Phenotype #0000157587

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00208980
Associated disease	EAOH
Phenotype details	see paper; ...
Diagnosis/Initial	early onset cerebellar ataxia associated with oculomotor apraxia.
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	EAOH
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2018-12-20 16:29:03 +01:00 (CET)
Date last edited	N/A

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