.109
247
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.109
248
P HYP076 Hyperthyroidism 55 0.109
249
PLM033 Pulmonary Embolism 60 0.109
250
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.108
251
CLN015 Colon Adenocarcinoma 65 0.108
252
HYP005 Hypokalemia 55 0.108
253
INT007 Intermediate Coronary Syndrome 58 0.108
254
P ALC033 Alcohol Use Disorder 58 0.108
255
P THL005 Thalassemia 62 0.108
256
ESP021 Esophageal Cancer 90 0.107
257
SVR004 Severe Combined Immunodeficiency 74 0.107
258
ANG054 Angina Pectoris 66 0.107
259
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.107
260
c ACT068 Acute Cystitis 63 0.107
261
ADR022 Adrenomyeloneuropathy 39 0.107
262
TRP004 Tropical Sprue 41 0.107
263
P NSP012 Nasopharyngeal Carcinoma 67 0.106
264
c HPT001 Hepatitis C 62 0.106
265
c DWL002 Dowling-Degos Disease 1 59 0.105
266
LYM019 Lymphosarcoma 48 0.105
267
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.105
268
P MNN013 Meningitis 67 0.105
269
P MPL001 Maple Syrup Urine Disease 68 0.105
270
OST003 Osteonecrosis 62 0.105
271
VCC001 Vaccinia 50 0.105
272
PLC008 Placenta Disease 51 0.105
273
ATX019 Ataxia with Vitamin E Deficiency 46 0.105
274
AST005 Asthma 80 0.104
275
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.104
276
DBT010 Diabetic Neuropathy 56 0.104
277
PPL022 Papilloma 56 0.104
278
P CRD132 Cardiac Conduction Defect 61 0.103
279
P MSC005 Muscular Dystrophy 68 0.103
280
P PNC044 Pancreatitis 61 0.102
281
P CNR004 Cone-Rod Dystrophy 2 72 0.102
282
IMM167 Immune Deficiency Disease 79 0.102
283
HLC007 Helicobacter Pylori Infection 61 0.102
284
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.101
285
P EXN002 Exanthem 58 0.101
286
P ENC004 Encephalitis 64 0.101
287
P GLM007 Glomerulonephritis 58 0.101
288
ANX010 Anxiety 75 0.100
289
P ATR011 Atrial Fibrillation 67 0.100
290
P LCT001 Lactic Acidosis 52 0.100
291
SQM002 Squamous Cell Papilloma 49 0.100
292
THY029 Thyroid Carcinoma 62 0.100
293
P PNM007 Pneumonia 71 0.100
294
CNS004 Constipation 59 0.100
295
TTN003 Tetanus 62 0.099
296
P BRS044 Breast Adenocarcinoma 59 0.099
297
MYL009 Myelodysplastic Syndrome 72 0.099
298
ADL002 Adult Syndrome 62 0.099
299
P INF038 Influenza 69 0.098
300
P ALP008 Alopecia 58 0.098
301
c GLY008 Glycogen Storage Disease Ii 68 0.098
302
BRN024 Bronchitis 70 0.098
303
P AST007 Astrocytoma 52 0.098
304
c MLG068 Malignant Glioma 46 0.098
305
ENT004 Enthesopathy 46 0.098
306
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.098
307
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.096
308
c HPT016 Hepatitis B 63 0.095
309
GST050 Gastrointestinal System Disease 57 0.095
310
CHR074 Choriocarcinoma 47 0.095
311
P PRP029 Porphyria 58 0.095
312
ALL014 Allergic Encephalomyelitis 40 0.095
313
LYS012 Lysosomal Acid Lipase Deficiency 63 0.094
314
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.094
315
P CYS018 Cystitis 59 0.094
316
P SCK005 Sickle Cell Disease 53 0.094
317
P GLY013 Glycogen Storage Disease 59 0.094
318
ACQ007 Acquired Immunodeficiency Syndrome 61 0.094
319
P MLN007 Male Infertility 57 0.093
320
c FNC043 Fanconi Anemia, Complementation Group E 64 0.093
321
c ATR087 Atrial Standstill 1 76 0.093
322
P ATR005 Atrophic Gastritis 49 0.093
323
P MSC003 Muscular Atrophy 52 0.093
324
TRN015 Transient Cerebral Ischemia 62 0.092
325
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.092
326
c VSC019 Vesicoureteral Reflux 1 62 0.092
327
HNS001 Hansen's Disease 35 0.092
328
P HDC001 Headache 59 0.091
329
P LPR021 Leprosy 3 67 0.091
330
CHL004 Cholelithiasis 50 0.091
331
P INS002 in Situ Carcinoma 55 0.091
332
NRL018 Neural Tube Defects, Folate-Sensitive 50 0.091
333
TXC005 Toxic Shock Syndrome 63 0.090
334
P MYC084 Mycobacterium Tuberculosis 1 69 0.090
335
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.090
336
P TRM003 Tremor 55 0.089
337
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.089
338
GST045 Gastroenteritis 60 0.089
339
P BNG032 Benign Mesothelioma 47 0.088
340
PRP030 Purpura 56 0.088
341
PSY004 Psychotic Disorder 68 0.088
342
SCK003 Sickle Cell Anemia 74 0.088
343
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.088
344
P RCT021 Rectum Cancer 54 0.088
345
STT004 Steatorrhea 39 0.088
346
PLC007 Placental Abruption 47 0.088
347
DPH001 Diphtheria 61 0.087
348
P CRD119 Cardiac Arrest 71 0.087
349
P ENC008 Encephalocele 47 0.087
350
P PLM037 Pulmonary Hypertension 69 0.087
351
CHL065 Cholangiocarcinoma 68 0.087
352
EXN003 Exencephaly 32 0.087
353
P URT039 Urticaria 61 0.086
354
P LNG064 Lung Cancer Susceptibility 3 79 0.086
355
c PRS136 Prostate Cancer, Hereditary, 6 34 0.086
356
c PRS130 Prostate Cancer, Hereditary, 8 33 0.086
357
P HYD006 Hydrocephalus 68 0.086
358
c CNG216 Congenital Hydrocephalus 55 0.086
359
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.086
360
P HML002 Hemolytic Anemia 64 0.085
361
INT079 Intrahepatic Cholangiocarcinoma 54 0.085
362
P PRK057 Parkinson Disease, Late-Onset 77 0.085
363
P HYP098 Hypereosinophilic Syndrome 67 0.085
364
IGR001 Ige Responsiveness, Atopic 61 0.085
365
c BSL007 Basal Cell Carcinoma 68 0.085
366
EYD002 Eye Disease 59 0.085
367
P RHN004 Rhinitis 59 0.085
368
c PRM038 Primary Agammaglobulinemia 45 0.085
369
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.084
370
P HYP265 Hypotonia 43 0.084
371
LSH001 Leishmaniasis 64 0.084
372
RNL077 Renal Fibrosis 49 0.084
373
P KLZ004 Kala-Azar 1 43 0.084
374
HMS001 Hemosiderosis 54 0.084
375
PLM031 Poliomyelitis 58 0.083
376
P CLC063 Celiac Disease 1 66 0.083
377
P INT068 Intestinal Disease 56 0.083
378
P ART023 Arthropathy 61 0.083
379
GRN017 Granulocytopenia 46 0.083
380
BRN004 Brain Edema 57 0.083
381
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.083
382
c LKM071 Leukemia, Chronic Lymphocytic 81 0.083
383
MYL020 Myelomeningocele 51 0.083
384
LNG031 Lung Benign Neoplasm 52 0.082
385
RSC001 Rosacea 55 0.082
386
BRN028 Brain Cancer 75 0.082
387
ZLL002 Zollinger-Ellison Syndrome 54 0.082
388
ENT011 Enterocolitis 51 0.082
389
c MCR129 Microvascular Complications of Diabetes 1 67 0.082
390
P PYL005 Pyelonephritis 58 0.082
391
PNG002 Pain Agnosia 52 0.081
392
c HPT003 Hepatitis a 60 0.081
393
HYP081 Hypolipoproteinemia 51 0.081
394
BLR008 Bilirubin Metabolic Disorder 58 0.081
395
P KDN017 Kidney Cancer 60 0.080
396
IRR002 Irritable Bowel Syndrome 65 0.080
397
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.080
398
P GRF003 Graft-Versus-Host Disease 71 0.080
399
PRP080 Peripheral Artery Disease 51 0.080
400
IMP005 Impotence 53 0.080
401
c SVR005 Severe Pre-Eclampsia 50 0.080
402
INS001 Insulinoma 60 0.079
403
VSC002 Vascular Dementia 57 0.079
404
END040 Endogenous Depression 55 0.079
405
ALL003 Allergic Rhinitis 69 0.079
406
P PLM036 Pulmonary Fibrosis 66 0.079
407
IDP011 Idiopathic Interstitial Pneumonia 65 0.079
408
SBC016 Subacute Delirium 43 0.079
409
P RRH023 Rare Hereditary Hemochromatosis 41 0.079
410
c HMC039 Hemochromatosis, Type 1 73 0.079
411
PRT013 Portal Hypertension 61 0.078
412
P MTH008 Methylmalonic Acidemia 50 0.078
413
DSS008 Disease of Mental Health 66 0.078
414
P END044 Endometriosis 63 0.078
415
c BTT014 Beta-Thalassemia 73 0.078
416
LPT014 Leptin Deficiency or Dysfunction 72 0.078
417
c LKM063 Leukemia, Chronic Myeloid 74 0.078
418
P ACT008 Actinic Keratosis 50 0.077
419
GNG013 Gingivitis 60 0.077
420
ACR006 Aceruloplasminemia 74 0.077
421
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.077
422
GTR002 Goiter 54 0.077
423
ORL011 Oral Cancer 62 0.077
424
CLF056 Cleft Lip with or Without Cleft Palate 42 0.077
425
c FML021 Familial Hypercholesterolemia 67 0.077
426
c PNS012 Paine Syndrome 61 0.076
427
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.076
428
SCH014 Schistosomiasis 57 0.076
429
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.076
430
P SRC025 Sarcoidosis 1 72 0.076
431
LYM133 Lymphoma, Hodgkin, Classic 70 0.076
432
P NPH012 Nephrotic Syndrome 65 0.076
433
MSL001 Measles 61 0.076
434
P CND004 Candidiasis 61 0.076
435
NRT001 Neurotic Disorder 53 0.076
436
RTN023 Retinitis 46 0.076
437
NRR001 Neuroretinitis 46 0.076
438
P HYP069 Hyperparathyroidism 64 0.075
439
ATS010 Autosomal Recessive Disease 49 0.075
440
CLF004 Cleft Lip/palate 55 0.075
441
CYS013 Cystinuria 66 0.075
442
MST005 Mastitis 55 0.075
443
c PLY105 Polycystic Ovary Syndrome 1 38 0.075
444
P OBS001 Obstructive Jaundice 49 0.075
445
RRS014 Rare Surgical Neurologic Disease 33 0.075
446
c LKM005 Leukemia, T-Cell, Chronic 35 0.075
447
OVR094 Ovarian Epithelial Cancer 39 0.075
448
P SYS005 Systemic Scleroderma 68 0.074
449
P RTN016 Retinal Degeneration 56 0.074
450
CLR109 Colorectal Adenocarcinoma 51 0.074
451
PNC001 Pancytopenia 54 0.074
452
CHR178 Chromosomal Triplication 36 0.074
453
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.074
454
ERY051 Erythroleukemia, Familial 58 0.074
455
P PRC031 Preeclampsia/eclampsia 1 42 0.074
456
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.074
457
OTT002 Otitis Media 71 0.073
458
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.073
459
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.073
460
P CTN015 Cutaneous T Cell Lymphoma 52 0.073
461
PST021 Postpartum Depression 51 0.073
462
TRN018 Transitional Cell Carcinoma 57 0.073
463
P RTN008 Retinitis Pigmentosa 77 0.073
464
PLY150 Polykaryocytosis Inducer 31 0.073
465
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.073
466
P GLM040 Glioma Susceptibility 1 68 0.072
467
P CNJ013 Conjunctivitis 67 0.072
468
c SCL052 Scleroderma, Familial Progressive 62 0.072
469
ORL015 Oral Squamous Cell Carcinoma 44 0.072
470
49X002 49,xxxxy Syndrome 39 0.072
471
DYS073 Dysphagia 52 0.072
472
DBT004 Diabetic Polyneuropathy 48 0.072
473
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.072
474
TLN003 Telangiectasis 53 0.072
475
c PSR017 Psoriasis 2 55 0.071
476
c PSR023 Psoriasis 1 50 0.071
477
c PSR028 Psoriasis 7 40 0.071
478
c PSR018 Psoriasis 13 40 0.071
479
c PSR032 Psoriasis 11 40 0.071
480
c FML035 Familial Hyperlipidemia 56 0.071
481
PNC129 Pancreatic Adenocarcinoma 69 0.070
482
P BRB001 Beriberi 41 0.070
483
TBR011 Tuberculous Meningitis 50 0.070
484
P VSC011 Vasculitis 64 0.070
485
DYS015 Dysentery 45 0.069
486
c CHR064 Chronic Monocytic Leukemia 43 0.069
487
P END033 Endocarditis 58 0.069
488
ALL006 Allergic Asthma 56 0.069
489
c MCR112 Microvascular Complications of Diabetes 2 42 0.069
490
CRH005 Crohn's Colitis 56 0.069
491
CHR073 Choreatic Disease 52 0.069
492
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.069
493
PPL001 Papillary Adenoma 42 0.069
494
VRC005 Varicose Veins 61 0.069
495
PST092 Posttransplant Acute Limbic Encephalitis 29 0.069
496
ANR040 Aneurysm 60 0.069
497
PRP036 Peripheral T-Cell Lymphoma 53 0.069
498
P PLY018 Polycythemia 56 0.068
499
P RTN018 Retinal Disease 53 0.068
500
P MJR007 Major Affective Disorder 1 44 0.068
501
c FML001 Familial Atrial Fibrillation 67 0.068
502
P OPN001 Open-Angle Glaucoma 50 0.068
503
P MDL005 Medulloblastoma 78 0.068
504
c PRD040 Periodontitis, Chronic 56 0.068
505
PRN019 Perinatal Necrotizing Enterocolitis 55 0.068
506
PYL006 Pyloric Stenosis 47 0.068
507
FDL002 Food Allergy 52 0.068
508
MSC007 Muscle Hypertrophy 65 0.068
509
PLG002 Plague 54 0.067
510
BRK010 Burkitt Lymphoma 68 0.067
511
IGG001 Iga Glomerulonephritis 50 0.067
512
KWS001 Kwashiorkor 46 0.067
513
MXD026 Mixed Glioma 36 0.067
514
P UVT001 Uveitis 58 0.067
515
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.067
516
P SHR001 Short Bowel Syndrome 50 0.066
517
P OPT006 Optic Nerve Disease 59 0.066
518
P VNT002 Ventricular Septal Defect 61 0.066
519
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.066
520
P FTL001 Fetal Alcohol Syndrome 56 0.066
521
AMN003 Amnestic Disorder 55 0.066
522
KPS004 Kaposi Sarcoma 75 0.066
523
HMT018 Hematopoietic Stem Cell Transplantation 54 0.066
524
SPL018 Splenomegaly 48 0.066
525
P DYS154 Dystonia 65 0.066
526
BCT002 Bacterial Vaginosis 52 0.066
527
c SPN225 Spondyloarthropathy 1 74 0.065
528
P BNC003 Bone Cancer 56 0.065
529
c WLM018 Wilms Tumor 5 63 0.065
530
PRT038 Protein-Energy Malnutrition 56 0.065
531
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.065
532
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.065
533
PTT037 Pituitary Tumors 47 0.065
534
HMG005 Hemoglobinopathy 57 0.065
535
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.065
537
SFT003 Soft Tissue Sarcoma 57 0.065
538
c GRV008 Graves Disease 1 55 0.065
539
P APL001 Aplastic Anemia 76 0.064
540
P PLL002 Pellagra 47 0.064
541
OST017 Osteomyelitis 65 0.064
542
CRN030 Coronary Stenosis 49 0.064
543
c MJR003 Major Affective Disorder 6 34 0.064
544
c MJR006 Major Affective Disorder 5 34 0.064
545
P ADL010 Adult Respiratory Distress Syndrome 61 0.064
546
P DNG005 Dengue Virus 57 0.064
547
HDN002 Head Injury 47 0.064
548
GST040 Gastric Adenocarcinoma 67 0.063
549
c ACT135 Acute Graft Versus Host Disease 52 0.063
550
LKP003 Leukoplakia 40 0.063
551
P PLY014 Polycystic Kidney Disease 61 0.063
552
c MJR008 Major Affective Disorder 2 35 0.063
553
c MJR023 Major Affective Disorder 7 34 0.063
554
c MJR004 Major Affective Disorder 4 29 0.063
555
P ALP009 Alopecia Areata 61 0.063
556
LYM027 Lymphopenia 58 0.063
557
GLS001 Gliosarcoma 56 0.063
558
SPS057 Spasticity 38 0.063
559
c JVN010 Juvenile Rheumatoid Arthritis 67 0.062
560
MSC157 Muscular Dystrophy, Duchenne Type 70 0.062
561
c HYP272 Hypercholesterolemia, Familial, 3 44 0.062
562
SCH003 Schizophreniform Disorder 49 0.062
563
P SLP006 Sleep Apnea 71 0.062
564
P HMP007 Hemophilia 58 0.062
565
GLS018 Glass Syndrome 51 0.062
566
P NRV007 Nervous System Disease 68 0.062
567
CRT017 Cartilage Disease 54 0.062
568
CHR100 Chronic Ulcer of Skin 53 0.062
569
P FNC004 Fanconi Syndrome 48 0.062
570
P FML011 Familial Adenomatous Polyposis 73 0.061
571
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.061
572
HYD002 Hydronephrosis 58 0.061
573
RHM001 Rheumatic Fever 56 0.061
574
PSR001 Psoriatic Arthritis 63 0.061
575
c OVR114 Ovarian Cancer 1 39 0.061
576
INT002 Intermittent Claudication 60 0.061
577
P THY023 Thymoma 64 0.061
578
c THY107 Thymoma, Familial 55 0.061
580
CRC021 Carcinosarcoma 62 0.061
581
KRT013 Keratolytic Winter Erythema 45 0.061
582
HYP141 Hyperphenylalaninemia 40 0.061
583
P PRS038 Personality Disorder 66 0.061
584
HYP017 Hypophosphatemia 48 0.060
585
ETN001 Eating Disorder 61 0.060
586
P HYP040 Hypospadias 54 0.060
587
MCR013 Microphthalmia 62 0.060
588
P GRV001 Graves' Disease 57 0.060
589
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 57 0.060
590
APH001 Aphthous Stomatitis 56 0.060
591
ART016 Aortic Aneurysm 71 0.060
592
MLN073 Melanosis, Neurocutaneous 45 0.060
593
SKN019 Skin Melanoma 68 0.060
594
P OLG002 Oligodendroglioma 67 0.060
595
THY030 Thyroid Gland Disease 53 0.060
596
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.060
597
TYP007 Typhoid Fever 61 0.060
598
P PRV006 Pervasive Developmental Disorder 58 0.060
599
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.059
600
THR004 Thrombocytosis 52 0.059
601
RDN001 Reading Disorder 42 0.059
602
P MYC008 Myocarditis 60 0.059
603
P MTR014 Motor Neuron Disease 66 0.059
604
ATN004 Autonomic Neuropathy 43 0.059
605
c MCL013 Mucolipidosis Iv 60 0.059
606
ABD010 Abdominal Wall Defect 37 0.059
607
URT010 Ureteral Obstruction 46 0.059
608
GRD007 Grade Iii Astrocytoma 59 0.059
609
P CHN012 Chondrosarcoma 57 0.059
610
P PTT006 Pituitary Adenoma 53 0.059
611
SCH012 Schizoaffective Disorder 50 0.059
612
P TRC086 Trichohepatoenteric Syndrome 1 57 0.059
613
ENH001 Enhanced S-Cone Syndrome 56 0.059
614
P ATX030 Ataxia-Telangiectasia 83 0.058
615
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.058
616
CNN005 Connective Tissue Disease 68 0.058
617
c ADL017 Adult T-Cell Leukemia 59 0.058
618
CHR066 Chronic Fatigue Syndrome 61 0.058
619
GNG012 Gingival Overgrowth 52 0.058
620
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 45 0.058
621
MLK006 Milk Allergy 44 0.058
622
TTH004 Tethered Spinal Cord Syndrome 33 0.058
623
c INF071 Inflammatory Bowel Disease 1 66 0.058
624
YLL002 Yellow Fever 58 0.058
625
SPN041 Spinal Cord Disease 57 0.058
626
HRT011 Heart Septal Defect 52 0.058
627
c MST023 Mesothelioma, Malignant 59 0.058
628
EXC002 Exocrine Pancreatic Insufficiency 41 0.058
629
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.058
630
c CHR682 Chronic Bilirubin Encephalopathy 36 0.057
632
PHR003 Pharyngitis 56 0.057
633
P MNC007 Monocytic Leukemia 52 0.057
634
c ALP101 Alpha-Thalassemia 63 0.057
635
c FTL006 Fetal Alcohol Spectrum Disorder 45 0.057
636
KHL003 Kohlschutter-Tonz Syndrome 63 0.057
637
LMY002 Leiomyoma 52 0.057
638
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.057
639
HPT022 Hepatoblastoma 58 0.057
640
c GLC092 Glaucoma, Primary Open Angle 63 0.057
641
ILS001 Ileus 51 0.057
642
FCT007 Factor Vii Deficiency 65 0.057
643
FBR047 Fibromyalgia 60 0.057
644
P TRT010 Teratoma 52 0.057
645
c ACT042 Acute Pyelonephritis 44 0.057
646
NRM005 Neuromuscular Disease 62 0.056
647
P RBL001 Rubella 56 0.056
648
MCR004 Macroglobulinemia 50 0.056
649
RTC005 Reticulosarcoma 48 0.056
650
ACR041 Acromelic Frontonasal Dysostosis 50 0.056
651
MNT001 Mantle Cell Lymphoma 69 0.056
652
PLS007 Plasmodium Falciparum Malaria 53 0.056
653
PRS047 Prostatitis 57 0.056
654
KRT006 Keratoconjunctivitis 53 0.056
655
DRY001 Dry Eye Syndrome 50 0.056
656
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.056
657
MYC006 Mycosis Fungoides 67 0.056
658
CYT008 Cytomegalovirus Infection 58 0.056
659
P ORF002 Orofacial Cleft 44 0.056
660
PLY001 Polycythemia Vera 70 0.056
661
P MYS003 Myasthenia Gravis 68 0.055
662
c MLG074 Malignant Mesenchymoma 50 0.055
663
P SNS001 Sensorineural Hearing Loss 62 0.055
664
AZS001 Azoospermia 51 0.055
665
KRT019 Keratitis, Hereditary 69 0.055
666
SPN051 Spondylitis 53 0.055
667
INF009 Inflammatory Spondylopathy 29 0.055
668
TRP009 Triple X Syndrome 42 0.055
669
P FLL037 Follicular Lymphoma 67 0.055
670
c MLG079 Malignant Pleural Mesothelioma 43 0.055
671
c SYS043 Systemic Lupus Erythematosus 1 39 0.055
672
c EXD008 Exudative Vitreoretinopathy 1 69 0.055
673
P LRY044 Larynx Cancer 59 0.055
674
c BCT007 Bacterial Meningitis 56 0.055
675
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.055
676
MCL006 Macular Retinal Edema 52 0.055
677
P HRD011 Hereditary Spherocytosis 59 0.055
678
P PRG092 Pregnancy Loss, Recurrent 1 40 0.055
679
P TXP001 Toxoplasmosis 61 0.054
680
ALC006 Alcoholic Hepatitis 60 0.054
681
GLB001 Gilbert Syndrome 58 0.054
682
CRB037 Cerebral Palsy 69 0.054
683
RBF001 Riboflavin Deficiency 46 0.054
684
AMN001 Amenorrhea 54 0.054
685
ACR007 Acromegaly 70 0.054
686
P MTC069 Mitochondrial Disorders 57 0.054
687
SPT004 Septic Arthritis 55 0.054
688
FCL014 Focal Epilepsy 56 0.054
689
BTN004 Biotin Deficiency 38 0.054
690
P SBS003 Substance Abuse 56 0.054
691
P MMP001 Mumps 57 0.054
692
NRT004 Neuritis 52 0.054
693
P CLL015 Collagen Disease 46 0.054
694
P LCH002 Lichen Planus 55 0.053
695
EWN003 Ewing Sarcoma 69 0.053
696
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.053
697
THY122 Thyroid Gland Cancer 59 0.053
698
IMM064 Immunodeficiency, Common Variable, 10 51 0.053
699
PYR016 Pyridoxine Deficiency 31 0.053
700
ECT026 Ectopic Pregnancy 50 0.053
701
OBS002 Obsessive-Compulsive Disorder 69 0.053
702
P HMR003 Hemorrhagic Disease 54 0.053
703
P CRB088 Cerebral Atrophy 43 0.053
704
NRN004 Neuroendocrine Tumor 59 0.053
705
PRD004 Prediabetes Syndrome 49 0.053
706
VRL011 Viral Infectious Disease 62 0.053
707
VSC003 Visceral Leishmaniasis 55 0.053
708
ACT058 Active Peptic Ulcer Disease 55 0.053
709
c HMG029 Hemoglobin Se Disease 40 0.053
710
SPR126 Superior Semicircular Canal Dehiscence 39 0.053
711
KRN002 Kearns-Sayre Syndrome 64 0.052
712
URN010 Urinary Tract Obstruction 59 0.052
713
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 0.052
714
MRG013 Mirage Syndrome 42 0.052
715
PYR009 Pyridoxine Deficiency Anemia 32 0.052
716
RNL065 Renal Cell Carcinoma, Papillary, 1 75 0.052
717
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.052
718
CTS005 Catastrophic Antiphospholipid Syndrome 44 0.052
719
CRD223 Cardiac Arrhythmia 61 0.052
720
P SLP005 Sleep Disorder 58 0.052
721
DWR001 Dwarfism 45 0.052
722
P VSC018 Visceral Steatosis 34 0.052
723
P EPN002 Ependymoma 61 0.052
724
P MYS005 Myositis 54 0.052
725
RFR010 Refractory Anemia 50 0.052
726
LNT004 Lentigines 47 0.052
727
STT009 Sutton Disease 2 31 0.052
728
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.052
729
BCT004 Bacteriuria 48 0.052
730
TND005 Tendinitis 45 0.052
731
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.052
732
P THY032 Thyroiditis 52 0.052
733
c SCN007 Secondary Hyperparathyroidism 52 0.052
734
P ANG001 Angelman Syndrome 65 0.051
735
c DNG003 Dengue Disease 61 0.051
736
P SPN237 Spina Bifida Aperta 21 0.051
737
INT075 Intracranial Hypertension 54 0.051
738
c BNG030 Benign Ependymoma 48 0.051
739
INT066 Interstitial Lung Disease 61 0.051
740
P HML001 Hemolytic-Uremic Syndrome 54 0.051
741
BRN056 Bronchopulmonary Dysplasia 57 0.051
742
P NRC002 Narcolepsy 56 0.051
743
MYL031 Myeloproliferative Neoplasm 66 0.051
744
P OCL013 Oculodentodigital Dysplasia 65 0.051
745
NWB001 Newborn Respiratory Distress Syndrome 58 0.051
746
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.051
747
P PNC025 Panic Disorder 53 0.050
748
ILT001 Ileitis 50 0.050
749
c INF145 Infantile Liver Failure Syndrome 1 50 0.050
750
ANP008 Anaplastic Oligoastrocytoma 31 0.050
751
P MCR010 Microcephaly 56 0.050
752
SNS003 Sensory Peripheral Neuropathy 56 0.050
753
P PRC012 Pericardial Effusion 51 0.050
754
HMP001 Hemopericardium 44 0.050
755
KRT001 Keratoconjunctivitis Sicca 53 0.050
756
MYL005 Myelofibrosis 69 0.050
757
CLL003 Cellulitis 56 0.050
758
P MTH007 Methemoglobinemia 47 0.050
759
HYP457 Hypertrophic Scars 44 0.050
760
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 33 0.050
761
HYP025 Hyperphosphatemia 47 0.050
762
BCK006 Back Pain 44 0.050
763
ANG046 Angioimmunoblastic T-Cell Lymphoma 49 0.050
764
c FLL041 Follicular Lymphoma 1 50 0.049
765
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.049
766
CHL061 Childhood Leukemia 49 0.049
767
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.049
768
ACT003 Acute Kidney Tubular Necrosis 42 0.049
769
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 51 0.049
770
ATM052 Autoimmune Disease 1 38 0.049
771
PPL049 Papillon-Lefevre Syndrome 63 0.049
772
RTN020 Retinal Vascular Disease 49 0.049
773
PRS063 Paresthesia 46 0.049
774
PRP016 Paraplegia 54 0.049
775
MSC190 Muscular Disease 54 0.049
776
TST015 Testicular Disease 49 0.049
778
P ANT006 Antiphospholipid Syndrome 56 0.049
779
CRV040 Cervix Carcinoma 52 0.049
780
BNM001 Bone Marrow Cancer 48 0.049
781
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 44 0.049
782
CRP001 Carpal Tunnel Syndrome 68 0.049
783
INC002 Inclusion Body Myositis 66 0.049
784
P CHR071 Charcot-Marie-Tooth Disease 65 0.049
785
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.049
786
P EPD016 Epidermolysis Bullosa 54 0.049
787
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.049
788
NNT012 Neonatal Jaundice 48 0.049
789
TTH006 Tooth Disease 47 0.049
790
ORL012 Oral Leukoplakia 42 0.049
791
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.049
792
P MYP006 Myopia 58 0.048
793
MLT157 Multiple System Atrophy 1 71 0.048
794
HMT002 Hematologic Cancer 64 0.048
795
DFF005 Diffuse Large B-Cell Lymphoma 56 0.048
796
INT067 Interstitial Nephritis 46 0.048
797
HPT082 Hepatic Adenomas, Familial 40 0.048
798
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 64 0.048
799
BLD131 Bladder Urothelial Carcinoma 62 0.048
800
P DRM010 Dermatomyositis 62 0.048
801
HRP004 Herpes Zoster 58 0.048
802
HYP043 Hyperandrogenism 48 0.048
803
PLC006 Placental Choriocarcinoma 33 0.048
804
HDG004 Hodgkin's Granuloma 27 0.048
805
HDG006 Hodgkin's Paragranuloma 23 0.048
806
GLS007 Glossitis 44 0.048
807
c PRM005 Primary Hyperparathyroidism 60 0.048
808
c CNT035 Central Nervous System Disease 56 0.048
809
ORT008 Orotic Aciduria 51 0.048
810
ATN005 Autonomic Dysfunction 48 0.048
811
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.048
812
END041 Endometrial Adenocarcinoma 64 0.048
813
BRS099 Breast Ductal Carcinoma 63 0.048
814
CMR002 Coumarin Resistance 56 0.048
815
P HMR005 Hemorrhoid 47 0.048
816
ART002 Arts Syndrome 63 0.047
817
ANG005 Anogenital Venereal Wart 51 0.047
818
CRT013 Carotid Stenosis 50 0.047
819
P HYP726 Hypercalcemia, Infantile, 1 58 0.047
820
TXC002 Toxic Encephalopathy 54 0.047
821
ASP007 Aspiration Pneumonia 46 0.047
822
P PMP001 Pemphigus 56 0.047
823
P NRV006 Nervous System Cancer 55 0.047
824
INT303 Intracranial Hypertension, Idiopathic 52 0.047
825
CHY002 Chylomicron Retention Disease 63 0.047
826
DBT002 Diabetic Autonomic Neuropathy 45 0.047
827
c WLM013 Wilms Tumor 1 69 0.047
828
P CHR012 Chronic Granulomatous Disease 69 0.047
829
HMR039 Hemorrhage, Intracerebral 59 0.047
830
DCT002 Ductal Carcinoma in Situ 57 0.047
831
c PRM092 Primary Lateral Sclerosis, Adult, 1 54 0.047
832
LYM009 Lymphocytic Choriomeningitis 45 0.047
833
AMN002 Amino Acid Metabolic Disorder 42 0.046
834
WLL004 Wallerian Degeneration 40 0.046
835
P BLD062 Bile Duct Cancer 66 0.046
836
GNT002 Giant Cell Glioblastoma 52 0.046
837
c CNT033 Central Nervous System Cancer 51 0.046
838
ASP004 Asphyxia Neonatorum 44 0.046
839
LYM048 Lymphoma, Large-Cell, Immunoblastic 30 0.046
840
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.046
841
BRN002 Bronchiolitis 60 0.046
842
P GLL020 Gallbladder Disease 60 0.046
843
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 52 0.046
844
ACT084 Acute Stress Disorder 42 0.046
845
c CHR418 Chronic Leukemia 52 0.046
846
MCL027 Macular Dystrophy, Dominant Cystoid 47 0.046
847
MTH047 Methanol Poisoning 31 0.046
848
PLS025 Plasmablastic Lymphoma 48 0.046
849
PST028 Post-Traumatic Stress Disorder 60 0.046
850
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.046
851
LPT006 Leptin Receptor Deficiency 47 0.046
852
AMN012 Aminoacidopathies 22 0.046
853
P OMP004 Omphalocele 51 0.045
854
THR013 Thoracic Outlet Syndrome 49 0.045
855
GST030 Gastrinoma 43 0.045
856
CRV038 Cervical Squamous Cell Carcinoma 58 0.045
857
P RST001 Restless Legs Syndrome 54 0.045
858
NPH003 Nephrocalcinosis 52 0.045
859
PNC034 Pancreas Disease 51 0.045
860
c XNT010 Xanthinuria, Type I 51 0.045
861
FSC004 Fasciitis 47 0.045
862
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 37 0.045
863
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.045
864
CLN045 Colonic Benign Neoplasm 52 0.045
865
VTM033 Vitamin K Deficiency Bleeding 47 0.045
866
c ATM006 Autoimmune Lymphoproliferative Syndrome 73 0.045
867
DCB001 Decubitus Ulcer 54 0.045
868
CLR030 Clear Cell Renal Cell Carcinoma 54 0.045
869
HMG002 Hemoglobinuria 49 0.045
870
TST014 Testicular Cancer 49 0.045
871
P ATR010 Atrial Heart Septal Defect 61 0.045
872
INT017 Intestinal Schistosomiasis 49 0.045
873
GLT005 Glutamate Formiminotransferase Deficiency 35 0.044
874
WST001 West Syndrome 61 0.044
875
LSC001 Lesch-Nyhan Syndrome 61 0.044
876
ALC009 Alcoholic Liver Cirrhosis 53 0.044
877
LMB062 Limb Ischemia 50 0.044
878
P RNL015 Renal Hypertension 47 0.044
879
P SBR004 Seborrheic Dermatitis 41 0.044
880
P PLY041 Polymyositis 57 0.044
881
ORL005 Oral Candidiasis 56 0.044
882
CHK001 Chikungunya 55 0.044
883
c PNC106 Pancreatic Agenesis 1 50 0.044
884
SKN013 Skin Benign Neoplasm 49 0.044
885
LWC001 Low Compliance Bladder 45 0.044
886
BRN032 Brain Glioma 44 0.044
887
P AVS003 Avascular Necrosis 43 0.044
888
GST020 Gastric Antral Vascular Ectasia 42 0.044
889
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 37 0.044
890
CYT018 Cytochrome P450 2d6 Variant 28 0.044
891
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 28 0.044
892
ATR057 Atrioventricular Block 56 0.044
893
c ACT020 Acute T Cell Leukemia 54 0.044
894
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.044
895
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.044
896
LRN003 Learning Disability 51 0.044
897
KWS002 Kawasaki Disease 65 0.044
898
BLL006 Bullous Pemphigoid 63 0.044
899
P TCD001 Tic Disorder 55 0.044
900
DBT006 Diabetic Macular Edema 46 0.044
901
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 44 0.044
902
HRN029 Hearing Loss, Noise-Induced 38 0.044
903
c TCL024 T-Cell Non-Hodgkin Lymphoma 37 0.044
904
ANS023 Anus, Imperforate 51 0.044
905
P ANR048 Aniridia 1 64 0.043
906
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 62 0.043
907
MSS001 Masa Syndrome 55 0.043
908
RST023 Resting Heart Rate, Variation in 43 0.043
909
c PRG106 Progressive Muscular Dystrophy 34 0.043
910
ORN001 Ornithosis 40 0.043
911
URN009 Urinary System Disease 52 0.043
912
THY121 Thyroid Gland Anaplastic Carcinoma 62 0.043
913
P STR020 Strabismus 57 0.043
914
c LKM070 Leukemia, Acute Monocytic 55 0.043
915
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.043
916
c BCT013 Bacterial Pneumonia 49 0.043
917
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 48 0.043
918
SKN005 Skin Atrophy 41 0.043
919
GRM010 Germ Cells Tumors 35 0.043
920
MCH006 Mechanical Strabismus 31 0.043
921
ACD008 Acid-Labile Subunit Deficiency 55 0.043
922
CRN017 Coronary Thrombosis 45 0.043
923
GST071 Gastrointestinal Carcinoma 42 0.043
924
SPR005 Superficial Basal Cell Carcinoma 36 0.043
925
P THR005 Thrombotic Thrombocytopenic Purpura 59 0.043
926
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.042
927
APN008 Apnea, Obstructive Sleep 64 0.042
928
PLL012 Pollen Allergy 46 0.042
929
RCT015 Reactive Arthritis 58 0.042
930
GLL018 Gallbladder Cancer 57 0.042
931
NRG002 Neurogenic Bladder 55 0.042
932
STP011 Stapes Ankylosis with Broad Thumbs and Toes 50 0.042
933
HMR023 Hemorrhagic Cystitis 40 0.042
934
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.042
935
HML018 Homologous Wasting Disease 22 0.042
936
EXF001 Exfoliation Syndrome 56 0.042
937
P PRP003 Porphyria Cutanea Tarda 66 0.042
938
ERY003 Erythema Multiforme 57 0.042
939
CRC006 Carcinoid Syndrome 55 0.042
940
CLN019 Colonic Disease 55 0.042
941
HLL004 Hellp Syndrome 53 0.042
942
MYM001 Myoma 52 0.042
943
P RTN022 Retinal Vein Occlusion 50 0.042
944
FTL021 Fetal Macrosomia 43 0.042
945
ADN011 Adenoid Cystic Carcinoma 71 0.042
946
c ART101 Aortic Valve Disease 2 67 0.042
947
NRF007 Neurofibroma 63 0.042
948
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.042
949
PMP006 Pemphigus Vulgaris, Familial 56 0.042
950
P SML001 Small Cell Carcinoma 55 0.042
951
P HST010 Histiocytosis 54 0.042
952
P THR015 Thrombophilia 51 0.042
953
VRS002 Virus-Associated Trichodysplasia Spinulosa 33 0.042
954
P HYP838 Hyperlipidemia, Familial Combined, 3 54 0.042
955
LPD009 Lipid Storage Disease 49 0.042
956
EPD015 Epidemic Typhus 47 0.042
957
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.042
958
BSL036 Basal Cell Nevus Syndrome 70 0.041
959
PRX085 Preaxial Hallucal Polydactyly 27 0.041
960
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.041
961
VRC001 Varicocele 51 0.041
962
P BRN035 Brain Stem Glioma 51 0.041
963
TRC008 Trachoma 49 0.041
964
c BSL024 Basal Cell Carcinoma 1 47 0.041
965
OST011 Osteomalacia 51 0.041
966
BRN009 Burning Mouth Syndrome 51 0.041
967
DGN001 Degenerative Disc Disease 49 0.041
968
CHL045 Choline Deficiency Disease 39 0.041
969
ADR054 Adrenocortical Carcinoma, Hereditary 68 0.041
970
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 58 0.041
971
ACT200 Acute Monoblastic Leukemia 56 0.041
972
NTR018 Neutrophilia, Hereditary 53 0.041
973
c DRM054 Dermatitis, Atopic, 2 45 0.041
974
NRD001 Neurodermatitis 40 0.041
975
MYF002 Myofascial Pain Syndrome 39 0.041
976
LNG039 Lung Squamous Cell Carcinoma 66 0.041
977
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.041
978
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 62 0.041
979
P EHL001 Ehlers-Danlos Syndrome 60 0.041
980
c HMN021 Human T-Cell Leukemia Virus Type 1 50 0.041
981
c JVN004 Juvenile Myelomonocytic Leukemia 68 0.040
982
P PTN014 Patent Ductus Arteriosus 1 60 0.040
983
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 56 0.040
984
EXP004 Exophthalmos 53 0.040
985
MCP006 Mucoepidermoid Carcinoma 53 0.040
986
MYL075 Myelodysplastic/myeloproliferative Neoplasm 50 0.040
987
CLS016 Clostridium Difficile Colitis 48 0.040
988
SPP008 Suppurative Otitis Media 46 0.040
989
BLR013 Biliary Tract Cancer 44 0.040
990
c SPR086 Spermatogenic Failure 3 41 0.040
991
KLB003 Klebsiella Pneumonia 36 0.040
992
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 32 0.040
993
SVR097 Severe Cutaneous Adverse Reaction 66 0.040
994
HRT012 Heart Valve Disease 56 0.040
995
PRM020 Premenstrual Tension 48 0.040
996
IRR003 Irritant Dermatitis 46 0.040
997
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.040
998
RTC010 Reticuloendotheliosis 37 0.040
999
P DRM007 Dermatitis Herpetiformis 50 0.040
1000
P RRT020 Rare Tumor 43 0.040
1001
SZR001 Sezary's Disease 59 0.040
1002
DFF036 Differentiated Thyroid Carcinoma 53 0.040
1003
GRW007 Growth Hormone Deficiency 48 0.040
1004
DMP001 Dumping Syndrome 44 0.040
1005
INT052 Intestinal Volvulus 44 0.040
1006
MCR011 Microinvasive Gastric Cancer 43 0.040
1007
MRS001 Marasmus 39 0.040
1008
ERY066 Erythema Multiforme Major 29 0.040
1009
P LYM033 Lymphoproliferative Syndrome 62 0.039
1010
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.039
1011
BWN001 Bowen-Conradi Syndrome 49 0.039
1012
EWN002 Ewing's Family of Tumors 48 0.039
1013
CLC006 Calcinosis 48 0.039
1014
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 46 0.039
1015
ANG049 Angioedema Induced by Ace Inhibitors 41 0.039
1016
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.039
1017
P URF003 Urofacial Syndrome 1 55 0.039
1018
PRL032 Perlman Syndrome 54 0.039
1019
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 48 0.039
1020
PNN001 Panniculitis 47 0.039
1021
P OCY003 Oocyte Maturation Defect 1 44 0.039
1022
PLS016 Plasma Cell Leukemia 41 0.039
1023
BCK003 Background Diabetic Retinopathy 37 0.039
1024
c DRM040 Dermatitis Herpetiformis, Familial 36 0.039
1025
SPC030 Specific Language Disorder 27 0.039
1026
GST049 Gastrointestinal System Cancer 49 0.039
1027
SPS019 Spastic Paraparesis 40 0.039
1028
c NRF024 Neurofibromatosis, Type I 72 0.039
1029
P OST001 Osteopetrosis 70 0.039
1030
c HYD046 Hydatidiform Mole, Recurrent, 1 62 0.039
1031
P MLN069 Melanoma, Uveal 59 0.039
1032
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 58 0.039
1033
PLM012 Pulmonary Sarcoidosis 54 0.039
1034
GST009 Gastroschisis 52 0.039
1035
c INF023 Inflammatory Breast Carcinoma 52 0.039
1036
AMB002 Amblyopia 51 0.039
1037
P HMN032 Human Herpesvirus 8 49 0.039
1038
NRN001 Neuroendocrine Carcinoma 48 0.039
1039
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 48 0.039
1040
GST010 Gestational Trophoblastic Neoplasm 46 0.039
1041
PRM003 Premature Ejaculation 44 0.039
1042
DFF003 Diffuse Scleroderma 43 0.039
1043
CRN020 Coronary Restenosis 40 0.039
1044
SPP007 Suppression Amblyopia 37 0.039
1045
c PNC108 Pancreatitis, Hereditary 70 0.038
1046
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.038
1047
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.038
1048
LMY014 Leiomyoma, Uterine 57 0.038
1049
P MTC133 Mitochondrial Myopathy 53 0.038
1050
THR016 Thrombophlebitis 50 0.038
1051
P END046 Endometritis 49 0.038
1052
ORL013 Oral Lichen Planus 47 0.038
1053
KRT008 Keratopathy 46 0.038
1054
c ACT004 Acute Diarrhea 38 0.038
1055
VGN019 Vaginal Discharge 35 0.038
1056
c SCH085 Schizophrenia 2 45 0.038
1057
P TTR001 Tetralogy of Fallot 70 0.038
1058
CMM004 Common Variable Immunodeficiency 69 0.038
1059
DBN001 Dubin-Johnson Syndrome 58 0.038
1060
PRM042 Primary Effusion Lymphoma 55 0.038
1061
HMT008 Hematuria, Benign Familial 53 0.038
1062
CYS036 Cystinosis, Nephropathic 53 0.038
1063
IMM136 Immune System Disease 52 0.038
1064
GRM005 Germ Cell Cancer 47 0.038
1065
NCR007 Necrotizing Fasciitis 47 0.038
1066
ANP009 Anaplastic Oligodendroglioma 44 0.038
1067
GST059 Gestational Trophoblastic Tumor 32 0.038
1068
CNN003 Conn's Syndrome 78 0.038
1069
P OPT009 Optic Neuritis 55 0.038
1070
MTC005 Mitochondrial Metabolism Disease 50 0.038
1071
RNL011 Renal Osteodystrophy 49 0.038
1072
OLG001 Oligospermia 44 0.038
1073
PRS042 Prostate Disease 42 0.038
1074
MST020 Mast Cell Activation Syndrome 28 0.038
1075
c FNC027 Fanconi Anemia, Complementation Group a 81 0.037
1076
AGM019 Agammaglobulinemia, X-Linked 71 0.037
1077
P AGM001 Agammaglobulinemia 66 0.037
1078
MGK001 Megakaryocytic Leukemia 65 0.037
1079
HYP063 Hypersplenism 51 0.037
1080
c PRM226 Primary Central Nervous System Lymphoma 50