Phenotypes for disease #00669 (USH2C (Usher syndrome,, type IIC (USH2C, GPR98/PDZD7 digenic)), OMIM:605472)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

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Phenotype/Onset     

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Owner     

Individual ID     
0000257298 Deafness, blurring of vision, generalised hypopigmentation, light coloured iris - - Familial, autosomal recessive - - - - - Anju Shukla 00361902
0000326718 Reduced visual acuity HP:0007663, Nyctalopia HP:0000662, Peripheral visual field loss HP:0007994, Retinitis pigmentosa HP:0000510, Moderate sensorineural hearing impairment HP:0008504 Usher syndrome # 605472 Familial, autosomal recessive 19y 45y 19y 19y - Rocio Villafuerte-de la Cruz 00436543
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