Phenotypes for disease #01473 (OPMD (dystrophy, muscular, oculopharyngeal (OPMD)), OMIM:164300)

140 entries on 2 pages. Showing entries 1 - 100.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000144116 asymptomatic (no muscles affected) - - Familial, autosomal dominant 50y - - unknown - Vered Raz 00183404
0000144117 asymptomatic (no muscles affected) - - Familial, autosomal dominant 54y - - unknown - Vered Raz 00183405
0000144118 mild (one muscle affected); diagnosis duration 5y - OPMD Familial, autosomal dominant 63y - - ptosis (HP:0000508) - Vered Raz 00183406
0000144119 mild (one muscle affected); diagnosis duration 6y - OPMD Familial, autosomal dominant 61y - - dysphagia (HP:0002015) - Vered Raz 00183407
0000144120 mild (one muscle affected); diagnosis duration 3y - OPMD Familial, autosomal dominant 54y - - dysphagia (HP:0002015) - Vered Raz 00183408
0000144121 mild (one muscle affected); diagnosis duration 7y - OPMD Familial, autosomal dominant 59y - - ptosis (HP:0000508) - Vered Raz 00183409
0000144122 asymptomatic (no muscles affected) - - Familial, autosomal dominant 57y - - unknown - Vered Raz 00183410
0000144123 asymptomatic (no muscles affected) - - Familial, autosomal dominant 66y - - unknown - Vered Raz 00183411
0000144124 mild (one muscle affected); diagnosis duration 7y - OPMD Familial, autosomal dominant 57y - - dysphagia (HP:0002015) - Vered Raz 00183412
0000144125 mild (one muscle affected); diagnosis duration 20y - OPMD Familial, autosomal dominant 60y - - unknown - Vered Raz 00183413
0000144126 mild (one muscle affected); diagnosis duration 55y - OPMD Familial, autosomal dominant 55y - - unknown - Vered Raz 00183414
0000144127 mild (one muscle affected); diagnosis duration 5y - OPMD Familial, autosomal dominant 64y - - dysphagia (HP:0002015) - Vered Raz 00183415
0000144128 mild (one muscle affected); diagnosis duration 10y - OPMD Familial, autosomal dominant 55y - - dysphagia (HP:0002015) - Vered Raz 00183416
0000144129 mild (one muscle affected); diagnosis duration 8y - OPMD Familial, autosomal dominant 51y - - ptosis (HP:0000508) - Vered Raz 00183417
0000144130 mild (one muscle affected); diagnosis duration 9y - OPMD Familial, autosomal dominant 59y - - dysphagia (HP:0002015) - Vered Raz 00183418
0000144131 mild (one muscle affected); diagnosis duration 24y - OPMD Familial, autosomal dominant 64y - - dysphagia (HP:0002015) - Vered Raz 00183419
0000144132 severe (two or more muscles affected); diagnosis duration 13y - OPMD Familial, autosomal dominant 50y - - unknown - Vered Raz 00183420
0000144133 mild (one muscle affected); diagnosis duration 7y - OPMD Familial, autosomal dominant 55y - - ptosis (HP:0000508) - Vered Raz 00183421
0000144134 mild (one muscle affected); diagnosis duration 13y - OPMD Familial, autosomal dominant 58y - - dysphagia (HP:0002015) - Vered Raz 00183422
0000144135 mild (one muscle affected); diagnosis duration 4y - OPMD Familial, autosomal dominant 53y - - ptosis (HP:0000508) - Vered Raz 00183423
0000144136 severe (two or more muscles affected); diagnosis duration 15y - OPMD Familial, autosomal dominant 75y - - leg weakness - Vered Raz 00183424
0000144137 mild (one muscle affected); diagnosis duration 1y - OPMD Familial, autosomal dominant 50y - - dysphagia (HP:0002015) - Vered Raz 00183425
0000144138 mild (one muscle affected); diagnosis duration 3y - OPMD Familial, autosomal dominant 63y - - ptosis (HP:0000508) - Vered Raz 00183426
0000144139 mild (one muscle affected); diagnosis duration 4y - OPMD Familial, autosomal dominant 63y - - ptosis (HP:0000508) - Vered Raz 00183427
0000144140 asymptomatic (no muscles affected); diagnosis duration 49y - - Familial, autosomal dominant 49y - - unknown - Vered Raz 00183428
0000144141 mild (one muscle affected); diagnosis duration 7y - OPMD Familial, autosomal dominant 55y - - dysphagia (HP:0002015) - Vered Raz 00183429
0000144142 severe (two or more muscles affected); diagnosis duration 42y - OPMD Familial, autosomal dominant 79y - - ptosis (HP:0000508) - Vered Raz 00183430
0000144143 mild (one muscle affected); diagnosis duration 6y - OPMD Familial, autosomal dominant 53y - - dysphagia (HP:0002015) - Vered Raz 00183431
0000144144 severe (two or more muscles affected); diagnosis duration 8y - OPMD Familial, autosomal dominant 52y - - leg weakness - Vered Raz 00183432
0000144145 mild (one muscle affected); diagnosis duration 7y - OPMD Familial, autosomal dominant 62y - - ptosis (HP:0000508) - Vered Raz 00183433
0000144146 mild (one muscle affected); diagnosis duration 2y - OPMD Familial, autosomal dominant 44y - - leg weakness - Vered Raz 00183434
0000144147 severe (two or more muscles affected); diagnosis duration 23y - OPMD Familial, autosomal dominant 73y - - dysphagia (HP:0002015) - Vered Raz 00183435
0000144148 mild (one muscle affected); diagnosis duration 16y - OPMD Familial, autosomal dominant 64y - - ptosis (HP:0000508) - Vered Raz 00183436
0000144149 mild (one muscle affected); diagnosis duration 25y - OPMD Familial, autosomal dominant 75y - - dysphagia (HP:0002015) - Vered Raz 00183437
0000144150 severe (two or more muscles affected); diagnosis duration 7y - OPMD Familial, autosomal dominant 74y - - ptosis (HP:0000508) - Vered Raz 00183438
0000144151 severe (two or more muscles affected); diagnosis duration 28y - OPMD Unknown 68y - - ptosis (HP:0000508) - Vered Raz 00183439
0000144152 mild (one muscle affected); diagnosis duration 8y - OPMD Unknown 62y - - dysphagia (HP:0002015) - Vered Raz 00183440
0000144153 mild (one muscle affected); diagnosis duration 4y - OPMD Unknown 51y - - dysphagia (HP:0002015) - Vered Raz 00183441
0000144154 mild (one muscle affected); diagnosis duration 5y - OPMD Unknown 54y - - dysphagia (HP:0002015) - Vered Raz 00183442
0000144155 mild (one muscle affected); diagnosis duration 5y - OPMD Unknown 49y - - dysphagia (HP:0002015) - Vered Raz 00183443
0000144156 severe (two or more muscles affected); diagnosis duration 20y - OPMD Unknown 73y - - leg weakness - Vered Raz 00183444
0000144157 mild (one muscle affected); diagnosis duration 7y - OPMD Unknown 63y - - leg weakness - Vered Raz 00183445
0000144158 mild (one muscle affected); diagnosis duration 4y - OPMD Unknown 77y - - dysphagia (HP:0002015) - Vered Raz 00183446
0000144159 mild (one muscle affected); diagnosis duration 59y - OPMD Unknown 59y - - unknown - Vered Raz 00183447
0000144160 mild (one muscle affected); diagnosis duration 7y - OPMD Unknown 62y - - ptosis (HP:0000508) - Vered Raz 00183448
0000144161 mild (one muscle affected); diagnosis duration 29y - OPMD Unknown 77y - - ptosis (HP:0000508) - Vered Raz 00183449
0000144162 mild (one muscle affected); diagnosis duration 11y - OPMD Unknown 59y - - ptosis (HP:0000508) - Vered Raz 00183450
0000144163 mild (one muscle affected); diagnosis duration 8y - OPMD Unknown 62y - - ptosis (HP:0000508) - Vered Raz 00183451
0000144164 mild (one muscle affected); diagnosis duration 17y - OPMD Unknown 67y - - ptosis (HP:0000508) - Vered Raz 00183452
0000144165 severe (two or more muscles affected); diagnosis duration 20y - OPMD Unknown 67y - - dysphagia (HP:0002015) - Vered Raz 00183453
0000144167 - - OPMD Unknown - - - - - Johan den Dunnen 00183462
0000144168 - - OPMD Unknown - - - - - Johan den Dunnen 00183463
0000144169 - - OPMD Unknown - - - - - Johan den Dunnen 00183464
0000144170 progressive ptosis, no histological evidence rimmed vacuoles/inclusion bodies OPMD? - Unknown - - - - - Johan den Dunnen 00183465
0000144171 - - OPMD Unknown - - - - - Johan den Dunnen 00183466
0000144172 - - OPMD Unknown - - - - - Johan den Dunnen 00183467
0000144173 - - OPMD Unknown - - - - - Johan den Dunnen 00183468
0000144174 - - OPMD Unknown - - - - - Johan den Dunnen 00183469
0000144175 - - OPMD Unknown - - - - - Johan den Dunnen 00183470
0000144176 - - OPMD Unknown - - - - - Johan den Dunnen 00183471
0000144177 - - OPMD Unknown - - - - - Johan den Dunnen 00183472
0000144178 - - OPMD Unknown - - - - - Johan den Dunnen 00183473
0000144179 - - OPMD Unknown - - - - - Johan den Dunnen 00183474
0000144180 - - OPMD Unknown - - - - - Johan den Dunnen 00183475
0000144181 - - OPMD Unknown - - - - - Johan den Dunnen 00183476
0000144182 - - OPMD Familial, autosomal dominant - - - - - Johan den Dunnen 00183477
0000144183 - - OPMD Familial, autosomal dominant - - - - - Johan den Dunnen 00183478
0000144184 - - OPMD Familial, autosomal dominant - - - - - Johan den Dunnen 00183479
0000144185 - - OPMD Familial, autosomal dominant - - - - - Johan den Dunnen 00183480
0000144186 late onset, progressive (biopsy proven - OPMD Isolated (sporadic) - - - - - Johan den Dunnen 00183481
0000144187 - - OPMD Unknown - - - - - Johan den Dunnen 00183482
0000144188 asymptomatic OPMD? - Unknown - - - - - Johan den Dunnen 00183483
0000144189 tongue weakness, speech problems OPMD? - Unknown - - - - - Johan den Dunnen 00183484
0000144190 - - OPMD Unknown - - - - - Johan den Dunnen 00183485
0000144191 - - OPMD Unknown - - - - - Johan den Dunnen 00183486
0000144192 - - OPMD Unknown - - - - - Johan den Dunnen 00183487
0000144193 neuromuscular disorder - OPMD Unknown - - - - - Johan den Dunnen 00183488
0000144194 - - OPMD Unknown - - - - - Johan den Dunnen 00183489
0000144195 - - OPMD Unknown - - - - - Johan den Dunnen 00183490
0000144196 - - OPMD Unknown - - 59y ptosis (HP:0000508) - Johan den Dunnen 00183491
0000144197 - - OPMD Unknown - - 63y ptosis (HP:0000508) - Johan den Dunnen 00183492
0000144198 - - OPMD Unknown - - 48y ptosis (HP:0000508) - Johan den Dunnen 00183493
0000144199 - - OPMD Unknown - - 53y limb girdle weakness - Johan den Dunnen 00183494
0000144200 - - OPMD Unknown - - 53y limb girdle weakness - Johan den Dunnen 00183495
0000144201 - - OPMD Unknown - - 58y ptosis (HP:0000508) - Johan den Dunnen 00183496
0000144202 - - OPMD Unknown - - 61y ptosis (HP:0000508) - Johan den Dunnen 00183497
0000144203 - - OPMD Unknown - - 64y ptosis (HP:0000508) - Johan den Dunnen 00183498
0000144204 - - OPMD Unknown - - 66y ptosis (HP:0000508) - Johan den Dunnen 00183499
0000144205 - - OPMD Unknown - - 66y ptosis (HP:0000508) - Johan den Dunnen 00183500
0000144206 - - OPMD Unknown - - 46y dysphagia (HP:0002015) - Johan den Dunnen 00183501
0000144207 - - OPMD Unknown - - 53y ptosis (HP:0000508) - Johan den Dunnen 00183502
0000144208 - - OPMD Unknown - - 55y ptosis (HP:0000508) - Johan den Dunnen 00183503
0000144209 - - OPMD Unknown - - 64y dysphagia (HP:0002015) - Johan den Dunnen 00183504
0000144210 - - OPMD Unknown - - 79y dysphagia (HP:0002015) - Johan den Dunnen 00183505
0000144211 - - OPMD Unknown - - 71y ptosis (HP:0000508) - Johan den Dunnen 00183506
0000144212 - - OPMD Familial, autosomal dominant - - - - - Johan den Dunnen 00183507
0000144213 - - OPMD Familial, autosomal dominant - - - - - Johan den Dunnen 00183508
0000144214 early onset - OPMD Familial, autosomal dominant - - - - - Johan den Dunnen 00183509
0000144217 - - OPMD Familial, autosomal dominant - - - - - Johan den Dunnen 00183512
0000144218 more sever phenotype - OPMD Familial, autosomal dominant - - - - - Johan den Dunnen 00183513
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