Phenotype #0000055482

Individual ID 00075707
Associated disease -
Phenotype details retinitis pigmentosa; progressive loss of visual acuity and peripheral fields posterior cortical cataracts, optic atrophy, attenuated retinal vasculature, and scattered bone spicule formation in each eye
Diagnosis/Initial retinitis pigmentosa
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 10y
Phenotype/Onset night blindness
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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