Phenotype #0000028467

Individual ID 00037924
Associated disease PPCRA
Phenotype details Presence of bilaterally symmetrical chorioretinal atrophy, with accumulation of bone corpuscle pigmentation along the retinal veins
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset ?
Protein -
Owner name Frans Cremers
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Frans Cremers
Date created 2015-05-01 22:00:00 +02:00 (CEST)
Date last edited N/A

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