Global Variome shared LOVD

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

Phenotype #0000283590 Individual ID 00390050 Associated disease SCA14 Phenotype details Ataxia, Cerebellar atrophy, Spastic paraplegia, Optic neuropathy, Dysarthria, Difficulty in tongue movements, Hyperreflexia; Son (untested) with similar symptoms Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis 30y Age/Onset - Phenotype/Onset - Protein - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2021-11-09 13:02:29 +01:00 (CET) Date last edited 2021-11-09 15:17:49 +01:00 (CET)

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