Global Variome shared LOVD

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

Phenotype #0000210617 Individual ID 00276061 Associated disease neuropathy, optic Phenotype details Optic atrophy (HP:0000648) Diagnosis/Initial - Diagnosis/Definite - Inheritance Familial, autosomal dominant Age/Examination 50y (50 years) Age/Diagnosis 50y Age/Onset - Phenotype/Onset - Protein - Owner name Khadidja Guehlouz Database submission license No license selected Created by Khadidja Guehlouz Date created 2020-01-24 11:38:09 +01:00 (CET) Date last edited 2020-08-25 21:27:59 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.