Global Variome shared LOVD

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

Phenotype #0000221098 Individual ID 00287363 Associated disease neuropathy, optic Phenotype details - Diagnosis/Initial - Diagnosis/Definite - Inheritance Familial, autosomal dominant Age/Examination 08y (8 years) Age/Diagnosis - Age/Onset 04y Phenotype/Onset - Protein - Owner name Khadidja Guehlouz Database submission license No license selected Created by Khadidja Guehlouz Date created 2020-02-14 11:41:14 +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.