Search results for Copper

1423 hits were found for Copper

# Family MCID Name MIFTS Score
1
MNK001 Menkes Disease 62 6.794
2
CPP001 Copper Deficiency, Familial Benign 18 4.912
3
CPP004 Copper Deficiency Myelopathy 28 3.327
4
IDP071 Idiopathic Copper-Associated Cirrhosis 7 3.111
5
WLS001 Wilson Disease 69 3.026
6
DSR031 Disorder of Copper Metabolism 29 2.461
8
CNG382 Congenital Cataracts, Hearing Loss, and Neurodegeneration 24 2.231
9
c ATS421 Autosomal Recessive Axonal Charcot-Marie-Tooth Disease Due to Copper Metabolism Defect 9 2.223
10
P LTR001 Lateral Sclerosis 56 0.273
11
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.272
12
LVR012 Liver Cirrhosis 67 0.254
13
P ALZ034 Alzheimer Disease 90 0.253
14
P LVR013 Liver Disease 71 0.243
15
IRN002 Iron Metabolism Disease 58 0.227
16
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.221
17
DFC004 Deficiency Anemia 77 0.218
18
P NTR004 Neutropenia 64 0.212
19
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.183
20
P PRN023 Prion Disease 57 0.182
21
PPL052 Papillomatosis, Confluent and Reticulated 34 0.178
22
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.174
23
HLX001 Helix Syndrome 46 0.172
24
48X005 48,xyyy 37 0.167
25
P NRB010 Neuroblastoma 1 66 0.162
26
CHL068 Cholestasis 61 0.162
27
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.157
28
P DRR001 Diarrhea 55 0.154
29
P PRM006 Primary Biliary Cirrhosis 54 0.152
30
HRW001 Hair Whorl 36 0.152
31
P ENC018 Encephalopathy 64 0.150
32
PRM236 Primary Biliary Cholangitis 57 0.150
33
HMS001 Hemosiderosis 54 0.148
34
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.148
35
P RRH023 Rare Hereditary Hemochromatosis 41 0.146
36
P HPT023 Hepatocellular Carcinoma 99 0.141
37
c HYP836 Hypercholesterolemia, Familial, 1 74 0.141
38
P OVR042 Ovarian Cancer 89 0.138
39
ATS010 Autosomal Recessive Disease 49 0.138
40
P RHM011 Rheumatoid Arthritis 82 0.129
41
P NRP001 Neuropathy 57 0.129
42
DRM006 Dermatitis 63 0.126
43
GLB002 Glioblastoma 74 0.122
44
GLB015 Glioblastoma Multiforme 60 0.122
45
FTT001 Fatty Liver Disease 63 0.120
46
OCC006 Occipital Horn Syndrome 51 0.120
47
ALC007 Alcohol Dependence 68 0.118
48
P HRD018 Hair Disease 43 0.118
49
P ART022 Arthritis 71 0.117
50
P PSR002 Psoriasis 63 0.115
51
PLV003 Pelvic Inflammatory Disease 54 0.115
52
PST011 Pustulosis of Palm and Sole 51 0.115
53
c PRC016 Pre-Eclampsia 63 0.113
54
P CLR023 Colorectal Cancer 100 0.110
55
c HMC039 Hemochromatosis, Type 1 73 0.110
56
PLM001 Pulmonary Tuberculosis 72 0.110
57
P HML002 Hemolytic Anemia 64 0.110
58
47X002 47,xyy 49 0.108
59
SCR011 Scrapie 37 0.108
60
P BRS047 Breast Cancer 99 0.106
61
P MTR014 Motor Neuron Disease 66 0.106
62
HYP266 Hypoxia 58 0.106
63
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.104
64
P BRS044 Breast Adenocarcinoma 59 0.104
65
HVY002 Heavy Metal Poisoning 23 0.104
66
MYL009 Myelodysplastic Syndrome 72 0.103
67
BCT022 Bacterial Infectious Disease 57 0.103
68
PNC001 Pancytopenia 54 0.103
69
AMN001 Amenorrhea 54 0.103
70
P HRT032 Heart Disease 78 0.101
71
ATH013 Atherosclerosis Susceptibility 68 0.101
72
P CTR002 Cataract 62 0.101
73
P INF032 Infertility 60 0.101
74
ORL004 Oral Submucous Fibrosis 55 0.101
75
P LYM118 Lymphoma 70 0.099
76
ACR006 Aceruloplasminemia 74 0.097
77
P KDN018 Kidney Disease 73 0.097
78
c ACT134 Acute Liver Failure 53 0.097
79
P LYM031 Lymphocytic Leukemia 56 0.095
80
GTR002 Goiter 54 0.095
81
P LNG032 Lung Cancer 99 0.093
82
ALL026 Allergic Hypersensitivity Disease 65 0.093
83
P VSC007 Vascular Disease 65 0.090
84
P PRP019 Peripheral Nervous System Disease 64 0.090
85
IRN001 Iron Deficiency Anemia 59 0.090
86
PST092 Posttransplant Acute Limbic Encephalitis 29 0.090
87
DWN001 Down Syndrome 70 0.088
88
P THL005 Thalassemia 62 0.088
89
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.088
90
CND006 Candida Glabrata 33 0.088
91
P GST053 Gastric Cancer 85 0.086
92
P HPT021 Hepatitis 69 0.086
93
HYP066 Hyperglycemia 63 0.086
94
c DWL002 Dowling-Degos Disease 1 59 0.086
95
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.086
96
SLC006 Silicosis 55 0.086
97
PLM017 Pulmonary Alveolar Microlithiasis 54 0.086
98
c PCH010 Pachyonychia Congenita 3 43 0.086
99
P PRS040 Prostate Cancer 97 0.084
100
P LNG064 Lung Cancer Susceptibility 3 79 0.084
101
P DBT009 Diabetes Mellitus 66 0.084
102
VTM002 Vitamin B12 Deficiency 48 0.084
103
CRV035 Cervical Cancer 77 0.081
104
P PRK057 Parkinson Disease, Late-Onset 77 0.081
105
P SCH015 Schizophrenia 76 0.081
106
c ATR087 Atrial Standstill 1 76 0.081
107
OST159 Osteogenic Sarcoma 67 0.081
108
P DYS154 Dystonia 65 0.081
109
P ADN016 Adenocarcinoma 65 0.081
110
c ACT073 Acute Leukemia 59 0.081
111
c VRL010 Viral Hepatitis 56 0.081
112
P PNC035 Pancreatic Cancer 86 0.079
113
LSH001 Leishmaniasis 64 0.079
114
P GLM045 Glioma 64 0.079
115
P CRN300 Coronary Heart Disease 1 59 0.079
116
CNT047 Contact Dermatitis 58 0.079
117
AGN016 Aging 58 0.079
118
GLC003 Glucose Intolerance 55 0.079
119
TLN003 Telangiectasis 53 0.079
120
GLL048 Glial Tumor 48 0.079
121
P KLZ004 Kala-Azar 1 43 0.079
122
STN013 Stenotrophomonas Maltophilia Infection 26 0.079
123
P LKM002 Leukemia 69 0.076
124
P ATS364 Autism 68 0.076
125
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.076
126
P TRM003 Tremor 55 0.076
127
SPP010 Suppressor of Tumorigenicity 3 54 0.076
128
BNR002 Bone Resorption Disease 51 0.076
129
ECT026 Ectopic Pregnancy 50 0.076
130
KWS001 Kwashiorkor 46 0.076
131
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.076
132
ANP008 Anaplastic Oligoastrocytoma 31 0.076
133
ARG004 Argyria 28 0.076
134
P MYC007 Myocardial Infarction 74 0.074
135
CRT072 Creutzfeldt-Jakob Disease 67 0.074
136
c ACT071 Acute Kidney Failure 60 0.074
137
c ACT075 Acute Myocardial Infarction 59 0.074
138
P FBR017 Fibrosarcoma 57 0.074
139
P OBS001 Obstructive Jaundice 49 0.074
140
HPT004 Hepatic Coma 42 0.074
142
MYL069 Myeloma, Multiple 85 0.071
143
OST012 Osteoarthritis 80 0.071
144
P NRF023 Neurofibromatosis, Type Ii 77 0.071
145
P HYP086 Hypothyroidism 70 0.071
146
RCK004 Rickets 70 0.071
147
CLN015 Colon Adenocarcinoma 65 0.071
148
SKN016 Skin Disease 64 0.071
149
LNG099 Lung Disease 62 0.071
150
ISC004 Ischemia 62 0.071
151
P PNC044 Pancreatitis 61 0.071
152
SQM006 Squamous Cell Carcinoma 60 0.071
153
P ALP008 Alopecia 58 0.071
154
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.071
155
HMC014 Homocysteinemia 54 0.071
156
P CHL066 Cholangitis 53 0.071
157
CYT002 Cytokine Deficiency 46 0.071
158
CCC002 Coccidiosis 46 0.071
159
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.071
160
P EPL164 Epilepsy 73 0.068
161
BRN024 Bronchitis 70 0.068
162
CNG034 Congestive Heart Failure 69 0.068
163
P HYP061 Hypertrophic Cardiomyopathy 68 0.068
164
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.068
165
P NPH012 Nephrotic Syndrome 65 0.068
166
ORL011 Oral Cancer 62 0.068
167
CHL123 Chlamydia 60 0.068
168
MST005 Mastitis 55 0.068
169
OST016 Osteochondrosis 55 0.068
170
PLR008 Pleurisy 50 0.068
171
P BLD134 Bladder Cancer 79 0.065
172
CRH001 Crohn's Disease 75 0.065
173
P DMN002 Dementia 68 0.065
174
P LKM062 Leukemia, Acute Lymphoblastic 68 0.065
175
MLN008 Melanoma 68 0.065
176
P LPR021 Leprosy 3 67 0.065
177
P CLC063 Celiac Disease 1 66 0.065
178
c RHB024 Rhabdomyosarcoma 2 64 0.065
179
P MYP004 Myopathy 63 0.065
180
P HYP750 Hypertriglyceridemia, Familial 62 0.065
181
HPT019 Hepatic Encephalopathy 60 0.065
182
P OPT006 Optic Nerve Disease 59 0.065
183
P ALC033 Alcohol Use Disorder 58 0.065
184
MTC097 Mitochondrial Complex Iv Deficiency 55 0.065
185
GST023 Gastric Ulcer 53 0.065
186
NNL006 Non-Alcoholic Steatohepatitis 53 0.065
187
MCR018 Microcytic Anemia 46 0.065
188
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.065
189
c ACT004 Acute Diarrhea 38 0.065
190
CHR178 Chromosomal Triplication 36 0.065
191
HNS001 Hansen's Disease 35 0.065
192
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.065
193
ESP021 Esophageal Cancer 90 0.062
194
ULC004 Ulcerative Colitis 75 0.062
195
c SPN225 Spondyloarthropathy 1 74 0.062
196
c ATS007 Autism Spectrum Disorder 69 0.062
197
P PLM037 Pulmonary Hypertension 69 0.062
198
P CRN018 Coronary Artery Anomaly 67 0.062
199
DPR016 Depression 64 0.062
200
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.062
201
P HMN010 Hemangioma 62 0.062
202
BLR008 Bilirubin Metabolic Disorder 58 0.062
203
PRT038 Protein-Energy Malnutrition 56 0.062
204
P ART021 Arteriosclerosis 56 0.062
205
P PLY019 Polyneuropathy 55 0.062
206
P ECL001 Eclampsia 53 0.062
207
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.062
208
ANX004 Anoxia 44 0.062
209
P HYP265 Hypotonia 43 0.062
210
PLY150 Polykaryocytosis Inducer 31 0.062
211
CRD009 Cardioencephalomyopathy 19 0.062
212
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.059
213
c HYP595 Hypertension, Essential 87 0.059
214
P OST002 Osteoporosis 79 0.059
215
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.059
216
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.059
217
SVR004 Severe Combined Immunodeficiency 74 0.059
218
P MLT020 Multiple Sclerosis 73 0.059
219
P HNT016 Huntington Disease 72 0.059
220
P PHC003 Pheochromocytoma 71 0.059
221
P GLM040 Glioma Susceptibility 1 68 0.059
222
P SKN015 Skin Carcinoma 67 0.059
223
P HRP006 Herpes Simplex 66 0.059
224
P ENC004 Encephalitis 64 0.059
225
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.059
226
CTN007 Cutaneous Leishmaniasis 61 0.059
227
NTR005 Nutritional Deficiency Disease 61 0.059
228
ART140 Arteries, Anomalies of 60 0.059
229
GST045 Gastroenteritis 60 0.059
230
ADN018 Adenoma 60 0.059
231
ERY051 Erythroleukemia, Familial 58 0.059
232
HPT022 Hepatoblastoma 58 0.059
233
P INF037 Inflammatory Bowel Disease 57 0.059
234
VSC002 Vascular Dementia 57 0.059
235
GLS001 Gliosarcoma 56 0.059
236
SPN051 Spondylitis 53 0.059
237
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.059
238
BLR001 Biliary Atresia 51 0.059
239
CLR109 Colorectal Adenocarcinoma 51 0.059
240
ADR040 Adrenal Gland Pheochromocytoma 51 0.059
241
P SHR001 Short Bowel Syndrome 50 0.059
242
c MCR120 Microvascular Complications of Diabetes 7 48 0.059
243
LGN006 Legionnaire Disease 48 0.059
244
ALB002 Albinism 48 0.059
245
P SCL009 Sclerosing Cholangitis 47 0.059
246
DYS015 Dysentery 45 0.059
247
ORL015 Oral Squamous Cell Carcinoma 44 0.059
248
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.059
249
c CHR576 Chronic Beryllium Disease 42 0.059
250
P BRY005 Beryllium Disease 40 0.059
251
HYP001 Hypochromic Microcytic Anemia 38 0.059
252
INF009 Inflammatory Spondylopathy 29 0.059
253
MTH071 Methane Production 26 0.059
254
c CRN216 Craniosynostosis 5 21 0.059
255
CYS001 Cystic Fibrosis 84 0.056
256
P RTN008 Retinitis Pigmentosa 77 0.056
257
c ATM006 Autoimmune Lymphoproliferative Syndrome 73 0.056
258
HMN044 Human Immunodeficiency Virus Type 1 73 0.056
259
P SRC025 Sarcoidosis 1 72 0.056
260
P AMY004 Amyloidosis 71 0.056
261
ART016 Aortic Aneurysm 71 0.056
262
P PNM007 Pneumonia 71 0.056
263
P SYS005 Systemic Scleroderma 68 0.056
264
SRC014 Sarcoma 67 0.056
265
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.056
266
c SML038 Small Cell Cancer of the Lung 67 0.056
267
CLT003 Colitis 63 0.056
268
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.056
269
P ART023 Arthropathy 61 0.056
270
MNT002 Mental Depression 60 0.056
271
P CTS001 Cutis Laxa 60 0.056
272
P EHL001 Ehlers-Danlos Syndrome 60 0.056
273
c HPT003 Hepatitis a 60 0.056
274
RHM027 Rheumatic Disease 56 0.056
275
P RTN016 Retinal Degeneration 56 0.056
276
DNT012 Dental Caries 52 0.056
277
BRN071 Brain Injury 51 0.056
278
RTN023 Retinitis 46 0.056
279
NRR001 Neuroretinitis 46 0.056
280
DMP001 Dumping Syndrome 44 0.056
281
GNT033 Genetic Prion Diseases 37 0.056
282
VGN019 Vaginal Discharge 35 0.056
283
c LKM061 Leukemia, Acute Myeloid 84 0.052
284
NRL016 Neural Tube Defects 83 0.052
285
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.052
286
P RSP003 Respiratory Failure 75 0.052
287
END057 Endometrial Cancer 74 0.052
288
c BTT014 Beta-Thalassemia 73 0.052
289
LPT014 Leptin Deficiency or Dysfunction 72 0.052
290
P MYC084 Mycobacterium Tuberculosis 1 69 0.052
291
P MSC005 Muscular Dystrophy 68 0.052
292
P THR014 Thrombocytopenia 67 0.052
293
P PLM036 Pulmonary Fibrosis 66 0.052
294
P PRD008 Periodontitis 66 0.052
295
IDP011 Idiopathic Interstitial Pneumonia 65 0.052
296
c ACT068 Acute Cystitis 63 0.052
297
RTN017 Retinal Detachment 62 0.052
298
THY029 Thyroid Carcinoma 62 0.052
299
P MYL006 Myeloid Leukemia 61 0.052
300
P SCL018 Scoliosis 61 0.052
301
PPT005 Peptic Ulcer Disease 60 0.052
302
BND020 Bone Disease 60 0.052
303
P MYP006 Myopia 58 0.052
304
GST033 Gestational Diabetes 58 0.052
305
P GST044 Gastritis 58 0.052
306
SCH014 Schistosomiasis 57 0.052
307
P MLN007 Male Infertility 57 0.052
308
P INT068 Intestinal Disease 56 0.052
309
c MCR113 Microvascular Complications of Diabetes 3 55 0.052
310
TRM010 Traumatic Brain Injury 54 0.052
311
THY030 Thyroid Gland Disease 53 0.052
312
P AST007 Astrocytoma 52 0.052
313
STM007 Stomatitis 51 0.052
314
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.052
315
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.052
316
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.052
317
HYP781 Hypoascorbemia 48 0.052
318
c HNT004 Huntington Disease-Like 2 48 0.052
319
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.052
320
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.052
321
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.052
322
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.052
323
HMP009 Haemophilus Influenzae 46 0.052
324
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.052
325
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.052
326
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.052
327
ACT055 Actinomycosis 43 0.052
328
c MCR130 Microvascular Complications of Diabetes 6 42 0.052
329
c MCR133 Microvascular Complications of Diabetes 4 42 0.052
330
MNT317 Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, and Keratoderma 42 0.052
331
GRD001 Giardiasis 42 0.052
332
MCR017 Macrocytic Anemia 41 0.052
333
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.052
334
c HNT011 Huntington Disease-Like 3 37 0.052
335
ACR005 Acrodermatitis 35 0.052
336
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.048
337
P HYD006 Hydrocephalus 68 0.048
338
P MCR115 Microvascular Complications of Diabetes 5 67 0.048
339
P NSP012 Nasopharyngeal Carcinoma 67 0.048
340
P ASP006 Aspergillosis 67 0.048
341
P CHR071 Charcot-Marie-Tooth Disease 65 0.048
342
LPD008 Lipid Metabolism Disorder 64 0.048
343
GT001 Gout 63 0.048
344
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.048
345
P BCL017 B-Cell Lymphoma 61 0.048
346
SPP011 Suppression of Tumorigenicity 12 61 0.048
347
ANR040 Aneurysm 60 0.048
348
P SZR006 Seizure Disorder 59 0.048
349
P SYP003 Syphilis 59 0.048
350
VSL002 Visual Epilepsy 58 0.048
351
P PRP029 Porphyria 58 0.048
352
GST050 Gastrointestinal System Disease 57 0.048
353
SPN035 Spindle Cell Sarcoma 57 0.048
354
ALL010 Allergic Contact Dermatitis 56 0.048
355
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.048
356
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.048
357
c CNG216 Congenital Hydrocephalus 55 0.048
358
P HYP076 Hyperthyroidism 55 0.048
359
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 54 0.048
360
OCL069 Ocular Motor Apraxia 53 0.048
361
P SCK005 Sickle Cell Disease 53 0.048
362
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.048
363
CRV040 Cervix Carcinoma 52 0.048
364
KRT009 Keratosis 52 0.048
365
OVR082 Overgrowth Syndrome 51 0.048
366
CVR006 Cavernous Hemangioma 49 0.048
367
P END046 Endometritis 49 0.048
368
SPL018 Splenomegaly 48 0.048
369
KRT002 Keratomalacia 47 0.048
370
TTH006 Tooth Disease 47 0.048
371
P MTH007 Methemoglobinemia 47 0.048
372
P SDR003 Sideroblastic Anemia 47 0.048
373
c MLG068 Malignant Glioma 46 0.048
374
ENT004 Enthesopathy 46 0.048
375
TNP001 Tinea Pedis 42 0.048
376
P CRV039 Cervicitis 42 0.048
377
END028 Endemic Goiter 37 0.048
379
PCD001 Pica Disease 33 0.048
380
HND015 Hand Skill, Relative 33 0.048
381
ENT007 Enteropathica 27 0.048
382
P ATX030 Ataxia-Telangiectasia 83 0.044
383
IMM167 Immune Deficiency Disease 79 0.044
384
INS024 Insulin-Like Growth Factor I 79 0.044
385
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.044
386
P APL001 Aplastic Anemia 76 0.044
387
BRN028 Brain Cancer 75 0.044
388
c LKM063 Leukemia, Chronic Myeloid 74 0.044
389
PRP027 Peripheral Vascular Disease 72 0.044
390
CRB039 Cerebrovascular Disease 71 0.044
391
P CRN037 Craniosynostosis 69 0.044
392
P INF038 Influenza 69 0.044
393
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.044
394
CHG001 Chagas Disease 66 0.044
395
ANR007 Anorexia Nervosa 64 0.044
396
MDD011 Mood Disorder 62 0.044
397
P ALP009 Alopecia Areata 61 0.044
398
P URT039 Urticaria 61 0.044
399
VRC005 Varicose Veins 61 0.044
400
P CND004 Candidiasis 61 0.044
401
c CHL119 Cholangitis, Primary Sclerosing 59 0.044
402
P GLM007 Glomerulonephritis 58 0.044
403
P PLY011 Polycystic Ovary Syndrome 58 0.044
404
P OCL002 Oculocutaneous Albinism 58 0.044
405
P EXN002 Exanthem 58 0.044
406
THR024 Thrombosis 58 0.044
407
P PYL005 Pyelonephritis 58 0.044
408
P TRC086 Trichohepatoenteric Syndrome 1 57 0.044
409
RHM001 Rheumatic Fever 56 0.044
410
P NRV006 Nervous System Cancer 55 0.044
411
DMY004 Demyelinating Disease 54 0.044
412
MYM001 Myoma 52 0.044
413
BCT002 Bacterial Vaginosis 52 0.044
414
OST011 Osteomalacia 51 0.044
415
c CNT033 Central Nervous System Cancer 51 0.044
416
AZS001 Azoospermia 51 0.044
418
c SVR005 Severe Pre-Eclampsia 50 0.044
419
HMG002 Hemoglobinuria 49 0.044
420
THR013 Thoracic Outlet Syndrome 49 0.044
421
c INV001 Invasive Aspergillosis 48 0.044
422
MTB004 Metabolic Acidosis 48 0.044
423
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.044
424
CHR074 Choriocarcinoma 47 0.044
425
ATX019 Ataxia with Vitamin E Deficiency 46 0.044
426
P SDR002 Siderosis 42 0.044
427
P TRC031 Trichorhinophalangeal Syndrome 41 0.044
428
ALL014 Allergic Encephalomyelitis 40 0.044
429
IDP070 Idiopathic Scoliosis 39 0.044
430
OVR094 Ovarian Epithelial Cancer 39 0.044
431
MRS001 Marasmus 39 0.044
432
P CRB059 Cerebellar Degeneration 38 0.044
433
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 38 0.044
434
CHL079 Children's Interstitial Lung Disease 27 0.044
435
URT049 Urate Oxidase, Pseudogene 26 0.044
436
MLR004 Malaria 82 0.039
437
c DLT002 Dilated Cardiomyopathy 81 0.039
438
c LKM071 Leukemia, Chronic Lymphocytic 81 0.039
439
ANX010 Anxiety 75 0.039
440
SCK003 Sickle Cell Anemia 74 0.039
441
PHN003 Phenylketonuria 73 0.039
442
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.039
443
SKN019 Skin Melanoma 68 0.039
444
P DRM053 Dermatitis, Atopic 68 0.039
445
c MCR129 Microvascular Complications of Diabetes 1 67 0.039
446
P MNN013 Meningitis 67 0.039
447
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.039
448
P ANR048 Aniridia 1 64 0.039
449
KHL003 Kohlschutter-Tonz Syndrome 63 0.039
450
c HPT016 Hepatitis B 63 0.039
451
P END044 Endometriosis 63 0.039
452
ADL002 Adult Syndrome 62 0.039
453
c PRG042 Progressive Familial Heart Block, Type Ia 62 0.039
454
BLD131 Bladder Urothelial Carcinoma 62 0.039
455
P LPS004 Lupus Erythematosus 62 0.039
456
ACN002 Acanthosis Nigricans 62 0.039
457
ATM095 Autoimmune Disease 62 0.039
458
TYP007 Typhoid Fever 61 0.039
459
ACQ007 Acquired Immunodeficiency Syndrome 61 0.039
460
CHL067 Cholecystitis 60 0.039
461
P KDN017 Kidney Cancer 60 0.039
462
LGN002 Legionellosis 60 0.039
463
END030 End Stage Renal Failure 60 0.039
464
P UVT001 Uveitis 58 0.039
465
TRN018 Transitional Cell Carcinoma 57 0.039
466
MCS002 Mucositis 56 0.039
467
P PMP001 Pemphigus 56 0.039
468
AVN001 Avian Influenza 56 0.039
469
c INT072 Intestinal Pseudo-Obstruction 55 0.039
470
P PNM006 Pneumoconiosis 55 0.039
471
SYN007 Synovitis 55 0.039
472
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.039
473
VSC003 Visceral Leishmaniasis 55 0.039
474
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.039
475
P SLM003 Salmonellosis 54 0.039
476
CHR100 Chronic Ulcer of Skin 53 0.039
477
P RTN018 Retinal Disease 53 0.039
478
LMY002 Leiomyoma 52 0.039
479
P HMC002 Homocystinuria 52 0.039
480
QDR001 Quadriplegia 51 0.039
481
IMM064 Immunodeficiency, Common Variable, 10 51 0.039
482
URM002 Uremia 50 0.039
483
LMB062 Limb Ischemia 50 0.039
484
RFR010 Refractory Anemia 50 0.039
485
SXL003 Sexual Disorder 49 0.039
486
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 0.039
487
P RNL007 Renal Tubular Acidosis 49 0.039
488
PRS034 Parasitic Helminthiasis Infectious Disease 48 0.039
489
P MRC003 Mercury Poisoning 47 0.039
490
P BNG032 Benign Mesothelioma 47 0.039
491
ANT018 Anthracosis 46 0.039
492
INT067 Interstitial Nephritis 46 0.039
493
PRS063 Paresthesia 46 0.039
494
DWR001 Dwarfism 45 0.039
495
CHR031 Chromoblastomycosis 44 0.039
496
c MCR112 Microvascular Complications of Diabetes 2 42 0.039
497
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.039
498
PRM329 Premature Aging 41 0.039
499
EXC002 Exocrine Pancreatic Insufficiency 41 0.039
500
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.039
501
LCH001 Leech Infestation 40 0.039
502
ATX010 Ataxia Neuropathy Spectrum 39 0.039
503
AMN006 Aminoaciduria 39 0.039
504
CRB004 Cerebral Artery Occlusion 38 0.039
505
SPS057 Spasticity 38 0.039
506
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.039
507
c LKM004 Leukemia, B-Cell, Chronic 35 0.039
508
c PRS136 Prostate Cancer, Hereditary, 6 34 0.039
509
c PRS130 Prostate Cancer, Hereditary, 8 33 0.039
510
SPN188 Spinal Muscular Atrophy, Distal, X-Linked 3 31 0.039
511
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.039
512
P ACT232 Acute Necrotizing Encephalopathy 28 0.039
513
BLD137 Blood Group--Ahonen 17 0.039
514
OBS532 Obsolete: Ehlers-Danlos Syndrome, Fibronectinemic Type 15 0.039
515
AST005 Asthma 80 0.034
516
c THR092 Thrombophilia Due to Thrombin Defect 74 0.034
517
OTT002 Otitis Media 71 0.034
518
P MJR001 Major Depressive Disorder 69 0.034
519
OBS002 Obsessive-Compulsive Disorder 69 0.034
520
HYP056 Hypoglycemia 68 0.034
521
P ATR011 Atrial Fibrillation 67 0.034
522
AND002 Androgen Insensitivity Syndrome 66 0.034
523
INC002 Inclusion Body Myositis 66 0.034
524
P TRN020 Turner Syndrome 66 0.034
525
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.034
526
P ANG001 Angelman Syndrome 65 0.034
527
OST017 Osteomyelitis 65 0.034
528
FCT007 Factor Vii Deficiency 65 0.034
529
LYM017 Lyme Disease 64 0.034
530
P HYP069 Hyperparathyroidism 64 0.034
531
c FNC043 Fanconi Anemia, Complementation Group E 64 0.034
532
TXC005 Toxic Shock Syndrome 63 0.034
533
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.034
534
SPN186 Spinal Cord Injury 63 0.034
535
HYP020 Hyperprolactinemia 62 0.034
536
NRM005 Neuromuscular Disease 62 0.034
537
BRC012 Brucellosis 62 0.034
538
TTN003 Tetanus 62 0.034
539
c HPT001 Hepatitis C 62 0.034
540
c SCL052 Scleroderma, Familial Progressive 62 0.034
541
c PNS012 Paine Syndrome 61 0.034
542
LKD001 Leukodystrophy 61 0.034
543
c LCL006 Localized Scleroderma 61 0.034
544
MSL001 Measles 61 0.034
545
ING001 Inguinal Hernia 61 0.034
546
P MYC008 Myocarditis 60 0.034
547
INT002 Intermittent Claudication 60 0.034
548
EYD002 Eye Disease 59 0.034
549
BRS051 Breast Disease 59 0.034
550
CNS004 Constipation 59 0.034
551
c ACT210 Acute Respiratory Distress Syndrome 59 0.034
552
NWB001 Newborn Respiratory Distress Syndrome 58 0.034
553
P AXN002 Axenfeld-Rieger Syndrome 58 0.034
554
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.034
555
LYM027 Lymphopenia 58 0.034
556
DSS009 Disseminated Intravascular Coagulation 58 0.034
557
CHL014 Cholera 58 0.034
558
RBS001 Rabies 57 0.034
559
P DNG005 Dengue Virus 57 0.034
560
P MTC069 Mitochondrial Disorders 57 0.034
561
SPN041 Spinal Cord Disease 57 0.034
562
BRN004 Brain Edema 57 0.034
563
PMP006 Pemphigus Vulgaris, Familial 56 0.034
564
PRP030 Purpura 56 0.034
565
CMR002 Coumarin Resistance 56 0.034
566
PHR003 Pharyngitis 56 0.034
567
PPL022 Papilloma 56 0.034
568
c PRD040 Periodontitis, Chronic 56 0.034
569
P VNS003 Venous Insufficiency 55 0.034
570
HYP005 Hypokalemia 55 0.034
571
P LCH002 Lichen Planus 55 0.034
572
P ICH004 Ichthyosis 55 0.034
573
PRN019 Perinatal Necrotizing Enterocolitis 55 0.034
574
c GRV008 Graves Disease 1 55 0.034
575
OCL022 Ocular Melanoma 54 0.034
576
c ACT020 Acute T Cell Leukemia 54 0.034
577
P MYS005 Myositis 54 0.034
578
PTH003 Pathologic Nystagmus 53 0.034
579
KRT006 Keratoconjunctivitis 53 0.034
580
ALC009 Alcoholic Liver Cirrhosis 53 0.034
581
c ALB020 Albinism, Oculocutaneous, Type Iii 53 0.034
582
STT041 Stuttering 53 0.034
583
c GLL024 Gallbladder Disease 1 53 0.034
584
LNG031 Lung Benign Neoplasm 52 0.034
585
PNG002 Pain Agnosia 52 0.034
586
c INF023 Inflammatory Breast Carcinoma 52 0.034
587
CRY005 Cryptococcosis 51 0.034
588
ENT011 Enterocolitis 51 0.034
589
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 51 0.034
590
P KRT007 Keratoconus 51 0.034
591
P DDN001 Duodenal Ulcer 50 0.034
592
VCC001 Vaccinia 50 0.034
593
MTC005 Mitochondrial Metabolism Disease 50 0.034
594
P INT099 Intrahepatic Cholestasis of Pregnancy 50 0.034
595
P LPM005 Lipomatosis 49 0.034
596
SQM002 Squamous Cell Papilloma 49 0.034
597
c HPT015 Hepatitis D 49 0.034
598
PRM020 Premenstrual Tension 48 0.034
599
ATN005 Autonomic Dysfunction 48 0.034
600
P NGH001 Night Blindness 48 0.034
601
CLC006 Calcinosis 48 0.034
602
BHR001 Behr Syndrome 47 0.034
603
P PLL002 Pellagra 47 0.034
604
PYL006 Pyloric Stenosis 47 0.034
605
ANR004 Anuria 47 0.034
606
CRN017 Coronary Thrombosis 45 0.034
607
c CPL013 Capillary Malformations, Congenital 44 0.034
608
HYP457 Hypertrophic Scars 44 0.034
609
HMP001 Hemopericardium 44 0.034
610
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.034
611
P CRB088 Cerebral Atrophy 43 0.034
612
ORL012 Oral Leukoplakia 42 0.034
613
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.034
614
ACT003 Acute Kidney Tubular Necrosis 42 0.034
615
FCL022 Focal Dystonia 41 0.034
616
LKP003 Leukoplakia 40 0.034
617
LPD014 Lipodermatosclerosis 40 0.034
618
c OVR114 Ovarian Cancer 1 39 0.034
619
c PRG020 Paragangliomas 3 36 0.034
620
c CHR682 Chronic Bilirubin Encephalopathy 36 0.034
621
CRD016 Cardiac Rupture 33 0.034
622
MTL005 Metal Allergy 32 0.034
623
ALR002 Al-Raqad Syndrome 32 0.034
624
HYP674 Hyperostosis Cranialis Interna 32 0.034
625
HMG010 Hemoglobinemia 29 0.034
626
FTL068 Fatal Infantile Cardioencephalomyopathy Due to Cytochrome C Oxidase Deficiency 28 0.034
627
P PLT008 Pili Torti 28 0.034
628
c RNG015 Ring Chromosome 2 27 0.034
629
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.034
630
LTH004 Lathyrism 16 0.034
631
XLN239 X-Linked Distal Hereditary Motor Neuropathy 12 0.034
632
HPP002 Huppke-Brendel Syndrome 7 0.034
633
P RTT002 Rett Syndrome 81 0.028
634
P MDL005 Medulloblastoma 78 0.028
635
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.028
636
P RTN024 Retinoblastoma 74 0.028
637
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.028
638
P CRD119 Cardiac Arrest 71 0.028
639
c PRM196 Premature Ovarian Failure 1 70 0.028
640
MSC157 Muscular Dystrophy, Duchenne Type 70 0.028
641
c PNC108 Pancreatitis, Hereditary 70 0.028
642
MNT001 Mantle Cell Lymphoma 69 0.028
643
CRB037 Cerebral Palsy 69 0.028
644
EWN003 Ewing Sarcoma 69 0.028
645
P MTC003 Metachromatic Leukodystrophy 69 0.028
646
CHL065 Cholangiocarcinoma 68 0.028
647
c CHR684 Chronic Kidney Disease 68 0.028
648
P NRV007 Nervous System Disease 68 0.028
649
P HYP098 Hypereosinophilic Syndrome 67 0.028
650
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.028
651
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.028
652
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.028
653
c NMN015 Niemann-Pick Disease, Type C1 67 0.028
654
GST040 Gastric Adenocarcinoma 67 0.028
655
PRT036 Peritonitis 66 0.028
656
P PRP003 Porphyria Cutanea Tarda 66 0.028
657
ANG054 Angina Pectoris 66 0.028
658
P SPN046 Spinal Muscular Atrophy 65 0.028
659
P FRD012 Friedreich Ataxia 1 65 0.028
660
TBC004 Tobacco Addiction 65 0.028
661
P VSC011 Vasculitis 64 0.028
662
FLL027 Fallopian Tube Carcinoma 64 0.028
663
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.028
664
LWC002 Lowe Oculocerebrorenal Syndrome 63 0.028
665
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.028
666
HSH003 Hashimoto Thyroiditis 63 0.028
667
ART002 Arts Syndrome 63 0.028
668
BLL006 Bullous Pemphigoid 63 0.028
669
P MVM001 Movement Disease 63 0.028
670
GLC006 Galactosemia 63 0.028
671
ALP103 Alpha-1-Antitrypsin Deficiency 63 0.028
672
c BRN108 Branchiootic Syndrome 1 62 0.028
673
P SNS001 Sensorineural Hearing Loss 62 0.028
674
TRN015 Transient Cerebral Ischemia 62 0.028
675
CRC021 Carcinosarcoma 62 0.028
676
SDD001 Sudden Infant Death Syndrome 61 0.028
677
INT066 Interstitial Lung Disease 61 0.028
678
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.028
679
P TXP001 Toxoplasmosis 61 0.028
680
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.028
681
c ACT027 Acute Pancreatitis 60 0.028
682
ART001 Arterial Tortuosity Syndrome 60 0.028
683
ALC006 Alcoholic Hepatitis 60 0.028
684
BRN002 Bronchiolitis 60 0.028
685
P OST009 Osteochondritis Dissecans 60 0.028
686
P RHN004 Rhinitis 59 0.028
687
P HDC001 Headache 59 0.028
688
P BPL003 Bipolar Disorder 59 0.028
689
P PRV006 Pervasive Developmental Disorder 58 0.028
690
CRV038 Cervical Squamous Cell Carcinoma 58 0.028
691
BRG013 Buerger Disease 58 0.028
692
HRP004 Herpes Zoster 58 0.028
693
GLB001 Gilbert Syndrome 58 0.028
694
TNS005 Tonsillitis 58 0.028
695
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 58 0.028
696
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.028
697
BRN045 Brunner Syndrome 57 0.028
698
BRN056 Bronchopulmonary Dysplasia 57 0.028
699
HMG005 Hemoglobinopathy 57 0.028
700
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.028
701
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.028
702
ANT024 Anthrax Disease 56 0.028
703
APH001 Aphthous Stomatitis 56 0.028
704
P MCR010 Microcephaly 56 0.028
705
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.028
706
FLR002 Filariasis 56 0.028
707
P PLY018 Polycythemia 56 0.028
708
c SVR001 Severe Acute Respiratory Syndrome 56 0.028
709
c CNT035 Central Nervous System Disease 56 0.028
710
DBT010 Diabetic Neuropathy 56 0.028
711
WST005 West Nile Virus 56 0.028
712
SNS003 Sensory Peripheral Neuropathy 56 0.028
713
P SBS003 Substance Abuse 56 0.028
714
DBL002 Double Outlet Right Ventricle 55 0.028
715
P PLM034 Pulmonary Emphysema 55 0.028
716
ASP002 Aspartylglucosaminuria 55 0.028
717
P ALP106 Alport Syndrome 1, X-Linked 55 0.028
718
END040 Endogenous Depression 55 0.028
719
LST001 Listeriosis 55 0.028
720
PRC002 Paracoccidioidomycosis 55 0.028
721
PRS045 Prostatic Hypertrophy 55 0.028
722
P INS002 in Situ Carcinoma 55 0.028
723
P OVR049 Ovarian Disease 55 0.028
724
DCB001 Decubitus Ulcer 54 0.028
725
DRR016 Diarrhea 2, with Microvillus Atrophy 54 0.028
726
INT079 Intrahepatic Cholangiocarcinoma 54 0.028
727
PRC013 Pericarditis 54 0.028
728
P MGL001 Megaloblastic Anemia 54 0.028
729
c PRM092 Primary Lateral Sclerosis, Adult, 1 54 0.028
730
CRT017 Cartilage Disease 54 0.028
731
P PNC025 Panic Disorder 53 0.028
732
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.028
733
P PRS049 Persistent Mullerian Duct Syndrome 53 0.028
734
HYP014 Hyperuricemia 52 0.028
735
FDL002 Food Allergy 52 0.028
736
c PST005 Posterior Uveitis 52 0.028
737
GNT002 Giant Cell Glioblastoma 52 0.028
738
P LCT001 Lactic Acidosis 52 0.028
739
P HMG032 Hemoglobin H Disease 52 0.028
740
P GNT009 Giant Axonal Neuropathy 52 0.028
741
P MSC003 Muscular Atrophy 52 0.028
742
c CHR418 Chronic Leukemia 52 0.028
743
PLC008 Placenta Disease 51 0.028
744
c INH020 Inherited Metabolic Disorder 51 0.028
745
PNC034 Pancreas Disease 51 0.028
746
ASC010 Ascaris Lumbricoides Infection 51 0.028
747
PRP080 Peripheral Artery Disease 51 0.028
748
PST021 Postpartum Depression 51 0.028
749
CHR005 Chorioamnionitis 51 0.028
750
HYP063 Hypersplenism 51 0.028
751
HYP080 Hypogonadism 51 0.028
752
P ACT008 Actinic Keratosis 50 0.028
753
ISL003 Isolated Growth Hormone Deficiency 50 0.028
754
c PNC106 Pancreatic Agenesis 1 50 0.028
755
P LNG035 Lung Large Cell Carcinoma 50 0.028
756
MNN009 Meningoencephalitis 50 0.028
757
c HNT010 Huntington Disease-Like 1 49 0.028
758
GST049 Gastrointestinal System Cancer 49 0.028
759
DRM011 Dermatophytosis 49 0.028
760
P BLR006 Biliary Tract Disease 49 0.028
761
DPM001 Dopamine Beta-Hydroxylase Deficiency 49 0.028
762
ENC055 Encephalopathy, Ethylmalonic 49 0.028
763
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.028
764
P CRV031 Cervical Adenocarcinoma 49 0.028
765
PST048 Postural Orthostatic Tachycardia Syndrome 49 0.028
766
CRN027 Corneal Neovascularization 48 0.028
767
BCT004 Bacteriuria 48 0.028
768
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 48 0.028
769
P FNC004 Fanconi Syndrome 48 0.028
770
P BLD051 Blood Coagulation Disease 48 0.028
771
P NRD007 Neurodegeneration with Brain Iron Accumulation 48 0.028
772
GRW007 Growth Hormone Deficiency 48 0.028
773
MYL001 Myelitis 48 0.028
774
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 48 0.028
775
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.028
776
SPN020 Spondylosis 48 0.028
777
P TRN034 Transverse Myelitis 48 0.028
778
ORL013 Oral Lichen Planus 47 0.028
779
ELS001 Eales Disease 47 0.028
780
P MYC033 Myoclonus 47 0.028
781
NCR007 Necrotizing Fasciitis 47 0.028
782
c VRL012 Viral Meningitis 47 0.028
783
FSC004 Fasciitis 47 0.028
784
EPD015 Epidemic Typhus 47 0.028
785
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.028
786
NDL007 Nodular Goiter 46 0.028
787
GRN017 Granulocytopenia 46 0.028
788
c FML008 Familial Retinoblastoma 46 0.028
789
MLT006 Multidrug-Resistant Tuberculosis 46 0.028
790
NPH010 Nephrosclerosis 46 0.028
791
LCK001 Locked-in Syndrome 46 0.028
792
P CLL015 Collagen Disease 46 0.028
793
EXS001 Exostosis 46 0.028
794
c ACT150 Acute Adrenal Insufficiency 46 0.028
795
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.028
796
KRT013 Keratolytic Winter Erythema 45 0.028
797
VGN020 Vaginal Disease 45 0.028
798
NWC001 Newcastle Disease 45 0.028
799
c PRS128 Persistent Mullerian Duct Syndrome, Types I and Ii 45 0.028
800
CRV043 Cervical Dystonia 45 0.028
801
FBR054 Fibroma 45 0.028
802
CYN002 Cyanosis, Transient Neonatal 45 0.028
803
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.028
804
GLC096 Galactorrhea 44 0.028
805
CHD004 Chudley-Mccullough Syndrome 44 0.028
806
BCK006 Back Pain 44 0.028
807
CRT015 Carotid Artery Occlusion 44 0.028
808
INT052 Intestinal Volvulus 44 0.028
809
FSC002 Fascioliasis 44 0.028
810
DSC009 Discoid Lupus Erythematosus 44 0.028
811
OLG001 Oligospermia 44 0.028
812
c ATS307 Autosomal Recessive Cerebellar Ataxia 44 0.028
813
c HMG003 Hemoglobin E Disease 43 0.028
814
CRB033 Cerebral Degeneration 42 0.028
815
c MJR024 Major Affective Disorder 9 42 0.028
816
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 42 0.028
817
c SPR086 Spermatogenic Failure 3 41 0.028
818
SKN005 Skin Atrophy 41 0.028
819
TRP004 Tropical Sprue 41 0.028
820
KLD004 Keloid Disorder 41 0.028
821
P SCL057 Scoliosis, Isolated 1 41 0.028
822
SNL007 Senile Cataract 41 0.028
823
MYP091 Myopathy, Congenital, with Fiber-Type Disproportion 41 0.028
824
BRY001 Berylliosis 41 0.028
825
CHR008 Choroiditis 41 0.028
826
CHP002 Chops Syndrome 41 0.028
827
MST004 Mast Cell Neoplasm 40 0.028
828
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 40 0.028
829
P MLT065 Multicentric Osteolysis, Nodulosis, and Arthropathy 40 0.028
830
c CNG497 Congenital Disorder of Glycosylation, Type Iio 40 0.028
831
GRS001 Gerstmann Syndrome 40 0.028
832
HYP064 Hypogonadotropism 40 0.028
833
c MJR022 Major Affective Disorder 8 39 0.028
834
MNR003 Mineral Metabolism Disease 39 0.028
835
EXT007 Extracutaneous Mastocytoma 39 0.028
836
EXT006 Extrahepatic Cholestasis 38 0.028
837
P PRG002 Progesterone-Receptor Positive Breast Cancer 38 0.028
838
KR002 Kuru 38 0.028
839
CRY036 Cryptogenic Cirrhosis 38 0.028
840
c CHR098 Chronic Pyelonephritis 38 0.028
841
P SPS008 Spastic Ataxia 37 0.028
842
BCK003 Background Diabetic Retinopathy 37 0.028
843
MYL074 Myelodysplastic Syndrome with Excess Blasts 37 0.028
844
NRN002 Neuronitis 37 0.028
845
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.028
846
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 36 0.028
847
CHN002 Chancroid 36 0.028
848
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.028
849
WRN004 Wrinkly Skin Syndrome 36 0.028
850
LYM011 Lymphogranuloma Venereum 36 0.028
851
RNL012 Renal Tuberculosis 36 0.028
852
OLV004 Oliver-Mcfarlane Syndrome 36 0.028
853
ASC001 Ascaridiasis 36 0.028
854
c AMY088 Amyotrophic Lateral Sclerosis 3 36 0.028
855
MXD026 Mixed Glioma 36 0.028
856
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.028
857
GNT167 Genetic Obesity 35 0.028
858
INT040 Intrinsic Asthma 34 0.028
859
c HYP716 Hypermanganesemia with Dystonia 1 34 0.028
860
HMC016 Homocystinuria Due to Cbs Deficiency 33 0.028
861
LYM035 Lymphangiectasis 33 0.028
862
ASH001 Asherman's Syndrome 33 0.028
863
PYR009 Pyridoxine Deficiency Anemia 32 0.028
864
c JVN024 Juvenile Hereditary Hemochromatosis 32 0.028
865
STT009 Sutton Disease 2 31 0.028
866
CRB009 Cerebritis 31 0.028
867
CHR028 Chronic Wasting Disease 30 0.028
868
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.028
869
SPN392 Spondylosis, Cervical 29 0.028
870
P DST101 Distal Hereditary Motor Neuropathies 29 0.028
871
CHL035 Cholinergic Urticaria 28 0.028
872
CYT018 Cytochrome P450 2d6 Variant 28 0.028
873
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 27 0.028
874
c CRN221 Craniosynostosis 4 27 0.028
875
c MYP018 Myopia 6 27 0.028
876
c TTH010 Tooth Agenesis, Selective, 1 26 0.028
877
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.028
878
IDP069 Idiopathic Avascular Necrosis 24 0.028
879
CPG001 Capgras Syndrome 23 0.028
880
c VSC053 Visceral Steatosis, Congenital 22 0.028
881
OST007 Ostertagiasis 19 0.028
882
SLN002 Selenium Poisoning 12 0.028
883
DSR036 Disorder of Mineral Absorption and Transport 5 0.028
884
c SYS001 Systemic Lupus Erythematosus 88 0.020
885
STR067 Stroke, Ischemic 82 0.020
886
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.020
887
PFF001 Pfeiffer Syndrome 79 0.020
888
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.020
889
KPS004 Kaposi Sarcoma 75 0.020
890
MRF001 Marfan Syndrome 75 0.020
891
c MNN043 Meningioma, Familial 74 0.020
892
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.020
893
P TBR001 Tuberous Sclerosis 72 0.020
894
P CNR004 Cone-Rod Dystrophy 2 72 0.020
895
P GRF003 Graft-Versus-Host Disease 71 0.020
896
ACR007 Acromegaly 70 0.020
897
c MGR028 Migraine with or Without Aura 1 70 0.020
898
P FML018 Familial Mediterranean Fever 70 0.020
899
LYM133 Lymphoma, Hodgkin, Classic 70 0.020
900
BHC003 Behcet Syndrome 70 0.020
901
c WLM013 Wilms Tumor 1 69 0.020
902
c EXD008 Exudative Vitreoretinopathy 1 69 0.020
903
P MLN066 Melanoma, Cutaneous Malignant 1 69 0.020
904
KRT019 Keratitis, Hereditary 69 0.020
905
PNC129 Pancreatic Adenocarcinoma 69 0.020
906
CMM004 Common Variable Immunodeficiency 69 0.020
907
P TMP003 Temporal Arteritis 68 0.020
908
CNN005 Connective Tissue Disease 68 0.020
909
BRK010 Burkitt Lymphoma 68 0.020
910
PSY004 Psychotic Disorder 68 0.020
911
P HMP002 Hemophagocytic Lymphohistiocytosis 68 0.020
912
c BSL007 Basal Cell Carcinoma 68 0.020
913
CRP001 Carpal Tunnel Syndrome 68 0.020
914
c FML001 Familial Atrial Fibrillation 67 0.020
915
c JVN010 Juvenile Rheumatoid Arthritis 67 0.020
916
c FML021 Familial Hypercholesterolemia 67 0.020
917
CLF027 Cleft Palate, Isolated 67 0.020
918
BRR014 Barrett Esophagus 67 0.020
919
MYC006 Mycosis Fungoides 67 0.020
920
GLL008 Gilles De La Tourette Syndrome 66 0.020
921
PRT037 Pertussis 66 0.020
922
c DPH024 Diaphragmatic Hernia, Congenital 66 0.020
923
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.020
924
P PRS038 Personality Disorder 66 0.020
925
P BLD062 Bile Duct Cancer 66 0.020
926
DSS008 Disease of Mental Health 66 0.020
927
c INF071 Inflammatory Bowel Disease 1 66 0.020
928
P OCL013 Oculodentodigital Dysplasia 65 0.020
929
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.020
930
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 65 0.020
931
c CNG006 Congenital Hypothyroidism 65 0.020
932
IRR002 Irritable Bowel Syndrome 65 0.020
933
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 64 0.020
934
CLR108 Colorectal Adenoma 64 0.020
935
LKC009 Leukocyte Adhesion Deficiency, Type I 64 0.020
936
KRN002 Kearns-Sayre Syndrome 64 0.020
937
END041 Endometrial Adenocarcinoma 64 0.020
938
P THY023 Thymoma 64 0.020
939
MNN042 Meningioma, Radiation-Induced 64 0.020
940
P HRM001 Hermansky-Pudlak Syndrome 64 0.020
941
P TST021 Testicular Germ Cell Tumor 63 0.020
942
P ART005 Arteriovenous Malformation 63 0.020
943
c ATM011 Autoimmune Hepatitis 63 0.020
944
c WLM018 Wilms Tumor 5 63 0.020
945
c ALP101 Alpha-Thalassemia 63 0.020
946
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.020
947
P LMY004 Leiomyosarcoma 63 0.020
948
PPL049 Papillon-Lefevre Syndrome 63 0.020
949
MCR013 Microphthalmia 62 0.020
950
OST003 Osteonecrosis 62 0.020
951
BDD001 Budd-Chiari Syndrome 62 0.020
952
PRP083 Porphyria, Acute Intermittent 62 0.020
953
GTL001 Gitelman Syndrome 62 0.020
954
P LYM033 Lymphoproliferative Syndrome 62 0.020
955
c HYD046 Hydatidiform Mole, Recurrent, 1 62 0.020
956
GRG001 Greig Cephalopolysyndactyly Syndrome 61 0.020
957
PTT048 Pituitary Adenoma, Prolactin-Secreting 61 0.020
958
c DNG003 Dengue Disease 61 0.020
959
WST001 West Syndrome 61 0.020
960
PRT013 Portal Hypertension 61 0.020
961
CHR066 Chronic Fatigue Syndrome 61 0.020
963
APP008 Appendicitis 61 0.020
964
HLC007 Helicobacter Pylori Infection 61 0.020
965
DPH001 Diphtheria 61 0.020
966
P ADL010 Adult Respiratory Distress Syndrome 61 0.020
967
P VNT002 Ventricular Septal Defect 61 0.020
968
c ANM038 Anemia, Autoimmune Hemolytic 61 0.020
969
P NMN002 Niemann-Pick Disease 60 0.020
970
GNG013 Gingivitis 60 0.020
971
PRT058 Pure Autonomic Failure 60 0.020
972
INS001 Insulinoma 60 0.020
973
STF001 Stiff-Person Syndrome 60 0.020
974
FBR086 Fibrolamellar Carcinoma 60 0.020
975
P NRM001 Neuromyelitis Optica 60 0.020
976
c PRM005 Primary Hyperparathyroidism 60 0.020
977
P GLL020 Gallbladder Disease 60 0.020
978
P INT070 Intestinal Obstruction 60 0.020
979
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.020
980
THY122 Thyroid Gland Cancer 59 0.020
981
RNL024 Renal Glucosuria 59 0.020
982
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 59 0.020
983
P GLY013 Glycogen Storage Disease 59 0.020
984
DNG002 Dengue Hemorrhagic Fever 59 0.020
985
NRN004 Neuroendocrine Tumor 59 0.020
986
END081 Endosteal Hyperostosis, Autosomal Dominant 59 0.020
987
c PTT056 Pituitary Adenoma 1, Multiple Types 59 0.020
988
P LRY044 Larynx Cancer 59 0.020
989
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.020
990
P HYP035 Hypophosphatasia 58 0.020
991
P END033 Endocarditis 58 0.020
992
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 58 0.020
993
PLM031 Poliomyelitis 58 0.020
994
HYD002 Hydronephrosis 58 0.020
995
YLL002 Yellow Fever 58 0.020
996
ERY029 Erythermalgia, Primary 58 0.020
997
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.020
998
ALK013 Alkaptonuria 57 0.020
999
CMM005 Common Cold 57 0.020
1000
EMB004 Embryonal Carcinoma 57 0.020
1001
GLL018 Gallbladder Cancer 57 0.020
1002
P CHN012 Chondrosarcoma 57 0.020
1003
APH002 Aphasia 56 0.020
1004
P BNC003 Bone Cancer 56 0.020
1005
PNM008 Pneumothorax 56 0.020
1006
c ALB009 Albinism, Oculocutaneous, Type Ia 56 0.020
1007
ALL006 Allergic Asthma 56 0.020
1008
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 56 0.020
1009
c BCT007 Bacterial Meningitis 56 0.020
1010
P RBL001 Rubella 56 0.020
1011
MNK003 Muenke Syndrome 56 0.020
1012
P SHR029 Short Syndrome 56 0.020
1013
JPN002 Japanese Encephalitis 56 0.020
1014
DFF005 Diffuse Large B-Cell Lymphoma 56 0.020
1015
P HYP024 Hypoparathyroidism 56 0.020
1016
GRN034 Grange Syndrome 55 0.020
1017
P TCD001 Tic Disorder 55 0.020
1018
CYS010 Cystinosis 55 0.020
1019
KLP010 Klippel-Trenaunay-Weber Syndrome 55 0.020
1020
ACD008 Acid-Labile Subunit Deficiency 55 0.020
1021
ANN002 Anencephaly 55 0.020
1022
CHK001 Chikungunya 55 0.020
1023
c THY107 Thymoma, Familial 55 0.020
1024
ADN027 Adenomyosis 55 0.020
1025
MSS001 Masa Syndrome 55 0.020
1026
CLF004 Cleft Lip/palate 55 0.020
1027
GNR004 Generalized Anxiety Disorder 55 0.020
1028
RSC001 Rosacea 55 0.020
1029
THY124 Thyroid Gland Papillary Carcinoma 54 0.020
1030
VSC044 Visceral Myopathy 54 0.020
1031
RHM028 Rheumatic Heart Disease 54 0.020
1032
HMT018 Hematopoietic Stem Cell Transplantation 54 0.020
1033
MBS002 Moebius Syndrome 54 0.020
1034
c INT064 Intermediate Uveitis 54 0.020
1035
P FBR031 Febrile Seizures 54 0.020
1036
PRP016 Paraplegia 54 0.020
1037
PLG002 Plague 54 0.020
1038
VGN023 Vaginitis 54 0.020
1039
INT075 Intracranial Hypertension 54 0.020
1040
P SJG002 Sjogren-Larsson Syndrome 54 0.020
1041
P RCT021 Rectum Cancer 54 0.020
1042
c CNG415 Congenital Disorder of Glycosylation, Type Ia 54 0.020
1043
P DBT005 Diabetes Insipidus 54 0.020
1044
TXC002 Toxic Encephalopathy 54 0.020
1045
P HML001 Hemolytic-Uremic Syndrome 54 0.020
1046
CLR030 Clear Cell Renal Cell Carcinoma 54 0.020
1047
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 54 0.020
1048
P HMR003 Hemorrhagic Disease 54 0.020
1049
PLS007 Plasmodium Falciparum Malaria 53 0.020
1050
INF034 Infective Endocarditis 53 0.020
1051
P PTS002 Ptosis 53 0.020
1052
P HYP083 Hypopituitarism 53 0.020
1053
EXP004 Exophthalmos 53 0.020
1054
DFF036 Differentiated Thyroid Carcinoma 53 0.020
1055
IMP005 Impotence 53 0.020
1056
TCK001 Tick-Borne Encephalitis 53 0.020
1057
HLL004 Hellp Syndrome 53 0.020
1058
c LRG017 Large Intestine Cancer 53 0.020
1059
P TMP001 Temporal Lobe Epilepsy 53 0.020
1060
CLF001 Cleft Lip 53 0.020
1061
AST006 Astigmatism 53 0.020
1062
P MTC133 Mitochondrial Myopathy 53 0.020
1063
P CRB045 Cerebellar Hypoplasia 53 0.020
1064
SPS003 Spastic Diplegia 53 0.020
1065
DYS073 Dysphagia 52 0.020
1066
c ACT135 Acute Graft Versus Host Disease 52 0.020
1067
CHR073 Choreatic Disease 52 0.020
1068
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 52 0.020
1069
LYS002 Lysosomal Storage Disease 52 0.020
1070
RGH009 Right Atrial Isomerism 52 0.020
1071
P THY032 Thyroiditis 52 0.020
1072
P MNC007 Monocytic Leukemia 52 0.020
1073
THR004 Thrombocytosis 52 0.020
1074
HST011 Histoplasmosis 52 0.020
1075
P CTN015 Cutaneous T Cell Lymphoma 52 0.020
1076
PRS021 Prostatic Adenoma 52 0.020
1077
P CHR345 Chronic Pain 52 0.020
1078
HRT011 Heart Septal Defect 52 0.020
1079
RDC002 Radiculopathy 51 0.020
1080
MYL020 Myelomeningocele 51 0.020
1081
DYS014 Dyspepsia 51 0.020
1082
ILS001 Ileus 51 0.020
1083
VRC001 Varicocele 51 0.020