Search results for erg

446 hits were found for erg

# Family MCID Name MIFTS Score
1
P PRS040 Prostate Cancer 97 6.279
2
EWN003 Ewing Sarcoma 69 6.214
3
P MYL006 Myeloid Leukemia 60 5.909
4
P LKM002 Leukemia 68 5.786
5
SRC014 Sarcoma 65 5.205
6
MYX005 Myxoid Liposarcoma 66 3.278
7
c RTN035 Retinal Cone Dystrophy 3b 32 3.151
8
PRS006 Prostatic Acinar Adenocarcinoma 27 2.346
9
EXT052 Extraskeletal Ewing Sarcoma 33 2.306
10
RTN023 Retinitis 46 0.268
11
NRR001 Neuroretinitis 42 0.268
12
P RTN008 Retinitis Pigmentosa 79 0.266
13
c LKM061 Leukemia, Acute Myeloid 84 0.257
14
P RTN016 Retinal Degeneration 53 0.226
15
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.215
16
P MCR115 Microvascular Complications of Diabetes 5 66 0.204
17
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.201
18
P NGH001 Night Blindness 48 0.201
19
P RTN018 Retinal Disease 53 0.198
20
RTN017 Retinal Detachment 61 0.173
21
P LKM062 Leukemia, Acute Lymphoblastic 69 0.160
22
P ADN016 Adenocarcinoma 64 0.160
23
P CNG010 Congenital Stationary Night Blindness 54 0.160
24
P CND005 Cone Dystrophy 43 0.152
26
P CTR002 Cataract 60 0.140
27
c ACT073 Acute Leukemia 58 0.136
28
DWN001 Down Syndrome 70 0.132
29
RTN209 Retinoschisis 1, X-Linked, Juvenile 62 0.132
30
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.127
31
P MYP006 Myopia 55 0.123
32
PTH003 Pathologic Nystagmus 52 0.123
33
AMB002 Amblyopia 49 0.118
34
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.118
35
SPP007 Suppression Amblyopia 39 0.118
36
P LNG028 Long Qt Syndrome 66 0.113
37
P OPT006 Optic Nerve Disease 60 0.113
38
P OPN001 Open-Angle Glaucoma 49 0.113
39
P ACH003 Achromatopsia 61 0.108
40
c CNT016 Central Retinal Vein Occlusion 53 0.108
41
SPN035 Spindle Cell Sarcoma 53 0.108
42
P RTN022 Retinal Vein Occlusion 53 0.108
43
SCT002 Scotoma 44 0.108
44
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.102
45
P OPT009 Optic Neuritis 57 0.102
46
NRT004 Neuritis 52 0.102
47
OCC002 Occult Macular Dystrophy 43 0.102
48
CHR178 Chromosomal Triplication 35 0.102
49
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 33 0.102
50
P MSC005 Muscular Dystrophy 66 0.096
51
MGK001 Megakaryocytic Leukemia 64 0.096
52
FND002 Fundus Dystrophy 55 0.096
53
PRS045 Prostatic Hypertrophy 53 0.096
54
OCL006 Ocular Hypertension 53 0.096
55
c INH030 Inherited Retinal Disorder 51 0.096
56
RTN003 Retinal Ischemia 50 0.096
57
P OGC005 Oguchi Disease 39 0.096
58
P CNR004 Cone-Rod Dystrophy 2 73 0.090
59
MSC157 Muscular Dystrophy, Duchenne Type 72 0.090
60
SPP011 Suppression of Tumorigenicity 12 59 0.090
61
PRS021 Prostatic Adenoma 51 0.090
62
P RTN014 Retinal Artery Occlusion 47 0.090
63
MCL003 Macular Holes 40 0.090
64
BRN026 Branch Retinal Artery Occlusion 40 0.090
65
c NGH029 Night Blindness, Congenital Stationary, Type 1e 37 0.090
66
ANG020 Angiosarcoma 64 0.083
67
FND001 Fundus Albipunctatus 60 0.083
68
P UVT001 Uveitis 57 0.083
69
MCL006 Macular Retinal Edema 55 0.083
70
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.083
71
KRT002 Keratomalacia 47 0.083
72
c CNT028 Central Retinal Artery Occlusion 43 0.083
73
PPL052 Papillomatosis, Confluent and Reticulated 33 0.083
74
c EXD008 Exudative Vitreoretinopathy 1 71 0.076
75
P LPS002 Liposarcoma 65 0.076
76
ENH001 Enhanced S-Cone Syndrome 57 0.076
77
PRS129 Prostatic Hyperplasia, Benign 49 0.076
78
47X002 47,xyy 49 0.076
79
ALB002 Albinism 46 0.076
80
RFR003 Refractive Error 43 0.076
81
P CNG024 Congenital Nystagmus 36 0.076
82
MLN046 Melanoma-Associated Retinopathy 24 0.076
83
P RTN024 Retinoblastoma 73 0.068
84
P NRB001 Neuroblastoma 72 0.068
85
c LNG047 Long Qt Syndrome 2 58 0.068
86
P NRP001 Neuropathy 56 0.068
87
OPT070 Optic Nerve Hypoplasia, Bilateral 56 0.068
88
c FML008 Familial Retinoblastoma 53 0.068
89
DBT006 Diabetic Macular Edema 48 0.068
90
RTN020 Retinal Vascular Disease 46 0.068
91
P EPT012 Epithelioid Sarcoma 44 0.068
92
CHL149 Childhood Acute Myeloid Leukemia 44 0.068
93
P SDR002 Siderosis 44 0.068
94
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.068
95
SMT004 Smith-Lemli-Opitz Syndrome 70 0.059
96
OST159 Osteogenic Sarcoma 66 0.059
97
MYL031 Myeloproliferative Neoplasm 66 0.059
98
KRN002 Kearns-Sayre Syndrome 63 0.059
99
P ANR048 Aniridia 1 63 0.059
100
P VSC007 Vascular Disease 63 0.059
101
P USH001 Usher Syndrome 60 0.059
102
ISC004 Ischemia 58 0.059
103
P STR022 Stargardt Disease 58 0.059
104
EYD002 Eye Disease 58 0.059
105
HYP266 Hypoxia 57 0.059
106
HPT046 Hepatic Veno-Occlusive Disease 56 0.059
107
ERY051 Erythroleukemia, Familial 56 0.059
108
P END047 Endophthalmitis 53 0.059
109
c CNR007 Cone-Rod Dystrophy 6 53 0.059
110
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.059
111
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.059
112
c LBR012 Leber Congenital Amaurosis 2 51 0.059
113
P HYP058 Hypervitaminosis a 48 0.059
114
KHN001 Kuhnt-Junius Degeneration 47 0.059
115
BST008 Bestrophinopathy, Autosomal Recessive 46 0.059
116
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.059
117
c RTN150 Retinitis Pigmentosa 10 45 0.059
118
c PLM170 Pulmonary Venoocclusive Disease 1, Autosomal Dominant 45 0.059
119
c PCH010 Pachyonychia Congenita 3 44 0.059
120
RTN187 Retinitis Pigmentosa-Deafness Syndrome 42 0.059
121
P PLM025 Pulmonary Venoocclusive Disease 42 0.059
122
MSN004 Mesenchymal Cell Neoplasm 41 0.059
123
ANX004 Anoxia 40 0.059
124
c MCR122 Microphthalmia, Isolated 5 39 0.059
125
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.059
126
c OGC001 Oguchi Disease 1 38 0.059
127
FST001 Foster-Kennedy Syndrome 36 0.059
128
CNC014 Cancer-Associated Retinopathy 34 0.059
129
MCL057 Macular Dystrophy with Central Cone Involvement 31 0.059
130
c CND012 Cone Dystrophy 4 30 0.059
131
P MCL035 Macular Dystrophy, Retinal, 2 26 0.059
132
P CNR040 Cone-Rod Dystrophy and Hearing Loss 1 25 0.059
133
c USH046 Usher Syndrome, Type 1m 15 0.059
134
P LNG032 Lung Cancer 98 0.048
135
MYL069 Myeloma, Multiple 85 0.048
136
CYS001 Cystic Fibrosis 81 0.048
137
OST012 Osteoarthritis 78 0.048
138
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.048
139
P SCH015 Schizophrenia 74 0.048
140
P MLT020 Multiple Sclerosis 72 0.048
141
P GRF003 Graft-Versus-Host Disease 72 0.048
142
MYL009 Myelodysplastic Syndrome 70 0.048
143
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.048
144
ART016 Aortic Aneurysm 69 0.048
145
P CRD119 Cardiac Arrest 67 0.048
146
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.048
147
ALS001 Alstrom Syndrome 64 0.048
148
P RHB003 Rhabdomyosarcoma 63 0.048
149
MSC152 Muscular Dystrophy, Becker Type 63 0.048
150
ACT119 Acute Promyelocytic Leukemia 63 0.048
151
RHB001 Rhabdoid Cancer 63 0.048
152
c GLC092 Glaucoma, Primary Open Angle 62 0.048
153
P ENC018 Encephalopathy 61 0.048
154
P HMN010 Hemangioma 61 0.048
155
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.048
156
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.048
157
SRC027 Sarcoma, Synovial 58 0.048
158
GYR004 Gyrate Atrophy of Choroid and Retina 57 0.048
159
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.048
160
P CHN012 Chondrosarcoma 56 0.048
161
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.048
162
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 55 0.048
163
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 54 0.048
164
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.048
165
P SML001 Small Cell Carcinoma 52 0.048
166
IMP005 Impotence 52 0.048
167
c LBR004 Leber Congenital Amaurosis 1 52 0.048
168
c ACT135 Acute Graft Versus Host Disease 52 0.048
169
OCL069 Ocular Motor Apraxia 51 0.048
170
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 50 0.048
171
TRT020 Tritanopia 49 0.048
172
CHL061 Childhood Leukemia 48 0.048
173
BRD025 Birdshot Chorioretinopathy 48 0.048
174
P CLR019 Color Blindness 48 0.048
175
MYP002 Myoepithelial Carcinoma 47 0.048
176
ATN005 Autonomic Dysfunction 46 0.048
177
c KNB006 Knobloch Syndrome 1 46 0.048
178
PTT037 Pituitary Tumors 44 0.048
179
c RTN172 Retinitis Pigmentosa 1 44 0.048
180
c NGH010 Night Blindness, Congenital Stationary, Autosomal Dominant 2 44 0.048
181
PRL047 Prolonged Electroretinal Response Suppression 42 0.048
182
SPN050 Spinocerebellar Degeneration 42 0.048
183
P VTL001 Vitelliform Macular Dystrophy 42 0.048
184
CLR033 Color Vision Deficiency 41 0.048
185
c ACH038 Achromatopsia 7 39 0.048
186
c RTN054 Retinitis Pigmentosa 25 39 0.048
187
c RTN048 Retinitis Pigmentosa 19 38 0.048
188
c CNR038 Cone-Rod Dystrophy, X-Linked, 3 38 0.048
189
c CND011 Cone Dystrophy 3 38 0.048
190
c NGH008 Night Blindness, Congenital Stationary, Autosomal Dominant 3 37 0.048
191
c RTN157 Retinitis Pigmentosa 37 36 0.048
192
P HRD217 Hereditary Optic Neuropathy 36 0.048
193
c RTN036 Retinal Cone Dystrophy 4 35 0.048
194
CNR033 Cone-Rod Synaptic Disorder, Congenital Nonprogressive 35 0.048
195
HRD016 Hereditary Retinal Dystrophy 35 0.048
196
BST007 Best Vitelliform Macular Dystrophy 34 0.048
197
BRN041 Bornholm Eye Disease 34 0.048
198
c NGH007 Night Blindness, Congenital Stationary, Type 1b 33 0.048
199
c CNR012 Cone-Rod Dystrophy 11 28 0.048
200
P ATM076 Autoimmune Retinopathy 27 0.048
201
c RTN213 Retinitis Pigmentosa 80 27 0.048
202
c RTN192 Retinitis Pigmentosa 77 23 0.048
203
c RTN230 Retinitis Pigmentosa 88 21 0.048
204
c RTN196 Retinitis Pigmentosa 78 21 0.048
205
c RTN217 Retinitis Pigmentosa 83 20 0.048
206
c NGH022 Night Blindness, Congenital Stationary, Type 1g 20 0.048
207
c RTN227 Retinitis Pigmentosa 86 19 0.048
208
RTN191 Retinal Dystrophy with or Without Extraocular Anomalies 19 0.048
209
c RTN219 Retinitis Pigmentosa 85 19 0.048
210
c CNR041 Cone-Rod Dystrophy and Hearing Loss 2 18 0.048
211
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 16 0.048
212
MCL029 Macular Degeneration, X-Linked Atrophic 14 0.048
213
P OVR042 Ovarian Cancer 88 0.034
214
P GST053 Gastric Cancer 83 0.034
215
MLR004 Malaria 81 0.034
216
GST019 Gastrointestinal Stromal Tumor 78 0.034
217
P PRK057 Parkinson Disease, Late-Onset 78 0.034
218
c NRF024 Neurofibromatosis, Type I 77 0.034
219
CRV035 Cervical Cancer 76 0.034
220
KPS004 Kaposi Sarcoma 75 0.034
221
GLB015 Glioblastoma Multiforme 75 0.034
222
P NJM001 Nijmegen Breakage Syndrome 74 0.034
223
SVR004 Severe Combined Immunodeficiency 73 0.034
224
SCH036 Scheie Syndrome 72 0.034
225
P FML011 Familial Adenomatous Polyposis 72 0.034
226
BHC003 Behcet Syndrome 71 0.034
227
P ATS364 Autism 70 0.034
228
MLT157 Multiple System Atrophy 1 70 0.034
229
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.034
230
P OST001 Osteopetrosis 70 0.034
231
P MYP004 Myopathy 70 0.034
232
P ASP006 Aspergillosis 69 0.034
233
P MLN008 Melanoma 69 0.034
234
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.034
235
P HYP086 Hypothyroidism 69 0.034
236
P LYM118 Lymphoma 68 0.034
237
P TMP003 Temporal Arteritis 68 0.034
238
SKN019 Skin Melanoma 68 0.034
239
P THR014 Thrombocytopenia 67 0.034
240
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.034
241
P PLM037 Pulmonary Hypertension 67 0.034
242
c RHB024 Rhabdomyosarcoma 2 67 0.034
243
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.034
244
c MCR129 Microvascular Complications of Diabetes 1 66 0.034
245
c MCL013 Mucolipidosis Iv 66 0.034
246
P BRD002 Bardet-Biedl Syndrome 66 0.034
247
P ART005 Arteriovenous Malformation 65 0.034
248
KRT019 Keratitis, Hereditary 65 0.034
249
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.034
250
HRL003 Hurler Syndrome 65 0.034
251
c WLM013 Wilms Tumor 1 65 0.034
252
P CHR071 Charcot-Marie-Tooth Disease 65 0.034
253
P DBT009 Diabetes Mellitus 64 0.034
254
P HRM001 Hermansky-Pudlak Syndrome 64 0.034
255
MSC007 Muscle Hypertrophy 64 0.034
256
HYP020 Hyperprolactinemia 64 0.034
257
P GLM045 Glioma 63 0.034
258
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.034
259
DPR016 Depression 63 0.034
260
IMM174 Immunodeficiency with Hyper-Igm, Type 1 63 0.034
261
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.034
262
P VSC011 Vasculitis 62 0.034
263
ATM095 Autoimmune Disease 62 0.034
264
ALL026 Allergic Hypersensitivity Disease 62 0.034
265
ATY005 Atypical Teratoid Rhabdoid Tumor 61 0.034
266
HYP066 Hyperglycemia 61 0.034
267
WST001 West Syndrome 61 0.034
268
c WLM018 Wilms Tumor 5 61 0.034
269
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.034
270
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.034
271
CRD223 Cardiac Arrhythmia 60 0.034
272
P SNS001 Sensorineural Hearing Loss 60 0.034
273
P OCL002 Oculocutaneous Albinism 60 0.034
274
P THL005 Thalassemia 60 0.034
275
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.034
276
CHL014 Cholera 59 0.034
277
PRT058 Pure Autonomic Failure 59 0.034
278
c LTN004 Late-Onset Retinal Degeneration 59 0.034
279
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.034
280
ANR040 Aneurysm 59 0.034
281
P BCL017 B-Cell Lymphoma 58 0.034
282
CRD132 Cardiac Conduction Defect 58 0.034
283
CHR072 Chordoma 58 0.034
284
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.034
285
CHR081 Choroideremia 57 0.034
286
c LKM070 Leukemia, Acute Monocytic 57 0.034
287
AYM001 Ayme-Gripp Syndrome 57 0.034
288
P BPL003 Bipolar Disorder 56 0.034
289
P SNR003 Senior-Loken Syndrome 1 56 0.034
290
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.034
291
P ISL078 Isolated Ectopia Lentis 56 0.034
292
P LBR014 Leber Congenital Amaurosis 4 56 0.034
293
c FRS014 Fraser Syndrome 1 56 0.034
294
AGN016 Aging 56 0.034
295
c CRD183 Ceroid Lipofuscinosis, Neuronal, 2 55 0.034
296
DFF005 Diffuse Large B-Cell Lymphoma 55 0.034
297
P STR020 Strabismus 55 0.034
298
HRL004 Hurler-Scheie Syndrome 55 0.034
299
P HYP076 Hyperthyroidism 55 0.034
300
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.034
301
DBF001 D-Bifunctional Protein Deficiency 54 0.034
302
c PST005 Posterior Uveitis 54 0.034
303
PNC001 Pancytopenia 54 0.034
304
c SPN294 Spinocerebellar Ataxia 1 53 0.034
305
c JBR041 Joubert Syndrome 3 53 0.034
306
P MNC007 Monocytic Leukemia 53 0.034
307
NVS001 Neovascular Glaucoma 53 0.034
308
INT075 Intracranial Hypertension 53 0.034
309
c FML191 Familial Long Qt Syndrome 53 0.034
310
OST011 Osteomalacia 52 0.034
311
APR001 Apraxia 52 0.034
312
ACT200 Acute Monoblastic Leukemia 52 0.034
313
DSM007 Desmoplastic Small Round Cell Tumor 52 0.034
314
ONC002 Onchocerciasis 52 0.034
315
P SPP010 Suppressor of Tumorigenicity 3 51 0.034
316
SRS007 Sorsby Fundus Dystrophy 51 0.034
317
ILS001 Ileus 51 0.034
318
P PRC012 Pericardial Effusion 51 0.034
319
HYP781 Hypoascorbemia 51 0.034
320
ALN001 Aland Island Eye Disease 50 0.034
321
CHR078 Chorioretinitis 50 0.034
322
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.034
323
CYT005 Cytomegalovirus Retinitis 50 0.034
324
P OBS001 Obstructive Jaundice 50 0.034
325
P CHR637 Choroidal Dystrophy, Central Areolar, 1 50 0.034
326
P MYT002 Myotonic Dystrophy 49 0.034
327
P MTC133 Mitochondrial Myopathy 49 0.034
328
MYL003 Myeloid Sarcoma 49 0.034
329
c BPL002 Bipolar I Disorder 49 0.034
330
INT054 Intraocular Lymphoma 48 0.034
331
ATS010 Autosomal Recessive Disease 48 0.034
332
c USH035 Usher Syndrome Type 2 48 0.034
333
SPL018 Splenomegaly 48 0.034
334
HMP001 Hemopericardium 48 0.034
335
AST006 Astigmatism 47 0.034
336
LNG020 Lung Oat Cell Carcinoma 47 0.034
337
RTN001 Retinal Vasculitis 47 0.034
338
PRX028 Peroxisomal Acyl-Coa Oxidase Deficiency 47 0.034
339
c STR084 Stargardt Disease 1 47 0.034
340
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.034
341
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.034
342
CD4003 Cd40 Ligand Deficiency 46 0.034
343
BCK003 Background Diabetic Retinopathy 46 0.034
344
c LBR005 Leber Congenital Amaurosis 10 45 0.034
345
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.034
346
c LBR018 Leber Congenital Amaurosis 8 45 0.034
347
P MNT185 Mental Retardation, Autosomal Dominant 7 45 0.034
348
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.034
349
c LBR016 Leber Congenital Amaurosis 6 44 0.034
350
SPN032 Spindle Cell Carcinoma 44 0.034
351
FBR054 Fibroma 44 0.034
352
CHN010 Chondroma 43 0.034
353
MYX004 Myxedema 43 0.034
354
P EPT020 Epithelioid Hemangioendothelioma 43 0.034
355
PRS042 Prostate Disease 43 0.034
356
P HYP265 Hypotonia 43 0.034
357
P MJR007 Major Affective Disorder 1 43 0.034
358
ONC003 Oncogenic Osteomalacia 42 0.034
359
c MCL066 Macular Dystrophy, Vitelliform, 2 42 0.034
360
c JBR013 Joubert Syndrome 8 42 0.034
361
EST005 Esotropia 42 0.034
362
c LBR009 Leber Congenital Amaurosis 14 42 0.034
363
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.034
364
MCH006 Mechanical Strabismus 42 0.034
365
P MSN005 Mesenchymal Chondrosarcoma 41 0.034
366
EST007 Estrogen Resistance 41 0.034
367
c MJR024 Major Affective Disorder 9 41 0.034
368
LYM116 Lymph Node Disease 41 0.034
369
c MCR112 Microvascular Complications of Diabetes 2 41 0.034
370
c CNG195 Congenital Disorder of Glycosylation, Type Id 40 0.034
371
c CNR014 Cone-Rod Dystrophy 16 40 0.034
372
c RTN114 Retinitis Pigmentosa 58 40 0.034
373
CHN053 Chondromyxoid Fibroma 39 0.034
374
BLT001 Bilateral Retinoblastoma 39 0.034
375
c RTN056 Retinitis Pigmentosa 28 39 0.034
376
c CNR005 Cone-Rod Dystrophy 3 39 0.034
377
c LBR017 Leber Congenital Amaurosis 7 38 0.034
378
c MJR022 Major Affective Disorder 8 38 0.034
379
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.034
380
MCP033 Mucopolysaccharidoses 38 0.034
381
CNT060 Central Serous Chorioretinopathy 38 0.034
382
PST036 Posterior Column Ataxia with Retinitis Pigmentosa 38 0.034
383
P CNR031 Cone-Rod Dystrophy, X-Linked, 1 37 0.034
384
CRT012 Cortical Blindness 37 0.034
385
c LBR011 Leber Congenital Amaurosis 16 37 0.034
386
PRR004 Preretinal Fibrosis 37 0.034
387
P CRB059 Cerebellar Degeneration 37 0.034
388
SVR002 Severe Nonproliferative Diabetic Retinopathy 37 0.034
389
c LBR006 Leber Congenital Amaurosis 11 36 0.034
390
c CNR013 Cone-Rod Dystrophy 12 36 0.034
391
CRB159 Cerebral Visual Impairment 35 0.034
392
c RTN180 Retinitis Pigmentosa 74 35 0.034
393
ASK001 Askin's Tumor 35 0.034
394
BTH002 Bothnia Retinal Dystrophy 35 0.034
395
RFM001 Roifman Syndrome 35 0.034
396
c CRD216 Ceroid Lipofuscinosis, Neuronal, 9 35 0.034
397
c MJR008 Major Affective Disorder 2 35 0.034
398
c MNS014 Monosomy 22 35 0.034
399
AMR003 Amaurosis Fugax 34 0.034
400
c CNR017 Cone-Rod Dystrophy 9 34 0.034
401
ACT177 Acute Basophilic Leukemia 34 0.034
402
CLR005 Clear Cell Chondrosarcoma 34 0.034
403
OPT001 Optic Disk Drusen 34 0.034
404
HMN016 Hemangioendothelioma 34 0.034
405
CRB006 Cribriform Carcinoma 33 0.034
406
c MJR023 Major Affective Disorder 7 33 0.034
407
c MSC045 Muscular Dystrophy-Dystroglycanopathy , Type a, 3 33 0.034
408
c MJR003 Major Affective Disorder 6 33 0.034
409
c MJR006 Major Affective Disorder 5 33 0.034
410
SSC001 Susac Syndrome 32 0.034
411
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.034
412
PLY150 Polykaryocytosis Inducer 31 0.034
413
CLR132 Colorblindness, Partial, Deutan Series 30 0.034
414
MNC001 Monocular Esotropia 30 0.034
415
CHN003 Chondroblastic Osteosarcoma 29 0.034
416
ISC001 Ischemic Neuropathy 29 0.034
418
PST092 Posttransplant Acute Limbic Encephalitis 29 0.034
419
c MJR004 Major Affective Disorder 4 28 0.034
420
MYP067 Myopathy, Distal, Tateyama Type 28 0.034
421
c NNS043 Nonsyndromic Retinitis Pigmentosa 27 0.034
422
AMT001 Ametropic Amblyopia 27 0.034
423
c SNR004 Senior-Loken Syndrome 4 26 0.034
424
c PRX066 Peroxisome Biogenesis Disorder 3b 26 0.034
425
XLN012 X-Linked Congenital Stationary Night Blindness 26 0.034
426
CRY010 Cryptophthalmos 25 0.034
427
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.034
428
c NGH030 Night Blindness, Congenital Stationary, Type 1f 25 0.034
429
c RTN032 Retinal Cone Dystrophy 1 24 0.034
430
c PRS134 Prostate Cancer, Hereditary, 3 24 0.034
431
SYN149 Syndromic Rod-Cone Dystrophy 22 0.034
432
c MCL061 Macular Dystrophy, Vitelliform, 4 21 0.034
433
RRV005 Rare Vascular Tumor 20 0.034
434
RTN037 Retinal Degeneration with Nanophthalmos, Cystic Macular Degeneration, and Angle Closure Glaucoma 19 0.034
435
LTT006 Littoral Cell Angioma of the Spleen 19 0.034
436
INT334 Intellectual Developmental Disorder and Retinitis Pigmentosa 19 0.034
437
PHC015 Phacoanaphylactic Uveitis 19 0.034
438
MYP155 Myopathy, Congenital, with Tremor 19 0.034
439
ACT235 Acute Macular Neuroretinopathy 19 0.034
440
EXT012 Extraskeletal Chondroma 19 0.034
441
RTC011 Reticular Dystrophy of Retinal Pigment Epithelium 18 0.034
442
NGH031 Night Blindness, Congenital Stationary, Type1i 18 0.034
443
RTN229 Retinitis Pigmentosa 87 with Choroidal Involvement 17 0.034
444
PRP099 Peripheral Cone Dystrophy 15 0.034
446
OPT069 Optic Atrophy with Negative Electroretinograms 9 0.034
Content
Loading form....