Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000254873 Individual ID 00359601 Associated disease LHON Phenotype details Optic neuropathy HP:0001138 Visual loss HP:0000572 Diagnosis/Initial Leber optic atrophy HP:0001112 Inheritance Maternal, mitochondrial Diagnosis/Definite - Age/Examination - Age/Diagnosis 20y-40y Age/Onset 20y-40y Phenotype/Onset - Protein - Owner name Daniele Ghezzi Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Daniele Ghezzi Date created 2021-03-30 12:29:48 +02:00 (CEST) Date last edited 2021-04-08 12:00:15 +02:00 (CEST)

Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.