Disease #06985 (SCA49 (ataxia, spinocerebellar, type 49), OMIM:619806)

Global Variome shared LOVD

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

Official abbreviation	SCA49
Name	ataxia, spinocerebellar, type 49
OMIM ID	619806
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SAMD9L
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-12-22 12:01:29 +01:00 (CET)
Date last edited	N/A

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