Search results for Copper

2300 hits were found for Copper

# Family MCID Name MIFTS Score
1
MNK001 Menkes Disease 64 55.400
2
WLS001 Wilson Disease 70 47.280
3
CPP001 Copper Deficiency, Familial Benign 16 24.855
4
DSR031 Disorder of Copper Metabolism 25 23.948
5
CPP004 Copper Deficiency Myelopathy 28 21.734
6
P LTR001 Lateral Sclerosis 58 17.250
7
c AMY091 Amyotrophic Lateral Sclerosis 1 88 17.227
8
IRN002 Iron Metabolism Disease 57 15.582
9
IDP071 Idiopathic Copper-Associated Cirrhosis 7 14.828
10
c ATS421 Autosomal Recessive Axonal Charcot-Marie-Tooth Disease Due to Copper Metabolism Defect 13 14.176
11
ATS010 Autosomal Recessive Disease 42 13.660
12
P LVR013 Liver Disease 69 13.110
13
CNG382 Congenital Cataracts, Hearing Loss, and Neurodegeneration 28 13.043
14
P ALZ034 Alzheimer Disease 87 12.880
16
DFC004 Deficiency Anemia 74 12.385
17
LVR012 Liver Cirrhosis 63 11.703
18
P PRN023 Prion Disease 60 11.294
19
OCC006 Occipital Horn Syndrome 54 11.179
20
RPD005 Rapidly Involuting Congenital Hemangioma 46 11.126
21
CHL068 Cholestasis 61 11.080
22
NNL005 Non-Alcoholic Fatty Liver Disease 63 10.927
23
P NRB001 Neuroblastoma 66 10.249
24
c ACT134 Acute Liver Failure 59 10.067
25
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 10.013
26
PRM236 Primary Biliary Cholangitis 60 9.973
27
PPL052 Papillomatosis, Confluent and Reticulated 34 9.731
28
ACR006 Aceruloplasminemia 63 9.724
29
HMS001 Hemosiderosis 48 9.656
30
HLX001 Helix Syndrome 48 9.586
31
P RRH023 Rare Hereditary Hemochromatosis 54 9.466
32
P NTR004 Neutropenia 63 9.310
33
48X005 48,xyyy 39 9.139
34
FTT001 Fatty Liver Disease 62 8.909
35
c DNT047 Dentinogenesis Imperfecta Type 2 35 8.777
36
c HYP836 Hypercholesterolemia, Familial, 1 73 8.690
37
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 8.282
38
P TRM003 Tremor 48 8.036
39
P BRS047 Breast Cancer 98 8.021
40
GLB002 Glioblastoma 67 8.015
41
P HML002 Hemolytic Anemia 62 7.912
42
c PLM127 Pulmonary Hypertension, Primary, 3 34 7.789
43
HRW001 Hair Whorl 35 7.677
44
P NRP001 Neuropathy 60 7.569
45
AGN016 Aging 54 7.471
46
P HRD018 Hair Disease 44 7.437
47
c HMC039 Hemochromatosis, Type 1 73 7.335
48
BCT022 Bacterial Infectious Disease 56 7.197
49
HYP266 Hypoxia 57 7.183
50
ALC007 Alcohol Dependence 66 7.146
51
P DBT009 Diabetes Mellitus 67 7.086
52
HVY002 Heavy Metal Poisoning 22 6.992
53
P MTR014 Motor Neuron Disease 65 6.838
54
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 6.779
55
PLV003 Pelvic Inflammatory Disease 55 6.701
56
P ENC018 Encephalopathy 62 6.594
57
P DYS154 Dystonia 64 6.464
58
P PRP019 Peripheral Nervous System Disease 58 6.444
59
IRN001 Iron Deficiency Anemia 58 6.412
60
SCR011 Scrapie 39 6.385
61
ORL004 Oral Submucous Fibrosis 56 6.213
62
c PRC016 Pre-Eclampsia 65 6.210
63
P DRR001 Diarrhea 55 6.096
64
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 6.094
65
P ATS364 Autism 69 6.026
66
VTM002 Vitamin B12 Deficiency 48 5.922
67
P GLM040 Glioma Susceptibility 1 71 5.878
69
P HPT023 Hepatocellular Carcinoma 96 5.832
70
P INF032 Infertility 57 5.826
71
P PRS040 Prostate Cancer 95 5.826
72
PNC001 Pancytopenia 53 5.791
73
P PNC035 Pancreatic Cancer 86 5.760
74
MLD018 Mild Cognitive Impairment 48 5.755
75
c TYP009 Type 2 Diabetes Mellitus 92 5.736
76
GLC003 Glucose Intolerance 54 5.690
77
P MYC084 Mycobacterium Tuberculosis 1 68 5.616
78
MYL009 Myelodysplastic Syndrome 67 5.553
79
MNT002 Mental Depression 57 5.544
80
ECT026 Ectopic Pregnancy 48 5.539
81
P ALC033 Alcohol Use Disorder 61 5.521
82
DWN001 Down Syndrome 70 5.498
83
DRM006 Dermatitis 62 5.443
84
ATH013 Atherosclerosis Susceptibility 63 5.422
85
DPR016 Depression 65 5.411
86
P PRK057 Parkinson Disease, Late-Onset 80 5.329
87
c ATS007 Autism Spectrum Disorder 72 5.320
88
P OVR042 Ovarian Cancer 88 5.315
89
P HYP265 Hypotonia 42 5.307
90
AMN001 Amenorrhea 54 5.306
91
HYP066 Hyperglycemia 61 5.249
92
CND006 Candida Glabrata 30 5.215
93
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 5.162
94
PST092 Posttransplant Acute Limbic Encephalitis 28 5.142
95
P VSC007 Vascular Disease 63 5.135
96
c DWL002 Dowling-Degos Disease 1 58 5.119
97
P CHL066 Cholangitis 52 5.071
98
ART140 Arteries, Anomalies of 53 5.059
99
KRT002 Keratomalacia 55 5.040
100
P THL005 Thalassemia 56 5.037
101
P ART022 Arthritis 71 5.032
102
c TYP008 Type 1 Diabetes Mellitus 70 5.007
103
PLM001 Pulmonary Tuberculosis 69 4.997
104
P BRS044 Breast Adenocarcinoma 58 4.974
105
P PNC044 Pancreatitis 61 4.973
106
c ATR087 Atrial Standstill 1 74 4.972
107
CNT047 Contact Dermatitis 57 4.963
108
HMC014 Homocysteinemia 52 4.958
109
P PRK039 Parkinsonism 55 4.958
110
MNT317 Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, and Keratoderma 45 4.923
111
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.918
112
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.918
113
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.918
114
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 4.918
115
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 4.918
116
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 4.918
117
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.918
118
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 4.918
119
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.918
120
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 4.918
121
CYS001 Cystic Fibrosis 78 4.824
122
MYL069 Myeloma, Multiple 77 4.815
123
NNL006 Non-Alcoholic Steatohepatitis 54 4.744
124
ALB002 Albinism 47 4.721
125
P MLN008 Melanoma 76 4.718
126
RCK004 Rickets 68 4.649
127
P LNG032 Lung Cancer 98 4.625
128
CRV035 Cervical Cancer 73 4.612
129
SVR001 Severe Acute Respiratory Syndrome 67 4.553
130
P LNG064 Lung Cancer Susceptibility 3 70 4.548
131
c PCH010 Pachyonychia Congenita 3 43 4.540
132
DSS032 Disease by Infectious Agent 55 4.531
133
ISC004 Ischemia 61 4.519
134
P KLZ004 Kala-Azar 1 41 4.517
135
LSH001 Leishmaniasis 64 4.517
136
P CTR002 Cataract 60 4.498
137
P EPL164 Epilepsy 68 4.483
138
P HYP750 Hypertriglyceridemia, Familial 62 4.458
139
CRT072 Creutzfeldt-Jakob Disease 68 4.451
140
47X002 47,xyy 48 4.449
141
STN013 Stenotrophomonas Maltophilia Infection 26 4.447
142
P ALP008 Alopecia 54 4.433
143
P SCH015 Schizophrenia 74 4.419
144
c SML038 Small Cell Cancer of the Lung 69 4.399
145
HPT004 Hepatic Coma 43 4.387
146
P ADN016 Adenocarcinoma 63 4.363
147
P SCL009 Sclerosing Cholangitis 48 4.317
148
DNT012 Dental Caries 53 4.310
149
P CLC063 Celiac Disease 1 66 4.307
150
CYT002 Cytokine Deficiency 43 4.277
151
HPT019 Hepatic Encephalopathy 59 4.247
152
P HNT016 Huntington Disease 73 4.238
153
ESP021 Esophageal Cancer 83 4.193
154
P DMN002 Dementia 66 4.186
155
ARG004 Argyria 26 4.181
156
P CRN300 Coronary Heart Disease 1 73 4.168
157
P SPP010 Suppressor of Tumorigenicity 3 51 4.165
158
P MVM001 Movement Disease 61 4.157
159
OST159 Osteogenic Sarcoma 66 4.157
160
GLL048 Glial Tumor 52 4.142
161
GLM045 Glioma 63 4.142
162
ORL011 Oral Cancer 60 4.135
163
P PSR002 Psoriasis 63 4.133
164
PST011 Pustulosis of Palm and Sole 52 4.133
165
CRH001 Crohn's Disease 80 4.130
166
c VRL010 Viral Hepatitis 53 4.128
167
ART016 Aortic Aneurysm 68 4.109
168
OST012 Osteoarthritis 77 4.104
169
LPP008 Lipoprotein Quantitative Trait Locus 65 4.098
170
LPD008 Lipid Metabolism Disorder 62 4.096
171
PRT251 Proteinuria, Chronic Benign 57 4.084
172
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 4.075
173
PLM129 Pulmonary Disease, Chronic Obstructive 74 4.047
174
P HYP086 Hypothyroidism 69 4.032
175
HMN044 Human Immunodeficiency Virus Type 1 78 4.032
176
P MLT020 Multiple Sclerosis 79 4.014
177
c MCR120 Microvascular Complications of Diabetes 7 47 4.012
178
P CLR023 Colorectal Cancer 100 3.996
179
P SHR001 Short Bowel Syndrome 53 3.990
180
OST016 Osteochondrosis 52 3.978
181
P OPT006 Optic Nerve Disease 58 3.959
182
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 3.931
183
DMP001 Dumping Syndrome 43 3.920
184
P INF037 Inflammatory Bowel Disease 53 3.908
185
BNR002 Bone Resorption Disease 47 3.902
186
P HRT032 Heart Disease 81 3.874
187
LNG099 Lung Disease 62 3.873
188
GTR002 Goiter 53 3.863
189
TLN003 Telangiectasis 51 3.842
190
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 3.829
191
NTR005 Nutritional Deficiency Disease 61 3.826
192
c CRN216 Craniosynostosis 5 21 3.825
193
ORL015 Oral Squamous Cell Carcinoma 43 3.825
194
c HYP595 Hypertension, Essential 85 3.818
195
c ACT071 Acute Kidney Failure 60 3.814
196
CHL123 Chlamydia 58 3.807
197
VRC005 Varicose Veins 60 3.786
198
P AMY004 Amyloidosis 70 3.757
199
PLY150 Polykaryocytosis Inducer 29 3.756
200
ULC004 Ulcerative Colitis 74 3.756
201
P OCL002 Oculocutaneous Albinism 59 3.744
202
GST033 Gestational Diabetes 61 3.734
203
SPL018 Splenomegaly 49 3.719
204
P MJR001 Major Depressive Disorder 68 3.708
205
PRT038 Protein-Energy Malnutrition 53 3.704
206
P SYS005 Systemic Scleroderma 74 3.690
207
P OST002 Osteoporosis 76 3.690
208
P PLY019 Polyneuropathy 52 3.678
209
MST005 Mastitis 53 3.662
210
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 3.653
211
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 3.653
212
ALL029 Allergic Disease 59 3.651
213
HYP781 Hypoascorbemia 52 3.642
214
P ART021 Arteriosclerosis 54 3.641
215
P MYP004 Myopathy 67 3.638
216
c ACT027 Acute Pancreatitis 60 3.633
217
P CTS001 Cutis Laxa 65 3.624
218
LGN006 Legionnaire Disease 52 3.621
219
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 3.620
220
P NPH012 Nephrotic Syndrome 60 3.610
221
LPT014 Leptin Deficiency or Dysfunction 78 3.586
222
c BTT014 Beta-Thalassemia 72 3.581
223
c CHL119 Cholangitis, Primary Sclerosing 58 3.569
224
P CRD246 Cardiovascular System Disease 56 3.562
225
c HPT003 Hepatitis a 63 3.562
226
P RHM011 Rheumatoid Arthritis 82 3.542
227
BLR008 Bilirubin Metabolic Disorder 57 3.540
228
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.529
229
CRB039 Cerebrovascular Disease 66 3.525
230
P HPT021 Hepatitis 69 3.518
231
P HRP006 Herpes Simplex 65 3.503
232
HPT022 Hepatoblastoma 54 3.501
233
P ACN011 Acne 57 3.488
234
CNG034 Congestive Heart Failure 69 3.476
235
P INT068 Intestinal Disease 53 3.476
236
P MRC003 Mercury Poisoning 49 3.471
237
SKN016 Skin Disease 63 3.469
238
GST050 Gastrointestinal System Disease 55 3.465
239
PLR008 Pleurisy 50 3.459
240
P HYP061 Hypertrophic Cardiomyopathy 69 3.449
241
SQM006 Squamous Cell Carcinoma 60 3.439
242
P EYD002 Eye Disease 57 3.421
243
P PLM036 Pulmonary Fibrosis 66 3.418
244
MCR018 Microcytic Anemia 47 3.405
245
CCC002 Coccidiosis 50 3.398
246
ANP008 Anaplastic Oligoastrocytoma 29 3.398
247
IMM167 Immune Deficiency Disease 78 3.397
248
c ACT004 Acute Diarrhea 40 3.382
249
P CND004 Candidiasis 58 3.377
250
ACR005 Acrodermatitis 38 3.371
251
PRP027 Peripheral Vascular Disease 71 3.370
252
P ECL001 Eclampsia 52 3.354
253
BRN024 Bronchitis 67 3.348
254
P HMN010 Hemangioma 62 3.348
255
c MCR130 Microvascular Complications of Diabetes 6 41 3.334
256
c MCR113 Microvascular Complications of Diabetes 3 52 3.334
257
c MCR133 Microvascular Complications of Diabetes 4 41 3.334
258
P FBR017 Fibrosarcoma 56 3.325
259
VGN023 Vaginitis 56 3.320
260
P KDN018 Kidney Disease 72 3.313
261
HYP001 Hypochromic Microcytic Anemia 37 3.311
262
GST045 Gastroenteritis 58 3.311
263
CRD009 Cardioencephalomyopathy 19 3.303
264
P RTN016 Retinal Degeneration 52 3.291
265
P URN019 Urinary Tract Infection 49 3.289
266
SLC006 Silicosis 56 3.282
267
MTB004 Metabolic Acidosis 48 3.267
268
CHR178 Chromosomal Triplication 34 3.266
269
P CHR071 Charcot-Marie-Tooth Disease 64 3.258
270
ANX004 Anoxia 40 3.257
271
CLN015 Colon Adenocarcinoma 65 3.251
272
P RSP003 Respiratory Failure 74 3.246
273
TTH006 Tooth Disease 51 3.232
274
P PRD008 Periodontitis 64 3.220
275
MLR004 Malaria 80 3.214
276
P PLT008 Pili Torti 30 3.213
277
VSC002 Vascular Dementia 60 3.197
278
P OVR082 Overgrowth Syndrome 49 3.195
279
P CRV039 Cervicitis 52 3.186
280
P SCL018 Scoliosis 57 3.171
281
NRL016 Neural Tube Defects 81 3.164
282
MLG169 Malignant Astrocytoma 57 3.161
283
ALL010 Allergic Contact Dermatitis 56 3.152
284
BLR001 Biliary Atresia 55 3.150
285
P SZR006 Seizure Disorder 70 3.144
286
P PLY011 Polycystic Ovary Syndrome 57 3.142
287
P ART023 Arthropathy 61 3.131
288
SVR004 Severe Combined Immunodeficiency 72 3.118
289
P LKM062 Leukemia, Acute Lymphoblastic 69 3.118
290
c MJR022 Major Affective Disorder 8 38 3.117
291
c MJR024 Major Affective Disorder 9 41 3.117
292
P BPL003 Bipolar Disorder 56 3.117
293
P ATT013 Attention Deficit-Hyperactivity Disorder 64 3.111
294
ENT007 Enteropathica 25 3.109
295
BCT002 Bacterial Vaginosis 53 3.107
296
MNN009 Meningoencephalitis 48 3.093
297
MTH071 Methane Production 25 3.087
298
PCD001 Pica Disease 38 3.086
299
P SDR003 Sideroblastic Anemia 51 3.077
300
P GST044 Gastritis 55 3.067
301
c MCR115 Microvascular Complications of Diabetes 5 65 3.066
302
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 56 3.064
303
P BND020 Bone Disease 59 3.044
304
P ASP006 Aspergillosis 72 3.020
305
STM007 Stomatitis 54 3.020
306
P SCK005 Sickle Cell Disease 56 3.020
307
c LKM061 Leukemia, Acute Myeloid 83 3.014
308
P SDR002 Siderosis 43 3.008
309
c DLT002 Dilated Cardiomyopathy 78 3.008
310
PRT036 Peritonitis 65 3.003
311
P RNL007 Renal Tubular Acidosis 50 2.992
312
MCR017 Macrocytic Anemia 44 2.990
313
c ACT073 Acute Leukemia 58 2.989
314
P EXN002 Exanthem 58 2.986
315
STR067 Stroke, Ischemic 80 2.984
316
CTN007 Cutaneous Leishmaniasis 62 2.983
317
c ACT075 Acute Myocardial Infarction 56 2.977
318
DMY004 Demyelinating Disease 50 2.976
319
c ACT068 Acute Cystitis 61 2.972
320
P DRM053 Dermatitis, Atopic 65 2.968
321
CVD001 Covid-19 57 2.968
322
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 2.956
323
P LPR021 Leprosy 3 71 2.954
324
P OBS001 Obstructive Jaundice 48 2.954
325
HNS001 Hansen's Disease 32 2.954
326
P ENC004 Encephalitis 61 2.953
327
P BCL017 B-Cell Lymphoma 59 2.950
328
P INF038 Influenza 68 2.948
329
P BLD134 Bladder Cancer 79 2.947
330
P EHL001 Ehlers-Danlos Syndrome 58 2.944
331
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 2.941
332
NRR001 Neuroretinitis 42 2.939
333
RTN023 Retinitis 46 2.939
334
GT001 Gout 64 2.939
335
OVR094 Ovarian Epithelial Cancer 39 2.937
336
P RTN008 Retinitis Pigmentosa 80 2.913
337
SPP011 Suppression of Tumorigenicity 12 61 2.905
338
P GST053 Gastric Cancer 83 2.905
339
P CRN037 Craniosynostosis 68 2.894
340
P TRC031 Trichorhinophalangeal Syndrome 38 2.894
341
PHN003 Phenylketonuria 76 2.876
342
RTN017 Retinal Detachment 60 2.872
343
P SKN015 Skin Carcinoma 71 2.871
344
c PLM128 Pulmonary Hypertension, Primary, 2 28 2.871
345
P PLM037 Pulmonary Hypertension 72 2.869
346
P MYC007 Myocardial Infarction 70 2.869
347
SPN051 Spondylitis 51 2.869
348
INF009 Inflammatory Spondylopathy 30 2.869
349
DYS073 Dysphagia 53 2.867
350
c CHR684 Chronic Kidney Disease 69 2.854
351
THY030 Thyroid Gland Disease 50 2.850
352
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 2.846
353
CHR100 Chronic Ulcer of Skin 57 2.846
354
SCH014 Schistosomiasis 56 2.846
355
END057 Endometrial Cancer 72 2.820
356
P END044 Endometriosis 62 2.809
357
P SRC025 Sarcoidosis 1 71 2.806
358
CRN017 Coronary Thrombosis 46 2.801
359
SCK003 Sickle Cell Anemia 74 2.797
360
TRM010 Traumatic Brain Injury 51 2.774
361
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 2.772
362
P MYP006 Myopia 56 2.766
363
ENT011 Enterocolitis 55 2.756
364
CHL014 Cholera 62 2.755
365
INV001 Invasive Aspergillosis 49 2.748
366
BRN071 Brain Injury 50 2.747
367
KRT078 Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Recessive 29 2.742
368
ACT098 Acute Erythroid Leukemia 55 2.725
369
P MLN007 Male Infertility 56 2.711
370
END086 End Stage Renal Disease 52 2.710
371
OTT002 Otitis Media 71 2.709
372
PRT013 Portal Hypertension 59 2.706
373
PRN019 Perinatal Necrotizing Enterocolitis 60 2.696
374
CLT003 Colitis 63 2.696
375
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.696
376
PRS063 Paresthesia 39 2.696
377
CHR576 Chronic Beryllium Disease 42 2.694
378
KRT009 Keratosis 53 2.694
379
P MTH007 Methemoglobinemia 46 2.694
380
BRN004 Brain Edema 54 2.686
381
c GLL024 Gallbladder Disease 1 52 2.685
382
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 2.683
383
P LKM002 Leukemia 67 2.683
384
SPN188 Spinal Muscular Atrophy, Distal, X-Linked 3 42 2.678
385
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 2.671
386
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 2.671
387
BLD131 Bladder Urothelial Carcinoma 60 2.665
388
P PHC003 Pheochromocytoma 69 2.663
389
ADR040 Adrenal Gland Pheochromocytoma 46 2.663
390
P BRY005 Beryllium Disease 39 2.663
391
HGH043 High Grade Glioma 45 2.663
392
CLR109 Colorectal Adenocarcinoma 50 2.659
393
c SPN225 Spondyloarthropathy 1 70 2.654
394
P MSC005 Muscular Dystrophy 67 2.654
395
GRD001 Giardiasis 46 2.654
397
GST023 Gastric Ulcer 52 2.632
398
KWS001 Kwashiorkor 45 2.631
399
SPS057 Spasticity 42 2.609
400
P KDN017 Kidney Cancer 61 2.609
401
TRN018 Transitional Cell Carcinoma 56 2.608
402
DCB001 Decubitus Ulcer 62 2.607
403
VGN019 Vaginal Discharge 47 2.595
404
VSC003 Visceral Leishmaniasis 55 2.587
405
THY029 Thyroid Carcinoma 51 2.582
406
XLN239 X-Linked Distal Hereditary Motor Neuropathy 12 2.574
407
c HPT016 Hepatitis B 62 2.561
408
LGN002 Legionellosis 62 2.556
409
P MSC003 Muscular Atrophy 52 2.544
410
P THR014 Thrombocytopenia 66 2.537
411
URL001 Urolithiasis 46 2.533
412
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.532
413
P GLM007 Glomerulonephritis 60 2.532
414
MDD011 Mood Disorder 62 2.529
415
c INH020 Inherited Metabolic Disorder 48 2.520
416
HYP056 Hypoglycemia 65 2.520
417
THR024 Thrombosis 56 2.515
418
P ICH004 Ichthyosis 56 2.511
419
P CRB088 Cerebral Atrophy 33 2.511
420
OST011 Osteomalacia 52 2.503
421
PPT005 Peptic Ulcer Disease 58 2.502
422
HND015 Hand Skill, Relative 30 2.492
423
P ALP009 Alopecia Areata 59 2.474
424
ANR040 Aneurysm 61 2.474
425
c BRN108 Branchiootic Syndrome 1 62 2.471
426
RFR010 Refractory Anemia 49 2.461
427
CHR031 Chromoblastomycosis 49 2.451
428
MCS002 Mucositis 56 2.450
429
P PMP001 Pemphigus 55 2.446
430
P BNG032 Benign Mesothelioma 53 2.446
431
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 2.444
432
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 2.440
433
CHR073 Choreatic Disease 54 2.440
434
HMP009 Haemophilus Influenzae 41 2.437
435
P THY032 Thyroiditis 57 2.435
436
HPP002 Huppke-Brendel Syndrome 7 2.431
437
CVR006 Cavernous Hemangioma 51 2.430
438
P LKM071 Leukemia, Chronic Lymphocytic 75 2.417
439
URM002 Uremia 47 2.417
440
CRY005 Cryptococcosis 60 2.403
441
GRN017 Granulocytopenia 42 2.403
442
P HYD006 Hydrocephalus 61 2.398
443
P NGH001 Night Blindness 52 2.396
444
SPN186 Spinal Cord Injury 61 2.388
445
HMG002 Hemoglobinuria 50 2.383
446
STT041 Stuttering 52 2.376
447
c HNT011 Huntington Disease-Like 3 34 2.368
448
INS024 Insulin-Like Growth Factor I 78 2.365
449
c HNT004 Huntington Disease-Like 2 52 2.365
450
P HYP076 Hyperthyroidism 53 2.365
451
ADN018 Adenoma 59 2.358
452
CRB033 Cerebral Degeneration 39 2.358
453
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 2.351
454
PST021 Postpartum Depression 50 2.336
455
PLC002 Plica Syndrome 35 2.327
456
SYN007 Synovitis 55 2.327
457
VCC001 Vaccinia 47 2.319
458
ING001 Inguinal Hernia 59 2.319
459
P ADL010 Adult Respiratory Distress Syndrome 71 2.319
460
P LCT001 Lactic Acidosis 51 2.314
461
P NSP012 Nasopharyngeal Carcinoma 61 2.311
462
c PRD040 Periodontitis, Chronic 52 2.296
463
TNP001 Tinea Pedis 48 2.296
464
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 2.296
465
SXL003 Sexual Disorder 49 2.286
466
CHR074 Choriocarcinoma 46 2.286
467
P URT039 Urticaria 58 2.286
468
HMN014 Human Immunodeficiency Virus Infectious Disease 54 2.283
469
CLC006 Calcinosis 47 2.278
470
P SLM003 Salmonellosis 54 2.265
471
BRS051 Breast Disease 58 2.265
472
LKP003 Leukoplakia 39 2.259
473
CRV040 Cervix Carcinoma 50 2.259
474
BTT017 Beta-Thalassemia Major 51 2.259
475
c SVR005 Severe Pre-Eclampsia 50 2.253
476
PLC008 Placenta Disease 49 2.246
477
P LKD001 Leukodystrophy 59 2.236
478
P RTN018 Retinal Disease 53 2.233
479
PMP006 Pemphigus Vulgaris, Familial 58 2.229
480
BRC012 Brucellosis 66 2.229
481
P SYP003 Syphilis 59 2.221
482
ACT055 Actinomycosis 55 2.221
483
P APL001 Aplastic Anemia 73 2.218
485
ATM095 Autoimmune Disease 61 2.202
486
PRS047 Prostatitis 58 2.201
487
FTL068 Fatal Infantile Cardioencephalomyopathy Due to Cytochrome C Oxidase Deficiency 35 2.198
488
OST017 Osteomyelitis 63 2.198
489
ORL012 Oral Leukoplakia 36 2.198
490
P VNS003 Venous Insufficiency 55 2.184
491
OCL069 Ocular Motor Apraxia 57 2.183
492
P CRB059 Cerebellar Degeneration 36 2.183
493
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 2.173
494
P MYC033 Myoclonus 47 2.173
495
MTC005 Mitochondrial Metabolism Disease 45 2.167
496
PNG002 Pain Agnosia 51 2.167
497
PTH003 Pathologic Nystagmus 52 2.167
498
ANR007 Anorexia Nervosa 60 2.166
499
ANT018 Anthracosis 51 2.166
500
EXC002 Exocrine Pancreatic Insufficiency 42 2.166
501
AVN001 Avian Influenza 61 2.146
502
MRS001 Marasmus 42 2.146
503
AZS001 Azoospermia 45 2.146
504
c SYS001 Systemic Lupus Erythematosus 87 2.135
505
P LPS004 Lupus Erythematosus 61 2.135
506
P PNM006 Pneumoconiosis 55 2.131
507
INT067 Interstitial Nephritis 46 2.131
508
LYM027 Lymphopenia 56 2.131
509
P NRV006 Nervous System Cancer 48 2.129
510
P END033 Endocarditis 58 2.112
511
URT049 Urate Oxidase, Pseudogene 24 2.109
512
CHG001 Chagas Disease 66 2.109
513
MYM001 Myoma 54 2.109
514
P PYL005 Pyelonephritis 57 2.109
515
c ATM011 Autoimmune Hepatitis 63 2.107
516
c HPT015 Hepatitis D 49 2.101
517
P RHN004 Rhinitis 57 2.101
518
P MYC008 Myocarditis 59 2.101
519
GLS001 Gliosarcoma 64 2.098
520
ANX010 Anxiety 70 2.096
522
P KRT007 Keratoconus 50 2.096
523
QDR001 Quadriplegia 50 2.096
524
AMN006 Aminoaciduria 37 2.096
525
DYS015 Dysentery 50 2.089
526
CRB037 Cerebral Palsy 67 2.083
527
P MCR129 Microvascular Complications of Diabetes 1 68 2.081
528
c MCR112 Microvascular Complications of Diabetes 2 42 2.081
529
P ATR011 Atrial Fibrillation 66 2.073
530
ALL014 Allergic Encephalomyelitis 34 2.071
531
P PRP029 Porphyria 60 2.068
532
P INT099 Intrahepatic Cholestasis of Pregnancy 62 2.068
533
SKN019 Skin Melanoma 71 2.061
534
DSS008 Disease of Mental Health 74 2.061
535
c PRG042 Progressive Familial Heart Block, Type Ia 66 2.060
536
INF034 Infective Endocarditis 54 2.050
537
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 2.050
538
P RTN024 Retinoblastoma 73 2.050
539
SNS003 Sensory Peripheral Neuropathy 52 2.050
540
P MCR010 Microcephaly 60 2.050
541
ATN005 Autonomic Dysfunction 46 2.045
542
c LCL006 Localized Scleroderma 65 2.043
543
P HYP083 Hypopituitarism 52 2.038
544
P NRD007 Neurodegeneration with Brain Iron Accumulation 52 2.033
545
P LCH002 Lichen Planus 54 2.033
546
SPN041 Spinal Cord Disease 55 2.027
547
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 2.022
548
P MYL006 Myeloid Leukemia 61 2.022
549
MDD018 Middle East Respiratory Syndrome 44 2.018
550
P TCD001 Tic Disorder 49 2.018
551
EXT006 Extrahepatic Cholestasis 40 2.018
552
ACQ007 Acquired Immunodeficiency Syndrome 59 2.016
553
ART002 Arts Syndrome 66 2.010
554
CNT033 Central Nervous System Cancer 47 1.999
555
CHR028 Chronic Wasting Disease 33 1.998
556
P END046 Endometritis 46 1.990
557
P SPN046 Spinal Muscular Atrophy 63 1.985
558
CRY036 Cryptogenic Cirrhosis 36 1.985
559
ENT004 Enthesopathy 51 1.985
560
MST021 Meester-Loeys Syndrome 42 1.961
561
HYP014 Hyperuricemia 51 1.961
562
LTH004 Lathyrism 15 1.961
563
c ALB009 Albinism, Oculocutaneous, Type Ia 53 1.961
564
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 1.960
565
LPD014 Lipodermatosclerosis 37 1.960
566
END028 Endemic Goiter 41 1.959
567
P SLP005 Sleep Disorder 61 1.951
568
c THR092 Thrombophilia Due to Thrombin Defect 74 1.951
569
c HPT001 Hepatitis C 62 1.951
570
P OST009 Osteochondritis Dissecans 62 1.951
571
P SNS001 Sensorineural Hearing Loss 59 1.951
572
HYP080 Hypogonadism 50 1.951
573
P NRV007 Nervous System Disease 67 1.951
574
IDP070 Idiopathic Scoliosis 42 1.947
575
P ERY036 Erythema Nodosum 49 1.944
576
P HMC002 Homocystinuria 53 1.944
577
CRB004 Cerebral Artery Occlusion 45 1.944
578
P UVT001 Uveitis 57 1.944
579
P CNJ013 Conjunctivitis 66 1.935
580
CHL065 Cholangiocarcinoma 58 1.930
581
IMP005 Impotence 52 1.930
582
INT079 Intrahepatic Cholangiocarcinoma 51 1.930
583
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.924
584
c MGR028 Migraine with or Without Aura 1 64 1.924
585
P HYP069 Hyperparathyroidism 62 1.924
586
PRP030 Purpura 54 1.924
587
P CHN012 Chondrosarcoma 57 1.917
588
DBT010 Diabetic Neuropathy 54 1.917
589
FDL002 Food Allergy 47 1.917
590
FBR047 Fibromyalgia 58 1.909
591
c SCL052 Scleroderma, Familial Progressive 61 1.903
592
P OVR046 Ovarian Cyst 46 1.898
593
c PRS136 Prostate Cancer, Hereditary, 6 33 1.889
594
c PRS130 Prostate Cancer, Hereditary, 8 32 1.889
595
P ATX030 Ataxia-Telangiectasia 80 1.886
596
PRC002 Paracoccidioidomycosis 54 1.886
597
NRM005 Neuromuscular Disease 63 1.886
598
PHR003 Pharyngitis 58 1.886
599
LNG031 Lung Benign Neoplasm 51 1.883
600
OBS002 Obsessive-Compulsive Disorder 68 1.873
601
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.860
602
P CHR345 Chronic Pain 50 1.858
603
PRM329 Premature Aging 36 1.857
604
c PNS012 Paine Syndrome 60 1.847
605
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.847
606
P LPM005 Lipomatosis 47 1.846
607
PPL022 Papilloma 53 1.846
608
SQM002 Squamous Cell Papilloma 46 1.846
609
PRM004 Primary Amebic Meningoencephalitis 27 1.845
610
P LMY004 Leiomyosarcoma 62 1.833
611
INT072 Intestinal Pseudo-Obstruction 62 1.816
612
LMY002 Leiomyoma 51 1.816
613
c LKM063 Leukemia, Chronic Myeloid 71 1.809
614
IDP069 Idiopathic Avascular Necrosis 23 1.807
615
PRC013 Pericarditis 53 1.807
616
MYL001 Myelitis 50 1.807
617
P FNC004 Fanconi Syndrome 60 1.807
618
c CNT035 Central Nervous System Disease 54 1.807
619
HYP020 Hyperprolactinemia 63 1.807
620
c OPT053 Optic Atrophy 1 62 1.805
621
P ANP001 Anaplastic Large Cell Lymphoma 61 1.799
622
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.799
623
CHL004 Cholelithiasis 49 1.799
624
BRN028 Brain Cancer 74 1.799
625
SYN005 Synostosis 43 1.799
626
P TRN034 Transverse Myelitis 47 1.783
627
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 39 1.783
628
c ALB020 Albinism, Oculocutaneous, Type Iii 49 1.773
629
PRS034 Parasitic Helminthiasis Infectious Disease 51 1.771
630
MTC208 Mitochondrial Complex Iv Deficiency, Nuclear Type 2 30 1.769
631
ALP103 Alpha-1-Antitrypsin Deficiency 68 1.769
632
RNL077 Renal Fibrosis 46 1.769
633
PRT037 Pertussis 65 1.769
634
CNS004 Constipation 56 1.769
635
ORL013 Oral Lichen Planus 46 1.769
636
MGL001 Megaloblastic Anemia 58 1.768
637
c HPT073 Hepatitis C Virus 71 1.765
638
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.762
639
MTL005 Metal Allergy 40 1.762
640
ACT003 Acute Kidney Tubular Necrosis 46 1.762
641
KRT006 Keratoconjunctivitis 53 1.762
642
LYM017 Lyme Disease 62 1.762
643
DSS009 Disseminated Intravascular Coagulation 57 1.762
644
WST001 West Syndrome 59 1.758
645
PSY004 Psychotic Disorder 66 1.758
646
P BLR024 Biliary Cirrhosis, Primary, 1 28 1.747
647
HYP005 Hypokalemia 55 1.744
648
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.738
649
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 1.735
650
c AMY088 Amyotrophic Lateral Sclerosis 3 31 1.729
651
ENC055 Encephalopathy, Ethylmalonic 51 1.729
652
P PRV006 Pervasive Developmental Disorder 52 1.729
653
c NMN014 Niemann-Pick Disease, Type C2 49 1.729
654
P PLM034 Pulmonary Emphysema 58 1.729
655
TXC005 Toxic Shock Syndrome 62 1.729
656
P CHN059 Chondrocalcinosis 52 1.729
657
LST001 Listeriosis 59 1.729
658
NCR007 Necrotizing Fasciitis 49 1.729
659
FSC004 Fasciitis 49 1.729
660
P TXP001 Toxoplasmosis 60 1.729
661
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 1.729
662
SYN036 Syncope 45 1.729
663
ART004 Aortic Atherosclerosis 47 1.729
664
MCR013 Microphthalmia 60 1.729
665
P RTT002 Rett Syndrome 79 1.729
666
SRC014 Sarcoma 65 1.726
667
P DNG005 Dengue Virus 56 1.718
668
PRM020 Premenstrual Tension 39 1.718
669
HLC007 Helicobacter Pylori Infection 67 1.693
670
CRV043 Cervical Dystonia 46 1.688
671
DRM011 Dermatophytosis 52 1.688
672
PYR009 Pyridoxine Deficiency Anemia 35 1.688
673
KLB003 Klebsiella Pneumonia 50 1.688
674
HMG005 Hemoglobinopathy 56 1.686
675
PRP080 Peripheral Artery Disease 54 1.677
676
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 1.677
677
CNT057 Central Centrifugal Cicatricial Alopecia 36 1.671
678
URT010 Ureteral Obstruction 45 1.656
679
MTC205 Mitochondrial Complex Iv Deficiency, Nuclear Type 1 57 1.646
680
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 1.646
681
CRT015 Carotid Artery Occlusion 45 1.646
682
P SBS003 Substance Abuse 54 1.646
683
VLV011 Vulvovaginal Candidiasis 49 1.646
684
OLG001 Oligospermia 45 1.646
685
P GNT009 Giant Axonal Neuropathy 46 1.646
686
c OVR114 Ovarian Cancer 1 59 1.644
687
ANT039 Antisynthetase Syndrome 55 1.644
688
PLS009 Plasma Cell Neoplasm 64 1.644
689
IRR002 Irritable Bowel Syndrome 65 1.636
690
FCL022 Focal Dystonia 42 1.624
691
c INF023 Inflammatory Breast Carcinoma 49 1.624
692
APH002 Aphasia 56 1.619
693
c CNG497 Congenital Disorder of Glycosylation, Type Iio 38 1.619
694
FBR086 Fibrolamellar Carcinoma 59 1.617
695
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 1.602
696
CRT084 Creatinine Clearance Quantitative Trait Locus 25 1.602
697
c CRN221 Craniosynostosis 4 29 1.602
698
VLV047 Volvulus of Midgut 52 1.602
699
ANG054 Angina Pectoris 66 1.602
700
P PRS049 Persistent Mullerian Duct Syndrome 52 1.602
701
P PLY018 Polycythemia 56 1.602
702
CRN027 Corneal Neovascularization 47 1.602
703
HYP063 Hypersplenism 52 1.602
704
SNL007 Senile Cataract 40 1.602
705
P BLR006 Biliary Tract Disease 46 1.602
706
BRN056 Bronchopulmonary Dysplasia 56 1.602
707
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 43 1.598
708
P MTC069 Mitochondrial Disorders 57 1.594
709
ETN001 Eating Disorder 59 1.594
710
INT002 Intermittent Claudication 61 1.588
711
BLD045 Bladder Diverticulum 39 1.581
712
SPN392 Spondylosis, Cervical 30 1.581
713
SPN020 Spondylosis 46 1.581
714
PLY100 Polyploidy 36 1.577
715
P HYP024 Hypoparathyroidism 55 1.577
716
CYS010 Cystinosis 62 1.577
717
GNG013 Gingivitis 59 1.577
718
HYP457 Hypertrophic Scars 42 1.573
719
MCR025 Microhydranencephaly 33 1.573
720
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 1.573
721
ANR004 Anuria 44 1.573
722
ALC009 Alcoholic Liver Cirrhosis 54 1.573
723
P DDN001 Duodenal Ulcer 53 1.573
724
MGB001 Megabladder, Congenital 23 1.561
725
CHL067 Cholecystitis 60 1.561
726
DWR001 Dwarfism 44 1.561
727
MSC157 Muscular Dystrophy, Duchenne Type 79 1.555
728
c PLM164 Pulmonary Hypertension, Primary, 1 76 1.555
729
FSC002 Fascioliasis 44 1.555
730
PNC129 Pancreatic Adenocarcinoma 65 1.555
731
TRN015 Transient Cerebral Ischemia 63 1.555
732
FLR002 Filariasis 55 1.555
733
PRM013 Premature Menopause 58 1.555
734
KLD004 Keloid Disorder 39 1.555
735
ELS001 Eales Disease 46 1.555
736
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 1.549
737
P OPN001 Open-Angle Glaucoma 55 1.536
738
P VSC011 Vasculitis 61 1.536
739
ILS001 Ileus 50 1.536
740
PRP016 Paraplegia 52 1.536
741
ECH003 Echinococcosis 53 1.536
742
P TBR001 Tuberous Sclerosis 69 1.536
743
P PNM007 Pneumonia 67 1.536
744
HST011 Histoplasmosis 55 1.536
745
PYR016 Pyridoxine Deficiency 29 1.536
746
P MYS005 Myositis 56 1.519
747
c PRG020 Paragangliomas 3 39 1.519
748
INC002 Inclusion Body Myositis 57 1.519
749
NWC001 Newcastle Disease 47 1.519
750
GRW007 Growth Hormone Deficiency 46 1.507
751
c SPR086 Spermatogenic Failure 3 46 1.507
752
ASP002 Aspartylglucosaminuria 58 1.507
753
c NMN015 Niemann-Pick Disease, Type C1 68 1.507
754
CMB007 Combined Immunodeficiency 57 1.507
755
TTN003 Tetanus 65 1.507
756
BCK006 Back Pain 47 1.507
757
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 1.507
758
c THY107 Thymoma, Familial 42 1.494
759
P AST005 Asthma 76 1.494
760
c CHL137 Cholestasis, Progressive Familial Intrahepatic, 3 53 1.494
761
CLF027 Cleft Palate, Isolated 64 1.494
762
MNL001 Monilethrix 49 1.494
763
P SLP003 Salpingitis 40 1.494
764
CHL061 Childhood Leukemia 47 1.494
765
BRN014 Bronchopneumonia 53 1.494
766
P CRD119 Cardiac Arrest 67 1.494
767
P THY023 Thymoma 64 1.494
768
PLM033 Pulmonary Embolism 58 1.494
769
P HDC001 Headache 57 1.494
770
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 1.494
771
P INT070 Intestinal Obstruction 57 1.473
772
c PLM121 Pulmonary Hypertension, Primary, 4 28 1.462
773
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 1.462
774
SMT007 Smith-Fineman-Myers Syndrome 32 1.456
775
P FRD001 Friedreich Ataxia 61 1.456
776
WST005 West Nile Virus 57 1.456
777
c MYP018 Myopia 6 27 1.456
778
P GLC113 Galactosemia I 66 1.456
779
TBC004 Tobacco Addiction 63 1.456
780
DPM001 Dopamine Beta-Hydroxylase Deficiency 53 1.456
781
CMM005 Common Cold 56 1.456
782
NDL007 Nodular Goiter 48 1.456
783
PRN071 Parenteral Nutrition-Associated Cholestasis 23 1.450
784
MTC211 Mitochondrial Complex Iv Deficiency, Nuclear Type 13 21 1.450
785
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.450
786
NPH003 Nephrocalcinosis 49 1.450
787
CLF001 Cleft Lip 53 1.450
788
P MTC133 Mitochondrial Myopathy 50 1.450
789
PNT001 Pontiac Fever 28 1.450
790
P NMN002 Niemann-Pick Disease 60 1.450
791
DPH001 Diphtheria 59 1.450
792
P BLP003 Blepharospasm 46 1.450
793
CYS008 Cystic Echinococcosis 57 1.450
794
HDN002 Head Injury 44 1.450
795
P DYS021 Dysautonomia 38 1.450
797
RHM001 Rheumatic Fever 59 1.445
798
TYP007 Typhoid Fever 64 1.433
799
MTN003 Motion Sickness 51 1.432
800
RHB024 Rhabdomyosarcoma 2 67 1.416
801
P CRB045 Cerebellar Hypoplasia 40 1.403
802
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 64 1.403
803
HPT067 Hepatocellular Adenoma 43 1.403
804
INT007 Intermediate Coronary Syndrome 54 1.403
805
P RBL001 Rubella 58 1.403
806
P ATR005 Atrophic Gastritis 50 1.403
807
MNG007 Manganese Poisoning 28 1.403
808
SDD001 Sudden Infant Death Syndrome 60 1.403
809
P HMG032 Hemoglobin H Disease 51 1.403
810
KRT019 Keratitis, Hereditary 66 1.403
811
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.403
812
FBR054 Fibroma 44 1.403
813
P HYP098 Hypereosinophilic Syndrome 66 1.403
814
OST007 Ostertagiasis 28 1.403
815
ALC006 Alcoholic Hepatitis 61 1.403
816
EXS001 Exostosis 49 1.403
817
PRS045 Prostatic Hypertrophy 53 1.403
818
HRP004 Herpes Zoster 61 1.403
819
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 1.401
820
P BNC003 Bone Cancer 58 1.401
821
MSL001 Measles 61 1.401
822
DSR036 Disorder of Mineral Absorption and Transport 5 1.401
823
P MTC003 Metachromatic Leukodystrophy 71 1.398
824
ADL002 Adult Syndrome 70 1.386
825
IMM140 Immunodeficiency 47 56 1.382
826
P PRS038 Personality Disorder 65 1.381
827
CRV038 Cervical Squamous Cell Carcinoma 58 1.364
828
ESP002 Esophageal Varix 51 1.362
829
P MNN013 Meningitis 65 1.362
830
LMB062 Limb Ischemia 55 1.359
831
LCH001 Leech Infestation 38 1.359
832
PLN026 Pilonidal Sinus 35 1.355
833
c GLC114 Glaucoma, Primary Closed-Angle 36 1.355
834
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 1.355
835
INS001 Insulinoma 59 1.355
836
P NRN021 Neuronal Ceroid Lipofuscinosis 65 1.355
837
ATH004 Athetosis 25 1.355
838
PRT058 Pure Autonomic Failure 58 1.355
839
DLS001 Delusional Disorder 45 1.354
840
GNT167 Genetic Obesity 30 1.346
841
SQM013 Squamous Cell Carcinoma, Head and Neck 73 1.346
842
EPD015 Epidemic Typhus 44 1.346
843
BTT018 Beta-Thalassemia Intermedia 31 1.346
844
VSC053 Visceral Steatosis, Congenital 34 1.346
845
P PRP003 Porphyria Cutanea Tarda 66 1.346
846
c HNT010 Huntington Disease-Like 1 55 1.346
847
P SPS008 Spastic Ataxia 41 1.346
848
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.346
849
LYM011 Lymphogranuloma Venereum 33 1.346
850
BCT004 Bacteriuria 47 1.346
851
c HMG003 Hemoglobin E Disease 42 1.346
852
CRT004 Carotid Artery Thrombosis 39 1.346
853
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.346
854
P OVR049 Ovarian Disease 52 1.346
855
P CLL015 Collagen Disease 48 1.346
856
HMP001 Hemopericardium 47 1.334
857
CRD016 Cardiac Rupture 34 1.334
858
PSR001 Psoriatic Arthritis 62 1.326
859
NPH009 Nephrolithiasis 54 1.326
860
c HYP716 Hypermanganesemia with Dystonia 1 34 1.306
861
WRN004 Wrinkly Skin Syndrome 36 1.306
862
CLF004 Cleft Lip/palate 57 1.304
863
HYP854 Hypopigmentation of the Skin 22 1.304
864
MYC006 Mycosis Fungoides 65 1.304
865
c EXD008 Exudative Vitreoretinopathy 1 71 1.304
866
END062 Endometrial Hyperplasia 48 1.304
867
P LYM118 Lymphoma 67 1.304
868
AND014 Androgenic Alopecia 47 1.304
869
KRN002 Kearns-Sayre Syndrome 63 1.304
870
CYS045 Cystinosis, Adult Nonnephropathic 32 1.304
871
c CND033 Candidiasis, Familial, 1 27 1.304
872
MSN001 Mesangial Proliferative Glomerulonephritis 44 1.304
873
P HMR005 Hemorrhoid 49 1.304
874
ASP007 Aspiration Pneumonia 49 1.304
875
DNG003 Dengue Disease 65 1.304
876
PRN009 Paranoid Schizophrenia 49 1.304
877
PRS021 Prostatic Adenoma 43 1.304
878
PPL002 Papillary Carcinoma 46 1.304
879
CRD001 Cardiac Tamponade 43 1.304
880
LYS002 Lysosomal Storage Disease 51 1.304
881
c FML021 Familial Hypercholesterolemia 72 1.304
882
HYP057 Hypervitaminosis D 37 1.304
883
c JVN010 Juvenile Rheumatoid Arthritis 66 1.304
884
CRL001 Cerulean Cataract 26 1.304
885
MYC019 Mycobacterium Marinum 29 1.304
886
SBC016 Subacute Delirium 43 1.304
887
P BRB001 Beriberi 44 1.289
888
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 1.288
889
KR002 Kuru 45 1.284
890
CYN002 Cyanosis, Transient Neonatal 43 1.284
891
P SCL057 Scoliosis, Isolated 1 40 1.284
892
GLB001 Gilbert Syndrome 53 1.284
893
c BSL007 Basal Cell Carcinoma 68 1.284
894
SPT004 Septic Arthritis 58 1.284
895
P INS002 in Situ Carcinoma 53 1.284
896
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 1.284
897
SPN035 Spindle Cell Sarcoma 54 1.262
898
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 1.261
899
RBS001 Rabies 58 1.261
900
ISL109 Isolated Cleft Lip 33 1.251
901
CYN003 Cyanide Poisoning 22 1.251
902
P ALP061 Alopecia, Androgenetic, 1 49 1.251
903
ADN027 Adenomyosis 57 1.251
904
P FML018 Familial Mediterranean Fever 73 1.251
905
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 1.251
906
BRK010 Burkitt Lymphoma 66 1.251
907
BRN032 Brain Glioma 45 1.251
908
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 1.251
909
SPN402 Spinal Muscular Atrophy, X-Linked 2 48 1.251
910
ERY029 Erythermalgia, Primary 58 1.251
911
ASB001 Asbestosis 47 1.251
912
P GLL020 Gallbladder Disease 56 1.251
913
CRN030 Coronary Stenosis 50 1.251
914
CRV002 Cervix Uteri Carcinoma in Situ 47 1.251
915
ASB003 Asbestos Intoxication 32 1.251
916
TLG001 Telogen Effluvium 31 1.251
917
P HRM001 Hermansky-Pudlak Syndrome 65 1.251
918
CNN005 Connective Tissue Disease 67 1.251
919
TRY001 Trypanosomiasis 50 1.251
920
CMM004 Common Variable Immunodeficiency 72 1.251
921
THR004 Thrombocytosis 53 1.251
922
BLN006 Blind Loop Syndrome 35 1.251
923
DBT007 Diabetic Cataract 36 1.251
924
CRV045 Cervical Intraepithelial Neoplasia 39 1.251
925
P AGN002 Agnosia 54 1.250
926
GST049 Gastrointestinal System Cancer 49 1.233
927
SLN002 Selenium Poisoning 10 1.218
928
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 1.218
929
CRC021 Carcinosarcoma 64 1.218
930
INT040 Intrinsic Asthma 36 1.218
931
END040 Endogenous Depression 55 1.218
932
P CRV031 Cervical Adenocarcinoma 48 1.218
933
GST040 Gastric Adenocarcinoma 67 1.218
934
c VRL012 Viral Meningitis 46 1.218
935
BRN002 Bronchiolitis 57 1.218
936
APH001 Aphthous Stomatitis 58 1.218
937
UTR043 Uterine Sarcoma 40 1.218
938
LYM035 Lymphangiectasis 30 1.218
939
PRN011 Pernicious Anemia 53 1.214
940
ATN004 Autonomic Neuropathy 42 1.214
941
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 1.194
942
BNG077 Benign Idiopathic Neonatal Seizures 23 1.194
943
c ANM038 Anemia, Autoimmune Hemolytic 64 1.194
944
c BLR016 Biliary Cirrhosis, Primary, 2 15 1.194
945
P CTN015 Cutaneous T Cell Lymphoma 48 1.194
946
P LYM033 Lymphoproliferative Syndrome 59 1.194
947
HSH003 Hashimoto Thyroiditis 60 1.194
948
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 1.194
949
c HYD046 Hydatidiform Mole, Recurrent, 1 59 1.194
950
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 47 1.194
951
INT075 Intracranial Hypertension 53 1.194
952
MTC004 Mitochondrial Encephalomyopathy 42 1.194
953
ALL006 Allergic Asthma 56 1.194
954
GST010 Gestational Trophoblastic Neoplasm 52 1.194
955
PNM008 Pneumothorax 54 1.194
956
DNG002 Dengue Hemorrhagic Fever 60 1.194
957
P