Phenotype #0000055620

Individual ID 00075845
Associated disease CORD
Inheritance Unknown
Diagnosis/Initial -
Age/Examination -
Diagnosis/Definite -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset unknown
Phenotype details cone-rod dystrophy (HP:0000510); central vision impairment and visual field changes, including central scotomas and peripheral field loss, light-adapted (cone) b-wave amplitudes were either more reduced than dark-adapted (maximal and rod-isolated) responses or both the light- and dark-adapted amplitude responses were similarly reduced, central and peripheral visual field loss
Protein -
Owner name Stéphanie Cornelis
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Stéphanie Cornelis
Date created 2016-02-22 12:22:09 +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.
  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.