Phenotype #0000272366

Individual ID 00377208
Associated disease -
Phenotype details see paper
Diagnosis/Initial retinal disease
Inheritance Familial, autosomal dominant
Diagnosis/Definite retinitis pigmentosa, type 27 (RP27)
Age/Examination 10y (10 years)
Age/Diagnosis 8y
Age/Onset 5y
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2021-07-16 14:18:12 +02:00 (CEST)
Date last edited N/A

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