Phenotype #0000129343

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	00164233
Associated disease	atrophy, cerebellar
Diagnosis/Initial	-
Diagnosis/Definite	-
Phenotype details	see paper; ..., cerebellar atrophy, spinal motor neuronopathy
Inheritance	Familial, autosomal recessive
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	1d
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2018-05-11 14:26:46 +02:00 (CEST)
Date last edited	N/A

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