Phenotype #0000317259

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00426109
Associated disease	ID
Diagnosis/Initial	intellectual disability
Diagnosis/Definite	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
Inheritance	Familial, autosomal recessive
Phenotype details	-
Age/Examination	27y (27 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2022-11-28 11:02:11 +01:00 (CET)
Date last edited	N/A

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