Phenotypes for disease #02332 (CORD5 (dystrophy, cone-rod, type 5 (CORD5)), OMIM:600977)

35 entries on 1 page. Showing entries 1 - 35.
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Phenotype details     

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Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Individual ID     
0000242738 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), Color vision defect (HP:0000551) cone-rod dystrophy CORD5 Familial, autosomal dominant 12y - - - - Mariah De Bruin 00324157
0000242739 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551) cone-rod dystrophy CORD5 Familial, autosomal dominant 25y - - - - Mariah De Bruin 00324158
0000242740 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551) cone-rod dystrophy CORD5 Familial, autosomal dominant 35y - - - - Mariah De Bruin 00324159
0000242741 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551) cone-rod dystrophy CORD5 Familial, autosomal dominant 26y - - - - Mariah De Bruin 00324160
0000242742 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551) cone-rod dystrophy CORD5 Familial, autosomal dominant 32y - - - - Mariah De Bruin 00324161
0000242743 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551) cone-rod dystrophy CORD5 Familial, autosomal dominant 32y - - - - Mariah De Bruin 00324162
0000242744 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551) cone-rod dystrophy CORD5 Familial, autosomal dominant 46y - - - - Mariah De Bruin 00324163
0000242745 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551) cone-rod dystrophy CORD5 Familial, autosomal dominant 32y - - - - Mariah De Bruin 00324164
0000242746 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), Color vision defect (HP:0000551) cone-rod dystrophy CORD5 Familial, autosomal dominant 27y - - - - Mariah De Bruin 00324165
0000242747 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), Color vision defect (HP:0000551) cone-rod dystrophy CORD5 Familial, autosomal dominant 44y - - - - Mariah De Bruin 00324166
0000242861 color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 53y - - - - Mariah De Bruin 00324300
0000242862 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 72y - - - - Mariah De Bruin 00324301
0000242863 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 51y - - - - Mariah De Bruin 00324302
0000242864 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 60y - - - - Mariah De Bruin 00324303
0000242865 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 64y - - - - Mariah De Bruin 00324304
0000242866 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 69y - - - - Mariah De Bruin 00324305
0000242867 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 71y - - - - Mariah De Bruin 00324306
0000242868 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 75y - - - - Mariah De Bruin 00324307
0000242869 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 21y - - - - Mariah De Bruin 00324326
0000242870 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 17y - - - - Mariah De Bruin 00324327
0000242871 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 22y - - - - Mariah De Bruin 00324328
0000242872 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 08y - - - - Mariah De Bruin 00324329
0000242873 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 32y - - - - Mariah De Bruin 00324330
0000242874 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 35y - - - - Mariah De Bruin 00324331
0000242875 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 28y - - - - Mariah De Bruin 00324332
0000242876 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 36y - - - - Mariah De Bruin 00324333
0000242877 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 23y - - - - Mariah De Bruin 00324334
0000242878 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 44y - - - - Mariah De Bruin 00324335
0000242879 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 56y - - - - Mariah De Bruin 00324336
0000242880 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 56y - - - - Mariah De Bruin 00324337
0000242927 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 60y - - - - Mariah De Bruin 00324387
0000242928 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 59y - - - - Mariah De Bruin 00324388
0000242929 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 61y - - - - Mariah De Bruin 00324389
0000242930 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 63y - - - - Mariah De Bruin 00324390
0000242931 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 cone-rod dystrophy CORD5 Familial, autosomal dominant 66y - - - - Mariah De Bruin 00324391
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