Disease #00062 (CLN8B (lipofuscinosis, ceroid, neuronal, type 8B (CLN-8, Northern epilepsy variant)), OMIM:610003)

Official abbreviation	CLN8B
Name	lipofuscinosis, ceroid, neuronal, type 8B (CLN-8, Northern epilepsy variant)
OMIM ID	610003
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CLN8
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-10-11 12:21:53 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD