Search results for Triglycerides Group C

670 hits were found for Triglycerides Group C

# Family MCID Name MIFTS Score
1
c HPT001 Hepatitis C 63 0.751
2
c HPT073 Hepatitis C Virus 70 0.715
3
P HYP750 Hypertriglyceridemia, Familial 61 0.572
4
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.537
5
P HPT021 Hepatitis 67 0.429
6
P CRN300 Coronary Heart Disease 1 63 0.420
7
LPD008 Lipid Metabolism Disorder 62 0.418
8
P LVR013 Liver Disease 68 0.413
9
FTT001 Fatty Liver Disease 61 0.398
10
c HYP836 Hypercholesterolemia, Familial, 1 72 0.393
11
48X005 48,xyyy 39 0.355
12
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.353
13
P CRN018 Coronary Artery Anomaly 63 0.339
14
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.332
15
LVR012 Liver Cirrhosis 63 0.319
16
P DBT009 Diabetes Mellitus 64 0.316
17
ATH013 Atherosclerosis Susceptibility 66 0.315
18
ART140 Arteries, Anomalies of 53 0.306
19
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.302
20
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.300
21
P KDN018 Kidney Disease 70 0.297
22
P HRT032 Heart Disease 75 0.293
23
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.284
24
P NTR004 Neutropenia 63 0.283
25
P BRS047 Breast Cancer 96 0.270
26
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.267
27
P VSC007 Vascular Disease 63 0.265
28
HMN044 Human Immunodeficiency Virus Type 1 71 0.255
29
P DRR001 Diarrhea 57 0.250
30
P LYM031 Lymphocytic Leukemia 55 0.248
31
ISC004 Ischemia 60 0.248
32
HYP066 Hyperglycemia 61 0.246
33
HYP060 Hyperinsulinism 54 0.242
34
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.238
35
P HPT023 Hepatocellular Carcinoma 100 0.236
36
c HPT016 Hepatitis B 59 0.235
37
c CHR684 Chronic Kidney Disease 66 0.232
38
P CLR023 Colorectal Cancer 98 0.228
39
c HYP595 Hypertension, Essential 84 0.228
40
c VRL010 Viral Hepatitis 51 0.227
41
P CRD246 Cardiovascular System Disease 56 0.223
42
P MYC007 Myocardial Infarction 70 0.220
43
CRB039 Cerebrovascular Disease 69 0.218
44
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.216
45
c HPT003 Hepatitis a 63 0.216
46
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.216
47
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.216
48
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.216
49
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.216
50
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.216
51
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.216
52
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.216
53
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.216
54
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.216
55
P ALZ034 Alzheimer Disease 88 0.213
56
DPR016 Depression 63 0.212
57
HLX001 Helix Syndrome 47 0.212
58
HYP056 Hypoglycemia 66 0.210
59
P LNG032 Lung Cancer 97 0.207
60
P LKM062 Leukemia, Acute Lymphoblastic 68 0.204
61
P NRB001 Neuroblastoma 71 0.203
62
CYS001 Cystic Fibrosis 80 0.203
63
END030 End Stage Renal Failure 58 0.203
64
c ACT075 Acute Myocardial Infarction 56 0.202
65
c ACT027 Acute Pancreatitis 59 0.201
66
TXC005 Toxic Shock Syndrome 61 0.199
67
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.198
68
ACQ007 Acquired Immunodeficiency Syndrome 60 0.198
69
IMM167 Immune Deficiency Disease 78 0.198
70
P OVR042 Ovarian Cancer 89 0.198
71
P HYP086 Hypothyroidism 68 0.194
72
MNT002 Mental Depression 57 0.194
73
GLC003 Glucose Intolerance 54 0.192
74
P ADN016 Adenocarcinoma 64 0.191
75
CNG034 Congestive Heart Failure 70 0.191
76
P BLD134 Bladder Cancer 78 0.190
77
c FML021 Familial Hypercholesterolemia 68 0.190
78
P NRP001 Neuropathy 56 0.188
79
NNL006 Non-Alcoholic Steatohepatitis 51 0.188
80
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.187
81
PRT037 Pertussis 65 0.186
82
P GST053 Gastric Cancer 83 0.186
83
47X002 47,xyy 49 0.186
84
INT007 Intermediate Coronary Syndrome 55 0.185
85
DWN001 Down Syndrome 70 0.185
86
c ATR087 Atrial Standstill 1 74 0.185
87
ANG054 Angina Pectoris 66 0.183
88
HYP081 Hypolipoproteinemia 50 0.183
89
P THR014 Thrombocytopenia 68 0.182
90
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.182
91
P PRS040 Prostate Cancer 97 0.181
92
P MYP004 Myopathy 64 0.179
93
P PNC044 Pancreatitis 61 0.178
94
STR067 Stroke, Ischemic 80 0.178
95
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.178
96
c PRC016 Pre-Eclampsia 63 0.176
97
ANX010 Anxiety 72 0.176
98
ATM095 Autoimmune Disease 61 0.174
99
P HYP061 Hypertrophic Cardiomyopathy 66 0.173
100
c THR092 Thrombophilia Due to Thrombin Defect 73 0.171
101
P PSR002 Psoriasis 62 0.169
102
ADL002 Adult Syndrome 69 0.169
103
PST011 Pustulosis of Palm and Sole 52 0.169
104
c RHB024 Rhabdomyosarcoma 2 65 0.168
105
DFC004 Deficiency Anemia 75 0.168
106
P TRN020 Turner Syndrome 65 0.168
107
ALL026 Allergic Hypersensitivity Disease 64 0.167
108
P LYN001 Lynch Syndrome 77 0.167
109
P PRD008 Periodontitis 62 0.167
110
P NRF023 Neurofibromatosis, Type Ii 76 0.166
111
INS024 Insulin-Like Growth Factor I 79 0.166
112
CYT002 Cytokine Deficiency 44 0.164
113
VSL002 Visual Epilepsy 58 0.164
114
CRH001 Crohn's Disease 74 0.164
115
c MCR113 Microvascular Complications of Diabetes 3 52 0.164
116
c SYS001 Systemic Lupus Erythematosus 86 0.163
117
c MCR120 Microvascular Complications of Diabetes 7 47 0.162
118
GST033 Gestational Diabetes 57 0.162
119
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.162
120
c MCR130 Microvascular Complications of Diabetes 6 41 0.162
121
c MCR133 Microvascular Complications of Diabetes 4 41 0.161
122
P ART021 Arteriosclerosis 54 0.158
123
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.158
124
BCT022 Bacterial Infectious Disease 56 0.158
125
ADN018 Adenoma 58 0.158
126
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.157
127
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.157
128
P ALC033 Alcohol Use Disorder 58 0.157
129
c HNT004 Huntington Disease-Like 2 49 0.156
130
ALC007 Alcohol Dependence 66 0.155
131
P MJR001 Major Depressive Disorder 68 0.154
132
P MCR115 Microvascular Complications of Diabetes 5 66 0.154
133
DRM006 Dermatitis 61 0.153
134
P THL005 Thalassemia 60 0.152
135
P RHM011 Rheumatoid Arthritis 80 0.152
136
PRP027 Peripheral Vascular Disease 71 0.152
137
c FML035 Familial Hyperlipidemia 55 0.152
138
ABT001 Abetalipoproteinemia 67 0.152
139
P SZR006 Seizure Disorder 58 0.151
140
P INF037 Inflammatory Bowel Disease 56 0.151
141
LYM133 Lymphoma, Hodgkin, Classic 69 0.150
142
c HNT011 Huntington Disease-Like 3 38 0.149
143
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.149
144
OST012 Osteoarthritis 78 0.149
145
P PRP019 Peripheral Nervous System Disease 57 0.148
146
P ART022 Arthritis 70 0.148
147
CHL068 Cholestasis 60 0.148
148
CHL123 Chlamydia 59 0.147
149
GST045 Gastroenteritis 59 0.146
150
PRP030 Purpura 55 0.146
151
P OST002 Osteoporosis 73 0.144
152
SRC014 Sarcoma 65 0.144
153
P SCH015 Schizophrenia 75 0.143
154
END057 Endometrial Cancer 74 0.142
155
SPN035 Spindle Cell Sarcoma 51 0.141
156
P EPL164 Epilepsy 71 0.140
157
P NPH012 Nephrotic Syndrome 63 0.140
158
THY029 Thyroid Carcinoma 59 0.140
159
c DLT002 Dilated Cardiomyopathy 79 0.140
160
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.139
161
P BPL003 Bipolar Disorder 56 0.139
162
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.139
163
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.138
164
HYP266 Hypoxia 56 0.138
165
c HYP272 Hypercholesterolemia, Familial, 3 43 0.138
166
P ALP008 Alopecia 56 0.138
167
CHL014 Cholera 55 0.138
168
c MJR024 Major Affective Disorder 9 41 0.137
169
c MJR022 Major Affective Disorder 8 38 0.137
170
P LPS004 Lupus Erythematosus 61 0.137
171
NTR005 Nutritional Deficiency Disease 61 0.137
172
P END033 Endocarditis 57 0.137
173
ATX019 Ataxia with Vitamin E Deficiency 48 0.136
174
PRT036 Peritonitis 65 0.134
176
ULC004 Ulcerative Colitis 73 0.134
177
P RSP003 Respiratory Failure 74 0.134
178
THR024 Thrombosis 56 0.134
179
IRN002 Iron Metabolism Disease 57 0.134
180
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.133
181
CNS004 Constipation 57 0.133
182
ATS010 Autosomal Recessive Disease 48 0.132
183
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.132
184
P CTR002 Cataract 60 0.132
185
P INF032 Infertility 57 0.132
186
P GRF003 Graft-Versus-Host Disease 71 0.131
187
P PNM007 Pneumonia 68 0.130
188
RCK004 Rickets 69 0.130
189
P PRS038 Personality Disorder 65 0.129
190
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.129
191
P RHN004 Rhinitis 57 0.128
192
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.128
193
CLT003 Colitis 62 0.128
194
P PLY011 Polycystic Ovary Syndrome 56 0.128
195
P ENC004 Encephalitis 61 0.128
196
DPH001 Diphtheria 60 0.127
197
P ENC018 Encephalopathy 61 0.127
198
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.126
199
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.126
200
P NMN002 Niemann-Pick Disease 60 0.126
201
SKN016 Skin Disease 63 0.125
202
ESP021 Esophageal Cancer 90 0.125
203
AGN016 Aging 56 0.123
204
P CRD119 Cardiac Arrest 67 0.123
205
P INS002 in Situ Carcinoma 52 0.123
206
c ACT071 Acute Kidney Failure 59 0.123
207
OCL069 Ocular Motor Apraxia 51 0.123
208
P MLT020 Multiple Sclerosis 72 0.122
209
END040 Endogenous Depression 54 0.122
210
P SLP006 Sleep Apnea 69 0.122
211
BRN071 Brain Injury 49 0.122
212
P DMN002 Dementia 67 0.121
213
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.120
214
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.120
215
c NMN015 Niemann-Pick Disease, Type C1 68 0.120
216
P GST044 Gastritis 55 0.118
217
c ACT068 Acute Cystitis 63 0.117
218
P HYP076 Hyperthyroidism 55 0.117
219
SPL018 Splenomegaly 48 0.116
220
P DRM053 Dermatitis, Atopic 66 0.116
221
P ZLL001 Zellweger Syndrome 64 0.115
222
HRW001 Hair Whorl 36 0.115
223
MDD011 Mood Disorder 62 0.115
224
P LTR001 Lateral Sclerosis 53 0.115
225
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.115
226
HYP014 Hyperuricemia 51 0.114
227
SPN186 Spinal Cord Injury 60 0.114
228
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.113
229
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.113
230
BNR002 Bone Resorption Disease 48 0.112
231
IDP011 Idiopathic Interstitial Pneumonia 63 0.112
232
CHL079 Children's Interstitial Lung Disease 27 0.112
233
P PLM036 Pulmonary Fibrosis 61 0.112
234
ANR007 Anorexia Nervosa 63 0.112
235
PLM033 Pulmonary Embolism 59 0.111
236
P SKN015 Skin Carcinoma 67 0.111
237
PLM001 Pulmonary Tuberculosis 70 0.111
238
ETN001 Eating Disorder 59 0.110
239
P OPN001 Open-Angle Glaucoma 49 0.110
240
HMS001 Hemosiderosis 54 0.110
241
URM002 Uremia 49 0.109
242
PSY004 Psychotic Disorder 67 0.109
243
P RCT021 Rectum Cancer 53 0.109
244
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.108
245
CNT047 Contact Dermatitis 57 0.108
246
c SPN225 Spondyloarthropathy 1 73 0.108
247
LSH001 Leishmaniasis 63 0.108
248
TRM010 Traumatic Brain Injury 53 0.107
249
P KLZ004 Kala-Azar 1 41 0.107
250
P DDN001 Duodenal Ulcer 50 0.107
251
c BTT014 Beta-Thalassemia 72 0.106
252
P AST007 Astrocytoma 50 0.106
253
c GLL024 Gallbladder Disease 1 52 0.106
254
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.106
255
P ECL001 Eclampsia 51 0.106
256
P CND004 Candidiasis 57 0.106
257
c SCL052 Scleroderma, Familial Progressive 62 0.106
258
P RRH023 Rare Hereditary Hemochromatosis 41 0.106
259
DNT012 Dental Caries 51 0.105
260
c ATM011 Autoimmune Hepatitis 62 0.105
261
DBT010 Diabetic Neuropathy 55 0.105
262
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.104
263
NTR007 Neutral Lipid Storage Disease with Myopathy 41 0.104
264
TRN018 Transitional Cell Carcinoma 56 0.104
265
PRP080 Peripheral Artery Disease 53 0.103
266
CRD132 Cardiac Conduction Defect 59 0.103
267
TRN015 Transient Cerebral Ischemia 62 0.103
268
DYS073 Dysphagia 50 0.103
269
PSR001 Psoriatic Arthritis 62 0.103
270
PPT005 Peptic Ulcer Disease 58 0.102
271
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 63 0.102
272
GT001 Gout 63 0.101
273
GST040 Gastric Adenocarcinoma 70 0.101
274
P LNG064 Lung Cancer Susceptibility 3 77 0.101
275
LPD009 Lipid Storage Disease 48 0.101
276
c HYP768 Hyperlipoproteinemia, Type I 52 0.100
277
P SCK005 Sickle Cell Disease 50 0.100
278
IRR002 Irritable Bowel Syndrome 63 0.100
279
P ATR011 Atrial Fibrillation 66 0.099
280
OST017 Osteomyelitis 64 0.098
281
c PRD040 Periodontitis, Chronic 54 0.098
282
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.098
283
CRN030 Coronary Stenosis 50 0.098
284
LYM019 Lymphosarcoma 47 0.098
285
c FML001 Familial Atrial Fibrillation 66 0.097
286
P APL001 Aplastic Anemia 74 0.097
287
SPN051 Spondylitis 52 0.097
288
LPT014 Leptin Deficiency or Dysfunction 73 0.097
289
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.097
290
CHL004 Cholelithiasis 49 0.097
292
INF009 Inflammatory Spondylopathy 32 0.096
293
P AMY004 Amyloidosis 70 0.096
294
c BRN108 Branchiootic Syndrome 1 61 0.096
295
IMP005 Impotence 52 0.096
296
ACT119 Acute Promyelocytic Leukemia 63 0.095
297
ART016 Aortic Aneurysm 68 0.095
298
VRC005 Varicose Veins 60 0.095
299
P ESP024 Esophagitis 62 0.095
300
GST092 Gastroesophageal Reflux 65 0.095
301
P ANR048 Aniridia 1 63 0.094
302
PRT013 Portal Hypertension 60 0.094
303
P MTR004 Maturity-Onset Diabetes of the Young 66 0.094
305
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.094
306
SCK003 Sickle Cell Anemia 72 0.093
307
ANR040 Aneurysm 58 0.093
308
PLY150 Polykaryocytosis Inducer 31 0.093
309
P KDN017 Kidney Cancer 61 0.093
310
c INF071 Inflammatory Bowel Disease 1 68 0.092
311
P PRM006 Primary Biliary Cirrhosis 61 0.092
312
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.092
313
c MCR129 Microvascular Complications of Diabetes 1 66 0.092
314
P TRC086 Trichohepatoenteric Syndrome 1 59 0.092
315
P SLP005 Sleep Disorder 59 0.092
316
PNC129 Pancreatic Adenocarcinoma 67 0.092
317
P CLC063 Celiac Disease 1 68 0.092
318
CHL065 Cholangiocarcinoma 67 0.091
319
INS001 Insulinoma 60 0.091
320
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.091
321
HPT022 Hepatoblastoma 56 0.091
322
P SYS005 Systemic Scleroderma 70 0.090
323
INT079 Intrahepatic Cholangiocarcinoma 50 0.090
324
CLN015 Colon Adenocarcinoma 63 0.090
325
P THY032 Thyroiditis 53 0.089
326
P PLY019 Polyneuropathy 56 0.089
327
c CNG006 Congenital Hypothyroidism 65 0.089
328
LYM027 Lymphopenia 57 0.088
329
MST005 Mastitis 53 0.088
330
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.087
331
BLR008 Bilirubin Metabolic Disorder 57 0.087
332
CMM005 Common Cold 56 0.087
333
P PRP029 Porphyria 62 0.087
334
P LMY004 Leiomyosarcoma 62 0.086
335
PPL022 Papilloma 54 0.086
336
ACN002 Acanthosis Nigricans 60 0.086
337
P ICH004 Ichthyosis 54 0.086
338
TNG002 Tangier Disease 65 0.086
339
EYD002 Eye Disease 58 0.085
340
ENT011 Enterocolitis 50 0.085
341
EXC002 Exocrine Pancreatic Insufficiency 41 0.085
342
HYP080 Hypogonadism 50 0.085
343
KHL003 Kohlschutter-Tonz Syndrome 64 0.085
344
HMC014 Homocysteinemia 53 0.085
345
P TRM003 Tremor 53 0.085
346
RTN017 Retinal Detachment 60 0.084
347
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.084
348
HYP064 Hypogonadotropism 40 0.084
349
P HYP069 Hyperparathyroidism 62 0.084
350
CLR108 Colorectal Adenoma 64 0.084
351
THR013 Thoracic Outlet Syndrome 53 0.083
352
RHM028 Rheumatic Heart Disease 53 0.083
353
DYS015 Dysentery 50 0.083
354
c SVR001 Severe Acute Respiratory Syndrome 55 0.083
355
SQM002 Squamous Cell Papilloma 42 0.082
356
GNG013 Gingivitis 59 0.082
357
P BND020 Bone Disease 59 0.082
358
P URT039 Urticaria 58 0.082
359
CYT008 Cytomegalovirus Infection 56 0.082
360
CRT013 Carotid Stenosis 50 0.082
361
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.082
362
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.081
363
P MYS005 Myositis 56 0.081
364
FML026 Familial Lipoprotein Lipase Deficiency 51 0.080
365
KRT002 Keratomalacia 48 0.080
366
LYS012 Lysosomal Acid Lipase Deficiency 64 0.080
367
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.079
368
c INH020 Inherited Metabolic Disorder 46 0.079
369
P MPL001 Maple Syrup Urine Disease 69 0.079
370
HDN002 Head Injury 45 0.078
371
BRD004 Borderline Personality Disorder 53 0.078
372
PPL052 Papillomatosis, Confluent and Reticulated 34 0.078
373
ART002 Arts Syndrome 63 0.078
374
SXL003 Sexual Disorder 48 0.078
375
HPT019 Hepatic Encephalopathy 60 0.077
376
HPT004 Hepatic Coma 43 0.077
377
CRH005 Crohn's Colitis 52 0.077
378
KRT009 Keratosis 53 0.077
379
P NRV007 Nervous System Disease 66 0.077
380
CHL147 Chlamydia Pneumonia 45 0.077
381
P FML018 Familial Mediterranean Fever 72 0.077
382
P PLY014 Polycystic Kidney Disease 59 0.076
383
MSC007 Muscle Hypertrophy 63 0.076
384
SCH012 Schizoaffective Disorder 50 0.076
385
ATX010 Ataxia Neuropathy Spectrum 38 0.076
386
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.076
387
P RTN008 Retinitis Pigmentosa 77 0.075
388
P PRP003 Porphyria Cutanea Tarda 67 0.075
389
c MCR112 Microvascular Complications of Diabetes 2 41 0.075
390
P HYD006 Hydrocephalus 65 0.075
391
ALL010 Allergic Contact Dermatitis 55 0.075
392
CHL067 Cholecystitis 58 0.075
393
P MLN007 Male Infertility 56 0.074
394
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.074
395
P LCT001 Lactic Acidosis 51 0.074
396
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.074
397
WRN001 Werner Syndrome 69 0.074
398
ANX004 Anoxia 42 0.073
399
P MSC003 Muscular Atrophy 52 0.073
400
P ADL010 Adult Respiratory Distress Syndrome 63 0.073
401
GRW007 Growth Hormone Deficiency 43 0.073
402
ADR007 Adrenoleukodystrophy 74 0.073
403
BRR014 Barrett Esophagus 64 0.072
404
PRN019 Perinatal Necrotizing Enterocolitis 54 0.072
405
PST092 Posttransplant Acute Limbic Encephalitis 29 0.072
406
P OVR082 Overgrowth Syndrome 50 0.072
407
c PNC108 Pancreatitis, Hereditary 69 0.072
408
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 0.071
409
SPS057 Spasticity 41 0.071
410
GST050 Gastrointestinal System Disease 56 0.071
411
CLR109 Colorectal Adenocarcinoma 50 0.071
412
MYL005 Myelofibrosis 67 0.071
413
BRS051 Breast Disease 58 0.071
414
IRN001 Iron Deficiency Anemia 58 0.070
415
ARG004 Argyria 28 0.070
416
INT002 Intermittent Claudication 61 0.069
417
P HYP265 Hypotonia 42 0.069
418
c MNN043 Meningioma, Familial 74 0.069
419
P PLY018 Polycythemia 55 0.069
420
RFR010 Refractory Anemia 48 0.069
421
HYP732 Hyperalphalipoproteinemia 1 56 0.069
422
P THY023 Thymoma 65 0.069
423
c THY107 Thymoma, Familial 54 0.069
424
VSC003 Visceral Leishmaniasis 55 0.069
425
P MLG056 Malignant Hyperthermia 67 0.069
426
PHN003 Phenylketonuria 75 0.069
427
ORL005 Oral Candidiasis 56 0.068
428
MTB004 Metabolic Acidosis 50 0.068
429
GST020 Gastric Antral Vascular Ectasia 41 0.068
430
BLD137 Blood Group--Ahonen 19 0.068
431
P SHR001 Short Bowel Syndrome 52 0.068
432
P ANT006 Antiphospholipid Syndrome 54 0.067
433
KRT006 Keratoconjunctivitis 53 0.067
434
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.067
435
PLY001 Polycythemia Vera 69 0.067
436
ALC006 Alcoholic Hepatitis 61 0.067
437
THY030 Thyroid Gland Disease 51 0.067
438
OST003 Osteonecrosis 61 0.067
439
P GLL022 Guillain-Barre Syndrome 59 0.067
440
ACT064 Acute Necrotizing Encephalitis 32 0.067
441
P ASP006 Aspergillosis 66 0.066
442
P MCR010 Microcephaly 58 0.066
443
PLC008 Placenta Disease 49 0.066
444
ESP020 Esophageal Atresia 62 0.066
445
KWS002 Kawasaki Disease 64 0.066
446
FDL002 Food Allergy 49 0.066
447
P BRS044 Breast Adenocarcinoma 59 0.066
448
P HYP121 Hypoalphalipoproteinemia 43 0.065
449
MNN042 Meningioma, Radiation-Induced 62 0.065
450
c CNG012 Congenital Generalized Lipodystrophy 54 0.065
451
AZS001 Azoospermia 50 0.064
452
SPN021 Spinal Meningioma 47 0.064
453
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.064
454
P TRC031 Trichorhinophalangeal Syndrome 40 0.064
455
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.064
456
P RTN016 Retinal Degeneration 53 0.064
457
SCR001 Secretory Meningioma 37 0.064
458
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.064
459
P FML011 Familial Adenomatous Polyposis 72 0.064
460
CRC021 Carcinosarcoma 61 0.064
461
VSC002 Vascular Dementia 57 0.063
462
PRP016 Paraplegia 53 0.063
463
SDD001 Sudden Infant Death Syndrome 61 0.063
464
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 0.063
465
c HYP739 Hyperlipoproteinemia, Type Iv 51 0.063
466
CHL045 Choline Deficiency Disease 39 0.063
467
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.062
468
P LYM025 Lymphedema 53 0.062
469
STT001 Status Epilepticus 59 0.062
470
GLL018 Gallbladder Cancer 56 0.062
471
IMP004 Impetigo 49 0.061
472
PRD004 Prediabetes Syndrome 47 0.061
473
CLR030 Clear Cell Renal Cell Carcinoma 53 0.061
474
FCL014 Focal Epilepsy 54 0.061
475
BRN056 Bronchopulmonary Dysplasia 57 0.061
476
P MTC069 Mitochondrial Disorders 56 0.061
477
P RTN022 Retinal Vein Occlusion 52 0.061
478
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.061
479
P INT068 Intestinal Disease 52 0.060
480
P PLY006 Polydactyly 58 0.060
481
LPT001 Leptospirosis 66 0.060
482
CRD223 Cardiac Arrhythmia 60 0.060
483
P GLY013 Glycogen Storage Disease 59 0.060
484
DRG003 Drug Dependence 47 0.059
485
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 63 0.059
486
OBS529 Obsolete: Combined Hyperlipidemia 22 0.058
487
P LPS002 Liposarcoma 65 0.058
488
P VSC018 Visceral Steatosis 33 0.058
489
P MTR003 Mitral Valve Stenosis 50 0.057
490
CRY005 Cryptococcosis 58 0.057
491
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 33 0.057
492
P DRM010 Dermatomyositis 61 0.057
493
BLR001 Biliary Atresia 50 0.057
494
KWS001 Kwashiorkor 45 0.057
495
P HYP730 Hypogonadotropic Hypogonadism 53 0.056
496
c SCN007 Secondary Hyperparathyroidism 50 0.056
497
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.056
498
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.056
499
VTM033 Vitamin K Deficiency Bleeding 48 0.056
500
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.056
501
WTH001 Withdrawal Disorder 48 0.055
502
PTH003 Pathologic Nystagmus 51 0.055
503
P AGM001 Agammaglobulinemia 65 0.055
504
ANL018 Analbuminemia 54 0.054
505
RST023 Resting Heart Rate, Variation in 41 0.054
506
c GRV008 Graves Disease 1 55 0.054
507
LYM035 Lymphangiectasis 30 0.054
508
GLM044 Glomerular Disease 39 0.054
509
c BLD140 Blood Group, I System 30 0.054
510
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.053
511
c SVR005 Severe Pre-Eclampsia 49 0.053
512
P LCT002 Lactose Intolerance 53 0.053
513
WLF001 Wolff-Parkinson-White Syndrome 65 0.053
514
P FML012 Familial Partial Lipodystrophy 55 0.053
515
HYP017 Hypophosphatemia 49 0.053
516
c HRD010 Hereditary Spastic Paraplegia 66 0.052
517
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.052
518
HYP043 Hyperandrogenism 48 0.052
519
ACT088 Acute Insulin Response 41 0.052
520
ERL001 Early Myoclonic Encephalopathy 61 0.052
521
ART004 Aortic Atherosclerosis 48 0.052
522
CRN239 Carnitine Deficiency, Systemic Primary 61 0.052
523
RTN020 Retinal Vascular Disease 48 0.051
524
LPT006 Leptin Receptor Deficiency 47 0.051
525
MYC088 Mycobacterium Avium Complex Infections 29 0.051
526
LPD004 Lipoid Nephrosis 47 0.051
527
ILT001 Ileitis 50 0.051
528
P RTN018 Retinal Disease 52 0.051
529
LGS001 Legius Syndrome 57 0.051
530
TRP009 Triple X Syndrome 42 0.051
531
ATN005 Autonomic Dysfunction 47 0.050
532
RYS001 Reye Syndrome 51 0.050
533
MTC005 Mitochondrial Metabolism Disease 48 0.050
534
c HYP839 Hyperlipidemia, Familial Combined, 1 28 0.050
535
DVR002 Diverticulitis 44 0.050
536
MMM001 Mammary Paget's Disease 53 0.050
537
ADR022 Adrenomyeloneuropathy 38 0.050
538
PYL006 Pyloric Stenosis 48 0.049
539
MSC190 Muscular Disease 51 0.049
540
SCH038 Schopf-Schulz-Passarge Syndrome 47 0.049
541
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.049
542
OBS524 Obsolete: Benign Exophthalmos Syndrome 15 0.049
543
c HYP841 Hypoalphalipoproteinemia, Primary, 1 37 0.048
544
PRT038 Protein-Energy Malnutrition 54 0.048
545
CRT016 Carotid Artery Disease 52 0.048
546
AND005 Androgen Insensitivity Syndrome, Mild 22 0.048
547
ASP007 Aspiration Pneumonia 48 0.048
548
c ART101 Aortic Valve Disease 2 63 0.047
549
CYN002 Cyanosis, Transient Neonatal 45 0.047
550
c LPD015 Lipodystrophy, Familial Partial, Type 2 62 0.047
551
P SPR086 Spermatogenic Failure 3 44 0.047
552
MNN034 Mannose-Binding Lectin Deficiency 45 0.047
553
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.047
554
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 50 0.047
555
ATN004 Autonomic Neuropathy 44 0.047
556
c HYP740 Hyperlipoproteinemia, Type V 54 0.046
557
NTR046 Neutrophil Migration 50 0.046
558
c INV001 Invasive Aspergillosis 48 0.046
559
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.046
560
PRT019 Protein-Losing Enteropathy 46 0.046
561
VLV047 Volvulus of Midgut 50 0.046
562
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.046
563
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 67 0.045
564
P CMP008 Compartment Syndrome 48 0.045
565
P SHR029 Short Syndrome 57 0.045
566
GLY014 Glycerol Kinase Deficiency 49 0.045
567
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.044
568
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.044
569
ASP026 Asplenia, Isolated Congenital 44 0.044
570
MTC027 Mitochondrial Trifunctional Protein Deficiency 56 0.044
571
FRZ001 Frozen Shoulder 53 0.044
572
ACT017 Acute Chest Syndrome 50 0.044
573
FRC011 Fructose Intolerance, Hereditary 56 0.044
574
CHR177 Chromophobe Renal Cell Carcinoma 56 0.044
575
CRN017 Coronary Thrombosis 47 0.044
576
P SBR004 Seborrheic Dermatitis 45 0.044
577
P MYT002 Myotonic Dystrophy 49 0.044
578
c VRL012 Viral Meningitis 48 0.043
579
c VRL007 Viral Encephalitis 51 0.043
580
P MYM013 Moyamoya Disease 1 54 0.043
581
ATN011 Autoinflammation with Infantile Enterocolitis 43 0.043
582
ONC002 Onchocerciasis 51 0.043
583
MNC019 Monocarboxylate Transporter 1 Deficiency 46 0.043
584
TRG002 Trigeminal Neuralgia 60 0.042
585
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.042
586
P OBS001 Obstructive Jaundice 48 0.042
587
FML235 Familial Combined Hyperlipoproteinemia 29 0.042
588
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.042
589
CHD004 Chudley-Mccullough Syndrome 44 0.042
590
CHL013 Cholecystolithiasis 37 0.042
591
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 51 0.042
592
P MTR012 Mitral Valve Disease 57 0.041
593
TXC020 Toxic Oil Syndrome 33 0.041
594
P NRM001 Neuromyelitis Optica 60 0.041
595
P HYP083 Hypopituitarism 53 0.041
596
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 27 0.041
597
FTL021 Fetal Macrosomia 42 0.041
598
c NMN014 Niemann-Pick Disease, Type C2 48 0.041
599
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.041
600
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.041
601
P RTN014 Retinal Artery Occlusion 46 0.040
602
BRN026 Branch Retinal Artery Occlusion 43 0.040
603
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 45 0.039
604
TBR011 Tuberculous Meningitis 48 0.039
605
GLC008 Glucose Metabolism Disease 40 0.039
606
FLL008 Folliculitis 46 0.038
607
LYM007 Lymphangioleiomyomatosis 68 0.038
608
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.038
609
P GLL020 Gallbladder Disease 58 0.038
610
KRN001 Korean Hemorrhagic Fever 34 0.038
611
LYM022 Lymphangioma 53 0.038
612
CHY002 Chylomicron Retention Disease 64 0.038
613
BLP005 Blepharitis 49 0.037
614
c NMN016 Niemann-Pick Disease, Type B 58 0.037
615
ACT162 Acute Sensory Ataxic Neuropathy 26 0.037
616
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.037
617
OVR063 Overnutrition 43 0.037
618
CRB009 Cerebritis 36 0.037
619
FLT006 Floating-Harbor Syndrome 48 0.037
620
P HYP024 Hypoparathyroidism 55 0.037
621
PRX001 Peroxisomal Disease 46 0.036
622
END072 Endotheliitis 35 0.036
623
PLC005 Placental Insufficiency 57 0.036
624
URT049 Urate Oxidase, Pseudogene 25 0.036
625
XNT003 Xanthomatosis 49 0.035
626
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.035
627
P PTY003 Pityriasis Rubra Pilaris 58 0.035
628
c RCR022 Recurrent Acute Pancreatitis 47 0.035
629
HYP006 Hypertensive Heart Disease 49 0.035
630
BLD063 Bile Duct Cysts 43 0.035
631
c ATM075 Autoimmune Encephalitis 38 0.035
632
ADS015 Aids Wasting Syndrome 22 0.035
633
DRM009 Dermatomycosis 36 0.035
634
ADL030 Adult-Onset Still's Disease 58 0.034
635
TRC005 Tracheal Stenosis 38 0.034
636
LNN001 Lennox-Gastaut Syndrome 57 0.034
637
MYC005 Myocardial Stunning 46 0.034
638
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 58 0.034
639
ACR041 Acromelic Frontonasal Dysostosis 52 0.034
640
SCT005 Scott Syndrome 48 0.033
641
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 61 0.033
642
c EXS019 Exostoses, Multiple, Type I 52 0.033
643
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 44 0.033
644
P RRL003 Rare Lymphatic Malformation 31 0.032
645
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.032
646
PYR016 Pyridoxine Deficiency 30 0.032
647
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.032
648
MYC019 Mycobacterium Marinum 29 0.031
649
BRR012 Berardinelli-Seip Congenital Lipodystrophy 48 0.030
650
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 39 0.030
651
P LPM005 Lipomatosis 45 0.030
652
P HYP058 Hypervitaminosis a 49 0.030
653
c FTL070 Fetal Akinesia Deformation Sequence 2 33 0.029
654
P FML187 Familial Hypertension 37 0.029
655
RTN021 Retinal Vascular Occlusion 44 0.029
656
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 0.028
657
EXT006 Extrahepatic Cholestasis 40 0.027
658
P HYP078 Hypertrophy of Breast 43 0.027
659
c NRM008 Neuromyelitis Optica Spectrum Disorder 31 0.027
660
MRS001 Marasmus 43 0.027
661
c CHL134 Cholestasis, Benign Recurrent Intrahepatic, 1 57 0.026
662
WDM005 Wiedemann-Rautenstrauch Syndrome 47 0.026
663
PLT031 Platelet Membrane Fluidity 28 0.026
664
EXF003 Exfoliative Dermatitis 27 0.026
665
VLL006 Villous Adenoma 38 0.026
666
ADR041 Adrenal Cortical Adenoma 43 0.025
667
ATP014 Atp8b1 Deficiency 25 0.025
668
SBL008 Sea-Blue Histiocyte Disease 43 0.024
669
ORG002 Organic Acidemia 43 0.024
670
P PLY188 Polyendocrinopathy 32 0.024
Content
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