Phenotype #0000326610

Individual ID 00436431
Associated disease -
Phenotype details Reduced visual acuity HP:0007663; Nyctalopia HP:0000662; Peripheral visual field loss HP:0007994; Retinitis pigmentosa HP:0000510
Diagnosis/Initial Retinitis pigmentosa
Inheritance Familial, autosomal recessive
Diagnosis/Definite RP69
Age/Examination 51y (51 years)
Age/Diagnosis 40y
Age/Onset 40y
Phenotype/Onset 40y
Protein -
Owner name Rocio Villafuerte-de la Cruz
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Rocio Villafuerte-de la Cruz
Date created 2023-09-15 20:12:08 +02:00 (CEST)
Date last edited 2023-09-18 16:35:58 +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.