Disease #06984 (SCA50 (ataxia, spinocerebellar), OMIM:620158)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SCA50
Name	ataxia, spinocerebellar
OMIM ID	620158
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NPTX1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-12-22 11:57:45 +01:00 (CET)
Date last edited	N/A

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