Phenotypes for disease #00698 (Stickler sydrome, type I, nonsyndromic ocular, OMIM:609508)

10 entries on 1 page. Showing entries 1 - 10.
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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     
0000020455 Predominant ocular - - Familial - - - - - Isabelle Touitou 00024337
0000020456 Predominant ocular - - Familial - - - - - Isabelle Touitou 00024338
0000020457 Predominant ocular - - Familial - - - - - Isabelle Touitou 00024339
0000020482 vitreoretinal degeneration, Wagner - - Unknown - - - - - Johan den Dunnen 00024364
0000020483 vitreoretinopathy with phalang; dysplasia, epiphysial - - Unknown - - - - - Johan den Dunnen 00024365
0000020575 Predominantly ocular - - Unknown 67y - - - - Isabelle Touitou 00024457
0000020576 Predominantly ocular - - Unknown 39y - - - - Isabelle Touitou 00024458
0000020623 Predominantly ocular - - Familial - - - - - Isabelle Touitou 00024505
0000020626 Predominantly ocular - - Familial - - - - - Isabelle Touitou 00024508
0000087517 severe myopia, cleft palate, Pierre Robin sequence - - Familial, autosomal dominant 03y06m 03y06m - - - Mouna Barat-Houari 00111434
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