Search results for Copper

1457 hits were found for Copper

# Family MCID Name MIFTS Score
1
MNK001 Menkes Disease 64 6.741
2
CPP001 Copper Deficiency, Familial Benign 18 4.883
3
CPP004 Copper Deficiency Myelopathy 30 3.301
4
IDP071 Idiopathic Copper-Associated Cirrhosis 6 3.089
5
WLS001 Wilson Disease 71 2.993
6
DSR031 Disorder of Copper Metabolism 27 2.439
7
CNG382 Congenital Cataracts, Hearing Loss, and Neurodegeneration 28 2.221
9
c ATS421 Autosomal Recessive Axonal Charcot-Marie-Tooth Disease Due to Copper Metabolism Defect 12 2.207
10
P LTR001 Lateral Sclerosis 54 0.269
11
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.268
12
LVR012 Liver Cirrhosis 62 0.245
13
P ALZ034 Alzheimer Disease 88 0.245
14
P LVR013 Liver Disease 68 0.234
15
IRN002 Iron Metabolism Disease 57 0.222
16
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.215
17
DFC004 Deficiency Anemia 70 0.205
18
P NTR004 Neutropenia 63 0.205
19
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.187
20
P PRN023 Prion Disease 57 0.180
21
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.180
22
PPL052 Papillomatosis, Confluent and Reticulated 33 0.177
23
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.169
24
HLX001 Helix Syndrome 47 0.166
25
48X005 48,xyyy 39 0.163
26
P NRB001 Neuroblastoma 72 0.159
27
CHL068 Cholestasis 61 0.159
28
HRW001 Hair Whorl 36 0.150
29
HMS001 Hemosiderosis 54 0.148
30
P PRM006 Primary Biliary Cirrhosis 62 0.147
31
P DRR001 Diarrhea 55 0.147
32
P RRH023 Rare Hereditary Hemochromatosis 41 0.147
33
P ENC018 Encephalopathy 61 0.145
34
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.145
35
P OVR042 Ovarian Cancer 88 0.142
36
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.140
37
P HPT023 Hepatocellular Carcinoma 100 0.139
38
ATS010 Autosomal Recessive Disease 48 0.138
39
c HYP836 Hypercholesterolemia, Familial, 1 73 0.136
40
P NRP001 Neuropathy 56 0.127
41
FTT001 Fatty Liver Disease 61 0.124
42
DRM006 Dermatitis 61 0.124
43
ALC007 Alcohol Dependence 66 0.121
44
P ART022 Arthritis 69 0.118
45
OCC006 Occipital Horn Syndrome 60 0.118
46
P RHM011 Rheumatoid Arthritis 80 0.116
47
GLB015 Glioblastoma Multiforme 75 0.116
48
PLV003 Pelvic Inflammatory Disease 55 0.116
49
ACR006 Aceruloplasminemia 65 0.115
50
47X002 47,xyy 49 0.115
51
P HRD018 Hair Disease 43 0.115
52
c PRC016 Pre-Eclampsia 63 0.111
53
P PSR002 Psoriasis 62 0.111
54
PST011 Pustulosis of Palm and Sole 52 0.111
55
PLM001 Pulmonary Tuberculosis 69 0.110
56
HYP266 Hypoxia 57 0.110
57
P BRS047 Breast Cancer 97 0.108
58
c HMC039 Hemochromatosis, Type 1 74 0.108
59
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.108
60
P HML002 Hemolytic Anemia 63 0.106
61
BCT022 Bacterial Infectious Disease 56 0.106
62
P CLR023 Colorectal Cancer 99 0.105
63
P HRT032 Heart Disease 75 0.105
64
P MTR014 Motor Neuron Disease 65 0.105
65
SCR011 Scrapie 39 0.105
66
HVY002 Heavy Metal Poisoning 22 0.105
67
MYL009 Myelodysplastic Syndrome 70 0.103
68
P BRS044 Breast Adenocarcinoma 59 0.103
69
P INF032 Infertility 57 0.101
70
AMN001 Amenorrhea 54 0.101
71
PNC001 Pancytopenia 54 0.099
72
P LYM118 Lymphoma 68 0.097
73
ATH013 Atherosclerosis Susceptibility 65 0.097
74
P CTR002 Cataract 60 0.097
75
ORL004 Oral Submucous Fibrosis 55 0.097
76
P KDN018 Kidney Disease 72 0.095
77
c ACT134 Acute Liver Failure 56 0.095
78
P VSC007 Vascular Disease 63 0.094
79
GTR002 Goiter 53 0.094
80
PST092 Posttransplant Acute Limbic Encephalitis 29 0.094
81
DWN001 Down Syndrome 70 0.090
82
P THL005 Thalassemia 60 0.090
83
IRN001 Iron Deficiency Anemia 59 0.090
84
P PRP019 Peripheral Nervous System Disease 58 0.090
85
CND006 Candida Glabrata 32 0.090
86
P LNG032 Lung Cancer 98 0.088
87
OST159 Osteogenic Sarcoma 66 0.088
88
ALL026 Allergic Hypersensitivity Disease 62 0.088
89
P LNG064 Lung Cancer Susceptibility 3 78 0.085
90
P ADN016 Adenocarcinoma 64 0.085
91
c DWL002 Dowling-Degos Disease 1 58 0.085
92
P PRS040 Prostate Cancer 97 0.083
93
P GST053 Gastric Cancer 83 0.083
94
P PRK057 Parkinson Disease, Late-Onset 78 0.083
95
HYP066 Hyperglycemia 61 0.083
96
SLC006 Silicosis 56 0.083
97
c PCH010 Pachyonychia Congenita 3 44 0.083
98
STN013 Stenotrophomonas Maltophilia Infection 25 0.083
99
c ATR087 Atrial Standstill 1 75 0.081
100
P SCH015 Schizophrenia 74 0.081
101
P HPT021 Hepatitis 67 0.081
102
P DBT009 Diabetes Mellitus 64 0.081
103
P GLM045 Glioma 63 0.081
104
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.081
105
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.081
106
c VRL010 Viral Hepatitis 52 0.081
107
VTM002 Vitamin B12 Deficiency 48 0.081
108
GLL048 Glial Tumor 45 0.081
109
P ATS364 Autism 70 0.079
110
P DYS154 Dystonia 65 0.079
111
c ACT073 Acute Leukemia 58 0.079
112
ISC004 Ischemia 58 0.079
113
CNT047 Contact Dermatitis 58 0.079
114
GLC003 Glucose Intolerance 54 0.079
115
ECT026 Ectopic Pregnancy 50 0.079
116
MYL069 Myeloma, Multiple 85 0.076
118
P PNC035 Pancreatic Cancer 84 0.076
119
P MYC007 Myocardial Infarction 70 0.076
120
LSH001 Leishmaniasis 63 0.076
121
TLN003 Telangiectasis 52 0.076
122
P KLZ004 Kala-Azar 1 41 0.076
123
CRT072 Creutzfeldt-Jakob Disease 70 0.074
124
CNG034 Congestive Heart Failure 69 0.074
125
P LKM002 Leukemia 68 0.074
126
RCK004 Rickets 68 0.074
127
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.074
128
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.074
129
AGN016 Aging 56 0.074
130
P TRM003 Tremor 54 0.074
131
P SPP010 Suppressor of Tumorigenicity 3 51 0.074
132
P OBS001 Obstructive Jaundice 50 0.074
133
BNR002 Bone Resorption Disease 48 0.074
134
KWS001 Kwashiorkor 44 0.074
135
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.074
136
ANP008 Anaplastic Oligoastrocytoma 30 0.074
137
ARG004 Argyria 27 0.074
138
OST012 Osteoarthritis 78 0.071
139
CRV035 Cervical Cancer 76 0.071
140
P HYP086 Hypothyroidism 69 0.071
141
CLN015 Colon Adenocarcinoma 65 0.071
142
P CRN300 Coronary Heart Disease 1 63 0.071
143
LNG099 Lung Disease 60 0.071
144
c ACT071 Acute Kidney Failure 60 0.071
145
P FBR017 Fibrosarcoma 56 0.071
146
HMC014 Homocysteinemia 53 0.071
147
CCC002 Coccidiosis 51 0.071
148
HPT004 Hepatic Coma 45 0.071
149
c NRF023 Neurofibromatosis, Type Ii 80 0.069
150
P MLN008 Melanoma 69 0.069
151
BRN024 Bronchitis 68 0.069
152
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.069
153
SKN016 Skin Disease 63 0.069
154
DPR016 Depression 63 0.069
155
SQM006 Squamous Cell Carcinoma 60 0.069
156
CHL123 Chlamydia 59 0.069
157
P ALC033 Alcohol Use Disorder 58 0.069
158
c ACT075 Acute Myocardial Infarction 57 0.069
159
P ALP008 Alopecia 54 0.069
160
MST005 Mastitis 53 0.069
161
P CHL066 Cholangitis 51 0.069
162
CRH001 Crohn's Disease 74 0.066
163
ULC004 Ulcerative Colitis 73 0.066
164
P LPR021 Leprosy 3 69 0.066
165
c ATS007 Autism Spectrum Disorder 67 0.066
166
c RHB024 Rhabdomyosarcoma 2 67 0.066
167
P PNC044 Pancreatitis 61 0.066
168
P NPH012 Nephrotic Syndrome 60 0.066
169
ORL011 Oral Cancer 60 0.066
170
MTC097 Mitochondrial Complex Iv Deficiency 59 0.066
171
OST016 Osteochondrosis 53 0.066
172
GST023 Gastric Ulcer 53 0.066
173
PLR008 Pleurisy 50 0.066
174
HNS001 Hansen's Disease 34 0.066
175
ESP021 Esophageal Cancer 90 0.063
176
P EPL164 Epilepsy 71 0.063
177
P HYP061 Hypertrophic Cardiomyopathy 70 0.063
178
P MYP004 Myopathy 70 0.063
179
ART016 Aortic Aneurysm 69 0.063
180
P LKM062 Leukemia, Acute Lymphoblastic 69 0.063
181
P CLC063 Celiac Disease 1 66 0.063
182
c SML038 Small Cell Cancer of the Lung 65 0.063
183
P HYP750 Hypertriglyceridemia, Familial 62 0.063
184
HPT019 Hepatic Encephalopathy 60 0.063
185
P OPT006 Optic Nerve Disease 60 0.063
186
MNT002 Mental Depression 58 0.063
187
PRT038 Protein-Energy Malnutrition 54 0.063
188
NNL006 Non-Alcoholic Steatohepatitis 54 0.063
189
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.063
190
P ECL001 Eclampsia 50 0.063
191
MCR018 Microcytic Anemia 47 0.063
192
CYT002 Cytokine Deficiency 42 0.063
193
c ACT004 Acute Diarrhea 39 0.063
194
CHR178 Chromosomal Triplication 35 0.063
195
PLY150 Polykaryocytosis Inducer 31 0.063
196
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.063
197
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.060
198
c HYP595 Hypertension, Essential 84 0.060
199
P GLM040 Glioma Susceptibility 1 81 0.060
200
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.060
201
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.060
202
c SPN225 Spondyloarthropathy 1 73 0.060
203
P MLT020 Multiple Sclerosis 72 0.060
204
HMN044 Human Immunodeficiency Virus Type 1 71 0.060
205
P AMY004 Amyloidosis 70 0.060
206
P PLM037 Pulmonary Hypertension 67 0.060
207
P DMN002 Dementia 66 0.060
208
P SKN015 Skin Carcinoma 66 0.060
209
LPP008 Lipoprotein Quantitative Trait Locus 62 0.060
210
NTR005 Nutritional Deficiency Disease 62 0.060
211
P HMN010 Hemangioma 61 0.060
212
BLR008 Bilirubin Metabolic Disorder 57 0.060
213
GLS001 Gliosarcoma 54 0.060
214
P INF037 Inflammatory Bowel Disease 54 0.060
215
P ART021 Arteriosclerosis 54 0.060
216
LGN006 Legionnaire Disease 52 0.060
217
CLR109 Colorectal Adenocarcinoma 51 0.060
218
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.060
219
BRN071 Brain Injury 49 0.060
220
c MCR120 Microvascular Complications of Diabetes 7 47 0.060
221
P HYP265 Hypotonia 43 0.060
222
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.060
223
ANX004 Anoxia 40 0.060
224
MTH071 Methane Production 26 0.060
225
CRD009 Cardioencephalomyopathy 19 0.060
226
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.057
227
P OST002 Osteoporosis 74 0.057
228
SVR004 Severe Combined Immunodeficiency 73 0.057
229
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.057
230
P HNT016 Huntington Disease 72 0.057
231
P PHC003 Pheochromocytoma 71 0.057
232
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.057
233
P PNM007 Pneumonia 68 0.057
234
P SYS005 Systemic Scleroderma 68 0.057
235
P PLM036 Pulmonary Fibrosis 65 0.057
236
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.057
237
P ART023 Arthropathy 62 0.057
238
CTN007 Cutaneous Leishmaniasis 62 0.057
239
P ENC004 Encephalitis 61 0.057
240
ADN018 Adenoma 59 0.057
241
GST045 Gastroenteritis 59 0.057
242
VSC002 Vascular Dementia 57 0.057
243
ERY051 Erythroleukemia, Familial 56 0.057
244
P PLY019 Polyneuropathy 56 0.057
245
HPT022 Hepatoblastoma 56 0.057
246
P SHR001 Short Bowel Syndrome 53 0.057
247
DNT012 Dental Caries 53 0.057
248
P INT068 Intestinal Disease 53 0.057
249
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.057
250
ART140 Arteries, Anomalies of 52 0.057
251
DYS015 Dysentery 52 0.057
252
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.057
253
SPN051 Spondylitis 51 0.057
254
P AST007 Astrocytoma 51 0.057
255
BLR001 Biliary Atresia 50 0.057
256
P SCL009 Sclerosing Cholangitis 48 0.057
257
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.057
258
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.057
259
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.057
260
ALB002 Albinism 46 0.057
261
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.057
262
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.057
263
ADR040 Adrenal Gland Pheochromocytoma 46 0.057
264
VGN019 Vaginal Discharge 46 0.057
265
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.057
266
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.057
267
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.057
268
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.057
269
ORL015 Oral Squamous Cell Carcinoma 43 0.057
270
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.057
271
c CHR576 Chronic Beryllium Disease 42 0.057
272
P BRY005 Beryllium Disease 40 0.057
273
HYP001 Hypochromic Microcytic Anemia 38 0.057
274
INF009 Inflammatory Spondylopathy 31 0.057
275
c CRN216 Craniosynostosis 5 21 0.057
276
c LKM061 Leukemia, Acute Myeloid 84 0.054
277
NRL016 Neural Tube Defects 82 0.054
278
CYS001 Cystic Fibrosis 81 0.054
279
P BLD134 Bladder Cancer 79 0.054
280
P RTN008 Retinitis Pigmentosa 79 0.054
281
c BTT014 Beta-Thalassemia 74 0.054
282
P SRC025 Sarcoidosis 1 70 0.054
283
P MYC084 Mycobacterium Tuberculosis 1 68 0.054
284
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.054
285
P NSP012 Nasopharyngeal Carcinoma 66 0.054
286
P HRP006 Herpes Simplex 65 0.054
287
GT001 Gout 64 0.054
288
c ACT068 Acute Cystitis 63 0.054
289
CLT003 Colitis 62 0.054
290
c HPT003 Hepatitis a 62 0.054
291
GST033 Gestational Diabetes 61 0.054
292
THY029 Thyroid Carcinoma 59 0.054
293
P RTN016 Retinal Degeneration 53 0.054
294
THY030 Thyroid Gland Disease 52 0.054
295
HYP781 Hypoascorbemia 51 0.054
296
P OVR082 Overgrowth Syndrome 50 0.054
297
P SDR003 Sideroblastic Anemia 49 0.054
298
RTN023 Retinitis 46 0.054
299
DMP001 Dumping Syndrome 44 0.054
300
MNT317 Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, and Keratoderma 43 0.054
301
NRR001 Neuroretinitis 42 0.054
302
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.051
303
P RSP003 Respiratory Failure 74 0.051
304
END057 Endometrial Cancer 74 0.051
305
LPT014 Leptin Deficiency or Dysfunction 74 0.051
306
CRB039 Cerebrovascular Disease 67 0.051
307
P MSC005 Muscular Dystrophy 66 0.051
308
P MCR115 Microvascular Complications of Diabetes 5 66 0.051
309
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.051
310
SRC014 Sarcoma 65 0.051
311
c DBT099 Diabetes Mellitus, Type I 65 0.051
312
P PRD008 Periodontitis 64 0.051
313
LPD008 Lipid Metabolism Disorder 62 0.051
314
RTN017 Retinal Detachment 61 0.051
315
P SCL018 Scoliosis 60 0.051
316
SPP011 Suppression of Tumorigenicity 12 59 0.051
317
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.051
318
P BND020 Bone Disease 59 0.051
319
PPT005 Peptic Ulcer Disease 59 0.051
320
P SYP003 Syphilis 58 0.051
321
P BCL017 B-Cell Lymphoma 58 0.051
322
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.051
323
SCH014 Schistosomiasis 57 0.051
324
P PLY011 Polycystic Ovary Syndrome 56 0.051
325
P GST044 Gastritis 56 0.051
326
P MLN007 Male Infertility 55 0.051
327
P MYP006 Myopia 55 0.051
328
BCT002 Bacterial Vaginosis 53 0.051
329
c MCR113 Microvascular Complications of Diabetes 3 52 0.051
330
CRV040 Cervix Carcinoma 51 0.051
331
c HNT004 Huntington Disease-Like 2 50 0.051
332
STM007 Stomatitis 50 0.051
333
P SCK005 Sickle Cell Disease 50 0.051
334
MTB004 Metabolic Acidosis 50 0.051
335
P CRV039 Cervicitis 49 0.051
336
P END046 Endometritis 49 0.051
337
SPL018 Splenomegaly 48 0.051
338
ACT055 Actinomycosis 47 0.051
339
KRT002 Keratomalacia 47 0.051
340
c MLG068 Malignant Glioma 46 0.051
341
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.051
342
URL001 Urolithiasis 45 0.051
343
GRD001 Giardiasis 45 0.051
344
MCR017 Macrocytic Anemia 44 0.051
345
HMP009 Haemophilus Influenzae 43 0.051
346
c MCR130 Microvascular Complications of Diabetes 6 41 0.051
347
c MCR133 Microvascular Complications of Diabetes 4 41 0.051
348
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.051
349
c HNT011 Huntington Disease-Like 3 38 0.051
350
ACR005 Acrodermatitis 38 0.051
351
IMM167 Immune Deficiency Disease 78 0.047
352
BRN028 Brain Cancer 74 0.047
353
PRP027 Peripheral Vascular Disease 71 0.047
354
P ASP006 Aspergillosis 69 0.047
355
P THR014 Thrombocytopenia 67 0.047
356
P HYD006 Hydrocephalus 66 0.047
357
P CHR071 Charcot-Marie-Tooth Disease 65 0.047
358
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.047
359
MDD011 Mood Disorder 62 0.047
360
P PRP029 Porphyria 62 0.047
361
VRC005 Varicose Veins 60 0.047
362
VSL002 Visual Epilepsy 59 0.047
363
ANR040 Aneurysm 59 0.047
364
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.047
365
P CND004 Candidiasis 58 0.047
366
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 57 0.047
367
P CRD246 Cardiovascular System Disease 57 0.047
368
CMR002 Coumarin Resistance 56 0.047
369
P SZR006 Seizure Disorder 56 0.047
370
ALL010 Allergic Contact Dermatitis 56 0.047
371
GST050 Gastrointestinal System Disease 56 0.047
372
CHR100 Chronic Ulcer of Skin 55 0.047
373
P HYP076 Hyperthyroidism 55 0.047
374
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.047
375
OCL069 Ocular Motor Apraxia 51 0.047
376
KRT009 Keratosis 51 0.047
377
TRM010 Traumatic Brain Injury 51 0.047
378
ENT004 Enthesopathy 49 0.047
379
CVR006 Cavernous Hemangioma 49 0.047
380
CNT033 Central Nervous System Cancer 47 0.047
381
TNP001 Tinea Pedis 46 0.047
382
TTH006 Tooth Disease 46 0.047
383
P MTH007 Methemoglobinemia 46 0.047
384
ATX019 Ataxia with Vitamin E Deficiency 42 0.047
385
PRS063 Paresthesia 41 0.047
386
PCD001 Pica Disease 41 0.047
387
OVR094 Ovarian Epithelial Cancer 38 0.047
388
END028 Endemic Goiter 37 0.047
390
HND015 Hand Skill, Relative 33 0.047
391
CHL079 Children's Interstitial Lung Disease 26 0.047
392
ENT007 Enteropathica 26 0.047
393
P ATX030 Ataxia-Telangiectasia 82 0.043
394
MLR004 Malaria 81 0.043
395
c DLT002 Dilated Cardiomyopathy 79 0.043
396
INS024 Insulin-Like Growth Factor I 79 0.043
397
P APL001 Aplastic Anemia 74 0.043
398
SCK003 Sickle Cell Anemia 74 0.043
399
ANX010 Anxiety 73 0.043
400
c LKM063 Leukemia, Chronic Myeloid 72 0.043
401
ADL002 Adult Syndrome 70 0.043
402
P CRN037 Craniosynostosis 68 0.043
403
SKN019 Skin Melanoma 68 0.043
404
P MJR001 Major Depressive Disorder 68 0.043
405
c MCR129 Microvascular Complications of Diabetes 1 66 0.043
406
CHG001 Chagas Disease 66 0.043
407
P MNN013 Meningitis 66 0.043
408
P DRM053 Dermatitis, Atopic 66 0.043
409
KHL003 Kohlschutter-Tonz Syndrome 65 0.043
410
ANR007 Anorexia Nervosa 63 0.043
411
P TRC086 Trichohepatoenteric Syndrome 1 62 0.043
412
BLD131 Bladder Urothelial Carcinoma 62 0.043
413
MSL001 Measles 62 0.043
414
P MYL006 Myeloid Leukemia 60 0.043
415
ACQ007 Acquired Immunodeficiency Syndrome 60 0.043
416
P ALP009 Alopecia Areata 60 0.043
417
RHM001 Rheumatic Fever 60 0.043
418
P OCL002 Oculocutaneous Albinism 60 0.043
419
c HPT016 Hepatitis B 59 0.043
420
P URT039 Urticaria 58 0.043
421
EYD002 Eye Disease 58 0.043
422
P GLM007 Glomerulonephritis 57 0.043
423
c CHL119 Cholangitis, Primary Sclerosing 57 0.043
424
P EXN002 Exanthem 57 0.043
425
P PYL005 Pyelonephritis 56 0.043
426
TRN018 Transitional Cell Carcinoma 56 0.043
427
MCS002 Mucositis 56 0.043
428
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.043
429
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.043
430
THR013 Thoracic Outlet Syndrome 54 0.043
431
MYM001 Myoma 54 0.043
432
SPN035 Spindle Cell Sarcoma 53 0.043
433
P RTN018 Retinal Disease 53 0.043
434
OST011 Osteomalacia 52 0.043
435
DMY004 Demyelinating Disease 52 0.043
437
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.043
438
c SVR005 Severe Pre-Eclampsia 50 0.043
439
AZS001 Azoospermia 50 0.043
440
HMG002 Hemoglobinuria 50 0.043
441
c INV001 Invasive Aspergillosis 49 0.043
442
RFR010 Refractory Anemia 48 0.043
443
P MRC003 Mercury Poisoning 48 0.043
444
SXL003 Sexual Disorder 47 0.043
445
CHR074 Choriocarcinoma 47 0.043
446
c DRR009 Diarrhea 6 46 0.043
447
P SDR002 Siderosis 44 0.043
448
SPN188 Spinal Muscular Atrophy, Distal, X-Linked 3 43 0.043
449
MRS001 Marasmus 42 0.043
450
IDP070 Idiopathic Scoliosis 42 0.043
451
c MCR112 Microvascular Complications of Diabetes 2 41 0.043
452
P TRC031 Trichorhinophalangeal Syndrome 40 0.043
453
ALL014 Allergic Encephalomyelitis 38 0.043
454
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 38 0.043
455
P CRB059 Cerebellar Degeneration 37 0.043
456
PRM329 Premature Aging 35 0.043
457
c PRS136 Prostate Cancer, Hereditary, 6 33 0.043
458
c PRS130 Prostate Cancer, Hereditary, 8 32 0.043
459
URT049 Urate Oxidase, Pseudogene 25 0.043
460
P LKM071 Leukemia, Chronic Lymphocytic 79 0.038
461
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.038
462
PHN003 Phenylketonuria 75 0.038
463
c THR092 Thrombophilia Due to Thrombin Defect 73 0.038
464
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.038
465
FCT007 Factor Vii Deficiency 67 0.038
466
P TRN020 Turner Syndrome 67 0.038
467
TTN003 Tetanus 65 0.038
468
P CTS001 Cutis Laxa 65 0.038
469
P ANR048 Aniridia 1 63 0.038
470
TYP007 Typhoid Fever 63 0.038
471
P END044 Endometriosis 63 0.038
472
c LCL006 Localized Scleroderma 62 0.038
473
c FNC043 Fanconi Anemia, Complementation Group E 62 0.038
474
c HPT001 Hepatitis C 62 0.038
475
c SVR001 Severe Acute Respiratory Syndrome 62 0.038
476
ATM095 Autoimmune Disease 62 0.038
477
TXC005 Toxic Shock Syndrome 62 0.038
478
INT002 Intermittent Claudication 61 0.038
479
c PNS012 Paine Syndrome 61 0.038
480
P LPS004 Lupus Erythematosus 61 0.038
481
LGN002 Legionellosis 60 0.038
482
P KDN017 Kidney Cancer 60 0.038
483
SPN186 Spinal Cord Injury 60 0.038
484
ACN002 Acanthosis Nigricans 60 0.038
485
PRN019 Perinatal Necrotizing Enterocolitis 59 0.038
486
AVN001 Avian Influenza 59 0.038
487
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.038
488
P EHL001 Ehlers-Danlos Syndrome 58 0.038
489
CNS004 Constipation 58 0.038
490
LYM027 Lymphopenia 58 0.038
491
P UVT001 Uveitis 57 0.038
492
CHL067 Cholecystitis 57 0.038
493
P HDC001 Headache 57 0.038
494
THR024 Thrombosis 57 0.038
495
c INT072 Intestinal Pseudo-Obstruction 56 0.038
496
P PNM006 Pneumoconiosis 56 0.038
497
BRN004 Brain Edema 56 0.038
498
HYP005 Hypokalemia 55 0.038
499
LMB062 Limb Ischemia 55 0.038
500
VSC003 Visceral Leishmaniasis 55 0.038
501
P VNS003 Venous Insufficiency 55 0.038
502
P SLM003 Salmonellosis 55 0.038
503
SYN007 Synovitis 54 0.038
504
P PMP001 Pemphigus 54 0.038
505
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.038
506
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.038
507
P HMC002 Homocystinuria 53 0.038
508
LMY002 Leiomyoma 52 0.038
509
PNG002 Pain Agnosia 51 0.038
510
ENT011 Enterocolitis 51 0.038
511
LNG031 Lung Benign Neoplasm 51 0.038
512
P RNL007 Renal Tubular Acidosis 51 0.038
513
BHR001 Behr Syndrome 51 0.038
514
END086 End Stage Renal Disease 51 0.038
515
PST021 Postpartum Depression 50 0.038
516
P KRT007 Keratoconus 50 0.038
517
OCL022 Ocular Melanoma 50 0.038
518
URM002 Uremia 49 0.038
519
QDR001 Quadriplegia 48 0.038
520
CLC006 Calcinosis 48 0.038
521
INT067 Interstitial Nephritis 48 0.038
522
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.038
523
ANT018 Anthracosis 48 0.038
524
CHR031 Chromoblastomycosis 47 0.038
525
P BNG032 Benign Mesothelioma 46 0.038
526
CRB004 Cerebral Artery Occlusion 45 0.038
527
SPS057 Spasticity 45 0.038
528
DWR001 Dwarfism 44 0.038
529
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.038
530
EXC002 Exocrine Pancreatic Insufficiency 42 0.038
531
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.038
532
c CHR682 Chronic Bilirubin Encephalopathy 39 0.038
533
LPD014 Lipodermatosclerosis 38 0.038
534
AMN006 Aminoaciduria 38 0.038
535
c OVR114 Ovarian Cancer 1 38 0.038
536
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.038
537
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.038
538
PLC002 Plica Syndrome 36 0.038
539
LCH001 Leech Infestation 35 0.038
540
ATX010 Ataxia Neuropathy Spectrum 34 0.038
541
ACT064 Acute Necrotizing Encephalitis 33 0.038
542
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.038
543
MGB001 Megabladder, Congenital 18 0.038
544
BLD137 Blood Group--Ahonen 16 0.038
545
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.033
546
P CNR004 Cone-Rod Dystrophy 2 73 0.033
547
OTT002 Otitis Media 72 0.033
548
c CHR684 Chronic Kidney Disease 70 0.033
549
P ANG001 Angelman Syndrome 69 0.033
550
OBS002 Obsessive-Compulsive Disorder 68 0.033
551
P INF038 Influenza 68 0.033
552
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.033
553
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.033
554
FLL027 Fallopian Tube Carcinoma 67 0.033
555
HYP056 Hypoglycemia 66 0.033
556
AND002 Androgen Insensitivity Syndrome 66 0.033
557
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.033
558
NRM005 Neuromuscular Disease 64 0.033
559
BRC012 Brucellosis 64 0.033
560
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.033
561
LYM017 Lyme Disease 64 0.033
562
HYP020 Hyperprolactinemia 64 0.033
563
OST017 Osteomyelitis 64 0.033
564
P HYP069 Hyperparathyroidism 63 0.033
565
P MVM001 Movement Disease 63 0.033
566
c OPT053 Optic Atrophy 1 63 0.033
567
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.033
568
P SPN046 Spinal Muscular Atrophy 62 0.033
570
c SCL052 Scleroderma, Familial Progressive 61 0.033
571
DRR016 Diarrhea 2, with Microvillus Atrophy 60 0.033
572
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.033
573
ING001 Inguinal Hernia 60 0.033
574
P MYC008 Myocarditis 59 0.033
575
P AXN002 Axenfeld-Rieger Syndrome 59 0.033
576
CHL014 Cholera 59 0.033
577
P LKD001 Leukodystrophy 59 0.033
578
P SLP005 Sleep Disorder 59 0.033
579
P DNG005 Dengue Virus 59 0.033
580
INC002 Inclusion Body Myositis 58 0.033
581
CRY005 Cryptococcosis 58 0.033
582
RBS001 Rabies 58 0.033
583
FBR047 Fibromyalgia 58 0.033
584
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.033
585
BRS051 Breast Disease 58 0.033
586
NWB001 Newborn Respiratory Distress Syndrome 58 0.033
587
CRV038 Cervical Squamous Cell Carcinoma 58 0.033
588
P BNC003 Bone Cancer 58 0.033
589
PMP006 Pemphigus Vulgaris, Familial 57 0.033
590
GLS018 Glass Syndrome 57 0.033
591
P RHN004 Rhinitis 57 0.033
592
DSS009 Disseminated Intravascular Coagulation 57 0.033
593
APH002 Aphasia 57 0.033
594
PHR003 Pharyngitis 57 0.033
595
P BPL003 Bipolar Disorder 56 0.033
596
P MYS005 Myositis 56 0.033
597
P MTC069 Mitochondrial Disorders 56 0.033
598
SPN041 Spinal Cord Disease 56 0.033
599
HMG005 Hemoglobinopathy 56 0.033
600
c GRV008 Graves Disease 1 56 0.033
601
NRN004 Neuroendocrine Tumor 55 0.033
602
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.033
603
BRN045 Brunner Syndrome 55 0.033
604
PRP030 Purpura 54 0.033
605
CRT017 Cartilage Disease 54 0.033
606
P ICH004 Ichthyosis 54 0.033
607
PPL022 Papilloma 54 0.033
608
PRC002 Paracoccidioidomycosis 54 0.033
609
P LCH002 Lichen Planus 53 0.033
610
KRT006 Keratoconjunctivitis 53 0.033
611
c PRD040 Periodontitis, Chronic 53 0.033
612
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.033
613
P PNC025 Panic Disorder 53 0.033
614
PRP080 Peripheral Artery Disease 53 0.033
615
ALC009 Alcoholic Liver Cirrhosis 53 0.033
616
c GLL024 Gallbladder Disease 1 53 0.033
617
STT041 Stuttering 52 0.033
618
P DDN001 Duodenal Ulcer 52 0.033
619
P MSC003 Muscular Atrophy 52 0.033
620
P NRD007 Neurodegeneration with Brain Iron Accumulation 52 0.033
621
PTH003 Pathologic Nystagmus 52 0.033
622
HYP014 Hyperuricemia 52 0.033
623
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.033
624
c ALB020 Albinism, Oculocutaneous, Type Iii 51 0.033
625
MGL001 Megaloblastic Anemia 51 0.033
626
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.033
627
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 51 0.033
628
GNT002 Giant Cell Glioblastoma 50 0.033
629
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.033
630
PLC008 Placenta Disease 50 0.033
631
c INF023 Inflammatory Breast Carcinoma 50 0.033
632
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.033
633
VGN020 Vaginal Disease 49 0.033
634
GST049 Gastrointestinal System Cancer 49 0.033
635
MTC005 Mitochondrial Metabolism Disease 49 0.033
636
c HPT015 Hepatitis D 49 0.033
637
VCC001 Vaccinia 49 0.033
638
P NGH001 Night Blindness 48 0.033
639
HMP001 Hemopericardium 48 0.033
640
PYL006 Pyloric Stenosis 48 0.033
641
CRN017 Coronary Thrombosis 47 0.033
642
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.033
643
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.033
644
P BLD051 Blood Coagulation Disease 46 0.033
645
ATN005 Autonomic Dysfunction 46 0.033
646
BCK003 Background Diabetic Retinopathy 46 0.033
647
P LPM005 Lipomatosis 46 0.033
648
KRT013 Keratolytic Winter Erythema 46 0.033
649
P PLL002 Pellagra 46 0.033
650
SQM002 Squamous Cell Papilloma 46 0.033
651
ANR004 Anuria 46 0.033
652
MXD026 Mixed Glioma 45 0.033
653
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.033
654
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.033
655
NWC001 Newcastle Disease 45 0.033
656
ACT003 Acute Kidney Tubular Necrosis 45 0.033
657
P CHR345 Chronic Pain 44 0.033
658
IMM064 Immunodeficiency, Common Variable, 10 44 0.033
659
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.033
660
HYP457 Hypertrophic Scars 42 0.033
661
P MLT065 Multicentric Osteolysis, Nodulosis, and Arthropathy 42 0.033
662
MTL005 Metal Allergy 41 0.033
663
c MJR024 Major Affective Disorder 9 41 0.033
664
FCL022 Focal Dystonia 41 0.033
665
PRM020 Premenstrual Tension 40 0.033
666
LKP003 Leukoplakia 39 0.033
667
c PRG020 Paragangliomas 3 39 0.033
668
ORL012 Oral Leukoplakia 39 0.033
669
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.033
670
c MJR022 Major Affective Disorder 8 38 0.033
671
CRD016 Cardiac Rupture 37 0.033
672
P CRB088 Cerebral Atrophy 37 0.033
673
CHR028 Chronic Wasting Disease 35 0.033
674
P PRG002 Progesterone-Receptor Positive Breast Cancer 35 0.033
675
ALR002 Al-Raqad Syndrome 33 0.033
676
HYP674 Hyperostosis Cranialis Interna 31 0.033
677
P PLT008 Pili Torti 31 0.033
678
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.033
679
FTL068 Fatal Infantile Cardioencephalomyopathy Due to Cytochrome C Oxidase Deficiency 30 0.033
680
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.033
681
c KRT078 Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Recessive 27 0.033
682
CYT018 Cytochrome P450 2d6 Variant 27 0.033
683
c RNG015 Ring Chromosome 2 26 0.033
684
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.033
685
LTH004 Lathyrism 16 0.033
686
XLN239 X-Linked Distal Hereditary Motor Neuropathy 12 0.033
687
HPP002 Huppke-Brendel Syndrome 7 0.033
688
STR067 Stroke, Ischemic 81 0.027
689
P RTT002 Rett Syndrome 80 0.027
690
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.027
691
P MDL005 Medulloblastoma 77 0.027
692
c MNN043 Meningioma, Familial 74 0.027
693
P RTN024 Retinoblastoma 73 0.027
694
MSC157 Muscular Dystrophy, Duchenne Type 72 0.027
695
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.027
696
P MTC003 Metachromatic Leukodystrophy 70 0.027
697
GST040 Gastric Adenocarcinoma 70 0.027
698
c PNC108 Pancreatitis, Hereditary 70 0.027
699
CRB037 Cerebral Palsy 69 0.027
700
P OCL013 Oculodentodigital Dysplasia 69 0.027
701
EWN003 Ewing Sarcoma 69 0.027
702
MNT001 Mantle Cell Lymphoma 69 0.027
703
c BSL007 Basal Cell Carcinoma 68 0.027
704
c NMN015 Niemann-Pick Disease, Type C1 68 0.027
705
PNC129 Pancreatic Adenocarcinoma 68 0.027
706
P CRD119 Cardiac Arrest 67 0.027
707
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.027
708
c INF071 Inflammatory Bowel Disease 1 67 0.027
709
P PRP003 Porphyria Cutanea Tarda 67 0.027
710
P HYP098 Hypereosinophilic Syndrome 67 0.027
711
P BLD062 Bile Duct Cancer 67 0.027
712
c MGR028 Migraine with or Without Aura 1 67 0.027
713
ANG054 Angina Pectoris 66 0.027
714
ART001 Arterial Tortuosity Syndrome 66 0.027
715
P ATR011 Atrial Fibrillation 66 0.027
716
P NRV007 Nervous System Disease 66 0.027
717
c FML001 Familial Atrial Fibrillation 65 0.027
718
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.027
719
KRT019 Keratitis, Hereditary 65 0.027
720
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.027
721
PND002 Pendred Syndrome 65 0.027
722
IRR002 Irritable Bowel Syndrome 65 0.027
723
P PRS038 Personality Disorder 65 0.027
724
PRT036 Peritonitis 64 0.027
725
TBC004 Tobacco Addiction 64 0.027
726
P GLC113 Galactosemia I 64 0.027
727
P FRD001 Friedreich Ataxia 64 0.027
728
ART002 Arts Syndrome 64 0.027
729
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.027
730
TRN015 Transient Cerebral Ischemia 63 0.027
731
c ALP101 Alpha-Thalassemia 62 0.027
732
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.027
733
c BRN108 Branchiootic Syndrome 1 62 0.027
734
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.027
735
BLL006 Bullous Pemphigoid 62 0.027
736
HSH003 Hashimoto Thyroiditis 62 0.027
737
MNN042 Meningioma, Radiation-Induced 62 0.027
738
CRC021 Carcinosarcoma 62 0.027
739
P OST009 Osteochondritis Dissecans 62 0.027
740
ASP002 Aspartylglucosaminuria 62 0.027
741
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 61 0.027
742
ALC006 Alcoholic Hepatitis 61 0.027
743
CHR066 Chronic Fatigue Syndrome 61 0.027
744
SDD001 Sudden Infant Death Syndrome 61 0.027
745
DCB001 Decubitus Ulcer 61 0.027
746
HRP004 Herpes Zoster 60 0.027
747
P TXP001 Toxoplasmosis 60 0.027
748
INT066 Interstitial Lung Disease 60 0.027
749
c ACT027 Acute Pancreatitis 60 0.027
750
P SNS001 Sensorineural Hearing Loss 60 0.027
751
P MCR010 Microcephaly 59 0.027
752
BRN002 Bronchiolitis 59 0.027
753
GLB001 Gilbert Syndrome 58 0.027
754
ANT024 Anthrax Disease 58 0.027
755
SPT004 Septic Arthritis 58 0.027
756
DSS008 Disease of Mental Health 58 0.027
757
BRG013 Buerger Disease 58 0.027
758
P GLL018 Gallbladder Cancer 57 0.027
759
BRN056 Bronchopulmonary Dysplasia 57 0.027
760
APH001 Aphthous Stomatitis 57 0.027
761
P PRV006 Pervasive Developmental Disorder 57 0.027
762
TNS005 Tonsillitis 57 0.027
763
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.027
764
CMM005 Common Cold 57 0.027
765
P PLY018 Polycythemia 56 0.027
766
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.027
767
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.027
768
LST001 Listeriosis 56 0.027
769
DBL002 Double Outlet Right Ventricle 56 0.027
770
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.027
771
IMM140 Immunodeficiency 47 56 0.027
772
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.027
773
P PLM034 Pulmonary Emphysema 55 0.027
774
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.027
775
P SBS003 Substance Abuse 55 0.027
776
FLR002 Filariasis 55 0.027
777
P ALP106 Alport Syndrome 1, X-Linked 55 0.027
778
END040 Endogenous Depression 55 0.027
779
ACD008 Acid-Labile Subunit Deficiency 54 0.027
780
TND005 Tendinitis 54 0.027
781
PRC013 Pericarditis 54 0.027
782
DBT010 Diabetic Neuropathy 54 0.027
783
c PST005 Posterior Uveitis 54 0.027
784
P LNG035 Lung Large Cell Carcinoma 54 0.027
785
WST005 West Nile Virus 54 0.027
786
SNS003 Sensory Peripheral Neuropathy 54 0.027
787
PRS045 Prostatic Hypertrophy 53 0.027
788
c HNT010 Huntington Disease-Like 1 53 0.027
789
P TCD001 Tic Disorder 53 0.027
790
P INS002 in Situ Carcinoma 53 0.027
791
ENC055 Encephalopathy, Ethylmalonic 53 0.027
792
INF034 Infective Endocarditis 53 0.027
793
HYP063 Hypersplenism 53 0.027
794
P ACT008 Actinic Keratosis 53 0.027
795
TXC002 Toxic Encephalopathy 53 0.027
796
c FML008 Familial Retinoblastoma 53 0.027
797
c CNT035 Central Nervous System Disease 52 0.027
798
EXP004 Exophthalmos 52 0.027
799
DRM011 Dermatophytosis 52 0.027
800
P CHN059 Chondrocalcinosis 52 0.027
801
P HMG032 Hemoglobin H Disease 52 0.027
802
P THY032 Thyroiditis 52 0.027
803
BWN001 Bowen-Conradi Syndrome 52 0.027
804
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 52 0.027
805
P OVR049 Ovarian Disease 52 0.027
806
c NMN014 Niemann-Pick Disease, Type C2 51 0.027
807
FDL002 Food Allergy 51 0.027
808
MYL001 Myelitis 51 0.027
809
PLS009 Plasma Cell Neoplasm 51 0.027
810
c PNC106 Pancreatic Agenesis 1 51 0.027
811
P LCT001 Lactic Acidosis 51 0.027
812
CHR005 Chorioamnionitis 51 0.027
813
P FNC004 Fanconi Syndrome 50 0.027
814
SPN021 Spinal Meningioma 50 0.027
815
P PRS049 Persistent Mullerian Duct Syndrome 50 0.027
816
FSC004 Fasciitis 50 0.027
817
ASC010 Ascaris Lumbricoides Infection 50 0.027
818
NPH010 Nephrosclerosis 50 0.027
819
OPT003 Opiate Dependence 50 0.027
820
HYP080 Hypogonadism 50 0.027
821
ISL003 Isolated Growth Hormone Deficiency 49 0.027
822
c CHR418 Chronic Leukemia 49 0.027
823
VLV011 Vulvovaginal Candidiasis 49 0.027
824
VLV047 Volvulus of Midgut 49 0.027
825
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.027
826
P CRV031 Cervical Adenocarcinoma 49 0.027
827
MNN009 Meningoencephalitis 49 0.027
828
BCT004 Bacteriuria 49 0.027
829
c ACT150 Acute Adrenal Insufficiency 48 0.027
830
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.027
831
NCR007 Necrotizing Fasciitis 48 0.027
832
VTM033 Vitamin K Deficiency Bleeding 48 0.027
833
PNC034 Pancreas Disease 48 0.027
834
c VRL012 Viral Meningitis 48 0.027
835
OPD006 Opioid Addiction 48 0.027
836
MLT006 Multidrug-Resistant Tuberculosis 48 0.027
837
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 47 0.027
838
CRN027 Corneal Neovascularization 47 0.027
839
P BLR006 Biliary Tract Disease 47 0.027
840
NDL007 Nodular Goiter 47 0.027
841
RNL077 Renal Fibrosis 47 0.027
842
P CLL015 Collagen Disease 47 0.027
843
KHN001 Kuhnt-Junius Degeneration 47 0.027
844
IRN004 Iron-Refractory Iron Deficiency Anemia 47 0.027
845
c INH020 Inherited Metabolic Disorder 47 0.027
846
GST071 Gastrointestinal Carcinoma 47 0.027
847
DPM001 Dopamine Beta-Hydroxylase Deficiency 47 0.027
848
RTN020 Retinal Vascular Disease 46 0.027
849
SPN020 Spondylosis 46 0.027
850
EXS001 Exostosis 46 0.027
851
CHD004 Chudley-Mccullough Syndrome 46 0.027
852
CHR008 Choroiditis 46 0.027
853
GRW007 Growth Hormone Deficiency 46 0.027
854
GST012 Gastroesophageal Junction Adenocarcinoma 46 0.027
855
P MYC033 Myoclonus 46 0.027
856
OPD001 Opioid Abuse 46 0.027
857
EPD015 Epidemic Typhus 45 0.027
858
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.027
859
ELS001 Eales Disease 45 0.027
860
P TRN034 Transverse Myelitis 45 0.027
861
OLG001 Oligospermia 45 0.027
862
RTR008 Root Resorption 45 0.027
863
P GNT009 Giant Axonal Neuropathy 45 0.027
864
CYN002 Cyanosis, Transient Neonatal 45 0.027
865
ORL013 Oral Lichen Planus 45 0.027
866
KR002 Kuru 45 0.027
867
c HMG003 Hemoglobin E Disease 45 0.027
868
CRT015 Carotid Artery Occlusion 45 0.027
869
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.027
870
CHP002 Chops Syndrome 44 0.027
871
GRN017 Granulocytopenia 44 0.027
872
c PRM038 Primary Agammaglobulinemia 44 0.027
873
c SPR086 Spermatogenic Failure 3 44 0.027
874
CVD001 Covid-19 44 0.027
875
FBR054 Fibroma 44 0.027
876
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 44 0.027
877
TND004 Tendinopathy 43 0.027
878
SKN005 Skin Atrophy 43 0.027
879
MYP091 Myopathy, Congenital, with Fiber-Type Disproportion 43 0.027
880
DSC009 Discoid Lupus Erythematosus 42 0.027
881
MST004 Mast Cell Neoplasm 42 0.027
882
TRP009 Triple X Syndrome 42 0.027
883
CRV043 Cervical Dystonia 42 0.027
884
SNL007 Senile Cataract 42 0.027
885
CRB033 Cerebral Degeneration 42 0.027
886
GLC096 Galactorrhea 42 0.027
887
MYF002 Myofascial Pain Syndrome 42 0.027
888
FSC002 Fascioliasis 42 0.027
889
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.027
890
LCN001 Lice Infestation 42 0.027
891
GST020 Gastric Antral Vascular Ectasia 41 0.027
892
49X006 49, Xxxxy Syndrome 41 0.027
893
P SCL057 Scoliosis, Isolated 1 41 0.027
894
KLB003 Klebsiella Pneumonia 41 0.027
895
SCR001 Secretory Meningioma 41 0.027
896
TRP004 Tropical Sprue 41 0.027
897
P SPS008 Spastic Ataxia 41 0.027
898
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.027
899
RDN001 Reading Disorder 40 0.027
900
CHN002 Chancroid 40 0.027
901
P FNC034 Fanconi Renotubular Syndrome 2 40 0.027
902
BRY001 Berylliosis 40 0.027
903
KLD004 Keloid Disorder 40 0.027
904
BLD045 Bladder Diverticulum 40 0.027
905
UTR043 Uterine Sarcoma 39 0.027
906
EXT006 Extrahepatic Cholestasis 39 0.027
907
c CNG497 Congenital Disorder of Glycosylation, Type Iio 39 0.027
908
MNR003 Mineral Metabolism Disease 39 0.027
909
EXT007 Extracutaneous Mastocytoma 38 0.027
910
P PRC031 Preeclampsia/eclampsia 1 38 0.027
911
c PLY105 Polycystic Ovary Syndrome 1 38 0.027
912
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.027
913
CNT060 Central Serous Chorioretinopathy 38 0.027
914
c CHR098 Chronic Pyelonephritis 38 0.027
915
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.027
916
CRB009 Cerebritis 37 0.027
917
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 37 0.027
918
CRR017 Curry-Jones Syndrome 37 0.027
919
GRS001 Gerstmann Syndrome 36 0.027
920
LYM011 Lymphogranuloma Venereum 36 0.027
921
CRY036 Cryptogenic Cirrhosis 36 0.027
922
WRN004 Wrinkly Skin Syndrome 36 0.027
923
PSD088 Pseudobulbar Affect 36 0.027
924
c AMY088 Amyotrophic Lateral Sclerosis 3 36 0.027
925
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.027
926
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.027
927
ASC001 Ascaridiasis 35 0.027
928
c HYP716 Hypermanganesemia with Dystonia 1 35 0.027
929
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.027
930
INT040 Intrinsic Asthma 34 0.027
931
PYR009 Pyridoxine Deficiency Anemia 34 0.027
932
GNT167 Genetic Obesity 33 0.027
933
RNL012 Renal Tuberculosis 33 0.027
934
P VSC018 Visceral Steatosis 33 0.027
935
P DST101 Distal Hereditary Motor Neuropathies 32 0.027
936
NRN002 Neuronitis 32 0.027
937
c CRN221 Craniosynostosis 4 31 0.027
938
LYM035 Lymphangiectasis 30 0.027
939
STT009 Sutton Disease 2 30 0.027
940
CHL035 Cholinergic Urticaria 30 0.027
941
SPN392 Spondylosis, Cervical 30 0.027
942
EPL149 Epilepsy, Hearing Loss, and Mental Retardation Syndrome 30 0.027
943
c INF078 Inflammatory Bowel Disease 2 29 0.027
944
c CNG496 Congenital Disorder of Glycosylation, Type Iiq 27 0.027
945
c MYP018 Myopia 6 27 0.027
946
c TTH010 Tooth Agenesis, Selective, 1 27 0.027
947
MLR020 Malaria, Mild 27 0.027
948
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.027
949
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 25 0.027
950
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.027
951
c VSC053 Visceral Steatosis, Congenital 25 0.027
952
CPG001 Capgras Syndrome 24 0.027
953
IDP069 Idiopathic Avascular Necrosis 23 0.027
954
OST007 Ostertagiasis 16 0.027
955
SLN002 Selenium Poisoning 11 0.027
956
DSR036 Disorder of Mineral Absorption and Transport 5 0.027
957
c SYS001 Systemic Lupus Erythematosus 86 0.019
958
PFF001 Pfeiffer Syndrome 79 0.019
959
MRF001 Marfan Syndrome 77 0.019
960
AST005 Asthma 76 0.019
961
KPS004 Kaposi Sarcoma 75 0.019
962
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.019
963
P FML018 Familial Mediterranean Fever 73 0.019
964
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.019
965
P GRF003 Graft-Versus-Host Disease 72 0.019
966
AGM019 Agammaglobulinemia, X-Linked 71 0.019
967
ACR007 Acromegaly 71 0.019
968
c EXD008 Exudative Vitreoretinopathy 1 71 0.019
969
BHC003 Behcet Syndrome 71 0.019
970
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.019
971
P TBR001 Tuberous Sclerosis 70 0.019
972
LYM133 Lymphoma, Hodgkin, Classic 69 0.019
973
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.019
974
P TMP003 Temporal Arteritis 68 0.019
975
CHL065 Cholangiocarcinoma 68 0.019
976
CMM004 Common Variable Immunodeficiency 68 0.019
977
CNN005 Connective Tissue Disease 68 0.019
978
BRK010 Burkitt Lymphoma 67 0.019
979
PSY004 Psychotic Disorder 67 0.019
980
CRP001 Carpal Tunnel Syndrome 67 0.019
981
c PRM196 Premature Ovarian Failure 1 67 0.019
982
MYC006 Mycosis Fungoides 66 0.019
983
GLL008 Gilles De La Tourette Syndrome 66 0.019
984
c FML021 Familial Hypercholesterolemia 66 0.019
985
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.019
986
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.019
987
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.019
988
GTL001 Gitelman Syndrome 65 0.019
989
P ART005 Arteriovenous Malformation 65 0.019
990
P AGM001 Agammaglobulinemia 65 0.019
991
PPL049 Papillon-Lefevre Syndrome 65 0.019
992
BRR014 Barrett Esophagus 65 0.019
993
PRT037 Pertussis 65 0.019
994
c WLM013 Wilms Tumor 1 65 0.019
995
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 65 0.019
996
P ADL010 Adult Respiratory Distress Syndrome 65 0.019
997
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.019
998
P THY023 Thymoma 65 0.019
999
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.019
1000
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.019
1001
P HRM001 Hermansky-Pudlak Syndrome 64 0.019
1002
CLF027 Cleft Palate, Isolated 64 0.019
1003
c JVN010 Juvenile Rheumatoid Arthritis 64 0.019
1004
CLR108 Colorectal Adenoma 64 0.019
1005
PRP083 Porphyria, Acute Intermittent 64 0.019
1006
c CNG006 Congenital Hypothyroidism 64 0.019
1007
PLM031 Poliomyelitis 64 0.019
1008
c DPH024 Diaphragmatic Hernia, Congenital 63 0.019
1009
KRN002 Kearns-Sayre Syndrome 63 0.019
1010
PLG002 Plague 63 0.019
1011
c MLG084 Malignant Fibrous Histiocytoma 63 0.019
1012
P SHR029 Short Syndrome 63 0.019
1013
END041 Endometrial Adenocarcinoma 63 0.019
1014
P LMY004 Leiomyosarcoma 63 0.019
1015
c ATM011 Autoimmune Hepatitis 63 0.019
1016
BDD001 Budd-Chiari Syndrome 63 0.019
1017
P VSC011 Vasculitis 62 0.019
1018
c ANM038 Anemia, Autoimmune Hemolytic 62 0.019
1019
MSS001 Masa Syndrome 62 0.019
1020
NRM001 Neuromyelitis Optica 61 0.019
1021
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 61 0.019
1022
OST003 Osteonecrosis 61 0.019
1023
P HYP035 Hypophosphatasia 61 0.019
1024
WST001 West Syndrome 61 0.019
1025
YLL002 Yellow Fever 61 0.019
1026
c WLM018 Wilms Tumor 5 61 0.019
1027
VRL011 Viral Infectious Disease 61 0.019
1028
FBR086 Fibrolamellar Carcinoma 61 0.019
1029
APP008 Appendicitis 61 0.019
1030
RGH009 Right Atrial Isomerism 60 0.019
1031
P TST021 Testicular Germ Cell Tumor 60 0.019
1032
DPH001 Diphtheria 60 0.019
1033
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.019
1034
P VNT002 Ventricular Septal Defect 60 0.019
1035
KFR001 Kufor-Rakeb Syndrome 60 0.019
1036
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.019
1037
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.019
1038
DNG002 Dengue Hemorrhagic Fever 60 0.019
1039
INS001 Insulinoma 60 0.019
1040
HYD002 Hydronephrosis 60 0.019
1041
STF001 Stiff-Person Syndrome 60 0.019
1042
P GLY013 Glycogen Storage Disease 60 0.019
1043
P RBL001 Rubella 59 0.019
1044
PRT013 Portal Hypertension 59 0.019
1045
c DNG003 Dengue Disease 59 0.019
1046
PLM033 Pulmonary Embolism 59 0.019
1047
PRT058 Pure Autonomic Failure 59 0.019
1048
P LYM033 Lymphoproliferative Syndrome 59 0.019
1049
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.019
1050
KLP010 Klippel-Trenaunay-Weber Syndrome 59 0.019
1051
GNG013 Gingivitis 59 0.019
1052
P NMN002 Niemann-Pick Disease 59 0.019
1053
CYS010 Cystinosis 59 0.019
1054
HLC007 Helicobacter Pylori Infection 59 0.019
1055
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 59 0.019
1056
MNK003 Muenke Syndrome 59 0.019
1057
RNL024 Renal Glucosuria 58 0.019
1058
P ANP001 Anaplastic Large Cell Lymphoma 58 0.019
1059
ALK013 Alkaptonuria 58 0.019
1060
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.019
1061
P INT070 Intestinal Obstruction 58 0.019
1062
ERY029 Erythermalgia, Primary 58 0.019
1063
c PTT056 Pituitary Adenoma 1, Multiple Types 58 0.019
1064
c PRM005 Primary Hyperparathyroidism 58 0.019
1065
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 57 0.019
1066
P GLL020 Gallbladder Disease 57 0.019
1067
P PLV020 Pelvic Organ Prolapse 57 0.019
1068
MCR013 Microphthalmia 57 0.019
1069
CHK001 Chikungunya 57 0.019
1070
MBS002 Moebius Syndrome 57 0.019
1071
P END033 Endocarditis 57 0.019
1072
c ALB009 Albinism, Oculocutaneous, Type Ia 57 0.019
1073
JPN002 Japanese Encephalitis 57 0.019
1074
PNM008 Pneumothorax 56 0.019
1075
P CHN012 Chondrosarcoma 56 0.019
1076
TCK001 Tick-Borne Encephalitis 56 0.019
1077
ALL006 Allergic Asthma 56 0.019
1078
ADN027 Adenomyosis 56 0.019
1079
GNR004 Generalized Anxiety Disorder 56 0.019
1080
SCH003 Schizophreniform Disorder 56 0.019
1081
ANN002 Anencephaly 56 0.019
1082
MTH009 Mouth Disease 56 0.019
1083