Phenotype #0000054927

Individual ID 00075152
Associated disease -
Phenotype details retinitis pigmentosa; progressive nightblindness, concentric reduction of the visual field, almost blind at 34y, fundus displays aspects of RP with pigmentary deposits all over the retina with choriocapillaris atrophy, severe concentric reduction of the visual field, unrecordable ERG
Diagnosis/Initial retinitis pigmentosa
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset <10y
Phenotype/Onset unknown
Protein -
Owner name Stéphanie Cornelis
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Stéphanie Cornelis
Date created 2016-02-22 12:22:09 +01:00 (CET)
Date last edited 2020-08-25 10:48:31 +02:00 (CEST)

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