Search results for Tocopherol

979 hits were found for Tocopherol

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.155
2
ATX019 Ataxia with Vitamin E Deficiency 42 0.149
3
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.142
4
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.130
5
ATH013 Atherosclerosis Susceptibility 65 0.124
6
P LVR013 Liver Disease 68 0.118
7
P PRS040 Prostate Cancer 97 0.112
8
P CRN300 Coronary Heart Disease 1 63 0.112
9
c HYP836 Hypercholesterolemia, Familial, 1 73 0.110
10
P MSC005 Muscular Dystrophy 66 0.110
11
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.105
12
P MYP004 Myopathy 70 0.103
13
P KDN018 Kidney Disease 72 0.100
14
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.100
15
48X005 48,xyyy 39 0.098
16
P CLR023 Colorectal Cancer 99 0.096
17
P ALZ034 Alzheimer Disease 88 0.096
18
HYP066 Hyperglycemia 61 0.096
19
c CHR684 Chronic Kidney Disease 70 0.093
20
P CTR002 Cataract 60 0.090
21
ISC004 Ischemia 58 0.090
22
P SKN015 Skin Carcinoma 66 0.088
23
FTT001 Fatty Liver Disease 61 0.088
24
HYP266 Hypoxia 57 0.088
25
AST005 Asthma 76 0.085
26
LVR012 Liver Cirrhosis 62 0.085
27
CYS001 Cystic Fibrosis 81 0.082
28
P ADN016 Adenocarcinoma 64 0.079
29
c PRC016 Pre-Eclampsia 63 0.079
30
P CRD246 Cardiovascular System Disease 57 0.079
31
END086 End Stage Renal Disease 51 0.079
32
HYP781 Hypoascorbemia 51 0.079
33
P BRS047 Breast Cancer 97 0.076
34
P DBT009 Diabetes Mellitus 64 0.076
35
P VSC007 Vascular Disease 63 0.076
36
OST003 Osteonecrosis 61 0.076
37
INT002 Intermittent Claudication 61 0.076
38
P RHN004 Rhinitis 57 0.076
39
HMS001 Hemosiderosis 54 0.076
40
ART140 Arteries, Anomalies of 52 0.076
41
P RRH023 Rare Hereditary Hemochromatosis 41 0.076
42
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.076
43
ABT001 Abetalipoproteinemia 69 0.073
44
ALL003 Allergic Rhinitis 67 0.073
45
PRT036 Peritonitis 64 0.073
46
CHL068 Cholestasis 61 0.073
47
VSL002 Visual Epilepsy 59 0.073
48
ADN018 Adenoma 59 0.073
49
ALL006 Allergic Asthma 56 0.073
50
P NRP001 Neuropathy 56 0.073
51
P SZR006 Seizure Disorder 56 0.073
52
CYT002 Cytokine Deficiency 42 0.073
53
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.073
55
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.069
56
P NRB001 Neuroblastoma 72 0.069
57
P HYP098 Hypereosinophilic Syndrome 67 0.069
58
ANG054 Angina Pectoris 66 0.069
59
LPP008 Lipoprotein Quantitative Trait Locus 62 0.069
60
ALL026 Allergic Hypersensitivity Disease 62 0.069
61
ORL011 Oral Cancer 60 0.069
62
P THL005 Thalassemia 60 0.069
63
MST005 Mastitis 53 0.069
64
c PCH010 Pachyonychia Congenita 3 44 0.069
65
P HPT023 Hepatocellular Carcinoma 100 0.066
66
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.066
67
MLR004 Malaria 81 0.066
68
OST012 Osteoarthritis 78 0.066
69
c BTT014 Beta-Thalassemia 74 0.066
70
DFC004 Deficiency Anemia 70 0.066
71
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.066
72
P HML002 Hemolytic Anemia 63 0.066
73
P HYP750 Hypertriglyceridemia, Familial 62 0.066
74
P ART021 Arteriosclerosis 54 0.066
75
P LTR001 Lateral Sclerosis 54 0.066
76
P PNC035 Pancreatic Cancer 84 0.062
77
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.062
78
P RSP003 Respiratory Failure 74 0.062
79
c RHB024 Rhabdomyosarcoma 2 67 0.062
80
c DBT099 Diabetes Mellitus, Type I 65 0.062
81
P PRD008 Periodontitis 64 0.062
82
LPD008 Lipid Metabolism Disorder 62 0.062
83
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.062
84
c ACT071 Acute Kidney Failure 60 0.062
85
c ACT073 Acute Leukemia 58 0.062
86
P HYP076 Hyperthyroidism 55 0.062
87
NNL006 Non-Alcoholic Steatohepatitis 54 0.062
88
OST115 Osteonecrosis of the Jaw 40 0.062
89
ESP021 Esophageal Cancer 90 0.058
90
P RTN008 Retinitis Pigmentosa 79 0.058
91
P PNM007 Pneumonia 68 0.058
92
DRM006 Dermatitis 61 0.058
93
P MYL006 Myeloid Leukemia 60 0.058
94
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.058
95
IGR001 Ige Responsiveness, Atopic 59 0.058
96
HLC007 Helicobacter Pylori Infection 59 0.058
97
P BCL017 B-Cell Lymphoma 58 0.058
98
P PRP019 Peripheral Nervous System Disease 58 0.058
99
PRS045 Prostatic Hypertrophy 53 0.058
100
BRN071 Brain Injury 49 0.058
101
RTN023 Retinitis 46 0.058
102
NRR001 Neuroretinitis 42 0.058
103
PRS063 Paresthesia 41 0.058
104
c PRS136 Prostate Cancer, Hereditary, 6 33 0.058
105
c PRS130 Prostate Cancer, Hereditary, 8 32 0.058
106
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.054
107
P GST053 Gastric Cancer 83 0.054
108
P HRT032 Heart Disease 75 0.054
109
MYL009 Myelodysplastic Syndrome 70 0.054
110
DWN001 Down Syndrome 70 0.054
111
BRN024 Bronchitis 68 0.054
112
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.054
113
P DMN002 Dementia 66 0.054
114
P DRM053 Dermatitis, Atopic 66 0.054
115
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.054
116
ATM095 Autoimmune Disease 62 0.054
117
NTR005 Nutritional Deficiency Disease 62 0.054
118
c ACT027 Acute Pancreatitis 60 0.054
119
IRN002 Iron Metabolism Disease 57 0.054
120
THR024 Thrombosis 57 0.054
121
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.054
122
BRN004 Brain Edema 56 0.054
123
AGN016 Aging 56 0.054
124
P GST044 Gastritis 56 0.054
125
TRD006 Tardive Dyskinesia 54 0.054
126
P ALP008 Alopecia 54 0.054
127
PRT038 Protein-Energy Malnutrition 54 0.054
128
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.054
129
c SVR005 Severe Pre-Eclampsia 50 0.054
130
47X002 47,xyy 49 0.054
131
c MCR120 Microvascular Complications of Diabetes 7 47 0.054
132
KRT002 Keratomalacia 47 0.054
133
c HNT011 Huntington Disease-Like 3 38 0.054
134
PLX004 Plexopathy 30 0.054
135
CYT018 Cytochrome P450 2d6 Variant 27 0.054
136
P LNG032 Lung Cancer 98 0.049
137
P OVR042 Ovarian Cancer 88 0.049
138
c NRF023 Neurofibromatosis, Type Ii 80 0.049
139
P BLD134 Bladder Cancer 79 0.049
140
SCK003 Sickle Cell Anemia 74 0.049
141
ULC004 Ulcerative Colitis 73 0.049
142
ANX010 Anxiety 73 0.049
143
c EXD008 Exudative Vitreoretinopathy 1 71 0.049
144
P MYC007 Myocardial Infarction 70 0.049
145
P FRG001 Fragile X Syndrome 70 0.049
146
P LKM062 Leukemia, Acute Lymphoblastic 69 0.049
147
RCK004 Rickets 68 0.049
148
CRB039 Cerebrovascular Disease 67 0.049
149
P TRN020 Turner Syndrome 67 0.049
150
P PLM037 Pulmonary Hypertension 67 0.049
151
P MCR115 Microvascular Complications of Diabetes 5 66 0.049
152
KHL003 Kohlschutter-Tonz Syndrome 65 0.049
153
P PLM036 Pulmonary Fibrosis 65 0.049
154
CLR108 Colorectal Adenoma 64 0.049
155
LSH001 Leishmaniasis 63 0.049
156
P GLM045 Glioma 63 0.049
157
ACT119 Acute Promyelocytic Leukemia 63 0.049
158
c ALP101 Alpha-Thalassemia 62 0.049
159
c HPT001 Hepatitis C 62 0.049
160
SPN186 Spinal Cord Injury 60 0.049
161
STT001 Status Epilepticus 60 0.049
162
PRN019 Perinatal Necrotizing Enterocolitis 59 0.049
163
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.049
164
EYD002 Eye Disease 58 0.049
165
P INF032 Infertility 57 0.049
166
c ACT075 Acute Myocardial Infarction 57 0.049
167
BCT022 Bacterial Infectious Disease 56 0.049
168
P HYP818 Hypobetalipoproteinemia, Familial, 1 56 0.049
169
P MLN007 Male Infertility 55 0.049
170
END040 Endogenous Depression 55 0.049
171
INT007 Intermediate Coronary Syndrome 55 0.049
172
DBT010 Diabetic Neuropathy 54 0.049
173
GST023 Gastric Ulcer 53 0.049
174
PRS021 Prostatic Adenoma 51 0.049
175
ENT011 Enterocolitis 51 0.049
176
TRM010 Traumatic Brain Injury 51 0.049
177
HYP081 Hypolipoproteinemia 51 0.049
178
c HNT004 Huntington Disease-Like 2 50 0.049
179
c HRD202 Hereditary Lymphedema I 50 0.049
180
PRS129 Prostatic Hyperplasia, Benign 49 0.049
181
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.049
182
RTN020 Retinal Vascular Disease 46 0.049
183
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.049
184
GLL048 Glial Tumor 45 0.049
185
c SPR086 Spermatogenic Failure 3 44 0.049
186
ENC005 Encephalomalacia 43 0.049
187
P KLZ004 Kala-Azar 1 41 0.049
188
ANX004 Anoxia 40 0.049
189
CRV045 Cervical Intraepithelial Neoplasia 39 0.049
190
BRC011 Brachial Plexus Neuropathy 39 0.049
191
ALL014 Allergic Encephalomyelitis 38 0.049
192
PST092 Posttransplant Acute Limbic Encephalitis 29 0.049
193
RDT004 Radiation Induced Brachial Plexopathy 17 0.049
194
c LKM061 Leukemia, Acute Myeloid 84 0.044
195
c HYP595 Hypertension, Essential 84 0.044
196
P PRK057 Parkinson Disease, Late-Onset 78 0.044
197
CRV035 Cervical Cancer 76 0.044
198
P OST002 Osteoporosis 74 0.044
199
c THR092 Thrombophilia Due to Thrombin Defect 73 0.044
200
P MLT020 Multiple Sclerosis 72 0.044
201
c LKM063 Leukemia, Chronic Myeloid 72 0.044
202
P PHC003 Pheochromocytoma 71 0.044
203
HMN044 Human Immunodeficiency Virus Type 1 71 0.044
204
PLM001 Pulmonary Tuberculosis 69 0.044
205
P HYP086 Hypothyroidism 69 0.044
206
P LKM002 Leukemia 68 0.044
207
c HYP768 Hyperlipoproteinemia, Type I 67 0.044
208
P HPT021 Hepatitis 67 0.044
209
OST159 Osteogenic Sarcoma 66 0.044
210
P MNN013 Meningitis 66 0.044
211
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.044
212
P ADL010 Adult Respiratory Distress Syndrome 65 0.044
213
SKN016 Skin Disease 63 0.044
214
DPR016 Depression 63 0.044
215
CLT003 Colitis 62 0.044
216
c HPT003 Hepatitis a 62 0.044
217
P PRP029 Porphyria 62 0.044
218
c PNS012 Paine Syndrome 61 0.044
219
P PNC044 Pancreatitis 61 0.044
220
P LPS004 Lupus Erythematosus 61 0.044
221
P NPH012 Nephrotic Syndrome 60 0.044
222
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.044
223
LNG099 Lung Disease 60 0.044
224
SQM006 Squamous Cell Carcinoma 60 0.044
225
c HPT016 Hepatitis B 59 0.044
226
P BRS044 Breast Adenocarcinoma 59 0.044
227
PPT005 Peptic Ulcer Disease 59 0.044
228
MNT002 Mental Depression 58 0.044
229
P EXN002 Exanthem 57 0.044
230
P HDC001 Headache 57 0.044
231
P FBR017 Fibrosarcoma 56 0.044
232
ERY051 Erythroleukemia, Familial 56 0.044
233
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.044
234
MCS002 Mucositis 56 0.044
235
VSC003 Visceral Leishmaniasis 55 0.044
236
FCT004 Factor Xii Deficiency 55 0.044
237
GLC003 Glucose Intolerance 54 0.044
238
P LCH002 Lichen Planus 53 0.044
239
GTR002 Goiter 53 0.044
240
NRT001 Neurotic Disorder 53 0.044
241
PRP080 Peripheral Artery Disease 53 0.044
242
c MCR113 Microvascular Complications of Diabetes 3 52 0.044
243
NTR018 Neutrophilia, Hereditary 52 0.044
244
ASP003 Aseptic Meningitis 51 0.044
245
P OVR082 Overgrowth Syndrome 50 0.044
246
RTN003 Retinal Ischemia 50 0.044
247
P ECL001 Eclampsia 50 0.044
248
P ATR005 Atrophic Gastritis 50 0.044
249
URM002 Uremia 49 0.044
250
VTM033 Vitamin K Deficiency Bleeding 48 0.044
251
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.044
252
SPL018 Splenomegaly 48 0.044
253
IGG001 Iga Glomerulonephritis 48 0.044
254
KHN001 Kuhnt-Junius Degeneration 47 0.044
255
ADR040 Adrenal Gland Pheochromocytoma 46 0.044
256
ORL013 Oral Lichen Planus 45 0.044
257
CRB004 Cerebral Artery Occlusion 45 0.044
258
ASP008 Aspiration Pneumonitis 45 0.044
259
P CHR345 Chronic Pain 44 0.044
260
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.044
261
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.044
262
c MCR130 Microvascular Complications of Diabetes 6 41 0.044
263
c MCR133 Microvascular Complications of Diabetes 4 41 0.044
264
RDN001 Reading Disorder 40 0.044
265
LKP003 Leukoplakia 39 0.044
267
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 31 0.044
268
ACT228 Acute Radiation Syndrome 29 0.044
269
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 28 0.044
270
CHL079 Children's Interstitial Lung Disease 26 0.044
271
DRG016 Drug Induced Dyskinesia 24 0.044
272
c SYS001 Systemic Lupus Erythematosus 86 0.038
273
STR067 Stroke, Ischemic 81 0.038
274
P LKM071 Leukemia, Chronic Lymphocytic 79 0.038
275
GST019 Gastrointestinal Stromal Tumor 78 0.038
276
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.038
277
P ATS364 Autism 70 0.038
278
CNG034 Congestive Heart Failure 69 0.038
279
P ART022 Arthritis 69 0.038
280
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.038
281
P LYM118 Lymphoma 68 0.038
282
P INF038 Influenza 68 0.038
283
P CRD119 Cardiac Arrest 67 0.038
284
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.038
285
ALC007 Alcohol Dependence 66 0.038
286
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.038
287
HYP056 Hypoglycemia 66 0.038
288
P MTR014 Motor Neuron Disease 65 0.038
289
LYS012 Lysosomal Acid Lipase Deficiency 65 0.038
290
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.038
291
MSC007 Muscle Hypertrophy 64 0.038
292
P NTR004 Neutropenia 63 0.038
293
c GLC092 Glaucoma, Primary Open Angle 62 0.038
294
c FNC043 Fanconi Anemia, Complementation Group E 62 0.038
295
c BRN108 Branchiootic Syndrome 1 62 0.038
296
TXC005 Toxic Shock Syndrome 62 0.038
297
MSL001 Measles 62 0.038
298
P ENC018 Encephalopathy 61 0.038
299
CHR066 Chronic Fatigue Syndrome 61 0.038
300
RTN017 Retinal Detachment 61 0.038
301
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.038
302
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.038
303
ACQ007 Acquired Immunodeficiency Syndrome 60 0.038
304
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.038
305
P OPT006 Optic Nerve Disease 60 0.038
306
P BND020 Bone Disease 59 0.038
307
PLM033 Pulmonary Embolism 59 0.038
308
GNG013 Gingivitis 59 0.038
309
P ALC033 Alcohol Use Disorder 58 0.038
310
BRS051 Breast Disease 58 0.038
311
c DWL002 Dowling-Degos Disease 1 58 0.038
312
P UVT001 Uveitis 57 0.038
313
MNR012 Meniere Disease 57 0.038
314
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.038
315
MCL006 Macular Retinal Edema 55 0.038
316
LMB062 Limb Ischemia 55 0.038
317
P DRR001 Diarrhea 55 0.038
318
NPH009 Nephrolithiasis 55 0.038
319
P RST001 Restless Legs Syndrome 54 0.038
320
P INF037 Inflammatory Bowel Disease 54 0.038
321
PLM010 Pulmonary Edema 54 0.038
322
AMN001 Amenorrhea 54 0.038
323
PNC001 Pancytopenia 54 0.038
324
P EPD016 Epidermolysis Bullosa 53 0.038
325
P RTN016 Retinal Degeneration 53 0.038
326
P SHR001 Short Bowel Syndrome 53 0.038
327
HMC014 Homocysteinemia 53 0.038
328
P RTN018 Retinal Disease 53 0.038
329
c VRL010 Viral Hepatitis 52 0.038
330
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.038
331
P DDN001 Duodenal Ulcer 52 0.038
332
P RCT021 Rectum Cancer 52 0.038
333
IMP005 Impotence 52 0.038
334
P MSC003 Muscular Atrophy 52 0.038
335
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.038
336
LMY002 Leiomyoma 52 0.038
337
KRT009 Keratosis 51 0.038
338
c PNC106 Pancreatic Agenesis 1 51 0.038
339
c PYR010 Peyronie's Disease 50 0.038
340
P SCK005 Sickle Cell Disease 50 0.038
341
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.038
342
PLC008 Placenta Disease 50 0.038
343
BLR001 Biliary Atresia 50 0.038
344
DYS073 Dysphagia 50 0.038
345
HYP080 Hypogonadism 50 0.038
346
P OPN001 Open-Angle Glaucoma 49 0.038
347
ATS010 Autosomal Recessive Disease 48 0.038
348
ASP007 Aspiration Pneumonia 48 0.038
349
P NGH001 Night Blindness 48 0.038
350
RFR010 Refractory Anemia 48 0.038
351
DBT006 Diabetic Macular Edema 48 0.038
352
PNC034 Pancreas Disease 48 0.038
353
P LYM024 Lymphatic System Disease 48 0.038
354
BNN003 Bone Inflammation Disease 48 0.038
355
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.038
356
DRY001 Dry Eye Syndrome 47 0.038
357
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.038
358
ANV001 Anovulation 47 0.038
359
MYC005 Myocardial Stunning 46 0.038
360
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.038
361
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.038
362
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.038
363
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.038
364
URT010 Ureteral Obstruction 45 0.038
365
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.038
366
c HMG003 Hemoglobin E Disease 45 0.038
367
CNT017 Central Nervous System Origin Vertigo 45 0.038
368
MYF001 Myofibroma 45 0.038
369
DBT008 Diabetic Angiopathy 44 0.038
370
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.038
371
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.038
372
CRB090 Cerebral Hypoxia 44 0.038
373
DBT002 Diabetic Autonomic Neuropathy 41 0.038
374
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.038
375
ANG049 Angioedema Induced by Ace Inhibitors 40 0.038
376
PRM020 Premenstrual Tension 40 0.038
377
ORL012 Oral Leukoplakia 39 0.038
378
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.038
379
HRN029 Hearing Loss, Noise-Induced 37 0.038
380
P HRD217 Hereditary Optic Neuropathy 36 0.038
381
HRW001 Hair Whorl 36 0.038
382
c PRG106 Progressive Muscular Dystrophy 33 0.038
383
P VSC018 Visceral Steatosis 33 0.038
384
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.038
385
PGM030 Pigmentation Anomaly of the Skin 26 0.038
386
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.038
387
NRL016 Neural Tube Defects 82 0.031
388
P ATX030 Ataxia-Telangiectasia 82 0.031
389
P RHM011 Rheumatoid Arthritis 80 0.031
390
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.031
391
ADR007 Adrenoleukodystrophy 75 0.031
392
BRN028 Brain Cancer 74 0.031
393
END057 Endometrial Cancer 74 0.031
394
P SCH015 Schizophrenia 74 0.031
395
CRH001 Crohn's Disease 74 0.031
396
SVR004 Severe Combined Immunodeficiency 73 0.031
397
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.031
398
P CNR004 Cone-Rod Dystrophy 2 73 0.031
399
SCH036 Scheie Syndrome 72 0.031
400
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.031
401
c HPT073 Hepatitis C Virus 72 0.031
402
WLS001 Wilson Disease 71 0.031
403
PRP027 Peripheral Vascular Disease 71 0.031
404
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.031
405
P EPL164 Epilepsy 71 0.031
406
P MTC003 Metachromatic Leukodystrophy 70 0.031
407
MYL005 Myelofibrosis 70 0.031
408
P OST001 Osteopetrosis 70 0.031
409
ADL002 Adult Syndrome 70 0.031
410
c PNC108 Pancreatitis, Hereditary 70 0.031
411
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.031
412
P KRB001 Krabbe Disease 69 0.031
413
PLY001 Polycythemia Vera 69 0.031
414
P MLN008 Melanoma 69 0.031
415
CRB037 Cerebral Palsy 69 0.031
416
P SLP006 Sleep Apnea 69 0.031
417
P OCL013 Oculodentodigital Dysplasia 69 0.031
418
P LPR021 Leprosy 3 69 0.031
419
ART016 Aortic Aneurysm 69 0.031
420
MNT001 Mantle Cell Lymphoma 69 0.031
421
P SYS005 Systemic Scleroderma 68 0.031
422
P MYC084 Mycobacterium Tuberculosis 1 68 0.031
423
c BSL007 Basal Cell Carcinoma 68 0.031
424
SKN019 Skin Melanoma 68 0.031
425
PNC129 Pancreatic Adenocarcinoma 68 0.031
426
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.031
427
P THR014 Thrombocytopenia 67 0.031
428
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.031
429
GST092 Gastroesophageal Reflux 67 0.031
430
c INF071 Inflammatory Bowel Disease 1 67 0.031
431
PSY004 Psychotic Disorder 67 0.031
432
c ATS007 Autism Spectrum Disorder 67 0.031
433
c MGR028 Migraine with or Without Aura 1 67 0.031
434
P CLC063 Celiac Disease 1 66 0.031
435
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.031
436
c FML021 Familial Hypercholesterolemia 66 0.031
437
P NSP012 Nasopharyngeal Carcinoma 66 0.031
438
c MCR129 Microvascular Complications of Diabetes 1 66 0.031
439
c MNN047 Mannosidosis, Alpha B, Lysosomal 66 0.031
440
P ATR011 Atrial Fibrillation 66 0.031
441
MYL031 Myeloproliferative Neoplasm 66 0.031
442
P NRV007 Nervous System Disease 66 0.031
443
c SML038 Small Cell Cancer of the Lung 65 0.031
444
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.031
445
TTN003 Tetanus 65 0.031
446
c FML001 Familial Atrial Fibrillation 65 0.031
447
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.031
448
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 65 0.031
449
ACR006 Aceruloplasminemia 65 0.031
450
PPL049 Papillon-Lefevre Syndrome 65 0.031
451
TNG002 Tangier Disease 65 0.031
452
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.031
453
PND002 Pendred Syndrome 65 0.031
454
HRL003 Hurler Syndrome 65 0.031
455
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.031
456
P PRS038 Personality Disorder 65 0.031
457
APN008 Apnea, Obstructive Sleep 64 0.031
458
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.031
459
NRM005 Neuromuscular Disease 64 0.031
460
P FRD001 Friedreich Ataxia 64 0.031
461
DGR001 Digeorge Syndrome 64 0.031
462
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.031
463
RFS006 Refsum Disease, Classic 64 0.031
464
OST017 Osteomyelitis 64 0.031
465
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.031
466
c DPH024 Diaphragmatic Hernia, Congenital 63 0.031
467
KRN002 Kearns-Sayre Syndrome 63 0.031
468
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.031
469
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.031
470
P HYP069 Hyperparathyroidism 63 0.031
471
CHN016 Cohen Syndrome 63 0.031
472
P MVM001 Movement Disease 63 0.031
473
TRN015 Transient Cerebral Ischemia 63 0.031
474
P END044 Endometriosis 63 0.031
475
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.031
476
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.031
477
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.031
478
c SVR001 Severe Acute Respiratory Syndrome 62 0.031
479
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 62 0.031
480
P ART023 Arthropathy 62 0.031
481
P VSC011 Vasculitis 62 0.031
482
PHL006 Phelan-Mcdermid Syndrome 62 0.031
483
BLD131 Bladder Urothelial Carcinoma 62 0.031
484
ASP002 Aspartylglucosaminuria 62 0.031
485
P DRM010 Dermatomyositis 61 0.031
486
c PRX045 Peroxisome Biogenesis Disorder 1b 61 0.031
487
FCS002 Fucosidosis 61 0.031
488
P SJG008 Sjogren Syndrome 61 0.031
489
SDD001 Sudden Infant Death Syndrome 61 0.031
490
VRL011 Viral Infectious Disease 61 0.031
491
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 61 0.031
492
PTN001 Patent Foramen Ovale 60 0.031
493
DRR016 Diarrhea 2, with Microvillus Atrophy 60 0.031
494
P TST021 Testicular Germ Cell Tumor 60 0.031
495
HPT019 Hepatic Encephalopathy 60 0.031
496
CRD223 Cardiac Arrhythmia 60 0.031
497
P ALP009 Alopecia Areata 60 0.031
498
LGG001 Legg-Calve-Perthes Disease 60 0.031
499
LBR030 Leber Optic Atrophy 60 0.031
500
RHM001 Rheumatic Fever 60 0.031
501
P PTN014 Patent Ductus Arteriosus 1 60 0.031
502
P CHR285 Chronic Myelomonocytic Leukemia 60 0.031
503
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.031
504
P LKD001 Leukodystrophy 59 0.031
505
THY029 Thyroid Carcinoma 59 0.031
506
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.031
507
c LTN004 Late-Onset Retinal Degeneration 59 0.031
508
AVN001 Avian Influenza 59 0.031
509
IRN001 Iron Deficiency Anemia 59 0.031
510
P NMN002 Niemann-Pick Disease 59 0.031
511
INC002 Inclusion Body Myositis 58 0.031
512
PST028 Post-Traumatic Stress Disorder 58 0.031
513
MTC027 Mitochondrial Trifunctional Protein Deficiency 58 0.031
514
CMP010 Complex Regional Pain Syndrome 58 0.031
515
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 58 0.031
516
c PRM005 Primary Hyperparathyroidism 58 0.031
517
CNT047 Contact Dermatitis 58 0.031
518
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.031
519
DSS008 Disease of Mental Health 58 0.031
520
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.031
521
GLS018 Glass Syndrome 57 0.031
522
P ZLL001 Zellweger Syndrome 57 0.031
523
BRN056 Bronchopulmonary Dysplasia 57 0.031
524
ARG007 Argininemia 57 0.031
525
BRD001 Brody Myopathy 57 0.031
526
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.031
527
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.031
528
AYM001 Ayme-Gripp Syndrome 57 0.031
529
P BPL003 Bipolar Disorder 56 0.031
530
P MYS005 Myositis 56 0.031
531
P PLY018 Polycythemia 56 0.031
532
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 56 0.031
533
P PLY011 Polycystic Ovary Syndrome 56 0.031
534
TRN018 Transitional Cell Carcinoma 56 0.031
535
c PRX059 Peroxisome Biogenesis Disorder 1a 56 0.031
536
LMY014 Leiomyoma, Uterine 56 0.031
537
P MTC069 Mitochondrial Disorders 56 0.031
538
GNR004 Generalized Anxiety Disorder 56 0.031
539
SCH003 Schizophreniform Disorder 56 0.031
540
PRS047 Prostatitis 56 0.031
541
GST050 Gastrointestinal System Disease 56 0.031
542
P LBR014 Leber Congenital Amaurosis 4 56 0.031
543
c FML035 Familial Hyperlipidemia 55 0.031
544
HYP005 Hypokalemia 55 0.031
545
NRN004 Neuroendocrine Tumor 55 0.031
546
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.031
547
P ANT006 Antiphospholipid Syndrome 55 0.031
548
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.031
549
P MYP006 Myopia 55 0.031
550
HRL004 Hurler-Scheie Syndrome 55 0.031
551
P VNS003 Venous Insufficiency 55 0.031
552
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.031
553
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.031
554
HYP060 Hyperinsulinism 54 0.031
555
RSC001 Rosacea 54 0.031
556
ACD008 Acid-Labile Subunit Deficiency 54 0.031
557
AMN003 Amnestic Disorder 54 0.031
558
CRT017 Cartilage Disease 54 0.031
559
PRT082 Preterm Premature Rupture of the Membranes 54 0.031
560
RFL001 Reflex Sympathetic Dystrophy 54 0.031
561
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.031
562
VLC001 Velocardiofacial Syndrome 54 0.031
563
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.031
564
HLL004 Hellp Syndrome 54 0.031
565
SNS003 Sensory Peripheral Neuropathy 54 0.031
566
GST009 Gastroschisis 53 0.031
567
MMM001 Mammary Paget's Disease 53 0.031
568
P INS002 in Situ Carcinoma 53 0.031
569
HRT012 Heart Valve Disease 53 0.031
570
KRT006 Keratoconjunctivitis 53 0.031
571
P HMC002 Homocystinuria 53 0.031
572
P MNC007 Monocytic Leukemia 53 0.031
573
CRH005 Crohn's Colitis 53 0.031
574
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.031
575
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.031
576
P ORL007 Oral Cavity Cancer 53 0.031
577
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.031
578
INT075 Intracranial Hypertension 53 0.031
579
P ACT008 Actinic Keratosis 53 0.031
580
TXC002 Toxic Encephalopathy 53 0.031
581
P INT068 Intestinal Disease 53 0.031
582
c OST131 Osteopetrosis, Autosomal Dominant 2 53 0.031
583
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 53 0.031
584
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.031
585
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 52 0.031
586
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.031
587
ACR041 Acromelic Frontonasal Dysostosis 52 0.031
588
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 0.031
589
CRT016 Carotid Artery Disease 52 0.031
590
THY030 Thyroid Gland Disease 52 0.031
591
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 52 0.031
592
P ACT105 Acute Mountain Sickness 52 0.031
593
BWN001 Bowen-Conradi Syndrome 52 0.031
594
TLN003 Telangiectasis 52 0.031
595
SPS003 Spastic Diplegia 51 0.031
596
OLG003 Oligohydramnios 51 0.031
597
P SPP010 Suppressor of Tumorigenicity 3 51 0.031
598
c NMN014 Niemann-Pick Disease, Type C2 51 0.031
599
FML026 Familial Lipoprotein Lipase Deficiency 51 0.031
600
FDL002 Food Allergy 51 0.031
601
CLR109 Colorectal Adenocarcinoma 51 0.031
602
LMB050 Limbal Stem Cell Deficiency 51 0.031
603
MGL001 Megaloblastic Anemia 51 0.031
604
THR016 Thrombophlebitis 51 0.031
605
LNG031 Lung Benign Neoplasm 51 0.031
606
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.031
607
P THR015 Thrombophilia 51 0.031
608
BHR001 Behr Syndrome 51 0.031
609
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.031
610
SKN013 Skin Benign Neoplasm 51 0.031
611
P CHL066 Cholangitis 51 0.031
612
c MTC055 Mitochondrial Dna Depletion Syndrome 4b 51 0.031
613
SCH012 Schizoaffective Disorder 50 0.031
614
c PRM012 Primary Polycythemia 50 0.031
615
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.031
616
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 50 0.031
617
CRT013 Carotid Stenosis 50 0.031
618
STM007 Stomatitis 50 0.031
619
c INF145 Infantile Liver Failure Syndrome 1 50 0.031
620
P KRT007 Keratoconus 50 0.031
621
NTR046 Neutrophil Migration 50 0.031
622
MTB004 Metabolic Acidosis 50 0.031
623
KRT001 Keratoconjunctivitis Sicca 49 0.031
624
c CHR431 Chronic Venous Insufficiency 49 0.031
625
GST049 Gastrointestinal System Cancer 49 0.031
626
BKR002 Baker-Gordon Syndrome 49 0.031
627
MTC005 Mitochondrial Metabolism Disease 49 0.031
628
BNR002 Bone Resorption Disease 48 0.031
629
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.031
630
SBS004 Substance Dependence 48 0.031
631
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.031
632
LPT006 Leptin Receptor Deficiency 48 0.031
633
INT010 Intracranial Embolism 48 0.031
634
HPR003 Heparin-Induced Thrombocytopenia 48 0.031
635
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.031
636
PRS127 Pearson Marrow-Pancreas Syndrome 47 0.031
637
SPH010 Sphingolipidosis 47 0.031
638
ACT084 Acute Stress Disorder 47 0.031
639
c INH020 Inherited Metabolic Disorder 47 0.031
640
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.031
641
ALP012 Alpha-Methylacyl-Coa Racemase Deficiency 47 0.031
642
GST071 Gastrointestinal Carcinoma 47 0.031
643
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.031
644
P BLD051 Blood Coagulation Disease 46 0.031
645
LYM019 Lymphosarcoma 46 0.031
646
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.031
647
ASP004 Asphyxia Neonatorum 46 0.031
648
ATN005 Autonomic Dysfunction 46 0.031
649
BCK003 Background Diabetic Retinopathy 46 0.031
650
CLN045 Colonic Benign Neoplasm 46 0.031
651
KRT013 Keratolytic Winter Erythema 46 0.031
652
TRP008 Tropical Calcific Pancreatitis 46 0.031
653
P BNG032 Benign Mesothelioma 46 0.031
654
P MTH007 Methemoglobinemia 46 0.031
655
P HMR005 Hemorrhoid 46 0.031
656
CRN019 Coronary Artery Vasospasm 46 0.031
657
HDN002 Head Injury 46 0.031
658
c DRR009 Diarrhea 6 46 0.031
659
PRX001 Peroxisomal Disease 46 0.031
660
HPT004 Hepatic Coma 45 0.031
661
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.031
662
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.031
663
P OCY003 Oocyte Maturation Defect 1 45 0.031
665
CLL014 Cll/sll 45 0.031
666
CRT015 Carotid Artery Occlusion 45 0.031
667
c ZLL011 Zellweger Spectrum Disorder 45 0.031
668
MLN073 Melanosis, Neurocutaneous 45 0.031
669
SPS057 Spasticity 45 0.031
670
ANS012 Anus Disease 45 0.031
671
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.031
672
SBC016 Subacute Delirium 44 0.031
673
IMM064 Immunodeficiency, Common Variable, 10 44 0.031
674
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 44 0.031
675
CRB008 Cerebral Atherosclerosis 44 0.031
676
P ATX024 Ataxia-Oculomotor Apraxia 3 44 0.031
677
PPL001 Papillary Adenoma 44 0.031
678
c HYP272 Hypercholesterolemia, Familial, 3 44 0.031
679
c PRM038 Primary Agammaglobulinemia 44 0.031
680
CVD001 Covid-19 44 0.031
681
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.031
682
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.031
683
RFR003 Refractive Error 43 0.031
684
c HYP575 Hypotrichosis 7 43 0.031
685
BNM001 Bone Marrow Cancer 43 0.031
686
c CHR546 Chronic Mountain Sickness 43 0.031
687
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.031
688
ORL015 Oral Squamous Cell Carcinoma 43 0.031
689
P HYP265 Hypotonia 43 0.031
690
P MJR007 Major Affective Disorder 1 43 0.031
691
HYP457 Hypertrophic Scars 42 0.031
692
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.031
693
URM005 Uremic Pruritus 42 0.031
694
TRP009 Triple X Syndrome 42 0.031
695
SNL007 Senile Cataract 42 0.031
696
YLL001 Yellow Nail Syndrome 42 0.031
697
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.031
698
P HYP087 Hypotrichosis 42 0.031
699
GST020 Gastric Antral Vascular Ectasia 41 0.031
700
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.031
701
49X006 49, Xxxxy Syndrome 41 0.031
702
c MJR024 Major Affective Disorder 9 41 0.031
703
c FML363 Familial Adult Myoclonic Epilepsy 41 0.031
704
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.031
705
c MCR112 Microvascular Complications of Diabetes 2 41 0.031
706
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.031
707
HPR006 Heparin Cofactor Ii Deficiency 40 0.031
708
ALC005 Alcoholic Pancreatitis 40 0.031
709
SPR126 Superior Semicircular Canal Dehiscence 40 0.031
710
GLC008 Glucose Metabolism Disease 40 0.031
711
P PRG092 Pregnancy Loss, Recurrent 1 40 0.031
712
KLD004 Keloid Disorder 40 0.031
713
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.031
714
ENT001 Enterocele 39 0.031
715
HYP344 Hyperthyroidism, Familial Gestational 39 0.031
716
c HMG029 Hemoglobin Se Disease 39 0.031
717
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.031
718
c CHR682 Chronic Bilirubin Encephalopathy 39 0.031
719
P PRC031 Preeclampsia/eclampsia 1 38 0.031
720
c PLY105 Polycystic Ovary Syndrome 1 38 0.031
721
c OVR114 Ovarian Cancer 1 38 0.031
722
ADR022 Adrenomyeloneuropathy 38 0.031
723
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.031
724
OVR094 Ovarian Epithelial Cancer 38 0.031
725
SPS019 Spastic Paraparesis 38 0.031
726
c SYS043 Systemic Lupus Erythematosus 1 38 0.031
727
c MJR022 Major Affective Disorder 8 38 0.031
728
MCP033 Mucopolysaccharidoses 38 0.031
729
CNT060 Central Serous Chorioretinopathy 38 0.031
730
MNT252 Mental Retardation, Skeletal Dysplasia, and Abducens Palsy 38 0.031
731
FRS019 Farsightedness 38 0.031
732
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.031
733
c LPR022 Leprosy 2 37 0.031
734
FST001 Foster-Kennedy Syndrome 36 0.031
735
JJN004 Jejunal Atresia 36 0.031
736
PRS011 Persian Gulf Syndrome 36 0.031
737
ABD010 Abdominal Wall Defect 36 0.031
738
MTG002 Mutagen Sensitivity 35 0.031
739
c GLC078 Glaucoma 1, Open Angle, F 35 0.031
740
NRX001 Neuroaxonal Dystrophy 35 0.031
741
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.031
742
c MJR008 Major Affective Disorder 2 35 0.031
743
ALC011 Alcoholic Neuropathy 34 0.031
744
HNS001 Hansen's Disease 34 0.031
745
c LKM005 Leukemia, T-Cell, Chronic 34 0.031
746
c RST012 Restless Legs Syndrome 1 34 0.031
747
c MJR023 Major Affective Disorder 7 33 0.031
748
PPL052 Papillomatosis, Confluent and Reticulated 33 0.031
749
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 33 0.031
750
c MJR003 Major Affective Disorder 6 33 0.031
751
c MJR006 Major Affective Disorder 5 33 0.031
752
PRD002 Periodic Limb Movement Disorder 33 0.031
753
c INF089 Inflammatory Bowel Disease 6 32 0.031
754
ALV001 Alveolar Periostitis 30 0.031
755
c INF078 Inflammatory Bowel Disease 2 29 0.031
756
c MJR004 Major Affective Disorder 4 28 0.031
758
VSD001 Vas Deferens, Congenital Bilateral Aplasia of, X-Linked 28 0.031
759
P OVR096 Overlap Myositis 27 0.031
760
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.031
761
MLR020 Malaria, Mild 27 0.031
762
URT049 Urate Oxidase, Pseudogene 25 0.031
763
PRN071 Parenteral Nutrition-Associated Cholestasis 25 0.031
764
INT074 Intracranial Arteriosclerosis 23 0.031
765
c CHR464 Chronic Intestinal Failure 22 0.031
766
c PRS080 Prostate Cancer, Hereditary, 7 22 0.031
767
MNS002 Mini Stroke 19 0.031
768
DSR072 Disorder of Energy Metabolism 12 0.031
769
MYL069 Myeloma, Multiple 85 0.022
770
c FNC027 Fanconi Anemia, Complementation Group a 81 0.022
771
c DLT002 Dilated Cardiomyopathy 79 0.022
772
INS024 Insulin-Like Growth Factor I 79 0.022
773
GLB015 Glioblastoma Multiforme 75 0.022
774
c ATR087 Atrial Standstill 1 75 0.022
775
LPT014 Leptin Deficiency or Dysfunction 74 0.022
776
P ALG028 Alagille Syndrome 1 73 0.022
777
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.022
778
P HNT016 Huntington Disease 72 0.022
779
OTT002 Otitis Media 72 0.022
780
P AMY004 Amyloidosis 70 0.022
781
GST040 Gastric Adenocarcinoma 70 0.022
782
P HYP061 Hypertrophic Cardiomyopathy 70 0.022
783
SMT004 Smith-Lemli-Opitz Syndrome 70 0.022
784
LYM133 Lymphoma, Hodgkin, Classic 69 0.022
785
CHL065 Cholangiocarcinoma 68 0.022
786
c NMN015 Niemann-Pick Disease, Type C1 68 0.022
787
CRP001 Carpal Tunnel Syndrome 67 0.022
788
c PRM196 Premature Ovarian Failure 1 67 0.022
789
c TYR012 Tyrosinemia, Type I 66 0.022
790
P CNJ013 Conjunctivitis 65 0.022
791
P PSD087 Pseudoxanthoma Elasticum 65 0.022
792
PRT037 Pertussis 65 0.022
793
P HRP006 Herpes Simplex 65 0.022
794
CHY002 Chylomicron Retention Disease 65 0.022
795
c WLM013 Wilms Tumor 1 65 0.022
796
KWS002 Kawasaki Disease 65 0.022
797
P THY023 Thymoma 65 0.022
798
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.022
799
MNK001 Menkes Disease 64 0.022
800
CLF027 Cleft Palate, Isolated 64 0.022
801
P MST009 Mastocytosis 64 0.022
802
TBC004 Tobacco Addiction 64 0.022
803
BRC012 Brucellosis 64 0.022
804
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.022
805
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.022
806
P PLY014 Polycystic Kidney Disease 62 0.022
807
P PSR002 Psoriasis 62 0.022
808
P SPN046 Spinal Muscular Atrophy 62 0.022
809
c NMN013 Niemann-Pick Disease, Type a 62 0.022
810
CRC021 Carcinosarcoma 62 0.022
811
MDD011 Mood Disorder 62 0.022
812
c SCL052 Scleroderma, Familial Progressive 61 0.022
813
ALC006 Alcoholic Hepatitis 61 0.022
814
c WLM018 Wilms Tumor 5 61 0.022
815
GST033 Gestational Diabetes 61 0.022
816
HRP004 Herpes Zoster 60 0.022
817
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.022
818
INS001 Insulinoma 60 0.022
819
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.022
820
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.022
821
SPP011 Suppression of Tumorigenicity 12 59 0.022
822
P SLP005 Sleep Disorder 59 0.022
823
DCT002 Ductal Carcinoma in Situ 59 0.022
824
P CYS018 Cystitis 59 0.022
825
P DNG005 Dengue Virus 59 0.022
826
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.022
827
c MCP044 Mucopolysaccharidosis, Type Iiib 59 0.022
828
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.022
829
P ANP001 Anaplastic Large Cell Lymphoma 58 0.022
830
P TYR004 Tyrosinemia 58 0.022
831
P INT070 Intestinal Obstruction 58 0.022
832
P URT039 Urticaria 58 0.022
833
CNS004 Constipation 58 0.022
834
LYM027 Lymphopenia 58 0.022
835
DSS009 Disseminated Intravascular Coagulation 57 0.022
836
P PRN023 Prion Disease 57 0.022
837
c MST023 Mesothelioma, Malignant 57 0.022
838
BLR008 Bilirubin Metabolic Disorder 57 0.022
839
VSC002 Vascular Dementia 57 0.022
840
c LKM070 Leukemia, Acute Monocytic 57 0.022
841
PLC005 Placental Insufficiency 57 0.022
842
SCH014 Schistosomiasis 57 0.022
843
SKN022 Skin Squamous Cell Carcinoma 57 0.022
844
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.022
845
c GRV008 Graves Disease 1 56 0.022
846
P PLY019 Polyneuropathy 56 0.022
847
HPT022 Hepatoblastoma 56 0.022
848
c CRD183 Ceroid Lipofuscinosis, Neuronal, 2 55 0.022
849
FLR001 Filarial Elephantiasis 55 0.022
850
ORP003 Oropharynx Cancer 55 0.022
851
ORL004 Oral Submucous Fibrosis 55 0.022
852
DFF005 Diffuse Large B-Cell Lymphoma 55 0.022
853
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.022
854
CHR100 Chronic Ulcer of Skin 55 0.022
855
FLR002 Filariasis 55 0.022
856
HRY003 Hairy Cell Leukemia 55 0.022
857
CLF004 Cleft Lip/palate 54 0.022
858
PRP030 Purpura 54 0.022
859
P ICH004 Ichthyosis 54 0.022
860
P TRM003 Tremor 54 0.022
861
CLL003 Cellulitis 54 0.022
862
ICH054 Ichthyosis, X-Linked 53 0.022
863
ECH003 Echinococcosis 53 0.022
864
MTN003 Motion Sickness 53 0.022
865
CLF001 Cleft Lip 53 0.022
866
NNT012 Neonatal Jaundice 53 0.022
867
ALC009 Alcoholic Liver Cirrhosis 53 0.022
868
LYS002 Lysosomal Storage Disease 52 0.022
869
PRP016 Paraplegia 52 0.022
870
P SML001 Small Cell Carcinoma 52 0.022
871
PST011 Pustulosis of Palm and Sole 52 0.022
872
DYS015 Dysentery 52 0.022
873
P NRC002 Narcolepsy 52 0.022
874
c THY107 Thymoma, Familial 52 0.022
875
HYP014 Hyperuricemia 52 0.022
876
ACT200 Acute Monoblastic Leukemia 52 0.022
877
P HMP007 Hemophilia 51 0.022
878
INT079 Intrahepatic Cholangiocarcinoma 51 0.022
879
P AST007 Astrocytoma 51 0.022
880
PNN001 Panniculitis 51 0.022
881
CRV040 Cervix Carcinoma 51 0.022
882
c ACT078 Acute Porphyria 51 0.022
883
c ALM001 Al Amyloidosis 50 0.022
884
PLR008 Pleurisy 50 0.022
885
RDC002 Radiculopathy 50 0.022
886
AZS001 Azoospermia 50 0.022
887
ASC010 Ascaris Lumbricoides Infection 50 0.022
888
P TMP001 Temporal Lobe Epilepsy 50 0.022
889
TRY001 Trypanosomiasis 50 0.022
890
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.022
891
HMG002 Hemoglobinuria 50 0.022
892
c CNG027 Congenital Hemolytic Anemia 50 0.022
893
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 49 0.022
894
VRC001 Varicocele 49 0.022
895
P END046 Endometritis 49 0.022
896
CHL004 Cholelithiasis 49 0.022
897
LRN003 Learning Disability 49 0.022
898
c BCT013 Bacterial Pneumonia 48 0.022
899
P HYP058 Hypervitaminosis a 48 0.022
900
CHL056 Cheilitis 48 0.022
901
HYP025 Hyperphosphatemia 48 0.022
902
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.022
903
P MRC003 Mercury Poisoning 48 0.022
904
P MYF003 Myofibrillar Myopathy 48 0.022
905
VTM002 Vitamin B12 Deficiency 48 0.022
906
ANT018 Anthracosis 48 0.022
907
RDT013 Radiation Proctitis 47 0.022
908
PPL002 Papillary Carcinoma 47 0.022
910
GLT007 Glutathione Synthetase Deficiency 47 0.022
911
PRC003 Proctitis 47 0.022
912
c SPN105 Spinocerebellar Ataxia 4 47 0.022
913
STM006 Stomach Disease 47 0.022
914
CHR074 Choriocarcinoma 47 0.022
915
P VTR007 Vitreoretinopathy 46 0.022
916
HMR023 Hemorrhagic Cystitis 45 0.022
917
ACT003 Acute Kidney Tubular Necrosis 45 0.022
918
RTR001 Retrograde Amnesia 44 0.022
919
CHP002 Chops Syndrome 44 0.022
920
LRY022 Laryngoonychocutaneous Syndrome 44 0.022
921
PTT037 Pituitary Tumors 44 0.022
922
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.022
923
P ORF002 Orofacial Cleft 44 0.022
924
KWS001 Kwashiorkor 44 0.022
925
P HYP111 Hyperprolinemia 44 0.022
926
SCT002 Scotoma 44 0.022
927
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.022
928
SKN005 Skin Atrophy 43 0.022
929
TST015 Testicular Disease 43 0.022
930
PRS036 Parasitic Protozoa Infectious Disease 43 0.022
931
c HYP597 Hyperprolinemia, Type Ii 43 0.022
932
MDD018 Middle East Respiratory Syndrome 43 0.022
933
DSC009 Discoid Lupus Erythematosus 42 0.022
934
MST004 Mast Cell Neoplasm 42 0.022
935
c RTN047 Retinitis Pigmentosa 18 42 0.022
936
MRS001 Marasmus 42 0.022
937
EXC002 Exocrine Pancreatic Insufficiency 42 0.022
938
c MLG079 Malignant Pleural Mesothelioma 42 0.022
939
OBS082 Obstructive Nephropathy 42 0.022
940
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.022
941
MSN004 Mesenchymal Cell Neoplasm 41 0.022
942
ELP001 Elephantiasis 41 0.022
943
OPS001 Opisthorchiasis 41 0.022
944
PLY021 Polyradiculopathy 41 0.022
945
ACT088 Acute Insulin Response 41 0.022
946
NNT008 Neonatal Abstinence Syndrome 41 0.022
947
CRD005 Cardia Cancer 40 0.022
948
P TRC031 Trichorhinophalangeal Syndrome 40 0.022
949
KRT063 Keratocystic Odontogenic Tumor 40 0.022
950
CHL045 Choline Deficiency Disease 39 0.022
951
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.022
952
EXT007 Extracutaneous Mastocytoma 38 0.022
953
HYP835 Hypothalamic Obesity 38 0.022
954
ISL109 Isolated Cleft Lip 38 0.022
955
CDQ001 Cauda Equina Syndrome 38 0.022
956
P CRB059 Cerebellar Degeneration 37 0.022
957
HYP114 Hypertensive Nephropathy 36 0.022
958
ATR003 Atrophic Rhinitis 35 0.022
959
KSH001 Keshan Disease 34 0.022
960
GLT039 Glutathione Peroxidase Deficiency 34 0.022
961
PRR001 Periarthritis 32 0.022
963
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.022
964
ASH001 Asherman's Syndrome 31 0.022
965
FTL004 Fetal Erythroblastosis 31 0.022
966
PLY150 Polykaryocytosis Inducer 31 0.022
967
PRC051 Paracetamol Poisoning 30 0.022
968
BLD041 Bladder Calculus 29 0.022
969
PRT025 Protein-Deficiency Anemia 27 0.022
970
PRQ002 Paraquat Poisoning 26 0.022
971
MTH071 Methane Production 26 0.022
972
c LPD044 Lipodystrophy, Familial Partial, Type 7 25 0.022
973
c VSC053 Visceral Steatosis, Congenital 25 0.022
974
AML013 Amelogenesis Imperfecta, Hypomaturation Type, Iia1 23 0.022
975
CRT011 Carotenemia 23 0.022
976
ORL006 Oral Mucosa Leukoplakia 23 0.022
977
HVY002 Heavy Metal Poisoning 22 0.022
978
OST173 Osteoradionecrosis of the Mandible 17 0.022
979
RDT016 Radiation-Induced Plexopathy 10 0.022
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