Phenotype #0000358375

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00473580
Associated disease	ataxia
Diagnosis/Initial	hereditary ataxia
Diagnosis/Definite	-
Phenotype details	Cerebellar ataxia; Hyporeflexia of upper and lower limbs; vitamin E treatment
Inheritance	Familial, autosomal recessive
Age/Examination	8y (8 years)
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2026-03-06 17:24:40 +01:00 (CET)
Date last edited	N/A

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