Phenotypes for disease #02318 (RP17 (retinitis pigmentosa, type 17 (RP17)), OMIM:600852)

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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     
0000326326 - retinitis pigmentosa RP17 Familial, autosomal dominant - - - - - Suzanne de Bruijn 00436142
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