Search results for Folic acid

1822 hits were found for Folic acid

# Family MCID Name MIFTS Score
1
FLC001 Folic Acid Deficiency Anemia 32 4.730
2
FLT009 Folate Malabsorption, Hereditary 50 3.839
3
P FRG001 Fragile X Syndrome 70 2.802
4
NRL016 Neural Tube Defects 82 0.577
5
DFC004 Deficiency Anemia 70 0.318
6
P LVR013 Liver Disease 68 0.309
7
HMC014 Homocysteinemia 53 0.306
8
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.287
9
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.287
10
P CLR023 Colorectal Cancer 99 0.285
11
P KDN018 Kidney Disease 72 0.274
12
FTT001 Fatty Liver Disease 61 0.257
13
LVR012 Liver Cirrhosis 62 0.252
14
P VSC007 Vascular Disease 63 0.248
15
IRN002 Iron Metabolism Disease 57 0.246
16
c PRC016 Pre-Eclampsia 63 0.236
17
P SZR006 Seizure Disorder 56 0.231
18
VTM002 Vitamin B12 Deficiency 48 0.230
19
HYP014 Hyperuricemia 52 0.227
20
CHL068 Cholestasis 61 0.226
21
P NRB001 Neuroblastoma 72 0.224
22
P DRR001 Diarrhea 55 0.224
23
P CRN300 Coronary Heart Disease 1 63 0.223
24
48X005 48,xyyy 39 0.220
25
ATH013 Atherosclerosis Susceptibility 65 0.217
26
LPP008 Lipoprotein Quantitative Trait Locus 62 0.217
27
VSL002 Visual Epilepsy 59 0.214
28
P LKM002 Leukemia 68 0.212
29
ACT119 Acute Promyelocytic Leukemia 63 0.210
30
LPD008 Lipid Metabolism Disorder 62 0.209
31
ISC004 Ischemia 58 0.208
32
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.207
33
P PSR002 Psoriasis 62 0.205
34
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.205
35
PST011 Pustulosis of Palm and Sole 52 0.203
36
ART140 Arteries, Anomalies of 52 0.200
37
P BRS047 Breast Cancer 97 0.200
38
HLX001 Helix Syndrome 47 0.200
39
c CHR684 Chronic Kidney Disease 70 0.195
40
c NRF023 Neurofibromatosis, Type Ii 80 0.193
41
ADN018 Adenoma 59 0.191
42
MTB004 Metabolic Acidosis 50 0.189
43
P GLM045 Glioma 63 0.189
44
CLT003 Colitis 62 0.189
45
PRN011 Pernicious Anemia 53 0.189
46
MGL001 Megaloblastic Anemia 51 0.188
47
GLL048 Glial Tumor 45 0.187
48
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.185
49
ANN002 Anencephaly 56 0.185
50
P HPT023 Hepatocellular Carcinoma 100 0.182
51
GST092 Gastroesophageal Reflux 67 0.181
52
OST012 Osteoarthritis 78 0.181
53
GT001 Gout 64 0.180
54
HYP066 Hyperglycemia 61 0.180
55
BNR002 Bone Resorption Disease 48 0.179
56
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.179
57
c HYP595 Hypertension, Essential 84 0.179
58
ULC004 Ulcerative Colitis 73 0.177
59
P INF037 Inflammatory Bowel Disease 54 0.177
60
P ATS364 Autism 70 0.177
61
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.174
62
P RHM011 Rheumatoid Arthritis 80 0.174
63
P HRT032 Heart Disease 75 0.173
64
P CRD246 Cardiovascular System Disease 57 0.173
65
DRM006 Dermatitis 61 0.173
66
END086 End Stage Renal Disease 51 0.170
67
P OVR042 Ovarian Cancer 88 0.169
68
c HYP836 Hypercholesterolemia, Familial, 1 73 0.169
69
P PRS040 Prostate Cancer 97 0.169
70
DWN001 Down Syndrome 70 0.169
71
P ART022 Arthritis 69 0.168
72
P NRP001 Neuropathy 56 0.168
73
DPR016 Depression 63 0.168
74
ALL026 Allergic Hypersensitivity Disease 62 0.167
75
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.167
76
P GST044 Gastritis 56 0.165
77
GLB015 Glioblastoma Multiforme 75 0.165
78
HYP056 Hypoglycemia 66 0.164
79
P ENC018 Encephalopathy 61 0.163
80
P MYC007 Myocardial Infarction 70 0.162
81
ATM095 Autoimmune Disease 62 0.162
82
P ADN016 Adenocarcinoma 64 0.162
83
NTR005 Nutritional Deficiency Disease 62 0.161
84
CRB039 Cerebrovascular Disease 67 0.160
85
P PRM006 Primary Biliary Cirrhosis 62 0.159
86
CLF027 Cleft Palate, Isolated 64 0.158
87
P DBT009 Diabetes Mellitus 64 0.157
88
P HYP750 Hypertriglyceridemia, Familial 62 0.156
89
PRT037 Pertussis 65 0.155
90
PPT005 Peptic Ulcer Disease 59 0.155
91
STR067 Stroke, Ischemic 81 0.154
92
P NTR004 Neutropenia 63 0.154
93
P LNG032 Lung Cancer 98 0.154
94
P OST002 Osteoporosis 74 0.153
95
HYP781 Hypoascorbemia 51 0.153
96
c ATS007 Autism Spectrum Disorder 67 0.152
97
ALC007 Alcohol Dependence 66 0.151
98
HRW001 Hair Whorl 36 0.150
99
c GLL024 Gallbladder Disease 1 53 0.150
100
PLM001 Pulmonary Tuberculosis 69 0.149
101
HMN044 Human Immunodeficiency Virus Type 1 71 0.148
102
P ALZ034 Alzheimer Disease 88 0.148
103
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.148
104
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.148
105
NNL006 Non-Alcoholic Steatohepatitis 54 0.147
106
MNT002 Mental Depression 58 0.145
107
c RHB024 Rhabdomyosarcoma 2 67 0.145
108
P MYL006 Myeloid Leukemia 60 0.144
109
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.144
110
P BPL003 Bipolar Disorder 56 0.144
111
c ACT071 Acute Kidney Failure 60 0.144
112
RCK004 Rickets 68 0.144
113
c MJR024 Major Affective Disorder 9 41 0.143
114
c MJR022 Major Affective Disorder 8 38 0.143
115
P EPL164 Epilepsy 71 0.143
116
HYP060 Hyperinsulinism 54 0.143
117
c ACT073 Acute Leukemia 58 0.143
118
CYS001 Cystic Fibrosis 81 0.143
119
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.142
120
P HNT016 Huntington Disease 72 0.141
121
OST159 Osteogenic Sarcoma 66 0.141
122
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.140
123
HYP266 Hypoxia 57 0.140
124
c ACT075 Acute Myocardial Infarction 57 0.139
125
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.139
126
CYT002 Cytokine Deficiency 42 0.139
127
P ECL001 Eclampsia 50 0.138
128
P PNC035 Pancreatic Cancer 84 0.138
129
47X002 47,xyy 49 0.138
130
CRV035 Cervical Cancer 76 0.137
131
P BLD134 Bladder Cancer 79 0.137
132
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.137
133
IRN001 Iron Deficiency Anemia 59 0.137
134
STM007 Stomatitis 50 0.137
135
PHN003 Phenylketonuria 75 0.136
136
CRH001 Crohn's Disease 74 0.136
137
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.135
138
P ESP024 Esophagitis 62 0.135
139
CNG034 Congestive Heart Failure 69 0.134
140
c MCR120 Microvascular Complications of Diabetes 7 47 0.134
141
c THR092 Thrombophilia Due to Thrombin Defect 73 0.133
142
STT001 Status Epilepticus 60 0.132
143
P INF032 Infertility 57 0.132
144
CLR108 Colorectal Adenoma 64 0.131
145
P GST053 Gastric Cancer 83 0.131
146
CHL079 Children's Interstitial Lung Disease 26 0.131
147
SKN016 Skin Disease 63 0.130
148
P HYP086 Hypothyroidism 69 0.130
149
c MCR113 Microvascular Complications of Diabetes 3 52 0.129
150
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.129
151
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.129
152
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.129
153
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.129
154
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.129
155
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.129
156
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.129
157
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.129
158
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.129
159
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.129
160
c MCR130 Microvascular Complications of Diabetes 6 41 0.129
161
c MCR133 Microvascular Complications of Diabetes 4 41 0.129
162
URM002 Uremia 49 0.128
163
P ART021 Arteriosclerosis 54 0.128
164
P DRM053 Dermatitis, Atopic 66 0.127
165
c PCH010 Pachyonychia Congenita 3 44 0.127
166
MCR017 Macrocytic Anemia 44 0.127
167
OCL069 Ocular Motor Apraxia 51 0.127
168
HPT004 Hepatic Coma 45 0.127
169
c HPT073 Hepatitis C Virus 72 0.126
170
P TRN020 Turner Syndrome 67 0.126
171
GST023 Gastric Ulcer 53 0.126
172
CLF001 Cleft Lip 53 0.124
173
P BND020 Bone Disease 59 0.124
174
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.124
175
MYL069 Myeloma, Multiple 85 0.123
176
P OVR082 Overgrowth Syndrome 50 0.123
177
P HMC002 Homocystinuria 53 0.123
178
P PRD008 Periodontitis 64 0.122
179
P THR014 Thrombocytopenia 67 0.122
180
c LKM061 Leukemia, Acute Myeloid 84 0.121
181
BCT022 Bacterial Infectious Disease 56 0.121
182
P PRP019 Peripheral Nervous System Disease 58 0.121
183
GLC003 Glucose Intolerance 54 0.121
184
c DBT099 Diabetes Mellitus, Type I 65 0.120
185
c SYS001 Systemic Lupus Erythematosus 86 0.120
186
P CHL066 Cholangitis 51 0.120
187
MLR004 Malaria 81 0.120
188
THR024 Thrombosis 57 0.120
189
MDD011 Mood Disorder 62 0.119
190
P SKN015 Skin Carcinoma 66 0.119
191
HPT019 Hepatic Encephalopathy 60 0.118
192
SQM006 Squamous Cell Carcinoma 60 0.118
193
CRB004 Cerebral Artery Occlusion 45 0.118
194
GST033 Gestational Diabetes 61 0.117
195
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.117
196
LNG099 Lung Disease 60 0.117
197
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.117
198
PPL052 Papillomatosis, Confluent and Reticulated 33 0.116
199
P SCH015 Schizophrenia 74 0.116
200
P LTR001 Lateral Sclerosis 54 0.116
201
P PLY011 Polycystic Ovary Syndrome 56 0.116
202
P MJR001 Major Depressive Disorder 68 0.116
204
P LKM062 Leukemia, Acute Lymphoblastic 69 0.115
205
MCS002 Mucositis 56 0.115
206
INS024 Insulin-Like Growth Factor I 79 0.115
207
P LYM118 Lymphoma 68 0.115
208
c MGR028 Migraine with or Without Aura 1 67 0.115
209
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.114
210
P CTR002 Cataract 60 0.114
211
P MYP004 Myopathy 70 0.114
212
SPN186 Spinal Cord Injury 60 0.114
213
P SPP010 Suppressor of Tumorigenicity 3 51 0.114
214
P MCR115 Microvascular Complications of Diabetes 5 66 0.114
215
P PLY019 Polyneuropathy 56 0.113
216
PRP027 Peripheral Vascular Disease 71 0.113
217
KRT002 Keratomalacia 47 0.113
218
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.112
219
CRV045 Cervical Intraepithelial Neoplasia 39 0.112
220
NPH009 Nephrolithiasis 55 0.112
221
c SML038 Small Cell Cancer of the Lung 65 0.112
222
P HRP006 Herpes Simplex 65 0.112
223
P BCL017 B-Cell Lymphoma 58 0.112
224
BRR014 Barrett Esophagus 65 0.111
225
P HPT021 Hepatitis 67 0.111
226
ADR007 Adrenoleukodystrophy 75 0.110
227
TRM010 Traumatic Brain Injury 51 0.110
228
P THL005 Thalassemia 60 0.110
229
AGN016 Aging 56 0.109
230
KRT009 Keratosis 51 0.109
231
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.108
232
BRN071 Brain Injury 49 0.108
233
CHL123 Chlamydia 59 0.108
234
P RTN024 Retinoblastoma 73 0.107
235
c VRL010 Viral Hepatitis 52 0.107
236
c FML008 Familial Retinoblastoma 53 0.107
237
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.107
238
c INH020 Inherited Metabolic Disorder 47 0.107
239
P LPS004 Lupus Erythematosus 61 0.106
240
PLM033 Pulmonary Embolism 59 0.106
241
HMP009 Haemophilus Influenzae 43 0.106
242
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.106
243
c DWL002 Dowling-Degos Disease 1 58 0.106
244
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.106
245
PLC008 Placenta Disease 50 0.106
246
TRP004 Tropical Sprue 41 0.106
247
INT007 Intermediate Coronary Syndrome 55 0.105
248
P HYP076 Hyperthyroidism 55 0.105
249
SRC014 Sarcoma 65 0.105
250
SPN035 Spindle Cell Sarcoma 53 0.105
251
c ACT027 Acute Pancreatitis 60 0.105
252
HYP005 Hypokalemia 55 0.105
253
P NSP012 Nasopharyngeal Carcinoma 66 0.105
254
SVR004 Severe Combined Immunodeficiency 73 0.104
255
P ALC033 Alcohol Use Disorder 58 0.104
256
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.104
257
P MLN008 Melanoma 69 0.104
258
ESP021 Esophageal Cancer 90 0.104
259
ANG054 Angina Pectoris 66 0.104
260
P DMN002 Dementia 66 0.103
261
c ACT068 Acute Cystitis 63 0.103
262
OST003 Osteonecrosis 61 0.103
263
ADR022 Adrenomyeloneuropathy 38 0.103
264
DBT010 Diabetic Neuropathy 54 0.103
265
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.102
266
c HPT001 Hepatitis C 62 0.102
267
LYM019 Lymphosarcoma 46 0.102
268
PPL022 Papilloma 54 0.102
269
ATX019 Ataxia with Vitamin E Deficiency 42 0.102
270
P BRS044 Breast Adenocarcinoma 59 0.102
271
VCC001 Vaccinia 49 0.101
272
P MNN013 Meningitis 66 0.101
273
AST005 Asthma 76 0.101
274
CRD132 Cardiac Conduction Defect 58 0.101
275
P MPL001 Maple Syrup Urine Disease 69 0.100
276
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.100
277
CLN015 Colon Adenocarcinoma 65 0.100
278
CNS004 Constipation 58 0.100
279
P MSC005 Muscular Dystrophy 66 0.100
280
P CNR004 Cone-Rod Dystrophy 2 73 0.100
281
BRN024 Bronchitis 68 0.100
282
HLC007 Helicobacter Pylori Infection 59 0.099
283
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.099
284
P EXN002 Exanthem 57 0.099
285
P ENC004 Encephalitis 61 0.099
286
P GLM007 Glomerulonephritis 57 0.098
287
SQM002 Squamous Cell Papilloma 46 0.098
288
P PNC044 Pancreatitis 61 0.098
289
THY029 Thyroid Carcinoma 59 0.098
290
P ALP008 Alopecia 54 0.097
291
RNL077 Renal Fibrosis 47 0.097
292
IMM167 Immune Deficiency Disease 78 0.097
293
P PRP029 Porphyria 62 0.097
294
P LCT001 Lactic Acidosis 51 0.097
295
P ATR011 Atrial Fibrillation 66 0.097
296
GST050 Gastrointestinal System Disease 56 0.097
297
TTN003 Tetanus 65 0.097
298
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.096
299
c GLY008 Glycogen Storage Disease Ii 70 0.096
300
URL001 Urolithiasis 45 0.096
301
ENT004 Enthesopathy 49 0.096
302
P PNM007 Pneumonia 68 0.095
303
MYL009 Myelodysplastic Syndrome 70 0.095
304
P MLN007 Male Infertility 55 0.095
305
P AST007 Astrocytoma 51 0.095
306
c MLG068 Malignant Glioma 46 0.095
307
ACQ007 Acquired Immunodeficiency Syndrome 60 0.095
308
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.095
309
P SCK005 Sickle Cell Disease 50 0.095
310
ALL014 Allergic Encephalomyelitis 38 0.093
311
ANX010 Anxiety 73 0.093
312
P MYC084 Mycobacterium Tuberculosis 1 68 0.093
313
CHR074 Choriocarcinoma 47 0.092
314
ADL002 Adult Syndrome 70 0.092
315
c HPT016 Hepatitis B 59 0.092
316
LYS012 Lysosomal Acid Lipase Deficiency 65 0.092
317
c FNC043 Fanconi Anemia, Complementation Group E 62 0.092
318
P CYS018 Cystitis 59 0.092
319
PNG002 Pain Agnosia 51 0.091
320
P INF038 Influenza 68 0.091
321
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.091
322
c SVR001 Severe Acute Respiratory Syndrome 62 0.091
323
P ATR005 Atrophic Gastritis 50 0.091
324
P GLY013 Glycogen Storage Disease 60 0.091
325
P MSC003 Muscular Atrophy 52 0.091
326
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.090
327
TXC005 Toxic Shock Syndrome 62 0.090
328
P INS002 in Situ Carcinoma 53 0.089
329
TRN015 Transient Cerebral Ischemia 63 0.089
330
c VSC019 Vesicoureteral Reflux 1 57 0.089
331
c ATR087 Atrial Standstill 1 75 0.089
332
SCK003 Sickle Cell Anemia 74 0.088
333
HNS001 Hansen's Disease 34 0.088
334
P PHC003 Pheochromocytoma 71 0.088
335
P ENC008 Encephalocele 47 0.088
336
P LPR021 Leprosy 3 69 0.088
337
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.088
338
ADR040 Adrenal Gland Pheochromocytoma 46 0.088
339
GST045 Gastroenteritis 59 0.088
340
c PRM038 Primary Agammaglobulinemia 44 0.088
341
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.088
342
CHL004 Cholelithiasis 49 0.087
343
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.087
344
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.087
345
CNT047 Contact Dermatitis 58 0.087
346
LSH001 Leishmaniasis 63 0.087
347
P HDC001 Headache 57 0.087
348
P KLZ004 Kala-Azar 1 41 0.087
349
PRP030 Purpura 54 0.086
350
PSY004 Psychotic Disorder 67 0.086
351
PLC007 Placental Abruption 48 0.086
352
P LNG064 Lung Cancer Susceptibility 3 78 0.086
353
P PLM036 Pulmonary Fibrosis 65 0.086
354
P HML002 Hemolytic Anemia 63 0.085
355
EYD002 Eye Disease 58 0.085
356
P RCT021 Rectum Cancer 52 0.085
357
P BNG032 Benign Mesothelioma 46 0.085
358
P CLC063 Celiac Disease 1 66 0.085
359
c PRS136 Prostate Cancer, Hereditary, 6 33 0.085
360
c PRS130 Prostate Cancer, Hereditary, 8 32 0.085
361
CHL065 Cholangiocarcinoma 68 0.085
362
DPH001 Diphtheria 60 0.085
363
c SVR005 Severe Pre-Eclampsia 50 0.085
364
P URT039 Urticaria 58 0.085
365
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.084
366
EXN003 Exencephaly 31 0.084
367
P RHN004 Rhinitis 57 0.084
368
INT079 Intrahepatic Cholangiocarcinoma 51 0.084
369
c BSL007 Basal Cell Carcinoma 68 0.083
370
P HYD006 Hydrocephalus 66 0.083
371
P CRD119 Cardiac Arrest 67 0.083
372
P HYP265 Hypotonia 43 0.083
373
P INT068 Intestinal Disease 53 0.083
374
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.083
375
IGR001 Ige Responsiveness, Atopic 59 0.083
376
P PRK057 Parkinson Disease, Late-Onset 78 0.083
377
HMS001 Hemosiderosis 54 0.082
378
P ART023 Arthropathy 62 0.082
379
P HYP098 Hypereosinophilic Syndrome 67 0.082
380
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.082
381
P PLM037 Pulmonary Hypertension 67 0.082
382
BRN004 Brain Edema 56 0.081
383
ENT011 Enterocolitis 51 0.081
384
MYL020 Myelomeningocele 51 0.081
385
GRN017 Granulocytopenia 44 0.081
386
RSC001 Rosacea 54 0.081
387
c MCR129 Microvascular Complications of Diabetes 1 66 0.081
388
PLM031 Poliomyelitis 64 0.081
389
LNG031 Lung Benign Neoplasm 51 0.081
390
BRN028 Brain Cancer 74 0.080
391
HYP081 Hypolipoproteinemia 51 0.080
392
IRR002 Irritable Bowel Syndrome 65 0.080
393
P CHR345 Chronic Pain 44 0.080
394
P PYL005 Pyelonephritis 56 0.079
395
ZLL002 Zollinger-Ellison Syndrome 55 0.079
396
P GRF003 Graft-Versus-Host Disease 72 0.079
397
P KDN017 Kidney Cancer 60 0.079
398
c DRR009 Diarrhea 6 46 0.079
399
P GLM040 Glioma Susceptibility 1 81 0.079
400
PRP080 Peripheral Artery Disease 53 0.079
401
IMP005 Impotence 52 0.078
402
VSC002 Vascular Dementia 57 0.078
403
SBC016 Subacute Delirium 44 0.078
404
NWC001 Newcastle Disease 45 0.077
405
INS001 Insulinoma 60 0.077
406
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.077
407
ALL003 Allergic Rhinitis 67 0.077
408
P RRH023 Rare Hereditary Hemochromatosis 41 0.077
409
c BTT014 Beta-Thalassemia 74 0.077
410
CLF056 Cleft Lip with or Without Cleft Palate 47 0.077
411
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.077
412
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.077
413
DSS008 Disease of Mental Health 58 0.076
414
PRT013 Portal Hypertension 59 0.076
415
c HMC039 Hemochromatosis, Type 1 74 0.076
416
GNG013 Gingivitis 59 0.076
417
LPT014 Leptin Deficiency or Dysfunction 74 0.076
418
P CND004 Candidiasis 58 0.076
419
SCH014 Schistosomiasis 57 0.076
420
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.076
421
PLS009 Plasma Cell Neoplasm 51 0.076
422
ORL011 Oral Cancer 60 0.075
423
MSL001 Measles 62 0.075
424
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.075
425
c FML021 Familial Hypercholesterolemia 66 0.075
426
c HPT003 Hepatitis a 62 0.075
427
MST005 Mastitis 53 0.075
428
GTR002 Goiter 53 0.075
429
CLF004 Cleft Lip/palate 54 0.074
430
P NPH012 Nephrotic Syndrome 60 0.074
431
ATS010 Autosomal Recessive Disease 48 0.074
432
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.074
433
CLR109 Colorectal Adenocarcinoma 51 0.074
434
P HYP069 Hyperparathyroidism 63 0.074
435
BLR008 Bilirubin Metabolic Disorder 57 0.073
436
c PLY105 Polycystic Ovary Syndrome 1 38 0.073
437
CYS013 Cystinuria 63 0.073
438
P PRC031 Preeclampsia/eclampsia 1 38 0.073
439
P SYS005 Systemic Scleroderma 68 0.073
440
c LKM005 Leukemia, T-Cell, Chronic 34 0.073
441
P OBS001 Obstructive Jaundice 50 0.073
442
49X006 49, Xxxxy Syndrome 41 0.072
443
END040 Endogenous Depression 55 0.072
444
P SRC025 Sarcoidosis 1 70 0.072
445
LYM133 Lymphoma, Hodgkin, Classic 69 0.072
446
c PNS012 Paine Syndrome 61 0.072
447
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.072
448
c FML035 Familial Hyperlipidemia 55 0.072
449
ORL015 Oral Squamous Cell Carcinoma 43 0.072
450
PNC001 Pancytopenia 54 0.072
451
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.072
452
P MTH008 Methylmalonic Acidemia 50 0.072
453
ERY051 Erythroleukemia, Familial 56 0.072
454
P CTN015 Cutaneous T Cell Lymphoma 49 0.072
455
OVR094 Ovarian Epithelial Cancer 38 0.072
456
PLY150 Polykaryocytosis Inducer 31 0.071
457
P RTN018 Retinal Disease 53 0.071
458
PST021 Postpartum Depression 50 0.071
459
ALL006 Allergic Asthma 56 0.071
460
c SCL052 Scleroderma, Familial Progressive 61 0.071
461
DBT004 Diabetic Polyneuropathy 49 0.071
462
CVD001 Covid-19 44 0.071
463
CHR178 Chromosomal Triplication 35 0.071
464
OTT002 Otitis Media 72 0.071
465
P CNJ013 Conjunctivitis 65 0.071
466
P FTL001 Fetal Alcohol Syndrome 57 0.070
467
P INT143 Interstitial Cystitis 61 0.070
468
TLN003 Telangiectasis 52 0.070
469
P HYP061 Hypertrophic Cardiomyopathy 70 0.070
470
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.070
471
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.070
472
DYS073 Dysphagia 50 0.070
473
P ADL010 Adult Respiratory Distress Syndrome 65 0.069
474
TRN018 Transitional Cell Carcinoma 56 0.069
475
PPL001 Papillary Adenoma 44 0.069
476
P END044 Endometriosis 63 0.069
477
NRT001 Neurotic Disorder 53 0.069
478
PNC129 Pancreatic Adenocarcinoma 68 0.068
479
c PRD040 Periodontitis, Chronic 53 0.068
480
c SPN225 Spondyloarthropathy 1 73 0.068
481
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.068
482
c MCR112 Microvascular Complications of Diabetes 2 41 0.068
483
P BRB001 Beriberi 46 0.068
485
P VSC011 Vasculitis 62 0.068
486
MTH086 Methotrexate Toxicity 33 0.068
487
PST092 Posttransplant Acute Limbic Encephalitis 29 0.068
488
P SCL018 Scoliosis 60 0.067
489
P MDL005 Medulloblastoma 77 0.067
490
ART016 Aortic Aneurysm 69 0.067
491
c MNN043 Meningioma, Familial 74 0.067
492
VRC005 Varicose Veins 60 0.067
493
c CHR064 Chronic Monocytic Leukemia 33 0.067
494
P BNC003 Bone Cancer 58 0.067
495
CRH005 Crohn's Colitis 53 0.067
496
CHR073 Choreatic Disease 52 0.067
497
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.067
498
P TYR004 Tyrosinemia 58 0.067
499
P END033 Endocarditis 57 0.067
500
P MJR007 Major Affective Disorder 1 43 0.067
501
P OPN001 Open-Angle Glaucoma 49 0.067
502
PYL006 Pyloric Stenosis 48 0.066
503
MSC007 Muscle Hypertrophy 64 0.066
504
CRN030 Coronary Stenosis 50 0.066
505
FDL002 Food Allergy 51 0.066
506
P SLP006 Sleep Apnea 69 0.066
507
ANR040 Aneurysm 59 0.066
508
P PLY018 Polycythemia 56 0.066
509
BCT002 Bacterial Vaginosis 53 0.066
510
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.066
511
c FML001 Familial Atrial Fibrillation 65 0.066
512
HMG005 Hemoglobinopathy 56 0.066
513
PLG002 Plague 63 0.066
514
P ANP001 Anaplastic Large Cell Lymphoma 58 0.065
515
P UVT001 Uveitis 57 0.065
516
c PSR017 Psoriasis 2 53 0.065
517
c PSR023 Psoriasis 1 52 0.065
518
c PSR032 Psoriasis 11 47 0.065
519
c PSR028 Psoriasis 7 42 0.065
520
c PSR018 Psoriasis 13 41 0.065
521
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.065
522
P DNG005 Dengue Virus 59 0.065
523
P OPT006 Optic Nerve Disease 60 0.065
524
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.065
525
P SHR001 Short Bowel Syndrome 53 0.065
526
P VNT002 Ventricular Septal Defect 60 0.065
527
KWS001 Kwashiorkor 44 0.064
528
SPL018 Splenomegaly 48 0.064
529
KPS004 Kaposi Sarcoma 75 0.064
530
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.064
531
MXD026 Mixed Glioma 45 0.064
532
P DYS154 Dystonia 65 0.064
533
AMN003 Amnestic Disorder 54 0.064
534
c WLM018 Wilms Tumor 5 61 0.064
535
VRL011 Viral Infectious Disease 61 0.064
536
SFT003 Soft Tissue Sarcoma 56 0.064
537
PTT037 Pituitary Tumors 44 0.064
538
PRP036 Peripheral T-Cell Lymphoma 53 0.064
539
RTN017 Retinal Detachment 61 0.063
540
WTH001 Withdrawal Disorder 48 0.063
541
PSR001 Psoriatic Arthritis 61 0.063
542
PRT038 Protein-Energy Malnutrition 54 0.063
543
CRT017 Cartilage Disease 54 0.063
544
c MJR003 Major Affective Disorder 6 33 0.063
545
c MJR006 Major Affective Disorder 5 33 0.063
546
c ACT135 Acute Graft Versus Host Disease 52 0.063
547
P PLY014 Polycystic Kidney Disease 62 0.063
548
P PRS038 Personality Disorder 65 0.063
549
OST017 Osteomyelitis 64 0.062
550
CHR100 Chronic Ulcer of Skin 55 0.062
551
GST040 Gastric Adenocarcinoma 70 0.062
552
P PLL002 Pellagra 46 0.062
553
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.062
554
c GRV008 Graves Disease 1 56 0.062
555
HDN002 Head Injury 46 0.062
556
c MJR008 Major Affective Disorder 2 35 0.062
557
c MJR023 Major Affective Disorder 7 33 0.062
558
c MJR004 Major Affective Disorder 4 28 0.062
559
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.062
560
DYS015 Dysentery 52 0.062
561
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.062
562
P ALP009 Alopecia Areata 60 0.062
563
LYM027 Lymphopenia 58 0.062
564
FBR047 Fibromyalgia 58 0.061
565
LKP003 Leukoplakia 39 0.061
566
P NRV007 Nervous System Disease 66 0.061
567
P FNC004 Fanconi Syndrome 50 0.061
568
SPS057 Spasticity 45 0.061
569
GLS001 Gliosarcoma 54 0.061
571
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.061
572
ETN001 Eating Disorder 60 0.061
573
c JVN010 Juvenile Rheumatoid Arthritis 64 0.060
574
MSC157 Muscular Dystrophy, Duchenne Type 72 0.060
575
P FML011 Familial Adenomatous Polyposis 72 0.060
576
c BRN108 Branchiootic Syndrome 1 62 0.060
577
P HMP007 Hemophilia 51 0.060
578
SCH003 Schizophreniform Disorder 56 0.060
579
SPN051 Spondylitis 51 0.060
580
INF009 Inflammatory Spondylopathy 31 0.060
581
GLS018 Glass Syndrome 57 0.060
582
IGG001 Iga Glomerulonephritis 48 0.060
583
P FNC034 Fanconi Renotubular Syndrome 2 40 0.060
584
ANR007 Anorexia Nervosa 63 0.060
585
P APL001 Aplastic Anemia 74 0.060
586
HYD002 Hydronephrosis 60 0.059
587
c HYP272 Hypercholesterolemia, Familial, 3 44 0.059
589
MLN073 Melanosis, Neurocutaneous 45 0.059
590
APH001 Aphthous Stomatitis 57 0.059
591
P HYP040 Hypospadias 51 0.059
592
SKN019 Skin Melanoma 68 0.059
593
RHM001 Rheumatic Fever 60 0.059
594
MCR013 Microphthalmia 57 0.059
595
HYP017 Hypophosphatemia 50 0.059
596
KRT013 Keratolytic Winter Erythema 46 0.059
597
HYP141 Hyperphenylalaninemia 39 0.059
598
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.059
599
c OVR114 Ovarian Cancer 1 38 0.059
600
INT002 Intermittent Claudication 61 0.059
601
P THY023 Thymoma 65 0.059
602
c THY107 Thymoma, Familial 52 0.059
603
P MNC007 Monocytic Leukemia 53 0.059
604
c ALP101 Alpha-Thalassemia 62 0.059
605
TYP007 Typhoid Fever 63 0.059
606
URT010 Ureteral Obstruction 45 0.059
607
CRC021 Carcinosarcoma 62 0.059
608
P PRV006 Pervasive Developmental Disorder 57 0.058
609
RDN001 Reading Disorder 40 0.058
610
GNG012 Gingival Overgrowth 51 0.058
611
P GRV001 Graves' Disease 55 0.058
612
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.058
613
TRP009 Triple X Syndrome 42 0.058
614
c MCL013 Mucolipidosis Iv 66 0.058
615
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.058
616
P CHN012 Chondrosarcoma 56 0.058
617
THY030 Thyroid Gland Disease 52 0.058
618
LMY002 Leiomyoma 52 0.058
619
P MYC008 Myocarditis 59 0.057
620
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.057
621
ABD010 Abdominal Wall Defect 36 0.057
622
c CHR682 Chronic Bilirubin Encephalopathy 39 0.057
623
P ATX030 Ataxia-Telangiectasia 82 0.057
624
P OLG002 Oligodendroglioma 67 0.057
625
P PTT006 Pituitary Adenoma 55 0.057
626
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.057
627
P ORF002 Orofacial Cleft 44 0.057
628
MLK006 Milk Allergy 48 0.057
629
P SNS001 Sensorineural Hearing Loss 60 0.057
630
THR004 Thrombocytosis 51 0.057
631
P MTR014 Motor Neuron Disease 65 0.057
632
GRD007 Grade Iii Astrocytoma 59 0.057
633
ATN004 Autonomic Neuropathy 45 0.057
634
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 0.057
635
CNN005 Connective Tissue Disease 68 0.057
636
c INF071 Inflammatory Bowel Disease 1 67 0.057
637
P TRC086 Trichohepatoenteric Syndrome 1 62 0.057
638
CHR066 Chronic Fatigue Syndrome 61 0.057
639
DRY001 Dry Eye Syndrome 47 0.056
640
HRT011 Heart Septal Defect 50 0.056
641
YLL002 Yellow Fever 61 0.056
642
P ADL017 Adult T-Cell Leukemia 56 0.056
643
SCH012 Schizoaffective Disorder 50 0.056
644
P MCR010 Microcephaly 59 0.056
645
c SYS043 Systemic Lupus Erythematosus 1 38 0.056
646
TTH004 Tethered Spinal Cord Syndrome 35 0.056
647
P PRG092 Pregnancy Loss, Recurrent 1 40 0.056
648
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.056
649
HMT002 Hematologic Cancer 62 0.056
650
c GLC092 Glaucoma, Primary Open Angle 62 0.055
651
c MST023 Mesothelioma, Malignant 57 0.055
652
FNG017 Fungal Infectious Disease 53 0.055
653
AZS001 Azoospermia 50 0.055
654
HPT022 Hepatoblastoma 56 0.055
655
SPR126 Superior Semicircular Canal Dehiscence 40 0.055
656
c HMG029 Hemoglobin Se Disease 39 0.055
657
PHR003 Pharyngitis 57 0.055
658
P MLG074 Malignant Mesenchymoma 40 0.055
659
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.055
660
P RBL001 Rubella 59 0.055
661
CYT008 Cytomegalovirus Infection 57 0.055
662
KRT019 Keratitis, Hereditary 65 0.055
663
PRS047 Prostatitis 56 0.055
664
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.055
665
FCT007 Factor Vii Deficiency 67 0.055
666
VGN023 Vaginitis 54 0.055
667
c ACT042 Acute Pyelonephritis 46 0.055
668
KRT006 Keratoconjunctivitis 53 0.054
669
PLS007 Plasmodium Falciparum Malaria 52 0.054
670
KHL003 Kohlschutter-Tonz Syndrome 65 0.054
671
P TRT010 Teratoma 52 0.054
672
MCR004 Macroglobulinemia 49 0.054
673
CRB037 Cerebral Palsy 69 0.054
674
c EXD008 Exudative Vitreoretinopathy 1 71 0.054
675
PRM003 Premature Ejaculation 44 0.054
676
P ANG001 Angelman Syndrome 69 0.054
677
NRM005 Neuromuscular Disease 64 0.053
678
MCL006 Macular Retinal Edema 55 0.053
679
P MYS003 Myasthenia Gravis 68 0.053
680
MYC006 Mycosis Fungoides 66 0.053
681
P MTC069 Mitochondrial Disorders 56 0.053
682
c BCT007 Bacterial Meningitis 55 0.053
683
P TXP001 Toxoplasmosis 60 0.053
684
GLB001 Gilbert Syndrome 58 0.053
685
RBF001 Riboflavin Deficiency 49 0.053
686
P FLL037 Follicular Lymphoma 67 0.053
687
ALC006 Alcoholic Hepatitis 61 0.053
688
P LRY044 Larynx Cancer 55 0.053
689
STT009 Sutton Disease 2 30 0.053
690
VSC003 Visceral Leishmaniasis 55 0.053
691
P LCH002 Lichen Planus 53 0.053
692
c MLG079 Malignant Pleural Mesothelioma 42 0.052
693
ACR007 Acromegaly 71 0.052
694
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.052
695
P MMP001 Mumps 58 0.052
696
NRN004 Neuroendocrine Tumor 55 0.052
697
ACT058 Active Peptic Ulcer Disease 55 0.052
698
FCL014 Focal Epilepsy 54 0.052
699
BTN004 Biotin Deficiency 38 0.052
700
OBS002 Obsessive-Compulsive Disorder 68 0.052
701
AMN001 Amenorrhea 54 0.052
702
SPT004 Septic Arthritis 58 0.052
703
SPN041 Spinal Cord Disease 56 0.052
704
PRD004 Prediabetes Syndrome 47 0.052
705
P ANT006 Antiphospholipid Syndrome 55 0.052
706
P CRB088 Cerebral Atrophy 37 0.052
707
P HMR003 Hemorrhagic Disease 53 0.052
708
ECT026 Ectopic Pregnancy 50 0.052
709
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.052
710
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.052
711
NRT004 Neuritis 52 0.052
712
P CLL015 Collagen Disease 47 0.052
713
PYR016 Pyridoxine Deficiency 30 0.052
714
CRD223 Cardiac Arrhythmia 60 0.052
715
c DNG003 Dengue Disease 59 0.051
716
URN010 Urinary Tract Obstruction 55 0.051
717
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.051
718
DWR001 Dwarfism 44 0.051
719
EWN003 Ewing Sarcoma 69 0.051
720
NWB001 Newborn Respiratory Distress Syndrome 58 0.051
721
P MYS005 Myositis 56 0.051
722
PYR009 Pyridoxine Deficiency Anemia 34 0.051
723
ACR041 Acromelic Frontonasal Dysostosis 52 0.051
724
P SLP005 Sleep Disorder 59 0.051
725
P SBS003 Substance Abuse 55 0.051
726
P VSC018 Visceral Steatosis 33 0.051
727
THY122 Thyroid Gland Cancer 57 0.051
728
INT066 Interstitial Lung Disease 60 0.050
729
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.050
730
P VTR007 Vitreoretinopathy 46 0.050
731
BRN056 Bronchopulmonary Dysplasia 57 0.050
732
P THY032 Thyroiditis 52 0.050
733
c SCN007 Secondary Hyperparathyroidism 51 0.050
734
P HRD011 Hereditary Spherocytosis 60 0.050
735
P BNG030 Benign Ependymoma 60 0.050
736
P SYP003 Syphilis 58 0.050
737
IDP070 Idiopathic Scoliosis 42 0.050
738
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.050
739
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.050
740
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.050
741
P SPN237 Spina Bifida Aperta 20 0.050
742
HYP025 Hyperphosphatemia 48 0.050
743
BCT004 Bacteriuria 49 0.050
744
RTN020 Retinal Vascular Disease 46 0.050
745
HYP457 Hypertrophic Scars 42 0.050
746
KRN002 Kearns-Sayre Syndrome 63 0.050
747
P HML001 Hemolytic-Uremic Syndrome 53 0.050
748
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.050
749
ATM052 Autoimmune Disease 1 37 0.050
750
KRT001 Keratoconjunctivitis Sicca 49 0.050
751
c JVN061 Juvenile Arthritis 60 0.049
752
CLL010 Cellular Ependymoma 54 0.049
753
ACN002 Acanthosis Nigricans 60 0.049
754
P NRC002 Narcolepsy 52 0.049
755
c INF145 Infantile Liver Failure Syndrome 1 50 0.049
756
ILT001 Ileitis 50 0.049
757
PLY001 Polycythemia Vera 69 0.049
759
PRP016 Paraplegia 52 0.049
760
ACT003 Acute Kidney Tubular Necrosis 45 0.049
761
TXC002 Toxic Encephalopathy 53 0.049
762
P MTH007 Methemoglobinemia 46 0.049
763
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.049
764
P PNC025 Panic Disorder 53 0.048
765
P OCL013 Oculodentodigital Dysplasia 69 0.048
766
PPL049 Papillon-Lefevre Syndrome 65 0.048
767
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.048
768
CHL061 Childhood Leukemia 48 0.048
769
P PRC012 Pericardial Effusion 51 0.048
770
HMP001 Hemopericardium 48 0.048
771
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.048
772
CLL003 Cellulitis 54 0.048
773
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.048
774
TST015 Testicular Disease 43 0.048
775
P CHR071 Charcot-Marie-Tooth Disease 65 0.048
776
P EPD016 Epidermolysis Bullosa 53 0.048
777
NNT012 Neonatal Jaundice 53 0.048
778
PRS063 Paresthesia 41 0.048
779
c PRM005 Primary Hyperparathyroidism 58 0.047
780
ACT084 Acute Stress Disorder 47 0.047
781
BCK006 Back Pain 42 0.047
782
P THR015 Thrombophilia 51 0.047
783
CRP001 Carpal Tunnel Syndrome 67 0.047
784
MYL031 Myeloproliferative Neoplasm 66 0.047
785
P ANR048 Aniridia 1 63 0.047
786
INC002 Inclusion Body Myositis 58 0.047
787
LYM009 Lymphocytic Choriomeningitis 47 0.047
788
TTH006 Tooth Disease 46 0.047
789
ORL012 Oral Leukoplakia 39 0.047
790
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.047
791
EXC002 Exocrine Pancreatic Insufficiency 42 0.047
792
GLS007 Glossitis 47 0.047
793
P NRF002 Neurofibromatosis 56 0.047
794
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.047
795
c FLL041 Follicular Lymphoma 1 49 0.047
796
HYP043 Hyperandrogenism 48 0.047
797
PLC006 Placental Choriocarcinoma 36 0.047
798
PST028 Post-Traumatic Stress Disorder 58 0.047
799
P MYP006 Myopia 55 0.047
800
ORT008 Orotic Aciduria 55 0.047
801
INT067 Interstitial Nephritis 48 0.047
802
P BLR006 Biliary Tract Disease 47 0.047
803
DBT002 Diabetic Autonomic Neuropathy 41 0.047
804
c CNT035 Central Nervous System Disease 52 0.046
805
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.046
806
BLD131 Bladder Urothelial Carcinoma 62 0.046
807
HRP004 Herpes Zoster 60 0.046
808
P PMP001 Pemphigus 54 0.046
809
P HMR005 Hemorrhoid 46 0.046
810
CRT013 Carotid Stenosis 50 0.046
811
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.046
812
MLT157 Multiple System Atrophy 1 70 0.046
813
CHY002 Chylomicron Retention Disease 65 0.046
814
BRN002 Bronchiolitis 59 0.046
815
ASP007 Aspiration Pneumonia 48 0.046
816
BRS099 Breast Ductal Carcinoma 62 0.046
817
P DRM010 Dermatomyositis 61 0.046
818
ANG005 Anogenital Venereal Wart 55 0.046
819
c CHR418 Chronic Leukemia 49 0.046
820
VRC001 Varicocele 49 0.046
821
P HYP726 Hypercalcemia, Infantile, 1 58 0.045
822
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.045
823
BRN038 Bronchial Disease 53 0.045
824
END041 Endometrial Adenocarcinoma 63 0.045
825
DCT002 Ductal Carcinoma in Situ 59 0.045
826
INT303 Intracranial Hypertension, Idiopathic 57 0.045
827
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.045
828
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.045
829
WLL004 Wallerian Degeneration 39 0.045
830
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.045
831
P CHR012 Chronic Granulomatous Disease 67 0.045
832
c WLM013 Wilms Tumor 1 65 0.045
833
CHK001 Chikungunya 57 0.045
834
CMR002 Coumarin Resistance 56 0.045
835
ORL005 Oral Candidiasis 56 0.045
836
CNT033 Central Nervous System Cancer 47 0.045
837
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.045
838
RFR010 Refractory Anemia 48 0.045
839
GNG003 Gingival Recession 44 0.045
840
MTH047 Methanol Poisoning 34 0.045
841
CLR030 Clear Cell Renal Cell Carcinoma 53 0.044
842
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.044
843
GNT002 Giant Cell Glioblastoma 50 0.044
844
PNC034 Pancreas Disease 48 0.044
845
LWC001 Low Compliance Bladder 43 0.044
846
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.044
847
P GLL020 Gallbladder Disease 57 0.044
848
P OMP004 Omphalocele 50 0.044
849
CRV038 Cervical Squamous Cell Carcinoma 58 0.044
850
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.044
851
INT017 Intestinal Schistosomiasis 48 0.044
852
P BLD062 Bile Duct Cancer 67 0.044
853
HMR039 Hemorrhage, Intracerebral 57 0.044
854
NPH003 Nephrocalcinosis 51 0.044
855
FSC004 Fasciitis 50 0.044
856
P END046 Endometritis 49 0.044
857
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.044
858
VTM033 Vitamin K Deficiency Bleeding 48 0.044
859
LPT006 Leptin Receptor Deficiency 48 0.044
860
GST030 Gastrinoma 45 0.044
861
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.043
862
ANG049 Angioedema Induced by Ace Inhibitors 40 0.043
863
LSC001 Lesch-Nyhan Syndrome 62 0.043
864
WST001 West Syndrome 61 0.043
865
P RNL015 Renal Hypertension 47 0.043
866
RST023 Resting Heart Rate, Variation in 41 0.043
867
c XNT010 Xanthinuria, Type I 53 0.043
868
c PNC106 Pancreatic Agenesis 1 51 0.043
869
HMG002 Hemoglobinuria 50 0.043
870
RTC005 Reticulosarcoma 47 0.043
871
TST014 Testicular Cancer 46 0.043
872
OLG001 Oligospermia 45 0.043
873
BRN032 Brain Glioma 45 0.043
874
P SCL057 Scoliosis, Isolated 1 41 0.043
875
THR013 Thoracic Outlet Syndrome 54 0.043
876
ALC009 Alcoholic Liver Cirrhosis 53 0.043
877
LRN003 Learning Disability 49 0.043
878
DCB001 Decubitus Ulcer 61 0.043
879
TRC003 Trichomoniasis 53 0.043
880
VGN019 Vaginal Discharge 46 0.043
881
GST020 Gastric Antral Vascular Ectasia 41 0.043
882
HRN029 Hearing Loss, Noise-Induced 37 0.043
883
ATR057 Atrioventricular Block 55 0.043
884
P RST001 Restless Legs Syndrome 54 0.043
885
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.043
886
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.043
887
HDG004 Hodgkin's Granuloma 23 0.043
888
HDG006 Hodgkin's Paragranuloma 22 0.043
889
MSS001 Masa Syndrome 62 0.042
890
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.042
891
ACD008 Acid-Labile Subunit Deficiency 54 0.042
892
SNS003 Sensory Peripheral Neuropathy 54 0.042
893
DGN001 Degenerative Disc Disease 48 0.042
894
ANS023 Anus, Imperforate 56 0.042
895
ADN011 Adenoid Cystic Carcinoma 70 0.042
896
c ART101 Aortic Valve Disease 2 65 0.042
897
P PLY041 Polymyositis 57 0.042
898
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.042
899
PPL002 Papillary Carcinoma 47 0.042
900
ASP004 Asphyxia Neonatorum 46 0.042
901
P AVS003 Avascular Necrosis 42 0.042
902
P ATR010 Atrial Heart Septal Defect 60 0.042
903
NRD004 Neurodegeneration Due to Cerebral Folate Transport Deficiency 39 0.042
904
ORN001 Ornithosis 38 0.042
905
LMB062 Limb Ischemia 55 0.042
906
HLL004 Hellp Syndrome 54 0.042
907
SPR005 Superficial Basal Cell Carcinoma 46 0.042
908
P SBR004 Seborrheic Dermatitis 45 0.042
909
c PRG106 Progressive Muscular Dystrophy 33 0.042
910
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.042
911
BLL006 Bullous Pemphigoid 62 0.042
912
P GLL018 Gallbladder Cancer 57 0.042
913
c BSL024 Basal Cell Carcinoma 1 56 0.042
914
NRG002 Neurogenic Bladder 55 0.042
915
SKN013 Skin Benign Neoplasm 51 0.042
916
c BCT013 Bacterial Pneumonia 48 0.042
917
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 40 0.042
918
CYT018 Cytochrome P450 2d6 Variant 27 0.042
919
MYL005 Myelofibrosis 70 0.042
920
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.042
921
CRC006 Carcinoid Syndrome 55 0.042
922
CRN017 Coronary Thrombosis 47 0.042
923
CLN045 Colonic Benign Neoplasm 46 0.042
924
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.042
925
CHL045 Choline Deficiency Disease 39 0.042
926
FTL021 Fetal Macrosomia 42 0.042
927
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.041
928
KWS002 Kawasaki Disease 65 0.041
929
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.041
930
c LKM070 Leukemia, Acute Monocytic 57 0.041
931
DBT006 Diabetic Macular Edema 48 0.041
932
HMR023 Hemorrhagic Cystitis 45 0.041
933
SKN005 Skin Atrophy 43 0.041
934
BNM001 Bone Marrow Cancer 43 0.041
935
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.041
936
HML018 Homologous Wasting Disease 22 0.041
937
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.041
938
LNG039 Lung Squamous Cell Carcinoma 66 0.041
939
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.041
940
P RTN022 Retinal Vein Occlusion 53 0.041
941
P PRP003 Porphyria Cutanea Tarda 67 0.041
942
APN008 Apnea, Obstructive Sleep 64 0.041
943
CLN019 Colonic Disease 47 0.041
944
GST071 Gastrointestinal Carcinoma 47 0.041
945
LPD009 Lipid Storage Disease 46 0.041
946
PLL012 Pollen Allergy 46 0.041
947
EPD015 Epidemic Typhus 45 0.041
948
NRF007 Neurofibroma 64 0.041
949
RCT015 Reactive Arthritis 61 0.041
950
PMP006 Pemphigus Vulgaris, Familial 57 0.041
951
P STR020 Strabismus 55 0.041
952
HST010 Histiocytosis 48 0.041
953
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.041
954
RTR008 Root Resorption 45 0.041
955
MYF002 Myofascial Pain Syndrome 42 0.041
956
MCH006 Mechanical Strabismus 42 0.041
957
KLB003 Klebsiella Pneumonia 41 0.041
958
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.041
959
EXF001 Exfoliation Syndrome 56 0.040
960
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.040
961
MCR011 Microinvasive Gastric Cancer 43 0.040
962
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.040
963
MST020 Mast Cell Activation Syndrome 26 0.040
964
PRX085 Preaxial Hallucal Polydactyly 28 0.040
965
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.040
966
c MLG084 Malignant Fibrous Histiocytoma 63 0.040
967
TRC008 Trachoma 53 0.040
968
P SML001 Small Cell Carcinoma 52 0.040
969
STP011 Stapes Ankylosis with Broad Thumbs and Toes 49 0.040
970
GRM010 Germ Cells Tumors 34 0.040
971
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.040
972
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.040
973
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.040
974
ERY003 Erythema Multiforme 58 0.040
975
OST011 Osteomalacia 52 0.040
976
BRN009 Burning Mouth Syndrome 50 0.040
977
DMP001 Dumping Syndrome 44 0.040
978
ATX010 Ataxia Neuropathy Spectrum 34 0.040
979
ACT064 Acute Necrotizing Encephalitis 33 0.040
980
BLD137 Blood Group--Ahonen 16 0.040
981
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.040
982
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.040
983
ORL004 Oral Submucous Fibrosis 55 0.040
984
BWN001 Bowen-Conradi Syndrome 52 0.040
985
c SPR086 Spermatogenic Failure 3 44 0.040
986
BLR013 Biliary Tract Cancer 42 0.040
987
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.039
988
BCK003 Background Diabetic Retinopathy 46 0.039
989
GST012 Gastroesophageal Junction Adenocarcinoma 46 0.039
990
P EHL001 Ehlers-Danlos Syndrome 58 0.039
991
LMY014 Leiomyoma, Uterine 56 0.039
992
OCL006 Ocular Hypertension 53 0.039
993
MYF001 Myofibroma 45 0.039
994
MRS001 Marasmus 42 0.039
995
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.039
996
AYM001 Ayme-Gripp Syndrome 57 0.039
997
EXP004 Exophthalmos 52 0.039
998
ACT200 Acute Monoblastic Leukemia 52 0.039
999
NTR018 Neutrophilia, Hereditary 52 0.039
1000
P BRN035 Brain Stem Glioma 52 0.039
1001
MCP006 Mucoepidermoid Carcinoma 50 0.039
1002
AMB002 Amblyopia 49 0.039
1003
CLS016 Clostridium Difficile Colitis 48 0.039
1004
SPP007 Suppression Amblyopia 39 0.039
1005
DFF036 Differentiated Thyroid Carcinoma 52 0.039
1006
PRM020 Premenstrual Tension 40 0.039
1007
RTC012 Reticuloendotheliosis, X-Linked 39 0.039
1008
BSL036 Basal Cell Nevus Syndrome 73 0.039
1009
P URF003 Urofacial Syndrome 1 57 0.039
1010
P DRM007 Dermatitis Herpetiformis 55 0.039
1011
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 52 0.039
1012
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.039
1013
URN009 Urinary System Disease 48 0.039
1014
LWR018 Lower Urinary Tract Obstruction, Congenital 40 0.039
1015
SPC030 Specific Language Disorder 26 0.039
1016
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.038
1017
SPP008 Suppurative Otitis Media 45 0.038
1018
c DRM054 Dermatitis, Atopic, 2 44 0.038
1019
VLV047 Volvulus of Midgut 49 0.038
1020
GRW007 Growth Hormone Deficiency 46 0.038
1021
c ACT004 Acute Diarrhea 39 0.038
1022
P OCY003 Oocyte Maturation Defect 1 45 0.038
1023
GRD001 Giardiasis 45 0.038
1024
P RRT020 Rare Tumor 41 0.038
1025
c DRM040 Dermatitis Herpetiformis, Familial 35 0.038
1026
GLT005 Glutamate Formiminotransferase Deficiency 41 0.038
1027
SVR097 Severe Cutaneous Adverse Reaction 69 0.038
1028
ART002 Arts Syndrome 64 0.038
1029
SZR001 Sezary's Disease 60 0.038
1030
THR016 Thrombophlebitis 51 0.038
1031
MTC005 Mitochondrial Metabolism Disease 49 0.038
1032
SPS019 Spastic Paraparesis 38 0.038
1033
P TTR001 Tetralogy of Fallot 70 0.038
1034
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.038
1035
P PTN014 Patent Ductus Arteriosus 1 60 0.038
1036
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.038
1037
GST009 Gastroschisis 53 0.038
1038
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.038
1039
CHR005 Chorioamnionitis 51 0.038
1040
PLP001 Pulpitis 49 0.038
1041
GST010 Gestational Trophoblastic Neoplasm 46 0.038
1042
DFF003 Diffuse Scleroderma 41 0.038
1043
CRN020 Coronary Restenosis 39 0.038
1044
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.038
1045
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.037
1046
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.037
1047
CRV040 Cervix Carcinoma 51 0.037
1048
KRT008 Keratopathy 47 0.037
1049
ORL013 Oral Lichen Planus 45 0.037
1050
ERY066 Erythema Multiforme Major 30 0.037
1051
PRL032 Perlman Syndrome 57 0.037
1052
PLS016 Plasma Cell Leukemia 53 0.037
1053
PNN001 Panniculitis 51 0.037
1054
c SCH085 Schizophrenia 2 33 0.037
1055
P OST001 Osteopetrosis 70 0.037
1056
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.037
1057
PLM012 Pulmonary Sarcoidosis 53 0.037
1058
c LRG001 Large Cell Carcinoma 50 0.037
1059
c INF023 Inflammatory Breast Carcinoma 50 0.037
1060
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.037
1061
NCR007 Necrotizing Fasciitis 48 0.037
1062
P HMN032 Human Herpesvirus 8 47 0.037
1063
MNN020 Meningococcal Infection 46 0.037
1064
P CRN024 Corneal Disease 44 0.037
1065
ANC001 Ancylostomiasis 43 0.037
1066
c PNC108 Pancreatitis, Hereditary 70 0.037
1067
P CYS039 Cystic Kidney Disease 54 0.037
1068
RNL011 Renal Osteodystrophy 50 0.037
1069
GST049 Gastrointestinal System Cancer 49 0.037
1070
c BPL002 Bipolar I Disorder 49 0.037
1071
EPL131 Epilepsy, Pyridoxine-Dependent 49 0.037
1072
MLT006 Multidrug-Resistant Tuberculosis 48 0.037
1073
KHN001 Kuhnt-Junius Degeneration 47 0.037
1074
GLC036 Glucagonoma 45 0.037
1075
PRS042 Prostate Disease 43 0.037
1076
MCR103 Microtia 43 0.036
1077
P HYP009 Hypertrophic Pyloric Stenosis 41 0.036
1078
CMM004 Common Variable Immunodeficiency 68 0.036
1079
FLL027 Fallopian Tube Carcinoma 67 0.036