Phenotype #0000302446

Individual ID 00410334
Associated disease RP
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details HP:0000546 - Retinal degeneration
HP:0000510 - Rod-cone dystrophy
Inheritance Familial, autosomal dominant
Age/Examination 06y (6 years)
Age/Diagnosis 12y
Age/Onset 06y
Phenotype/Onset -
Protein -
Owner name Alaaeldin Fayez
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Alaaeldin Fayez
Date created 2022-05-24 13:04:08 +02:00 (CEST)
Date last edited 2022-05-26 12:07:03 +02:00 (CEST)

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.