Global Variome shared LOVD

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Phenotype #0000067430 Individual ID 00087906 Associated disease RPar Phenotype details Nustagmus,low visual acuity,nyclatopia, retinal dystrophy Diagnosis/Initial retinitis pigmentosa Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset ? Phenotype/Onset Nystagmus, low visual acquity,nyclatopic since infancy Protein - Owner name Raheel Qamar Database submission license No license selected Created by Raheel Qamar Date created 2012-09-06 09:49:02 +02:00 (CEST) Date last edited 2020-09-04 12:50:01 +02:00 (CEST)

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