Search results for Glutamic acid

3286 hits were found for Glutamic acid

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 46 42.080
2
LPD008 Lipid Metabolism Disorder 62 41.176
3
NNL005 Non-Alcoholic Fatty Liver Disease 63 39.482
4
FTT001 Fatty Liver Disease 62 38.944
5
GLT005 Glutamate Formiminotransferase Deficiency 42 38.855
6
P SZR006 Seizure Disorder 70 38.846
7
GST092 Gastroesophageal Reflux 61 38.756
8
HLX001 Helix Syndrome 48 38.621
9
c GLY008 Glycogen Storage Disease Ii 72 38.359
10
LYS012 Lysosomal Acid Lipase Deficiency 65 37.754
11
CHL068 Cholestasis 61 35.271
12
P MPL001 Maple Syrup Urine Disease 70 35.083
13
P NRB001 Neuroblastoma 66 34.875
14
c AMY091 Amyotrophic Lateral Sclerosis 1 88 34.616
15
P LTR001 Lateral Sclerosis 58 34.481
16
P LVR013 Liver Disease 69 34.372
17
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 56 33.452
18
P FRS004 Free Sialic Acid Storage Disorders 41 33.189
19
GLM045 Glioma 63 32.593
20
GLL048 Glial Tumor 52 32.577
21
P ENC018 Encephalopathy 62 32.282
22
INF159 Infantile Sialic Acid Storage Disease 41 31.996
23
PRT037 Pertussis 65 31.633
24
MTB004 Metabolic Acidosis 48 31.098
25
HYP014 Hyperuricemia 51 30.971
26
P SCH015 Schizophrenia 74 30.950
27
c TYP008 Type 1 Diabetes Mellitus 70 30.721
28
ISC004 Ischemia 61 30.024
29
P HNT016 Huntington Disease 73 29.832
30
P EPL164 Epilepsy 68 29.598
31
P DBT009 Diabetes Mellitus 67 29.181
32
MNT002 Mental Depression 57 29.093
33
DPR016 Depression 65 28.986
34
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 28.702
35
P ALZ034 Alzheimer Disease 87 28.583
36
RFS006 Refsum Disease, Classic 63 28.555
37
c TYP009 Type 2 Diabetes Mellitus 92 28.487
38
P BPL003 Bipolar Disorder 56 28.371
39
HYP066 Hyperglycemia 61 28.052
40
NRL016 Neural Tube Defects 81 28.048
41
48X005 48,xyyy 39 27.974
42
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 27.887
43
c MJR022 Major Affective Disorder 8 38 27.824
44
c MJR024 Major Affective Disorder 9 41 27.824
45
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 27.744
46
HYP266 Hypoxia 57 27.556
47
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 27.543
48
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 27.543
49
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 27.541
50
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 27.541
51
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 27.535
52
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 27.535
53
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 27.535
54
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 27.535
55
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 27.535
56
LVR012 Liver Cirrhosis 63 27.513
57
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 27.473
58
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 27.444
59
BRN071 Brain Injury 50 27.051
60
HYP056 Hypoglycemia 65 26.990
61
GT001 Gout 64 26.738
62
TRM010 Traumatic Brain Injury 51 26.632
63
HPT004 Hepatic Coma 43 26.577
64
ALC007 Alcohol Dependence 66 26.348
65
P MJR001 Major Depressive Disorder 68 26.344
66
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 26.326
67
DCR008 Dicarboxylic Aminoaciduria 40 26.196
68
CLT003 Colitis 63 26.103
69
HPT019 Hepatic Encephalopathy 59 26.082
70
AGN016 Aging 54 25.654
71
BNR002 Bone Resorption Disease 47 25.611
72
STT001 Status Epilepticus 59 25.514
73
GLB002 Glioblastoma 67 25.394
74
HYP060 Hyperinsulinism 54 25.377
75
HMN044 Human Immunodeficiency Virus Type 1 78 25.278
76
ALL029 Allergic Disease 59 24.680
77
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 24.584
78
CRB004 Cerebral Artery Occlusion 45 24.510
79
P HYP750 Hypertriglyceridemia, Familial 62 24.434
80
c HYP836 Hypercholesterolemia, Familial, 1 73 24.392
81
P CRN300 Coronary Heart Disease 1 73 24.296
82
P BRS047 Breast Cancer 98 23.997
83
c MGR028 Migraine with or Without Aura 1 64 23.972
84
c ATS007 Autism Spectrum Disorder 72 23.625
85
P DDN001 Duodenal Ulcer 53 23.455
86
P ATS364 Autism 69 23.400
87
P TMP001 Temporal Lobe Epilepsy 49 23.367
88
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 23.252
89
ALK013 Alkaptonuria 59 23.069
90
AMN002 Amino Acid Metabolic Disorder 39 23.023
91
ACT119 Acute Promyelocytic Leukemia 62 22.834
92
CHL014 Cholera 62 22.808
93
MDD011 Mood Disorder 62 22.806
94
ANX004 Anoxia 40 22.781
95
c CHR684 Chronic Kidney Disease 69 22.547
96
OST012 Osteoarthritis 77 22.530
97
SPN186 Spinal Cord Injury 61 22.483
98
P NRP001 Neuropathy 60 22.071
99
HRT031 Hartnup Disorder 52 22.061
100
P DRR001 Diarrhea 55 22.018
101
P ENC004 Encephalitis 61 22.007
102
ISV001 Isovaleric Acidemia 54 21.999
103
ATH013 Atherosclerosis Susceptibility 63 21.993
104
NNL006 Non-Alcoholic Steatohepatitis 54 21.991
105
LPP008 Lipoprotein Quantitative Trait Locus 65 21.917
106
P GST044 Gastritis 55 21.764
107
ARG002 Argininosuccinic Aciduria 61 21.748
108
PRM236 Primary Biliary Cholangitis 60 21.727
109
P INF038 Influenza 68 21.430
110
P LKM002 Leukemia 67 21.411
111
DFC004 Deficiency Anemia 74 21.357
112
PPL052 Papillomatosis, Confluent and Reticulated 34 21.297
113
P PRS040 Prostate Cancer 95 21.270
114
CYT002 Cytokine Deficiency 43 21.240
115
IMM167 Immune Deficiency Disease 78 21.227
116
P ESP024 Esophagitis 60 21.138
117
P KDN018 Kidney Disease 72 21.115
118
P CLR023 Colorectal Cancer 100 21.087
119
OCL069 Ocular Motor Apraxia 57 21.053
120
HMC014 Homocysteinemia 52 21.030
121
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 20.933
122
P ALC033 Alcohol Use Disorder 61 20.906
123
c GLL024 Gallbladder Disease 1 52 20.831
124
MNS015 Monosodium Glutamate Sensitivity 18 20.808
125
P HPT021 Hepatitis 69 20.777
126
IRN002 Iron Metabolism Disease 57 20.761
127
P HRP006 Herpes Simplex 65 20.560
128
ULC004 Ulcerative Colitis 74 20.555
129
P PRK039 Parkinsonism 55 20.546
130
CYS001 Cystic Fibrosis 78 20.543
131
P INF037 Inflammatory Bowel Disease 53 20.490
132
P ACN011 Acne 57 20.460
133
P CHR345 Chronic Pain 50 20.383
134
P MYC084 Mycobacterium Tuberculosis 1 68 20.355
135
ATM095 Autoimmune Disease 61 20.335
136
P ATT013 Attention Deficit-Hyperactivity Disorder 64 20.262
137
47X002 47,xyy 48 20.254
138
P HPT023 Hepatocellular Carcinoma 96 20.152
139
PPT005 Peptic Ulcer Disease 58 20.078
140
P FRG001 Fragile X Syndrome 70 20.059
141
P MYP004 Myopathy 67 19.924
142
c PRC016 Pre-Eclampsia 65 19.897
143
TTN003 Tetanus 65 19.826
144
ORG002 Organic Acidemia 44 19.823
145
STF001 Stiff-Person Syndrome 58 19.782
146
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 19.679
147
STR067 Stroke, Ischemic 80 19.652
148
PHS025 Phosphatase, Acid, of Tissues 28 19.635
149
P GLM040 Glioma Susceptibility 1 71 19.549
150
CTR172 Citrullinemia, Classic 65 19.538
151
P OST002 Osteoporosis 76 19.520
152
ART140 Arteries, Anomalies of 53 19.512
153
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 19.488
154
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 19.488
155
P HRT032 Heart Disease 81 19.410
156
P MLT020 Multiple Sclerosis 79 19.356
157
PHN003 Phenylketonuria 76 19.079
158
P PRP019 Peripheral Nervous System Disease 58 19.056
159
P PNC035 Pancreatic Cancer 86 19.013
160
P GCH001 Gaucher's Disease 70 19.005
161
P LNG032 Lung Cancer 98 18.858
162
GBM001 Gaba Aminotransferase Deficiency 29 18.711
163
INS024 Insulin-Like Growth Factor I 78 18.667
164
HRW001 Hair Whorl 35 18.631
165
P PHC003 Pheochromocytoma 69 18.627
166
P TRM003 Tremor 48 18.598
167
CRH001 Crohn's Disease 80 18.472
168
c HPT073 Hepatitis C Virus 71 18.339
169
c MCR115 Microvascular Complications of Diabetes 5 65 18.249
170
P ART022 Arthritis 71 18.222
171
OST159 Osteogenic Sarcoma 66 18.165
172
P VSC007 Vascular Disease 63 18.153
173
P PRD008 Periodontitis 64 18.132
174
c ACT027 Acute Pancreatitis 60 18.039
175
ALL014 Allergic Encephalomyelitis 34 18.015
176
ADR040 Adrenal Gland Pheochromocytoma 46 17.903
177
P LCT001 Lactic Acidosis 51 17.860
178
NPH009 Nephrolithiasis 54 17.818
179
c HYP595 Hypertension, Essential 85 17.815
180
BRN004 Brain Edema 54 17.701
181
c HPT001 Hepatitis C 62 17.638
182
KRT002 Keratomalacia 55 17.636
183
GLC003 Glucose Intolerance 54 17.612
184
BCT022 Bacterial Infectious Disease 56 17.608
185
P CHL066 Cholangitis 52 17.513
186
P PNC044 Pancreatitis 61 17.503
187
P MYC007 Myocardial Infarction 70 17.462
188
ANX010 Anxiety 70 17.443
189
P BND020 Bone Disease 59 17.408
190
ADR007 Adrenoleukodystrophy 73 17.355
191
c ACT071 Acute Kidney Failure 60 17.309
192
GYR004 Gyrate Atrophy of Choroid and Retina 58 17.238
193
P BCL017 B-Cell Lymphoma 59 17.226
194
P HYP086 Hypothyroidism 69 17.223
195
P PSR002 Psoriasis 63 17.173
196
P MLN008 Melanoma 76 17.102
197
P ADN016 Adenocarcinoma 63 17.090
198
c INH020 Inherited Metabolic Disorder 48 17.041
199
MLG169 Malignant Astrocytoma 57 17.035
200
c LKM061 Leukemia, Acute Myeloid 83 16.994
201
DRM006 Dermatitis 62 16.970
202
PRT251 Proteinuria, Chronic Benign 57 16.780
203
GST023 Gastric Ulcer 52 16.760
204
GBT001 Gaba-Transaminase Deficiency 37 16.726
205
GLT033 Glutamic Acid Decarboxylase, Brain, Membrane Form 4 16.708
206
c HPT016 Hepatitis B 62 16.651
207
P OVR042 Ovarian Cancer 88 16.565
208
P PRK057 Parkinson Disease, Late-Onset 80 16.494
209
HGH043 High Grade Glioma 45 16.487
210
c DVL036 Developmental and Epileptic Encephalopathy 39 39 16.463
211
PLM001 Pulmonary Tuberculosis 69 16.463
212
PST011 Pustulosis of Palm and Sole 52 16.444
213
MYL069 Myeloma, Multiple 77 16.422
214
VTM009 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1 31 16.324
215
CRB039 Cerebrovascular Disease 66 16.199
216
P MYL006 Myeloid Leukemia 61 16.184
217
P DRM053 Dermatitis, Atopic 65 16.178
218
P LPS004 Lupus Erythematosus 61 16.112
219
DWN001 Down Syndrome 70 16.111
220
P GST053 Gastric Cancer 83 16.088
221
c SYS001 Systemic Lupus Erythematosus 87 15.983
222
PLM129 Pulmonary Disease, Chronic Obstructive 74 15.948
223
SKN016 Skin Disease 63 15.948
224
VCC001 Vaccinia 47 15.930
225
c ACT134 Acute Liver Failure 59 15.888
226
PRT036 Peritonitis 65 15.830
227
P RTN016 Retinal Degeneration 52 15.817
228
TRC120 Tricarboxylic Acid Cycle, Defect of 16 15.735
229
P SLL003 Salla Disease 45 15.724
230
HMP009 Haemophilus Influenzae 41 15.643
231
BRR014 Barrett Esophagus 66 15.555
232
STM007 Stomatitis 54 15.542
233
P RHM011 Rheumatoid Arthritis 82 15.511
234
END086 End Stage Renal Disease 52 15.392
235
URM002 Uremia 47 15.254
236
CHL123 Chlamydia 58 15.244
237
ACQ007 Acquired Immunodeficiency Syndrome 59 15.210
238
MLR004 Malaria 80 15.196
239
P BLD134 Bladder Cancer 79 15.184
240
SVR001 Severe Acute Respiratory Syndrome 67 15.135
241
DBT010 Diabetic Neuropathy 54 15.117
242
INT323 Intraocular Pressure Quantitative Trait Locus 64 15.098
243
ADN018 Adenoma 59 15.063
244
URT049 Urate Oxidase, Pseudogene 24 15.058
245
NCT003 N-Acetylglutamate Synthase Deficiency 43 15.054
246
PNG002 Pain Agnosia 51 15.024
247
EMB004 Embryonal Carcinoma 56 14.990
248
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 14.978
249
P OVR082 Overgrowth Syndrome 49 14.975
250
c MCR120 Microvascular Complications of Diabetes 7 47 14.945
251
GST033 Gestational Diabetes 61 14.943
252
P URN019 Urinary Tract Infection 49 14.917
253
HLC007 Helicobacter Pylori Infection 67 14.872
254
P INF032 Infertility 57 14.851
256
GLT040 Glutamate-Cysteine Ligase Deficiency 31 14.835
257
P AST005 Asthma 76 14.823
258
c MCR113 Microvascular Complications of Diabetes 3 52 14.810
259
IRR002 Irritable Bowel Syndrome 65 14.778
260
c ACT068 Acute Cystitis 61 14.759
261
P DMN002 Dementia 66 14.744
262
P HYP265 Hypotonia 42 14.737
263
ADR022 Adrenomyeloneuropathy 39 14.735
264
NRR001 Neuroretinitis 42 14.717
265
CRV035 Cervical Cancer 73 14.716
266
RTN023 Retinitis 46 14.714
267
INS001 Insulinoma 59 14.683
268
OBS002 Obsessive-Compulsive Disorder 68 14.654
269
RCK004 Rickets 68 14.651
270
c PCH010 Pachyonychia Congenita 3 43 14.639
271
P MSC005 Muscular Dystrophy 67 14.635
272
c MCR133 Microvascular Complications of Diabetes 4 41 14.633
273
c MCR130 Microvascular Complications of Diabetes 6 41 14.628
274
ATS010 Autosomal Recessive Disease 42 14.612
275
P MSC003 Muscular Atrophy 52 14.578
276
GMM011 Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due to 25 14.562
277
TXC005 Toxic Shock Syndrome 62 14.547
278
PLY150 Polykaryocytosis Inducer 29 14.470
279
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 14.450
280
URL001 Urolithiasis 46 14.368
281
P HDC001 Headache 57 14.344
282
HDN002 Head Injury 44 14.282
283
DNT012 Dental Caries 53 14.210
284
P DYS154 Dystonia 64 14.179
285
LNG099 Lung Disease 62 14.176
286
CNG034 Congestive Heart Failure 69 14.109
287
PPT001 Peptic Esophagitis 52 14.045
288
SQM006 Squamous Cell Carcinoma 60 14.030
289
c HPT003 Hepatitis a 63 13.987
290
P CTR002 Cataract 60 13.982
291
PSY004 Psychotic Disorder 66 13.941
292
P RTN024 Retinoblastoma 73 13.939
293
P AMY004 Amyloidosis 70 13.893
294
DSS032 Disease by Infectious Agent 55 13.815
295
RNL114 Renal Cell Carcinoma, Nonpapillary 80 13.815
296
AMN003 Amnestic Disorder 54 13.804
297
PRP001 Propionic Acidemia 65 13.804
298
P RTN008 Retinitis Pigmentosa 80 13.797
299
c SML038 Small Cell Cancer of the Lung 69 13.788
300
AMN012 Aminoacidopathies 20 13.748
301
c ATR087 Atrial Standstill 1 74 13.694
302
P CRD119 Cardiac Arrest 67 13.685
303
SVR004 Severe Combined Immunodeficiency 72 13.685
304
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 13.653
305
c ACT075 Acute Myocardial Infarction 56 13.648
306
KRT009 Keratosis 53 13.647
307
NPH091 Nephrolithiasis, Calcium Oxalate 61 13.637
308
P MTH008 Methylmalonic Acidemia 52 13.614
309
P LKM062 Leukemia, Acute Lymphoblastic 69 13.582
310
CNS004 Constipation 56 13.495
311
c DNT047 Dentinogenesis Imperfecta Type 2 35 13.418
312
SRC014 Sarcoma 65 13.377
313
P ADL010 Adult Respiratory Distress Syndrome 71 13.316
314
P RSP003 Respiratory Failure 74 13.301
315
SPN035 Spindle Cell Sarcoma 54 13.220
316
VTM002 Vitamin B12 Deficiency 48 13.203
317
P LYM118 Lymphoma 67 13.199
318
P LNG064 Lung Cancer Susceptibility 3 70 13.195
319
MLD018 Mild Cognitive Impairment 48 13.188
320
GST045 Gastroenteritis 58 13.188
321
P INT099 Intrahepatic Cholestasis of Pregnancy 62 13.185
322
P ECL001 Eclampsia 52 13.141
323
CLN015 Colon Adenocarcinoma 65 13.118
324
P THR014 Thrombocytopenia 66 13.110
325
MTH071 Methane Production 25 13.100
326
PST028 Post-Traumatic Stress Disorder 59 13.038
327
THY029 Thyroid Carcinoma 51 12.987
328
P MTR014 Motor Neuron Disease 65 12.984
329
P PLY019 Polyneuropathy 52 12.982
330
ESP021 Esophageal Cancer 83 12.977
331
URC002 Urea Cycle Disorder 51 12.921
332
BRN024 Bronchitis 67 12.915
333
AVN001 Avian Influenza 61 12.866
334
P SKN015 Skin Carcinoma 71 12.858
335
TRN015 Transient Cerebral Ischemia 63 12.848
336
P RHN004 Rhinitis 57 12.836
337
GST050 Gastrointestinal System Disease 55 12.835
338
TRT001 Teratocarcinoma 42 12.798
339
CYS013 Cystinuria 66 12.775
340
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 12.751
341
DPH001 Diphtheria 59 12.717
342
c VRL010 Viral Hepatitis 53 12.610
343
FLT009 Folate Malabsorption, Hereditary 49 12.587
344
HYP005 Hypokalemia 55 12.533
345
PST092 Posttransplant Acute Limbic Encephalitis 28 12.519
346
CHL004 Cholelithiasis 49 12.503
347
P RTN018 Retinal Disease 53 12.475
348
P ATR011 Atrial Fibrillation 66 12.473
349
c FTL070 Fetal Akinesia Deformation Sequence 2 36 12.438
350
PLM010 Pulmonary Edema 55 12.427
351
P MVM001 Movement Disease 61 12.396
352
P THL005 Thalassemia 56 12.389
353
P BRS044 Breast Adenocarcinoma 58 12.345
354
P EXN002 Exanthem 58 12.306
355
P SCL009 Sclerosing Cholangitis 48 12.260
356
c DWL002 Dowling-Degos Disease 1 58 12.245
357
P HYP076 Hyperthyroidism 53 12.214
358
MTH009 Mouth Disease 57 12.171
359
P MNN013 Meningitis 65 12.122
360
ANG054 Angina Pectoris 66 12.105
361
P GLY013 Glycogen Storage Disease 60 12.104
362
P MYC033 Myoclonus 47 12.080
363
P FBR017 Fibrosarcoma 56 12.063
364
OST003 Osteonecrosis 61 12.045
365
P HYP098 Hypereosinophilic Syndrome 66 12.035
366
MYL009 Myelodysplastic Syndrome 67 12.031
367
P ART021 Arteriosclerosis 54 11.998
368
BRN028 Brain Cancer 74 11.987
369
WTH001 Withdrawal Disorder 48 11.972
370
CLF027 Cleft Palate, Isolated 64 11.957
371
P ZLL001 Zellweger Syndrome 65 11.924
372
RYS001 Reye Syndrome 49 11.899
373
P SCK005 Sickle Cell Disease 56 11.789
374
BLR008 Bilirubin Metabolic Disorder 57 11.762
375
HNS001 Hansen's Disease 32 11.733
376
c NMN013 Niemann-Pick Disease, Type a 63 11.729
377
P NTR004 Neutropenia 63 11.725
378
END040 Endogenous Depression 55 11.674
379
FBR047 Fibromyalgia 58 11.669
380
P LPR021 Leprosy 3 71 11.660
381
P PLM037 Pulmonary Hypertension 72 11.652
382
P GLM007 Glomerulonephritis 60 11.643
383
ARG004 Argyria 26 11.634
384
PRS047 Prostatitis 58 11.579
385
DBT084 Diabetes Mellitus, Ketosis-Prone 60 11.562
386
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 11.557
387
HMS001 Hemosiderosis 48 11.554
388
P INB001 Inborn Amino Acid Metabolism Disorder 11 11.497
389
P HMC002 Homocystinuria 53 11.496
390
CRD132 Cardiac Conduction Defect 60 11.492
391
DYS073 Dysphagia 53 11.480
392
P PLM036 Pulmonary Fibrosis 66 11.467
393
P EYD002 Eye Disease 57 11.459
394
P OBS001 Obstructive Jaundice 48 11.457
395
c BRN108 Branchiootic Syndrome 1 62 11.451
396
P CYS018 Cystitis 59 11.441
397
P PLY011 Polycystic Ovary Syndrome 57 11.436
398
P THY032 Thyroiditis 57 11.392
399
FCL014 Focal Epilepsy 53 11.365
400
PRP027 Peripheral Vascular Disease 71 11.323
401
LPT014 Leptin Deficiency or Dysfunction 78 11.309
402
THR024 Thrombosis 56 11.307
403
NTR005 Nutritional Deficiency Disease 61 11.305
404
SPS057 Spasticity 42 11.277
405
CRV045 Cervical Intraepithelial Neoplasia 39 11.274
406
CRV002 Cervix Uteri Carcinoma in Situ 47 11.271
407
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 11.256
408
CHR073 Choreatic Disease 54 11.256
409
P PRS038 Personality Disorder 65 11.255
410
CRB037 Cerebral Palsy 67 11.221
411
P CLC063 Celiac Disease 1 66 11.187
412
P KDN017 Kidney Cancer 61 11.179
413
P ALP008 Alopecia 54 11.153
414
PRS045 Prostatic Hypertrophy 53 11.148
415
P CRD246 Cardiovascular System Disease 56 11.143
416
P KLZ004 Kala-Azar 1 41 11.141
417
LSH001 Leishmaniasis 64 11.141
418
ANT024 Anthrax Disease 58 11.074
419
DMY004 Demyelinating Disease 50 11.053
420
LMB024 Limbic Encephalitis 43 11.045
421
NWC001 Newcastle Disease 47 11.012
422
PRX001 Peroxisomal Disease 46 11.007
423
P NPH012 Nephrotic Syndrome 60 10.974
424
CHL065 Cholangiocarcinoma 58 10.920
425
P CND004 Candidiasis 58 10.898
426
INT079 Intrahepatic Cholangiocarcinoma 51 10.874
427
P RRH023 Rare Hereditary Hemochromatosis 54 10.851
428
MSL001 Measles 61 10.829
429
P PRP029 Porphyria 60 10.812
430
P PNM007 Pneumonia 67 10.789
431
P SBS003 Substance Abuse 54 10.781
432
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 59 10.763
433
P NMN002 Niemann-Pick Disease 60 10.752
434
VSC002 Vascular Dementia 60 10.747
435
CNT047 Contact Dermatitis 57 10.727
436
ADG002 Audiogenic Seizures 25 10.702
437
P INS002 in Situ Carcinoma 53 10.689
438
ALL003 Allergic Rhinitis 67 10.682
439
P HML002 Hemolytic Anemia 62 10.675
440
P LKM071 Leukemia, Chronic Lymphocytic 75 10.667
441
LYS002 Lysosomal Storage Disease 51 10.627
442
IRN001 Iron Deficiency Anemia 58 10.625
443
MCS002 Mucositis 56 10.605
444
CRB011 Cerebrotendinous Xanthomatosis 65 10.587
445
CRT015 Carotid Artery Occlusion 45 10.582
446
P PRN023 Prion Disease 60 10.551
447
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 10.549
448
P CNJ013 Conjunctivitis 66 10.544
449
P ART023 Arthropathy 61 10.531
450
c ACT073 Acute Leukemia 58 10.523
451
PPL022 Papilloma 53 10.507
452
PLM033 Pulmonary Embolism 58 10.476
453
ACT084 Acute Stress Disorder 54 10.469
454
MDD018 Middle East Respiratory Syndrome 44 10.424
455
RLP002 Relapsing-Remitting Multiple Sclerosis 56 10.423
456
P MLN007 Male Infertility 56 10.419
457
P SPP010 Suppressor of Tumorigenicity 3 51 10.418
458
P NSP012 Nasopharyngeal Carcinoma 61 10.338
459
DSR078 Disorder of Branched-Chain Amino Acid Metabolism 9 10.325
460
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 10.207
461
ISL099 Isolated Methylmalonic Acidemia 36 10.207
462
P TRN020 Turner Syndrome 67 10.203
463
PRS021 Prostatic Adenoma 43 10.171
464
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 10.165
465
LTN029 Latent Autoimmune Diabetes in Adults 38 10.154
466
ENT004 Enthesopathy 51 10.144
467
KPS004 Kaposi Sarcoma 77 10.128
468
CHG001 Chagas Disease 66 10.124
469
SQM002 Squamous Cell Papilloma 46 10.114
470
c LKM005 Leukemia, T-Cell, Chronic 34 10.104
471
INT007 Intermediate Coronary Syndrome 54 10.094
472
c DLT002 Dilated Cardiomyopathy 78 10.074
473
P HYP069 Hyperparathyroidism 62 10.065
474
P RTT002 Rett Syndrome 79 10.052
475
P ATR005 Atrophic Gastritis 50 10.002
476
ANN002 Anencephaly 57 9.969
477
SBC016 Subacute Delirium 43 9.962
478
LYM133 Lymphoma, Hodgkin, Classic 74 9.947
479
P SLP006 Sleep Apnea 69 9.933
480
P HYD006 Hydrocephalus 61 9.915
481
P MDL005 Medulloblastoma 75 9.907
482
P URT039 Urticaria 58 9.903
483
MST005 Mastitis 53 9.876
484
c SCN036 Secondary Progressive Multiple Sclerosis 55 9.868
485
SCR011 Scrapie 39 9.862
486
RTN003 Retinal Ischemia 49 9.826
487
ENT011 Enterocolitis 55 9.817
488
ORL011 Oral Cancer 60 9.815
489
AMN007 Aminoacylase 1 Deficiency 33 9.815
490
ACY011 Acyl-Coa Dehydrogenase Deficiency 30 9.810
491
BLR001 Biliary Atresia 55 9.784
492
RTN017 Retinal Detachment 60 9.754
493
AMN006 Aminoaciduria 37 9.747
494
PRS129 Prostatic Hyperplasia, Benign 49 9.743
495
SCH014 Schistosomiasis 56 9.733
496
c SPN258 Spinocerebellar Ataxia, Autosomal Recessive 13 38 9.728
497
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 9.727
498
PRP030 Purpura 54 9.710
499
XNT003 Xanthomatosis 49 9.708
500
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 9.695
501
GLT035 Glutaric Acidemia I 57 9.657
502
LYM019 Lymphosarcoma 46 9.644
503
CRB090 Cerebral Hypoxia 42 9.624
504
P DNG005 Dengue Virus 56 9.621
505
P NRV007 Nervous System Disease 67 9.598
506
ORL015 Oral Squamous Cell Carcinoma 43 9.588
507
P BRB001 Beriberi 44 9.576
508
P SYS005 Systemic Scleroderma 74 9.573
509
P VSC011 Vasculitis 61 9.573
510
P INT068 Intestinal Disease 53 9.556
511
c SPN292 Spinocerebellar Ataxia, Autosomal Recessive 18 31 9.521
512
P GRF003 Graft-Versus-Host Disease 71 9.519
513
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 9.518
514
CHR074 Choriocarcinoma 46 9.491
515
CVD001 Covid-19 57 9.471
516
PRP016 Paraplegia 52 9.455
517
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 9.454
518
CHC001 Chickenpox 57 9.451
519
c LKM063 Leukemia, Chronic Myeloid 71 9.431
520
P MCR010 Microcephaly 60 9.423
521
ACT098 Acute Erythroid Leukemia 55 9.393
522
c THR092 Thrombophilia Due to Thrombin Defect 74 9.386
523
c FML021 Familial Hypercholesterolemia 72 9.384
524
P SLP005 Sleep Disorder 61 9.374
526
RSC001 Rosacea 55 9.368
527
END057 Endometrial Cancer 72 9.351
528
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 9.341
529
PRN011 Pernicious Anemia 53 9.337
530
PNC041 Pancreatic Ductal Adenocarcinoma 51 9.329
531
CLR108 Colorectal Adenoma 64 9.322
532
ETN001 Eating Disorder 59 9.319
533
P ANP001 Anaplastic Large Cell Lymphoma 61 9.293
534
GNG013 Gingivitis 59 9.293
535
P GRV001 Graves' Disease 55 9.281
536
PTH003 Pathologic Nystagmus 52 9.263
537
P RCT021 Rectum Cancer 54 9.263
538
P OPT006 Optic Nerve Disease 58 9.252
539
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 9.234
540
P SHR001 Short Bowel Syndrome 53 9.218
541
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 65 9.207
542
SCK003 Sickle Cell Anemia 74 9.197
543
PRT013 Portal Hypertension 59 9.167
544
P TBR001 Tuberous Sclerosis 69 9.163
545
P BNG032 Benign Mesothelioma 53 9.154
546
ALL006 Allergic Asthma 56 9.146
547
MSC157 Muscular Dystrophy, Duchenne Type 79 9.145
548
NRT001 Neurotic Disorder 56 9.110
549
P SRC025 Sarcoidosis 1 71 9.100
550
P ANR048 Aniridia 1 64 9.086
551
P PYL005 Pyelonephritis 57 9.067
552
LYS003 Lysinuric Protein Intolerance 57 9.029
553
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 9.027
554
TBC004 Tobacco Addiction 63 9.024
555
MNN043 Meningioma, Familial 79 9.023
556
HMN014 Human Immunodeficiency Virus Infectious Disease 54 9.013
557
P MCR129 Microvascular Complications of Diabetes 1 68 8.995
558
P PLY014 Polycystic Kidney Disease 69 8.990
559
c PRD040 Periodontitis, Chronic 52 8.982
560
TLN003 Telangiectasis 51 8.977
561
TRD006 Tardive Dyskinesia 53 8.966
562
RBS001 Rabies 58 8.965
563
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 8.956
564
MGL001 Megaloblastic Anemia 58 8.955
565
P RNL007 Renal Tubular Acidosis 50 8.954
566
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 8.901
567
c BTT014 Beta-Thalassemia 72 8.897
568
ADL002 Adult Syndrome 70 8.883
569
SCR001 Secretory Meningioma 40 8.841
570
LYM002 Lymphoplasmacyte-Rich Meningioma 35 8.841
571
SPN021 Spinal Meningioma 50 8.841
572
P LKD001 Leukodystrophy 59 8.824
573
P END044 Endometriosis 62 8.812
574
DYS015 Dysentery 50 8.807
575
MLT157 Multiple System Atrophy 1 69 8.799
576
ANR007 Anorexia Nervosa 60 8.796
577
P UVT001 Uveitis 57 8.793
578
MSC007 Muscle Hypertrophy 64 8.790
579
BRK010 Burkitt Lymphoma 66 8.744
580
P RHB003 Rhabdomyosarcoma 66 8.734
581
RHB024 Rhabdomyosarcoma 2 67 8.734
582
RNL077 Renal Fibrosis 46 8.728
583
c PLM164 Pulmonary Hypertension, Primary, 1 76 8.721
584
FDL002 Food Allergy 47 8.718
585
TND005 Tendinitis 54 8.705
586
JPN002 Japanese Encephalitis 61 8.700
587
HYP080 Hypogonadism 50 8.699
588
ANT039 Antisynthetase Syndrome 55 8.687
589
P MJR007 Major Affective Disorder 1 42 8.683
590
OTT002 Otitis Media 71 8.656
591
PRT038 Protein-Energy Malnutrition 53 8.577
592
c BCT007 Bacterial Meningitis 55 8.568
593
P ACT008 Actinic Keratosis 54 8.566
594
P FTL001 Fetal Alcohol Syndrome 55 8.535
595
c SCL052 Scleroderma, Familial Progressive 61 8.530
596
P NRN021 Neuronal Ceroid Lipofuscinosis 65 8.505
597
CHR178 Chromosomal Triplication 34 8.500
598
P TYR004 Tyrosinemia 50 8.497
599
P SCL018 Scoliosis 57 8.487
600
IGR001 Ige Responsiveness, Atopic 59 8.468
601
CHL067 Cholecystitis 60 8.447
602
P FML011 Familial Adenomatous Polyposis 71 8.441
603
P BNC003 Bone Cancer 58 8.414
604
P INT143 Interstitial Cystitis 60 8.408
605
PLC002 Plica Syndrome 35 8.386
606
SYN007 Synovitis 55 8.386
607
P HYP061 Hypertrophic Cardiomyopathy 69 8.369
608
P TRT010 Teratoma 51 8.361
609
SPL018 Splenomegaly 49 8.357
610
PNC129 Pancreatic Adenocarcinoma 65 8.338
611
c CNT035 Central Nervous System Disease 54 8.324
612
CRT072 Creutzfeldt-Jakob Disease 68 8.290
613
c PNS012 Paine Syndrome 60 8.269
614
HND015 Hand Skill, Relative 30 8.269
615
FRN006 Frontotemporal Dementia 68 8.261
616
c ATM011 Autoimmune Hepatitis 63 8.245
617
INT075 Intracranial Hypertension 53 8.233
618
P SNS001 Sensorineural Hearing Loss 59 8.208
619
CLR109 Colorectal Adenocarcinoma 50 8.197
620
LNG031 Lung Benign Neoplasm 51 8.171
621
P HMP007 Hemophilia 52 8.112
622
c ATM075 Autoimmune Encephalitis 40 8.110
623
TYP007 Typhoid Fever 64 8.099
624
VRC005 Varicose Veins 60 8.091
625
HYP141 Hyperphenylalaninemia 42 8.072
626
OCL006 Ocular Hypertension 53 8.047
627
P MYC008 Myocarditis 59 8.042
628
P SPN046 Spinal Muscular Atrophy 63 8.022
629
PYR009 Pyridoxine Deficiency Anemia 35 8.007
630
OST017 Osteomyelitis 63 8.000
631
MMM001 Mammary Paget's Disease 53 7.997
632
WST005 West Nile Virus 57 7.976
633
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 34 7.969
634
P NRC002 Narcolepsy 56 7.968
635
c TBR025 Tuberous Sclerosis 1 84 7.953
636
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 7.947
637
TND004 Tendinopathy 45 7.946
638
P PNC025 Panic Disorder 52 7.927
639
PRN019 Perinatal Necrotizing Enterocolitis 60 7.916
640
c BSL007 Basal Cell Carcinoma 68 7.915
641
P FNC004 Fanconi Syndrome 60 7.866
642
LYM143 Lymphoma, Non-Hodgkin, Familial 75 7.848
643
SCH012 Schizoaffective Disorder 50 7.846
644
CMM005 Common Cold 56 7.840
645
P MYS003 Myasthenia Gravis 68 7.811
646
CLF001 Cleft Lip 53 7.798
647
YLL002 Yellow Fever 61 7.797
648
P FBR031 Febrile Seizures 52 7.778
649
DRG003 Drug Dependence 46 7.769
650
GST040 Gastric Adenocarcinoma 67 7.757
651
HYP017 Hypophosphatemia 49 7.751
652
DSS009 Disseminated Intravascular Coagulation 57 7.705
653
PLG002 Plague 58 7.698
654
KRT006 Keratoconjunctivitis 53 7.671
655
P MTC069 Mitochondrial Disorders 57 7.664
656
P MYS005 Myositis 56 7.629
657
ALC006 Alcoholic Hepatitis 61 7.622
658
ANR040 Aneurysm 61 7.618
659
ATN004 Autonomic Neuropathy 42 7.617
660
P THY023 Thymoma 64 7.616
661
c THY107 Thymoma, Familial 42 7.611
662
ORT008 Orotic Aciduria 57 7.593
663
IGG001 Iga Glomerulonephritis 50 7.568
664
CRH005 Crohn's Colitis 53 7.564
665
BRT054 Brittle Bone Disorder 74 7.560
666
IMP005 Impotence 52 7.560
667
CCN001 Cocaine Dependence 48 7.556
668
GTR002 Goiter 53 7.541
669
NRT004 Neuritis 53 7.519
670
P SMK004 Smoking As a Quantitative Trait Locus 3 44 7.501
671
DWR001 Dwarfism 44 7.486
672
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 7.461
673
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 7.461
674
c MCR112 Microvascular Complications of Diabetes 2 42 7.461
675
ART016 Aortic Aneurysm 68 7.455
676
P CTR177 Citrullinemia, Type Ii, Adult-Onset 55 7.430
677
FML035 Familial Hyperlipidemia 55 7.429
678
CCN002 Cocaine Abuse 49 7.427
679
KRT019 Keratitis, Hereditary 66 7.425
680
P OPN001 Open-Angle Glaucoma 55 7.424
681
c 2HY001 2-Hydroxyglutaric Aciduria 38 7.420
682
LSC001 Lesch-Nyhan Syndrome 62 7.418
683
PLS011 Plasmacytoma 56 7.415
684
MRP001 Morphine Dependence 42 7.390
685
VRL011 Viral Infectious Disease 61 7.367
686
PLM031 Poliomyelitis 63 7.355
687
PST021 Postpartum Depression 50 7.354
688
CNV004 Canavan Disease 62 7.349
689
ERL001 Early Myoclonic Encephalopathy 62 7.348
690
PLC008 Placenta Disease 49 7.347
691
P END033 Endocarditis 58 7.345
692
P ICH004 Ichthyosis 56 7.335
693
CND006 Candida Glabrata 30 7.297
694
ATN005 Autonomic Dysfunction 46 7.292
695
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 7.285
696
ALL010 Allergic Contact Dermatitis 56 7.277
697
CNN005 Connective Tissue Disease 67 7.268
698
PLM134 Pulmonary Fibrosis, Idiopathic 76 7.268
699
HPT022 Hepatoblastoma 54 7.257
701
P PLY018 Polycythemia 56 7.234
702
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 7.226
703
VGN023 Vaginitis 56 7.216
704
BCK006 Back Pain 47 7.215
705
MNN009 Meningoencephalitis 48 7.203
706
P ANG015 Angioedema 56 7.184
707
P HYP111 Hyperprolinemia 45 7.168
708
P TCD001 Tic Disorder 49 7.150
709
P OLG002 Oligodendroglioma 66 7.150
710
PRV004 Periventricular Leukomalacia 52 7.126
711
CYS010 Cystinosis 62 7.117
712
OVR094 Ovarian Epithelial Cancer 39 7.113
713
P SJG008 Sjogren Syndrome 61 7.109
714
VSC003 Visceral Leishmaniasis 55 7.108
715
NRN004 Neuroendocrine Tumor 59 7.101
716
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 7.087
717
MCR013 Microphthalmia 60 7.057
718
P MGR001 Migraine Without Aura 49 7.043
719
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 7.039
720
P SLM003 Salmonellosis 54 7.031
721
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 7.018
722
HSH003 Hashimoto Thyroiditis 60 7.004
723
P NRF002 Neurofibromatosis 57 7.003
724
c ESS001 Essential Tremor 57 6.998
725
PTT037 Pituitary Tumors 44 6.994
726
SQM013 Squamous Cell Carcinoma, Head and Neck 73 6.990
727
THY030 Thyroid Gland Disease 50 6.990
728
TRN018 Transitional Cell Carcinoma 56 6.989
729
CMB007 Combined Immunodeficiency 57 6.985
730
MNG007 Manganese Poisoning 28 6.979
731
P TXP001 Toxoplasmosis 60 6.962
732
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 6.930
733
P CTN015 Cutaneous T Cell Lymphoma 48 6.913
734
TBR011 Tuberculous Meningitis 48 6.893
735
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 6.866
736
MST004 Mast Cell Neoplasm 42 6.854
737
WST001 West Syndrome 59 6.845
738
EXT007 Extracutaneous Mastocytoma 38 6.840
739
c HNT011 Huntington Disease-Like 3 34 6.839
740
OPT003 Opiate Dependence 49 6.835
741
GLS001 Gliosarcoma 64 6.835
742
ILS001 Ileus 50 6.820
743
LWC002 Lowe Oculocerebrorenal Syndrome 68 6.808
744
CHR066 Chronic Fatigue Syndrome 60 6.806
745
SPN051 Spondylitis 51 6.793
746
INF009 Inflammatory Spondylopathy 30 6.793
747
PRP080 Peripheral Artery Disease 54 6.792
748
KWS001 Kwashiorkor 45 6.763
749
PHR003 Pharyngitis 58 6.762
750
DRY001 Dry Eye Syndrome 50 6.749
751
PLC005 Placental Insufficiency 56 6.742
752
PRP083 Porphyria, Acute Intermittent 65 6.731
753
KRN002 Kearns-Sayre Syndrome 63 6.727
754
LMY002 Leiomyoma 51 6.725
755
HVY002 Heavy Metal Poisoning 22 6.723
756
ALX003 Alexander Disease 61 6.718
757
PRD004 Prediabetes Syndrome 52 6.714
758
P MGR003 Migraine with Aura 52 6.711
759
HMG005 Hemoglobinopathy 56 6.705
760
P CHN012 Chondrosarcoma 57 6.700
761
CHR100 Chronic Ulcer of Skin 57 6.695
762
P CRV039 Cervicitis 52 6.676
763
SFT003 Soft Tissue Sarcoma 57 6.672
764
DBT004 Diabetic Polyneuropathy 50 6.668
765
PNC001 Pancytopenia 53 6.649
766
P NGH001 Night Blindness 52 6.648
767
P FML355 Familial Intrahepatic Cholestasis 42 6.641
768
EPL131 Epilepsy, Pyridoxine-Dependent 45 6.640
769
LRN003 Learning Disability 49 6.630
770
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 52 6.613
771
SLP001 Sleeping Sickness 56 6.602
772
CRC021 Carcinosarcoma 64 6.598
773
P SPR120 Supranuclear Palsy, Progressive, 1 69 6.593
774
GLL008 Gilles De La Tourette Syndrome 65 6.587
775
NRN005 Neuronal Ceroid-Lipofuscinoses 61 6.570
776
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 6.569
777
ART002 Arts Syndrome 66 6.568
778
c HYP724 Hyperlipoproteinemia, Type Iii 67 6.565
779
c THY109 Thyroid Cancer, Nonmedullary, 1 55 6.549
780
P RBL001 Rubella 58 6.545
781
ASP007 Aspiration Pneumonia 49 6.544
782
P CHR071 Charcot-Marie-Tooth Disease 64 6.538
783
TRY001 Trypanosomiasis 50 6.523
784
BTN004 Biotin Deficiency 45 6.521
785
SDD001 Sudden Infant Death Syndrome 60 6.516
786
c HNT004 Huntington Disease-Like 2 52 6.500
787
P PTS002 Ptosis 52 6.499
788
SKN019 Skin Melanoma 71 6.488
789
HYD002 Hydronephrosis 58 6.468
790
ANP008 Anaplastic Oligoastrocytoma 29 6.452
791
HRN029 Hearing Loss, Noise-Induced 37 6.451
792
URT010 Ureteral Obstruction 45 6.447
793
CRC006 Carcinoid Syndrome 55 6.443
794
P RST001 Restless Legs Syndrome 52 6.424
795
P MMP001 Mumps 57 6.423
796
HMP005 Hemiplegia 54 6.417
797
P ATM019 Autoimmune Polyendocrine Syndrome 46 6.412
798
P ATX030 Ataxia-Telangiectasia 80 6.410
799
c HPT015 Hepatitis D 49 6.410
800
P CRN037 Craniosynostosis 68 6.405
801
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 6.393
802
P OLV001 Olivopontocerebellar Atrophy 51 6.387
803
c GRV008 Graves Disease 1 54 6.384
804
VTM033 Vitamin K Deficiency Bleeding 48 6.382
805
P MYP006 Myopia 56 6.357
806
c L2H001 L-2-Hydroxyglutaric Aciduria 49 6.350
807
P DST107 Distal Renal Tubular Acidosis 48 6.350
808
VLV047 Volvulus of Midgut 52 6.345
809
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 63 6.345
810
LYM027 Lymphopenia 56 6.343
811
c NMN015 Niemann-Pick Disease, Type C1 68 6.340
812
STN013 Stenotrophomonas Maltophilia Infection 26 6.337
813
c BLD140 Blood Group, I System 46 6.331
814
DSS008 Disease of Mental Health 74 6.331
815
PLS007 Plasmodium Falciparum Malaria 52 6.327
816
HYP025 Hyperphosphatemia 48 6.304
817
SPS019 Spastic Paraparesis 38 6.292
818
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 6.289
819
NRM005 Neuromuscular Disease 63 6.280
820
c SPN225 Spondyloarthropathy 1 70 6.264
821
CHK001 Chikungunya 60 6.261
822
DFF005 Diffuse Large B-Cell Lymphoma 54 6.248
823
c HMP029 Hemophilia a 68 6.245
824
RTN020 Retinal Vascular Disease 46 6.220
825
P MTC133 Mitochondrial Myopathy 50 6.215
826
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 6.192
827
INT002 Intermittent Claudication 61 6.191
828
P SYP003 Syphilis 59 6.187
829
ARG007 Argininemia 58 6.181
830
PLS009 Plasma Cell Neoplasm 64 6.178
831
PYR016 Pyridoxine Deficiency 29 6.170
832
TTH006 Tooth Disease 51 6.161
833
THY111 Thyroid Carcinoma, Familial Medullary 67 6.153
834
ANP005 Anaplastic Astrocytoma 57 6.146
835
P CNR004 Cone-Rod Dystrophy 2 74 6.146
836
KRT001 Keratoconjunctivitis Sicca 50 6.144
837
P HYP761 Hypouricemia, Renal, 1 44 6.129
838
P LCH002 Lichen Planus 54 6.087
839
HMN047 Human Cytomegalovirus Infection 57 6.084
840
c EXD008 Exudative Vitreoretinopathy 1 71 6.055
841
P ASP006 Aspergillosis 72 6.050
842
INT066 Interstitial Lung Disease 60 6.047
843
TRP006 Tarp Syndrome 58 6.038
844
GNR004 Generalized Anxiety Disorder 55 6.031
845
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 6.031
846
DBT002 Diabetic Autonomic Neuropathy 41 6.029
847
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 58 6.028
848
P MRC003 Mercury Poisoning 49 6.028
849
EXT006 Extrahepatic Cholestasis 40 6.028
850
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 6.011
851
P CRB088 Cerebral Atrophy 33 6.008
852
c JVN010 Juvenile Rheumatoid Arthritis 66 5.999
853
CMP010 Complex Regional Pain Syndrome 60 5.999
854
P PTT006 Pituitary Adenoma 55 5.991
855
CRN030 Coronary Stenosis 50 5.991
856
ACR007 Acromegaly 70 5.985
857
TNS005 Tonsillitis 57 5.983
858
INT067 Interstitial Nephritis 46 5.976
859
EXC002 Exocrine Pancreatic Insufficiency 42 5.975
860
CRD223 Cardiac Arrhythmia 63 5.968
861
GLY010 Glycine Encephalopathy 57 5.965
862
c GLC092 Glaucoma, Primary Open Angle 62 5.963
863
OPD006 Opioid Addiction 48 5.959
864
AZS001 Azoospermia 45 5.957
865
c HMC039 Hemochromatosis, Type 1 73 5.955
866
BRD004 Borderline Personality Disorder 53 5.948
867
P PLL002 Pellagra 46 5.946
868
SNS003 Sensory Peripheral Neuropathy 52 5.927
869
P PRM002 Primary Hyperoxaluria 65 5.921
870
NNT012 Neonatal Jaundice 53 5.919
871
LST001 Listeriosis 59 5.906
872
SCH003 Schizophreniform Disorder 55 5.904
873
P INT070 Intestinal Obstruction 57 5.894
874
DDN006 Duodenitis 50 5.892
875
P PGT001 Paget's Disease of Bone 61 5.891
876
CLR030 Clear Cell Renal Cell Carcinoma 54 5.888
877
P CRB059 Cerebellar Degeneration 36 5.887
878
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 5.877
879
ESP002 Esophageal Varix 51 5.873
880
HRY003 Hairy Cell Leukemia 61 5.869
881
PYR037 Pyruvate Carboxylase Deficiency 45 5.859
882
BRC012 Brucellosis 66 5.851
883
c PRM005 Primary Hyperparathyroidism 59 5.845
884
P DBT005 Diabetes Insipidus 54 5.844
885
P VNW001 Von Willebrand's Disease 65 5.835
886
P MLT074 Multiple Endocrine Neoplasia 59 5.830
887
NRM001 Neuromyelitis Optica 61 5.801
888
P VTR007 Vitreoretinopathy 46 5.800
889
BRN056 Bronchopulmonary Dysplasia 56 5.795
890
c HPT007 Hepatitis E 51 5.795
891
c SCN007 Secondary Hyperparathyroidism 51 5.783
892
PRM329 Premature Aging 36 5.779
893
P GNG009 Gangliosidosis 44 5.779
894
c BPL002 Bipolar I Disorder 47 5.769
895
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 5.769
896
P CRP001 Carpal Tunnel Syndrome 66 5.753
897
c SVR005 Severe Pre-Eclampsia 50 5.752
898
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 64 5.749
899
ALP103 Alpha-1-Antitrypsin Deficiency 68 5.742
900
MTC027 Mitochondrial Trifunctional Protein Deficiency 57 5.741
901
P D2H002 D-2-Hydroxyglutaric Aciduria 1 52 5.738
902
THR004 Thrombocytosis 53 5.736
903
APH002 Aphasia 56 5.736
904
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 5.733
905
ASP026 Asplenia, Isolated Congenital 43 5.713
906
ADS004 Aids Dementia Complex 40 5.712
907
RDC002 Radiculopathy 52 5.708
908
CTN007 Cutaneous Leishmaniasis 62 5.704
909
CHY002 Chylomicron Retention Disease 64 5.701
910
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 5.699
911
P ANT006 Antiphospholipid Syndrome 55 5.681
912
P GLL022 Guillain-Barre Syndrome 60 5.670
913
c MST023 Mesothelioma, Malignant 56 5.669
914
LYM017 Lyme Disease 62 5.649
915
P ADL017 Adult T-Cell Leukemia 56 5.647
916
P FCL005 Focal Segmental Glomerulosclerosis 57 5.645
917
PLR008 Pleurisy 50 5.645
918
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 5.644
919
P OPT009 Optic Neuritis 57 5.637
920
SPP011 Suppression of Tumorigenicity 12 61 5.635
921
P PLM034 Pulmonary Emphysema 58 5.618
922
c TYR012 Tyrosinemia, Type I 61 5.607
923
LWC001 Low Compliance Bladder 45 5.591
924
GRN017 Granulocytopenia 42 5.587
925
ACT003 Acute Kidney Tubular Necrosis 46 5.583
926
P DRM010 Dermatomyositis 61 5.580
927
THY125 Thyroid Gland Medullary Carcinoma 48 5.573
928
P TRC031 Trichorhinophalangeal Syndrome 38 5.565
929
P CHR012 Chronic Granulomatous Disease 69 5.565
930
HPT014 Hepatorenal Syndrome 49 5.560
931
XRD010 Xeroderma Pigmentosum, Variant Type 73 5.554
932
PLY001 Polycythemia Vera 69 5.554
933
MCR017 Macrocytic Anemia 44 5.547
934
KWS002 Kawasaki Disease 65 5.544
935
FCT001 Factor Viii Deficiency 60 5.537
936
SPN050 Spinocerebellar Degeneration 39 5.524
937
MYL020 Myelomeningocele 51 5.524
938
HYP020 Hyperprolactinemia 63 5.523
940
OCL052 Ocular Dominance 40 5.512
941
TCK001 Tick-Borne Encephalitis 59 5.496
942
DNG003 Dengue Disease 65 5.489
943
P EPD016 Epidermolysis Bullosa 53 5.486
944
OVR063 Overnutrition 42 5.482
945
CRY003 Cryptosporidiosis 56 5.480
946
CHD004 Chudley-Mccullough Syndrome 48 5.480
947
GRD001 Giardiasis 46 5.470
948
ASP004 Asphyxia Neonatorum 50 5.467