Global Variome shared LOVD

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

Phenotype #0000138577 Individual ID 00168059 Associated disease ataxia Diagnosis/Initial Cerebellar Ataxia Diagnosis/Definite - Phenotype details Reading difficulty, dysarthria, UL & LL ataxia, Inheritance Familial, autosomal recessive Age/Examination - Age/Onset 34y Phenotype/Onset - Protein - Owner name Inge Meijer Database submission license No license selected Created by Inge Meijer Date created 2018-07-27 19:07:22 +02:00 (CEST) Date last edited N/A

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