Global Variome shared LOVD

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Phenotype #0000055631 Individual ID 00075856 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 International Created by Stéphanie Cornelis Date created 2016-02-22 12:22:09 +01:00 (CET) Date last edited N/A

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