Phenotypes for disease #03596 (WFSL (Wolfram-like syndrome, autosomal dominant (WFSL)), OMIM:614296)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

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Owner     

Individual ID     
0000050852 - - - Familial, autosomal dominant - - - - - Andreas Laner 00037405
0000326755 Reduced visual acuity HP:0007663, Nyctalopia HP:0000662, Peripheral visual field loss HP:0007994, Retinitis pigmentosa HP:0000510, Moderate sensorineural hearing impairment HP:0008504, Optic atrophy HP:0000648 Usher syndrome # 614296 Familial, autosomal dominant 13y 50y 13y 13y - Rocio Villafuerte-de la Cruz 00436608
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