Global Variome shared LOVD

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

Phenotype #0000141837 Individual ID 00177026 Associated disease ataxia Diagnosis/Initial Ataxia and Neuropathy Diagnosis/Definite - Phenotype details Developpemental delay, Mild ID, Cerebellar atrophy Inheritance Familial, autosomal recessive Age/Examination - Age/Onset <01y Phenotype/Onset - Protein - Owner name Inge Meijer Database submission license No license selected Created by Inge Meijer Date created 2018-08-16 18:01:05 +02:00 (CEST) Date last edited N/A

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