Phenotype #0000154774

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	00206984
Associated disease	CLN
Phenotype details	progressive cognitive decline and motor deterioration, epilepsy, chorea
Diagnosis/Initial	late infantile NCL
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	CLN-2
Age/Examination	-
Age/Onset	4y
Phenotype/Onset	-
Protein	-
Owner name	Sara Mole
Database submission license
Created by	Johan den Dunnen
Date created	2018-10-31 15:35:34 +01:00 (CET)
Date last edited	N/A

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