Phenotype #0000057997

Individual ID 00078222
Associated disease -
Phenotype details retinitis pigmentosa; Night blindness, peripheral vision loss, and ocular fundus alteration and reduced scotopic response.
Diagnosis/Initial retinitis pigmentosa
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
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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