Phenotype #0000307985

Individual ID 00416220
Associated disease -
Phenotype details best corrected visual acuity right/left eye: 0.5 / 0.6; fundus features: bilateral attenuation of retinal arterioles, widespread retinal pigment epithelium degeneration mixed with gray dots deposition
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite retinitis pigmentosa
Age/Examination 41y (41 years)
Age/Diagnosis -
Age/Onset <18y
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-08-25 12:55:56 +02:00 (CEST)
Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.