Phenotypes for disease #02289 (RP14 (retinitis pigmentosa, type 14 (RP14)), OMIM:600132)

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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     
0000318800 Myopia; Two uncles (maternal side) retinitis pigmentosa, one with variant TULP1 NM_003322.6 c.1082G>A p.(Arg361Gln) in homozygous state - - Familial 32y - - - - Andreas Laner 00427828
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