Phenotype #0000287543

Individual ID 00394339
Associated disease -
Phenotype details SD, symptoms 35 y, also hearing impairment
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite Stargardt disease
Age/Examination -
Age/Diagnosis -
Age/Onset 35y
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2021-12-01 10:17:04 +01:00 (CET)
Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.