Phenotypes for disease #02387 (RP19 (retinitis pigmentosa, type 19 (RP19)), OMIM:601718)

6 entries on 1 page. Showing entries 1 - 6.
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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     
0000242342 - RP RP Familial, autosomal recessive - - - - - Zixi Sun 00320328
0000242343 - RP RP Familial, autosomal recessive 20y - - - - Zixi Sun 00320329
0000242344 - RP RP Familial, autosomal recessive 47y - 09y - - Zixi Sun 00320330
0000243062 - RP RP19 Familial, autosomal recessive 34y 34y 27y - - Qing Zhu 00324518
0000245457 rod-cone dystrophy rod-cone dystrophy rod-cone dystrophy Familial, autosomal recessive 18y 18y 14y nyctalopia, peripheral field loss ARL3 Leming Fu 00326994
0000300905 - - (RP19) Familial, autosomal recessive - - - - - Nancy Xilotl de Jesús 00408787
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