Search results for erg

1558 hits were found for erg

# Family MCID Name MIFTS Score
1
P PRS040 Prostate Cancer 95 49.298
2
EWN003 Ewing Sarcoma 70 41.052
3
P LKM002 Leukemia 67 29.932
4
P MYL006 Myeloid Leukemia 61 29.638
5
SRC014 Sarcoma 65 26.962
6
NRR001 Neuroretinitis 42 18.591
7
RTN023 Retinitis 46 18.591
8
P RTN008 Retinitis Pigmentosa 80 17.912
9
P RTN016 Retinal Degeneration 52 16.377
10
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 16.138
11
MYX005 Myxoid Liposarcoma 65 14.504
12
P NGH001 Night Blindness 52 14.412
13
P RTN018 Retinal Disease 53 13.325
14
c MCR115 Microvascular Complications of Diabetes 5 65 12.714
15
c RTN035 Retinal Cone Dystrophy 3b 32 12.472
16
PRS006 Prostatic Acinar Adenocarcinoma 25 11.782
17
P CNG010 Congenital Stationary Night Blindness 56 11.773
18
c LKM061 Leukemia, Acute Myeloid 83 11.615
20
P CND005 Cone Dystrophy 47 9.986
21
INT323 Intraocular Pressure Quantitative Trait Locus 64 9.883
22
RTN017 Retinal Detachment 60 9.616
23
c NRF024 Neurofibromatosis, Type I 72 9.599
24
P RTN209 Retinoschisis 1, X-Linked, Juvenile 60 9.513
25
EXT052 Extraskeletal Ewing Sarcoma 30 9.210
26
PTH003 Pathologic Nystagmus 52 8.952
27
P JVN042 Juvenile Retinoschisis 39 8.702
28
P MYP006 Myopia 56 8.157
29
SPN035 Spindle Cell Sarcoma 54 8.086
30
P CNR004 Cone-Rod Dystrophy 2 74 7.868
31
P LKM062 Leukemia, Acute Lymphoblastic 69 7.778
32
SCT002 Scotoma 42 7.763
33
RTN003 Retinal Ischemia 49 7.728
34
c INH030 Inherited Retinal Disorder 28 7.359
35
FND002 Fundus Dystrophy 55 7.338
36
P RTN022 Retinal Vein Occlusion 54 7.027
37
CNT016 Central Retinal Vein Occlusion 54 6.982
38
XLN247 X-Linked Congenital Retinoschisis 20 6.790
39
MCL006 Macular Retinal Edema 57 6.779
40
P OPT006 Optic Nerve Disease 58 6.774
41
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 6.754
42
P ACH003 Achromatopsia 62 6.691
43
P ADN016 Adenocarcinoma 63 6.664
44
P UVT001 Uveitis 57 6.475
45
c ACT073 Acute Leukemia 58 6.469
46
RFR003 Refractive Error 41 6.246
47
OCL006 Ocular Hypertension 53 6.244
48
P LNG032 Lung Cancer 98 6.241
49
P CTR002 Cataract 60 6.041
50
P MSC005 Muscular Dystrophy 67 5.945
51
P OPN001 Open-Angle Glaucoma 55 5.934
52
DWN001 Down Syndrome 70 5.910
53
SPP007 Suppression Amblyopia 38 5.756
54
AMB002 Amblyopia 50 5.756
55
NRT004 Neuritis 53 5.750
56
P OGC005 Oguchi Disease 45 5.748
57
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 5.737
58
SPP011 Suppression of Tumorigenicity 12 61 5.554
59
c NGH029 Night Blindness, Congenital Stationary, Type 1e 37 5.530
60
P STR022 Stargardt Disease 61 5.528
61
SML031 Small Cell Carcinoma of the Bladder 46 5.493
62
RTN020 Retinal Vascular Disease 46 5.485
63
OCC002 Occult Macular Dystrophy 46 5.430
64
LBR036 Leber Plus Disease 66 5.345
65
P OPT009 Optic Neuritis 57 5.327
66
MSC157 Muscular Dystrophy, Duchenne Type 79 5.325
67
KRT002 Keratomalacia 55 5.319
68
P RTN024 Retinoblastoma 73 5.318
69
P GST053 Gastric Cancer 83 5.263
70
ENH001 Enhanced S-Cone Syndrome 58 5.245
71
FND001 Fundus Albipunctatus 55 5.182
72
PRS045 Prostatic Hypertrophy 53 5.150
73
P BLD134 Bladder Cancer 79 5.117
74
c EXD008 Exudative Vitreoretinopathy 1 71 5.016
75
P USH001 Usher Syndrome 64 4.999
76
MCL003 Macular Holes 44 4.993
77
P EYD002 Eye Disease 57 4.984
78
P SML001 Small Cell Carcinoma 52 4.976
79
PRS021 Prostatic Adenoma 43 4.913
80
P RTN014 Retinal Artery Occlusion 47 4.889
81
BRN026 Branch Retinal Artery Occlusion 41 4.889
82
MLN046 Melanoma-Associated Retinopathy 24 4.757
83
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 4.754
84
ANG020 Angiosarcoma 64 4.742
85
END057 Endometrial Cancer 72 4.737
86
47X002 47,xyy 48 4.672
87
CHR178 Chromosomal Triplication 34 4.625
88
P LNG028 Long Qt Syndrome 64 4.620
89
P NRP001 Neuropathy 60 4.504
90
CNC014 Cancer-Associated Retinopathy 42 4.469
91
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 30 4.424
92
P MCR129 Microvascular Complications of Diabetes 1 68 4.422
93
c MCR112 Microvascular Complications of Diabetes 2 42 4.422
94
P END047 Endophthalmitis 53 4.408
95
BST008 Bestrophinopathy, Autosomal Recessive 46 4.377
96
CNT028 Central Retinal Artery Occlusion 43 4.356
97
PRS129 Prostatic Hyperplasia, Benign 49 4.255
98
MNN043 Meningioma, Familial 79 4.108
99
ALB002 Albinism 47 4.008
100
OPT070 Optic Nerve Hypoplasia, Bilateral 56 3.976
101
GST040 Gastric Adenocarcinoma 67 3.875
102
P LNG064 Lung Cancer Susceptibility 3 70 3.875
103
ADN011 Adenoid Cystic Carcinoma 68 3.863
104
P LPS002 Liposarcoma 64 3.834
105
c GLC092 Glaucoma, Primary Open Angle 62 3.830
106
BRD025 Birdshot Chorioretinopathy 48 3.810
107
SVR004 Severe Combined Immunodeficiency 72 3.807
108
c OGC001 Oguchi Disease 1 39 3.740
109
P CNG024 Congenital Nystagmus 36 3.696
110
GST103 Gastric Cancer, Hereditary Diffuse 68 3.689
111
P OVR042 Ovarian Cancer 88 3.629
112
CHR081 Choroideremia 58 3.568
113
ATM076 Autoimmune Retinopathy 27 3.564
114
ISC004 Ischemia 61 3.561
115
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 63 3.559
116
P EPT012 Epithelioid Sarcoma 41 3.557
117
P SCH015 Schizophrenia 74 3.550
118
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 3.548
119
P LYM118 Lymphoma 67 3.521
120
HYP066 Hyperglycemia 61 3.499
121
GLM045 Glioma 63 3.495
122
P NRN021 Neuronal Ceroid Lipofuscinosis 65 3.474
123
KHN001 Kuhnt-Junius Degeneration 48 3.473
124
ACT250 Acute Megakaryocytic Leukemia 60 3.457
125
DBT006 Diabetic Macular Edema 48 3.401
126
HYP266 Hypoxia 57 3.398
127
P VTL001 Vitelliform Macular Dystrophy 46 3.364
128
P STR020 Strabismus 56 3.361
129
MCH006 Mechanical Strabismus 40 3.361
130
SKN019 Skin Melanoma 71 3.358
131
P GLM040 Glioma Susceptibility 1 71 3.351
132
P MLT020 Multiple Sclerosis 79 3.317
133
P CLR019 Color Blindness 48 3.317
134
OST159 Osteogenic Sarcoma 66 3.313
135
MSN004 Mesenchymal Cell Neoplasm 42 3.306
136
P VTR007 Vitreoretinopathy 46 3.292
137
c PCH010 Pachyonychia Congenita 3 43 3.279
138
P SDR002 Siderosis 43 3.279
139
RPD005 Rapidly Involuting Congenital Hemangioma 46 3.197
140
HMN016 Hemangioendothelioma 34 3.184
141
PPL052 Papillomatosis, Confluent and Reticulated 34 3.183
142
BCK003 Background Diabetic Retinopathy 47 3.173
143
ACT098 Acute Erythroid Leukemia 55 3.148
144
MSC152 Muscular Dystrophy, Becker Type 69 3.148
145
SML009 Small Intestine Adenocarcinoma 57 3.144
146
P BRS047 Breast Cancer 98 3.097
147
c STR084 Stargardt Disease 1 53 3.067
148
XLN012 X-Linked Congenital Stationary Night Blindness 28 3.067
149
FST001 Foster-Kennedy Syndrome 39 3.066
150
ACT120 Acute Zonal Occult Outer Retinopathy 24 3.059
151
AGN016 Aging 54 3.054
152
AST006 Astigmatism 47 3.044
153
CHL152 Childhood Acute Lymphocytic Leukemia 50 3.024
154
P BRD002 Bardet-Biedl Syndrome 66 3.019
155
CLR033 Color Vision Deficiency 40 3.019
156
LNG039 Lung Squamous Cell Carcinoma 57 3.004
157
CLN015 Colon Adenocarcinoma 65 2.973
158
PTT037 Pituitary Tumors 44 2.952
159
ATS010 Autosomal Recessive Disease 42 2.920
160
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.906
161
CNT060 Central Serous Chorioretinopathy 38 2.895
162
P TMR010 Tumor Predisposition Syndrome 67 2.882
163
ADN089 Adenosquamous Lung Carcinoma 49 2.882
164
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 2.882
165
c BRN108 Branchiootic Syndrome 1 62 2.872
166
P EPT020 Epithelioid Hemangioendothelioma 44 2.843
167
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 2.832
168
c NNS043 Nonsyndromic Retinitis Pigmentosa 27 2.817
169
c NGH007 Night Blindness, Congenital Stationary, Type 1b 42 2.813
170
TRT020 Tritanopia 50 2.801
171
c SML038 Small Cell Cancer of the Lung 69 2.797
172
KRN002 Kearns-Sayre Syndrome 63 2.769
173
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 2.768
174
c CLR087 Colorectal Cancer 12 34 2.768
175
P HMN010 Hemangioma 62 2.767
176
c LBR004 Leber Congenital Amaurosis 1 52 2.764
177
PRL047 Prolonged Electroretinal Response Suppression 43 2.738
178
c USH035 Usher Syndrome Type 2 52 2.708
179
c PST005 Posterior Uveitis 54 2.708
180
P SNS001 Sensorineural Hearing Loss 59 2.708
181
MYL031 Myeloproliferative Neoplasm 66 2.704
182
CHL149 Childhood Acute Myeloid Leukemia 43 2.697
183
c RTN150 Retinitis Pigmentosa 10 44 2.693
184
48X005 48,xyyy 39 2.680
185
c LNG047 Long Qt Syndrome 2 59 2.661
186
WST001 West Syndrome 59 2.652
187
PST092 Posttransplant Acute Limbic Encephalitis 28 2.652
188
BLC001 Blue Cone Monochromacy 45 2.649
189
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.645
190
P RHB003 Rhabdomyosarcoma 66 2.645
191
P VSC007 Vascular Disease 63 2.645
192
c LBR012 Leber Congenital Amaurosis 2 52 2.615
193
c MJR022 Major Affective Disorder 8 38 2.615
194
c MJR024 Major Affective Disorder 9 41 2.615
195
P BPL003 Bipolar Disorder 56 2.615
196
c GLM047 Glioma Susceptibility 3 33 2.567
197
c MSM022 Mismatch Repair Cancer Syndrome 1 70 2.567
198
c GLM025 Glioma Susceptibility 2 30 2.567
199
c GLM043 Glioma Susceptibility 9 30 2.567
200
P OLG002 Oligodendroglioma 66 2.567
201
CYT005 Cytomegalovirus Retinitis 50 2.565
202
NRN005 Neuronal Ceroid-Lipofuscinoses 61 2.554
203
P HRD217 Hereditary Optic Neuropathy 36 2.548
204
P MLN008 Melanoma 76 2.530
205
STR046 Stargardt Macular Degeneration 27 2.530
206
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.515
207
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.515
208
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.515
209
PLY150 Polykaryocytosis Inducer 29 2.515
210
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 2.515
211
MYL009 Myelodysplastic Syndrome 67 2.515
212
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.515
213
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 2.515
214
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.515
215
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 2.515
216
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.515
217
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.515
218
P VSC011 Vasculitis 61 2.505
219
P HYP265 Hypotonia 42 2.505
220
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 2.456
221
c NGH010 Night Blindness, Congenital Stationary, Autosomal Dominant 2 46 2.446
222
P NRB001 Neuroblastoma 66 2.446
223
IMP005 Impotence 52 2.446
224
CHR078 Chorioretinitis 51 2.443
225
c RTN172 Retinitis Pigmentosa 1 44 2.441
226
ALN001 Aland Island Eye Disease 55 2.411
227
P MJR001 Major Depressive Disorder 68 2.406
228
CRB159 Cerebral Visual Impairment 34 2.379
229
P CHN012 Chondrosarcoma 57 2.374
230
GYR004 Gyrate Atrophy of Choroid and Retina 58 2.374
231
RHB024 Rhabdomyosarcoma 2 67 2.373
232
c NGH026 Night Blindness, Congenital Stationary, Type 1a 47 2.307
233
SRC027 Sarcoma, Synovial 58 2.300
234
OCL069 Ocular Motor Apraxia 57 2.294
235
c MCL066 Macular Dystrophy, Vitelliform, 2 48 2.293
236
BRS099 Breast Ductal Carcinoma 61 2.286
237
MNC001 Monocular Esotropia 30 2.278
238
EST005 Esotropia 43 2.278
239
ALL029 Allergic Disease 59 2.278
240
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 2.278
241
c MCR122 Microphthalmia, Isolated 5 39 2.264
242
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 2.261
243
P ANR048 Aniridia 1 64 2.251
244
c CHR095 Chronic Progressive External Ophthalmoplegia 49 2.251
245
NVS001 Neovascular Glaucoma 52 2.243
246
PHC015 Phacoanaphylactic Uveitis 18 2.221
247
VTR003 Vitreous Detachment 41 2.219
248
P THL005 Thalassemia 56 2.208
249
P BCL017 B-Cell Lymphoma 59 2.208
250
HYP056 Hypoglycemia 65 2.208
251
LTN004 Late-Onset Retinal Degeneration 60 2.201
252
c PLM164 Pulmonary Hypertension, Primary, 1 76 2.180
253
ACT119 Acute Promyelocytic Leukemia 62 2.180
254
P EPL164 Epilepsy 68 2.172
255
P FLL037 Follicular Lymphoma 74 2.153
256
P OCL002 Oculocutaneous Albinism 59 2.135
257
MCP033 Mucopolysaccharidoses 44 2.135
258
P DBT009 Diabetes Mellitus 67 2.134
259
PRP099 Peripheral Cone Dystrophy 14 2.122
260
ACT235 Acute Macular Neuroretinopathy 16 2.097
261
P MYP004 Myopathy 67 2.097
262
CMB007 Combined Immunodeficiency 57 2.097
263
SPN050 Spinocerebellar Degeneration 39 2.095
264
c PRS134 Prostate Cancer, Hereditary, 3 20 2.095
265
c USH036 Usher Syndrome, Type I 61 2.076
266
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.076
267
ANX004 Anoxia 40 2.063
268
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 2.058
269
SPL018 Splenomegaly 49 2.058
270
ART016 Aortic Aneurysm 68 2.051
271
RHB001 Rhabdoid Cancer 68 2.051
272
OST012 Osteoarthritis 77 2.051
273
P ART022 Arthritis 71 2.046
274
c CNR007 Cone-Rod Dystrophy 6 52 2.029
275
BRN041 Bornholm Eye Disease 34 2.019
276
c RTN032 Retinal Cone Dystrophy 1 24 2.018
277
DSM007 Desmoplastic Small Round Cell Tumor 54 2.018
278
c RNG015 Ring Chromosome 2 22 2.016
279
SMT004 Smith-Lemli-Opitz Syndrome 70 2.011
280
ANR040 Aneurysm 61 2.004
281
ALS001 Alstrom Syndrome 65 2.002
282
c BRD010 Bardet-Biedl Syndrome 1 64 1.985
283
INT082 Intraocular Retinoblastoma 29 1.985
284
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 1.978
285
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.978
286
DFF005 Diffuse Large B-Cell Lymphoma 54 1.978
287
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.978
288
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 1.957
289
MYL069 Myeloma, Multiple 77 1.957
290
ATN005 Autonomic Dysfunction 46 1.957
291
P CLR023 Colorectal Cancer 100 1.954
292
KRT019 Keratitis, Hereditary 66 1.936
293
KPS004 Kaposi Sarcoma 77 1.936
294
c NGH025 Night Blindness, Congenital Stationary, Type 2a 44 1.922
295
P PNC035 Pancreatic Cancer 86 1.920
296
HRD016 Hereditary Retinal Dystrophy 34 1.907
297
PRS047 Prostatitis 58 1.906
298
HPT046 Hepatic Veno-Occlusive Disease 62 1.900
299
ADN018 Adenoma 59 1.893
300
INT054 Intraocular Lymphoma 48 1.893
301
RTN001 Retinal Vasculitis 46 1.893
302
P MYT002 Myotonic Dystrophy 51 1.893
303
c CND011 Cone Dystrophy 3 40 1.891
304
c TYP008 Type 1 Diabetes Mellitus 70 1.890
305
HLX001 Helix Syndrome 48 1.890
306
P RHM011 Rheumatoid Arthritis 82 1.857
307
c OPT053 Optic Atrophy 1 62 1.857
308
CLB010 Coloboma of Macula 53 1.857
309
CYS001 Cystic Fibrosis 78 1.855
310
MYP002 Myoepithelial Carcinoma 46 1.855
311
P CHR637 Choroidal Dystrophy, Central Areolar, 1 49 1.848
312
CHL014 Cholera 62 1.848
313
c LBR016 Leber Congenital Amaurosis 6 42 1.834
314
BTT001 Bietti Crystalline Corneoretinal Dystrophy 48 1.823
315
ACT038 Acute Retrobulbar Neuritis 24 1.823
316
c CRD183 Ceroid Lipofuscinosis, Neuronal, 2 56 1.808
317
c RTN054 Retinitis Pigmentosa 25 42 1.806
318
CLR132 Colorblindness, Partial, Deutan Series 30 1.802
319
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 58 1.802
320
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 1.801
321
MLR004 Malaria 80 1.801
322
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 1.801
323
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 53 1.801
324
CHL061 Childhood Leukemia 47 1.801
325
c MGR028 Migraine with or Without Aura 1 64 1.789
326
SFT003 Soft Tissue Sarcoma 57 1.789
327
c RTN162 Retinitis Pigmentosa 2 45 1.754
328
MCR013 Microphthalmia 60 1.754
329
MTR001 Mature Cataract 29 1.754
330
MSC012 Muscular Dystrophy, Duchenne and Becker Type 33 1.754
331
SYN149 Syndromic Rod-Cone Dystrophy 21 1.754
332
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.754
333
OPT001 Optic Disk Drusen 34 1.754
334
CHN010 Chondroma 43 1.754
335
P BNC003 Bone Cancer 58 1.754
336
CND006 Candida Glabrata 30 1.754
337
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 15 1.744
338
MCL057 Macular Dystrophy with Central Cone Involvement 28 1.729
339
P PLM025 Pulmonary Venoocclusive Disease 44 1.707
340
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.705
341
CHN053 Chondromyxoid Fibroma 39 1.705
342
HRL003 Hurler Syndrome 66 1.705
343
CRD223 Cardiac Arrhythmia 63 1.705
344
CHR072 Chordoma 57 1.705
345
FBR054 Fibroma 44 1.705
346
P MSN005 Mesenchymal Chondrosarcoma 47 1.705
347
P ENC018 Encephalopathy 62 1.705
348
CNR033 Cone-Rod Synaptic Disorder, Congenital Nonprogressive 35 1.698
349
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 1.693
350
c ATM099 Autoimmune Uveitis 45 1.683
351
P PLY006 Polydactyly 59 1.683
352
CRH001 Crohn's Disease 80 1.683
353
CRN030 Coronary Stenosis 50 1.683
354
IRD001 Iridocyclitis 53 1.683
355
VNH007 Von Hippel-Lindau Syndrome 73 1.672
356
MCL029 Macular Degeneration, X-Linked Atrophic 17 1.668
357
SHR107 Short Stature-Obesity Syndrome 25 1.653
358
c SPN294 Spinocerebellar Ataxia 1 53 1.653
359
HYP020 Hyperprolactinemia 63 1.653
360
P THR014 Thrombocytopenia 66 1.653
361
EXT012 Extraskeletal Chondroma 17 1.653
362
CLR005 Clear Cell Chondrosarcoma 37 1.653
363
OST011 Osteomalacia 52 1.653
364
BLT001 Bilateral Retinoblastoma 35 1.653
365
CHN003 Chondroblastic Osteosarcoma 30 1.653
366
PSR001 Psoriatic Arthritis 62 1.646
367
c ATS169 Autosomal Recessive Congenital Stationary Night Blindness 30 1.646
368
c MCL013 Mucolipidosis Iv 65 1.646
369
c CNR038 Cone-Rod Dystrophy, X-Linked, 3 36 1.623
370
c NGH008 Night Blindness, Congenital Stationary, Autosomal Dominant 3 36 1.623
371
c DWL002 Dowling-Degos Disease 1 58 1.608
372
P MYC084 Mycobacterium Tuberculosis 1 68 1.608
373
CLT003 Colitis 63 1.608
374
P HNT016 Huntington Disease 73 1.608
375
P KRT007 Keratoconus 50 1.608
376
VGT001 Vogt-Koyanagi-Harada Disease 56 1.608
377
P PLM037 Pulmonary Hypertension 72 1.599
378
SVR002 Severe Nonproliferative Diabetic Retinopathy 36 1.599
379
RRV005 Rare Vascular Tumor 17 1.599
380
ILS001 Ileus 50 1.599
381
P CRN026 Corneal Edema 42 1.599
382
ONC003 Oncogenic Osteomalacia 42 1.599
383
SKN022 Skin Squamous Cell Carcinoma 54 1.577
384
LBL001 Lobular Neoplasia 55 1.577
385
MYL005 Myelofibrosis 71 1.573
386
P RRT020 Rare Tumor 39 1.569
387
P JBR020 Joubert Syndrome 1 74 1.569
388
c TYP009 Type 2 Diabetes Mellitus 92 1.569
389
DGN002 Degenerative Myopia 31 1.569
390
c INT064 Intermediate Uveitis 54 1.569
391
PTT063 Pattern Dystrophy 36 1.569
392
c CND012 Cone Dystrophy 4 30 1.563
393
TTR011 Tetraploidy 43 1.542
394
c LKM070 Leukemia, Acute Monocytic 56 1.542
395
MLT157 Multiple System Atrophy 1 69 1.542
396
SCH036 Scheie Syndrome 73 1.542
397
P ISL078 Isolated Ectopia Lentis 58 1.542
398
PRS042 Prostate Disease 42 1.542
399
INT075 Intracranial Hypertension 53 1.542
400
P MTC133 Mitochondrial Myopathy 50 1.542
401
SRC030 Sarcomatoid Carcinoma 42 1.542
402
SCR001 Secretory Meningioma 40 1.542
403
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.542
404
P MNC007 Monocytic Leukemia 47 1.542
405
PNC001 Pancytopenia 53 1.542
406
ATY005 Atypical Teratoid Rhabdoid Tumor 69 1.542
407
SPN021 Spinal Meningioma 50 1.542
408
ACT200 Acute Monoblastic Leukemia 41 1.542
409
c ATS007 Autism Spectrum Disorder 72 1.529
410
P MGR001 Migraine Without Aura 49 1.529
411
P PNV001 Panuveitis 49 1.529
412
LKS001 Leukostasis 41 1.529
413
RTN021 Retinal Vascular Occlusion 45 1.529
414
ESP021 Esophageal Cancer 83 1.514
415
END041 Endometrial Adenocarcinoma 64 1.514
416
c PRS097 Prostate Cancer, Hereditary, 1 39 1.490
417
c PRS070 Prostate Cancer, Hereditary, 12 22 1.490
418
c PRS071 Prostate Cancer, Hereditary, 13 25 1.490
419
c PRS117 Prostate Cancer, Hereditary, 11 24 1.490
420
c PRS114 Prostate Cancer, Hereditary, 2 33 1.490
421
PRS015 Prostate Signet Ring Cell Adenocarcinoma 25 1.490
422
PRP030 Purpura 54 1.489
423
LYS002 Lysosomal Storage Disease 51 1.489
424
P PTS002 Ptosis 52 1.489
425
c ATS168 Autosomal Dominant Congenital Stationary Night Blindness 24 1.489
426
ONC007 Oncocytoma 50 1.481
427
APR001 Apraxia 52 1.481
428
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.481
429
P CHR071 Charcot-Marie-Tooth Disease 64 1.481
430
P HYP086 Hypothyroidism 69 1.481
431
P ART005 Arteriovenous Malformation 65 1.481
432
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.481
433
BTH002 Bothnia Retinal Dystrophy 35 1.452
434
FML292 Familial Drusen 34 1.447
435
RTN078 Retinoschisis of Fovea 19 1.447
436
P AST005 Asthma 76 1.447
437
c CNG411 Congenital Disorder of Glycosylation, Type in 67 1.447
438
PPL021 Papilledema 49 1.447
439
MNT002 Mental Depression 57 1.447
440
ALT003 Alternating Exotropia 33 1.447
441
P MCR010 Microcephaly 60 1.447
442
EXT022 Exotropia 42 1.447
443
DPR016 Depression 65 1.447
444
CRV035 Cervical Cancer 73 1.417
445
ASK001 Askin's Tumor 32 1.417
446
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 1.417
447
GST019 Gastrointestinal Stromal Tumor 78 1.417
448
PST048 Postural Orthostatic Tachycardia Syndrome 46 1.417
449
CRT012 Cortical Blindness 42 1.417
450
P CRB059 Cerebellar Degeneration 36 1.417
451
c PRS136 Prostate Cancer, Hereditary, 6 33 1.409
452
c PRS130 Prostate Cancer, Hereditary, 8 32 1.409
453
c STR040 Stargardt Disease 3 34 1.404
454
c THY107 Thymoma, Familial 42 1.404
455
c RTN058 Retinitis Pigmentosa 3 43 1.404
456
ANG054 Angina Pectoris 66 1.404
457
P OCL001 Ocular Albinism 48 1.404
458
c RTN066 Retinitis Pigmentosa 4 42 1.404
459
P EXD001 Exudative Vitreoretinopathy 56 1.404
460
P ATR011 Atrial Fibrillation 66 1.404
461
c SPN291 Spinocerebellar Ataxia 7 53 1.404
462
P MYC007 Myocardial Infarction 70 1.404
463
CRN019 Coronary Artery Vasospasm 47 1.404
464
P THY023 Thymoma 64 1.404
465
P MCL035 Macular Dystrophy, Retinal, 2 27 1.378
466
c USH046 Usher Syndrome, Type 1m 17 1.378
467
ATM095 Autoimmune Disease 61 1.359
468
PRS012 Pars Planitis 47 1.359
469
THR100 Thrombocytopenic Purpura, Autoimmune 61 1.359
470
P PSR002 Psoriasis 63 1.359
471
PST011 Pustulosis of Palm and Sole 52 1.359
472
TLN003 Telangiectasis 51 1.359
473
P NPH005 Nephronophthisis 56 1.359
474
P LBR033 Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy 22 1.359
475
MSC007 Muscle Hypertrophy 64 1.349
477
P NJM001 Nijmegen Breakage Syndrome 76 1.349
478
c WLM013 Wilms Tumor 1 66 1.349
479
P SPP010 Suppressor of Tumorigenicity 3 51 1.349
480
CRB006 Cribriform Carcinoma 34 1.349
481
GLB002 Glioblastoma 67 1.349
482
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 1.349
483
ACT113 Acute Myeloblastic Leukemia with Maturation 46 1.349
484
LYM116 Lymph Node Disease 42 1.349
485
CHR167 Chorioretinal Atrophy, Progressive Bifocal 27 1.335
486
c RTN036 Retinal Cone Dystrophy 4 35 1.335
487
RTN191 Retinal Dystrophy with or Without Extraocular Anomalies 19 1.317
488
P SZR006 Seizure Disorder 70 1.313
489
CRT072 Creutzfeldt-Jakob Disease 68 1.313
490
c MCR130 Microvascular Complications of Diabetes 6 41 1.313
491
P FTL001 Fetal Alcohol Syndrome 55 1.313
492
IMM167 Immune Deficiency Disease 78 1.313
493
c MCR120 Microvascular Complications of Diabetes 7 47 1.313
494
P HMC002 Homocystinuria 53 1.313
495
c MCR113 Microvascular Complications of Diabetes 3 52 1.313
496
c MCR133 Microvascular Complications of Diabetes 4 41 1.313
497
c PRC016 Pre-Eclampsia 65 1.313
498
P PLY019 Polyneuropathy 52 1.313
499
SQM006 Squamous Cell Carcinoma 60 1.313
501
P GRF003 Graft-Versus-Host Disease 71 1.299
502
c CNR013 Cone-Rod Dystrophy 12 36 1.295
503
P SNR003 Senior-Loken Syndrome 1 58 1.295
504
CRD132 Cardiac Conduction Defect 60 1.274
505
HRL004 Hurler-Scheie Syndrome 57 1.274
506
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 61 1.274
507
SVR001 Severe Acute Respiratory Syndrome 67 1.274
508
P HRM001 Hermansky-Pudlak Syndrome 65 1.274
509
P NPH012 Nephrotic Syndrome 60 1.274
510
P OST001 Osteopetrosis 71 1.274
511
LTT006 Littoral Cell Angioma of the Spleen 18 1.274
512
PRT058 Pure Autonomic Failure 58 1.274
513
P ATS364 Autism 69 1.265
514
RTN208 Retinopathy, Pericentral Pigmentary, Autosomal Recessive 16 1.265
515
ALC007 Alcohol Dependence 66 1.265
516
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.265
517
P RTN034 Retinal Cone Dystrophy 3a 28 1.265
518
TRM010 Traumatic Brain Injury 51 1.265
519
P HYP087 Hypotrichosis 42 1.265
520
c HPT001 Hepatitis C 62 1.265
521
CRT015 Carotid Artery Occlusion 45 1.265
522
P TRT010 Teratoma 51 1.265
523
KRT001 Keratoconjunctivitis Sicca 50 1.265
524
CLR030 Clear Cell Renal Cell Carcinoma 54 1.238
525
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 1.226
526
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 1.226
527
SQM013 Squamous Cell Carcinoma, Head and Neck 73 1.215
528
c CNR003 Cone-Rod Dystrophy 1 31 1.215
530
c BTT014 Beta-Thalassemia 72 1.215
531
P NNP021 Nanophthalmos 39 1.215
532
P MTH008 Methylmalonic Acidemia 52 1.215
533
P ANT006 Antiphospholipid Syndrome 55 1.215
534
XRP001 Xerophthalmia 41 1.215
535
GT001 Gout 64 1.215
536
HYP008 Hypertensive Retinopathy 39 1.215
537
STT001 Status Epilepticus 59 1.215
538
SNL007 Senile Cataract 40 1.215
539
P VTR008 Vitreoretinal Degeneration 29 1.215
540
P HDC001 Headache 57 1.215
541
P GNG009 Gangliosidosis 44 1.215
542
P CNR031 Cone-Rod Dystrophy, X-Linked, 1 37 1.201
543
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 1.201
544
P LBR014 Leber Congenital Amaurosis 4 56 1.201
545
c NGH030 Night Blindness, Congenital Stationary, Type 1f 25 1.201
546
P BLD062 Bile Duct Cancer 67 1.197
547
P LNG021 Lung Occult Small Cell Carcinoma 20 1.197
548
LNG019 Lung Combined Type Small Cell Carcinoma 32 1.197
549
CVD001 Covid-19 57 1.191
550
P GLL032 Galloway-Mowat Syndrome 46 1.191
551
EST007 Estrogen Resistance 41 1.191
552
P HMN036 Hemangiopericytoma, Malignant 58 1.191
553
MYL003 Myeloid Sarcoma 48 1.191
554
c RTN048 Retinitis Pigmentosa 19 39 1.189
555
c RTN230 Retinitis Pigmentosa 88 23 1.189
556
c RTN233 Retinitis Pigmentosa 89 20 1.189
557
NRR002 Norrie Disease 61 1.164
558
c USH037 Usher Syndrome, Type Iia 48 1.164
559
P LKM071 Leukemia, Chronic Lymphocytic 75 1.164
560
MCL069 Macular Dystrophy, Retinal, 1, North Carolina Type 38 1.164
561
P LSS002 Lissencephaly 50 1.164
562
DFC004 Deficiency Anemia 74 1.164
563
P MCL001 Mucolipidosis 49 1.164
564
P RBL001 Rubella 58 1.164
565
P CHL066 Cholangitis 52 1.164
566
SKN016 Skin Disease 63 1.164
567
CRT013 Carotid Stenosis 51 1.164
568
P SCL009 Sclerosing Cholangitis 48 1.164
569
THR004 Thrombocytosis 53 1.164
570
P BLP003 Blepharospasm 46 1.164
571
HYP080 Hypogonadism 50 1.164
572
P LMY004 Leiomyosarcoma 62 1.164
573
c RNG021 Ring Chromosome 5 20 1.164
574
MTH021 Methylmalonic Acidemia with Homocystinuria 44 1.164
575
PRR004 Preretinal Fibrosis 34 1.127
576
HYP781 Hypoascorbemia 52 1.119
577
MTH047 Methanol Poisoning 37 1.110
578
P ALZ034 Alzheimer Disease 87 1.110
579
P PHC003 Pheochromocytoma 69 1.110
580
ATR057 Atrioventricular Block 54 1.110
581
DBT090 Diabetes and Deafness, Maternally Inherited 45 1.110
582
NRN008 Neuronal Intranuclear Inclusion Disease 47 1.110
583
MYP106 Myopathy, Myosin Storage, Autosomal Recessive 33 1.110
584
ADR040 Adrenal Gland Pheochromocytoma 46 1.110
585
SCR011 Scrapie 39 1.110
586
P ALP008 Alopecia 54 1.110
587
P CRN024 Corneal Disease 44 1.110
588
P NTR004 Neutropenia 63 1.110
589
P SBS003 Substance Abuse 54 1.110
590
ABS022 Absolute Glaucoma 33 1.110
592
c MNS014 Monosomy 22 35 1.097
593
P TMP003 Temporal Arteritis 69 1.097
594
LNG099 Lung Disease 62 1.097
595
DNG001 Dengue Shock Syndrome 40 1.097
596
P DNG005 Dengue Virus 56 1.097
597
DNG002 Dengue Hemorrhagic Fever 60 1.097
598
HMP001 Hemopericardium 47 1.097
599
P PRC012 Pericardial Effusion 50 1.097
600
P HYP076 Hyperthyroidism 53 1.097
601
DBF001 D-Bifunctional Protein Deficiency 55 1.089
602
SRS007 Sorsby Fundus Dystrophy 51 1.089
603
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 1.089
604
c LBR005 Leber Congenital Amaurosis 10 45 1.075
605
c LBR018 Leber Congenital Amaurosis 8 47 1.075
606
c LBR006 Leber Congenital Amaurosis 11 35 1.075
607
c LBR017 Leber Congenital Amaurosis 7 37 1.075
608
LYM133 Lymphoma, Hodgkin, Classic 74 1.053
609
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.053
610
c FML294 Familial Short Qt Syndrome 43 1.053
611
INS024 Insulin-Like Growth Factor I 78 1.053
612
c USH038 Usher Syndrome, Type Iiia 51 1.053
613
c SPN225 Spondyloarthropathy 1 70 1.053
614
FTL006 Fetal Alcohol Spectrum Disorder 43 1.053
615
c SHR030 Short Qt Syndrome 44 1.053
616
c BRD017 Bardet-Biedl Syndrome 5 38 1.053
617
c CHL119 Cholangitis, Primary Sclerosing 58 1.053
618
ALL006 Allergic Asthma 56 1.053
619
ULC004 Ulcerative Colitis 74 1.053
620
SPN051 Spondylitis 51 1.053
621
ADN009 Adenosquamous Carcinoma 48 1.053
622
c DLT002 Dilated Cardiomyopathy 78 1.053
623
DNG003 Dengue Disease 65 1.053
624
INF009 Inflammatory Spondylopathy 30 1.053
625
DBT008 Diabetic Angiopathy 45 1.053
626
DMY004 Demyelinating Disease 50 1.053
627
KRT008 Keratopathy 46 1.053
628
HYP060 Hyperinsulinism 54 1.053
629
P NRF002 Neurofibromatosis 57 1.053
630
c NNS007 Nonsyndromic Deafness 33 1.053
631
P MTC069 Mitochondrial Disorders 57 1.053
632
c ACT135 Acute Graft Versus Host Disease 51 1.042
633
P CNR040 Cone-Rod Dystrophy and Hearing Loss 1 26 1.027
634
CLP005 Ciliopathy 41 0.992
635
c MCP050 Mucopolysaccharidosis, Type Ii 74 0.992
636
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.992
637
c ATR087 Atrial Standstill 1 74 0.992
638
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.992
639
MNT001 Mantle Cell Lymphoma 67 0.992
640
c NGH027 Night Blindness, Congenital Stationary, Type 1c 36 0.992
641
P CTN015 Cutaneous T Cell Lymphoma 48 0.992
642
CRH005 Crohn's Colitis 53 0.992
643
c LBR015 Leber Congenital Amaurosis 5 42 0.992
644
c BRD011 Bardet-Biedl Syndrome 10 49 0.992
645
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.992
646
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 0.992
647
c ACH020 Achromatopsia 2 48 0.992
648
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.992
649
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.992
650
OPT010 Optic Papillitis 38 0.992
651
c CHR684 Chronic Kidney Disease 69 0.992
652
SCH012 Schizoaffective Disorder 50 0.992
653
NRM001 Neuromyelitis Optica 61 0.992
654
GLL048 Glial Tumor 52 0.992
655
DBT010 Diabetic Neuropathy 54 0.992
656
MYP060 Myopic Macular Degeneration 19 0.992
657
P FBR017 Fibrosarcoma 56 0.992
658
P CND004 Candidiasis 58 0.992
659
P LCT001 Lactic Acidosis 51 0.992
660
P SYP003 Syphilis 59 0.992
661
P ACN011 Acne 57 0.992
662
RDG001 Red-Green Color Blindness 28 0.992
663
PRS025 Presbyopia 38 0.992
664
UNL002 Unilateral Retinoblastoma 37 0.992
665
DRM006 Dermatitis 62 0.992
666
TXC008 Toxic Optic Neuropathy 27 0.992
667
CHR073 Choreatic Disease 54 0.992
668
ENT004 Enthesopathy 51 0.992
669
c HPT016 Hepatitis B 62 0.992
670
P ACT105 Acute Mountain Sickness 52 0.992
671
BRN071 Brain Injury 50 0.992
672
P MYC033 Myoclonus 47 0.992
673
ACT177 Acute Basophilic Leukemia 34 0.985
674
DRM014 Dermatofibrosarcoma Protuberans 65 0.985
675
P SYS005 Systemic Scleroderma 74 0.985
676
AMT001 Ametropic Amblyopia 26 0.985
677
VSC002 Vascular Dementia 60 0.985
678
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.985
679
AMR003 Amaurosis Fugax 33 0.985
680
c SNR004 Senior-Loken Syndrome 4 26 0.944
681
c MSC045 Muscular Dystrophy-Dystroglycanopathy , Type a, 3 36 0.944
682
c LBR011 Leber Congenital Amaurosis 16 38 0.944
683
c LBR009 Leber Congenital Amaurosis 14 41 0.944
684
HPT070 Hepatosplenic T-Cell Lymphoma 36 0.940
685
P DBT005 Diabetes Insipidus 54 0.928
686
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 34 0.928
687
SHK001 Shaken Baby Syndrome 21 0.928
688
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.928
689
DNN001 Danon Disease 59 0.928
690
MYC006 Mycosis Fungoides 65 0.928
691
c USH041 Usher Syndrome, Type if 47 0.928
692
HMC014 Homocysteinemia 52 0.928
693
BRK010 Burkitt Lymphoma 66 0.928
694
c THR092 Thrombophilia Due to Thrombin Defect 74 0.928
695
HMN044 Human Immunodeficiency Virus Type 1 78 0.928
696
P ANP001 Anaplastic Large Cell Lymphoma 61 0.928
697
P SLP006 Sleep Apnea 69 0.928
698
P INF037 Inflammatory Bowel Disease 53 0.928
699
c RTN044 Retinitis Pigmentosa 14 37 0.928
700
P TYS001 Tay-Sachs Disease 69 0.928
701
LGH007 Leigh Syndrome 70 0.928
702
c USH020 Usher Syndrome, Type Iic 45 0.928
703
P PRN026 Porencephaly 55 0.928
704
PRT037 Pertussis 65 0.928
705
P PRK039 Parkinsonism 55 0.928
706
MTC004 Mitochondrial Encephalomyopathy 42 0.928
707
P HYP098 Hypereosinophilic Syndrome 66 0.928
708
P RRH023 Rare Hereditary Hemochromatosis 54 0.928
709
NRN001 Neuroendocrine Carcinoma 47 0.928
710
P OLV001 Olivopontocerebellar Atrophy 51 0.928
711
P PNC025 Panic Disorder 52 0.928
712
P MGR003 Migraine with Aura 52 0.928
713
HMS001 Hemosiderosis 48 0.928
714
CHR008 Choroiditis 48 0.928
715
CYS010 Cystinosis 62 0.928
716
LVR012 Liver Cirrhosis 63 0.928
717
OPT007 Optic Nerve Glioma 40 0.928
718
MDD011 Mood Disorder 62 0.928
719
DSR002 Disorders of Intracellular Cobalamin Metabolism 29 0.928
720
PRS063 Paresthesia 39 0.928
721
ALL014 Allergic Encephalomyelitis 34 0.928
722
MLN065 Melanocytic Nevus Syndrome, Congenital 62 0.888
723
PLS025 Plasmablastic Lymphoma 56 0.888
724
MLT165 Multilocular Cystic Renal Neoplasm of Low Malignant Potential 28 0.888
725
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 32 0.888
726
OVR062 Ovary Serous Adenocarcinoma 25 0.888
727
PRM126 Primary Peritoneal Carcinoma 62 0.888
728
NGH031 Night Blindness, Congenital Stationary, Type1i 19 0.862
729
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.859
730
CTS003 Coats Disease 53 0.859
731
ACR008 Acrocallosal Syndrome 70 0.859
732
ANG004 Angioid Streaks 40 0.859
733
MNK001 Menkes Disease 64 0.859
734
HYP332 Hypotrichosis, Congenital, with Juvenile Macular Dystrophy 41 0.859
735
KSH004 Kashin-Beck Disease 38 0.859
736
VTR010 Vitreoretinochoroidopathy 49 0.859
737
c HYP836 Hypercholesterolemia, Familial, 1 73 0.859
738
c BRD013 Bardet-Biedl Syndrome 12 44 0.859
739
NRT011 Neurotrophic Keratopathy 36 0.859
740
c LRG001 Large Cell Carcinoma 48 0.859
741
INT007 Intermediate Coronary Syndrome 54 0.859
742
LRN003 Learning Disability 49 0.859
743
P SKN015 Skin Carcinoma 71 0.859
744
P DMN002 Dementia 66 0.859
745
BLR001 Biliary Atresia 55 0.859
746
HYD002 Hydronephrosis 58 0.859
747
P STC001 Stickler Syndrome 60 0.859
748
TRC008 Trachoma 53 0.859
749
P SHR001 Short Bowel Syndrome 53 0.859
750
HYD001 Hydranencephaly 43 0.859
751
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.859
752
P KDN017 Kidney Cancer 61 0.859
753
c GM2006 Gm2 Gangliosidosis 46 0.859
754
P TMP001 Temporal Lobe Epilepsy 49 0.859
755
LST001 Listeriosis 59 0.859
756
c MCP001 Mucopolysaccharidosis Iii 69 0.859
757
c LKM005 Leukemia, T-Cell, Chronic 34 0.859
758
MCL079 Macular Telangiectasia Type 2 27 0.859
759
MLT035 Multifocal Choroiditis 31 0.859
760
ORN004 Ornithinemia 13 0.859
761
P KNB001 Knobloch Syndrome 38 0.859
762
P HYP058 Hypervitaminosis a 47 0.847
763
CLL002 Collecting Duct Carcinoma 54 0.846
764
ACR014 Acral Lentiginous Melanoma 52 0.846
765
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.846
766
PPL004 Papillary Squamous Carcinoma 39 0.846
767
PNS010 Penis Squamous Cell Carcinoma 45 0.846
768
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 21 0.846
769
PNS005 Penis Mixed Squamous Cell Carcinoma 12 0.846
770
SSC001 Susac Syndrome 32 0.840
771
c OPT051 Opitz Gbbb Syndrome, Type I 46 0.840
772
P PRK057 Parkinson Disease, Late-Onset 80 0.840
773
P FML011 Familial Adenomatous Polyposis 71 0.840
774
MYP067 Myopathy, Distal, Tateyama Type 28 0.840
775
CD4003 Cd40 Ligand Deficiency 54 0.840
776
P ASP006 Aspergillosis 72 0.840
777
IMM174 Immunodeficiency with Hyper-Igm, Type 1 64 0.840
778
ISC001 Ischemic Neuropathy 27 0.840
780
c ACH038 Achromatopsia 7 37 0.839
781
c NGH022 Night Blindness, Congenital Stationary, Type 1g 20 0.839
782
c CNR012 Cone-Rod Dystrophy 11 27 0.839
783
KNB006 Knobloch Syndrome 1 43 0.839
784
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.839
785
c RTN192 Retinitis Pigmentosa 77 22 0.839
786
c RTN196 Retinitis Pigmentosa 78 20 0.839
787
c RTN219 Retinitis Pigmentosa 85 18 0.839
788
CNR041 Cone-Rod Dystrophy and Hearing Loss 2 19 0.839
789
c RTN157 Retinitis Pigmentosa 37 34 0.839
790
c RTN227 Retinitis Pigmentosa 86 21 0.839
791
RTN232 Retinal Dystrophy, Optic Nerve Edema, Splenomegaly, Anhidrosis, and Migraine Headache Syndrome 25 0.839
792
c RTN213 Retinitis Pigmentosa 80 27 0.839
793
c RTN217 Retinitis Pigmentosa 83 20 0.839
794
c RTN234 Retinitis Pigmentosa 90 23 0.839
795
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.814
796
ACT201 Acute Posterior Multifocal Placoid Pigment Epitheliopathy 21 0.785
797
OPT077 Optic Disc Pit 17 0.785
798
c TRN053 Transient Pseudohypoaldosteronism 24 0.785
799
OCL015 Oculomotor Apraxia 39 0.785
800
SPS057 Spasticity 42 0.785
801
P OVR082 Overgrowth Syndrome 49 0.785
802
LRY022 Laryngoonychocutaneous Syndrome 43 0.785
803
SCH018 Schizencephaly 52 0.785
804
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.785
805
c BRD015 Bardet-Biedl Syndrome 3 48 0.785
806
c RTN069 Retinitis Pigmentosa 7 44 0.785
807
OCL008 Oculopharyngeal Muscular Dystrophy 53 0.785
808
c MCL059 Macular Dystrophy, Patterned, 1 29 0.785
809
P ATX030 Ataxia-Telangiectasia 80 0.785
810
LNN001 Lennox-Gastaut Syndrome 61 0.785
811
c OGC002 Oguchi Disease 2 35 0.785
812
BRN032 Brain Glioma 45 0.785
813
GNY003 Guanylate Cyclase 2e, Pseudogene 12 0.785
814
c BRD019 Bardet-Biedl Syndrome 7 43 0.785
815
c DFN093 Deafness, Autosomal Recessive 23 38 0.785
817
c ALB009 Albinism, Oculocutaneous, Type Ia 53 0.785
818
MTC027 Mitochondrial Trifunctional Protein Deficiency 57 0.785
819
NRM019 Neuraminidase Deficiency 48 0.785
820
P PSD087 Pseudoxanthoma Elasticum 67 0.785
821
PTR032 Peters-Plus Syndrome 63 0.785
822
c BRD014 Bardet-Biedl Syndrome 2 53 0.785
823
ADN001 Adenosine Deaminase Deficiency 59 0.785
824
P HRD018 Hair Disease 44 0.785
825
CLR017 Clear Cell Sarcoma 44 0.785
826
P PRD008 Periodontitis 64 0.785
827
P HYP061 Hypertrophic Cardiomyopathy 69 0.785
828
CNS004 Constipation 56 0.785
829
P DMN001 Diamond-Blackfan Anemia 71 0.785
830
c BSL007 Basal Cell Carcinoma 68 0.785
831
MLG169 Malignant Astrocytoma 57 0.785
832
PRT018 Portal Vein Thrombosis 50 0.785
833
ASP004 Asphyxia Neonatorum 50 0.785
834
ACQ002 Acquired Night Blindness 20 0.785
835
P PRP019 Peripheral Nervous System Disease 58 0.785
836
c GM1007 Gm1 Gangliosidosis 65 0.785
837
GLY031 Glycoproteinosis 49 0.785
838
P BNG032 Benign Mesothelioma 53 0.785
839
VSC006 Vascular Cancer 46 0.785
840
HST011 Histoplasmosis 55 0.785
841
P INS002 in Situ Carcinoma 53 0.785
842
MSC077 Muscle Eye Brain Disease 52 0.785
843
MSL001 Measles 61 0.785
844
MCR055 Microcephaly Nonsyndromal 9 0.785
845
PCH002 Pachygyria 32 0.785
846
RTC011 Reticular Dystrophy of Retinal Pigment Epithelium 18 0.724
847
c CNR005 Cone-Rod Dystrophy 3 40 0.724
848
c CNR014 Cone-Rod Dystrophy 16 42 0.724
849
ADR022 Adrenomyeloneuropathy 39 0.702
850
c RRR006 Rare Retinal Disorder 8 0.702
851
MTR087 Maternal Uniparental Disomy 28 0.702
852
c JVN041 Juvenile Nephronophthisis 43 0.702
853
CNG506 Congenital Amyoplasia 27 0.702
854
BTT011 Butterfly-Shaped Pigment Dystrophy 31 0.702
855
ATX010 Ataxia Neuropathy Spectrum 34 0.702
856
OLG014 Oligocone Trichromacy 25 0.702
857
c NRF023 Neurofibromatosis, Type Ii 71 0.702
858
ATH013 Atherosclerosis Susceptibility 63 0.702
859
DRV001 Dravet Syndrome 69 0.702
860
MST006 Mast Syndrome 40 0.702
861
ADR007 Adrenoleukodystrophy 73 0.702
862
c RTN053 Retinitis Pigmentosa 24 27 0.702
863
c DFN146 Deafness, X-Linked 3 27 0.702
864
c MCL046 Mucolipidosis Iii Alpha/beta 60 0.702
865
c MCL016 Mucolipidosis Iii Gamma 50 0.702
866
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 60 0.702
867
c RTN068 Retinitis Pigmentosa 6 27 0.702
868
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.702
869
c CRD185 Ceroid Lipofuscinosis, Neuronal, 6 53 0.702
870
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.702
871
P KLZ004 Kala-Azar 1 41 0.702
872
MCL027 Macular Dystrophy, Dominant Cystoid 51 0.702
873
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 0.702
874
P DST002 Distal Arthrogryposis 65 0.702
875
MRG003 Marginal Zone B-Cell Lymphoma 52 0.702
876
c LNG050 Long Qt Syndrome 5 46 0.702
877
c RTN143 Retinitis Pigmentosa 47 41 0.702
878
c NGH028 Night Blindness, Congenital Stationary, Type 1d 26 0.702
879
BTT017 Beta-Thalassemia Major 51 0.702
880
c USH040 Usher Syndrome, Type Id 47 0.702
881
P FRD001 Friedreich Ataxia 61 0.702
882
LYM143 Lymphoma, Non-Hodgkin, Familial 75 0.702
883
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 34 0.702
884
c NNP011 Nanophthalmos 2 26 0.702
885
c RTN133 Retinitis Pigmentosa 43 29 0.702
886
MGL003 Megalocornea 47 0.702
887
CHN016 Cohen Syndrome 60 0.702
888
GLC012 Galactosialidosis 56 0.702
889
PGM007 Pigmented Paravenous Chorioretinal Atrophy 42 0.702
890
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.702
891
GLC003 Glucose Intolerance 54 0.702
892
PRM329 Premature Aging 36 0.702
893
THY029 Thyroid Carcinoma 51 0.702
894
XLN228 X-Linked Recessive Disease 24 0.702
895
P NRD007 Neurodegeneration with Brain Iron Accumulation 52 0.702
896
c CRD179 Ceroid Lipofuscinosis, Neuronal, 7 49 0.702
897
P RNG032 Ring Chromosome 39 0.702
898
P ZLL001 Zellweger Syndrome 65 0.702
899
P FBR003 Fibrous Histiocytoma 43 0.702
900
GLC001 Glaucomatocyclitic Crisis 27 0.702
901
KRT006 Keratoconjunctivitis 53 0.702
902
P HRP006 Herpes Simplex 65 0.702
903
LSH001 Leishmaniasis 64 0.702
904
P TRM003 Tremor 48 0.702
905
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 45 0.702
906
P TXC009 Toxic Maculopathy 21 0.702
907
SPS087 Spasmus Nutans 21 0.702
908
PNM008 Pneumothorax 54 0.702
909
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.702
910
SMN007 Seminoma 42 0.702
911
P GRV001 Graves' Disease 55 0.702
912
c SCN007 Secondary Hyperparathyroidism 51 0.702
913
PRP026 Peripheral Retinal Degeneration 29 0.702
914
P HYP069 Hyperparathyroidism 62 0.702
915
RBS002 Rubeosis Iridis 32 0.702
916
P ECL001 Eclampsia 52 0.702
917
ACC002 Accommodative Spasm 25 0.702
918
P PRN023 Prion Disease 60 0.702
919
P INT068 Intestinal Disease 53 0.702
920
ERL001 Early Myoclonic Encephalopathy 62 0.702
921
P CPL006 Capillary Hemangioma 53 0.702
922
LNS001 Lens Subluxation 39 0.702
923
DBT007 Diabetic Cataract 36 0.702
924
P ACT028 Acute Closed-Angle Glaucoma 32 0.702
925
LKC002 Leukocoria 33 0.702
926
SLR002 Solar Retinopathy 28 0.702
927
RTN004 Retinal Microaneurysm 33 0.702
928
DBT004 Diabetic Polyneuropathy 50 0.702
929
CRB033 Cerebral Degeneration 39 0.702
930
HDR002 Hidradenitis Suppurativa 54 0.702
931
HDR003 Hidradenitis 50 0.702
932
IRN002 Iron Metabolism Disease 57 0.702
933
NRN004 Neuroendocrine Tumor 59 0.702
934
P MRQ003 Morquio Syndrome 35 0.702
935
PLM033 Pulmonary Embolism 58 0.702
936
DYS032 Dystrophinopathies 47 0.702
938
STM007 Stomatitis 54 0.702
939
P SCK005 Sickle Cell Disease 56 0.702
940
MYT011 Myotonia 39 0.702
941
PRN039 Paraneoplastic Syndromes 37 0.702
942
FRS019 Farsightedness 36 0.702
943
P NNS072 Nonsyndromic Hearing Loss